Search Results (248)

This study explored the utilization of coal gangue with high iron content to synthesize poly-ferric-alum-sulfate (PAFS) and coal gangue leaching residue-PAFS (CG@PAFS) coagulants, which were subsequently applied to treat landfill leachate and its concentrate. The results demonstrated that the PAFS coagulant exhibited notable removal efficiency for key pollutants, including chemical oxygen demand (COD) and total phosphorus (TP), with removal rates of 23.8% and 77.5%, respectively. Its performance was comparable to polyferric sulfate (PFS) and superior to aluminum polysulfate (PAS). Mechanistic investigations revealed that Fe³⁺ in the PAFS coagulant reacted chemically with phosphate ions, forming insoluble precipitates and facilitating phosphate removal through flocculation. Furthermore, PAFS also exhibited moderate removal efficiency for COD and ammonia nitrogen (NH₃-N) via flocculation processes. From a sustainability perspective, this study advances a circular economy model by simultaneously addressing two pressing environmental challenges: the valorization of coal gangue (a massive industrial solid waste) and the treatment of landfill leachate (a hazardous wastewater). Importantly, the post-treatment sludge, rich in available phosphorus and silicon, demonstrates promising potential for beneficial reuse as a soil conditioner, thereby closing the material loop and reducing reliance on virgin chemical resources. This integrated waste-to-resource approach aligns with multiple Sustainable Development Goals (SDGs), particularly SDG 6 (Clean Water and Sanitation), SDG 11 (Sustainable Cities and Communities), and SDG 12 (Responsible Consumption and Production). Overall, this study provides valuable insights into the resource-efficient utilization of coal gangue and presents an effective, low-carbon, and sustainable approach for landfill leachate management. Full article

The development of efficient technologies for processing secondary technogenic raw materials represents a promising approach to replenishing vanadium resources. This study investigates the processes of sulfuric acid reductive leaching of vanadium from spent vanadium catalysts using oxalic acid and metallic iron as reducing agents. It was established that oxalic acid provides vanadium extraction of up to 95.2%, whereas the use of metallic iron (2–3 wt.% of the catalyst mass) enables a vanadium recovery rate of 91–92% at a solid-to-liquid ratio of 1:7 and pH 1.3–1.5, offering a more cost-effective alternative. Thermodynamic modeling of the V–Fe–P–SO₄–C₂O₄–H₂O system was performed using the Medusa software package over a pH range of 0–3. The results showed that vanadium(IV) predominantly exists as the VOSO₄ complex in sulfuric acid solutions, whereas the formation of oxalate and phosphate complexes is thermodynamically insignificant. Iron(III) was found to exhibit a strong affinity toward phosphate ions, promoting their selective precipitation as an iron phosphate phase while maintaining vanadium in solution. The obtained results provide a scientific basis for the efficient preliminary separation of iron and vanadium and for improving the selectivity of subsequent vanadium sorption. Full article

The application of a huge number of lithium-ion batteries (LIBs) to electric vehicles has produced much solid waste. If not disposed properly, the solid waste may cause environmental pollution and is, per se, a waste of resources. Therefore, recycling valuable metals from LIBs is considered an ideal option for preventing environmental pollution and alleviating waste. Taking sulfuric acid (H₂SO₄) as the leaching agent and glucose (C₆H₁₂O₆) as the reducing agent, the ultrasonic-assisted reducing leaching was used to recycle lithium (Li) and iron (Fe) from spent lithium iron phosphate (LFP) batteries. Based on experimental results of conventional leaching, the research aimed to examine the influence of ultrasonic treatment on leaching rates of Li and Fe. Results show that the leaching rates of Li and Fe are separately 96.53% and 96.8% when the concentration of H₂SO₄ is 2 mol/L, the concentration of C₆H₁₂O₆ is 2 mol/L, the liquid–solid ratio is 15 mL/g, leaching temperature is 70 °C, leaching time is 60 min, and ultrasonic power is 100 W. Compared with conventional leaching, the leaching rates of Li and Fe separately increase by 10.84% and 12.33% through ultrasonic-assisted leaching under the same experimental conditions. Kinetics analysis of ultrasonic-assisted reducing leaching indicates that the activation energies of Li and Fe are 10.84 kJ/mol and 16.24 kJ/mol, respectively. The ultrasonic-assisted reducing leaching process of Li and Fe from LFP batteries is controlled by diffusion. Full article

Phosphate tailings (PTs), a solid waste generated from phosphate flotation, are a low-grade phosphate resource rich in quartz and dolomite. Their long-term accumulation leads to both resource loss and environmental risks, making valorization increasingly important for the sustainable development of the phosphorus chemical industry. In this study, calcareous–magnesian PTs were used as raw materials, and selective hydrothermal leaching with weakly acidic AlCl₃ solution was employed to separate the dolomite phase and directly construct a Ca-Mg-Al precursor solution for layered double hydroxides (LDHs). The LDHs were subsequently synthesized by co-precipitation and evaluated for phosphate removal from wastewater. The results showed that the precipitation pH markedly affected the phase composition and platelet morphology of the LDHs, while appropriate aging conditions further improved their adsorption performance. Under the optimal conditions of pH 12, aging at 40 °C for 2 h, the obtained LDHs exhibited the best phosphate uptake. Adsorption kinetics followed the pseudo-second-order model, and the maximum adsorption capacity calculated from the Langmuir model reached 38.61 mg-P/g. Characterization by XRD, FTIR, TG-DTA, point of zero charge, and XPS indicated that phosphate removal was dominated by surface complexation, accompanied by anion exchange, ionic precipitation, and electrostatic attraction. Full article

Tetracycline-class antibiotics are persistent contaminants in aquatic environments and are difficult to remove by conventional treatment processes. In this study, a recoverable granular MIL-101(Fe)/γ-Al₂O₃ catalyst was prepared through ligand anchoring followed by secondary Fe-MOF growth on spherical γ-Al₂O₃ and applied to catalytic ozonation of tetracycline (TC) under ordinary-bubble and microbubble-assisted operation. Structural characterization supported the formation of Fe-containing MOF domains on the alumina support, accompanied by an increase in BET surface area from 164.28 to 210.05 m² g⁻¹ and enhanced Lewis-acid-related pyridine-IR signals. Under conventional bubbling ozonation, the optimized catalyst achieved 67.93% apparent UV–Vis-based TC removal during an overall 50 min run consisting of 30 min dark adsorption followed by 20 min ozonation. In a 12 L microbubble reactor, the catalyst-assisted system reached 93.74% apparent UV–Vis-based TC removal at pH 6 with 100 g catalyst and 6 mg min⁻¹ fed ozone, showing higher apparent removal than ordinary ozonation, microbubble ozonation, and ordinary-bubble catalytic ozonation under the tested configuration. Phosphate-blocking and radical-quenching experiments were consistent with the involvement of Lewis-acid-related sites, hydroxyl radicals, and superoxide-related pathways, but these tests are interpreted as indirect mechanistic evidence. LC-MS analysis suggested possible hydroxylation, demethylation, deamidation, ring opening, and low-molecular-weight product formation. The system also transformed chlortetracycline, oxytetracycline, and doxycycline and reduced COD and TOC in a simulated mixed-antibiotic matrix. Because parent-compound HPLC/LC-MS time-series quantification, ozone utilization/off-gas ozone measurement, bubble-size/kLa analysis, and ICP-based Fe loading/leaching data were not available, the present work is positioned as an apparent catalyst–reactor coupling study rather than a complete catalytic, hydrodynamic, or process-level demonstration. Full article

The wet recovery of spent lithium iron phosphate (LFP) batteries is severely hindered by the low efficiency of copper removal. Here, a new process has been developed using a copper-removing chelating resin with pyridine nitrogen, carboxyl, and hydroxyl groups for the selective separation of copper ions. This copper chelating resin achieved a copper removal efficiency of 96.99% and reduced the residual copper content to below 10 milligrams per liter, significantly outperforming the traditional iron powder method. The adsorption process is highly sensitive to pH, with the highest efficiency at pH 1.75. A concentration of 2.0 moles per liter of H₂SO₄ can achieve a desorption rate of approximately 95%. The adsorption process follows the Langmuir isothermal equation and the pseudo-second-order kinetic model, corresponding to single-layer chelated chemical adsorption. Mechanism studies have confirmed that the synergistic coordination effect of the multifunctional groups helps in the efficient capture of copper ions. This copper chelating resin exhibits excellent stability, reversibility, and reusability, providing a promising method for efficient copper removal and recovery in the wet metallurgical recycling of LFP. Full article

Flotation tailings and metallurgical slags from mining often contain toxic Pb, Cd, and Zn. In this study, we evaluated the in situ immobilization of Pb, Cd, and Zn in a Pb–Zn flotation tailing and a smelting slag by adding representative amendments: phosphate-based (ammonium phosphate, phosphoric acid, glassy fertiliser), cementitious (Portland cement), and iron-based (bog iron ore) materials at 1–10% (w/w). Treated samples underwent EPA-TCLP and pH-dependent leaching tests (pH 3–10), with Pb, Cd, and Zn measured by atomic absorption spectroscopy. The untreated tailing leached hazardous Pb (~60 mg/L) and elevated levels of Cd (~0.7 mg/L) and Zn (~53 mg/L), whereas the untreated slag leached negligible metal concentrations. All amendments reduced metal release in a dose-dependent manner. Phosphate amendments were most effective (e.g., 10% H₃PO₄ cut tailing Pb by 80%, Cd by 60%, and Zn by 30%), while cement and iron additions had much weaker effects. Solid-phase XRD and SEM-EDS analyses indicated the formation of stable calcium–phosphate minerals on sulfide surfaces after phosphate treatment. These findings suggest that low-cost phosphate additives (~5–10%) can substantially immobilize Pb, Cd, and Zn in such wastes. However, under strongly acidic conditions (pH < 3), some remobilization occurred, highlighting the need for further validation. This work provides practical guidance for waste managers on selecting in situ stabilization strategies for Pb–Zn mine wastes. Full article

Green roofs offer significant potential for urban stormwater management, yet their capacity to improve runoff water quality is constrained by the limited pollutant retention of conventional substrates and inherent nutrient leaching risks. This critical review synthesizes recent advances in substrate engineering and phytoremediation to establish an integrated framework for transforming green roofs into active bio-filtration systems. Our analysis reveals that amending conventional substrates with waste-derived biosorbents substantially enhances heavy metal and nutrient retention through complementary mechanisms of surface complexation, ion exchange, and microprecipitation. When strategically coupled with hyperaccumulator plant species and rhizospheric microbial communities, these amended substrates significantly reduce contaminant loads in urban runoff while maintaining hydraulic functionality. We critically evaluate standard growing media versus substrates amended with targeted biosorbents: biochar, which enhances heavy metal retention and hydraulic conductivity via surface complexation; seaweed biomass, which provides superior water retention and cation exchange while reducing synthetic fertilizer dependence; and chitin-rich crab shell waste, which promotes microprecipitation of metals and phosphates while valorizing marine waste. The novelty resides not in the materials themselves, but in their synergistic combination and the systematic comparative analysis of their retention mechanisms under green roof hydrological conditions. This review further identifies critical engineering trade-offs, including biosorbent-induced hydraulic conductivity reductions and long-term adsorption site saturation, and provides actionable design thresholds for amendment dosing, substrate depth, and species selection. Ultimately, this work establishes a mechanistic and practical roadmap for next-generation green roofs that simultaneously optimize stormwater retention, runoff quality, and circular economy valorization, highlighting priority research directions for long-term field validation and climate-adaptive standardization. Full article

The accelerated deployment of hydrogen technologies is widely discussed as a pathway to mitigate climate change and reduce environmental pollution associated with fossil fuel use. In this context, intermediate-temperature proton-exchange membranes that operate in the 120–200 °C window, similar to the one characterizing liquid-acid PAFC systems (much larger in their power range), are sought as a bridge between low-temperature PFSA-based PEMFCs and low-temperature PCFs, thus combining reduced sensitivity to external humidification with solid-electrolyte handling. This Part I review surveys phosphate- and silicate-based glassy proton conductors as single-anion baseline matrices and organizes the literature around a mechanistic screening framework that links processing fingerprints—particularly sol–gel hydrolysis/condensation conditions, aging, drying, and thermal treatment—to pore architecture, hydration state, and the dominant proton-transport regime. Across both families, conductivity is governed by coupled variables: network chemistry (acidic site density and connectivity), water activity (RH), and microstructure-controlled percolation and retention. Reported σ values can arise from fundamentally different regimes, ranging from hopping-dominated transport supported by dense hydrogen-bond networks and proton-bearing groups to carrier-assisted, water-mediated transport in connected porosity, with distinct humidity dependence and stability implications. Accordingly, the review treats σ(T,RH) and activation energy together with hydration/porosity indicators as primary screening metrics, and it records missing durability and device-level information—chemical stability (hydrolysis and leaching/acid migration), mechanical robustness and cycling response, and current/power density where available—as explicit knowledge gaps. While substantial progress has been achieved within single-anion phosphate and silicate glasses, particularly through engineered acidity and microstructural control, most systems remain limited by hydration drift under gradients, thermal/humidity cycling stability, and electrode/electrolyte interfacial constraints when evaluated against intermediate-temperature membrane requirements. These conclusions establish a quantitative baseline and comparison rules for Part II, which will assess mixed-network, composite, and hybrid strategies designed to decouple conductivity from water-retention and durability trade-offs. Full article

This study investigates the leaching behavior of the LiNi_0.65Co_0.25Mn_0.10O₂ cathode material in a phosphoric acid medium, with metallic copper recycled from spent battery components serving as a reducing agent. The aim was to develop an efficient approach for the recovery of Li, Ni, Co, and Mn while providing a mechanistic understanding. Leaching experiments were performed by varying key parameters, including copper addition, acid concentration (0.2–0.8 mol·L⁻¹), cathode mass (0.2–1.0 g), stirring rate (0–600 rpm), and temperature (35–80 °C). Thermodynamic analysis, supported by Pourbaix and species distribution diagrams, was used to interpret metal behavior. The results show that lithium is readily dissolved, whereas the extraction of Ni, Co, and Mn depends on the presence of copper, which enables their reduction and dissolution. Optimal conditions (0.4 mol·L⁻¹ H₃PO₄, 0.2 g Cu, 600 rpm, 80 °C) enabled rapid extraction, exceeding 90% within 30 min, while near-complete extraction (~100%, 99%, 99%, and 97% for Li, Ni, Co, and Mn) was achieved after 60 min. Structural analysis revealed a transformation from the layered structure to spinel-like intermediates, followed by their dissolution and formation of copper phosphate phases. The proposed system represents an efficient approach for the sustainable recycling of NMC cathodes. Full article

To promote the resource recovery of phosphate mine tailings and alleviate the pressure caused by the growing scarcity of river sand, this study employs a research methodology combining macroscopic performance analysis with microscopic testing to systematically investigate the effects of three types of recycled sand containing varying proportions of phosphate mine tailings (flint (FS), phosphorite flint (PFS) and dolomitic limestone (DLS)) on the performance of mortar. The study focused on assessing the impact of recycled sand on the workability of mortar, water absorption, mechanical properties, pore structure, cement hydration characteristics, and environmental safety, and conducted a comprehensive evaluation of the project’s feasibility in conjunction with a cost analysis. The effect of DLS was most pronounced in terms of setting time. Water absorption tests show that when the proportions of FS, PFS, and DLS are all 25%, the mortar’s water absorption reaches its minimum value. In terms of mechanical properties, DLS showed a more pronounced increase in early-stage flexural strength, whilst PFS and FS demonstrated a more significant increase in later-stage strength. In terms of compressive strength improvement, PFS outperformed both FS and DLS. XRD and TG-DTA test results show that the three kinds of recycled sand have no adverse effect on cement hydration. SEM and MIP results confirmed that compared with river sand, the porosity of mortar mixed with FS was smaller and the pore structure was denser. Environmental safety assessments have shown that the heavy metal leaching concentrations in the mortar made from the three types of recycled sand are all significantly below the national limits, indicating good environmental compatibility. An economic analysis indicates that the “25% river sand + 75% FS” alternative offers the best economic benefits, resulting in cost savings of 93.27 CNY per cubic metre. In summary, the use of recycled sand derived from phosphate ore tailings as a substitute for river sand in the preparation of mortar is feasible from technical, environmental, and economic perspectives. This approach facilitates the recovery of solid waste resources, conserves natural resources, reduces the environmental burden, and promotes cost optimisation. Full article

Soil and water contamination with high nutrient concentrations from swine farms poses a risk to human and animal health. This study investigated the effects of biochar derived from young aromatic coconut husk (CH), coconut shell (CS), and their mixture (CHCS) on nutrient retention in biochar-amended soil columns for variable synthetic swine wastewater (SW) loading based on water use for piglets and fattening stalls. A 0.9 L leaching test column contained 3 g of each biochar type mixed with 300 g of soil. It was loaded daily with synthetic SW for 42 days at loading rates of 30 mL/day (piglet SW) and 60 mL/day (fattening SW). CH-amended soil was then selected to investigate the effect of rainfall rates at 0 (R0), 25 (R25), 70 (R70) and 140 (R140) mL/4 days on soil nutrient retention. Leachate was collected every 7 days to analyze nitrogen and phosphorus concentrations. The results showed that CH-amended soil had the highest retention of total nitrogen (TN) and phosphate among all treatments. For piglet SW, TN retention in CH-amended soil was 1.4–1.6 times higher than with CS and CHCS treatments, probably due to enhanced ammonium retention on exchangeable sites associated with the high cation exchange capacity of CH. High phosphate retention in CH-amended soil was linked to Ca²⁺ release from CH, facilitating phosphate precipitation. Moreover, CH-amended soil at R25 showed the highest ammonium retention but inhibited seed germination. Overall, CH-amended soil effectively retained nutrients and was suitable as a seedling growth medium, except under the R25 rainfall condition. Full article

This paper presents an analysis of the physicochemical and biological properties of the developed composite zinc phosphate cement modified with bismuth oxide and phosphorus slag additives. The powder phase was synthesized by sintering a frit with an optimal composition (ZnO, MgO, SiO₂, Bi₂O₃) using phosphorus slag as the active component. The study included an assessment of the microstructure, chemical resistance in aggressive environments (5% NaCl solution, 10% lactic acid, carbonated water), solubility in artificial saliva, and cytotoxicity in human fibroblasts. The addition of phosphorus slag was found to promote the formation of low-melting eutectics, which reduces the sintering temperature by 100 °C and increases the material’s whiteness to 97.8%. X-ray diffraction analysis confirmed the presence of zincite, quartz, and periclase phases, forming a dense microstructure without pronounced pores or cracks. The experimental cement demonstrated high acid resistance: the maximum weight loss in lactic acid was 8%, while the leaching of toxic elements (Pb, As, Cr, etc.) remained extremely low (10–67 ppm), confirming the material’s environmental safety. Testing of the composite zinc phosphate cement in artificial saliva revealed minimal weight loss compared to similar products. Biological testing showed that the cement’s cytotoxicity is dose-dependent; at a 0.3 g dose and a 1:4 dilution, the material loses its toxic properties and becomes safe for living tissue. The developed zinc phosphate composite cement composition offers improved aesthetic and mechanical properties, high chemical stability, and biocompatibility at working concentrations, making it promising for use in clinical dentistry. Full article

This study presents a comprehensive investigation of OPE residues, distribution patterns, and dietary exposure risks in crustaceans from southeast China. OPEs were detected in over 90% of samples, with mean total concentrations (ΣOPEs) of 5.80 μg/kg wet weight (ww) in freshwater shrimp, 6.52 μg/kg ww in marine prawn, and 1.25 μg/kg ww in marine crab. Tributyl phosphate (TiBP), triethyl phosphate (TEP), and tris(2-chloroethyl) phosphate (TCEP) emerged as the dominant congeners, accounting for 68.1% of ΣOPEs, which indicates inputs from industrial emissions, plastic waste leaching, and aquaculture equipment. Spatial analysis revealed striking regional differences: coastal industrial cities (Zhoushan, Taizhou) exhibited ΣOPE levels up to 12-fold higher than inland mountainous areas (Quzhou, Lishui), while no significant temporal variations were observed. Human health risk evaluation, based on estimated daily intake (EDI) and target hazard quotient (THQ), demonstrated negligible non-carcinogenic risks for the general population (HI < 1), though children and frequent seafood consumers have slightly elevated exposure. These findings indicate the value of crustaceans as bioindicators for OPE contamination and require long-term monitoring of emerging OPEs and their synergistic effects with co-occurring pollutants. Full article

The efficient recovery of rare earth elements from associated rare-earth-bearing phosphate ores is of paramount importance for expanding the supply of rare earth resources. In contrast to conventional studies that focus on extracting rare earths either from phosphate concentrates or from phosphogypsum generated during the sulfuric acid wet-process, this study takes as its subject the rare-earth-enriched residue—an intermediate product obtained after the selective leaching of phosphorus via the hydrochloric acid route—from a rare-earth-bearing phosphate ore in Zhijin, Guizhou Province. The occurrence states, leaching behavior, and kinetic mechanisms of rare earth elements within this residue were systematically elucidated. Analyses using scanning electron microscopy coupled with energy-dispersive spectroscopy (SEM–EDS) and aberration-corrected scanning transmission electron microscopy (STEM) reveal that rare earth elements are hosted in residual fluorapatite and newly formed CaF₂ through isomorphic substitution. The substitution of REE³⁺ for Ca²⁺ induces lattice contraction in CaF₂, with the interplanar spacing decreasing from 0.27 nm to 0.26 nm. Through single-factor experiments and response surface methodology (RSM) optimization, the optimal leaching conditions were determined to be a temperature of 80 °C, a leaching time of 120 min, a hydrochloric acid dosage of 160% of the theoretical requirement, a solid–liquid ratio of 1:6, and a agitation speed of 500 r·min⁻¹. Under these conditions, the leaching efficiency of rare earth elements reached as high as 92.69%. Kinetic analysis indicates that the leaching process follows the shrinking-core model, with the rate controlled by diffusion through the solid product layer. The apparent activation energy was calculated to be 37.2 kJ·mol⁻¹, characteristic of a diffusion-controlled process. Furthermore, response surface analysis of variance confirms that leaching temperature and time are the most significant factors influencing rare earth leaching. This study elucidates, from multiple perspectives, the leaching mechanism of rare earth elements from enriched residues within a hydrochloric acid system, thereby providing important theoretical support for the efficient recovery and process optimization of rare earth resources from associated phosphate ores. Full article