Publication:
Direct stepwise oxidation of methane to methanol over Cu-SiO2

dc.contributor.coauthorSot, Petr
dc.contributor.coauthorNachtegaal, Maarten
dc.contributor.coauthorRanocchiari, Marco
dc.contributor.coauthorVan Bolchoven, Jeroen A.
dc.contributor.coauthorMesters, Carl
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.kuauthorBozbağ, Selmi Erim
dc.contributor.kuprofileResearcher
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.date.accessioned2024-11-09T12:16:09Z
dc.date.issued2018
dc.description.abstractCu supported on SiO2 can be used to directly convert methane to methanol in a stepwise process with no intrinsic need for a zeolite support. Effects of parameters such as the O-2 activation temperature, activation time, CH4 reaction temperature, CH4 partial pressure (pCH(4)), and Cu wt % on methanol yield were investigated. Increasing the O-2 activation temperature in the 200-800 degrees C range significantly improved the methanol yield, and when carried out at 800 degrees C, a methanol yield of 11.5 mu mol/g(ctalyst) was obtained after reaction with methane at 200 degrees C for the sample with 2 wt % Cu. Yield per mole of Cu increased exponentially from 1.0 to 59.1 mmol with decreased Cu wt % from 30 to 1, respectively. The increase in the O-2 activation time also strongly influenced the yield which corresponded to the increase in yield by a factor of >2 between 1 and 8 h. Increasing PCH4 from 0.05 to 1 atm resulted in a 5-fold increase in yield after activation at 450 degrees C; however, it resulted in at least 20% lower yields after activation at 800 degrees C showing that active sites of different nature were formed at different activation temperatures. The increase in yield with ramped O-2 activation temperature correlated with the dehydration of the samples as evidenced by X-ray absorption near-edge spectroscopy (XANES) and via mass spectroscopy (MS) traces of H2O during the O-2 activation step.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.issue7
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorshipTurkish Scientific and Technological Research Council (Scientific and Technological Research Council of Turkey (TÜBİTAK))
dc.description.versionAuthor's final manuscript
dc.description.volume8
dc.formatpdf
dc.identifier.doi10.1021/acscatal.8b01021
dc.identifier.eissn2155-5435
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR01549
dc.identifier.issn2155-5435
dc.identifier.linkhttps://doi.org/10.1021/acscatal.8b01021
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85047385822
dc.identifier.urihttps://hdl.handle.net/20.500.14288/1373
dc.identifier.wos438475100008
dc.keywordsMethane to methanol
dc.keywordsSilica
dc.keywordsCopper
dc.keywordsActivation temperature
dc.keywordsXRD
dc.keywordsXAS
dc.languageEnglish
dc.publisherAmerican Chemical Society (ACS)
dc.relation.grantno2219
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/8199
dc.sourceACS Catalysis
dc.subjectChemistry
dc.titleDirect stepwise oxidation of methane to methanol over Cu-SiO2
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorBozbağ, Selmi Erim
relation.isOrgUnitOfPublicationc747a256-6e0c-4969-b1bf-3b9f2f674289
relation.isOrgUnitOfPublication.latestForDiscoveryc747a256-6e0c-4969-b1bf-3b9f2f674289

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