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TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase

The commercial P25 titania has been modified with transition metallic species (Cr, Co, Ni, and Cu), added by impregnation with aqueous solutions of the corresponding nitrates. The preparation procedure also includes a heat treatment (500 °C) in argon to decompose the nitrates, remove impurities and...

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Autores principales: Amorós-Pérez, Ana, Cano-Casanova, Laura, Castillo-Deltell, Ana, Lillo-Ródenas, María Ángeles, Román-Martínez, María del Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337716/
https://www.ncbi.nlm.nih.gov/pubmed/30583575
http://dx.doi.org/10.3390/ma12010040
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author Amorós-Pérez, Ana
Cano-Casanova, Laura
Castillo-Deltell, Ana
Lillo-Ródenas, María Ángeles
Román-Martínez, María del Carmen
author_facet Amorós-Pérez, Ana
Cano-Casanova, Laura
Castillo-Deltell, Ana
Lillo-Ródenas, María Ángeles
Román-Martínez, María del Carmen
author_sort Amorós-Pérez, Ana
collection PubMed
description The commercial P25 titania has been modified with transition metallic species (Cr, Co, Ni, and Cu), added by impregnation with aqueous solutions of the corresponding nitrates. The preparation procedure also includes a heat treatment (500 °C) in argon to decompose the nitrates, remove impurities and to strengthen the metal–TiO(2) interaction. The catalysts have been thoroughly characterized using N(2) adsorption, scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-visible diffuse-reflectance spectroscopy (UV-vis DRS) and X-ray photoelectron spectroscopy (XPS), and have been tested in the aqueous phase decomposition of acetic acid and in the gas phase oxidation of propene, using an irradiation source of 365 nm in both cases. The photocatalytic activity of the four metal-containing catalysts varies with the nature of the metallic species and follows a similar trend in the two tested reactions. The effect of the nature of the added metallic species is mainly based on the electrochemical properties of the supported species, being Cu/P25 (the sample that contains copper) the best performing catalyst. In the photodecomposition of acetic acid, all the metal-containing samples are more active than bare P25, while in the gas phase oxidation of propene, bare P25 is more active. This has been explained considering that the rate-determining steps are different in gas and liquid media.
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spelling pubmed-63377162019-01-22 TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase Amorós-Pérez, Ana Cano-Casanova, Laura Castillo-Deltell, Ana Lillo-Ródenas, María Ángeles Román-Martínez, María del Carmen Materials (Basel) Article The commercial P25 titania has been modified with transition metallic species (Cr, Co, Ni, and Cu), added by impregnation with aqueous solutions of the corresponding nitrates. The preparation procedure also includes a heat treatment (500 °C) in argon to decompose the nitrates, remove impurities and to strengthen the metal–TiO(2) interaction. The catalysts have been thoroughly characterized using N(2) adsorption, scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-visible diffuse-reflectance spectroscopy (UV-vis DRS) and X-ray photoelectron spectroscopy (XPS), and have been tested in the aqueous phase decomposition of acetic acid and in the gas phase oxidation of propene, using an irradiation source of 365 nm in both cases. The photocatalytic activity of the four metal-containing catalysts varies with the nature of the metallic species and follows a similar trend in the two tested reactions. The effect of the nature of the added metallic species is mainly based on the electrochemical properties of the supported species, being Cu/P25 (the sample that contains copper) the best performing catalyst. In the photodecomposition of acetic acid, all the metal-containing samples are more active than bare P25, while in the gas phase oxidation of propene, bare P25 is more active. This has been explained considering that the rate-determining steps are different in gas and liquid media. MDPI 2018-12-23 /pmc/articles/PMC6337716/ /pubmed/30583575 http://dx.doi.org/10.3390/ma12010040 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Amorós-Pérez, Ana
Cano-Casanova, Laura
Castillo-Deltell, Ana
Lillo-Ródenas, María Ángeles
Román-Martínez, María del Carmen
TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase
title TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase
title_full TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase
title_fullStr TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase
title_full_unstemmed TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase
title_short TiO(2) Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase
title_sort tio(2) modification with transition metallic species (cr, co, ni, and cu) for photocatalytic abatement of acetic acid in liquid phase and propene in gas phase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337716/
https://www.ncbi.nlm.nih.gov/pubmed/30583575
http://dx.doi.org/10.3390/ma12010040
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