Enhanced densification of ultrafine Ti(C, N)-based cermets based on grain-growth induced liquid-phase pore filling mechanism

被引:6
|
作者
Zhou, Sheng-Jian [1 ,2 ]
Ouyang, Jia-Hu [1 ,2 ]
Yu, Yong-Bo [1 ]
Wang, Yu-Jin [1 ,2 ]
Chen, Lei [1 ,2 ]
Liu, Zhan-Guo [1 ]
Zhou, Yu [1 ]
机构
[1] Harbin Inst Technol, Inst Adv Ceram, Sch Mat Sci & Engn, Harbin 150001, Peoples R China
[2] Jilin Changyu Adv Mat Co Ltd, Changchun 130000, Peoples R China
基金
中国国家自然科学基金;
关键词
Ti(C; N)-based cermets; Liquid phase sintering; Densification behavior; Pore-filling theory; Cutting tools; SINTERED WC-CO; TI(C; N)-BASED CERMETS; CEMENTED CARBIDE; POWDER SIZE; MICROSTRUCTURE; BEHAVIOR; PRECIPITATION; TEMPERATURE; ADDITIONS; SUPPORT;
D O I
10.1016/j.jallcom.2024.174141
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The composition complexity of Ti(C, N)-based cermets poses a great challenge to the controllability of their sintering process. The effects of both refractory TaC addition and original particle size of starting materials on densification behavior and microstructural evolution of Ti(C, N)-based cermets were investigated during liquid phase sintering. The particle rearrangement only plays a very limited role in promoting densification of Ti(C, N)based cermets at the initial stage of liquid phase sintering, whereas the pore-filling in the presence of liquid phase becomes a dominant densification mechanism in the middle stage or even earlier. Enhanced densification of ultrafine Ti(C, N)-based cermets is realized by introducing refractory TaC additive based on the grain growthinduced liquid phase pore-filling mechanism, which is also verified by an extended study using other refractory carbide additives such as NbC, ZrC and HfC. This work provides a novel idea for the development of fully densified ultrafine Ti(C, N)-based cermets with outstanding mechanical properties, which are highlighted in machining applications of difficult-to-machine materials as well as other wear-resistant parts operating in hightemperature and high-stress environments.
引用
收藏
页数:14
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