Calcium Ion Mixing Modes Govern Membrane Fouling Mitigation During Membrane-Based Recovery of Extracellular Polymeric Substances

钙离子混合模式控制膜法回收胞外聚合物过程中膜污染的缓解

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Abstract

Recycling extracellular polymeric substances (EPSs) from excess sludge in wastewater treatment plants has garnered significant research attention. Membrane separation offers a promising approach for EPS concentration; however, membrane fouling remains a critical challenge. Previous studies demonstrate that Ca(2+) addition effectively mitigates membrane fouling. This study reveals that Ca(2+) mixing modes govern membrane fouling in the dead-end ultrafiltration of both the practical EPS and model EPS [sodium algiante (SA)]. The interaction mechanisms between Ca(2)(+) and the EPS under varied mixing conditions and their impact on filtration performance were systematically investigated. At a low Ca(2+) concentration, the addition sequence critically influenced colloidal particle sizes formed via Ca(2)(+)-EPS interactions, altering the cake layer structure governing filtration resistance; these effects diminished at higher Ca(2+) concentrations. In suspensions prepared by adding EPS to Ca(2+) solution (EPS-Ca), a portion of the EPS became encapsulated within an EPS-Ca layer formed through Ca(2+) EPS binding, reducing free EPS concentration and enlarging colloidal aggregates. This encapsulation reduced EPS-mediated membrane fouling, thereby lowering filtration resistance. Conversely, in suspensions prepared by adding Ca(2+) to EPS solution (Ca-EPS), more complete Ca(2+) EPS interactions formed a dense crosslinked structure with smaller colloids on membrane surfaces, intensifying fouling and resistance. Additionally, EPS-Ca exhibited higher compressibility than Ca-EPS, though both exhibited comparable filtration resistance under high-pressure conditions. These results offer critical insights into optimizing EPS ultrafiltration concentration to mitigate membrane fouling through Ca(2+) addition strategies.

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