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Thixoforming : Semi-solid Metal Processing

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52j 3 Material Aspects of Steel <strong>Thixoforming</strong><br />

Figure 3.7 Simplified schematic <strong>solid</strong>ification or concentration<br />

development of steel with 1% carbon [21].<br />

centre of the primary crystals changes only slightly during <strong>solid</strong>ification, so that the<br />

average concentration is below equilibrium. For aluminium alloys with an element<br />

concentration below the maximum solubility, the formation of brittle secondary<br />

phases even has to be expected. This is the case, for example, for the forming of the<br />

magnesium alloys AZ91 or AM60 by means of thixo- or pressure die casting. Despite<br />

a maximum solubility of 12.6% Al, these alloys show a significant fraction of brittle,<br />

eutectic b-phase (Mg17Al12) [17].<br />

For the development of the conventional thixoforming process of steel, especially<br />

the carbon concentration and the local carbon distribution exert a crucial influence on<br />

the fusion behaviour during reheating. In Figure 3.7, micro-segregations for a steel<br />

with a carbon concentration of 1% are depicted schematically under the assumption<br />

that the carbon does not diffuse in the <strong>solid</strong> phase. Hence micro-segregations also<br />

results in a shift of the <strong>solid</strong>us line to lower temperatures and a broadening of the<br />

<strong>solid</strong>ification interval. The chemical homogeneity adjusted during the primary<br />

material production therefore has a considerable influence on the fusion behaviour<br />

and the suitability of a material for thixoforming.<br />

For the development of rheo-processes, accurate knowledge of the nucleation and<br />

nucleus growth process is necessary. Typically, a dendritic structure of the <strong>solid</strong> phase<br />

is formed during the <strong>solid</strong>ification process of metals due to the constitutional<br />

undercooling of the liquid phase. In most cases, the temperature gradient in the<br />

liquid state is not sufficient or the <strong>solid</strong>ification rate is not high enough to avoid<br />

dendritic <strong>solid</strong>ification. To obtain a globular instead of a dendritic microstructure, the<br />

<strong>solid</strong>ifying alloy has to be specially treated. For all primary material routes, local<br />

concentration differences have to be avoided because they can lead to undercooling<br />

and superheating in different areas of the liquid, leading to an inhomogeneous<br />

distribution of the <strong>solid</strong> and liquid phases.<br />

In order to understand the nucleation and crystal growth processes, numerical<br />

modelling techniques are applied [22]. Here local undercooling is seen to be responsible<br />

for the formation of a dendritic structure. The growth rate of a dendrite barb

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