2 to 3 h. A dissolution-precipitation mechanism of synthesis of TiC by MSS was established based on these observed results."/>

最新色国产精品精品视频,中文字幕日韩一区二区不卡,亚洲有码转帖,夜夜躁日日躁狠狠久久av,中国凸偷窥xxxx自由视频

+Advanced Search
Synthesis of stoichiometric titanium carbide by a combination of carbothermal reduction and the molten salt method and its characterization
DOI:
Author:
Affiliation:

The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology,,,,

Clc Number:

Fund Project:

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

    This paper presents a novel method of preparing stoichiometric titanium carbide (TiC) powders by combining carbothermal reduction and molten salt synthesis (MSS) from raw starting materials of titanium oxide (anatase), C (carbon black), and sodium chloride. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), laser particle size analysis, energy spectrum analysis (EDS), and thermodynamic analysis were used to characterize the powders. The effects of heating temperatures and molar ratios of titania to carbon black on the preparation of TiC are discussed. Results showed that the use of MSS to reduce the synthesis temperatures of both stoichiometric and pure TiC from 1700°C to 1550°C and the time required for synthesis decreased from 10 h for conventional carbothermal reduction of TiO2 to 3 h. A dissolution-precipitation mechanism of synthesis of TiC by MSS was established based on these observed results.

    Reference
    Related
    Cited by
Get Citation

[SongYunfei, Zhu Hongxi, Deng Chengji, Yuan Wenjie, Ding Jun. Synthesis of stoichiometric titanium carbide by a combination of carbothermal reduction and the molten salt method and its characterization[J]. Rare Metal Materials and Engineering,2018,47(4):1082~1088.]
DOI:[doi]

Copy
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:May 09,2016
  • Revised:August 15,2016
  • Adopted:October 18,2016
  • Online: May 31,2018
  • Published: