Controlling the selectivity and deactivation of H-ZSM-5 by tuning b-axis channel length for glycerol dehydration to acrolein
[Display omitted] •A series of H-ZMS-5 with well controlled b-axis channels of 60–250nm were prepared.•Much better catalytic performance was obtained with H-ZSM-5 of 60nm b-axis channels.•Less coking and lower rate of deactivation was realized by shortening the b-axis channels.•Coking behaviors were...
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Published in: | Journal of industrial and engineering chemistry (Seoul, Korea) Vol. 88; pp. 127 - 136 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier B.V
25-08-2020
한국공업화학회 |
Subjects: | |
Online Access: | Get full text |
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Summary: | [Display omitted]
•A series of H-ZMS-5 with well controlled b-axis channels of 60–250nm were prepared.•Much better catalytic performance was obtained with H-ZSM-5 of 60nm b-axis channels.•Less coking and lower rate of deactivation was realized by shortening the b-axis channels.•Coking behaviors were discovered by UV-Raman spectra, TGA, EDS and iDPC-STEM.
Glycerol dehydration to value-added acrolein over zeolite catalysts is a useful approach to offer a sustainable economic route for the biodiesel industry. Glycerol dehydration over H-ZSM-5 with conventional morphology often exhibits a significant mass transfer limitation and inhibits the access to active sites in the micropores, which causes low activity, selectivity, and severe catalyst deactivation. In this study, a significant impact of b-axis channel length on acrolein selectivity and catalyst activity was revealed by using H-ZSM-5 synthesized with varied channel length in b-axis of 60, 130, 180, and 250nm. Complete glycerol conversion and high acrolein selectivity (88%) were observed over H-ZSM-5 with 60nm channels length in b-axis, due to high availability of active sites and enhanced diffusion through the shortest channels, which dramatically suppressed the coke formation. The catalysts with long b-axis channels exhibited a slow internal diffusion, leading to increased polymerization side reactions and coke formation. |
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ISSN: | 1226-086X 1876-794X |
DOI: | 10.1016/j.jiec.2020.03.037 |