Department of Civil and Environmental Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Water Res. 2017 Sep 1;120:146-155. doi: 10.1016/j.watres.2017.04.080. Epub 2017 May 3.
The application of ozone pre-treatment for ultrafiltration (UF) in drinking water treatment has been studied for more than 10 years, but its performance in mitigating or exacerbating membrane fouling has been inconclusive, and sometimes contradictory. To help explain this, our study considers the significance of the influent organic matter and its interaction with ozone on membrane fouling, using solutions of two representative types of extracellular polymeric substances (EPS), alginate and bovine serum albumin (BSA), and samples of surface water. The results show that at typical ozone doses there is no measurable mineralization of alginate and BSA, but substantial changes in their structure and an increase in the size of nano-particle aggregates (micro-flocculation). The impact of ozonation on membrane fouling, as indicated by the membrane flux, was markedly different for the two types of EPS and found to be related to the size of the nano-particle aggregates formed in comparison with the UF pore size. Thus, for BSA, ozonation created aggregate sizes similar to the UF pore size (100 k Dalton) which led to an increase in fouling. In contrast, ozonation of alginate created the nano-particle aggregates greater than the UF pore size, giving reduced membrane fouling/greater flux. For solutions containing a mixture of the two species of EPS the overall impact of ozonation on UF performance depends on the relative proportion of each, and the ozone dose, and the variable behaviour has been demonstrated by the surface water. These results provide new information about the role of nano-particle aggregate size in explaining the reported ambiguity over the benefits of applying ozone as pre-treatment for ultrafiltration.
臭氧预处理在饮用水处理中的超滤(UF)中的应用已经研究了超过 10 年,但它在减轻或加剧膜污染方面的性能尚无定论,有时甚至相互矛盾。为了帮助解释这一点,我们的研究考虑了进水有机物及其与臭氧相互作用对膜污染的重要性,使用了两种代表性的胞外聚合物(EPS)——藻酸盐和牛血清白蛋白(BSA)的溶液以及地表水样本。结果表明,在典型的臭氧剂量下,藻酸盐和 BSA 没有可测量的矿化,但它们的结构发生了实质性变化,纳米颗粒聚集体(微絮凝)的尺寸增加。通过膜通量表示的臭氧处理对膜污染的影响,对于两种类型的 EPS 明显不同,并且发现与形成的纳米颗粒聚集体的尺寸与 UF 孔径的关系有关。因此,对于 BSA,臭氧处理会产生与 UF 孔径(100kDalton)相似的聚集体尺寸,从而导致污染增加。相比之下,臭氧处理藻酸盐会产生大于 UF 孔径的纳米颗粒聚集体,从而减少膜污染/增加通量。对于含有两种 EPS 混合物的溶液,臭氧处理对 UF 性能的整体影响取决于每种物质的相对比例、臭氧剂量,并且地表水已经证明了这种可变行为。这些结果提供了有关纳米颗粒聚集体尺寸在解释报道的臭氧作为超滤预处理的好处方面的模糊性的新信息。