摘要
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 ℃. The decomposition reaction of nitrogen is conducted sharply at 1 300 ℃. However, the decomposition of nitrogen is inhibited while the liquid phase appears, and then begins again above 1 500 ℃. The solution reaction of TaC and Mo2C into ring phase starts at 1 200 ℃, and WC into ring phase at 1 300 ℃ is finished. Therefore, the heating rate during sintering of cermets between 900 ℃ and 1 350 ℃ is important.
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 ℃. The decomposition reaction of nitrogen is conducted sharply at 1 300 ℃. However, the decomposition of nitrogen is inhibited while the liquid phase appears, and then begins again above 1 500 ℃. The solution reaction of TaC and Mo2C into ring phase starts at 1 200 ℃, and WC into ring phase at 1 300 ℃ is finished. Therefore, the heating rate during sintering of cermets between 900 ℃ and 1 350 ℃ is important.
出处
《中国有色金属学会会刊：英文版》
CSCD
2009年第S3期696-700,共5页
Transactions of Nonferrous Metals Society of China
