首页> 外文期刊>Journal of Cleaner Production >Simultaneous magnesia regeneration and sulfur dioxide generation in magnesium-based flue gas desulfurization process
【24h】

Simultaneous magnesia regeneration and sulfur dioxide generation in magnesium-based flue gas desulfurization process

机译:基于镁的烟气脱硫过程中同时氧化镁再生和二氧化硫产生

获取原文
获取原文并翻译 | 示例
       

摘要

A method was proposed for simultaneously regenerating magnesia from the Mg-based flue gas desulfurization byproducts in the power plant and generating the high concentration of sulfur dioxide. Elemental sulfur particles were evaporated to sulfur vapor and the latter one was used as the reductive agent to regenerate magnesia from the magnesium gypsum. The experiments were carried out in a successive fixed-bed system to study the concentration of sulfur dioxide in the exhaust gas and the activity of the regenerated magnesia under different reaction conditions. Sulfur vapor effectively reduced the magnesia regeneration temperature from above 950 degrees C to merely 650 degrees C. The concentration of sulfur dioxide in the exhaust gas could achieve 20% by volume when the sulfur vapor partial pressure was 1674 Pa, the regeneration temperature was 750 degrees C, the gas hourly space velocity was 1200 h(-1) and the loading of the reaction materials in the regeneration reactor was 16 g, respectively. The activity of the regenerated magnesia after the decomposition of the magnesium gypsum at 750 degrees C was satisfactory. Both the magnesium gypsum and the regenerated magnesia were characterized using X-ray fluorescence spectroscopy, thermogravimetric analyzer, X-ray diffraction spectroscopy, BET surface area analyzer, scanning electron microscopy, high resolution transmission electron microscopy, and X-ray photoelectron spectroscopy. The kinetics of the magnesia regeneration from the magnesium gypsum in the presence of the sulfur vapor was analyzed and the nucleation model was determined to be the most appropriate kinetic model. The activation energy and the pre-exponential factor were determined to be 76.51 kJ/mol and 228.66 min(-1), respectively. All the results demonstrate that there is considerable potential for the application of this proposed method in flue gas desulfurization process. (C) 2020 Elsevier Ltd. All rights reserved.
机译:提出了一种用于从发电厂的MG基烟气脱硫副产物同时再生氧化镁,并产生高浓度的二氧化硫。将元素硫颗粒蒸发至硫蒸汽,后者用作还原剂以从镁石膏中再生氧化镁。在连续的固定床系统中进行实验,以研究废气中二氧化硫的浓度以及在不同的反应条件下再生氧化镁的活性。硫蒸汽从950℃的高于950℃有效地降低了镁质再生温度,仅为650℃。当硫部分压力为1674Pa时,废气中的二氧化硫浓度可以达到20%,再生温度为750度C,气体小时空间速度为1200小时(-1),再生反应器中的反应材料的负载分别为16g。在750℃下分解镁石膏后再生氧化镁的活性令人满意。使用X射线荧光光谱法,热重分析仪,X射线衍射光谱,BET表面积分析仪,扫描电子显微镜,高分辨率透射电子显微镜和X射线光电子能量,镁石膏和再生氧化镁。分析了在硫蒸汽存在下从镁石膏中再生的镁质再生的动力学,并确定核切割模型是最合适的动力学模型。激活能量和预指数因子分别测定为76.51 kJ / mol和228.66分钟(-1)。所有结果表明,在烟道气脱硫过程中,这种提出方法应用了相当大的潜力。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Journal of Cleaner Production》 |2021年第15期|124720.1-124720.14|共14页
  • 作者单位

    Qingdao Univ Sci & Technol Coll Chem Engn State Key Lab Base Ecochem Engn Qingdao 266042 Peoples R China;

    Qingdao Univ Sci & Technol Coll Chem Engn State Key Lab Base Ecochem Engn Qingdao 266042 Peoples R China;

    Qingdao Univ Sci & Technol Coll Chem Engn State Key Lab Base Ecochem Engn Qingdao 266042 Peoples R China;

    Qingdao Agr Univ Coll Resources & Environm Qingdao 266109 Peoples R China;

    Qingdao Univ Sci & Technol Coll Chem Engn State Key Lab Base Ecochem Engn Qingdao 266042 Peoples R China;

    Ningxia Univ State Key Lab High Efficiency Utilizat Coal & Gre Yinchuan 750021 Ningxia Peoples R China;

    Ningxia Univ State Key Lab High Efficiency Utilizat Coal & Gre Yinchuan 750021 Ningxia Peoples R China;

    Henan Acad Sci Energy Res Inst Co Ltd Zhengzhou 450008 Peoples R China;

    Qingdao Univ Sci & Technol Coll Chem Engn State Key Lab Base Ecochem Engn Qingdao 266042 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Magnesia; Desulfurization; Regeneration; Sulfur vapor; SO2 concentration;

    机译:镁质;脱硫;再生;硫蒸气;SO2浓度;
  • 入库时间 2022-08-19 01:51:43
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