Controlling the selectivity and deactivation of H-ZSM-5 by tuning b-axis channel length for glycerol dehydration to acrolein

被引:36
作者
Ali, Babar [1 ]
Lan, Xiaocheng [1 ]
Arslan, Muhammad Tahir [1 ]
Gilani, Syed Zulfiqar Ali [1 ]
Wang, Huanjun [1 ]
Wang, Tiefeng [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green React Engn & Technol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Glycerol dehydration; Acrolein; ZSM-5; zeolites; b-Axis channels; Diffusion; GAS-PHASE DEHYDRATION; LONG-LIFE CATALYST; LEWIS-ACID SITES; COKE FORMATION; HYDROCARBONS CONVERSION; SUSTAINABLE PRODUCTION; HYDROTHERMAL SYNTHESIS; PORE CONDENSATION; MOLECULAR-SIEVES; HZSM-5; ZEOLITE;
D O I
10.1016/j.jiec.2020.03.037
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 250 nm. Complete glycerol conversion and high acrolein selectivity (88%) were observed over H-ZSM-5 with 60 nm 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. (C) 2020 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 136
页数:10
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