Search Results (1,419)

The present study showed that it is possible add value to eucalyptus harvest waste, obtained in large quantities, from the cellulose industries, without known economic use, for the production of an activated biochar. The biochar, produced from the impregnation of eucalyptus harvest waste with H₃PO₄, and subsequently pyrolyzed at 600 °C for 1 h, was successfully used as a bioadsorbent in the removal of paracetamol, an emerging pollutant present in wastewater. The biochar showed a high specific surface area with micro- and mesopores and functionalized surface. The optimal conditions for the removal of paracetamol achieve an efficiency around 88–93%. The Langmuir and the pseudo-first-order models best fit the experimental data, with a maximum adsorption capacity of approximately 27.8 mg g⁻¹, at 25 °C. The thermodynamic showed that adsorption occurred spontaneously, endothermally and randomly at the solid–liquid interface. In addition, the bioadsorbent showed excellent reusability and no significant difference in adsorption capacity was observed in more complex aqueous matrices. Thus, the activated biochar produced in this study proved to be an efficient, low-cost and environmentally friendly bioadsorbent, capable of removing paracetamol from contaminated water, with great potential for use in water treatment plants, on a large scale and economically, contributing to the improvement of water quality and minimizing residual biomass in the environment. Full article

This study developed a novel adsorbent for Cr (VI) removal from wastewater by grafting N-[(dimethylamino)methylene]thiourea (TUFA) onto lignin. The resulting TUFA-functionalized lignin adsorbent AL was comprehensively characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), and X-ray photoelectron spectroscopy (XPS). Batch adsorption experiments systematically evaluated the influence of solution pH, contact time, temperature, initial Cr (VI) concentration, and adsorbent dosage. AL exhibited high adsorption capacity (593.9 mg g⁻¹ at 40 °C), attributed to its abundant nitrogen and sulfur-containing functional groups. Kinetic analysis revealed that the adsorption process followed pseudo-second-order kinetics. Equilibrium isotherm data were best described by the Langmuir model, indicating predominant monolayer chemisorption. Thermodynamic parameters demonstrated that Cr (VI) adsorption onto AL is spontaneous, endothermic, and entropy-driven. The adsorption mechanism involves membrane diffusion and intra-particle diffusion processes. This work successfully synthesized a stable, effective, and low-cost adsorbent (AL) using an amine agent incorporating both nitrogen and sulfur functional groups, offering a promising approach for treating Cr (VI)-contaminated wastewater. Full article

Electrochemical reduction processes enable the CO to be converted into a useful chemical fuel. Our study employs density functional theory calculations to analyze the (110) facets of the transition metal carbide surfaces for CO capture, incorporating the Mars–van Krevelen (MvK) mechanism. All the possible adsorption sites on the surface, including carbon, metal, and bridge sites, were fully investigated. The findings indicate that the carbon site is more active relative to the other adsorption sites examined. The CO hydrogenation paths have been comprehensively investigated on all the surfaces, and the free energy diagrams have been constructed towards the product. The results conclude that the TiC is the most promising candidate for the formation of methane, exhibiting an onset potential of −0.44 V. The predicted onset potential for CrC, MoC, NbC, VC, WC, ZrC, and HfC are −0.86, −0.61, −0.61, −0.93, −0.87, −0.61, and −0.81 V, respectively. Our calculated results demonstrate that MvK is selectively relevant to methane synthesis. Additionally, we investigated the stability of these surfaces against decomposition and conversion to pure metals concerning thermodynamics and kinetics. It was found that these carbides could remain stable under ambient conditions. The exergonic adsorption of hydrogen on carbon sites, requiring smaller potential values for product formation, and stability against decomposition indicate that these surfaces are highly suitable for CO reduction reactions using the MvK mechanism. Full article

Addressing the challenge of sulfonated lignite (SL) removal from oilfield wastewater, this study introduces a novel hierarchical MgFe-layered double hydroxide (LDH) adsorbent. The material was fabricated via in situ co-precipitation, utilizing a template formed by the NaCl-induced co-assembly of oleylaminopropyl betaine (OAPB) and sodium dodecyl sulfate (SLS) into zwitterionic, anionic, shear-responsive viscoelastic gels. This gel-templating approach yielded an LDH structure featuring a hierarchical pore network spanning 1–80 nm and a notably high specific surface area of 199.82 m²/g, as characterized by SEM and BET. The resulting MgFe-LDH demonstrated exceptional efficacy, achieving a SL removal efficiency exceeding 96% and a maximum adsorption capacity of 90.68 mg/g at neutral pH. Adsorption kinetics were best described by a pseudo-second-order model (R² > 0.99), with intra-particle diffusion identified as the rate-determining step. Equilibrium adsorption data conformed to the Langmuir isotherm, signifying monolayer uptake. Thermodynamic analysis confirmed the process was spontaneous (ΔG < 0) and exothermic (ΔH = −20.09 kJ/mol), driven primarily by electrostatic interactions and ion exchange. The adsorbent exhibited robust recyclability, maintaining over 79% of its initial capacity after three adsorption–desorption cycles. This gel-directed synthesis presents a sustainable pathway for developing high-performance adsorbents targeting complex contaminants in oilfield effluents. Full article

Excessive phosphorus emissions are a significant driver of severe eutrophication in water bodies, and developing an efficient and cost-effective adsorbent for phosphorus removal is imperative. In this study, a Na-type zeolite was synthesized from coal gangue sourced from an open-pit mine in Xinjiang province, China. The synthesis process involved drying, crushing, alkali activation, aging, hydrothermal crystallization, and Na⁺ ion exchange. Orthogonal design identified the optimal synthesis parameters: an alkali-to-ash ratio of 1:1, aging at 20 °C for 12 h, and crystallization at 130 °C for 12 h. Aging time exerted the greatest influence on the phosphate removal efficiency. The optimized zeolite exhibited excellent phosphate adsorption performance, achieving a removal efficiency of up to 96% and a capacity of 16 mg/g. The adsorption kinetics followed both pseudo-first-order and pseudo-second-order models, indicating processes governed by combined physical and chemical mechanisms. Isotherm data fitting with Freundlich and Langmuir models suggested the presence of both homogeneous and heterogeneous active sites. Thermodynamic studies confirmed a spontaneous and endothermic process, increasingly favorable at higher temperatures. Characterizations via scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray fluorescence (XRF) spectroscopy, and Fourier transform infrared (FTIR) spectroscopy confirmed the formation of Na-type zeolite and revealed structural and compositional changes following phosphate adsorption. Aluminum and calcium binding played key roles in the chemical adsorption mechanisms. This work not only offers a high-efficiency, low-cost solution for phosphorus removal from wastewater but also provides a sustainable pathway for the valorization of coal gangue in the Zhundong area of Xinjiang, China. Full article

Dry ice, the solid form of carbon dioxide (CO₂), is widely used in cold chain logistics, industrial cleaning, and biomedical preservation. Its production, however, is closely linked to carbon capture, energy-intensive liquefaction, and solidification processes. This review critically evaluates and compares the existing methods of CO₂ capture, including chemical absorption, physical absorption, adsorption, and membrane-based separation as they pertain to dry ice production. This study further assesses liquefaction cycles using refrigerants such as ammonia and R744, highlighting thermodynamic and environmental trade-offs. Solidification techniques are examined in the context of energy consumption, process integration, and product quality. The comparative analysis is supported by extensive tabulated data on operating conditions, CO₂ purity, and sustainability metrics. This review identifies key technical and environmental challenges, such as solvent regeneration, CO₂ leakage, and energy recovery. Thus, it also explores emerging innovations, including hybrid cycles and renewable energy integration, to advance the sustainability of dry ice production. This, in turn, offers strategic insight for optimizing dry ice manufacturing in alignment with low-carbon industrial goals. Full article

Water pollution by organic dyes poses serious environmental and health challenges, demanding efficient and selective remediation methods. In this study, we engineered tailored organo-clay nanocomposites by modifying montmorillonite with hexadecyltrimethylammonium bromide (HTAB) and intercalating polyethylene glycol (PEG) chains of two distinct molecular weights (PEG200 and PEG4000). Comprehensive characterization techniques (XRD, FTIR, SEM, zeta potential, and TGA) confirmed the successful modification of the composites. Notably, PEG4000 promoted significant interlayer expansion, as evidenced by the shift of the (00l) reflection corresponding to the basal spacing d, indicating an increase in basal spacing. This expansion contributed to the formation of a well-ordered porous framework with uniformly distributed pores. In contrast, PEG200 produced smaller pores with a more uniform distribution but induced less pronounced interlayer expansion. Adsorption tests demonstrated rapid kinetics, achieving equilibrium in under 15 min, and impressive capacities: 420 mg/g of methylene blue (MB) adsorbed on PEG200/MMT@HTAB, and 385 mg/g of Congo red (CR) on PEG4000/MMT@HTAB. The crucial role of PEG chain length in adsorption selectivity was assessed, showing that shorter PEG chains favored methylene blue adsorption by producing narrower pores and faster kinetics, while longer PEG chains enhanced CR uptake via a stable, interconnected pore network that facilitates diffusion of larger dye molecules. Thermodynamic and Dubinin–Radushkevich analyses confirmed that the adsorption was spontaneous, exothermic, and predominantly driven by physical adsorption mechanisms involving weak van der Waals and dipole interactions. These findings highlight the potential of PEG-modified montmorillonite nanocomposites as cost-effective, efficient, and tunable adsorbents for rapid and selective removal of organic dyes in wastewater treatment. Full article

Heparin, an essential plasma-derived therapy, acts as a naturally occurring anticoagulant and is essential in various physiological processes. Due to its complex structure, repeating units of sulfated glycosaminoglycan, it attracts attention in the field of commercial pharmaceuticals. In recent decades, significant advancements have been made in the development of economical adsorbents designed especially for the extraction of heparin from the intestinal mucosa of pigs, as evidenced by investments from various pharmaceutical industries. This requirement arises from the demand for efficient, scalable extraction methods for natural sources. In this study, we investigated the application of beta zeolites to increase the recovery of heparin from real porcine mucosa samples, emphasizing materials with greater adsorption surfaces, higher thermal stability, and increased porosity. According to our research, the zeolite CP814E’s macropores and huge surface area allow it to adsorb up to 20.6 mg·g⁻¹ (39%) of heparin from actual mucosa samples. We also investigated the adsorbent’s surface conditions, which are essential for efficient heparin recovery, and adjusted temperature and pH to enhance heparin uptake. These findings demonstrate that zeolite-based adsorbents can enhance the extraction of heparin effectively for use in medicinal applications. Full article

Fluoroquinolone antibiotics (FQs) are widely applied in veterinary practice and animal husbandry and frequently persist in organic waste liquids (OWLs), creating substantial environmental and health risks when untreated. A high-capacity mesoporous silica aerogel (SA-60) was produced via a cost-effective sol–gel route from water glass, followed by ambient pressure drying at 60 °C for 6 h. SA-60 exhibited pronounced selectivity, providing a maximum adsorption capacity of 630.18 mg·g⁻¹ for enrofloxacin (ENR) in acetonitrile. Adsorption efficiency was weakly dependent on pH. Mechanistic analysis indicated combined physical and chemical interactions, with intra-particle diffusion governing the overall rate. Thermodynamic evaluation showed a spontaneous and endothermic process for ENR adsorption. Organic solvent type and water content were major determinants of adsorption efficiency. Durable performance was observed, with capacity retention above 80% after five adsorption-desorption cycles. The mesoporous architecture (surface area 249.21 m²·g⁻¹; average pore diameter 10.81 nm) supported the high uptake. These results identify SA-60 as a sustainable adsorbent for removing hazardous FQs from OWLs, offering a simple, energy-efficient approach for the source-level control of antibiotic pollution and improved environmental management. Full article

Sewage sludge, a byproduct of wastewater treatment, can be converted into biochar, offering a sustainable solution for waste management and water treatment. Although biochars from biomass have been widely studied, sewage sludge-derived biochars remain underexplored. This study investigated the use of alkaline-treated sewage sludge-derived biochar (AlBC) as an adsorbent for three water pollutants: caffeine (CAF), carbamazepine (CBZ), and 17α-ethinyl estradiol (EE2). A comprehensive analysis was conducted to explore the kinetic and thermodynamic behaviors of these pollutants under varying conditions, such as different adsorbent dosage, temperature, and water matrix values. The AlBCSS showed enhanced surface area and improved adsorption capacity, with EE2 being preferentially adsorbed (q_e: 9.51 mg g⁻¹), followed by CAF (6.12 mg g⁻¹) and CBZ (4.58 mg g⁻¹). Adsorption followed the Langmuir isotherm for CAF and CBZ, and the Freundlich isotherm for EE2, while kinetics were best described by the pseudo-second-order and Elovich models. Thermodynamic analysis revealed that the adsorption process was spontaneous, primarily driven by physical interactions. Factors such as dosage, temperature, and pollutant concentration influenced adsorption, with no saturation observed at higher concentrations. The natural water matrix had a minimal effect on removal efficiency (40–100%), whereas AlBC exhibited promising results after four adsorption cycles. These results highlight the potential of sewage sludge-derived biochar as a sustainable adsorbent for emerging water pollutants, supporting circular economy practices in wastewater management. Full article

The study aims to promote environmental restoration by shedding light on the potential use of moringa waste as an inexpensive, eco-friendly adsorbent for treating wastewater contaminated with Chromium (VI). FTIR was used to characterise the surface functional groups of moringa waste. The one-factor-at-a-time method was used to study the initial concentration in milligrams per litre, contact time in minutes, temperature in degrees Celsius, pH, and adsorbent dosage in milligrams per litre. The output was the removal percentage. Furthermore, adsorption isotherms, kinetics, and thermodynamic models were applied to understand the process behaviour. FTIR examination revealed the moringa waste structure’s stability and aromaticity, confirmed by peaks located around 1596 cm⁻¹ and the stretching of the hydroxyl group around 3321 cm⁻¹, which are important for enhancing Cr (VI) adsorption due to their capability to establish strong bonds with metal ions. Aromatic rings contribute to a large surface area and porosity and are stable; this is important for adsorption applications. At 60 min of contact time with a pH of 6 and 0.5 g of adsorbent dosage at 45 °C for a concentration of 100 mg/L, the highest removal percentage was found to be 77.03%. Adsorption data values indicated a good fit to the Langmuir isotherm model. The thermodynamic study showed that the process is endothermic and spontaneous, hence making the application of moringa waste in wastewater treatment viable. Full article

Efficient and selective separation of gallium (Ga(III)) from alkaline industrial waste streams remains a significant challenge due to the coexistence of chemically similar ions such as Al(III) and V(V). In this study, a novel ion-imprinted chitosan-based adsorbent (CS/(H-CGCS)-Ga-IIP) was synthesized via a hybrid cross-linking strategy using glutaraldehyde and siloxane-modified chitosan. The optimized material exhibited a high adsorption capacity of 106.31 mg·g⁻¹ for Ga(III) at pH 9, with fast adsorption kinetics reaching equilibrium within 60 min. Adsorption behavior followed the pseudo-second-order kinetic and Langmuir isotherm models, and thermodynamic analysis indicated a spontaneous and endothermic process. In simulated Bayer mother liquor systems, the material demonstrated outstanding selectivity and a distribution coefficient ratio k_d-Ga/k_d-Al = 146.9, highlighting its strong discrimination ability toward Ga(III). Mechanistic insights from SEM-EDS, FTIR, and XPS analyses revealed that Ga(III) adsorption occurs via electrostatic interaction, ligand coordination, and structural stabilization by the siloxane network. The material maintained good adsorption performance over three regeneration cycles, indicating potential for reuse. These findings suggest that CS/(H-CGCS)-Ga-IIP is a promising candidate for the sustainable recovery of gallium from complex alkaline waste streams such as Bayer process residues. Full article

The rational design of functional and sustainable polymers is central to addressing global environmental challenges. In this context, unmodified lignin derived from Sarkanda grass (Tripidium bengalense), an abundant agro-industrial lignocellulosic byproduct, was systematically investigated as a natural polymeric adsorbent for the remediation of aqueous media contaminated with heavy metals. The study evaluates lignin’s behavior toward nine metal(loid) ions: arsenic, cadmium, chromium, cobalt, copper, iron, nickel, lead, and zinc. Adsorption performance was systematically investigated under static batch conditions, optimizing key parameters, with equilibrium and kinetic data modeled using established isotherms and rate equations. Surface characterization and seed germination bioassays provided supporting evidence. Unmodified Sarkanda grass lignin demonstrated effective adsorption, exhibiting a clear preference for Cu(II) followed by other divalent cations, with lower capacities for As(III) and Cr(VI). Adsorption kinetics consistently followed a pseudo-second-order model, indicating chemisorption as the dominant mechanism. Thermodynamic studies revealed spontaneous and endothermic processes. Bioassays confirmed significant reduction in aqueous toxicity and strong metal sequestration. This work positions unmodified Sarkanda grass lignin as a bio-based, low-cost polymer platform for emerging water treatment technologies, contributing to circular bioeconomy goals and highlighting the potential of natural polymers in sustainable materials design. Full article

The pharmaceutical contamination of water, especially by widely used drugs, presents important environmental and health concerns due to the inefficiency of conventional treatment methods. The present study proposes a sustainable solution using biochar (Bch) obtained from tomato waste, functionalized with Fe₃O₄ and MnO₂ nanoparticles, for the removal of paracetamol from aqueous solutions. The composite materials were synthesized, characterized, and evaluated under varying conditions, including pH, temperature, contact time, initial drug concentration, and adsorbent dose. The materials exhibited porous structures with wide pore size distributions. Optimal removal efficiency was achieved for 30 mg L⁻¹ paracetamol concentration, pH 2, 25 °C, 0.3 g L⁻¹ adsorbent dose, and 20 min contact time. The Freundlich isotherm provided the best fit for the adsorption data. Kinetic studies revealed that the pseudo-second-order model best described the adsorption process. Thermodynamic parameters indicated that the process was spontaneous, feasible, and exothermic. Compared with similar materials derived from agricultural waste, the tomato waste-based composites demonstrated competitive adsorption capacities. These findings suggest that Bch-HCl/MnO₂ and Bch-HCl/Fe₃O₄/MnO₂ are promising, cost-effective adsorbents for mitigating pharmaceutical pollutants in wastewater. Full article

Phosphates are key pollutants involved in the eutrophication of water bodies, creating the need for efficient and low-cost strategies for their removal in order to meet environmental quality standards. This study presents a comparative thermodynamic evaluation of phosphate ion adsorption from aqueous solutions using two sustainable and readily available materials: autoclaved aerated concrete (AAC) and pumice stone (PS). Batch experiments were conducted under acidic (pH 3) and alkaline (pH 9) conditions to determine equilibrium adsorption capacities, and kinetic experiments were carried out for the best-performing adsorbent. Adsorption data were fitted to the Langmuir and the Freundlich isotherm models, while kinetic data were evaluated using pseudo-first-order and pseudo-second-order models. The Freundlich model showed the best correlation (R² = 0.90 − 0.97), indicating the heterogeneous nature of the adsorbent surfaces, whereas the Langmuir parameters suggested monolayer adsorption, with maximum capacities of 1006.69 mg/kg for PS and 859.20 mg/kg for AAC at pH 3. Kinetic results confirmed a pseudo-second-order behavior, indicating chemisorption as the main mechanism and the rate-limiting step in the adsorption process. To the best of our knowledge, this is the first study to compare the thermodynamic performance of AAC and PS for phosphate removal under identical experimental conditions. The findings demonstrate the potential of both materials as efficient, low-cost, and thermodynamically favorable adsorbents. Furthermore, the use of AAC, an industrial by-product, and PS, a naturally abundant volcanic material, supports resource recovery and waste valorization, aligning with the principles of the circular economy and sustainable water management. Full article