dc.creatorFenoglio, Rosa Juana
dc.creatorMassa, Paola Andrea
dc.creatorIvorra, Fernando Daniel
dc.creatorHaure, Patricia Monica
dc.date.accessioned2019-02-18T20:45:03Z
dc.date.accessioned2022-10-14T22:54:41Z
dc.date.available2019-02-18T20:45:03Z
dc.date.available2022-10-14T22:54:41Z
dc.date.created2019-02-18T20:45:03Z
dc.date.issued2007-05
dc.identifierFenoglio, Rosa Juana; Massa, Paola Andrea; Ivorra, Fernando Daniel; Haure, Patricia Monica; Conventional and wet proofed CuO/Al2O3 catalysts for phenol oxidation: Deactivation studies in a trickle bed reactor; John Wiley & Sons Ltd; Journal of Chemical Technology and Biotechnology; 82; 5; 5-2007; 481-487
dc.identifier0268-2575
dc.identifierhttp://hdl.handle.net/11336/70406
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4316365
dc.description.abstractA large variety of catalytic systems have been studied for the catalytic wet air oxidation of phenolic solutions. Most of them show good activity, but serious stability problems. In this contribution, stability studies were performed over CuO/Al2O3 conventional (CNT) and polytetrafluorethylene coated (C3T) catalysts used for the oxidation of 5 g L-1 phenol solutions in a trickle bed reactor (140 °C and 7 atm of oxygen pressure). For the hydrophilic catalyst, phenol conversion decreased with usage due to the formation of Cu2O and copper oxalate phases. For the wet proofed catalyst, the hydrophobic layer prevented the appearence of those phases, and conversion levels remained practically constant with reaction time. After usage, both catalysts were oxidized at 400 °C and tested for reaction: in the case of the C3T catalyst, the phenol conversion was increased over its initial level; for CNT catalyst, the phenol conversion was also increased, but initial levels were not completely restored. The deactivation mechanism of the CNT catalyst is associated with the formation of the Cu2O and copper oxalate phases during reaction. For catalyst C3T, practically no deactivation was observed.
dc.languageeng
dc.publisherJohn Wiley & Sons Ltd
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/jctb.1694
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jctb.1694
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCOPPER OXALATE
dc.subjectCU2O
dc.subjectCUO CATALYSTS
dc.subjectHYDROPHOBIC CATALYSTS
dc.subjectPHENOL OXIDATION
dc.titleConventional and wet proofed CuO/Al2O3 catalysts for phenol oxidation: Deactivation studies in a trickle bed reactor
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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