Search Results (843)

The sorption process is most commonly described by Langmuir isotherms, which can be calculated from either a non-linear form or various linear forms. Despite the fact that the non-linear model is now preferred, articles using linear models continue to be submitted to journals. On the basis of 68 isotherms, it was found that the linear Hanes–Woolf model (the most commonly used) gives the most similar q_m and K_L values to the non-linear model. The largest differences were obtained by determining the isotherm from the non-linear and linear forms of the Lineweaver–Burk model (this is the model often used by researchers). The evaluation of isotherms should not be performed solely on the basis of the coefficient of determination R², which was intended for linear equations. Statistical measures such as the mean relative error, sum of squares of errors, chi-square statistic, sum of absolute errors, hybrid fractional error function, mean squared error were analysed. On the basis of the coefficient of determination, the Hanes–Woolf linear model was found to best describe the actual results, and on the basis of the other statistical measures, the isotherm determined from the non-linear form was found to be the best fit for the study. 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

We studied the adsorption thermodynamics and mechanism behind the binding of nitric oxide (NO) in the interior surfaces and structural fragments of the high metal center density microporous Metal-Organic Framework (MOF) CPO-27-Cu, by gas sorption, at a series of temperatures. For the purpose of comparison, we also measured the corresponding CO₂ adsorption isotherms, and as a result, the isosteric heats of adsorption for the two studied adsorptives were derived, being in the range of 12–15 kJ/mol for NO at loadings up to 0.5 NO molecules per formula unit (f.u.) of the bare compound (C₄O₃HCu), and 23–25 kJ/mol CO₂ in the range 0–1 CO₂ per f.u. Microscopically, the mode of NO binding near the square pyramid Cu(II) centers was directly accessed with the use of in situ NO gas adsorption X-ray Absorption Spectroscopy (XAS). Additionally, during the vacuum/temperature activation of the material and consequent NO adsorption, the electronic state of the Cu-species was monitored by observing the corresponding X-ray Near Edge Spectra (XANES). Contrary to the previously anticipated chemisorption mechanism for NO binding at Cu(II) species, we found that at slightly elevated temperatures, under ambient, but also cryogenic conditions, only relatively weak physisorption takes place, with no evidence for a particular adsorption preference to the coordinatively unsaturated Cu-centers of the material. Full article

In this study, we tested a flexible polyurethane (PU) foam, synthesized from bio-based components, for the removal of petroleum-derived fuels from water samples. The PU was synthesized via the prepolymer method through the reaction of PEG 400 with L-lysine ethyl ester diisocyanate (L-LDI), followed by chain extension with 2,5-bis(hydroxymethyl)furan (BHMF), a renewable platform molecule derived from carbohydrates. Freshwater and seawater samples were artificially contaminated with commercial diesel, gasoline, and kerosene. Batch adsorption experiments revealed that the total sorption capacity (S, g/g) of the PU was slightly higher for diesel in both water types, with values of 67 g/g in freshwater and 70 g/g in seawater. Sorption kinetic analysis indicated that the process follows a pseudo-second-order kinetic model, suggesting strong chemical interactions. Equilibrium data were fitted using Langmuir and Freundlich isotherm models, with the best fit achieved by the Langmuir model, supporting a monolayer adsorption mechanism on homogeneous surfaces. The PU foam can be regenerated up to 50 times by centrifugation, maintaining excellent performance. This study demonstrates a promising application of this sustainable and bio-based polyurethane foam for environmental remediation. Full article

This study reported covalent organic frameworks (COFs) and their hybrid composites with two-dimensional materials, graphene oxide (GO), graphitic carbon nitride (g-C₃N₄), and boron nitride (BN), to examine their structural, textural, and gas adsorption properties. Material characterization confirmed the crystallinity of COF-1 and the preservation of framework integrity after integrating the 2D nanomaterials. FT-IR spectra exhibited pronounced vibrational fingerprints of imine linkages and validated the functional groups from the COF and the integrated nanomaterials. TEM images revealed the integration of the two components, porous, layered structures with indications of interfacial interactions between COF and 2D nanosheets. Nitrogen adsorption–desorption isotherms revealed the microporous characteristics of the COFs, with hysteresis loops evident, indicating the development of supplementary mesopores at the interface between COF-1 and the 2D materials. The BET surface area of pristine COF-1 was maximal at 437 m²/g, accompanied by significant micropore and Langmuir surface areas of 348 and 1290 m²/g, respectively, offering enhanced average pore widths and hierarchical porous strcuture. CO₂ adsorption tests were investigated showing maximum adsorption capacitiy of 1.47 mmol/g, for COF-1, closely followed by COF@BN at 1.40 mmol/g, underscoring the preserved sorption capabilities of these materials. These findings demonstrate the promise of designed COF-based hybrids for gas capture, separation, and environmental remediation applications. Full article

Rare earth metals (REMs) are vital for high-tech industries, but their extraction from secondary sources is challenging due to environmental and technical constraints. This study investigates the ion-exchange extraction of light REMs (neodymium, praseodymium, and samarium) from sulfuric and phosphoric acid solutions, modeling industrial leachates from apatite concentrates and phosphogypsum. The study considers the use of anion- and cation-exchange resins with different functional groups for efficient and environmentally safe REM separation. Experimental sorption isotherms were obtained under static conditions at 298 K and analyzed using a thermodynamic model based on the linearization of the mass action equation. Equilibrium constants and Gibbs energy were calculated, which reveals the spontaneity of the processes. Cation-exchange resins demonstrated high selectivity towards individual REMs, while anion-exchange resins were suitable for group extraction. Infrared spectral analysis confirmed the presence of sulfate and phosphate complexes in the resin matrix, clarifying the ion-exchange mechanisms. Thermal effect measurements indicated exothermic sorption on anion-exchange resins with negative entropy and endothermic sorption on cation-exchange resins with positive entropy. The findings highlight the potential of ion-exchange resins for selective and sustainable REM recovery, offering a safer alternative to liquid extraction and enabling the valorization of industrial wastes like phosphogypsum for resource recovery. Full article

Waste and chemicals generated from industry have been a major source of pollution and a prominent threat to human health via the food chain; hence, an efficient and durable material that can be used to detoxify polluted soil and water bodies is necessary to attain ecosystem equity and security. This study hypothesized that biochar (BC) made from poultry manure (PM) through pyrolysis and fortification with iron (Fe–BC) can be used to remove methyl orange dye from aqueous solution. Furthermore, this study evaluated the effect of solution pH on the sorption of methyl orange through batch sorption studies. The similarity in the modeled data and experimental data was measured by the standard error of estimate, whereas sorption isotherms were examined using nonlinear forms of different sorption equations. With the use of Langmuir models, a maximum sorption capacity of 136.25 mg·g⁻¹ and 98.23 mg·g⁻¹ was recorded for Fe–BC and BC, respectively. Fe–BC possessed a higher adsorption ability in comparison to BC. The pseudo-second-order best described the sorption kinetics of both adsorbents at R² = 0.9973 and 0.9999, indicating a strong interaction between MO and Fe–BC. Furthermore, the efficiency with which MO was removed by the absorbent was highest at lower pH (pH = 4). It is therefore concluded that Fe–BC can be used as an effective and environmentally friendly material for detoxification of wastewater; however, further research on the application and usage of biochar modified techniques for enhancing adsorption efficacy on a large scale should be encouraged. Full article

Herein, a novel super-hygroscopic material, steam-exploded modified corn stalk pith (SE-CSP), was developed from corn stalk pith (CSP) via the steam explosion (SE) method, and its hygroscopic properties and mechanisms were evaluated. The results confirmed that SE effectively removed lignin and hemicellulose, disrupted the thin cell walls of natural CSP, and formed an aligned porous structure with capillary channels. SE changed the bonding distribution and surface morphology, and enhanced the crystallinity and thermal stability of CSP. The equilibrium hygroscopic percentage of SE-CSP (62.50%) was higher than that of CSP (44.01%) at 25 °C and 80% relative humidity (RH), indicating significantly greater hygroscopicity. The hygroscopic process of SE-CSP followed a Type III isotherm and fitted the Guggenheim–Anderson–de Boer (GAB), Peleg, and pseudo-first-order kinetic models. This process exhibited multi-layer adsorption with enthalpy-driven, exothermic behavior, primarily through physical adsorption involving hydrogen bonds and van der Waals forces. This work offered a new approach for advancing sorption dehumidification technology. Full article

Developing sustainable packaging materials has become a global priority in response to environmental concerns associated with conventional plastics. This study used a wheat flour byproduct (glue flour, GF) and poly(butylene adipate-co-terephthalate) (PBAT) to produce films via blown extrusion, incorporating rosemary extract (RE) at 2% (FRE2) and 4% (FRE4) (w/w). A control film (FCO) was formulated without RE. The physicochemical, thermal, mechanical, and biodegradation properties of the films were evaluated. FCO, FRE2, and FRE4 exhibited tensile strength (TS) values between 8.16 and 9.29 MPa and elongation at break (ELO) above 889%. Incorporating 4% RE decreased luminosity (91.38 to 80.89) and increased opacity (41.14 to 50.95%). A thermogravimetric analysis revealed a main degradation stage between 200 °C and 450 °C, with FRE2 showing the highest residual mass (~15% at 600 °C). Sorption isotherms indicated enhanced hydrophobicity with RE, thereby reducing the monolayer moisture content from 5.23% to 3.03%. Biodegradation tests revealed mass losses of 64%, 58%, and 66% for FCO, FRE2, and FRE4, respectively, after 180 days. These findings demonstrate that incorporating RE into GF/PBAT blends via blown extrusion is a promising strategy for developing biodegradable films with enhanced thermal behavior, mechanical integrity, and water resistance, contributing to the advancement of sustainable packaging materials. Full article

Sugarcane bagasse-derived biochars, produced at 350 °C (B350) and 600 °C (B600), were evaluated for their capacity to modify the sorption behavior of the herbicide sulfentrazone (SFZ) in Red–Yellow Latosol (RYL) and to serve as carriers for its controlled release. Batch sorption experiments indicated that SFZ exhibits low affinity for soil and undergoes sorption–desorption hysteresis. Adding B350 biochar (up to 0.30%) did not significantly affect the herbicide sorption, whereas B600 enhanced its retention. Sequential desorption assays were conducted by incorporating SFZ either directly into the soil or into the biochars, which were subsequently blended into the soil (at 0.15% w/w). The SFZ desorbed more rapidly from the soil than from the biochars, suggesting that the pyrogenic material has potential for modulating herbicide release. Phytotoxicity assessments using Sorghum bicolor confirmed that only SFZ incorporated into B350 (at 0.15% w/w) retained herbicidal efficacy comparable to its direct application in soil. These findings underscore the potential of B350 biochar as a controlled-release carrier for SFZ without compromising its weed control effectiveness. Full article

Occupational exposure to commercial formic and acetic acids through dermal contact and inhalation during rubber sheet processing poses significant health risks to workers. Additionally, the use of these acids contributes to environmental pollution by contaminating water sources and soil. This study investigates the potential of three types of wood vinegar—derived from para-rubber wood, bamboo, and eucalyptus—obtained through biomass pyrolysis under anaerobic conditions, as sustainable alternatives to formic and acetic acids in the production of ribbed smoked sheets (RSSs). The organic constituents of each wood vinegar were characterized using gas chromatography and subsequently mixed with fresh natural latex to produce coagulated rubber sheets. The physical and chemical properties, equilibrium moisture content, and drying kinetics of the resulting sheets were then evaluated. The results indicated that wood vinegar derived from para-rubber wood contained a higher concentration of acetic acid compared to that obtained from bamboo and eucalyptus. As a result, rubber sheets coagulated with para-rubber wood and bamboo vinegars exhibited moisture sorption isotherms comparable to those of sheets coagulated with acetic acid, best described by the modified Henderson model. In contrast, sheets coagulated with eucalyptus-derived vinegar and formic acid followed the Oswin model. In terms of physical and chemical properties, extended drying times led to improved tensile strength in all samples. No statistically significant differences in tensile strength were observed between the experimental and reference samples. The concentration of acid was found to influence Mooney viscosity, the plasticity retention index (PRI), the thermogravimetric curve, and the overall coagulation process more significantly than the acid type. The drying kinetics of all five rubber sheet samples displayed similar trends, with the drying time decreasing in response to increases in drying temperature and airflow velocity. Full article

Chabazite, a tectosilicate mineral, belongs to the zeolite group and has been widely used for the adsorptive removal of a number of cationic contaminants from the aqueous phase. However, a negatively charged chabazite surface can be altered by chemical modification in order to change its adsorption abilities towards anions. This study reports the potential for the removal of hexavalent chromium ions from aqueous solutions by modified chabazite. In this regard, natural chabazite was modified by the immobilization of HDTMA-Br to achieve double-layer coverage on its surface, defined as the double external cation exchange capacity. Next, a batch adsorption system was applied to study the adsorption of inorganic Cr(VI) anions from aqueous solutions. The process equilibrium was described by 11 theoretical isotherm equations, while 6 adsorption kinetics were represented by four models. Among those tested, the most appropriate model for the description of the studied process kinetics was the pseudo-second order irreversible model. The obtained results suggest that Cr(VI) adsorption takes place according to a complex mechanism comprising both Langmuir-type sorption with the maximum adsorption capacity of modified chabazite, approx. 9.3–9.9 mg g⁻¹, and the trapping of Cr(VI) inside the capillaries of the amorphous sorbent, making it a viable option for water treatment applications. Full article

The removal of mercury(II) from aquatic environments using polyurea-crosslinked calcium alginate (X-alginate) aerogels was investigated through batch-type experiments, focusing on low mercury concentrations (50–180 μg·L⁻¹), similar to those found in actual contaminated environments. Within this concentration range, the metal retention was very high, ranging from 85% to quantitative (adsorbent dosage: 0.6 g L⁻¹). The adsorption process followed the Langmuir isotherm model with a sorption capacity of 4.4 mmol kg⁻¹ (883 mg kg⁻¹) at pH 3.3. Post-adsorption analysis with EDS confirmed the presence of mercury in the adsorbent and the replacement of calcium in the aerogel matrix. Additionally, coordination/interaction with other functional groups on the adsorbent surface may occur. The adsorption kinetics were best described by the pseudo-first-order model, indicating a diffusion-controlled mechanism and relatively weak interactions. The adsorbent was regenerated via washing with a Na₂EDTA solution and reused at least three times without substantial loss of sorption capacity. Furthermore, X-alginate aerogels were tested for mercury removal from an industrial wastewater sample (pH 7.75) containing 61 μg·L⁻¹ mercury (and competing ions), achieving 71% metal retention. These findings, along with the stability of X-alginate aerogels in natural waters and wastewaters, highlight their potential for sustainable mercury removal applications. Full article

The snack market is shifting toward healthier options, leading to a growing interest in organic snacks. Dried fruits are particularly popular due to their long shelf life and convenience. Freeze-drying helps preserve both the taste and nutrients of these fruits. Among them, peaches are noteworthy for their antioxidant and anti-inflammatory properties. The research assessed the impact of lactic fermentation using Lactiplantibacillus plantarum (P_LP) and Fructilactobacillus fructivorans (P_FF), followed by freeze-drying, on the physicochemical, structural, and sensory properties of peach slices. Fermentation increased acidity (>22 mg/kg), decreased sugars (up to 43.5%), and raised salt content (to ~0.5%), effectively altering the fruit’s chemical profile. Dry matter content decreased by 6.0% (P_LP) and 7.2% (P_FF), while water activity remained low (0.13–0.15). Color parameters changed notably: L* values decreased, and a* values increased, with total color differences (ΔE) exceeding 15. Structural changes included higher porosity (to 71.4% in P_LP and 72.8% in P_FF) and reduced hardness from 50.1 N (control) to 35.7 N (P_LP) and 28.2 N (P_FF), which may benefit processing. Water sorption isotherms suggested improved stability under elevated humidity. However, sensory analysis showed lower consumer acceptance of the fermented samples due to reduced sweetness, crunchiness, and overall palatability, along with undesirable flavors from F. fructivorans. While lactic fermentation holds the potential for creating fruit snacks with better functional value, further optimization is needed to enhance sensory appeal and market potential. Full article

Microplastic (MPs) pollution has emerged as a critical environmental issue due to its persistent accumulation in ecosystems, posing risks to aquatic life, food safety, and human health. In this study, magnetic Fe₃O₄ nanoparticles functionalized with citric acid (Fe₃O₄@AC) were used to remove high-density polyethylene (HDPE), low-density polyethylene (LDPE), and polypropylene (PP) MPs from an aqueous medium. Fe₃O₄@AC was synthesized via the coprecipitation method and characterized by morphology (SEM), crystalline phases (XRD), chemical aspects (FTIR), and surface area (nitrogen sorption isotherms). The MPs removal efficiency of Fe₃O₄@AC was evaluated based on the initial concentration, contact time, and pH. The adsorption isotherm and kinetics data were best described by the Sips and pseudo-second-order models, respectively. Fe₃O₄@AC removed 80% of the MPs at a pH of 6. Based on experimental observations (zeta potential, porosity, and SEM) and theoretical insights, it was concluded that hydrogen bonding, pore filling, and van der Waals forces governed the adsorption mechanism. Reusability tests showed that Fe₃O₄@AC could be reused up to five times, with a removal efficiency above 50%. These findings suggest that Fe₃O₄@AC is a sustainable and promising material for the efficient removal of microplastics from wastewater, offering a reusable and low-impact alternative that contributes to environmentally responsible wastewater treatment strategies. Full article