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在海水预处理中使用亚铁/过氧乙酸对超细微塑料和有机物共污染物进行协同减污。

Synergistic fouling mitigation of co-contaminants of ultrafine microplastics and organics in seawater pretreatment using ferrous iron/peracetic acid.

作者信息

Li Zihao, Xu Boyan, Hao Anni, Hong Seungkwan, Ng How Yong

机构信息

Center for Water Research, Advanced Institute of Natural Sciences, Beijing Normal University, Zhuhai 519087, China.

Center for Water Research, Advanced Institute of Natural Sciences, Beijing Normal University, Zhuhai 519087, China.

出版信息

Water Res. 2025 Jul 13;286:124227. doi: 10.1016/j.watres.2025.124227.

Abstract

The increasing occurrence of ultrafine microplastics (MPs, 3 μm) and algal organic matter (AOM), such as humic acid (HA), in seawater poses a growing challenge to conventional desalination pretreatment, as their interactions can lead to MP-HA co-contaminants that significantly reduce the effectiveness of traditional coagulants (e.g., FeCl). Furthermore, ultrafiltration (UF) of MP-HA co-contaminants showed a synergistic increase in the modified fouling index (MFI), exceeding the sum of individual effects. This intensified fouling was due to MPs serving as scaffolds for HA, which was immobilized through non-covalent interactions such as hydrogen bonding, π-π stacking, and electrostatic attraction, resulting in reduced porosity and a denser cake layer. To address this issue, this study proposed an advanced coagulation using ferrous iron/peracetic acid (Fe/PAA) for the treatment of MP-HA (20 mg/L HA and 10 mg/L MPs) in seawater (both synthetic seawater and real seawater). At an optimal dosage of 0.2 mM Fe/0.1 mM PAA, the Fe/PAA system demonstrated superior coagulation performance compared to 0.2 mM Fe, achieving more effective charge neutralization (Fe: -14.7 mV; Fe/PAA: -5.8 mV) and forming larger, denser flocs (Fe: 74.2 μm; Fe/PAA: 104 μm), resulting in significantly improved coagulation performance (e.g., turbidity removal of 83.9 %; 19.0 % for Fe). Regarding the unique mechanisms of Fe/PAA in seawater, we found that a high Cl concentration of 25 g/L (428 mM) markedly influenced the dominant reactive species by scavenging •OH radicals, thereby increasing the proportion of FeO from 13.7 % to 40.3 %, highlighting the critical role of FeO in enhancing coagulation performance. Furthermore, compared to Fe, Fe/PAA primarily mitigated membrane fouling caused by cake layer formed by MP-HA, resulting in a 1.8-fold improvement in membrane flux by the end of filtration. Crucially, trials in real natural seawater demonstrated that Fe/PAA preserved its enhanced coagulation and fouling-control effectiveness under authentic marine conditions. Collectively, this study reveals the synergistic fouling effects of MP-HA in seawater desalination and offers theoretical and technical guidance for applying Fe/PAA to address this emerging challenge.

摘要

海水中超细微塑料(MPs,粒径3μm)和藻类有机物(AOM)如腐殖酸(HA)的出现频率不断增加,这给传统海水淡化预处理带来了越来越大的挑战,因为它们之间的相互作用会导致MP-HA共污染物的产生,从而显著降低传统混凝剂(如FeCl)的有效性。此外,对MP-HA共污染物进行超滤时,改性污染指数(MFI)呈现协同增加,超过了各自单独作用的总和。这种强化的污染是由于微塑料作为腐殖酸的支架,腐殖酸通过氢键、π-π堆积和静电吸引等非共价相互作用固定在微塑料上,导致孔隙率降低和滤饼层更致密。为了解决这个问题,本研究提出使用亚铁/过氧乙酸(Fe/PAA)进行深度混凝处理海水中的MP-HA(20mg/L HA和10mg/L MPs,包括合成海水和实际海水)。在0.2mM Fe/0.1mM PAA的最佳剂量下,与0.2mM Fe相比,Fe/PAA系统表现出卓越的混凝性能,实现了更有效的电荷中和(Fe:-14.7mV;Fe/PAA:-5.8mV),并形成更大、更致密的絮体(Fe:74.2μm;Fe/PAA:104μm),从而显著提高了混凝性能(例如,浊度去除率为83.9%;Fe为19.0%)。关于Fe/PAA在海水中的独特作用机制,我们发现25g/L(428mM)的高Cl浓度通过清除•OH自由基显著影响了主要的活性物种,从而使FeO的比例从13.7%增加到40.3%,突出了FeO在增强混凝性能中的关键作用。此外,与Fe相比,Fe/PAA主要减轻了由MP-HA形成的滤饼层引起的膜污染,在过滤结束时膜通量提高了1.8倍。至关重要的是,在实际天然海水中的试验表明,Fe/PAA在真实海洋条件下仍保持其增强的混凝和污染控制效果。总的来说,本研究揭示了海水中MP-HA的协同污染效应,并为应用Fe/PAA应对这一新兴挑战提供了理论和技术指导。

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