Electrospun cellulose acetate supported Ag@AgCl composites with facet-dependent photocatalytic properties on degradation of organic dyes under visible-light irradiation

被引:82
作者
Zhou, Zidan [1 ]
Peng, Xinwen [1 ]
Zhong, Linxin [1 ]
Wu, Lan [2 ]
Cao, Xuefei [3 ]
Sun, Run Cang [1 ,3 ]
机构
[1] S China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou 510641, Guangdong, Peoples R China
[2] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510641, Guangdong, Peoples R China
[3] Beijing Forestry Univ, Beijing Key Lab Lignocellulos Chem, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrospun cellulose acetate; Composites; Silver chloride; Visible light; Dye degradation; HIGHLY EFFICIENT; METHYLENE-BLUE; GRAPHENE OXIDE; AG/AGCL; NANOCOMPOSITE; NANOPARTICLES; PERFORMANCE; NANOFIBERS; MICROCRYSTALS; NANOWIRES;
D O I
10.1016/j.carbpol.2015.09.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Electrospun cellulose acetate (CA) membrane was employed as a support that provided sites for AgCl crystals in situ growth. The Ag@AgCl crystals on electrospun CA composites with exposed {100} and {111} facets were fabricated at room temperature by a double diffusion technique. The crystal structure, morphology, composition, and absorption light ability of CA supported Ag@AgCl were characterized utilizing X-ray powder diffraction (XRD), scanning electron microscopy (SEM), attenuated total reflection-infrared intensity (ATR-IR), X-ray photoelectron spectroscopy measurements (XPS), energy dispersive spectrometer (EDS) and ultraviolet-visible (UV-vis) diffuse reflectance spectra, respectively. The photocatalytic activity of the catalysts was evaluated using methyl orange (MO) as a target. The CA supported cubic Ag@AgCl catalyst exhibited much higher catalytic activity than octahedral catalyst in terms of the degradation of MO under visible light. The 10 mg CA based cubes could completely degrade MO (10 mg L-1) in 160 min. The photocatalyst still exhibited a good catalytic ability after three times. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:322 / 328
页数:7
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