Development of a predictive framework to assess the removal of trace organic chemicals by anaerobic membrane bioreactor

被引:100
作者
Wijekoon, Kaushalya C. [1 ]
McDonald, James A. [2 ]
Khan, Stuart J. [2 ]
Hai, Faisal I. [1 ]
Price, William E. [3 ]
Nghiem, Long D. [1 ]
机构
[1] Univ Wollongong, Sch Civil Min & Environm Engn, Strateg Water Infrastruct Lab, Wollongong, NSW 2522, Australia
[2] Univ New S Wales, Sch Civil & Environm Engn, Sydney, NSW 2052, Australia
[3] Univ Wollongong, Sch Chem, Strateg Water Infrastruct Lab, Wollongong, NSW 2522, Australia
基金
澳大利亚研究理事会;
关键词
Anaerobic membrane bioreactor (AnMBR); Trace organic chemicals (TrOCs); Hydrophobicity; Functional groups; Biodegradation/transformation; WASTE-WATER TREATMENT; ENDOCRINE DISRUPTING COMPOUNDS; PERSONAL CARE PRODUCTS; PHARMACEUTICALS; FATE; MBR; MICROPOLLUTANTS; DIGESTION; SYSTEM;
D O I
10.1016/j.biortech.2015.04.034
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
This study aims to develop a predictive framework to assess the removal and fate of trace organic chemicals (TrOCs) during wastewater treatment by anaerobic membrane bioreactor (AnMBR). The fate of 27 TrOCs in both the liquid and sludge phases during AnMBR treatment was systematically investigated. The results demonstrate a relationship between hydrophobicity and specific molecular features of TrOCs and their removal efficiency. These molecular features include the presence of electron withdrawing groups (EWGs) or donating groups (EDGs), especially those containing nitrogen and sulphur. All seven hydrophobic contaminants were well removed (>70%) by AnMBR treatment. Most hydrophilic TrOCs containing EDGs were also well removed (>70%). In contrast, hydrophilic TrOCs containing EWGs were mostly poorly removed and could accumulate in the sludge phase. The removal of several nitrogen/sulphur bearing TrOCs (e.g., linuron and caffeine) by AnMBR was higher than that by aerobic treatment, possibly due to nitrogen or sulphur reducing bacteria. Crown Copyright (C) 2015 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:391 / 398
页数:8
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