dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorValentini, A.
dc.creatorCarreño, N. L. V.
dc.creatorLeite, E. R.
dc.creatorGonçalves, R. F.
dc.creatorSoledade, L. E. B.
dc.creatorManiette, Y.
dc.creatorLongo, Elson
dc.creatorProbst, L. F. D.
dc.date2014-05-27T11:21:07Z
dc.date2016-10-25T18:19:44Z
dc.date2014-05-27T11:21:07Z
dc.date2016-10-25T18:19:44Z
dc.date2004-07-01
dc.date.accessioned2017-04-06T01:09:46Z
dc.date.available2017-04-06T01:09:46Z
dc.identifierLatin American Applied Research, v. 34, n. 3, p. 165-172, 2004.
dc.identifier0327-0793
dc.identifierhttp://hdl.handle.net/11449/67800
dc.identifierhttp://acervodigital.unesp.br/handle/11449/67800
dc.identifierS0327-07932004000300005
dc.identifier2-s2.0-3142734563.pdf
dc.identifier2-s2.0-3142734563
dc.identifierhttp://www.scielo.org.ar/scielo.php?pid=S0327-07932004000300005&script=sci_arttext
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/889211
dc.descriptionThe CO2 reforming of CH4 was carried out over Ni catalysts supported on γ-Al2O3 and CeO 2-promoted γ-Al2O3. The catalysts were characterized by means of surface area measurements, TPR, CO2 and H2 chemisorption, XRD, SEM, and TEM. The CeO2 addition promoted an increase of catalytic activity and stability. The improvement in the resistance to carbon deposition is attributed to the highest CO2 adsorption presented by the CeO2 addition. The catalytic behavior presented by the samples, with a different CH4/CO2 ratio used, points to the CH4 decomposition reaction as the main source of carbon deposition.
dc.languageeng
dc.relationLatin American Applied Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCarbon formation
dc.subjectCeO2
dc.subjectDry reforming
dc.subjectMethane
dc.subjectSyngas
dc.subjectAlumina
dc.subjectCarbon dioxide
dc.subjectCerium
dc.subjectChemisorption
dc.subjectDeposition
dc.subjectNickel
dc.subjectReforming reactions
dc.subjectScanning electron microscopy
dc.subjectTemperature programmed desorption
dc.subjectTransmission electron microscopy
dc.subjectX ray diffraction analysis
dc.subjectCarbon formations
dc.subjectGreenhouse gases
dc.subjectCatalyst activity
dc.titleImproved activity and stability of Ce-promoted Ni/γ-A1 2O3 catalysts for carbon dioxide reforming of methane
dc.typeOtro


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