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Multivariate curve resolution analysis applied to time-resolved synchrotron X-ray Absorption Spectroscopy monitoring of the activation of copper alumina catalyst

dc.contributor.authorCassinelli, Wellington H. [UNESP]
dc.contributor.authorMartins, Leandro [UNESP]
dc.contributor.authorPassos, Aline R. [UNESP]
dc.contributor.authorPulcinelli, Sandra Helena [UNESP]
dc.contributor.authorSantilli, Celso Valentim [UNESP]
dc.contributor.authorRochet, Amelie
dc.contributor.authorBriois, Valerie
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionSynchrotron SOLEIL
dc.date.accessioned2014-12-03T13:08:38Z
dc.date.available2014-12-03T13:08:38Z
dc.date.issued2014-06-15
dc.description.abstractThe pure X-ray Absorption (XAS) spectral constituents and related concentration profiles characterizing the reduction of a copper-based catalyst supported on hierarchically porous alumina were disentangled from a set of time-resolved Quick-XAS using a Multivariate Curve Resolution-methodology. First, the number of components involved in the data set and the range of existence of intermediate species were determined by Principal Component Analysis (PCA). Then, a Multivariate Curve Resolution with Alternating Least Squares fitting of the set of time-resolved Quick-XANES was performed using the constraints of non-negativity of both absorption and concentration and of closure of concentration. Consideration about the strategy of use of the chemometric methods and robustness regarding the reliability of results for time-resolved XAS data is discussed. The intermediate copper species determined by MCR-ALS is at the monovalent oxidation state and characterized by a local order of 2 oxygen atoms at 1.915 angstrom. Upon isothermal treatment under 60% H-2/He at 250 degrees C for 30 min, the intermediate species appears quite resistant to complete copper reduction. Copper speciation obtained using MCR-ALS method leads to very different results than those obtained using bulk CuO, Cu2O and metallic Cu as constituents, MCR-ALS concentration profile so-determined being fully consistent with the reducibility of the catalyst measured by TPR. (C) 2013 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv Estadual Paulista, UNESP, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationSynchrotron SOLEIL, F-91192 Gif Sur Yvette, France
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 07/53073-4
dc.description.sponsorshipIdFAPESP: 13/50023-7
dc.description.sponsorshipIdFAPESP: 13/05346-2
dc.format.extent114-122
dc.identifierhttp://dx.doi.org/10.1016/j.cattod.2013.10.077
dc.identifier.citationCatalysis Today. Amsterdam: Elsevier Science Bv, v. 229, p. 114-122, 2014.
dc.identifier.doi10.1016/j.cattod.2013.10.077
dc.identifier.issn0920-5861
dc.identifier.lattes5782696565602340
dc.identifier.lattes9971202585286967
dc.identifier.lattes5584298681870865
dc.identifier.orcid0000-0002-8356-8093
dc.identifier.urihttp://hdl.handle.net/11449/111409
dc.identifier.wosWOS:000333450100014
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofCatalysis Today
dc.relation.ispartofjcr4.667
dc.relation.ispartofsjr1,347
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectTime-resolved XASen
dc.subjectMCR-ALSen
dc.subjectPCAen
dc.subjectCopper speciationen
dc.titleMultivariate curve resolution analysis applied to time-resolved synchrotron X-ray Absorption Spectroscopy monitoring of the activation of copper alumina catalysten
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes5782696565602340
unesp.author.lattes9971202585286967
unesp.author.lattes5584298681870865[5]
unesp.author.orcid0000-0002-8356-8093[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentBioquímica e Tecnologia - IQARpt
unesp.departmentFísico-Química - IQARpt

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