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Thixoforming : Semi-solid Metal Processing

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_g ¼ ffiffi p<br />

3 _Eeq, where _ 226j 7 A Physical and Micromechanical Model for <strong>Semi</strong>-<strong>solid</strong> Behaviour<br />

Eeq is the macroscopic von Mises equivalent strain rate.<br />

As a consequence, the steady-state <strong>solid</strong> fraction in the active zone is calculated<br />

by [25]<br />

f s<br />

A ¼<br />

f s<br />

f s þ Kdg s<br />

ð1fÞðÞ _g<br />

n<br />

Kag<br />

ð7:3Þ<br />

It is worth noting that Equation 7.3 provides a macroscopic description of the<br />

strain-ratedependenceoftheinternalstructure.<br />

To improve the description of relationships between local deformation mechanisms<br />

and microstructure evolution, we incorporate the fact that the relevant shear rate<br />

is not the overall one but the local one within the <strong>solid</strong> bonds. We postulate that the<br />

<strong>solid</strong> bonds break as soon as the local shear reaches a critical value g c. To do so,<br />

Equation 7.2 is rewritten as<br />

_f A<br />

s ¼ Kag f s 1 f A<br />

s 1 f s<br />

_g bonds<br />

f<br />

gc A<br />

s<br />

ð7:4Þ<br />

The shear rate within the <strong>solid</strong> bonds is naturally given by the micro–macro<br />

modelling (see Equation 7.11 where the medium B is the active zone A) and is<br />

equal to<br />

_g bonds ¼ ffiffiffi p<br />

s<br />

3 _e ð7:5Þ<br />

A eq<br />

During deformation, it is admitted that the kinetics of the agglomeration process are<br />

much lower than the kinetics of the deagglomeration process (Martin et al., 1994).<br />

Consequently, for isothermal thixoforming, we can neglect the agglomeration term<br />

in comparison with the deagglomeration term, so that<br />

_f A<br />

s ¼ 1 f s<br />

_g bonds<br />

f<br />

gc A<br />

s<br />

ð7:6Þ<br />

For non-isothermal processing when the dies are colder than the slug, an increase in<br />

<strong>solid</strong> fraction related to <strong>solid</strong>ification due to thermal exchanges at the tool–slug<br />

interface is observed. As a result, the <strong>solid</strong> particles are more agglomerated. In order<br />

to incorporate this agglomeration–<strong>solid</strong>ification phenomenon, we introduce a<br />

phenomenological term in Equation 7.4 accounting for the increase in the <strong>solid</strong><br />

fraction within the active zone when temperature decreases. It is written as<br />

_f A<br />

s<br />

A<br />

¼ a 1 f s f sðTÞj_ Tj b<br />

1 f s<br />

_g bonds<br />

f<br />

gc A<br />

s<br />

where a and b are two positive material parameters.<br />

ð7:7Þ<br />

7.3.1.3 Local Behaviours<br />

The description of the RVE requires liquid and <strong>solid</strong> behaviour representation. The<br />

liquid phase is regarded as a Newtonian fluid. The <strong>solid</strong> phase is regarded as a<br />

viscoplastic material, the consistency of which may depend on temperature. Solid

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