Synthesis of tungsten carbide nanopowders by direct carbonization of tungsten oxide and carbon: Effects of tungsten oxide source on phase structure and morphology evolution

被引:24
作者
Wu, Haoyang [1 ]
Wang, Qianyu [1 ]
Qin, Mingli [1 ,2 ]
Yin, Ruowei [1 ]
Zhang, Ziyue [1 ]
Jia, Baorui [1 ]
Qu, Xuanhui [1 ,2 ]
机构
[1] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing 100083, Peoples R China
[2] Univ Sci & Technol Beijing, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China
关键词
Tungsten carbide; Nanopowder synthesis; Tungsten oxide source; Carbothermal reduction; Morphology; CO COMPOSITE POWDER; NANO-WC; REDUCTION; CARBURIZATION; ULTRAFINE; TRIOXIDE; COBALT; ROUTE;
D O I
10.1016/j.ceramint.2019.12.118
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In the paper, WC nanopowders are successfully prepared by carbothermal reduction method, and the effect of tungsten oxide source on the phase structure evolution and products properties of the as-synthesized WC nanopowders has been investigated. Four tungsten oxide powders are chosen as tungsten oxide sources, e.g., rods-like WO3, WO3 nanopartiles, WO3 micro-particles and WO2.9 micro-particles. Compared with other three tungsten oxide sources, the WO3 micro-particles possesses small particle size, less agglomerates and good dispersity and the uniform tungsten oxide-carbon mixture after ball milling can be easily obtained. The appropriate tungsten oxide source can result in lower processing temperature (<= 1200 degrees C) and shorter holding time (<= 3 h). Single-phase WC powders with average particle size of 100 nm and uniform particle distribution can be achieved by micro-particle-like WO3 at 1100 degrees C for 3 h. The as-prepared WC products by other three tungsten oxide sources exhibit problems of more aggregates, non-uniform particle size and large particle size (250 nm), respectively. In addition, the method can provide a facile, low-cost, efficient, and industrially feasible pathway for large scale preparation of WC nanopowders.
引用
收藏
页码:8787 / 8795
页数:9
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