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Review Open access Aug 2026

Microalgae-based bioremediation of heavy metals: Mechanisms, optimization, and environmental applications.

Heavy metal (HM) contamination in aquatic environments remains a persistent global challenge driven by industrialization, mining activities, and agricultural runoff. Microalgae-based remediation has emerged as a sustainable and cost-effective technology, utilizing both passive surface biosorption and active intracellular bioaccumulation mechanisms. This review comprehensively synthesizes recent advances in microalgae-mediated HM removal by integrating mechanistic insights at molecular, cellular, and process aspects. The performance of dried, living, and chemically modified biomass is comparatively evaluated across major HMs, including Cd, Pb, Cr, Cu, Hg, Ni, Zn, and As, under varying operational conditions. Microalgae are categorized into four major phyla to comparatively evaluate their HM adsorption capacities. Quantitatively analysis indicates that biosorption onto cell surfaces is the predominant mechanism while bioaccumulation, i.e., the uptake of HM into cells, is in general secondary but in some cases substantial. Transporter-regulated uptake and intracellular detoxification mechanisms are also discussed. Kinetic, isotherm, and thermodynamic modeling approaches are examined comprehensively, despite recurring inconsistencies in model selection, parameter interpretation, and reporting practices in the literature. Adsorption enhancement strategies, including physical and physiological conditioning, chemical modification, immobilization, biofilm cultivation, and multi-species co-cultivation, are assessed for their roles in improving HM removal efficiency, regeneration stability, and system robustness. By bridging mechanistic understanding with engineering implementation, this review provides a comprehensive framework to advance microalgae-based HM remediation.

Siwei Gu, Weihao Meng, Chuhui Zhang et al. · 0 citations
Open access Aug 2026

Hydrophobic Ion Pairing with Cationic Surfactant Modifies Surface Activity and Colloidal Behavior of PFAS

Quaternary ammonium compounds (QACs) are increasingly used to enhance the removal of per- and polyfluoroalkyl substances (PFAS), particularly short-chain compounds, through hydrophobic ion pairing (HIP). Here, we investigated how HIP with cetyltrimethylammonium chloride (CTAC) influences the interfacial and colloidal behavior of selected PFAS at low-micromolar concentrations below reported critical micelle concentrations (CMCs) and across varying solution chemistries (pH, ionic strength, and natural organic matter) using surface tension measurements, dynamic light scattering (DLS), ζ-potential analysis, and transmission electron microscopy (TEM). Relative to the corresponding PFAS-only controls, CTAC (6.66 μM) reduced the surface tension of PFBA, PFBS, and PFOA solutions (3.33 μM each) by 24.64, 45.71, and 70.17%, respectively. PFOS exhibited little additional surface-tension response to CTAC but responded strongly to a shorter-chain QAC (C12), indicating that interfacial behavior depends on fluorocarbon–hydrocarbon chain-length compatibility. Targeted DLS, ζ-potential, and TEM characterization identified detectable bulk coassembly in selected PFAS–QAC systems at concentrations of 3.33–33.30 μM. Electrolyte addition produced PFAS-dependent changes in interfacial behavior, while NOM reduced the interfacial activity of several mixtures. These findings provide mechanistic insight into PFAS–QAC behavior relevant to the development of QAC-assisted PFAS separation processes.

B. Pandey, Ligaya Manalastas, Afaq Ahmad et al. · 0 citations

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