Comparing the degradation of acetochlor to RhB using BiOBr under visible light: A significantly different rate-catalyst dose relationship

被引:41
作者
Peng Yi-Zhu [1 ,2 ]
Ma Wan-Hong [1 ]
Jia Man-Ke [1 ,2 ]
Zhao Xiao-Rong [1 ,2 ]
Johnson, David M. [1 ,2 ]
Huang Ying-Ping [1 ,2 ]
机构
[1] Innovat Ctr Geohazards & Ecoenvironm Three Gorges, Yichang 443002, Hubei Province, Peoples R China
[2] China Three Gorges Univ, Minist Educ, Engn Res Ctr Ecoenvironm Gorges Reservoir Reg 3, Yichang 443002, Peoples R China
基金
中国国家自然科学基金;
关键词
Bismuth oxide bromide; Acetochlor; RhB; Unique adsorption behavior; Photodegradation; PHOTOCATALYTIC DEGRADATION; CHLOROACETANILIDE HERBICIDES; MESOPOROUS BIOBR; OXIDATION; TIO2; PRODUCTS; PHOTODEGRADATION; IDENTIFICATION; IRRADIATION; PATHWAY;
D O I
10.1016/j.apcatb.2015.08.002
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
In this study, a weakly polar pesticide acetochlor in water was tried to degrade by BiOBr catalysts under visible light irradiation. Its degradation reaction rate increased exponentially with increasing catalyst dosage, which was significantly different from conventional photocatalytic patterns established for polar or water-soluble pollutants. Thus, the rate-dosage relationship of BiOBr/acetochlor was compared to that of BiOBr/Rhodamine B (RhB) (a typical strong polar dye pollutant in water) at different BiOBr dosages. The degradation rate of RhB increased with the BiOBr dosage and then plateaued due to more catalyst particles blocking the light into the inner solution, which is a typical behavior for heterogeneous photocatalysis of polar organic compounds in aqueous solution. While acetochlor behaved differently, its degradation rate increased exponentially with the BiOBr dosage, and no plateau was observed even up to 9.0 g/L BiOBr dosage. This special rate-dose relationship for weakly polar acetochlor was correlated with a unique adsorption property of BiOBr to acetochlor in water solution. There was a re-distribution effect that always exclude excessive acetochlor adsorbed on BiOBr surface regardless either substrates or BiOBr overdose. This finally resulted in every BiOBr particle having enough adsorption sites available for dissolved dioxygen to function thereby accelerate the degradation of weakly polar organic compounds in water. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:517 / 523
页数:7
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