+Advanced Search
Low Temperature Preparation of ZrB2-SiC Composite Powders by a Combined Molten Salt and Carbothermal/magnesium Reduction Method
DOI:
Author:
Affiliation:

The State Key Laboratory of Refractories and Metallurgy,,The State Key Laboratory of Refractories and Metallurgy

Clc Number:

Fund Project:

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    ZrB2-SiC composite powders were prepared in NaCl-KCl flux using zirconium, silica, boron oxide as main raw materials, magnesium powder as reducing agent by a combined molten salt and carbothermal/magnesium reduction method. The phase compositions of the resulted powders were investigated by X-ray diffraction. The influences of molar ratio of Zr/Si, content of activated carbon, silica and boron oxide on the phase composition and contents of the crystalline phase of ZrB2-SiC composite powders were investigated. The results show that high purity ZrB2-SiC composite powders can be synthesized with the molar ratio of n(Zr)/n(Si) is 1 and the amount of activated carbon, silica and boron oxide was respectively 120 mol%, 120 mol% and 150 mol% in NaCl-KCl flux with the molar ratio of n(NaCl)/n(KCl) is 1 at 1 200 ℃ for 2 h, and the amount of ZrB2 and SiC was calculated as 59 wt% and 35 wt% in the prepared powders. FE-SEM results show that there exits aggregation in the final powders with the particle size of about 0.5μm. Compared with the conventional carbothermal/magnesium reduction method, the synthesis temperature of ZrB2-SiC composite powders was reduced about 200 ℃ in the present work.

    Reference
    Related
    Cited by
Get Citation

[Li Faliang, Li Wen, Zhang Haijun. Low Temperature Preparation of ZrB2-SiC Composite Powders by a Combined Molten Salt and Carbothermal/magnesium Reduction Method[J]. Rare Metal Materials and Engineering,2018,47(S1):185~189.]
DOI:[doi]

Copy
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:June 18,2017
  • Revised:June 18,2017
  • Adopted:January 29,2018
  • Online: October 22,2018
  • Published: