Effect of 1.5TiC/1.5TiC+0.6 Ce2O3 addition on the oxidation behavior of WC-Cu-10Ni-5Mn-3Sn cemented carbides

被引:0
|
作者
Li, Xiulan [1 ]
Jiang, Xiao [1 ]
Zhou, Xinjun [1 ]
Li, Xuan [1 ]
Zhang, Xudong [1 ]
机构
[1] Sichuan Univ Sci & Engn, Fac Mech Engn, Yibin 644000, Peoples R China
来源
INTERNATIONAL JOURNAL OF REFRACTORY METALS & HARD MATERIALS | 2025年 / 126卷
关键词
WC; TiC; Pressureless melt infiltration; Oxidation; HIGH-TEMPERATURE OXIDATION; WC-CO; MECHANICAL-PROPERTIES; MICROSTRUCTURE; RESISTANCE; KINETICS; TUNGSTEN; METALS; NI;
D O I
10.1016/j.ijrmhm.2024.106957
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The oxidation experiments on WC-Cu-10Ni-5Mn-3Sn-1.5TiC and WC-Cu-10Ni-5Mn-3Sn-1.5TiC-0.6Ce2O3 materials were carried out for 2 h, 4 h, 6 h, 8 h, and 10 h in the temperature range of 500-800 degrees C, respectively, to elucidate the effects of oxidation temperatures and times on the properties of cemented carbides. The evolution laws of oxidation products and oxide layer microstructure of WC-Cu-10Ni-5Mn-3Sn-1.5TiC-0.6 Ce2O3 cemented carbide material with the change of temperature and time were mainly investigated. The oxidation behavior and oxidation mechanism were analyzed in combination with the oxidation kinetics and thermodynamics of the formation of oxidation products. The results revealed that the addition of Ce2O3 improved the oxidation resistance of the cemented carbide material at 500-800 degrees C after 2-10 h of heat treatment. With the increase of oxidation temperature or the prolongation of oxidation time at the same temperature, the oxidation resistance of the cemented carbide material decreased. The cemented carbides were shown to withstand a long-term oxidation at 500 degrees C. However, the surface of the material was completely oxidized even after 2 h of oxidation at the temperature of 800 degrees C. The products of the interaction between O 2- and metal ions appeared in the following order: Cu2O, WO2, WO3 + Mn3O4 + MnO, CuO, W 18 O 49 , and Mn2O3 + MnO2. Moreover, the oxidation products of the same element changed from low to high valence. However, the high-valence oxidation was also reduced to a low-valence state in the complex oxidation process involving many elements. Meanwhile, the oxidation products with greater thermodynamic driving force were not detected in the oxide layer due to the influence of element diffusion, the ionization energy and the competition with O2 during the formation and growth of oxides.
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页数:15
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