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Remarkable enhancement of catalytic activity and selectivity of MSE-type zeolite by post-synthetic modification

Paper ID Volume ID Publish Year Pages File Format Full-Text
54360 47007 2015 7 PDF Available
Title
Remarkable enhancement of catalytic activity and selectivity of MSE-type zeolite by post-synthetic modification
Abstract

•MSE-type zeolites (MCM-68, YNU-3, and MSEOSDAF) were successfully synthesized.•Each material was used as a solid acid catalyst for hexane cracking.•Al-rich version of the MSE-type zeolites caused rapid deactivation by heavy coking.•Framework Al atoms were properly removed by adequate acid treatments.•Dealuminated MSE-type zeolites showed sufficient activity and coke durability.

Besides conventional MCM-68, Al-rich MSE-type zeolites with a 12-10-10-ring micropore system were successfully synthesized in a remarkably short crystallization period by some different synthetic methods: (1) hydrothermal conversion of an FAU-type zeolite with the aid of the dipyrrolidinium-type organic structure-directing agent (OSDA) and (2) hydrothermal synthesis without using any OSDA with the aid of seed crystals. The dealumination behaviors during post-synthetic acid treatments as well as the properties of the products differed depending on the synthetic method. The dealuminated version of each Al-rich MSE-type zeolite showed a high level of coking resistance in addition to a significant yield of propylene in the hexane-cracking reaction, and the MSE synthesized under OSDA-free conditions showed the best catalytic performance among three different MSE-type zeolites after post-synthetic modification. The Al-rich MSE products obtained in this work are promising parent materials for industrial applications as highly selective and long-lived catalysts.

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Keywords
MSE-type zeolite; Organic structure-directing agent; OSDA-free synthesis; Dealumination; Hexane cracking; Coking resistance.
First Page Preview
Remarkable enhancement of catalytic activity and selectivity of MSE-type zeolite by post-synthetic modification
Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Today - Volume 243, 1 April 2015, Pages 85–91
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis