Search Results (3,147)

This study presents a plant-fabricated nanoparticle system of zirconia (ZrO₂) using Sonchus asper plant extract, compared with conventionally synthesized ZrO_2, for their efficacy in Cr(VI) removal from aqueous solutions. The nanoparticles were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS) for elemental composition, Fourier-transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analysis. The plant-fabricated ZrO₂ exhibited mesoporosity and enhanced surface functionality, attributed to bioactive compounds from Sonchus asper, which improved adsorption performance via increased surface area and residual organic functional groups. Batch adsorption experiments showed that Cr(VI) removal was optimized at 100 mg/L Cr(VI), 300 mg/L adsorbent dosage, pH 5, and 30 min reaction time at 25 °C. Adsorption followed the Langmuir isotherm and pseudo-second-order kinetics models. According to Langmuir model fitting, the maximum adsorption capacity (qmax) reached 142.24 mg/g for PF-ZrO₂ NPs and 133.11 mg/g for conventional ZrO₂ NPs, indicating the superior adsorption performance of the green-synthesized material. This work highlights the sustainable potential of plant-fabricated ZrO₂ nanoparticles as cost-effective and environmentally friendly nano-adsorbents for heavy metal remediation, contributing to the achievement of UN SDG No. 6 by providing clean water solutions. Full article

Boric acid/β-CD-based polymers (BA-CD) possess hierarchical porous structures and efficient functional groups for further molecular recognition, which are used for the adsorption of a series of cationic and anionic organic dyes. The effects of pH, contact time, initial concentration of solution, and temperature on the adsorption performance were experimentally investigated in detail. Surprisingly, the adsorption capacities of BA-CD towards RB exhibited a higher value of 733.2 mg g⁻¹ among a series of cationic and anionic dyes. The adsorption kinetics further indicated that the adsorption of dyes by BA-CD belonged to a quasi-second-order kinetic model, while the adsorption isotherms demonstrated the adsorption process as the Langmuir isotherm model. The characterization of the adsorption process was performed in the presence of monomolecular layer chemisorption. In addition, the reusability test showed that BA-CD had a high reusability rate of 90% in MG after five cycles, indicating its future potential for the treatment of dye wastewater. 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

This study developed a beta-cyclodextrin polymer crosslinked with citric acid (CDCAPol) for removing water contaminants using methylene blue (MB) as a model compound. The polymer, which features free carboxyl groups and cyclodextrin cavities, demonstrated high adsorptive capacity. Under optimal conditions (0.01 g adsorbent, pH 6, and 50 mg/dm³ MB), a removal efficiency of 99.2% was achieved, with a maximum adsorption capacity of 126.58 mg/g as determined by the Langmuir isotherm. Kinetic data fit the best to the pseudo-second-order model, highlighting strong interactions between MB and the polymer. This promising material may find applications in wastewater treatment and environmental protection. 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

Pharmaceutical contaminants such as ibuprofen are increasingly detected in water sources due to widespread use and insufficient removal by conventional treatment processes. Given its persistence and adverse effects on human health and aquatic ecosystems, efficient removal technologies are needed. This study reports the synthesis of a Mg/Al-layered double hydroxide (LDH) hybridized with carbon quantum dots (CQDs) via in situ co-precipitation to enhance adsorptive performance. The hybrid (LDH-CQD) was characterized by FTIR, XRD, DSC, TGA-DTG, SEM-EDS, BET, and pH in the point of zero charge (pH_PZC) analysis. Results indicated a marked increase in surface area (2.89 to 66.9 m²/g), a shift in surface charge behavior (pHpzc from 8.57 to 6.21), and improved porosity. Adsorption experiments using ibuprofen as a model contaminant revealed superior performance of the hybrid compared to pristine Mg/Al-LDH, with a maximum capacity of 22.13 mg·g⁻¹ (% Removal = 88.53%) at 25 ppm, and in lower concentrations (5 and 10 ppm), the hybrid showed 100% removal. Kinetic modeling followed a pseudo-second-order mechanism, and the isotherm was the SIPS model (maximum adsorption capacity = 24.150 mg.g⁻¹). These findings highlight the potential of LDH-CQD hybrid as efficient and tunable adsorbents for removing emerging pharmaceutical pollutants from aqueous media. 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

Natural zeolites have gained attention as low-cost adsorbents for the removal of heavy metals (HMs) from wastewater. However, their performance can be compromised by the presence of competing cations such as ammonium (NH₄⁺). This study investigated the competitive adsorption and desorption dynamics of NH₄⁺ and six HMs (Cd, Cr, Cu, Ni, Pb, and Zn) on two natural zeolites. Batch and column experiments using synthetic wastewater were conducted to evaluate the effects of different NH₄⁺ concentrations, pH, and particle size on HM removal efficiency and desorption effects. Results showed that increasing NH₄⁺ concentrations significantly reduce HM adsorption, with total capacity decreasing by ~45% at 100 mg/L NH₄-N in kinetic tests. Adsorption isotherms of the HM mixture for both zeolite types followed a clear sigmoidal trend, which was captured well by the Hill model (R² = 0.99), with loading rates up to 56.14 mg/g. Pb consistently exhibited the highest affinity for zeolites, while Cd, Cr, Ni, and Zn were most affected by NH₄⁺ competition in the column tests. Desorption tests confirmed that NH₄⁺ rapidly re-mobilises adsorbed metals, in particular Cd, Cu, and Zn. Slightly acidic to neutral pH conditions were optimal for minimising HM remobilisation. These findings underscore the need to consider competitive interactions and operational conditions when applying natural zeolites for HM removal, especially in ammonium-rich environments such constructed wetlands, soil filters, or other decentralised applications. Full article

Protein adsorption on dental zirconia (ZrO₂) surfaces plays a crucial role in plaque formation, tissue healing, and bone osseointegration. This study investigated and compared the adsorption behavior of three salivary antimicrobial proteins—peroxidase, lactoferrin, and lysozyme—on a ZrO₂ sensor and an Au sensor using a quartz crystal microbalance (QCM) operating at 27 MHz. Protein adsorption was determined from frequency decreases, and the apparent reaction rate constant (k_obs) was calculated by fitting frequency–time curves to a kinetic model. The amount of lactoferrin adsorbed on the ZrO₂ sensor was significantly higher than that of peroxidase and lysozyme (p < 0.05). Significantly smaller amounts of peroxidase and lysozyme were adsorbed onto the ZrO₂ sensor than the Au sensor (p < 0.05). The k_obs for lysozyme on the Au sensor was significantly higher than those for lactoferrin on sensors and for peroxidase on the Au sensor (p < 0.05). Differences in salivary antimicrobial protein adsorption between Au and ZrO₂ surfaces were influenced, in part, by electrostatic interactions between the proteins and the material surface. Full article

Understanding the differences in the adsorption behaviors of tetrabromobisphenol A (TBBPA) and tetrabromobisphenol S (TBBPS) on soils is critical for assessing their environmental mobility and risks. This study investigated the adsorption characteristics and patterns of TBBPA/S across various soil types. Adsorption kinetics analysis indicated that the adsorption of TBBPA/S on soils followed pseudo-secondary-order kinetics. Isotherm results revealed that the Langmuir model described TBBPA adsorption more accurately, while the Freundlich model was a better fit for TBBPS adsorption, suggesting distinct adsorption mechanisms due to their differing properties. Correlation analysis and principal component analysis (PCA) were performed to identify the key soil physicochemical properties influencing TBBPA/S adsorption. The results showed that TBBPA adsorption was inversely correlated with soil pH and positively correlated with clay content. In contrast, TBBPS adsorption displayed negative correlations with soil pH and sand content, and positive correlations with amorphous iron, amorphous aluminum, and free iron content. Further analysis of different treated soil fractions demonstrated that soil organic matter dominated the adsorption of TBBPA/S, with humic acid playing a more significant role than humin. The adsorption behavior characteristics of TBBPA/S on different soils provide fundamental data for understanding their environmental fate in soil systems. Full article

Formo-phenolic-like resins were synthesized by replacing phenol with phloroglucinol, a biobased and biocompatible compound, and using different aldehydes, such as biomass-derived furaldehyde and glyoxal. Studies on the adsorption of rare earth elements from an aqueous organic acid solution indicate that these resins follow the Langmuir isotherm model, with maximum adsorption capacities ranging from 0.38 to 0.75 mmol/g. Adsorption was temperature-independent but strongly influenced by pH, with an up to fourfold increase between pH 2 and 5. Extraction kinetics were rapid, reaching equilibrium within two hours. Complete metal recovery was achieved within ten minutes using a 1 mol/L HCl desorption solution. Selectivity also varied with pH; glyoxal- and furfural-based resins showed superior separation performance at pH 2–3 and 3–4, respectively. The application of this method to real-world samples, including permanent magnet and red mud organic acid leachates, demonstrated effective extraction of rare earth elements and promising selectivity over iron (Fe), cobalt (Co), and nickel (Ni). Full article

Empty pinecones are a largely available byproduct of Pinus pinea L. nut production, mostly concentrated in the Mediterranean area; e.g., in Portugal, around 70,000 tons of pinecones are produced annually. One valorization line for residual biomass is its use as biosorbents for the removal of contaminants in effluents and water courses which are an increasing environmental problem. This study explores the biosorbent potential of pinecones to remove zinc ions from aqueous solutions. We analyzed the morphology and chemical composition of pinecones (9.4% extractives, 37.0% lignin, 68.6% holocellulose, 1.4% ash). The effect of pH and adsorbent dose on the adsorption process was studied, as were the sorption kinetics and isotherms. The pinecones showed good potential to remove Zn ions, with 96% removal at pH 7 and a maximum adsorption capacity of 7.92 mg g⁻¹. The process followed the Freundlich isotherm model, indicating a heterogeneous surface and multilayer adsorption, and the pseudo-second-order kinetic model, suggesting chemisorption as the dominant mechanism. The use of pinecones as bio-adsorbent is therefore a green and low-cost alternative for environmental remediation and biomass waste management. Full article