4.7 Review

Oxidation of ultra-high temperature transition metal diboride ceramics

期刊

INTERNATIONAL MATERIALS REVIEWS
卷 57, 期 1, 页码 61-72

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1179/1743280411Y.0000000012

关键词

Zirconium diboride; Hafnium diboride; Oxidation; Review

资金

  1. UHTCs at Missouri University of Science and Technology
  2. US Air Force Office of Scientific Research/NASA National Hypersonic Science Center for Materials and Structures [FA9550-09-10477]
  3. US National Science Foundation [DMR-0906584]
  4. US Air Force Office of Scientific Research [FA9550-09-1-0168]
  5. Direct For Mathematical & Physical Scien
  6. Division Of Materials Research [0906584] Funding Source: National Science Foundation

向作者/读者索取更多资源

The oxidation behaviour of transition metal diboride ceramics is reviewed with emphasis on the performance of zirconium diboride and hafnium diboride. First, the oxidation behaviour of nominally pure diborides is discussed, focusing on the transition to linear mass gain kinetics at temperatures above similar to 1100 degrees C. Next, the use of SiC and other additives that produce silica based scales when oxidised is reviewed. These additives improve oxidation protection due to the formation/stability of the outer layer of borosilicate glass that acts as a barrier to diffusion of oxygen to the substrate. However, elevated temperatures (>1650 degrees C) and/or the combination of aerodynamic flow, high heat flux and reactive atmosphere associated with hypersonic flight destabilises the outer oxide and decreases oxidation protection. Other additives that affect the composition and structure of the crystalline oxide scale without forming an outer glassy layer are a promising approach to improving oxidation behaviour of diborides. These additives require further research to understand the mechanisms of improved protection and further optimise the protective behaviour. While the oxidation of ultra-high temperature diborides has been studied for many years, several possible areas for future research are identified.

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