Selective conversion of CO2 and H2 into aromatics
Transformation of greenhouse gas CO 2 and renewable H 2 into fuels and commodity chemicals is recognized as a promising route to store fluctuating renewable energy. Although several C 1 chemicals, olefins, and gasoline have been successfully synthesized by CO 2 hydrogenation, selective conversion of...
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Published in | Nature communications Vol. 9; no. 1; pp. 1 - 7 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
27.08.2018
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Transformation of greenhouse gas CO
2
and renewable H
2
into fuels and commodity chemicals is recognized as a promising route to store fluctuating renewable energy. Although several C
1
chemicals, olefins, and gasoline have been successfully synthesized by CO
2
hydrogenation, selective conversion of CO
2
and H
2
into aromatics is still challenging due to the high unsaturation degree and complex structures of aromatics. Here we report a composite catalyst of ZnAlO
x
and H-ZSM-5 which yields high aromatics selectivity (73.9%) with extremely low CH
4
selectivity (0.4%) among the carbon products without CO. Methanol and dimethyl ether, which are synthesized by hydrogenation of formate species formed on ZnAlO
x
surface, are transmitted to H-ZSM-5 and subsequently converted into olefins and finally aromatics. Furthermore, 58.1%
p
-xylene in xylenes is achieved over the composite catalyst containing Si-H-ZSM-5. ZnAlO
x
&H-ZSM-5 suggests a promising application in manufacturing aromatics from CO
2
and H
2
.
Selective conversion of CO
2
and H
2
into aromatics remains challenging due to the high unsaturation degree and complex structure of aromatics. Here the authors report a composite catalyst of ZnAlO
x
and H-ZSM-5 which promotes the formation of aromatics with high selectivity while inhibiting CO and CH
4
formation in CO
2
hydrogenation reactions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-018-05880-4 |