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Enhanced photocatalytic performance of Hemin (chloro(protoporhyinato) iron(III)) anchored TiO2 photocatalyst for methyl orange degradation: A surface modification method

机译:增强光催化性能的氯化(氯(原甲酸)铁(III))锚定TiO2光催化剂对甲基橙降解的影响:表面改性方法

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摘要

TiO2 was prepared by sol-gel method through the hydrolysis of TiCl4 and its surface derivatization was carried out with molecular catalyst like Hemin (chloro(protoporhyinato)iron(III)). Catalyst was characterized by various analytical techniques like UV-vis spectroscopy, FT-IR, FE-SEM and XRD. The anchoring of Hemin on titania surface is confirmed by FT-IR spectra through the linkage of OCOTi bond and also by TGA-DSC and elemental analysis. The photocatalytic activity of the surface modified catalyst is tested for the degradation of methyl orange (MO) as a model compound under UV light. The Hemin impregnated TiO2 (H-TiO2) in presence of H 2O2 shows an excellent photocatalytic activity compared to pristine TiO2, Hemin, H2O2, TiO 2/H2O2, and Hemin/H2O2 systems. The enhancement in the photocatalytic activity is attributed to the presence of iron (III) porphyrin ring on the TiO2 surface, which reduces the electron-hole recombination rate and also by acting as a mediator for continuous production of enriched concentration of hydroxyl radicals along with various other reactive free radicals. © 2013 Elsevier B.V. All rights reserved.
机译:TiO2是通过溶胶-凝胶法通过水解TiCl4制备的,其表面衍生化是通过分子催化剂如Hemin(氯(原卟啉)铁(III))进行的。催化剂通过各种分析技术进行表征,例如紫外可见光谱,FT-IR,FE-SEM和XRD。 Hemin在二氧化钛表面的锚固通过FT-IR光谱通过OCOTi键的键合以及TGA-DSC和元素分析得到证实。测试了表面改性催化剂的光催化活性,以分析在紫外光下作为模型化合物的甲基橙(MO)的降解情况。与原始TiO2,Hemin,H2O2,TiO 2 / H2O2和Hemin / H2O2系统相比,在H 2O2存在下用Hemin浸渍的TiO2(H-TiO2)具有出色的光催化活性。光催化活性的提高归因于在TiO2表面上存在铁(III)卟啉环,这降低了电子-空穴的复合率,并且还充当了连续产生富集浓度的羟基自由基以及各种不同形式的介质的媒介。其他反应性自由基。 ©2013 Elsevier B.V.保留所有权利。

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