The influence of textural and compositional characteristics of Nafion/silica composites on isobutane/2-butene alkylation

被引:48
作者
Botella, P [1 ]
Corma, A [1 ]
López-Nieto, JM [1 ]
机构
[1] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
关键词
isobutane/2-butene alkylation; Nafion; Nafion/silica composites; H-beta; sulfated zirconia;
D O I
10.1006/jcat.1999.2502
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
Nafion/silica composites of different surface areas and polymer contents were prepared using a sol-gel technique. Their catalytic behavior was measured for the liquid phase alkylation of isobutane with 2-butene. A maximum initial (TOS = 1 min) activity and selectivity to trimethylpentanes as well as slower decay were detected for the sample with the smallest surface area (10 m(2) g(-1)) and a Nafion content of 20 wt%. Catalysts with the same polymer content but a larger surface area showed a considerably lower initial activity and selectivity; deactivation was faster. This can be explained by the fact that, in composites with a greater surface area-highly dispersed Nafion-the sulfonic groups of the polymer interact to a greater extent with the silanol groups of the silica, resulting in a decrease in the activity of the sulfonic groups. In the same way, when the Nafion content is varied in those composites with a large and similar BET area, the rates of deactivation are inversely proportional to the amount of resin in the sample. Moreover, a silica-supported Nafion catalyst, prepared by impregnation, has given results as good as those obtained with the more active Nafion/silica composite. The effect of the process variables (TOS, temperature, and isoparaffin/olefin molar ratio) on the activity and selectivity of these catalysts was studied as well. Comparison of these catalysts with other solid acid materials, such as an II-Beta zeolite and a sulfated zirconia, shows that the Nafion/silica samples behave more like H-Beta than like the sulfated zirconia catalyst. (C) 1999 Academic Press.
引用
收藏
页码:371 / 377
页数:7
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