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A Novel CFC-12 Hydrolysis Catalyst: WO_3/SnO_2 被引量:1
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作者 Zhen MA wei ming hua +1 位作者 Yi TANG Zi GAO (Department of Chemistry, Fudan University, Shanghai 200433) 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第1期87-88,共2页
The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over WO_3/SnO_2 solid acid which was prepared by impregnating Sn(OH)_4 with aqueous ammonium metatungstate followed by evaporating, drying ... The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over WO_3/SnO_2 solid acid which was prepared by impregnating Sn(OH)_4 with aqueous ammonium metatungstate followed by evaporating, drying and calcining in air. The CFC-12 conversion over WO_3/SnO_2 at 330'C remained above 99.5% during 150 h on stream, however, parent metal oxides showed rare catalytic decomposition activity. 展开更多
关键词 Environmental catalysis Freon decomposition WO_3/SnO_2 catalyst.
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Catalytic hydrolysis of CFC-12 over solid acid Ti(SO_4)_2 被引量:1
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作者 Zhen MA wei ming hua +1 位作者 Yi TANG Zi GAO (Department of Chemistry. Fudan University. Shanghai 200433) 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第4期311-314,共4页
The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1... The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1). the CPC-12 conversion at 310C over Ti(SO_4)_2 calcined at 350C remained about 98.5% during 360 h on stream. and the selectivity to by-products remained zero. The findings enlarged the scope of traditional catalyst systems for the CFCs decomposition. 展开更多
关键词 Chlorofluorocarbons. catalytic decomposition. solid acid Ti(SO_4)_2.
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A Novel Way to Prepareγ-A1_2O_3 Supported SO_4^(2-)/ZrO_2 Solid Superacid Catalysts for n-Butane Isomerization
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作者 Ting LEI Yi TANG +2 位作者 wei ming hua Jin Suo XU Zi GAO (Department of Chemistry, Fudan University, Shanghai 200433) 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第1期89-92,共4页
Highly active solid superacid catalysts for n-butane isomerization, SZ/A1_2O_3-P, were prepared by supporting SO-(4-2)/ZrO2, (SZ) on y-A1_2O_3 carrier using a precipitation method. The activities of some catalysts wer... Highly active solid superacid catalysts for n-butane isomerization, SZ/A1_2O_3-P, were prepared by supporting SO-(4-2)/ZrO2, (SZ) on y-A1_2O_3 carrier using a precipitation method. The activities of some catalysts were enhanced significantly j The activity of the most active sample. 60%SZ/Al_2O3-P, was even about 2 times more active than that of the SZ catalyst. 展开更多
关键词 SO_4^(2-)/ZrO_2 n-Butane Isomerization γ-A1_2O_3 supported superacid catalysts.
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