Search Results (6,718)

Depression is becoming more common in the face of modern life’s obstacles. Antidepressants are a fast-expanding pharmaceutical category. Antidepressant residues in water must be closely monitored and kept at levels that do not endanger human health, just like those of other psychotropic medications. Additionally, research has shown that these pollutants severely hinder aquatic life’s ability to migrate, reproduce, and interact with one another when they enter natural ecosystems. Antidepressants released into the natural environment can therefore be expected to have an impact on exposed fish and other aquatic species. There is a lot of information available about how exposure affects fish, but much of it is for exposure levels higher than those seen in their natural habitats. Antidepressants can bioaccumulate in fish tissues, and some behavioral effects have been documented for exposures that are relevant to the environment. As a result, antidepressant residue removal methods must be incorporated into contemporary wastewater treatment plant technology. In addition to covering a wide range of suggested treatment options and their ecotoxicological consequences on non-target organisms, this study discusses recent efforts to accomplish this goal. First, a thorough analysis of the harmful impacts on non-target people is provided. This work describes a variety of adsorptive methods that can make use of modern materials like molecularly imprinted polymers or ion-exchange resins or can rely on well-known and efficient adsorbents like silicates or activated carbon. Although extractive methods are also taken into consideration, they are now impractical due to the lack of reasonably priced and ecologically suitable solvents. Lastly, sophisticated oxidation methods are discussed, such as electrochemical alternatives, UV and gamma radiation, and ozone therapy. Notably, some of these techniques could totally mineralize antidepressant toxicants, either alone or in combination. Lastly, the topic of biological treatment with microorganisms is covered. This method can be very specific, but it usually prevents full mineralization. Full article

The reverse water–gas shift (RWGS) reaction efficiently converts CO₂ to CO, with vital applications in carbon emission reduction and Fischer-Tropsch chemical production. This study used density functional theory (DFT) to investigate CO₂ adsorption and activation on CeO₂, oxygen-vacancy CeO₂ (CeO_2−x), and single-atom Ni-loaded CeO₂ (Ni/CeO₂). Adsorption energy analysis indicates that CO₂ preferentially adsorbs at the intermediate oxygen sites on CeO₂ and Ni/CeO₂, but on CeO_2−x, it preferentially adsorbs at the oxygen vacancies. Mulliken charge and band gap results indicate that CeO_2−x and Ni/CeO₂ exhibit higher activity than pure CeO₂. Density of states studies indicate that CeO₂, CeO_2−x, and Ni/CeO₂ can activate CO₂ to varying degrees; strong hybridization between Ni’s d-orbitals and CO₂’s O p-orbitals is key to Ni/CeO₂’s high activity. Mechanistically, CeO_2−x follows the RWGS redox mechanism, while Ni/CeO₂ follows the formate-associated mechanism. This work innovatively clarifies differential CO₂ adsorption-activation by vacancies and Ni in CeO₂-based catalysts, providing a theoretical basis for RWGS catalyst design and supporting low-energy carbon conversion development. Full article

The main goal of this study is to address the problem of environmental water pollution caused by organic dyes through waste valorization by synthesizing geopolymer-based adsorbents. In this work, geopolymers were synthesized using fly ash modified with chitosan and polyvinyl alcohol as a starting material. The obtained materials were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and determination of the point of zero charge. We examined the adsorption potential for organic dye (methylene blue, brilliant green, crystal violet) removal through the influence of contact time, initial pH and concentration of adsorbate solution, and temperature on adsorption. The obtained results were analyzed using theoretical kinetics and isotherm models. Interpretation of the obtained results was performed using the Box–Behnken design and chemometric methods of multivariate analysis. The findings showed that modification with chitosan significantly enhanced the adsorption efficiency of the synthesized materials up to 95.9% for methylene blue adsorption. The parameters identified as having the greatest influence on the adsorption process were contact time, pH-value, initial dye concentration, and the type of dye being adsorbed. Full article

Efficient coalbed methane (CBM) recovery combined with carbon dioxide (CO₂) sequestration is a promising strategy for sustainable energy production and greenhouse gas mitigation. However, the molecular mechanisms controlling pressure-dependent CH₄ displacement by CO₂ in coal nanopores remain insufficiently understood. In this study, molecular dynamics simulations were conducted to investigate CO₂-driven CH₄ recovery in a slit-pore coal model under driving pressures of 15, 20, and 25 Mpa. The simulations quantitatively captured the competitive adsorption, diffusion, and migration behaviors of CH₄, CO₂, and water, providing insights into how pressure influences enhanced coalbed methane (ECBM) recovery at the nanoscale. The results show that as the pressure increases from 15 to 25 Mpa, the mean residence time of CH₄ on the coal surface decreases from 0.0104 ns to 0.0087 ns (a 16% reduction), reflecting accelerated molecular mobility. The CH₄–CO₂ radial distribution function peak height rises from 2.20 to 3.67, indicating strengthened competitive adsorption and interaction between the two gases. Correspondingly, the number of CO₂ molecules entering the CH₄ region grows from 214 to 268, demonstrating higher invasion efficiency at elevated pressures. These quantitative findings illustrate a clear shift from capillary-controlled desorption at low pressure to pressure-driven convection at higher pressures. The results provide molecular-level evidence for optimizing CO₂ injection pressure to improve CBM recovery efficiency and CO₂ storage capacity. Full article

This study compares the operational performance of membrane capacitive deionization (MCDI) and circulation-MCDI (C-MCDI) under symmetric (2/2, 3/3, 4/4 min) and asymmetric (5/2, 5/3, 5/4 min) adsorption/desorption cycles to identify efficient operating conditions at the pilot scale. A pilot system was tested with a NaCl solution of about 1000 mg/L, and 15 consecutive cycles were conducted to evaluate removal efficiency, specific energy consumption (SEC), and stability. MCDI consistently achieved over 90% removal efficiency with SEC below 0.6 kWh/m³ across all modes, maintaining stable performance over 15 cycles. The 2/2 condition provided the shortest cycle time and the highest treated water productivity, making it the most efficient condition for the pilot-scale MCDI tested. C-MCDI showed stronger dependence on operating conditions, with the number of stable cycles ranging from 3 to 7 depending on desorption duration. Nevertheless, the 5/2 condition achieved about 91% removal efficiency with 0.58 kWh/m³ SEC, and its extended adsorption period yielded about 2.5 times more treated water per cycle than the 2/2 case. Overall, this work provides a comparative pilot-scale evaluation of MCDI and C-MCDI, highlighting their advantages, limitations, and potential applications, and offering practical insights for energy-efficient and sustainable desalination strategies. Full article

Investigating ecological irrigation risks associated with mine water utilization is of great significance for alleviating water resource shortages in arid mining regions of western China, thereby supporting efficient coal extraction and coordinated ecological development. In this study, a representative mining area in Xinjiang was investigated to reveal the evolution patterns of mine water quality under arid geo-environmental conditions in western China and to systematically assess environmental risks induced by ecological irrigation. Surface water, groundwater, and mine water samples were collected to study ion ratio coefficients, hydrochemical characteristics, and evolution processes. Based on this, a multi-index analysis was employed to evaluate ecological irrigation risks and establish corresponding risk control measures. The results show that the total dissolved solids (TDS) of mine water in the study area are all greater than 1000 mg/L. The evolution of mine water quality is mainly controlled by water–rock interaction and is affected by evaporation and concentration. The main ions Na⁺, Cl⁻, Ca²⁺, and SO₄²⁻ originate from the dissolution of halite, gypsum, and anorthite. If the mine water is directly used for irrigation without treatment, the soluble sodium content, sodium adsorption ratio, salinity hazard, and magnesium adsorption ratio will exceed the limits, leading to the accumulation of Na⁺ in the soil, affecting plant photosynthesis, and posing potential threats to the groundwater environment. Given the evolution process of mine water quality and the potential risks of direct use for irrigation, measures can be taken across three aspects: nanofiltration combined with reverse osmosis desalination, adoption of drip irrigation and intermittent irrigation technologies, and selection of drought-tolerant vegetation. These measures can reduce the salt content of mine water, decrease the salt accumulation in the soil layer, and lower the risk of groundwater pollution, thus reducing the environmental risks of ecological irrigation with mine water. The research will provide an important theoretical basis for the scientific utilization and management of mine water resources in arid areas by revealing the evolution law of mine water quality in arid areas and clarifying its ecological irrigation environmental risks. Full article

Fly ash from coal-fired power plants is a promising precursor for zeolite synthesis due to its aluminosilicate-rich composition. However, its direct utilization is often limited by impurities and a low silicon-to-aluminum ratio (SAR). This study demonstrates the conversion of Class C fly ash from the Soma thermal power plant (Turkey) into FAU- and CHA-type zeolites through optimized acid leaching and hydrothermal synthesis. Acid treatment increased the SAR from 1.33 to 2.85 and effectively reduced calcium-, sulfur-, and iron-bearing impurities. The SAR enhancement by acid leaching was found to be reproducible among Class C fly ashes, whereas Class F materials exhibited a limited response due to their acid-resistant framework. Subsequent optimization of alkaline fusion-assisted synthesis enabled selective crystallization of FAU and CHA, while GIS and MER appeared under prolonged crystallization or higher alkalinity. SEM revealed distinct morphologies, with MER forming rod-shaped clusters, and CHA exhibiting disc-like aggregates. Water sorption analysis showed superior uptake for metastable FAU (~23 wt%) and CHA (~18 wt%) compared to stable GIS and MER (~12–13 wt%). Overall, this study establishes a scalable and sustainable route for producing high-performance zeolites from industrial fly ash waste, offering significant potential for adsorption-based applications in dehumidification, heat pumps, and gas separation. Full article

Coalbed methane (CBM) development involves multiple interacting physical fields, and different coupling schemes can lead to distinctly different production behaviors. A thermo-hydro-mechanical model accounting for gas–water two-phase flow and matrix dynamic diffusion (TP-D-THM) is developed and validated, achieving an error rate below 10%. By embedding the numerically estimated reservoir physical parameters of the Qinshui Basin into the numerical model, multi-field couplings during CBM production, the evolution of physical parameters, and the depth-dependent effects on production characteristics were revealed. The main findings are as follows: The inhibitory effect of water on CBM recovery consistently exceeds the promoting effect of temperature. As burial depth expands, the inhibitory effect first diminishes, then intensifies, ranging from 19.73% to 28.41%, while the thermal promotion effect exhibits a monotonically increasing trend, fluctuating between 8.55% and 16.33% and stabilizing below 1000 m. Temperature and burial depth do not alter the trend in gas production rate. For equilibrium permeability, reproducing a decrease–increase–decrease rate pattern requires explicit inclusion of water and matrix-fracture mass exchange terms, which can explain why different scholars obtained varying gas production rate trends using the THM model. Matrix adsorption-induced strain is the primary control on permeability evolution, and temperature amplifies the magnitude of permeability change. The critical depth essentially reflects the statistical characteristics of reservoir petrophysical properties. A dimensionless critical depth criterion has been proposed, which comprehensively considers reservoir pressure, permeability, and a fractional coverage index. For burial depths ranging from 650 to 1350 m, the TP-D-THM model can be simplified to the gas-mechanical model accounts for matrix dynamic diffusion (D-HM) with an error below 5%, indicating that thermal and water effects nearly cancel each other. Full article

An integrated analysis including total organic carbon (TOC), X-ray diffraction (XRD), scanning electron microscopy (SEM), and gas adsorption experiments was conducted on core samples from the deep Wufeng–Longmaxi (WF-LMX) Formation in the Zigong area to characterize its lithofacies and reservoir characteristics and their influencing factors. The results suggest that eight distinct lithofacies are distinguished and argillaceous/calcareous mixed siliceous shale lithofacies (S-1) is the most optimal lithofacies. The pore surface fractal dimension (D) was derived by applying the Frenkel–Halsey–Hil (FHH) model to low-temperature N₂ adsorption (LTNA) data. The meso-macropore regime shows higher heterogeneity than the micropore regime (since D₂ > D₁). Both D₁ and D₂ show a significant positive relation with TOC and carbonate content, a slight negative correlation with quartz content, and no clear link with clay content. In the initial depositional stage of the LMX Formation, a low-energy, stagnant, and strongly reducing environment facilitated the accumulation of siliceous biogenic sediments, leading to the formation of siliceous shale characterized by high paleoproductivity. In the middle to late stages of LMX Formation deposition, increased input of terrigenous clastic material, shallower water depths, and the gradual disruption of the anoxic conditions resulted in diminished paleoproductivity, causing a transition from siliceous shale to a mixed shale lithofacies. Increased TOC and carbonate content enhance pore heterogeneity, with TOC predominantly influencing micropores and carbonates controlling macropores. In contrast, higher quartz content inhibits pore development. Full article

This study presents the valorisation of cocoa waste (CW) by transforming it into edible packaging films using apple pectin (AP) as a gelling agent. Several properties, including microstructure, optical characteristics, sorption, wetting, barrier functionality, mechanical strength, structure, and antioxidant activity, were investigated. The analyses concluded that increasing the concentration of CW from 0 to 50% in pectin films enhanced UV light protection and caused a reorganisation in the film’s microstructure, resulting in both higher surface roughness and improved mechanical resistance. Specifically, the tensile strength increased from 7.28 to 19.14 MPa. The addition of CW reduced the lightness (parameter L*) from 82.58 to 28.58, making the films darker. Measurements of the water contact angle, which was in the range of 38.25 to 73.23; gas permeability, in the range from 5.53 to 19.52 × 10⁻¹⁶ g/m·Pa·s for oxygen and from 9.62 to 40.82 × 10⁻¹⁶ g/m·Pa·s for carbon dioxide; and adsorption indicated a reduction in water vapour sorption rates, suggesting that the films have average barrier properties against moisture. Fourier-transform infrared spectroscopy analysis confirmed no interactions between CW and the polymer matrix, showing the typical functional groups of pectin, such as carbonyl (C=O) and hydroxyl (-OH) groups. The incorporation of CW significantly increased the antioxidant properties of the developed films, attributed to the bioactive compounds present in CW. These films have potential for use as active food packaging thanks to the CW addition. They could be particularly beneficial for extending the shelf life of products sensitive to oxidation, such as oily products. Excellent sealability indicated suitability for use as pouches for fried products, such as instant coffee or powders. This study underscores the possibility of using apple pectin films with cocoa waste as sustainable components in eco-friendly packaging materials. This idea aligns with circular economic and waste reduction principles. This approach contributes to the development of innovative solutions for sustainable food packaging. Full article

Bacterial cellulose (BC) is a type of biomass composed entirely of cellulose. This characteristic favors the presence of a multitude of active sites, which facilitate the exchange of heavy metals present in polluting effluents. Upon contact with water contaminated with metals such as chromium, arsenic, and lead, among others, this biomass offers a potential solution to the environmental problem of industrial pollutants in water. This is particularly pertinent given the well-documented harmful effects of heavy metals in aquatic ecosystems. In this context, the objective is to determine the impact of temperature on Cr (IV) adsorption using bacterial cellulose biomass as an adsorbent, under different temperature scenarios, similar to the conditions of discharge of contaminated effluents into rivers, lagoons, and wetlands. In this study, the biomass was previously characterized through FTIR and SEM images, and isothermal models were subsequently evaluated along with batch adsorption kinetics. The findings demonstrate that bacterial cellulose biomass has great potential for Cr (VI) removal at various temperatures, with an adsorption capacity of 140 mg/g at high temperatures and a reduction of up to 125 mg/g at low temperatures. The findings of this study constitute a valuable contribution to decision-making when considering the expansion of these treatment processes, facilitating this task by offering a comparative analysis of effluent discharge conditions in relation to various scenarios involving contaminated liquid temperatures. The use of this biomaterial in an environmental sustainability initiative focused on water resource conservation is a very promising prospect. Full article

The effectiveness of periodate-assisted photocatalysis in removing the cationic dye Safranin O (SO) was evaluated using a UV/TiO₂/IO₄⁻ process operated at room temperature under near-neutral pH conditions. Under base conditions ([IO₄⁻] = 0.15 mM, [TiO₂] = 0.4 g/L, [SO] = 10 mg/L), the ternary system achieved a pseudo-first-order rate constant of 0.6212 min⁻¹, outperforming the UV/TiO₂ and UV/IO₄⁻ processes by approximately 21- and 29-fold, respectively. This yielded a synergy ratio of about 12 compared to the sum of the binary processes. Targeted quenching experiments revealed the operative pathways. Strong inhibition by ascorbic acid and phenol indicates that interfacial holes and ^•OH are key oxidants. Methanol caused a moderate slowdown, consistent with ^•OH and hole scavenging. Benzoquinone and oxalate suppressed removal by intercepting the electron and O₂^•− pathways, respectively. Dichromate markedly inhibited the process via optical screening and competition for electrons. Azide had little effect, suggesting a minor role for singlet oxygen. Matrix studies showed progressively slower kinetics from deionized water to mineral water to seawater. This was due to halides, sulfate, alkalinity, and TiO₂ aggregation driven by ionic strength. Additional tests confirmed that the dominant modulators of performance were humic acid (site fouling and light screening), chloride and sulfate (radical speciation and surface effects), nitrite (near-diffusion radical quenching), and bicarbonate at pH 8.3 (conversion of ^•OH to CO₃^•−). Nonionic surfactants (Tween 80, Triton X-100) also depressed SO removal through micellar sequestration and competitive adsorption on TiO₂. The study confirms the potential of UV/TiO₂/IO₄⁻ as a tunable AOP capable of delivering rapid and reliable dye degradation under a wide range of water quality conditions. The mechanistic mapping unifies two roles for IO₄⁻, an electron acceptor that inhibits recombination and a photochemical precursor of iodine centered and ^•OH radicals and connect these roles to the observed synergy and to the trend across deionized water, mineral water, and seawater. The scavenger outcomes assign the main oxidant flux to holes and ^•OH radicals with a contributory electron or O₂^•− branch from IO₄⁻ reduction. Full article

This study presents the fabrication and chemical modification of titanium meshes produced by nanosecond laser drilling, tailored for advanced photocatalytic and surface-enhanced Raman scattering (SERS) applications. Titanium meshes were fabricated via pulsed laser ablation (TM_1) and subsequently modified either by deposition of silver nanoparticles through irradiation (TM_2) and sonication (TM_3) or by surface oxidation using hydrogen peroxide (TM_4). Morphological and compositional analyses revealed that these modifications lead to distinct Ag nanoparticle morphologies and significant increases in surface oxygen content, notably enhancing photocatalytic performance. Photocatalytic tests demonstrated that the TM_4 mesh achieved the highest degradation rate of methylene blue, underscoring the critical role of surface oxygen enrichment. In contrast, TM_2 and TM_3 exhibit strong potential as surface-enhanced Raman scattering (SERS) substrates due to the well-distributed plasmonic silver nanostructures that enhance local electromagnetic fields. Their three-dimensional porous architecture facilitates high surface area and efficient analyte adsorption (MB), further improving SERS sensitivity. These findings establish nanosecond laser-processed titanium meshes, particularly those that are chemically modified, as promising, scalable materials for efficient water purification and effective SERS substrates for molecular sensing. Full article

In line with the circular economy approach and the pursuit of sustainable solutions for spent coffee grounds, this study investigates the valorization of spent coffee grounds as a source of cellulose-based enzyme immobilization carriers. Considering that global coffee consumption generates approximately 6.9 million tonnes of spent coffee grounds annually, their disposal represents both an environmental challenge and an opportunity for value-added applications. A multistep extraction process, including Soxhlet extraction followed by sequential subcritical extraction with ethanol and water, and alkaline treatment, led to the production of cellulose-enriched carriers. The carriers obtained were characterized by their morphology, porosity and surface properties and subsequently used for the two lipases immobilization, Burkholderia cepacia (BCL) and Pseudomonas fluorescens (PFL), using three techniques: adsorption and covalent binding via direct and indirect methods. The immobilized lipases were analyzed for key biochemical and operational properties and compared with each other and with their free enzymes. Based on their stability, catalytic activity, and reusability, the lipases immobilized by adsorption were identified as the most efficient biocatalysts. These immobilized enzymes were then used in two selected reactions to demonstrate their practical utility: cocoa butter substitute synthesis using PFL and the enzymatic pretreatment of wastewater from the oil processing industry using BCL. Both immobilized lipases showed excellent catalytic performance and maintained their high activity over four consecutive reuse cycles. Full article

Background/Objectives: The oral administration of chemopreventive agents for colorectal cancer (CRC) remains limited by their low solubility, instability, and limited intestinal absorption. This study develops sodium carboxymethyl cellulose (CMC)-stabilised water-in-oil-in-water (W/O/W) multiple emulsions as pH-responsive carriers for co-delivery of resveratrol and selenium—two complementary chemopreventive compounds. Methods: Multiple emulsions differing in droplet size (small-droplet emulsions, SDE; large-droplet emulsions, LDE) and CMC concentration (0.0–0.5% w/w) are prepared in a Couette–Taylor Flow contactor. The study involves physicochemical characterisation of emulsions (droplet size, stability, rheological behaviour, ζ-potential, encapsulation efficiency), evaluation of release profiles under simulated gastric pH (2.0) and intestinal pH (7.0) conditions, including pathological environments (pH = 5.5), and ex vivo assessment of mucoadhesion using porcine intestinal tissue. Results: SDE and LDE containing CMC (0.0–0.5% w/w) exhibit a complex “drop-in-drop” structure, with Sauter mean diameters of approximately 9–12 μm and 23–25 μm, respectively, and high encapsulation efficiencies (>91%). Increasing CMC concentration enhances viscosity and induces more negative ζ-potential, confirming polymer adsorption at the oil–water interface. Under simulated gastric pH = 2.0, compound release remains limited (≤15%), whereas gradual/sustained release is observed under simulated intestinal pH (5.5/7.0). Mucoadhesion increases with polymer concentration, reaching ~90% for SDE and ~70% for LDE at 0.5% w/w CMC, and remains above 50% under simulated pathological conditions. Conclusions: The study demonstrates that CMC incorporation improves the structural stability, modulates the release behaviour, and enhances the mucoadhesive properties of W/O/W multiple emulsions. These findings suggest that CMC-stabilised emulsions may be further explored as oral delivery vehicles for CRC chemoprevention. Full article