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第 36 卷第 6 期                             精   细   化   工                                  Vol.36, No.6
             201 9 年 6 月                             FINE CHEMICALS                                 June    2019


              催化与分离提纯技术
                         FeCoY 催化剂的催化还原脱硫脱硝性能



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                      庞子涛 ,程   亮            1,2 ,宋永吉 ,王新承 ,李翠清 ,王   虹
                 (1.  北京石油化工学院  化学工程学院  燃料清洁化及高效催化减排技术北京市重点实验室,北京
                 102617; 2.  北京化工大学  化学工程学院,北京    100029)
                 摘要:以 CO 为还原剂,FeCoY 为活性组分,采用等体积浸渍法制备了一系列不同负载量、不同载体的催化剂
                 FeCoY/AC,并在微型固定床反应器上探讨催化剂同时脱硫脱硝活性及抗氧化性。通过 XRD、BET、H 2 -TPR 对
                 催化剂进行了表征。结果表明:经过硝酸预处理的催化剂能显著提高催化剂的性能;通过同时脱硫脱硝正交实
                 验,得到活性组分 Fe、Co、Y 分别占载体质量 10%、6%、3%的催化剂 10Fe6Co3Y/AC 为最优组合,脱硫脱硝
                 转化率均能达 100%,T 90% (脱硫脱硝转化率同时达到 90%时的温度)约为 218 ℃。XRD 结果表明:催化剂具
                 有尖晶石结构。抗氧化性实验初步判断脱硫过程遵循 Redox-COS 协同作用机理,而脱硝仅遵循 COS 机理,体
                 积分数为 1%的 O 2 对 NO 和 SO 2 的活性位点表现出不同的毒害作用。
                 关键词:同时脱硫脱硝;FeCoY;预处理;抗氧化性;反应机理;催化剂
                 中图分类号:X511; O463.36      文献标识码:A      文章编号:1003-5214 (2019) 06-1111-07


                             Catalytic Reduction Proerties of FeCoY Catalysts for
                                        Desulfurization and Denitrification


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                             PANG Zi-tao , CHENG Liang , SONG Yong-ji , WANG Xin-cheng ,
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                                                LI Cui-qing , WANG Hong
                 (1. Beijing Key Laboratory of Fuels Cleaning and Advanced  Catalytic Emission Reduction Technology, College of
                 Chemical Engineering, Beijng Institute of Petrochemical Technology, Beijing 102617, China; 2. College of Chemical
                 Engineering, Beijing University of Chemical Technology, Beijing 100029, China)
                 Abstract: A series of catalysts with different loading amount and different supports were prepared by equal
                 volume impregnation method using FeCoY as active component. Their simultaneous desulfurization and
                 denitration  activities  and  oxidation  resistance  were  studied  in  an  atmospheric  pressure  micro  fixed  bed
                 reaction device using CO as reducing agent. The catalysts were characterized by XRD, BET and H 2-TPR.
                 The results show that pretreatment of activated carbon (AC) with nitric acid can improve the performance
                 of the catalyst. The catalyst 10Fe6Co3Y/AC (the active components Fe, Co and Y are 10%, 6% and 3% of
                 the  supports  mass,  respectively)  is  the  best  combination  and  the  desulfurization  and  denitrification
                 efficiencies  can  reach  100%.  T 90%  (the  temperature  at  which  the  desulfurization  and  denitrification
                 efficiencies reach 90% simultaneously) is about 218 ℃. XRD results demonstrate that the catalyst has a
                 spinel  structure.  From  the  results  of  oxidation  resistance  experiments,  it  is  preliminarily  judged  that  the
                 desulfurization process follows the Redox-COS synergistic mechanism, while the denitration only follows
                 the COS mechanism. Oxygen with a volume fraction of 1% exhibits different toxic effects on the active
                 sites of NO and SO 2.
                 Key  words:  simultaneous  denitrification  and  desulfurization;  FeCoY;  pretreatment;  oxidation  resistance;
                 reaction mechanism; catalyst
                 Foundation item: National Natural Science Foundation of China (20176012, 21076025)



                 收稿日期:2018-08-11;  定用日期:2019-02-01; DOI: 10.13550/j.jxhg.20180590
                 基金项目:国家自然科学基金项目(20176012,21076025)
                 作者简介:庞子涛(1994—),男,硕士生。联系人:宋永吉(1963—),男,教授,博士生导师,E-mail:songyongji@bipt.edu.cn。
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