Insight into the effect of UVC-based advanced oxidation processes on the interaction of typical microplastics and their derived disinfection byproducts during disinfection

化学 吸附 微塑料 环境化学 浸出(土壤学) 有机化学 土壤水分 环境科学 土壤科学
作者
Juanjuan Yao,Hanyang Qian,Zhi‐Hao Yan,Xiong Zhao,Naiyun Gao,Zhi Zhang
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:472: 134597-134597 被引量:15
标识
DOI:10.1016/j.jhazmat.2024.134597
摘要

10 μm polystyrene (PS) and polyethylene-terephthalate microplastics (PET MPs), prevalent in finished drink water, were employed to investigate the effect of normal dosage UVC-based-advanced-oxidation-processes (UVC-AOPs) on the interaction between MPs and their derived disinfection-byproducts (DBPs) during subsequent chlorination-disinfection, in the presence of Br-, for the first time. The results indicated that UVC/H2O2 caused higher leaching of microplastic-derived-organic-matter (MP-DOM), with smaller and narrower molecular-weight-distribution than UVC and UVC/peroxymonosulfate (UVC/PMS). The trihalomethanes (as dominant DBPs) molar-formation-potentials (THMs-MFPs) for MP-DOM leached in different UVC-AOPs followed the order of UVC/H2O2>UVC/PMS>UVC. The adsorption of formed THMs, especially Br-THMs, back on MPs was observed in all MPs suspensions with or without UVC-AOPs pre-treatment. The Cl-THMs adsorption by MPs is more sensitive to UVC-AOPs than Br-THMs. The adsorption kinetic, isotherm and thermodynamic experiments indicated that UVC-AOPs reduce the capacity but increase the rate of THMs adsorption by MPs, suggesting the halogen and hydrogen bonding forces governed the THMs adsorption-rate while hydrophobic interaction determines their adsorption-capacity. The UVC-AOPs pre-treatment sharply increased the total yield of THMs via both indirectly inducing MP-DOM leaching and directly increasing the THMs-MFPs of MPs by oxidation. 21.36-41.96% of formed THMs adsorbed back on the UVC-AOPs-pretreated MPs, which might increase the toxicity of MPs. Microplastics (MPs) through Conventional-Drinking-Water-Treatments can cause the leaching of MP-derived dissolved-organic-matter (MP-DOM) during subsequent ultraviolet advanced oxidation processes (UV-AOPs) and increase the disinfection byproducts (DBPs) formation during disinfection in Drink-Water-Treatment-Plants. This study first investigated the MP-DOM leaching during UV-AOPs, the DBP formation during disinfection, and the MP-DOM derived-DBPs adsorption on UV-AOP treated MPs. In UV-AOPs, smaller-sized MPs released more MP-DOM, whereas bromine could increase DBP formation during disinfection by generating more Br-DBPs which were adsorbed by MPs more than Cl-DBPs. The findings could provide valuable information for the safety of drinking water treatment as MPs are present.
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