Search Results (2,069)

In this study, particles of ground grape seeds were utilized to adsorb phosphate ions from a prepared solution, aiming to reduce phosphate concentration. Through a series of adsorption experiments, the effects of the adsorbent concentration, initial phosphate ion concentration, temperature, and pH on the phosphate ion uptake were studied. The removal efficiency of the phosphate ion decreased from 77 to 61% as a 25 to 45 °C increment in temperature was observed, which indicated the exothermicity in the adsorption process. The phosphate ion movement onto the adsorbent surface that exhibited the highest uptake value favored a neutral reaction environment with a pH value of seven. The experimental results, when compared using different adsorption isotherms, showed that the best fit was exhibited by the Jovanovic isotherm, which was further confirmed owing to its high 0.974 R² value. Intraparticle diffusion and pseudo second order models describe the kinetics of phosphate adsorption onto grape seeds, with reaction constants of 8.8 × 10⁻³ (mg/g min) and 0.412 (mg/g·min^0.5), respectively. The adsorption was physiosorptive, spontaneous, exothermic, and favorable. Furthermore, the negative entropy with a value of −0.0887 kJ/mol·K revealed reduced randomness in the adsorption process system. Full article

The continuous occurrence of steroidal pharmaceutical dexamethasone (DXM) in aqueous environments indicates the need for an efficient removal technology. The frequent detection of DXM in surface water could be substantially reduced by the application of photo-induced advanced oxidation technology. In the present study, Fe²⁺ and UVA-light activated peroxo compounds were applied for the degradation and mineralization of a glucocorticoid, 25.5 µM DXM, in ultrapure water (UPW). The treatment efficacies were validated in real spring water (SW). A 120 min target pollutant degradation followed pseudo first-order reaction kinetics when an oxidant/Fe²⁺ dose 10/1 or/and UVA irradiation were applied. Acidic conditions (a pH of 3) were found to be more favorable for DXM oxidation (≥99%) regardless of the activated peroxo compound. Full conversion of DXM was not achieved, as the maximum TOC removal reached 70% in UPW by the UVA/H₂O₂/Fe²⁺ system (molar ratio of 10/1) at a pH of 3. The higher efficacy of peroxymonosulfate-based oxidation in SW could be induced by chlorine, bicarbonate, and carbonate ions; however, it is not applicable for peroxydisulfate and hydrogen peroxide. Overall, consistently higher efficacies for HO^•-dominated oxidation systems were observed. The findings from the current paper could complement the knowledge of oxidative removal of low-level DXM in real water matrices. Full article

In this work, the biosorption potential of Spirulina sp. as an effective and eco-friendly biosorbent for the removal of Ni(II) and Pb(II) ions from aqueous solutions was investigated. Detailed characterization of the biosorbent was carried out, including surface morphology, chemical composition, particle size, zeta potential, crystallinity, zero-point charge, and functional group analysis. Batch tests were performed to determine the kinetic constants and adsorption equilibrium of the studied ions. The adsorption behavior of Spirulina sp. was described using six adsorption isotherms. The best fit was obtained for the Redlich-Peterson and Langmuir isotherms, indicating that monolayer adsorption occurred. The maximum biosorption capacities for Ni(II) and Pb(II) were 20.8 mg·g⁻¹ and 93.5 mg·g⁻¹, respectively, using a biosorbent dose of 10 g·L⁻¹, initial metal concentrations ranging from 50 to 5000 mg·L⁻¹, at pH 6, 20 °C, and a contact time of 120 min. Low values of the mean free energy of adsorption (E) in the Dubinin–Radushkevich and Temkin model (0.3 and 0.1 kJ·mol⁻¹ for Pb(II) and 0.35 and 0.23 kJ·mol⁻¹ for Ni(II)) indicate the dominance of physical processes in the ion binding mechanism. The adsorption of Pb(II) ions was more effective than that of Ni(II) ions across the entire range of tested concentrations. At low initial concentrations, the removal of Pb(II) reached 94%, while for Ni(II) it was 80%. Full article

Background: Influenza A viruses (IAV) cause seasonal flu and occasional pandemics. In addition, the potential for the emergence of new strains presents unknown challenges for public health. Face masks and other personal protective equipment (PPE) can act as barriers that prevent the spread of these viruses. Metal ions embedded into PPE have been demonstrated to inactivate respiratory viruses, but the underlying mechanism of inactivation and potential for resistance is presently not well understood. Methods: In this study, we used hemagglutination assays to quantify the effect of zinc ions on IAV sialic acid receptor binding. We varied the zinc concentration, incubation time, incubation temperature, and passaged IAV in the presence of zinc ions to investigate if resistance to zinc ions could evolve. Results: We found that zinc ions impact the ability of IAV particles to hemagglutinate and observed inhibition within 1 min of exposure. Maximum inhibition was achieved within 1 h and sustained for at least 24 h in a concentration-dependent manner. Inhibition was also temperature-dependent, and optimal above room temperature. Serial passaging of IAV in the presence of zinc ions did not result in resistance. Conclusions: e conclude that zinc ions prevent IAV hemagglutination in a concentration and temperature-dependent manner for at least 24 h. Overall, these findings are in line with previous observations indicating that zinc-embedded materials can inactivate the IAV hemagglutinin and SARS-CoV-2 spike proteins, and they support work toward developing robust, passive, self-cleaning antiviral barriers in PPE. Full article

Aimed at developing an economical and efficient biosorbent for the adsorption and separation of rare earth ions, this study employed Spirulina dry powder biomass as a biosorbent to investigate its removal performance for Pr³⁺ in aqueous solutions. Experimental results demonstrated that under optimized conditions (pH = 5, adsorbent dosage = 2.0 g/L, initial Pr³⁺ concentration = 100 mg/L, and adsorption time = 60 min), the removal efficiency of Pr³⁺ reached 79.0%. FT-IR and XPS characterization confirmed the participation of various functional groups on the Spirulina surface in the adsorption process. When 0.1 mol/L HNO₃ was used as the desorption agent, the desorption rate of Pr³⁺ from Spirulina reached 91.7%, demonstrating excellent regeneration performance. At different temperatures (298–318 K), the adsorption data were fitted using Langmuir, Freundlich, Dubinin–Radushkevich, and Redlich–Peterson models. Among them, the Langmuir model (R² ranged from 0.993 to 0.999) provided the best fit, and the adsorption capacity of Spirulina for Pr³⁺ was in the range of 51.10 to 55.31 mg/g. Kinetic studies revealed that the pseudo-second-order model (R² = 0.999) best described the adsorption process, with a rate constant of 0.054 g/(mg·min) (R² was 0.999) at an initial Pr³⁺ concentration of 300 mg/L, indicating chemisorption-controlled behavior. Thermodynamic parameter analysis showed that within the experimental temperature range, ΔG⁰ < 0 and ΔS⁰ > 0, confirming that the adsorption process was spontaneous and endothermic. This study provides a novel technical approach for the green recovery of rare earth elements and highlights the potential of Spirulina biomass in rare earth resource recycling. Full article

Spores of filamentous fungi are common biological particles in indoor air that can negatively impact human health, particularly among immunocompromised individuals and patients with chronic respiratory conditions. Airborne viruses represent an equally pervasive threat, with some carrying the potential for pandemic spread, affecting both healthy individuals and the immunosuppressed alike. This study investigated the abundance and diversity of airborne fungal spores in both hospital and residential environments, using custom designed air samplers with or without the presence of negative air ions (NAIs) inside the sampler. The main purpose of investigation was the assessment of biological effects of NAIs on fungal spore viability, deposition, mycelial growth, and sporulation, as well as airborne viral load. The precise assessment of mentioned biological effects is otherwise difficult to carry out due to low concentrations of studied specimens; therefore, specially devised and designed, ion-bioaerosol interaction air samplers were used for prolonged collection of specimens of interest. The total fungal spore concentrations were quantified, and fungal isolates were identified using cultural and microscopic methods, complemented by MALDI-TOF mass spectrometry. Results indicated no significant difference in overall spore concentration between environments or treatments; however, presence of NAIs induced a delay in the sporulation process of Cladosporium herbarum, Aspergillus flavus, and Aspergillus niger within 72 h. These effects of NAIs are for the first time demonstrated in this work; most likely, they are mediated by oxidative stress mechanisms. A parallel experiment demonstrated a substantially reduced concentration of aerosolized equine herpesvirus 1 (EHV-1) DNA within 10–30 min of exposure to NAIs, with more than 98% genomic load reduction beyond natural decay. These new results on the NAIs interaction with a virus, as well as new findings regarding the fungal sporulation, resulted in part from a novel interaction setup designed for experiments with the bioaerosols. Our findings highlight the potential of NAIs as a possible approach for controlling fungal sporulation and reducing airborne viral particle quantities in indoor environments. Full article

This study presents the development of a novel Cu–Co–O-codoped graphitic carbon nitride (g-C₃N₄) catalyst for efficient peroxymonosulfate (PMS) activation to degrade sulfamethoxazole (SMX) in aqueous environments. The synthesized Cu–Co–O-g-C₃N₄ catalyst demonstrated exceptional catalytic performance, achieving 90% SMX removal within 10 min—significantly outperforming pristine g-C₃N₄ (14%) and O-doped g-C₃N₄ (22%)—with a reaction rate constant of 0.63 min⁻¹. The superior activity was attributed to the synergistic effects of Cu-Co bimetallic doping and oxygen incorporation, which enhanced the active sites, stabilized metal ions, and minimized leaching. Mechanistic studies revealed a dual-pathway degradation process: (1) a radical pathway dominated by sulfate radicals (SO₄•⁻) and (2) a non-radical pathway driven by singlet oxygen (¹O₂), with the latter identified as the dominant species through quenching experiments. The catalyst exhibited broad pH adaptability and optimal performance at neutral to alkaline conditions. Characterization techniques (XRD, FTIR, XPS) confirmed successful doping and revealed that oxygen incorporation modified the electronic structure of g-C₃N₄, improving charge carrier separation. This work provides a sustainable strategy for antibiotic removal, addressing key challenges in advanced oxidation processes (AOPs), and highlights the potential of multi-heteroatom-doped carbon nitride catalysts for water purification. Full article

Chestnut (Castanea sativa Mill.) is an edible nut recognized for its nutritional attributes, particularly its elevated levels of carbohydrates (starch) and proteins. Chestnuts are popular for their health-promoting properties and hold significant environmental and economic importance in Europe. During this study, after the characterization of the fruit, attention was directed toward the valorization of chestnut shells, a predominant by-product of industrial chestnut processing that is typically discarded. Valuable bioactive compounds were extracted from the shells using Pressurized Liquid Extraction (PLE), a green, efficient, scalable method. Response surface methodology (RSM) was utilized to determine optimal extraction conditions, identified as 40% v/v ethanol as the solvent at a temperature of 160 °C for 25 min under a constant pressure of 1700 psi. High total polyphenol content (113.68 ± 7.84 mg GAE/g dry weight) and notable antioxidant activity—determined by FRAP (1320.28 ± 34.33 μmol AAE/g dw) and DPPH (708.65 ± 24.8 μmol AAE/g dw) assays—were recorded in the optimized extracts. Ultrahigh-performance liquid chromatography coupled with a hybrid trap ion mobility-quadrupole time-of-flight mass spectrometer (UHPLC-TIMS-QTOF-MS) was applied to further characterize the compound profile, enabling the identification of phenolic and antioxidant compounds. These findings highlight the possibility of using chestnut shell residues as a long-term resource to make valuable products for the food, medicine, cosmetics, and animal feed industries. This study contributes to the advancement of waste valorization strategies and circular bioeconomy approaches. Full article

Nanotechnology plays an increasingly important role in the economy and human life, which means that more and more amounts of nanosubstances, including nanoparticles of metal oxides, together with wastewater, end up in the environment. This study aimed to study the impact of iron(III) oxide nanoparticles (n-Fe₂O₃), which have magnetic properties, on the efficiency of the Anammox wastewater treatment process. The results indicate that n-Fe₂O₃ in the range of low concentrations may have a positive effect on nitrogen metabolism, increasing the efficiency of NH₄-N removal to 98% in 120 min and at 30 °C. During the first 30 min of the process, when almost anaerobic conditions arose, nanoparticles of Fe₂O₃, stabilized the system by producing ROS. However, a constant control of TOC and pH is necessary because of the constant increase in the amount of organic compounds and H⁺ ions during the reaction. However, a longer contact of n-Fe₂O₃ with biomass causes the efficiency to decrease, and, as a result, the efficiency is lower compared to the system containing only Anammox. Full article

In this study, an efficient and cost-effective nanocomposite material based on Opuntia ficus indica (cactus) powder modified with iron oxide nanoparticles was developed as an adsorbent for the removal of methylene blue (MB), a common water pollutant. The nanocomposite was synthesized through the co-precipitation method of Fe²⁺ and Fe³⁺ ions and characterized using Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS) and thermogravimetric analysis (TGA). Batch adsorption experiments were conducted over 24 h, varying different operational conditions, such as pH, temperature and initial pollutant concentration. Furthermore, a Box–Behnken design was employed to develop an empirical model for predicting removal efficiency and optimizing the adsorption conditions. The effects of adsorption variables including contact time (1–60 min), initial MB concentration (20–100 mg/L), pH (2–12), adsorbent dosage (2–6 g/L) and temperature (25–55 °C) on the removal capacity were examined. Under optimal conditions, the maximum removal efficiency of MB reached approximately 96%, with a maximum adsorption capacity of 174 mg/g, as predicted by the Langmuir model. The synthesized cactus/iron oxide nanocomposite demonstrated significant potential as an adsorbent for treating MB-contaminated water. Full article

Electrocoagulation is rapidly gaining prominence in wastewater treatment due to its capabilities and less reliance on additional chemicals. While a lot of research efforts have been focused on the influence of the anode material, power supply, and reactor design, the contribution of the cathode to contaminant removal has been less explored. In this study, we investigated the performance of stainless steel (SS-304) and aluminium (Al-6061) electrodes in both similar and dissimilar configurations for a 120 min electrocoagulation treatment of spent machinery coolant. The anode–cathode configurations, including SS-SS, Al-Al, SS-Al and Al-SS, have been investigated. Additionally, we examined the effects of the initial pH and agitation methods on the process performance. Our findings indicated that the type of cathode could significantly affect the floc formation and contaminant removal. Notably, the combination of an Al anode and SS cathode (Al(A)-SS(C)) demonstrated a synergistic improvement in the Chemical Oxygen Demand (COD), with a removal of 84.3% within a short treatment time (<20 min). The final COD removal of 91.4% was achieved with a turbidity level close to 12 Nephelometric Turbidity Units (NTU). The Al anode readily released the Al ions and formed light flocs at the early stage of electrocoagulation, while the SS cathode generated heavy Fe hydroxides that mitigated the flotation effect. These results demonstrated the cathode’s significant contribution in electrocoagulation, leading to potential savings in the treatment time required. Full article

Due to their biocompatibility, biodegradability, injectability, and self-setting properties, calcium–magnesium phosphate cements (MCPCs) have proven to be effective biomaterials for bone defect filling. Two types of MCPC powders based on the magnesium whitlockite or stanfieldite phases with MgO with different magnesium contents (20 and 60%) were synthesised. The effects of magnesium ions (Mg²⁺) on functional properties such as setting time, temperature, mechanical strength, injectability, cohesion, and in vitro degradation kinetics, as well as cytocompatibility in the MG-63 cell line and the osteogenic differentiation of BM hMSCs in vitro, were analysed. The introduction of NaHA into the cement liquid results in an increase in injectability of up to 83%, provides a compressive strength of up to 22 MPa, and shows a reasonable setting time of about 20 min without an exothermic reaction. These cements had the ability to support MG-63 cell adhesion, proliferation, and spread and the osteogenic differentiation of BM hMSCs in vitro, stimulating ALPL, SP7, and RUNX2 gene expression and ALPL production. The combination of the studied physicochemical and biological properties of the developed cement compositions characterises them as bioactive, cytocompatible, and promising biomaterials for bone defect reconstruction. Full article

The application of high-performance liquid chromatography with tandem mass spectrometry (HPLC-MS/MS) in the analysis of peptide therapeutics demonstrates its capacity to achieve high sensitivity and selectivity, which are essential qualities for the expanding peptide therapeutic industry. Given the challenges posed by hydrophilic peptides in reversed-phase chromatography, we investigated the necessity of a derivatization procedure to improve chromatographic separation and quasimolecular ion fragmentation during MS/MS detection. We investigated how eight different derivatizing agents react with a hydrophilic lysine- and arginine-containing human ezrin peptide-1 (HEP-1) to identify the most suitable one. The results showed that the reaction of HEP-1 with propionic anhydride proceeds most rapidly and completely, providing a high and reproducible yield of the product, which has sufficient retention on the RP column. The 4-propionylated derivative of HEP-1, compared to the other derivatives considered, demonstrates the most pronounced MS/MS fragmentation. The retention time of 2.42 min allows the separation of the substance from the interfering components of the blood plasma matrix and provides a limit of quantification of 5.00 ng/mL, which allows the use of this derivatizing agent for subsequent applications in pharmacokinetic studies, and this approach can improve the analytical parameters of similar peptides in other HPLC-MS/MS studies. Full article

Due to its health-promoting properties, resveratrol is one of the most desirable compounds in many industries. Hence, this work focused on finding the conditions of its extraction from Japanese knotweed which could be used on an industrial scale to obtain extracts with the best antioxidant properties. The contribution of polyphenolics to the activity of the obtained isolates was also assessed in this study. Ultrasound-assisted solvent extraction was used to prepare extracts in various solvents under conditions differing in extraction time, temperature, and ultrasound frequency. The extracts were tested for their ability to neutralize radicals and reduce metal ions. It was shown that although the best extractant was the same water–alcohol mixture, the optimal conditions for the extraction of resveratrol and polyphenols were different: 10 min, 50 °C and 80 kHz for resveratrol (for which the highest contents of resveratrol equals 0.91 mg/g was obtained) and 20 min, 25 °C and 37 kHz for polyphenolics (for which the total phenolic content equals 31.28 mg of gallic acid/g was determined) Under the latter conditions, one of the best antioxidant activities was also obtained. The results confirm that Japanese knotweed, despite its bad reputation in Europe as a very invasive species, can be used as a source of sought-after resveratrol and polyphenols. Full article

The present study compared the adsorption properties of two plant materials and the waste products after their essential oil extraction for removing Cu(II) ions from contaminated water. Methods like SEM, XRD, nitrogen adsorption, DTA, TGA, FTIR, and XPS were used for characterization of the materials. All materials showed similar porosity and structure, favoring Cu(II) biosorption. The effects of contact time, pH, temperature, sample amount, and initial metal concentration on Cu(II) removal were examined. Optimal pH was 4, with equilibrium reached in less than 10 min. Temperature and sample amount do not significantly influence the biosorption. The experimental data were fitted to the Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models, and maximum adsorption capacities were calculated. The four plant materials proved to be effective biosorbents for removing copper ions from contaminated water. Desorption experiments using 1 M HNO₃ and 0.1 M EDTA showed 100% recovery. The reusability of the most effective biosorbent was confirmed through four adsorption/desorption cycles with EDTA. This material was also used to study the possibilities of purifying a real sample of contaminated water. Full article