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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Bibliographic Details
Published inNature communications Vol. 9; no. 1; pp. 1 - 7
Main Authors Ni, Youming, Chen, Zhiyang, Fu, Yi, Liu, Yong, Zhu, Wenliang, Liu, Zhongmin
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 27.08.2018
Nature Publishing Group
Nature Portfolio
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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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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-018-05880-4