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Pt/TiO₂特性对可见光诱导光催化邻甲酚分解时间行为的影响。

Effect of Pt/TiO2 characteristics on temporal behavior of o-cresol decomposition by visible light-induced photocatalysis.

作者信息

Chen Hua-Wei, Ku Young, Kuo Yu-Lin

机构信息

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan.

出版信息

Water Res. 2007 May;41(10):2069-78. doi: 10.1016/j.watres.2007.02.021. Epub 2007 Apr 5.

Abstract

Platinum deposited TiO(2) films were prepared on quartz substrates by dip-coating process for the photodecomposition of o-cresol. The characteristics of Pt/TiO(2) and the temporal behavior of o-cresol decomposition by Pt/TiO(2) photocatalysis under visible light irradiation were investigated. Platinum deposited on TiO(2) photocatalysts was characterized by Brunauer-Emmett-Teller (BET) surface area measurement, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), diffuse reflectance UV-Vis spectra (DRS) and photoluminescence (PL) emission spectra. The results indicated that the deposition of platinum on TiO(2) promoted the optical absorption in the visible region and made it possible to be excited by visible light. The decomposition rate of o-cresol under visible light irradiation from a fluorescent lamp was enhanced to noticeably extents for experiments conducted with Pt/TiO(2) containing platinum up to 0.50wt% platinum because of the presence of Ti(3+) resulted from the platinum deposited on the TiO(2) surface; and the formation of Schottky Barrier between platinum and TiO(2) preventing the recombination of electric holes and electrons. Specifically, the reaction rate of o-cresol photodegradation at pH 9 using the 0.50wt% Pt/TiO(2) was 4.8 times than that of using pure TiO(2). The intermediates identified by GC/MS spectroscopy during the photocatalytic oxidation of o-cresol. The proposed kinetic model could be adequately applied to describe the temporal behavior of the o-cresol decomposition with and without the dosage of Pt on TiO(2) in aqueous solution by UV/TiO(2) process.

摘要

通过浸涂工艺在石英衬底上制备了用于邻甲酚光催化分解的铂负载二氧化钛薄膜。研究了Pt/TiO₂的特性以及在可见光照射下Pt/TiO₂光催化分解邻甲酚的时间行为。通过布鲁诺尔-埃米特-泰勒(BET)表面积测量、X射线衍射(XRD)、X射线光电子能谱(XPS)、扫描电子显微镜(SEM)、漫反射紫外-可见光谱(DRS)和光致发光(PL)发射光谱对负载在TiO₂光催化剂上的铂进行了表征。结果表明,铂在TiO₂上的沉积促进了可见光区域的光吸收,并使其能够被可见光激发。由于沉积在TiO₂表面的铂导致Ti(3+)的存在,对于含铂量高达0.50wt%铂的Pt/TiO₂进行的实验,在荧光灯光照下邻甲酚的分解速率有显著提高;并且铂与TiO₂之间形成肖特基势垒,阻止了空穴和电子的复合。具体而言,使用0.50wt% Pt/TiO₂在pH 9条件下邻甲酚光降解的反应速率是使用纯TiO₂的4.8倍。通过气相色谱/质谱(GC/MS)光谱鉴定了邻甲酚光催化氧化过程中的中间产物。所提出的动力学模型能够充分应用于描述在水溶液中通过紫外/TiO₂工艺在有无铂负载在TiO₂上的情况下邻甲酚分解的时间行为。

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