Zeolite-based catalysts for oxidative upgrading of methane: design and control of active sites

被引:6
|
作者
Yabushita, Mizuho [1 ]
Osuga, Ryota [2 ]
Yokoi, Toshiyuki [3 ]
Muramatsu, Atsushi [4 ,5 ]
机构
[1] Tohoku Univ, Sch Engn, Dept Appl Chem, 6 6 07 Aoba,Aramaki,Aoba ku, Sendai, Miyagi 9808579, Japan
[2] Hokkaido Univ, Inst Catalysis, Kita 21 Nishi 10,Kita ku, Sapporo, Hokkaido 0010021, Japan
[3] Tokyo Inst Technol, Inst Innovat Res, 4259 Nagatsuta cho,Midori ku, Yokohama, Kanagawa 2268503, Japan
[4] Tohoku Univ, Int Ctr Synchrotron Radiat Innovat Smart, 2 1 1 Katahira,Aoba ku, Sendai, Miyagi 9808577, Japan
[5] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, 2 1 1 Katahira,Aoba ku, Sendai, Miyagi 9808577, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
SOLID-STATE NMR; TEMPERATURE SELECTIVE OXIDATION; EXCHANGED ZEOLITES; MECHANISTIC INSIGHTS; DIRECT CONVERSION; AL DISTRIBUTION; MFI ZEOLITES; ACETIC-ACID; CU; FRAMEWORK;
D O I
10.1039/d3cy00482a
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
Oxidative upgrading of methane into carbon monoxide, methanol, lower hydrocarbons (such as ethane and ethylene), and other oxygenates has been achieved at relatively low temperatures over zeolite-based catalysts. The high tunability afforded by the framework structures of zeolites offers a unique and precious opportunity for the design of active species, resulting in outstanding catalytic performance. Thus, we categorize the various reported active species in zeolite-based catalysts into three groups in terms of their origin, viz., active species originated from intra-framework heteroatoms, active species introduced by ion-exchange, and active species prepared by impregnation. We present an overview of the performance, structure, and catalysis of each category and comment on the general outlook.
引用
收藏
页码:4020 / 4044
页数:25
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