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Thixoforming : Semi-solid Metal Processing

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3.4 Structural Parameter Development and Material Selectionj71<br />

are still connected to each other (black areas), whereas they exist isolated at a lower<br />

threshold of 200 (light green and blue areas). The difference of the measured <strong>solid</strong>phase<br />

fraction in the depicted image is about 5%, whereas the influence on the<br />

average grain size (Ddm ¼ 20 mm) and the contiguity of the <strong>solid</strong> phase (DCf ¼ 0.1) is<br />

considerably larger. Even at a threshold of 200, globulites are still connected to each<br />

other (yellow areas), which are regarded as separate particles by the automatic image<br />

recognition and have to be corrected by hand according to the experiences of the<br />

metallographer.<br />

It can be noted that the structural parameters of X210CrW12 samples quenched<br />

from the three-phase area (austenite–carbide–cast) can be determined allowing for<br />

diverse factors of influence, because the austenite can be distinguished relatively<br />

clearly from the eutectic. It cannot be ruled out that the globulites grow marginally<br />

during quenching and that, therefore, higher <strong>solid</strong>-phase contents are measured.<br />

However, this effect is overridden by the systematic errors during structure detection.<br />

A metallographic determination of the carbide content is not possible because the<br />

carbides occur mostly at the phase boundaries and cannot be differentiated from the<br />

quenched eutectic. In the determination of the structural parameters, the most<br />

important factors of influence are the thresholds set by the user for the detection of<br />

the different phases and the minimal particle size (number of pixels) for the<br />

consideration of a particle. The minimum number of pixels for the consideration<br />

of a particle can be discounted if the existing eutectic is very fine. In addition to the<br />

evaluation-specific inaccuracy, the determined liquid phase content is also dependent<br />

on the particular observed sample area. Therefore, the deviation of different images<br />

of the same sample can vary widely, which is also depicted by the dispersion bars in<br />

Figure 3.15.<br />

3.4.1.2 <strong>Metal</strong>lographic Analysis of Quenched Specimens from the Two-Phase Area<br />

Representative structural images of the quenched samples and the determined<br />

liquid-phase contents of the quenching experiments above the three-phase area are<br />

summarized in Figure 3.20. The structural images show that above a temperature of<br />

1300 C secondary austenite accumulates at some austenite particles and protuberance<br />

formation occurs. Furthermore, at this temperature the development of fine,<br />

secondary austenite (highlighted by arrows) starts in large liquid-phase areas. At a<br />

temperature of 1325 C, coarse, secondary austenite is increasingly formed. If the<br />

primary austenite grains lie close to each, other the secondary austenite adheres to the<br />

large primary grains. If the diffusion paths become long enough in larger liquidphase<br />

areas, the coarse secondary austenite exists isolated in the dark matrix and only<br />

adheres to the large austenite grains in the boundary areas. This phenomenon<br />

intensifies with rising temperature, so that a sharp boundary between primary and<br />

secondary austenite can no longer be drawn, which becomes apparent from the<br />

quenched sample of 1350 C. At temperatures of up to about 1325 C, the protuberance-formed<br />

accumulating austenite and the fine secondary austenite isolated in<br />

the liquid can be considered without large errors and disposed of during image<br />

re-editing. At higher temperatures, the distinction is no longer possible, because on<br />

the one hand the eutectic coarsens with increasing temperature and on the other the

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