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Direct conversion of carbon dioxide into liquid fuels and chemicals by coupling green hydrogen at high temperature

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Direct conversion of carbon dioxide into liquid fuels and chemicals by coupling green hydrogen at high temperature

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dc.contributor.author Li, Yubing es_ES
dc.contributor.author Zeng, Lei es_ES
dc.contributor.author Pang, Ge es_ES
dc.contributor.author Wei, Xueer es_ES
dc.contributor.author Wang, Mengheng es_ES
dc.contributor.author Cheng, Kang es_ES
dc.contributor.author Kang, Jincan es_ES
dc.contributor.author Serra Alfaro, José Manuel es_ES
dc.contributor.author Zhang, Qinghong es_ES
dc.contributor.author Wang, Ye es_ES
dc.date.accessioned 2024-04-16T18:02:37Z
dc.date.available 2024-04-16T18:02:37Z
dc.date.issued 2023-05-05 es_ES
dc.identifier.issn 0926-3373 es_ES
dc.identifier.uri http://hdl.handle.net/10251/203534
dc.description.abstract [EN] The chemical conversion of CO2 into hydrocarbon fuels and chemicals using green hydrogen not only utilizes abundant CO2 as a carbon feedstock but also enables the storage of hydrogen. Herein, we investigate the direct hydrogenation of CO2 to gasoline and olefins over a series of bifunctional iron-zeolite tandem catalysts operated at high temperatures (> 300 degrees C). This process may efficiently utilize CO2 discharged from industrial combustion and green H2 produced by solid oxide electrolytic cells (SOEC). The optimized FeMnK+H-ZSM-5 catalyst offers a 70% selectivity of C5-C11 range hydrocarbons together with a 17% selectivity of C2-C4 lower olefins at 320 degrees C. The CO2 conversion levels and the aromatics contents could be greatly enhanced as the temperature increases from 320 degrees C to 400 degrees C. The hydrocarbon distribution is mainly determined by the micropore size of the zeolites. The dynamic evolution of bifunctional catalysts and its impact on bifunctional catalysis was systematically investigated. es_ES
dc.description.sponsorship This work was supported by the National Key Research and Devel- opment Program of Ministry of Science and Technology (No. 2019YFE0104400) , the National Natural Science Foundation of China (Nos. 91945301, 22121001, 22222206, 22072120, and 22202165) , and the China Postdoctoral Science Foundation (No. 2021M702733) . es_ES
dc.language Inglés es_ES
dc.publisher Elsevier es_ES
dc.relation.ispartof Applied Catalysis B Environmental es_ES
dc.rights Reconocimiento - No comercial - Sin obra derivada (by-nc-nd) es_ES
dc.subject Zeolite es_ES
dc.subject Liquid fuels es_ES
dc.subject CO2 reduction es_ES
dc.subject Bifunctional es_ES
dc.subject Hydrogen storage es_ES
dc.title Direct conversion of carbon dioxide into liquid fuels and chemicals by coupling green hydrogen at high temperature es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1016/j.apcatb.2022.122299 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/NSFC//22121001/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/NSFC//22222206/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/NSFC//22072120/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/NSFC//22202165/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/NSFC//91945301/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/NKRDPC//2019YFE0104400/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/China Postdoctoral Science Foundation//2021M702733/ es_ES
dc.rights.accessRights Embargado es_ES
dc.date.embargoEndDate 2024-12-31 es_ES
dc.description.bibliographicCitation Li, Y.; Zeng, L.; Pang, G.; Wei, X.; Wang, M.; Cheng, K.; Kang, J.... (2023). Direct conversion of carbon dioxide into liquid fuels and chemicals by coupling green hydrogen at high temperature. Applied Catalysis B Environmental. 324. https://doi.org/10.1016/j.apcatb.2022.122299 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.1016/j.apcatb.2022.122299 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 324 es_ES
dc.relation.pasarela S\510770 es_ES
dc.contributor.funder China Postdoctoral Science Foundation es_ES
dc.contributor.funder National Natural Science Foundation of China es_ES
dc.contributor.funder National Key Research and Development Program of China es_ES


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