Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, No.27 Shanda South Road, Jinan, 250100, People's Republic of China.
Key Laboratory for Special Functional Aggregated Materials of Education Ministry, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, People's Republic of China; Environmental Engineering Research Centre, Department of Civil Engineering, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region.
Chemosphere. 2018 Apr;196:418-428. doi: 10.1016/j.chemosphere.2017.12.198. Epub 2018 Jan 5.
Cyanobacterial bloom causes the release of algal organic matter (AOM), which inevitably affects the treatment processes of natural organic matter (NOM). This study works on treating micro-polluted surface water (SW) by emerging coagulant, namely titanium sulfate (Ti(SO)), followed by Low Pressure Ultrafiltration (LPUF) technology. In particular, we explored the respective influence of extracellular organic matter (EOM) and intracellular organic matter (IOM) on synergetic EOM-NOM/IOM-NOM removal, functional mechanisms and subsequent filtration performance. Results show that the IOM inclusion in surface water body facilitated synergic IOM-NOM composite pollutants removal by Ti(SO), wherein loosely-aggregated flocs were produced, resulting in floc cake layer with rich porosity and permeability during LPUF. On the contrary, the surface water invaded by EOM pollutants increased Ti(SO) coagulation burden, with substantially deteriorated both UV-represented and dissolved organic matter (DOC) removal. Corresponded with the weak Ti(SO) coagulation for EOM-NOM removal was the resultant serious membrane fouling during LPUF procedure, wherein dense cake layer was formed due to the compact structure of flocs. Although the IOM enhanced NOM removal with reduced Ti(SO) dose and yielded mitigated membrane fouling, larger percentage of irreversible fouling was seen than NOM and EOM-NOM cases, which was most likely due to the substances with small molecular weight, such as microcystin, adhering in membrane pores. This research would provide theoretical basis for dose selection and process design during AOM-NOM water treatment.
蓝藻水华会导致藻源有机物(AOM)的释放,这不可避免地会影响天然有机物(NOM)的处理过程。本研究采用新兴的混凝剂硫酸钛(Ti(SO))处理微污染地表水(SW),然后采用低压超滤(LPUF)技术。特别是,我们探索了细胞外有机物(EOM)和细胞内有机物(IOM)对协同 EOM-NOM/IOM-NOM 去除、功能机制和后续过滤性能的各自影响。结果表明,地表水体内的 IOM 有利于 Ti(SO)对协同 IOM-NOM 复合污染物的去除,其中形成了松散聚集的絮体,导致 LPUF 过程中形成了具有丰富孔隙度和渗透性的絮体层。相反,受 EOM 污染物侵袭的地表水增加了 Ti(SO)的混凝负担,导致 UV 代表的和溶解有机物(DOC)的去除明显恶化。与 Ti(SO)对 EOM-NOM 去除的弱混凝相对应的是 LPUF 过程中严重的膜污染,由于絮体结构紧凑,形成了致密的滤饼层。尽管 IOM 通过减少 Ti(SO)剂量增强了 NOM 的去除,并减轻了膜污染,但与 NOM 和 EOM-NOM 情况相比,不可逆污染的比例更大,这很可能是由于分子量较小的物质,如微囊藻毒素,附着在膜孔中。本研究将为 AOM-NOM 水处理过程中的剂量选择和工艺设计提供理论依据。