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dc.contributor.author
D'ippolito, Silvana Andrea  
dc.contributor.author
Ballarini, Adriana Daniela  
dc.contributor.author
Pieck, Carlos Luis  
dc.date.available
2018-04-24T20:08:28Z  
dc.date.issued
2017-04  
dc.identifier.citation
D'ippolito, Silvana Andrea; Ballarini, Adriana Daniela; Pieck, Carlos Luis; Influence of Support Acidity and Ir Content on the Selective Ring Opening of Decalin over Ir/SiO 2 –Al 2 O 3; American Chemical Society; Energy & Fuels (print); 31; 5; 4-2017; 5461-5471  
dc.identifier.issn
0887-0624  
dc.identifier.uri
http://hdl.handle.net/11336/43344  
dc.description.abstract
The influence of the addition of HCl and Ir (1 wt %) to different SiO2−Al2O3 supports of varying silica content was studied in the reaction of selective ring opening of decalin. The addition of HCl to silica−alumina supports containing 70 and 80 wt % SiO2 was found to have little influence in the distribution of reaction products compared to the calcined supports. The incorporation of Ir to the silica−alumina catalysts has a beneficial effect, increasing the decalin conversion, being this effect more noticeable in the low acidity supports, i.e., those containing 30−40 wt % SiO2. The iridium-containing materials display the highest yield of cracking products, ring opening products, and ring contraction products. Increasing the reaction temperature promotes cracking and dehydrogenation but markedly decreases the selectivity to ring contraction products. At 350 °C a slight decrease in selectivity to ring opening products occurs, though the overall increase in conversion results in an increased yield of these products. An optimum ratio between the acid sites and metal activity that favors the formation of ring opening products was found. At lower acid sites/metal activity ratios the isomerization reaction which leads to C5 cycle isomers is low, and ring opening by hydrogenolysis is limited as a consequence. On the other hand, at high acid sites/metal activity ratios the cracking reactions are favored, decreasing the yield of RO products.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Chemical Society  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Selective Ring Opening  
dc.subject
Decalin  
dc.subject
Ir/Sio2−Al2o3  
dc.subject.classification
Otras Ingeniería Química  
dc.subject.classification
Ingeniería Química  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Influence of Support Acidity and Ir Content on the Selective Ring Opening of Decalin over Ir/SiO 2 –Al 2 O 3  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-04-13T13:57:11Z  
dc.journal.volume
31  
dc.journal.number
5  
dc.journal.pagination
5461-5471  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: D'ippolito, Silvana Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.description.fil
Fil: Ballarini, Adriana Daniela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.description.fil
Fil: Pieck, Carlos Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.journal.title
Energy & Fuels (print)  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/acs.energyfuels.7b00451  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1021/acs.energyfuels.7b00451