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"An ounce of careful plant design is worth ten pounds of reconstruction.

"

LECTURE 12: LABORATORY AND INDUSTRIAL CATALYTIC REACTORS: SELECTION, APPLICATIONS, AND DATA ANALYSIS
I. Introduction
A. B. C. D. Why study reactors? Definition and classification of reactors Reactor/process design perspective: from the laboratory to the full-scale plant Selection of reactors in the laboratory and plant

II. III.

Laboratory and Bench Scale Reactors


A. Kinds B. Criteria for selection of lab/bench scale reactors; applications

Plant Reactors
A. B. C. D. Common types Fixed catalyst bed reactors: characteristics, advantages, limitations Fluidized beds: characteristics, advantages, limitations Criteria for selection General approach and guidelines Criteria for choosing catalyst form and pretreatment, reaction conditions Choosing mode of reactor operation; differential and integral reactors Analyzing and reporting data from laboratory reactors 1. Analysis of rate data: objectives and approach 2. Integral analysis 3. Differential analysis

IV.

Collecting, Analyzing and Reporting Data from Laboratory Reactors


A. B. C. D.

V.

Examples

New HDS Unit, ARCO Carson, CA Refinery

I.

Introduction

A. Why study reactors?


1. The design of catalyst and reactor
are closely interrelated. 2. Design of catalytic processes requires a knowledge reactor design, operation optimization and selection 3. Progress in improving our standard of living depends on our ability to design reactors 4. Our personal existence depends on controlling cellular reactions in our body while that of the human race hangs on the outcome of enormous global reactions.

B. Definition and Classification of Reactors


1. What is a Reactor?
a. A device that encloses the reaction space, and which houses the
catalyst and reacting media.

b. A container to which reactants are fed and products removed, that provides for the control of reaction conditions.

2. Classification of Reactors
a. b. c. d.
Size Methods of charging/discharging: batch or steady-state flow Motion of particles with respect to each other Fluid flow type: tubular or mixed-fluid

Table 12.1 Classification of Catalytic Reactors


Basis for Classification Size Classes Laboratory Bench scale Pilot scale Plant scale Batch Flow, steady state Examples 0.5 cm diam. tubular microreactor (0.1-1 g catalyst) 2.5 cm diam. x 30-50 cm long tubular reactor (50-200 g catalyst) 7.5 cm diam x 6-10 m long tubular reactor (20-100 kg catalyst) 1-6 m diam x 20-50 m long tubular reactor (20-100 metric tons cat.) Stirred liquid and solids a. tubular, fixed catalyst bed b. slurry, mixed fluid, mixed solids Tubular fixed solids (fixed bed) a. fluidized bed b. slurry bubble column Turbulent gas in tubular fixed bed Slurry reactor with mechanical stirring

Methods of charging and discharging

Motion of catalyst particles relative to each other Fluid flow

Fixed Relative motion

Tubular, plug flow Mixed fluid flow

Hardware and Software

Scientific & Engineering Tasks


Discover Reaction

Scientific & Engineering Disciplines

C. Reactor/process design perspective

Laboratory Reactor
Intrinsic Kinetics

Chemical Kinetics
Catalyst P rop. and Catalys is Diff., Mass Trans

Kinetic Model Development Reaction Engineering & Mathematics Reactor Model Development

Rate/Selectivity & Rate Equation

Reactor Model

Reactor /Proces s Des ign Catalytic Reactor Design

Fig. 12.1

Structure of Catalytic Process Development [adapted from J. M. Smith, Chem. Eng. Prog., 64, 78 (1968)].
Pilot Plant Reactor

Proces s Design Economic s Finl. Plant Des ign & Economic Studies

Large Scale Plant

D. Choosing reactors in the lab and plant


Reactors are used for many different purposes:
1. to study the mechanisms and kinetics of chemical reactions to
provide data for validation of process simulations 2. to investigate process performance over a range of process variables 3. to obtain design data 4. to produce energy, materials and products.

Choosing the right reactor is critical to the engineering process and is dictated by many different variables such as

reaction type rate of deactivation economics other process requirements

II. Common Lab and Bench Scale Reactors

1. 2. 3. 4. 5.

fixed bed tubular

stirred gas, fixed bed stirred liquid/gas, stirred catalyst fluid bed fixed bed, transient gas flow

Laboratory and bench-scale reactors vary greatly in size, complexity, cost, and application.

Table 12.2 Laboratory and Bench-Scale Catalytic Reactors


Classes
Fixed bed tubular

Class Examples
Laboratory differential/integral Bench-scale integral Stirred batch Batch recycle Berty Carberry

Features
0.5 cm diam tubular microreactor (0.1-1 g catalyst, solid catalyst, gas fluid; glass or metal 2.5 cm diam. x 30-50 cm long tubular reactor (50-200 g catalyst); solid catalyst, gas or liquid fluid; metal microreactor, 1 g catalyst, glass or met. microreactor, 1 g catalyst, glass or met. bench-scale, 2-200 g cat., 10-100 atm, stainless steel, circulating gas bench-scale, 2-200 g cat., 10-100 atm, stainless steel, spinning catalyst basket

Stirred gas, fixed bed

Stirred liquid/gas, stirred catalyst


Fluid bed

Stirred batch Bubble slurry


Laboratory Bench-scale transport Recirculating transport Pulse flow TPD/TPSR Radio tracer exchange MS/Transient response Frequency response

bench-scale, 2-50 g cat., 1-200 atm, glass or metal heterogeneous or homogeneous catalyst
microreactor, 1-5 g cat, 1 atm, glass bench-scale, 50200 g catal, 1-10 atm, metal

Fixed bed, transient gas flow

microreactor, 0.1-1 g catalyst, glass or metal, 1 atm

Fig. 12.2

Features of representative laboratory reactors [Levenspiel, 1979].

10/30 female joint

10/30 male joint

9 mm O-ring joint

4 ft. preheater coil of 2 mm capillary tubing Thermocouple guide of 2mm capillary tubing

7"

Figure 12.3
Catalyst space

Laboratory Pyrex FBR reactor (courtesy of the BYU Catalysis Laboratory).

Fritted disc

Figure 12.4 Berty internal recycle reactor.

Gas-Liquid CSTR (UCSB)

Batch Reactor (UCSB)

Bench scale reactor


(courtesy of Shell Corp.)

II. Laboratory and Bench Scale Reactors


B. Criteria for selection of lab and bench-scale reactors;
applications
1. 2. 3. 4. 5. 6.
Satisfying intended application Avoiding deactivation Avoiding inter- and intra- particle heat and mass transport limitations Minimizing temperature and concentration gradients Maintaining ideal flow patterns Maximizing the accuracy of concentration and temperature measurements 7. Minimizing construction and operating costs

Table 12.3 Seven Criteria for Selection of Laboratory and Bench-Scale


Catalytic Reactors
Criterion 1. Satisfy purpose of measurement (i.e., application) Issues Involved/Measures of/Methods to Meet Criterion Measure: (1) intrinsic activity/selectivity, (2) kinetics of reaction and deactivation Obtain mechanistic understanding Simulate process See Chap. 5 (B&F) on avoiding different kinds of catalyst deactivation Fast decay causes activity and selectivity disguises and requires use of transient or transport reactor Slow decay best studied using CSTR or differential reactor Thiele modulus less than 0.5; small particles or thin catalyst layer Minimize film thickness with high flow rates, turbulence Operate at low conversions Use CSTR or differential reactor Gradients cause activity and selectivity disguises Maximize mixing in batch reactor and CSTR; use inerts Use CSTR or differential reactor where possible

2. Avoid catalyst deactivation where possible; where not, decide if fast or slow 3. Avoid inter- and intra-particle heat and mass transport limitations

4. Minimize temperature and concentration gradients

5. Maintain ideal flow patterns

Minimize mixing and laminar flow in tubular reactors; Maximize mixing and minimize gradients in CSTR Avoid gas or liquid holdup in multi-phase reaction systems
Sensitive analytical methods and well-placed, sensitive probes Sufficiently high product concentrations Select the least expensive reactor that will satisfy the other criteria Consider ways of minimizing size of catalyst and volume of reactant gas

6. Maximize accuracy of concentration and temperature measurements 7. Minimize construction and operating costs

Table 12.4 Applications of Lab/Bench Test Reactors


Reactor Type Catalyst Selection Activity/Selectivity Reactor/Design Life Kinetics Fundamental Mechanism Process Simulation

Integral
Adiabatic Isothermal Differential Single Pass Recycle Stirred gas Fluid bed/ Transport Micro-pulse Transient X (intrinsic) X (intrinsic) X (intrinsic) X (fast deact.) X (comparative, initial) X (elem. steps) X (kinetics) X (fast deact.) X (intrinsic) X (intrinsic) X (intrinsic) X (fast deact.) X X X (model) X (eliminate) X (eliminate) X (eliminate) X (model) X X (overall avg. conv.) X (overall conv. at T) X X X X

Common Types of Catalytic Plant Reactors


1. Fixed-bed Reactors
a. b. c. d.
Packed beds of pellet or monoliths Multi-tubular reactors with cooling Slow-moving pellet beds Three-phase trickle bed reactors

2. Fluid-bed and Slurry Reactors


a. Stationary gas-phase b. Gas-phase c. Liquid-phase
i. Slurry ii. Bubble Column iii. Ebulating bed

Table 12.5 Characteristics of Plant-Scale Fixed Bed Reactors


Advantages 1. Ideal plug (or mixed) flow 2. Simple analysis 3. Low cost, low maintenance 4. Little loss or attrition 5. Greater variation in operating conditions and contact times is possible 6. Usually a high ratio of catalyst to reactants long residence time complete reaction 7 Little wear on catalyst and equipment 8. Only practical, economical reactor at very high pressures Disadvantages 1. Poor heat transfer in a large fixed bed. a. Temp. control and measurement difficult b. Thermal catalyst degradation c. Non uniform rates. 2. Non uniform flow patterns e.g. channeling 3. Swelling of the catalyst; deformation of the reactor 4. Regeneration or replacement of the catalyst is difficult - shut down is required. 5. Plugging, high pressure drop for small beads or pellets - P is very expensive. 6. Pore diffusional problems intrude in large pellets

Overcoming the Disadvantages 1. Monolithic supports overcome disadvantages 2, 5 & 6 2. Temperature control problems are overcome with: a. Recycle b. Internal and external heat exchanges c. Staged reactors d. Cold shot cooling e. Multiple tray reactor - fluid redistributed & cooled between stages. Catalyst is easily removed - varied from tray to tray. f. Use of diluents g. Temperature self regulation with competing reactions, one endo and one exothermic. h. Temp control by selectivity and temporarily poisoning the catalyst

B. Fixed-bed reactors: characteristics, advantages, limitations


Advantages:
Flexible- large variation in operating conditions and contact times
is possible Efficient- long residence time enables a near complete reaction Generally low-cost, low-maintenance reactors

Disadvantages:
Poor heat transfer with attendant poor temperature control Difficulty in regenerating or replacing spent catalyst

a..

Reactants Inlet

Feed

Liquid Or Gaseous Bath

Inert balls Catalyst


Gas Or Liquid Flow

Reactor Tube

Reactor Tube

Outlet Product

Product

Figure 12.5 Commercial


fixed-bed, adiabatic catalytic reactor.

Fig. 12.6 Commercial fixed-bed reactor designs for controlling


temperature: (a) multi-tubular heat-exchange reactor, (b) series of fixed-bed, adiabatic reactors with interstage heating or cooling.

Table 12.6 Characteristics of Plant-Scale Fluidized and Slurry Bed Reactors


Advantages
1. Frequent regeneration of the catalyst possible. 2. Rapid mixing of solids in fluid beds means uniform gas composition. 3. Isothermal operation and efficient temperature control is practical. 4. Small-diameter particles in fluid minimize pore diffusional resistance. 5. Improved thermal efficiency because of high heat transfer rates. 6. In the case of highly exothermic, liquid phase reactions, slurry reactors are less complex and less expensive than heatexchange-tubular systems.

Disadvantages
1. Fluidized beds are complicated systems involving multiple reactors, heat exchangers, extensive valving and piping to provide continuous system. 2. $$ Extensive investment. Maintenance is high.

3. Fluid flow is complex in fluidized and slurry bubble columns - less than ideal contacting. Product distribution is changed - less intermediate formed in a series reaction.
4. Only a small variation in residence time possible. Low residence times. Conversion may be limited. 5. Attrition & loss of Catalyst.

Figure 12.7 Liquid-phase slurry reactors: (a) forced-circulation,


slurry-bed reactor, (b) bubble-column, slurry-bed reactor.

Figure 12.8 Batch-slurry reactor for hydrogenation


of specialty chemicals.

Fig. 12.9 Design of typical FCC transfer-line (riser)


reactor with fluidized-bed regenerator.

a. Cyclone Flue gas Regenerator Overflow well

Products Riser reactor Catalyst stripper Steam

b. Flue gas

Products Cyclone Reactor Catalyst stripper Steam

Regenerator Reactor feed Air Steam Reactor feed

Air

Figure 12.10 Commercial FCC riser reaction designs (a) Exxon, (b) UOP.

Fluid Cat Cracker (Chevron)

Stacked Fluid Cat Cracker (UOP)

Shell Cat-Cracker

All-riser Cracking FCC Unit

Criteria for Selection of Plant Reactors


1. General Criteria.
a. deactivation rate and regeneration policy b. reaction conditions c. catalyst strength and attrition resistance d. process economics

2. Role of Cp/(-DHr)

Fig. 12.11 (a) Operating line for a


highly exothermic reaction in an ideal tubular reactor with pure reactant and (b) corresponding reciprocal rate versus conversion curve and area V/FAo for a CSTR. (c) Operating line for a highly exothermic reaction in an ideal tubular reactor with dilute reactant and (d) corresponding reciprocal rate versus conversion curve and area V/FAo for a PFR.

3. Optimal Temperature Progression

Figure 12.12 Optimum temperature progression (and locus of


maximum rates) of (a) reversible endothermic reaction and (b) reversible exothermic reactions.

Fig. 12.13 (a) Use of staged adiabatic tubular fixed-bed reactors with interstage cooling to achieve optimum
temperature progression in the cases of exothermic reversible, exothermic irreversible and endothermic reactions. (b) Design schematic for staged adiabatic fixed-bed reactors with interstage furnace heating for a strongly endothermic reaction such as reforming of methane.

Collecting, Analyzing and Reporting Data from Laboratory Reactors


Different purposes:
1. activity/selectivity and life data for catalyst selection 2. chemical reaction mechanistic and kinetic data for understanding the
reaction at a fundamental level, modeling the reaction process, and/or designing reactors

3. process variable data over a wide range of conditions for purposes of


designing large-scale reactors, experimentally validating models and optimizing the catalytic process.

Data collection typically involves three major steps (Fig. 12.14):


1. selection of a reaction and catalyst 2. selection of a reactor type 3. analysis of the data

new experiments Select Reaction and Catalyst Select reactor and conditions Batch Flow CSTR Plug - integral or differential Data Analysis Data Integral Differential Initial Rates mechanism rate expression process optimization

Criteria

Figure 12.14 Process of obtaining rate and kinetic data; note that
statistical methods are used in Steps 2 and 3 and in the recycle process.

Table 12.7 Proposed Guidelines for Choosing Catalyst Form, Pretreatment, and
Reaction Conditions and for Reporting of Data [Ribiero et al., 1996].

1. Catalyst Properties and Characterization


a. Catalysts/surfaces should be carefully prepared and pretreated so as to be free of solid contaminants such as sulfur, chlorides, and carbon that might affect activity. b. Support effects should be avoided by studying reactions on single crystals of the active catalytic phase, e.g., metal, metal films, and/or relatively highlyconcentrated, poorly-dispersed supported metals. Preparation methods should be used which minimize decoration of the metal surface, e.g., decomposition of metal carbonyls on supports. Supported base metal catalysts need to be wellreduced to avoid complications due to unreduced metal oxides. c. In the case of structure-sensitive reactions, effects of surface structure and/or dispersion need to be taken into account. d. Metal dispersion/surface area should be measured using proven and/or standard (ASTM) methods, e.g., hydrogen chemisorption or titration rather than CO chemisorption for metals. e. Methods of preparation and characterization should be reported in detail. Methods for calculating surface area and dispersion should also be carefully reported. Reporting these methods and the surface area or dispersion of catalyst samples should be a requirement for publication of specific activity data.

Table 12.7 Continued


2. Reaction Conditions
a. TOF and kinetic data must be measured in the absence of pore diffusional restrictions, film mass transfer limitations, and heat transfer limitations (generally at low temperature and low conversion). Experimental evidence and calculations based on well-known criteria (e.g., the Thiele modulus for pore diffusional resistance) should be provided in publications to demonstrate that the data were obtained in the absence of these effects. b. TOF and kinetic data must be measured in the absence of deactivation effects, e.g., poisoning, coking, and sintering. The burden of proof that such effects are absent should be on the authors of a publication. c. TOF data should be collected over wide ranges of temperature and reactant concentrations to facilitate valid comparison with data from other laboratories and to provide meaningful data for determining temperature and concentration dependencies. d. TOF data should be reported at specified conditions of temperature, reactant concentrations, and conversion. These specifications should be used by reviewers and editors as a minimum reporting requirement for publication in a journal.

Analyzing and reporting data from laboratory reactors


1. Analysis of rate data: objectives
a. finding a rate equation b. determining catalyst activity, selectivity and activity stability c. determining the effects of important process variables such as
temperature, pressure, reactant concentrations, and space velocity on activity, selectivity and stability

2. Extracting rate constants and concentration dependencies


a. Integral analysis b. Differential analysis

Figure 12.15
Test for integral analysis of rate data involving plot of W/FAo versus integrated reciprocal rate.

W F x

x x

Integral Analysis of Rate Data


Integral analysis of rate data involves the following steps:

x dx o (-rA)

1. A series of runs are made in a packed bed at a fixed initial concentration CAo and a fixed temperature while varying the catalyst mass W and/or the initial molar flow rate FAo to generate a range of W/FAo values at different conversions (XA). 2. A candidate rate equation is selected for testing using the design equation for plug flow. First try simpler rate equations, e.g. zero-, first- and second-order irreversible and use differential analysis to scope out possible reaction orders. 3. The left-hand side (W/FAo) and right-hand side (the integral of 1/rA) of the design equation are each evaluated numerically and plotted against each other, as shown in Figure 4.19 to test for linearity. 4. Linearity of the plot (e.g. Figure 12.15) is used as the criterion for judging if the candidate rate equation is a useful model of the data, i.e. consistent with the data. 5. This should be followed by a nonlinear regression with statistical analysis to determine kinetic parameters.

1.0
Fig. 12.16
(a) Differential analysis to obtain reaction rates. (b) Plot to obtain reaction orders.

slope = -rA' X X X X

b X X X ln (-rA) X X

slope = X X

XA 0.5 X X 0

Differential Analysis of Rate Data

W/FA0

ln CA

Differential analysis of rate data involves the following steps: 1. The identical series of runs (as in integral analysis) are made in a packed bed at a fixed initial concentration CAo and fixed temperature while varying the catalyst mass W and/or the initial molar flow rate FAo to generate a range of W/FAo values at different conversions (XA). 2. A plot of conversion XA versus W/FAo data is made for each set of runs at a fixed temperature. A best fit of the data is made using a simple quadratic or cubic equation, and the corresponding curve is plotted on the same figure, as illustrated in Figure 4.20(a). 3. Tangents to the curve are drawn at regular intervals along the curve corresponding to the best fit, and the slopes of these tangents are evaluated (Figure 12.16a); the slopes on this plot correspond to the reaction rate, i.e. dXA = (rA)[d(W/F)]. Tangents can be evaluated more accurately by differentiating the equation for the best fit of the data and evaluating the derivative at various intervals over the data set. 4. Values of rA versus XA are plotted on linear or log-log plots to determine reaction orders. For example, for an irreversible reaction in which data are fitted by a simple power rate law, rA = k CA , a plot of ln(rA) versus ln(CA) is linear with a slope (Figure 12.16b). 5. Differential analysis is a useful scoping tool to explore forms of the rate expression; however, in the end a nonlinear regression and rigorous statistical analysis is required to obtain kinetic parameters with acceptable accuracy.

References
1. O. Levenspiel, Chemical Reaction Engineering, 2nd and 3rd Eds., John Wiley and Sons, 1972, 1999. 2. O. Levenspiel, The Chemical Reactor Minibook, OSU Bookstores, 1979. 3. J.M. Smith, Chemical Engineering Kinetics, 3rd Ed., McGraw Hill, 1981. 4. "Reactor Technology," Kirk-Othmer: Encyclopedia of Chemical Technology, Vol. 19, 3rd Ed, John Wiley, 1982, pp. 880-914. 5. G.F. Froment and K.B. Bischoff, Chemical Reactor Analysis and Design, John Wiley, 1990. 6. O. Levenspiel, The Chemical Reactor Omnibook, 1993, OSU Bookstores, 1993. 7. C. H. Bartholomew and R. J. Farrauto, Fundamentals of Industrial Catalytic Processes, Chapman and Hall, 2005, Chap. 4.