Removal of Estrogenic Compounds from Filtered Secondary Wastewater Effluent in a Continuous Enzymatic Membrane Reactor. Identification of Biotransformation Products

漆酶 化学 流出物 色谱法 生物转化 废水 电喷雾电离 液相色谱-质谱法 质谱法 污水处理 雌酮 膜反应器 催化作用 有机化学 生物化学 废物管理 工程类 激素
作者
L. Lloret,Gemma Eibes,Marı́a Teresa Moreira,Gumersindo Feijóo,Juan M. Lema
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:47 (9): 4536-4543 被引量:99
标识
DOI:10.1021/es304783k
摘要

In the present study, a novel and efficient technology based on the use of an oxidative enzyme was developed to perform the continuous removal of estrogenic compounds from polluted wastewaters. A 2 L enzymatic membrane reactor (EMR) was successfully operated for 100 h with minimal requirements of laccase for the transformation of estrone (E1), 17β-estradiol (E2), and 17α-ethinylestradiol (EE2)from both buffer solution and real wastewater (filtered secondary effluent). When the experiments were performed at high and low concentrations of the target compounds, 4 mg/L and 100 μg/L, not only high removal yields (80-100%) but also outstanding reduction of estrogenicity (about 84-95%) were attained. When the EMR was applied for the treatment of municipal wastewaters with real environmental concentrations of the different compounds (0.29-1.52 ng/L), excellent results were also achieved indicating the high efficiency and potential of the enzymatic reactor system. A second goal of this study relied on the identification of the transformation products to elucidate the catalytic mechanism of estrogens' transformation by laccase. The formation of dimers and trimers of E1, E2, and EE2, as well as the decomposition of E2 into E1 by laccase-catalyzed treatment, has been demonstrated by liquid chromatography atmospheric pressure chemical ionization (LC-APCI) analysis and confirmed by determination of accurate masses through liquid chromatography electrospray time-of-flight mass spectrometry (LC-ESI-TOF). Dimeric products of E2 and EE2 were found even when operating at environmental concentrations. Moreover, the reaction pathways of laccase-catalyzed transformation of E2 were proposed.
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