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低温等离子体协同Ag/Al_2O_3选择性催化丙烯还原氮氧化物反应的原位红外光谱研究 被引量:5

In Situ DRIFTS Study on Non-thermal Plasma-Assisted NO_x Reduction by Propene over Ag/Al_2O_3 Catalyst
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摘要 研究了稀燃条件下低温等离子体(NTP)协同丙烯在Ag/Al2O3催化剂上选择性催化还原NOx反应,通过原位漫反射傅里叶变换红外光谱(DRIFTS)对NTP协同前后反应气中NO和C3H6的吸附以及丙烯选择性催化还原反应进行了表征.结果表明,丙烯的活化是Ag/Al2O3上选择性催化还原反应的关键步骤.NTP活化反应气体后,Ag/Al2O3表面-NCO、R-NO2和有机酸根等物种的数量大幅度增加,并且其催化还原NOx的低温(<350℃)活性也显著提高.在NTP协同前后,选择性催化还原过程可能存在两条反应路径,较低温度下主要是-NCO生成N2,而较高温度下则是-CN向N2转化. The non-thermal plasma (NTP)-assisted selective catalytic reduction (SCR) of NO, by propene over the Ag/Al2O3 catalyst was investigated. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) studies were carried out on the NO and C3H6 adsorption and SCR reactions over Ag/Al2O3 with or without NTP pretreatment. The results showed that the low-temperature activity of C3H6-SCR was remarkably enhanced with the assistance of NTP in the presence of excess oxygen. The activation of propene was the key step in C3H6-SCR over Ag/Al2O3. After the application of NTP, the amount of -NCO, R-NO2 and organic acid species over Ag/Al2O3 significantly increased, which caused a high catalytic activity at low temperatures (〈350℃ ). Two reaction paths were proposed in both SCR and NTP-SCR. At low reaction temperatures, -NCO was the key intermediate to generate N2, while it was -CN at high reaction temperatures.
出处 《催化学报》 SCIE CAS CSCD 北大核心 2005年第11期951-955,共5页
基金 国家高技术研究发展计划(863计划)项目(2004AA649150) 国家自然科学基金重点项目(20437010)资助
关键词 低温等离子体 氧化铝 选择性催化还原 稀燃 氮氧化物 原位漫反射傅里叶变换红外光谱 non-thermal plasma, silver, alumina, selective catalytic reduction, lean burn, nitrogen oxide, in situ diffuse reflectance infrared Fourier transform spectroscopy
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  • 1Koebel M, Elsener M, Kleemann M. Catal Today, 2000,59(3-4) : 335. 被引量:1
  • 2Burch R, Breen J P, Meianier F C. Appl Catal B, 2002,39(4) : 283. 被引量:1
  • 3LiJ H, HaoJ M, FuLX, ZhuTL, LiuZM, CuiXY.Chin Chem Lett, 2004, 15(6) : 695. 被引量:1
  • 4LiJ H, HaoJ M, FuLX, LiuZM, CuiX Y. Catal Today, 2004, 90(3-4): 215. 被引量:1
  • 5Li J H, Hao J M, Fu L X. React Kinet Catal Lett, 2004,81(2) : 265. 被引量:1
  • 6Li J H, Hao J M, Fu LX, ZhuT L. TopCatal, 2004,30-31(1-4): 81. 被引量:1
  • 7Li J H, Hao J M, FuLX, ZhuTL, Liu Z M, Cui X Y.React Kinet Catal Lett , 2003, 80(1): 75. 被引量:1
  • 8Li J H, Hao J M, Fu L X, Zhu T L, Liu Z M, Cui X Y.Appl Catal A, 2004, 265(1) : 43. 被引量:1
  • 9Ycon S, Panov A G, Tonkyn R G, Ebeling A C, Barlow S E, Balmer M L. Catal Today, 2002, 72(3-4) : 251. 被引量:1
  • 10Tran D N, Aardahl C L, Rappe K G, Park P W, Boyer C L. Appl Catal B, 2004, 48(2) : 155. 被引量:1

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