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dc.contributor.author
Cuesta Zapata, Pablo Martín  
dc.contributor.author
Parentis, Monica Liliana  
dc.contributor.author
Gonzo, Elio Emilio  
dc.contributor.author
Bonini, Norberto Alejandro  
dc.date.available
2019-09-23T17:33:07Z  
dc.date.issued
2013-04-24  
dc.identifier.citation
Cuesta Zapata, Pablo Martín; Parentis, Monica Liliana; Gonzo, Elio Emilio; Bonini, Norberto Alejandro; Acid sites development on Cr3+/SiO2 catalysts obtained by the sol-gel method and hydrothermal treatment: Effect of calcination temperature; Elsevier Science; Applied Catalysis A: General; 457; 24-4-2013; 26-33  
dc.identifier.issn
0926-860X  
dc.identifier.uri
http://hdl.handle.net/11336/84140  
dc.description.abstract
Cr/SiO2 catalysts (4-8% Cr, w/w), obtained from Cr(III) salts and tetraethylortosilicate (TEOS), were prepared by the sol-gel method. After TEOS hydrolysis in ammoniacal solution (pH: 9.5), the gel was treated under hydrothermal conditions at 120-220 C. The solids were characterized by N 2 sorptometry, TG-DTA, DRUV-vis, XRD, and FTIR. In vacuum or N 2 atmosphere, Cr3+ ions were stable up to 450 C. However, calcination in air promotes the partial oxidation of Cr3+ to Cr 6+ as the temperature increases from 200 to 450 C. The amount of Cr6+ formed depends on the temperature of the hydrothermal treatment. 2,6-Lutidine adsorption allows to determine the evolution, with respect to calcination temperature, of both Lewis and Brönsted acid centers. Cr 3+ ions were related to the presence of Lewis sites, and Cr 6+ ions to the development of weak Brönsted acid sites. Accordingly, the 2-propanol dehydration reaction rate shows an increase when the catalysts are treated in N2 at 450 C, while catalysts calcined in air develop a lower acidity. The dehydration reaction is attributed to the presence of Lewis acid centers.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
Cr/Sio2  
dc.subject
Sol-Gel  
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2,6-Lutidine  
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Druv-Vis  
dc.subject.classification
Otras Ingeniería Química  
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Ingeniería Química  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.subject.classification
Otras Nanotecnología  
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Nanotecnología  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Acid sites development on Cr3+/SiO2 catalysts obtained by the sol-gel method and hydrothermal treatment: Effect of calcination temperature  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-06-10T20:35:00Z  
dc.journal.volume
457  
dc.journal.pagination
26-33  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Cuesta Zapata, Pablo Martín. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina  
dc.description.fil
Fil: Parentis, Monica Liliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina  
dc.description.fil
Fil: Gonzo, Elio Emilio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina  
dc.description.fil
Fil: Bonini, Norberto Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina  
dc.journal.title
Applied Catalysis A: General  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apcata.2013.02.028  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X13001191