Influence of quaternary ammonium compounds on the microbial reductive dechlorination of pentachloroaniline

被引:10
|
作者
Hong, Jinglan [1 ,2 ]
Tezel, Ulas [1 ,3 ]
Tas, Didem Okutman [1 ,4 ]
Paulostathis, Spyros G. [1 ]
机构
[1] Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
[2] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Peoples R China
[3] Bogazici Univ, Inst Environm Sci, TR-34342 Istanbul, Turkey
[4] Istanbul Tech Univ, Dept Environm Engn, TR-34469 Istanbul, Turkey
关键词
Quaternary ammonium compounds; Dechlorination; Inhibition; Methanogenesis; Chlorinated anilines; ACTIVATED-SLUDGE; BENZALKONIUM CHLORIDE; CATIONIC SURFACTANTS; WASTE-WATER; CHLORINATED ETHENES; BIODEGRADATION; PENTACHLORONITROBENZENE; DEGRADATION; SEDIMENT; TOXICITY;
D O I
10.1016/j.watres.2013.09.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The inhibitory effect of two widely used quaternary ammonium compounds (QACs) - alkyl benzyl dimethyl (AB) and hexadecyl trimethyl (HD) ammonium chloride - on fermentation, methanogenesis and pentachloroaniline (PCA) dechlorination was assessed using a mixed, methanogenic, PCA-dechlorinating culture amended with AB or HD at a concentration range from 5 to 70 mu M. PCA dechlorination was inhibited at 5 mu M AB and was completely inhibited at 25 or 5 mu M by AB or HD, respectively. However, the PCA dechlorination pathway was the same in both the QACs-free and QACs-amended culture series. Fermentation (acidogenesis) and methanogenesis were inhibited by both AB and HD at and above 25 mu M but to a lesser degree than PCA dechlorination. Overall, HD resulted in a more severe inhibition of the mixed culture than AB. Adsorption of both QACs to the mixed culture biomass followed the Freundlich isotherm model. The adsorption affinity of HD for the mixed culture biomass was significantly higher than that of AB, which may be related to the observed higher inhibitory effects of HD compared to AB. Both AB and HD were not degraded in the mixed, dechlorinating culture used in this study. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6780 / 6789
页数:10
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