Synthesis of hierarchical SAPO-34 to improve the catalytic performance of bifunctional catalysts for syngas-to-olefins reactions

被引:40
|
作者
Wang, Mengheng [1 ]
Wang, Ziwei [1 ]
Liu, Suhan [1 ]
Gao, Runtian [1 ]
Cheng, Kang [1 ]
Zhang, Lei [2 ]
Zhang, Guoquan [2 ]
Min, Xiaojian [2 ]
Kang, Jincan [1 ]
Zhang, Qinghong [1 ]
Wang, Ye [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Mat, State Key Lab Phys Chem Solid Surfaces,Natl Engn, Xiamen 361005, Peoples R China
[2] Shaanxi Coal & Chem Technol Inst Co Ltd, State Energy Key Lab Clean Coal Grading Convers, Xian 710070, Peoples R China
基金
中国国家自然科学基金;
关键词
Syngas; Lower olefins; Mesoporous SAPO-34; Bifunctional catalysis; Reaction coupling; Methanol conversion; Zeolite deactivation; Shape catalysis; FISCHER-TROPSCH SYNTHESIS; HIGHLY SELECTIVE CONVERSION; LIGHT OLEFINS; ENHANCED LIFETIME; METHANOL; HYDROCARBONS; ZEOLITE; AROMATICS; DESIGN; OXIDE;
D O I
10.1016/j.jcat.2020.08.020
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
Bifunctional process integrating methanol synthesis and methanol-to-olefins conversion provides a new synthetic strategy for lower olefins (C-2-C-4(=)), whereas designing matchable zeolite components is still challenging due to the harsh reaction conditions. Here, a hierarchical SAPO-34 zeolite with a sandglass-like hollow structure is synthesized from an aluminum-rich precursor gel, which provides an abundance of crystal defects during zeolite crystallization. The bifunctional catalyst obtained by integrating the hierarchical SAPO-34 and ZnO-ZrO2 oxide offers a C-2-C-4(=) selectivity of 80% at 25% CO conversion with excellent stability in syngas conversion. We demonstrate that in the presence of high-pressure hydrogen, a moderate density of acid sites is the prerequisite for obtaining high C-2-C-4(=) selectivity in syngas/methanol conversion, because the olefins are easily hydrogenated into alkanes by excessive Bronsted acid sites. The hierarchical architecture significantly prolongs the lifetime of bifunctional catalysts, by facilitating C-2-C-4(=) desorption and slowing down the coking rate. (c) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:181 / 192
页数:12
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