首页> 外文期刊>材料とプロセス: 日本鉄鋼協会講演論文集 >Thermodynamic modeling of P2O5 containing oxide system for De-P process in steelmaking: Preliminary thermodynamic modeling results
【24h】

Thermodynamic modeling of P2O5 containing oxide system for De-P process in steelmaking: Preliminary thermodynamic modeling results

机译:炼钢De-P工艺含P2O5氧化物体系的热力学建模:初步热力学建模结果

获取原文
获取原文并翻译 | 示例
           

摘要

The CaO-FeO-Fe2O3-MgO-SiO2-P2O5 oxide system is a basic oxide system for the Basic Oxygen Furnace (BOF) process as well as the hot metal de-phosphorization process. Great amount of investigations on this oxide system are being carried out, particularly in Japan, to find out an advanced process route for P removal from molten iron. In the case of the BOF process, the utilization of a large liquid miscibility gap in the CaO-FeO-Fe2O3-P2O5 system is a new interesting route for the de-phosphorization of molten iron. As the Ca2SiO4 phase in the oxide system can dissolve a considerable amount of P2O5 under the steelmaking condition, it can enhance the de-phosphorization of molten iron during the hot metal pretreatment process. Since Fe has two valence states, Fe2+ and Fe3+, the phase equilibrium in the oxide system can vary strongly with oxygen partial pressures, which induces a difficulty in the phase diagram measurement.
机译:CaO-FeO-Fe2O3-MgO-SiO2-P2O5氧化物系统是用于碱性氧气炉(BOF)工艺以及铁水脱磷工艺的碱性氧化物系统。目前正在对这种氧化物体系进行大量研究,特别是在日本,以寻找从铁水中去除P的先进工艺路线。对于BOF工艺,在CaO-FeO-Fe2O3-P2O5系统中利用大的液体混溶性间隙是铁水脱磷的新途径。由于在炼钢条件下,氧化物体系中的Ca2SiO4相可以溶解大量P2O​​5,因此可以在铁水预处理过程中增强铁水的除磷效果。由于Fe具有Fe2 +和Fe3 +两个价态,因此氧化物体系中的相平衡会随着氧分压而发生很大变化,这会导致相图测量方面的困难。

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