Quantification of Nanoscale Silver Particles Removal and Release from Municipal Wastewater Treatment Plants in Germany

被引:160
|
作者
Li, Lingxiangyu [1 ]
Hartmann, Georg [1 ]
Doeblinger, Markus [2 ,3 ]
Schuster, Michael [1 ]
机构
[1] Tech Univ Munich, Dept Chem, D-85747 Garching, Germany
[2] Univ Munich, Dept Chem, D-81377 Munich, Germany
[3] Univ Munich, Ctr NanoSci CeNS, D-81377 Munich, Germany
关键词
CLOUD POINT EXTRACTION; METAL NANOPARTICLES; TITANIUM-DIOXIDE; TOXICITY; FATE; AGGREGATION; SPECIATION; DYNAMICS; SAMPLES; IMPACT;
D O I
10.1021/es3041658
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The majority of pure silver nanoparticles in consumer products are likely released into sewer systems and usually end up in wastewater treatment plants (WWTPs). Research investigating the reduction in nanoscale silver particles (n-Ag-Ps) has focused on the biological treatment process, generally in controlled laboratory experiments. This study, analyzing the field-collected samples from nine municipal WWTPs in Germany, is the first to evaluate the reduction in n-Ag-Ps by mechanical and biological treatments in sequence in WWTPs. Additionally, the concentration of n-Ag-Ps in effluent was determined through two different methods that are presented here: novel ionic exchange resin (IER) and cloud point extraction (CPE) methods. The n-Ag-Ps concentrations in influent were all low (<1.5 mu g/L) and decreased (average removal efficiency of similar to 35%) significantly after mechanical treatment, indicating that the mechanical treatment contributes to the n-Ag-Ps removal. Afterward, more than 72% of the remaining n-Ag-Ps in the semi treated wastewater (i.e., wastewater after mechanical treatment) were reduced by biological treatment. Together, these processes reduced 95% of the n-Ag-Ps that entered WWTPs, which " resulted in low concentration of n-Ag-Ps in the effluents (<12 ng/L). For a WWTP with 520000 t/d treatment capacity, we estimated that the daily n-Ag-Ps load in effluent discharge equated to about 4.4 g/d. Obviously, WWTPs are not potential point sources for n-Ag-Ps in the aquatic environment.
引用
收藏
页码:7317 / 7323
页数:7
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