Catalytic photodegradation of dyes by in situ zeolite-supported titania

Detalhes bibliográficos
Autor(a) principal: Petkowicz, Diego Ivan
Data de Publicação: 2010
Outros Autores: Pergher, Sibele Berenice Castellã, Silva, Carlos Daniel Silva da, Rocha, Zênis Novais da, Santos, João Henrique Zimnoch dos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/29122
Resumo: The degradation of dyes (methylene blue, direct blue 71, direct yellow 8) by a series of titania-supported catalysts generated in situ via the impregnation of TiCl4 onto a series of zeolite, which was synthesized using rice husks as the silicon source, was individually evaluated. After calcination, the resulting supported catalysts were characterized by X-ray diffraction spectrometry, ultraviolet–visible diffuse reflectance spectroscopy, diffuse reflectance and transmittance infrared Fourier transform spectroscopy, energy dispersive X-ray scanning electron microscopy, small angle X-ray scattering and differential pulse voltammetry. The titania generated is present in the anatase phase, without affecting the zeolite framework. Catalyst activity was shown to be comparable to that of the commercial P-25 catalyst after 1 h of UV light exposition. Monitoring the catalyst performance of several batches of material showed that P-25 provided the highest photodecomposition until the third cycle. On the other hand, the activity of the in situ-supported titania catalyst, in spite of showing lower catalytic activity, remained roughly constant up to the fifth cycle. This suggests that the catalyst generated in situ is more suitable for both filtering and reuse.
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spelling Petkowicz, Diego IvanPergher, Sibele Berenice CastellãSilva, Carlos Daniel Silva daRocha, Zênis Novais daSantos, João Henrique Zimnoch dos2020-06-03T02:00:09Z2020-06-03T02:00:09Z2010-04-15PETKOWICZ, Diego Ivan; PERGHER, Sibele B. C.; SILVA, Carlos Daniel Silva da; ROCHA, Zênis Novais da; SANTOS, João H. Z. dos. Catalytic photodegradation of dyes by in situ zeolite-supported titania. Chemical Engineering Journal, [s. l.], v. 158, n. 3, p. 505-512, abr. 2010. ISSN 1385-8947. DOI https://doi.org/10.1016/j.cej.2010.01.039. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S1385894710000604?via%3Dihub. Acesso em: 16 maio 2020.1385-8947https://repositorio.ufrn.br/jspui/handle/123456789/2912210.1016/j.cej.2010.01.039ElsevierPhotocatalysisTitaniaZeolite NaADyeRice huskCatalytic photodegradation of dyes by in situ zeolite-supported titaniainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleThe degradation of dyes (methylene blue, direct blue 71, direct yellow 8) by a series of titania-supported catalysts generated in situ via the impregnation of TiCl4 onto a series of zeolite, which was synthesized using rice husks as the silicon source, was individually evaluated. After calcination, the resulting supported catalysts were characterized by X-ray diffraction spectrometry, ultraviolet–visible diffuse reflectance spectroscopy, diffuse reflectance and transmittance infrared Fourier transform spectroscopy, energy dispersive X-ray scanning electron microscopy, small angle X-ray scattering and differential pulse voltammetry. The titania generated is present in the anatase phase, without affecting the zeolite framework. Catalyst activity was shown to be comparable to that of the commercial P-25 catalyst after 1 h of UV light exposition. Monitoring the catalyst performance of several batches of material showed that P-25 provided the highest photodecomposition until the third cycle. On the other hand, the activity of the in situ-supported titania catalyst, in spite of showing lower catalytic activity, remained roughly constant up to the fifth cycle. 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dc.title.pt_BR.fl_str_mv Catalytic photodegradation of dyes by in situ zeolite-supported titania
title Catalytic photodegradation of dyes by in situ zeolite-supported titania
spellingShingle Catalytic photodegradation of dyes by in situ zeolite-supported titania
Petkowicz, Diego Ivan
Photocatalysis
Titania
Zeolite NaA
Dye
Rice husk
title_short Catalytic photodegradation of dyes by in situ zeolite-supported titania
title_full Catalytic photodegradation of dyes by in situ zeolite-supported titania
title_fullStr Catalytic photodegradation of dyes by in situ zeolite-supported titania
title_full_unstemmed Catalytic photodegradation of dyes by in situ zeolite-supported titania
title_sort Catalytic photodegradation of dyes by in situ zeolite-supported titania
author Petkowicz, Diego Ivan
author_facet Petkowicz, Diego Ivan
Pergher, Sibele Berenice Castellã
Silva, Carlos Daniel Silva da
Rocha, Zênis Novais da
Santos, João Henrique Zimnoch dos
author_role author
author2 Pergher, Sibele Berenice Castellã
Silva, Carlos Daniel Silva da
Rocha, Zênis Novais da
Santos, João Henrique Zimnoch dos
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Petkowicz, Diego Ivan
Pergher, Sibele Berenice Castellã
Silva, Carlos Daniel Silva da
Rocha, Zênis Novais da
Santos, João Henrique Zimnoch dos
dc.subject.por.fl_str_mv Photocatalysis
Titania
Zeolite NaA
Dye
Rice husk
topic Photocatalysis
Titania
Zeolite NaA
Dye
Rice husk
description The degradation of dyes (methylene blue, direct blue 71, direct yellow 8) by a series of titania-supported catalysts generated in situ via the impregnation of TiCl4 onto a series of zeolite, which was synthesized using rice husks as the silicon source, was individually evaluated. After calcination, the resulting supported catalysts were characterized by X-ray diffraction spectrometry, ultraviolet–visible diffuse reflectance spectroscopy, diffuse reflectance and transmittance infrared Fourier transform spectroscopy, energy dispersive X-ray scanning electron microscopy, small angle X-ray scattering and differential pulse voltammetry. The titania generated is present in the anatase phase, without affecting the zeolite framework. Catalyst activity was shown to be comparable to that of the commercial P-25 catalyst after 1 h of UV light exposition. Monitoring the catalyst performance of several batches of material showed that P-25 provided the highest photodecomposition until the third cycle. On the other hand, the activity of the in situ-supported titania catalyst, in spite of showing lower catalytic activity, remained roughly constant up to the fifth cycle. This suggests that the catalyst generated in situ is more suitable for both filtering and reuse.
publishDate 2010
dc.date.issued.fl_str_mv 2010-04-15
dc.date.accessioned.fl_str_mv 2020-06-03T02:00:09Z
dc.date.available.fl_str_mv 2020-06-03T02:00:09Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.citation.fl_str_mv PETKOWICZ, Diego Ivan; PERGHER, Sibele B. C.; SILVA, Carlos Daniel Silva da; ROCHA, Zênis Novais da; SANTOS, João H. Z. dos. Catalytic photodegradation of dyes by in situ zeolite-supported titania. Chemical Engineering Journal, [s. l.], v. 158, n. 3, p. 505-512, abr. 2010. ISSN 1385-8947. DOI https://doi.org/10.1016/j.cej.2010.01.039. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S1385894710000604?via%3Dihub. Acesso em: 16 maio 2020.
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/29122
dc.identifier.issn.none.fl_str_mv 1385-8947
dc.identifier.doi.none.fl_str_mv 10.1016/j.cej.2010.01.039
identifier_str_mv PETKOWICZ, Diego Ivan; PERGHER, Sibele B. C.; SILVA, Carlos Daniel Silva da; ROCHA, Zênis Novais da; SANTOS, João H. Z. dos. Catalytic photodegradation of dyes by in situ zeolite-supported titania. Chemical Engineering Journal, [s. l.], v. 158, n. 3, p. 505-512, abr. 2010. ISSN 1385-8947. DOI https://doi.org/10.1016/j.cej.2010.01.039. Disponível em: https://www.sciencedirect.com/science/article/abs/pii/S1385894710000604?via%3Dihub. Acesso em: 16 maio 2020.
1385-8947
10.1016/j.cej.2010.01.039
url https://repositorio.ufrn.br/jspui/handle/123456789/29122
dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv Elsevier
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