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dc.contributor.authorFonseca, Juliana da Silva Lima-
dc.contributor.authorFaro Júnior, Arnaldo da Costa-
dc.contributor.authorGrau, Javier Mario-
dc.contributor.authorVarela, Maria do Carmo Rangel Santos-
dc.creatorFonseca, Juliana da Silva Lima-
dc.creatorFaro Júnior, Arnaldo da Costa-
dc.creatorGrau, Javier Mario-
dc.creatorVarela, Maria do Carmo Rangel Santos-
dc.date.accessioned2012-04-12T19:15:09Z-
dc.date.issued2010-
dc.identifier.issn0926-860X-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/5611-
dc.descriptionAcesso restrito: Texto completo. p. 201-210.pt_BR
dc.description.abstractPlatinum catalysts supported on zeolite KY (Si/Al = 12.7), modified with magnesium, calcium or barium,were evaluated in n-octane reforming to produce ethylbenzene. The catalysts were characterized by nitrogen adsorption, 27Al and 29Si solid state nuclear magnetic resonance, Fourier transform infrared spectroscopy using carbon monoxide or pyridine, metal dispersion measurements and programmed temperature oxidation. No significant structural change was noted for the solids due to the dopants except for barium, which decreased the specific surface area, due to the partial blockage of the zeolite channels by the large size ions. However, a decrease was noted for all samples due to platinum, which partially blocked the zeolite channels. Barium also decreased the crystallinity while platinum caused this effect only for calcium and barium-containing samples, due to the structure partial collapse. Metallic platinum species in several electronic states were detected in the cages of zeolite, barium-containing catalyst showing the most electron-enriched platinum atoms. The amount of Lewis and Brønsted acid sites increased due to magnesium and calcium but barium increased only the amount of Lewis acid sites, as compared to potassium-containing solid. The catalysts with magnesium and barium showed the same platinum dispersion, which was higher than the one containing calcium. All catalysts were active in n-octane reforming at 723K and selective to ethylbenzene, but the conversion dropped with time reaction due to the decrease of specific surface area and to coke deposition. The calcium-containing sample produced the hardest coke, which led to the highest drop in conversion. The n-octane conversion was supposed to occur by a monofunctional mechanism but the bifunctional mechanism also seemed to occur due to the residual acidity of the catalysts. The calcium and barium-containing catalysts were the most selective to ethylbenzene, due to electron-enriched platinum species related to promoters, but the low ethylbenzene selectivity for the magnesium-containing catalyst was compensated by its high conversion, resulting in similar yields for all catalysts.pt_BR
dc.language.isoenpt_BR
dc.sourceDOI: 10.1016/j.apcata.2010.07.056pt_BR
dc.subjectn-Octane reformingpt_BR
dc.subjectY zeolitept_BR
dc.subjectEthylbenzenept_BR
dc.subjectCokept_BR
dc.subjectBariumpt_BR
dc.subjectCalciumpt_BR
dc.subjectMagnesiumpt_BR
dc.titleEthylbenzene production over platinum catalysts supported on modified KY zeolitespt_BR
dc.title.alternativeApplied Catalysis A-Generalpt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 386, n. 1-2pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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