期刊文献+

原位合成含钛陶瓷相增强Fe基合金熔覆层研究 被引量:1

Fe-Based Alloy Clad Coatings Reinforced by in Situ Synthesized Ceramic Phases Containing Titanium
原文传递
导出
摘要 以Fe901、Ti、B_4C和h-BN粉为原料,采用反应等离子熔覆方法在Q235钢基本上原位合成了含钛陶瓷相增强Fe基合金熔覆层。研究表明:相比B_4C,Fe更易与h-BN反应形成铁硼化物,当同时添加B_4C和h-BN时,B_4C/h-BN比减小至一定值后将导致熔覆层中Fe B含量升高和Ti_2N、Ti B等中间产物形成,但却可抑制陶瓷相长大。熔覆层显微组织均具有梯度分布特征,Ti B_2大小和形态受熔池温度和成分影响。熔覆层显微硬度随h-BN添加量增加而降低,Ti:B_4C:BN摩尔比为3:1:0时熔覆层近表面层HV_(0.2)显微硬度可高达11.26 GPa。 The Fe-based alloy coatings reinforced with in situ synthesized ceramic phases containing titanium were prepared on Q235 steel by a reactive plasma cladding process using Fe901, Ti, B4C and h-BN powders as raw materials. The results show that Fe is apt to react with h-BN to produce Fe B comparing with B4C. When both of B4C and h-BN are added as reactants, the B4C/h-BN ratio decreases to a certain value; as a result, the content of FeB increases and the Ti2N and Ti B intermediates occur in the coatings. However, it can depress the growth of ceramic phases. The microstructure of the clad coatings exhibits an obvious gradient distribution along the depth direction. The size and morphology of TiB2 change with the temperature and composition of the molten pool. Increasing h-BN amount results in the decrease of microhardness of the coatings. The high HV0.2 microhardness value 11.26 GPa can be achieved in the layer near the surface for the coating at Ti:B4C:h-BN=3:1:0.
出处 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2016年第9期2342-2346,共5页 Rare Metal Materials and Engineering
基金 江苏省自然科学基金(BK2011250) 江苏省博士后科学基金(1101017C) 中国博士后科学基金(20100481079)
关键词 Fe基合金涂层 等离子熔覆 原位合成 TiB2-TiC TiB2-TiN Fe-based alloy coating plasma cladding in situ synthesis TiB2-TiC TiB2-TiN
  • 相关文献

参考文献15

  • 1Liu J, Wang L, Li H. ApplSurfSci[J], 2009, 255:4921.
  • 2Chen D, Liu D, Liu Yet al. Surf Coat Technol[J], 2014, 239: 28.
  • 3刘均波,王立梅,黄继华.反应等离子熔覆(Cr,Fe)_7C_3/γ-Fe金属陶瓷复合材料涂层的耐磨性[J].北京科技大学学报,2007,29(1):50-54. 被引量:9
  • 4Li H, Li G; Wang H et al. MaterDes[J], 2011, 32:3004.
  • 5吴玉萍,彭竹琴,林萍华.等离子原位合成TiC颗粒增强Ni基复合涂层[J].材料科学与工艺,2004,12(4):429-432. 被引量:22
  • 6Zhang L, Sun D, Yu H. Mater Sci EngA[J], 2008, 490:57.
  • 7Wang X, Shun H, Li C et al. Surf Coat Technol[J], 2006, 201: 2500.
  • 8Wu Yuping, Lin Pinghua, Wang Zehua. Trans Nonferrous Met Soc China[J], 2004, 14(8): 1335.
  • 9Li M, Huang J, Zhu Y et al. Surf Coat Technol[J], 2012, 206: 4021.
  • 10Wang Zhenting, Zhou Xiaohui, Zhao Guogang. Trans Nonfer- rous Met Soc China[J], 2008, 18(4): 831.

二级参考文献18

  • 1SHANGGUANG D,AHUJA S, et al. An analytical model for the interaction between particle and advacing solid\liquid interface[ J ]. Metal Trans,1992,32A :669 -680.
  • 2HITOSHI H, TAKASHI I, SHIGEHARU K, et al.Fabrication of NiTi intermetallic compound coating made by laser plasma hybrid spraying of mechanically alloyed powders [J]. Surface and Coatings Technology,2001,139:93 - 100.
  • 3BRICE J C. The Growth of Crystals from Liquids[ M].Amsterdam: North - Holland, 1977.
  • 4DING X Y,FAN P, WANG W Z. Thermodynamic calculation for alloy systems [ J ]. Metallurgical and Materials Transactions, 1999,30B (4) :271 - 277.
  • 5ZHAO C,TIAN F, Hongrui PENG H R, et al. Nontransferred arc plasma cladding of Stellite Ni60 alloy on steel[J]. Surface and Coatings Technology, 2002,155:80 - 84.
  • 6YAN M, ZHU W Z. Surface remelting of Ni -Cr- B -Si cladding with a micro-beam plasma arc [J]. Surface and Coating Technology, 1997, 92:157 - 163.
  • 7PEI Y T, ZUO T C. Gradient microstructure in laser clad TiC - reinforce Ni-alloy composite coating [J]. Materials Science and Engineering,1998 ,A241 ( 1 -2) :259 -263.
  • 8NUKAMI T, FLEMINGS M C. In situ synthesis of TiC particulate reinforced aluminum matrix composites [J].Metal Mater Trans, 1995,26A (7): 1877 - 1884.
  • 9MITRA R,FINE M E,WEERTMAN J R. Chemical reaction strengthening of Al/TiC MMCs by isothermal heat treatment at 913K[J].J Mater Res,1993,8(9) :2370-2379.
  • 10La P Q,Xue Q J,Liu W M.Effects of boron doping on tribological properties of Ni3A1-Cr7C3 coatings under dry sliding.Wear,2001,249:93

共引文献28

同被引文献9

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部