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MoSi2和(Mo,W)Si2涂层的宽温域氧化过程

  • 毛绍宝 杨英 李海庆 张世宏
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  • 1. 安徽工业大学材料科学与工程学院,安徽 马鞍山 243002 2. 安徽工业大学现代表界面工程研究中心,安徽 马鞍山 243002 3. 中国运载火箭技术研究院航天材料及工艺研究所,北京 100076

收稿日期: 2018-11-10

  修回日期: 2019-01-18

  网络出版日期: 2019-08-15

基金资助

自修复硅氧烷/NiAl-NiCr-Cr3C2多层梯度复合涂层结构调控及荷温耦合作用失效机理研究

Oxidation processes of MoSi2 and (Mo,W)Si2 coatings in wide temperature range

  • Shaobao MAO Ying YANG Haiqing LI Shihong ZHANG
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  • 1. School of Material Science and Engineering, Anhui University of Technology, Ma?anshan, Anhui 243002, China 2. Research Center of Modern Surface and Interface Engineering, Anhui University of Technology, Ma?anshan, Anhui 243002, China 3. Aerospace Research Institute of Materials & Processing Technology, China Academy of Launch Vehicle Technology, Beijing 100076, China

Received date: 2018-11-10

  Revised date: 2019-01-18

  Online published: 2019-08-15

Supported by

Structural modulation and influencing mechanism of both load and temperature of self-repairing silicone/NiAl-NiCr-Cr3C2 multilayer gradient composite coatings

摘要

采用包渗法在Mo及Mo?W基体上分别制备MoSi2及(Mo,W)Si2涂层,研究了W掺杂对MoSi2涂层抗氧化性能的影响规律和作用机理。结果表明,W元素固溶到MoSi2涂层中,形成(Mo,W)Si2固溶体,涂层微观结构更加致密化。在1600℃高温下静态氧化,(Mo,W)Si2涂层抗氧化失效时间长达70 h,1200℃下氧化1000 h仍具有良好的防护性能,抗氧化性能大幅提升。加入W元素阻碍了Si元素与基体间的扩散反应,降低了涂层中Si元素的消耗速率,显著增强了(Mo,W)Si2涂层抗高温氧化性能。在500℃低温下静态氧化50 h,与MoSi2涂层相比,(Mo,W)Si2涂层氧化产生明显的“Pest”现象,涂层严重粉化失效。加入W元素降低了涂层中Si元素的扩散速率,导致低温下涂层表面无法形成致密氧化层,加剧涂层的快速氧化。

本文引用格式

毛绍宝 杨英 李海庆 张世宏 . MoSi2和(Mo,W)Si2涂层的宽温域氧化过程[J]. 过程工程学报, 2019 , 19(4) : 826 -835 . DOI: 10.12034/j.issn.1009-606X.218310

Abstract

MoSi2 and (Mo,W)Si2 coatings were prepared on Mo and Mo?W substrates respectively by means of pack cementation, and the effects and mechanisms of W element doping on the oxidation resistances of MoSi2 coating were investigated systematically. XRD, SEM and EDS were used to determine the phase structure, morphology and composition of the coatings. The results showed that W element was dissolved in MoSi2 coating in the form of (Mo,W)Si2 solid solution, and the microstructure of (Mo,W)Si2 coating was denser compared with that of MoSi2 coating as a result of W element doping. After static oxidation at 1600℃, the antioxidant life of (Mo,W)Si2 coating reached 70 h, while MoSi2 coating was failed after 25 h oxidation due to severe weight loss. Moreover, (Mo,W)Si2 coating exhibited excellent high-temperature protection performance after oxidation at 1200℃ for 1000 h. At the initial stage of the oxidation, the oxidation rate of (Mo,W)Si2 coating was higher than that of MoSi2 coating owing to W element doping, which led to lower formation velocity of dense oxide layer on the surface of (Mo,W)Si2 coating. After the dense SiO2 covering the surface completely, the oxidation rate of (Mo,W)Si2 coating decreased dramatically. The diffusion reaction between the Si element and the substrate was hindered by the addition of W element, the consumption rate of Si element in the coating was reduced remarkably, and the high-temperature oxidation resistance of (Mo,W)Si2 coating was enhanced significantly. After static oxidation at 500℃, comparing with MoSi2 coating, (Mo,W)Si2 coating exhibited a typical “Pest” phenomenon after oxidation for 50 h, and the coating failed in the form of disintegration. The addition of W element reduced the diffusion rate of Si element in the coating, therefore, a dense oxide layer could not be formed on the coating surface at low-temperature, which caused the rapid oxidation of the coating.

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