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Characterization of phase transformation and microstructure of nano hard phase Ti(C,N)-based cermet by spark plasma sintering 被引量:4

Characterization of phase transformation and microstructure of nano hard phase Ti(C,N)-based cermet by spark plasma sintering
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摘要 By means of optical microscope , scanning electron microscope (SEM) and transmission electron microscope (TEM), the process of densification, the characterization of phase transformation and the microstructure for spark plasma sintering (SPS) nano hard phase Ti(C,N)-based cermet were investigated. It is found that the spark plasma sintering (SPS) enables the nano hard phase Ti(C,N)-based cermet to densify rapidly, however, the full densification of the sintered samples can not be obtained. The rate of phase transformation is significantly quick. When being sintered at 1 200 ℃ for 8 min, Mo2C is completely dissolved, and TiN dissolves into TiC entirely and disappears. Above 1 200 ℃, Ti(C,N) begins to decompose and the atoms of C and N separate from Ti(C,N) resulting in the generation of N2 and the graphite. Due to the denitrification and the graphitization, the density and the hardness of sintered samples are rather low. The distribution of grain size of the sample sintered at 1 350 ℃ covers a wide range of 90500 nm, and most of the grain size are about 200 nm. The hard phase is not of typical core-rim structure. Oxides on the surface of particles can not be fully removed and present in sample as titanium oxide TiO2. Graphite exists in band-like shape. By means of optical microscope , scanning electron microscope (SEM) and transmission electron microscope (TEM), the process of densification, the characterization of phase transformation and the microstructure for spark plasma sintering (SPS) nano hard phase Ti(C,N)-based cermet were investigated. It is found that the spark plasma sintering (SPS) enables the nano hard phase Ti(C,N)-based cermet to densify rapidly, however, the full densification of the sintered samples can not be obtained. The rate of phase transformation is significantly quick. When being sintered at 1 200 ℃ for 8 min, Mo_2C is completely dissolved, and TiN dissolves into TiC entirely and disappears. Above 1 200 ℃, Ti(C,N) begins to decompose and the atoms of C and N separate from Ti(C,N) resulting in the generation of N_2 and the graphite. Due to the denitrification and the graphitization, the density and the hardness of sintered samples are rather low. The distribution of grain size of the sample sintered at 1 350 ℃ covers a wide range of 90500 nm, and most of the grain size are about 200 nm. The hard phase is not of typical core-rim structure. Oxides on the surface of particles can not be fully removed and present in sample as titanium oxide TiO_2. Graphite exists in band-like shape.
出处 《中国有色金属学会会刊:英文版》 CSCD 2004年第3期510-515,共6页 Transactions of Nonferrous Metals Society of China
基金 Project(5 0 0 740 17)supportedbytheNationalNaturalScienceFoundationofChina ProjectsupportedbytheStateKeyLabo ratoryofAdvancedTechnologyforMaterialsSynthesisandProcessingofWuhanUniversityofTechnology ,China
关键词 火花等离子烧结 金属陶瓷 粉末冶金 相变 显微结构 硬质相 TEM SPS 纳米相 Ti(C,N)-based cermet nano phase spark plasma sintering phase transformation microstructure
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  • 1郑勇,赵兴中,胡镇华,崔崑.Ti(C,N)基金属陶瓷烧结过程中的相变[J].硬质合金,1995,12(4):203-206. 被引量:12
  • 2熊惟皓.华中理工大学博士学位论文[M].,1994,7..
  • 3郑勇.华中理工大学硕士学位论文[M].,1993,4..
  • 4熊惟皓,博士学位论文,1994年
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