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Biodegradation of the artificial sweetener acesulfame in biological wastewater treatment and sandfilters

机译:人工甜味剂乙酰磺胺胺在生物废水处理和沙滤池中的生物降解

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摘要

A considerable removal of the artificial sweetener acesulfame (ACE) was observed during activated sludge processes at 13 wastewater treatment plants (WWTPs) as well as in a full-scale sand filter of a water works. A long-term sampling campaign over a period of almost two years revealed that ACE removal in WWTPs can be highly variable over time. Nitrifying/denitrifying sequencing batch reactors (SBR) as well as aerobic batch experiments with activated sludge and filter sand from a water works confirmed that both activated sludge as well as filter sand can efficiently remove ACE and that the removal can be attributed to biologically mediated degradation processes. The lab results strongly indicated that varying ACE removal in WWTPs is not associated with nitrification processes. Neither an enhancement of the nitrification rate nor the availability of ammonium or the inhibition of ammonium monooxygenase by N-allylthiourea (ATU) affected the degradation. Moreover, ACE was found to be also degradable by activated sludge under denitrifying conditions, while being persistent in the absence of both dissolved oxygen and nitrate. Using ion chromatography coupled with high resolution mass spectrometry, sulfamic acid (SA) was identified as the predominant transformation product (TP). Quantitative analysis of ACE and SA revealed a closed mass balance during the entire test period and confirmed that ACE was quantitatively transformed to SA. Measurements of dissolved organic carbon (DOC) revealed an almost complete removal of the carbon originating from ACE, thereby further confirming that SA is the only relevant final TP in the assumed degradation pathway of ACE. A first analysis of SA in three municipal WWTP revealed similar concentrations in influents and effluents with maximum concentrations of up to 2.3 mg/L. The high concentrations of SA in wastewater are in accordance with the extensive use of SA in acid cleaners, while the degradation of ACE in WWTPs adds only a very small portion of the total load of SA discharged into surface waters. No removal of SA was observed by the biological treatment applied at these WWTPs. Moreover, SA was also stable in the aerobic batch experiments conducted with the filter sand from a water works. Hence, SA might be a more appropriate wastewater tracer than ACE due to its chemical and microbiological persistence, the negligible sorbing affinity (high negative charge density) and its elevated concentrations in WWTP effluents.
机译:在13个废水处理厂(WWTP)以及自来水厂的大型滤砂机中,在活性污泥处理过程中观察到大量的人造甜味剂乙酰舒泛(ACE)去除。在将近两年的时间里进行的长期抽样调查显示,污水处理厂中ACE的去除随时间变化很大。硝化/脱氮定序分批反应器(SBR)以及从水厂进行的活性污泥和滤砂的好氧分批实验证实,活性污泥和滤砂都可以有效去除ACE,并且去除可以归因于生物介导的降解流程。实验结果强烈表明,污水处理厂中不同的ACE去除与硝化过程无关。 N-烯丙基硫脲(ATU)的硝化速率的提高,铵的可用性或对铵单加氧酶的抑制都不会影响降解。此外,发现ACE在脱氮条件下也可被活性污泥降解,而在不存在溶解氧和硝酸盐的情况下仍可保持持久性。使用离子色谱与高分辨率质谱联用,确定了氨基磺酸(SA)是主要的转化产物(TP)。 ACE和SA的定量分析显示,在整个测试期间,质量平衡是封闭的,并证实ACE已定量转化为SA。溶解有机碳(DOC)的测量表明几乎完全清除了源自ACE的碳,从而进一步证实SA是假定的ACE降解途径中唯一相关的最终TP。对三个市政污水处理厂中SA的首次分析显示进水和出水中的浓度相似,最大浓度高达2.3 mg / L。废水中高浓度的SA符合酸性清洁剂中SA的广泛使用,而污水处理厂中ACE的降解仅增加了排放到地表水中的SA总负荷的很小一部分。在这些污水处理厂进行的生物处理未观察到SA的去除。此外,在自来水厂的滤砂进行的好氧分批实验中,SA也是稳定的。因此,由于SA的化学和微生物持久性,可忽略的吸附亲和力(高负电荷密度)和在WWTP废水中的较高浓度,因此它可能比ACE更适合作为废水示踪剂。

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