首页> 外文期刊>ISIJ international >Activity Measurement of the CaS–MnS Sulfide Solid Solution and Thermodynamic Modeling of the CaO–MnO–Al2O3–CaS–MnS–Al2S3 System
【24h】

Activity Measurement of the CaS–MnS Sulfide Solid Solution and Thermodynamic Modeling of the CaO–MnO–Al2O3–CaS–MnS–Al2S3 System

机译:CaS–MnS硫化物固溶体的活性测定和CaO–MnO–Al 2 O 3 –CaS–MnS–Al 2 S 3 系统

获取原文
       

摘要

In order to provide a prediction tool for sulfide/oxide/oxysulfide inclusion evolution in Mn–Al steel with a Ca addition/CaO-based flux, a comprehensive thermodynamic database for the inclusion system composed of CaO–MnO–Al_(2)O_(3)–CaS–MnS–Al_(2)S_(3) was developed in the present study. Activity of MnS in a CaS–MnS sulfide solid solution was experimentally determined by employing a chemical equilibrium technique at 1400°C and 1500°C. The measured activity exhibits a positive deviation from an ideal behavior, which is in consistent with the known two-phase separation of the sulfide solid solution at lower temperature (T_(cr) = ~ 1200°C). Based on the activity and the phase diagram data available in literature, a thermodynamic modeling of the CaS–MnS system was carried out. The following excess Gibbs free energy of the CaS–MnS sulfide solid solution was obtained:Furthermore, using available thermodynamic modeling results for other constituent sub-systems, a larger thermodynamic database of the CaO–MnO–Al_(2)O_(3)–CaS–MnS–Al_(2)S_(3) system was developed. A Modified Quasichemical Model in the quadruplet approximation was used to model the Gibbs free energy of the oxysulfide liquid solution. Comparisons between the model calculation and available experimental data show good agreement. The developed thermodynamic model and the database were used to predict unexplored phase diagrams with various n _(Mn)/(n _(Ca) + n _(Mn)) ratio, and sulfide capacity of the CaO–MnO–Al_(2)O_(3) oxide liquid phase. The database can be used along with software for Gibbs free energy minimization in order to calculate any phase diagram section or thermodynamic property.
机译:为了提供一个基于钙添加量/基于CaO的助熔剂的Mn-Al钢中硫化物/氧化物/氧硫化物夹杂物演变的预测工具,由CaO-MnO-Al_(2)O_( 3)–CaS–MnS–Al_(2)S_(3)在本研究中得到了发展。 CaS–MnS硫化物固溶体中的MnS活性是通过采用化学平衡技术在1400°C和1500°C下实验确定的。测得的活性显示出与理想行为的正偏差,这与在较低温度(T_(cr)=〜1200°C)下硫化物固溶体的已知两相分离相一致。根据文献中的活性和相图数据,对CaS-MnS系统进行了热力学建模。获得了CaS–MnS硫化物固溶体的以下过量吉布斯自由能:此外,利用其他组成子系统的可用热力学建模结果,获得了较大的CaO–MnO–Al_(2)O_(3)–热力学数据库开发了CaS–MnS–Al_(2)S_(3)系统。使用四重近似中的改进的拟化学模型来建模氧硫化物液体溶液的吉布斯自由能。模型计算与可用实验数据之间的比较显示出很好的一致性。使用已开发的热力学模型和数据库来预测具有各种n _(Mn)/(n _(Ca)+ n _(Mn))比率和硫化物容量的未探索相图。 CaO–MnO–Al_(2)O_(3)氧化物液相。该数据库可与用于Gibbs自由能最小化的软件一起使用,以便计算任何相图截面或热力学性质。

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