Abstract
The widespread use of plastics has inevitably led to the accumulation of persistent plastic debris in aquatic systems, where gradual fragmentation generates microplastics (MPs) that threaten ecological and biological health. Their small size, chemical stability, and resistance to degradation make effective removal particularly challenging. In this work, a composite adsorbent was fabricated through the in situ solvothermal growth of Materials of Institute Lavoisier 100 (Iron) (MIL-100(Fe)) onto coconut shell-derived activated carbon (CSAC), yielding a monolithic material denoted as CSAC@MIL-100(Fe). The integration of porous C with a metal-organic framework created a hierarchically structured adsorbent rich in accessible binding sites. The composite achieved a maximum polystyrene (PS) removal efficiency of 97.4% and maintained 91.44% efficiency after seven regeneration cycles. Stable adsorption performance was observed across a broad pH range. Structural and chemical analyses (scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS)) combined with adsorption modeling revealed heterogeneous multilayer adsorption behavior consistent with the Freundlich isotherm and pseudo-second-order kinetics. π-π interactions, electrostatic attraction, and coordination effects jointly governed PS capture. The Langmuir maximum adsorption capacity reached 746.27 mg/g. These findings demonstrate a practical and recyclable strategy for efficient MP remediation in aquatic environments.