Search Results (468)

Sorption and advanced oxidative processes (AOPs) are potential strategies for the removal of organic compounds, such as caffeine, from aqueous media. Such strategies tend to be more promising when combined with biopolymeric membranes as sorbents and photocatalyst supports. Therefore, the aim of the present study was to investigate sorption and AOP parameters in the performance of chitosan membranes and chitosan/TiO₂ composite membranes in individual and hybrid systems involving the photolysis, photocatalysis, and sorption of caffeine. Caffeine degradation by photolysis was 19.51 ± 1.14, 28.61 ± 0.05, and 30.64 ± 6.32%, whereas caffeine degradation by photocatalysis with catalytic membrane was 18.33 ± 2.20, 20.83 ± 1.49, and 31.41 ± 3.08% at pH 6, 7, and 8, respectively. In contrast, photocatalysis with the dispersed catalyst achieved degradation of 93.56 ± 2.12, 36.42 ± 2.59, and 31.41 ± 1.07% at pH 6, 7, and 8, respectively. These results indicate that ions present in the buffer solutions affect the net electrical charge on the surface of the composite biomaterial with the change in pH variation, occupying active sorption sites in the structure of the biomaterial, which was characterized by Fourier transform infrared spectrometry, thermogravimetric analysis, differential scanning thermogravimetry, and X-ray diffraction. Thus, it is verified that in a combined process of caffeine removal under UV irradiation and use of chitosan/TiO₂ composite membranes in phosphate-buffered medium, the photolysis mechanism is predominant, with little or no contribution from sorption, and that the TiO₂ catalyst promotes a significant reduction in the percentage of pollutant in the medium only when used dispersed and at low pH. Full article

The exponential increase in electronic waste (e-waste) from end-of-life electrical and electronic equipment presents a growing environmental challenge. E-waste contains high concentrations of rare earth elements (REEs), which are classified as critical raw materials (CRMs). Their removal and recovery from contaminated systems not only mitigate pollution but also support resource sustainability within a circular economy framework. The present study proposed the use of hazelnut shells as a biosorbent to reduce water contamination and recover REEs. The sorption capabilities of this lignocellulosic material were assessed and optimized using the response surface methodology (RSM) combined with a Box–Behnken Design (three factors, three levels). Factors such as pH (4 to 8), salinity (0 to 30), and biosorbent dose (0.25 to 0.75 g/L) were evaluated in a complex mixture containing 9 REEs (Y, La, Ce, Pr, Nd, Eu, Gd, Tb and Dy; equimolar concentration of 1 µmol/L). Salinity was found to be the factor with greater significance for REEs sorption efficiency, followed by water pH and biosorbent dose. At a pH of 7, salinity of 0, biosorbent dose of 0.75 g/L, and a contact time of 48 h, optimal conditions were observed, achieving removals of 100% for Gd and Eu and between 81 and 99% for other REEs. Optimized conditions were also predicted to maximize the REEs concentration in the biosorbent, which allowed us to obtain values (total REEs content of 2.69 mg/g) higher than those in some ores. These results underscore the high potential of this agricultural waste with no relevant commercial value to improve water quality while providing an alternative source of elements of interest for reuse (circular economy). Full article

A facile method was adopted to fabricate β-C₃N₄, and it was then doped with manganese and tellurium to obtain novel 10%MnTeO₃@β-C₃N₄ (10%MnTe@β) and 20%MnTeO₃@β-C₃N₄ (20%MnTe@β) nanohybrids. The β-C₃N₄, 10%MnTe@β, and 20%MnTe@β showed surface areas of 85.86, 97.40, and 109.54 m² g⁻¹, respectively. Using ciprofloxacin (CIP) as a pollutant example, 10%MnTe@β and 20%MnTe@β attained equilibrium at 60 and 45 min with q_t values of 48.88 and 77.41 mg g⁻¹, respectively, and both performed better at pH = 6.0. The kinetic studies revealed a better agreement with the pseudo-second-order model for CIP sorption on 10%MnTe@β and 20%MnTe@β, indicating that the sorption was controlled by a liquid film mechanism, which suggests a high affinity of CIP toward 10%MnTe@β and 20%MnTe@β. The sorption equilibria outputs indicated better alignment with the Freundlich and Langmuir models for CIP removal by 10%MnTe@β and 20%MnTe@β, respectively. The thermodynamic analysis revealed that CIP removal by 10%MnTe@β and 20%MnTe@β was exothermic, which turned more spontaneous as the temperature decreased. Applying 20%MnTe@β as the best sorbent to groundwater and seawater spiked with CIP resulted in average efficiencies of 94.8% and 91.08%, respectively. The 20%MnTe@β regeneration–reusability average efficiency was 95.14% within four cycles, which might nominate 20%MnTe@β as an efficient and economically viable sorbent for remediating CIP-contaminated water. Full article

This study presents research on the production of activated biocarbons derived from herbal waste. Sage stems were chemically activated with two activating agents of different chemical natures—H₃PO₄ and K₂CO₃—and subjected to two thermal treatment methods: conventional and microwave heating. The effect of the activating agent type and heating method on the basic physicochemical properties of the resulting activated biocarbons was investigated. These properties included surface morphology, elemental composition, ash content, pH of aqueous extracts, the content and nature of surface functional groups, points of zero charge, and isoelectric points, as well as the type of porous structure formed. In addition, the potential of the prepared carbonaceous materials as adsorbents of model organic (represented by Triton X-100 and methylene blue) and inorganic (represented by iodine) pollutants was assessed. The influence of the initial adsorbate concentration (5–150 (dye) and 10–800 mg/dm³ (surfactant)), temperature (20–40 °C), and pH (2–10) of the system on the efficiency of contaminant removal from aqueous solutions was evaluated. The adsorption kinetics were also investigated to better understand the rate and mechanism of contaminant uptake by the prepared activated biocarbons. The results showed that materials activated with orthophosphoric acid exhibited a significantly higher sorption capacity for all tested adsorbates compared to their potassium carbonate-activated counterparts. Microwave heating was found to be more effective in promoting the formation of a well-developed specific surface area (471–1151 m²/g) and porous structure (mean pore size 2.17–3.84 nm), which directly enhanced the sorption capacity of both organic and inorganic contaminants. The maximum adsorption capacities for iodine, methylene blue, and Triton X-100 reached the levels of 927.0, 298.4, and 644.3 mg/g, respectively, on the surface of the H₃PO₄-activated sample obtained by microwave heating. It was confirmed that the heating method used during the activation step plays a key role in determining the physicochemical properties and sorption efficiency of activated biocarbons. Full article

The use of widespread and inexpensive clay minerals as adsorptive agents, as well as materials obtained by their chemical modification, can contribute to the solution of the problem of environmental pollution with antibiotics. This review considers the structural features of various natural clay minerals and the effect of these features on their sorption capacity. Based on the analysis of available papers (over the last 15 years, also including some fundamental basics over the last 20–30 years), it has been established that the main property of an antibiotic molecule affecting the ability to be adsorbed by a clay mineral is the hydrophilicity of the organic substance molecule. The leading properties that determine the ability of clays to adsorb antibiotics are the charge and area of their surfaces. The ability of antibiotic molecules to protonate and a partial change in the edge charge of mineral layers is determined by the acidity of the sorption solution. In addition, empirical evidence is provided that the most important factors affecting adsorption are the ionic strength of the sorption solution, the concentration of the adsorbent and adsorbate, and the interaction temperature. The diversity of the composition, structure, and properties of clay minerals allows them to be effective sorbents for a wide range of antibiotics. Full article

This study aims to evaluate the potential of Lemna minor (common duckweed) for the removal of galaxolide (HHCB) from polluted water, a compound commonly used in consumer products such as perfumes and detergents. The focus was to identify the optimal conditions for removal, determine the removal efficiency, and elucidate the mechanisms involved. The experiment was conducted by cultivating Lemna minor using as a cultivation medium synthetic sewage and laboratory solutions (MilliQ water) containing galaxolide at two levels of concentration (1034 µg·L⁻¹ and 2326 µg·L⁻¹). The plants were exposed to light for 16 h a day and grown at pH 5. Removal efficiency was assessed through liquid chromatography (HPLC) with fluorescence detection (FLD). Kinetics of observed process was modelled using a pseudo-first-order equation. The study of the HHCB decay mechanism included determining the contributions to the final effect of the following processes occurring simultaneously: sorption on the plant surface, photodegradation, and uptake by Lemna. The removal efficiency (RE%) of galaxolide by Lemna minor was 99.7% when aqueous standard solution was used as the cultivation medium after 14 days, and between 97.8% and 98.6% in the case of wastewater samples. Sorption onto plants surface, photodegradation, and uptake by the plants were identified as the primary mechanisms for HHCB removal. Toxicity studies revealed that galaxolide exposure adversely affected Lemna minor growth, altering photosynthetic pigments (chlorophyll and carotenoid) levels. Full article

Globally, phosphogypsum (PG) is the primary by-product of the phosphorus industry. Aspergillus niger (A. niger), one of the most powerful types of phosphate-solubilizing fungi (PSF), can secrete organic acids to dissolve the phosphates in PG. This study investigated heavy metal (HM) remediation by PG and A. niger under the co-existence of Pb and Cd. It demonstrated that 1 mmol/L Pb²⁺ stimulated the bioactivity of A. niger during incubation, based on the CO₂ emission rate. PG successfully functioned as P source for the fungus, and promoted the growth of the fungal cells. Meanwhile, it also provided sulfates to immobilize Pb in the solution. The subsequently generated anglesite was confirmed using SEM imaging. The immobilization rate of Pb reached over 95%. Under co-existence, Pb²⁺ and 0.01 mmol/L Cd²⁺ maximized the stimulating effect of A. niger. However, the biotoxicity of Pb²⁺ and elevated Cd²⁺ (0.1 mmol/L) counterbalanced the stimulating effect. Finally, 1 mmol/L Cd²⁺ dramatically reduced the fungal activity. In addition, organic matters from the debris of A. niger could still bind Pb²⁺ and Cd²⁺ according to the significantly lowered water-soluble Pb and Cd concentrations. In all treatments with the addition of Cd²⁺, the relatively high biotoxicity of Cd²⁺ induced A. niger to absorb more Pb²⁺ to minimize the sorption of Cd²⁺ based on the XRD results. The functional group analysis of ATR-IR also confirmed the phenomenon. This pathway maintained the stability of Pb²⁺ immobilization using the fungus and PG. This study, hence, shed light on the application of A. niger and solid waste PG to remediate the pollution of Pb and Cd. 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

Activated carbon prepared from coconut shell was characterized using SEM/EDS, N₂-sorption, XRD analysis, Raman, and FTIR spectroscopy. It was then evaluated in terms of its capacity to adsorb nitrobenzene, a priority pollutant, from water samples with varying pH levels. Initial studies revealed high adsorption capacity; further studies were broadened to include nitrobenzene derivative, dinitrobenzene, as real samples are expected to contain a mixture of these pollutants. The maximum amount of adsorbed adsorbate increased notably with temperature, reaching 12.88 mg g⁻¹ and 42.75 mg g⁻¹ for nitrobenzene and dinitrobenzene, respectively, at 35 °C. Thermodynamic considerations and determined values of ∆G⁰ and ∆S⁰ indicated that the adsorption process of both nitrobenzene and dinitrobenzene is spontaneous and ∆H⁰ value indicated that it is endothermic in the studied temperature range. A study of the simultaneous adsorption of nitrobenzene and dinitrobenzene indicated a higher affinity toward dinitrobenzene. This study pointed out that coconut shell-derived activated carbon holds high potential as an adsorbent for removing nitrobenzene and its derivatives from water samples. Full article

High levels of pesticide use are associated with intensive crop production. Pesticides are increasingly prevalent in surface and groundwater, which is a major environmental concern. Various methods have been proposed to improve the retention and/or degradation of pesticides in soils. These methods are mainly based on soil adaptation with organic wastes to mitigate soil and water pollution. In addition, there has recently been increased interest in assessing the influence of organic waste additions on pesticide movement in soils with low contents of organic matter. Agriculture and related industries generate large amounts of waste each year. Because of their components, they have the great ability to produce high-value products for environmental restoration. This study reports on the influence of four different agro-industrial wastes (orange peel, beer bagasse, grape pomace, and gazpacho waste) used as organic amendments on the leaching of metobromuron and chlorbromuron (phenylurea herbicides) on a silty clay loam soil (gypsic–calcaric regosol) with low organic matter contents from a semiarid area (southeastern Spain). The adsorption, leaching, and dissipation processes of these herbicides were evaluated on a laboratory scale in amended and unamended soils. In addition, the main leaching indices (GUS, LIX, LEACH, M LEACH, LIN, GLI, HI, and ELI) commonly used to assess groundwater protection against pesticide pollution were evaluated. The sorption coefficients (K_OC) increased in the amended soils. Metobromuron was found in leachates in all cases, although a marked reduction was observed in amended soils, while chlorbromuron was mainly retained in soils, especially in the top layer. The disappearance time (DT₅₀) for metobromuron and chlorbromuron in soil ranged from 11 to 56 d and 18 to 95 d, respectively. All indices except GLI categorize metobromuron as mobile or very mobile in unamended soil. For chlorbromuron, GUS, LIX, LEACH, MLEACH, and Hornsby classify this compound as a medium-to-high leache, while GLI and ELI classify it as having low mobility. In amended soils, most indices classify metobromuron as transitioning to mobile, while most indices catalog chlorbromuron as immobile/transition. 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

Water contamination with toxic pollutants such as heavy metals, oil spills, organic and inorganic dyes, pesticides, etc., causes severe environmental and human health pollution. Aerogels have gained increasing attention in recent years as promising adsorbents due to their outstanding properties. This paper critically evaluates the recent advancements in aerogel-based materials, highlighting their challenges, limitations, and practical applications in large-scale experiments. The influence of key parameters such as adsorbent dosage, solution pH, ionic strength, and temperature is also discussed. Integrating nanotechnology and advanced manufacturing methods, a new generation of high-performance adsorbents with increased sorption capacity and reusability could be developed. Additionally, pilot studies and field trials are highlighted in this review, showing aerogels’ practical and real-world applications. Although various gaps in the production process that limit aerogel implementation in the market still exist, the research progress in the field shows that novel aerogels could be used in real wastewater treatment in the future. This review underscores the need for future research to develop advanced aerogel-based materials using green and sustainable synthesis methods that can lead to full-scale application. 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

This review reports some aspects of soil contaminant chemistry and its fundamental role in shaping the soil–human health relationship. Exposure to soil contaminants can occur through direct pathways, such as ingestion, inhalation, and dermal contact, as well as indirect pathways, including food chain contamination via plant uptake or groundwater leaching. The mobility and persistence of organic and inorganic pollutants in soil are primarily controlled by sorption–desorption processes, which involve a complex interplay of physical and chemical mechanisms. Soil properties, such as pH, organic matter content, clay minerals, and oxide hydroxides, play a crucial role in regulating these processes and determining contaminant behavior. A high sorption capacity enhances the soil’s ability to mitigate pollutant mobility, thereby reducing their infiltration into groundwater and accumulation in the food chain. Soils rich in organic matter and fine-textured minerals, such as clay, can effectively immobilize contaminants, limiting their bioavailability and potential harm to human health. A deeper understanding of how soil characteristics influence contaminant mobility and bioavailability is critical to addressing the hazards of soil pollution for human health. Beyond merely assessing contaminant concentrations, it is essential to consider the dynamic processes governing pollutant fate in soil, as they ultimately shape exposure pathways and health risks. This knowledge is the key to developing more effective strategies for mitigating soil contamination and protecting public health. Full article