Influence of the Synthesis Method on the Preparation Composites Derived from TiO2-LDH for Phenol Photodegradation

J. C. Contreras-Ruiz, S. Martínez-Gallegos, J. L. García-Rivas, J. C. González-Juárez, E. Ordoñez
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引用次数: 1

Abstract

Three different TiO2 catalysts are prepared using different methods. MgAl-CO3 layered double hydroxides (LDH) were obtained by the sol-gel method. In the preparation of the composites, the three photocatalysts were combined with LDH following different methodologies. The composites were characterized using X-ray diffraction (XRD), specific surface area (SA), atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). The influence of the synthesis method on the preparation of the composites was evaluated by analyzing their photocatalytic activity against phenol as a model organic pollutant under UV irradiation. The photocatalytic activity of the composites improves when the chemical interaction, determined by XPS, between the TiO2 and the LDH decreases. The same happens when the ratio of the anatase-rutile phases, determined by XRD, approaches optimum (80:20%). The effect of the composite concentration in the solution (0.5–2.0 g/L) was investigated, and the light-shielding phenomenon due to high composite concentration decreases the phenol photodegradation. The reduction of photocatalytic activity in reuse cycles is due to loss and partial deactivation of the material. The elimination of phenol is attributed primarily to the photocatalytic process due to the generation of ●OH radicals and to a lesser extent the adsorption process also present in the samples.
合成方法对制备TiO2-LDH光降解苯酚复合材料的影响
采用不同的方法制备了三种不同的TiO2催化剂。采用溶胶-凝胶法制备了MgAl-CO3层状双氢氧化物(LDH)。在复合材料的制备中,采用不同的方法将三种光催化剂与LDH结合。采用x射线衍射(XRD)、比表面积(SA)、原子力显微镜(AFM)和x射线光电子能谱(XPS)对复合材料进行了表征。通过分析复合材料在紫外光照射下对典型有机污染物苯酚的光催化活性,评价了合成方法对复合材料制备的影响。通过XPS测定,TiO2与LDH之间的化学相互作用减小,复合材料的光催化活性提高。当XRD测定锐钛矿与金红石相的最佳比例(80:20%)时,也会发生同样的情况。考察了复合材料浓度(0.5 ~ 2.0 g/L)对苯酚光降解的影响,发现高复合材料浓度导致的遮光现象降低了苯酚的光降解。在重复使用循环中,光催化活性的降低是由于材料的损失和部分失活。苯酚的消除主要归因于光催化过程,由于产生了●OH自由基,在较小程度上吸附过程也存在于样品中。
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