Enhanced transformation of diphenylarsinic acid in soil under sulfate-reducing conditions

被引:13
作者
Guan, Ling [2 ]
Hisatomi, Shihoko [2 ]
Fujii, Kunihiko [3 ]
Nonaka, Masanori [1 ]
Harada, Naoki [1 ]
机构
[1] Niigata Univ, Fac Agr, Nishi Ku, Niigata 9502181, Japan
[2] Niigata Univ, Grad Sch Sci & Technol, Nishi Ku, Niigata 9502181, Japan
[3] Niigata Univ, Off Environm & Safety, Nishi Ku, Niigata 9502181, Japan
基金
日本学术振兴会;
关键词
Biotransformation; Carbon source; LC-ICPMS; Specific inhibitor; Sulfate reduction; CHEMICAL WARFARE AGENTS; ARSENIC SPECIATION; CONTAMINATED SOILS; HEAVY-METALS; REDUCTION; RICE; DEGRADATION; GROUNDWATER; OXIDATION; BACTERIA;
D O I
10.1016/j.jhazmat.2012.09.054
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Diphenylarsinic acid (DPAA) is known to be the major contaminant in soils where diphenylchloroarsine and diphenylcyanoarsine were abandoned after World Wars I and II. In this study, experimental model studies were performed to elucidate key factors regulating the transformation of DPAA under anaerobic soil conditions. The elimination of DPAA in Gleysol soils (Qiqihar and Shindori soils) was more rapid than in Mollisol and Regosol soils (Heihe and lkarashi soils, respectively) during a 5-week incubation. No clear relationship between decreasing rates of DPAA concentrations and soil Eh values was found. The Ikarashi soil showed the slowest decrease in DPAA concentrations among the four soils, but the transformation of DPAA was notably enhanced by addition of exogenous sulfate together with acetate, cellulose or rice straw. Addition of molybdate, a specific inhibitor of sulfate reduction, resulted in the stagnation of DPAA transformation, suggesting that indigenous sulfate reducers play a role in DPAA transformation under anaerobic conditions. Arsenate, phenylarsonic acid, phenylmethylarsinic acid, diphenylmethylarsine oxide and three unknown compounds were detected as metabolites of DPAA. This is the first study to reveal enhancement of DPAA transformation under sulfate-reducing conditions. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:355 / 362
页数:8
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