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Direct conversion of CO and H2O into liquid fuels under mild conditions.

Authors :
Xu, Yao
Li, Jing
Li, Wenjing
Li, Weizhen
Zhang, Xiaochen
Zhao, Yue
Xie, Jinglin
Wang, Xiaoping
Liu, Xi
Li, Yongwang
Xiao, Dequan
Yin, Zhen
Cao, Yong
Ma, Ding
Source :
Nature Communications; 3/27/2019, Vol. 10 Issue 1, pN.PAG-N.PAG, 1p
Publication Year :
2019

Abstract

Although enormous progress has been made in C<subscript>1</subscript> chemistry and CO<subscript>2</subscript> conversion in recent years, it is still a challenge to develop new carbon resource transformation protocols especially those lead to the production of liquid fuels with high selectivity under mild conditions (e.g., under low temperature and using benign solvent). Herein, we present a novel and energy-efficient catalytic route to directly transform CO and H<subscript>2</subscript>O to liquid fuels (i.e., liquid hydrocarbons) at low temperature (≤200 °C) in aqueous phase (i.e., in a benign solvent), in which H<subscript>2</subscript>O served as both hydrogen source and solvent for the liquid fuel production. The key to the catalytic process is the construction of a highly efficient tandem catalyst Pt-Mo<subscript>2</subscript>C/C + Ru/C, which can directly convert CO and H<subscript>2</subscript>O in aqueous phase to liquid hydrocarbons with a production rate of 8.7 mol<subscript>-CH2-</subscript> mol<subscript>Ru</subscript><superscript>−1</superscript> h<superscript>−1</superscript> and selectivity up to 68.4% of C<subscript>5+</subscript> hydrocarbons at 200 °C. Developing new carbon resource transformation protocols leading to the production of liquid fuels with high selectivity under mild conditions remains challenging. Here the authors present a novel and energy-efficient catalytic route to directly transform CO and H<subscript>2</subscript>O to liquid fuels at low temperature in aqueous phase. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
10
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
135579483
Full Text :
https://doi.org/10.1038/s41467-019-09396-3