Materials for engineering, 3rd Edition - (Malestrom)
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76<br />
<strong>Materials</strong> <strong>for</strong> <strong>engineering</strong><br />
the temperature of working, there<strong>for</strong>e, the grain size of the final product may<br />
be controlled.<br />
Hot working a material that may undergo a phase change on cooling, such<br />
as steel, presents a further, powerful means of grain size control. Controlled<br />
rolling of steel is an example of this, whereby the steel is de<strong>for</strong>med above<br />
the γ trans<strong>for</strong>mation temperature: dynamic recrystallization produces a fine<br />
γ grain size, which, on air-cooling, is trans<strong>for</strong>med to an even finer α grain<br />
size. Sophisticated process control is necessary to produce material consistently<br />
with the desired microstructure, but, in principle, controlled rolling constitutes<br />
a very attractive means of achieving this.<br />
3.1.3 Alloy hardening<br />
Work hardening and grain-size strengthening, which we have considered so<br />
far, can be applied to a pure metal. The possibility of changing the composition<br />
of the material by alloying presents further means of strengthening. We will<br />
consider two ways in which alloying elements may be used to produce<br />
strong materials: solute hardening and precipitation hardening.<br />
Solute hardening<br />
We have shown in Fig. 1.10(a) and 1.10(b) that two types of solid solution<br />
may be <strong>for</strong>med, namely interstitial and substitutional solutions. The presence<br />
of a ‘<strong>for</strong>eign’ atom in the lattice will give rise to local stresses which<br />
will impede the movement of dislocations, hence raising the yield stress of<br />
the solid.<br />
This effect is known as solute hardening, and its magnitude will depend<br />
on the concentration of solute atoms in the alloy and also upon the magnitude<br />
of the local misfit strains associated with the individual solute atoms. It is<br />
also recognized that the solubility of an element in a given crystal is itself<br />
dependent upon the degree of misfit – indeed, if the atomic sizes of the<br />
solute and solvent differ by more than about 14%, then only very limited<br />
solid solubility occurs. There must thus be a compromise between these two<br />
effects in a successful solution-hardened material – i.e. there must be sufficient<br />
atomic misfit to give rise to local lattice strains, but there must also be<br />
appreciable solubility.<br />
A theoretical approach expresses the increase in shear yield stress, ∆τ y , in<br />
terms of a solute atom mismatch parameter, ε, in the <strong>for</strong>m:<br />
∆τ y = Gε 3/2 bc 1/2 [3.3]<br />
where G is the shear modulus, b the dislocation Burgers vector and c the<br />
concentration of solute atoms.