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.

The sludge-derived biochar is considered an effective emerging contaminants adsorbent for wastewater treatment. In this paper, red mud and steel slag (RMSS) was used for improving sludge dewaterability and enhancing the sludge-derived biochar adsorption capacity. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and a scanning electron microscope (SEM) were employed to comprehensively characterize the mineral composition, functional group, and morphology of the adsorbent. RMSS was able to improve the sludge dewatering performance by providing a skeleton structure to promote drainage and Fe(III) to decrease the Zeta potential. The dosage of 20 mg/g RMSS was able to reduce the specific resistance to filtration (SRF) and the Zeta potential of sludge from 1.57 × 10¹³ m/kg and −19.56 mV to 0.79 × 10¹³ m/kg and −9.10 mV, respectively. The co-pyrolysis of RMSS and sludge (2:8) induced the formation of biochar containing FeAl₂O₄ (PS80). The PS80 exhibited a large surface area (46.40 m²/g) and high tetracycline (TC) removal capacity (98.87 mg/g) when combined with H₂O₂ (PS80-H₂O₂). The adsorption process of TC onto PS80 and PS80-H₂O₂ was well described by the pseudo-first-order and pseudo-second-order kinetic model, indicating physisorption and chemisorption behavior. The results indicated that co-pyrolysis of RMSS sludge PS80-H₂O₂ could enhance the biochar adsorption capacity of TC, attributable to the degradation by ·OH generated by the heterogeneous Fenton reaction of FeAl₂O₄ and H₂O₂, the release of adsorbed sites, and the improvement of the biochar pore structure. This study proposed a novel method for the use of RMSS to dewater sludge as well as to induce the formation of FeAl₂O₄ in biochar with effective TC removal by providing a Fe and Al source, achieving a waste-to-resource strategy for the integrated management of industrial solid waste and sewage sludge.

The reaction tank of process wastewater, as one of the key pieces of equipment for wastewater treatment, is exposed to an acidic and alkaline wastewater immersion environment for a long time and is prone to the influence of complex ions in water, resulting in concrete shedding and steel bar corrosion, which seriously affect service performance. To address the issue of ionic erosion in process wastewater reaction tanks, a silicon–oxygen grid substrate was constructed with ethyl orthosilicate, and graphene oxide was used as the corrosion-resistant functional component to prepare GO/SiO₂ corrosion-resistant films under acid-catalyzed conditions. Extreme corrosion environments were designed to evaluate the corrosion resistance of GO/SiO₂ films. The results showed that the permeability of the uncoated samples decreased significantly, and the ion concentration leached in the corrosive medium was higher. The permeability of the GO/SiO₂-coated samples did not decrease significantly, and the ion leaching concentration in the corrosive medium gradually decreased with the increase in GO content, verifying the positive correlation between GO content and corrosion resistance and GO’s use in the field of corrosion resistance in water treatment facilities.

The degradation of stone surfaces resulting from natural aging and environmental factors poses significant challenges to material durability and esthetics. This review systematically summarizes recent advances in composite protective materials designed to enhance stone surface preservation. It focuses on the classifications and fundamental properties of organic polymer-based materials, inorganic nanocomposites, and multifunctional protective coatings, emphasizing their physicochemical, mechanical, and environmental performance. The review further analyzes case studies across various stone substrates, such as marble, limestone, sandstone, and granite, highlighting substrate-specific coating compatibility and protective effectiveness against water ingress, biological colonization, graffiti, and pollutant deposition. Critical factors influencing protective performance, including stone mineralogy, coating composition, environmental conditions, and application protocols, are elucidated. Finally, existing challenges and future research directions are identified, underscoring the need for environmentally friendly, multifunctional, and durable composite coatings with enhanced substrate adaptability and simplified application processes.

Rapid growth of water conservancy/hydropower projects has spurred rising demand for sand-gravel aggregates. Under strict water use and zero-waste policies, treating wet-process aggregate washing wastewater is challenging. Flocculants—key chemicals in this process—directly influence treatment efficiency and operational costs via their type, dosage, and efficacy. Further development of the intelligent control system for flocculant dosing can reduce flocculant consumption by 50% to 67%. However, existing studies have an insufficient understanding of the identification of emerging contaminants in aggregate washing wastewater and the migration of flocculants in multi-medium environments, as well as a lack of research on the synergistic effects of multiple flocculants. Another key core challenge lies in the accurate identification of the impact of flocculant residues on concrete performance, along with the problems of high cost and poor adaptability of intelligent systems. Future research directions will focus on precise flocculation, residue control and resource utilization to drive the development of efficient and environmentally friendly treatment technologies.

A novel and rapid ball-milling approach was developed in this study to efficiently intercalate hexadecyltrimethylammonium bromide (HDTMA-Br) into vermiculite (VMT) within only 15 min. The raw granular VMT (2–3 mm) was first ground into fine powder using an airflow pulverizer. A suspension containing VMT and HDTMA-Br (1 CEC) in deionized water was then subjected to planetary ball milling at 450 r/min (25 °C), followed by washing and drying to obtain organo-vermiculite (OVMT) with a particle size of 44–5 µm. X-ray diffraction, Fourier-transform Infrared Spectroscopy and Thermogravimetric Analysis analyses confirmed successful intercalation, with the basal spacing $d_{\left(001\right)}$ expanding from 1.46 nm to 4.51 nm. Transmission Electron Microscopy observations further revealed partial delamination of lamellar structures and a pronounced reduction in particle size, supporting the structural reorganization induced by the mechanochemical process. In addition, nitrogen adsorption analysis showed that the BET surface area decreased by 4.05 m²·g⁻¹, while the average pore diameter increased by 3.2 nm, indicating the development of a more hydrophobic interlayer environment. Overall, this approach offers a practical route for producing organophilic silicate materials and shows strong potential for wastewater treatment applications, particularly for the adsorption of organic pollutants and heavy-metal ions.