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dc.contributor.authorRout, Kumar Ranjan
dc.contributor.authorGil Matellanes, Maria Victoria
dc.contributor.authorChen, De
dc.date.accessioned2020-07-07T08:35:37Z
dc.date.available2020-07-07T08:35:37Z
dc.date.created2019-11-23T23:16:17Z
dc.date.issued2019
dc.identifier.citationCatalysis science & technology. 2019, 9 (15), 4100-4107.en_US
dc.identifier.issn2044-4753
dc.identifier.urihttps://hdl.handle.net/11250/2660914
dc.description.abstractThe development of an energy-efficient and cost-effective technology for the purification of a hydrogen rich stream to achieve a CO concentration below 10 ppm, suitable for low temperature fuel cell applications, is one of the major objectives of energy research. Here we report the sorption enhanced Boudouard (SEB) reaction as an effective route for pure hydrogen production on metal-free catalysts by the highly selective removal of CO and CO2 from a hydrogen rich stream, where CaO serves as both a catalyst and a CO2 sorbent. We reveal that the in situ generated oxygen vacancy by CO adsorption on CaO catalyzes the sorption enhanced Boudouard reaction, hence the Boudouard reaction and CO2 removal occur simultaneously in a single step. The capture of CO2 in the presence of H2 by the solid sorbent shifts the chemical equilibrium towards complete CO conversion. The results demonstrate a remarkable decrease in the CO concentration from 0.5% in a hydrogen rich stream to less than 5 ppm, suitable for low temperature fuel cells. It avoids a subsequent preferential oxidation process or methanation reaction, as well as an additional CO2 capture process. The feasibility of applying the sorption enhanced Boudouard reaction in the production of highly pure hydrogen (CO content less than 10 ppm) was demonstrated by multicycle tests of Boudouard-carbonation/regeneration on Ca-based oxides with stable cyclic operation.en_US
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleHighly selective CO removal by sorption enhanced Boudouard reaction for hydrogen productionen_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber4100-4107en_US
dc.source.volume9en_US
dc.source.journalCatalysis science & technologyen_US
dc.source.issue15en_US
dc.identifier.doi10.1039/c9cy00851a
dc.identifier.cristin1751396
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2019 by Royal Society of Chemistry -en_US
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode0


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