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用过渡金属物种(铬、钴、镍和铜)对二氧化钛进行改性以光催化去除液相中的乙酸和气相中的丙烯。

TiO₂ Modification with Transition Metallic Species (Cr, Co, Ni, and Cu) for Photocatalytic Abatement of Acetic Acid in Liquid Phase and Propene in Gas Phase.

作者信息

Amorós-Pérez Ana, Cano-Casanova Laura, Castillo-Deltell Ana, Lillo-Ródenas María Ángeles, Román-Martínez María Del Carmen

机构信息

MCMA Group, Department of Inorganic Chemistry and Materials Institute, University of Alicante, E-03080 Alicante, Spain.

出版信息

Materials (Basel). 2018 Dec 23;12(1):40. doi: 10.3390/ma12010040.

DOI:10.3390/ma12010040
PMID:30583575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6337716/
Abstract

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⁻TiO₂ interaction. The catalysts have been thoroughly characterized using N₂ 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.

摘要

商用P25二氧化钛已用过渡金属物种(铬、钴、镍和铜)进行了改性,通过用相应硝酸盐的水溶液浸渍添加。制备过程还包括在氩气中进行热处理(500℃)以分解硝酸盐、去除杂质并增强金属⁻TiO₂相互作用。使用N₂吸附、扫描电子显微镜(SEM)、X射线衍射(XRD)、紫外可见漫反射光谱(UV-vis DRS)和X射线光电子能谱(XPS)对催化剂进行了全面表征,并在两种情况下均使用365nm的辐照源对乙酸的水相分解和丙烯的气相氧化进行了测试。四种含金属催化剂的光催化活性随金属物种的性质而变化,并且在两个测试反应中遵循相似的趋势。添加金属物种的性质的影响主要基于负载物种的电化学性质,其中Cu/P25(含铜样品)是性能最佳的催化剂。在乙酸的光分解中,所有含金属样品都比纯P25更具活性,而在丙烯的气相氧化中,纯P25更具活性。考虑到气液介质中速率决定步骤不同,对此进行了解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/da4f97697010/materials-12-00040-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/a23cd34dd9e5/materials-12-00040-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/dd45c0fac241/materials-12-00040-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/c48b956303be/materials-12-00040-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/814151de040c/materials-12-00040-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/4edfca227b35/materials-12-00040-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/686d1393aa55/materials-12-00040-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/da4f97697010/materials-12-00040-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/a23cd34dd9e5/materials-12-00040-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/dd45c0fac241/materials-12-00040-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/c48b956303be/materials-12-00040-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/814151de040c/materials-12-00040-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/4edfca227b35/materials-12-00040-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/686d1393aa55/materials-12-00040-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1f/6337716/da4f97697010/materials-12-00040-g007.jpg

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