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Improved Photocatalytic Degradation of Methyl Orange by Polyoxometalates Supported on Titanium Dioxide Doping with Rare Earth

机译:通过稀土化掺杂二氧化钛掺杂的多氧化钛的光催化降解甲基橙

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Dye wastewater pollution has become a global issue with the development of textile industry. Polyoxometalates photocatalysis is an effective process in degradation of dye wastewater. This paper is to develop a novel supported polyoxometalates photocatalytic material. The H3PW12O40-Y2O3-TiO2 nano photocatalyst was prepared by impregnation method while the Y2O3-TiO2 support was synthesized via sol-gel technology for the first time. The compound was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), nitrogen adsorption-desorption determination and scanning electron microscopy (SEM). The measurements results demonstrate that the original Keggin structure of the polyoxometalates remained intact and there exist anatase phase in the prepared material. The photocatalytic degradation of azo-dye, Methyl Orange (MO) under UV light (λ≥365 nm) in the presence of H3PW12O40-Y2O3-TiO2 photocatalyst in aqueous solution had been investigated and compared with the photodegradation by TiO2 and Y2O3-TiO2 suspensions. The supported polyoxometalates exhibited excellent photocatalytic activity due to the fact that MO was almost completely degraded in 20 min with initial pH=1.0. The photocatalytic activity of polyoxometalates was greatly enhanced, comparing with the staring polyoxometalates, by the synergistic effect between polyoxometalates and anatase Y2O3-TiO2 as well as the increased surface area. Leakage of H3PW12O40 from the compound was hardly observed during catalytic tests, which attributes to the strong chemical but not simply physical interaction between the Keggin units and the Y2O3-TiO2 support. The prepared material is insoluble and easily separated from reaction system for recovery. Any drop of the photocatalytic activity after 8 times’ cyclic operation was not found, revealing that the prepared catalysts are stable.
机译:染料废水污染已成为纺织行业发展的全球性问题。多金属氧酸盐光催化是染料废水的降解的有效方法。本文旨在开发一种新型多金属氧酸盐支持的光催化材料。的H3PW12O40-Y2O3二氧化钛纳米光触媒的制备是通过浸渍方法而Y 2 O 3 TiO 2载体经溶胶 - 凝胶技术合成首次。该化合物的特征是傅里叶变换红外光谱(FTIR),X射线衍射(XRD),氮吸附 - 脱附测定和扫描电子显微镜(SEM)。测量结果表明,该多金属氧酸盐的原始Keggin结构保持完整并在制备的材料存在的锐钛矿相。偶氮染料下在水溶液H3PW12O40-Y2O3二氧化钛光催化剂的存在下UV光(λ≥365纳米)的光催化降解,甲基橙(MO)进行了调查,并与由TiO 2和Y 2 O 3的TiO 2悬浮液的光降解相比。所支持的多金属氧酸盐由于以下事实:MO是在20分钟,初始pH = 1.0几乎完全降解表现出优异的光催化活性。多金属氧酸盐的光催化活性被大大增强,与多金属氧酸盐盯着比较,由金属氧酸盐和锐钛矿Y2O3二氧化钛以及增加的表面积之间的协同效应。从化合物H3PW12O40的泄漏期间催化试验中几乎没有观察到,这归因于强化学但Keggin结构单元和Y 2 O 3 TiO 2载体之间不是简单的物理相互作用。将所制备的材料是不溶性的,并从反应体系中容易地分离回收。 8次循环操作后的光催化活性的任何下降没有被发现,其显露制备的催化剂是稳定的。

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