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Sintering technology of Ti(C, N) base cermets

机译:Ti(C,N)基金属陶瓷的烧结技术

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The variations of chemical compositions, phases, microstructure evolution and shrinking of cermets compact debinded in H2 or in vacuum and sintered subsequently in vacuum were studied systematically using chemical analysis, back scattering scanning electron microscopy (SEM), and X-ray diffractometry (XRD). The total carbon of cermets debinded in H2 is lower than that debinded in vacuum by 0.4%-0.5%. The contents of carbon and oxygen are decreased sharply when being sintered at 1 100-1 300 °C. The decomposition reaction of nitrogen is conducted sharply at 1 300 °C. However, the decomposition of nitrogen is inhibited while the liquid phase appears, and then begins again above 1 500 °C. The solution reaction of TaC and Mo2C into ring phase starts at 1 200 °C, and WC into ring phase at 1 300 °C is finished. Therefore, the heating rate during sintering of cermets between 900 °C and 1 350 °C is important.
机译:使用化学分析,系统地研究了化学组成,阶段,在真空中逐渐变得紧凑,然后在真空中烧结并在真空中烧结的变化,然后用化学分析研究,后散射扫描电子显微镜(SEM)和X射线衍射法(XRD) 。 CERMETS在H 2中逐渐变化的总碳低于真空逐渐变慢0.4%-0.5%。当在1 100-100℃下烧结时,碳和氧的含量急剧下降。氮的分解反应在100℃下急剧进行。然而,在出现液相的同时抑制氮的分解,然后再次高于1 500℃。将TAC和MO2C转化为环相的溶液反应在1±200℃下开始,并完成100℃的环相。因此,在900℃和1 350℃之间烧结金属陶瓷期间的加热速率是重要的。

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