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富氧条件下Mn/ZSM-5选择催化CH_4还原NO 被引量:23

Selective Catalytic Reduction of NO in Excess Oxygen by Methane over Mn/ZSM-5 Catalysts
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摘要 考察了富氧条件下Mn/ZSM-5催化剂上CH4选择催化还原NO反应,并采用H2程序升温还原、SO2程序升温表面反应和NO程序升温脱附等手段对催化剂进行了表征.结果表明,催化剂活性与制备方法和Mn负载量密切相关.离子交换法制备的Mn/ZSM-5催化剂活性明显优于浸渍法制备的催化剂;NO转化率随着Mn负载量的增加而增加,至2.06%时达到最大值(57.3%),然后随着Mn负载量的增加而降低.采用离子交换法或较低Mn负载量(≤2.06%)抑制了催化剂中非化学计量的MnOx(1.5<x<2)物种的形成,减缓了CH4的氧化燃烧反应,因而CH4还原NO的选择性提高.在含SO2体系中,Mn/ZSM-5活性在550oC以下时明显下降,但在600oC以上基本不受影响.这是由于在550oC以下时SO2在Mn/ZSM-5表面形成了稳定的吸附硫物种,覆盖了部分活性位,导致催化剂活性降低;而在600oC以上时含硫物种基本脱附完全,因而对催化剂活性影响不大. The selective catalytic reduction of NO in excess O2 by CH4 was investigated over a series of ZSM-5-supported manganese catalysts(Mn/ZSM-5).The catalytic activity depended on preparation method and Mn loading.An ion exchange method resulted in a higher activity than an impregnation method.Catalytic activity increased with increasing Mn loading until a Mn loading of 2.06% that gave a maximum NO conversion of 57.3%.H2 temperature-programmed reduction results showed that the ion exchange method and low Mn loadings(≤ 2.06%) restricted the formation of non-stoichiometric MnOx(1.5 〈x〈 2) species that have higher oxidative activity,and thus suppressed the combustion of CH4 by O2,which increased the selectivity for NO reduction.In a SO2 containing stream,a substantial decrease in NO conversion was seen at ≤ 550 ℃ but not at ≥ 600 ℃.SO2 temperature-programmed surface reaction and NO temperature-programmed desorption demonstrated that sulfur species were formed at temperature ≤ 550 ℃,and these covered active sites and decreased the catalytic activity.The sulfur species desorbed at ≥ 600 ℃,thus the addition of SO2 did not have a significant impact on the catalytic activity.
出处 《催化学报》 SCIE EI CAS CSCD 北大核心 2010年第9期1107-1114,共8页
基金 国家自然科学基金(20876102) 高等学校博士学科点专项科研基金(200801120006) 山西省自然科学基金(2008011022)
关键词 一氧化氮 甲烷 选择催化还原 ZSM-5 二氧化硫 nitrogen oxide methane selective catalytic reduction manganese ZSM-5 sulfuric dioxide
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