Dye adsorption by magnetic modified biochar has now received growing interest due to its excellent adsorption performance and facile separation for recycling. In this study, nano iron oxide–modified biochar was fabricated via the successive hydrothermal-pyrolyzing method using Chlorella vulgaris (Cv) and FeSO₄·7H₂O as raw materials, and its adsorption on Rhodamine B (RhB) in aqueous solution was studied. Multiple techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), vibrating sample magnetometry (VSM) and X-ray photoelectron spectroscopy (XPS) were employed to comprehensively characterize the structure, morphology and physicochemical properties of the adsorbent. The as-synthesized nano iron oxide–modified biochar (CBC-Fe(II)) exhibited a large surface area (527.6 m²/g) and high magnetic saturation value (13.7 emu/g) to facilitate magnetic separation. Compared with CBC and CBC-Fe(III), CBC-Fe(II) exhibited superior adsorption ability towards RhB in aqueous solution, with a maximum adsorption capacity of 286.4 mg/g. The adsorption process of RhB onto CBC-Fe(II) was well described by the pseudo-second-order kinetic model and Langmuir isotherm model, indicating monolayer chemisorption behaviors for the adsorption system. Facile preparation, great adsorption performance and magnetic recovery properties endow CBC-Fe(II) to be a promising adsorbent for dye removal.

Polymer-based wastewater disinfection, which is typically performed using chemical oxidation or irradiation, can result in various toxic byproducts and corrosion under harsh environments. This study introduces a robust bio-adsorbent prepared from naturally abundant polydopamine-modified medical stone (MS@PDA) for the high-efficiency removal of bacteria from water. The PDA nanocoating can be easily applied through an in situ self-polymerization process, resulting in a considerably high bacterial adsorption capacity of 6.6 k pcs mm⁻² for Staphylococcus aureus. A cyclic flow-through dynamic filtration and a disinfection system was implemented using an MS@PDA porous filter with an average pore size of 21.8 ± 1.4 µm and porosity of ~83%, achieving a 5.2–6.0-fold enhancement in the cumulative removal efficiency for MS@PDA₂. The underlying mechanisms were elucidated through the synergistic effects of interfacial bio-adsorption and size-dependent interception. Notably, the bacteria captured on the surface could be killed using the enhanced photothermal effects of the PDA nanocoating and the inherent antimicrobial properties of the mineral stone. Thus, this study not only provides a new type of advanced bio-adsorbent but also provides new perspectives on an efficient and cost-effective approach for sustainable wastewater treatment.

Municipal solid waste incineration fly ash (MSWIFA) can be reused as an admixture in cementitious materials, but its low activity limits its utilization as a resource. In this study, we systematically investigated the mineral and grinding characteristics of MSWIFA and then studied its pretreatment and activation via mechanical force–surface modification. The results indicate that the fineness and angle of repose of MSWIFA during grinding are inversely proportional to grinding time, while specific surface area and powder fluidity increase. Agglomeration occurs in the later stage, and particle size fluctuates. Gray correlation analysis shows that MSWIFA powder with a particle size of 16–45 μm contributes most to compressive strength improvement. The composite surface modifier TEA-STPP benefits grinding, shortens ball-milling time, and increases active particle size content, thereby promoting hydration activity. The best process regarding the modifier was determined. MSWIFA and blast furnace slag (BFS) accelerate early hydration of ordinary Portland cement (OPC) and increase its reaction participation, promoting the generation of calcium chloroaluminate (Friedel’s salt) and monosulfate-aluminate phases (SO₄-AFm) and significantly enhancing the hydration of tricalcium aluminate (C₃A) in OPC.

Phosphogypsum, the primary solid waste from the wet-process phosphoric acid industry, poses significant environmental and health risks due to large-scale stockpiling. To promote its resource utilisation, this study systematically evaluated the solidification and stabilisation performance of phosphogypsum–coal fly ash cementitious material (PAC) for Cr(VI)-contaminated soil under high-chloride conditions. Phosphogypsum reactivity was enhanced via mechanical activation and high-temperature calcination. An orthogonal experimental design was employed to analyse the effects of multiple factors—including calcination temperature and duration—on compressive strength and heavy metal leaching behaviour. Results show that PAC prepared from coal ash calcined at 600 °C for 3 h exhibits excellent mechanical properties and Cr(VI) stabilisation efficacy under high-chloride conditions, achieving a maximum compressive strength of 28.75 MPa and a Cr(VI) leaching concentration as low as 15.69 μg/L. Microstructural characterisation revealed the synergistic formation of a dense framework between C–S–H gel and calcium aluminate, conferring superior mechanical strength. Substitution and chelation mechanisms of Cl⁻ ions played a key role in enhancing corrosion resistance. This study provides theoretical support and technical guidance for the high-value utilisation of phosphogypsum-based materials in remediating saline–alkali-contaminated soils.