Ismail L F M, Emara M M, El-Moselhy M M, Maziad N A, Hussein O K
Al-Azhar University, Faculty of Science (Girls), Chemistry Department, Nasr City, Cairo, Egypt.
Al-Azhar University, Faculty of Science (Boys), Chemistry Department, Nasr City, Cairo, Egypt; Science Center for Detection and Remediation of Environmental Hazards (SCDREH), Al-Azhar University, Nasr City, Cairo, Egypt.
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Oct 15;131:158-68. doi: 10.1016/j.saa.2014.03.041. Epub 2014 Apr 21.
Silica-coating ZnO nanoparticles were prepared using the hydrothermal method. The prepared nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray Spectroscopy (EDX). It was found that ultrafine core/shell structured silica-coating ZnO nanoparticles were successfully obtained. TEM analysis revealed a continuous and uniform silica coating layer of about 8nm in thickness on the surface of ZnO nanoparticles. The photocatalytic performance of silica-coating ZnO core/shell nanoparticles in methylene blue aqueous solution was investigated. The effects of some operational parameters such as pH value, nanocatalyst loading and initial MB concentration on the degradation efficiency were discussed. Kinetic parameters were experimentally determined and a pseudo-first-order kinetic was observed. Thus, the main advantage of the coating is the stability of the photocatalysts and the better performance in acidic or alkaline solutions. Compared to ZnO the maximum apparent rate constant is obtained at pH 8.5 (pH 11.5 in case of bare ZnO). Moreover, the Langmuir adsorption model was applied to describe the equilibrium isotherm at different MB concentration. The applicability of the Langmuir isotherm suggests monolayer coverage of the MB onto surface of silica-coating ZnO nanoparticles. The kinetics of the adsorption with respect to the initial dye concentration, were also investigated. The pseudo-first-order and second-order kinetic models were used and the rate constants were evaluated. The kinetic studies revealed that the pseudo-second-order kinetic model better represented the adsorption kinetics, suggesting that the adsorption process may be chemisorption.
采用水热法制备了二氧化硅包覆的氧化锌纳米颗粒。通过X射线衍射(XRD)、透射电子显微镜(TEM)、扫描电子显微镜(SEM)和能量色散X射线光谱(EDX)对制备的纳米颗粒进行了表征。结果表明,成功获得了超细核壳结构的二氧化硅包覆氧化锌纳米颗粒。TEM分析显示,在氧化锌纳米颗粒表面有一层厚度约为8nm的连续且均匀的二氧化硅包覆层。研究了二氧化硅包覆氧化锌核壳纳米颗粒在亚甲基蓝水溶液中的光催化性能。讨论了pH值、纳米催化剂负载量和初始MB浓度等操作参数对降解效率的影响。通过实验确定了动力学参数,并观察到了准一级动力学。因此,包覆的主要优点是光催化剂的稳定性以及在酸性或碱性溶液中的更好性能。与氧化锌相比,在pH 8.5时获得最大表观速率常数(裸氧化锌在pH 11.5时)。此外,应用朗缪尔吸附模型描述了不同MB浓度下的平衡等温线。朗缪尔等温线的适用性表明MB在二氧化硅包覆氧化锌纳米颗粒表面的单层覆盖。还研究了吸附相对于初始染料浓度的动力学。使用了准一级和二级动力学模型并评估了速率常数。动力学研究表明,准二级动力学模型能更好地表示吸附动力学,表明吸附过程可能是化学吸附。