Redox and Nonredox CO2 Utilization: Dry Reforming of Methane and Catalytic Cyclic Carbonate Formation

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dc.contributor.authorSubramanian, Saravananko
dc.contributor.authorSong, Youngdongko
dc.contributor.authorKim, Doyunko
dc.contributor.authorYavuz, Cafer T.ko
dc.date.accessioned2020-06-22T05:20:17Z-
dc.date.available2020-06-22T05:20:17Z-
dc.date.created2020-06-15-
dc.date.created2020-06-15-
dc.date.created2020-06-15-
dc.date.created2020-06-15-
dc.date.issued2020-05-
dc.identifier.citationACS ENERGY LETTERS, v.5, no.5, pp.1689 - 1700-
dc.identifier.issn2380-8195-
dc.identifier.urihttp://hdl.handle.net/10203/274759-
dc.description.abstractCO2 emissions are too large to tackle with a single process, but a combination of avoidance with chemical utilization may be able to slow global warming. In this Focus Review, we identify two large-scale CO2 conversion processes based on their viability and opposite energy requirements. In the high-energy, stationary path, CO2 reforming of methane could provide gigatons of CO2 utilization through synthesis gas. The main problem is the lack of a durable, effective, low-cost dry reforming catalyst. The exothermic cyclic carbonate formation from CO2 and organic epoxides offers a low-energy, mobile, nonredox route. The catalysts, however, must be metal-free and robust, have a high surface area, and be low-cost while being easily scalable. These two processes could potentially address at least a quarter of all current CO2 emissions.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleRedox and Nonredox CO2 Utilization: Dry Reforming of Methane and Catalytic Cyclic Carbonate Formation-
dc.typeArticle-
dc.identifier.wosid000535176100041-
dc.identifier.scopusid2-s2.0-85120951235-
dc.type.rimsART-
dc.citation.volume5-
dc.citation.issue5-
dc.citation.beginningpage1689-
dc.citation.endingpage1700-
dc.citation.publicationnameACS ENERGY LETTERS-
dc.identifier.doi10.1021/acsenergylett.0c00406-
dc.contributor.localauthorYavuz, Cafer T.-
dc.contributor.nonIdAuthorSubramanian, Saravanan-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordPlusSYNTHESIS GAS-
dc.subject.keywordPlusCHEMICAL FIXATION-
dc.subject.keywordPlusPARTIAL OXIDATION-
dc.subject.keywordPlusIONIC LIQUIDS-
dc.subject.keywordPlusBIMETALLIC CATALYSTS-
dc.subject.keywordPlusSUPPORTED CATALYSTS-
dc.subject.keywordPlusORGANIC FRAMEWORK-
dc.subject.keywordPlusNI/MGO CATALYSTS-
dc.subject.keywordPlusHIGHLY EFFICIENT-
dc.subject.keywordPlusNOBLE-METALS-
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