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University of Wollongong

Research Online
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1992

Flow assessment of powders in pneumatic


conveying : a bench top assessment
Mukeshchandra Kantilal Desai
University of Wollongong

Recommended Citation
Desai, Mukeshchandra Kantilal, Flow assessment of powders in pneumatic conveying : a bench top assessment, Doctor of Philosophy
thesis, Department of Mechanical Engineering, University of Wollongong, 1992. http://ro.uow.edu.au/theses/1579

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University of Wollongong. For further information contact Manager
Repository Services: morgan@uow.edu.au.
FLOW ASSESSMENT OF POWDERS
IN PNEUMATIC CONVEYING
- A BENCH TOP ASSESSMENT

A thesis submitted in fulfilment of the


requirements for the award of the degree of

DOCTOR OF PHILOSOPHY

from

THE UNIVERSITY OF WOLLONGONG

IVVOUONGO**
by \ UBfc^l

MUKESHCHANDRA KANTILAL DESAI


B.E.(MECH.), M.E.(HONS.), M.I.E. (AUST.

DEPARTMENT OF MECHANICAL ENGINEERING


1992
CERTIFICATE

This is to certify that this work has not been submitted

for a degree to any other university or institution.

(Mukeshchandra K.Desai)
To my parents
iv

ACKNOWLEDGEMENTS

The author extends his most sincere thanks and appreciation to his thesis
supervisor, Dr. A . G . M c L e a n , for the skillful guidance, the deep interest and
enthusiasm, numerous invaluable comments and encouragement throughout the course
of this investigation as well as for his personal generosity and assistance.

Thanks are also due to Prof. P. C. Arnold, Head of Department of Mechanical


Engineering for his assistance and support for this study.

The author wishes to thank the laboratory and workshop staff for helping to
construct and revise the experimental equipment.

The author wishes to convey his appreciation for moral support, patience and
understanding from his wife Dipika, daughter Ashka and son Vishal w h o have missed
week-end fun for years.

The scholarship provided by the Wollongong University which enabled me to


pursue this study is gratefully acknowledged.
v

ABSTRACT

This thesis outlines the use of powder properties, determined from bench tests to
predict powder flow behaviour in pneumatic conveying particularly in dense phase and
super dense phase systems. The bench test powder properties examined included,
particle size and distribution, bulk density and particle density, surface characteristics,
fluidization and deaeration characteristics, powder cohesiveness, tensile strength and
wall friction characteristics.

The surface characteristics of various powders pneumatically conveyed were


observed by an Electron Scanning Microscope. This information provides a good insight
into flow characteristics. Differences in shape and surface explain vastly different
conveying characteristics of supposedly similar powders.

Particle size and distribution of various powders were measured by a Malvern


Particle Sizer. It was found that particle size determines, to a large extent, powder
cohesiveness, fluidization and deaeration characteristics. Furthermore, the effect of
particle density, bulk density, permeability and compressibility on flow behaviour were
examined. These properties were determined using a B e c k m a n Pycnometer, a Jenike
Compressibility Tester and a Jenike Permeability Tester. The observed fluidization
characteristics not only revealed the powder classification with respect to Geldart's
diagram, but also revealed the extent of powder cohesiveness and ease of segregation.

An estimate of a powder's cohesion was conveniently evaluated by use of an


Arch Tester. This tester consists of a perspex silo with a variable width slotted outlet
opened by a chain drive mechanism. The powder remains undisturbed as the outlet is
opened. Each powder bed examined was subject to a set deaeration time before opening
the outlet. These results were compared with the cohesion measured in a direct shear
tester. It w a s found that arch length and deaeration characteristics assists prediction of
powder behaviour and cohesion.

Tensile strengths were measured using an Ajax W.S.L. Tensile Tester under
different extents of consolidation. This property was found to indicate cohesiveness and
indirectly the air retention capacity of powders.

The deaeration characteristics of powders were observed in a perspex cylinder


suitably instrumented. In particular, pressure transducers were connected at the middle
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and bottom of the cylinder fitted with permeable and impermeable bases, respectively.
For effective measurement of deaeration characteristics, it was found that the fill rate
should be as fast as possible. These characteristics are important for assessing air
retention characteristics of powders.

Knowledge of the powder velocity is very important parameter in pneumatic


conveying. For instance, if powders travel too slow, they drop out from the suspension
and settle at the bottom of the pipe. This m a y lead to a blockage. Hence, it is necessary to
convey powders above the critical settling velocity and they should not be conveyed
with excessive velocity, which leads to powder degradation, pipeline wear and increased
energy consumption. %

To effect velocity measurement, an optical fibre probe was developed on the


cross-correlation principle using two sensing probes, a fixed distance apart. The probe
consisted of eight fibres in total. Six projector fibres are connected to a light source,
which emits light to the powder passing through a sight glass fitted in the conveying
line. In this case, the conveying line formed part of an actual pilot scale pneumatic
conveying rig. Reflected light from the travelling powder was transmitted by two
receiver fibres and cross-correlated, using a H P 3 7 2 1 A correlator, to determine the
particle transit time between the two fibres and thus predict the powder velocity.

Wall friction is another important factor contributing to the pressure drop in dense
phase pneumatic conveying. The frictional properties of powders have an adverse effect
in pneumatic conveying. These properties were evaluated under aerated conditions in a
perspex tube by pushing powders upwards for different column lengths.

Due to the importance of cohesion in governing a powder's dense phase flow


characteristics or whether it can be transported by pneumatic conveying, the cohesion
strengths predicted by the Arch Tester, Jenike Shear Tester and the Tensile Tester.
Hence, cohesiveness ranking of the various powders tested was possible.

A new phase diagram incorporating powder properties is proposed to predict a


powder's an optimal pneumatic conveying mode.

This thesis concludes by correlating the described bench measured powder


properties with reported actual powder pneumatic conveying characteristics. T h e
identified correlations provide useful information for future pneumatic conveying system
designs.
vii

TABLE OF CONTENTS
Page

ACKNOWLEDGEMENT iv
ABSTRACT v
TABLE OF CONTENTS vii
LIST OF FIGURES x
LIST OF PLATES xvi
LIST OF TABLES xvii

CHAPTER 1 INTRODUCTION
1.1 Introduc tion 1
1.2 Pneumatic Conveying Systems 1
1.3 Flow Patterns 2
1.4 Types of Dense Phase Pneumatic Conveying Systems 6
1.5 Advantages and Disadvantages of Pneumatic Conveying
Systems 8
1.6 Powder Properties 9
1.7 The Objectives of the Research 10

CHAPTER 2 BLOW TANKS, DENSE PHASE FLOW AND


WALL FRICTION
2.1 Blow Tank 13
2.2 System Design 20
2.3 Dense Phase and Super Dense Phase Flow 20
2.4 Powder Properties 24
2.5 Wall Friction 27

CHAPTER 3 PNEUMATIC CONVEYING SYSTEM


3.1 Gas Solid Suspension 37
viii

3.2 Instability 39

3.3 Pneumatic Conveying Models 39

3.4 Particle Velocity 42

3.5 Particle Concentration 47

CHAPTER 4 COEFFICIENT OF RESTITUTION, BENDS


AND WEAR
4.1 Coefficient of Restitution 49

4.2 Bends 56
4.3 Wear and Abrasion 61

4.4 Attrition 62

4.5 Piping 65

CHAPTER 5 POWDER PROPERTIES


5.1 Introduction 68
5.2 Salient Powder Properties 68

CHAPTER 6 TEST EQUIPMENT AND PROCEDURES


6.1 Pneumatic Conveying Rigs 96

6.2 Velocity Measurement 103


6.3 Powder Concentration Ill

6.4 Hewlett Packard 3497A Data Acquistion System 112

6.5 Test Procedures for Pneumatic Conveying Rigs 117

6.6 Wall Friction Rig 120

6.7 Coefficient of Restitution Rig 122

6.8 Solid Density, Loose Poured Bulk Density and...

Compressibility Tests 122

6.9 Particle Size Measurement 128

6.10 Jenike Direct Shear Tester 130


ix

6.11 Tensile Tester 131

6.12 Cohesion Arch Tester 133

6.13 Deaeration Tester 135

6.14 Fluidization Rig 135

CHAPTER 7 RESULTS
7.1 Scanning Electron Microscope Photographs 139

7.2 Coefficient of Restitution 157

7.3 Particle Size Analysis 161

7.4 Bulk Density I66


7.5 Solids Density 168
7.6 Arch Length and Drained Angle of Repose 168

7.7 Flow Function 180

7.8 Tensile Strength 182


7.9 Wall Friction 191

7.10 Deaeration 204


7.11 Fluidization and Deaeration 211
7.12 Pneumatic Conveying Flow Characteristics 217

CHAPTER 8 DISCUSSION 235


CHAPTER 9 CONCLUSIONS 304
BIBLIOGRAPHY 315
PUBLICATIONS 329
APPENDICES 330
X

LIST OF FIGURES
FIGURE DESCRIPTION PAGE NO.
NO.
1.1 Basic Components of Pneumatic Conveying Systems 2
1.2 Pneumatic Conveying System Layout 3
1.3 Phase Diagram for Pneumatic Conveying of Solids 5
1.4 Flow Patterns in a Horizontal Pipe 5
1.5 Classification of Dense Phase Pneumatic Conveying Systems 7
2.1 A Single Blow Tank System 14
2.2 Parallel Arrangement 17
2.3 Series Arrangement 17
2.4 Aerated Blow Tank 19
2.5 Column of Material 29
2.6 Pressure Distribution 29
2.7 Force Analysis of a Column of Bulk Material 29
2.8 Forced Flow Apparatus 34
2.9 Conveying Force Results for Millet 35
2.10 Rademacher Wall Friction Tester 35
2.11 Front View of the Coefficient of Friction Test Rig 36
2.12 Variation of Frictional Force and the Normal Load for Brown Coal 36
4.1 Variation of the Coefficient of Restitution of Perspex with Temperature 54
4.2 Particle Trajectories for Quartz and Lime Impacting Various Pipe 54
Materials
4.3 Variation of Coefficient of Restitution versus Impact Height 55
4.4 Test Rig for Particle/Wall Collision 55
4.5 Variation of Coefficient of Restitution versus Impact Angle 56
4.6 Examples of Bend Geometries 59
5.1 Critical Arching Diameters 91
5.2 Critical Arching Diameters 91
5.3 Tensile Tester 92
5.4 Geldart's Classification of Powders 92
5.5 Deaeration Test Rig 93
5.6 Deaeration Experiment 93
5.7 Filling-Deaeration Plot for Zyolite Powder 94
5.8 Pressure Variation in a Hopper; Permeable and Impermeable Base 94
5.9 Deaerated Bed Settling for Group A Powder 95
5.10 Deaerated Bed Settling for Group C Powder 95
6.1 Configuration of Sturtevant Blow Tank 97
XI

6.2 Schematic Layout of the Sturtevant Pneumatic Conveying Test Rig 99


6.3 Types of Bends 100
6.4 L o w Velocity Rig Blow Tank 102
6.5 L o w Velocity Test Rig Layout 105
6.6 T.200 Series Transducer Block Schematic 106
6.7 Pin Diode Amplifier Circuit 111
6.8 The Block Schematic of the T.300 Transducer 113
6.9 The Layout of the Front Panel T.300 Concentration Meter 114
6.10 T.300 Transducer Board 115
6.11 Jenike Compressibility Tester 127
6.12 Jenike Permeability Tester « 127
7.1 Coefficient of Restitution Rig 157
7.2 Coefficient of Restitution of Wheat, Millet and Bean (Co-rotation) 159
7.3 Coefficient of Restitution of Coal, Sinter and Sodium Ferrite 160
(Co-rotation)
7.4 Coefficient of Restitution of Wheat, Millet and Coal (Counter- 160
rotation)
7.5 Particle Size Distribution versus % Undersize of Fly Ash A', 164
'B', C and 'D'
7.6 Particle Size Distribution versus % Undersize of Fly Ash 'E',
*F\ 'G' and 'H' 164
7.7 Variation of Frequency versus Particle Size for Fly Ash 'A', 'B' and 'C 165
7.8 Variation of Frequency versus Particle Size for Fly Ash 'D' and 'E' 165
7.9 Variation of Frequency versus Particle Size for Fly Ash'F and 'G' 166
7.10 Variation of Frequency versus Particle Size for Cement, P V C Powder
and Sand 166
7.11 Arch Tester 169
7.12 Tester for Measuring the Drained Angle of Repose 170
7.13 Arch Length versus Deaeration Time for Fly Ash 'A' 175
7.14 Arch Length versus Deaeration Time for Fly Ash 'C 175
7.15 Arch Length versus Deaeration Time for Cement 176
7.16 Arch Length versus Deaeration Time for Cement, Fly Ash 'A' and 'B' 176
7.17 Arch Length versus Deaeration Time for Fly Ash 'B', *C\ 'D', 'E'
and 'F 177
7.18 Arch Length versus Bed Height for Cement 177
7.19 Arch Length versus Particle Size Variation for the Powders Tested 178
7.20 Variation of Drained Angle of Repose with Bed Height for Cement 178
7.21 Variation of Drained Angle of Repose Versus Deaeration Time for the
xii

Fly Ash Tested 179


7.22 Variation of Drained Angle of Repose versus Deaeration Time for
Cement 179
7.23 Variation of Drained Angle of Repose versus M e a n Particle Size 180
7.24 Powder Flow Functions 180
7.25 Tensile Tester 182
7.26 Tensile Strength versus Consolidation Force for Fly Ash 'A', 'B' and
C 183
7.27 Tensile Strength versus Consolidation Force for Fly Ash 'D', 'E' and
F 183
7.28 Tensile Strength versus Consolidation Force for Fly Ash 'A', 'B' and
'C with 15 minutes Deaeration 184
7.29 Tensile Strength versus Consolidation Force for Fly Ash 'D', 'E' and
F with 15 minutes Deaeration 184
7.30 Tensile Strength versus Voidage for Fly Ash A', 'B' and C 185
7.31 Tensile Strength versus Voidage for Fly Ash 'D', 'E' and F 185
7.32 Tensile Strength versus Bulk Density for the Fly Ash Tested 186
7.33 Tensile Strength versus Voidage for Fly ash 'A', 'B' and 'C with
15 minutes Deaeration 186
7.34 Tensile Strength versus Voidage for Fly Ash 'D', 'E' and F with
15 minutes Deaeration 187
7.35 Tensile Strength versus Bulk Density for the Fly Ash Tested with 15
minutes Deaeration 187
7.36 Tensile Strength versus Consolidation Force for Light Soda Ash,
Dense Soda Ash, P V C Powder and Castor Sugar 188
7.37 Tensile Strength versus Voidage for Light Soda Ash, Dense Soda Ash
and P V C Powder 188
7.38 Tensile Strength versus Consolidation Force for Fly Ash 'J' 189
7.39 Tensile Strength versus Consolidation Force for Fly Ash 'H', T and 'J' 189
7.40 Tensile Strength versus Consolidation Force for Cement 190
7.41 Wall Friction Rig 191
7.42 Frictional Force versus Aeration Air Pressure for Brown Rice 192
7.43 Frictional Force versus Aeration Air Pressure for White Rice 192
7.44 Frictional Force versus Aeration Air Pressure for Rice Flakes 193
7.45 Frictional Force versus Aeration Air Pressure for Millet 193
7.46 Frictional Force versus Aeration Air Pressure for Wheat 194
7.47 Frictional Force versus Aeration Air Pressure for Sand 194
xin

7.48 Frictional Force versus Aeration Air Pressure for Shirley Phosphate 195
7.49 Frictional Force versus Column Length for Brown Rice 195
7.50 Frictional Force versus Column Length for White Rice 196
7.51 Frictional Force versus Column Length for Rice Flakes 196
7.52 Frictional Force versus Column Length for Millet 197
7.53 Frictional Force versus Column Length for Wheat 197
7.54 Frictional Force versus Column Length for Sand 198
7.55 Shear Stress versus Air Pressure for Brown Rice 198
7.56 Shear Stress versus Air Pressure for White Rice 199
7.57 Shear Stress versus Air Pressure for Rice Flakes 199
7.58 Shear S tress versus Air Pressure for Millet , 200
7.59 Shear Stress versus Air Pressure for Sand 200
7.60 Shear Stress versus Air Pressure for Shirley Phosphate 201
7.61 Aeration Air Pressure versus Wall Friction Factor uk for Brown Rice 201
7.62 Aeration Air Pressure versus Wall Friction Factor uk for White Rice 202
7.63 Aeration Air Pressure versus Wall Friction Factor uk for Rice Flakes 202
7.64 Aeration Air Pressure versus Wall Friction Factor uk for Millet 203
7.65 Aeration Air Pressure versus Wall Friction Factor uk for Wheat 203
7.66 Deaeration Tester 204
7.67 Pressure Variation During Filling; Permeable Base 205
7.68 Deaeration Time of Fly Ash A', F and 'G'; Permeable Base 205
7.69 Deaeration Behaviour of Fly Ash 'A', F and 'G'; Permeable Base 206
7.70 Pressure Variation During Filling; Impermeable Base 206
7.71 Deaeration Time of Fly Ash 'A', F and 'G'; Impermeable Base 207
7.72 Deaeration Time of Fly ash 'C ; Impermeable Base 207
7.73 Deaeration Behaviour of Fly ash A', F and 'G'; Impermeable Base 208
7.74 Deaeration of Fly Ash 'A', F and 'G'; Permeable Base 208
7.75 Deaeration of Fly Ash'E'; Permeable Base 209
7.76 Deaeration of Fly Ash A'and'G'; Permeable Base 209
7.77 A Filling-Deaeration Graph for Fly Ash 'A'; Impermeable Base 210
7.78 Fluidization Rig
7.79 Geldart's Fluidization Diagram Showing the Classification of Fly Ash 212
7.80 Fluidization Analysis of Fly Ash A ' 212
7.81 Fluidization Analysis of Fly Ash 'C 213
7.82 Fluidization Analysis of Fly Ash A', "C and 'E 213
7.83 Fluidization Analysis of Alumina 214
7.84 Fluidization Analysis of Sand 214
7.85 Fluidization Analysis of P V C Powder 215
7.86 Deaeration of Fly Ash 'A' in Fluidization Rig 215
7.87 Deaeration of Fly Ash 'C in Fluidization Rig 216
7.88 Deaeration of Fly Ash *F in Fluidization Rig 216
7.89 Friction Loop 217
7.90 Exploded View of a Typical Pipeline Air Pressure Tapping Location 218
7.91 Transducer Air Pressure versus Distance from Blow Tank 229
7.92 Transducer Air Pressure versus Distance from Blow Tank 229
7.93 Transducer Air Pressure versus Distance from Blow Tank 230
7.94 Transducer Air Pressure versus Distance from Blow Tank 230
7.95 Transducer Air Pressure versus Distance from Blow Tank 231
7.96 Transducer Air Pressure versus Distance from Blow Tank 231
8.1 Variation of Specific Surface versus M e a n Particle Size for the Fly Ash
Tested 237
8.2 Variation of M e a n Particle Size versus Characteristic Dimensions of Fly
Ash 239
8.3 Variation of Average Characteristic Dimensions versus M e a n Particle
Size 239
8.4 Variation of M e a n Size versus % < 5.8 p m for Fly Ash Tested 240
8.5 Variation of M e a n Size versus Particle Size Distribution Span for Fly
Ash Tested 240
8.6 Variation of M e a n Size versus Average % < 5.8 p m and Particle Size
Distribution Span for the Fly Ash Tested 241
8.7 Bulk Density versus Major Consolidation Stress 242
8.8 Bulk Density versus Major Consolidation Stress 242
8.9 Compressibility Coefficient Variation versus M e a n Particle Size 243
8.10 The Ratio of Packed to Loose Poured Bulk Density versus Particle Size
for the Fly Ash and Cement Tested 245
8.11 Variation of M e a n Particle Size versus Hausner Ratio 245
8.12 Variation of Hausner Ratio versus Different Particle Size Span 246
8.13 Variation of Hausner Ratio versus Average Particle Size Distribution
Span 246
8.14 Voidage versus M e a n Particle Size for the Fly Ash and Cement Tested 248
8.15 Variation of Ratio of Packed to Loose Poured Bulk Density versus
Drained Angle of Repose for the Powders Tested 251
8.16 Variation of Effective Angle of Friction from Experiment and Shear
Tester 253
8.17 Variation of Internal Angle of Friction from Experiment and Shear
Tester 254
XV

8.18 Flowability Index of Fly Ash and Cement versus Arch Length 255
8.19 Variation of Adhesion Force versus Consolidation for Fly Ash 256
8.20 Variation of Adhesion Force versus Consolidation for Fly Ash with
Deaeration 257
8.21 Wall Yield Loci for Fly A s h 'A', V and 'D' for Stainless Steel 259
8.22 Variation of Deaeration Time Constant versus M e a n Particle Size for
Impermeable and Permeable Bases 261
8.23 Variation of Deaeration Time Constant versus Particle Size Distribution
Span for Impermeable and Permeable Bases 262
8.24 Variation of Dense Phase Voidage versus Particle Density 263
8.25 Deaeration Behaviour of Fly A s h 'A', 'C and 'E' 265
8.26 Variation of Permeability Factor versus M e a n Size for Fly Ash Tested 266
8.27 Permeability of the Fly Ashes Tested 267
8.28 Variation of Permeability Coefficient versus M e a n Particle Size for Fly
Ash Tested 268
8.29 Variation of Permeability Coefficient versus Pressure Gradient for Fly
Ash Tested 268
8.30 Variation of Permeability Coefficient a and Compressibility Coefficient
b versus M e a n Particle Size for Fly Ash Tested 269
8.31 Factors Affecting Powder Flow Characteristics 273
8.32 Pneumatic Conveying Phase Diagram 276
8.33 Pneumatic Conveying Phase Diagram (Alternate View) 277
8.34 Schematic Presentation of the Variation of Cohesion and
Permeability with Particle Size 279
8.35 Schematic Presentation of the Variation of Cohesion and
Deaeration versus Particle Size 279
8.36 Variation of Reciprocal of Arch Length and Hausner Ratio with
Particle Size of Fly Ash Tested 280
8.37 Mechanical Interlocking 281
8.38 Schematic Representation of the Variation of Permeability versus
Mechanical Interlocking 281
8.39 Specific Examples of Powder Properties with respect to the
Proposed Powder Conveying Phase Diagram 284
8.40 Variation of Particle Velocity with Time for Cement 289
8.41 Variation of Particle Velocity with Time for Cement 289
8.42 Variation of Particle Velocity with Time for Wheat 289
8.43 Variation of Volumetric Air Flow Rate with Time for Cement 290
8.44 Variation of Mass Flow ratio with Solids Mass Flow Rate for Cement
and Wheat 290
8.45 Variation of Solids Flow Rate versus Air Mass Flow Rate 291
8.46 Variation of Experimental versus Predicted Solids Velocity for Sand 292
8.47 Variation of Particle Velocity versus Time 292
8.48 Variation of Particle Velocity versus Time 293
8.49 Variation of Slip Velocity versus (1- Voidage) for Sand 296
8.50 Variation of Superficial Air Velocity versus (1-Voidage) for Sand 296
8.51 Variation of Superficial Air Velocity versus Mass Flow Ratio for Sand 297
8.52 Variation of Pipeline Pressure Drop versus Air Mass Flow Rate for Sand 297
8.53 Variation of Mass Flow Ratio versus Initial Blow Tank Pressure for
Sand . 298
8.54 Solid-Air Ratio Variation with Initial Blow Tank Pressure for Wheat 300
8.55 Mass Flow Rate of Solids with Initial Blow Tank Pressure for Wheat 300
8.56 Solids Mass Flow Rate versus Air Mass Flow Rate of Wheat 302
8.57 Average Blow Tank Pressure versus Air Mass Flow Rate for Wheat 302
8.58 Pipeline Pressure Drop versus Air Mass Flow Rate for Wheat 303
9.1 Recommended Sequence of Powder Tests 307
A. 1 Settling Velocity in Still Air of Spherical Particles with Diameter d 332
A.2 Settling Velocity in Still Air of Spherical Particles with Diameter d 333
A.3 M o o d y Diagram 334
B.l Typical Slugging Diagram 356
C. 1 Calibration Plot 360
C.2 Typical Calibration Graph 361
C.3 Typical Calibration Graph 363
C.4 Concentration Graph 364

LIST OF PLATES
6.1 Control Panel 98
6.2 Blow Tank 101
6.3 Receiving Hopper 102
6.4 L o w Velocity Rig Blow Tank 104
6.5 H P 3721A Correlator connected to Tealgate T.200 Series Transducer 108
6.6 Fibre Optic Probe with H P 3721A Correlator 109
6.7 Fibre Optic Probe Located on Sight Glass 110
6.8 Chart Recorder Connected to the T.300 Concentration Meter 115
6.9 Data Acquisition System (DAS) 116
6.10 Wall Friction Rig 121
6.11 Coefficient of Restitution Rig 123
6.12 Beckman Pycnometer for Measuring Solid Density 125
6.13 Jenike Compressibility Tester 125
6.14 Malvern Particle Sizer 129
6.15 Jenike Direct Shear Tester 129
6.16 Ajax Tensile Tester 132
6.17 (A) Cohesion Arch Tester (B) Deaeration Tester 134
6.18 Fluidization Rig 137
7.1 S E M Photograph of Raw Sugar Grains (X= 14) 139
7.2 S E M Photograph of Raw Sugar Grains (X= 30) 140
7.3 S E M Photograph of Raw Sugar Grains (X= 144) 140
7.4 S E M Photograph of Raw Sugar Grains (X= 1440) - 141
7.5 S E M Photograph of Light Soda Ash (X= 162) 141
7.6 S E M Photograph of Light Soda Ash (X=780) 142
7.7 S E M Photograph of Dense Soda Ash (X= 180) 142
7.8 S E M Photograph of Dense Soda Ash (X=600) 143
7.9 S E M Photograph of Zinc Fume (X= 90) 143
7.10 S E M Photograph of Zinc Fume (X= 600) 144
7.11 S E M Photograph of Zinc Fume (X= 6000) 144
7.12 S E M Photograph of P V C Powder (X= 360) 145
7.13 S E M Photograph of P V C Powder (X= 1800) 145
7.14 S E M Photograph of Pulverised Coal - Tallawarra (X= 60) 146
7.15 S E M Photograph of Pulverised Coal -Tallawarra (X=600) 146
7.16 S E M Photograph of Pulverised Coal - Tallawarra (X= 2100) 147
7.17 S E M Photograph of Petroleum Coke (X= 12) 147
7.18 S E M Photograph of Petroleum Coke (X= 120) 148
7.19 S E M Photograph of Petroleum Coke (X=600) 148
7.20 S E M Photograph of Petroleum Coke (X= 3000a) 149
7.21 S E M Photograph of Petroleum Coke (X= 3000b) 149
7.22 S E M Photograph of Eraring Fly Ash (X= 1320) 150
7.23 S E M Photograph of Liddell Fly Ash (X= 1320) 150
7.24 S E M Photograph of Liddell Fly Ash (X= 6600) 151
7.25 S E M Photograph of Vales Point Fly Ash (X=468) 151
7.26 S E M Photograph of Vales Point Fly Ash (X= 6600) 152

LIST OF TABLES
1.1 Data for Pneumatic Conveying Systems for a Pipe Diameter of 100 m m 4
2.1 Blow Tank Characteristics and Operation - Literature Survey 15
2.2 Dense Phase Flow - Literature Survey 22
2.3 Powder Characteristics 26
2.4 Wall Friction - Literature Survey 30
3.1 Pneumatic Conveying Models - Literature Survey 40
3.2 Solids Velocity Measurement Techniques 43
3.3 Concentration Measurement 48
4.1 Coefficient of Restitution - Literature Survey 50
4.2 Bend Characteristics and Application 58
4.3 Bend Pressure-drop Factors for Use in Equn. (4.8) 60
4.4 Service Life of Long Radius Bends and Blind Tees Conveying
Zirconium Sodium 61
4.5 Variables affecting Attrition - 63
4.6 Assessment of Attrition 63
4.7 Types of Attrition Tests 64
4.8 Surface Roughness of Various Piping Materials 65
4.9 Piping Materials 66
5.1 List of Salient Powder Properties 69
5.2 Powder Properties 70
5.3 Mohs' Scale of Hardness 75
5.4 The General Relationships between Angle of Repose and the
Flowability of Materials 75
5.5 Particle Shape and Flow Characteristics 76
5.6 Angle of Repose - Literature Survey 77
5.7 Cohesion - Literature Survey 79
5.8 Tensile Strength - Literature Survey 82
5.9 Fluidization - Literature Survey 85
5.10 Deaeration - Literature Survey 87
7.1 Observations from Scanning Electron Microscope Photographs 153
7.2 Coefficient of Restitution 158
7.3 Particle Size Analyses 161
7.4 Size Analysis of Sand 161
7.5 Size Analysis of Brown Rice (I) 162
7.6 Size Analysis of Brown Rice (II) 163
7.7 Size Analysis of White Rice 163
7.8 Bulk Density 167
7.9 Loose Poured Bulk Density 167
7.10 Solids Density 168
7.11 Arch Length and Drained Angle of Repose of Cement, Fly Ash and
Sodium Ferrite 171
7.12 Instantaneous Yield Loci 181
7.13 Tensile Strength Versus Consolidation Stress 190
7.14 Deaeration Time Constant and Exponents 210
7.15 Air Pressure Channels 219
7.16 Transducer Locations 219
7.17 Material Flow Properties 219
7.18 Air Pressure Channels and Transducer Location 220
7.19 Conveying Characteristics - Cement 221
7.20 Conveying Characteristics - Wheat 222
7.21 Conveying Characteristics of Sand 223
7.22 Transducer Air Pressures 227
7.23 Bend Air Pressure 228
7.24 Data Channel Details 232
7.25 Pipeline Details 232
7.26 L o w Velocity Conveying Rig - Wheat 233
8.1 Effects of Different Lenses on Particle Size Distribution 238
8.2 Compressibility of Materials 243
8.3 Density Parameters 248
8.4 Wall Friction Tests of Fly Ash 258
8.5 Wall Friction Angles 259
8.6 Deaeration Factor 263
8.7 Collapse Air Velocity and Dense Phase Parameters 263
8.8 Permeability Factor 265
8.9 Ranking of Fly Ash Properties Based O n Bench Tests 271
8.10 Recommended Powder Property Bench Tests for Assessment of
Pneumatic Conveying Suitability 274
8.11 Factors Influencing the M e a n Interparticle Spacing 281
8.12 Pressure Differential for Friction Loop 287
8.13 Air Velocity, Slip Velocity and Froude Number 294
8.14 Plug Velocity and Length 301
A.l Friction Factor 335
A.2 Bend Loss Coefficient for 90 Degrees Bends 337
C. 1 Typical Calibration Values 359
C.2 Calibration Results 360
1

CHAPTER 1
INTRODUCTION
1.1 INTRODUCTION:
In the last century, fans were used as primemovers to convey light powders and
dusts through pipes. The application of pneumatic conveying, on a large scale,
commenced in early as 1890. The necessary machines and controls were perfected in
several developmental stages in the process industries with automated installations. With
the development of fans, roots type blowers and rotary feed valves, pneumatic conveying
technology has developed quickly. B y the end of the first war, a device called the Fuller-
Kinyon p u m p had been invented making it possible to convey materials like cement and
fly ash at higher concentrations than that possible using simple fan technology. This
was the birth of modern dense phase conveying.

Recently, there has been an increasing interest in dense phase and super dense
phase pneumatic conveying. The latter is defined as the conveying of powders by air or
gas along a pipe which is more or lessfilledwith powders at one or more cross-sections.
The successful development of commercial conveying systems, during the 1960's like
the simple pressure pulse phase and bypass systems and the need to feed particles such as
coal or cracking catalyst into fiuidized beds, with the m i n i m u m amount of air, created
increased interest in dense phase systems.

1.2 PNEUMATIC CONVEYING SYSTEMS:


A pneumatic conveying system consists of four zones namely prime mover,
feeder, conveying and separation (Figure 1.1). A range of compressors, blowers and
fans are available as primemovers. For the design of a pneumatic conveying system, the
required gas flow rate and pressure should be determined. Feeding powders to the
conveying gas is critical. W h e n the powders are fed to the pipeline, they are initially
stationary and a large m o m e n t u m change from the conveying gas is necessary to
accelerate the solids. Once accelerated, the powders convey in the pipeline and at the end
of the pipeline are separated from the conveying gas. Cyclone and bag filters are used to
separate the gas and powder to keep dust free. A typical pneumatic conveying system
layout with all the necessary components is shown in Figure 1.2. Conveying pressure
loss is dependent on m a n y factors such as particle wall interaction, particle-particle
interaction, conveying gas, powder properties, moisture content, pipe roughness, etc.
2

1.3 FLOW PATTERNS;


The design of a pneumatic conveying system strongly depends on powder
properties, the particle size distribution and the mass flow rate of gas and the solids. The
following table categorizes the various conveying systems [Bohnet, (1985)]. A phase
diagram for the pneumatic conveying system showing the flow patterns named in Table
1.1 is presented in Figure 1.3 .

Conveying
SEPARATION
Piping
Cyclone
JJ Bends
Bag Filter
Cleaning;
^Diverter
Mechanical
Reverse Jet
-JT- Coupling

Feeding, Mixing, Wear Resistance


Acceleration

Prime Mover
\r Venturi

Fan
CY Rotary Valve

<3>
Compressor
Blower
/I/I/I/I
Scre
*
Reciprocating
Screw Blow Tank

Figure 1.1: Basic Components of Pneumatic Conveying Systems [ Chambers, 1987].


3

Storage
Hopper C o a r s e and
Fine
Particles

Prime Mover
Acceleration
O ^^^T^rr^f « r Z o n e j . 1.1.'j.i.».!. i.i.i
end F l o v

O Feeding Zone
C o n v e q i n q P r e s s u r e Loss.
B e n d Acceleration
Particle- Zone
./ Y | Vail Interaction

Particle- Particle
> Interaction
Variables
"ohesive,Humidity, Electro-
Air/Solids Seperation
static,Pipe R o u g h n e s s
/fl*
Stepped Pipe
\Q7 To S l o v Conveying
Velocity
Discharge
Hoppei ear and
jjmyy-y-y-'-y-yy-'Mm
Degradation
O t II I I » I I I I I I I I I I I I I I I I L I I ifc i i r r -

4—-Dense Phase Dilute Phase—f

Figure 1.2: Pneumatic Conveying System Layout [ Chambers, 1987].


4

Table 1.1: Data for pneumatic conveying systems for a pipe diameter of 100 m m .

Type of Gas velocity Solid to gas Particle Solids mass


conveying m/sec. velocity ratio size flow ratio

Dilute phase 15-35 0.3 - 0.7 coarse 30


SUdingbed 5-20 0.1 - 0.5 fine 100
Plug flow 2-6 0.6 - 0.9 coarse 50-100
Plug flow 3-10 0.2 - 0.8 fine 100-500
with bypass
Plug flow 5-15 0.2 - 0.8 fine 100-500
with controlled
secondary gas
Extrusion flow 0.4-4 0.6 - 0.9 fine 400-800

Typical flow patterns in a horizontal pipe are shown in Figure 1.4. Dilute phase
conveying is a fully suspended flow generated by large volumes of gas at high velocities.
The flow pattern in dense phase flow can vary from an unstable flow to a stable flow
depending on gas velocity, powder characteristics, flow rate, pipe roughness and
diameter. Flow patterns for dense phase conveying vary from conditions in which the
solids completely pack sections of the pipe and move as a continuous plug to conditions
where the solids on the bottom of the pipe move as a series of dunes with a dilute phase
layer of solids flowing above the dunes.

At high solid loading ratio conveying occurs as plugs of coarse powder with high
pressure gradient but low velocities. Obviously, the specific energy consumption required
for dense phase flow will be low, if fine powders are conveyed which are fiuidizable.

In dense phase flow proper, the material fills completely the pipeline cross
section. A reduction of the gas velocity less than a critical value to keep the particles in
suspension results in a non uniform distribution of powders over the conveying pipeline
cross section. This critical velocity is termed as the saltation velocity for horizontal
conveying and choking velocity for vertical conveying.
5

Loading of solids
U.-W)
'30

Dilute-phase conveying

1 10 100 m / s
Gas velocity w —

Figure 1.3: Phase Diagram for Pneumatic Conveying of Solids [ Bohnet, 1985].

Homogeneous Flow Immature Slug Flow


7*T^f+T^^Ti^^T^^*^^*T^

»______

Degenerate Slug Flow


Homogeneous Flow
nrrrrr

^^i'^-Ai^iSirtr»^rtiiS«w*

Immature Dune Flow Degenerate Slug Flow


^^T*T*^^^?*^^T*mT^.

\__£k&sm&ik

Dune Flow Ripple Flow


*r^^T*^T**?^^*T^^^Tm*^?

Degenerate Dune Flow Pipe Plugged

Figure 1.4: Flow Patterns in a Horizontal Pipe [ W e n , 1959].


6

1.4 TYPES OF DENSE PHASE PNEUMATIC CONVEYING SYSTEMS:


The various dense phase pneumatic conveying systems are characterized by the
system pressure and plug location along the pipeline. Variation of the plug location can be
controlled by parallel gas booster supply lines or gas bypass arrangements.

Gas bypass systems are employed for impermeable products, which tend to form
solid plugs when conveyed at low velocities. W h e n a plug forms in the conveying line,
the gas bypasses and reenters where the resistance of the plug is less than in the bypass
line. A long plug of material is thus divided into shorter plugs and material transport is
thus reestablished. In general, dense phase pneumatic conveying systems are categorized
into four types. These being:
1.4.1 CONTROLLED PLUG FORMATION:
The natural plug formation of coarse-grained powders is induced by generating
plugs into the conveying pipe, e.g. this natural plug formation process occurs when
conveying Wheat, Rice, Millet, etc.
1.4.2 CONTROLLED PLUG BREAK-UP;
This method consists of localizing plugs in their initial stages and breaking them
up before a critical length is exceeded. A disadvantage of this system is the possibility of
powder penetrating into the internal or external by-pass lines.
1.4.3 SUSPENSION METHOD;
Such systems exploit the high gas retention capacity of some powders. The gas
and solids are mixed at regular intervals to restore fluidization of the slow moving
powder.
1.4.4 C O M B I N A T I O N S :
Other systems combine the latter two methods. All practical systems can be
categorized into one of the four groups mentioned above. Harder et al. (1988a) provides
an excellent summary of dense phase pneumatic conveying system classification as
presented in Figure 1.6. Without the knowledge of the powder behaviour, it is not
possible to design dense phase conveying systems for reliable operation. The usual feeder
for dense phase conveying systems is the pressure vessel or blow tank. These feeders
are capable of achieving any required conveying pressure without uncontrolled gas losses
or leakage.

All conveying requirements may not be solved using dense phase conveying
systems and for this reason dilute phase conveying systems still have their field of
application. These fields include for example, conveying systems with frequently
changing solids or very cohesive powders, where high velocities are necessary to
overcome the interparticle forces.
Dense phase conveying methods
I
£
Dense phase conveying Dense phase conwying
conventional with stabilization

tf
I
Solids with high gas Solids with tow gas
permeability / permeability /
low gas holding high gas holding
capacity capacity
J
S£<r

S.5CT

Strand conveyance, Conveyance with Conveyance with Suspension method


dunes, conglobations controlled slug controlled slug of conveyance
production degradation

e.g. e.g. Fluidstat Twistcon/CPAG


CPAG. Pulsecon/CPAG
— •
^mSO
5SW^S*SB*^< ^-F^F Turbuflow
____&(&
Pneumosplit

Uncontrolled slug
degradation* suspen=
sion effect

System Gattys

is*&3t£'

Fluidschub

e.t.c.
y^

Figure 1.5: Classification of Dense Phase Pneumatic Conveying Systems


[Harderetal. (1988a)]
8

1.5 ADVANTAGES AND DISADVANTAGES OF PNEUMATIC


CONVEYING SYSTEMS:
15.1 ADVANTAGES:
The advantages of pneumatic conveying, in general, include:
[1] Clean transportation of a large variety of powders;
[2] Relatively simple system;
[3] Flexibility in routing- it is possible to convey vertically or horizontally by the
simple addition of bends;
[4] Distribution of powder to different areas within a plant and the ability to pick up
powder from several locations;
[5] L o w maintenance and manpower costs;
[6] Multiple use - a single pipeline can be used for a variety of powders;
[7] Security where the pipeline is used to convey valuable powders;
[8] Lower initial cost, savings of bulk shipments, totally enclosed, less maintenance,
easy to automate.

1.5.2 DISADVANTAGES:
Unfortunately, pneumatic conveying systems incur the following disadvantages:
[1] High operating pressure;
[2] High energy consumption;
[3] Possibility of complete pipeline blockage;
[4] Difficult to predict the nature of the flow;
[5] W e a r and abrasion of system components;
[6] Conveying distance is presently limited to a few kilometers;
[7] Cost of transportation increases with the addition of bends;
[8] The allowable powder mass flow rate decreases with increasing conveying
length.

1.5.3 ADVANTAGES OF DENSE PHASE CONVEYING:


The notable advantages of dense phase conveying include:
[1] The energy required per kg. of solids and metre of conveyor length is less than
that of comparable dilute phase conveying.
[2] Smaller air powder separators are required
[3] The total pressure drop does not vary as widely with air flow rate, as it does for
dilute phase systems.
[4] System operation is more stable;
[5] The air velocities are generally in the range of (or less than) the choking or
saltation velocities in dilute phase conveying.
9

1.5.4 DISADVANTAGES;
In c o m m o n with all pneumatic systems, dense phase conveying incurs the
following disadvantages:
[1] The problem of feeding large quantities of solids from an atmospheric
environment to a high pressure pipeline generally means that rotary valves are
not suitable.
[2] In general, single blowtanks are used to feed the solids which necessitates batch
m o d e operation.
[3] Not all powders which can be pneumatically conveyed are conveyed satisfactorily
in dense phase.

1.5.5 ADVANTAGES OF LOW VELOCITY CONVEYING:


The advantages of low velocity conveying or super dense phase conveying
include:
[1] L o w rates of pipeline wear and powder degradation;
[2] Minimal segregation of conveyed powder;
[3] M i n i m u m conveying air requirements.
The need to minimize conveying air volume is highhghted as follows:
[1] Blower power requirements increase approximately as the cube of the air
velocity.
[2] Pipe erosion increases approximately as the cube of the air velocity.
[3] Powder degradation occurs at high velocity.

Hence, there is a clear trend, within the pneumatic conveying industry, towards
dense phase and low velocity conveying. This trend is consistent with the distinct
advantages of these systems. However, use of dilute phase system will be continued for
the reasons discussed earlier.

Due to the above features, pneumatic conveying is one of the fastest developing
methods for the transportation of bulk solids. This method is proving to be cheaper,
easier and more convenient than m a n y other more conventional methods of transporting
bulk solids including belt conveyors and mechanical conveyors. Air is relatively cheap
and easy to obtain in large quantities. Furthermore, the escape of air contaminated with
dust particles usually causes only minimal environmental damage.

1.6 POWDER PROPERTIES:


The important properties of powders, governing pneumatic conveying
characteristic include,
10

[1] Particle Size and Distribution


[2] Particle Shape and Structure
[3] Bulk Density
[4] Particle Hardness
[5] Permeability
[6] De-aeration
[7] Floodability
[8] Corrosiveness
[9] Cohesiveness
[10] Explosibility
[11] Moisture Absorbancy
[12] Toxicity
[ 13] Angle of Repose
[14] Electrostatics

As can be seen the large number of powder variables causes pneumatic conveying
to be an extremely complex phenomenon. T o partially overcome this complexity
improved knowledge of the interaction between powder properties and conveying
characteristics is sought. T o this end, the effects of a number of powder properties on
pneumatic conveying characteristics were selected for further examination. Actual details
of this examination are summarized in the following section.

1.7 THE OBJECTIVES OF THE RESEARCH:


The broad aim of this thesis is to gain further insight into dense phase and super
dense phase pneumatic conveying processes, to improve the design procedures for the
conveying of various powders and to develop standard bench tests to assess material
pneumatic conveying characteristics.

Particular effort will be devoted to the latter since pneumatic conveying is not
fully understood in regard to the conveyability of a powder on the basis of properties
determined from bench tests. In regard to bench test development, this work studies in
detail the cohesive arch behaviour, measurement of tensile stress, fluidization and
deaeration properties, wall friction of aerated powders, surface characteristics, bulk
density, solid density, flow properties, particle size analysis and powder coefficient of
restitution. The properties so measured are then correlated with pneumatic powder flow
behaviour in dilute phase, dense phase and super dense phase flow systems.
11

The need to assess the foregoing properties to successfully design a pneumatic


conveying system is highlighted by the following. Firstly, wall friction is an important
factor contributing to the pressure drop in dense phase pneumatic conveying. Obviously,
the frictional properties of powders have an adverse effect in pneumatic conveying. A s an
initial quantification of wall friction effects during pneumatic conveying, wall friction
measurements were evaluated under aerated conditions in a perspex tube by pushing
powders upwards at different column lengths.

Secondly, the internal friction angle, shearing cohesiveness and tensile strength of
powders are significant parameters during dense phase and super dense phase conveying.
Notably, in these modes, the creation and breakage of plugs depends on powder
cohesiveness. In fact, m a n y problems, associated with powder handling, originate from
the influence of the cohesive forces on the flow behaviour of powders.

To assess the effect of cohesion, the arching dimension and hence cohesive
strength were evaluated in a purpose built Cohesive Arch Tester for various powders.
The cohesive strength so measured was then compared to that measured using the Jenike
Direct Shear Tester. T o further elucidate powder cohesive properties, the tensile strength
was evaluated for various powders. This powder property was measured using an Ajax
Tensile Tester at different consolidation levels.

Thirdly, as previously indicated, powder fluidization characteristics, air


permeability and air retention characteristics of powders are important considerations in
pneumatic conveying. Since these properties are intimately related to the particle size
distribution, measurement of the same was evaluated using a Malvern Particle Sizer. The
particle size distribution, so measured, was also correlated to other powder characteristics
assessed in this investigation. The particle size distribution also governs its air
permeability and air retention characteristics. The latter properties were evaluated and
assessed by conducting measurements in fluidization columns and deaeration rigs.

Fourthly, the surface characteristics of powders are important in regard to powder


degradation and pipeline wear in pneumatic conveying systems. Furthermore, surface
characteristics contribute to the powder's internal and wall frictional behaviour. T o obtain
knowledge of the powder surface characteristics Electron Scanning Microscope
observations were conducted. These examinations revealed a host of information
concerning expected powder behaviour.
12

Fifthly, bulk density, permeability and solid density bear an important influence
on the flow behaviour in pneumatic conveying systems. These important parameters
were determined using a Jenike Compressibility Tester, Jenike Permeability Tester and
Beckman Pycnometer, respectively.

Finally, the coefficient of restitution is very important in governing the flow of


granular materials during dilute phase flow. This coefficient was determined for several
particulate materials using a basic rotating disk technique. Since the coefficient of
restitution is of secondary importance in regard to dense phase conveying, minimal
discussion of this coefficient is presented.

Powder properties determined from bench tests provide convenient and rapid
assessment of a powder's flowability. This assessment is useful for ranking of different
powders and identification of the optimum m o d e of pneumatic conveying. A n e w phase
diagram is proposed incorporating powder properties such as cohesion, deaeration,
permeability and mechanical interlocking to indicate pneumatic conveying flow
behaviour.

In regard to powder flow behaviour in actual conveying systems, the following


was conducted. Actual system performance was determined using a suitably configured
pneumatic conveying pilot scale test system. This closed circuit system comprised a
Sturtevant blow tank feeding a m a x i m u m of 71 meters of 50 m m nominal bore tubing
discharging into a receiving hopper. Initially, a friction loop was installed to measure
system pressure drop. Subsequent improvements to the system included measurements of
powder velocity and concentration by use of Tealgate T.200 and 300 series transducers
[Beck etal. (1971,1982)].

In the latter phases of the performance tests, the effect of bend geometry on the
flow characteristics was examined. In particular, two different bends were used namely,
long radius and vortice elbow. This examination was followed by the development of a
fibre optic probe to measure powder velocity. Subsequent testing, using this velocity
probe was conducted at different air flow rates.

The results of the above investigation yield useful information in regard to


pneumatic conveying flow behaviour of powders in general, and for the prediction and
design of practical pneumatic conveying systems in particular.
13

CHAPTER 2
BLOW TANKS, DENSE PHASE FLOW
AND WALL FRICTION

2.1 BLOWTANK:
2.1.1 INTRODUCTION:
A blow tank is essentially a pressure vessel configured with powder inlet and
discharge ports and valves, a pressurization port and a vent port, refer Figure 2.1. The
basic operating cycle of a blow tank comprises filling, pressurizing and conveying.
During filling, the powder inlet valve is open and the discharge valve closed. In this
phase, powder feeds into the blow tank (usually by gravity from a feed hopper). W h e n
the blow tank is full, the inlet valve is closed allowing pressurization. Once pressurized
to the required system pressure, the discharge valve is opened to supply powder to the
conveying pipeline.

Blow tanks may also incorporate fluidization, conveying and secondary air flow
systems. There are two types of blow tanks, the top discharge and the bottom discharge
also k n o w n as the Fluxo and Cera type, respectively. Blow tanks are pressure vessels
which have to be designed in accordance with the pressure vessel code according to A S
1210 in Australia. Because they work under internal pressure, they require a certificate of
fitness at regular intervals to ensure safe operation. A summary of blow tank
characteristics and operation, as found in the literature, is presented in Table 2.1.

2.1.2 ADVANTAGES:
The advantages of blow tank feeders include:
[1] High solids to gas ratios;
[2] Small pipelines;
[3] Small dust filtration systems;
[4] N o moving parts;
[5] M i n i m u m powder degradation and segregation;
[6] Simple control of flowrate;
[7] Higher conveying capacities;
[8] Long conveying distance possible;
[9] M i n i m u m bend and pipeline wear;
[10] Can convey hot powders;
[11] N o difficulty in feeding against adverse pressure gradient.
14

Vent line Feeding hopper


Control valves
Inlet gate

From
Level indicator
compressed air
supply
Blow tank

Conveying

ine

Figure 2.1: A Single Blow Tank System.

2.1.3 LIMITATIONS:
The limitations or disadvantages of blow tanks include,
[1] System conveying rate is limited by blow tank size;
[2] They operate in batch mode in most situations;
[3] M i n i m u m product cooling (low gas to solid ratio);
[4] They are of high pressure design;
[5] D u e to the use of high pressure, the conveying velocity increases with
distance; down the pipeline due to expansion of the compressed conveying gas.

Since the blow tank discharges product to the conveying line in batches, two blow
tanks m a y be used to operate in sequence, so that one is being recharged, while the other
is discharging.
15

TABLE 2.1 B L O W TANK CHARACTERISTICS AND OPERATION


- LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1972 Rain Reviewed c o m m o n configurations of blow tanks and their


fields of applications.

1978 Shepherd Reported the difficulty of dense phase conveying of w o o d


etal. pulp due to hold up and blow hole formation. Conveyed
either by a higher initial pressure in the blow tank or
alternate pulsing of the inlet and discharge valves.

1982 Tomita Measured the velocity profiles of non cohesive granular


etal. materials at different flow rates in a top discharge blow j
tank. Found similarity between the gravity discharge of
solids from an orifice to that of the flow of solids in the
blow tank. Observed that the material flow was not affected
by the air flow except near the pipe inlet and is independent
of the pipeline pressure drop.

1982 Hitt Applied the time derivative of the ideal gas law to the blow
tank discharge flow to calculate solids loading ratio, to
predict pressurization transient and conveying characteristics.

1984 Lohrmann Reported experimental results of Group A powders using a


etal. bottom discharge blow tank. Examined the influence of
initial blow tank pressurization, chargingfraction,air flow
rate and total length by testing Lime, Portland Cement and
fly ash. Observed that Group A powders are good
candidates for dense phase conveying, are easily fluidizable
and retain fluidization air.

1985 McLean Analyzed blow tank design using the principles of gravity
flow bins taking into account the fluid pressure gradient.
16

Recommended critical dimensions and main design


considerations to determine the geometry of blow tank for
reliable flow.

1986 McLean Presented expressions of steady state blow tank


characteristics applicable to both Fluxo and Cera type blow
tanks conveying either cohesive or non-cohesive bulk solids.

1987 Kennedy Investigated the effects of different methods of air injection


etal. on the performance of bottom distharge blow tanks. Found
that this can have a significant effect on the overall
performance of pneumatic conveying system.

1988b Harder Described criteria for blow tank design, various possible
etal. arrangements and alternative feeders for dense and dilute
phase conveying.

2.1.4 PARALLEL ARRANGEMENT:


In this system, one blow tank discharges powder into the conveying pipe, while
the other receives powder from the hopper. Hence, by alternate sequencing of this cycle
continuous powder conveying is possible (Figure 2.2). W h e n installed with individual
feed hoppers, each blow tank m a y all handle the same material or they m a y alternately
handle different types of material.

2.1.5 SERIES ARRANGEMENT:


In the series arrangement, each blow tank is separated or isolated from each other
by isolation gates and each blow tank have their o w n venting and pressurizing
connections. T h e lower blow tank pressure is selected to be slightly higher than the
operating pressure to ensure a uniform gravity flow of powder from the blow tank to the
conveying pipe. T h e upper blow tank is alternately pressurized so that powder can be
discharged batchwise to the lower blow tank or it is vented so that powder can be charged
into it from the hopper. T h e bottom blow tank, however, conveys more or less
continuously (Figure 2.3).
Figure 2.2: Parallel Arrangement [ Reed, 1989 ].

Hopper
S/enV line

Pressure
balance Conveying
and vent" line

/.ir supply

Figure 2.3: Series Arrangement [ Reed, (1989)].


18

2.1.6 CAPACITY:
The approximate capacity of a blow tank system can be calculated from the
equation (Kraus, 1983),

8.156 x IO-4 ph V
Pb
C= 1 (2.1)

where, C = capacity, tonnes / hr.,


Pb = loose poured bulk density, kg / m 3
V = blow tank volume, m 3
t = total cycle time, sees.
The system capacity can be increased by selecting a series or parallel arrangement.

2.1.7 AIR REQUIREMENTS:


Air requirements depend upon the characteristics of the powder, the distance to
be conveyed and the diameter of the pipe line.

2.1.8 SECONDARY AIR:


Secondary or supplementary air is required to promote the powder flow in the
conveying pipe. As the slug moves through the conveying pipe, it tends to compact due
to the frictional forces or from the loss of air due to its leakage through the material.
When this happens, additional air can be introduced to break down the plug and to
promote flow.

2.1.9 VENTING:
Proper venting is important for smooth blow tank operation. If the blow tank is
not vented, a large adverse pressure gradient occurs, which prevents further material flow
into the blow tank. The existence of this adverse pressure gradient severely retards infill
flow rates of both cohesive and low density powders.

2.1.10 AERATION AND FLUIDIZATION: /


The flowability of powders can be increased by aeration. This is the injection of
air upwards through the powder. Low pressure differentials are sufficient for aeration. At
higher air velocity, the powder will be suspended and fluidized.

A common aeration device is the plenum chamber through which air can
and supports a permeable or porous membrane (Figure 2.4). The plenum chamber is
bolted to the bottom of the hopper of the blow tank.
19

Figure 2.4: Aerated B l o w Tank [ Reed, (1985)].

2.1.11 BLOW TANK PERFORMANCE CHARACTERISTICS:


Jotaki et al. (1978) studied conveying characteristics of the Fluxo type of blow
tank, w h e n conveying P V C powder and polyethylene pellets. The blow tank solids
mass flow rate is evaluated by knowledge of the superficial air velocity at the pipe inlet
and is independent of the pipeline pressure drop. They stated that the relation between
the solids mass flow rate and the superficial air velocity at the pipeline inlet can be taken
as a blow tank characteristic curve. Furthermore, secondary air in the pipeline has no
effect on this relation in so far as it only reduces the solids concentration. The discharge
characteristics of a fluxo blow tank for coarse granular solids are adequately described by
(McLean, 1986),

u.
Ms = 0.988 ps 7T ( D - 1.9 d )25 g?5 -1 (2.2)

where Ms = solids flow rate from blow tank, kg s"1;


p s = solid density of bulk solids, kg n r 3 ;
d = diameter of solid particles, m ;
g a = effective gravitational acceleration - 9.81 m s 2 ;
D - inside diameter of blow tank delivery tube, m ;
u 0 = superficial gas velocity through solids bed, m s - 1 ;
u0* = characteristic velocity of powder at channel outlet, m sr1.
20

2.2 SYSTEM nFfiTQl^


The design of a pneumatic conveying system involves the specification of:
1. Route of the pipe;
2. Type of conveying system to be used (e.g. vacuum or positive pressure; low,
medium or high pressure; closed or open loop);
3. Details of individual components (feeding and discharge mechanism, valves,
cyclones, bagfilters,types of bends, materials of construction);
4. Flow pattern in the pipe (dilute phase, dense phase or moving bed);
5. Pipe size;
6. Solid mass flow rate;
7. Air flow rate;
8. Horizontal and vertical distances of pipeline;
9. Particle density of the powder and its particle size distribution;
10. Overall pressure drop;
11. Determination of power consumption;
12. Air blower / compressor;
13. Determination of the critical velocity.

Generally, the design of pneumatic conveying systems is based on rules of thumb,


previous operating experience and know-how of specialist companies. A summary of the
design procedure for dilute phase conveying was recommended by Bandrowski et al.
(1981). The basic parameters required to effect optimal powder conveyance (minimum
power consumption, m a x i m u m throughput of solids and longest possible life of pipes
and equipment) should be determined in the design phase. The methods for increasing
the effectiveness of pneumatic conveying systems include achievement of the m a x i m u m
flow concentration and assurance conditions for its maintenance for the longest possible
time.

The important parameters are the capacity to be conveyed, the distance over which
the powder will be conveyed and the number of bends involved. Since bends create large
pressure drops, it is highly desirable to minimize their number. Furthermore, the
required velocity must be determined. The solids mass flow rate should be continuous to
minimize energy consumption.

2.3 DENSE PHASE AND SUPER DENSE PHASE FLOW :


Dense phase conveying occurs, when the conveying velocity is below the saltation
or choking velocity. In this phase, the mass flow ratio is high and significant pressure
21

fluctuations occur due to the existence of dunes and slugs. Dense phase conveying can
used for powder and granular materials, but blockages may occur. Hence, the
conveying velocity is an important consideration.

Dense-phase conveying in the form of plugs is the most economical f


conveying. In this mode of conveying, the pressure drop across a plug is approximate
proportional to its length, provided the particles forming the plugs do not exhibit
decreasing permeability with increasing consolidation. For such powders, discontinuous
phase conveying is feasible. In general, plugs of large, mono sized particles exhibit
linear pressure drops. For such powders, the permeability of the plug is insensitive t
bed consolidation.

2.3.1 CLASSIFICATION OF DENSE PHASE FLOW:


Types of dense phase conveying systems are discussed in Chapter 1. Dense
phase flow can be classified into continuous phase, where the powder moves by saltatio
over a stationary or sliding bed and discontinuous phase, where powders move as slugs.
This classification can be further subdivided into pulse phase for granular materials an
plug phase for powders. In the latter case, powder plugs are essentially extruded
through the pipe.

2.3.1.1 CONTINUOUS SYSTEMS:


Non ..ohesive powders may be conveyed over short distances using continuous
phase flow systems. These systems usually consist of a conventional blow tank
supplying a standard pipeline arrangement. Hence, this mode is non optimal in solids
mass flow loading and tend to exhibit non stable flow characteristics. This flow type als
characterizes dilute phase systems operating non optimally. Hence, continuous phase
systems have limited practical significance.

2.3.1.2 DISCONTINUOUS-PHASE SYSTEMS:


Most systems use some form of air injection to fluidize the powder and prevent
wedging between particles. Some provision is made to break up long plugs, but plu
formation is not directly controlled. Plug-forming systems create small plugs at the f
point. Other systems destroy plugs on formation and operate in dune phase.

In the pulse phase system, air knife is used to seperate plugs by


periodically. The advantage of this system is that the pressure drop, when conveying
series of discrete plugs is less than the pressure differential required to transport a s
continuous compact material plug over the same conveying length. In the former case,
22

the pressure drop is equal to the summation of the pressure drop of the individual plugs
in the conveying pipeline. A s long as the plugs are stable and do not join together and
block the pipe, discrete plug flow conveying is very efficient. This system can be used
for fine cohesive powders.

Due to high pressure losses in discrete dense phase powder plugs, air expands
significantly along the pipe and the conveying velocity increases. A s a result of this
increase in air velocity along the pipe, tensile forces are produced in the powder plugs,
which tends to tear them apart. T o prevent disintegration of the discrete powder plugs, a
valve or orifice must be located at the end of the conveying pipeline to provide a system
back pressure.

Air boosters positioned along the conveying pipeline sense the pressure at each
stage and adjust the pipeline pressure to convey granular materials smoothly and prevent
high back pressures. For very cohesive powders, a booster line m a y be added to pulse
phase system for continuous plug flow. Details of dense phase flow and super dense
flow systems is presented by Klinthworth et al. (1985). A literature survey summary
relating to dense phase flow is presented in Table 2.2.

TABLE 2.2 DENSE PHASE F L O W - LITERATURE SURVEY

1980 Konrad et al. Evaluated the pressure drop required to m o v e a plug in a


horizontal pipe. Using the packed bed theory, he predicted
an expression for the pressure drop for a cohesionless
material. For fine powders, he suggested that the pressure
drop across a plug varies exponentially with plug length.

1981 Chan et al. Considered one dimensional plug flow. Examined stability
criteria by considering the axial interparticle stresses within
single plugs and the effect of wall friction.

1981 Wilson Considered the effects of stress on deformation within a


plug. H e stated that this deformation effects the
permeability of the plug, the pressure gradient and the
stresses along its length.
23
1981 Klinzing et Applied porous media and turbulent flow concepts to
al. extrusion flow. Suggested a permeability factor for low
gas velocities.

1981 Tomita et al. Observed wavelike slug motion of polyethylene pellets in a


horizontal pipeline. Found the pressure drop caused by the
wavelike slug motion is estimated by the Ergun eqn.

1982 Tsuji et al. Observed plug conveying of coarse particles in a horizontal


pipe with secondary air injection. Studied the effects of
particle size and number of injection holes. Experimental
results deviated from Ergun's eqn.

1982 Hitt et al. Studied two models of slugging, shearing type and full bore
flow in a horizontal pipe and compared predictions with
experiments.

1983 Tsuji Reported that the pressure drop across a moving plug was
less than across a packed bed of the same particles. It was
noted that turbulence and vibration prevented wedging of
the conveyed powders.

1983 Werner Reported the influence of particle size distribution on dense


phase pneumatic conveying in vertical and horizontal pipes.
Studied the difference between the conveying of uniform
sized powders and powders having a wide size distribution.

1986a Konrad Discussed the similarity of plug conveying of cohesive


powders to the arch formation theory of material flowing
out of a hopper (Jenike, 1967) neglecting the effect of
gravity and presented an excellent review of dense phase
pneumatic conveying.

1986b Konrad Considered the effect of air compressibility on the pressure


drop in dense phase pneumatic conveying.

1987 Hauser et al. Observed that abrasion of agglomerated lectose can be


24
reduced in plug conveying by using a back pressure system
aimed at reducing the volume expansion of air.

1987 Zheng Reported the relationship between pressure drop and plug
length to be an approximate linear relationship.

1987 Borzone Suggested that the pressure drop was found to be


etal independent of the air flow rate and to vary linearly with
plug length. The plug velocity was independent of the plug
length and for vertical plug flow at low velocities,
gravitational forces are significant.

1988 Aziz et al. Indicated that the pressure drop variation is linear with plug
length. Found particle size distribution and cohesion govern
plug formation and stability. Proposed a pressure drop
model for plug flow and found wall shear stress was
important for controlling the flow in horizontal and inclined
pipes.

1988a Harder et Discussed the effect of powder properties on dense phase


al. conveying and energy optimization with respect to
industrial applications.

2.4 POWDER PROPERTIES:


The suitability of powders for discontinuous dense phase conveying (pulse, slug
and solid phase) depends on numerous physical powder properties. These are particle
size distribution, particle shape, hardness, compressibility, adhesiveness, cohesion, de-
aeration, coefficient of friction and coefficient of restitution which also control, to a
large extent, the system pressure drop.

For super dense phase conveying, air permeability, air retention capability,
particle size distribution, density, wall friction, internal friction and product adhesion are
important powder considerations. Super dense phase pneumatic conveying exhibits
greater stability at high solids loading compared to that w h e n conducted at low solids
loading. However, occasionally powder plugs consolidate to form immovable plugs.
25

W h e n powder permeable to air are transported, the conveying air is able to


penetrate into the plug of material, fluidizing it and so limit the plug formation process.
In addition, pressure compensation between the individual pockets of air and the slugs of
material is possible without the aid of bypass or parallel booster lines.

When conveying powders exhibiting low air retention characteristics, additional


facilities have to be provided to prevent the particles packing together and forming
immovable plugs. For such materials, bypass pipes m a y be used. These bypass pipes
increase the turbulence and mixing in the flowrate [ Klintworth et al. (1985)]. Bypass
pipes with regular connections can be used internal or external to the conveying pipeline

The need to prevent formation of plugs is particularly relevant for low air retentive
cohesive powders. Conveying of such powders, with limited overall pressure drops, is
possible by keeping the plug length short. It should be noted that the wall friction is also
reduced by preventing unlimited plug formation.

As the conveying velocity is reduced, the strand characteristics of continuous


dense phase conveying changes to moving dunes. These dunes m a y subsequently form
into plugs which will fill the pipe. During dune flow, efficiency is reduced due to
continual deceleration and reacceleration of the particles. Furthermore, wall friction
provides a major energy loss during plug conveying. In this m o d e of conveying, powder
properties and size distribution are important considerations.

The powder characteristics governing horizontal dense phase conveying system


characteristics are summarized in Table 2.3.
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27

2.5 W A L L FR1CTTON:
2.5.1 INTRODUCTION:
The wall friction is an important design parameter in pneumatic conveying. In
solids handling, it is usual to assume that the shearing of granular material along a surface
is similar to the solid body friction along a surface. Hence, it is usual to apply Amonton-
Coulomb's law. In investigations, concerning the frictional forces between a granular
material and a surface, most researchers assume that the friction force to be of the same
form as solid body friction and apply the Coulomb friction law to describe the same.
However, other researchers [Platonov et al. (1969)] consider the resistance to slip as a
combination of an adhesive force, which is independent of the normal pressure and a
shearing force proportional to the normal pressure. Wherein the characteristics of both
friction components would be dependent solely on the materials interacting at the surface.

The total resistance to sliding of powders against a boundary surface is a


combination of the force due to external and internal friction. Under the action of a load,
the powders change their density and this creates difficulty in formulating a theory of
frictional contact of powders and in calculation of the actual contact area on which
frictional force is realized.

2.5.2 THE FRICTION OF SMOOTH AND ROUGH PARTICLES:


For smooth particles the real area of contact m a y be less than that for the rough
particles. The frictional force F is the product of the shear strength x and the real contact
of area A ,
F - t A (2.3)

For smooth elastic spheres, the magnitude of the contact surface area A at the wall
can be obtained from the Hertz equation,

( 1 2 , 2 V1
?* — 1-V- 1 - V2 (2.5)
V — cTi + Tr
z_ J

where R = radius of the sphere,


W = the normal force,
V; = the Poisson's ratio, and
Ej = Young's modulus for the sphere and the flat surface, respectively.
28

For rough particles, the real area of contact increases at least linearly with the
applied normal force. The problem of computing the actual magnitude of the contact area
is complicated and requires details of the surface topography. For instance, the frictional
force for rough particles is directly proportional to load.

Many studies have been done to evaluate the wall friction of powders under de-
aerated conditions, but very little research has been undertaken to evaluate the frictional
coefficient variations under aerated conditions. T h e friction angles determined in shear
cell tests appropriate to hopper design [ Arnold et al. (1980) ] are not directly applicable
for powders pneumatically conveyed. A literature survey s u m m a r y relating to wall
friction of powders is depicted in Table 2.4.

2.5.3 ANALYSIS:
Considering the fact that frictional resistance of the container walls offer support
to the material in the vertical direction (Figure 2.5) and assuming equilibrium of an
elemental strip of thickness dz; Figure 2.7, the following equation was derived for the
pressure drop variation,

Solution to this equation gives:

P =J5_
(2.7) l - e x p [ - ^ —
z
4pk

The distribution described by equation (2.7) is shown in Figure 2.6. T h e above


analysis assumes the following conditions:
1. T h e coefficient of friction p is constant;
2. The ratio of lateral pressure to vertical pressure k = P r / P z is constant;
3. The pressure distribution over the surface of the piston is constant;
4. The tube bore is perfectly parallel
5. T h e grain is incompressible.

It therefore follows that the conveying force necessary to move a column of


material up a cylindrical tube can be evaluated by the following expression,
77tD3 f4ukL^
F z == exi -1 (2.8)
l6TIkL \—J
D!
iliJHljljljlHJltJliY

dz'
T
Figure 2.5: Column of Material. Figure 2.6: Pressure Distribution.

Column of
Material

if *•••*•*"*••••••••••'•-•-•-'---*••-•-•-•-•-•-•-•---- •»-- • •-•---r>-.-.-w-"---*---'-i

Piston

V
Figure 2.7: Force Analysis of a Column of Bulk Material.

[ Arnold et al. (1980) ].


30

T A B L E 2.4 W A L L FRICTION - LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1958 Barth Reported the value of the coefficient of friction for cokes,
coal and for crushed Wheat based on experiments in
vertical pipes.

1959 Muschel- Obtained the value of the coefficient of friction by


knautz measuring the rebound motion of solid particles from a
rotating disk surface, when dropped vertically.

1960 Zenz Conducted experiments to measure solid-wall friction. The


bed of powders rested on afixedpiston. The pressure
exerted at the bottom of the powder bed was measured by
means of a pressure gauge. The frictional force between the
solids and tube wall was taken as the difference between the
pressure exerted on the powder bed, when m o v e d upwards
and that when it was stationary. The experiments were
performed with and without powder aeration and tube
diameter was varied from 8.9 m m to 14.0 m m inner
diameter. The tube was raised by hand and the rate of
movement was recorded by high speed motion pictures.

1966 Roberts Studied the forced flow of Millet in a 3.66 m . long and 44.5
m m . diameter perspex tube fitted with a perforated piston
and piston rod to force columns of material upwards
(Figure 2.8). Resistance strain gauges were used to
measure the conveying force. The upward movement of the
piston was effected by mechanical means. His results for
different column lengths are shown in Figure 2.9.

1969 Platonov Developed a testrigfor measuring the coefficient of


etal. friction between a granular material and a solid surface.
31

They found that the coefficient of friction was dependent


on the normal pressure of the granular material and
furthermore that the deviation from Amonton-Coulomb's
friction law varied also with normal pressure. They also
reported that the Amonton-Coulomb theory has not been
verified under experimental conditions, as it has not been
possible to identify and measure individual friction
components.

Their testrigis considered to simulate accurately the


real process of slip between a surface and a material.
Experimental investigations using granular materials
including Iron ore, Polysterene, Wheat, Glass bead and
Millet revealed that the coefficient of friction to shear for all
materials tested was not constant and depended
considerably on the normal pressure of the granular
material.

1978 Rademacher Observed that during the flow of coarse granular materials
along a surface essentially translational particle motion
occurs. H e reported that the dead load method for
measuring friction coefficients between a bulk solid and a
surface, suggested by Brubaker et al. (1965) and Platonov
et al. (1969), does not simulate the actual phenomenon
correctly. Such methods almost eliminate the rotational
m o v e m e n t of granules. H e observed such granular materials
microscopically and concluded that this process would
result in a flattened particle surface. Hence, the results
under dead load conditions can't be considered as a true
representation of the actual friction coefficient.

His testrigeliminated the deficiencies associated


with dead load methods. It consists of two parts: a fixed
vertical tube and a horizontal disc, which is driven by a
fixed variable speed motor, as shown in Figure 2.10. Since
the test rig provided consistent results, it became apparent
that the friction coefficients along the tube walls and on the
32

disc would follow by simple calculations. This evaluation


requires that the geometry of the granular mass, the angular
speed co and the m o m e n t required to drive the disc be
known. T o facilitate this evaluation, the original unit was
replaced by a vertical motor - gear box combination with
cushioned air bearings.

The experimental investigation of three different .


materials, namely, Rape-seed, Vetch and Millet using the
latter test equipment produced very consistent results. The
observed coefficient of friction between steel disc surface
and Millet seed compared favourably to that obtained using
the dead load method and other reported research work
[ Brubaker et al. (1965)]. This favourable comparision m a y
be due to the fact that the coefficient of friction between
Millet and the surface does not vary significantly with slip
velocity.

His method is useful for measuring the kinetic


coefficient of friction between granules and a surface.
However, the method is not suitable for testing cohesive
powders nor aerated powders. Further, it can't be used to
determine the wall friction parameter (fik) applicable to
powder column conveying.

1983 Thompson Measured the wall friction coefficient of Wheat using the
etal. test rig shown in Figure 2.11. In their testrig,a flexible
pressure diaphragm near the walls was used to exert a
k n o w n force on the grain mass to simulate the pressure;
which occur in a grain bin. T o determine the friction
coefficient for a given pressure, the force required to pull a
metal blade through the grain mass was measured. They
found that the coefficient of wall friction for W h e a t on Steel
varies with moisture content, overburden pressure and
sliding velocity. For an increase of moisture content of
Wheat from 8 to 2 0 % , the coefficient of friction increased.
33

However, it decreased as the overburden pressure increased


from 7 to 172 kPa.

1984 Kano Investigated the wall friction factor in a vibratoryfieldusing


a shear cell like testrig.A sample of Millet, packed in a
cubic acrylic vessel on an acrylic plate, was vibrated by
means of a vibrator and the wall friction factor was obtained
from knowledge of the horizontal force required to m o v e
the vessel horizontally.

1987 Berkovich Reported methods to estimate wall frictional force of


powders based on the calculation of actual contact area. H e
found that under conditions of powder elastic and plastic
deformations at low pressure, the frictional force is close to
that predicted from the monomial Amonton's law. At high
pressures and with constant nominal contact area, the actual
contact area is completely saturated and the formula for the
frictional force is transformed into the binomial Coulomb's
law. H e also reported the effect of humidity on frictional
properties of powders. His experimental finding is
presented in Figure 2.12.

1988 Morikawa Reported that the aerated coefficient of wall friction was
independent of solid loading and Froude number defined by
pipe diameter and m e a n particle velocity for Lupin, C o m ,
Wheat, Polystyrene pellets, Steel balls, Glass beads in steel
pipes 5, 10 and 20 cm. inside diameter.
___^_^<l___7<y
Scorn

Pressore Prop
Across Co/___o

^ p___*£___\_J__i_______c

F/osv Meter

vppj'-t jkqo/eifbr

se

Figure 2.8: Forced Flow Apparatus [ Roberts, (1966) ].


80 -,
I5j* COLUMN

I2> COLUMNi

8 COLUMN!
6" COLUMM
~ i —
4?"-^OLOMivj

10 15
TIME. -- S ECS

Figure 2.9: Conveying Force Results for Millet [ Roberts, (1966) ].

Figure 2.10: Rademacher Wall Friction Tester.


(a) Original with Variable Transmission and Electric Motor in Fixed Position
(b) Modified with Measuring A r m [ Rademacher, (1978) ].
36
GALVANIZED
STEEL BLADE

REMOVABLE
SLIDE GATE

VERTICAL ROLLER
OUDE ASSEMBLY

AIR INTAKE
SYSTEM

RUBBER PR
DIAPHRAGM

REMOVABLE
-1 SLIDE
GATE

Figure 2.11: Front View of the Coefficient of Friction Test Rig


[ Thompson et al., (1983) ].

1, 2, 3, 4 - Relative Humidity: 10.3, 15.7, 18.7 28.7 %.


Figure 2.12: Variation of Frictional Force and the Normal Load for Brown Coal
[ Berkovich, (1987) ].
37

CHAPTER 3
PNEUMATIC CONVEYING SYSTEM

3.1 GAS-SOLID SUSPENSION:


The motion of a fluid m a y occur under the influence of the force of gravity or
pressure created by an air blower or fan. In pneumatic conveying systems, the energy
expended in flow must originate from the air stream (Clark, et al. 1952).

Evaluation of system pressure drop is paramount for the determination of powe


requirements and specifications of prime movers. The total pressure drop consists of that
frictional losses due to gas flow alone and an additional pressure drop caused by the
presence of the solid particles.

Air friction is affected by the presence of solids because of the degree of


turbulence of the fluid and pressure at any point will be influenced by the presence of
solids. Furthermore, diminishing pipe cross section will be available for the air flow, if
the concentration of solids is high.

The additional pressure drop arises because energy is transferred from the ai
the particles. Firstly, to overcome the inertia and to accelerate the particles and secondly,
to compensate for energy losses occurring when particles collide with the wall or with
each other. Since the drag force on the particles is a function of their relative velocity in
the air stream, the rate of transfer of energy will be a maximum, when the particles have
to be accelerated from rest and will decrease, as the velocity of the particles increases.

The viscous forces perform friction work against the walls and in the formati
of a continuous velocity field in the flow, absorbs the flow's mechanical energy. The
motion of the fluid is therefore accompanied by dissipation of energy. Energy obtained
from the flow must be used to overcome those forces, which tend to force the solids to
the boundaries of the system. Such forces m a y include electrostatic attraction,
hydrodynamic wall interaction forces, gravity forces, etc.. If the suspension is flowing
vertically, the fluid drag on each particle must be greater than the force of gravity.

When a fluid flow acts upon a particle lying on the bottom of a pipe, three t
of particle motion are possible depending on its particle size and the mean flow speed.
38

These three types are rolling or sliding motion, separation from the flow suspension with
repeated m o v e m e n t in jumps or steady motion in the suspended state. These types of
motion characterize the mechanism of suspension and transfer of the particles. A n
excellent discussion of the flow type and phenomena in lean phase systems is presented
bySmoldyrev (1980).

In pneumatic conveying for fully developed flow in a horizontal pipe, the


additional pressure drop is essentially due to the collision between particles and the
surface of the pipewall. W h e n the moving particles collide with the wall, some of their
kinetic energy will be lost. This lost energy has to be offset by the gas in order to
maintain steady flow. Hence, the particles are conveyed colliding with the pipe wall and
assume various velocities. Large particles m a y loose only a part of their velocity at the
wall. Small particles m a y loose all their m o m e n t u m through impact and adhesion with the
wall. Moreover, elastic collisions are expected for fine particles (Boothroyd, 1969). H e
concluded that inelasticity of impacts, rotation of particles of irregular shape, influence of
velocity gradient and other factors decrease the interaction of colliding particles.

The slip velocity is caused by velocity losses due to collisions of the particles with
the wall and sliding friction between the wall and particles at the points of contact.
Interaction of the translational movement of the fluid and the rotational movement of the
particle generate a M a g n u s force. The strength and the direction of this M a g n u s force is
determined by the conditions prevailing at the point of contact and can be given by:

Fm= 0.5pfVf d3u3p (3.1)

where d = particle diameter, (m)


p f = fluid density, (kg/m 3 )
V f = superficial fluid velocity, (m/sec.)
(jop - angular velocity of particle, (rad/sec.)

The strength of the Magnus force may be important in regard to the angle of
reflection and the shape of the particle trajectory.

A sufficiently robust and accurate model to calculate the pipeline pressure loss for
dilute phase pneumatic conveying systems is presented in Appendix A for completeness.
39

3.2 INSTABILITY:
Flow instability in dense phase flow investigations were conducted by Myler et.
al. (1986). In this investigation the stability of pneumatic conveying systems in terms of
flow behaviour, choking and saltation and a linear solution to the unsteady force balance,
was examined. Subsequent observations and experimental data revealed that a wide range
of instabilities are possible in a pneumatic conveying system. For instance, as the gas
velocity decreases, the balance of forces occurs by a decrease in voidage. At a certain
instant, the drag force is insufficient to balance the force of gravity, friction and pressure
and instability occurs termed choking in vertical systems and saltation in horizontal
systems. Jones et al. (1978) compared various correlations for determining the saltation
velocity. They suggested the Rizk correlation defined thus,

R (1.1 D p+ 2.5) (3-2)


U8Sait -CgD»5
(0.1)AM D „ + 1.96

where D p = particle diameter in mm.,


Ugsait - Superficial gas velocity at saltation,
D t = Pipe diameter, to be the most accurate correlation.

The stability of a pneumatic conveying system can be described by the use of the
basic dynamic equations of theflow.The velocities of the gas and solid can be expressed
as a steady state component plus a fluctuation from that steady state that is,
U p - Up. + Op (3-3)
U g - U g . + Ug (3.4)
where U p = Particle velocity,
U g = Superficial gas velocity,
Up- = Steady state particle velocity,
U g s - Steady state gas velocity,
Up = Particle velocity fluctuation,
u g = Gas velocity fluctuation.

In terms of flow fluctuations, if the fluctuating terms decay, then the flow is said
to be stable, whereas, if thefluctuatingterms grow the flow is said to be unstable.

3.3 PNEUMATIC CONVEYING MODELS;


A literature survey summary of pneumatic conveying models is presented in
Table 3.1.
40

TABLE 3.1 PNEUMATIC CONVEYING MODELS - LITERATURE


REVIEW

YEAR AUTHOR COMMENTS

1958 Barth Proposed a model based on the forces acting on the


1959 Muschelknautz particles during lean phase pneumatic conveying. They used
a rotating disk on which particles could be dropped at
various speeds. In this way, very large angles of incidence
which occur during pneumatic conveying could be
simulated.

1965 Julian et al. Suggested that for dilute phase conveying, the presence
of solids is reflected by modification of the local turbulence
in the gas phase. This effect causes an increase in turbulent
fluctuations, mixing length and eddy viscosity and frictional
pressure drop.

1978 C r o w e et al. Developed a particle trajectory model based on treating the


particles as being equivalent to a gaseous phase. They also
developed an implicit quasi one dimensional numerical
formulation for two phase flow.

1980 Molerus Derived the energy conservation law for particle motion in
pipeline. Dimensionless equations for the additional
pressure drop in the conveying of coarse and fine powders
are derived from the energy loss between the fluid and
particle. Contributions of particle / wall friction of sliding
particles and losses due to particle / wall and / or particle /
particle collisions are included in the total pressure drop
equation.

1980 Wheeldon Analyzed the fundamental equation of motion by selecting


etal. particle velocity data from the literature and examined their
influence on particle velocity and the additional pressure
41

drop. H e has shown that the coefficient of restitution is the


most significant variable in predicting these parameters.

1984 Shen et al. Modelled the particle collisions of rough, inelastic discs
by considering the geometry of particle trajectories before
and after collision, and computing statistical averages. A
strong dependence on volume fraction was found.

1984 Michaelides Presented a two-dimensional model based on a turbulence


model. H e considered the eddy viscosity taking into account
the Reynolds stress changing with both velocity and density
gradient. A s a result of this work he calculated the Reynolds
stress according to the mixing length hypothesis.

1985 Tsuji et al. Proposed a model for abnormal bouncing and found that the
particle flow predicted by his simulation agreed with
measurements regarding particle distribution, pressure drop
and particle velocities including angular velocities. Studied
also the effects of particle size, pipe diameter, particle
density, etc.

1986 Doss et al. Formulated a model to consider wall friction for


multispecies. The expressions for the friction factor, to
simulate the effect of particle-wall interaction with a single
solid species, have been extended to model the wall shear
stress for multispecies solid-gas flows. This model can be
used to study the effect of particle-wall interactions on flow
characteristics.

1986 A d e w u m i et al. Presented a two-dimensional steady state hydrodynamic


model for vertical pneumatic conveying. They considered
viscous dissipation in terms of the gas and particulate phase.

1986 Edwards Developed a three dimensional computer model for dilute


phase pneumatic conveying in a circular pipe. This model
takes into account the particle-particle interaction and
particle-wall interactions.
42

3.4.1 PARTICLE VELOCITY:


Measurement of the particle velocity in pneumatic conveying is necessary for
evaluation of the optimum gas velocity for stable operation, system pressure drop and
the solids residence time [ Matsumoto et al. (1982)]. Unfortunately, direct particle
velocity measurement is difficult due to the complex gas-solid flow existing.

The particle velocity is governed by many factors such as air velocity, solid / air
ratio and type of solids. T h e distribution of the solids is not uniform and is changed by
the flow pattern. T h e complexity of this flow is highlighted by the particle-particle,
particle-gas and particle-wall interactions present. These individual interactions are
difficult to separate experimentally. Furthermore, knowledge of the particle velocity is an
important parameter for estimating energy requirements and frictional losses in pneumatic
conveying systems.

Boothroyd (1971) reviewed solid velocity measurement techniques. In general, he


concluded that measurement of the mass flow rates of gas and solid are simple and
accurate, but the direct measurement of solids velocity is somewhat difficult. T h e
different techniques for measuring solids velocity are summarized in Table 3.2.

3.4.2 INDIRECT METHODS:


T h e solids velocity can be determined from knowledge of the volumetric
concentration of solids in the pipe and volumetric flux of the solids. The latter quantity is
usually determined easily.

3.4.3 FIBRE OPTIC TECHNIQUE:


For the last 15 years, measurement of particle velocities using optical fibres has
been reported in the field of fluidization. This measuring method can be classified into
two types; one based on the correlation technique [ Oki et al. (1977)] and the other based
on the space filtering in which the frequency is proportional to the particle velocity
[Morikawa et al. (1986)]. Davies (1984) and Matsumoto et al. (1986) used photo-cells
based on the cross-correlation to determine particle velocities.

The method used by the author is likewise based on the correlation technique.
T h e fibre optic probe consists of a pair of bundles each consisting of small polymer
fibres. Within each bundle, three fibres are used to illuminate the flow stream and a
fourthfibreto detect the light signals reflected by the travelling particles. T h e detected
light signals are then cross-correlated to find the transit time (t m ) between the two
43

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Photographic Two photographs superimposed on same Local solids velocity Required special Jotaki etal. (1971)
Stroboscopic Method photographic negative, velocity calculated can be obtained. viewing window, Jodlowski (1976)
from the displacement of the particle in the average solid velocity
negative, stroboscope used as a light can't be determined.
source, interval being determined by a
multivibrator.

3
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Solids velocity measured by comparing Required special

"CL,

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the progress of coloured granules, frame viewing window, Reddy etal. (1969),
by frame against a metered scale. can't be used for Jodlowski (1976),
small particles owin^ Jotakiet al. (1971),
to rapid dispersion Tokar etal. (1983)
of coloured particles.

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Disturbance of flow,

E
cr

Quick Closing Valve Valves installed at two ends of the test

"ex
Technique section to hold up particles. After valves time consuming. Mehta etal. (1957),
closed, particles removed and weighed. Capes et al. (1973),
Velocity determinedfrommass flow rate Ostrovskii et al. (1976)
of solids, weight of solids and test section
length.
44
Laser Doppler Particle intercepted by a laser beam Can be used for wide Required special Riethmuller etal. (1973),
Velocimetry (LDV) with a shift in a frequency which is then range of velocities, viewing window, Birchenough et al. (1976),
related to particle velocity. calibration not expensive. Scott (1978), Lee et al.
required, accurate (1978, 1982), Tsuji et al.
results for dilute (1982), Davies (1984).
phase flow.

X
Hamid etal. (1975),

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particle velocity obtained from doppler calibration.
frequency shift of transmitted and reflected
signal.
46

detecting points and thus solids velocity can be calculated using the following
relationship.

Vs= (3 5)
h '
where L = the distance between detecting points and t m the transit time.

The size of the probe must be sufficiently small to detect the reflected light signals
from the individual particles. More complete details of the fibre optic probe used in this
investigation are presented in Chapter 6.

The advantages and disadvantages of the fibre optic probe technique will now be
briefly discussed.

3.5.4.1 ADVANTAGES:
The advantages of the fibre optic probe include:
1. It can be used for both dilute and dense phase flows;
2. L o w cost instrumentation;
3. The probe is external, readily moved to a desired position and does not induce
flow disturbances;
4. The strength of the reflected light signals can be calibrated to solids
concentration.

3.5.4.2 DISADVANTAGES:
The disadvantages of thefibreoptic probe include:
1. Limited application depending on concentration;
2. Not applicable for measuring particle velocity at the top of pipes due to the
low concentration in this location;
3. Only surface particle velocity is measured;
4. Not applicable forflowswhere in a stationary layer forms on the inside of the
pipe.

3.5.4.3 CROSS-CORRELATION TECHNIQUE:


In the correlation technique, two sensors are used to convert the random
fluctuations of a physical property of the conveyed solids into stochastic voltage signals
X(t) and Y(t). These physical properties may be for instance temperature, permittivity,
conductivity, porosity or permeability variations in the flow as detected by suitable
sensors. The variations in flow properties used for cross correlation must be of random
stochastic structure. If the distance L between the sensors is not too large, both signals
47

are very similar. Under ideal conditions they are identical and shifted by the transit time
t m of the solids from thefirstsensor to the downstream sensor.

The transit time (tm) can be found by computing the cross-correlation function
over a time period T. The cross-correlation function is defined by,

R x y (0 = Y £ X (t - x) Y(t) dt (3.6)

where t = the adjustable time delay.

It has been proved [Beck et al. (1968)] that the value of the cross-correlation
function reaches a m a x i m u m , when the delay time (T) equals the transit time (tm). Hence,
the solids velocity can be easily calculated by using eqn. (3.5).

There are many advantages in the cross-correlation method for velocity


measurement. T h e principal advantage is that calibration of sensors is not required
because the time delay is measured with reference to a crystal controlled time standard in
the cross-correlator, secondly cross-correlation rejects the effect of spurious interference
on the signals.

Bitz (1983) designed a microprocessor based correlator and in combination with


an electrostatic sensor conducted experiments to measure velocity and mass flow rate of
Coal. Recent developments in large-scale integrated circuits and microprocessors enable
simple, fast and reliable cross correlators to be designed at a cost that is acceptable for
industrial use. B y use of cross-correlation velocity and flowmeters a wide range of
industrial and environmental measurement problems can be solved (Beck, 1981).

3.6 PARTICLE CONCENTRATION:


Usually, the particle density p s of the conveyed solids is normally k n o w n and the
velocity v is calculated by one of the correlation methods. Hence, measurement of the
solids concentration C s remains. Optical, capacitive and radiometric methods have been
used for this measurement. Unfortunately, for very low concentrations capacitive and
radiometric sensors do not work properly.

The conveyed mass flow rate ms is,


m s = Ps C s A v (3.7)

The different techniques for measuring solids concentration are summarized in


Table 3.3.
48

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49

CHAPTER 4
COEFFICIENT OF RESTITUTION,
BENDS AND WEAR

4.1 COEFFICIENT OF RESTITIJTION(C.O.R.):


The theory of impact is based on the impulse-momentum law forrigidbodies. For
perfectly elastic impact of two bodies, the law of conservation of mechanical energy can
be used to determine thefinalvelocities. The resilience of a particle is defined as the
ability of the material to resist conversion of kinetic energy to other forms of energy on
impact

When the impact produces a permanent deformation, this relation can be replaced
by a coefficient of restitution, e, for the process. This coefficient describes the degree of
plasticity of the collision. Theory and experimental data indicate that a definite value for
the coefficient of restitution can't be assigned to the impact of bodies unless their size,
material and impact velocity are specified initially.

The coefficient of restitution is an important parameter in predicting particle


velocities and additional pressure drops in lean phase horizontal and vertical pneumatic
conveying. It is a measure of the kinetic energy exchange between the two bodies upon
impact and it gives a good indication of the particle-wall interaction. It is a measure of the
elasticity of collision. It is defined as the ratio of the relative normal velocity components
of the two colliding particles after impact to the normal velocity components before
impact.

(v'2n- v'ln) (4.1)


e=
( V 2n ~ V ln )

The loss of kinetic energy may be expressed by the following equation


(Konno etal. 1969),

E = -|mi(yJ-vf) + ^(cD?-cn|) ^

where m_ = mass of colliding body, kg.


Vj = velocity of colliding body before impact, m/s.
v 2 = velocity of colliding body after impact, m/s.
50

coj = angular velocity of colliding body before impact, rad/sec.


o>2 = angular velocity of colliding body after impact, rad/sec.
I = m o m e n t of inertia of colliding body, kg-m 2 .

For completely elastic collisions (e=l) there is no kinetic energy loss, whereas for
completely inelastic impact (e=0) there is appreciable loss of kinetic energy. Hence, the
values of e=l arid e = 0 denote the idealized concept of perfectly elastic and plastic
impact, respectively.

Neglecting the air drag on a falling particle, the coefficient of restitution is simpl
the square root of the ratio of rebound height to initial height.

Rebound
e=
si- h.
initial
(4.3)

Because of the scatter in the height after impact due to the irregular shape of
particles, e-values must be averaged to obtain a representative value of the coefficient of
restitution. A literature survey s u m m a r y declaring coefficient of restitution investigations
is presented in Table 4.1.

T A B L E 4.1 COEFFICIENT O F RESTITUTION -


LITERATURE SURVEY

YEAR AUTHOR MATERIAL COMMENTS


TESTED

1954 Tillet Steel balls C.O.R.impacting on Glass-0.985,


on Glass and Perspex- 0.95, Glycerol sextol
Plastic plates phthalate-0.94, Steel- 0.95; Time of
contact for 1/4 in. dia. Steel ball with
velocity of 0.9 m/sec, w h e n
impacting Perspex - 73 x 10"" sec.,
Glass- 32 xlO' 6 sec, Steel - 21 x
10"6 sec.. Typical variation with
temperature over the range 20° and
51

90° C for an 1/8 in. diameter ball


impacting on 2 in. thick perspex,
refer Figure 4.1.

1957 Adam Quartz and Lime Studied particle trajectories with pipe
materials namely Glass, Rubber and
Lead by use of high speed motion
pictures. Figure 4.2 depicts the
observed particle trajectories showing
the impact and rebound angles.

1959 Muschel- Granular Used a rotating disk technique onto


-knautz materials which the particles are allowed to
drop from a certain height (< 5 cm.).
The disc's material, particles ( > 2
m m . ) and speed (< 4 m/s.) were
changed and the rebound height,
torque and reflected angles measured.

1960 Ranz et al. Plastic, Studied particle collision of shot gun


Rubber, Lucite projected particles against a hard
surface at varying incident angles.
H e noted rebound trajectory scatter
due to impact friction and particle
shape.

1961 Macre et al. Steel, Glass, Studied the effect of the coefficient
Poly styrene, of restitution for various materials as
Phosphor a function of height, refer Figure
Bronze 4.3.

1970a Matsumoto Glass beads Simulated irregular bouncing model


1970b etal. of ellipsoid particles and found e =
0.97. Found from experiments using
photographic techniques that particles
flowing in the duct were rotating at
high speeds of 1000 r.p.s. or more.
52

Presented an alternate model based


on wall roughness.

1970 Maeda Polyvinyl Used photographic techniques to


etal. Chloride and study particle trajectories of both
Polyethylene 150 n m m e a n size polyvinyl chloride
particles and 100 |im mean size
Polyethylene particles impacting flat
plates at 20° and 10°, found that
particle-particle collisions seldom
occur and if they collide with each
other the m o m e n t u m losses are
negligibly small.

1976 Matsumoto Ellipsoid Simulated in a circular pipe in terms


etal. particles of concentration distribution, particle
velocity, additional pressure drop and
frequency of particle collisions with
the pipe wall.

1978 Tsuji et al. Coarse particles Calculatedfrictionloss due to


collision of the particles with the
pipe wall using the impulsive
equations.

1978 Scott Rubber Used rotating disk technique, drop


pellets height 100 m m and impact impart
Aluminium. Observed e= 0.8 and
f = 1.5 (±0.5).

1980 Tabakoff Quartz and Used a Laser Doppler Velocimeter


coal ash (L.D.V.) system, particles of 0.5 to
60 particles microns in size colliding
with Aluminium, Stainless Steel and
Titanium alloys plates. Measured
normal and tangential components.
Concluded that the coefficient of
53

restitution for particles below 30


microns in size can only be measured
with a L.D.V. system.

1980 Brauer Steel Used photographic techniques to


particle observe Steel 6 m m . spheres
impacting on various wall materials,
refer Figure 4.4. Found that for the
twelve different wall materials tested,
the coefficient of restitution generally
decreases, with increasing impact
angle, refer Figure 4.5.

1981 Sabbaghian Coal Studied effect of angle of impact,


particle size, particle concentration
and shape impacting on Stainless
Steel.

1981 Ottjes Polypropylene Developed a detector to measure


Steel and Rubber particle / wall collisions in a
pneumatic conveyingrigand
expressed collision measurements
in terms of pressure loss.

1982 Ottjes Polypropylene, Used a rotating disk technique, disk


Nylon and diameter of 0.3 m. and speed of
Rubber 2990 r.p.m., e= 0.6 with a standard
deviation of 0.2 for impact velocities
in the range of 1.2 - 2.5 m / s . ,

/
1987 Devas within Sand Used a sand-shot blasting machine
etal. ( < 400 n m ) impact on a mild steel
plate, velocity 68 - 92 m / s., impact
angles 30° and 40°.
54

0-95
e
0-9

Temperature (°c)

Figure 4.1: Variation of the Coefficient of Restitution of Perspex with Temperature

[ Tillet, (1954) ].

100 m m
Materials:
Fbrticle /Pipewal
Quartz /Glass

Lime A3 lass

Lime /Rubber

Quartz/Lead

Figure 4.2: Particle Trajectories for Quartz and L i m e Impacting

Various Pipe Materials [ Adam, (1957) ].


10 "•«---rc—o Steel
-Q--
c •-• • -a- GJQSS_tQ
+
o --
~ 0-9 V--...^
in
ff
0-8
" ^ - r .
.. Polystyrene

Phosphor bronze
.!§ 0 7 "* *—-.-„
--x-
o
ri-

8 0 6

0-5

12 18 2-, 30 36
Height of drop, (inches)

Figure 4.3: Variation of Coefficient of Restitution versus Impact Height


[ Macre, (1961) ].

-P- i

Figure 4.4: Test Rig for Particle / Wall Collision [ Brauer, (1980) ].
56

1.0

0.8

i
3*
H
CJ

? 0.6
,4*
.U
QJ
O
<J
C
.g

a?
0 IS 30 iS 60 75 90
impac zngte a, ["}

Figure 4.5: Variation of Coefficient of Restitution versus Impact A

[ Brauer, (1980)].

4.2 BENDS:
4.2.1 INTRODUCTION:
Bend geometry has a strong influence on the performance of a pneumatic
conveying system. Space limitations usually make the use of bends essential in
pneumatic conveying. The usual method of calculating energy losses in bends for single
phaseflowis to obtain a factor by which the diameter of the pipe is multiplied to obtain
an equivalent length of straight pipe. Due to convenience, this method has been
extrapolated to two phase flow.

In general, visual observation of powder flow in bends reveals that


flow occurs: in the first powder slides around the outer radius of the bend at a slower
velocity than the conveying gas, whereas, in the second the powder makes a number of
collisions in traversing the bend. The particle trajectories between the particle-wall
impacts are sometimes reported as straight lines andfrequentlyas distinct curves. The
flow pattern in bends is complicated by secondary flow of the conveying gas induced by
centrifugal effects. Twin eddies are formed in the radial plane and in combination with
the main flow creates a double spiral motion downstream. Deceleration and acceleration
of the powder occurs as well as segregation of the powders by the sliding and erosion of
the pipewall. Hence, the pressure loss across bends is larger than that across an
equivalent length of straight horizontal pipe.
57

4.2.2 TYPES OF BENPS;


Bends in pneumatic conveying systems usually have the following forms.
1. Long radius bend - Most widely used
2. Short radius bend - Available as a standard
3. Blinded Tee bend - Excellent wear properties
4. W e a r back bend - Commonly accepted method of reinforcing a bend
5. Impact bend - High pressure loss
6. Vortice Elbow - Lower pressure loss

A complete discussion of the flow mechanism in the various bend types,


geometries and their application is presented by Hilbert(l--83). A summary of this
discussion is presented in Table 4.2.

To reduce the extent of erosion in bends various wear prevention techniques are
employed. C o m m o n wear prevention techniques include bend lining materials, bends
with drop out boxes, etc.. Lining materials used to date include various refractory
materials, ceramics and epoxy resin mixed with high abrasionfillers.Various bend
geometries and types commonly used in pneumatic conveying systems are shown in
Figure 4.6.

4.2.3 PRESSURE DROP CORRELATIONS:


Ito (1960)reporteda suitable correlation for the long radius bend as,
/2RBV>-9
A _ 0.248 a i - p -
A
PB V D — (4.4)
A C ., 2 r, 0.2
0.5 p f vf Re

-1.96
f2R B
where, a = 0.95 + 17.2 (4.5)
ID
R e = Reynolds number,
pf = density of gas, and
Vf = gas velocity.

Schuchart (1968) evaluated an experimental correlation on pressure losses in


bends as,
APB (2RBV115 ,.,.
Apst = 210K—-=.
D (4.6)
58

J-l
CO .2? -_0
9 ie •S
CO
(SO
o
E .S 53 §
co •a
i* Sj>
60

s J
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59

Wear Backed
Long Radius Bend

Long Radius Bend

^
Short Radius Bend
Impact Bend

Blinded Tee

Vortice Elbow

Figure 4.6: Examples of Bend Geometries [ Arnold, 1989 ].


60
where A p B = pressure drop in a bend conveying powders,
A Pst = pressure drop of solids of an equivalent length of straight pipe,
R B = radius of curvature of the bend, and
D = diameter of the pipe.

For fine particles, Muley et al. (1982) developed an experimental correlation as,

A P
bends 1_,7f2RBy0-64
— —_i3S7[—) (4.7)
r
^ st. pipe >

Mason et al. (1973) data on the flow of fine particles 15, 40 and 70 micron in
diameter through long radius bends having a diameter ratio D B / D of 20 found that
existing bend pressure drop correlations overestimate the pressure drop.

Scott (1977) suggested a simple approach to evaluate the overall system pressure
by treating the flow as fully accelerated flow and then to add an appropriate additional
pressure drop for each bend. This extra pressure drop arises from the need to reaccelerate
the solid particles after they have been slowed d o w n by the bend.

Alternatively, to estimate the bend pressure drop the concept of an equivalent pipe
length, using factors derived from experimental work can be used. In this procedure the
pressure drop is expressed as,

(48
Apt>= 2 >
where p s = density of the gas / solids suspension,
k b = a coefficient,
Vf = gas velocity.

TABLE 4.3: BEND PRESSURE-DROP FACTORS FOR USE IN


EQUN. (4.8)

Bend ratio (= 2 x radius of bend/ diameter of pipe) Bend pressure-drop factor k b

4 1.50
8 0.75
12 0.50
61

From the Table 4.3, it can be seen that, in general, the sharper the bend radius,
the higher the pressure loss. Unfortunately, the information presented in Table 4.3 is
particular to a specific experimental set up and hence application of the bend pressure
factor presented to other application situations is limited.

In another experimental investigation, Hilbert (1983) compared the service


between blinded tees and long radius bends, when conveying zirconium sodium. His
findings are summarized in Table 4.4.

T A B L E 4.4: SERVICE LIFE O F L O N G RADIUS BENDS


A N D BLIND TEES C O N V E Y I N G ZIRCONIUM SODIUM.

Bend Type Service Life (Hrs.)

Long radius R/D = 8 8


Long radius R/D=12 14
Long radius R/D= 16 15
Long radius R/D= 24 26
Blinded Tee 487

4.3 W E A R A N D ABRASION:
It is generally considered that wear in pneumatic conveying systems is largely
dependent on material, hardness, particle size and concentration. Furthermore, wear of
pneumatic conveying lines is aggravated by the following factors:
1. High abrasiveness of conveying material;
2. Inadequate selection of conveying equipment;
3. Poor pipeline design;
4. Excessive conveying velocity and
5. Inadequate pipeline installation.

To decrease the degree of abrasion in a pipeline, the following is recommend


(Stankovich, 1985):
1. Use dense-phase pneumatic conveying systems where possible and applicable.
2. Use the lowest possible conveying velocities consistent with transportation
limits. The need to operate conveying systems at the minimum transport velocity
is apparent from the following simple abrasive wear correlations,
Abrasion W = k v 3 for straight pipelines (4.9)
62

and W = k- v 4 for fittings, (4.10)


where k and kx = coefficients related to the material conveyed and pipe
characteristics (material, hardness) and v = the conveying velocity.
3. Use continuous conveying (e.g. double blow tanks) whenever possible and
practical to eliminate the filling and pipeline purging phases of the conveying
cycle. It is found that most pipeline abrasion wear occurs during these phases of
the conveying cycle. In particular, it is usual to observe very high transient
transport velocities during these phases.
4. Use purpose designed abrasive-resistant pipes and fittings m a d e of abrasive-
resistant iron and steel alloys, ceramics, with wear-backs, replaceable back bends
with longer ends to remove their joints from wear impact zones as m u c h as
possible and practical.
5. Use larger size pipe and fittings at the pipeline terminal than that for the main
pipeline section to minimize the effect of the terminal velocities caused by air
expansion,
6. Whenever possible and practical, use a smaller pipe size to minimize the effect
of material pulsing and minimize flow instabilities.
7. Properly support all pipe joints and fittings to avoid vibrations and pipe
misalignment.

4.4 ATTRITION:
Particle attrition generally arises from mechanical forces, thermal forces, chemical
stress or pressure changes between the inside and outside of particles. The attrition is
caused by collisions between particles and collisions between particles and the pipe
walls. A s the particle velocity increases, the degree of fragmentation of the particles also
increases. Attrition is manifested through particle size reduction and particle shape
deformation (Bridgewater, 1987).

First order kinetic formulations for this phenomenon have been reported in the
literature. The rate of loss of material in a certain size interval is proportional to the
amount of material in that size-interval. However, this is not generally true. G w y n
(1969) suggested a time dependent formulation for attrition to be,
W = ktm (4-n)
where W = the weightfractionattrited,
t = the time,
k = a constant and is a function of the initial particle size, and
m = an exponent.
63
H e found the value of m to be about 0.46 for the catalyst particles used in his
experimental investigation. Variables affecting particle attrition, different methods of
assessment for particle attrition and types of attrition tests are shown in Tables 4.5, 4.6
and 4.7 respectively (Bemrose et al., 1987).

TABLE 4.5: VARIABLES AFFECTING ATTRITION

Particle properties Environment properties

Size Time
Shape Velocity
Surface Pressure
Porosity Shear
Hardness Temperature
Cracks Micro structure

TABLE 4.6: ASSESSMENT OF ATTRITION

Individual particles Group of particles Bulk material

Particle shape N u m b e r concentration Settling density


Particle size Surface area Tap density
Particle size distribution Flowability
Indices: Packing index
Attrition index Angle of internal
Hardgrove index friction
W o r k index
Elutriation rate
Breakage and selection
functions
64

TABLE 4.7: TYPES OF ATTRITION TESTS

Single particle Multi-particle Possible tests


(Fragmentation) (Fragmentation
and abrasion)

Crushing Fluidizedbed Chemical reaction


Impact Shear cell Pressure change
Rotating drum Heating
Grindability Fluid Transport
Vibration
Drop shatter
Paddle wheel
Enhanced sieving

F r o m the various research work conducted on attrition, it can be concluded that


1. It increases if the particles are subjected to impact.
2. It is m a x i m u m at particle to surface impact angles of 30°-50° from the plane
of the surface.
3. It occurs mainly from breakage of the coarser particles.
4. The rate of attrition for spherical particles is approximately one-half of the
rate for nonspherical particles. In particular sharp, angular particles erode
more than do rounded particles [ Tilly (1969)].

The impaction of particles onto components of the pneumatic system results in


contamination and attrition of the conveyed material. Powder attrition can cause problems
due to changes in particle shape and particle size distribution which effect flow
characteristics. Plant operating difficulties are experienced because of the fines produced,
particularly with filtration equipment. In the latter equipment thefiltercloth and screens
tend to block due to the high flow rate of fine powder. This increases the pressure drop
across the filter reducing the pressure drop available for conveying. These effects
combine to reduce the conveying rate. Therefore, it is essential that powder attrition be
minimized.
65

Properties of materials like internal angle of friction, particle size distribution,


shape, surface area, bulk density and minimum fluidizing velocity change due to
attrition. Loss of material occurs due to change in particle size which, in turn, generate a
dust pollution problem. Sometimes this fine material can be recovered and recycled by
agglomeration into large particles.

Attrition can be minimized by operation at minimum transport velocity, the use of


streamlining the system and elimination of unnecessary components and bends, smooth
internal surfaces and gradual change of internal cross sectional areas and the
maintenance of high system pressure.

4.5 PIPING:
The correct installation of piping is most important and where possible
misalignment should be avoided. Furthermore, the pipe should be free from blemishes
and be undented. Obviously, any irregularity in the piping will promote wear in that
particular area.

In dilute phase systems and dense phase systems it is normal to use standard
medium gauge or steam piping. The c o m m o n methods for connecting these pipes include
welding, slip-on couplings and screwed flanges. Compression-type sleeve coupling
allow easy rotation to equalize wear. They are often butt-welded. However, although
convenient welded pipe joints are undesirable, especially if maintenance woi*. is
required on a particular section of pipe. Typical details of surface roughness and piping
materials are presented in Table 4.8 and Table 4.9, respectively.

TABLE 4.8: SURFACE ROUGHNESS OF VARIOUS PIPING


MATERIAL

Material Surface roughness m m .

Concrete 0.3-3
Cast Iron 0.26
Galvanized Iron 0.15
Commercial Steel 0.045
Wrought Iron 0.045
Drawn Tubing 0.0015
66

TABLE 4.9 - PIPING MATERIALS

PIPING M A T E R I A L CHARACTERISTICS A N D
APPLICATIONS

Seamless mild steel Rust contamination, Commonly used except


in the food industry

Stainless steel Corrosion resistant material, Used for


chemically active material like food
substances, plastics,resinsand similar soft
materials.

Carbon steel Suitable for inert materials, ductile,


weldable, cheap.

Spun sand cast chrome iron alloy Used for ash handling

Plastic Suitable for food substances and/or


chemically corrosive materials. Less wear
compared to steel and rubber-lined pipes.
Disadvantages are high cost, problems of
static charge generation and inability to
withstand high temperature.

Glass Chemical resistant, clean and transparent

Carbon-based antistatic plastic Used essentially to combat the static


electricity problem.

Rubber, various rubber G o o d abrasion and impactresistance,but the


compounds disadvantage is a highfrictionalresistance;
Synthetic rubber has wear resistance
comparable to natural rubber. Used for
67

bends and flexible situations and for long


horizontal / vertical runs.

Pipe lined with ceramics Developed essentially to provide long service


life, highly wear resistant.

Pipe lined with Alumina oxide Developed to withstand high temperature


and impact ceramics.

Silicon carbide ceramics lined These pipes are suitable for fine, extremely
abrasive particles, however these pipes are
expensive.

Basalt lined pipe High resistance to sliding wear and erosion.

Shot blasted Aluminium Used in the plastic industry for good wear
characteristics and ehmination of electrostatic
charges due to high conductivity. Light
weight.

Special pipe lined with Ideal wearresistance,commonly used in the


Asbestos-cement cement industry.

Abrasion-resistant lining special Used for very abrasive conditions


pipe
68

CHAPTER 5
POWDER PROPERTIES

5.1 INTRODUCTION;
T h e following properties should be considered to ascertain or predict the flow of
powders in pneumatic conveying systems:

1. Particle Properties 1.1 Solid


1.2 Surface
2. Bulk or Particle Assembly Properties 2.1 Assembly Characteristics
2.2 Interparticle Forces
2.3 Particle Property Distribution
3. Fluid Phase Interactions 3.1 Fluid Properties
3.2 Individual Particle
Interactions
3.3 Bulk Interactions
4. Synergetic Properties 4.1 Flowability
4.2 Slugging andDuning
4.3 Segregation
4.4 Electrostatic
4.5 Explosibility

Obviously, these properties interact with each other in a very complex manner to
generate actual powder pneumatic conveying flow characteristics. Unfortunately, the full
description and analysis of the forestated powder properties is beyond the scope of this
work. In view of this difficulty, brief details of the salient powder properties effecting
pneumatic conveying flow characteristics is n o w presented. M o r e complete details of the
powder properties and their assessment is presented in Appendix 'B'.

5.2 SALIENT POWDER PROPERTIES:


Table 5.1 provides a list of the salient powder properties effecting powder flow
and Table 5.2 presents the powder properties assessed in Appendix 'B'.
69

TABLE 5.1: SALIENT P O W D E R PROPERTIES

1. Individual 2. Bulk 3. Fluid Interactions 4. Synergetic

Particle Properties

1.1 Solid 2.1 Assembly 3.1 Fluid Properties 4.1 Flowability

Hardness Characteristics Buoyancy Force 4.2 Slugging &

Attrition Packing Viscosity Duning

Degradation Porosity Surface Tension 4.3 Segregation

Porosity Bulk Density Compressibility 4.4 Electrostatic

Size Compressibility 3.2 Individual 4.5 Explosibility

Coefficient of - 2.2 Interparticle Force Particle

Restitution Internal & Wall Friction Interactions

Elasticity Agglomeration Drag Coefficient

Abrasion Contact Stresses Turbulence

Combustibility Shear Strength 3.3 Bulk Interactions

Fabric Yield Strength Permeability

Shape Cohesion Moisture Content

Structure Angle of Repose Flow Resistance

1.2 Surface Tensile Strength Deaeration

Surface Energy 2.3 Particle Property -

Surface - Distributions

Electrostatic Flow Capillary -

Surface Profile Distribution

Surface Area Distribution of Solids

Roughness Particle Size Distribution

Void Space Distribution

Contact N o . Distribution
70

1 oc (N cn >-0
CQ CQ
i p-lB CQ CQ

5-
r-H

_ o

1.9 c

m
&

a
5.
I eU
sin
trQ
Cfl B
.S e- -ir-rl

w <P oQ C-H
HH > rC
B
H §
Pr. B
u -a
(U
•S
cd
C-r
1.
-- c«
•> <->
Cr c/5

o l-H r (U u
r-S S3, g e
Om CM o OH
PH
X US ! fix *>
w § V. 5P r
Q 3 rr §
Sr,
a U '3
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EM
« -a
1/3 TZT
cu
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-J
<+-i J-5
CQ

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*-> oi o>
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ln -oa
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.a i R -S
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B
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e 5
w
3
71
Depends on particle size, shape and effect of
consolidation.
.—i
i—1

i
CQ

Compressi- Describes the variation of bulk density Indicates indirectly particle size distribution, powder
bility with consolidation. packing, particle hardness, surface area.
pd

CO
ti
IT}

Describes the spatial arrangement and Influencesflowability,packing and interaction with


•s

1
orientation of the particle matter. fluid flows.
Difficult to measure.
PQ
"ft
T—1

Intraparticle porosity describes the void Influence the moisture adsorption characteristics, the

i
PL,
space within individual particles, whereas relative density of particles and flow behaviour.
interparticle porosity describes the void
space between particles.
i—i

CQ

B
"fr

OH

Refers to the arrangement of particles Influences the particle density, interparticle porosity and

(JO
within the powder. permeabihty.
1
CQ

Interparticle Caused by molecular, capillary, electrical Determines a powder's cohesive properties, extent of
Forces and coulomb forces. Difficult to isolate. adhesion of particles on the pipe walls and
agglomeration characteristics.
72
Angle of Describes the angle of incUnation of the Used to indicate the flowabiUty of a powder. Varies with Table 5.4 B.17
Repose powder free surface when poured onto the particle size, shape, degree of segregation and and 5.6 (a.l)
aflatsurface. aeration,moisture content, cohesion, intemal friction and
compaction.
CO
CQ

H
i-H
1—1
oo

ett

Tensile Is the minimum force required to separate Used to measure the degree of cohesion and
Strength a powder bed and is a fundamental failure agglomeration of powders.
property.
CQ
/ - r \

Internal and Internal friction determines the shear Friction angles are important in the design of powder Chapter
WaU Friction resistancewithin powder beds, whereas storage,handUng and transportation equipment Depends 2.5
waU friction determines the shear on particle size, tensile strength, cohesion, shape, surface
resistance between the powder bed and properties and bulk density.
the container waUs.
p
<—1
Xi

CQ

P
Determines type of system, feeder type and dimensions

CM

U
>i-H
g
r-;

Defined as the molecular attraction by

o
which particles of a powder are held and need for discharge aids in bins and hopper.
together. Paramount in regard toflowabiUtyof a powder.
i—i

CQ

'

p
Used for measuring surface area of the powder. Strongly

Om
Describes the extent of fluid flow through

£
•a
a powder bed. influenced by porosity of the powder & particle size
distribution.
73
74

ON rH
1—1
tN
PQ CQ

u
r-i
Os
wn </"i
rH p
x> rQ
c. C-
H H
>>
<->
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-B
rO
CM

"3
CM
•B 9„
«-N S-P
P
o
r H

33 a" V
rB P
S3
bfl

*- <_. B
trO -B .3
1 8
Powders c be classified accon
behaviour to free-flowing and

I to
B
•rH

g >^
•B P 1
o
e
TJ
p
rB
3 •-* •+-1
43 D
CX
O p
CM
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CM
§ B
rH
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l cd
&

6 •*-»

5
T3 P •a
p
2 bO
P CM .S .3
n of a settl
d like mas

CM
3
ca
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6
P .3
w.

B
2 3 o -8 *->
2p
S aed rp-T
H
§ Q
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*->
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•a
l B ^ "8 1
i. fe 5-
Sr ^ 3 CM P 'S
•S € "2
S "a9 8
P
B

1 I
1E P
l"
75

TABLE 5.3: MOHS' SCALE OF HARDNESS

M o h s Scale Material Explanation


Hardness
1. Talc Very soft, can be powdered with the fingers
2. Gypsum Moderately soft, can scratch lead
3. Calcite Can scratch a fingernail
4. Fluorite Can scratch copper
5. Apatite Can scratch a knife blade with difficulty
6. Feldspar Can scratch a knife blade
7. Quartz
8. Topaz All products harder than
9. Corundum Feldspar will scratch glass
10. Diamond

TABLE 5.4: THE GENERAL RELATIONSHIPS BETWEEN


ANGLE OF REPOSE AND THE FLOWABILITY OF MATERIALS
[Carr, (1976)]

Angle of Repose Characteristic of Material

25-35° Very free-flowing; noncohesive; for granular material


25-35° Veryfloodabletofloodable;for fine powders
35-45° Free-flowing; some cohesiveness; for granular material
35-45° Fluidizable powders; some cohesiveness
45-55° Non-free flowing; cohesive ,
55-65° Very non free-flowing; very cohesive /
65-75° Very, very, non free-flowing; very, very cohesive
TABLE 5.4: PARTICLE SHAPE AND FLOW CHARACTERISTICS

TERM MEANING FLOW


CHARACTERISTICS

Acicular Needle shape Poor- interlocking


Angular Sharp edged or having Fair
rough polyhedral shape
CrystaUine O f geometric shape, freely Fair - poor
developed in afluidmedium
Dendritic Having a branched Poor - interlocking
crystalline shape
Fibrous Regularly or irregularly Poor - interlocking
threadlike
Flaky Platelike Poor - extreme interlocking
strongly anisotropic
Granular Having approximately Good to fair
equi-dimensional,
but irregular shape
Irregular Lacking any symmetry Poor
Nodular Having a round, Fair
irregular shape
Spherical Globule shape Good
TABLE 5.6 ANGLE OF REPOSE - LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1952 Dawes Reported angles ofreposemeasured for cohesive powders


including coal and siUca sand using afixedcone method.
Observed the angle to be 50° or more at a mean particle size near
100 [tm. Furthermore, observed variation of angle of repose with
tensile strength.

1958 Train Used four methods to measure angle ofreposenamely fixed


height cone, fixed base cone,tiltingtable and rotating cyUnder.

1960 Zenz et al. Determined angle ofreposeof a wide range of different materials.

1961 Brown Reported that the variation of angle ofreposefor materials of


different particle size increased with increased cohesion.

1967 Bruff et al. Used a conical funnel of ^0 cm. long to measure the poured angle
ofreposeof anthracite in various gas media. Observed that in
hydrogen, (low viscosity) the angle of repose was highest and
equal to 31°, in carbon dioxide (medium viscosity) the angle was
smaller, while in air (high viscosity) the angle was lowest. This
suggests that at higher gas viscosity, anthracite has a tendency to
spread, whereas at low gas viscosity, it settles rapidly.

1974 Fryman Measured the poured angle ofreposefor potash peUets and
suggested to increase the angle by preventing rolling of the
particles in the top layer and use of a light spray of water to the
surface.

1976 Cartensen Reported arelationbetween particle size and angle ofreposeof


etal. powders consisting of mono sized cohesive spherical particles.
The angle ofreposewas observed to decrease with increasing
particle diameter. H erelatedthe angle of repose to the cohesion
force and the coefficient of internal friction.

1982 Tuzun Observed drained angle of repose for glass ballotini inflatbottom
etal. bin in the range of 35°- 45°. Suggested that for simplified bin
design the angle of internal friction bereplacedby the drained
angle of repose to evaluate the hopper half angle.

1984 Cheremi- Reported that for monosized particles or particles with a narrow
sinoff size distribution, the drained and poured angles are approximately
etal. the same, whereas, for powders with a wide size distribution, the
drained angle is higher than the poured angle.

1985 Augwood Observed the effect of aeration and deaeration on the angle of
repose. Reported that deaerated powders exhibit angles of repose
higher than aerated powders.

1985 Kalson Reported experimental measurements of the angle of repose as a


etal. function of hopper angle and of the critical drainage angle for
several granular bulk solids in a wedge-shaped hopper.

1986 Kraus Reported that the angle of repose is used for the design of bins
and hoppers and to select the type of flow inducers in a
pneumatic conveying system.

1990 Geldart Developed a tester to measure the poured angle of repose of soda
ash to assessflowabiUty.Evaluated the effect of size and size
distribution on angle of repose.
79

TABLE 5.7 COHESION - LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1957 Langmaid Performed experiments on wedge shaped and conical


etal. hoppers with non-cohesive granular material. Presented
correlations for the critical hopper outlet width and diameter.
Found variation in results due to differing material shape.

1961 Jenike Considered stability of a self-supporting cohesive arch of


unit thickness and stated that the force tending to break the
arch is due to the weight of the material within it. This is the
worst case for maintaining flow.

1963 Jenike et al. Extended the arch analysis to include the variation of
thickness of the arch.

1966 Richards Presented a summary of the equations for minimum


cohesive arch length of smooth and rough w a U suggested
by various authors. Discussed saUent features of bunker
design.

1969 Stepanoff Reported large arch lengths for cohesive powders.


Suggested scale factors for arching of the prototype and
model for the same cohesive powders.

1973 Wright Evaluated the Jenike design method by performing


experiments on iron ores using wedge shaped and conical
bunkers. Found that the Jenike method does not consider
impact fiUing.

1974 Ecknoff Compared the m i n i m u m outlet slot width and the minimum
etal. hopper wall slope for mass flow predicted by the Jenike
method to that observed in a silo with symmetrical wedge-
shaped hopper. Found that the Jenike method overdesigned
80

the critical hopper slope by 8-10° and the slot width from
0-100% depending on the extent of extrapolation of the
flow function.

1975 Jenike Suggested the m i n i m u m outlet dimension required to


maintain flow from a mass flow hopper as a measure of
flowabiUty of powders.

1966 Walker Derived a force balance of the weight of material in the arch
relative to the shear stress in the material at its periphery.

1967 Walker Arching testresultsand predictions from his theory are


shown in Figure 5.1, whereas, his results and predictions
from Jenike's theory are shown in Figure 5.2.

1975 Enstad M a d e an extensive investigation of critical hopper outlet


openings, took into account vertical pressure acting on the
arch and claims to have reduced overdesign, but still a
considerable difference was found between calculated and
experimentaUy observed outlet openings.

1982 Borg Calculated critical arching outlet diameters for many


powders of varying degrees of cohesiveness. Studied effect
of time consolidation, moisture, temperature, particle size
on critical arching diameter.

1982 Molerus Reviewed flow behaviour of cohesive materials. Used a


centrifuge bunker to study critical outlet ciimension
requirements. Found that the initiation of flow depends on
previous consolidation.

1983 Yamashiro Studied compressibility,fluidityand cohesion of single and


etal. mixed powders using a K Y T - 1 0 0 0 commercial tap density
meter.

1984 Geldart et al. Suggested that a smaU change in particle size and other
parameters which affect interparticle forces can transform a
81

free flowing powder into a cohesive one. This property was


assessed by measuring the ratio of tapped to aerated bulk
density.

1984 Piepers et al. Measured the cohesion constant of the powder using a
tilting bed technique, theresultsfrom whichrevealedthat
the cohesion constant increases with increasing pressure
and dependence of pressure was observed with the
increasing bed expansion, adsorption of gas to the soUd
and the increasing elasticity modulus.

1985 Scott et al. Studied the effect of moisture, clay content and chemical
composition on cohesive critical arch dimensions of a
steaming coal.

1985 Novosad Developed an arch tester to measure critical outlet openings


etal. in mass flow hoppers. Indicated that the overdesign in the
Jenike method is due to extrapolation of the flow function in
the design process.

1987 Reinhold Applied statistical powder theory to arching by calculating


etal. arching probability.

1987 Luqing et al. Analyzed the pressure drop in horizontal plug pneumatic
conveying for both cohesive and non-cohesive powders.

1988 Knight Measured the powder cohesive strength of five different


etal. powders ranging from slightly cohesive to highly cohesive
with a penetrometer and compared results with cohesive /
strength measurements obtained using a shear ceU. /

1988 Aziz et al. Observedfinecohesive coals conveying in half or full plug


forms depending on gas velocity and plug length.

1990 BeU Discussed the effect of cohesion, moisture content,


permeabiUty, airretentionand other powder properties on
pneumatic conveying system design.
82

T A B L E 5.8 TENSILE S T R E N G T H - LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1952 Dawes Used a spUt-glass plate technique to measure the tensile


strengths of cohesive powders.

1970 Rumpf Suggested a model for tensile strength of soUds arising out
of the forces acting between individual particles in terms of
mean bonding force at contact points, void fraction and
particle diameter.

1964 Ashton Developed a basic tensile tester driven by a motor with


etal. constant speed with notiltingof the specimen. A probe is
attached that stops the motor after the ring has traveUed a
certain distance,referFigure 5.3. This reduces the problem
of visually observing whether the sample has sheared or
not The tester was used in conjunction with the Jenike
Direct Shear Tester to examine, for a number of powders,
that the yield loci, at constant bulk density, follow the
proposed power law relationships with the applied
compressive stress. H e found that the tensUe strength
increases logarithmically with packing fraction.

1965 Farely Presented a design method to calculate slot outlet opening


etal. for arching and rathoUng from data obtained by use of the
Tensile Tester and Jenike Direct Shear Tester. They
developed a yield locus equation and measured the tensile
strength of different plastic materials.

1973 Stainforth ! Evaluated four constants to describe flowabiUty of powders


etal. based on the Warren Spring Yield Locus equation (refer
Ashton et al. (1964)).

1973 Kocova et Conducted tensile and shear tests on narrow size fractions
al. of powders and mixtures of different size fractions.
83

Evaluated parameters for both types of powders to study


flow and failure properties.

1974 Turner et Performed tensile strength experiments on dry small


al. spherical glass beads. Found that the particle-particle bond
strength for a cubic packing from R u m p f s model is
approximately 1 p:N. This suggested that the bond strength
developed by van der Waals forces, electrical forces and
capiUary forces were smaU compared to mechanical forces
like friction, interlocking and arching.

1975 Molerus Assumed the stress force relation expressed by R u m p f only


appUes under isotropic or hydrostatic pressure conditions
and applied this conclusion to the analysis of the shearing
mechanism. Furthermore, he extended the analysis to
predict the yield locus of cohesive powders.

1976 Turner et Measured tensile strength of limestone powder using the


al. Shinohara and Tanaka compaction ceU and the Warren
Spring Laboratory Tester. Presented the results in terms of
the void fraction and moisture content of the sample. Found
the tensile strength is dependent on the particular properties
of the tester.

1978 Eckhoff et Combined tensile strength data of powders and failure loci
al. from Jenike Shear Tester Cell tests. Reported that tensile
strength results are not sufficiently accurate and
considerable over-designresultswith the Jenike theory in
regard to arching.

1982 Yokoyama Reported a dimensionless number expressing the ratio of


etal. the cohesive force to the gravity force on a single particle
and related this number with the floodabiUty index evaluated
by Carr's method. This indirectly suggests that tensile
strength is related to particle size. Powderfillingwas
effected by a spatula and a 10 minutes deaeration time was
allowed.
84

1983 Chen Investigated the tensile strength of both single powders and
etal. binary mixtures. Developed equations whichrelatetenstte
strength, particle size parameters and the composition of
binary mixtures.

1984 Tsubaki Indicated that therelationshipbetween tensile stress and


porosity should be a straight line on a serm-logarithmic
paper. Presented expressions for the tensile strength and
consolidating pressure in terms of porosity and provided an
excellent review of powder bed mechanics.

1984 Tsubaki Proposed experimental equations to correlate the tensUe


et. al. strength of a powder bed measured by spUt-ceU methods
with powder bed porosity. Found that the pre-compressive
force at the interparticle contact point effects the tensile
strength more strongly than porosity.

1986 Terasbita Conductedflowabilityassessment of dry and wetfinecoals


etal. by evaluating powder properties namely intemal friction,
cohesion and tensile strength. Found flowabiUty can be
more readily and accurately assessed by tensile strength and
cohesion compared to the assessment using internal friction.
In particular, he measured the tensile strength by use of a
hanging-type cohesion tester. Assessed theflowabilityof
fly ash to be higher than that exhibited by fine coal. They
stated the lower values of internal friction factor and tensile
strength offlyash m a y be due to the loss offixedcarbon
and volatile matter and the sphericity offlyash particles
resultingfromhigh-temperature combustion. H e found that
the tensUe strength offlyash increased dramaticaUy with a
slight increase in water content. This highlights that the
flowabiUty offlyash is effected by environmental humidity.

1988 Nikolakakis Studied the effect of particle shape and size on the powder
etal. tensile strength and proposed correlations of tensUe strength
in terms of particle shape, particle size and packing
fraction.
85

TABLE 5.9 FLUIDIZATION - LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1973 Geldart Developed a classification system for the fluidization


properties and behaviour of particles, refer Figure 5.4.

1979 Dixon Developed a slugging diagram for different pipe diameter


systems based on the Geldart's fluidization diagram.

1982 Molerus Proposed a similar classification to that of Geldart.


Attributed the differences in behaviour between Group A , B
and C powders to the relative magnitude of adhesive forces
between the particles dominated by local deformations of
the contact areas. Treatment in terms of adhesive forces
constitutes a quantitative justification of Geldart's
boundaries. Deduced a combination of the variables
defining lines of similar slope working backwards
from Geldart's laboratory scale observations.

1982 Obata et al. Reported a method of particle size distribution measurement


for binary and tertiary mixtures using information from a
fluidization curve.

1984 Zenz Reviewed the classification suggested by Geldart in


relation to solids incipient fluidization velocity, solids
surface tension, solids viscosity and the powderiness
i versus granularity classification.

1984 Rietema Presented Geldart's classification of A , B and C powders in


dimensionless form by the consideration of the parameters
of cohesion, gas viscosity and gravitational acceleration.

1988 Kretschmer Reported experimental data on fluidization and correlated


this with dense phase pneumatic conveying characteristics.
86

Presented expression for flowability in terms of potential


and kinetic energy.

1988 Clark et al. Suggested a numerical representation to Geldart's


classification of powders by assigning arbitrary
classification numbers and correlated with Geldart's
and Molerus powder classification.

»
87

TABLE 5.10 DEAERATION - LITERATURE SURVEY

YEAR AUTHOR COMMENTS

1953 Diekman Observed that powders exhibiting smaU viscosity (or


etal. permeabiUty) changes with deaeration display good flow
characteristics.

1972 Johanson Conducted an analysis of powder deaeration based on


etal. continuity of the gas and solids and the equilibrium of the
forces acting on the solid. They accounted for the variation
of powder permeabUity and bulk density with consoUdation,
gas compressibUity and w a Ufriction.The model was
numericaUy solved using finite difference methods with the
results presented in dimensionless form.

1973, Sutton Conducted deaeration tests by observing the collapse of a


1976 etal. fluidized powder column. In particular, column height with
time on coUapse was observed using video techniques.
Their experimentrigis depicted in Figure 5.5. B y extensive
experimental work, he classified powders according to
deaeration properties.

1977 Farley Observed the effect of deaeration on the strength of


powders. Stated that if the powder deaerates slowly, the
pressure distribution wiU be hydrostatic and decaying and
hence the containing bin walls should be designed for this /
pressure. Also, the strength of the powder tends to mcrjeiase
as it losses air.

1980 Rietema, Suggested that deaeration is slow, if the powder consists


etal. of fine particles. O n ceasing aeration, any bubbles first
leave the bed while an expanded dense phase is left At the
bottom of the bed, the relative gas flow is zero. The bed
settling starts from the base and maintains a relative gas
88

velocity at the top, where the powder is stiU fluidized.


Henceforth, a packed bed of increasing thickness is created
from the base upwards, while the total bed height decreases
and continues decreasing until the deaeration is completed,
refer Figure 5.6.

1980 Murfitt Stated two drainage mechanism namely, double drainage


etal. and single drainage. A cyUnder with an open top and a
permeable basefiUedwith powder approximates to double
drainage. Hence, if the base has lowfluidresistanceor
permeabiUty, the permeable base oase corresponds to the
single drainage case of double height They suggested that
the rate of collapse of the powder in a fluidized bed is one
w a y of measuring the rate of deaeration.

1980 Abrahamsen Used the coUapse rate technique to predict the average
etal. dense phase properties in bubbling beds of fine powders.
They also observed the effect of fines ( < 45 p.m), bed
height, distributor detaUs on fluidization characteristics.
They observed that the average dense phase voidage of
Group A powder increases as the particle density and mean
particle size decreases. Likewise the voidage increases as
thefractionoffines< 45 p>m, gas viscosity (temperature)
and gas density (pressure) increases.

1983 Dry etal. Reported bed collapse experiments using powders of


particle size 12-67 |J,m in a 140 cm. column and they found
that the dense phase voidage (for class A C powders)
depends on the extent of fines.

1984 Zenz Reported a classification of powders based on their


deaeration times for pneumatic conveying.

1984 Piepers Reported deaeration tests in which they calculated the height
etal. of the dense phase, the dense phase gas velocity and the
bubble hold up. In their tests, the powder bed was fluidized
89

for several minutes at a superficial gas velocity higher than


Ubp after which the air supply was suddenly shut off and
the bed height was found to decrease quickly to a certain
value because of the quick escape of bubbles. After this
phase, the deaeration was found to be m u c h slower. They
conducted experiments at pressures up to 15 bar using N 2
and Ar. The time and bed height were recorded on
videofilm.

1984 Geldart Reported the difference between cohesive (Group C ) and


etal. less cohesive (Group A ) powders by examining the
deaeration characteristics of powders. They observed that
by ignoring the data for the first two seconds, when the
bubbles in the bed escape to the top, less cohesive powders
deaerate at a constant rate. Whereas, the cohesive powders
deaerate faster for the first ten seconds and afterwards at a
slow rate. The powder mass then remains in a sUghdy
deaerated state for a considerable time with the pressure at
the bottom of the bed decreasing very slowly. In the case of
cohesive powder, the gas flows through cracks and
microvoids. W h e n moistioned, Group A powders exhibit a
deaeration curve sirmlar to Group C powders.

1985 Tardos et al. Observed that the pressure profiles remain approximately
the same shape throughout the deaeration process and
indicate a decreasing pressure gradient with depth below
the top surface. A typicalfilUng-deaerationcurve for the
pressure variation at the base of the hopper versus time is
shown in Figure 5.7, for a m a x i m u mfillingheight of 15
cm.. ThefiUingcurve is not smooth because inflowing
powder impacts on existing settled powder. Also, some
deaeration takes place during thefiUingphase. This non
uniform characteristic m a y also be due to sUp stick w a U
friction characteristics.

1985 Kirby In regard to pressure profiles in collapsing bed, he reported


that m a x i m u m air pressure occurs at the base, when the
90

hopper is impermeable and somewhere in the lower half for


a permeable base, refer Figure 5.8.

1985 Geldart Conducted an extensive series of deaeration tests. A typical


coUapse curve for a Group A powder is shown in Figure
5.9. Thetimerequiredfor Group A powders to deaerate is
dependent not only on the coUapse rate, but also on the
height through which the bed surface has to faU. Cohesive
powders in Group C display a different coUapse rate as
shown in Figure 5.10. For these powders, the bed doesn't
bubble evenly and bed expansion is caused by the presence
of cavities and cracks of various inclinations. W h e n the
gas supply is stopped, the large cracks close up rapidly and
further coUapse proceeds more slowly, as in the final
consoUdation stage of Group A powders. They found that
the bed height decreases linearly with the time for Group A
powders, whereas for Group C powders it decreases
exponentially.

1987 Rathone, Conducted a theoretical analysis of powder deaeration.


etal. G o o d model experimental correlation was observed
particularly for Group A powders. However, Group C
powders deviated considerably due to channeUing.
91

Predicted f r o m Walker theory


using ring cell shear strengths

Experimental results

\Y\W\
30 Experimental
\ \ \ \ \

15 Experimental
' / / /

3 4 5 6 7 8 9 10 11 12 13 14 15 16 17
% Moisture content
l.D.F coal

Figure 5.1: Critical Arching Diameters [ Walker, (1967) ].

Predicted from
36
34
32
o Jenike theory and
Jenike shear celt
Experimental
resuLts
©
30
30" No
solution
~" 26
2 24
t
v

l~
•o 2 0
cn
c 18 \\\\f A
t 16 30 Experimental
S
14
3 12
Z. 10
/////
' >15 Experimental
° 8
6 // / 7 / /
4
2

3 4 5 6 7 8 9 10 11 12 13 14 15 16 17
•/. Moisture content
IDF coal

Figure 5.2: Critical Arching Diameters [ Walker, (1967) ].


Figure 5.3: Tensile Tester [ Ashton et. al. (1964) ].

Key
Group C properties
reported
a Baerns
v Brekken et aJ
c de Jong et al
Group A properties
reported
& Baerns
a Davies et a!
a Rietema
B de Jong et ai
D Godarti et ai
« Oltrogge
* Kehoe
» de Groot
» This wcrk
Group 8 properties
reported
* de Grooi
• This work

oroep D properties
reported
x. Mathur

20 50 100 200 500 1000


Mean particle size d.v ( p m )

Figure 5.4: Geldart's Classification of Powders [ Geldart, (1973) ].


Fi«*4 sc«l«
Paro(ltl--i-<4
Conta-Mf
PeralM-sidcd (FV-poc b«U
container
l-IOJJ pifK)

P»wd*r

Sinttf«d
plastic bos*

Snt*r*4
-f aji pad

Figure 5.5: Deaeration Test Rig [ Sutton et. al. (1976) ].

(a) Before shutting of the air supply (b) After shutting of air supply

(c) Deaeration completed

Figure 5.6: Deaeration Experiment [ Rietema et. al. (1980) ].


94

D •i~- t - i — r 1- 1 T T T 1 1 1 1 1

M
5 ASSUMED PROFILE
E f\ -o- MEASURED PROFILE -
*4 •

a.
O
?4 \V
1 <5
Q 3
ill 11
1

1
EC 1
1
r . 2
1 \
UJ p
GC
"1 1
t

• s — • 1. , — . - • — i 1 1 • 1 H T - T T T V O —r-l
l-fl-'l 1 • 1
20 40 60 80 100 120 140
TIME, sec

Figure 5.7: Filling-Deaeration Plot for Zyolite Powder


[ Tardos et. al. (1985) ].

Figure 5.8: Pressure Variation in a Hopper; Permeable and Impermeable Bases


[ Kirby, (1985) ].
95

Bubble escape stage

Hindered settling
stoge; slope-U c

I ing bed<K

iSSetU

l<0 H-U

Figure 5.9: Deaerated Bed Settling for Group A Powder


[ Geldart et. al. (1985) ].

He

H.

t-0 tc

t<0 -lc

Figure 5.10: Deaerated Bed Settling for Group C Powder


[ Geldart et. al. (1985) ].
96

CHAPTER 6
TEST EQUIPMENT AND
PROCEDURES

6.1 PNEUMATIC CONVEYING RIGS:


6.1.1 STURTEVANT PULSE PHASE RIG:
This rig consists of a 0.425 m 3 Sturtevant pulse phase blow tank with a
m a x i m u m safe working pressure of 350 kPa (Figure 6.1). In addition, blow tank top air,
fluidizing ring air and conveying air facilities are incorporated
- A n electro-pneumatic control cabinet housing all the necessary control equipment for
conveyor operation (Plate 6.1);
- 7 1 m . and 61 m . total effective length of 50 m m Schedule 40 (52 m m I.D.) conveyor
pipeline (Figure 6.2);
- 3.6 m vertical lift pipe section (located 5.4 m from the blow tank outlet);
- T w o blinded-tee bends connected to the vertical pipe. In later testing, the blinded-tee
bends were changed to long radius bends and then to vortice elbows (Figure 6.3);

The blowtank has a butterfly-type discharge valve mounted at the bottom of the
vessel whic^ is supported by four shear-beam-type load cells to measure the si <ply
solids mass flow rate (Plate 6.2). In addition, the receiving hopper, which is mounted
directly above the blow tank is supported by tension load cells to monitor the rate of
solids discharging from the end of the pipeline (Plate 6.3).

The air supply consists of an Atlas Copco Model GA308 rotary screw
compressor, an S M C Model L D P - 1 5 0 S refrigerated air dryer and two air receivers
totalling 7.8 m 3 volumetric capacity. The capacity of the compressor is 3.1 N m 3 min' 1
(free air delivery) with a m a x i m u m pressure head of 800 kPa. Orifice plates with D and
D / 2 tappings (designed according to B.S. 1042 : Part 1 : 1964) measure air flow rates
during the conveying cycles.

The reverse-jet air filter consists of carbon-impregnated Goretex™ filter bags


earthed to the filter housing, a horizontal upstandfittedwith an explosion relief panel, an
exhaust fan to provide a vacuum in the receiving hopper and thefilterhousing and a
discharge duct to provide venting of any explosion directly to atmosphere.
97

Material Vent Air


Inlet
Top Air

Fluidising
Ring Air

Discharge
Valve

Conveying

Figure 6.1: Configuration of Sturtevant Blow Tank


Plate 6.1: Control Panel
A - HOPPER METER
B - BLOW TANK DISCHARGE VALVE
C - HOPPER INLET VALVE
D - FLUIDIZING RING AIR VALVE
E - AIR REGULATOR
F - CONVEYING AIR VALVE
G - HOPPER CONTROL VALVE
H - VIBRATOR ACTIVATION SWITCH
99
100

\u VORTEX ELBOW

Blind Tee

Elbow

fr Short Radius
*' »-•

Lon^ Radius

Figure 6.3: Types of Bends


101

iai»^M^g-^#/^

Plate 6.2: Blow Tank


A - L O A D CELL
102

rtJto. ----1 -l •<WUj ; ^rA

•pr^r-,F>-^-1» u t u r UtiUUhi J J
i] .^ i'jn /.Ml' !-Wi'R|l|
"... ^rSE- ' 1 '

iW*K.-'^>>'i«E-1.*.*^A*i "#""'

Plate 6.3: Receiving Hopper


A - HOPPER LOAD CELL

Material
Inlet

Top Air

Aeration
Air Low Velocity
Attachment

Supplementary Air Pipeline

Figure 6.4: Low Velocity Rig Blow Tank


103

6.1.2 L O W VELOCITY RTf>


The testrigconsists of the following components:
- 0.9 m 3 blow tank (700 k P a m a x i m u m safe working pressure) with low-velocity
attachment air to fluidize the solids as it is fed into the pipeline, refer Figure 6.4 and
Plate 6.4.
- mild steel conveying pipeline (L = 97.10 m and 51.3 m , D = 105 m m )
- six or eleven l m radius 90° bends;
-1 m 3 receiving silo;
- Atlas Copco Rotary-screw air compressor (3.1 m 3 m i n - 1 free air delivery, 800 kPa
m a x i m u m pressure head) connected to arefrigeratedair dryer and an air receiver.
A schematic layout of this testrigis shown in Figure 6.5.

The following conveying parameters were recorded using a portable HP data


acquisition system:
- blow tank top air pressure;
- two downstream intermediate pipeline air pressures;
- mass of solids discharged from the blow tank;
- mass of solidsreturnedto the silo;
- air mass flowrate via orifice plate measurements.

6.2 VELOCITY MEASUREMENT:


6.2.1 TEALGATE T.20Q SERTES TRANSDUCERS;
The Tealgate electro-dynamic T.200 series transducer is a continuous on-line
solids velocity measurement test unit. This unit is a solid state electronic device capable
of detecting the velocity of dry particulate material. There are three basic components to
the T.200 series system namely the electrode, the transducer and the display unit. The
schematic block diagram is shown in Figure 6.6.
Electrode: T h e electrode is a leakagefieldtype which forms part of the pipe wall. A
small section of the pipe wall is insulated from the main body of the pipe thereby creating
an electrode which does not interfere with the particulate material flow. The electrode
forms a complete circumferential section of the pipe.
Transducer: In the electro-dynamic transducer, the principle employed is that of
electro-dynamic induced charge, by which a charged particle brought close to a surface
induces a charge on that surface. T h e change in charge which occurs w h e n particles
m o v e through the pipe is detected. A n input capacitor acts as a charge to voltage
converter. T h e A.C. components of the signal voltage are used for velocity measurement
utilizing the cross-correlation technique. T h e material conveyed must be dry, either
conducting or non-conducting and the transducer must be free from vibration.
104

Plate 6.4: L o w Velocity Rig Blow Tank


105
106

A
r

•a

a
CO
o
li on
J-l
PP
S3
o
3
•a
ti

•g
CO
CN
H
*
o
HH-
u
Q)
CD -P
O hO U rX)
h O CO CD
U -P > it
03 rH fl
r-J O O
O > O

L_ J
107

Display unit: The display unit is housed in a self contained instrument case, which
requires a standard 240 V A.C. mains supply. The facia panel incorporates a power
supply switch and indicator, a 0 - 1 0 0 % analogue meter, a response switch, a range
selector switch, two B N C sockets and a 3.5 m m jack socket (Plate 6.5).

The T.200 transducers were separated by a distance of 70 mm, about three meters
downstream from the blow tank discharge valve and a H P 3 7 2 1 A cross-correlator is used
to cross-correlate the transducer outputs. The product of the selected time scale and the
horizontal displacement from the y-axis to the most dominant peak of the correlogram is
the transit time (t^ of the flow between the transducers. Since, the distance L between
the transducers is k n o w n the solids velocity is given by,

_. L 70 x 10~3 _! .
Vs= — = ms (6.1;

6.2.2 FIBRE OPTIC PROBE;


A fibre optic probe was developed to measure the velocity of the particulate flow
in the dilute phase conveyor system. This probe consisted of two bundles of polymer
fibres with each bundle comprising three emittingfibresand one receivingfibre.The two
fibre bundles were mounted so that the receiving fibres were 13.5 m m apart. The
reflected light signal, detected and transmitted by each receiving fibre was then converted
to a voltage and amplified in separate pin diode amplifier circuits (Figure 6.7). The
amplified voltage outputs from these circuits were then cross-correlated using a H P
3721A correlator to determine the transit time (tm) for the particle to travel the reference
distance. Since thereferencedistance was 13.5 m m , the solids velocity at the test section
is given by,

_. L 13.5 x 10"3 _i (fx ^


Vs = — = ms (6.2J
TTl TTl

Details of the probe configured in the actual rig are shown in Plates 6.6 and 6.7.
The light source used was a Tungsten Quartz Halogen 12 V , 100 W L a m p with a
operating temperature range between-30 degree Celsius to +85 degree Celsius. A lens
was used to concentrate the light. The optical fibres are 2.25 m m . in overall diameter and
1 m m . core diameter. The numerical aperture ( N A ) is 0.47 for normal use and for low
attenuation, 150 d B / k m max.(600 n m ) .
«
108

9
Ijn^o^*
wm

•'•"•;'' ,' • ..

Plate 6.5: H P 3721A Correlator connected to the Tealgate

T.200 Series Transducer


109

f7
•i
-f
A
1 * —
1
1
\
-

ri
wtbij • "ISH
MiumTmfflHwtwwvwmvv^^^
«
- ^ * -
&]&<&&ri tfiStTVQ /-—- 1

M
D
1
IffJfcJS-fc.,-', ,v%p t ^ B

:Z±':1 | IB ~ B I
fl
^ r- r
f^J

Plate 6.6: Fibre Optic Probe with HP 3721A Correlator


A - PROBE
B - HP 3721A CORRELATOR
C - AMPLIFIER
D - LIGHT UNIT
110

!>-=.'J. .

Plate 6.7: Fibre Optic Probe Located on Sight Glass

A - FIBRE OPTIC PROBE


B - SIGHT GLASS
C - MILD STEEL PIPE
D - FLEXIBLE COUPLING
Ill

1 Mil lMfl
PIN
DIODE
+15 +15
10KO. o.l u f

n> -15
h
C ^1-15
OUTPUT

10 K G
-15
VOLTS

I
Figure 6.7: Pin Diode Amplifier Circuit.

6.2.3 HEWLETT-PACKARD 3721A CORRELATOR:


The H P 3721A correlator is a digital instrument designed to compute and display
probability, auto-correlation and cross-correlation functions. The computed function is
displayed on the internal C R T using 100 points. The horizontal axis of the display is
scaled in millimeters. B y selecting a suitable sec / m m time scale from the correlator, a
correlogram can be obtained. T h e time scale can be varied from 1 pis to 1 s. In
particular, the H P 3721A correlator was connected to the T.200 Tealgate transducer or
fibre optic probe for solids velocity measurement. The front panel of the correlator
consists of various selection knobs. During the cross-correlation process, the function
knob was set to A delayed or B delayed cross-correlation and averaging function knob to
summation. The V 2 / cm. knob was set at a suitable value to suit the correlogram on the
display using A input and B input switches.

6.3 P O W D E R CONCENTRATION:
This was measured by using a T.300 Tealgate series transducer connected to a
display unit. There are three basic components in the system namely the sensor, the
transducer proper and the display unit.
6.3.1 Sensor: T h e sensor is a leakagefieldtype device, which forms part of the pipe
wall. A small section of the pipe wall is insulated from the main body of the pipe, thereby
creating capacitance between the insulated ring and the remainder of the pipe, the sensor
forms a complete circumferential section of the pipe.
6.3.2 Transducer: The principle used is to measure the capacitance of the sensor with
the material being monitored as the dielectric. The sensor is one arm of a bridge network
112

and the amount of imbalance created by the presence of material is measured. If the
relative dielectric permeability of the material is known, the capacitance measured is
related to the solids concentration of the material. Figure 6.8 depicts a block schematic
of the T.300 transducer.
6.3.3 Display unit: It is housed in a self contained 30 x 42 H P module, which will
fit into a standard 19" sub-rack. It requires a 240 volt A.C. mains input. The facia panel
incorporates a flat analogue meter, three flow level indicators and two ten turn vernier
controls. The meter gives a continuous indication of the solids concentration on a 0-
1 0 0 % scale. A chart recorder can be connected to measure the variation in solids
concentration.

The layout of the front panel is shown in Figure 6.9. Particular details are
declared in Figure 6.10 revealing the T.300 transducer board. The display meter was
calibrated to a chartrecorderto obtain steady state readings. Details of the recorder set up
are revealed in Plate 6.8.

6.4. HEWLETT PACKARD 3497A DATA ACQUISITION SYSTEM:


The H P 3497A Data Acquisition System was used in combination with a H P 85B
computer and a Tektronics 4923 tape deck. The H P 3497A can datalog up to 20 channel
transducer inputs and can be used to measure various parameters such as voltage,
pressure, temperature, resistance and frequency (Plate 6.9). The H P 85B computer was
used to set up the required experiment parameters. These include; experiment date,
number of channels used by the H P 3497A, number of scans and time lapse between
each scan. By entering the maximum and minimum pressure in the conveying system to
the H P 85B, it is possible to obtain the calibration factors for each transducer. In addition
to this, the H P 85B can be used to check transducerresponses.The data processed by the
H P 3497A and H P 85B were recorded to tape using the T E X 4923 tape deck. The
recorded data was transferred to the University's mainframe computer ( U N I V A C ) via a
Tektronics T E X 4010 terminal to obtain computer plots.

All the important conveying parameters such as blow tank top air pressure,
pipeline air pressure, supply / delivery mass of solids and supply air mass flow rate are
recorded withrespectto cycletimeusing the Data Acquisition System. Typical transducer
input channels, recorded with respect to cycle time, included blow tank air pressure;
pipeline air pressure; upstream pipeline and differential air pressures and the mass of
material entering thereceivinghopper and / or leaving the blow tank.
113

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115

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Figure 6.10: T.300 Transducer Board [ Tealgate Manual ]

Plate 6.8: Chart Recorder connected to the T.300 Concentration Meter


116

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___________

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-8-1-1-1=1=)

Plate 6.9: Data Acquisition System

A - H P 3497A Data Acquisition System

B - HP 85B Desk Top Calculator

C - TEKTRONICS 4923 Tape Deck


117

6.5 TEST PROCFXHTRFS FOR PNEUMATIC CONVEYING RIGS:


6.5.1 INTRODUCTION!
The test procedures for the experiments involve the following phases: transducer
calibration, blow tank pressurization, material conveying and data logging. Before
commencing the experiments, the following checks are conducted;
1. All transducers are connected to the proper channels of the data acquisition system
(DAS);
2. T.200 system is properly connected to the correlator;
3. T.300 system is connected to the chart recorder.
Also, atmospheric pressure, temperature and relative humidity readings should be
recorded from the gauges provided in the laboratory.

6.5.2 CALIBRATIONi
Transducer calibration and T.300 system calibration should be done at the
beginning of each experimental session, refer Plate 6.1.
Transducer calibration:
1. Set the H P 85B in calibration m o d e and zero the H P 3054A Data Acquisition
System (DAS). Material should be in the hopper ( check meter reading A ) .
2. Open blow tank discharge valve (Switch B ) and close the hopper inlet valve
(Switch C ) .
3. Connect the pressure meter to the pipeline.
4. Pressurize the blow tank and the pipeline to 100-200 kPa (Switch D and air
regulator E).
5. W h e n the pressure reading is steady, read the pressure meter. This pressure is the
m a x i m u m pipeline pressure.
6. Depressurize the blow tank by opening the blow tank vent valve and read the
pressure meter. This pressure is the minimum pipeline pressure.
6. Enter the above selected m a x i m u m and minimum pressure into the H P 85B and
run the D A S . Get the print out of the calibration values from the H P 85B.

6.5.3 T ™n SERIES SYSTEM C^JJLBRAIIQNI


In c o m m o n with other instruments, this device requires calibration. Calibration of
this instrument is effected as follows. Initially, the display meter reading is set up to 0 %
with no flow in the conveying pipeline. Then, for a fully packed condition in the pipeline
the display meter is set to 100%. These display meter readings can be set by adjusting
the trimmer capacitor switch, which isfixedonto the transducer board.
118

The actual calibration operating procedure is as follows.


Open the conveying air valve (Switch F) to give a high air flow rate across the
T.300 transducer.
Close the conveying air valve and set the T.300 display reading to zero by
adjusting the trimmer capacitor switch.
Convey material with a low air flow rate to effect a solids blockage condition near
the T.300 transducer. This can be checked from the sight glass.
Set the T.300 display reading to 1 0 0 % by adjusting the switch 1 or 2 and the
vernier scales.
Convey material into the hopper and calibrate the T.300 display reading to a chart
recorder to obtain the steady state concentration range.

5.4 OPERATION:
(a) Feed material into the blow tank:
Close the blow tank discharge valve and open the hopper inlet valve.
Open the blow tank inlet valve (Switch C ) and allow material to flow into the
blow tank. W h e n the material stops flowing i.e. meter reading A steady, lift the
hopper (Switch G ) and vibrate (Switch H ) for about 30 seconds to allow the
remaining material to fall into the blow tank. Using the switch (G), put the hopper
down.
(b) Pressurize the blow tank:
Using switch (D), pressurize the blow tank.
Adjust the blow tank pressure to a required value by using the air regulators
(Switch E ) for topringand probe air system.
(c) Set the D A S to run:
Follow the instructions appearing on the H P 85B screen and enter all required
values and data required by the D A S .
Just before commencement of material conveying, start the data logging process.
Also start a stop watch to record the experimental time.
(d) Start conveying:
Open the conveying air valve (F) slowly and steadily.
Open the blow tank discharge valve to convey material.
Take correlogram readings and T.300 display meter readings.
(e) Correlogram measurement:
Just after the conveying cycle starts, take correlogram measurements from the H P
3721A correlator every 15 seconds timed with a stopwatch.
T o get the correlogram into the display screen, press the m n button on the
correlator. Select a suitable time scale from the correlator and measure the
119

horizontal displacement (in m m . ) of the most dominant peak of the correlogram


from the Y-axis.
(0 Solids concentration measurement from the T.300 system:
Just after the conveying cycle starts, take the steady state solids concentration
measurement from the chart recorder.
T o run the chart recorder, select a suitable sweep rate setting on the chart recorder
and press the start button.
(g) Stop conveying:
After conveying all the material into the receiving hopper (conveying cycle
completed), depressurise the blow tank using the switch.
Close the conveying air valve gradually.
Close the blow tank discharge valve.
(h) Data transferring:
Follow the instruction appearing on the H P 8 5 B screen and record the data onto a
tape using T E X 4923 tape deck.
Transfer the recorded data to the University's mainframe computer ( U N I V A C ) via
the Tektronix 4010 terminal for final processing and graphical output.

TEST PROCEDURE FOR LOW VELOCITY RIG:


The valves controlling the distribution of air to the blow tank (top air, aeration
and low velocity attachment air) were first set for each experiment.
The pressure regulator controlling the air supply to the blow tank was set at a
predetermined level.
Under these conditions the air supply to the vessel was actuated and conveying
commenced.
During this time, the various conveying parameters were recorded via the data
acquisition system.
In addition, the amount of material remaining in the blow tank was regularly
monitored so that the air supply could be turned off before the blow tank was
empty.
After the air supply was shut off, the material continued conveying as the residual
air pressure in the vessel and pipeline dissipated.
120

6.6.1 W A L L FRTCTTOV RTrT;


The testrigwas designed to measure the force required to convey a column of
material along a cylindrical perspex tube. B y using a permeable piston, it was possible to
measure the variation of conveying force for both aerated and non-aerated conditions. A
schematic of the wall frictionrigis shown in Plate 6.10.

The rig consists of a 100 mm inner bore perspex tube fixed to a vertical square
section steelframe.The perspex tube, in which the 99.7 m m diameter piston arrangement
travels is mounted vertically during operation. T o facilitate the distribution of air over the
top of the piston, concentric grooves are used. Pressurized air supplied to the piston,
flows into the tube by permeating through a V y o n -D plate fitted to the top of the piston.
The piston m a y be used to convey the column of material along the pipe test section. The
movement of the piston and material column along the tube is effected by a screw-bar,
powered by a variable speed D C motor, which m n s through a ballscrew nut. The motor is
supported on a guide roller mechanism, which allows vertical movement. This
arrangement causes linear motion of the piston whenever the reversible motor is actuated.
Rotational movement of the piston is prevented by a guide bar, which runs through a
linear bearing for the full length of the screw bar. The m a x i m u m linear speed attained by
the piston is 35.2 c m / min.

Two foam rubber piston rings are used to prevent powder loss down the side of
the piston, restrict the downward flow of air as well as to provide a smooth surface for
the piston travel. Initially, these foam rings were adequate w h e n testing granular
materials. However, w h e n testing fine materials, the foam rubber piston rings were
replaced by Teflonringsto minimize leakage of the material through the piston rings.

The whole arrangement of the tube, piston, screw bar and motor is pivoted about a
horizontal axis through the main frame. This pivot allows the tube to be rotated in a
vertical plane parallel to the main frame. This rotational arrangement assists the loading
and unloading of materials into the tube. A locating pin at the bottom end of the frame
and a bracket fitted to the ground locks the whole arrangement in the vertical position
during testing. T o minimize the electrostatic charge, a wire was wrapped around the
perspex tube.

To facilitate the measurement of the load acting on the piston, a load cell is
mounted between the piston and the back up plate fixed to the end of a screw bar. The
output from the load cell is connected to a chart recorder via a control unit. A platform is
fixed to the vertical frame so that loading and unloading of the material and calibration of
121

Plate 6.10: Wall Friction Rig

A - PERSPEX T U B E
B - D.C. MOTOR
C - CONTROL UNIT
D - CHART RECORDER
122
the load cell can be effected. The air supply is connected through a pressureregulatorand
a rotameter to the distributor/piston by means of aflexibleplastic tube.

6.6.2 OPERATION:
First the load cell was calibrated using known weights and recording the chart
recorder readings. The piston was then returned to the lowest position in the tube and the
force required to convey the piston alone in the tube recorded. The test material was then
loaded into the perspex tube. The column length of the material was recorded before
observing the force necessary to convey the column upwards with the motor actuated.
The observations are recorded during the piston movement over a selected test section of
the tube. The piston was then returned to its original position by reversing the motor.
Before commencing the next test, a selected air flow was supplied to the piston. The
supply air pressure and air flow rate were recorded before observing the upward
conveying force, when the motor was actuated. This procedure was repeated for selected
supply air pressures. The expansion of the powder bed was noted by measuring the
expanded heights for each supply pressure.

6.7 COEFFICIENT OF RESTITUTION RIG:


Basically therigconsists of:
- a rotating backing disk direct mounted on a high speed trunnion mounted D.C.
motor. The motor is trunnion mounted to allow tilting of the impact surface.
- a clamp mechanism to maintain the selectedtiltangle during testing.
- a protactor to measure the tilt angle.
- a variable drop height granular material gravity feed arrangement
- a background grid of non reflective coating to measure the granular material rebound
height.

The actual test impact surface is changed by fixing disks of the test surface
material to the backing plate. In this test series, various granular material were caused to
impact selected rotating surfaces at preselected tilt angles and rotational speeds. The
rebound height of the material stream was recorded using video equipment and the results
analyzed by slow motion of the video cassette (Plate 6.11).

6.8.1.1 SOLID DENSITY:


Powder solids density was measured using a Beckman Model 930 air-
comparison pycnometer. This instrument measures the true particle volume of a powder
sample of known mass. The solids density, p s is the ratio of mass and particle volume.
This instrument consists basically of two chambers and two pistons (one measuring and
123

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=*£

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.,«#>*•»-

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• •

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*®&*^ f t M ,

Plate 6.11: Coefficient of Restitution Rig


A - D.C. MOTOR
B - WALL SURFACE
C - PROTACTOR
D - FEED ARRANGEMENT
F - BACKGROUND GRID
G - HANDLE
H - LOCKING DEVICE
124

onereference),a valve connecting the two chambers, a differential pressure indicator


and a digital counter calibrated forreadingsin cubic centimeters (Plate 6.12). The two
pistons are moved together to ensure no differential pressure between the chambers. The
distance, the measuring piston differsfromitsreferenceposition before inserting the
powder sample is proportional to the volume being measured
6.8.1.2 TESTING PROCEDURE;
- Close gauge valve.
- Rotate handwheels to counterclockwise extreme.
- Turn measuring handwheel clockwise until starting number is set on the counter which
is 108.68.
- Place sample of powder in cup, insert cup in compartment, lock sample cup in place
by pressing clamping lever down firmly.
- Wait 15 seconds, then close the coupling valve.
- Turn both handwheels simultaneously or alternately until reference handwheel rests
against stop. Keep pointer on scale during this operation.
- Wait 10 seconds, bring pointer to zero with measuring handwheel.
- Open coupling valve andreadsample volume on counter directly in cubic centimeters.

6.8.2 LOOSE POURED BULK DENSITY:


This was measured by placing a sample of known mass in a measuring cylinder.

6.8.3.1 COMPRESSIBILITY TEST:


The bulk density of a powder was determined using a compressibility tester, the
arrangement of which is depicted in Plate 6.13 (A) and Figure 6.11. The tester consists
of a 63.5 m m diameter x 19 m m deep cell which is filled with a sample of powder. A lid
is placed on top of the sample. Loads are applied to the lid by means of a weight carrier
and the compression of the sample measured with a dial gauge. Knowledge of the mass
of the sample, the volume of the sample and the vertical loads applied allows the
relationship between bulk density (pb) and consolidation (a) to be determined. The
resulting variation can be presented using either a linear scale or logarithmic scales.
6.8.3.2 TESTING PROCEDURE:
Indicator calibration:
Place the gauge block in the cell. Place the cover over it and set indicator
holder on the cell. The indicator should read 0.75".
Filling of Base:
Spoon the material into the cell, taking care not to pack the material during the
filling process. Place the cover on the material. Clean the top surface of the cell with a
small brush.
125

Plate 6.12: Beckman Pycnometer for measuring Solid Density

Plate 6.13: Jenike Compressibilty and Permeability Tester.


A - Jenike Compressibilty Tester B - Jenike Permeability Tester
126

Compaction and measurement:


Place the indicator holder on the cell. Using the twisting bar, apply 30 twists (back
and forth) of about 10° amplitude. R e m o v e the twisting bar and record the indicator
reading for a load of 0.12 kg. Place the combination weight hanger on the cover and
indicator holder on the cell over the weight hanger. Repeat previous steps six times by
adding the weight hanger equal to 0.5 kg; then by doubling the total weight (including
weight hanger) each time (i.e. 1, 2, 4, 8, 16 kilograms). The total load is equal to the
weight of the cover, the weight hanger and any weights placed on the weight hanger. A n
indicator reading is taken for each vertical load applied. R e m o v e the indicator holder,
weights, weight hanger and cover. Weigh the cell and its contents. The net weight of the
powder sample is this figure less 243.4 grams (the weight of the base).

6.8.4.1 PERMEABILITY TESTER:


The tester consists of a cabinet and a stainless steel test cylinder, cover and dial
indicator with holder, refer Plate 6.13(B) and Figure 6.12. The powder is placed in the
cylinder and compacted to various increasing densities. The height of the sample is
measured with a dial indicator. Air is blown into the bottom of the cylinder to flow
through the sample. The pressure drop is set at a value slightly less than that which will
lift the powder. F r o m knowledge of the mass of sample, a permeability versus
consolidation relationship can be determined.
6.8.4.2 TESTING P R O C E D U R E :
Filling of Cylinder:
Place the material in the test cylinder with a spoon, layer after layer. Scrape off the
excess material. Weigh the material before and after filling to determine the actual material
mass in the cylinder, refer Figure 6.12
Air Pressure:
Back off regulator R 2 by turning counter-clockwise. Open toggle valve V (gauge
Gi should read 11 psi). Determine the optimum air pressure P 0 to be applied to the
cylinder full of material using P 0 = W t / 80.6 where W t i s the net weight (in grams) of the
material in the test cylinder and P 0 is in inches of water. Slowly increase the air pressure P
at the base of the test cylinder using regulator R 2 and gauge G 2 . Try to m a k e P = P 0 .
Record the value of P which is finally used.
Packing and M e a s u r e m e n t :
Place the cover over the material. A plastic h a m m e r is used to pack the material.
Use sharp blows on both sides of the lower part of the cylinder. Measure the height using
the indicator after each packing. The height is measured with the cover on the sample. The
height of the material in the test cylinder is equal to the dial reading plus 3.00 inches.
After the indicator reading has been taken, set air pressure P and read the flow rate.
127

DIAL INDICATOR

INDICATOR HOLDER

COVER

"/////////////////////
SAMPLE

WEICHT CARRIER-

Figure 6.11: Jenike Compressibility Tester [ Arnold et al. (1980)]

Se: air
Air Pressure Gauge
0-) Rotameters

supply to
11 psig
f,5 F» ^•s*
First stage
regulator
G.
o c
dia.
~1 Test Cylinder

5,
o
o
X
o
o
X
•H
e
O
u
1 r
Air supply
Ov © O O O
<

Regulator
L- • Yjr'. Sample ' </ I.
r/ .,'
g i
iv/-:?./;-!
cdifrJb->fioo

Figure 6.12: Jenike Permeability Tester


[Arnoldetal. (1980)]
128

6.9 PARTICLE SIZE MEASUREMENT.


6.9.1.1 SIEVE ANALYSTS-
Sieve analyses of various materials were conducted The equipment used included:
1. Selection of clean dry sieves of different sizes,
2. Endecotts (Soilcrete) mechanical test sieve shaker, and
3. Mettler P C 4400 top pan directreadingbalance,
6.9.1.2 OPERATION:
The sieves were assembled in ascending order with a catch pan and lid having first
been weighted empty. A net weight of dried sample of powder was placed in the top sieve
before the lid w a s placed and top clamps of the sieve shaker were put to seal the sieve
assembly. T h e shaker w a s activated for 10 minutes, after which the sieves were
dismantled Their weights were recorded and the net weight of size fraction obtained.

6.9.2.1 PARTICLE SIZER:


Particle size distribution was measured using a Malvern 3600 E C particle sizer.
In the Malvern particle sizer, Fraunhofer diffraction is applied to determine the particle
size analysis. The sample is illuminated by a low-power laser (1 m W H e - N e laser). The
particles scatter some of this light at angles, which are characteristic of their sizes forming
a series of diffraction patterns, each consisting of concentric bright and darkrings.This
scattered light is collected by the Fourier optical system and focused onto a radial diode
array detector. The signal, which is derived from each detector element and which varies
according to the intensity of the light falling on it, is collected, amplified and digitized for
processing by the in built computer (Plate 6.14).
6.8.2.2 OPERATION:
The E A S Y - S I Z E R software has been designed for use with the Malvern particle
sizer. It consists of four special function keys, which normally performs a measurement.
These are:
Sample details F2 Allows entry of sample details for annotation of prints.
Set zero F3 Measures the diffracted light with no sample present to
establish the base line.
Check sample F4 Gives a dynamic display of the diffracted light and the
concentration sample loading with an indication of
acceptable values.
Measure sample F5 Measures the diffractedtightfrom the sample, corrects for
and analyse the base line, analyses and presents the results.
129

Plate 6.14: Malvern Particle Sizer

Plate 6.15: Jenike Direct Shear Tester.


Shear Cell C - Load Tranducer Output
B - Drive Mechanism D - Chart Recorder
130

These keys m a k e up the measurement sequence and are used in numerical order
for user interactive single measurements. W h e n changes to the optical system have been
made, it is necessary to check and adjust the optical alignment. This is achieved by
pressing the key "a" (for alignment). Access to the disc transfer system is effected by
pressing the key "d" (for disc). This allows the storage of data on the disc for later recall
and re-analysis. Access to the package M A S T E R - S I Z E R is possible by pressing the key
"m" to use the full range of M A S T E R - S I Z E R options.

6.10.1 JENIKE DIRECT SHFAR TESTER-


The main features of the Jenike Direct Shear Tester are as follows:
1. Circular shaped shear cells.
2. Normal loads are applied to the cell by means of gravity vertical loading.
3. The shearing action is by means of an electromechanical drive moving a load
sensing stem horizontally at a certain velocity.
4. The shear force is sensed by the load sensing stem and readings displayed on a
chart recorder (Plate 6.15).
5. T w o different size shear cells are used namely: for low pressure consolidation a
95.3 m m I.D.(cross sectional area of 1 / 1 4 0 m 2 ) cell is used, whereas for high pressure
consolidation a 63.5 m m I.D. (cross sectional area of 1 / 315 m 2 ) cell is used.

Use of the Jenike Direct Shear Tester, is that of producing instantaneous yield loci
in order to determine the instantaneous flow function. The yield loci are determined for
different consolidation loads (usually 3 loci). Jenike Direct Shear testing was conducted
in accordance with the procedure declared in the text by Arnold et al. (1980).

6.10.2 Effective yield locus:


The straight line through the origin and tangent to the major M o h r circle of stress
is called the Effective Yield Locus. The angle 5 m a d e by this line to the horizontal axis is
the effective angle of friction. For yield loci at different consolidation, 5 is approximately
constant or it m a y decrease with increasing consolidation.

6.10.3 Flow function:


The instantaneous yield loci are used to determine the bulk solids flow function.
The flow function is a plot of the unconfined yield stress o c versus the major
consolidating stress 0\. These two parameters are obtained from the relevant yield loci.
The flow function is dependent on several factors including duration of consolidation,
moisture content, particle size and distribution, mechanical vibration, etc.
131

6.11.1 T E N S I L E TESTER-
The tensile tester used was manufactured by Ajax Equipment (Bolton) Co. Ltd.,
England and is k n o w n as the Ajax-W.S.L. Tensile Tester. It consists of a split cylindrical
cell with one half fixed and attached to the main body of the machine, whilst the other
half is mounted on a pivoting block supported by low friction radial bearings. The
pivoting block is balanced by means of two opposing springs that are tensioned by
screwed spindles. The front spindle has a counter attached that is set to zero and the rear
spindle is adjusted until the two halves of the cell just touch, thus being the position of
null-balance (Plate 6.16).
6.11.2 OPERATION:
Choose two springs from the selection given and attach to the underside of the
tester. Adjust the front hand wheel until the counter is showing '000'. Turn the rear
wheel until the pivoted cell half just parts. Screw the clamping screw onto the top of the
tester to hold the cell firmly together.

Place the top ring over the cell. Powder is then placed in the cell until the level
reaches approximately halfway up the topring.Place the compaction plunger on the ring
and apply four to five twists of about 30° each. Once the powder has been compacted,
the plunger and compaction ring are removed, with the excess powder being scraped off
level with the top of the cell. The sample is n o w ready to test.

The clamping screw is unlocked and a load applied to the pivoting block by means
of turning the screwed spindle which extends a spring attached to the block. Once the
shearing action hasfinished,indicated by a split forming in the prepared cell, the figure is
read from the counter on the spindle and the tensile stress is found by referring this
reading to the calibration graph supplied with the machine.

Three different test series were conducted. Firstly, a test series was conducted
immediately after sample preparation, a second series of testing was conducted
incorporating 15 minutes deaeration time. In thefinaltest series, the tester cell was filled
using a screen vibrator. O n completion of testing, the powder sample tested is weighed.
This mass was then divided by the volume of the cell to obtain the sample bulk density.
For this determination a mass balance accurate to the nearest O.lg was used.
132

'•N.

Plate 6.16: Ajax Tensile Tester


A - SPLIT CYLINDRICAL CELL
B - CLAMPING S C R E W
C - SPINDLES
D - COMPACTION RING
E - COMPACTION PLUNGER
F - COUNTER
G - SCREEN
133
6.12 COHESION ARCH TESTER:
The arch tester basically consists of squat perspex silo which height is 500 m m .
and side length and width are 250 mm., fitted with a novel oudet gate arrangement. The
latter slotted outlet can be operated by a hand drive chain mechanism that symmetrically
opens the oudet gates without disturbing the material. The m a x i m u m opening size of the
slot is 100 m m . A graduated scale is fitted to measure the arch length.

The silo was filled up by using a hand pouring or mechanical feed techniques.
Initial experiments were performed by hand pouring the powder, but later the silo was
filled up by raining the powder through a 3 m m . or 4 m m . aperture sieves to intersect the
flow stream to ensure uniform powder distribution and consolidation stresses. This
procedure was also adopted by Novosad et al. (1985). In the latter part of the testing,
powder was hand poured onto a conveyor belt discharging into the arch tester (Plate
6.17). Using this technique, thefillingtime was selected to be about 5 minutes.

A set deaeration time is allowed before opening the outlet. The recorded
deaeration time includes the time for filling and the deaerationtimenecessary to dissipate
the entrapped air. Thefillingtime was varied between 0 and 28 minutes, followed by a
deaeration time proper, which varied between 0 and 62 minutes. Eckhoff et al. (1974)
also allowed a deaeration time of 30 minutes.

The drained angle of repose made by the remaining powder in the silo with the
horizontal was also measured. After discharge, the powder was collected in a receiving
binfittedbelow the tester. O n complete discharge of the gravity activated material, the
drained angle ofrepose,the angles formed between the four flow channels boundary silo
wall interface and the horizontal were measured.

The advantages of the arch tester include:


1. Convenience of measurement;
2. Effect of deaeration could be observed;
3. L o w stress levels in powder bed.
Unfortunately, the tester exhibits the following disadvantages:
1. Actual consolidation level unknown;
2. Unknown internal friction;
3. Limited arch dimension;
4. Limited consolidation stresses.
Plate 6.17: (A) Cohesion Arch Tester
(B) Deaeration Tester
C - SQUAT PERSPEX SILO G - DEAERATION CYLINDER
D - CHAIN DRIVE MECHANISM H - PRESSURE TAPPING
E - RECEIVING BIN I - GRADUATED SCALE
J - STAND
K - CHART RECORDER
135

6.13 DEAERATION TESTER:


The deaeration tester consists of:
a perspex cylinder fitted with detachable permeable and impermeable bases;
a pressure transducer connected at the bottom for impermeable base testing
and at the middle of the cylinder for permeable base testing;
a graduation scale to measure the settling bed height;
a chart recorder to record the pressure variation duringfillingand deaeration.

The experimental time was recorded with a stop watch. The pressure transducer
outputs were calibrated by use of a pressurized tank. Controlledfillingwas effected by
directing the discharge from an elevated belt conveyor into the cylinder. In each test, the
conveyor was loaded with a k n o w n mass of powder (Plate 6.17). For all deaeration
experiments, the chartrecorderspeed was 6 cm. / min. The length of deaeration cylinder
was 94 cm. In all tests, the approximate filling time was noted.

Initially, in trial runs filling was effected slowly by pouring material on the
conveyor belt. For example for fly ash 'E' with a filling time of 6 minutes, no
observation for deaeration interstitial pressures were possible using a slow filling
procedure. W h e n fastfilled,pressure peaks of magnitude between 5 kPa to 20 kPa were
observed.

6.14.1 FLUIDIZATION RIG:


The fluidizationrigconsists of:
- a plenum chamber base with a retaining assembly to house the 6 m m thick P o r e x ™ gas
distributor;
- a permeable plastic (6 m m , 35 m m P o r e x ™ ) gas distributor covered with a carbon-
impregnated G o r e t e x ™filtermaterial to prevent particulate penetration into the gas
distributor and to allow the discharge of excessive electrostatic charge;
- a 102 m m internal diameter pyrex vertical column (750 m m long)fittedwith a
graduation scale for bed height measurement;
- the air line pressure is regulated using a Fairchild, Kendal Model 10 regulator (Max.
supply 700 kPa);
- the air flow is measured using Fischer-Porter rotameters series 10A3000 with the
following ranges;
Rotameter 1-1.47 litres min -1 (full scale)
Rotameter 2 - 7.372 litres min" 1
Rotameter 3 - 22.653 liters min' 1
Rotameter 4 - 86.083 liters min" 1
136

- the rotameter operating pressure is measured using a Eicon Instruments S R I 200 kPa
(Max. 350 kPa) pressure gauge;
- the air isregulatedusing two flow control valves in parallel, viz; a 6 m m Parker and 13
mm Flutec valve;
- two Rosemount Model 1151 D P differential pressure transmitters (0 to 152 m m H 2 0
and 0 to 762 m m H 2 0 ) for direct measurement of the pressure drop across the bed via
Goretex™ protected pressure tappings;
A n illustration of the test facility is presented in Plate 6.18.

6.14.2 TEST PROCEDURE:


A test procedure is conducted as follows:
- Place the test powder of k n o w n weight into the testrig,usually between
1.5 to 3.0 kg.
- Bolt on the perspex cap with the Goretex™ filter.
- Switch on the power source for the differential pressure meters and connect the
pressure taps onto the test rig.
- Adjust the airregulatorto read approximately 50 kPa.
- The air flow is regulated via the flow control valves and measured using rotameter 1,
2, 3 and 4, as appropriate.
- The air flow is increased to allow the material to be fully fluidized.

The following parameters were recorded for each sample.


- Height of material above the P o r e x ™ gas distributor, H b (cm),
- Air pressure drop across the bed of material, A p b ( m m H 2 0 ) ,
- Volumetric flow rate of air passing through the rotameter, Q f (cm 3 s"1),
- Operating conditions of the rotameter (i.e. air pressure and temperature), and
atmospheric conditions (i.e. air pressure, temperature and relative humidity).

For each value of Qf, the corresponding value of mf was calculated using the
operating conditions of the rotameter. The superficial velocity of air, V f (cm s _1 ), leaving
the bed of material was also determined. The variation of the average air pressure
gradient, A p b / H b ( m m H 2 0 cm" 1 ), with respect to V f was plotted for each sample and
the resulting fluidization curve plotted.
137

9 r

g£vT f
7$ •
* "-•" ;ft
."-.ilk-*
!V JE_5;

"^pl^

mm
i>-_ if
oj,.»«Mm

- . * . . < • . ; - • , ; v ......... -. , -

StK-Ss«l83

Plate 6.18: Fluidization Rig

A - Plenum Chamber

B - Flow Rotameters

C - Flow Regulators

D - Differential Pressure Transmitter


138

CHAPTER 7
RESULTS

In this chapter, the observations and results obtained from the bench tests
conducted on the various powders tested and the observed flow characteristics in actual
pneumatic conveyingrigsare discussed. In summary, the bench tests included;

[1] Scanning Electron Microscope (SEM) photographs of the pneumatically


conveyed powders at various magnifications,referSection 7.1;
[2] Coefficient of restitution of various granular materials measured using a bench
scale tester based on the rotating disk technique, refer Section 7.2;
[3] Particle size analysis of various powders obtained by sieve analysis and the
Malvern Particle Sizer,referSection 7.3;
[4] Loose poured bulk density and compressibility evaluated by a measuring
cylinder technique and Jenike Compressibility Tester,referSection 7.4;
[5] Powder solids density as measured using the Beckman Pycnometer, refer
Section 7.5;
[6] Arch dimension and drained angle of repose of various powders measured using
the bench scale Arch Tester, refer Section 7.6;
[7] Flow function measured using the Jenike Direct Shear Tester,referSection 7.7;
[8] Tensile strength measured using the Ajax W.S.L. Tensile Tester, refer Section
7.8;
[9] Wall friction behaviour of aerated powders evaluated from the bench scale Wall
Friction Test Rig, refer Section 7.9;
[10] Deaeration behaviour of various powders measured in both a permeable and an
impermeable base deaeration cylinder,referSection 7.10;
[11] Fluidization and deaeration behaviour observed using a Fluidization Rig, refer
Section 7.11;
[12] Permeability measured using the Jenike Permeabihty Tester, refer Section 8.12;

In regard to observation of powder flow characteristics, the actual conveying rigs


used included;

(A) Sturtevant Pneumatic Conveying Rig:


- friction loop;
- particle velocity obtained from the T.200 Tealgate velocity sensor and a fibre
optic probe developed in combination with H P 3 7 2 1 A Correlator;
139

- particle concentration obtained from the T.300 Tealgate concentration sensor,


- long radius and vortice elbow bends.

(B) Low Velocity Rig:


- Conveying characteristics of Wheat at different airflowrates and pipeline
lengths.

The results and observations from this test work now follow:

7.1 SCANNING ELECTRON MICROSCOPE(SEM) PHOTOGRAPHS;


The powders tested were selected torepresenta range of different conveying
characteristics, particle shape and surface characteristics. Details of the observations are
presented in Table 7.1. For each powder examined, a number of S E M photographs
were taken at various magnification levels in each case to highlight paramount features.

Plate 7.1: S E M Photograph of R a w Sugar Grains (X = 14).


Plate 7.2: S E M Photograph of Raw Sugar Grains (X = 30).

Plate 7.3: S E M Photograph of R a w Sugar Grains (X = 144).


141

Plate 7.4: S E M Photograph of Raw Sugar Grains (X = 1440).

* »

..,

.:-A

***--_*

| 216 u m |

?->
Plate 7.5: S E M Photograph of Light Soda Ash (X = 162).
Plate 7.6: S E M Photograph of Light Soda Ash (X = 780).

— ^

>

& * -'•• 4r
f
c -

113!?pml ^ '

Plate 7.7: S E M Photograph of Dense Soda Ash (X = 180).


143

Plate 7.8: S E M Photograph of Dense Soda Ash (X = 600).

Plate 7.9: S E M Photograph of Zinc Fume (X = 90).


144

Plate 7.10: S E M Photograph of Zinc Fume (X = 600).

Plate 7.11: S E M Photograph of Zinc Fume (X = 6000).


145

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Plate 7.12: S E M Photograph of P V C Powder (X = 36Q).

Plate 7.13: S E M Photograph of P V C Powder (X = 1800).


146

Plate 7.14: S E M Photograph of Pulverised Coal - Tallawarra (X = 60).

Plate 7.15: S E M Photograph of Pulverised Coal - Tallawarra (X = 600).


147

Plate 7.16: S E M Photograph of Pulverised Coal - Tallawarra (X = 2100).

Plate 7.17: S E M Photograph of Petroleum Coke (X = 12).


148

Plate 7.18: S E M Photograph of Petroleum Coke (X = 120).

Plate 7.19: S E M Photograph of Petroleum Coke (X = 600).


149

Plate 7.20: S E M Photograph of Petroleum Coke (X = 3000a).

Plate 7.21: S E M Photograph of Petroleum Coke (X = 3000b).


Plate 7.22: S E M Photograph of Eraring Fly Ash (X = 1320).

Plate 7.23: S E M Photograph of Liddell Fly Ash (X = 1320).


Plate 7.24: S E M Photograph of Liddell Fly Ash (X = 6600).

Plate 7.25: S E M Photograph of Vales Point Fly Ash (X = 468).


152

\
«'• '+•';•_

^ ... , r»*t-vW;^
v
" • > - • • "<w • -

Plate 7.26: S E M Photograph of Vales Point Fly Ash (X = 6600).


153

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Considerable Very rough, Vesicular Some sharp Individual Small particles Prone to Highly cohesive,

1
7.10 particle fluffy surface edges and particles have not weU degradation ratholing tend-
7.11 porosity, corners formed cemented. At encies in blow
At high agglomerates higher magni- tanks, inter-
magnification fication locking
reveals the particles tendency
extent of pore consist of fused
volume rhombus crystals

o
CO
7.12 Polyvinyl Macroscopic Uneven, Very rough Rounding of A fractured, rough Individual No, hard Static electricity
7.13 chloride indentations irregular, and uneven edges and fused subparticle particles incompressible iffects conveying,
C»vc) visible undulations, surface at comers agglomerate particles tendency to plug,
cauhflower high mag- generaUy interlocking
appearance nification individual tendency,
particles. effective volume
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present volume

O
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Si
7.14 Pulverized Highly angu- Fractured Sharp edges No agglomerates, Individual No, individual Good conveying

1
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7.16 Tallawarra rough from grinding varying in but definite
surface at operation size edges suggest
154
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nification abrasion

6
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CO

co
2
7.17 Petroleum Angular, Visible, Highly Cracks/ Sharp edges, Cleating and

: E
bo

1
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7.18 coke very irregu- cleated, conchoidal fracture prone to flakiness
7.19 lar uneven structure extreme characteristics,
7.20 surface degradation very abrasive
7.21

CS
CS
3

I/O
co
Eraring fly Spherical Smooth No edges Partial agglo- Larger Submicron Degradation

r-
I
1
ash particles and or comers meration of particles particles increases the
sintered different sized surrounded by dislodge from submicron
surface, small particles smaller the large loading (HI
particles particle surface downstream
during dust collection
pneumatic facilities. This
conveying fly ash fluidizes
& conveys weU

7.23 Liddell fly 2-22 nm Low permea- Spherical Some No edges or Partial agglome- Micron and Significant Unsteady
7.24 ash smaller in bility, signi- particles, particles comers ration of small & submicron due to conveying
155
156

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157

7.2 COEFFTCTFNT OF RFSTTTTTTTON;


The details and operating procedure for this rig are described in Section 6.6. A
schematic of this rig is presented in Figure 7.1. Observations and results from the
various experiments are declared in Table 7.2 and are depicted graphically in Figures
7.2, 7.3 and 7.4. In this test series, different wall surfaces namely, Mild Steel and
Stainless Steel were used. The wall surfaces were tilted, during impact, both in (
denoted by C O in Table 7.2) and counter ( denoted by C O U N T in Table 7.2 ) to the
direction of rotation of motor.

FEEDER
/
INCIDENT PRRTICLES

R E B O U N D PRRTICLES
\ :
L-
-
\

REFERENCE
GRID —

'!
DISK

W A L L SURFRCE

FLEKIBLE SHAFT

HANDLE
D.C.

a
PROTRCTOR
\


MOTOR

BRSE

Figure 7.1: Coefficient of Restitution Rig.


158

TABLE 7.2 COEFFICIENT OF RESTITUTION

SR. MATERIAL COEFFICIENT STD. ANGLE WALL DISK DISK


NO OF RESTITU- DEVIATI- OF MATERIAL R.P.M. TILT
TION e ON IMPACT
1. WHEAT 0.628 0.159 0 MILD STEEL 2632 CO
2. 0.618 0.192 10 2757
3. 0.635 0.147 15 2649
4. 0.655 0.174 20 2649
5. 0.675 0.161 5 2655 COUNT
6. 0.665 0.217 10 2660
7. 0.674 0.195 15 2660
8. 0.674 0.202 20 2675
9. 0.585 0.174 0 STAINLESS 2606 COUNT
10. 0.611 0.164 5 STEEL 2603
11. 0.648 0.196 10 2652
12. 0.569 0.161 15 2711
13. 0.647 0.191 20 2146
14. MILLET 0.551 0.17 0 MILD STEEL 2265 COUNT

15. 0.55 0.17 5 2611

16. 0.57 0.15 10 2603

17. 0.59 0.15 15 2620

18. 0.56 0.18 5 2634 CO

19. 0.57 0.15 10 2146

20. 0.59 0.14 15


21. MUNGBEAN 0.60 0.178 0 S. S.
22. 0.63 0.177 5 2621

23. 0.623 0.155 10 2730

24. 0.64 0.146 15


25. 0.574 0.169 20
26. COAL 0.589 0.089 0 M. S.
27. 0.61 0.093 5 2611 CO

28. 0.62 0.071 10 2615

29. 0.656 0.076 15


30. 0.569 0.109 20
159

31. 0.589 0.086 5 2727 COUNT


32. 0.695 0.099 10 2738
33. 0.645 0.093 15 2750
34. 0.692 0.087 20 2652
35. 0.529 L 0.064 0 s. s. 2682 CO
36. 0.467 0.056 5 2725
37. 0.489 0.051 10 2709
38. 0.539 0.099 15 2774
39. COKE 0.536 0.109 0 s. s. 2497
40. SINTER 0.573 0.048 5 s. s. 2670 COUNT
*
41. 0.53 0.052 10 2683
42. 0.574 0.093 15 2672
43. SODIUM- 0.548 0.132 0 s. s. 2779 COUNT
44. FERRITE 0.509 0.108 10 2649
45. 0.579 0.070 15 2706
46. SUGAR 0.531 0.147 0 M. S.
47. PLASTIC 0.7085 0.120 0 M. S. 2740
BALLS

U.bb- •
z • •
0.64-
O
11
F 0.62-

8 LEGEND
r-
00 • Q WHEAT M.S.
LU 0.60" » • WHEAT S.S.
CC • B MILLET M.S.
LL D
O
i O BEAN S.S.
0.58- Q
Z D •
LU
O 0.56-
LL l•
LU
D
LU 1
0.54 -* ... ,
O 0 10 20 30
O ANGLE OF IMPACT, DEGRESS
Figure 7.2: Coefficient of Restitution of Wheat, Millet and Bean (Co-rotation).
160

z
o
H LEGEND
t
Q COAL M.S.
to • COAL S.S.
LU D SINTER S.S.
Ul
CC • FERRITE S.S.
o
Ul
o
i i r
o 10 20 30
ANGLE OF IMPACT, DEGREES

Figure 7.3: Coefficient of Restitution of Coal, Sinter and Sodium Ferrite (Co-rotation).

z
O

LEGEND
Ul
oc • WHEAT M.S.
u. • MILLET M.S.
oUJ • COAL M.S.

u
LL
U-
Ul
O
O
T • r
0 10 20
ANGLE OF IMPACT, DEGREES
Figure 7.4: Coefficient of Restitution of Wheat, Millet and Coal (Counter-rotation).
161

7.3 P A R T I C L E S I Z E ANAI.VSF.fi;
The particle size analyses of the various powders and granular materials tested are
declared in Tables 7.3 to 7.7. This information is presented graphically in Figures 7.5 to
7.10.

T A B L E 7.3 P A R T I C L E SIZE A N A L Y S E S

Sr. Material d50 d90 dlO D(4,3) D(3,2) Specific


No. Lim um Lim Lim Um surface
sq.m / cc.
1.1 Fly ash 'A' 16.9 56.7 4.8 24.4 11.1 0.10
.11 15.1 64.8 4.7 26.6 10.2 0.06
2.1 Fly ash 'B' 15.0 65.8 4.1 26.7 9.7 0.07
.11 14.3 61.9 3.9 22.6 9.4 0.08
3. Fly ash 'C 9.2 30.3 3.1 13.9 6.6 0.12
4.1 Fly ash 'D' 10.0 64.5 3.2 22.3 7.2 0.06
.11 11.8 84.0 3.0 28.5 7.7 0.05
5.1 Fly ash *E' 5.4 27.1 2.0 10.2 3.6 0.18
6.1 Fly ash F 13.8 64.5 3.5 22.7 8.5 0.07
.11 14.0 65.4 3.6 25.1 8.7 0.07
7.1 Fly ash 'G* 14.9 83.5 2.8 26.3 7.8 0.06
.11 13.9 75.0 3.2 28.2 7.8 0.06
.III 13.8 74.8 3.2 28.0 7.9 0.06
8. Cement 18.3 55.1 5.2 25.7 11.5 0.08
9. Sand 209.5 364.6 105.4 221.6 120.4 0.02
10. P V C Powder 149.6 221.7 123.5 163.7 151.8 0.03

T A B L E 7.4 SIZE A N A L Y S I S O F S A N D

Mesh size, Tare.g Weight, g Weight %


Um fraction, g
1000 440.00 447.1 7.1 1.42
850 423.00 428.4 5.4 1.08
710 421.4 432.8 11.4 2.28
500 406.9 453.0 46.1 9.21
425 386.4 440.5 54.1 10.8
300 329.2 473.8 144.6 28.88
212 360.9 487.4 126.5 25.26
1% 333.0 438.1 105.1 20.99
180 302.4 352.7 50.3 10.05

150 348.8 386.4 37.6 7.50

125 302.3 313.7 11.4 2.28

106 344.2 348.3 4.1 0.82

90 475.9 477.3 1.4 0.28

75 267.6 267.9 0.3 0.06

45 340.1 340.3 0.2 0.04

22.5 334.7 334.9 0.2 0.04

Surface to volume mean diameter = = 305 \im


V ^ weight fraction
------ mean diameter

TABLE 7.5 SIZE ANALYSIS O F B R O W N RICE (I)

Mesh size Tare,g Weight, g Weight %

mm fraction, g

3.35 493.1 493.4 0.3 0.003

2.80 489.4 492.6 3.2 0.003

2.36 427.1 1160.4 733.3 0.78

2.0 412.7 572.9 160.2 0.171

1.4 444.6 481.3 36.7 0.039

1.18 389.6 390.8 1.2 0.001

1.0 386.2 387.0 0.8 0.001

850 u m 423.1 423.7 0.6 0.001

425 urn 334.6 337.5 2.9 0.003

1
Surface to volume mean diameter = = 2.0 m m
weight fraction
mean diameter
TABLE 7.6 SIZE ANALYSIS OF B R O W N RICE (II)

Mesh size Tare, g Weight, g Weight %


mm fraction, g
2.80 489.4 492.6 3.2 0.005
2.36 427.1 816.4 389.3 0.633
2.0 412.7 607.5 194.8 0.317
1.4 444.6 469.7 25.1 0.041
1.18 389.6 390.3 0.7 0.001
1.0 386.2 386.7 0.5 0.001
500LUT1 334.6 336.3 1.7 0.003

1
Surface to volume mean diameter = = 2.42 m m
weight fraction
mean diameter

TABLE 7.7 SIZE ANALYSIS OF W H I T E RICE

Mesh size Tare.g Weight, g Weight %


mm fraction, g
2.8 489.6 492.3 2.9 0.004
2.36 427.1 878.4 451.3 0.651
2.0 412.7 633.0 220.3 0.318
1.4 444.6 454.9 10.3 0.015
1.18 389.6 391.0 1.4 0.002
1.0 386.2 387.4 1.2 0.002
500um 334.2 340.0 5.8 0.008

1
Surface to volume mean diameter = = 2.49 m m
weight fraction
mean diameter
1

Ul LEGEND
N FLY ASH
eo
-B- 'A'
DC
Ul
-D- 'C
o
••- -D'
Z
3
as

PARTICLE SIZE (nm)

Figure 7.5: Particle Size Distribution versus % Undersize of Fly Ash 'A', 'B',
'D'.

ui
N LEGEND
<7i FLY ASH
cc -O- '£<
ui
Q •+• V
HB- 'G'
z -••CEMENT
3

PARTICLE SIZE (um)

Figure 7.6: Particle Size Distribution versus % Undersize of Fly Ash 'E, 'F, 'G' and
Cement.
165

> •

o
ui
3
O
Ul
CC

PARTICLE SIZE (um)

Figure 7.7: Variation of Frequency versus Particle Size of Fly Ash 'A', 'B*

LEGEND
> •

ui FLY ASH
o -a- 'D'
z •+- 'E'
Ul
3
o
Ul
DC

PARTICLE SIZE (^m)

Figure 7.8: Variation of Frequency versus Particle Size of Fly Ash 'D* and 'E'.
166

LEGEND
>-
o FLY ASH
z -a- 'F
Ul •o-'G-
3
O

PARTICLE SIZE (um)

Figure 7.9: Variation of Frequency versus Particle Size of Fly Ash

>-
o
LEGEND
z
Ul •o-CEMENT
3 -#- PVC
a -B- SAND
ui
DC
LL

10' 10'
PARTICLE SIZE (um)
Figure 7.10: Variation of Frequency versus Particle Size of
Cement, PVC Powder and Sand.

7.4 B U L K DENSITY
The observed powder bulk density and loose poured bulk density propert
summarized in Table 7.8 and 7.9, respectively.
167

T A B L E 7.8 BULK DENSITY

Sr. Material Po Oo constant b correl.


No. kg/m 3 kPa coeffi.
1. Fly ash 'A' 1032 6.458 0.0417 0.99
2. Fly ash "B' 1134 6.458 0.0598 0.98
3. Fly ash 'C 944 6.458 0.0554 0.74
4. Fly ash 'D' 1088 6.458 0.049 0.95
5. Fly ash 'E 975 6.566 0.057 0.99
6. Fly ash "F 1275 6.458 0.0584 0.98
7. Fly ash *G' 1294 6.458 0.053 0.98

8. Cement 1312 6.458 0.0557 0.99

9. Wheat 868 6.458 0.0021 0.99

10. White Rice 865 6.458 0.0018 0.99

11. Brown Rice 825 6.458 0.0016 1.00

12. Sand 1502 6.458 0.011 0.98

13. Sugar 883 6.458 0.0023 0.98

14. P V C Powder 649 6.458 0.0084 0.99

15. Sodium Ferrite 1512 6.458 0.0314 0.99

TABLE 7.9 LOOSE POURED BULK DENSITY

Material Loose Packed Material Loose Packed

Poured to Loose Poured to Loose

Bulk Poured
Bulk Poured
Density, B.D. Density, B.D.

kg/m 3 kg/m3 kg/m3 kg/m3

Fly ash 'A' 769 1.342 Cement 950 1.381

Fly ash *B' 750 1.512 Sand 1424 1.055

Fly ash 'C 520 1.815 P V C Powder 575 1.129

Fly ash 'D* 703 1.548 Wheat 709 1.224

Fly ash *E' 617 1.58 Brown Rice 703 1.173

Fly ash T 965 1.321 White Rice 751 L152


168

7.5 SOLIDS DENSITY.


The observed particle solids density of the materials tested are summarized in Table
7.10.

TABLE 7.10 SOLIDS DENSITY

Material Solids Density, Material Solids Density,


kg/m 3 kg/m 3
White Rice 1478 Fly ash 'A' 2130
Brown Rice 1579 Fly ash 'B' 2492
Riceflakes 1579 Fly ash 'C 2195
Wheat 1380 Fly ash 'D' 2624
Millet 1550 Fly ash 'E* 2536
Castor Sugar 1500 Fly ash F 2537
Light soda ash 2454 Fly ash *G' 2391
Dense soda ash 2508 Cement 3100
P V C Powder 1378 Sand 2735
Sodium Ferrite 1147

7.6 A R C H L E N G T H A N D DRAINED A N G L E O F REPOSE:


The details and operating procedure for the Arch Tester shown in Figure 7.11
are provided in Section 6.12. This same tester was also used for measuring the drained
angle of repose as shown in Figure 7.12.

Table 7.11 summarize the observed critical arch dimensions as measured in the
Arch Tester. In addition, this Table represent a comparison of the predicted arclf
dimension assuming rough wall boundaries apply in the Jenike (1970) and Walker (1966)
analysis, refer Section B.17 (b). In this latter evaluation, the assumed powder flow
function information is presented in Table 7.13 and graphically in Figure 7.24.

Figures 7.13 to 7.15 represent the variation of arch length versus deaeration time
with different relative humidity for fly ash 'A', 'C and Cement, respectively. Figures
7.16 and 7.17 reveal the variation of arch length versus deaeration time for Cement and
fly ash, respectively. Figure 7.18 depicts the variation of bed height versus arch length
for Cement, whereas, Figure 7.19 represents the variation of mean particle size versus
arch length for the different powders tested in the Arch Tester.
169

Furthermore, the observed drained angle of repose at the four flow channel
boundaries are presented in Table 7.11. Figure 7.20 represents the variation of drained
angle of repose with bed height for Cement, whereas variation of drained angle of repose
versus deaeration time for fly ash and Cement are depicted in Figures 7.21 and 7.22,
respectively. Figure 7.23 represents the variation of mean particle size versus drained
angle of repose for the different powders tested.

DUST COUER

CHAIN P E R S P E K SILO
DRIUE

ROTATING HANDLE

SCALE

SIGHT GLASS DISCHARGE BIN

Figure 7.11: Arch Tester.


170

DUST COVER

PERSPEX SILO
POWDER

SLIDE GATES

DRAINED ANGLE
OF REPOSE

SIGHT GLASS RECEIVING BIN

Figure 7.12: Tester for Measuring the Drained Angle of Repose.


171

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173

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NO P- O ^ <N H- HH CS CO CO Tt NO CS Tf P-

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oo
m
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CO CS O r^ >n r-.
"" S r-l -— I-, -"* °° -** r~- °° CS r-t r-t

r—1
P- y
174

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OO 00 vo ~ P- ON ON NO r-r Tt NO

in
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00 00 Tl" ON CO CO CO in pr- in NO

in in
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NO NO P- Pr- t~- P~ Pr- |-~ P- in in

00 00 o O o o o O o o m
CO CO O ON vo
cs m in — CO o cs

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pr- ON 00 oo ON ON oo r-- in p- r-

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o o o o o o O O o in o
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o o o o O O O O Q in O
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r- oo CO Tt cir ;_; r-- oo oo co co co in in co
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in o O Pr- O O O Tt in o O in o
CS NO CN CN Tt m
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° 5 in
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co «n
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cs — m ^ -H -H CN

B 2
Q oi
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175

FLY ASH 'A'

LEGEND
RELATIVE HUMIDTY
H 55%
• 59%

i ' r
20 40 60
Deaeration time, minutes

Figure 7.13: Arch Length versus Deaeration Time for Fly Ash 'A'.

FLY A ? H '<•?'

LEGEND
RELATIVE HUMIDITY
B 67%
• 73%

-, i 1 • I
20 40 60
Deaeration time, minutes

Figure 7.14: Arch Length versus Deaeration Time for Fly Ash 'C.
176

/u -

0
60-

• LEGEND
50- B B
D • • REL HUM.
•a 56%
40 - e B • B • 61%
• B 66%
a • 70%
30- <r
• •
a
1 i 1
2\J - T 1 •

20 40 60 80
Deaeration time, min.

Figure 7.15: Arch Length versus Deaeration Time for Cement

LEGEND
B Cement
• Fly ash *A'
B B'

Deaeration time, mins.

7.16: Arch Length versus Deaeration Time for Cement, Fly Ash 'A' and 'B'.
LEGEND
Fly ash
B 'C
e 'D'
B 'E'
• F

- i — i — i — | — i -

10 20 30 40 50 60 70
Deaeration time, mins.

Figure 7.17: Arch Length versus Deaeration Time for Fly Ash
*B\ 'C, T>\ 'E' and 'F.

CEMENT
ou -
B
B
50-
B • LEGEND
B EXP.

B 1
40-
• 2
B
B 3

30-
B

i • 1 *
100 200 300 400 500
Bed height, mm.

Figure 7.18: Arch Length versus Bed Height for Cement


178

120

E
E
o>
c
©
X
<

Mean particle size, micron

Figure 7.19: Arch Length versus Particle Size Variation for the Powders Tested.

B4 -
B B
82-
? • Q
LEGEND
•a REL HUM
80- B
H 75%
i • • 74%
o 78- • • 66%
Q.
s
r-
76-
o
EI Q
e
cn T l i 1
74 i
c 100 200 300 400 500
a
c Bed height, mm.

Figure 7.20: Variation of Drained Angle of Repose with Bed Height for Cement
179

100
8
&
LEGEND
S? FLY ASH
TJ
80- B 'B'
8 • B
• 'C
o B 'D'
Q. 70-
B B B • 'E'
&
o B V
-2 60-
cn
B
c 50
• "•——i > r- —1 1
20 40 60 80
Deaeration time, mins.

Figure 7.21: Variation of Drained Angle of Repose versus Deaeration Time for
Fly Ash Tested.

e
LEGEND
t? REL. HUM.
•o 90- • a 56%
8" o
• 61%
o B 66%
a • D BB • 70%
£ 80- a B 74%
r— DO • • a 75%
O B 1 • El •
c
• «
# D DD
8
c B
5a 70- i • l • l

0 20 40 60 80
Deaeration time, mins.

Figure 7.22: Variation of Drained Angle of Repose versus Deaeration Time for Cement
CO 100
0
e
-.
cn
e
TJ
o
»
o
Q.
0
O)
c
a
CO
e
100
Mean particle size, microns

Figure 7.23: Variation of Drained Angle of Repose versus Mean Particle Size.

7.7 F L O W FIJNCTTON:
The observed powder flow functions are summarized in Table 7.12.
Alternatively, these flow functions are plotted in Figure 7.24.

a
a.
LEGEND
n
cn El CEMENT
a • FLY ASH 'A'
T>
B •B'
• •C'
>N B •D'
TJ • •E'
C A 'F
c
o
o
c 2 4 6 8
z>
Major consolidating stress, kPa

Figure 7.24: Powder Flow Functions.


181

TABLE 7.12: INSTANTANEOUS YIELD LOCI DATA

Sr. Material ai(kPa) <-c(kPa) 5(degree <|>(degre< -) oi/cc Slope of F.F.

1. Cement 8.55 2.21 43.64 37.13 3.869 0.293

10.46 2.51 45.15 39.35 4.167

5.78 1.14 46.20 41.66 5.070

2. Fly ash 'A' 6.51 3.2 42.22 31.20 2.726 0.464

8.53 3.64 54.13 21.47 1.294

4.12 1.80 41.69 28.37 2.299

3. Fly ash •B' 6.46 1.55 38.55 32.14 4.168 0.31

9.19 2.34 39.15 32.33 3.927

4.68 1.10 39.30 33.08 4.255

4. Fly ash 'C 6.82 2.29 40.27 30.75 2.978 0.195

8.41 2.48 44.13 36.50 3.391

4.53 1.85 36.69 23.75 2.449

5. Fly ash 'D' 5.91 2.61 41.27 27.58 2.264 0.222

8.05 2.92 43.21 33.07 2.757

4.14 2.07 43.80 27.84 2.00

6. Fly ash E' 7.37 5.06 57.84 35.56 1.457 0.923

9.23 6.92 56.38 27.70 1.334

4.59 2.96 52.08 30.05 1.551

7. Fly ash "F 5.94 3.82 35.28 31.67 1.457 0.6

7.93 4.72 38.53 33.26 1.334

4.59 2.96 38.45 35.06 1.551


182

7.8 T E N S U E STRENGTH-

clamping screw
/

S= -T—V\±—
^JVV7/-.--V-V-\/V2. /•• $S-J\r„%^j. -L
•%-»•

^pivot point

pivoting block

Figure 7.25: Tensile Tester

The details and operating procedure for this tester are described in Section 6.11
and Appendix B.2.4. A schematic of this tester is presented in Figure 7.25.

The observed tensile stress versus consolidation stress for the powders tested are
depicted in Figures 7.26 and 7.27. T h e tt nsiL tests of the same powders when tested
with a deaeration time of about 15 minutes are shown in Figures 7.28 and 7.29. The
observed voidage variation versus tensile strength of the various fly ash tested are shown
in Figures 7.30,7.31,7.33 and 7.34, whereas, the observed bulk density variation are
shown in Figures 7.32 and 7.35. The observed tensile stress versus consolidation stress
and voidage for light soda ash, dense soda ash, P V C powder and castor sugar are
depicted in Figures 7.36 and 7.37, respectively.

T o observe the effect of the filling procedure on the measured tensile stress versus
consolidation stress, two different procedures were used. In particular, in one
experiment, a screen vibrator was used and in another experiment spoon filling of the cell
was used. In each experiment an approximate deaeration time of 15 minutes was allowed.
The comparison of filling procedure for fly ash 'J' is depicted in Figure 7.38, whereas,
tensile stress versus consolidation stress for fly ash 'H, T and 'J' are shown in Figures
7.39 and 7.40, respectively.
183

(B LEGEND
O.
FLY ASH
B TV
Si • 'B'
B 'C
c

0 20 40 60 80 100 120
Consolidation Stress, kPa

Figure 7.26: Tensile Stress versus Consolidation Stress for Fly Ash 'A', 'B'
and C.

CO LEGEND
a FLY ASH

a •D'
? • 'E'
to B •F
"35
c

0 20 40 60 80 100 120
Consolidation Stress, kPa

Figure 7.27: Tensile Stress versus Consolidation Stress for Fly Ash 'D, 'E
and 'F.
184

(B
a LEGEND
FLY ASH
B 'A'
CO • 'B'
B 'C

20 40 60 80 100 120
Consolidation Stress, kPa

Figure 7.28: Tensile Stress versus Consolidation Stress for Fly Ash 'A', 'B' and
'C with 15 minutes Deaeration.

a LEGEND
o. FLY ASH
-t
j£ a 'D'
S> • 'E"
c
B F
£ 1-
55
CO
c
e
r
T ' I
20 40 60 80 100 120
Consolidation Stress, kPa

Figure 7.29: Tensile Stress versus Consolidation Stress for Fly ash 'D', 'E' and
'F with 15 minutes Deaeration.
185

a
OL LEGEND
FLY ASH
• .A.
e 'B'
0
B •<_'
"35
c

Voidage

Figure 7.30: Tensile Stress versus Voidage for Fly Ash 'A', *B' and 'C.

CB LEGEND
a.
FLY ASH
• 'D'
• 'E"
B T
c

0.7

Figure 7.31: Tensile Stress versus Voidage for Fly Ash 'D, *F and 'F.
186

\£V '
u e
100 - LEGEND
B fl 0 • DI FLY ASH
8. 80- B 'A'
B B » » D • 'B'
60- B

•c
B • 0 • D B •D'
B •E"
c 40-
D •F
e B B e •a B
20-
B B D •
• 1 • i 1 1 1 1 1 1
1
600 700 800 900 1000 1100 1200
Bulk Density kg/m3

Figure 7.32: Tensile Stress versus Bulk Density for the Fly Ash Tested.

LEGEND
2. FLY ASH
-C
B TV
• 'B"
• B 'C
tt
c
tt

0.50 0.55 0.60 0.65 0.70


Voidage

Figure 7.33: Tensile Stress versus Voidage for Fly Ash 'A', 'B' and 'C with
15 minutes Deaeration.
1

CB
Q. LEGEND
FLY ASH
B 'D'
CO • "E"

•35
B *F
c
tt

0.8

Figure 7.34: Tensile Stress versus V o i d a g e for Fly A s h 'D', 'E' and 'F with 15
minutes Deaeration.

LEGEND
CB 3- B FLY ASH
• a 'A'
• I B B o • 'B'
a
2- e •• B 'C
co •n • 'D'
B 'E'
c 03 D 'F'
tt

700 800 900 1000 1100


Bulk Density, kg/m3

Figure 7.35: Tensile Stress versus B u l k Density for Fly A s h Tested with 15
minutes Deaeration.
188

OL
LEGEND
BLIGHT SODA ASH
2- •DENSE SODA ASr
B PVCPOWDER
c • CASTOR SUGAR

20 40 60 80 100
Consolidation Stress, kPa

Figure 7.36: Tensile Stress versus Consolidation Stress for Light Soda Ash,
Dense Soda Ash, PVC Powder and Castor Sugar.

CB LEGEND
CL
e •
SODA ASH
• B a LIGHT
! 2- •DENSE
55 e B PVC
tt
tt B POWDER
c

0.3 0.4 0.5 0.6 0.7


Voidage

Figurte 7.37: Tensile Stress versus Voidage for Light Soda Ash, Dense Soda Ash
and PVC Powder.
189

CL LEGEND
FLY ASH 'J'
B NODEAERA.
55 • SCREEN VIBR.
o B SPOON
«
c
tt
»-
-i 1 1 1 1 | 1 — r
20 40 60 80 100 120
Consolidation Stress, kPa

Figure 7.38: Tensile Strength versus Consolidation Stress for Fly Ash 'J'.

LEGEND
FLY ASH
B 'H'
s • T
55 B 'J'
on
c
e

20 40 60 80 100
Consolidation Stress, kPa

Figure 7.39: Tensile Strength versus Consolidation Stress for Fly Ash
'H, T and T.
190

CEMENT
2.4

a 2.2-
a.

-- 2.0-
CO

n 1.8-
c

1.6H—.—i—r -J i 1 1 i r-
0 20 40 60 80 100
Consolidation Strees, kPa

Figure 7.40: Tensile Strength versus Consolidation Stress for Cement

It should be noted that the observed tensile strength variations are plotted using a
standard Macintosh computer software package with the observations correlated to
exponential regression curve fits. The values of the empirical constants, so evaluated and
slope of the tensile strength curve are presented in Table 7.13.

TABLE 7.13: TENSILE STRESS VERSUS CONSOLIDATION


STRESS

Material Exponent Slope Material Exponent Slope


Fly ash 'A' 0.0017 L 0.632 Light soda ash 0.006 1.04
Fly ash 'B' 0.0029 0.214 Dense soda ash 0.0019 0.314
Fly ash C - 0.741 P V C powder 0.0017 0.244
Fly ash TV 0.0021 0.474 Castor sugar 0.0023 0.458
Fly ash 'E' 0.0025 0.666 Fly ash 'H' 0.0038 0.306
Fly ash T 0.0032 0.957 Fly ash T 0.0046 0.533
Cement - 0.682 Fly ash T 0.0039 0.413
191

7.9 W A L L FRTCTTON-

PRESSURE GAUGE

PRESSURE REGULATOR

' & - COMPRESSED


AIR SUPPLY

.100 mm <t> PERSPEX TUBE

X
\
ROTAMETER

^PERSPEX DISTRIBUTOR

i EK
• i *. i
LOAD CELL
i
SCREW BAR!
y
CONTROL;
UNIT :
CONTROL UNIT WITH
FORWARD/REVERSE
CHART
SWITCH/ I
RECORDER
DC MOTOR

Figure 7.41: Wall Friction Rig

The details and operating procedure for this rig are described in Chapter 6.6. A
schematic of this rig is presented in Figure 6.39. The observed wall friction force versus
piston aeration air pressure for different column lengths are depicted in Figures 7.42 to
7.48, whereas variation of column length and frictional force at different aeration air
pressure are depicted in Figures 7.49 to 7.54.

Average shear stress which is the ratio of the frictional force to the contact area
versus aeration pressure are depicted in Figures 7.55 to 7.60. Using the analysis
presented in Section 2.5, the evaluated wall friction factor u k versus piston aeration air
pressure for different column lengths are depicted in Figures 7.61, 7.62, 7.63, 7.64 and
7.65 for B r o w n Rice, White Rice, Rice Flakes, Millet and Wheat, respectively.
BROWN RICE

CD LEGEND
o COLUMN HEIGHT
o • 80 mm.
LL • 120 mm.
CO
C o 160 mm.
o « 200 mm.
r—

T 1 1 1 r
100 200 300 400
Air Pressure, kPa

Figure 7.42: Frictional Force versus Aeration Air Pressure for Brown Rice.

WHITE RICE

LEGEND
COLUMN HEIGHT
u • 80 mm
• 120 mm
a 160 mm
CO
• 200 mm
c
o
o
LL

100 200 300 400 500


Air Pressure, kPa

Figure 7.43: Frictional Force versus Aeration Air Pressure for White Rice.
RICE FLAKES

LEGEND
COLUMN HEIGHT
B 80 mm.
• 120 mm.
B 160 mm.
• 200 mm.

-r
100 200 300 400
Air Pressure, kPa

Figure 7.44: Frictional Force versus Aeration Air Pressure for Rice Flakes.

MILLET

LEGEND
COLUMN HEIGHT
B 80 mm.
e 120 mm.
a 160 mm.
• 200 mm.

100 200 300 400 500


Air Pressure, kPa

Figure 7.45: Frictional Force versus Aeration Air Pressure for Millet
194

LEGEND
COLUMN HEIGHT
B 80 mm.
• 120 mm.
B 160 mm.
• 200 mm.

100 200 300 400


Air Pressure, kPa

Figure 7.46: Frictional Force versus Aeration Air Pressure for Wheat.

SAND
300

LEGEND
200- COLUMN HEIGHT
B 80 m m
• 125 m m
B 165 m m
100-

T
100 200 300
Air Pressure, kPa

Figure 7.47: Frictional Force versus Aeration Air Pressure for Sand.
195

LEGEND
o
COLUMN HEIGHT
B 55 mm
CO • 80 mm
c
o
u

100 200 300 400


Air Pressure, kPa

Figure 7.48: Frictional Force versus Aeration Air Pressure for Shirley Phosphate.

BROWN RICE

LEGEND
AERATION
0)
o PRESSURE
B o
o
LL • 113
CO B 197
C
• 281
o kPa
o
'Z
LL
• i i

100 150 200 250


Column Length, mm.

Figure 7.49: Frictional Force versus Column Length for Brown Ric
WHITE RICE
-H. -
I LEGEND
AERATION

PRESSURE
30- B o
B
• 71
B B 113
• 197
B 281
20-
e n 366
§ kPa

10- • i i i i i i

50 100 150 200 250


Column Length, m m .

Figure 7.50: Frictional Force versus Column Length for White Rice.

RICE FLAKES
4U -
LEGEND
B AERATION
30-
o PRESSURE
B B 0
o • 113
20- e
D
B • B 197
• 323
n
i kPa
10-

0- —7—1- 1 • i • • •— T — | — 1 1

50 100 150 200 250


Column Length, m m .

Figure 7.51: Frictional Force versus Column Length for Rice Flakes.
MILLET

LEGEND
AERATION
PRESSURE
B 0
• 113
B 197
• 323
B 408
kPa

• • •

150 200 250


Column Length, m m .

Figure 7.52: Frictional Force versus Column Length for Millet.

WHEAT

LEGEND
AERATION
PRESSURE
B 0
• 70
B 113
• 197
B 281
B
kPa

. -
i | i i i

100 150 200 250


Column Length, m m .

Figure 7.53: Frictional Force versus Column Length for Wheat.


SAND
300
LEGEND
AERATION
CD
O 200- PRESSURE
o B o
LL • 70
CO B 113
C • 197
o 100-
B 281
o kPa
iZ
LL

T • I ' I • I r
60 100 120 140 160 180
Column Length, m m .

Figure 7.54: Frictional Force versus Column Length for Sand.

BROWN RICE
n -in -
CB
Q.
._- ii
(0 LEGEND
OT • O •
LU 0.45- COLUMN HEIGHT

OC il • B 80 mm.
tr i' B • « 120 mm.
<
LU a B B B B 160 mm.
X 0.40 - • B P 200 mm.

CO B • •
LU • O
B
(3
< B B B
OC
LU 0.35-f T T
>
<
100 200 300 400
Air Pressure, kPa

Figure 7.55: Shear Stress versus Air Pressure for Brown Rice.
199

WHITE RICE
CO u.o-
OL

• • •
CO
(A 07- B
LEGEND
CD
r .
1f COLUMN HEIGHT
B
tin B 80 mm.
P B B • 120 mm.
CO 0.6- B B
0)
1i
9 • P B 160 mm.
JZ
B B •
B B B B B • 200 mm.
(0 B
<> • • • •
a> 0.5- • • • •
at
to
w
0) 0.4- —r
>
< 100 200 300 400
Air Pressure, kPa

Figure 7.56: Shear Stress versus Air Pressure for White Rice.

RICE FLAKES
CO U.b-; >
a. 1 > 5 B B
-C i
o • ft Q
<n B P LEGEND
B B G Q
</> 1 B
0 0.4- • B COLUMN HEIGHT

</5 B B 80 mm.
• m
• P B • 120 mm.
CO B B 160 mm.
0)
JC • 200 mm.
Ui 0.3 J
Q> • •
at
co
_.
0) l r
> 0.2- T 1"
< 100 200 300 400
Air Pressure, kPa

Figure 7.57: Shear Stress versus Air Pressure for Rice Flakes.
200

co I
a.
-C
1.0-
CO LEGEND
n 0.8- B COLUMN HEIGHT
CD B B B 80 mm.
i-
B B • 120 mm.
55 0.6-
CO B B 160 mm.
o B
0.4- ; :
: • • 200 mm.
£ • Q B
B H • • •
CO
0) 0.2-
B B 1 • i i»
B
cs
CO 0.0- -" 1 i — r r r 1
i_
0) 100 200 300 400 500
> Air Pressure, kPa
<

Figure 7.58: Shear Stress versus Air Pressure for Millet.

SANP
CO 10
D. B
-e
co 8-
co a LEGEND
0) • • • COLUMN HEIGHT
tm
<0 6-
B a B B 80 mm.
CO • 125 mm.
o
x: B
a 165 mm.
Ui
0
at 2-\
CO
-.
0 0 1 • 1
> 100 200 300
< Air Pressure, kPa

Figure 7.59: Shear Stress versus Air Pressure for Sand.


201

SHIRLEY PHOSPHATE

CO
CL
-C

CO
0
4- LEGEND
B COLUMN HEIGHT
CO
B 55 mm.
V
3- • 80 mm.
JC
CO • B . • •
0>
O)
2-
CO
tm
0
> — I *- T
100 200 300 400
Air Pressure, kPa

Figure 7.60: Shear Stress versus Air Pressure for Shirley Phosphate.

B R O W N RICE
0.08-

1 LEGEND
0.06-
COLUMN HEIGHT
i1
B 80 mm
mm 0.04-
• 120 mm
B 8 B

e a B 160 mm
l 8 • • • 200 mm
0.02- • •
• •

B B

0.00-1 Tr"— 1 i
100 200 300 400
Air Pressure, kPa

Figure 7.61: Aeration Air Pressure versus Wall Friction Factor \ik for Brown Rice.
202

U.f-

B LEGEND
0.3- COLUMN HEIGHT
I B B
B B a B 80 mm.
-C • 120 mm.
a 160 mm.
0.2- • 200 mm.

• P • #
• •
9 •
B 8 8 8
0.1 - 5100
9
—r
200 — i
300 * > -
B
'f — •
400 500
Air Pressure, kPa

Figure 7.62: Aeration Air Pressure versus Wall Friction Factor uk for White Rice.

RICE FLAKES

LEGEND
COLUMN LENGTH
B 80 mm.
• 120 mm.
It, B 160 mm.
O 200 mm.

200 400
Air Pressure, kPa

Figure 7.63: Aeration Air Pressure versus Wall Friction Factor uk for Rice Flakes.
203

0.5

0.4- LEGEND
B B COLUMN LENGTH
0.3- B 80 mm.
mm • 120 mm.
0.2 B 160 mm.
• 200 mm.

0.1 -
P

0.0 I P
B
100


200 300 400
Air Pressure, kPa

Figure 7.64: Aeration Air Pressure versus Wall Friction Factor |ik for Millet.

WHEAT

LEGEND
COLUMN HEIGHT
B 80 mm.
• 120 mm.
B 160 mm.
O 200 mm.

200 300 400


Air Pressure, kPa

Figure 7.65: Aeration Air Pressure versus Wall Friction Factor u\k for Wheat
7.10 DEAERATTONr

SCALE

PRESSURE TRANSDUCER (PERMEABLE BASE

DEEAERATION
T
CHART
CYLINDER RECORDER
Z E R O CONDITIONING UNIT
STAND
P R E S S U R E T R A N S D U C E R (IMPERMEABLE BASE)

Figure 7.66: Deaeration Tester.

The details and operating procedure for this test and test rig are described in
Chapter 6.13. Figure 7.65 depicts a typical pressure variations during filling of fly ash
'A', 'F and 'G' for a permeable base. The subsequent respective, deaeration
characteristics of the powders tested in Figure 7.67 are depicted in Figure 7.68, when
tested with a permeable base, whereas Figure 7.67 depicts the combined filling and
deaeration pressure variations.

In comparison, the filling and deaeration pressure variations of the fly


tested in the deaeration cylinder with a impermeable base are depicted in Figures 7.70,
7.71, 7.72 and 7.73. The observed bed height versus deaeration time variation for the
fly ash studied when tested with permeable and impermeable bases are shown in Figures
7.74, 7.75 and 7.76.
205

PERMEABLE BASE
ou -
a B
40- a
B LEGEND
• B FLY ASH
30-
B 'A'
D B

• F
20- B 'G'
B
D
10-
B
B
0- B J_ —r- 1
10 20 30
Filling Time, sec.

Figure 7.67: Pressure Variation During Filling; Permeable Base.

PERMEABLE BASE

LEGEND
FLY ASH
-B- TV
•P- F
•a- 'G'

T
100 200
Deaeration Time, sec.

Figure 7.68: Deaeration Time of Fly Ash 'A', 'F and 'G'; Permeable Base.
PERMEABLE BASF

CO LEGEND
0.
FLY ASH
0 -a- 'A'
m. -p- F
3
CO -a- 'G
CO
a>

T
100 200
Deaeration Time, sec.

Figure 7.69: Deaeration Behaviour of Fly Ash 'A', 'F and 'G'; Permeable Base.

IMPERMEABLE BASE
DV -

B F
40 - B
co LEGEND
0. D
• D FLY ASH
30-
B TV
D B
3

• F
CO 20-
(0 B 'G'
0 •

t
10-

B
D n
1 • i •

10 20 30
Filling Time, sec.

Figure 7.70: Pressure Variation During Filling; Impermeable Base.


IMPERMEABLE BASE

co
a. FLY ASH
-B- •A'
3 -•- F
CO
(0 * •G'
0

-i | i 1 1 | i—i r-
0 20 40 60 80 100 120
Deaeration Time, sec.

Figure 7.71: Deaeration Time of Fly Ash'A','F and'G'; Impermeable Base.

FLY ASH 'C

co
a
-C

3
CO
CO
0

T
100 200
Deaeration Time, sec.

Figure 7.72: Deaeration T i m e of Fly A s h 'C; Impermeable Base.


50 -i

40- wr\.
CO
Q.
LEGEND
30- FLY ASH
0 -B- 'A'
m.
3 *T \|ID -»- F
CO
20- •»• 'G'
w
km
0.
0
10-
IB ^^^><^^ k " , *SL_
0 -1
r • , - i |
C» 100 20 0

Deaeration Time, sec.


Figure 7.73: Deaeration Behaviour of Fly Ash 'A', 'F and 'G'; Impermeable Ba

PERMEABLE BASE

E LEGEND
E FLY ASH
JZ -a- 'A'
OJ
0
•P- 'F
-B-'G'
z
TJ
0
OQ

0 100 200 300 400


Deaeration Time, sec.

Figure 7.74: Deaeration of Fly Ash 'A', 'F and 'G'; Permeable Base.
E
E
x
o
z
TJ
0
OQ

40 60 80 100 120 140 160


Deaeration Time, sec.

Figure 7.75: Deaeration of Fly Ash 'E; Permeable Base.

IMPERMEABLE BASE

E LEGEND
E FLY ASH
-B- 'A'
"0 -«- 'GV
X ••- 'G2'
TJ
0
m

100 200 300


Deaeration Time, sec.

Figure 7.76: Deaeration of Fly Ash *A' and 'G'; Impermeable Base.
210

A typical filling-deaeration graph obtained from the Deaeration Tester is revealed

in Figure 7.77 for fly ash 'A*.

--t— ••-.

—[— . .... .
'. J
' L"
1
i i
' !. !
mU
m\ :i
V
1 V [
J N
,
j .
V •«. "
• i

sV j]
t1f
;
,i- •->

£:
£-- , i

t
1
1
1
.r=f— 4


1
/ , —--
• • - • *
*~_,_» :--i ^ 1 - — 1 t~-\ 1 -1. -- < r- "1 . —-*.» ~-1f — f --
1 1 -— — -_ ... .
t
i I 1
1 _j. _l
— 1 — . t j
— i —

( ' 1 ( 1

Figure 7.77: A FiUing-deaeration Graph for Fly Ash 'A'; Impermeable base.

Fly ash deaeration behaviour with time are correlated with exponential regres
curve fits (y = a* 1 0 * ) . The time constants, exponents a, b and regression coefficients
are presented in Table 7.14.

TABLE 7.14: DEAERATION TIME CONSTANT AND EXPONENTS

M A T E R I A ^ E X P O N E N T S a, band R E G R E S S I O N TIME CONSTANT,

COEFFICIENTS Seconds

PERM. BASE IMPERM. BASE PERM. IMPERM.

a b R a b _R_ BASE BASE

38.90 0.0096 0.99 88 _33.


Fly ash 'A' 28.10 0.0054 0.95
16_
Fly ash 'F 23.50 0.0043 0.95 30.92 0.0121 0.98 j60_
65 23
B y ash 'G' 14.88 0.0019 0.96 32.28 0.0079 0.97
211

7.11 FLUIDIZATION AND DFAFR ATTnjy;

-10mm Dia. Holes


/:
jbnnna-r-_Perspex
•**!• il'-^^Flanges

.102mm 1.0.
Transmitter, Pyrex Tube
©0

Perspex
Flange
Air
102mm 1.0.
Supply
Steel Pipe Gas Distributor
Plenum Assembly
Chamber
Pressure Irri
Meter — H U J

Figure 7.78: Fluidization Rig. [ W y p y c h etal. (1987)]

The details and operating procedure for this rig are described in Chapter
6.14. A schematic of this rig is presented in Figure 7.78. The location of the fly
ash tested when plotted on the Geldart diagram are as shown in Figure 7.79.

Fluidization analysis of the powders tested are depicted in Figures 7.80 to


7.85, whereas, Figures 7.86 to 7.88 depict the deaeration behaviour of the fly ash
tested in fluidization rig.
1 10 100 1000 10000
Mean particle size, micron

Figure 7.79: Geldart Fluidization Diagram Showing


the Classification of Fly Ash.

FLY ASH A'

60
50 -

40 -

30 -

20-

10-

0 -T-""?
2 4 6
Superficial Velocity, cm/sec.

Figure 7.80: Fluidization Analysis of Fly Ash 'A'.


FLY ASH 'F
E
o
o
CM
X
E
Ec
•o
CD
O
m
m.
3
n
n 0 2 4 6
Superficial Velocity, cm/sec.

Figure 7.81: Fluidization Analysis of Fly Ash 'E'.

E
o
o
CM
z
E
E
c
0
TJ
CO
o
3
.)
<A
0

2 4 6
SUPERFICIAL VELOCITY, CM/S.

Figure 7.82: Fluidization Analysis of Fly Ash 'A', C and 'E*.


214

8- ^ • — M - M M

6-

4-
r
2-
J
•* • .
u
) 1 2
(
Superficial Velocity, cm/s.

Figure 7.83: Fluidization Analysis of Alumina.

SANP

Superficial Velocity, cm/s.

Figure 7.84: Fluidization Analysis of Sand.


PVC POWDER

Superficial Velocity, cm/s.

Figure 7.85: Fluidization Analysis of P V C Powder.

600

500 -?

400-

300

DEAERATION TIME, SECS.

Figure 7.86: Deaeration of Fly Ash *A' in Fluidization Rig.


510

500- LEGEND
EXP. NO.
490- B 1
• 2
B 3
480- • 4
B 5
470

460 —I 1 \ 1 1—
20 40 60 80
DEAERATION TIME, SECS.

Figure 7.87: Deaeration of Fly Ash 'C in Fluidization Rig.

510-IT

500- LEGEND
EXP. NO.
B 1
490- • 2
B 3
• 4
480-

470
20 40 60 80
DEAERATION TIME, SECS.

Figure 7.88: Deaeration of Fly Ash 'F in Fluidization Rig.


217

7.12 PNEUMATIC CONVEYING FLOW CHARArTERTSTTrs-


(A. STURTEVANT PNFTTMATIC CONVEYING RTOr
FRICTION LOOP-
LEGEnD
O— Pressure
Transducer
1.91 m.
Channel Ilo.

JJ -o-
0.4 m.

1.41 m.

3
--c*
1.41 m.

-ilo- 1 11
o-
0.4 m .

Figure 7.89: Friction Loop.

A schematic of this test rig is depicted in Figure 7.89. This rig incorporates seven
air pressure tapping locations. Six of these pressure tappings were used in the friction
loop as shown in Figure 7.89. In these tapping locations, pressure transducers were
installed with the transducer output recorded using a Data Acquisition System.

The pressure tapping details are shown in Figure 7.90, whereas the Data
Acquisition Channels details are summarized in Table 7.15. The transducer locations,
measured from the blow tank, are declared in Table 7.16.

The materials tested in the friction loop were cement and W h e a t The flow
properties of these materials are declared in Table 7.17.
218

Pressure
Transducer

Quick-Connect
Coupling

1/4" BSPT
Thread

Retaining
Screw
O-Ring
Porex
Disc

1/4" BSP
Socket

52mm I.D.
Pipeline

Figure 7.90: Exploded View of a Typical Pipeline Air Pressure Tapping Location.
TABLE 7.15 - AIR PRESSURE CHANNELS

Channel N a m e of channels
number
0 Blow tank pressure
1 First pipeline pressure
2 First friction loop pressure
3 Secondfrictionloop pressure
4 Thirdfrictionloop pressure
5 Fourth friction loop pressure
6 Fifth friction loop pressure
7 Air supply pressure (orifice plate)
8 Differential pressure
9 Silo load cells
10 Blow tank load cells
11 Sixthfrictionloop pressure

TABLE 7.16 - TRANSDUCER LOCATIONS

Transducer Downstream
location, m .
First transducer 0.15 m .
Firstfrictionloop transducer 4.68 m .
Secondfrictionloop transducer 6.06 m .
Third friction loop transducer 7.45 m .
Fourth friction loop transducer 10.17 m .
Fifth friction loop transducer 11.55 m.
Sixth friction loop transducer 12.94 m.

TABLE 7.17 - MATERIALS FLOW PROPERTIES

Material Solid density, Loose poured d50,


kg/m3 bulk density, |j,m

kg/m3
Cement 3100 950 30
Wheat 1380 864 313
220

A summary of the test results are summarized in Tables 7.19 and 7.20. In this test
series, the particle velocity was measured by using a Tealgate T.200 series transducer in
combination with a Hewlett Packard Correlator, refer Chapter 6.2.

For the next test series, the air pressure channels and transducer locations details
are shown in Table 7.18, whereas Tables 7.21 and 7.22 summarize the results of
conveying characteristics of sand. The flow properties of sand are declared in Sections
7.3 to 7.5.

For experiment No. 1 to 49, the Tealgate T.200 series transducer was used in
combination with a Hewlett Packard Correlator, whereas for experiment N o . 50 to 82, a
purpose built fibre optic velocity probe w a s used, refer Section 6.2.2. The variation of
transducer air pressure for sand versus distance from blow tank are shown in Figures
7.91 to 7.98.

T A B L E 7.18 - AIR P R E S S U R E C H A N N E L S A N D T R A N S D U C E R
LOCATIONS

Channel Name of channels Transducer Downstream


number No. location, m .
0 B l o w tank pressure 0 0
1 First pipeline pressure 1 0.15
2 Second pipeline pressure 2 3.51
3 Third pipeline pressure 3 4.22
4 Fourth pipeline pressure 4 6.44
5 Fifth pipeline pressure 5 14.76
6 Sixth pipeline pressure 6 18.08
7 Air supply pressure (orifice plate) 7 -

8 Differential pressure _ .

9 Silo load cells 9 .

10 B l o w tank load cells 10 -

11 Seventh pipeline pressure 11 25.37


12 Eighth pipeline pressure 12 29.62
221

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TABLE 7.22: TRANSDUCER AIR PRESSURES, kPa

EXP. CHANNEL NO.


NO. 0 1 2 3 4 5 6 11 12
21. 110 107 120 85 65 62 56 46 42
22. 120 117 130 100 75 70 60 50 46
23. 113 110 120 85 70 65 55 46 39
24. 105 101 115 75 60 56 60 42 38
25. 105 101 115 75 60 56 60 42 38
26. 120 115 125 85 68 65 60 46 42
28. 80 72 88 50 47 45 40 31 29
29. 105 102 110 70 40 38 50 40 37
30. 95 90 105 65 55 52 45 36 34
31. 112 107 120 75 57 55 52 42 38
33. 100 96 105 65 55 52 50 38 34
35. 95 90 100 60 50 48 42 32 30
37. 105 103 110 70 60 58 50 38 35
38. 105 101 107 70 60 58 50 39 36
39. 90 84 90 53 50 48 40 32 28
40. 80 75 78 50 45 42 38 28 26
41. 75 65 80 . 40 38 35 . .

42. 86 80 95 55 48 45 40 - -

43. 76 82 48 44 42 38 25 29
44. 102 98 110 70 60 55 50 . -

45. 85 81 110 70 60 55 48 32 28
46. 113 70 62 60 55 42 40
47. 84 82 90 50 42 40 35 28 26
49. 90 82 50 1
45 40 34 28
50. 130 126 120 112 i 75 68 62 48 42
51. 90 85 50 ! 45 40 34 26
52. 155 148 140 133 90 80 70 50 40
53. 152 148 138 I 87 ! 80 70 55 50

57. 100 98 91 90 56 53 50 36 33

58. 124 120 112 110 70 67 60 46 42

62. 146 136 127 125 80 75 . 56 48

63. 129 125 123 121 78 70 68 48 42


228
64. 115 112 107 105 70 65 60 46 40
66. 100 90 85 83 50 47 43 34 30
67. 110 106 97 95 62 56 52 40 34
70. 72.5 70 66 64 42 38 34 28 23
71. _ 100 97 65 ., _ 33 29
72. 87.1 85 80 78 50 47 44 . .

73. 100 97 89 87 56 52 48 36 33
74. 130 122 113 111 70 66 62 48 44
75. 115 112 105 103 63 60 55 42 38
76. 132 129 120 118 75 70 65 52 44
77. 132 128 120 117 75 70 65 52 44
78. 123 120 110 106 66 60 55 46 40
79. 115 111 106 105 ! 65 i 60 56 44 40
80. 70 68.6 64 61 40 37 34 _ _

81. 92 86.6 80 78 50 46 44 34 28
82. 105 98.3 90 88 56 54 50 38 32

PARTICLE CONCENTRATION:
This was calculated by using eqn. (C.5), refer Appendix C with the evaluated
values declared in Table 7.21. Also, a typical solids concentration variation during
experiments obtainedfromthe Tealgate T.300 concentration sensor are depicted in
Appendix C.

BENDS:
The pressure drop obtained using two different bends, namely long radius and
vortice elbow are shown in Table 7.23. As evident in Table 7.22, air pressure channels
No. 11 and No. 12 for experiments 24 to 82 are for vortice elbow bend.

TABLE 7.23: BEND AIR PRESSURE, kPa

Exp. No. Channel No. 11 Channel No. 12 Type of Bend


51 48 40 Long Radius
56 34 29 Long Radius
20 38 33 Long Radius
21 46 42 Vortice
22 50 46 Vortice
23 46 42 Vortice
CB 140
0-

120-.
a
M 100 LEGEND
Exp. No.
0
0 80-

60-
f B 21
• 24
a 29
0
O

J
40
a
•o
n 20
—r-
c 10
a
20 30
Distance from blow tank, m.
I-

Figure 7.91: Transducer Air Pressure versus Distance from Blow Tank.

a 140
a.
mm
120
3 LEGEND
0 100-
3
Exp. No.
0
0
B 35
80-
• 40
• 74
60-
* B B
o 40 P
3 P
TJ 5 I
M 20 —r~
C
0 10
10 20 30
a
Distance from blow tank, m.
Figure 7.92: Transducer Air Pressure versus Distance from Blow Tank.
0 uu -
Q.
-c
1
3 80- 1 P
0 • LEGEND
]
0 1 Exp. No.
0 r
B 28
60-
• 41
a B 47
B •
O 40-
O I I Q
D
3 B
•o E
0 B B
1
c 1
0 10 20 30
Distance from blow tank, m.

Figure 7.95: Transducer Air Pressure versus Distance from Blow Tank.

0
CL
100
-C

3 LEGEND
at
0 Exp. No.
0
B 42
• 72
B 82
o
o
3
•o
0
C
0
Distance from blow tank, m.

Figure 7.96: Transducer Air Pressure versus Distance from Blow Tank.
LEGEND
Exp. No.

h 1
B
e
B
26
46
79

-1—
10 20 30
Distance from blow tank, m.

Figure 7.93: Transducer Air Pressure versus Distance from Blow Tank.

\&J -

100 -1 B
LEGEND
• i u
80- Exp. No.
B 71
B e 73
60- B 81

40-
'' - 8
B 41
El B
i • i

C 10 20 30
Distance from blow tank, m.
Figure 7.94: Transducer Air Pressure versus Distance from Blow Tank.
232

(B) L O W VELOCITY CONVFYTNC- pTrrT


The relevant test conditions for this test series including data channel details and
pipeline details are declared in Tables 7.24 and 7.25, respectivelty. A summary of the
test results for the low velocity conveying rig are shown in Table 7.26.

TABLE 7.24: DATA CHANNEL DETAILS

CHANNEL N A M E OF CHANNELS
NOS.
0 Blow tank top air pressure
1 First pipeline air pressure
2 Second pipeline air pressure
7 Orifice plate upstream static pressure
8 Differential pressure !
9 Blow tank load cell
10 Silo load cell

TABLE 7.25: PIPELINE DETAILS

Series Experiment Horizontal pipeline length, Vertical Bend Details


No. m. pipeline, Number Equivalent
First loop Second loop length, m . length, m .

A Experiment 1 to 20 3.11 87.51 6.48 11 44

B Experiment 21 to 30 3.11 41.71 6.48 7 28


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235

CHAPTER 8
DISCUSSION

8.1 SCANNING ELECTRON MICROSCOPE:


S E M photographs revealed important powder features including particle size, particle
porosity, surface roughness, edge description, the existence of agglomerates, interparticle
contact details, etc.. For example, from S E M photographs observations, the sharp and
angular edges of raw sugar grains, dense soda ash, zinc fume and pulverized coal suggest
that such materials m a y cause excessive wear and damage to pipes, blow tank and filtration
equipment. In comparison, the large rough surfaces of P V C powder suggest this powder is
prone to interlocking during dense phase conveying. In regard to fly ash, the significant
degradation observed during conveying (Wypych, 1986) is consistent with the existence of
loosely agglomerated macro particles. Hence, this information is vital for explaining both
directly and indirectly unusual flow behaviour, poor system performance, blockage, wear
and erosion characteristics. This information related to particle characteristics is summarized
in Chapter 7, Table 7.1.

8.2 COEFFICIENT OF RESTITUTION:


Figure 7.2 depicts the observed variation of the angle of impact versus coefficient of
restitution for Wheat impacting on Mild Steel and Stainless Steel wall surfaces, Millet on Mild
Steel and Bean seed on a Stainless Steel wall surface. The observed range of the coefficient
of restitution, 0.55 to 0.65, is typical for these particle wall contacts (Ottjes, 1982).

It should be noted that both Bean and Millet seeds are spherical granular particulates.
It was found that Millet has a lower coefficient of restitution compared to that for both the
spherical Beans and Wheat. This trend was attributed to the smaller particle size of Millet. In
this series of tests, the coefficient of restitution was measured with the disc tilted in the
direction of rotation.

In Figure 7.3, which depicts the variation of coefficient of restitution tilted in the
flow direction, the observed range was 0.44 to 0.65. For coal, the coefficient of restitution is
higher, when impacting on Mild steel (Initial drop height = 10.6 cm.) compared to that
when impacting on Stainless Steel. For Sinter and Sodium Ferrite, the observed coefficient
of restitution ranged from 0.52 to 0.58.
236

In Figure 7.4, the coefficient of restitution was measured with the impact disc tilted
against the direction of rotation. In this configuration, the coefficient of restitution ranged
between 0.56 to 0.69. A n examination of this Figure clearly reveals that Millet has a lower
coefficient of restitution compared to that observed for Wheat and Coal.

The coefficient of restitution for Coke impacting on Stainless Steel was found to be
0.54, Sugar on Mild Steel 0.53 and plastic balls on Mild Steel 0.71 which is relatively high
compared to the other materials tested. The latter coefficient of restitution was the highest
observed coefficient of restitution.

It was found that the coefficient of restitution was lower on Stainless Steel compared
to that for Mild Steel. T h e latter suggests that for a given system a lower pressure drop will
result when using Stainless Steel pipe compared to that for a Mild Steel pipe. However, this
operation advantage must be compared with the additional capital cost associated with the use
of Stainless Steel pipes. Obviously, for food standard systems the use of Stainless Steel
pipework is mandatory.

The use of Stainless Steel may also be warranted for materials exhibiting high
coefficients of restitution and hence high system pressure drops w h e n conveying in dilute
phase in Mild'Steel pipe systems. In these situations, the lower wall friction characteristics of
Stainless Steel m a y also be an advanatage.

As stated, the aforesaid pressure difference will be more significant for dilute phase
systems. This implies, in turn, that knowledge of the coefficient of restitution is more
important in dilute phase systems, in regard to explaining unusual flow behaviour, high
system pressure drops or in systems operating at low flow rate.

8.3 PARTICLE SIZE ANALYSIS;


F r o m an examination of Table 7.3, which presents the size characteristics of the fly
ash and cement tested, it is apparent that fly ash 'E' and 'C display the smaller Sauterpaean
diameter D(3, 2) and the m e a n diameter D(4, 3) derived from the volume distribution
compared to the other fly ash tested. In particular, fly ash 'E' has a m e a n Sauter diameter
of 10.2 |im, whereas the next finest, fly ash 'C, has a m e a n Sauter diameter of 13.9 ,am.
The m e a n diameter for fly ash 'E' and 'C are 10.2 and 13.9 |J.m. Furthermore, Table 7.3
reveals that fly ash 'E' has the lowest m e a n particle size of 5.4 |im. In comparison, the
mean particle size of fly ash 'A' is 16.9 |im and cement 18.3 |im.
237
Fly ash 'E' a n d ' C have the higher specific surface of 0.18 sq. m / cc and 0.12
sq. m / c c , whereas S a n d and P V C p o w d e r have lower specific surface areas of 0.02 and
0.03 sq. m / c c , respectively. Figure 8.1 depicts the variation of specific surface versus
m e a n particle size for the fly ash tested for all measurement runs. It can be seen from this
Figure that as the m e a n particle size increases, the specific surface decreases.

o
ti

VI

ft
u
L
3
(0
ti
u
ft I I—I I I—I—I I I I I I—I I I—I I I—I-
o- 6 8 10 12 14 16 18
(0
Mean Particle Size d50. "im

Figure 8.1: Variation of Specific Surface versus M e a n Particle Size for the Fly Ash
Tested.

The particle size analysis of Sand, Brown Rice and White Rice, as declared in
Tables 7.4 to 7.7, reveal that these materials are granular materials somewhat coarser than
fly ash samples and cement powders.

Figures 7.5 and 7.6 which compare the particle size distributions of all materials
tested, indicate that all fly ash tested possess particle size distributions with similar slope
over the d6o- d 4 0 range with fly ash 'E' displaying a slightly steeper slope. This
tendency suggests that the formation process of the various fly ash powders tested were
similar.

The above trends are reinforced in Figures 7.7 to 7.10, which depict the log
normal distribution plotted as a relative percentage frequency distribution using a
logarithmic scale for particle size of the powders tested.
238

TABLE 8.1 EFFECTS OF DIFFERENT LENSES ON


PARTICLE SIZE DISTRIBUTION

Material Obscu- Focal Geomertic Volume Beam Distri- Log


ration Length Volume Concen- Length bution Error
'mm) Median -tration Width
Dia. (mm) (Span)

Cement 0.1752 100 18.3 0.0052 14.3 2.7 3.74


Fly ash 'E' 0.1867 63 5.4 0.0018 14.3 4.6 2.46
Fly ash 'D' 0.1726 300 11.8 0.0037 14.3 6.9 2.08
Fly ash 'D' 0.4830 100 8.8 0.0094 14.3 6.5 2.68
Fly ash 'D' 0.2017 100 10.0 0.0037 14.3 6.1 2.57
Fly ash 'G' 0.1599 300 14.9 0.0037 14.3 5.4 2.84
Fly ash'G' 0.1685 100 13.8 0.0033 14.3 5.2 2.66
Fly ash'G' 0.2335 100 13.9 0.0048 14.3 5.2 2.67
Fly ash 'F 0.1795 100 14.0 0.004 14.3 4.4 2.78
Fly ash 'F 0.156 100 13.8 0.0034 13.8 4.4 2.52
Fly ash 'C 0.302 100 9.2 0.0054 9.2 3.0 2.97
Fly ash 'B' 0.1323 100 14.3 0.0032 14.3 4.1 2.96
Fly ash *B' 0.1184 100 15.0 0.0028 14.3 4.1 2.91
Fly ash 'A' 0.1941 100 15.1 0.0051 14.3 4.0 3.19
Fly ash W 0.2026 63 16.9 0.006 14.3 3.1 3.41

Proper selection of the Malvern particle sizer lens is important. In particular,


particles outside the range of the lens, lead to erroneous results. Table 8.1 shows
variation of m e a n particle size with respect to different lenses and the effects of sample
concentration on the m e a n size.

Figure 8.2 shows the variation of mean particle size versus characteristic
dimensions for the fly ash with different measurement runs. Figure 8.3 shows the
variation of average characteristic dimensions of each fly ash versus mean particle size.
From both Figures, it is revealed that fly ash 'E' and 'C have the lowest characteristic
dimensions of the fly ash samples tested.
239

100
'D' T* >B> >A'
G 'G* D
80
'D' ID
.2 8 'A' B D(v,0.9)
** =i • D(4,3)
•2 . 60 H
L. e • D(3,2)
ft e • D(v,0.1)
* * i ^
'E'
ti w • D(v,0.5)
*• _- 40
L * w V
*G
ua I! D
O «w t - •"—r
20 H4 6 8 10 12 14 16 18 20
Mean Size, d50, |im

Figure 8.2: Variation of Mean Particle Size versus Characteristic Dimensions of Fly
Ash.

OM ~

•a*
•D'
60 - •
T' LEGEND
>r* H 'B* 'A'
*- _± • D(v,0.9)
L e • 0(4,3)
40 -
ft e •c n D(3,2)
'E'
•* '^
• •
o D(v,0.1)
o w • • • D(v,0.5)
?0 - • •
*"- ? ••• •
rr S • • •
u a 1 D o
O
o- T"»T "•!'—!— 0
I ' ' i i r-T- i i i i i l ' '
6 8 10 12 14 16 18
Mean Size, d50, |im

Figure 8.3: Variation of Average Characteristic Dimensions versus M e a n Particle Size.

Figures 8.4 and 8.5 reveal the variation of m e a n size versus % < 5.8 u m and
particle size distribution span, respectively for all measurement runs. The particle size
distribution span measures the spread between the 10% and 90% points of the cumulative
undersize distribution, scaled in terms of the 50% point and defined as the ratio of
D(v,0.9) - D (v,0.1)/D(v,0.5) pm. Figure 8.6 reveals the variation of mean particle size
versus average % < 5.8 pm and particle size distribution span. It is revealed from these
Figures that fly ash _* has the highest % < 5.8 pm as compared to other fly ash,
whereas fly ash 'D' has the highest particle size distribution span.
240

60

50 -

09
10 30 -
v
tf 20 - B' -A'

10 -

—i I i I i I i I i I » l •
4 6 8 10 12 14 16 18
D(v,0.5), |im

Figure 8.4: Variation of Mean Size versus % < 5.8 pm for Fly Ash Tested.

5 -
a.
(0 4 -

3 -

- I — • 1 1 1 • I • 1 — • -
8 10 12 14 16 18
D(v,0.5), pm
Figure 8.5: Variation of M e a n Size versus Particle Size Distribution for Fly Ash Tested.
241

60

50 - -6

40 - 'E' e LEGEND
CO -5 «
IO <3 % < 5.8ipm
Ok
v Vt • PSD.span
30 H M 8
tf

20 H -3

10 I • • l • • I • • l l ' ' I ' -


4 6 8 10 12 14 16 18
D(V,0.5), p m

Figure 8.6: Variation of M e a n Size versus Average % < 5.8 p m and


Particle Size Distribution Span for the Fly Ash Tested.

The above Figures confirm clearly identifiable property differences between the
powders tested. In some cases differences in the numerical values for the properties
approaching an order of magnitude were apparent. These differences are mainly due to
differences in the particle size distributions and are strongly dependent on mean particle
size.

8.4 PACKED BULK DENSITY, LOOSE POURED BULK DENSITY,


COMPRESSIBILITY:
Figures 8.7 and 8.8 depict the variation of bulk density with major consolidation
stress for the fly ash and cement tested. This testing revealed that fly ash 'C and 'E' had
the lower bulk density a m o n g the fine powders tested. Furthermore, it is evident from
Table 7.8 that the bulk density empirical coefficients ranged from 649 to 1512 kg/m 3 and
0.0016 to 0.0598 for p 0 and b, respectively. The empirical coefficient b is highest for fly
ash 'B' (0.0598) followed closely, in turn, by that for Light Soda ash, fly ash 'F, 'E'
and 'C (0.0554).

Such high numerical values for the coefficient b suggest that these powders are
highly compressible. In comparison, low values of b were observed for materials such
as Wheat, Rice and Millet. This clearly indicates that these materials are relatively
incompressible. All fly ash and cement have a higher value of b compared to other
granular materials. Unfortunately, Figure 8.9 which reveals the variation of b versus
mean particle size dso, reveals no apparent trend.
242

1300

Major Consolidation Stress (kPa)

Figure 8.7: Bulk Density versus Major Consolidation Stress.

1600

1400 LEGEND
FLY ASH
B E
1200- • F
n G
• CEMENT
1000-

800
0 10 20
Major Consolidation Stress (kPa)

Figure 8.8: Bulk Density versus Major Consolidation Stress.


243

u.ui -

ft 'B'
0.06 - •F'
e 'E' •
"C" • CEMENT
ti
'G'

VI
'D1
0.05 -
Yl •
ft
L •A'
a
E U.\J*V 1
e 10 20
u Mean particle size, microns
Figure 8.9: Compressibility Coefficient Variation versus Mean Particle Size.

TABLE 8.2 COMPRESSIBILITY OF MATERIALS.

Material Compressibility, % Material Compressibility, %

Fly ash 'A' 25 Cement 28


Fly ash 'B' 34 Sand 5
Fly ash 'C 45 P V C powder 11
Fly ash 'D' 35 Wheat 18
Fly ash 'E' 37 Brown Rice 15
Fly ash 'F 24 White Rice 13

The compressibility, as the difference between the packed bulk density and the
loose poured bulk density, divided by the packed bulk density times 100, are shown in
Table 8.2. It can be seen that compressibility values of Sand, P V C powder, Brown Rice,
White Rice varies in between 5 to 15 percent and having free flow powder
characteristicks. For cement,flyash 'A' and fly ash 'F the compressibility values range
from 24 to 28 percentage, whereas forflyash 'B\ fly ash 'D\ fly ash 'E' the range is
from 34 to 37 and for fly ash 'C it has a value of 45.
244

From Table 7.9, it is evident that the ratio of packed to loose poured bulk density is
highest for fly ash 'C compared to the other fly ash tested. The loose poured bulk density of
the powders tested is the average of three observations. This value is closely followed by
that for fly ash 'E', 'D', 'B', 'A', cement, fly ash 'F, Wheat, B r o w n Rice, White Rice,
P V C powder and Sand, in that order. This ratio is a good indication of cohesion and
fluidization characteristics, with a higher value indicating greater cohesiveness and hence
decreasing flowability. In particular, Geldart et al. (1984) reported the ratio of tapped and
aerated bulk density is less than 1.25 for group A , from 1.25 to 1.4 for group A C and greater
than 1.4 for group C powders. The ratio of the packed and loose poured bulk density is also
known as the Hausner ratio.

Figure 8.10 which depicts the variation of the Hausner ratio (ratio of packed to loose
poured bulk density) with dso, indicates this ratio increases with decreasing particle size. A
closer examination of this Figure suggests that the Hausner ratio is relatively high for fly ash
'C. This high numerical value is consistent with the higher cohesiveness exhibited by this fly
ash. The same also suggests that fly ash 'C will display greater tendencies for flow
fluctuations and flow difficulties from blow tank especially in dense phase systems. The
exponential trend correlation for this Figure is y = 2.2877 x"0-173 where x = dso-

Figure 8.11 shows the variation of mean particle size versus all Hausner ratio data
obtained from experiments with 1 % error bars. Figure 8.12 shows the variation of Hausner
ratio versus particle size span for the fly ash tested, whereas Figure 8.13 shows the variation
of Hausner ratio versus average particle size distribution span. It is revealed from Figure 8.13
that fly ash 'C has the highest Hausner ratio with least span, whereas fly ash 'D' has
highest particle size span and an intermediate Hausner ratio.
M
o
5 >.
o "n
*- c
o
o
• - - _ *

o —
a 3
a. .a
O 3
~ 2
a a
K Mean particle size, microns

Figure 8.10: The Ratio of Packed to Loose Poured Bulk Density versus
Particle Size for the Fly Ash and Cement Tested.

1.9
1.8- 9
o 'E'
«
r->
(0 1-7 H •c
OC •D' •B'
1.6
co i
« 1-5"
X
1.4 H

1.3 - 1 — i — | — i-+
! — i — r — i — i — • — i •—

6 8 10 12 14 16 18
Mean Particle Size, microns

Figure 8.11: Variation of Mean Particle Size versus Hausner Ratio.


/ -1 El

6- •
'D'
5- 'E1
CO
'A' ,B. •
a
4- B •
oo

3- B

2- • 1 -
• i • i —* — 1 ' 1
1.3 1.4 1.5 1.6 1.7 1.8 1.9
H. R.

Figure 8.12: Variation of the Hausner Ratio versus Particle Size Span.

i.a -
•c
1.8- B

1.7-
'E'
1.6- B 'D'
'B' EI
1.5- •

1.4- TV
'F

B
i 1
1 .o "1 ' 1 •
' 1 1
2 3 4 5 6 7
PSD, Span

Figure 8.13: Variation of Hausner Ratio versus Average Particle


Size Distribution Span for the Fly Ash Tested.
247
8.5 S O L I D S D E N S I T Y -

From Table 7.10, it is evident that the solid density observed for the materials
tested ranged from 1147 to 2735 kg/m3. This range is described more fully in Table 8.3
which depicts the density and density related values for the powders tested.

From bulk and particle densities, the voidage e can be calculated. Apparent
specific volume V s is the bulk volume of powder of unit weight, which is the inverse of
bulk density. Bulkiness is the bulk volume of powders, which is the inverse of packing
density. Greater bulkiness reveals lessflowability,whereas less bulkiness require less
storage. Voidratiois the ratio of the void volume to the net volume of powders.

The equations for the above parameters are shown at the top of the following
Table 8.3. This Table reveals that significant variations occur between the numerical
values of density and density related values for apparently similar powders. These
significant numerical differences, for the various parameters, reflect complex differences
in powder packing arrangement and particle shape. The same m a y also indicate test
deviations.

Fly ash 'E' having greatest bulkiness (2.604), exhibits less flowability, whereas
Wheat with lowest bulkiness (1.59) requires less free volume. Furthermore, it is revealed
from Table 8.3 that fly ash 'E' has the highest voidage and the lowest packing density,
whereas Wheat has the lowest voidage and the highest packing density.

An initial implication of the practical significance of these vast numerical


difference is the implied differences in blow tank volume system requirements. A further
significant variation is the variation of voidage versus mean particle size dso which is
revealed in Figure 8.14. The exponential trend correlation for this Figure is y = 0.77618 -
o. 143 w here x = dso.

It is observed that fly ash 'G' and cement revealed greatest variation from the
observed trend as voidage is strongly effected by particle size distribution and packing
mechanisms.
248

TABLE 8.3 DENSITY PARAMETERS

Material Po Voidage Packing Specific Bulki- Void ratio


kg/m 3 e = density volume ness (|)v=e/ 1-e
(Ps - Pb)/ Pi <J)p=l-e V s = 1/Pb <t>b=l/<t>p

Fly ash 'A' 1032 0.515 0.485 9.689 x IO"4 2.062 1.062
Fly ash 'B* 1134 0.545 0.455 8.818 x IO"4 2.198 1.198
Fly ash C 944 0.57 0.43 10.593 x IO"4 2.326 1.325
Fly ash 'D' 1088 0.585 0.415 9.191 x 10-4 2.41 1.409
Fly ash *E' 975 0.616 0.384 10.256 x IO"4 2.604 1.604
Fly ash T 1275 0.497 0.503 7.843 x IO"4 1.988 0.988
Fly ash 'G' 1294 0.459 0.541 7.843 x IO"4 1.988 0.988
Cement 1312 0.577 0.423 7.621 x IO"4 2.364 1.364
Sand 1502 0.451 0.549 6.657 x IO"4 1.821 0.821
P V C powder 649 0.529 0.471 15.408 x IO"4 2.123 1.123
Sodium Ferrite 1512 0.411 0.589 6.613 x IO"4 1.698 0.698
Wheat 868 0.371 0.629 11.52x IO"4 1.59 0.59
White Rice 865 0.415 0.585 11.56x IO"4 1.709 0.709
Brown Rice 825 0.478 0.522 12.121 x IO'4 1.916 0.916
Sugar 883 0.411 0.589 11.325x10-4 1.698 0.698

u.i -

\ E'
0.6- 'C* 'D* CEfvENT
ffi B ,B. Q
cn
r-T^El
co
o
0.5- -F Q 'A'
>
'G' B

0.4-
10 20
Mean particle size, microns
Figure 8.14: Voidage versus Mean Particle Size for the Fly Ash and Cement Tested.
249

8-6 COHESIVE ARCH LF-NOTH AND DRATNED ANGLE OF RF.POSF..


8.6.1 COHESIVE ARCH l.RNOTH;
Since the ratio of the silo width to m a x i m u m outlet opening span of the Arch Tester is
2.5 : 1, plane strain conditions are assumed to apply during gravity discharge (Figure 7.11).
Hence, the Arch Tester can be used to measure the plane flow outlet span necessary to attain
reliable gravity discharge in a funnel flow channel. This span is commonly known as the
critical cohesive plane flow arching dimension for rough walls (Jenike, 1970). Unfortunately
for very cohesive powders, arching prevents realistic measurement of this arching dimension
and obviously, the drained angle of repose.

From the results, it was revealed that, in general the Jenike and Walker methods give
arch lengths m u c h higher than those observed in the experiments. But for fly ash 'C and
'E', the difference between the experimental arch lengths and that predicted from the Jenike
and Walker methods were m u c h less.

The Arch Tester may give the lower bound on the critical arch opening, whereas the
Jenike method the upper bound. T h e overdesign of over 1 0 0 % associated with Jenike's
method m a y be useful to account for initial filling conditions and other factors like increase in
moisture content. The correct determination of the flow function from shear strength
measurement with the Jenike shear cell m a y be an important factor generating this
overdesign.

The arch length for fly ash 'A' was tested on two days having different relative
humidity, namely 5 5 % and 5 9 % , refer Figure 7.13. A n examination of this Figure reveals
that the arch length increased significantly with increasing relative humidity and the arch
length increased as the deaeration time including filling was increased. This observation is
consistent with that of Molerus et al. (1982).

Further evidence for the increase in cohesive arch length with increasing relative
humidity was clearly apparent from the arch tests conducted on fly ash 'C and cement, refer
Figure 7.14 and 7.15, respectively. This m a y be due to capillary condensation of water in the
void between two particles resulting in a component additional to the van der Waals attraction
(Visser, 1989). Thus, the environmental relative humidity strongly influences cohesive arch
length and hence cohesive properties of powders during transport.
250
From the Table 7.11, it is evident that for fly ash, cement and Sodium Ferrite, the
arch length increased with increasing deaeration time. It was observed that fly ash 'F
becomes cohesive after considerable deaeration. In fact, the cohesive arch formed was so
strong that no flow occurred and extended some 30 m m high across the outlet. Since, fly
ash 'E' exhibited the smallest m e a n particle size, the observed trend in the arch length
suggested that as the m e a n particle size decreases, the cohesive arch length increases.

Fly ash 'E' and 'C have higher arch length than other fly ash and cement, refer
Figures 7.16 and 7.17. Figure 7.19 depicts the variation of mean particle size versus arch
length for theflyash tested. This Figure reveals that as the mean particle size dso decreases,
the arch length increases. This trend is consistent with that observed by Borg (1982).

The relatively large cohesion force observed for fly ash 'E' deviates from the
cohesive strength trend predicted by Molerus et al. (1982). This deviation highlights that the
particle size distribution and packing in addition to the m e a n particle size significantly
controls a powder's cohesion. Hence, fly ash 'E' with the smallest particle size and largest
% -10 p m material displays the highest cohesion of the powders tested.

Fly ash 'B' was found to be relatively free flowing compared to the other fly ash. In
comparison, fly ash 'C was very cohesive. In fact, the powder tends to form vertical flow
channels after long deaeration times. Furthermore, this powder tended to form arch across
the tester outlet. In particular after considerable deaeration, measurement of the cohesive arch
length was impossible due to the occurrence of cohesive arch.

In addition, testing with the Arch Tester indicated that the arch length was dependent
on the depth of material in the tester. This trend is evident in Figure 7.18 as observed for
cement.

Unfortunately, results from the cohesive arch tester proved to be highly sensitive to
test conditions including ambient relative humidity,fillingprocedure and extent of deaeration.
Hence, at best the Arch Tester should only be used for indicating the cohesiveness of various
powders or to indicate the relative differences in cohesiveness between seemingly similar
powders.
251

8.6.2 DRAINED ANGLE OF REPOSE:


Figure 7.20 depicts the variation of drained angle of repose versus bed height for
cement at differing relative humidity. The trend that the angle of repose increases with
increasing storage time is clearly evident in Figure 7.21 which depicts the variation of drained
angle of repose versus deaeration time for various fly ash. These effects compound when
both the deaeration time and relative humidty increases as shown in Figrue 7.22 for cement.

A further interesting trend is evident in Figure 7.23 which depicts the variation of
particle size versus drained angle of repose for the powders tested. This Figure reveals that
the drained angle of repose increases as the m e a n particle size dso decreases. This is
consistent with the trend reported by B r o w n (1961).

-00-i

90- B 'E' ,
°S
^—'•'""ETC -
C TO
n •r
80- ^*^*^
• BT^^^
£ o.
a «> 70 - B B 'B*
CEMENT

60 H i 1 • i « I • I • I '—
1.4 1.5 1.6 1.7 1.8 1.9
Ratio of packed to loose
poured bulk density

Figure 8.15: Variation of Ratio of Packed to Loose Poured Bulk Density


versus Drained Angle of Repose for the Powders Tested.

An increasing trend is evident from Figure 8.15, which reveals the variation of
drained angle of repose versus ratio of packed to loose poured bulk density of powders
tested. This trend is consistent with that observed by Grey et al. (1968).

It was observed that the drained angle of repose increased with deaeration time. For
fly ash 'D', the average front angle of repose was 65°, back angle of repose was 75° for 20
minutes filling and deaeration time, whereas for 27 minutes filling and deaeration time, the
average front angle of repose was 70° and back angle of repose w a s 85°. In this case, filling
was conducted by mechanical means.
252

A s noted from Figure 7.21 generally, the drained angle of repose increased with
increasing deaeration time. Furthermore, the experimental work also suggested in a
qualitative matter, that the drained angle of repose increases with increasing powder
cohesion. This trend is consistent with the trend predicted by Molerus et al. (1982). Hence, a
small change in fine particle content results in measurable change in cohesiveness. In
particular, fly ash 'E' was found to be the most cohesive of the powders tested. For this
powder, of m e a n particle size 5.4 p m , the angle of repose for all flow channel boundaries
was 90°. Particularly, in one test a drained angle of repose of 110° was noted. Testing was
conducted on two days at relative humidity of 7 3 % and 7 8 % , respectively. For all
observations, recorded angles of repose in excess of 90° were noted. After significant
deaeration, determination of drained angle of repose was not possible due to the tendency of
the powder to arch.

One powder, cement, however deviated from the general strength versus particle size
trend. It is considered that the hygroscopic nature of cement caused this powder to display
higher drained angle of repose compared to the observed general trend. This tendency to
absorb moisture, obviously, increased the powder's cohesiveness. This, in turn, suggests
that the drained angle of repose displayed by hygroscopic materials is dependent on test
relative humidity. Therefore, for hygroscopic powders the relative humidity must be
controlled and specified and be representative of actual plant conditions. This clearly suggests
that cement must be pneumatically conveyed with dry air.

Although variations with drained angle of repose were noted for the various powders,
no consistent trend was observed. For this reason, the angle of repose at best is a crude
simple indicator of a powder's cohesiveness.

8.7 FLOW FUNCTION:


Here, cohesion is indicated by the intercept formed by the powder flow function and
the unconfined yield stress axis. It should be noted that the flow function, also called the
failure function, can be used to characterize the flowability of powders (Jenike, 1970) since
it is a property of the bulk material and its degree of compaction.

The flow function of powders were determined in a Jenike Direct Shear


various consolidation loads. This testing revealed that fly ash 'E' to be the most
253

and cement to be least cohesive of the powders tested. The other fly ash exhibited
intermediate cohesive strength as revealed in Figure 7.25 and Table 7.12.

A further characteristic of the flow function is its slope. In general, an increasing


function slope indicates decreasing stability and reduced suitability for pneumatic conveying.
From Table 7.15, it is evident that fly ash 'E' has the highest slope of 0.923. Furthermore,
powders exhibiting steep flow functions have a greater strength and ability to support an arch
and strong tendency to form plugs during pneumatic conveying [Thompson, (1984)]. These
plugs will possess considerable strength and be hard to dislodge due to the consolidation
effect caused by the action of the significant body forces present during the plug formation
process.

The trend between effective angle of friction 6 observed from the Arch Tester and 8
from shear tester is good, as shown in Fig. 8.16. However, the trend between internal angle
of friction 0 observed from Arch Tester and (J) from the shear tester is not as consistent, refer
Fig. 8.17. This is expected because the actual powder yield locus must take into account the
cohesion C of the powder.

100 -•

E 90-
_>
E
Q)
S* 80-
LU
E
2 70-

60 -
30 40 50 60
From Shear Tester

Figure 8.16: Variation of Effective Angle of Friction from Experiment and Shear Tester
254

c
tt
E
"
u
a.
xE
LU
o

i i i i i i i i i i i

28 30 32 34 36 38 40
From Shear Tester

Figure 8.17: Variation of Internal Angle of Friction from Experiment and Shear Tester

In regard to the correlation between the flowability index suggested by Tsunakawa et


al. (1988), defined as the ratio of the unconfined yield strength to the bulk density, an
observed arch length of fly ash and cement minimum significance was observed, refer Figur
8.18. However, it should be noted that cement and fly ash 'C deviate the greatest from th
apparent trend. Fly ash 'E' has the highest flowability index.

120

100 -
E
E

cn
c
tt
u
<

0.1 0.2 0.3 0.4 0.5 0.6


Flowability Index

Figure 8.18: Flowability Index of Fly A s h and Cement versus Arch Length.
255

8.8 TENSILE STRENGTH;


The observed tensile strength versus consolidation variations lbr the powders tested
are depicted in Figures 7.26 and 7.27. In comparison the observed strengths, w h e n subject
to a deaeration time of about 15 minutes, are s h o w n in Figures 7.28 and 7.29. A n
examination of the tensile strength variations depicted in these Figures suggest that the 'y-
axis' intercept indicates the cohesiveness of a powder. Noting this for the fly ash tested, fly
ash 'E' exhibits the greatest strength whilst fly ash 'F the least. Relative ranking of the
intermediate fly ash is also clearly evident. Furthermore, the powders exhibiting tensile
strength variations of high slope display significant strength, w h e n consolidated.

The observed voidage variation versus tensile strength of the various fly ash tested are
shown in Figures 7.30 and 7.31 for instantaneous conditions and Figures 7.34 and 7.35 for
a deaeration time of about 15 minutes. A n examination of these figures clearly highlight that
the tensile strength decreases as the voidage increases. Here, fly ash 'E' and 'C of smaller
mean particle size, display high voidage, yet fly ash 'E' exhibits the highest tensile strength.

The observed tensile strength versus bulk density variations for the fly ash tested are
depicted in Figure 7.32 and Figure 7.33 for instantaneous conditions and w h e n subject to a
deaeration time of 15 minutes, respectively. A s a comparison, the observed tensile strength
versus consolidation for light soda ash, dense soda ash, P V C powder and castor sugar are
depicted in Figure 7.36, whereas the voidage variations are depicted in Figure 7.37. It
should be noted that the relatively high tensile strength of castor sugar evident in these
Figures was due to the presence of absorbed moisture. Furthermore, P V C powder exhibited
minimal strength with dense soda ash and light soda ash displaying intermediate tensile
strengths.

The effect of the filling procedure on the measured tensile strength is revealed in
Figure 7.37. In particular, both a screen vibrator and spoon cell filling procedure was used.
From an examination of Figure 7.38, it is apparent that at high consolidation, the observed
tensile strength is the same for each filling procedure. Whereas, at low consolidation the
observed tensile strength is relatively sensitive to the filling procedure used. The tensile
strength is small at lower consolidation as the particles are not closely packed consistent with
their low bulk density. Furthermore, at low consolidation the screen filled values are higher
than the spooned values. This observation confirms that of Y o k o y a m a et al. (1982) w h o
likewise have shown the importance of filling procedure on the tensile strength observations.
256

O n identifying the suitability of the screen vibrator procedure, fly ash 'H', T
and 'J' were tested using thisfillprocedure incorporating the necessary consolidation and
twists. These small samples of fly ash were received from Queensland Electricity
Commission. The results are depicted in Figure 7.39. From an examination of this
Figure, it is evident thatflyash T exhibits the highest tensile strength and fly ash 'H
has the lowest.

The range of consolidation stresses for tensile strength test was 11.31 kPa to
107.647 kPa, whereas the tensile strength measured range was 0.672 kPa to 4.56 kPa.
The highest tensile strength of 4.56 kPa was measured with fly ash 'H\ Moreover, the
range of voidage was 0.0483 with P V C powder to 0.72 with fly ash 'E\ Also, the bulk
density ranged between 1311 kg/m 3 for P V C powder to 733 kg/m 3 for fly ash *E\

The adhesion forces forflyash for instantaneous conditions and with 15 minutes
deaeration are determined from R u m p f s (1970) equation which can be revealed in
Figures 8.19 and 8.20. Adhesion force increases with consolidation force which is in
agreement with thefindingsof Tsubaki et al. (1984). It is also revealed that fly ash 'E'
has the lowest adhesion force. Unfortunately in both Figures 8.19 and 8.20 extrapolation
to zero consolidation force is difficult. From Figure 8.20, it is revealed that with fly ash
'B' and 'D' at higher consolidation adhesion force decreased.

Oi
6 BUU ~

LEGENC)
600 - FLY ASH
A
o • B
L D C
400 -
e D
• — E
tt D F
200 -
•a •
—• —m- -m- _ •
<
0 - -r——f I— , — - V — r — " I ' 1 1 1
0 10 20 30 40 50 60
Consolidation, N
Figure 8.19: Variation of Adhesion Force versus Consolidation for Fly Ash.
257

o.
I
o LEGEND
FLY ASH
—B— A
—*— B
tt
u —n— D
—P— E
- —•— F
o
CO
tt
X
•a
< 0 10 20 30 40 50 60
Consolidation Force, N
Figure 8.20: Variation of Adhesion Force versus Consolidation for
Fly Ash with Deaeration

The foregoing examination suggests that the tensile tester provides the most evident
distinction between various yet seemingly similar powders. Hence, in view of the convenient
use and clearly evident ranking of powder properties, this test should provide useful
information regarding rapid assessment of a powder's cohesiveness.

8.9 WALL FRICTION:


The necessary calibration procedure and data for this test rig are presented in
Appendix 'C. O n using this information Figures 7.42 to 7.48 result. These figures
summarize the observed wall friction force variations for the various granular materials
tested under differing conditions of the slug length ( 80 to 200 m m . ) and applied slug
aeration air pressure in the range of 0 to 400 kPa. A n examination of these figures reveal
that, in general, the frictional force increases with increasing column height. This is in
agreement with the finding of Roberts (1966).

Furthermore, for Millet and Rice Flakes, at high air pressure, a rapid decrease in
frictional force w a s noted, whereas, for B r o w n Rice, White Rice and W h e a t a small
decrease in the frictional force occurred. This suggests that super dense phase flow or plug
flow will exhibit relatively low wall friction retardation effects. This reconfirms the
favourable flow characteristics of this flow mode.
258

It w a s revealed that under the same conditions of air pressure and column height,
White Rice has higher frictional force as compared to B r o w n Rice, refer Figures 7.42 and
Fig. 7.43. It should be noted that the frictional force for W h e a t is slightly higher-than that
observed for Millet. This m a y be due to a particle shape difference between the two grains, in
particular the Millet is spherical whereas W h e a t is m o r e angular. Also, at higher air
pressures the frictional force decreased for Millet, whereas for W h e a t a slight decrease was
observed. This further confirms the favourable spherical particle shape of Millet

For sand, an opposite trend was observed. In particular at higher air pressure, the
frictional force increased. This increase m a y be due to particular powder characteristics
notably particle abrasiveness and angularitiy and testrigor procedure shortcomings.

The subsequent Figures 7.49 to 7.54 depict the variation of frictional force versus
column length for the materials tested, whereas, Figures 7.55 to 7.60 depict the average
shear stress versus aeration pressure. O n the other hand, Figures 7.61 to 7.65 depict the
evaluated wallfrictionfactor uk for the respective materials tested. These figures reveal the
value of p k decreases generally with both increasing air pressure and column height. It is
interesting to note that this value is higher for Millet and B r o w n Rice as compared to that for
Wheat and White Rice, respectively.

W h e n performing wall friction tests using fine materials, the following results are
observed (Table 8.4). Furthermore, it w a s noted that fly ash 'A' and 'D' tended to form
plugs at air pressure of 1 and 13.78 kPa, respectively.

TABLE 8.4: W A L L FRICTION TESTS OF FLY ASH

SR. NO. MATERIAL AIR PRESSURE FRICTIONAL COLUMN uk


kPa FORCE, N LENGTH, mm
1. FLY ASH 'A' 1 29.43 60 0.79
2. FLY ASH 'D' 0 14.225 80 _

69.9 47.088 80 0.53


13.78 63.078 130 0.27
3. FLY ASH *F 0 13.244 80 0.322
69.9 329.468 80 _

110 355.286 80 -
259
Wall friction angles of fly ash using Stainless Steel as a wall surface were
evaluated using the Jenike Direct Shear Tester (Table 8.5). The details of the tester and
operating procedure are provided by Arnold et al. (1980). The observed wall yield loci
using this test procdeure offlyash are shown in Figure 8.21. A n examination of this
Figure suggests that the wall yield loci are generally convex from above. A similar trend
has been reported for cohesive powders by Roberts et al. (1984).

GL LEGEND
-i
FLY ASH
Vt
VI —B 'A'
4
k. » 'D'
*r
—• "F
(0
L
*
-fi
CO

0 10 20 30
Normal Stress, kPa
Figure 8.21: Wall Yield Loci for Fly Ash 'A', 'F and 'D' on Stainless Steel.

TABLE 8.5: WALL FRICTION


ANGLES

Material Angle of wall


friction
(degrees)
Fly ash'A' 39
Fly ash 'D' 37
Fly ash *F 37

Unfortunately, the attainment of useful information regarding wall friction for


fine materials was marred by test difficulties. These difficulties included the tendency for
some powders to form plugs and separate from the piston. Whereas in other cases
powder plugs formed and broke up again with increasing air pressure. Hence, at best the
wall friction rig can only provide a crude assessment of the extent of wall friction between
a powder plug and a cylindrical wall surface.
260

provide a crude assessment of the extent of wall friction between a powder plug and a
cylindrical wall surface.

In view of these problems, it was considered that the familiar Jenike Direct Shear
Tester provides the best and most useful indication of a powder's wallfrictioncharacteristics,
refer Table 8.5. This latter tester obviously does not provide any indication of a powder's
plug formation tendencies.

The rig, does however, provide useful observations of plug formation of powders
and frictional forces of granular materials. The results obtained indicate the necessary
frictional force required to convey a plug of granular material in super dense phase pneumatic
conveying. This information ranges for different granular materials and column height,
which indirectly indicate pressure drop in low velocity conveying.

8.10 DEAERATION:
Pressure variations during filling and deaeration for fly ash 'A', 'F and 'G', for a
permeable base are shown in Figures 7.67 to 7.69. A n examination of Figures 7.68 and 7.69
suggest that fly ash 'A' has the most air retentive characteristics of the powders tested. In
comparison, the filling and deaeration pressure variations of the powders tested with the
impermeable base are depicted in Figures 7.70 to 7.72. From Figures 7.69 and 7.73, it is
observed that with fly ash, the m a x i m u m interstitial pressures ranged from 20 to 23 kPa for
the permeable base and from 42 to 44 kPa for the impermeable base.

The decay of the deaeration graph is more rapid, included intermittent bed dropping
and greater oscillations during filling when using a deaeration tester with an impermeable
base as compared to that when using a permeable base. Moreover, the peak of filling and
deaeration transition is sharp with an impermeable base, whereas it is smooth and non
distinct with a permeable base. This suggests that it is best to determine the deaeration
characteristics of powders using an impermeble base.

Figures 7.71 and 7.73 reconfirm that fly ash 'A' exhibits the strongest long term ai
retention characteristics. O n the other hand, fly ash 'F and 'G' display relatively rapid
deaeration. Figure 7.72 reveals the deaeration pressure variation for fly ash 'C. From Table
7.14, it can be seen that the exponent obtained from the exponential curve fitting of data
points is lowest for fly ash 'G' under conditions of both permeable and impermeable bases.
261

Also, the deaeration time constant is highest for fly ash A', intermediate for fly ash 'G' and
lowest for fly ash 'F w h e n tested using permeable and impermeable bases.

In regard to powder deaeration, the time constant obtained from decay curve of
interstitial pressure or bed height versus time indicates whether a powder is air retentive or
will rapidly deaerate. In particular, powders exhibiting large numerical values for the time
constant retain air for a significant time. These powders with slow deaeration rate retains
interstitial air maintaining separation of the powder plug. This allows easy conveying in
pipelines without interparticle interlockings. In comparison, powders with small numerical
values for the time constant deaerate rapidly.

Figure 8.22 reveals the variation of deaeration time constant versus mean particle size
of fly ash tested in a deaeration tester for impermeable and permeable bases. It reveals that the
deaeration time constant increases with m e a n particle size. Figure 8.23 reveals the variation
of deaeration time constant versus particle size span for impermeable and permeable bases.
It reveals that fly ash 'G' and 'F have higher particle size distribution span as compared to
fly ash 'A'.

o
jz tt LEGEND
B PERMEABLE
O *-
• IMPERMEABLE
a a
l_ «H BASE
a c
e o
a a

13 14 15 16 17
D(v,0.5), p m
Figure 8.22: Variation of Deaeration T i m e Constant versus M e a n Particle
Size for Impermeable and Permeable Bases.

Figures 7.74,7.75 and 7.76 depict the bed height variation versus deaeration time for
fly ash tested under conditions of both permeable and impermeable bases. Initially, the bed
262
level falls rapidly as the bubbles leave the bed. Then the bed level falls slowly at a constant
rate. This characteristic is consistent with that of cohesive powders [ Geldart et al. (1984)].

Figure 7.77 reveals a typical filling-deaeration graph for fly ash 'A' with an
impermeable base. T h e filling pressure trace is not smooth suggesting the filling process
takes place in a series of steps. This observed trend is consistent with that observed by
Tardos et al. (1985).

100n

80-
tt
E w
— o •

1- tt 60 - LEGEND
C •
• PERMEABLE
0 «-r
tr- C • IMPERMEABLE
-. *H 40 -
0) 0) . BASE
CO c
tt o •

Q O 20-

0 -
3 4 5 6
Particle Size Distribution Span, p m
Figure 8.23: Variation of Deaeration Time Constant versus Particle Size Distribution
Span for Impermeable and Permeable Bases.

The deaeration parameters evaluated from a plot of bed height versus time include the
intercept U_, k n o w n as the dense phase bed height and the dense phase deaeration time. The
former corresponds to the y intercept obtained by drawing a tangent to the deaeration graph,
whereas the latter is the x axis intercept of the same tangent line. Bubble hold up, which is
defined as thefractionbubble volume / bed volume, m a y be evaluated from the ratio of the
difference in actual bed height and dense phase bed height to the actual bed height.

Deaeration parameters including deaeration factor, collapse rate air velocity, dense
phase voidage, dense phase bed height, dense phase deaeration time and bubble hold up for
the fly ash tested are declared in Tables 8.6 and 8.7. Variation of dense phase voidage
versus particle density is revealed in Figure 8.24. It is noted that the dense phase voidage is
higher w h e n using a permeable base compared to that observed w h e n using an impermeable
263

base. Moreover, the dense phase deaeration time and bubble hold up for fly ash 'E' with
permeable base are the lowest.

u.ou -
El
«
0.59 -
cn
a
o •
0.58- LEGEND
>
co B PERMEABLE
a 0.57- • IMPERMEABLE
x
BASE
0. •
tt 0.56-
CO
- •
tt
0.55-1 i 1 r- 1 1 1 r
a 2100 2200 2300 2400 2500 2600
Particle Density, kg/m3

Figure 8.24: Variation of Dense Phase Voidage versus Particle Density.

TABLE 8.6: DEAERATION FACTOR


Material Deaeration Factor (mbar.s/m.) Deaeration Factor / Particle Density
Permeable Base Impermeable Base Permeable Base Impermeable Base
Fly ash 'A' 12170 7091 3.33 5.71
Fly ash 'C - 1891 0.86 .

Fly ash 'E' _ . 0.643 _

Fly ash 'F 11539 4762 1.88 4.55


Fly ash 'G' 14037 7460 5.87 3.14

TABLE 8.7: COLLAPSE AIR VELOCITY AND DENSE PHASE


PARAMETERS

Material Collapse air Dense Phase Dense Phase Dense Phase Bubble
Deaeration Hold up
velocity, c m /s voic age Bed Ht. m m . time, sec.
Base P.B. LB. P.B. LB. P.B. LB. P.B. LB. P.B. LB.
Fly ash 'A' 0.086 0.09 0.595 0.582 80 83 350 250 0.05 0.02
264

Fly ash'E 0.077 - 0.643 - 72 . 195 . 0.01 .

Fly ash 'F 0.063 - 0.553 - 74 - 340 - 0.03 .

Fly ash'G' 0.055 0.07 0.564 0.554 71 71 350 346 0.04 0.03

8.11 FLUIDIZATION AND DEAERATION:


Figures 7.80 and 7.81 depict thefluidizationbehaviour of fly ash 'A' and 'E' for
different experimental runs, whereas Figure 7.82 depicts the comparison of fluidization
behaviour of fly ash 'A', 'C and 'E', respectively. A n examination of this Figure
suggests thatflyash 'E' and 'C exhibit more severe channelling than that exhibited by
fly ash 'A'.

During fluidization testing of fly ash 'A', a plug of 170 mm.; fly ash 'E' a plug of
175 m m formed due to the presence of strong interparticle forces and small mass of
particles. The high initial pressure gradient influidizationm a y be due to the presence of
segregated fines at the top of column. In particular, the behaviour offlyash 'A' and *E'
was typical of that for Group C powders which exhibit cohesive tendencies. With
increased air flow, the air opens the channels that extend from the air distributor to the
surface. If channels are not formed, the whole bed will lift as a plug.

Figures 7.83, 7.84 and 7.85 depict the fluidization characteristics of Alumina,
Sand and P V C powder, respectively. These powders are free flowing as compared to fly
ash, hence they can fluidize easily. The minimumfluidizationvelocity for Sand, Alumina
and P V C powders are 5, 1.22 and 1.37 cm/sec, respectively.

Figures 7.86 to 7.88 represent the deaeration behaviour of fly ash in the
fluidization rig. S o m eflyash were tested a number of times for successive deaeration and
refluidization. It can be seen that in all experiments by repeating the deaeration on the
same sample the bed height variation decreased and the powder exhibits decreasing air
retentive properties. This trend confirms the existence offinesentrainment in the
fluidization air emitting the bed and the tendency for thefinesto segregate at the top of the
column.

The implication of this finding is that the fluidization testing should be rapidly
conducted on a single undisturbed sample. Moreover, if the particle bed consists of a
wide particle sizerange,fluidizationtesting m a y not be practical or m a y be prone to error.
265

550

E 500 LEGEND
E
FLY ASH
X a 'A'
450 -
g • 'C
LU n 'E'
X
Q 400 -
LU
m

350
40 60 80
DEAERATION TIME, Sees.

Figure 8.25: Deaeration Behaviour of Fly Ash 'A', C and 'E'.

Figure 8.25 depicts the deaeration behaviour of fly ash 'A', C and 'E' observed in
the fluidization rig. It is clearly evident that fly ash 'E' and 'C have deaerated slowly due to
their small particle size as compared to fly ash 'A. The exponential trend correlations for this
Figure are y = 543.91 x"8-443, 516.53 x"1-546 and 514.79 x'1-365 for the fly ash 'A', 'C* and
'E' respectively. This Figure also reveals that fly ash 'E' has deaerated slightly slower than
fly ash 'C.

The following Table 8.8 depicts the permeability factor obtained from the fluidization
tests. Based on the Mainwaring et al. (1987) classification, all powders can be conveyed in
either dense phase moving bed type flow or can't be conveyed in dense phase at all, whereas
the same classification system suggests that fly ash 'E' can be conveyed in plug type mode of
dense phase conveying.

TABLE 8.8: PERMEABILITY FACTOR


Sr. NOJ Powder Permeability factor, m2bar/s
1. Sand 0.67
2. Fly ash 'A' 0.61
3. Fly ash C 0.86
4. Fly ash 'E 2.96
5. Alumina 0.52
6. P V C powder 0.71
266

Figure 8.26 shows the variation of permeability factor versus mean particle size
for fly ash 'A', *C and 'E' tested in the fluidizationrig.It reveals that fly ash 'C and
'E' have higher permeability factors compared to fly ash 'A'.

Vt
• 3 - tr
-
_a 'E'
-%
CM
E 2 -
L
e
'C
1 -
'A'
Dl

E
L n - 1 1 1 1 i I • • 1 • • 1 • • | i i | — i — i — |
tt
6 8 10 12 14 16 18
Q.
D(v,0.5), p m
Figure 8.26: Variation of Permeability Factor versus M e a n Size for Fly Ash Tested.

Jones et al. (1989) revealed that the powders having high values of permeability
factor will exhibit poor air retention characteristics. This trend was observed with fly ash
'E\

Although the concept of fluidization is straightforward, the measurement of the


fluidization characteristics of cohesive powders, powders possessing a wide particle size
distribution or powders possessing ultrafines is difficult. For this reason the description,
interpretation, reporting and subsequent classification of fluidization characteristics of
such powders should be viewed with caution. Noting these difficulties various
techniques have been attempted to overcome the same. These techniques include poured
fluidization testing, vibrated and mechanical agitatedfluidizationcolumns. Unfortunately,
the success of these alternate procedures has been limited [ Geldart et al. (1984)].

Similar problems also occur with cohesive powders or powders with wide
particle size consists during quantification of deaeration characteristics. Notably
channelling of cohesive powder beds causes such powder beds to collapse at extremely
high rates, whereas the loss of fines and ultrafine particles from some powder beds
causes an incorrect assessment of the deaeration constant.
267
With these difficulties aside thefluidizationand deaeration characteristics. of
powders are vital parameters for classifying the flow characteristics of powders especially
in regard to dense phase pneumatic conveying. This classification has been successfully
effected by Mainwaring et al. (1987).

8.12: PERMEABILITY:
The permeability of theflyashes were determined using a Jenike Permeability
Tester as described in Chapter 6.8. T h e results are shown in Figure 8.27 as follows. It
reveals thatflyash ' C and 'B' exhibits the highest and lowest permeability coefficient,
respectively of theflyashes tested.

£
LEGEND
FLY ASH
vt • -A-
• 'B'
D 'C
P 'D'
E • 'F
-
tt
CL

1.0 1.2 1.4 1.6 1.8


Major Consolidation Stress, kPa

Figure 8.27: Permeability of the Fly Ashes Tested.

Figure 8.28 reveals the variation of permeability coefficient versus mean particle
size for the fly ashes tested. Figure 8.29 reveals the variation of permeability coefficient
versus pressure gradient evaluated from fluidizationrigfor the fly ashes tested. It reveals
that the pressure gradient for fly ash 'E' and ' C are lower than fly ash 'A'. Figure 8.30
reveals the variation of both the permeability coefficient a and compressibility coefficient
b versus the m e a n particle size for theflyashes tested.
268

10'
1 'A'
10 -4 •j B
•c
10 1 D

1 IO-6 1

o 10 -7 ^1 'D'
o •
10 •1
•F'
10 -9 • •E' 'B'
B El
10 10 ' 1 ' 1 • 1 1 i —\ r•

8 10 12 14 16 18
D(v,0.5), p m
Figure 8.28: Variation of Permeability Coefficient versus M e a n Particle Size
for Fly Ash Tested.

r- 10
-3
(0
c 10 -4 El 'A'

E 10' • 'C

o
u
10 -6
— 10 -7 ;i

o 10"8 \
u
E 10 "9 •
a • 'E'
Q. 10 10
1000 2000
dp/dl, mbar/m

Figure 8.29: Variation of Permeability Coefficient versus Pressure Gradient


for Fly Ash Tested.
269

10 -J

1 "
a
'B'
.1 - 'F'
• •

w
• • • i • i • i • i • — \ — • — i — i — |

4 6 8 10 12 14 16 18
D(v,0.5), Lim
Figure 8.30: Variation of Permeability Coefficient a and Compressibility
Coefficient b versus M e a n Particle Size for Fly Ash Tested.

8.13: RANKING OF POWDER PROPERTIES-


The observed ranking of powder properties appropriate to pneumatic conveying
determined from bench top tests, is presented in Table 8.9.

The arch length and drained angle of repose ranking is determined from
observations with m a x i m u m deaeration time. Unfortunately, clear ranking of the cohesive
powders using these bench tests is difficult. However, relative comparison of
cohesiveness can be m a d e for seemingly similar powders. It is revealed from the table
thatflyash 'E' and 'C have higher arch lengths and drained angle of repose as compared
with other fly ash. Fly ash 'D' and 'B' have high ranks for drained angle of repose as
compared with arch length. Likewise, fly ash 'F' has higher rank for arch length in
comparision with the drained angle of repose.

Ranking from tensile strength and slope indicate that fly ash 'C\ 'A' and 'D' have
the same rank in terms of both parameters. Fly ash 'F' has lowest rank in tensile
strength, but exhibits the highest flow function slope. Fly ash 'E' has highest rank of
tensile strength, but third rank of slope.

Ranking from flow function and slope indicate that fly ash 'E' has the highest
rank. Ranking from deaeration tests influidizationcolumn is not easy as similar
deaeration behaviour was observed forflyash 'E' and 'C\ However, from the results of
the purpose built deaeration tester, clear ranking was possible forflyash 'A', 'F and
'G'.
270
Clear ranking is possible with the Jenike Direct Shear Tester. Clear ranking was
not evident from the permeability tests since during testing of cohesive fly ash 'E' plugs
formed.

In regard to a particular material this Table suggest that mean particle size is an
accuratefirstbasis indicator for ranking. Other characteristic dimension numbers derived
from particle size distribution also give clear ranking.

Out of eighteen columns of the table, twelve columns indicate highest rank of fly
ash 'E', followed by fly ash 'C indicated by six columns. Similarly, lowest rank of fly
ash 'A' is indicated by six columns out of thirteen columns.

Simple bench top tests like mean particle size, bulk density, Hausner ratio and
tensile strength are easy to perform and clear ranking of similar powders can be
evaluated, whereas rough andfirstindications of cohesion can be evaluated from the
bench top tests such as arch length and the drained angle of repose. Wall friction
properties can be evaluated from aerated piston tester or shear cell. Deaeration behaviour
m a y be evaluated fromfluidizationcolumn or purpose built tester.

Actual pneumatic conveying flow characteristics of the fly ashes have shown
good dense phase conveyability [ Arnold et al. (1986) ]. Allflyash have more irregular
flow characteristics and higher pressure drop, tendency to block and fluctuation in
pressure drop except fly ash 'F.

It is important to know whether a powder is suitable for conveying. Some


powders are difficult to convey, whereas some m a y have unstable flow characteristics.
After conveying, a large range and number of powders, adverse powders should be
identified. The reasons for the poor system performance of those powders should be
understood.

Simple non cohesive powders can be conveyed pneumatically in either plug or


moving bed depending upon the powder's deaeration and permeability characteristics.
Increasing cohesion results in greater instabilities during pneumatic conveying and more
attention should be given to pipeline details e.g. bends,flanges,pipe internal smoothness
and blow tank design.
271

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272
Location of aeration points is important. Obviously, unstable flow and blockages
are relavent w h e n transporting powders with considerable cohesion. For such cohesive
powders, pneumatic conveying is possible by applying vibration or using by pass, pulse
dense phase and controlled slug techniques. Thus, cohesive powders can be maintained
in a fluidized state, offsetting to some extent, the deaeration of the powder. If aeration can
be effected, difficulties associated with pneumatic conveying of cohesive powders can be
reduced.

With incresed cohesion, only dilute phase is possible. Standard pneumatic


conveying systems are generally not suitable with extreme cohesion. For such materials,
reliable and consistent feeding is difficult. Hence, cohesion is an important powder
property w h e n selecting a powder's optimal pneumatic conveying mode.

At present, flow assessment of powders is evaluated from pilot scale plant tests.
From these tests, pressure drop, air flow rate, solids flow rate and particle velocity are
obtained. However, information m a y be obtained from bench tests regarding selection of
conveying phase and system components. The powder property evaluation from bench
tests is very important to identify adverse flow behaviour before running a full scale plant
in view of a possible failure. Emphasis should be placed on powder properties from
bench top tests and correlations to determine conveyability in dilute, dense and super
dense phase pneumatic conveying. In view of the significance of the powder properties
examined the important powder property bench tests and their ranking to assess
pneumatic conveying suitability are shown in Table 8.10, whereas factors affecting
powder flow characteristics are shown in Figure 8.31.
gravity assist
smooth surface
air retentive
characteristics
low compressibility
constant permeability
m o n o sized particles
spherical

POSITIV E EFFECTS

CONSOLIDATION PERMEABILITY

N E G A T V E EFFECTS

rougli surface
pressure gradient
cohesiveness
wall friction
acceleration
force
gravity
high compressibility
sensitive permeability
degradation
wide particle size
distribution

Figure 8.31: Factors affecting Powder Flow Characteristics.


274

TABLE 8.10: R E C O M M E N D E D P O W D E R PROPERTY BENCH TESTS


FOR ASSESSMENT OF PNEUMATIC CONVEYING SUITABILITY.

Property Crude Assessment Accurate Assessment

M e a n Particle Size Visual Particle Size Analysis, Sieving


Laser Particle Size Analyser
M e a n Particle Density Estimate Pycnometer
Particle Shape Visual or assumed
Basic Chemical Specified
Composition
Loose Poured and Simple Test Jenike Compressibility Tester
Packed Bulk Density
Extent of cohesion Hand Squeeze Test Moisture Test
due to moisture content, Moisture Test
due to particle size (a) Ranking (b) System Design
distribution and individual (i) Hausner Slope and
powder properties Ratio intercept
f*
of the yield loci
(ii) Angle of (c) Fundamental
Repose Knowledge
(iii) Arch (i) Tensile Tester
Tester (ii) Cohesion Tester
(iv) Tensile Tester
L o w Cohesion Powders
Fluidization * Fluidization Column
Deaeration * Deaeration Tester
Vibrated Fluidization column
Permeability * Permeability Tester
Slugging * Develop suitable test
Particle Size Distribution Particle Size Analyses, Sieving
Laser Particle Size Analyser
Safety and System
Properties
275

Toxicity
Contamination Tolerance
Radioactivity
W e a r Considerations
Hardness M o h s Hardness Scale Vickers Micro Hardness Scale
Abrasiveness
Dustiness (Dust collector Pilot Tests Particle Size Analysis
sizing)
Particle Shape (for W e a r Optical Scanning Electron Microscope
and Mechanical Inter- (SEM)
locking considerations)
Tendency for Mechanical Visual SEM
interlocking
Tendency for Degradation Pilot Tests Pilot Tests and SEM
Tendency for Segregation Pilot Tests Particle Size Analysis
Tendency for Agglomerate Pilot Tests Pilot Tests
Removal from Dust Wall Friction Test
Filter Media

I*

* Observe extent of segregation, stratification and fines elutriation from bed,


tendency to slug, channelling and bed collapse during testing.
* Tests should only be conducted on powders of low cohesiveness.
276

8.14 A N E W PHASE DIAGRAM FOR PNEUMATIC CONVEYING OF


POWDERS:
8.14.1 INTRODUCTION:
Powders are in two forms dry and moist. Depending on their internal properties,
powders will be either free flowing or cohesive. A free flowing and dry powder can be
conveyed successfully in a pneumatic conveying system, whereas moist and cohesive
powders are difficult to convey. In particular, cohesive powders m a y stick or clog in
pneumatic conveying system components.

This suggests that cohesion be included in a phase diagram for pneumatic


conveying. For fine powders, the effect of permeability and deaeration is well known
(Mainwaring et al. 1987, Jones et al. 1989) and have already been incorporated into a
phase diagram for pneumatic conveying. The present investigation suggests that this
phase diagram is incomplete and should be supplemented by the inclusion of cohesion for
fine powders and the effects of mechanical interlocking for coarse materials or materials
possessing high permeability and rapid deaeration. The resultant proposed complete
phase diagram is presented in Figure 8.32, whereas Figure 8.33 shows the phase
diagram from another orientation.

Mechanical
Interlocking t
N o Flow or
Unstable
Reliable
Plug Flow

Dilute Phase
Conveying
Reliable Moving
Bed Flow

Deaeration Permeability

Figure 8.32: Pneumatic Conveying Phase Diagram.


277

A n examination of this Figure suggests that for fine low permeability materials,
cohesion, deaeration and permeability should receive primary attention. If the extent of
deaeration decreases, the powder can be easily m o v e d in the form of a moving bed flow.
Unfortunately for extremely fine low permeability powders, as shown in the phase
diagram, excessive cohesive forces exceed the otherwise slow deaeration and low
permeability. Powders in this zone can only be conveyed by dilute phase conveying if at
all.

Whereas, for coarse materials, permeability and mechanical interlocking, in


particular, should be considered. For these materials, the high permeability generates
m i n i m u m air flow resistance and hence m i n i m u m flow body forces. T h e high
permeability is also associated with low air retention and rapid deaeration characteristics.
For these materials, mechanical interlocking causes flow difficulties. The high values of
permeability suggests that these materials can be conveyed in slug type flow or super
dense phase pneumatic conveying.

Cohesion
Mechanical
i Interlocking

1
Large particles
Deaeration strong mechanical
interlocking

Permeability

Figure 8.33: Pneumatic Conveying Phase diagram (Alternate View).

8.14.2 EFFECT OF COHESION ON THE PHASE DIAGRAM POWDER


PROPERTIES:
8.14.2.1 Permeability:
Permeability is a function of the overall packing, the size of void channels and the
shape of the voids. In some situations, large particles act as a filter membrane during the
flow mechanism. This causes the permeability to decrease. This action is compounded by
the tendency for the slip velocity of coarse particles to be high and of fine particles to be
278

low. However, if sufficient air flow can percolate the bed, bed expansion of the air inside
the voids will keep the powder bed in tension and hence counteract the effect of cohesion.
In view of the above trends, the following can be declared.
(i) H i g h permeability;
Powders with high permeability are conveyed easily but rapidly deaerate. For
these powders, considerable powder expansion due to air expansion, percolation of air
into the powder plug act to reduce the frictional forces and prevent formation of immobile
powder slugs. However, formation of immobile slugs is promoted by the decrease in the
mean particle separation due to wall friction and the pressure driving force. This suggests
that coarse particles can be conveyed in slug m o d e and super dense phase pneumatic
conveying provided the wall friction is minimal.
(ii) E x t r e m e permeability:
For very coarse particles, insufficient motive forces are generated by the fluid
drag effect relative to weight and frictional forces. Hence, these materials are difficult to
convey. For these very coarse particles, blockages due to mechanical interlocking is very
common.
(iii) L o w permeability:
Coarse powders with low permeability are difficult to convey using slug m o d e
conveying. However, fine low permeability powders exhibiting low deaeration rate can
be easily conveyed using fluidized moving bed technique. Furthermore, increasing fine
decreases permeability and increase cohesion. The low air permeability demands that
short lengths be used. Insufficient air flow and air expansion keep the powder bed from
compacting during dense phase fluidized bed conveying. In general,finepowders with
low permeability will exhibit high cohesion. Hence, such powders m a y be more difficult
to convey. Figure 8.34 shows the variation of the reciprocal of cohesion and
permeability with particle size.
(iv) Constant permeability:
If a powder exhibits constant permeability, no blockages are expected since the
mean particle separation will increase during conveying.
279

1/Cohesion
and
Permeability

Particle size, d

Figure 8.34: Schematic Presentation of the Variation of Cohesion


and Permeability with Particle Size.

8.14.2.2 Deaeration:
With cohesive powders the deaeration rate is fast initially then exponential,
whereas for free flowing powders deaeration rate is fast. However, with less cohesive
powders, deaeration rate is slow and linear generally. Such powders will be easy to
convey in the form of a moving bed. O n the other hand, the effect of cohesion is to cause
strongly cohesive powders to deaerate rapidly due to the formation of capillaries and
cracks within the bed. For these cohesive powders with high de-aeration rate a by-pass
system is used for conveying.

Reciprocal of
Cohesion Uariation

Resulting Optimal
Trend
1/Cohesion — I / d2
and
Deaeration

Particle size, d

Figure 8.35: Schematic Representation of the Variation of Cohesion


and Deaeration versus Particle Size.
280

Figure 8.35 shows the variation of reciprocal of cohesion and deaeration versus
particle size, whereas the variation of reciprocal of arch length and Hausner ratio with
particle size of theflyashes tested are depicted in Figure 8.36.

In regard to flow characterization, powders having a wide particle size distribution


generally exhibit segregation effects and higher cohesion. Fine particles with a wide
particle size distribution have a poor air retention capacity and are not suitable for super
dense phase pneumatic conveying.

0.03

e
-
0.02 - tl
o
L
< X
w
Vl 0.01 - e
* o
e VI
*
u -fi
0.00 e
8 10 12 14 u
Particle Size, p m
Figure 8.36: Variation of Reciprocal of Arch Length and Hausner
Ratio with Particle Size of Fly A s h Tested.

8.14.2.3 M e c h a n i c a l Interlocking:
Noting that the air pressure gradient and air flow drag provide the motive forces
in pneumatic conveying. This suggests that for extremely permeable powders mechanical
interlocking, refer Figure 8.37 becomes the predominant factor causing slug formation or
the occurrence of a pipe blockage. For these powders any factor which causes the
interparticle spacing to decrease m a y result in a pipe blockage or require the use of a slug
creation or slug length control techniques to maintain flow. Factors which m a y cause the
interparticle spacing to decrease include wall friction, pipe irregularities, bends, etc. The
parameters controlling the m e a n interparticle spacing are summarized in Table 8.11.

Figure 8.38 shows the variation of permeability versus the expected extent of
mechanical interlocking. In particular, this Figure reveals that large particles exhibiting
high permeability have a strong tendency for mechanical interlocking and hence are
difficult to convey in pneumatic conveying.
281

O 0 Q QZ5.0 MECHANICAL
INTERLOCKING

00(7 0
Figure 8.37: Mechanical Interlocking.

TABLE 8.11: FACTORS INFLUENCING


THE MEAN INTERPARTICLE SPACING

Increasing Decreasing
L o w cohesion Strong cohesion
Gas expansion Long slug length
Gas viscosity High bulk density
Fluid turbulence Wall friction
High permeability L o w permeability
Smooth surfaces Rough surfaces
Uniform particle size Wide particle size
L o w consolidation High consolidation
Insensitive properties Sensitive properties

Mechanical
Interlocking

Resulting
Optimal Trend

Mechanical
Interlocking

Permeability
Figure 8.38: Schematic Representation of the Variation of Permeability versus
Mechanical interlocking
282

8.14.3 I N F L U E N C E S O N COHESION-
The following powder properties, which influence cohesion/ flowability, are
briefly described as follows:.
1 • Moisture Content: A slight increase of moisture to a dry powder can transform it
into a cohesive powder e.g. the addition of as little as 0.6 % moisture to dry sand will
change freeflowingdry sand into a cohesive material.
2. Hygroscopicity: Powders having a hygroscopic nature tend to be very cohesive
especially if they absorb moisture from the conveying air. Hence, hygroscopic powders
are difficult to convey pneumatically. To prevent this absorption, it is recommended that
dry conveying air and a closed system should be used.
3. Agglomeration: Agglomeration of particles results in larger particles, changes in
shape and porosity.
4. Thermoplastics: Powders which are thermoplastics may be extremely cohesive
during flow due to the softening effects associated with thermal, friction or impact
stresses during flow.

8.14.4 TESTS TO ASSESS COHESION:


The following bench tests can be used to assess cohesion / flowability
characteristics of powders which can be divided into two categories, namely direct and
indirect tests.
(A) Direct Tests:
1. Hand Squeeze Test:
This is a simple qualitative test forflowability/cohesion assessment of powders.
In this crude test, a powder sample is squeezed by hand to observe whether the sample
divides easily or remains as a lump.
2. Angle of Repose:
This simple test provides an qualitative and partial indication of cohesion /
flowability. Unfortunately, for cohesive powders, test results are highly variable with the
result that is is difficult torankmeasurements.

More quantitative methods/tests to assess cohesion now follow:


3. Arch Tester:
The minimum width required to assume flow from a mass or plane flow hopper/
bin reveals a direct measure of flowability/cohesion of powders and other bulk solids. B y
the use of thisrig,it is convenient to compare seemingly similar cohesive powders.
283

4. Direct Shear Tests:


Cohesion can be assessed from the instantaneous yield loci obtained from shear
tests. Simple testers like the Uniaxial Compression Tester can also be used for relative
measurements. O n e advantage of the information gained from shear tests is that, in
particular, that from the Jenike Shear Tester, the same information can be used in the
geometric design of blow tanks and storage vessels. Here, the relevant parameters are the
slope of the flow function and its intercept with the unconfined yield strength axis. Here,
the relevant parameters are the slope of the flow function and its intecept with the
unconfined yield stress axis.
5. Tensile Tester:
Tensile strength can be assessed from the various tensile strength testers
depending on the direction of pull with respect to the applied consolidation force. In
particular in the split cell testers, the sample is subject to tensile forces perpendicular to
the direction of consolidation. In comparison, other testers exert tensile forces on the
powder in the same direction as that of the applied consolidation force.

(B) Indirect Tests:


1. Compressibility Constant (b): O n e of the indirect tests to assess cohesion is
the slope of compressibility versus consolidation stress variation plotted on a log-log
basis. This slope is referred to as the powder's compressibility (b).
2. S l o p e of F l o w Function: A steep flow function slope indicates high powder
strength sensitivity with increasing consolidation.
3. H a u s n e r Ratio: This is a simple and rapid test for evaluation of a powder's
cohesion / flowability for seemingly similar powders based on bulk density
measurements. The use of this ratio of the packed to loose poured bulk density to indicate
a powder's cohesiveness wasfirstsuggested by Geldart et al. (1984).
4. W a l l friction: Based on the simple assumption that cohesive powders exhibit large
wall friction angles. It is suggested that wall friction properties evaluated from an
aerated piston tester or shear cell be used to assess the extent of cohesion.

8.15 TEST PTFFTCITI TIES:


8.15.1 Aicliiii&i
For very cohesive powders, arching occurs across the outlet of the tester and
renders measurement of the arch length impossible.
8.15.2 Deaeration:
Difficulties experienced during the conduction of the deaeration tests include
powder lining the inside of the tube wall. Furthermore, since the top surface of the
powder bed level fallsrapidly,measurement of the bed height using a video camera is
284

recommended. However, in a large scale deaeration test, visual bed height measurement
may be possible.
8.15.3 Fluidization:
For cohesive Group C powders, fluidization is difficult. During testing,
channelling, slugging and lifting as a plug occur. For fluidization testing of cohesive
powders, it is suggested that the column be closed with a sealed porous end creating
high resistance to prevent fine and submicron particles leaving the bed. For extremely
cohesive powders fluidization testing of powders is not practical nor meaningful.
8.15.4 C o h e s i o n :
S o m e low permeability powders m a y rapidly deaerate due to cohesion. The
measurement of the permeability of such powders is difficult to measure due to strong
cohesive forces. Such powders m a y locate in zone T in the phase diagram (Figure
8.39). But they are expected to be located in moving bed flow zone as shown '2' in the
diagram.

Figure 8.39: Specific Examples of Powder Properties with respect to the


Proposed Powder Conveying Phase Diagram.

8.15.5 Permeability:
T w o main problems associated with the conduction of the Jenike Permeability
Test result from the effect of cohesion. In particular, strongly cohesive powders will
form a plug and extrude from the tester on application of the pressure differential.
Whereas powders with low cohesion m a y exhibit segregation effects at low
consolidation. This segregation m a y result in fines leaving the powder bed. One
alternative procedure, to partially overcome' these problems, is to evaluate a powder's
285

nominal permeability from the fluidization column. Unfortunately, such a evaluation does
not provide knowledge of the permeability variation with consolidation.

8.16 EFFECT ON CONVEVINO-


8.16.1 Particle Shape;
Particle shape and surface characteristics of powders can be examined with a
Scanning Electron Microscope. Intuition suggests that irregular, sharp and angular
shaped particles are associated with high pressure drops. Furthermore, fragile and brittle
powders exhibit increasing fines percentage which, in turn, results in increasing
cohesion and decreasing permeability. Likewise, afibrouspowder is difficult to control
in a blow tank system. Powders having considerable flakiness and hence strong
tendency to mechanical interlocking are also difficult to convey.

Obviously, particle shape significantly controls the wear of compressor


components (in vacuum systems), rotary feeders and venturi feeders. In particular, sharp
edged hard particlesrapidlywear the same, whereas soft spherical particles effect reduced
wear on system components directly exposed to the particle stream.

8.16.2 Air Compressibility:


The pressurized air will expand as the air pressure decreases along the conveying
pipe. This expansion imposes tensile stress in the flowing powder. The existence of
tensile forces in the flowing powder implies increasing m e a n interparticle distance. This
increasing interparticle distance generally promotes stable flow. The maintenance of
stable flow b y the generation of tensile forces in the powder bed is the basis of by pass
secondary air techniques. However, it should be noted that secondary air can generate
compressive forces, if the b y pass line becomes blocked downstream and the material
conveyed is cohesive or exhibits high wall friction and low permeability.

Air expansion along the pipeline causes an increase of superficial air velocity
which results in m o r e energy consumption and wear of system components. For short
pipelines with low pressure drops, air can be considered as an incompressible fluid but
for long pipelines due to air expansion and increase of superficial velocity, it is c o m m o n
to design the pipeline with increasing pipeline diameters to control velocity near the end
of pipeline.
286

8.17: OTHER CONSIDERATIONS:


1. Toxicity: For toxic powders, precautions should be taken in the design of system
components and strict control is required for conveying operation. A vacuum and closed
system is required for toxic powders to prevent leakage to the atmoshphere.
2. Combustibility: Closed system should be used for powders having
combustibility property. Alternatively, inert gas conveying is necessary. Inert gases
include nitrogen, combustion gas C O 2 suitably cooled and dehumidified.
3. Hardness: Harder particles have more flowability. In general, hard incompressible
particles exhibit high internal friction angles and wall friction angles.
4. Wear: Large diameter pipes should be used near the end of conveying line. The
conveying velocity should be low to reduce wear. Harder particles increases wear.
5. DegradLaliojoi Powders which degrade during flow effectively becomefineand
hence more cohesive as they are conveyed. T o prevent breakage of particles, low velocity
conveying and m i n i m u m number of bends should be used. Sharp changes and
discontinuity in pipeline or rough sections should be avoided.
6. Electrostatics: A n electrostatic powder usually exhibit unexpectedly high
cohesion and wall friction due to the occurrence of localized zones of oppositely charged
particles or wall boundaries. These powders m a y stick or clog in blow tanks, pipeline
andfilters.Static eliminators provided in cyclone and bag-filters prevent build up of
powder. A static inhibitor coating can be used. For conveying of plastics, pipeline should
be grounded to earth.
6. Hygroscopicity: D r y conveying air should be used to convey hygroscopic
powders. These powders will cake and create problems in conveying.
287

8-18 PNEUMATIC CONVEYING CHARACTERISTICS:


The experiments were performed to obtain the steady state operating conditions. The
conveying characteristics results for cement and Wheat are tabluated in Tables 7.19 and
7.20, respectively. The air flow valve setting was used in the range of 0.05 - 0.09 kg/sec. It
was revealed, from experiments N o . 21 to 25, refer Table 7.20 that as the air flow rate
increases, the powder velocity also increases. The solids flow rate was evaluated from the
slope of the load cell response graph.

The pressure differentials of a friction loop for cement and Wheat conveying
upwards are shown in Table 8.12. Furthermore, in this series of experiments, air pressure
fluctuating and unsteady flow were observed.

TABLE 8.12: PRESSURE DIFFERENTIALS FOR FRICTION


LOOP

Exp. Pressure differential Exp. Pressure differential


No. conveying upwards, kPa No. conveying upwards, kPa
Material: cement Material: Wheat
5 8 22 4
<
12 18 23 7
13 10 25 10
14 5 31 4
15 8 34 4
16 11 35 2

Particle velocity w a s measured experimentally by using a Tealgate 200 series


transducer in combination with a Hewlett Packard Correlator as described in Section 6.2. The
transducer was located some 3 m . from the blow tank so that suspension flow is fully
developed. The particle velocity was obtained during the conveying cycle from the cross
correlation signal appearing on a Hewlett Packard Correlator screen before averaging out the
observations noted during the conveying cycle. The correlator time scale selected was 333
ps / m m .

Typical variations of the particle velocity during a conveying cycle for cement and
Wheat are graphically revealed in Figures 8.40 to 8.42. It is revealed from these Figures that
288

particle velocity variations are periodic cyclic oscillations. Particle velocity variation during
the conveying cycle is an indirect indication of the extent of steady state flow.

The variation of volumetric air flow rate with time for cement is shown in Figure
8.43. Figure 8.44 shows the variation of solids flow rate versus air mass flow rate for
cement and Wheat. T h e solids flow rate increases with increasing air flow rate. It can be
revealed that cement can be conveyed with less air mass flow rate as compared with Wheat.

The solids mass flow rate and mass flow ratio variations for cement and Wheat are
shown in Figure 8.44. In particular, the air mass flow rate for cement and Wheat was in the
range of 0.011 - 0.63 and 0.05 -0.0635 kg/sec, respectively. It can be seen that cement for
the flow conditions observed has higher mass flow ratio as compared to that for Wheat.

u
<_

u
0
>

CO
O-

Time, Sec.
Figure 8.40: Variation of Particle Velocity with Time for Cement.
Time, Sec.

Figure 8.41: Variation of Particle Velocity with Time for Cement.

LEGEND
Exp. No.
- a — 21
-P 22
-B— 23
-p 25

Time, Sec.

ure 8.42: Variation of Particle Velocity with Time for Wheat.


LEGEND
Exp. No.
-B 31
—•— 32
-a— 34
—0 35

400

gure 8.43: Variation of Volumetric Air Flow Rate with Time for Cement.

-
3U



40 i •
LEGEND
• P Material

30 - P • Wheat
• Cement
B _ _

20- ••QD

• • l i • I • • 1 1 i i | i i
'l
0.2 0.4 0.6 0.8 1.0 1.2 1.4
Solids Mass Flow Rate, kg/sec
Figure 8.44: Variation of Mass Flow Ratio with Solids Mass Flow Rate
for Cement and Wheat.
291

CO
CC
LEGEND
EI Cement
5
o • Wheat
(0
32
o
w
-i 1 r-
0.01 0.02 0.03 0.04 0.05 0.06 0.07
Air Mass Flow Rate, kg/s

Figure 8.45: Variation of Solids Flow Rate versus Air Mass Flow Rate.

Tables 7.21 and 7.22, refer Chapter 7 summarize the conveying characteristics of
sand. A t higher air flow rates, as can be seen from experiments 25 to 29, 34, 35, 41, 46, 47
powder velocity increases and with m e d i u m air flow rate such as in experiments 3 0 to 33,45,
79 and low air flow rate, experiments 43, 44, 51, 52, 71, 80, 81, lower particle velocity w a s
observerd. '

The variation of particle velocity obtained experimentally and predicted for low,
m e d i u m and high air flow rate is depicted in Figure 8.46. T h e predicted velocity w a s
calculated from the equation s h o w n in Appendix C. F r o m an examination of Figure 8.46, it
is apparent that the actual observed particle velocity deviated increasingly from the predicted
velocity with increasing air flow rate.

Cycle time is effected by blow tank pressurization which is revealed in experiments


29, 30, 3 4 to 37 and 39 with a blow tank pressure of 150 kPa. Here, the experiment cycle
time average w a s 3 min., 3 2 sec, whereas at lower blow tank pressure of 125 kPa,
experiments 41, 42, 43, 47 the average cycle time w a s 4 min. and 6 sec.

Figure 8.47 reveals the particle velocity variations with time during experiments 54,
53 and 7 7 at an initial blow tank pressures of 180, 175 and 175 kPa, respectively, whereas
Figure 8.48 reveals the particle velocity variation with time during experiments 74,75 and 7 6
at the initial blow tank pressure of 150 kPa.
292

The air mass flow rate as per valve setting for both Figures were 0.09, 0.085 and
0.0635 kg/sec, respectively. A higher particle velocity with increased air mass flow
trend is generally evident from Figures 8.47 and 8.48 even though the Figures indica
considerable scatter.

o
0) 30
(0

LEGEND
u 20 - AIR FLOW
o
> • HIGH
• MEDIUM
CO
T3 a L£W
o 10 -
CO
•o

5 10 15
Experimental Solids Velocity, m/sec.

Figure 8.46: Variation of Experimental versus Predicted Solids Velocity for

u
9)
0) LEGEND
Exp. No.
-v— 54
O -•— 53
O
ti -fl— 77
>

o
(0
Q.

0 20 40 60 80 100 120 140


Time, Sec.
Figure 8.47: Variation of Particle Velocity versus Time.
293

<-U -
o
-2
LEGEND
E
EXP. No.
Ss
mm
• B •
B 74
o 10- • B D
• 75
o • B • • • B 76 '
"3 B • B D B B
>
73
"«H

a
Q.
i | i i i i | i

C) 50 100 150
Time, Sec.

Figure 8.48: Variation of Particle Velocity versus Time.

Transducer air pressure variation versus distance from blow tank are shown in
Figures 7.91 to 7.96. Details of transducer distances from blow tank are shown in Table
7.18. Figure 7.91 and 7.92 depict the variation of air pressure with initial blow tank pressure
of 150 kPa, whereas Figure 7.93 depicts with 175 kPa of high air flow rate. Figures 7.94,
7.95 and 7.96 depict the variation of air pressure at the initial blow tank pressure of 125 kPa
with low, high and m e d i u m air flow rate, respectively.

Table 8.13 presents the calculated values of superficial air velocity, actual air
velocity, voidage, slip velocity and Froude number derived from Table 7.21. Also, the
friction factor, calculated using the K o n n o et al. (1969) correlation, is included to indicate the
considerable range of test conditions.

To understand the variation of flow parameters with voidage during flow various
phase diagrams were prepared. In particular, Figure 8.49 depicts the variation of slip velocity
versus ( 1 - voidage ) for three different but almost constant solids mass flow rates. With
low solids mass flowrate,it is revealed that slip velocity decreases with (1 - voidage),
whereas with a high solids flow rate slip velocity increases. This trend is similar to that
reported by Klinzing et al. (1986).
294
T A B L E 8.13: AIR VELOCITY, SLIP VELOCITY AND FROUDE
NUMBER
Material: Sand

Exp. Superficial air E Vf Slip velocity Froude Friction


No. velocity m / sec. m / sec. number factor
Vf rn/sec.
23 33.18 0.843 39.359 27.079 46.456 0.0066
24 40.51 0.788 51.409 34.963 56.714 0.0049
25 40.51 0.791 51.214 34.998 56.714 0.005
26 44.369 0.863 51.413 35.745 62.116 0.0052
28 40.51 0.882 45.93 28.286 56.714 0.0046
29 41.282 0.788 52.388 35.879 57.795 0.0049
30 39.353 0.804 48.946 37.184 55.094 0.0069
31 38.969 0.763 51.072 36.014 54.556 0.0054
33 35.881 0.796 45.077 29.066 50.233 0.0051
35 31.251 0.775 40.324 22.294 43.751 0.0045
37 30.865 0.775 39.826 23.073 43.211 0.0048
38 28.936 0.767 37.726 22.013 40.51 0.0052
39 25.85 0.801 32.272 18.06 50.685 0.0057
40 26.621 0.847 31.43 37.269 37.269 0.0046
41 28.628 0.849 33.72 14.935 40.079 0.0043
42 28.55 0.772 36.982 20.295 39.97 0.0049
43 25.464 0.832 30.606 16.067 35.649 0.0056
44 6.559 0.741 8.852 -3.882 9.183 0.0064

45 27.779 0.831 33.428 22.206 38.891 0.0072

46 32.409 0.721 44.95 28.608 45.372 0.005

47 29.708 0.829 35.836 16.671 41.591 0.0042


0.828 - - -
49 - -

50 27.393 0.748 36.622 25.22 38.35 0.0071

51 21.721 0.824 26.36 15.414 30.409 0.0074

52 22.377 0.686 32.62 20.554 31.328 0.0067

53 27.393 0.704 38.911 26.073 38.35 0.0063



58 - 0.734 -
'
295

62 11.767 0.675 17.433 16.474


63 26.814 0.614 43.671 - 37.539 .
64 32.794 0.78 42.044 - 45.911 -
66 28.55 - - - 39.97 -
67 23.843 0.706 33.772 - 33.38 -
70 - 0.839 - - - -
71 24.306 0.696 34.922 27.557 34.028 0.0111
72 28.55 0.797 35.822 26.835 39.97 0.0091
73 - 0.828 - - - 0.0095
74 32.409 0.745 43.502 33.367 45.372 0.008
75 30.865 0.816 37.825 29.341 43.211 0.0096
76 24.692 0.667 37.019 29.586 34.568 0.0109
77 26.621 0.817 32.584 25.103 37.269 0.0108
78 31.637 0.835 37.889 - 44.292 0.0109
79 31.637 0.812 38.962 29.773 44.292 0.0088
80 23.535 0.853 27.591 19.717 32.949 0.0103
81 23.535 0.801 29.382 20.673 32.949 0.0093
82 28.55 0.757 37.715 28.621 39.97 0.0089

Furthermore, Figures 8.50 and 8.51 reveal the variation of superficial air velocity
versus (1- voidage) and mass flow ratio, respectively. The scatter in the results depicted
in Figures 8.50 to 8.51 appears to depend on many parameters including particle
diameter, density, shape, air velocity, particle-wall interactions, pipe diameter, etc..

Figure 8.52 shows the variation of pipeline pressure drop versus air mass flow ra
initial blow tank pressures of 125, 150 and 175 kPa, respectively. Pipeline pressure drop
was evaluated by taking first pipeline air pressure differential alone, which can be
approximated as the experimental pipeline pressure drop [ Arnold et al., (1986)]. This series
of experiments indicated that with increasing initial blow tank pressure, an increase of
pipeline pressure drop results. However, no clear trend was evident.

Figure 8.53 shows the variation of mass flow ratio versus initial blow tank press
of 120-125 and 170-175 kPa. It is suggested, from the limited observations, that the mass
flow ratio increases with an increase in initial blow tank pressure.
29

-HJ -

nn LEGEND
SOLIDS MASS
30-
FLOWRATE
B 0.857 - 0.886

• • 0.957 - 0.984
• ""- 1.214-1.234
20- •
kg/sec

10 i • 1 I i i 1 i • i • i

0.14 0.20 0.22


(1 - Voidage)

Figure 8.49: Variation of Slip Velocity versus (1 - Voidage) for Sand.

DU ~

LEGEND
SOLIDS MASS
40 - DB
FLOWRATE
B 0.857-0.886
• 0.957-0.984
• B 1.214-1.234
30- kg/sec

B

Q

20 - 1 1 T— ' " ' 1 ' • I • • —


0.14 0.16 0.18 0.20 0.22
(1 - Voidage )

Figure 8.50: Variation of Air Superficial Velocity versus (1 - Voidage) for Sand.
1

u
ti
in

LEGEND
SOLIDS MASS
u FLOWRATE
o •0.857-0.886
ii
> -•—0.957-0.984
-fl—1.214 - 1.234
kg/sec
ra
o
0)
Q.
cn
Mass Flow Ratio

Figure 8.51: Variation of Superficial Air Velocity versus Mass Flow Ratio for
Sand.

(0
a 140
-C
a. LEGEND
o 120 -
Initial Blow
Tank Pressure
-
to
B 125
(0 100 - • 150
ai
fl 175
0) kPa

"3
a.

ca
H- 0.06 0.07 0.08 0.09 0.10 0.11 0.12
o
Air Mass Flow Rate, kg/sec.

ure8 52: Variation of Pipeline Pressure Drop versus Air Mass Flow Rate for Sand.
298

26-

24-
0 • LEGEND
r H
22- •
• Initial Blow
CaC . * Tank Pressure
3 20-
0 . B B 120-125
LU 18- B • 170-175
n , kPa
co 16-
S
14-

12- ->—r
110 120 130 140 150 160 170 180
Initial Blow Tank Pressure, kPa
Figure 8.53: Variation of Mass Flow Ratio versus Initial Blow Tank Pressure for
Sand.

8.18.1 BEND PRESSURE DIFFERENTIAL OBSERVATIONS:


As stated in Section 7, two bends types were examined namely long radius and
vortice elbow, refer Table 7.23. For experiments 51, 56 and 20, the observed pressure
differential across the long radius bend was 8, 5 and 5 kPa, respectively. In comparison,
for the vortice elbow the pressure differential was 4 kPa as revealed in experiments 21,22
and 23.

This observation is consistent with that of Paulson et al. (1983) who al


that vortice elbow bends give slightly less pressure drop than long radius bends.This increa
may be due to the considerable pipe length in the latter. Obviously, the pressure drop in a
radius bend will depend upon the ratio of the bend diameter to the pipe diameter, surface
roughness and actual pipe length around the bend.

8.18.2 CONCENTRATION:
From the concentration variation observed in experiments 24 and 26, the
concentration peaks were higher for experiment 26 as compared to 24 due to the higher initial
blow tank pressure and air mass flow rate. For experiments 28, 29 and 30, it was observed
that the powder concentration was highest for experiment 30. Here, the blow tank pressure
was 150 kPa and air flow rate 39.94 m3/hour.
299

Surprisingly, a lower concentration was observed in experiment 29 even though the


blow tank pressure was 150 kPa. However, the air flow rate was higher at 43.3 m3/hour.
This higher air flow rate results in more dilute flow compared to that for experiment 30. In
comparison, in experiment 28 the blow tank pressure was lower at 125 kPa and the solids
concentration was less.

In experiment 32, the blow tank pressure was 130 kPa, average air flow rate was
34.8 m3/hour. For this experiment, the concentration was observed to exhibit very uneven
peaks which, in turn, indicates the flow to be unsteady. For experiment 33, the blow tank
pressure was 140 kPa and average air flow rate 37.6 m 3 /hour. In this case, higher
concentration peaks were observed.

In experiment 36, higher concentration was observed compared to experiment 34 and


35, under relatively similar experimental conditions. However, in experiment 39, the
powder concentration was higher compared to experiment 40 and lowest for experiment 37.
In experiment 39, unstable flow was observed due to the high mass flow ratio.

In experiment 42, the concentration was higher compared to that in experiment 41.
This higher concentration m a y be due to the higher solid to air mass flow ratio of 17.9 as
compared to* 11.8 with experiment 41. In experiment 48, high concentration and unsteady
flow was observed compared to that for experiment 47. The initial blow tank pressure was
the same in both experiments. These trends are probably due to the reduced air flow rate.

8.18.3 LOW VELOCITY CONVEYING:


From Table 7.26, refer Chapter 7, it is evident that the increase in air supply
pressure results in a higher air mass flow rate. The range of mass flow ratio in this test series
was from 13 to 53. Obviously, an increase in air pressure and blow tank pressure results in
increased tonnage of material conveyed.

Figure 8.54 reveals the variation of solid to air ratio versus initial blow tank pre
whereas Figure 8.55 reveals the variation of mass flow rate of solids versus initial blow tank
pressure for Wheat. In particular, the observed range was from 120-200 and 200 - 300 kPa
under both low and high pressure conditions. It is evident from Figure 8.54 that at the higher
initial blow tank pressure i.e. 200 - 300 kPa, the solid-air ratio was less than that observed
when the initial blow tank pressure range was 120 - 300 kPa. Unfortunately, no clear trend
300

was evident for the variation in mass flow rate of solids versus with initial blow tank
pressure, refer Figure 8.55.

ou - B
LEGEND
40- • INITIAL B L O W
cc B TANK PRESSURE

30- B 120-200
< • • 200-300
• kPa
o •
20-
cn B
H • • •
10 - —,— ,. r ,,. 1

100 200 300 400


Initial Blow Tank Pressure, kPa

Figure 8.54: Solid-Air Ratio Variation with Initial Blow Tank Pressure for Wheat.

cfl LEGEND
O INITIAL B L O W
TANK PRESSURE
B 120-200
m* • 200-300
co kPa
0C
o

c/>
its
CO
100 200 300 400
Initial Blow Tank Pressure, kPa

Figure 8.55: Mass Flow Rate of Solids with Initial Blow Tank Pressure for Wheat.

Furthermore, from Table 7.26, it is revealed a reduced solids mass flow rate was
observed at the higher set pressure for experiments 5 and 8. These experiments were
performed at constant blow tank pressure (220 kPa) but with set pressures of 300 and 450
kPa, respectively This indicates that higher set pressure results in a reduced solids flow rate.
301
It should be noted that the set pressure provides the necessary aeration of material in pipeline
to be conveyed at low velocity.

Further information concerning the flow behaviour was gained by visual obser
of the plug flow behaviour. This observation was made using the sight glass located along
the low velocity conveying rig. This also facilitated measurement of the time taken for each
plug to pass through the sight glass. The observations are tabulated in Table 8.14. From
Table 8.14, it is evident that the plug velocity during low velocity conveying ranged between
0.66 - 1.02 m / sec. This velocity range is much lower than the observed dilute phase
conveying range of 7 -19 m/sec, refer Table 7.21.

TABLE 8.14: PLUG VELOCITY AND LENGTH


Material: Wheat
Experiment Plug Velocity No. of Plug Length No. of
No. m / sec. observations cm. observations
22 0.8 13 11.07 6
23 1.02 15 12.8 9
25 0.8 6 10.0 2
26 1.0 10 11.5 2 I
27 0.7 9 12.25 4
28 1.02 8 13.17 3
29 0.7 3 13.25 4
30 0.7 5 13.25 4

These observations are consistent with the fact that Wheat locates in Group B of the
Dixon diagram and it is a good candidate for low velocity dense phase conveying with strong
axisymmetric plugs. In this super dense phase conveying, Wheat was transported at
extremely high levels of volumetric concentration which are not possible in conventional
pneumatic conveying systems. In this mode, air pushes the plugs and percolates through
them. Also, towards the end of the conveying cycle high velocity purging was not present. It
is interesting to note that the conveying cycle is able to be stopped and restarted at any time.
This can be achieved due to the low velocities that are used during the conveying cycle and
the high permeability of the slug consist.
302
Figure 8.56 shows the variation of solids mass flow rate versus air mass flow rate for
two different test series (A and B) with two pipeline lengths, namely 97 and 51.3 m,
respectively, whereas Figure 8.57 shows the variation of average blowtank pressure ve
air mass flow rate. Full test details are presented in Table 7.25. In particular, a hi
solids mass flow rate and a lower average blowtank pressure were observed with the sma
pipeline length test series.

*H
CO LEGEND
CC
Test Series
5
o 3- B A
lo- • B
co
co
co 2-
S
CO
•v
o 1
CO 0.01 0.02 0.03
Air Mass Flow Rate, kg/sec.

Figure 8.56: Solids Mass Flow Rate versus Air Mass Flow for Wheat.

ra
a 300
-i

-
CO
CO LEGEND
Test Series
-t
B A
c 200 -
ca • B
3
o
CO
©
cn
a 100
»- 0.02 0.03 0.04 0.05
0)
> mf, kg/s
<
Figure 8.57: Average Blow Tank Pressure versus Air Mass Flow Rate for Wheat.
303

Figure 8.58 shows the variation of pipeline pressure drop versus air mass flow rate
for solids mass flow rate in the range 0.47 - 0.69 and 0.9 - 1.01 kg / sec. Here, the pipeline
pressure drop w a s approximated by taking air pressure measurements near the blow tank
outlet. Unfortunately, no clear trend was evident in this Figure.

CO 300
O.
LEGEND
a.
Solids Mass
o
Flow Rate
200 - B 0.471 - 0.692
CO
co • 0.902-1.014
cu kg/sec.
0)
c
0)
a.
100
0.02 0.03 0.04 0.05
Air Mass Flow Rate, kg/sec.

Figure 8.58: Pipeline Pressure Drop versus Air M a s s Flow Rate for Wheat.
304

CHAPTER 9
CONCLUSIONS

9.1 GENERAL CONCLUSIONS:


General conclusions drawn from the investigations include:

[1] Scanning Electron Microscope observations are a very useful tool for revealing
vital information concerning powder properties particularly size, distribution, surface
characteristics, surface roughness, shape, porosity, pore shape, ease of degradation, the
presence of sharp or cutting edges promoting erosion, presence offineor ultra fine
particles,fineparticle agglomerates, effective transport volume of particles, etc. Hence,
information from Electron Microscope provides a good insight into and understanding of
powder flow characteristics during pneumatic conveying. A s this information provides
fundamental details of powder properties, it is recommended that w h e n additional
knowledge of powder pneumatic conveying flow behaviour is required, the powder
should be examined under a Scanning Electron Microscope.

[21 In pneumatic conveying, particle density, bulk density, compressibility,


permeability and particle size are important parameters. Knowledge of these powder
properties is essential for predicting pneumatic conveying behaviour. These are simple
and rapid powder properties to evaluate and compare flowability of seemingly similar
powders. Furthermore, particle size plays a significant role in determining a powder's
cohesiveness, fluidization and deaeration characteristics.

[3] The mean particle size and deaeration time are very important parameters
influencing the magnitude of the drained angle of repose. In general, for the powders
tested the drained angle of repose increased as the powder m e a n particle size decreased.
Also, the drained angle of repose increased as the deaeration and fill time increased.
Furthermore, the angle of repose exhibited by hygroscopic powders is sensitive to the
test ambient relative humidity conditions. In particular, the drained angle of repose
increases as the test environment relative humidity increases.
305

[4] For hygroscopic powders, pneumatic conveying should be effected by using dry
conveying air or gas.

[5] Usually, powders displaying high cohesive strength exhibit flow problems. On the
other hand, powders displaying minimal cohesive strength present few difficulties. Powders
which are cohesive also display a tendency to form ratholes in blow tanks during discharge.
Cohesive powders m a y stick in discharge hoppers, feeders and conveying pipelines.
Strongly cohesive powders usually exhibit plug behaviour during pneumatic conveying.

[6] For cohesive powders, the deaeration rate is fast initially and exponential. Deaeratio
behaviour indicates the air retentive properties of powder wjuch indicates the ease or
otherwise of pneumatic conveying by slug or plug flow. Generally, powders with long
deaeration times are good candidates for moving bed flow pneumatic conveying.

[7] In general, on the basis of powder properties determined from bench tests, the
flowability of powders in pneumatic conveying systems can be predicted as follows:

high cohesion, rough particle surface, wall friction, increasing particle density,
increasing particle size, high coefficients of restitution, high drained angle of repose are
material parameters which act as flow resistances in pneumatic conveying.

slow deaeration, smooth particle surface, low packed bulk density are material
parameters which promote flow in moving bed flow.

high permeability, smooth particle surface, incompressible, consolidation stress,


insensitive properties promote conveyance by low velocity conveying.

[8] For powders exhibiting intermediate and extreme values of cohesion, wall friction,
particle size, particle density and permeability; prime mover, blow tank, aeration device/s
(primary, secondary and tertiary (along pipe)), air addition location and method (e.g.
annular), pipe details (number of bends, bend radii, steps, divergence, joints, etc.) and
discharge arrangement characteristics are paramount in determining pneumatic conveying
characteristics.

[9] Pneumatic conveying of powders is complex due to the interaction of a vast number
of individual powder properties. Assessment of pneumatic conveying characteristics can be
306

effected by performing pilot scale tests on pneumatic conveying rigs with the
observations and results suitably scaled up for actual plant conditions. However, for
dense phase and super dense phase pneumatic conveying emphasis should be placed on
powder properties determined from bench tests. These tests should include the specified
tests listed in Table 8.10. This Table also indicates the order of priority for conduction of
the test based on findings from this investigation. This ranking is given with the aim to
determine and identify as accurately and quickly as possible whether a given material will
be suitable for conveying or not. If conveyable, the tests should also be used as a guide
to select the most suitable m o d e of conveying. The implications of the test results are also
declared in Figure 9.1.

9.2 SPECIFIC CONCLUSIONS:


Specific conclusions drawn from this investigation include:

[1] The ratio of packed to loose poured bulk density or Hausner ratio is an relatively
simple bench test to compare cohesion of seemingly similar powders. The
compressibility offinermaterials can be distinquished easily from packed bulk density
test.

[21 Measurement of characteristic dimensions from a particle sizer based on the


principle of Fraunhofer diffraction can indicate indirectly pneumatic conveying flow
behaviour of powders.

[3] Generally, the Jenike and Walker methods provide arch length higher than from
the Cohesive Arch Tester experiments.

[4] The Cohesive Arch Tester provides convenient comparative assessment or


ranking of a powder's cohesive strength. In this tester, significant cohesiveness is
indicated by the tendency of a powder to arch in the tester. Powders possessing such
cohesiveness are usually difficult to convey pneumatically.

[5] The Tensile Tester also conveniently reveals the ranking of powders in regard to
cohesion compared to that measured using the Direct Shear Tester. The latter requires
considerable experience to operate. T o attain uniform porosity with m i n i m u m operator
care,fillingof the tensile tester with a screen vibrator is recommended.

[6] For extremely cohesive powders, it is difficult to test the drained angle of repose.
This suggests that the drained angle of repose is an useful yet crude indicator of the
307
M e a n Particle Size

M e a n Particle Density
I
Estimate of Particle Shape

Basic Chemical Composition


I
Loose Poured and Packed Bulk Density

Lou- Intermediate Extreme

Dense Phase Conueying Possible Dilute Phase


1
Ewtent of Cohesion Unsuitable

Moisture Content

Low Intermediate High

Dense Phase Conueying Possible Dilute Phase

Increasing % M . C. causes increasing Unsuitable


instabilities during flow or special
m o d e of conueging is required e.g.
extrusion flow

Cohesion due to Particle Size Distribution and


Indiuidual Particle Properties

I Intermediate High
Low

[Dense Phase Conueying Possible Dilute Phase Unsuitable

*,
308
Improued Knowledge of Particle Size Distribution

Fluidization
Select m o d e These tests are
I
of conueying Deaeration not meaningful
according to I for powders with
Permeability
Mainwaring
I intermediate
and Jones Slugging
and high extents
Phase Diagram
I Plug Wall Friction of cohesion

Paramount Safety and


System Properties

Toxicity Unusual Powder


Contamination Tolerance
Combustability and/or Properties
Explosiueness
Radioactiuity
Hygroscopicity Thermoplasticity
Hardness and Particle Shape Pjpzosoftening
Rbrasiueness
Thermal Softening
Thixotropic Softening

r
Elastic Properties
Extreme Particle Shape Equiualent to
Fluffy, Flaky and Stringy increasing
Particle Shape cohesion and
Extreme Particle Density wall friction
Swelling Tendency
Extreme LLVall Friction

Figure 9.1: Recommended Sequence of Powder Tests.


309
flowability. Hence, flowability or cohesion of powders can be assessed in regard to
reliable pneumatic conveying characteristics.

[7J In view of the observed rapid gain in strength of fine powders with deaeration
time, m i n i m u m deaeration times should be effected in pneumatic conveying systems to
minimize powder strength. Hence, short cycle times are advantageous in pneumatic
conveying systems handling fine cohesive powders.

[83 It is recommended that the mechanized fill method be used for assessing
deaeration characteristics of powders having segregation tendencies. Thefillrateshould
be as fast as possible and the actual rate should be determined by a trial and error
procedure.

[9] Deaeration cylinders with permeable bases should not be used for assessing
deaeration characteristics since a more complex deaeration pressure variation results.
This variation is difficult to describe empirically.

[ 10] In this investigation, various fly ash of small particle size classified as Group C
powders in Geldart's classification, were found to exhibit poor fluidization
characteristics, whereas, Sand, Alumina and P V C powder were fluidized easily. D u e to
cohesive effects, no clear m i n i m u m fluidization velocity were observed for the fly ash
samples tested.

[11] The determination of the fluidization properties of powders with a wide particle
size consist is difficult to test due to segregation effects. Elutriation offinesfrom the bed
and stratification of different particle size fractions result in changing powder
characterisitcs.

[12] The Jenike Direct Shear Tester can be used to evaluate both the powders internal
and wall friction characteristics, whereas the wall frictionrigindicates a powder's plug
formation tendencies and plug wall friction characteristics for both aerated and deaerated
conditions.

[13] In general, the frictional force in the wall friction rig increases with increasing
column height, whereas the wall friction parameter pk decreases with both increasing air
pressure and column height.
310
[14] The developed fibre optic probe was found to be accurate and convenient for
measuring the powder velocity in actual lean phase pneumatic conveying systems.
However, it is only suitable for granular materials or powders which do not coat the
probe view ports. Obviously, the necessity of the view ports severely restricts the use of
this device. However, this m a y not be a significant disadvantatge as an increasing
number of pneumatic conveying systems are being installed with sight glass sections for
operational control.

[15] Due to difficulties encountered in calibrating the Tealgate T.300 concentration


meter, inaccurate results were obtained. D u e to this reason, the device was only suitable
for indicating whether the flow was unstable or steady during each pneumatic conveying
cycle.

[16] A higher particle velocity is evident with increased mass flow rate as observed
with pneumatic conveying of sand.

[17] During the experimental phase, higher pressure drops were observed in the
vortice elbow bend compared to that in long radius bends, w h e n conveying sand at
solids loading upto 30.

[18] In low velocity conveying of Wheat, an increase in air supply pressure and blow
tank pressure results in more tonnage of material conveyed.

[19] The proposed phase diagram of powder properties is a very important tool to
evaluate and predict the general material flow behaviour in dense phase and super dense
phase pneumatic conveying. B y assessing important powder properties like cohesion,
deaeration, permeability, mechanical interlocking and particle size, flow behaviour of
powders in pneumatic conveying can be predicted. This information is summarized in
Figure 9.1. However, there are limitations in general application of this phase diagram as
not all the powder properties affecting the flow behaviour are included.

[20] Powder properties evaluation from bench tests which are both simple and
convenient indicate fundamental and individual powder properties and allow ranking of
the same. In particular, the properties presented in Table 8.10 should be considered fully
before a system design is contemplated.

[21] Various bench tests provide qualitative and quantitative evaluation of powder
cohesiveness. Depending upon the requirements, selection of suitable bench tests should
311

be made. Qualitative tests are simple and convenient but for accurate measurement,
quantitative bench tests should be used. After conducting a series of bench tests for
different similar powders, mean ranking of cohesiveness should be made to indicate the
relative cohesion. Hence, for ranking of powders, a compromise should be m a d e
between convenient qualitative and accurate quantitative bench tests selection. This
compromise is summarized in Table 8.10.

[22] The various powder properties determined from bench tests provide convenient
and rapid assessment of a powder's flowability, refer Figure 9.1 and Table 8.10. This
assessment is particularly useful forrapidrelative flowability evaluation and ranking of
different powders. The powder properties determined from bench tests yield useful
information in regard to pneumatic conveying flow behaviour of powders in general, and
for the prediction and design of practical pneumatic conveying systems in particular.

9.3 SUGGESTIONS FOR FUTURE WORK:

[1] The Arch Tester should be modified by the installation of pressure tappings on
both sides 50 m m above the bottom. These pressure tappings should be of similar design
to those used on the deaeration cylinder with V y o n D low resistance plugs to prevent
powder ingress into the same. These pressure tappings should, in turn, be connected to
pressure transducers to measure interstitial air pressure during filling and deaeration of
the powder before the conduction of arch measurements.

[2] The maximum outlet opening dimension of the Arch Tester should be increased
as the present 100 m m severely restricts the assessment of powder cohesiveness. In
particular with very cohesive fly ash 'E' of arch length more than 100 m m , actual
measurement was not possible with this Tester.

[3] Additional arching tests should be conducted on various powders under


differing bed heights and different ambient test conditions.

[4] Determination of a powder's tensile strength should be effected utilizing a


differential velocity split cell linear tester. Modified Tensile Testers in which both sides of
the split cell are movable and which incorporate at least four sensitive load cells should be
used to extend the measuring range of the powder bed porosity and the tensile strength.
This suggestion is m a d e to overcome the deficiencies of the Tensile Tester used in this
work.
312
[5] Tensile tests should be performed on powders consisting of different mean size
and actual distribution. These parameters were not considered in the present work.

[6] Cohesion and Tensile strength tests should be performed under controlled
atmosphere conditions wherein temperature and relative humidity can be varied as these
powder properties are strongly affected by moisture content and to a lesser extent by
temperature.

[7] Cohesion and Tensile strength tests should be performed at high pressure to
evaluate the effect of air pressure on cohesion. This high pressure testing should aim to
evaluate conditions in actual pneumatic conveying systems.

[8] Likewise, techniques should be developed to measure powder permeability under


pressurized conditions. The selected test pressure should be consistent with the actual
blow tank and pipeline operation pressures. This information would be extremely useful
in the design of high pressure dense phase pneumatic systems.

[9] Cohesion and Tensile strength tests should be performed by using other Cohesion
and Tensile testers including the Ajax Cohesion Tester.

[10] The unconfined yield strength should be evaluated by performing tests on the
annular shear tester to cover large shear displacements. This tester has a constant area of
shear and flow properties can be evaluated after repeated failure of the same sample. The
observations so obtained should be compared to those assessed using the Jenike Direct
Shear Tester.

[11] The unconfined yield strength should be evaluated by performing uniaxial


compaction tests. The evaluation of this test is simple compared to using the Jenike
Direct Shear Tester as the unconfined yield strength is determined by simply applying a
compressive vertical load on the compacted specimen.

[12] The present wall friction rig should be modified to measure wall friction for
slugging materials by observing the characteristics of the slug motion. The actual slug
motion could be observed by sonic, optic, laser or electrical techniques. The pressure
necessary to achieve constant velocity for slug movement should also be obtained from
experiments. This pressure drop will be useful for evaluating the pressure drop in dense
phase pneumatic conveying systems.
313

[13] The wall friction rig should be replaced by a ring torque measuring apparatus
wherein the ring is immersed at the top of a suitably fluidized powder bed. Also, the
effect of different shaped rings on the frictional force and torque should be observed.

[ 14] Wall friction tests should be performed on other wall materials including Mild
Steel, Polished Stainless Steel by the replacement of the existing Perspex tube with tube
constructed of the relevant material.

[15] Deaeration tests should be conducted using Group A powders and compared with
that of Group C powder deaeration behaviour for differing bed heights to evaluate the
effect of both consolidation and cohesion.

[16] Deaeration tests should be conducted using a video camera to observe accurate
bed height and other dense phase parameters. With a larger size of deaeration column,
rapid bed height observations would be possible without loss of accuracy.

[17] Fluidization of cohesive powders should be effected by the use of mechanical


stirrers or vibrators as the conduction of this test for typical practical powders is difficult.

[18] To consider the effect of particle size distribution in a Geldart's diagram, the
mean particle size should be replaced by the material characteristic dimension such as
particle size distribution span.

[19] Compressibility tests on powders should be conducted at different deaeration


times to observe the significance of deaeration on the compressibility and hence on the
flow properties. This information should then, be used to predict the pneumatic
conveying characteristics of powders.

[20] The fibre optic probe developed for velocity measurement in this work should be
utilized to measure powder concentration in combination with the Hewlett Packard
Correlator and Spectrum Analyzer as well as to study the flow patterns in pneumatic
conveying of powders.

[21] The fibre optic probe should be utilized to measure the rebound particle motion on
the coefficient of restitutionrig.In this work, the rebound particle motion w a s measured
by use of video equipment.
314
[22] The fibre optic probe should be located on various positions of sight glass for
velocity measurement such as in vertical and inclined directions on horizontal pipeline,
on vertical pipeline and after bends. Furthermore, it should be located after the
accleration zone immediately downstream of each system discontinuity.

[23] A data base of powder properties should be developed to assist pneumatic


conveying selection and design. This data base of powder pneumatic conveying
characteristics should be prepared incorporating a large range and number of powders.
M a n y powder properties can be characterized and appreciated by an examination of the
powder's surface, particle shape and form based on S E M photographs. Furthermore,
powder exhibiting adverse flow characteristics and reasons for poor system performance
should be identified. Greater importance should be given to powder properties
determined from simple bench tests like particle size, Hausnerratio(ratio of packed to
loose poured bulk density), compressibility, particle size, tensile strength, deaeration to
determine suitability and ranking of powder properties. This data base should also be
used in a regression analysis to ascertain the significance both qualified and quantified,
of the various powder properties. This regression should also be used to indicate a
powder's suitability or otherwise for lean phase, dense phase and super dense phase
pneumatic conveying. Information so gained should also be used to confirm the proposed
phase diagram for pneumatic conveying.
315

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PUBLICATIONS

During the course of this research programme, the following co-authore


papers were written.

Desai M. K. and McLean A. G., "Convenient Methods to assess Pneumatic


Conveying Characteristics of Powders", Proc. Third Int. Conf. on Bulk
Materials Storage. Handling and Transportation. Newcastle, N S W , Australia,
27-29 June 1989, 98-103.

Desai M. K. and McLean A. G., "Convenient Methods to assess Cohesion fo


Selecting powder's Optimal Pneumatic Conveying Mode", Proc. 19th Aust.
Chem. Eng. Conf. - C H E M E C A 91. Newcastle, N S W , Australia, 18-20
September, 1991, 817-824.

Desai M. K. and McLean A. G., "Deaeration of Powders", To be submitted


to Indian Journal of Engineering.

Desai M. K. and McLean A. G., "Effect of Cohesion on Pneumatic


Conveying Characteristics of Powders" To be submitted to Indian Journal of
Engineering.
330

APPENDIX 'A'
PRESSURE DROP
A model to calculate the pipeline pressure loss for a pneumatic conveying system
including the solids friction component as proposed by Weber (1982) and Chambers
(1986) for circular pipes is presented below for completeness.

A.1 SUPERFICIAL TRANSPORT VELOCITY:

where ms = solids mass flow rate (kgs-1),


m * = m s / m f = phase density of the solids / gas flow,
mf = air mass flow rate (kgs-1),
Pf = air density (kg nr 3 ),
A = 7iD 2 /4( m 2),and
D = internal diameter of pipeline (m).

A.2 FREE SETTLING VELOCITY OR TERMINAL VELOCITY OF


POWDER: vb„
Since the velocity of a single particle flowing vertically upwards often is defined
as the difference between the gas superficial velocity and the particle's terminal velocity.
It is appropriate to discuss briefly this characteristic velocity. This velocity has
paramount significance in governing the behaviour of powders in fluidized beds,
standpipes and flow of powders from orifices and hopper outlets. For these situations
the particle terminal velocity indirectly indicates the Froude Number applicable to the
flow situation. A s will be shown shortly, the Froude No. is an important dimensionless
parameter in pneumatic conveying analysis.
For spheres,

4gd(pbd-pf)
v
b~ = (A.2)
3CDpf

The drag coefficient C o has been shown to correlate with the Reynolds number.
In flow situations involving gas solids flow it is usual to adopt the following definition
for the Reynolds number,
R e ^ - - - ^ (A.3)
331

where Pf = absolute viscosity of air Pa-s, and


d = mean particle diameter, m
In regard to the drag coefficient for spheres the following correlations apply,
CD= Re
IR^:A1+"1O-J' b~^*° CA.4)
26 A
CD=0.4+--^, l<Reboo<104 (A.5)
Reb«
C D = 0.4, 104<Reboo<105 (A.6)
where p b l = loose poured bulk density of solid (kgm"3)

By use of equations (A.2) and (A.6) v ^ can be evaluated. Obviously, in this


evaluation iterations are necessary. Assuming air at atmospheric pressure (101 kPa abs.),
air temperature at 293° K and spherical particles, the relationship between v ^ and d can
be plotted as shown in Figures A.l and A.2, the same can be used to determine v ^ .

A.3 FRICTION COEFFICIENTS:


A.3.1 Darcv Friction Factor for Air : X{
For air flow alone knowledge of the relative roughness of a pipe allows
evaluation of Xf from the M o o d y diagram (Figure A.3). For laminar and turbulent flows
in smooth pipes, dimensional analysis indicates that the pipe friction is a function of the
flow Reynold's number Re.

For a laminar flow, Xf = 64 / Re (A.7)


and for turbulent flow in smooth pipes Blasius derived that,
Xf = 0.316 /ReO- 2 * (A.8)

The Darcy-Weisback equation predicts the pipeline pressure loss due to air
friction to be,

2
PfVf
LXf
A
Pf= 2D (A 9)
'
where Xf = friction factor due to air only,
Vf = the gas velocity
or
A p f = 500[(1012 + 0.004567 m/"85 L D " 5 ) 0 5 - 101 ] Pa (A.10)
Voo (m/s)

t 5 6 7 10 *- IC4

d(pm)

Figure A.2: Settling Velocity in still air of Spherical Particles with Diameter d
Voo (m/s)

d (pm)

Figure A.l: Settling Velocity in still air of Spherical Particles with Diameter d
334

A.3.2 Effective friction coefficient due to solids. Xs


Stegmaiker (1978) determined a mean value for this coefficient by correlating the
data from a number of fine powder flow experiments and applying the mechanics of
similitude. The correlation was found to be,
Xs = 2.1 (m*) - 0 ' 3 Fr -1 Fr,0"25 (^) , d < 0.0005 m (A.l 1)

Xs = 0.082 (m*)-0'3 Fr-0"86 Fif25 (^) ' , d > 0.0005 m (A.12)


where, Froude number = Fr = Vf 2 / g D and (A. 13)
Fr^v^/go * (A.14)

A number of research workers have analyzed the friction factor and reported
correlations for the same in the literature, a small number of which are presented in Table

Figure A.3: Moody Diagram.


TABLE A.1: FRICTION FACTOR

Research worker Expression Friction factor

2fspp(l-e)v
Stemerding (1962) pw W T P 0.003
D
2fsPp(l-£)vg
Reddy and Pei (1969) 0.046vp - 1
D

sPp p
Capes and Nakamura (1973) ^ 0.046vp-1.22

2fsPp(l-e)vg
Konno and Saito (1969)
D 0.028(gD)°-5vD-l

2fsPp(l-e)vg -.-0.979
Yang(vertical)(1978) 0.0315
D

2fsPp(l-e)vp2
Yang(horizontal) (1978) 0.0293
D

p p 55.5Dt'l.i
Mathur and Klinzing (1981) -
D .0.64 pJ3.26
J4). 2 6 .C0.91
g H Pp
-0.1
2fsPp(l-e)v2 -T, 0.25nV
m. - . . - U . - T - "1,-. r
-
Stegmaiker (dense) (1978)
D 2.1p Fr Frs
s
UJ
-1-1.28
2fsPpa-e)vg 1.05 Vf-vp
Muley, Mathur and Klinzing 0.0172(l-e)
D 05
L(gD)
(1982)

[After Klinzing et al. (1987) ]

A.4 ACCELERATION PRESSURE DROP DUE TO FLUID. An.f


The acceleration pressure drop for the transport fluid alone is,
PfVf
A
P_f = (A.15)
336

A.5 ACCELERATION PRESSURE DROP DUE TO SOLIDS. An,.


When solids are transported in a transport fluid an additional acceleration pressure
drop occurs. This pressure drop is expressed by,
APas = m * p f V f v s (A. 16)
where v s and Vf are in ms -1 , d is in m m . and p s is in kgm-3.

Wherein the particle velocity vs can also be calculated from the voidage e an
solids mass flow rate m s using the following equation,
mc
v.= ,_ ,' .
' s ~(1-e) p s A
(A.17)

where p s = the density of solid and %

A = cross sectional area of the pipe.

Moreover, the particle velocity can be determined from experimental techniqu


discussed in Section 3.4.

Obviously, the superficial velocity Vf can be calculated from the system supp
flowmeter reading and the knowledge of the diameter of pneumatic conveying test rig.
From the superficial velocity V f and the voidage e, the actual air velocity can be
calculated, viz.
vf = V f / e (A-18)

A.6 FRICTIONAL PRESSURE DROP. Apf


The friction generated pressure drop Ap f can be evaluated using the expression,
p f V?L7if m*pfV2LXs (A19)
Apf +
~ 2D 2D
where L = L^ + L v (m)
L h = total effective length of horizontal pipes (m),
L v = total effective length of vertical pipes (m).

A.7 GRAVITATION^ PRESSURE DROP. AP-.


For vertical upwards pneumatic conveying system legs the pressure loss can be
evaluated using the same equations for horizontal pipes by taking into account an
additional term due to the pressure loss of lifting the solids against gravity. This term is
given by,
KA ZV)
A p ^ d + m^PfgL, -
where Ly = vertical length of pipe
337

Obviously, when conveying vertically downwards this pressure loss provides


assistive effort.
A-8 PRESSURE DROP DUE TO RENfng, A p b
The pressure drops associated with bends can be evaluated using the following
correlation,
BNB(l+m*)pfVf2
Apb= 5 (A.21)
where B = Bend coefficient,
R g = Centreline radius of bend, and
N B = Number of bends.

For 90° bends in circular pipes the following bend coefficients apply as a function
ofRg/D.
TABLE A.2: BEND LOSS COEFFICIENT FOR 90° BENDS

Bend radius / pipe diameter B

2 1.5
4 0.75
6 or more 0.5

A.9 TOTAL PRESSURE DROP. Ap


A s can be appreciated this initial simplified correlation lacks theoretical basis nor
does it account for actual bend configuration. With knowledge of the individual
component pressure drop, the overall total system pressure drop is evaluated using,

Ap = APaf + APas + Apf + Apg + Apb (A.22)

Frictional pressure drop due to solids in dense phase conveying can be given as
(Wen et al. 1959),

A p s = 4.27 L Pds vs0"45 ( § ) ° ' 2 5 (A.23)

where d = the average particle diameter,


Pd- = the dispersed solids density.
338
APPENDIX 'B'
POWDER PROPERTIES

B.l INTRODUCTION:
The purpose of this appendix is to present important aspects of powder properties
which were m a d e during the literature survey for this investigation to which reference
was made. Inclusion of this information is considered appropriate to ensure the reader is
familiar with the numerous powder properties which characterize powder and to highlight
the complexity of powder properties and behaviour. Obviously, for brevity reasons not
all powder properties are discussed in this Appendix. Likewise space restriction prevents
discussion and mention of all terms used to describe powders. For a more complete
discussion the reader should consult the nomograph by Svarovsky (1987).

A brief discussion of the characteristics and significance of powder properties in


regard to pneumatic conveying is n o w presented.

B.2 PARTICLE HARDNESS:


The hardness of a particle depends upon the type of structure and bonding, radii
distance of the atoms, relative atom or molecular size, the valence value and the continuity
of the bonding. In general, the harder the particle surface, the lower the interparticle
contact possible suggesting good flowability.

A knowledge of particle hardness is important for the design of pneumatic


conveying systems. It gives an indication of the extent of abrasion and erosion to key
components. Individual particles are small and the commercial equipment to measure
hardness like Vickers, Rockwell and Brinell types are not suitable for the powders. Since
scratching is the major mechanism of abrasive wear, scratch hardness can be used to
indicate the resistance of a metal of k n o w n hardness to abrasive wear. Thus, scratch
hardness is a suitable method for the measurement of hardness of powders. Particle
hardness is paramount for selecting the pneumatic conveying system piping material,
bearing and bearing seal requirements for rotary feeders.

B.3 ABRASIVENESS:
In the design of pneumatic conveying system equipment to protect against wear, it
is important to have knowledge of a material's abrasiveness. Coke and foundary sand
will wear hoppers and pneumatic conveying systems. In dry wear situations, hardened
steels, wear-resistant liners and high-density plastics should be considered for contact
materials.
339

B.4 ELASTICITY:
Particle elasticity has an important role in pneumatic conveying. Elasticity
influences the rate of loss of kinetic energy during the interparticle collisions occurring
during flow and has some control on the duration of any particular collision.

B.5 ELECTROSTATIC PROPERTIES:


If the powder exhibits a tendency toward static electricity, it m a y be necessary to
install static eliminators in the filter receivers, cyclones or elsewhere to keep the powder
from building up on the filter bags or walls of thefilter-receiver.It m a y also be necessary
to add moisture to the conveying air to reduce the static properties.

Electrostatic effects have been reviewed by Boothroyd (1971) and Soo (1971).
The use of dense phase conveying reduce the problems created by static electricity due to
lower conveying velocities and greatly reduced tendency of particle collisions as
suggested from the work conducted by Lippert (1966). The significance of electrostatic
charging is further supported by observations m a d e by Clark (1952) that the pressure
drop increased, in some cases was up to 10 times, whenever powders were conveyed for
long periods.

B.6 EXPLQSIQN^CJIARAmTiRISTlCSi
W h e n conveying combustible materials the combinations of high concentrations of
solids in air mixtures in bins and pneumatic conveying systems and ideal ignition sources
giveriseto frequent dangerous dust fires and dust explosions, if proper precautions are
not taken. Pneumatic conveying systems generally operate with a solid to mass ratio
considerably above the upper explosible limits and if the conveying velocity is kept as
high as possible, then the time of exposure of the dust particles to an ignition spark is
minimal. There are a variety of preventive measures for dilute phase pneumatic
conveying.
- avoiding dangerous material concentration
- avoiding ignition sources
- avoiding oxygen concentrations that render ignition possible
- by using special construction and protective barriers.

B.7 PARTJCJJEJSIZE_ANA_Jl^I^
A simple technique to determine the particle size analysis is to sieve the sample
powder into different fractions and weight average the results according to the sieve
openings. The distribution of particles over varying size ranges can be presented on a
340

mass or number basis. In particular, a sieve analysis presents the particle size information
on a mass basis, whereas, optical sizing is on a number basis.

The diameter of a particle is usually based on an equivalent sphere of the same


volume or mass. The sieve diameter is the width of the minimum square aperture through
which the particle will pass. Microscopic techniques m a y characterize particle size based
on the use of the m e a n value of the distance between pairs of parallel tangents to the
projected outline of the particles (Feret diameter) or the mean chord length of the
projected outline of the particle (Martin's diameter). This characterization of particle size
is further complicated by the fact that various forms of averaging are possible. The Sauter
mean diameter is a measure of the ratio of the total volume of particles to the total surface
area. The mean diameter is derived from the volume distribution. In general, powders
exhibiting bimodal distributions tend to be more cohesive and less permeable than
monosized powders of the same mean particle size.

B.8 SUREACE^AREA^i
O n e further important characteristics of the fine powders is the specific surface
area. This is a measure of the fineness and porosity of the powder. The specific surface
area increases with decreasing particle size.

The specific surface can be converted into an equivalent mean spherical diameter
XgV using the equation,
XsV = 6/S v , (B.l)
where S v = volume specific surface.

Some methods of measuring surface area are: permeametry, gas adsorption,


dynamic gas adsorption, gas diffusion, hindered settling, adsorption from solution, flow
microcalorimetry, dye adsorption and porosimetry. The actual method used to measure
surface area is selected depending on the purpose of the measurement.

The size of a particle relates to its surface area. The interrelationship of particl
size, surface area and porosity will determine the flow characteristic of a powder. In
general, a powder with large particle size and small surface area will be free flowing,
whereas a powder with small size and large surface area will be cohesive. Fine particles
with high porosity will also tend to be more floodable. Furthermore, a powder with large
surface area will display increased hygroscopicity, electrostatic activity, agglomeration,
solubility, deformability and reactivity.
341
B.9 PARTICLE nFMSITY-
This is the true density of a single particle. It is the density of a particle including
the pores or voids within the individual solids. It is defined as the weight of the particle
divided by the volume occupied by the entire particle. In general, dense particles do not
cohere to other particles and tend to be more free flowing than less dense particles. In
the design of pneumatic conveying system, this powder property controls, to a
significant extent, the conveying air pressure and volumetric requirements. In the design
of low velocity dense phase systems, particle density is an important parameter.

B.10 BULK DFNSTTY-


A powder consists of many particles grouped to form a bulk. This powder will
have an apparent bulk density, i.e. the mass of the bulk divided by the volume of particles
and voids contained. It is the overall density of the loose powder including the
interparticle distance of separation. This bulk density is dependent on the particle size and
size distribution, the particle shape, the particle density, moisture content, particle
packing, method of filling and the interparticle separation. Obviously, bulk density is
related to particle density through the interparticle void fraction.

It is important to recognize that bulk density does not have a unique value for a
particular bulk material, but will vary with the condition of the material. For example a
material that has just been pneumatically conveyed m a y be aerated and have a
considerably lower bulk density than when allowed to de-aerate.

The bulk density used to size a specific item of equipment in a pneumatic


conveying system should be relative to the condition of the powder at that point in the
system. T h e latter is not always easy to determine as most methods of evaluating bulk
density which, in turn, determines the change in volume of the powder, requires
knowledge of the changing consolidation conditions. Here, tests where both the poured
or aerated volume and the deaerated or settled volume are measured for a known mass of
powder provide useful benchmarks bulk density values for pneumatically conveyed
powders.

Ravenet (1983) stated three different bulk density values should be determined
experimentally to characterize powders. These are apparent density (without compression
or compaction), density under compression and density under compaction. For granular
products, the variation between apparent density and density under compaction is
between 9 and 21 per cent, while for cohesive powders, the difference is greater,
varying from between 22 and 87 per cent.
342

Seville (1987) has indicated that the Hausner ratio is an indirect measure of
interparticle forces. Harnby et al. (1987) also reported the variation of the Hausner ratio
with relative humidity for Ballotini. In particular, an increase of the Hausner ratio was
evident with a decrease in particle size and an increase in relative humidity.

B.ll COMPRESSIBTI.TTY-
Compressibility is a simple way of measuring indirectly the following
characteristics of flow:
- bulk density,
- uniformity in size and shape, %

- hardness,
- surface area,
- relative moisture content, and
- cohesiveness.

A simple quantification of compressibility is to define compressibility as the


difference between the aerated bulk density and the packed bulk density, divided by the
packed bulk density, times 100. This numerical value is referred to as the powder's
compressibility. This value varies, in general, with a powder's flow characteristics as
follows:
5 to 15 percent for free flowing granules - excellent flow
12 to 16 percent for free flowing powdered granules - good flow
18 to 21 percent for fair flow
23 to 28 percent poor flow
28 to 35 percent poor flow, fluidizable cohesive powders
33 to 38 percent for very poor flow, fluidizable cohesive powders
> 40 percent for very very poor flow cohesive powders.

The compressibility of a powder results in two effects: increase of bulk density


which affects the amount of powder held and an increase of cohesive strenguVwhich
affects the flowability of the powder. In general, a powder of wide size range is less
compressible than a powder of narrow-size range because of the increased number of
interparticle contacts. However, for the former case the powder m a y exhibit high
compressibility if the particles are fragile or soft. Obviously, the higher the relative
porosity, the lower the compressibility.
343
B.12 PARTICLE SHAPF-
Particle shape has a significant effect on the energy required to convey the powder
efficiently through the pipeline. Measurement of particle shape is difficult because of the
three dimensionality of particles and nonuniformity of size. Obviously, a particle that
has m a n y irregular protrusions on its surface will have different flow behaviour to that of
a spherical particle. In general, irregular particles will join together and behave as a single
particle more easily than spherical particles. This tendency is reinforced by the fact that
irregular shaped particles have m a n y points of contact. Hence, they display significant
surface forces. This suggests that as the size of the particles decreases, the importance of
shape becomes less. In general, the particles of powders vary not only in size but also in
shape. The qualitative terms used to describe powder particle shape and general flow
characteristics are presented in Table 5.5.

In general, spherical particles flow in pneumatic conveying without degradation


compared to the extent of degradation experienced w h e n conveying sharp angular
particles, especially if the latter have a tendency to interlock. Yuasa et al. (1983) reported
that rougher particles have a higher interparticle coefficient of friction and are less likely to
pack as densely as less rough particles. Rough surface particles also display an increased
friction between the particles and the pipewall which reduces their flowability.

B.13 SURFACE PROPERTIES:


A knowledge of the general shape and structure of the particles comprising the
powder can be obtained by micrographs from either optical or electron microscopy.
Information in this visual form can provide the designer with information on the product
to be conveyed which can be linked to experience in handling similar shaped powders.
For example, the shape and structure of the particles m a y appear to be fragile indicating
that severe particle degradation m a y occur during transportation. A fibrous, thread-like
shape will indicate that the particles m a y lock together precipitating flow problems. The
sharp crystalline edges of a hard material m a y indicate the possibility of erosion of the
pipeline and system components.

The classification of surfaces on the basis of roughness depends on the scale of


observation. Surfaces appearing smooth from macroscopic examination by eye m a y
appear very rough under a high resolution microscope.

The use of microscope techniques to observe particle surfaces and shape provides
a powerful tool in modern particle technology studies. Use of microscopic techniques has
344

been facilitated by the development of modern electron microscopes access to which is


n o w c o m m o n place.

However, the observation of powder surfaces by optical microscope is limited


clue to short length of focus. Whereas, in the electron transmission microscope, it is
limited by the sample preparation technique. Furthermore, the particles m a y alter during
examination by evaporation or decomposition of the particles which are opaque to
electrons. These effects results in the recording of shadowgrams.

Electron Microscopes take one of two forms; scanning (SEM) and transmission
( T E M ) . In respect to application to powder technology, the advantages of the Electron
Scanning Microscope are:
- direct examination;
- a large depth of focus (about 300 times that of an optical microscope) at resolutions of
15-20 n m as compared to 0.3-0.5 n m for the Transmission Electron Microscope (TEM);
- a higher range of magnification, 20 x to 100000 x is possible;
- minimal or no sample preparation, except for coating of nonmetallic specimens;
- a low specimen current;
- easy to operate;
- faster and more three dimensional details than T E M ; and
- samples as large 25 m m x 25 m m can be observed.

In view of the above ad/antages, it is apparent that the Electron Scanning


Microscope provides an excellent technique to observe powder size, shape, surface
roughness and texture, porosity and pore shape, microstructure and agglomeration
tendencies.

The only drawback to the wider application of SEM techniques is the need to
vapor-deposit a thin layer of metallic coating to prevent charging of the specimen.
Usually this metallic coating is gold.

In the scanning electron microscope, an electron beam of medium energy (5-50


keV) produced with an electron gun, is focused on the specimen through condenser and
objective lenses. These electrons interact with the sample and produce more electrons
which are classified as low-energy secondary electrons whose energy is less than 50 e V
and back scattered electrons of energy between 50 e V and the energy of incident
electrons. These secondary electrons and back scattered electrons are detected, amplified
345
and displayed on the screen of a cathode ray tube. Generally, these examination
made on photographic records of the screen.

B.14.1 POROSITY-
Porosity or voidage is defined as the volume of the voids within the powder bed.
The void volume includes the pores if particles are porous. It can be measured indirectly
from particle and bulk densities.

B.14.2 PACKING;
The packing of solids in a material determines its porosity, permeability and the
bulk density. Moreover, the extent of packing and porosity is partly dependent on the
shape, size and size distribution of the particles. If the surface of the particles is rough,
then the interparticle friction may be greater and so prevent a denser packing condition.

The critical values of void ratio are dependent on particle geometry and the
interparticle friction angle. A powder bed or aggregate formed from equal spheres
exhibiting higher interparticle friction angle will have a critical voidratiohigher than
aggregates formed from the same mono size spheres exhibiting lower interparticle
friction angle. W h e n attractive forces exist between the spheres closer packing, higher
number of contacts and a lower voidratioresults. Whereas, when repulsive forces exist
more separated packing, reduced number of contacts and higher voidratioresults. In
general, powders having a wide particle size distribution exhibit closer packing and lower
porosity [Wood, (1986)].

B.15 THE FLOW OF FLUIDS THROUGH PARTICLE RF.ns-


B.15.1 INTRODUCTION:
The flow of fluids through powder beds is controlled by the permeability of the
packing which depends to a significant extent, on the external surface of the particles.
The external surface area of the particulate system may be calculated from the Kozeny-
Carman equation by measuring the linear rate of flow and pressure drop of a fluid
through a particulate packing at various porosities. The permeability is low when the
particles consisting the bed have rough, porous surfaces and the calculated surface area
high.

B.15.2 PERMEAMETRY:
Permeametry is generally suitable for powders of average particle size between
0.2 and 50 microns but it can be also used with coarse particles, say upto 1000 microns
in size using a suitably scaled up test equipment. At low gas flow rates, therateof gas
346

flow through a packed bed increases linearly with applied pressure drop. Bed
permeability or the permeability factor is the gas flow rate (m3/s) per unit pressure drop
(N/m 2 ), per unit cross sectional area of the bed (m 2 ) times the bed depth (m), giving the
final units for this factor in m4/N.s. This factor also depends on the gas viscosity.

In general, all permeametry methods are based on the Carman-Kozeny equation


which relates the superficial approach velocity u to the porosity of the powder e and the
specific surface of the sample S w .

The measurement of permeability of a packed bed of powder can be conducted for


laminar gas flow. It can be measured either using continuous, steady-state flow (constant
pressure drop) or using variable flow (constant volume) instruments.
(a) Constant flow instruments:
The Lea and Nurse apparatus and Fisher Sub-sieve sizer are examples of
commercially available constant flow instruments.
(b) Variable flow instruments:
The most c o m m o n variable flow instruments are the Griffin and George (oil
suction) and the Reynolds and Branson (mercury suction) permeameters.

B.16 INTERPARTICLE FORCES:


Adhesion is the phenomenon observed when particles stick to solid surfaces.
This is undesirable and must be accounted for in pneumatic conveying systems.
(a) V A N D E R W A A L ' S F O R C E S :
The molecular forces of adhesion are determined by Van der Waal's forces of
interaction between particle molecules and the supporting surface. They depend on the
properties and geometry of the contacting bodies, the roughness of the supporting
surface and the area of contact.
(b) CAPILLARY FORCES:
Capillary forces of adhesion are due to the condensation of water vapor into the
pores of loose solids. A liquid meniscus develops between the particles and the pipe wall,
resulting in the formation of surface forces. These forces press the solids onto the
pipewall. Capillary forces m a y be reduced by increasing the hydrophobicity of the
surface (i.e. by making it moisture resistant) through the addition of a liquid surface-
active agent in the loose material.
(c) ELECTROSTATIC FORCES:
Electrical forces of adhesion occur only during direct contact between particles and
the pipewall. During flow, the particles rub against each other and with the walls. This
creates electrical charges, causing a potential difference with the result that the particles
347

agglomerate. The greater the contact potential difference, the greater are the electrical
adhesion forces. The contact potential difference depends on the amount of charge on the
particle's surfaces and the supporting surface.

Coulomb's forces of adhesion arise, when charged particles approach the


pipewall. W h e n this happens, on the opposite side of the pipewall, charges are generated
that are equal to the particle charges, but are of opposite sign. The higher the wall's
conductivity, the less pronounced are Coulomb's forces and consequently, the smaller the
forces of adhesion. Surface wetness also promotes this process.
(d) V A R I A T I O N W I T H P A R T T C I . E ST7E-
Each type of adhesion force has a different effect dependent on particle size. In
terms of particle radius, the relationship are as follows:
Coulomb's forces are proportional to 1/r 2;
electrical forces, to r °-7;
molecular forces to r ;
capillary forces, r p (1 - r p x l ) , for exponent x > 1.
(e) VARIATION WITH P O W D E R PROPERTIES:
Because of the radically different natures of the adhesion component forces, a
universal method for minimizing them is not possible. For example, while the
hydrophobilization of the pipewall decreases capillary forces, it tends to increase electrical
and coulombic forces; whereas increasing wetness decreases electrical and Coulomb's
forces but increases capillary forces. In comparison, Van-der Waals forces are
strengthened by adsorption layers; electrostatics and magnetic forces; liquid bridges and
solid bridges due to partial melting or crystallization of dissolved substance.

B.17 POWDER FLOWABILITY:


B.17.1 INTRODUCTION:
Two factors friction and cohesion act during the flow of solid bodies. They
correspond to two types of strength, shear and tensile. These strengths are directly based
on the packing structure of the particle assemblage through the degree of mechanical
interlocking a m o n g particles and the coordination number. A s one expects the handling of
powders is associated with the frictional and cohesive properties and are fundamental to
the interpretation of particle behaviour.
(a) FRICTION:
For cohesive powders three angles of friction are important.
- The effective angle of friction, 8
- The angle of internal friction, ty
- The angle of internal friction between the powder and the wall, <j>w
348

These angles are functions of the size distribution, shape, surface properties of the
powders, bulk density, normal compressive stress. Knowledge of these friction angles
are important in the design of powders storage, handling and transportation equipment.

The angle of internal friction determines the stress distribution within a bed of
powder undergoing strain. Whereas, the angle of wall friction describes the stress
condition acting between the material bed and the walls of the container.

Since, the temperature and humidity can change the surface and frictional
properties of a material, atmospheric conditions will also affect the flow properties of a
bulk solid.

The internal and wall coefficients of friction of a powder may be determined by


shear tester and a M o h r circle stress analysis (Arnold et al. 1980). In regard to
determination of the internal friction, the frictional force, F required to shear a
consolidated powder sample under various normal loads, W , is measured. B y repetition
of the shear procedure on different consolidated samples a powder yield locus is
obtained,
x = f(G) (B.2)
where x = the shear stress parallel to the plane and
a = the compressive stress normal to the plane.
The slope of the powder yield locus determines the coefficient of internal friction,
p = tan<j) (B.3)
where <J)-= the angle of internal friction.

To determine the coefficient of the wall friction, pw, the base of the cell is
effectively lined with the wall material to be tested. The resulting yield locus is k n o w n as
the wall yield locus. T h e slope of the wall yield locus determines the coefficient of wall
friction,
p w = tan <|>w, (B.4)
where <J>W -= the angle of wall friction.

The accuracy of the measurements depend largely on the creation and maintenance
of a well defined failure plane within the cell. Modifications of the conventional shear
testers are the biaxial and triaxial testers.

Evaluation of results from wall friction tests is simple. The shear force necessary
to m o v e the loaded cell is plotted against the applied normal load (note that both the axes
349
should have the same scale) and, where appropriate, a straight line is drawn through the
plot. The angle subtended by this line with the x-axis is the angle of wall friction.
Sometimes, there is a strong cohesion between the powder and the wall and this leads to
the above plot showing an intercept.
(a.l) ANGLE QF REPOSE;
The angle of repose is that formed, when a sample of the powder is poured onto a
flat surface. It is used sometimes to indicate the type of metering and feeding devices for
bins or hoppers. Furthermore, the internal angle of friction can be approximated by the
angle of repose. This is a reasonable assumption only when the cohesive strength of the
powder is low.

Two methods for measuring this angle exist, namely discharging from a f
bottom container or forming a heap on a horizontal surface. In first method, the angle of
repose is the angle formed between the surface of the powder remaining in the container
and the bottom wall. In the second method, the half angle of a heap formed on a flat
surface, measured at the top is taken as the angle of repose. As the measurements are
done at rest, these angles provide an indication of the static value of the internal angle of
friction of the powder.
(a.2) A N G L E O F SLIDE:
The angle of slide on a plate provides a convenient assessment of the angle of wall
friction.This convenience results from the fact that the tangent of the angle of slide
approximates the coefficient of friction of the product on the plate.
(a.3) C A S C A D I N G A N G L E :
The cascading angle represents the flowing state of powder rather than the
assembly at rest. It is defined as the angle formed by the inclined surface of a flowing
powder inside a horizontal rotating cylinder, and the horizontal. This angle is affected by
moisture content, particle size, shape and roughness (Yamashiro et al., 1982) and also
dependent on wall friction (Briscoe et al., 1985).

(b) COHESION:
Cohesion is a fundamental property and hence is evaluated directly as a powder
flow property. The presence of cohesion in a powder causes the powder to stick together
to form a powder mass. Obviously, the higher the apparent surface cohesion of a
powder, the less the flowability and vice versa.

A relative measure of cohesion can be determined by extrapolating the


by a straight line across the low-stress region to intercept the shear stress axis. This
350

intercept is a measure of the shear stress at zero normal stress. This cohesion results
from the interparticle forces discussed in Section B.6.

Cohesive powders behave as rigid-plastic Coulomb solid. A rigid-plastic solid


possesses a yield locus which defines the limits of a range of stresses that cause no
permanent deformation, whereas stresses equal to the limiting cause either failure or
plastic flow. For a Coulomb powders the yield locus can be represented by:
T = C + CT tan <|> (B.5)
giving a linear relation between the shear stress, x, and the normal stress,CT.Thus, the
cohesion, C, and tensile strength, x, can be correlated with the angle of friction, <{>.

For different consolidations of a powder, there will be different yield loci.


Usually, powders display non linear yield loci. However, over a limited range of
consolidation, the yield locus can be approximated by straight lines. Furthermore, the end
points of the individual yield loci approximately lie on a straight line which goes through
origin. With cohesive powders the individual yield loci are a strong function of the
interstitial voidage, e of the bulk.

In practical terms, the cohesiveness of a powder is evaluated by evaluating the


flow function of a solid. In this evaluation,CTiis major consolidating stress and CTC the
unconfined yield strength of the powder. The ratio
ff c = CTl/ CTC, (B.6)
is defined as the flow function and is a measure of powder's flowability.
The larger the function ffc and the smaller the strengthCTC, the better is the flowability of
a powder. If,
ffc < 2 then the powder is very cohesive and non flowing
2 < ffc < 4 then the powder is cohesive
4 < ffc < 10 then the powder is easy flowing and
10 < ffc then the powder is free flowing

By using a flow - no flow concept, gravity flow channel outlets can be sized for
reliable flow. In this concept, the strength of the powder is compared with the stresses
causing the powder to flow. Flow will occur w h e n (Ti > CTC . That is the cohesive arch
across the outlet will fail since the stress CTi imposed by the hopper exceeds the
unconfined yield stress of the powder CTC. The critical value of CTi occurs at the
intersection point of the flowfactor and the powder flow function. That is for the flow to
be continuous.
351

A cohesive powder can support a static shear stress with no normal load applied.
For arching to be prevented and flow to be continuous, the strength of any arch must be
less than the forces tending to break it. In most situations, these forces only represent the
gravitational forces. However in some situations, there m a y be an additional force due to
a differential gas pressure across the arch.

In a free arch, both the shear and normal stresses in the plane tangential to the
arch must be zero, so that the stresses at any point on the surface of an arch must be
represented by a M o h r circle passing through the origin; this M o h r circle which touches
the material yield locus represent the stresses at a point in a powder on the verge of
failure. -

This limiting circle also defines the unconfined yield strength, CTC, of the powder
for a particular consolidation. This property is the yield strength that can be measured by
causing a radially unconfined cylindrical plug of preconsolidated powder to fail in axial
compression. T h e relation between the unconfined yield strength, the cohesion and
internal angle of friction, for a linear yield locus is approximately linear is,
c_oc(l-gin4>) (B?)

2 cos(t)
In the limiting case, the m a x i m u m shear strength possible is, 1/2 o c (B.8)

In this initial simple model, Jenike and Walker assume the point G(=l/2 CTC,)
which gives the most difficult and conservative case for maintaining flow.

Jenike's theory in combination with powder properties measured in the shear cell
predicts the arching dimension larger than the arching dimension found experimentally
as reported by Walker (1967). However, it is advisable to have a overdesign to be on the
safe side. In particular, Walker's equation for arching is,
CTC sin 2 (a + (j)) ( B9 )
R = —————^——
Pb
which considers the walls to be steep and smooth.

However, engineers who apply the Jenike method in practice consider the method
to be reliable and claim it is advisable to have a certain overdesign to be on the safe
side.The overdesign of 1 0 0 % is probably necessary to account for initial filling
conditions and other unaccounted factors (e.g. increase in moisture content, etc.).
Obviously more accurate outlet sizing can be determined using full scale experimental
facilities. Such testing would provide a lower bound to the expected critical outlet opening
dimension and the Jenike method the upper bound. T o approximate full scale
352

experimental facilities a novel arch tester was developed. Details of this arch tester is
outlined in Chapter 6. 12.

Using this tester, the unconfined powder yield strength was then evalu
knowledge of the observed opening span to effect flow, by use of the well known Jenike
critical outlet dimension equation (Jenike, 1970), viz.
H (a) CTi
BorD= (BI0)
"^i-
where H(a) = function of a
a = hopper half angle
CTi = major principal consolidating stress
Pb = bulk density
In this evaluation the channel boundaries were assumed to be rough.

B.18 TENSILE STRENGTH:


B.18.1 INTRODUCTION:
Powder tensile strength is a fundamental failure property. Since this powder
property bears a strong relationship to powder cohesiveness, the tensile strength of a
powder is important during handling and processing of cohesive powders. The tensile
strength has been estimated from the failure curve obtained from shear tests or three
dimensional compression tests. Alternatively, it may be measured by purpose built
powder testers.

Rumpf (1970) suggested a model for tensile strength of solids arising


forces between individual particles. Rumpf s equation for tensile strengthCTZis,
CTz=^k| (B.ll)

where e = porosity
k = average coordination number
H = cohesive force at a contact point
dp = particle diameter

B.18.2 YIELD LOCUS EQUATION:


Farely (1965) reported that for any powder there exists a series of yield loci with
a state of compaction measured as bulk density as a parameter. It has been found that the
yield loci can be represented by the following equation:

where x = shear stress,


353

T = Ultimate tensile strength,


C = cohesion,
CT = compressive stress,
and n = shear index.

It was shown experimentally that this relationship holds for a large number of
powders tested. The value of the constant n varies between 1 and 2, being just over 1 for
free flowing powders and approaching 2 for cohesive powders. For a free flowing
powder, n = 1, T = C = 0 and the eqn.. (B.29) reduces to,
T= K
° (B.13)
where K = a value similar to the internal friction of the powde*

Nedderman (1978) has shown that the value of the constant n can not be larger
than two if Mohr's circle is to be tangential to the material yield locus.

Jimbo et al. (1984) confirmed experimentally by testing many powders that the
relationship between the tensile strength CTZ and the porosity e can be expressed by the
following equation over a wide range of porosity, except for agglomeration
phenomenon.
a z = kx exp ( ~ ^- J (B.14)
where ki and b are empirical constants.

The expression relating the tensile strength CTZ, and pre-compression stress p can
be written as:
CTz = k 2 p m (B.15)
where k2 and m are empirical constants.

They also found that the porosity e can be correlated to the pre-compressive stress
p by the following equation.

p = k3exp(-~) (B.16)

where k3 and c are constants.

Moreover, Jimbo et al. (1984) found that the behaviour of powders can be
approximated, in the porosity range of about 0.4 ~ 0.9 by the expression,
(-i-~-)=10exp(-4.5e) (B.17)
354

In this range of porosity, the semi-theoretical equation proposed by Tsubaki et al.


(1984) to relate a powder tensile strength to bed porosity, pre-compression stress and
m e a n particle size as,
m
•--(¥) -.dp;
(B.18)

where P is the pre-compression force.

T o overcome the limitations of the W.S.L. tester, notably the narrow limit of the
range of porosity of the powder bed, Jimbo et al. (1984) developed modified testers in
which both sides of the split cell are mounted on ball bearings incorporating a pushing
mechanism to reduce friction in the bearings. *

The tensile tester provides values of the powder's uniaxial tensile strength, in
comparison to that predicted from the Jenike's method which gives powder behaviour
when subject to a biaxial stress state.

C.19 FLUIDIZATTON:
Fluidization is the transformation of a static bed of particles into a liquid like mass
system induced by the flow of a gas or liquid. In most fluidization systems, the
fluidizing agent is air or a gas. In essence, particulate masses m a y range in characteristics
from static beds, through fluidized beds, through, in turn, fast fluidized to dilute
suspended particulate streams as those occurring in dilute pneumatic conveying.

In regard to fluidization behaviour, powders can be classified into two groups,


namely : Free-flowing and cohesive powders. With free flowing powders, the forces of
attraction between the particles are negligible, so that the powder can flow easily under
the action of gravity, e.g.dry Silica, Sand, dry Wheat. These powders give few problems
in regard to design and operation of pneumatic conveying systems. For cohesive
powders, there is more frictional resistance to flow and in some cases this resistance is
strong enough to prevent movement. These powders exhibit significant interparticle
forces and hence these powders are troublesome, w h e n pneumatically conveyed. For
this reason, cohesion directly relates to the flowabiUty of a powder.

Thus, a free flowing powder is fluidized without any difficulty, whilst the
fluidization of cohesive powders is normally difficult and can require the modification of
either the flow properties of the powder or of the fluidization equipment. Further
classification of powders are:
1 free-flowing 6 fluidizable, high air retention
355

2 less free-flowing 7 very cohesive


3 fluidizable 8 abrasive
4 fluidizable, low air retention 9 friable
5 fluidizable, moderate air retention

The inter-particle forces that cause poor fluidization characteristics are small
particle sizes, strong electrostatic charges or the presence of moisture in the bed. Hence,
in regard to fluidization, the most important powder properties and their effects are n o w
listed.
Particle size: thefinerthe particles the stronger the interaction between the fluidizing
gas and the particles.
Flowability: the more flowable a fine powder, the more fluid-like and hence the more
readily it can be fluidized.
Hardness: controlsrateof system wear, m i n i m u m effect with respect to fluidization.
Hygroscopicity: moisture works against fluidization.
Dispersibility: the less cohesion, the more readily fluidized the powder
Compressibility: the less the compressibility of a fine powder, the more fluidizable
the powder.
Size distribution: the wider the distribution, the less definite the fluidization and
greater tendency to segregate in the bed.
Particle shape: the more spherical the particle, the easier the fluidization. Irregular
shaped particles tend to interlock and hence tend to be difficult to fluidize.
C o h e s i o n a n d particle friction: the stronger these forces, the more difficult the
fluidization.

Geldart (1973) suggested that powder particle size and density be used as a
criteria to classify various powders into four groups having different gas-fluidization
behaviour.

Group A powders are slightly cohesive and exhibit large bed expansion after
m i n i m u m fluidization and before the c o m m e n c e m e n t of bubbling. Group B powders
bubble at m i n i m u m fluidization velocity with small bed expansion. Group C powders
are cohesive and difficult to fluidize, whereas Group D powders can form stable spouted
beds if the gas is admitted through a centrally positioned hole.

Group A powders deaerate at a constant rate, Group B powders deaerate rapidly,


Group C powders deaerate faster than Group A powders but remain in an aerated state
356

for a considerable time, decaying pressure at the base of the bed very slowly. In view of
this correlation, the deaeration rate is important in characterizing powders.

B.20 SLUGGING:
Dixon (1979) proposed slugging diagram (Figure B.l) based on Geldart's
fluidization diagram to predict the behaviour of powders in dense phase systems.

\

V
K\-
v\
\
\ V\
s,\ \
\
' (?) D
*
\ <°>
NO \ ^WEAK \ STROI IG
* SLl GC IN 3 \SYM MET lie 1*> AXISY MME1 RIC
/ JLUG5 ^ SLUG!

_ *•
v',
— 5—-J
- /
w "'.
'.-
;
/>-,
•>
s
->. \
\
\

20 50
Fg JI ( 3 - 4 INCHPIPIr SL JG< !>IN G D>» G H A W

100 600
\
1000
N
M E A N PARTICLE SIZE d (pml

Figure B.l: Typical Slugging Diagram [ Dixon, (1979) ].

In Figure B.l, Group A powders are the best candidates for dense phase
conveying. They are not natural sluggers but can be made to slug by using slug forming
techniques. Group B powders give problems if high solid gas loadings are used.
Group C powders are less suitable for dense phase conveying, whereas Group D
powders are good candidates which have natural slugging behaviour.

Flatt (1980) reported a graph for selection of dense phase systems whether by
pass or pulse phase systems taking into account the particle size distribution, whereas
Klintworth et. al. (1985) revealed particle size variation against mean particle size
indicating four classification zones for selecting discontinuous phase systems.
B.21 DEAERATION:
A n important property of fine powders is their ability to retain air within the voids.
W h e n powders are filled into containers, a large volume of air is entrapped within the
voids. O n settling, this air slowly dissipates and the level of powder drops, until it comes
to a s o m e steady state level. After which time consolidation at almost constant voidage
commences.

Deaeration can be defined by noting the change in bed height with time after
aeration ceases or by noting the change in pressure differential across a unit of height of
powder with time. In regard to the observation of bed height, this apparently simple task
often proves difficult for m a n y powders, as some powders tend to coat the interior of the
testrigwith fine particles. ,

All powders that have been fluidized will deaerate over a certain period of time
during which their bulk density increases. The rate of deaeration process is important in
regard suitability for dense phase conveying. In practical filling operations, deaeration
takes place during the filling process.

The deaeration process forms the initial stage in time consolidation. Hence, to
prevent time consolidation, it is necessary to prevent the initial de-aeration. This can be
effected by passing air through an air distributor at the bottom of the bin. A t the same
time, the formation of consolidation zones within the bed can be prevented. T h e
existence of these zones causes channelling, ii the powder is allowed to consolidate and
the air is introduced before powder filling commences. The powder contains zones of
higher bulk density and w h e n air is passed, these zones will tend to separate causing the
fluid flow to channel through the less dense zones in the bed. T h e rate of diffusion
depends on the interparticle forces, size, shape and packing properties of the powder.

The quantity of air dissipated from the bed during deaeration is equivalent to the
volumetric change of the void during densification. Under most circumstances, the
voidage distribution settles d o w n rapidly to steady state level, since most of the air is
dissipated while the permeability is still large. Thereafter, the deaeration is relatively
slow. Here, the displaced fluid caused by the change in bulk density percolates slowly
through the compacted bed.

Sutton described empirically the variation depicted by,


H = Hoe-k't (B.19)
where k' is diffusion coefficient
358

F r o m these tests a value of k' was derived. Powders with k' > 100 cm/s are
unsuitable for aerated discharge, while powders which are aeratable i.e. deaerate slowly
have values of k' < 30 cm/s. This factor provides a measure of the tendency of the
particles to form agglomerates in the bed by interparticle attraction and which have a
structure different from the rest of the bed.

By use of a pressure transducer and recorder device, the time variation of column
base pressure can be observed and recorded. The relationship between the pressure drop
per unit length and time is of the form

Af = t . Ap/L , (B.20)
where A p = pressure drop per unit length L of the bed
t = time in seconds
A f = a constant defined as the deaeration factor with units of mbar.s/m

Mainwaring et al. (1987) proposed the permeability and air retention are two
important parameters in regard to feasibility of a powder in dense phase pneumatic
conveying. They developed the plot of the permeability factor, pf, versus quasi-steady
pressure drop per unit length corresponding to the fluidized condition, (Ap /L) c T h e
results for a number of powders tested by them indicate that powders exhibiting high
values of permeability factor generally convey in a plug type m o d e of dense phase
conveying, while powders exhibiting low permeability were conveyed in either a dense
phase moving bed type flow or could not be conveyed in dense phase at all.

This approach of utilizing the permeability and deaeration factors of the powder to
be conveyed ensures that the influence of the size distribution rather than a mean particle
size is used to categorize a powder for its likely conveying characteristics.
359

APPENDIX 'C

Cl CALIBRATION OE TRANSDUCER CHANNELS:

When conducting experiments on both the Sturtevant rig and low velocity rig, the
pressure transducers were calibrated before commencing each experimental run. Typical
values from the calibration are as follows, refer Table C l .

TABLE Cl: TYPICAL CALIBRATION VALUES

(A) (B)
Sturtevant Rig L o w Velocity Rig *
Channel No. Calibration Values Channel No. Calibration Values

0 0.223 0 0.510
1 0.251 1 0.287
2 0.354 2 0.204
3 0.293 3 0.117
4 0.298 4 0.48
5 0.309 5 -

6 0.293 6 -

7 0.228 7 0.486
8 0.009 8 0.009
9 7.809 9 182.0
10 95.61 10 356.1
11 0.299
12 0.330
13 0.305
14 0.311
15 0.139

C.2 CALIBRATION OF WALL FRICTION RTO LOAD CELL:

This was calibrated by loading the piston with different weights and observing the
corresponding chart recorder readings. A typical calibration plot is presented in Figure
Cl.
360

8-j — .

-35 -/.

UJ J3

o-l . , • , ,
0 100 200 300
NUMBER OF DIVISIONS - m m

Figure C. 1: Calibration Plot.

C.3 CALIBRATION OF PRESSURE GAUGE IN WALL FRICTION RIG:

To measure the air pressure in the wall friction rig, a pressure gauge No. P /
2125 - 466 of capacity 0 - 700 kPa x 254 m m . diameter was used. Before commencing
the experiments, it was calibrated by a static pressurized tank system, the results of which
are stated below, refer Table C.2.

T A B L E C.2: CALIBRATION RESULTS

Test Pressure, Gauge Reading, Calibrated Pressure,


kPa kPa kPa

60 57.2 59.9
110 106.1 109.9
160 156.4 159.9
210 206.7 209.9
260 254.9 259.8
310 305.2 309.8
360 356.9 359.7
410 405.1 409.8
510 504.4 509.6
610 604.9 609.6
660 654.6 659.5
361
C.4 CALIBRATION OF THE DEAERATION RIG PRESSURE
TRANSDUCERS:

The calibration of the pressure transducers used in the deaeration rig to record the
interstitial air pressure, was effected using the Sturtevant blow tank as a pressurization
tank. A typical calibration recording is presented in Figure C.2.

Figure C.2: Typical Calibration Graph.

C.5 POWDER CONCENTRATION:


This can be measured using a T.300 Tealgate transducer or calculated using the
data observed during each experimental run. In particular, the powder concentration can
be calculated using the equation :

C- = ^ (CD

where Vs = Volume of solids and


362
V t = Volume of solids + air = total volume = V s + V f (C.2)
V f = Volume of fluid (air)
Since, volume is related to mass M and density p,

Ms
Vs - — (C3)
KS

Mf
Vf = - 1 (c.4)
Pf
Therefore, the powder concentration,
Ms
Ps
r ( -.
s CC5J
Ms Mf
P7 P7
Simplifying eqn. (C5) gives,

1
c = (C6)
* 1—wt:
+
M p s f
where pf = air density = Patal + p f / R T
where P atm and pf are equal to the atmospheric pressure and the operating air pressure at
the point closest to the measuring instruments, respectively.
R = gas constant (for air, R=0.287 kJ/kg/K)

T = operating air temperature.

C.6 CALIBRATION OF THE T.300 SERIES TRANSDUCER:

To measure powder concentration, the T.300 series transducer was


Sturtevant pneumatic conveying testrigsystem. A typical observed calibration graph is
presented in Figure C.3. Values of the transducer output corresponding to 30%, 5 0 %
and 8 0 % concentration peaks are evaluated from the calibration graph for particular
reference. A typical concentration variation obtained by use of a Tealgate T.300
transducer is presented in Figure C 4 .

C.7 POWDER VELOCITY:


With knowledge of the particle concentration, the velocity of the conveyed
powder can be calculated as follows.
363

Since, the powder concentration is as per eqn. (Cl),

Ms
Cs (C 7)
" V^ ~ Ps V, A '
where V s = volume of powder
V t = volume of powder and air
It follows that the powder velocity can be calculated from a rearrangement of
equ. (C.7), viz.

Ms
(C.S)
V = —
s
PsACs

Figure C.3: Typical Calibration Graph.


364

ut«M tthV^^9'*npmiM%f^%pp%mptmmm9W9'Pmumm»mpmt»»M»vt>mi*im99paimtPP»»imamnmmtt3nii

iinuiHitirMMiiMtMMMii iv 4tiiiMi---WrWi«niitii<ir'wii»iiW*<'IWfiM winiiiwi


«-+
*
4-1 ___:
1 -T
1 ttt
tct *IS33
S 3"- mix
-£ ^r
nil IIS ill t
-t
ca n;cr;S -8
trip

-3-t
c-i
3? 1 at m wm
Figure C.4 : Concentration Graph.

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