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Enhanced photocatalytic degradation of caffeine as a model pharmaceutical pollutant by Ag-ZnO-Al_2O_3 nanocomposite

机译:Ag-ZnO-Al_2O_3纳米复合材料增强的咖啡因作为模型药物污染物的光催化降解

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In this paper, an Ag-ZnO-Al2O3 nanocomposite with enhanced photocatalytic activity has been obtained by calcination of an Ag-loaded zinc/aluminum layered double hydroxide (LDH). First, LDH materials intercalated by carbonates ions (Zn-Al-CO3) were synthesized by the co-precipitation method at a Zn/Al molar ratio of 3 and were calcined at different temperatures (300, 400, 500, 600, 800, and 1000 degrees C). Thereafter, in order to increase photocatalytic activity, catalysts obtained at optimal temperature were doped by Ag noble metal with various amounts (1, 3, and 5 wt %) using a ceramic process. Samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy coupled to energy dispersive X-ray spectroscopy (SEM/EDX). The photocatalytic activity was evaluated for the degradation of caffeine as a model of pharmaceutical pollutant in aqueous solutions under UV irradiation. The effect of irradiation time, initial concentration of caffeine, catalyst dosage, solution pH, and reuse were investigated. The Ag-doped calcined LDH materials showed significantly higher photocatalytic activity compared with undoped and standard Degussa P-25 titanium dioxide. The photocatalytic degradation of caffeine was increased with an increase in the Ag-loaded amounts. The photocatalyst showed high stability after three regeneration cycles.
机译:通过负载载银的锌/铝层状双氢氧化物(LDH)的煅烧,获得了具有增强的光催化活性的Ag-ZnO-Al2O3纳米复合材料。首先,通过共沉淀法以Zn / Al摩尔比为3合成由碳酸根离子(Zn-Al-CO3)嵌入的LDH材料,并在不同温度(300、400、500、600、800和800 1000摄氏度)。此后,为了提高光催化活性,使用陶瓷工艺将在最佳温度下获得的催化剂用各种量(1、3和5重量%)的Ag贵金属掺杂。通过X射线衍射(XRD),傅立叶变换红外光谱(FTIR)和耦合到能量色散X射线光谱(SEM / EDX)的扫描电子显微镜对样品进行表征。评价咖啡因的降解的光催化活性,作为咖啡因在紫外线照射下的水溶液模型。研究了辐照时间,咖啡因的初始浓度,催化剂用量,溶液pH值和再利用的影响。与未掺杂和标准的Degussa P-25二氧化钛相比,掺Ag的煅烧LDH材料显示出明显更高的光催化活性。咖啡因的光催化降解随着载银量的增加而增加。在三个再生循环后,光催化剂显示出高稳定性。

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