State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Science, Chinese Academy of Sciences, Beijing 100085, China.
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Science, Chinese Academy of Sciences, Beijing 100085, China; Institute of Environment and Health, Jianghan University, Wuhan, Hubei Province 430056, China.
Sci Total Environ. 2016 Feb 15;544:262-70. doi: 10.1016/j.scitotenv.2015.11.112. Epub 2015 Dec 3.
Although organophosphate esters (OPEs) in the ambient environment are from sewage treatment plants due to the discharge of effluent and application of sludge, the distribution, degradation and fate of OPEs in advanced municipal sewage treatment plants remain unclear. This work focused on the use of mass flow and mass balance analysis to understand the behaviors and fate of 14 OPEs in an advanced municipal sewage treatment plant. OPEs were detected in all sewage water and sludge samples with total OPEs (ΣOPEs) concentrations of 1399 ± 263 ng/L in raw sewage aqueous phase, 833 ± 175 ng/L in tertiary effluent aqueous phase, and 315 ± 89 ng/g dry weight in dewatered sludge. The dissolved concentrations of ΣOPEs significantly decreased during biological treatment, whereas negligible decrease was observed in mechanical and physical-chemical treatments. For individual OPE, the chlorinated tris(2-chloroethyl) phosphate (TCEP) and tris(2-chloroisopropyl) phosphate (TCPP) did not decrease but increased during both biological treatment and physical-chemical treatment. Mass flow analysis indicated the total removal efficiency of ΣOPEs in aqueous phase was 40.5%, and the polarity-specific removal efficiencies for individual OPE were positively related to their solid-water partition coefficients (Kd). Furthermore, mass balance results showed that 53.1% and 6.3% of the initial OPE mass flow were eventually transferred to the effluents and dewatered sludge, respectively, while the remaining 39.9% and 0.7% were lost due to biodegradation and physical-chemical treatment, respectively. It was indicated that the activated sludge treatment system with anaerobic/anoxic/aerobic bioreactors was a major factor in the removal of OPEs from the raw sewage, while transfer to dewatered sludge governed by hydrophobic interactions was limited during the sewage treatment. Meanwhile, the degradation difference of OPEs in activated sludge treatment was more related with their molecular structure over their hydrophobicity.
尽管环境中的有机磷酸酯 (OPE) 是由于污水处理厂的污水排放和污泥应用,但先进的城市污水处理厂中 OPE 的分布、降解和归宿仍不清楚。本工作重点采用质量流和质量平衡分析来了解 14 种 OPE 在先进城市污水处理厂中的行为和归宿。在所有污水和污泥样品中均检测到 OPE,原污水水相中的总 OPEs(ΣOPEs)浓度为 1399±263ng/L,三级出水水相中的浓度为 833±175ng/L,脱水污泥中的浓度为 315±89ng/g 干重。ΣOPEs 的溶解浓度在生物处理过程中显著降低,而在机械和物理化学处理过程中几乎没有降低。对于个别 OPE,氯化三(2-氯乙基)磷酸酯 (TCEP) 和三(2-氯异丙基)磷酸酯 (TCPP) 在生物处理和物理化学处理过程中均未减少反而增加。质量流分析表明,ΣOPEs 在水相中的总去除效率为 40.5%,各 OPE 的极性特异性去除效率与其固-水分配系数(Kd)呈正相关。此外,质量平衡结果表明,初始 OPE 质量流的 53.1%和 6.3%最终分别转移到废水中和脱水污泥中,而其余 39.9%和 0.7%分别由于生物降解和物理化学处理而损失。这表明具有厌氧/缺氧/好氧生物反应器的活性污泥处理系统是从原污水中去除 OPEs 的主要因素,而在污水处理过程中,受疏水性相互作用的限制,向脱水污泥的转移是有限的。同时,OPE 在活性污泥处理中的降解差异与其分子结构更相关,而与其疏水性关系不大。