Search Results (569)

Chitosan (CS) was employed to modify coconut shell activated carbon (CAC) to fabricate a composite adsorbent for wastewater treatment. By integrating the functional groups of CS with the high specific surface area of CAC through chemical modification, the resulting CS-AC composite exhibited significantly enhanced adsorption performance toward hexavalent chromium (Cr(VI)) in aqueous solutions. The effects of key parameters, including adsorbent dosage, initial Cr(VI) concentration, contact time, temperature, and solution pH on the adsorption efficiency were systematically investigated. Under optimal conditions, the CS-AC composite achieved a Cr(VI) removal efficiency of up to 99.04%. Kinetic and isotherm modeling revealed that the adsorption process followed the pseudo-second-order kinetic model and was well described by the Langmuir isotherm. Regeneration studies conducted over five consecutive adsorption-desorption cycles demonstrated that the composite retained a high removal efficiency of 98.10%, indicating excellent reusability. These findings suggest that the CS-AC composite is a promising and effective adsorbent for the removal of Cr(VI) from contaminated water. Full article

The discharge of metal-complex dyes from textile industries poses significant environmental challenges due to their chemical stability and resistance to conventional biological treatment. This study examined the degradation of Acid Black 194 (AB–194), a 1:2 chromium-complex azo dye, using Co²⁺-activated peroxymonosulfate (PMS). A central composite design based on response surface methodology was used to evaluate the effects of Co²⁺ (5.93–20.07 µM), PMS (1.67–7.33 mM), and dye (13.79–56.21 mg L⁻¹) concentrations on decolorization and mineralization. The polynomial models demonstrated strong predictive accuracy (R² > 0.9896), identifying Co²⁺ and dye concentrations as the most influential factors. Under optimal conditions (18.0 µM Co²⁺, 6.5 mM PMS, 20.0 mg L⁻¹ dye), 99.19% decolorization was achieved at 30 min and 41.43% TOC removal at 240 min. Degradation kinetics were described by a mechanistic model incorporating 15 elementary reactions that comprise the Co²⁺/Co³⁺ redox cycle, radical generation, and dye oxidation, yielding a global R² of 0.9617. Estimated rate constants for dye oxidation (k₁₄ = 3.52 × 10⁹ M^–1 s^–1 for and k₁₅ = 2.00 × 10¹⁰ M^–1 s^–1 ) were consistent with values reported for aromatic compounds in sulfate radical systems. Radical contribution analysis confirmed sulfate radicals as the principal oxidizing species, accounting for 96.75% of the overall process. Full article

Heavy metal pollution remains a major global environmental challenge due to persistent ecological risks and potential threats to food safety. Microbial remediation and phytoremediation represent sustainable alternatives to conventional treatments; however, their effectiveness is strongly influenced by number of factors including nutrient availability. This review critically examines how nutritional regulation governs microbial metabolism, plant physiological responses, and rhizosphere interactions to enhance heavy metal transformation and removal. Metal bioavailability depends on type, concentration, soil pH, redox potential, and microbial processes. Interventions including fertilizers, chelating agents, inoculation with arbuscular mycorrhizal fungi and plant-growth-promoting rhizobacteria enhance phytoremediation processes through regulating plant nutrient and heavy metal uptake, while selection between ammonium/nitrate changes rhizosphere pH consequently affects plant metal uptake. Similarly, nutrients, i.e., phosphate, iron, zinc and manganese competitively affect metal uptake. Organic amendments enhance phytostabilization, especially for selenium and mercury, while enhancing chromium reduction. Sulfur-reducing bacteria precipitate metals as insoluble sulfides with 90% efficiency. In addition, soil amendments including plant-growth-promoting rhizobacteria, arbuscular mycorrhizal fungi, and metal-chelating agents can be strategically used to enhance the phytoextraction from metal from contaminated soils. We suggest that the future integration of modern approaches such as multi-omics and cisgenesis supported by artificial intelligence tools can help to accurately predict the efficiency of nutrient regulation strategies and their remediation outcomes, thereby supporting evidence-based soil management. Full article

Porous glycidyl methacrylate-based copolymers crosslinked with ethylene glycol dimethacrylate (EGDMA) and trimethylolpropane trimethacrylate (TMPTMA) were synthesized via suspension–emulsion polymerization and subsequently functionalized with triethylenetetramine. The effect of the monomer composition on the epoxy group content and porous structure was systematically investigated by varying the GMA-to-crosslinker molar ratio from 1:1 to 5:1. Increasing the GMA fraction enhanced the epoxy group content (2.8–5.0 mmol/g) but significantly reduced the specific surface area (333–23 m²/g), indicating a trade-off between functionality and porosity. ATR-FTIR and elemental analysis confirmed successful amine functionalization while preserving a considerable degree of porosity. The modified copolymers were evaluated for Cr(VI) removal, showing strong pH dependence, with maximum efficiency at pH 3 due to electrostatic interactions between protonated amine groups and HCrO₄⁻ ions. Equilibrium studies revealed saturation-type behavior, with a maximum sorption capacity of 165.47 mg/g for TMPTMA-based copolymers. Despite the higher nitrogen content in EGDMA-based materials, TMPTMA-crosslinked copolymers exhibited a superior adsorption performance, demonstrating that pore accessibility, rather than functional group density alone, governs adsorption efficiency. These findings provide insight into the rational design of amine-functionalized porous polymer sorbents for efficient chromium(VI) removal. Full article

Coagulation-based technologies are increasingly recognized as key for controlling fluoride and hexavalent chromium in urban water and wastewater. Combined geogenic and industrial sources often drive chronic exposure and create an underrecognized public health burden. This review synthesizes current knowledge on the occurrence, speciation, and toxicology of F⁻ and Cr(VI) in urban systems, links regulatory targets to health outcomes, and critically examines conventional, advanced, and electrochemical coagulation processes for their removal under realistic water-quality conditions. Mechanistic sections describe how aluminum-, iron-, magnesium- and zirconium-based coagulants, including pre-polymerized and composite formulations (e.g., IPC-type coagulants, PSiFAC-Mg, ZrCl₄), remove fluoride via Al–F complexation, Al–F–OH co-precipitation, ion exchange, and sweep flocculation, while Cr(VI) control relies on Fe(II)-mediated reduction to Cr(III), followed by adsorption and co-precipitation with metal hydroxides. The review assesses how water chemistry and operating conditions affect single- and multi-contaminant removal, highlighting competition among fluoride, Cr(VI), nutrients, and other oxyanions. Performance data from bench-, pilot-, and selected full-scale studies show that optimized coagulation and electrocoagulation can substantially reduce fluoride and Cr(VI) (to drinking-water-relevant levels) in diverse urban waters, but also reveal persistent issues of sludge generation and stability, residual metals, process robustness, and cost. The review identifies priorities, including long-term urban-scale assessments, low-toxicity green coagulants, life-cycle and health impact assessments, and real-time coagulation control for fluoride and Cr(VI). Full article

Hydrothermally treated chitosan/polyvinyl alcohol beads (H-CS/PVA) were used as filler material in a fixed-bed column for continuous Cr (VI) removal. The effects of main operational parameters, namely bed height, initial concentration and flow rate, were evaluated in the respective ranges of 2–6 cm, 20–60 mg/L and 2.5–7.5 mL/min. Maximum removal efficiency and adsorption capacity were calculated as 64.2% and 15.53 mg/g, respectively. The corresponding breakthrough curves were analyzed by Yoon–Nelson, Adams–Bohart, Thomas and BDST (Bed Depth–Service Time) models, out of which the highest consistency was achieved with the Yoon–Nelson model for all studied conditions. The adsorbent maintained strong reusability, showing minimal loss (~2.5%) in desorption efficiency across three successive regeneration cycles with 0.1 M NaOH as the eluent. SEM and SEM–EDX analyses confirmed the presence of chromium on the H-CS/PVA surface at an elemental fraction of 1.03% (w.). Furthermore, FTIR and XPS analyses verified the role of amine and hydroxyl functionalities in the complexation and adsorption of Cr (VI). Overall, a column system operated under optimal conditions (H_bed: 6 cm, C₀: 40 mg/L, and column diameter: 2.5 cm) and regenerated three times can efficiently treat 20 L of Cr (VI)-contaminated wastewater, resulting in an associated environmental impact of 0.896 kg CO₂-eq. Full article

Soil contamination by heavy metals is a significant sustainability and ecological issue, impacting on the health of ecosystems and groundwater. This study assessed the efficacy of malic acid as a biodegradable and environmentally benign agent for the remediation of soils contaminated with cadmium, chromium, copper, and zinc. Two soils with contrasting textures were treated with a 10% malic acid solution at solid/liquid ratios of 1:5 and 1:10 for contact times of 2, 4, 6, and 8 h. The extraction efficiency varied depending on metal type, soil texture, and washing conditions. Cadmium removal ranged from 26% to 55%, zinc removal ranged from 10% to 25%, while copper showed variable extraction (5–45%) depending on initial soil concentration. Chromium exhibited the highest removal efficiency (30–90%), quantified as total chromium; however, the absence of speciation analysis (Cr(III)/Cr(VI)) represents a key limitation and may affect the interpretation of the removal performance. FTIR and UV–Vis analyses confirmed the formation of metal–carboxylate complexes and changes in soil functional groups during the washing process. In addition, significant mobilization of nitrogen and potassium was observed, whereas phosphorus remained relatively stable. The results highlight the influence of soil texture and multi-metal interactions on malic acid washing efficiency and provide a laboratory-scale environmental assessment of malic acid as a sustainable remediation alternative for soil remediation, while emphasizing the need for further evaluation regarding chromium speciation and post-treatment soil quality and sustainability impacts. Full article

This study investigates the synthesis and kinetic behavior of a magnetic biochar derived from avocado seed biomass for the removal of hexavalent chromium (Cr(VI)) from aqueous solutions. Magnetite (Fe₃O₄) was synthesized through different routes, including nitrogen-assisted coprecipitation, redox-controlled coprecipitation, polyol, sol–gel, and sonochemical methods, to evaluate their structural properties and iron incorporation efficiency. Based on compositional and crystallographic analyses, the coprecipitation under an inert atmosphere exhibited improved phase purity and higher Fe₃O₄ content, which was selected for in situ incorporation onto biochar produced by pyrolysis at 450 °C. The resulting magnetic material and composite were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDS), confirming the suitability of the synthesis method and the successful deposition of magnetite onto the porous carbon matrix while preserving its structural integrity. Batch adsorption experiments were conducted at pH 2.0 to evaluate the effect of adsorbent dose and initial Cr(VI) concentration. The adsorption process reached equilibrium within 120 min and was better described by the pseudo-second-order kinetic model (R² ≥ 0.98), suggesting that chemisorption governs the rate-controlling step, with diffusion phenomena contributing but not dominating the overall mechanism. The maximum adsorption capacity predicted by the kinetic model reached 42.49 mg g⁻¹ at an initial concentration of 100 mg L⁻¹. The results demonstrate that avocado-seed-derived magnetic biochar represents a sustainable and effective material for chromium-contaminated water treatment, integrating agro-industrial waste valorization with enhanced adsorption performance and magnetic separability. Full article

The textile industry consumes a significant quantity of water and produces effluent containing water-soluble dyes and heavy metals such as Lead (Pb), Cadmium (Cd), Chromium (Cr), Copper (Cu), and Zinc (Zn), among others. Heavy metal contamination of water bodies and their impact on aquatic life, as well as on human health, is of prime importance. This review examined the potential of phytoremediation, a low-cost and eco-friendly process for removing contaminants from textile effluent. This review also investigated the impact of heavy metal toxicity on aquatic plants used for biogas production post phytoremediation application. This review evaluated textile effluent characteristics, efficiency evaluation of phytoremediation of textile wastewater, metal uptake mechanisms of aquatic plants, and anaerobic digestion processes with emphasis on Water hyacinth (Eichhornia crassipes), Duckweed (Lemna minor), and Water lettuce (Pistia stratiotes). The findings indicated that these aquatic plants possess immense potential for removing heavy metals and other impurities by employing phytoextraction and rhizofiltration methods. Their rapid growth rate makes them preferred candidates for anaerobic digestion. However, accumulation of heavy metals in plant tissues inhibits microbial activities during anaerobic digestion, resulting in fluctuations in biogas and methane production. Findings also showed that these aquatic plants are efficient in the removal of heavy metals in water while yielding considerable biomass that can be used to produce bioenergy through anaerobic digestion. However, the sequestration of heavy metals in plant biomass may affect the rate of methane generation efficiency. The findings of this review suggest that phytoremediation has promising potential for the recycling of textile wastewater and, when coupled with biogas production, contributes towards a circular bioeconomy, an approach that integrates closed-loop resource utilization with renewable biological systems to minimize waste. Full article

Aligned CS/Rx aerogels were fabricated by inducing non-directional ice growth (freeze-molding) followed by low-temperature curing, resulting in monoliths with interconnected channels, a high void fraction, and moldability. The swelling index (S%) was calculated to be 1029, the apparent density 0.496 g·cm⁻³, and the estimated porosity 90% based on micrographic analysis. Aerogels have mechanical behavior Shore A hardness greater than 25. Batch metal removal tests were performed (10 mL, 100 mg·L⁻¹ Cr(VI), 0.19 g adsorbent, 24 h, and pH 5–5.5), and the material achieved 95% metal removal. Additional kinetic and isothermal results were obtained using CS85R15 on a packed column (20 to 140 mg·L⁻¹, 1000 mL Cr(VI), 0.80 g adsorbent, 24 h, and pH 5–5.5). Equilibrium data were consistent with a heterogeneous surface hosting a specific site, as reflected in the joint Freundlich/Langmuir fit (q_max 100.8 mg·g⁻¹ for Langmuir). This confirmed the preservation of chitosan functionalities (–OH/–NH) after processing, while XPS detected chromium on the surface with signals consistent with the partial reduction of Cr(VI) to Cr(III) on the aerogel surface. This highlights the relevance of adsorption-based technologies for water remediation, where high-porosity and low-density materials allow for short diffusion pathways and capture electrostatics by protonated amines and redox conversion of hazardous substances. The soft-cure freeze-molding technique is simple, scalable, and compatible with packed-bed/column operation, providing a material platform for tailoring the microstructure (sheets and channels) and surface chemistry to regenerable sorbents for industrial wastewater treatment. Full article

Heavy metal contamination of drinking water remains a persistent global challenge, exacerbated by salinity, industrial discharge, and the limitations of existing membrane technologies that are constrained by permeability–selectivity trade-offs. In this study, we develop a hybrid thin film nanocomposite (TFN) forward osmosis (FO) membrane by incorporating a zirconium-based metal–organic framework (UiO-66) and its conductive polymer-functionalized analogue (PANI@UiO-66) into the polyamide active layer via interfacial polymerization. The incorporation of UiO-66 enhances water transport through the introduction of hydrophilic microporous domains, while the polyaniline coating modulates nanoscale transport pathways and interfacial interactions. Systematic variation in filler type and loading reveals distinct functional roles of the two fillers. Membranes incorporating bare UiO-66 exhibit increased water flux, attributed to facilitated transport through MOF-derived nanochannels, but show a moderate increase in reverse solute flux. In contrast, PANI@UiO-66 incorporation results in reduced water flux but significantly suppresses reverse solute flux and enhances chromium rejection, indicating improved control over selective transport. At an optimal loading of 0.15 wt% (TFN-PU3), the membrane demonstrates an improved balance between water permeability and solute selectivity compared to the pristine thin film composite (TFC) membrane under FO conditions. The observed performance is attributed to the combined effects of modified transport pathways and interfacial interactions introduced by the hybrid filler system. The results highlight the potential of conductive polymer–MOF hybridization as a strategy for tuning membrane performance. This work provides a practical framework for designing TFN membranes for selective heavy-metal removal in saline and complex water environments. Full article

Selective laser melting (SLM) is an additive manufacturing method based on powder bed fusion that has gained prominence in prosthodontics for its capability to create intricate, patient-specific metal restorations with precision and consistency. SLM has become an important part of digital dental workflows, allowing for the direct creation of dental frameworks from computer-aided design (CAD), offering advantages over traditional casting and subtractive milling techniques. This review outlines the fundamentals of SLM, the dental alloys commonly employed, and the microstructural characteristics that affect mechanical properties, corrosion resistance, and biocompatibility. It explores current uses in removable partial denture frameworks, fixed dental prostheses, metal–ceramic restorations, implant-supported prosthetics, and maxillofacial rehabilitation. Alloys based on cobalt–chromium and titanium produced through SLM exhibit strong mechanical properties, fatigue resistance, and biological compatibility when suitable post-processing is conducted. Despite these advantages, issues such as surface roughness, porosity, anisotropy, powder handling, and high costs remain, and there is a lack of extensive long-term clinical data. Ongoing process refinement and clinical validation are crucial for the wider integration of SLM into standard prosthodontic practice. Full article

Objectives: This study aimed to compare the retention and fit precision of removable partial denture circumferential clasps fabricated from cast cobalt–chromium, 3D-printed cobalt–chromium, and polyether ether ketone. Methods: A maxillary right first premolar abutment was prepared. Eighty circumferential clasps were allocated into three material groups: cast Co–Cr (n = 20), 3D-printed Co–Cr (n = 20), and PEEK (n = 40). The terminal third of metal retentive clasps was designed to engage 0.25 mm and 0.50 mm undercuts. PEEK clasps were fabricated with two designs: partial (two-thirds) and full-arm undercut engagement. Each group was examined for retentive forces after 1440 cycles (simulating 1 year). Initial and final retentive forces were recorded. Clasp deformation was assessed by measuring inter-arm distance before and after cycling using digital photography and ImageJ software. Results: All clasp groups demonstrated a statistically significant reduction in retention after 1440 cycles (p < 0.05). At both undercut depths, cast and 3D-printed Co–Cr clasps exhibited significantly higher retentive forces than PEEK (p < 0.001). Within the PEEK group, full-arm engagement showed significantly higher retention than partial engagement at the 0.25 mm undercut (p < 0.001), whereas no significant difference was observed between designs at the 0.50 mm undercut (p = 0.406). Fit precision revealed a significant increase in inter-arm distance after cycling (p < 0.05). PEEK clasps exhibited significantly smaller dimensional changes than Co–Cr clasps (p < 0.02). Conclusions: Clasp material, undercut depth, and design significantly influenced retention and fit precision. Co–Cr clasps maintained higher retentive forces, whereas PEEK clasps demonstrated reduced deformation after cycling. Full article

Heavy metal contamination of freshwater systems represents a persistent environmental challenge due to metal toxicity, non-biodegradability, and bioaccumulation potential. This study compared the phytoremediation performance of Eichhornia crassipes, Pistia stratiotes, and Chrysopogon zizanioides for the removal of chromium (Cr), copper (Cu), cadmium (Cd), and lead (Pb) from contaminated water under controlled conditions. Plants were exposed to aqueous solutions containing 5 mg L⁻¹ of the four metals for 45 days. Metal concentrations in roots and shoots were determined by wavelength-dispersive X-ray fluorescence, translocation factor (TF), bioconcentration factor (BCF), and removal efficiency (RE) were calculated. TF values (0.02–2.90) varied across species, metals, and experimental conditions, indicating a general tendency for metal retention in roots, although translocation to shoots occurred in several cases. BCF values (0.04–87.55) were significantly influenced by species, exposure time, and treatment (p < 0.05), with P. stratiotes showing higher accumulation under specific conditions (Cu = 87.55; Pb = 44.56). In contrast, RE showed high variability (−616.21 to 72.72%) and no significant differences among experimental factors. Overall, the results demonstrate context-dependent variation in metal uptake and translocation, highlighting the potential of aquatic macrophytes as low-cost alternatives for the treatment of metal-contaminated wastewater systems. Full article

Ion-imprinting technology based on biosorbents via sorption demonstrates potential for the selective removal of metal ions from water and wastewater. This offers both high sorption capacity and selectivity for specific metals. Current research trends are toward the development of sorbents with minimal environmental impact. Among the most rapidly evolving classes of sorbents are those derived from biopolymers, such as chitosan—a natural derivative of chitin that can be readily functionalized. Due to the growing interest in this topic, it is necessary to summarize the current knowledge. In this article, we provide a comprehensive overview of the latest advances in ion-imprinted chitosan-based materials designed for the purification of metal-contaminated aqueous systems. We conduct a bibliographic analysis and describe a variety of chitosan-based materials exhibiting selectivity toward heavy metals, including chromium Cr(III/VI), cobalt Co(II), nickel Ni(II), copper Cu(II), zinc Zn(II), arsenic As(III/V), cadmium Cd(II), mercury Hg(II), and lead Pb(II). Finally, we discuss future prospects and highlight current research gaps, aiming to guide further scientific exploration and innovation in this promising field. Full article