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Occurence of benzothiazoles in municipal wastewater and their fate in biological treatment

机译:市政废水中苯并噻唑的发生及其在生物处理中的命运

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摘要

A number of 2-substituted benzothiazoles that are known to be used as fungicides, corrosion inhibitors and vulcanization accelerators in industry have been analyzed in municipal wastewater and the effluents of activated sludge and membrane bioreactor (MBR) treatment over a three month period. All six analytes were regularly detected in the municipal wastewater by liquid chromatography-mass spectrometry and amount to a total concentration of 3.4 mug/L. Of these compounds benzothiazole-2-sulfonic acid (1,700 ng/L), benzothiazole (850 ng/L) and 2-hydroxybenzothiazole (500 ng/L) were most prominent. The source of the benzothiazole emission is yet unknown. Activated sludge treatment did not reduce total benzothiazole concentration significantly. Removals of the individual compounds ranged from 90% for 2-mercaptobenzothiazole and 70% for hydroxybenzothiazole to 40% for benzothiazole. The concentration of benzothiazole-2-sulfonic acid increased by 20%, whereas 2-methylthiobenzothiazole increased by 160% during activated sludge treatment, likely due to the methylation of mercaptobenzothiazole. Total benzothiazole removal in two parallely operated MBRs was significantly better (43%) than in the conventional activated sludge treatment. Namely benzothiazole and benzothiazole-2-sulfonic acid were more effectively removed. This first systematic study on the occurrence of benzothiazoles in municipal wastewater has shown that this is a relevant class of trace contaminants in municipal wastewater which is only incompletely removed in biological wastewater treatment. Emission from sewage treatment is dominated by the most polar benzothiazole-2-sulfonic acid. MBR treatment may reduce but cannot avoid this emission.
机译:在三个月的时间里,已经对市政废水以及活性污泥和膜生物反应器(MBR)的废水进行了分析,分析了许多在工业上用作杀菌剂,腐蚀抑制剂和硫化促进剂的2-取代苯并噻唑。通过液相色谱-质谱法在市政废水中定期检测所有六种分析物,总浓度为3.4杯/升。在这些化合物中,苯并噻唑-2-磺酸(1,700 ng / L),苯并噻唑(850 ng / L)和2-羟基苯并噻唑(500 ng / L)最突出。苯并噻唑的排放来源尚不清楚。活性污泥处理不会显着降低总苯并噻唑浓度。单个化合物的去除范围从2-巯基苯并噻唑的90%和羟基苯并噻唑的70%到苯并噻唑的40%。在活性污泥处理期间,苯并噻唑-2-磺酸的浓度增加了20%,而2-甲硫基苯并噻唑的浓度增加了160%,这可能是由于巯基苯并噻唑的甲基化。在两个并行操作的MBR中,总苯并噻唑的去除率明显好于传统的活性污泥处理(43%)。即,更有效地除去了苯并噻唑和苯并噻唑-2-磺酸。对市政废水中苯并噻唑的发生进行的首次系统研究表明,这是市政废水中相关的一类微量污染物,在生物废水处理中只是不完全清除了。污水处理的排放主要由极性最强的苯并噻唑-2-磺酸决定。 MBR处理可能会减少但无法避免这种排放。

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