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Research Article | Open Access

Preparation of ZrB2-MoSi2 high oxygen resistant coating using nonequilibrium state powders by self-propagating high-temperature synthesis

Menglin ZHANGXuanru REN( )Mingcheng ZHANGSongsong WANGLi WANGQingqing YANGHongao CHUPeizhong FENG( )
School of Materials and Physics, China University of Mining and Technology, Xuzhou 221116, China
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Abstract

To achieve high oxygen blocking structure of the ZrB2-MoSi2 coating applied on carbon structural material, ZrB2-MoSi2 coating was prepared by spark plasma sintering (SPS) method utilizing ZrB2-MoSi2 composite powders synthesized by self-propagating high-temperature synthesis (SHS) technique as raw materials. The oxygen blocking mechanism of the ZrB2-MoSi2 coatings at 1973 K was investigated. Compared with commercial powders, the coatings prepared by SHS powders exhibited superior density and inferior oxidation activity, which significantly heightened the structural oxygen blocking ability of the coatings in the active oxidation stage, thus characterizing higher oxidation protection efficiency. The rise of MoSi2 content facilitated the dispersion of transition metal oxide nanocrystals (5-20 nm) in the SiO2 glass layer and conduced to the increasing viscosity, thus strengthening the inerting impact of the compound glass layer in the inert oxidation stage. Nevertheless, the ZrB2-40 vol%MoSi2 coating sample prepared by SHS powders presented the lowest oxygen permeability of 0.3% and carbon loss rate of 0.29×10-6 g·cm-2·s-1. Owing to the gradient oxygen partial pressure inside the coatings, the Si-depleted layer was developed under the compound glass layer, which brought about acute oxygen erosion.

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Journal of Advanced Ceramics
Pages 1011-1024

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Cite this article:
ZHANG M, REN X, ZHANG M, et al. Preparation of ZrB2-MoSi2 high oxygen resistant coating using nonequilibrium state powders by self-propagating high-temperature synthesis. Journal of Advanced Ceramics, 2021, 10(5): 1011-1024. https://doi.org/10.1007/s40145-021-0485-y

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Received: 30 January 2020
Revised: 31 March 2021
Accepted: 16 April 2021
Published: 15 September 2021
© The Author(s) 2021

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