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57]67
K.L. EdwardsU
Elmac Group Limited, Northern Works, Appletongate, Newark-on-Trent, Nottinghamshire, NG24 1LR, UK
Abstract
The influence of polymers on modern product design is unprecedented and in many cases is the only material suitable. Today,
the range of polymer materials is vast and, at the same time, bewildering to designers new to these materials. This article contains
an essential summary of salient information on polymer technology formatted for use by engineering designers considering
product designs which comprise of or contain parts made from polymer materials. The information is structured around
materials, processes, properties and applications for thermoplastics, thermosets and rubbers. Q 1998 Elsevier Science Ltd. All
rights reserved.
2.1. Thermoplastics
2.1.1.3. Polypropylene (PP). This material is available 2.1.2.3. Polystyrene (PS). This material is easy to
in many grades and also as a copolymer Žethylenerpro- process and is available in a range of grades. Polystyrene
pylene.. PP possesses good strength, stiffness and excel- is also available in expanded form for packaging and
lent fatigue and chemical resistance. Applications in- thermal insulation.
clude, automotive components, television cabinets, tool 2.1.2.4. Acrylonitrile-butadiene-styrene (ABS). This
handles, integral hinges, etc. PP is also available as a material has very high strength, stiffness and toughness
fibre and as a film. properties compared to most other plastics. It com-
2.1.1.4. Polyamides (nylons). There are many types of pares well with nylons and acetals in many applications,
nylon, but all of them possess high strength, stiffness but is generally less expensive. It is attacked by chlori-
and toughness. Unfortunately, nylons absorb moisture nated solvents, esters, ketones, acids and alkalis.
with an associated dimensional stability problem, but in 2.1.2.5. Polycarbonate. This material has very high
glass-reinforced form this problem is reduced and a toughness. It is also transparent and has a very high
very strong material results. Nylons are regularly used temperature-resistance, but is attacked by alkaline so-
for gears, bearings, housings, etc. lutions and hydrocarbon solvent.
2.1.1.5. Acetals. These materials possess high 2.1.2.6. Poly-ether-sulphone (PES). This material has
strength, stiffness and toughness, and low moisture high load-bearing and operating-temperature capability
absorption. Acetals are available in two forms: a ho- Žup to 1808C. and low flammability, dimensional stabil-
mopolymer and a copolymer. The homopolymer is ity and electrical properties Žup to 2008C..
stiffer and stronger, while the copolymer has better
temperature performance. 2.2. Thermosets
2.1.1.6. Poly-tetra-fluoro-ethylene (PTFE). This mate-
rial possesses excellent chemical resistance and a very 2.2.1. Aminos
low coefficient of friction. It is used in bearings, gas- There are two basic types: urea-formaldehyde and
kets, diaphragms and non-stick surfaces, particularly if melamine formaldehyde. They are hard and rigid with
the environment is aggressive. good abrasion resistance. Mechanical properties are
2.1.1.7. Thermoplastic polyesters. These materials pos- good up to 1008C.
sess high strength, toughness, abrasion and chemical
resistance, and a low coefficient of friction. 2.2.2. Phenolics
Phenol-formaldehyde was one of the first regularly-
1. Poly-ethylene-terephthalate ŽPET. is available in used thermosets Žtrade name Bakerlite..
two forms: in a moulded form, which is used in
carbonated ‘lemonade’ bottles, and in fibre form, 2.2.3. Polyurethanes
e.g. under the trade name Terylene. These are available in three forms: elastomers, flex-
2. Poly-butylene-teraphthalate ŽPBT. is used for ible foams and rigid foams. They have high strength
lightly-loaded gears, bearings, housings, etc. and good chemical and abrasion resistance.
The properties of rubber are improved by vulcanising 3. Stabilising. The third stage is stabilising the shape
Žcross-linking or curing.. This is mostly achieved by established in the previous stage. This is normally
additions of sulphur and the application of heat. Also achieved for thermoplastics by cooling and solidify-
by mixing rubber with carbon-black, effectively a rein- ing, or, for thermosets, by chemical cross-linking
forcement, its mechanical properties are enhanced, its Žhot or cold..
degradation due to sunlight and ozone reduced and its
liquid absorption reduced. The main types of rubber
are as follows: 3.1. Mixing processes
Natural rubber: This rubber has high strength, good 3.1.1. Intensi¨ e mixing
fatigue resistance and low temperature-stability. The intensive mixer comprises of two counter-rotat-
Styrene-butadiene rubber ŽSBR.: This rubber has a ing rotors revolving inside the cavity of a housing the
better abrasion and fatigue resistance than natural shape of two interconnected cylinders. A combination
rubber. of drag flow between the casing and the rotors and
Chloroprene rubber: The physical properties of this shear flow between the rotors causes mixing of the
rubber are inferior to natural rubber, but better ingredients. The ingredients are fed into the mixer via
ozone, chemical, oil and high-temperature resistance. an aperture at the top Žwhich can be sealed to create
Nitrile rubber ŽNBR.: This rubber has improved oil pressure in the cavity. and the compound after the
resistance and reduced resilience and low-tempera- mixing is drawn off through a port at the bottom. A
ture flexibility with increasing acrylonitrile content. capacity limit of up to 500 kg is typical.
Ethylene-propylene rubber ŽEPM. and ethylene-pro-
pylene diene terpolymer ŽEPDM.: These rubbers are 3.1.2. Two-roll milling
comparable to SBR but with much better resistance The two-roll mill comprises of two counter-rotating
to atmospheric ageing, ozone and oxidation. EPM cylindrical rolls separated by a narrow gap, or ‘nip’.
has slightly better weather-resistance. The feed Žpossibly partly mixed from an intensive mixer.
Butyl rubber: This rubber has good ozone, weather- is introduced between the rolls and is dragged with
ing, heat and chemical resistance, extremely low gas high laminar shear through the nip and adheres as a
permeability, high damping capacity at room temper- band to one of the rolls. A capacity limit of up to 500
ature. kg is typical.
Butadiene rubber: This rubber has low hysteresis,
good low-temperature flexibility and abrasion resis- 3.2. Extrusion processes
tance, and poor tear resistance.
Thermoplastic rubbers: These rubbers have similar The extrusion processes provide continuous constant
properties to SBR except the upper temperature section products.
limit is approx. 508C.
3.2.1. Calandering
The normal arrangement of a calander consists of
four horizontally mounted counter-rotating cylindrical
3. Polymer-processing methods rolls. The first two rolls are analogous to the two-roll
mill. The compound is drawn through the first nip and
The processing of polymers w2]4,6x can be con- is transferred via adhesion to one roll on the second
sidered to take place in three distinct and broadly nip. The second nip is smaller than the first nip and
defined stages: therefore reduces the thickness of the compound. There
is a further reduction in the third and final nip. The
1. Mixing and converting into a melt. The first stage resulting sheet can be approx. 1 m wide and up to a few
involves dispersion of additives such as stabilisers millimetres in thickness.
and pigments into the polymer, removal of air and
volatiles, transformation of solid polymer feedstock 3.2.2. Screw extrusion
Žif powder or granules. into a ‘melt’, and achieving The essential parts of a screw extruder are: the
a fluid state which is uniform in composition tem- extruder, the die and the ancillaries, the haul-off mech-
perature and deformation history. anism and the supporting device for the product or
2. Shaping. The second stage is shaping, using ‘extrudate’. The extruder consists of a screw rotating
processes which are discussed in more detail below. inside a heated close-fitting constant-diameter barrel.
The shaping processes may be divided into batch The screws function is to pump Žby drag flow between
flow Že.g. moulding. or continuous flow Že.g. extru- the screw and the barrel., melt and mix the polymer to
sion.. such a condition that it will pass through a die. The
K.L. Edwards r Materials and Design 19 (1998) 57]67 61
screw is held at one end in a thrust bearing and technique is also widely used for moulding Sheet
rotationally driven by an electric motor via a gearbox. Moulding Compound ŽSMC. and Dough Moulding
The screw is normally of constant pitch, but its depth Compound ŽDMC.. These are compounds based on
changes from being constant and greatest in the feed thermosetting resin Žnormally polyester. combined with
zone, tapering down in the compression zone to a filler Žnormally calcium carbonate., short glass fibres
constant and smaller depth in the metering zone. The and modifying agents in varying proportions. Complex
ingredients are normally fed into the feed zone via a shaped mouldings are possible, but flow-induced orien-
hopper and pass out of the metering zone via a heated tation of the fibres leads to varying mechanical proper-
die which has the shape of the desired cross-section of ties. Compression moulding is also the key process in
the product. The extrusion of profiles, tubes and sheet rubber tyre manufacture.
are facilitated by a haul-off and support system and
either cut to finite lengths or rolled on to drums. 3.2.5. Transfer moulding
In transfer moulding, the compound is melted in a
3.2.3. Moulding processes separate chamber and then transferred under pressure
In contrast to the continuous processes described through a channel or ‘runner’ to the mould impression
above, moulding is a discontinuous process, but can be for shaping and cross-linking. The advantages of this
a repetitive cycle. The steps in the process are essen- process are the charge is already in a molten state
tially delivery of a shapable compound to a mould so when it enters the mould, so it can flow easily, espe-
that a product can be made, or moulded, and its shape cially around inserts. However, when fibre-filled plas-
stabilised. The moulds can be ‘open’ type, in male or tics are used, the fibres can easily be damaged passing
female form, that define one surface of a mould Žcon- through the runner and tend to become aligned with
tact moulding.. The moulds can be two matched female the flow direction.
half-moulds for hollow products. The moulds can also
be matched male and female pairs which have a cavity 3.2.6. Injection moulding
that can be filled with compound. The shaping is nor- In injection moulding, a polymer melt Žthermoplas-
mally achieved by applying pressure to cause the fluid tic, cross-linked plastic or rubber compound. is injected
to conform to one or both of the mould surfaces into the cavity of a closed split mould. The main
depending on the type of mould. equipment necessary for injection moulding are an
injection machine, a split mould and a system for
3.2.4. Compression moulding opening, closing and holding closed the mould. The
In compression moulding, a male, or projecting core, injection machine is similar to an extruder, except the
mould is brought together with a complementary fe- die is replaced by a valve nozzle and the screw can also
male, or cavity, mould such that a space or ‘impression’ move axially to act as a piston to pump the melt. The
is created between them. The mould pair are usually mould normally has a vertical part-line with no flash
held between the platens of a ‘press’ to create the clearance and a runner system connecting the injection
pressure necessary to cause the plastic compound to machine to the impression. Opening and closing the
flow and fill the cavity. To ensure alignment of the mould is achieved hydraulically. A system of mould
moulds when being brought together, guide or dowel locking, temperature control, guide pins and ejector
pins are used. It is also necessary to incorporate injec- pins are also necessary. The injection pressures are
tion pins and generous tapers or drafts to mould sur- typically above 100 MN my2 with injection rates of
faces to facilitate removal of mouldings which shrink 0.0003 m3 sy1 and greater. Obviously, the injection
considerably during moulding. The techniques can be machine and the moulds have to be robustly con-
used for small mouldings using multi-impression structed to resist the high pressures if unacceptably
moulds. Metal inserts can also be included. large distortions are to be avoided. This will make the
The process of compression moulding is widely used capital costs of the equipment high, but this can be
for moulding cross-linked polymers where the moulds amortised over large production runs.
are heated. The moulds are normally steel to withstand
the pressures which can be up to 50 MN my2 . The 3.2.7. Blow moulding
‘charge’ can be granules, a preform or rubber com- In blow moulding, a uniform thick-walled molten
pound which is placed in the cavity. Under pressure thermoplastic ‘parison’ is extruded vertically down-
and temperature, the charge melts and spreads to fill wards between the open faces of a cool matched fe-
the cavity. To ensure complete filling and removal of male or split mould. The mould is then closed and the
air, the charge is slightly larger than the cavity will sealed parison is inflated pneumatically Žat 0.25 MN
permit and the excess is forced along a very narrow gap my2 . so that the outside of the tube conforms to the
or clearance between the two moulds. This results in shape of the surface of the mould cavity. The mould
‘flash’ which can be easily removed after moulding. The has only to withstand the inflation pressure and there-
62 K.L. Edwards r Materials and Design 19 (1998) 57]67
Table 1
Applications and properties of thermoplastics
Table 1 Ž Continued.
fore can be less robust than the mould used for injec- The variation in wall thickness is a problem with blow
tion moulding and correspondingly less expensive. The moulding, being thinnest in the corners where the
moulding produced will have only one ‘good’ surface, plastic under goes a high degree of stretching. A char-
the outside surface, which is in contact with the mould. acteristic feature of blow moulding is the scar left by
64 K.L. Edwards r Materials and Design 19 (1998) 57]67
Table 1 Ž Continued.
the seal, which has to be strategically placed to disguise and changes of properties with quite small changes of
it. The protruding ends of the moulding have also to be temperature. The incorporation of fibres into a po-
trimmed, but by granulating they can be recycled. lymer matrix to form a composite will considerably
improve the stiffness and strength properties.
3.2.8. Thermoforming
In thermoforming, a sheet of thermoplastic is heated 4.2. Thermal properties
Žradiant or oven. above an open mould. The softened
sheet is then drawn down on to the mould either by The thermal properties of polymers are generally
compressed air, vacuum or plunger so that it conforms those expected from organic substances. Thermal con-
to the shape of the mould surface. As with blow mould- ductivity in polymers is low compared to metals. Con-
ing there is significant stretching of the sheet resulting versely, thermal expansion and contraction are high
in variable wall thicknesses and only one surface Žnext compared to metals Ž30]100 = 10y6 8Cy1 ..
to the mould. is ‘good’. The whole process though is
relatively inexpensive compared to all the techniques 4.3. Melt properties
described above. However, the process tends to be slow
and requires a trimming operation, generating scrap
Thermoplastics have relatively low melting points
which can be recycled.
Ž- 2508C. and can therefore be shaped via the applica-
tion of heat and stabilised by cooling. Thermosets are
shaped in low molecular weight form and stabilised by
4. Properties of polymer materials chemical cross-linking. The fluidity of each type of
polymer material dictates the type of processing.
Compared to metals, polymers have the attractive
properties w1,7]9x of low weight, corrosion resistance, 4.4. Chemical properties
ease of manufacture and aesthetics. However, design-
ing with polymers demands special attention. In partic- The chemical properties of polymers can be derived
ular, polymers exhibit viscoelastic behaviour, and this from either physical phenomena or chemical reaction.
occurs at low temperatures. The former includes the permeation of fluids and the
swelling Žfor thermosets. and solution Žfor thermoplas-
4.1. Mechanical properties tics. effects of solvents. A chemical reaction causes
permanent change to the polymer. The transmission of
Most unreinforced synthetic polymers Žthermoplastic fluids through plastics results from its relatively open
and thermoset. are regarded as low strength and stiff- structure as a consequence of its low density. There are
ness materials, but because of their low densities several important classes of chemical reaction in po-
Žaround 1 Mg my3 ., the strength- and stiffness-to- lymers. ‘Ageing’ is a deterioration of performance with
weight ratios are high. Typically, tensile strengths for time and can also result from physical change. ‘En-
polymers range from 10 to 90 MPa and modulus of vironmental stress cracking’ is premature brittle failure
elasticity from 1 to 3 GPa. The mechanical properties, under stress. Both phenomena result from exposure
however, are time-dependent and temperature sensi- and reaction to environmental factors such as tempera-
tive. The materials are therefore susceptible to creep ture, moisture, light, etc.
K.L. Edwards r Materials and Design 19 (1998) 57]67 65
4.5. Electrical properties ity and are therefore excellent materials for insulation
purposes. The dielectric properties, i.e. relative permit-
tivity and power factor, are typical of those found in
Most polymers are very poor conductors of electric- low-molecular-weight organic materials.
Table 2
Applications and properties of thermosets
Table 3
Applications and properties of rubbers
Truck tyres, radial side walls, Natural rubber and Elastic, translucent, durable,
resilient mountings, medical polyisoprene excellent strength, resilience and
adhesives and sealants, abrasion resistance, very good
insulated cables, flexible hoses electrical and low temperature
performance, low cost
Car tyres, shoe soles and heels, Styrene butadiene Elastic, translucent, good
automotive extrusions, cables coploymer mechanical properties, superior
and belting ageing properties, very low cost
Roofing and reservoir sheeting, Butyl Elastic, translucent, low
inner tubes, chemical vessel resilience, excellent electrical
linings insulation, low gas permeability
Tyre treads Žin blends with Butadiene Elastic, translucent, high
NRrSBC. golf balls, equipment resilience, good abrasion resistance
mounts, shoe soles, tubing and low temperature properties
Belting, gaskets, radiator hoses, Chloroprene Temperature resistance up to
wet suits, adhesives, weather- 1008C, exceptional low
and oil-resistant mouldings, temperature flexibility, self
sponge, automotive weather extinguishing
strip and sheeting
Rollers, coatings, membranes, Nitrile Žbutadiene Oil and petrol resistant mouldings
conveyor belts, flooring screeds, acrylonitrile and extrusions, good temperature
hydraulic components, fuel hoses, copolymer. resistance
refrigerant liners
Wire and cable insulation, roof Ethylene propylene General moulding and sheeting
membranes, steam hoses, flexible with good mechanical properties,
parts for washers and dryers, car outstanding ozone and weather
bumper pans, injection mouldings resistance, wide range of
temperature resistance
Žy70]2008C.
Table 3 Ž Continued.