Search Results (171)

Polypyrrole, which belongs to the conducting polymer family, has demonstrated profound potential in advanced water purification applications due to its inherent electrical conductivity, environmental stability, and tunable surface chemistry. As a sorbent, PPy exhibits high sorption capacity for aquatic contaminants, including heavy metals, pharmaceutical compounds, and their metabolites, as well as synthetic dyes. The removal efficiency is correlated to a complex interaction mechanism involving electrostatic attractions, redox activity, and π–π stacking. Recent advances have expanded the utility by further developing nanostructured PPy-based (nano)composites, which elevate sorption performance by increasing surface area, mechanical integrity, and selective affinity. In addition, its integration into membrane technologies has enabled the design of an effective filtration system with improved selectivity and regeneration capabilities. Moreover, PPy is effective in electrochemical processes of water treatment, including capacitive deionization and electrochemically assisted sorption, opening novel paths towards energy-efficient pollutant removal. The multifunctionality of PPy as a sorbent material highlights its value as an important material for water treatment, with the capability of extended modification tailored for emerging environmental needs revised in this work. Full article

Nitrate (NO₃⁻) and cadmium (Cd²⁺) are common water pollutants with distinct chemical behaviors, often requiring different removal strategies. This study presents a low-cost synthesis of carbonated hydroxyapatite nanopowder (cHA), Ca₅(PO₄)_3-y(CO₃)_y(OH) (y = 0.13–0.17), using eggshell waste as a calcium precursor, aimed at removing both NO₃⁻ and Cd²⁺ from wastewater. SEM and TEM analyses revealed a porous nanostructure with an average particle size of 13.53 ± 6.43 nm and a specific surface area of 7.568 m²/g. Adsorption experiments were conducted under varying conditions, including contact time (0.3–3 h), dosage (0.3–2 g/L), initial concentrations (10–100 mg/L for NO₃⁻; 5–15 mg/L for Cd²⁺), and temperature (22 and 50 ± 2 °C). Cd²⁺ removal reached up to 99% at pH 2–4.5, while NO₃⁻ removal peaked at 38% in competitive systems, within 30 min. In single-ion systems, maximum nitrate uptake was 19.14 mg/g at 50 °C. Characterization using FT-IR, EDS, and XRD (with Rietveld refinement) confirmed carbonate B-type substitution and structural changes due to ion exchange and chemisorption. The results demonstrate that cHA derived from food waste is an efficient and sustainable sorbent, particularly for cadmium removal in contaminated water. Full article

Carbonaceous sorbents were prepared from Chlorella vulgaris via hydrothermal carbonization (200 °C and 250 °C) and slow pyrolysis (300–500 °C) to assess their effectiveness in removing the herbicide metribuzin from water. The biomass was cultivated under controlled laboratory conditions, allowing for consistent feedstock quality and traceability throughout processing. Using a single microalgal feedstock for both thermal methods enabled a direct comparison of hydrochar and pyrochar properties and performance, eliminating variability associated with different feedstocks and allowing for a clearer assessment of the influence of thermal conversion pathways. While previous studies have examined algae-derived biochars for heavy metal adsorption, comprehensive comparisons targeting organic micropollutants, such as metribuzin, remain scarce. Moreover, few works have combined kinetic and isotherm modeling to evaluate the underlying adsorption mechanisms of both hydrochars and pyrochars produced from the same algal biomass. Therefore, the materials investigated in the present work were characterized using a combination of standard physicochemical and structural techniques (FTIR, SEM, BET, pH, ash content, and TOC). The kinetics of sorption were also studied. The results show better agreement with the pseudo-second-order model, consistent with chemisorption, except for the hydrochar produced at 250 °C, where physisorption provided a more accurate fit. Freundlich isotherms better described the equilibrium data, indicating heterogeneous adsorption. The hydrochar obtained at 200 °C reached the highest adsorption capacity, attributed to its intact cell structure and abundance of surface functional groups. The pyrochar produced at 500 °C exhibited the highest surface area (44.3 m²/g) but a lower affinity for metribuzin due to the loss of polar functionalities during pyrolysis. This study presents a novel use of Chlorella vulgaris-derived carbon materials for metribuzin removal without chemical activation, which offers practical benefits, including simplified production, lower costs, and reduced chemical waste. The findings contribute to expanding the applicability of algae-based sorbents in water treatments, particularly where low-cost, energy-efficient materials are needed. This approach also supports the integration of carbon sequestration and wastewater remediation within a circular resource framework. Full article

This study investigates the hydrothermal synthesis of calcium silicate hydrate (C-S-H) from photovoltaic (PV) waste glass and carbide sludge as a strategy for resource recovery and sustainable chromium removal from wastewater. Waste-derived precursors were co-ground, blended at controlled Ca/Si molar ratios (0.8, 1.0, 1.2), and hydrothermally treated at 180 °C for 96 h to yield C-S-H with tunable morphology and crystallinity. Comprehensive characterization using XRD, FT-IR, SEM-EDX, and UV-Vis spectroscopy revealed that a Ca/Si ratio of 1.0 produced a well-ordered tobermorite/xonotlite structure with a high surface area and fibrous network, which is optimal for adsorption. Batch adsorption experiments showed that this material achieved rapid and efficient Cr(III) removal, exceeding 90% uptake within 9 h through a combination of surface complexation, ion exchange (Ca²⁺/Na⁺ ↔ Cr³⁺), and precipitation of CaCrO₄ phases. Morphological and structural evolution during adsorption was confirmed by SEM, FT-IR, and XRD, while EDX mapping established the progressive incorporation of Cr into the C-S-H matrix. These findings highlight the viability of upcycling industrial waste into advanced C-S-H sorbents for heavy metal remediation. Further work is recommended to address sorbent regeneration, long-term stability, and application to other contaminants, providing a foundation for circular approaches in advanced wastewater treatment. Full article

This study investigates the potential of biochars derived from agricultural waste biomass for the removal of heavy metal ions from aqueous solutions. Biochars were produced via slow pyrolysis at 793 K using almond shells (AS), walnut shells (WS), pistachio shells (PS), and rice husks (RH) as feedstocks. The physicochemical properties and adsorption performance of the resulting materials were evaluated with respect to Cd(II), Mn(II), Co(II), Ni(II), Zn(II), total Iron (Fe_tot), total Arsenic (As_tot), and total Chromium (Cr_tot) in model solutions. Surface morphology, porosity, and surface chemistry of the biochars were characterized by scanning electron microscopy (SEM), nitrogen adsorption at 77 K (for specific surface area and pore structure), Fourier-transform infrared spectroscopy (FTIR), and determination of the point of zero charge (pH_pzc). Based on their textural properties, biochars derived from WS, PS, and AS were classified as predominantly microporous, while RH-derived biochar exhibited mesoporous characteristics. The highest Brunauer–Emmett–Teller (S_BET) surface area was recorded for PS biochar, while RH biochar showed the lowest. The pistachio shell biochar exhibited the highest specific surface area (440 m²/g), while the rice husk biochar was predominantly mesoporous. Batch adsorption experiments were conducted at 25 °C, with an adsorbent dose of 3 g/L and a contact time of 24 h. The experiments in multicomponent systems revealed removal efficiencies exceeding 87% for all tested metals, with maximum values reaching 99.9% for Cd(II) and 97.5% for Fe_tot. The study highlights strong correlations between physicochemical properties and sorption performance, demonstrating the suitability of these biochars as low-cost sorbents for complex water treatment applications. Full article

Porphyrins and their derivatives are excellent materials with specific physical and photochemical properties in medical, chemical, and technological applications. In chemistry, their properties are applied to create new functional materials with specific characteristics, such as porphyrin-based sorbents combined with porous organic polymers, silica, carbon nanostructures, or metal–organic frameworks. This review covers the applications of porphyrins and metalloporphyrins in preparing and using sorbents for metal ion enrichment and their separation. Uncommon applications that utilize specific properties of porphyrins, such as light-enhanced processes and redox properties for selective sorption and photocatalytic conversion of metal ions, are also discussed. These applications suggest new fields of use, such as the removal or recycling of metals from electronic waste or the selective elimination of heavy metals from the environment. Full article

This study focuses on the synthesis and characterization of a cationic ion-exchange sorbent derived from vermiculite and epoxy acrylate copolymers, designed to address freshwater scarcity by removing toxic metal ions from aqueous environments. The sorbent was engineered to preserve the chemical integrity of freshwater while adhering to environmental safety standards. Vermiculite served as the base material, modified with glycidyl methacrylate (GMA), acrylonitrile (ACN), and orthophosphoric acid (H₃PO₄) in a mass ratio of 1:0.35:0.15:3. Optimization experiments explored varying H₃PO₄ proportions (two- and threefold increases) to refine the synthesis conditions. The materials underwent microwave irradiation at 300 W for 10 min. Infrared (IR) spectroscopy confirmed the presence of functional groups (P=O, P−O−C), enhancing sorption capacity, while scanning electron microscopy (SEM) revealed a porous structure crucial for adsorption. Sorption properties, assessed via atomic emission spectroscopy, demonstrated capacities of 39.80 mg/g for MoO₄²⁻ and 39.06 mg/g for ReO₄⁻, with extraction efficiencies of 79% and 78%, respectively. Chemical stability tests indicated the sorbent retained up to 90% of its functionality in aggressive environments, highlighting its robustness. The developed sorbent offers a high-performance, cost-effective solution for heavy metal removal from wastewater, advancing sustainable water purification technologies. Full article

This study presents a sustainable approach to recycling exhausted etching solutions through ferritization, using various activation methods and aeration rates. The process transforms industrial waste into valuable magnetic sorbents, supporting circular economy principles. Structural and chemical analysis of the ferritization products revealed the formation of ferromagnetic crystalline phases, including lepidocrocite (ɣ-FeOOH), ferrooxygite (δ-FeOOH), and magnetite (Fe₃O₄). Increasing the aeration rate and use of ultrasound treatment enhances Fe₃O₄ content and iron ion removal efficiency. The adsorption capacity of the recycled materials for Zn²⁺ removal was assessed under different pH conditions using mechanical mixing and ultrasound treatment. The highest level of Zn²⁺ removal (92.0%) was achieved at pH 8 with ultrasound-activated sorbents containing 61.3% δ-FeOOH and 38.7% Fe₃O₄. At pH 10, magnetite-based sorbents achieved over 98.9% Zn²⁺ removal, enabling the treated water’s reuse in industrial rinsing processes. Electron microscopy and X-ray fluorescence confirmed the presence of fine, spherical magnetite and zinc ferrite particles. These findings underscore the potential of ferritization-based recycling as an eco-friendly and efficient strategy for heavy metal removal from galvanic wastewater. Full article

To develop a strategy for sustainable bioremediation of heavy metal-contaminated environments, it is necessary to understand the mechanisms of remediation using microorganisms. A huge bioremediation potential is possessed by fungi. Fusarium culmorum, with their wide range of plant hosts, can be the basis for creating sustainable phytoremediation technologies and for creating sustainable agriculture methods. Exopolymers (EPSs) produced by F. culmorum can be excellent metal sorbents and basic factors in the biosorption mechanism. The sorption capacities of zinc, lead, and cadmium by the EPS of a pathogenic DEMFc37 strain and two non-pathogenic strains (PGPF-DEMFc2 and DRMO-DEMFc5) were compared, and the effects of these metals on EPS synthesis by the three strains was determined. EPS samples were chemically characterised in regards to their sugar, protein, and phenolic compound contents and used to study metal binding. The concentrations of metals bound/adsorbed to EPS were determined by Atomic Absorption Spectroscopy. The EPSs of all the strains bound more than 80% of Zn, as well as 64–84% of Cd and 74–79% of Pb. Thus, it has been clearly shown that the use of F. culmorum EPSs can be the basis for creating sustainable bioremediation, including phytoremediation. Full article

N-isopropylacrylamide and methacrylic acid were copolymerized by a free radical polymerized mechanism. The obtained hydrogel poly(N-isopropylacrylamide-co-methacrylic acid) hydrogels, poly(NIPAM-co-MAA), were utilized as sorbent material for removal Cr(VI), Mn(II), and Pb(II) ions from simulated aqueous solutions. Hydrogel structures before and after heavy metal sorption are characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The swelling results indicate that poly(NIPAM-co-MAA) hydrogels are pH- and temperature-sensitive and have high swelling reversibility through three swelling/contraction cycles. The studied parameters of heavy metal sorption include the effect of pH, the initial concentration of heavy metal, the effect of temperature, and the desorption of metal ions. The maximum sorption capacities of poly(NIPAM-co-MAA) hydrogels were determined at pH 4.5 and 25 °C, and they are, for Cr(VI), Mn(II), and Pb(II) ions, 289.35 mg/g, 190.59 mg/g, and 349.71 mg/g, respectively. The pseudo-second-order model and the Langmuir adsorption isotherm best describe the sorption of heavy metal ions onto hydrogels. The removal of heavy metals is an exothermic reaction, and the interaction mechanism between the metal and the hydrogel is primarily physical in nature. Results of three sorption/desorption cycles show a good desorption ratio and sorption capacity of poly(NIPAM-co-MAA) hydrogels. Full article

Adsorption represents an effective strategy for water remediation applications, particularly when utilising eco-friendly materials in a circular economy framework. This approach offers significant advantages, including low cost, material availability, ease of operation, and high efficiency. Herein, the performance of cadmium ion adsorption onto hydroxyapatites, derived through a calcination-free process from shells of two mollusc species, Queen Scallop (Aequipecten opercularis) and Pacific Oyster (Magallana gigas), is examined. The phase and morphology of the synthesised adsorbents were investigated. The results showed that hydroxyapatites obtained from mollusc shells are characterised by high efficiency regarding cadmium removal from water, exhibiting rapid kinetics with equilibrium achieved within 5 min and high adsorption capacities up to 334.9 mg g⁻¹, much higher than many waste-based adsorbents reported in literature. Structural investigation revealed the presence of Cadmium Hydrogen Phosphate Hydrate in the hydroxyapatite derived from oyster shells loaded with Cd, indicating the formation of a solid solution. This finding suggests that the material not only has the capability to decontaminate but also to immobilise and store Cd. Overall, the results indicate that hydroxyapatites prepared via a synthetic route in mild conditions from waste shells are an economical and efficient sorbent for heavy metals encountered in wastewater. Full article

(1→3)-α-d-Glucan is an important component of the cell wall of most fungi. The polymer has many applications, including as a therapeutic agent in the prevention or treatment of various diseases, as well as a heavy metal sorbent and a component of new materials used in the plastics industry. The presence of (1→3)-α-d-glucan (water-insoluble, alkali-soluble polysaccharide) in the cell wall of Pleurotus djamor (pink oyster mushroom) was confirmed using specific fluorophore-labeled antibodies. Therefore, the water-insoluble fraction (WI-ASF) of P. djamor B123 fruiting bodies was isolated by alkaline extraction and used for further analyses. The structural features of the WI-ASF were determined by composition analysis, linkage analysis, Fourier transform infrared and Raman spectroscopy, ¹H and ¹³C nuclear magnetic resonance spectroscopy, scanning electron microscopy, as well as viscosity, specific rotation, and gel permeation chromatography. These studies revealed the presence of glucose units linked by α-glycosidic bonds and scanty amounts of mannose and xylose. Furthermore, methylation analysis of WI-ASF demonstrated that the (1→3)-linked glucopyranose (Glcp) is the primary moiety (86.4%) of the polymer, while the 3,4- and 3,6-substituted hexoses are the branching residues of the glucan. The results of chemical and spectroscopic investigations indicated that the analyzed WI-ASF is a (1→3)-linked α-d-glucan type with a molecular weight of 552 kDa. Full article

The presence of heavy metals in groundwater and wastewater has been a concern for health organizations. This study investigated the effectiveness of activated carbon derived from various natural precursors, including acorns from red oak trees (Quercus rubra), date seeds, and peach seeds, employing the thermal activation method for the removal of heavy metals from aqueous solutions. Batch adsorption tests investigated the effects of sorbent quantity, pH levels, disinfectant presence, and dissolved organic matter (DOM) on the removal efficiency of Pb and Cu. Characterization of the prepared activated carbon was conducted using scanning electron microscopy (SEM). Lead removal efficiency diminished at pH 7 relative to pH 3 and 5, but copper exhibited superior removal efficiencies at pH 7 compared to pH 5. The addition of monochloramine at 4 parts per million (ppm) effectively eliminated lead from the solution. A rise in free chlorine concentration from 2 to 4 mg/L led to a reduction in metal removal from water by 20 to 60%. DOM at concentrations of 1 and 6 mg/L reduced metal removal efficacy relative to DOM at 3 mg/L. Date seed-activated carbons underscore their distinctive potential, offering useful insights for the enhancement of water and wastewater treatment systems. Full article

As a cost-effective sorbent, modified biochar has received increasing attention for the removal of heavy metal contaminants. Among several chemical modification methods, introducing thiol functional groups onto the surface of biochar has been identified as an effective enhancement approach for the heavy metal sorption and removal capacity of this porous adsorbent material. In general, chemical impregnation is a widely used method to graft thiol groups onto the surface of carbon-based materials. However, limited comparative data are available on the efficacy of the present biochar thiolation methods. In this study, the biochar of nine different organic sources was modified by two frequently used agents with distinct thiolation mechanisms: 3-Mercaptopropyltrimethoxysilane (3-MPTS) and β-mercaptoethanol. In addition to chemical impregnation, the ball milling method, a simple and environmentally friendly alternative thiolation method, was also evaluated. A comprehensive structural characterization of the biochar samples was completed before and after thiolation. A higher concentration of sulfur on the surface of the biochar was achieved through thiolation with β-mercaptoethanol, in which the thiolation mechanism is performed through an esterification reaction with the carboxylic acid functional groups of the activated biochar. Chemical impregnation was found to be a more effective thiolating method than ball milling using the same thiolating agent. Full article

Heavy metal cations such as Ag⁺, Pb²⁺, and Hg²⁺ can accumulate in living organisms, posing severe risks to biological systems, including humans. Therefore, removing heavy metal cations from wastewater is crucial before discharging them to the environment. However, trace levels and high-capacity removal of the heavy metals remain a critical challenge. This work demonstrates the synthesis and characterization of [Mo₂S₁₂]²⁻ intercalated cobalt aluminum-layered double hydroxide, CoAl―Mo₂S₁₂―LDH (CoAl―Mo₂S₁₂), and its remarkable sorption properties for heavy metals. This material shows high efficiency for removing over 99.9% of Ag⁺, Cu²⁺, Hg²⁺, and Pb²⁺ from 10 ppm aqueous solutions with a distribution constant, K_d, as high as 10⁷ mL/g. The selectivity order for removing these ions, determined from the mixed ion state experiment, was Pb²⁺ < Cu²⁺ ≪ Hg²⁺ < Ag⁺. This study also suggests that CoAl―Mo₂S₁₂ is not selective for Ni²⁺, Cd²⁺, and Zn²⁺ cations. CoAl―Mo₂S₁₂ is an efficient sorbent for Ag⁺, Cu²⁺, Hg²⁺, and Pb²⁺ ions at pH~12, with the removal performance of both Ag⁺ and Hg²⁺ cations retaining > 99.7% across the pH range of ~2 to 12. Our study also shows that the CoAl―Mo₂S₁₂ is a highly competent silver cation adsorbent exhibiting removal capacity (q_m) as high as ~918 mg/g compared with the reported data. A detailed mechanistic analysis of the post-treated solid samples with Ag⁺, Hg²⁺, and Pb²⁺ reveals the formation of Ag₂S, HgS, and PbMoO₄, respectively, suggesting the precipitation reaction mechanism. Full article