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dc.contributor.author
Fornero, Esteban Luis  
dc.contributor.author
Chiavassa, Dante Luis  
dc.contributor.author
Bonivardi, Adrian Lionel  
dc.contributor.author
Baltanas, Miguel Angel  
dc.date.available
2017-12-22T11:04:33Z  
dc.date.issued
2017-12  
dc.identifier.citation
Baltanas, Miguel Angel; Bonivardi, Adrian Lionel; Chiavassa, Dante Luis; Fornero, Esteban Luis; Transient analysis of the reverse water gas shift reaction on Cu/ZrO2 and Ga2O3/Cu/ZrO2 catalysts; Elsevier; Journal of CO2 Utilization; 22; 12-2017; 289-298  
dc.identifier.issn
2212-9820  
dc.identifier.uri
http://hdl.handle.net/11336/31346  
dc.description.abstract
The performance of two copper-based catalysts, Cu/ZrO2 and Ga2O3/Cu/ZrO2, in regards the reverse water gas shift (RWGS) reaction as compared with their reaction rates for the methanol synthesis reaction (RCH3OH) was studied using H2/CO2 mixtures at 1.6 and 0.1 MPa, at 498 K. The reactivity studies were carried out using a Carberry-type microcatalytic reactor operated in the batch (transient) mode after H2 prereduction at 523 K (2 h). Measurements of the catalytic activity were also made using D2/CO2 mixtures (0.1 MPa, 498 K) to assess isotope effects. For Cu/ZrO2, the initial RWGS reaction rate using D2 instead of H2 was slightly higher whereas such rate was about equal for the ternary catalyst. Kinetic rate expressions obtained from the Langmuir-Hinshelwood-Hougen-Watson formalism were used to model and analyze the experimental results and the reaction mechanism(s) of the RWGS on these catalysts. Congruence was found between the experimental results and a reaction mechanism where (predominantly) CO2 adsorbs dissociatively on the Cu particles (rate-determining step). The reduction of (ad)oxygen and surface hydroxyls follow afterwards.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Associative Mechanisms  
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Co2 Hydrogenation  
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Methanol Synthesis  
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Redox Mechanism  
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Supported Copper  
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Water Gas Shift  
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Otras Ingeniería Química  
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Ingeniería Química  
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INGENIERÍAS Y TECNOLOGÍAS  
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Ingeniería Medioambiental y Geológica, Geotécnicas  
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Ingeniería del Medio Ambiente  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Transient analysis of the reverse water gas shift reaction on Cu/ZrO2 and Ga2O3/Cu/ZrO2 catalysts  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-12-19T18:30:20Z  
dc.journal.volume
22  
dc.journal.pagination
289-298  
dc.journal.pais
Países Bajos  
dc.description.fil
Fil: Fornero, Esteban Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina  
dc.description.fil
Fil: Chiavassa, Dante Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina  
dc.description.fil
Fil: Bonivardi, Adrian Lionel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina  
dc.description.fil
Fil: Baltanas, Miguel Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina  
dc.journal.title
Journal of CO2 Utilization  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.jcou.2017.06.002