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Cu/Al-Ce-PILC在丙烯选择性催化还原NO反应中的失活研究
摘要点击 1976  全文点击 1093  投稿时间:2006-04-12  修订日期:2006-06-12
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中文关键词  Cu/Al-Ce-PILC  氮氧化物  丙烯  选择性催化还原  失活
英文关键词  Cu/Al-Ce-PILC  nitric oxides  propylene  selective catalytic reduction  deactivation
作者单位
林绮纯 清华大学环境科学与工程系北京100084 
郝吉明 清华大学环境科学与工程系北京100084 
李俊华 清华大学环境科学与工程系北京100084 
傅立新 清华大学环境科学与工程系北京100084 
林维明 广州大学化工系广州510405 
中文摘要
      采用聚合羟基复合阳离子合成交联黏土Al-Ce-PILC,经SO2-4改性后,以浸渍法制备了铜基交联黏土催化剂Cu/Al-Ce-PILC,并将其应用于C3H6选择性催化还原NO的反应,350℃时NO转化率达到最大值56%,700℃时下降至22%.为探究催化剂高温失活的原因,采用XPS、TPR、TGA、Py-IR和DSC对反应前后催化剂的物化性能进行了表征.结果表明,经过H2预处理活化后活性组分Cu物种以Cu+形式存在,而高温反应后Cu物种除以Cu+和Cu2+ 2种形式存在外,还出现了少量CuO物种;高温反应过程中Al-Ce-PILC上结构羟基和SO2-4流失导致催化剂表面酸性减弱;此外,还存在表面积炭覆盖了部分活性中心并堵塞了催化剂孔道的现象.这三者的共同影响促进了C3H6深度氧化,抑制了NO还原,从而导致催化剂的失活.
英文摘要
      New pillared clay catalysts were studied for NO removal by hydrocarbon in the presence of oxygen. The purpose of this work is to study the deactivation of Cu/Al-Ce-PILC in the SCR of NO. Montmorillonite was pillared by multi oligomeric hydroxyl cation to synthesize Al-Ce-PILC and treated by (NH4)2SO4, then it was used as catalyst support. Cu/Al-Ce-PILC catalyst was prepared by impregnation and applied to the SCR of NO by C3H6.The NO conversion to N2 reached its maximum of 56% at 350℃ and decreased to 22% at 700℃. To study the deactivation of Cu/Al-Ce-PILC in the SCR of NO at high temperature, the fresh and post-reaction catalysts were characterized by XPS, TPR, TGA, Py-IR and DSC. The results showed that only Cu+ species existed on the fresh catalyst pretreated in hydrogen, while another species CuO was detected on the post-reaction catalyst. The loss of structural hydroxyl and SO2-4 on Al-Ce-PILC weakened the surface acidity of the catalyst at high reaction temperature. Furthermore, the coke deposition on the catalyst covered part of the active sites and blocked the pores of the catalyst. The deactivation of Cu/Al-Ce-PILC may be due to the combined effects of CuO formation, the decrease on acidity and the coke deposition, which facilitated propylene combustion and inhibited NO reduction.

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