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Materials for engineering, 3rd Edition - (Malestrom)

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168<br />

<strong>Materials</strong> <strong>for</strong> <strong>engineering</strong><br />

Toughening of polymers<br />

The moderate ductility apparent in curve 3 in Fig. 5.4 is more difficult to<br />

achieve. One approach is to prepare a two-phase material by a technique<br />

known as copolymerization. An example of this is acrylonitrile–butadiene<br />

styrene which consists of spheroidal inclusions of the soft elastomeric<br />

polybutadiene in a matrix of the relatively rigid styrene acrylonitrile (SAN)<br />

copolymer. When the material is strained, stress concentrations <strong>for</strong>m in the<br />

matrix around the inclusions. Defects then grow from the inclusions, absorbing<br />

extra energy as they do so, the process being known as elastomer toughening,<br />

although the overall tensile modulus of the material is reduced by the change<br />

in microstructure.<br />

Another approach has been to synthesize new polymers based on different<br />

kinds of repeat units, <strong>for</strong> example the use of amorphous polycarbonate. This<br />

contains rigid aromatic groups in the molecular backbone and exhibits<br />

mechanical toughness well below its glass-transition temperature. This may<br />

again arise by the <strong>for</strong>mation of energy-absorbing defects as happens in<br />

‘elastomer toughening’ described above.<br />

5.4.4 Material data <strong>for</strong> polymers<br />

In contrast to the properties of metals and alloys, the properties of a given<br />

polymer made by different manufacturers may well differ significantly. This<br />

arises <strong>for</strong> several reasons: firstly, all polymers contain a range of molecular<br />

lengths (see Fig. 1.22) and slight changes in processing will change this<br />

spectrum and also the degree of crystallinity in the product. The properties<br />

will also be changed by mechanical processing. Again, as already discussed,<br />

the mechanical properties of polymers are time- and temperature-dependent,<br />

so that the data obtained will depend on the testing conditions of temperature<br />

and strain-rate. The following compilation of data (where they are available)<br />

must there<strong>for</strong>e be regarded as approximate and, in designing a product,<br />

reference should always be made to the data provided by the individual<br />

manufacturers. We have included the representative polymers listed at the<br />

start of this chapter, Table 5.1<br />

5.4.5 Fracture<br />

Crazing<br />

If a brittle transparent polymer such as polystyrene (widely used <strong>for</strong> the<br />

manufacture of rulers and the bodies of ballpoint pens) is loaded in tension<br />

at room temperature, plastic de<strong>for</strong>mation leads to the appearance of small,<br />

white, crack-shaped features called crazes, typically some 5 µm in thickness.<br />

Crazes usually develop at orientations which are at right-angles to the principal<br />

stress axis, but they are not in fact cracks rather a precursor to fracture.

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