Professional Documents
Culture Documents
vii
Editorial Board
Editors
Bryan Ellis
Formerly Sheffield University, UK
Dr. Ray Smith
University of London, UK
Advisory Editor
Dr. Howard Barth
Formerly DuPont, US
Executive Editors
Dr. Fiona Macdonald
CRC Press, Boca Raton, US
Dr. Matt Griffiths
CRC Press, London, UK
Contributing Editors
Dr. Paul Tindal
Dr. Martin Edwards
Dr. Philip Drachman
Additional data collected by contributors to the CRC Chemical Database.
ix
Introduction
Those of us who work with polymers and polymeric materials rely heavily on data regarding solution and bulk
properties, and manufacturing procedures. These parameters usually can be found spread over different
handbooks, encyclopedias, and the Internet. However, Polymers: A Property Database is one-stop shopping,
whereby this information is now available from a single source. Entries range from a few lines for research
polymers to encyclopedic submissions for more common polymers. (An online version of the Database for
simplified data retrieval and entry updates is now available from Taylor & Francis Group.)
To produce this comprehensive Database, which conveniently can be used as a desk reference book, a double-
column format was used with small, but easy to read font with spaced-out tables. Because main-chain or common
polymer names are used as headers, arranged alphabetically in dictionary style, the Database is practical to use.
(IUPAC approved nomenclature is given under a separate heading). To quickly locate a polymer, a comprehensive
polymer name index is available.
The Database contains a listing of polymer properties that are, for the most part, associated with polymer
manufacturing, processing, and applications. As such, the Database contains other useful information in addition
to polymer properties, not found in other source books; an example of this is given for nylon 6,6, a well-studied
commercial polymer:
The Database also lists many types of polysaccharides, modified cellulosics, and other important biopolymers.
Different types of polymers and polymeric structures are presented, such as inorganic polymers, blends, block
copolymers, graft polymers, ionomers, elastomers, fibers, hydrogels, interpenetrating networks, structural foams,
polymer composites, polysiloxanes, resins, and natural rubbers.
For this second edition, an introductory chapter has been added that reviews polymer complexity as it relates
to polymer properties. Furthermore, tabulated lists of polymer properties are given to serve as a guide in selecting
appropriate test procedures.
xi
Polymer property data are now available on the Internet in a variety of tabular forms. The advantages and
convenience of having a desk reference book of the magnitude of Database cannot be overstated. No other
reference handbooks contain the caveats, descriptions, and explanations that are found in Polymers: A Property
Database as exemplified in the above table.
B. POLYMER COMPLEXITY
Because of polymer complexity, property variability must be taken into consideration. In this section, we will
discuss possible sources of polymer inconsistency and offer suggestions to recognize and reduce these errors.
Chemical or compositional heterogeneity refers to the chemical or structural difference among chains of the
same polymer. Thus, a measured property of a chemically heterogeneous sample will be an averaged value
dependent upon sample source. For chemically homogeneous samples, property variability will not be a concern.
In a similar fashion, polymers that are polydisperse in molecular weight have averaged property values, while
monodisperse samples will give accurate data. Obviously, samples that are both chemically homogeneous and
monodisperse will give the most accurate and precise values.
Compared to synthetic polymers, almost all nucleic acids and mammalian proteins are compositionally
(chemically) homogeneous and monodisperse. If not, there would be no life; biopolymers carry highly specific and
selective information. Mammalian polysaccharides, for the most part, are also compositionally homogeneous, but
are polydisperse in molecular weight; whereas plant polysaccharides are polydisperse. Chemically modified
cellulose (cellulosics) are typically both compositionally heterogeneous and polydisperse in molecular weight.
Starches (a-amylose and amylopectin), another major class of polysaccharides, are highly polydisperse in
molecular weight, but quite compositionally homogeneous. In addition, amylopectin and many other
polysaccharides are highly branched, which may further complicate listed property values.
Synthetic polymers can be quite complex and, as such, tabulated and measured property data must be interpreted
with care. Homogeneous synthetic polymers are those produced from condensation polymerization reactions, in
which all polymer chains are chemically indistinguishable from another. Even though these types of polymers show a
finite polydispersity of two, accuracy and precision will not be compromised because all samples (and reference
standards) will have the same degree of polydispersity. Lastly, synthetic polymers produced by addition
polymerization (i.e., ionic, complex coordination catalytic or free-radical copolymerization) will have the greatest
amount of compositional heterogeneity and, with the exception of anionically polymerized samples, will also have a
large molecular weight polydispersity. For these polymers, tabulated data must be interpreted with caution, unless
users establish their own data sets with reference polymers obtained from the same polymerization conditions.
Sequence distribution or polymer microstructure is the next higher level of complexity in which the average
arrangement of monomers along a chain is considered. The polymerization mechanism and reactivity ratios of
xii
monomers dictate this parameter. Monomers can be randomly arranged along chains in the case of statistic or
random copolymers or, in the extreme form, as block copolymers. In any event, the microstructure of reference
polymers should be defined when properties are listed.
Next in line of complexity is macromolecular architecture, or polymer configuration, in which the topological
nature of the chain is of interest. Thus polymer branching can take on a wide range of configurations including
short- and long-chain branching, and comb, star, and dendritic structures with or without comonomer
segregation or blockiness. Because of the strong influence of polymer configuration on properties, this parameter
needs to be defined and care taken when comparing tabulated data to those of actual samples.
In summary, polymers may have up to two or more distributed characteristics depending on the number of
different monomers used in the polymerization, the type of polymerization mechanism, and whether or not the
sample was fractionated during isolation. As a rough estimate, polymer ‘‘complexity’’ increases exponentially
with the number of distributive properties, making it more difficult to measure accurate polymer properties.
Some polymers are modified after polymerization; however, this process can be somewhat difficult to control
because polymer chain segments can influence the chemistry of a neighboring groups. Chemical modifications are
done mainly on cellulosics and other polysaccharides to tailor-make specific property characteristics. Thus
tabulated property data given for cellulosics and polysaccharides represent average values of the entire sample
ensemble of polymer chains that differ in composition. To complicate matters further, insoluble gels, comprised of
three-dimensional networks, may form if chains are allowed to chemically or physically (via hydrogen bonding)
react with one another, either during or after polymerization.
Post-polymerization processes are also accomplished via vulcanization, irradiation, or through the addition of
a low molecular weight cross-linking agent. The resulting polymer (i.e., rubber, elastomer, resin, or gel) in
essence, is one super or giant molecule approaching infinite molecular weight. These viscoelastic materials have
wonderful consumer, industrial, and aerospace end-use applications when properly formulated.
The next level of polymer complexity is polymer blends and multicomponent systems. To adjust the glass-
transition temperature, plasticizers are added, often times at high concentrations. To increase polymer strength,
reinforced polymeric materials are used that consist of added inorganic material, the most common being carbon
black or glass fibers. Laminated structures are also produced for increased material strength.
High-value added, specialty products with controlled molecular weight, branching, or architecture are being
developed for high-technology industries, most notably electronic and optical devices, printing inks, and coatings
in the aerospace industry. Because of their specialized uses, most of these polymeric materials are not listed in this
compilation.
C. REGULATORY AGENCIES
Most industries issue testing protocols and polymer property specifications to the trade. To ensure uniformity,
national regulatory agencies have formed to deal with standardized methods and testing approaches. In the
United States, ASTM is the most prominent independent agency supported by industry with about 100 test
methods in place specifically for polymers and polymeric materials. API specializes in the development of
procedures for petroleum products, some of which are polymeric. In Britain, BSI is the key agency for testing,
while in Europe, DIN procedures are followed. Many of these agencies are overseen by ISO, a federation of
national regulatory bodies. (See Table 1 for complete names and acronyms.)
Governmental departments of commerce, defense, and military are also involved in issuing protocols and
specifications. For example, the FDA is responsible for establishing acceptable limits of extractable components
from polymeric materials in contact with food and drugs.
Table 1. Key agencies involved in standardized testing of polymersand polymeric materials under the umbrella of ISO
Abbreviation Organization
xiii
D. REFERENCE POLYMERS AND SPECIALTY MATERIALS
Sources of reference polymer standards that can be used for instrument calibration and validating methods are
listed in Table 2. In the United States NIST is responsible for distributing a number of well-characterized
polymer standards.
These standards have well-defined chemical composition and molecular weight, and are also suitable for
formulating materials for R&D. All reference standards and polymeric material should come with certificates of
analysis. (Because water content in polymers, especially hydrophilic ones and polysaccharides, may affect
properties, it is advisable to vacuum dry and properly store them to prevent moisture buildup and degradation.)
Table 2. Sources of polymer standards used for instrument calibration, method development and verification, and formulating
R&D samples
E. POLYMER PROPERTIES
In this section we discuss and list polymer properties that are included in data tables of this book. Some properties
reviewed in this section are not listed in this text, but they are included for completeness. Specific properties for
certain classes of polymers are not given, especially those used for optical, electronic and magnetic devices.
Much of this section and the book’s content is based on van Krevelen’s (1976) property schemes, with
modification. His book should be consulted for more detailed discussions. Other books of interest are listed at
the end of this chapter.
Basic information that characterizes polymers is listed in Table 3. These properties can be estimated from the
expected outcome of the polymerization, measured, or calculated from group contributions (see van Krevelen,
xiv
1976). Methods for measuring these properties can be found in the reference list (for example, see Barth and
Mays 1991; Brady 2003; Wu 1995). Some of the more important properties will be considered here.
The most useful average molecular weights are the number- (Mn), weight- (Mw), and z-averages (Mz). These
averages are easily determined from the molecular weight distribution obtained using size exclusion
chromatography (Mori and Barth 2001). Oftentimes just the viscosity-average molecular weight (Mv) is
available, which can be conveniently determined from the measured intrinsic viscosity of the polymer in a given
solvent at a specified temperature using tabulated MarkHouwink coefficients. Alternatively, Mw can be
determined from light scattering and Mn from osmometry.
Branching, molecular topology, and comonomer sequence distribution along the chain are more difficult to
estimate; these properties are best estimated by the chemistry of the polymerization procedure, with support from
NMR measurements. Polymer toxicity and stability must be known or at least estimated from functional group
and comonomer chemistry. It should be realized that polymer toxicity, to a first approximation, is lower than the
corresponding comonomer toxicity; because of the low polymer diffusion coefficient, macromolecules cannot
readily pass through biomembranes, thus have limited bioavailability.
The effect of molecular weight of a polymer in solution on its colligative properties, summarized in Table 4, is
a well-established phenomenon. These properties are dependent on the number of macromolecules in solution,
which independent on molecular weight and chemical composition. In fact, the number-average molecular weight
of a polymer can be determined by measuring one of its colligative properties.
Table 5 lists volumetric properties of polymers in the liquid or solid state as a function of temperature; these
properties are related to the compactness of chains and the interaction of comonomers within and among
neighboring chains. These properties are more dependent on chemical composition, than molecular weight.
Volumetric properties also depend on factors influenced by comonomer sequence distribution, such as tacticity,
branching, and polymer crystallinity.
Table 6 lists thermodynamic and calorimetric attributes of a polymer, while Table 7 deals with polymer
solubility and cohesive energy. Except for molar entropy, all these properties depend mainly of chemical
composition, rather than molecular weight. Furthermore, polymer crystallinity, in addition to the chemical
nature of a polymer, plays a major role in dictating solubility behavior. In order to effect solubility in the case of
crystalline or semicrystalline polymers, the solution must be heated near or above its melting point to break up
crystalline regions.
Light scattering and inherent viscosity measurements made at infinite dilution are used to determine polymer
size parameters, conformation, second virial coefficient, weight-average molecular weight, and long-chain
branching parameters (Table 8). These are fundamental parameters that allow us to probe structural features of
polymer molecules. These properties are dependent on molecular mass and shape, rather than polymer
composition.
xv
Table 6. Calorimetric and thermodynamic properties including transitiontemperatures
Molar entropy
Molar enthalpy
Molar heat capacity
Latent heat of crystallization
Thermal conductivity
Melting temperature, Tm Disappearance of polymeric crystalline phase
Glass-transition temperature, Tg Onset of extensive macromolecular motion
Secondary transition temperatures Other than Tm and Tg
Deflection temperature (heat distortion) Highest continuous temperature material will withstand
Vicat softening point Temperature at which a needle penetrates material
Brittleness temperature
Cohesive energy
Cohesive energy density Related to the ‘‘internal pressure’’ of a polymer in solution
Surface and interfacial energy
Solubility parameter Equal to the square root of the cohesive energy density
Good Solvency Good solvent imparts solubility via polymer solvation
Nonsolvency Poor solvent cannot solvate polymer
Theta temperature The temperature at which polymerpolymer, polymersolvent, and solventsolvent interactions are equal
Theta solvent A solvent in which polymerpolymer, polymersolvent, and solventsolvent interactions are equal
Intrinsic viscosity Measured quantity related to the hydrodynamic shape and molecular
volume of a polymer in solution
MarkHouwink coefficients Coefficients related to the shape of macromolecules in solution.
Molecular conformation Molecular shape parameter
Specific refractive index Parameter needed for calculating Mw from light scattering data
Polymer-solvent 2nd virial coefficient Determined from light scattering measurements
Radius of gyration Macromolecular size parameter
End-to-end distance Macromolecular size parameter
Hydrodynamic volume Macromolecular volume parameter
Melt index and viscosity are critical parameters needed for polymer processing. These and other polymer
transport properties are listed in Table 9. As in the case of other viscosity measurements, these properties depend
mainly on higher statistical molecular weight averages, such as Mw and Mz.
Tables 10 to 13 list polymer characteristics directly involved with end-use properties: mechanical properties
(Table 10), electric and magnetic properties (Table 11), optical properties (Table 12), and polymer stability (Table
13). (A more complete discussion of these properties is given in selected references at the end of this chapter.)
xvi
Table 10. Mechanical properties
Adhesion (tackiness)
Ball indentation hardness
Bulk modulus (reciprocal of compressibility)
Coefficient of friction
Compression strength Force needed to rupture material
Tensile creep Shape change of material caused by suspended weight
Damping Absorption or dissipation of vibrations
Dynamic mechanical behavior
Elastic modulus
Elongation
Fatigue Number of cycles required for fracture
Flexural stiffness
Flexural strength at break Amount of stress needed to break material
Fracture mechanical properties Fracture energy, fatigue resistance, fatigue crack growth, void coalescence
Friction abrasion and resistance
Hardness Resistance to compression, indentation, and scratch
Impact strength Energy absorbed by sample prior to fracture
Indention hardness
Load deformation
Mar resistance
Mold shrinkage
Poisson’s ratio
Scratch resistance
Shear strength Maximum load to produce a fracture by shearing
Surface abrasion resistance
Tear resistance
Tensile strength break (yield) See Young’s modulus
Toughness Amount of energy to break a material (area under stress-strain curve)
Ultimate strength
Viscoelastic behavior
Young’s modulus
(Tensile strength) Modulus of elasticity or tensile modulus
Arc resistance Time needed for current to make material surface conductive because of carbonization
Dielectric constant Ability of material to store electric energy for capacitor application
Dielectric permittivity
Dielectric strength Voltage required to break down or arc material
Dissipation power factor (loss tangent) Watts (power) lost in material used as insulator
Insulation resistance
Magnetic susceptibility
Resistivity
Volume resistivity
Color Physiological response; measured using three parameters: lightness, chroma, and delta
Luminous transmittance Measure of plastic haze or clarity
Molar refraction
Percent transmission Transparency
Refractive index
Specular gloss Surface ‘‘flatness’’; mirror ‘‘finish’’
Total internal reflectance
UV-visible absorbance spectrum
xvii
Table 13. Polymer stability
CONCLUSIONS
Polymer science can be viewed as an applied branch of chemistry based on deliverable properties. It is of interest
to note that most of these properties depend on just four attributes: (1) polymer molecular weight, (2)
crystallinity, (3) chemical composition, and (4) macromolecular topology or architecture; furthermore, these
parameters interact with one another in a complex manner. By varying these parameters, polymers can be tailor-
made to fit a list of desirable characteristics.
It is hoped that this polymer property database will serve as a guideline to help pave the way for the
development of newer materials of improved characteristics.
General Description
Volumetric and Calorimetric Properties
Surface Properties and Solubility
Transport Properties
Mechanical Properties
Electrical Properties
Optical Properties
Polymer Stability
Applications and Commercial Products
References
Upon entering the database you will be presented with the polymer search screen illustrated below (Figure 1).
It is from here that searches will be performed.
xviii
Figure 1
From the search window, design your search profile using text, numerical fields or a combination of both.
Once your search has been performed the resultant hits are listed alphabetically by polymer name in the hit
list window. Clicking on any one of the hits in the hit list window will result in that entry being displayed
(Figure 2).
xix
Figure 2
In addition, the online version also contains a searchable monomers database. Monomers may be searched by
a combination of text and structure searching via a downloadable browser plug-in (Figure 3).
xx
Figure 3
xxi
SELECTED REFERENCES
Billmeyer, F. W., Textbook of Polymer Science, 3rd ed., Interscience Publishers, 1984 (classic book with excellent
treatment of polymer properties).
Barth, H. G. and Mays, J. W., Eds., Modern Methods of Polymer Characterization, New York: Wiley, 1991
(covers latest developments at the time of most methods).
Brady, Jr., R. F., Ed., Comprehensive Desk Reference of Polymer Characterization and Analysis, American
Chemical Society-Oxford, 2003 (survey of characterization and analytical methods).
Brandrup, J., Immergut, E. H.,Grulke, E. A., Abe, A, and Bloch, D. R., Eds., Polymer Handbook, 4th ed., New
York: John Wiley & Sons, 2005 (premier handbook of polymer science, listing virtually all polymer characteristics
for most polymers).
Brydson, J. A., Plastics Materials, Butterworth Heinemann, 2000 (comprehensive treatment of plastics, their
synthesis, properties, and applications).
Bueche, F., Physical Properties of Polymers, Krieger Publishing, 1979 (emphasis is on polymer physics).
Cowie, J.M.G. and Arrighi, V., Polymers: Chemistry and Physics of Modern Materials, 3rd ed., CRC Press, 2008
(excellent discussion of physical properties and applications).
Heimenz, P.C. and Lodge, T. P., Polymer Chemistry, 2nd ed., CRC Press, 2007 (comprehensive treatment of
polymer chemistry*synthesis and physical chemistry).
Mark, J.E., Allcock, H. R., and West, R., Inorganic Polymers, Oxford, 2005 (physical chemistry and properties of
inorganic polymers).
Mark, J. E., Ed., Polymer Data Handbook, Oxford, 1999 (compilation of major classes of polymers and their
physical properties).
Mori, S. and Barth, H. G., Size Exclusion Chromatography, Springer-Verlag, 1999 (comprehensive treatment of
SEC, theory and applications).
Munk, P. and Aminabhavi, T. M., Introduction to Macromolecular Science, 2nd ed., New York: John Wiley &
Sons, 2002 (emphasis on polymer physical chemistry).
Nielsen, L. E., Polymer Rheology, Marcel Dekker, 1977 (introductory text on polymer rheology).
Richardson, T. L. and Lokensgard, E., Industrial Plastics: Theory and Applications, Delmar, 1996 (practical
overview of some important properties and polymer processing).
Carraher, Jr., C. E., Seymour/Carraher’s Polymer Chemistry, 7th ed., CRC Press, 2007 (popular introduction to
polymer chemistry).
Seymour, R. B., Engineering Polymer Sourcebook, McGraw-Hill, 1990 (good overview of physical properties of
engineering polymers).
Sperling L. H., Introduction to Physical Polymer Science, 2nd ed., Wiley-Interscience, 1992 (good treatment of
polymer physics and properties).
van Krevelen, D. W., Properties of Polymers, 3rd ed., Elsevier, 1990 (in-depth treatment of polymer properties,
best resource available).
Whistler, R., Industrial Gums, 2nd ed., Academic Press, 1973 (although outdated, gives solid background on the
chemistry and properties of cellulosics and polysaccharides).
Wu, C. S., Ed., Handbook of Size Exclusion Chromatography, 2nd ed., Marcel Dekker, 2003 (covers all aspects of
this important technique).
xxii
ABS, Blow moulding ABS, Carbon reinforced A-1 A-2
A-1
ABS,
A-1 Blow moulding A-1 Deflection Temperature:
Monomers: Acrylonitrile, 1,3-Butadiene, Styrene
Material class: Thermoplastic, Copolymers No. Value Note
Polymer Type: ABS 1 808C 1.8 MPa, ASTM D648 [3]
CAS Number:
2 908C 0.45 MPa, ASTM D648 [3]
CAS Reg. No.
9003-56-9
Surface Properties & Solubility:
Solvents/Non-solvents: Sol. polar solvents, esters, ketones and
some chlorinated hydrocarbons [5]
Applications/Commercial Products:
Transport Properties:
Trade name Supplier Transport Properties General: Exhibits viscoelastic behaviour in
both the melt and solid states. Like other thermoplastics, it may be
Cycolac MSB General Electric Plastics described as exhibiting non-Newtonian behaviour; viscosity
Cycolac MSC General Electric Plastics decreases due to increasing shear rate [2]
Water Absorption:
Cycolac MSD General Electric Plastics
Cycolac MSL General Electric Plastics No. Value Note
1 0.3 % 24h, ASTM D570 [3]
A-2 2 0.75 % saturation, ASTM D570 [3]
ABS, Carbon reinforced A-2
Synonyms: Acrylonitrile-butadiene-styrene copolymer. Acryloni-
trile-butadiene-styrene terpolymer. Poly(2-propenenitrile-co-1,3-
Mechanical Properties:
Mechanical Properties General: Has high impact resistance over a
butadiene-co-ethenylbenzene)
wide temp. range, with very good rigidity and toughness. Its
Related Polymers: ABS
tensile and flexural strength, tensile and flexural moduli are all
Monomers: Acrylonitrile, 1,3-Butadiene, Styrene
higher than those of unreinforced ABS. Has very low notched
Material class: Composites, Copolymers, Thermoplastic
Izod impact strength compared to that of unreinforced ABS
Polymer Type: ABS
grades. Elongation at break 1 2% (ASTM D638). [3]
CAS Number:
Glass-Transition Temperature: Impact Strength: Izod 60 J m-1 (notched, ASTM D256) [3],
280 J m-1 (unnotched, ASTM D256) [3]
No. Value Note Hardness: Rockwell M90 (ASTM D785) [3]
Fracture Mechanical Properties: Shear strength 45 MPa (ASTM
1 100 1108C [4] D732) [3]. Coefficient of friction 0.2 (static) (LNP SOP) 0.15,
(dynamic) (LNP SOP) [3]
Friction Abrasion and Resistance: Coefficient of friction 0.2 (static,
(LNP SOP), 0.15 (dynamic, LNP SOP) [3]
1
ABS, Extrusion, Unfilled A-3 A-3
2
ABS, Extrusion, Unfilled A-3 A-3
Transport Properties:
Transport Properties General: ABS exhibits viscoelastic behaviour Miscellaneous Moduli:
in both the melt state and the solid state. Like other
thermoplastics, it may be described as exhibiting non-Newtonian No. Value Note Type
behaviour; viscosity decreases due to increasing shear rate [2]. 1 1250 1400 MPa 50.5% elongation, tensile creep
Melt Flow Index: 1000h, ISO/IEC 899 [4] modulus
Flexural Modulus:
Dielectric Strength:
No. Value Note
No. Value Note
1 1800 2400 MPa 2 mm min-1, ISO 178 [3]
1 34 85 kV.mm-1 IEC 243-1 [3,4]
Compressive Modulus:
Arc Resistance:
No. Value Note
No. Value Note
1 1030 2690 MPa ASTM D695 [5]
1 50 90s [2]
Elastic Modulus:
3
ABS Flame retardant A-4 A-4
4
ABS Flame retardant A-4 A-4
5
ABS Flame retardant A-4 A-4
Decomposition Details: Thermal decomposition of the fire Cycolac CKM1, CKM2 General Electric Plastics
retardant additives can occur at temps. in excess of 2408 or during Cycolac K25, KJL General Electric Plastics
long residence times. In addition to the constituent monomers,
antimony compounds, brominated hydrocarbons and hydrogen GPC Delta D-1000 H Simex International
bromide might also be released [4] Lastilac LATI Industria
Flammability: Flammability rating V0 (1.57 3.2 mm thick, Thermoplastics S.p.A.
UL 94) [4, 6]; 5VA (2.5 3.2 mm thick, UL 94) [4, 6]. Glow wire
test, wire applied during 30 seconds, extinguishing time 5 5 s Lustran Bayer Inc.
(1.5 3.2 mm, 9608, IEC 695-2-1/1) [4]. Limiting oxygen index 27 Lustran ABS 911, 914HM Monsanto Chemical
30% (ASTM D2863, ISO4589 IV) [4, 6]
Environmental Stress: Resistance to weathering and Uv is poor Magnum Dow
unless protected. Undergoes stress cracking when in contact with Novodur L3FR, M3FR Bayer Inc.
certain chemical agents under stress. ABS polymeric components
differ in oxidative stability. The rubber phase in ABS oxidises Novodur Bayer Inc.
more rapidly than the rigid component. Oxidation of polybuta- RESIN RX1-550FR Resin Exchange
diene results in embrittlement of the rubber [2]. May discolour in
sunlight [2, 8] RXI-500 Resin Exchange
Chemical Stability: Undergoes stress cracking when in contact Ronfalin DSM
with certain chemical agents. Resistant to mineral and vegetable
oils, waxes and related household and commercial materials. High Sinkral PDFRI-UV Enichem America
resistance to staining agents in household applications. Attacked Starflam ABS Ferro Corporation
by conc. nitric acid, sulfuric acid. Unaffected by weak acids, weak
and strong bases up to 658. Poor resistance to most organic Terluran BASF
solvents [2,8]
Thermofil ABS Thermofil
Biological Stability: Is biologically inert [4]
Recyclability: Can be recycled. The scrap should be clean, Toyolac Toray
uncontaminated, and free from degradation. Normally the
VP II Diamond Polymers
content of the reground material should not exceed 20 25 % [4]
Stability Miscellaneous: Sufficiently stable during processing
provided that processing temp. is kept as low as conveniently
possible and residence times are kept to an absolute minimum [4]
6
ABS General purpose A-5 A-5
1 0.2 W/mK DIN 52612 [4] 3 CO2 3.54 4.72 cm3 mm/(m2 day atm)
7
ABS General purpose A-5 A-5
8
ABS, Glass fibre reinforced ABS, Heat Resistant A-6 A-7
9
ABS, Heat Resistant A-7 A-7
Volumetric & Calorimetric Properties: region associated with particle-particle interactions. As the
Density: grafting degree increases the viscoelastic functions first decrease
and then increase. The minima in the functions occurs at the
No. Value Note grafting degree of about 0.45 for ABS having rubber particles of
3
170 nm [16]
1 d 1.06 g/cm ISO 1183 [5] Water Absorption:
Flexural Modulus:
Melting Temperature:
No. Value Note
No. Value Note
1 2500 2800 MPa 2 mm min-1, ISO 178 [5]
1 2408C [4,5]
Transport Properties:
Transport Properties General: Exhibits viscoelastic behaviour in Flexural Strength Yield:
both the melt and solid states. Like other thermoplastics, it may be
described as exhibiting non-Newtonian behaviour; viscosity No. Value Note
decreases due to increasing shear rate 1 75 85 MPa 5 mm min-1, ISO 178 [5]
Melt Flow Index:
10
ABS, Heat Resistant A-7 A-7
11
ABS, High impact A-8 A-8
Glass-Transition Temperature:
Bibliographic References
[1] Kirk-Othmer Encycl. Chem. Technol., Vol. 1, 4th edn., (ed.
J.I.Kroschwitz), Wiley Interscience, 1991, 391 No. Value Note
[2] Encycl. Polym. Sci. Eng., Vol. 1, 2nd edn. (ed. J.I. Kroschwitz), John 1 91 1108C [14]
Wiley & Sons, 1985, 388
[3] Brydson, J.A., Plast. Mater., 5th edn., Butterworths, 1988
[4] DSM Polymers, DSM, 1995, (technical datasheet) Deflection Temperature:
[5] Lustran ABS, Novadur ABS, Application Technology Information,
Bayer, 1997, (technical datasheet)
[6] The Plastics Compendium, Key Properties and Sources, (ed. R. No. Value Note
Dolbey), Rapra Technology Ltd., 1995, 1 1 89 1018C 120 K h-1, 1.8 MPa, ISO 75/A [3,4]
[7] Harper, C.A., Handb. Plast. Elastomers, (ed. C.A. Harper), McGraw-
Hill, 1975 2 988C 0.45 MPa [5]
[8] Terluran, BASF Plastics, (technical datasheet)
[9] Casale, A. and Salvatore, O., Polym. Eng. Sci., 1975, 15, 286
[10] Hayes, R.A. and Futamura, S., J. Polym. Sci., Polym. Chem. Ed., 1981, Vicat Softening Point:
19, 985
[11] Brydon, A., Burnett, G.M. and Cameron, C.G., J. Polym. Sci., Polym. No. Value Note
Chem. Ed., 1974, 12, 1011
[12] Allen, P.W., Ayrey, G. and Moore, C.G., J. Polym. Sci., 1959, 36, 55 1 91 1008C 50 K h-1, 50 N, ISO 306B [3,4]
[13] Odian, G., Principles of Polymerization, McGraw-Hill, 1970
[14] Pillichody, C.T. and Kelley, P.D., Handbook of Plastic Materials and
Technology, (ed. I.I.Rubin), Wiley Interscience, 1990, (stress-strain
behaviour, creep, stress relaxation, fatigue) Surface Properties & Solubility:
[15] Guide to Plastics, Property and Specification Charts, (ed W.A. Kaplan) Solvents/Non-solvents: Sol. polar solvents, esters, ketones and
McGraw-Hill, 1991, 68, 11 some chlorinated hydrocarbons [6]
[16] Aoki, Y., Macromolecules, 1987, 20, 2208, (dynamic viscoelastic and
steady-flow props) Transport Properties:
Transport Properties General: Exhibits viscoelastic behaviour in
A-8 both the melt state and the solid state. Like other thermoplastics,
ABS, High impact A-8 it may be described as exhibiting non-Newtonian behaviour;
Synonyms: Acrylonitrile-butadiene-styrene copolymer. Acryloni- viscosity decreases due to increasing shear rate [2]
trile-butadiene-styrene terpolymer. Poly(2-propenenitrile-co-1,3- Melt Flow Index:
butadiene-co-ethenylbenzene)
Related Polymers: ABS No. Value Note
Monomers: Acrylonitrile, 1,3-Butadiene, Styrene 1 4.5 17 g/10 min 2208, 10 kg, ISO 1133 [3,4]
Material class: Thermoplastic, Copolymers
Polymer Type: ABS
CAS Number: Polymer Melts: Storage shear modulus and loss shear modulus as
a function of angular frequency, and shear stress as a function of
CAS Reg. No. shear rate depend strongly on grafting degree in the long-time
region associated with particle-particle interactions. As the
9003-56-9 grafting degree increases, the viscoelastic functions first decrease
and then increase. The minima in these functions occurs at the
Molecular Formula: [(C8H8)(C4H6)(C3H3N)]n grafting degree of about 0.45 for ABS having a rubber particle size
Fragments: C8H8 C4H6 C3H3N of 170 nm [8]
General Information: An amorph. thermoplastic that combines Water Absorption:
high performance with design versatility and easy processability
No. Value Note
Volumetric & Calorimetric Properties:
Density: 1 0.2 0.3 % 238, 24h, DIN 53495 [3,5]
12
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DANCE ON STILTS AT THE GIRLS’ UNYAGO, NIUCHI
I see increasing reason to believe that the view formed some time
back as to the origin of the Makonde bush is the correct one. I have
no doubt that it is not a natural product, but the result of human
occupation. Those parts of the high country where man—as a very
slight amount of practice enables the eye to perceive at once—has not
yet penetrated with axe and hoe, are still occupied by a splendid
timber forest quite able to sustain a comparison with our mixed
forests in Germany. But wherever man has once built his hut or tilled
his field, this horrible bush springs up. Every phase of this process
may be seen in the course of a couple of hours’ walk along the main
road. From the bush to right or left, one hears the sound of the axe—
not from one spot only, but from several directions at once. A few
steps further on, we can see what is taking place. The brush has been
cut down and piled up in heaps to the height of a yard or more,
between which the trunks of the large trees stand up like the last
pillars of a magnificent ruined building. These, too, present a
melancholy spectacle: the destructive Makonde have ringed them—
cut a broad strip of bark all round to ensure their dying off—and also
piled up pyramids of brush round them. Father and son, mother and
son-in-law, are chopping away perseveringly in the background—too
busy, almost, to look round at the white stranger, who usually excites
so much interest. If you pass by the same place a week later, the piles
of brushwood have disappeared and a thick layer of ashes has taken
the place of the green forest. The large trees stretch their
smouldering trunks and branches in dumb accusation to heaven—if
they have not already fallen and been more or less reduced to ashes,
perhaps only showing as a white stripe on the dark ground.
This work of destruction is carried out by the Makonde alike on the
virgin forest and on the bush which has sprung up on sites already
cultivated and deserted. In the second case they are saved the trouble
of burning the large trees, these being entirely absent in the
secondary bush.
After burning this piece of forest ground and loosening it with the
hoe, the native sows his corn and plants his vegetables. All over the
country, he goes in for bed-culture, which requires, and, in fact,
receives, the most careful attention. Weeds are nowhere tolerated in
the south of German East Africa. The crops may fail on the plains,
where droughts are frequent, but never on the plateau with its
abundant rains and heavy dews. Its fortunate inhabitants even have
the satisfaction of seeing the proud Wayao and Wamakua working
for them as labourers, driven by hunger to serve where they were
accustomed to rule.
But the light, sandy soil is soon exhausted, and would yield no
harvest the second year if cultivated twice running. This fact has
been familiar to the native for ages; consequently he provides in
time, and, while his crop is growing, prepares the next plot with axe
and firebrand. Next year he plants this with his various crops and
lets the first piece lie fallow. For a short time it remains waste and
desolate; then nature steps in to repair the destruction wrought by
man; a thousand new growths spring out of the exhausted soil, and
even the old stumps put forth fresh shoots. Next year the new growth
is up to one’s knees, and in a few years more it is that terrible,
impenetrable bush, which maintains its position till the black
occupier of the land has made the round of all the available sites and
come back to his starting point.
The Makonde are, body and soul, so to speak, one with this bush.
According to my Yao informants, indeed, their name means nothing
else but “bush people.” Their own tradition says that they have been
settled up here for a very long time, but to my surprise they laid great
stress on an original immigration. Their old homes were in the
south-east, near Mikindani and the mouth of the Rovuma, whence
their peaceful forefathers were driven by the continual raids of the
Sakalavas from Madagascar and the warlike Shirazis[47] of the coast,
to take refuge on the almost inaccessible plateau. I have studied
African ethnology for twenty years, but the fact that changes of
population in this apparently quiet and peaceable corner of the earth
could have been occasioned by outside enterprises taking place on
the high seas, was completely new to me. It is, no doubt, however,
correct.
The charming tribal legend of the Makonde—besides informing us
of other interesting matters—explains why they have to live in the
thickest of the bush and a long way from the edge of the plateau,
instead of making their permanent homes beside the purling brooks
and springs of the low country.
“The place where the tribe originated is Mahuta, on the southern
side of the plateau towards the Rovuma, where of old time there was
nothing but thick bush. Out of this bush came a man who never
washed himself or shaved his head, and who ate and drank but little.
He went out and made a human figure from the wood of a tree
growing in the open country, which he took home to his abode in the
bush and there set it upright. In the night this image came to life and
was a woman. The man and woman went down together to the
Rovuma to wash themselves. Here the woman gave birth to a still-
born child. They left that place and passed over the high land into the
valley of the Mbemkuru, where the woman had another child, which
was also born dead. Then they returned to the high bush country of
Mahuta, where the third child was born, which lived and grew up. In
course of time, the couple had many more children, and called
themselves Wamatanda. These were the ancestral stock of the
Makonde, also called Wamakonde,[48] i.e., aborigines. Their
forefather, the man from the bush, gave his children the command to
bury their dead upright, in memory of the mother of their race who
was cut out of wood and awoke to life when standing upright. He also
warned them against settling in the valleys and near large streams,
for sickness and death dwelt there. They were to make it a rule to
have their huts at least an hour’s walk from the nearest watering-
place; then their children would thrive and escape illness.”
The explanation of the name Makonde given by my informants is
somewhat different from that contained in the above legend, which I
extract from a little book (small, but packed with information), by
Pater Adams, entitled Lindi und sein Hinterland. Otherwise, my
results agree exactly with the statements of the legend. Washing?
Hapana—there is no such thing. Why should they do so? As it is, the
supply of water scarcely suffices for cooking and drinking; other
people do not wash, so why should the Makonde distinguish himself
by such needless eccentricity? As for shaving the head, the short,
woolly crop scarcely needs it,[49] so the second ancestral precept is
likewise easy enough to follow. Beyond this, however, there is
nothing ridiculous in the ancestor’s advice. I have obtained from
various local artists a fairly large number of figures carved in wood,
ranging from fifteen to twenty-three inches in height, and
representing women belonging to the great group of the Mavia,
Makonde, and Matambwe tribes. The carving is remarkably well
done and renders the female type with great accuracy, especially the
keloid ornamentation, to be described later on. As to the object and
meaning of their works the sculptors either could or (more probably)
would tell me nothing, and I was forced to content myself with the
scanty information vouchsafed by one man, who said that the figures
were merely intended to represent the nembo—the artificial
deformations of pelele, ear-discs, and keloids. The legend recorded
by Pater Adams places these figures in a new light. They must surely
be more than mere dolls; and we may even venture to assume that
they are—though the majority of present-day Makonde are probably
unaware of the fact—representations of the tribal ancestress.
The references in the legend to the descent from Mahuta to the
Rovuma, and to a journey across the highlands into the Mbekuru
valley, undoubtedly indicate the previous history of the tribe, the
travels of the ancestral pair typifying the migrations of their
descendants. The descent to the neighbouring Rovuma valley, with
its extraordinary fertility and great abundance of game, is intelligible
at a glance—but the crossing of the Lukuledi depression, the ascent
to the Rondo Plateau and the descent to the Mbemkuru, also lie
within the bounds of probability, for all these districts have exactly
the same character as the extreme south. Now, however, comes a
point of especial interest for our bacteriological age. The primitive
Makonde did not enjoy their lives in the marshy river-valleys.
Disease raged among them, and many died. It was only after they
had returned to their original home near Mahuta, that the health
conditions of these people improved. We are very apt to think of the
African as a stupid person whose ignorance of nature is only equalled
by his fear of it, and who looks on all mishaps as caused by evil
spirits and malignant natural powers. It is much more correct to
assume in this case that the people very early learnt to distinguish
districts infested with malaria from those where it is absent.
This knowledge is crystallized in the
ancestral warning against settling in the
valleys and near the great waters, the
dwelling-places of disease and death. At the
same time, for security against the hostile
Mavia south of the Rovuma, it was enacted
that every settlement must be not less than a
certain distance from the southern edge of the
plateau. Such in fact is their mode of life at the
present day. It is not such a bad one, and
certainly they are both safer and more
comfortable than the Makua, the recent
intruders from the south, who have made USUAL METHOD OF
good their footing on the western edge of the CLOSING HUT-DOOR
plateau, extending over a fairly wide belt of
country. Neither Makua nor Makonde show in their dwellings
anything of the size and comeliness of the Yao houses in the plain,
especially at Masasi, Chingulungulu and Zuza’s. Jumbe Chauro, a
Makonde hamlet not far from Newala, on the road to Mahuta, is the
most important settlement of the tribe I have yet seen, and has fairly
spacious huts. But how slovenly is their construction compared with
the palatial residences of the elephant-hunters living in the plain.
The roofs are still more untidy than in the general run of huts during
the dry season, the walls show here and there the scanty beginnings
or the lamentable remains of the mud plastering, and the interior is a
veritable dog-kennel; dirt, dust and disorder everywhere. A few huts
only show any attempt at division into rooms, and this consists
merely of very roughly-made bamboo partitions. In one point alone
have I noticed any indication of progress—in the method of fastening
the door. Houses all over the south are secured in a simple but
ingenious manner. The door consists of a set of stout pieces of wood
or bamboo, tied with bark-string to two cross-pieces, and moving in
two grooves round one of the door-posts, so as to open inwards. If
the owner wishes to leave home, he takes two logs as thick as a man’s
upper arm and about a yard long. One of these is placed obliquely
against the middle of the door from the inside, so as to form an angle
of from 60° to 75° with the ground. He then places the second piece
horizontally across the first, pressing it downward with all his might.
It is kept in place by two strong posts planted in the ground a few
inches inside the door. This fastening is absolutely safe, but of course
cannot be applied to both doors at once, otherwise how could the
owner leave or enter his house? I have not yet succeeded in finding
out how the back door is fastened.