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Influence of Brazing Process on the Microstructure and Wear Resistance of Diamond Composite Coating on TC4
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1.State Key Laboratory of Advanced Brazing Filler Metals and Technology, China Academy of Machinery Zhengzhou Research Institute of Mechanical Engineering Co., Ltd, Zhengzhou 450001, China;2.Ningbo Intelligent Machine Tool Research Institute Co., Ltd. of China National Machinery Institute Group, Ningbo 315709, China;3.University of Science and Technology Beijing, Beijing 100083, China

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TG425

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    Abstract:

    In order to improve the surface wear resistance of titanium alloys, TC4 (Ti-6Al-4V) was selected as the matrix material, and diamond particles (20%, mass fraction) and CuTi alloy powder (10%, mass fractions) were added to Al-12Si filler metal. The diamond composite wear-resistant brazing coating on TC4 surface was prepared by induction brazing under argon protection. The effects of particle size of CuTi alloy, brazing temperature, and isothermal reaction time on the microstructure and wear resistance of composite coatings were studied. The results indicate that the composite coating is mainly composed of α-Al, Ti(Al1-xSix)3, CuAl2, and diamond particles. Reducing the particle size of CuTi alloy powder and increasing the brazing temperature can promote its full reaction with the brazing alloy. With the increase in temperature and insulation time, the CuAl2 phase at the grain boundary between α-Al and Ti(Al1-xSix)3 gradually disperses, improving the hardness of the brazing alloy coating. However, excessive insulation can cause the CuAl2 phase to start growing and to overlap with each other to form a coarse network structure, resulting in a significant increase in brittleness and a decrease in wear resistance of the brazed coating alloy.

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[Sun Huawei, Liu Pan, Zhang Lei, Qin Jian, Zhu Hongtao, Jing Peiyao. Influence of Brazing Process on the Microstructure and Wear Resistance of Diamond Composite Coating on TC4[J]. Rare Metal Materials and Engineering,2025,54(2):481~489.]
DOI:10.12442/j. issn.1002-185X.20240426

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History
  • Received:July 14,2024
  • Revised:December 18,2024
  • Adopted:December 19,2024
  • Online: February 25,2025
  • Published: February 20,2025