Tandem Catalysis of Direct CO2 Hydrogenation to Higher Alcohols

被引:49
|
作者
Xu, Di [1 ]
Yang, Hengquan [2 ]
Hong, Xinlin [1 ]
Liu, Guoliang [1 ]
Tsang, Shik Chi Edman [3 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Shanxi Univ, Sch Chem & Chem Engn, Inst Mol Sci, Taiyuan 030006, Peoples R China
[3] Univ Oxford, Wolfson Catalysis Ctr, Dept Chem, Oxford OX1 3QR, England
来源
ACS CATALYSIS | 2021年 / 11卷 / 15期
基金
中国国家自然科学基金;
关键词
higher alcohols; CO2; hydrogenation; multifunctional catalyst; synergistic effect; proximity effect; SELECTIVE CONVERSION; METHANOL SYNTHESIS; ETHANOL; SYNGAS;
D O I
10.1021/acscatal.1c01610
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
Direct CO2 hydrogenation to higher alcohols (HA) is highly attractive but remains a huge challenge due to the low HA productivity. Herein we develop a highly active multifunctional catalyst composed of CuZnAl and K-CuMgZnFe oxides which significantly improve the HA space time yield (STY) to 106.5 mg g(cat)(-1) h(-1) (2.24 mmol g(cat)(-1) h(-1)) with more than 90% of the HA fraction in total alcohol products. A strong synergistic effect occurs when these two components are in proper proximity and at an appropriate mass ratio, which can efficiently facilitate the conversion of CO2 to HA by promoting the formation of a *CO intermediate via the reverse water gas shift reaction over CuZnAl and subsequently the *CO migration and conversion on K-CuMgZnFe.
引用
收藏
页码:8978 / 8984
页数:7
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