Eawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland.
Water Res. 2011 Jan;45(2):605-17. doi: 10.1016/j.watres.2010.07.080. Epub 2010 Aug 5.
The kinetics of oxidation and disinfection processes during ozonation in a full-scale reactor treating secondary wastewater effluent were investigated for seven ozone doses ranging from 0.21 to 1.24 g O(3) g(-1) dissolved organic carbon (DOC). Substances reacting fast with ozone, such as diclofenac or carbamazepine (k(P, O3) > 10(4) M(-1) s(-1)), were eliminated within the gas bubble column, except for the lowest ozone dose of 0.21 g O(3) g(-1) DOC. For this low dose, this could be attributed to short-circuiting within the reactor. Substances with lower ozone reactivity (k(P, O3) < 10(4) M(-1) s(-1)) were only fully eliminated for higher ozone doses. The predictions of micropollutant oxidation based on coupling reactor hydraulics with ozone chemistry and reaction kinetics were up to a factor of 2.5 higher than full-scale measurements. Monte Carlo simulations showed that the observed differences were higher than model uncertainties. The overestimation of micropollutant oxidation was attributed to a protection of micropollutants from ozone attack by the interaction with aquatic colloids. Laboratory-scale batch experiments using wastewater from the same full-scale treatment plant could predict the oxidation of slowly-reacting micropollutants on the full-scale level within a factor of 1.5. The Rct value, the experimentally determined ratio of the concentrations of hydroxyl radicals and ozone, was identified as a major contribution to this difference. An increase in the formation of bromate, a potential human carcinogen, was observed with increasing ozone doses. The final concentration for the highest ozone dose of 1.24 g O(3) g(-1) DOC was 7.5 μg L(-1), which is below the drinking water standard of 10 μg L(-1). N-Nitrosodimethylamine (NDMA) formation of up to 15 ng L(-1) was observed in the first compartment of the reactor, followed by a slight elimination during sand filtration. Assimilable organic carbon (AOC) increased up to 740 μg AOC L(-1), with no clear trend when correlated to the ozone dose, and decreased by up to 50% during post-sand filtration. The disinfection capacity of the ozone reactor was assessed to be 1-4.5 log units in terms of total cell counts (TCC) and 0.5 to 2.5 log units for Escherichia coli (E. coli). Regrowth of up to 2.5 log units during sand filtration was observed for TCC while no regrowth occurred for E. coli. E. coli inactivation could not be accurately predicted by the model approach, most likely due to shielding of E. coli by flocs.
在处理二级废水的全尺寸反应器中进行臭氧化时,研究了七种臭氧剂量(范围为 0.21 至 1.24 g O3 g(-1) 溶解有机碳(DOC))的氧化和消毒过程动力学。与臭氧快速反应的物质,如双氯芬酸或卡马西平(k(P, O3) > 10(4) M(-1) s(-1)),除了最低的臭氧剂量为 0.21 g O3 g(-1) DOC 外,在气泡柱内被消除。对于这个低剂量,可以归因于反应器内的短路。臭氧反应性较低的物质(k(P, O3) < 10(4) M(-1) s(-1))仅在较高的臭氧剂量下才能完全消除。基于耦合反应器水力学、臭氧化学和反应动力学的预测,微污染物氧化的预测值比全尺寸测量值高出高达 2.5 倍。蒙特卡罗模拟表明,观察到的差异高于模型不确定性。对微污染物氧化的高估归因于微污染物与水胶体相互作用,从而免受臭氧攻击。使用来自同一全尺寸处理厂的废水进行实验室规模的批量实验,可以在全尺寸水平上预测缓慢反应的微污染物的氧化,预测值与实际值的比值在 1.5 倍以内。Rct 值,即实验确定的羟基自由基和臭氧浓度之比,被确定为这种差异的主要贡献。随着臭氧剂量的增加,观察到溴酸盐(一种潜在的人类致癌物)的形成增加。最高臭氧剂量为 1.24 g O3 g(-1) DOC 的最终浓度为 7.5 μg L(-1),低于饮用水标准 10 μg L(-1)。在反应器的第一隔室中观察到高达 15 ng L(-1)的 N-亚硝基二甲胺(NDMA)形成,随后在砂滤中略有消除。可同化有机碳(AOC)增加到 740 μg AOC L(-1),与臭氧剂量没有明显的相关性,在砂滤后减少了高达 50%。根据总细胞计数(TCC),臭氧反应器的消毒能力评估为 1-4.5 个对数单位,而对于大肠杆菌(E. coli)则为 0.5 至 2.5 个对数单位。TCC 在砂滤中观察到高达 2.5 个对数单位的再生,而 E. coli 则没有发生再生。大肠杆菌的失活不能通过模型方法准确预测,最有可能是由于絮体对大肠杆菌的屏蔽。