Complete low-barrier side-chain route for olefin formation during methanol conversion in H-SAPO-34

被引:99
作者
De Wispelaere, Kristof
Hemelsoet, Karen
Waroquier, Michel
Van Speybroeck, Veronique [1 ]
机构
[1] Univ Ghent, CMM, B-9052 Zwijnaarde, Belgium
基金
欧洲研究理事会;
关键词
Methanol to olefin; Heterogeneous catalysis; Side-chain mechanism; Zeolites; First-principle kinetics; H-SAPO-34; ZEOLITE-CATALYZED METHYLATION; REACTION-MECHANISMS; SHAPE-SELECTIVITY; REACTION CENTERS; MTO CONVERSION; HYDROCARBONS; INSIGHTS; SAPO-34; ETHENE; IONS;
D O I
10.1016/j.jcat.2013.04.015
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 methanol to olefins process is an alternative for oil-based production of ethene and propene. However, detailed information on the reaction mechanisms of olefin formation in different zeolite is lacking. Herein, a first-principle kinetic study allows elucidating the importance of a side-chain mechanism during methanol conversion in H-SAPO-34. Starting from the experimentally observed hexamethylbenzene, a full low-barrier catalytic cycle for ethene and propene formation is found. The olefin elimination steps exhibit low free energy barriers due to a subtle interplay between a sp(3) carbon center of the organic intermediate, stabilizing non-bonding interactions and assisting water molecules in the zeolite material. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:76 / 80
页数:5
相关论文
共 35 条
[1]  
[Anonymous], J CHEM PHYS
[2]   Theoretical investigation of arene alkylation by ethene and propene over acidic zeolites [J].
Arstad, B ;
Kolboe, S ;
Swang, O .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (07) :2300-2308
[3]   Theoretical study of the methylbenzene side-chain hydrocarbon pool mechanism in methanol to olefin catalysis [J].
Arstad, B ;
Nicholas, JB ;
Haw, JF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (09) :2991-3001
[4]   The reactivity of molecules trapped within the SAPO-34 cavities in the methanol-to-hydrocarbons reaction [J].
Arstad, B ;
Kolboe, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (33) :8137-8138
[5]   The methanol-to-hydrocarbons reaction:: insight into the reaction mechanism from [12C]benzene and [13C]methanol coreactions over zeolite H-beta [J].
Bjorgen, M ;
Olsbye, U ;
Petersen, D ;
Kolboe, S .
JOURNAL OF CATALYSIS, 2004, 221 (01) :1-10
[6]   Coke precursor formation and zeolite deactivation: mechanistic insights from hexamethylbenzene conversion [J].
Bjorgen, M ;
Olsbye, U ;
Kolboe, S .
JOURNAL OF CATALYSIS, 2003, 215 (01) :30-44
[7]   A computational study of methanol-to-hydrocarbon conversion - Towards the design of a low-barrier process [J].
Chan, Bun ;
Radom, Leo .
CANADIAN JOURNAL OF CHEMISTRY, 2010, 88 (08) :866-876
[8]   Recent advancements in ethylene and propylene production using the UOP/Hydro MTO process [J].
Chen, JQ ;
Bozzano, A ;
Glover, B ;
Fuglerud, T ;
Kvisle, S .
CATALYSIS TODAY, 2005, 106 (1-4) :103-107
[9]   Fate of Bronsted Acid Sites and Benzene-Based Carbenium Ions During Methanol-to-Olefin Conversion on SAPO-34 [J].
Dai, Weili ;
Scheibe, Matthias ;
Guan, Naijia ;
Li, Landong ;
Hunger, Michael .
CHEMCATCHEM, 2011, 3 (07) :1130-1133
[10]  
Frisch M. J., 2016, Gaussian 03 Revision B.03