Effect of operational key parameters on photocatalytic degradation of phenol using nano nickel oxide synthesized by sol-gel method

被引:91
作者
Hayat, Khizar [3 ]
Gondal, M. A. [1 ,2 ]
Khaled, Mazen M. [3 ]
Ahmed, Shakeel [4 ]
机构
[1] King Fahd Univ Petr & Minerals, Laser Res Grp, Dept Phys, Dhahran 31261, Saudi Arabia
[2] King Fahd Univ Petr & Minerals, CENT, Dhahran 31261, Saudi Arabia
[3] King Fahd Univ Petr & Minerals, Dept Chem, Dhahran 31261, Saudi Arabia
[4] King Fahd Univ Petr & Minerals, Ctr Refining & Petrochem, Res Inst, Dhahran 31261, Saudi Arabia
关键词
Nano nickel oxide; Heterogeneous photocatalysis; Phenol; Waste water treatment; Nanoparticles; HETEROGENEOUS PHOTOCATALYSIS; AQUEOUS-SOLUTION; SEMICONDUCTOR PHOTOCATALYSIS; THERMAL-DECOMPOSITION; TITANIUM-DIOXIDE; ZNO NANOWIRES; THIN-FILMS; AZO DYES; NIO; OXIDATION;
D O I
10.1016/j.molcata.2010.12.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic oxidation of phenol was studied using nickel oxide (NiO) nanoparticles synthesized by sol-gel method. The morphology of synthesized catalyst was studied by using field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX) and high resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD). The average particle size was 6.5 nm as estimated by Scherrer formula and was confirmed by HRTEM and FESEM analysis. The photocatalytic activity of NiO was evaluated by degradation of phenol under irradiation of unique source like UV laser. The influence of various key parameters such as amount of photocatalyst, initial solution pH and the initial concentration of phenol was investigated. The operational parameters show the expected influence regarding the efficiency of the photocatalytic degradation process. The photocatalytic degradation efficiency of NiO was found to decrease with the increase in the initial solution pH. The degradation of the phenol followed a pseudo first-order rate kinetics with k = 5.7 x 10(-2) min(-1). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 71
页数:8
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