Deactivation pathways in zeolite-catalyzed isobutane/butene alkylation

被引：87

作者：

Feller, A ^{[1
]}

Barth, JO ^{[1
]}

Guzman, A ^{[1
]}

Zuazo, I ^{[1
]}

Lercher, JA ^{[1
]}

机构：

[1] Tech Univ Munich, Lehrstuhl Tech Chem 2, D-85747 Garching, Germany

来源：

JOURNAL OF CATALYSIS | 2003年 / 220卷 / 01期

关键词：

isobutane/butene alkylation; zeolites; deactivation; coke analysis; MALDI; LDI;

D O I：

10.1016/S0021-9517(03)00251-3

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 deactivation of rare-earth-exchanged zeolite X as catalysts in isobutane/2-butene alkylation between 40 and 130 degreesC was studied. The deactivated samples and the isolated deposits were analyzed by a range of techniques, including for the first time (matrix assisted) laser desorption/ionization time-of-flight mass spectroscopy (MALDI-TOF MS, LDI-TOF MS). The compounds found in the deactivated zeolites are, in addition to large alkanes and alkenes, highly unsaturated and highly branched species containing cyclic structures, which are increasingly aromatic as the reaction temperature increased. The deposits in part interact strongly with the acid sites and block the sites for further alkylation reactions. Their structure and route of formation resemble those of conjunct polymers formed in liquid acid-catalyzed alkylation. (C) 2003 Elsevier Inc. All rights reserved.

引用

页码：192 / 206

页数：15

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