Influence of thermal hydrolysis-anaerobic digestion treatment of wastewater solids on concentrations of triclosan, triclocarban, and their transformation products in biosolids

被引:34
|
作者
Armstrong, Dana L. [1 ]
Rice, Clifford P. [2 ]
Ramirez, Mark [3 ]
Torrents, Alba [1 ]
机构
[1] Univ Maryland, Dept Civil & Environm Engn, 1173 Glenn L Martin Hall, College Pk, MD 20742 USA
[2] USDA ARS, Sustainable Agr Syst Lab, Beltsville, MD USA
[3] Dist Columbia Water & Sewer Author, DCWater, Washington, DC USA
关键词
Biosolids; Triclosan; Triclocarban; Cambi; Thermal hydrolysis; Anaerobic digestion; PERSONAL CARE PRODUCTS; METHYL TRICLOSAN; SEWAGE-SLUDGE; FATE; PHARMACEUTICALS; BIOACCUMULATION; METHYLTRICLOSAN; NONYLPHENOL; DEGRADATION; SEDIMENTS;
D O I
10.1016/j.chemosphere.2016.12.122
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The growing concern worldwide regarding the presence of emerging contaminants in biosolids calls for a better understanding of how different treatment technologies at water resource recovery facilities (WRRFs) can influence concentrations prior to biosolids land application. This study focuses on the influence of solids treatment via the Cambi Thermal Hydrolysis Process " in conjunction with anaerobic digestion (TH-AD) on concentrations of triclosan (TCS), triclocarban (TCC), and their transformation products in biosolids and sludges. Concentrations of the target analytes in biosolids from the TH-AD process (Class A), sludges from the individual TH-AD treatment steps, and limed biosolids (Class B) from the same WRRF were compared. TCC concentrations were significantly lower in Class A biosolids than those in the Class B product - a removal that occurred during thermal hydrolysis. Concentrations of TCS, methyl triclosan, and 2,4-dichlorophenol, conversely, increased during anaerobic digestion, leading to significantly higher concentrations of these compounds in Class A biosolids when compared to Class B biosolids. Implementation of the TH-AD process had mixed effect on contaminant concentrations. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:609 / 616
页数:8
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