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Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/12387
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dc.contributor.authorQuadro, Emerentino Brazil-
dc.contributor.authorDias, Maria de Lourdes Ribeiro-
dc.contributor.authorAmorim, Adelaide Maria Mendonça-
dc.contributor.authorVarela, Maria do Carmo Rangel Santos-
dc.creatorQuadro, Emerentino Brazil-
dc.creatorDias, Maria de Lourdes Ribeiro-
dc.creatorAmorim, Adelaide Maria Mendonça-
dc.creatorVarela, Maria do Carmo Rangel Santos-
dc.date.accessioned2013-07-31T19:37:20Z-
dc.date.available2013-07-31T19:37:20Z-
dc.date.issued1999-
dc.identifier.issn0103-5053-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/12387-
dc.descriptionp. 51-59pt_BR
dc.description.abstractCopper and chromium-doped magnetite was prepared to be used as catalysts, in the active phase, in the high temperature shift (HTS) reaction. Samples were produced by heating a mixed hydrate ferric oxyhydroxide (IHA) in the range of 150-400 °C and characterized by means of chemical analysis, X-ray diffraction, thermal analysis (DSC and TG), infrared spectroscopy, surface area measurements, scanning electron microscopy and X-ray microanalysis. It was found that copper favors magnetite formation but does not affect significantly the crystallinity of the solids. Both chromium and copper improve the performance of the catalysts towards the HTS reaction: chromium acts as a stabilizer whereas copper increases the intrinsic activity. However, copper favors sinterization leading to solids with low surface areas. The increase in the catalytic activity and in the surface area of the solids reflects the synergy of these dopants.pt_BR
dc.language.isoenpt_BR
dc.publisherJournal of the Brazilian Chemical Societypt_BR
dc.sourcehttp://dx.doi.org/10.1590/S0103-50531999000100009pt_BR
dc.titleChromium and Copper-Doped Magnetite Catalysts for the High Temperature Shift Reactionpt_BR
dc.title.alternativeJournal of the Brazilian Chemical Societypt_BR
dc.typeArtigo de Periódicopt_BR
dc.description.localpubSão Paulopt_BR
dc.identifier.numberv. 10, n. 1pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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