Solar photocatalytic degradation of sulfanilamide by BiOCl/reduced graphene oxide nanocomposites: Mechanism and degradation pathways

被引:98
作者
Dong, Shuying [1 ]
Pi, Yunqing [1 ]
Li, Qilu [1 ]
Hu, Limin [1 ]
Li, Yukun [2 ]
Han, Xiao [1 ]
Wang, Jingzhen [1 ]
Sun, Jianhui [1 ]
机构
[1] Henan Normal Univ, Henan Key Lab Environm Pollut Control, Key Lab Yellow River & Huai River Water Environm, Sch Environm,Minist Educ, Xinxiang 453007, Henan, Peoples R China
[2] Hohai Univ, Sch Environm, Key Lab Integrated Regulat & Resource Dev Shallow, MOE, Nanjing 210098, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
BiOCl/RGO; Sulfanilamide; Natural sunlight; Photocatalytic; Mechanism; RESISTANCE GENES; FACILE SYNTHESIS; MICROSPHERES; TIO2; PHOTODEGRADATION; SULFADIAZINE; SULFONAMIDES; PERFORMANCE; OXIDATION; REMOVAL;
D O I
10.1016/j.jallcom.2015.12.027
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
Flower-like bismuth oxychloride (BiOCl) catalysts were synthesized with a facile hydrolysis reaction, where the synthesized BiOCl products were further decorated with the prepared graphene oxide (GO) to form novel BiOCl/reduced graphene oxide (BiOCl/RGO) composites. The as-synthesized materials were well characterized with the aid of various techniques, before they were used as photocatalysts for the degradation of sulfanilamide (SN) aqueous solution. The BiOCl/RGO composites contained 1 wt% RGO exhibited superior photocatalytic response, where the degradation rate of SN at 82.7% stayed 30% higher than that of pure BiOCl. The enhanced photocatalytic performances of BiOCl/RGO composites were neither related to the surface area values nor the bandgap of the fabricated photocatalysts, but associated with the enhanced visible light absorption and advanced electron transfer ability. On a basis of the analysis on the SN intermediate products by HPLC, IC, FTIR, H-1 NMR, C-13 NMR and MS, the degradation pathway of SN was speculated, where it was confirmed that the main intermediate product of SN was sulfanilic acid. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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