Increased photocatalytic activity of NiO and ZnO in photodegradation of a model drug aqueous solution: Effect of coupling, supporting, particles size and calcination temperature

被引:327
作者
Derikvandia, Hadis [1 ,2 ]
Nezamzadeh-Ejhieh, Alireza [1 ,2 ,3 ]
机构
[1] Islamic Azad Univ, Shahreza Branch, Dept Chem, POB 311-86145, Shahreza, Isfahan, Iran
[2] Islamic Azad Univ, Shahreza Branch, Young Researchers & Elite Club, Shahreza, Iran
[3] Islamic Azad Univ, Shahreza Branch, RCRC, Esfahan, Iran
关键词
Heterogeneous photodegradation; Clinoptilolite nanoparticles; Calcination temperature; Metronidazole; NiO-ZnO semiconductors; CLINOPTILOLITE NANO-PARTICLES; METRONIDAZOLE DEGRADATION; OPTICAL-PROPERTIES; NANOPARTICLES; LIGHT; REMOVAL; PHOTOLUMINESCENCE; FABRICATION; SURFACTANT; ZEOLITES;
D O I
10.1016/j.jhazmat.2016.09.056
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Mechanically ball-mill prepared clinoptilolite nanoparticles (NC) were used for increasing photocatalytic activity of NiO and ZnO as alone and binary systems. The semiconductors were supported onto the zeolite during calcination of Ni(II)-Zn(II)-exchanged NC at different calcinations temperatures. XRD, FTIR, SEM-EDX, X-ray mapping, DRS, TEM and BET techniques were used for characterization of the samples. The calcined catalysts at 400 degrees C for 4h showed the best photocatalytic activity for metronidazole (MNZ) in aqueous solution. The mole ratio of ZnO/NiO affected the photodegradation efficiency because activity of the coupled catalysts depends to the both e/h production and electron scavenging processes. In the used system, NiO acted as e/h production source and ZnO as an electron sink. Red shifts in band gaps of the supported coupled semiconductors was observed whit respect to monocomponent one, confirming formation of nanoparticles of the semiconductors onto the zeolitic bed. The best activities were obtained for the NiO1.3-ZnO1.5N/C (NZ-NC) and NiO0.7-ZnO4.3/NC (NZ(3)-NC) catalysts at pH 3,1.2 g L-1 of the catalysts and 1 g L-1 of MNZ. (C) 2016 Elsevier B.V. All rights reserved.
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页码:629 / 638
页数:10
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