Search Results (45)

Chiral pharmaceuticals (CPs) have gained growing attention in environmental studies regarding the differential behavior of individual enantiomers in racemic mixtures. This study investigates the stereoselectivity and efficiency of montmorillonite (MMT), a natural and low-cost adsorbent, for the removal of a wide group chiral pharmaceuticals and metabolites (atenolol, propranolol, metoprolol, fluoxetine, venlafaxine, norfluoxetine, and O-desmethylvenlafaxine). The effects of adsorption conditions including initial CP concentration, contact time, adsorbent dose, solution pH, and humic acid content were evaluated. In most adsorption experiments, no significant stereoselective behavior was observed, except for the case where a low adsorbent dose was applied. Interestingly, as the solution humic acid content increased (up to 40 mg/L), the adsorption capacity was increased for most of the target CPs. Isotherm studies revealed that the Freundlich model described the experimental data well and the process was favorable. Adsorption mechanism was interpreted by material characterization before and after adsorption. High removal efficiencies (88.0 to 99.8%) and the non-enantioselective behavior of MMT indicate that it can be used effectively for the simultaneous removal of both enantiomeric forms of various chiral pharmaceuticals from aqueous matrices. Full article

In this study, phenol adsorption from aqueous solutions was investigated using a carbonized adsorbent derived from a 1:1:1 mixture of banana, carrot, and potato peels, representing a major fraction of municipal bio-waste in Serbia. The material (CARB_BCP) was characterized by pH_pzc, SEM, FTIR, and BET analyses. The results indicated a highly porous structure with developed micro- and mesoporosity and a high specific surface area (S_BET = 483 m²/g). FTIR confirmed the formation of a stable aromatic carbon structure, while the high pH_pzc value (10.55) suggested a limited role of electrostatic interactions. Adsorption experiments performed at an initial phenol concentration of 1858 mg/L, room temperature, and an adsorbent dose of 0.1 g achieved a removal efficiency of 20.5%. The Langmuir model provided the best fit, indicating monolayer adsorption, with good agreement between theoretical (≈187 mg/g) and experimental (≈190 mg/g) capacities. Kinetic analysis followed the pseudo-second-order model, suggesting chemisorption as the rate-controlling step. The adsorption mechanism was mainly governed by π–π interactions, hydrophobic effects, and hydrogen bonding. These results demonstrate that CARB_BCP, derived from biodegradable waste, is a promising low-cost adsorbent for wastewater treatment. Full article

In this work, sustainable aluminum-modified orange peels functionalized with graphene oxide (OP-Al-GO) were synthesized and evaluated for the removal of Methylene Violet (MV) and Reactive Red 120 (RR120) from aqueous solutions. Adsorption performance was systematically investigated in single-dye systems, binary dye mixtures, and real textile wastewater samples, and compared with that of orange peels (OP), orange peel–aluminum composite (OP-Al), and graphene oxide (GO). pH_pzc analysis clarified the surface charge of the adsorbent, while SEM and FTIR showed that the incorporation of aluminum and GO increased roughness and functional groups appearance, enhancing dye adsorption and confirming successful interactions. The OP-Al-GO composites exhibited improved removal efficiency for both dyes (64.8% for RR120 and 96.2% for MV) at pH 3.0. The presence of aluminum improved structural stability and surface charge regulation, while graphene oxide contributed to multiple adsorption mechanisms, including electrostatic attraction and π–π interactions. The adsorption kinetics were found to follow a pseudo-second-order (PSO) kinetic model for RR120 and an intraparticle-diffusion model (IPD) for MV, while isotherm analysis revealed a Langmuir behavior for MV and a Freundlich behavior for RR120. Langmuir maximum adsorption capacities were 298.7 and 10.8 mg/g for MV and RR120, respectively. High removal efficiency was maintained in binary dye mixtures, with OP-Al-GO achieving 96.9% removal of MV and 85.7% of RR120. Furthermore, the proposed adsorbent was tested on real wastewater samples, and the results highlight that the proposed adsorbents are promising, low-cost, and environmentally sustainable for textile wastewater treatment. Full article

Hydrogen energy is acknowledged as being the cleanest energy source. As hydrogen fuel cell technology advances, the development of low-cost, high-quality hydrogen purification technologies has grown increasingly critical. Targeting the separation of steam methane reforming gas mixture with a typical composition of H₂/CO₂/CH₄/CO = 76%/20%/3.5%/0.5%, a 6-bed-13-step pressure-swing adsorption process featuring four pressure-equalization steps was designed, in which a multi-layer adsorbent packing strategy was adopted to investigate the purification performance. The effects of feed flow rate, adsorbent packing combination, and purge-to-feed ratio on hydrogen purity and recovery, and on the impurity content level were analyzed. Furthermore, the gas-phase and solid-phase concentration distributions of each adsorbent layer under cyclic steady state were studied in detail, and the variation characteristics of their adsorption–desorption behaviors were systematically elaborated. Eventually, the optimal adsorbent combination and process condition configurations were determined. The results show that the proposed process can achieve a hydrogen purity of 99.99971%, with a concentration of CO of less than 0.2 ppm, which meets the fuel cell-grade hydrogen standard. Full article

Dyes are widely used in textile processing and are frequently discharged without adequate treatment, posing risks to aquatic ecosystems through reduced water quality, toxicity to organisms, and long-term environmental degradation. To address the need for sustainable remediation solutions, this study investigated the use of pine bark (Pinus pinaster), an abundant forestry byproduct, as a low-cost biosorbent for textile dye removal. Powdered (<0.5 mm) and granular (>1 mm) bark fractions were washed, dried, and modified through iron impregnation (10 wt.% Fe) via sonication in an FeCl₃·6H₂O solution, with one iron-coated variant subsequently subjected to thermal treatment at 400 °C under nitrogen (1 h) and hydrogen (3 h). Adsorption performance was evaluated using synthetic effluents containing Sirius Blue, Astrazon Red, and Sirius Yellow, individually and as a ternary mixture (80 mg/L each), with added NaCl and NaHCO₃ to simulate realistic conditions. Thermally treated granular iron-coated bark showed the highest removal efficiency, achieving >90% dye elimination within 24 h without detectable iron leaching, along with strong iron retention (~80%) and a 53% thermal-treatment yield. Maximum adsorption reached 15.51 mg/g at 5.0 g/L, while lower adsorbent doses increased capacity (26.8 mg/g) but reduced overall removal (~83%). Kinetic analysis was dose-dependent: the pseudo-first-order model provided the best fit at 5.0 g/L, reflecting the rapid approach to equilibrium, whereas the Elovich model fitted best at 2.5 g/L (R > 0.99), consistent with heterogeneous surface interactions under limited adsorbent availability. These results demonstrate the potential of thermally treated iron-coated pine bark as an efficient and sustainable biosorbent for textile wastewater treatment. Full article

Chlorpyrifos (CHP) is a persistent organophosphate pesticide whose presence in water poses serious ecological and health risks. Here, we report a sustainable adsorbent obtained by high-temperature carbonization of immature walnuts (Juglans regia). The adsorbent’s structure, surface chemistry, and charge properties were comprehensively characterized using FTIR, SEM-EDX, zeta potential measurement, BET analysis, and XPS. The synthesis yielded a mesoporous carbon material with a BET surface area of 303 m² g⁻¹. Its performance in CHP removal was assessed under batch and dynamic conditions. Adsorption followed pseudo-second-order kinetics (k₂ = 0.122 mg min⁻¹ g⁻¹; contact time 0–120 min). Isotherm experiments performed at 20, 25, and 30 °C, with equilibrium data best described by the Langmuir and Sips models, reaching a maximum capacity of 43.2 mg g⁻¹. Thermodynamic analysis indicated a spontaneous and endothermic process. The adsorbent demonstrated selectivity for CHP over chlorpyrifos-oxon (CPO) in binary mixtures, retained its efficiency over at least ten regeneration cycles with ethanol, and removed up to 90% of CHP toxicity, as measured by acetylcholinesterase inhibition. Dynamic filtration confirmed its applicability under flow conditions. These findings demonstrate that the investigated adsorbent is an effective, reusable, and selective adsorbent, offering a low-cost and eco-friendly approach to pesticide removal from contaminated waters. 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

In this work, biochars were produced by pyrolysis of exhausted olive pomace and evaluated as low-cost adsorbents for the removal of methylene blue (MB) from aqueous solutions. The biochar obtained at 400 °C for 1 h, which exhibited the best adsorption performance, was characterized by FTIR, N₂ adsorption–desorption isotherms, SEM-EDX, and proximate analysis, revealing a mesoporous structure with a relatively low specific surface area but enriched in surface functional groups, likely due to the partial degradation of lignocellulosic components. Adsorption experiments were conducted to optimize operational parameters such as solid particle size (2–3 mm), agitation speed (75 rpm), and bioadsorbent dosage (1 g per 0.05 L of MB solution), which allowed for dye removal efficiencies close to 100%. Kinetic studies showed that MB adsorption followed a pseudo-second-order model, while equilibrium data at 30 °C were best described by the Langmuir isotherm (R² = 0.999; SE = 4.25%), suggesting monolayer coverage and strong adsorbate–adsorbent affinity. Desorption trials using water, ethanol, and their mixtures resulted in low MB recovery, whereas the addition of 10% acetic acid significantly improved desorption performance. Under optimal conditions, up to 52% of the retained dye was recovered. Full article

Cellulose has been identified as a medium for heavy metal removal due to its high adsorption capacity in relation to these contaminants. Furthermore, cellulose is abundant and can be obtained in a practical and easy way. A notable example is E. crassipes biomass, which is abundant in wetlands and has not yet been efficiently and sustainably removed. Another biomass that has been used in heavy metal removal projects is bacterial cellulose. Generating this biomass in a laboratory setting is imperative, given its 100% cellulose composition, which ensures optimal adsorption capacities during the development of heavy metal adsorbent systems. Therefore, the objective of this project was to design biomass adsorbents that combine the properties of bacterial and E. crassipes cellulose for Cr(VI) removal. The rationale for combining these two materials is based on the premise that it will produce optimal results, a hypothesis supported by the documented efficiency of bacterial cellulose and the formidable resilience of E. crassipes biomass to elution processes. The second-order model and the Langmuir isotherm fit proved to be the most suitable, indicating that there an occurred interaction between the adsorption sites of these biomasses and Cr (VI). This suggests the presence of a significant number of active sites on the surface of these materials. The EC(50)+BC(50) biomass, with an adsorption capacity of 42 g of Cr(VI) per dollar, is the most cost-effective due to the low cost of E. crassipes and the high capacity of bacterial cellulose. It is a mixture that guarantees high adsorption capacities and facilitates up to seven reuse cycles through elutions with ethylenediaminetetraacetic acid (EDTA). This finding emphasizes the potential of this material for implementation in environmental sustainability initiatives, particularly those focused on the removal of heavy metals, including Cr(VI). Full article

Natural gas purification and the mitigation of carbon dioxide (CO₂) emissions from flue gases are critical steps in alleviating the greenhouse effect and significantly mitigate multiple environmental challenges associated with global warming. Hypercrosslinked polymers (HCPs) have become a hot topic as prospective adsorbents for gas purification and separation, owing to their low cost and scalability. Hence, TPB-Ben, TPB-Nap, and TPB-Ant were synthesized through a solvent knitting strategy, with the modification in the size of the monomers serving as a distinctive feature. This alteration aimed to explore the impact of phenyl ring quantity on the polymers’ gas adsorption and separation efficiency. All HCPs showed outstanding selective separation capability of CO₂ from CO₂/CH₄ and CO₂/N₂ mixtures, such as TPB-Ben-3-2 (CO₂/CH₄: 10.77; CO₂/N₂: 59.72), TPB-Nap-3-2 (CO₂/CH₄: 9.12; CO₂/N₂: 61.31), and TPB-Ant-3-2 (CO₂/CH₄: 10.00; CO₂/N₂: 62.89), which could be potential candidate adsorbents for natural gas purification and CO₂ capture. Considering the mild reaction conditions, low cost, efficient gas adsorption, and the potential for scalable production, these polymers are considered ideal selective solid adsorbents for capturing CO₂. This further highlights the significance of the solvent knitting strategy. Full article

In this study, we demonstrate a new all bio-based adsorbent material by treating Enteromorpho prolifera (EP) fibers with tannic acid-ferric chloride complex and then grafting hydrophobic group octadecylamine. All raw materials are easily available, low-cost, and safe. The modified EP fibers have approximately 63.4 g ${\mathrm{g}}^{-1}$ of oil absorption and 1.4 g ${\mathrm{g}}^{-1}$ of water absorption, which is an 62.8% increase in oil absorption and an 82% increase in hydrophobicity over that of untreated EP fibers, respectively, exhibiting high hydrophobicity and oleophilicity. The affinity discrimination to water and oil enables hydrophobic algae candidate materials to separate oils and water efficiently, both in an oil–water mixture and a water-in-oil emulsion. In summary, the as-synthesized modified EP demonstrates a broad application prospect in the treatment of oil spill accidents and oily wastewater. Full article

The global challenge of oil spill treatment has been addressed using nanocomposite-based natural fibers. These materials offer great potential in oil spill cleanup and are considered due to their environmental friendliness, high efficiency, and low cost. Thus, the current study reports a novel composite fabricated from date palm fiber (DPF) and recycled polyethylene terephthalate (rPET) with a proper combination of a mixture of carbon nanotubes (CNTs) and graphene nanosheets (GNSs) for oil removal. The established nanocomposite (DPF-rPET/CNT/GNS) was fabricated via physical mixing of various quantities (0.9, 0.8, and 0.7 g) of PET, along with varying loads of DPF at different proportions of CNT:GNS. The prepared nanocomposite (DPF-rPET/CNT/GNS) was fully characterized using scanning electron microscopy–energy dispersive X-ray (SEM-EDX) analysis, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analysis. In static experiments and under the optimal parameters of pH, sorbent doze, shaking time, and quantity of diesel oil), the established sorbent (DPF-rPET/CNT-GNS nanocomposite) displayed excellent adsorption capacity (98 mg/g). This study also expands the utility of the sorbent for the reusability of the oil adsorption, maintaining performance after five cycles. The adsorption data fitted well with the Langmuir isotherm model with a correlation coefficient (R²) of 0.99 and maximum adsorption capacity of 99.7 mg/g, indicating monolayer adsorption. Additionally, the adsorption kinetics followed a pseudo-second-order model, with an R² near unity and an adsorption capacity of 99.09 mg/g. This study highlights the promising potential of the DPF-rPET/CNT-GNS composite as an effective adsorbent for treating oily water. Full article

The global increase in antibiotics consumption has caused hazardous concentrations of these antimicrobials to be present in soils, mainly due to the spreading of sewage sludge (or manure or slurry) and wastewater, and they could enter the food chain, posing serious risks to the environment and human health. One of these substances of concern is cefuroxime (CFX). To face antibiotics-related environmental pollution, adsorption is one of the most widely used techniques, with cost-effective and environmentally friendly byproducts being of clear interest to retain pollutants and increase the adsorption capacity of soils. In light of this, in this work, three low-cost bioadsorbents (pine bark, oak ash, and mussel shell) were added to different soil samples (at doses of 12 and 48 t/ha) to study their effects on the adsorption of CFX. Specifically, batch experiments were carried out for mixtures of soils and bioadsorbents, adding a range of different antibiotic concentrations at a fixed ionic strength. The results showed that the addition of pine bark (with pH = 3.99) increased the adsorption to 100% in most cases, while oak ash (pH = 11.31) and mussel shell (pH = 9.39) caused a clearly lower increase in adsorption (which, in some cases, even decreased). The Freundlich and linear models showed rather good adjustment to the experimental data when the bioadsorbents were added at both doses, while the Langmuir model showed error values which were too high in many cases. Regarding desorption, it was lower than 6% for the soils without bioadsorbents, and there was no desorption when the soils received bioadsorbent amendments. These results show that the addition of appropriate low-cost bioadsorbents to soils can be effective for adsorbing CFX, helping in the prevention of environmental pollution due to this emerging contaminant, which is a result of clear relevance to environmental and human health. Full article

Dyes provide a notable environmental issue as a result of their intrinsic poisonous and carcinogenic characteristics. An estimated 60,000 metric tons of dyes has been discharged into the environment, leading to a substantial increase in water pollution. The mitigation of these dyes is a substantial and intricate challenge. The primary objective of this research is to conduct a comprehensive analysis of the adsorption of cationic dyes containing positively charged groups such as sulphonates, amines, and triphenylmethanes. The adsorption study was carried out using four different low-cost adsorbents derived from biowaste, specifically Groundnut Shell (GS), Mosambi Peel (MP), Mango Bark (MBARK), and Mango Leaves (ML). The adsorbent materials were characterized using FTIR, UV–Vis spectroscopy, scanning electron microscopy (SEM), point-of-zero charge (PZC), and BET techniques. The adsorption capacity was found to be between 1.5 and 2.2 mg/gm for Groundnut Shell, Mosambi Peel, Mango Bark, and Mango Leaves for individual dye removal (Crystal violet, Methylene blue, Rhodamine B, and Malachite green). It was observed that adsorbent derived from mango bark showed excellent adsorption (%) in a mono-component dye system and, thus, was explored for the simultaneous removal of a mixture of the same dyes. MBARK exhibited an excellent overall dye removal efficiency of 94.44% (Q_e = 2.7 mg/g) for the dye mixture in 60 min. From a detailed kinetic investigation, it was concluded that the adsorption followed the pseudo-second-order model (R²= 0.99963 to 1 for different dyes and adsorbents) hinting at chemisorption. The effect of the pH of the analyte solution and the dosage of adsorbent was also studied for simultaneous removal. The isothermal studies demonstrated that the Langmuir adsorption model (R² = 0.99416) was the best-fitted model, suggesting monolayer adsorption. The adsorption process was predicted to be governed by ion exchange, electrostatic interaction, hydrogen bonding, pi–pi interaction, etc., based on charge, functional groups, and pH of dyes and adsorbent. Thus, this study highlights the application of low-cost biowaste as a potential adsorbent for the mitigation of toxic industrial dyes present in wastewater. Full article

The hydrolysis of cellulose using ionic liquid (IL) has been extensively studied but there is limited understanding of the removal of IL from the biomass hydrolysate. Finding a suitable method for the recovery and reuse of IL is one of the biggest challenges before its large-scale application. Selecting an appropriate combined recovery process is very important. This study proposed a facile ion-exchange combined method for the recovery of IL from the modeled cellulose hydrolysate mixture containing sugars as well as γ-valerolactone (GVL) via an adsorption–desorption mechanism using sulfonic acid cation-exchange (Amberlyst 15 (H)) resin. The results showed that the resin could adsorb more than 94% of 1-ethyl-3-methylimidazolium chloride [Emim]Cl IL at ambient conditions within a contact time of 20 min. The other coexisting constituents like glucose and GVL have no significant effect on the adsorption efficiency of IL. The adsorption of IL on Amberlyst 15 (H) resin was observed to be pseudo-second-order adsorption. The regeneration of the adsorbed IL was possible up to 70% using low-cost, easily available sodium chloride (NaCl) solution. Similarly, despite the interference of other unwanted byproducts in the real biomass hydrolysate sample, an IL adsorption efficiency up to 51% was reached under similar operating conditions. This study thus opens the facile possibility of extracting and recycling IL used in the biomass hydrolysis process. Full article