Studies on adsorption of NO on Cu-ZSM-5/cordierite and mechanism of NO decomposition by IR spectroscopy
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Guan, NJ
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Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Guan, NJ
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Shan, XL
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机构:Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Shan, XL
Zeng, X
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机构:Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Zeng, X
Xiang, SH
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机构:Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Xiang, SH
Trunschke, A
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机构:Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Trunschke, A
Baerns, M
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机构:Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
Baerns, M
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[1] Nankai Univ, Coll Chem, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
The adsorption of NO on in-situ synthesized Cu-ZSM-5/cordierite monolithic catalyst samples with different Si/Al ratios is studied by diffuse reflectance Fourier transform infrared spectroscopy at different NO partial pressure from omega =5 x 10(-4) to 2 x 10(-3) and temperatures from 298 K to 773 K. The Cu exists mainly in Cu2+ state even at room temperature. No Cu+-NO is found under the conditions. Several N2O species are observed on the catalyst surface as well as on the Cu/cordierite sample. It is supposed that there exists a copper-zeolite-substrate interaction on the in-situ synthesized monolithic catalyst. The band at 2133 cm(-1) is attributed to NO+-O-lattice and only related to the zeolite matrix. A possible mechanism of NO decomposition over the Cu-ZSM-5/cordierite monolithic catalyst is drawn.