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dc.creatorDevard, Alejandra Veronica-
dc.creatorPujro Tarquino, Richard Alfonzo-
dc.creatorde la Puente, Gabriela-
dc.creatorSedran, Ulises Anselmo-
dc.date2018-07-17T14:21:38Z-
dc.date2018-07-17T14:21:38Z-
dc.date2012-07-
dc.date2018-07-11T14:09:54Z-
dc.date.accessioned2019-04-29T15:29:20Z-
dc.date.available2019-04-29T15:29:20Z-
dc.date.issued2018-07-17T14:21:38Z-
dc.date.issued2018-07-17T14:21:38Z-
dc.date.issued2012-07-
dc.date.issued2018-07-11T14:09:54Z-
dc.identifierDevard, Alejandra Veronica; Pujro Tarquino, Richard Alfonzo; de la Puente, Gabriela; Sedran, Ulises Anselmo; Hydrocarbon Yield Structure in the Conversion of Heavy Model Molecules (Quinolin-65) on Fluidized Catalytic Cracking Catalyst; American Chemical Society; Energy & Fuels (print); 26; 7-2012; 5015-5019-
dc.identifier0887-0624-
dc.identifierhttp://hdl.handle.net/11336/52358-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/295068-
dc.descriptionThe reactivity of a heavy model molecule (quinolin-65, named Q65, a 2,3,7,8-dibenzopyrene derivative) over two different equilibrium fluidized catalytic cracking catalysts of the conventional and resid types was studied at 550 °C and with reaction times that varied from 5 to 20 s, in a batch fluidized-bed laboratory reactor. Two types of experiments were performed to determine the hydrocarbon products resulting from the conversion of Q65. This compound is solid at room temperature, and a solution of Q65 at 4.6 wt % in toluene and pure toluene were used. Conversions and yields were assessed by means of careful mass balances. The product distributions showed that Q65 produced a wide range of hydrocarbons from C1 to C20. These distributions were different according to the formulations of the catalysts. Olefins were predominant among gases and, neatly, aromatics among liquids. Coke yields were high, exceeding 12 wt %. The characteristics of the catalysts were also revealed through the higher activity and hydrogen-transfer ability of the conventional catalyst and the better coke selectivity of the resid catalyst. It was shown that both the linear alkyl chain and the multi-ring core react.-
dc.descriptionFil: Devard, Alejandra Veronica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina-
dc.descriptionFil: Pujro Tarquino, Richard Alfonzo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina-
dc.descriptionFil: de la Puente, Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina-
dc.descriptionFil: Sedran, Ulises Anselmo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina-
dc.formatapplication/pdf-
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dc.formatapplication/pdf-
dc.languageeng-
dc.publisherAmerican Chemical Society-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/journal/enfuem-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org//10.1021/ef300474f-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.subjectFCC-
dc.subjectResids-
dc.subjectQ65-
dc.subjectFuels-
dc.subjectOtras Ingeniería Química-
dc.subjectIngeniería Química-
dc.subjectINGENIERÍAS Y TECNOLOGÍAS-
dc.titleHydrocarbon Yield Structure in the Conversion of Heavy Model Molecules (Quinolin-65) on Fluidized Catalytic Cracking Catalyst-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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