首页> 外文期刊>Vacuum: Technology Applications & Ion Physics: The International Journal & Abstracting Service for Vacuum Science & Technology >Thermodynamic analysis and experimental rules of vacuum decomposition of molybdenite concentrate
【24h】

Thermodynamic analysis and experimental rules of vacuum decomposition of molybdenite concentrate

机译:辉钼矿精矿真空分解的热力学分析和实验规律

获取原文
获取原文并翻译 | 示例
           

摘要

Vacuum decomposition process of molybdenite concentrate was investigated under pressure of 5-35 Pa for 15-120 min at the temperature range 1473 K-1973 K. The theoretical and experimental results showed that Gibbs free energy of vacuum decomposition reactions and evaporation rate of pure sulfur provided the theoretical calculation basis for temperature and heat preservation time selection in vacuum decomposition experiments of molybdenite concentrate. Melting points and saturated vapor pressures of pure substances and compounds predicted the evaporation behavior of impurity elements and its compounds during the experimental process. Both Cu and Fe could partly evaporate into condensate and Cu had better evaporation ability than Fe. MoO3 could easily and Al2O3, SiO2 could partly evaporate into the condensate. Kilo-scale experiment was performed based on the small experiments and its results showed that the Mo content of molybdenum metal product was 92.38% and the S content of sulfur product was 96.28%, and the molybdenum recovery rate reached to 95.94%. Both the theoretical and experimental results proved that it was feasible to produce crude molybdenum and sulfur from molybdenite concentrate through vacuum decomposition. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在1473 K-1973 K的温度范围内,在5-35 Pa的压力下,对辉钼矿精矿的真空分解过程进行了15-120分钟的研究。理论和实验结果表明,吉布斯真空分解反应的自由能和纯硫的蒸发速率为辉钼矿精矿真空分解实验中温度和保温时间的选择提供了理论计算依据。纯物质和化合物的熔点和饱和蒸气压预测了实验过程中杂质元素及其化合物的蒸发行为。 Cu和Fe都可以部分蒸发成冷凝物,并且Cu具有比Fe更好的蒸发能力。 MoO3很容易蒸发,而Al2O3,SiO2可能会部分蒸发到冷凝物中。在小实验的基础上进行了公斤级试验,结果表明,金属钼产品的钼含量为92.38%,硫产品的硫含量为96.28%,钼的回收率达到95.94%。理论和实验结果均证明,通过减压分解由辉钼矿精矿生产粗钼和硫是可行的。 (C)2015 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号