Hydroisomerization of n-butane over sulfated zirconia catalysts promoted by alumina and platinum

被引:39
|
作者
Hua, WM [1 ]
Sommer, J [1 ]
机构
[1] Univ Strasbourg 1, Inst Chim, Lab Physicochim Hydrocarbures, UMR 7513, F-67070 Strasbourg, France
关键词
butane activation; Pt-promoted SZA; strong acids; initiation step; protolysis; H/D exchange;
D O I
10.1016/S0926-860X(01)00945-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The isomerization of n-butane over Pt-promoted/Al2O3-promoted sulfated zirconia (Pt/SZA) catalyst in comparison with SZA was studied in the presence of H-2 at 250degreesC. Catalysts prepared using IN H2SO4 are slightly more active than those prepared using 2N H2SO4. The optimum calcination temperature for Pt/SZA was found to be 650degreesC, same as for SZA catalyst. The presence of platinum improves the catalytic stability and isomerization selectivity of SZA catalyst, particularly at low H-2/n-butane ratio. Comparing the maximum activity displayed by both catalysts, Pt/SZA is more active than SZA for n-butane isomerization, especially at the steady state. Pre-treating the Pt/SZA catalyst in H-2 at 350 degreesC before the reaction results in a significant loss in activity. The mechanical mixture of Pt/Al2O3 and SZA exhibits much higher activity than Pt/SZA catalyst, probably due to a change of reaction mechanism from monofunctional over the latter catalyst to bifunctional over the former. The initiation step of n-butane isomerization over SZA catalyst is discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:279 / 286
页数:8
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