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dc.contributor.author
Albornoz, L.L  
dc.contributor.author
da Silva, S.W.  
dc.contributor.author
Bortolozzi, Juan Pablo  
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Banus, Ezequiel David  
dc.contributor.author
Brussino, Paula  
dc.contributor.author
Ulla, Maria Alicia del H.  
dc.contributor.author
Bernardes, Andrea Moura  
dc.date.available
2021-10-29T16:20:43Z  
dc.date.issued
2021-04  
dc.identifier.citation
Albornoz, L.L; da Silva, S.W.; Bortolozzi, Juan Pablo; Banus, Ezequiel David; Brussino, Paula; et al.; Degradation and mineralization of erythromycin by heterogeneous photocatalysis using SnO2-doped TiO2 structured catalysts: Activity and stability; Pergamon-Elsevier Science Ltd; Chemosphere; 268; 4-2021; 1-47  
dc.identifier.issn
0045-6535  
dc.identifier.uri
http://hdl.handle.net/11336/145495  
dc.description.abstract
Heterogeneous photocatalysis was used for the degradation and mineralization of erythromycin (ERY), with a consequent production of carboxylic acids. For that, a series of TiO2 and Ti1-xSnxO2 structured catalysts, namely M1 to M5, was prepared using the washcoating method, with the catalytic coatings being deposited onto stainless steel meshes. Besides, the catalytic activity of the prepared systems was compared to that of the commercial mesh (CM). The results showed that the prepared TiO2 structured catalyst (M1) presented better ERY oxidation than the CM one, what was associated to the higher catalyst load and to the anatase/rutile ratio. Considering the Sn-doped structured catalysts, for M2, M4 and M5 catalysts, lower ERY mineralization and high formation of carboxylic acids were found, when compared to the M3 catalyst. The improved M3 activity was attributed to the formation of a staggered gap (type II heterojunction), providing better charge separation. In this situation, a high generation of hydroxyl radicals is obtained, resulting on a higher ERY mineralization. By the obtained results it is possible to determine that the addition order and the type of Sn compound added in the washcoating process, affects the catalytic activity due to the formation of a solid solution and to the type of produced heterostructures. The M3 catalyst also showed high stability in long-term tests up to 44 h of reaction. The results provide insights into the development of an inexpensive structured catalyst production method and its influence in the stability of the photocatalyst, as well as in its applicability on water/wastewater treatment.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Pergamon-Elsevier Science Ltd  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
ERYTHROMYCIN  
dc.subject
PHOTOCATALYSIS  
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SHORT CARBOXYLIC ACIDS  
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TI1-XSNXO2  
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WASHCOATING  
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Ingeniería de Procesos Químicos  
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Ingeniería Química  
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INGENIERÍAS Y TECNOLOGÍAS  
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Recubrimientos y Películas  
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Ingeniería de los Materiales  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Degradation and mineralization of erythromycin by heterogeneous photocatalysis using SnO2-doped TiO2 structured catalysts: Activity and stability  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2021-09-07T14:33:13Z  
dc.journal.volume
268  
dc.journal.pagination
1-47  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: Albornoz, L.L. Universidade Federal do Rio Grande do Sul; Brasil  
dc.description.fil
Fil: da Silva, S.W.. Universidade Federal do Rio Grande do Sul; Brasil  
dc.description.fil
Fil: Bortolozzi, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.description.fil
Fil: Banus, Ezequiel David. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.description.fil
Fil: Brussino, Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.description.fil
Fil: Ulla, Maria Alicia del H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina  
dc.description.fil
Fil: Bernardes, Andrea Moura. Universidade Federal do Rio Grande do Sul; Brasil  
dc.journal.title
Chemosphere  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0045653520330563  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.chemosphere.2020.128858