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Kinetic study and H2S effect on refractory DBTs desulfurization in a heavy gasoil

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dc.contributor.author Kallinikos, LE en
dc.contributor.author Jess, A en
dc.contributor.author Papayannakos, NG en
dc.date.accessioned 2014-03-01T01:33:41Z
dc.date.available 2014-03-01T01:33:41Z
dc.date.issued 2010 en
dc.identifier.issn 0021-9517 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/20531
dc.subject Desulfurization en
dc.subject Dibenzothiophenes en
dc.subject Hydrogen sulfide effect en
dc.subject Refractory compounds en
dc.subject Spiral mini-bed reactor en
dc.subject.classification Chemistry, Physical en
dc.subject.classification Engineering, Chemical en
dc.subject.other Active site en
dc.subject.other Bed reactors en
dc.subject.other Commercial operation en
dc.subject.other Deep desulfurization en
dc.subject.other Dibenzothiophenes en
dc.subject.other Heavy gasoil en
dc.subject.other Hydrotreating en
dc.subject.other Inhibiting effect en
dc.subject.other Kinetic study en
dc.subject.other Liquid hourly space velocity en
dc.subject.other Refractory compounds en
dc.subject.other S effect en
dc.subject.other Spiral mini-bed reactor en
dc.subject.other Sulfur component en
dc.subject.other Tetramethyl en
dc.subject.other Total pressure en
dc.subject.other Total sulfur en
dc.subject.other Trimethyl en
dc.subject.other Activation energy en
dc.subject.other Catalysts en
dc.subject.other Hydrodesulfurization en
dc.subject.other Hydrogen en
dc.subject.other Hydrogen sulfide en
dc.subject.other Hydrogenation en
dc.subject.other Liquids en
dc.subject.other Organic polymers en
dc.subject.other Refractory materials en
dc.subject.other Sulfur en
dc.subject.other Sulfur determination en
dc.subject.other Chemical contamination en
dc.title Kinetic study and H2S effect on refractory DBTs desulfurization in a heavy gasoil en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.jcat.2009.11.005 en
heal.identifier.secondary http://dx.doi.org/10.1016/j.jcat.2009.11.005 en
heal.language English en
heal.publicationDate 2010 en
heal.abstract The removal evolution of six refractory individual S-compounds, i.e. DBT, 4-methyl-DBT, 4,6-dimethyl-DBT, 4-ethyl-6-methyl-DBT, 2,4,6-trimethyl-DBT, and 2,4,6,8-tetramethyl-DBT, and five groups of S-compounds with one to four substitutions has been studied during the deep desulfurization process of a heavy gasoil in a mini scale-structured bed reactor. The reactivity of the sulfur compounds was investigated by hydrotreating the gasoil with a commercial NiMo/gamma-Al2O3 catalyst under commercial operation conditions of temperature (563-623 K), total pressure (50 x 10(5) Pa), liquid hourly space velocity (LHSV) (0.7-3 h(-1)), and gas-to-liquid ratio (400-600 Nm(H2)(3)/m(oil)(3)). Moreover, the inhibiting effect of the hydrogen sulfide on the hydrodesulfurization rates of the S-compounds has been studied by performing tests with various H2S partial pressures. The results showed that the most refractory sulfur component is the 4,6-dimethyl-DBT constituting the major compound in the hydrotreated product with 50 ppm total sulfur and practically the only S-compound in the product with 10 ppm total sulfur. It has been verified that differences in HDS reactivity among DBT, 4-methyl-DBT, and 4,6-dimethyl-DBT in the real feed are lower than those commonly referred to in model feeds. The reactivity of the S-compounds is affected by the presence of the adsorbed on the catalyst active sites hydrogen sulfide and this effect appears decreasing with the number of the substituents of DBTs. The activation energy of DBTs obtained in the current work appears to be higher for the non-substituted DBT, which mainly reacts through the hydrogenolysis route, and to decrease for the substituted DBTs, which react through the hydrogenation route. (c) 2009 Elsevier Inc. All rights reserved. en
heal.publisher ACADEMIC PRESS INC ELSEVIER SCIENCE en
heal.journalName Journal of Catalysis en
dc.identifier.doi 10.1016/j.jcat.2009.11.005 en
dc.identifier.isi ISI:000274042600019 en
dc.identifier.volume 269 en
dc.identifier.issue 1 en
dc.identifier.spage 169 en
dc.identifier.epage 178 en


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