首页> 外文期刊>International journal of hydrogen energy >Kinetic analysis of gasification reaction of coke with CO2 or H2O
【24h】

Kinetic analysis of gasification reaction of coke with CO2 or H2O

机译:焦炭与CO2或H2O气化反应的动力学分析

获取原文
获取原文并翻译 | 示例
           

摘要

Using granular coke gasification reaction equipment and an unreacted core shrink model, this study examined the gasification reaction and conducted kinetic analysis of coke under CO2 and H2O atmospheres. Results show that in CO2 or H2O, solution loss rate increases with increasing temperature. The reaction rate of coke with H2O is approximately two to four times faster than that with CO2 at the same temperature. From 1173 K to 1373 K, the apparent activation energies of the gasification reaction of coke with CO2 and H2O are 143.33 kJ mol(-1) and 104.53 kJ mol(-1), respectively. The internal diffusion resistance in H2O was far below that in CO2, demonstrating that the gasification reaction rate between H2O and coke was quicker. In CO2 at low temperatures (<= 1273 K), coke gasification was controlled by interfacial reaction during the early stage, interfacial reaction and gas diffusion in the middle stage, and gas diffusion in the final stage. At high temperatures (>1273 K), gasification was controlled by interfacial reaction. However, coke gasification in H2O at low temperatures (1173 K) was controlled by interfacial reaction during the early stage, and was under mixed control by interfacial reaction and gas diffusion during the final stage. At high temperatures (>= 1223 K), gasification was controlled by interfacial reaction. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:本研究使用粒状焦气化反应设备和未反应的堆芯收缩模型,研究了气化反应并在CO2和H2O气氛下进行了焦炭的动力学分析。结果表明,在CO2或H2O中,溶液损失率随温度升高而增加。在相同温度下,焦炭与H2O的反应速率比与CO2的反应速率快约2-4倍。从1173 K到1373 K,焦炭与CO2和H2O的气化反应的表观活化能分别为143.33 kJ mol(-1)和104.53 kJ mol(-1)。 H2O中的内部扩散阻力远低于CO2中的内部扩散阻力,表明H2O和焦炭之间的气化反应速率更快。在低温(<= 1273 K)的CO2中,焦炭的气化受早期阶段的界面反应,中间阶段的界面反应和气体扩散以及最终阶段的气体扩散控制。在高温(> 1273 K)下,通过界面反应控制气化。然而,在低温(1173 K)下,H2O中的焦炭气化在早期受到界面反应的控制,在最后阶段受到界面反应和气体扩散的混合控制。在高温(> = 1223 K)下,通过界面反应控制气化。 Hydrogen Energy Publications,LLC版权所有(C)2015。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2015年第39期|13306-13313|共8页
  • 作者单位

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China|Anhui Univ Technol, Maanshan 243002, Anhui, Peoples R China;

    Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China|Qingdao Iron & Steel Grp, Qingdao 266043, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Coke; Gasification reaction; Kinetic; Pore structure;

    机译:焦炭气化反应动力学孔结构;

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