Synthesis of WO3 nanoparticles by citric acid-assisted precipitation and evaluation of their photocatalytic properties

被引:82
|
作者
Sanchez-Martinez, D. [1 ]
Martinez-de la Cruz, A. [2 ]
Lopez-Cuellar, E. [2 ]
机构
[1] Fac Ingn Civil UANL, Dept Ecomat & Energia, San Nicolas De Los Garza 66451, NL, Mexico
[2] Univ Autonoma Nuevo Leon, Fac Ingn Mecan & Elect, San Nicolas De Los Garza 66451, NL, Mexico
关键词
Oxides; Chemical synthesis; X-ray diffraction; Catalytic properties; TITANIUM-DIOXIDE; THIN-FILMS; DEGRADATION; WATER; DYES; TIO2;
D O I
10.1016/j.materresbull.2012.11.024
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
WO3 nanoparticles were synthesized by citric acid-assisted precipitation method using a 1:1.5 molar ratio of ammonium paratungstate hydrate (H42N10O42W12.xH(2)O):citric acid (C6H8O7). The formation of monoclinic crystal structure of WO3 at different temperatures was confirmed by X-ray powder diffraction (XRD). The characterization of the samples synthesized was complemented by transmission electron microscopy (TEM), Brunauer-Emmitt-Teller surface area (BET) and diffuse reflectance spectroscopy (DRS). According to the thermal treatment followed during the synthesis of WO3, the morphology of the nanoparticles formed was characterized by rectangular and ovoid shapes. The photocatalytic activity of WO3 obtained under different experimental conditions was evaluated in the degradation of rhodamine B (rhB), indigo carmine (IC), methyl orange (MO), and Congo red (CR) in aqueous solution under UV and UV-vis radiation. The highest photocatalytic activity was observed in the sample obtained by thermal treatment at 700 degrees C. In general, the sequence of degradation of the organic dyes was: indigo carmine (IC) > rhodamine B (rhB) > methyl orange (MO) > Congo red (CR). The mineralization degree of organic dyes by WO3 photocatalysts was determined by total organic carbon analysis (TOC) reaching percentages of mineralization of 82% (rhB), 85% (IC), 28% (MO), and 7% (CR) for 96 h of lamp irradiation. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:691 / 697
页数:7
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