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Optimization of Solar Photocatalytic Degradation of Chloroxylenol Using TiO 2 , Er 3+ /TiO 2 , and Ni 2+ /TiO 2 via the Taguchi Orthogonal Array Technique

机译:Taguchi正交阵列技术优化TiO 2,Er 3+ / TiO 2和Ni 2+ / TiO 2的太阳光催化降解氯代木酚

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In this study, the optical properties of a TiO 2 photocatalyst were enhanced with various impregnations of Er 3+ and Ni 2+ separately, using the impregnation method as photocatalysts for the direct solar photolysis degradation of chloroxylenol. The synthesized Er 3+ /TiO 2 and Ni 2+ /TiO 2 catalysts were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX), metal mapping, and ultraviolet visible (UV–Vis) spectroscopy. The results showed that the Er 3+ /TiO 2 and Ni 2+ /TiO 2 nano-particles have the same structures of TiO 2 nano-particles with little difference in particle size. The Er 3+ and Ni 2+ ions were well-distributed on the TiO 2 surface, and it was found that the maximum band gap decreased from 3.13 eV for intrinsic TiO 2 to 2.63 eV at 1.8 wt % Er 3+ /TiO 2 and to 2.47 eV at 0.6 wt % for Ni 2+ /TiO 2 . The initial concentration of chloroxylenol, catalyst loading, and pH of the solution are the most important factors affecting the solar photocatalytic degradation efficiency that were optimized using Design Expert software (version 6.0.10, Minneapolis, MN, USA, 2003). The results showed that the optimal conditions for chloroxylenol degradation include a pH of 4, TiO 2 loading at 3 g/L, and a chloroxylenol concentration of 50 mg/L. These conditions resulted in a degradation efficiency of 90.40% after 60 min of direct solar irradiation, wherein the solar energy recorded during a clear sunny day is 1000 W/m 2 . However, some experiments were conducted on a semi-cloudy day to cover all weather stated and to study the degradation kinetics. During semi-cloudy day experiments, using Er 3+ /TiO 2 and Ni 2+ /TiO 2 with a solar irradiation activity of 600 W/m 2 for a 60 min exposure at optimal conditions increased the degradation efficiency from 68.28% for intrinsic TiO 2 to 82.38% for Er 3+ /TiO 2 and 80.70% for Ni 2+ /TiO 2 .
机译:本研究采用Er 3+和Ni 2+的不同浸渍方式,分别采用浸渍法作为光催化剂直接降解氯氧lenol,从而提高了TiO 2光催化剂的光学性能。利用X射线衍射(XRD),场发射扫描电子显微镜(FESEM),能量色散X射线(EDX),金属制图和紫外光谱对合成的Er 3+ / TiO 2和Ni 2+ / TiO 2催化剂进行了表征。可见(UV-Vis)光谱。结果表明,Er 3+ / TiO 2和Ni 2+ / TiO 2纳米颗粒具有与TiO 2纳米颗粒相同的结构,粒径差异很小。 Er 3+和Ni 2+离子均匀分布在TiO 2表面上,发现最大带隙从本征TiO 2的3.13 eV降至1.8 wt%Er 3+ / TiO 2和2.63 eV。 Ni 2+ / TiO 2的含量为0.6 wt%时为2.47 eV。使用设计专家软件(版本6.0.10,明尼阿波利斯,明尼苏达州,美国,2003年)优化过的氯氧亚麻酸的初始浓度,催化剂的负载量和溶液的pH值是影响太阳光催化降解效率的最重要因素。结果表明,降解氯氧亚麻酚的最佳条件包括:pH为4,TiO 2负载量为3 g / L和氯氧亚麻酚浓度为50 mg / L。这些条件导致直接太阳光照射60分钟后的降解效率为90.40%,其中在晴朗的晴天记录的太阳能为1000 W / m 2。但是,在半阴天进行了一些实验,以覆盖所有规定的天气并研究降解动力学。在半阴天实验中,使用Er 3+ / TiO 2和Ni 2+ / TiO 2在最佳条件下暴露60分钟的太阳辐照活性为600 W / m 2时,降解效率从68.28%提高到本征TiO Er 3+ / TiO 2为2至82.38%,Ni 2+ / TiO 2为80.70%。

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