Search Results (4,460)

Diesel is a major soil contaminant that poses significant environmental risks, making its removal essential. This study investigates the synergistic application of thermal desorption (TD) and thermal plasma for the remediation of diesel-contaminated soil, while simultaneously converting desorbed contaminants into valuable gaseous products. Artificially contaminated soil (25 g/kg) was treated by TD at 250–300 °C and the resulting off-gas and volatilized diesel were subsequently processed in a thermal plasma system. Soil samples were characterized using CHNS, EDX, FTIR, and TGA/DTG analyses, while gas composition was determined using a gas analyzer. The results demonstrate that TD achieved diesel removal efficiencies of up to 86% at 300 °C and 65% at 250 °C. TD off-gas and volatilized diesel were predominantly converted into synthesis gas (H₂ + CO) in a thermal plasma environment, with H₂ and CO concentrations reaching up to 15.49 vol% and 7.61 vol%, respectively, depending on the plasma-forming gas, carrier gas flow rate, and remediation temperature. Thermal treatment of diesel-contaminated soil significantly altered key physicochemical properties, including reduced organic matter content, increased soil compaction, and temperature-dependent shifts in pH and nitrogen speciation (decreased NO₃⁻-N and increased NH₄⁺-N). These changes were accompanied by enhanced phosphorus availability, indicating substantial thermally induced transformation of soil nutrients. Phytotoxicity assessment using Lepidium sativum in a soil leachate-based bioassay indicated that higher treatment temperature (300 °C) increased toxicity and inhibited plant growth, whereas treatment at 250 °C resulted in lower phytotoxicity. These findings highlight the adaptability of the proposed combination of methods enabling effective soil remediation while supporting energy recovery. Full article

This study investigates the corrosion behaviour of a WC–6Co cemented carbide (94 wt% WC, 6 wt% Co) in acidic (pH 2) and alkaline (pH 13) electrolytes used for industrial PVD coating removal. The removal of the coating was not investigated, since no coatings were applied or analysed in this study. The objective was exclusively to simulate the corrosion response of the exposed substrate after the coating had been removed during electrochemical stripping. Potentiodynamic polarisation measurements were performed from OCP −0.2 V to +3 V at a scan rate of 1 mV·s⁻¹, followed by surface characterisation using SEM/EDS and laser profilometry to identify corrosion mechanisms and quantify material degradation. In an acidic solution, corrosion was dominated by cobalt dissolution, followed by the formation of a W–O-rich corrosion-product layer, as indicated by increased tungsten and oxygen contents in SEM/EDS analyses. The layer became increasingly porous and mechanically unstable at higher potentials. Progressive thickening of the corrosion-product layer and subsequent breakdown resulted in significant material loss, including surface abrasion up to ~8 µm. In alkaline electrolytes, SEM/EDS analyses revealed a Co–O-rich surface layer, suggesting cobalt-containing hydroxide/oxide corrosion products. These results suggest that surface-layer formation on WC–Co does not necessarily provide reliable corrosion protection, as stability and morphology strongly depend on pH. These findings provide valuable guidance for the use of cemented carbides in electrochemical stripping processes for PVD coating removal. Full article

Calcium carbide slag is a highly alkaline solid waste generated during acetylene production, but its long-term accumulation causes land occupation and persistent environmental risks such as soil alkalinization and water pollution. To support circular economy and carbon emission reduction goals, in this study, we develop an integrated physical decontamination–mineralization process combining calcination, magnetic separation, sedimentation, and CO₂ mineralization. After calcination, magnetic separation, and 8 h of gravity sedimentation, the removal efficiency of Si reaches about 67% (residual Si content reduces to 0.43%), while those of Fe and Al are 75.4% and 74.2%, respectively. The purified calcium-rich slurry is then used for CO₂ mineralization. Under a solid-to-liquid ratio of 10% and a CO₂ flow rate of 0.4 L/min, CO₂ is fixed as carbonate solids, yielding calcite-type CaCO₃ with 97.88% ± 0.35% purity. This process is centered on physical separation and uses no acids, alkalis, or ammonium salts, avoiding secondary pollution while achieving waste valorization and permanent CO₂ sequestration. In this study, we provide a scalable, low-impact pathway for alkaline solid waste valorization and carbon emission reduction, contributing to sustainable consumption and production (SDG 12) and climate action (SDG 13). Full article

Background: The relationship between allergic status, SARS-CoV-2 infection, Long COVID, and post-restriction respiratory outcomes in children remains incompletely understood. This study aimed to explore the associations between allergic status and Long COVID, as well as between SARS-CoV-2 vaccination and post-restriction changes in allergic rhinitis (AR), asthma, and upper respiratory infections, in a pediatric tertiary-care cohort. Methods: We conducted a single-center, questionnaire-based observational study involving children aged 0–16 years, who were followed at the Pediatric Allergy Clinic of Umberto I Hospital in Rome. Parents completed an email-based questionnaire addressing SARS-CoV-2 infection, vaccination, persistent post-infectious symptoms, allergic diseases, and respiratory infections following restrictions. Analyses of Long COVID were limited to children with confirmed SARS-CoV-2 infection. Results: A total of 214 questionnaires were analyzed. Allergic status was not significantly associated with SARS-CoV-2 infection in the overall cohort. Among infected children, allergic status was independently associated with higher odds of Long COVID (adjusted OR 3.12, 95% CI 1.20–8.09; p = 0.019). Severe acute infection was also strongly associated with Long COVID (adjusted OR 6.84, 95% CI 2.72–17.21; p < 0.001). Complete vaccination was associated with lower odds of SARS-CoV-2 infection in the overall sample (adjusted OR 0.20, 95% CI 0.09–0.46; p < 0.001) but was not independently associated with Long COVID among infected children. After the removal of COVID-19 restrictions, 90.1% of allergic children reported worsening AR and 52.0% reported worsening asthma, with no significant association with SARS-CoV-2 infection or Long COVID. Group A Streptocossus (GAS) pharyngitis was reported in 50.0% and viral pharyngitis in 10.7% of the cohort, with no significant differences between allergic and non-allergic children. Conclusions: In this single-center, questionnaire-based pediatric cohort, allergic status was correlated with increased likelihood of Long COVID among children with confirmed SARS-CoV-2 infection; however, it was not associated with a higher risk of infection itself. Complete vaccination was linked to a reduced risk of infection, whereas no independent correlation with Long COVID was identified. Post-restriction exacerbation of allergic respiratory symptoms was prevalent, while the incidence of bacterial and viral pharyngitis did not vary significantly according to allergic status. Full article

Incretin receptor agonists (IRAs) such as GLP-1-based therapies improve metabolic and cognitive outcomes and enhance brain insulin signaling. One way that IRAs could have these actions is by affecting the blood–brain barrier (BBB); however, IRA-BBB interactions are poorly studied. Here, we examined the ability of insulin and IRAs to affect each other’s transport across the BBB in lean mice. We found that intracerebroventricular (ICV) administration of the insulin receptor antagonist S961 did not affect the blood-to-brain transport of the bioactive fragment of the IRA, ¹²⁵I-dulaglutide (BAF). In contrast, ¹²⁵I-dulaglutide (BAF) co-administered with intravenous (IV) insulin significantly enhanced ¹²⁵I-dulaglutide (BAF) BBB transport into whole brain, olfactory bulb, parietal cortex, and pons, demonstrating insulin-dependent modulation of IRA BBB transport. Regional transport rates for ¹²⁵I-dulaglutide (BAF) across the brain varied by ~2.5-fold, with the fastest transport into the olfactory bulb, frontal cortex, cerebellum, and pons. Co-administration of IV dulaglutide (BAF) did not alter ¹²⁵I-insulin BBB transport rates (K_i) but did reduce reversible insulin binding (V_i) at the BBB by >50%, suggesting rapid effects on BBB insulin receptors. To explore the effects of chronic IRA administration, lean mice were treated with semaglutide for two weeks. Body weight and food intake were unchanged, but female mice showed reduced fasting levels of serum insulin and GLP-1 and decreased insulin transport into whole brain, while male mice showed a reduction in insulin binding at the BBB. Chronic semaglutide also reduced ¹²⁵I-insulin BBB transport in female mice when studied with in situ perfusion, a procedure that removes the immediate influence of serum factors. Together, these findings demonstrate reciprocal and female-selective interactions between IRAs and insulin at the BBB. Acute insulin enhances the BBB transport of an IRA in female mice, whereas chronic IRA exposure selectively impairs insulin BBB transport in females, highlighting the BBB as a dynamic and hormone-sensitive interface with implications for long-term treatment in mouse models and potential for translation impact in humans. Full article

Cobalt oxide (Co₃O₄), a transition metal oxide with a cubic spinel structure, shows high potential in peroxymonosulfate (PMS) activation, while its catalytic efficiency is often limited by sluggish interfacial charge transfer. In this study, a chlorine-doped Co₃O₄ (Cl-Co₃O₄) was synthesized via a hydrothermal method for the degradation of bisphenol A (BPA) through PMS activation. Systematic characterizations and electrochemical tests demonstrated that chlorine doping could effectively modulate the surface electronic structure of the catalyst, significantly reducing the interfacial charge transfer resistance. Degradation performance evaluations revealed that, compared to pristine Co₃O₄, Cl-Co₃O₄ exhibited a significantly enhanced BPA degradation, achieving near-complete removal of BPA within 15 min under neutral to weakly alkaline conditions. The optimal operational parameters were determined as catalyst dosage of 0.20 g/L, PMS concentration of 0.10 mM and initial pH of 7.0–9.0, with the pseudo-first-order rate constant reaching 0.37 min⁻¹. High-concentration NO₃⁻ showed weak inhibition, while Cl⁻ showed moderate inhibition; 50 mM HCO₃⁻ drastically reduced the rate constant to 0.05 min⁻¹ and almost completely suppressed the reaction. Sulfate (SO₄•⁻) and superoxide (O₂•⁻) radicals were the primary reactive species in this system, explicitly excluding the role of the non-radical electron transfer pathway. Furthermore, three plausible BPA degradation pathways involving C-C bond cleavage, hydroxylation and C-O bond breakage were proposed with 19 intermediates identified. Ecotoxicological assessments based on ECOSAR verified that both acute and chronic toxicity of the intermediates to fish, daphnid and green algae decreased gradually, and the final small-molecule products exhibited significantly lower toxicity than the parent BPA. This study provides a novel strategy for enhancing the PMS activation performance of cobalt-based catalysts by modulating their electronic structures via halogen doping. Full article

p-nitrophenol (p-NP) is a pollutant with environmental persistence, bioaccumulation potential, and significant health risks, and is widely dispersed in wastewater, so efficient removal of p-NP is imperative. Among the various methods, the catalytic reduction of p-NP to p-aminophenol (p-AP) using sodium borohydride (NaBH₄) is a particularly promising one and, herein, catalysts play a crucial role. Among the various metals, Au shows unique catalytic activity for p-NP reduction. However, nanosized Au often exhibit limited activity and stability due to their high surface free energy. To address this challenge, we designed and synthesized Au-SnO_x hybrid nanoparticles confined within hollow mesoporous silica nanoreactors (Au-SnO_x@hm-SiO₂) via a soft-template-assisted co-adsorption strategy. The resulting bimetallic Au-SnO_x@hm-SiO₂ nanoreactor showed significantly enhanced catalytic activity toward the NaBH₄-mediated reduction of p-nitrophenol (p-NP) compared with its monometallic Au@hm-SiO₂ counterpart, owing to the synergistic effect between Au and SnO_x. Among various Au/Sn ratios, the catalyst with an Au/Sn molar ratio of 1:0.1 demonstrated the highest activity, achieving complete conversion of p-NP within 5 min at a p-NP/Au molar ratio of 529:1—a tenfold improvement over Au@hm-SiO₂. Moreover, the catalyst maintained high efficiency over six consecutive cycles, with only slight deactivation, benefiting from the protective silica shell. Full article

In this study, manganese ferrite was grown on the surface of a low-cost powder substrate of a guava leaf using the co-precipitation method. The resulting material was characterized using various spectroscopic and microscopic techniques. The composite was formed through the electrostatic and non-electrostatic interactions between the manganese ferrite nanoparticles, and the functional groups present on the guava leaf substrate; consequently, a high content of functional groups was observed in the synthesized composite through the Fourier transform infrared spectroscopy. The average size of the nanoparticles grown on the guava leaf substrate was determined to be between 3 and 5 nanometers. The synthesized composite material was utilized for adsorption applications, employing Methylene blue dye as a model adsorbate. Methylene blue was removed from the aqueous solutions under various conditions—including variations in the pH, contact time, temperature, and concentration. Under optimal conditions, it was observed that an adsorbent dosage of 2 g L⁻¹ was capable of removing approximately 99% of the dye from a 10 mg L⁻¹ dye solution at pH 7. The dye removal efficiency (%) decreased with the increasing temperature, indicating an exothermic process; this was further confirmed by the thermodynamic parameter analysis (specifically, the change in enthalpy, or ΔH), which yielded a negative value. Gibbs Free Energy (ΔG) also yielded a negative value, signifying the feasibility and spontaneity of the adsorption process. In this study, the adsorption process followed the Freundlich isotherm model, with the value of ‘n’ falling between 1 and 10, which is indicative of heterogeneous adsorption. The adsorption kinetics were determined to follow a pseudo-second-order model, and the overall rate-limiting step of the process was identified as intraparticle diffusion. To assess the sustainability and stability of the adsorbent, regeneration and reusability experiments were conducted. The results revealed that the modified guava leaf performed effectively for up to five cycles, achieving an adsorption efficiency of approximately 24% after the final cycle. Thus, the developed adsorbent proved to be an effective material for the removal of Methylene blue dye. Full article

Self-grooming is a fundamental and evolutionarily conserved behavior and is essential for removing Varroa destructor in honeybees (Apis mellifera). However, its molecular and neural regulation remains poorly understood. This study identifies a microRNA-mediated neuromodulatory pathway that governs the intensity of self-grooming behavior in A. mellifera. Comparative behavioral analyses revealed pronounced differences in grooming intensity between bees exhibiting strong (MS) and weak (MW) grooming phenotypes. Liquid chromatography detection and pharmacological experiments demonstrated that octopamine (OA) levels are significantly different between MS and MW bees, and OA enhances grooming behavior. Small RNA sequencing revealed differentially expressed miRNAs in the brains of MS versus MW bees, leading to the identification of miR-281-x as a candidate associated with OA regulation. Functional validation showed that overexpression of miR-281-x significantly reduces grooming behavior, whereas inhibition of miR-281-x enhances grooming. Mechanistically, bioinformatics prediction and experimental validation confirmed that miR-281-x directly targets the tdc2, which encodes tyrosine decarboxylase 2 in OA biosynthesis. Fluorescence in situ hybridization (FISH) revealed co-localization of miR-281-x and tdc2 in Kenyon cells of the mushroom bodies. RNAi-mediated knockdown of tdc2 significantly reduced grooming intensity and rescue experiments confirmed the miR-281-x–tdc2–OA regulatory axis. Together, our findings uncover a post-transcriptional modulatory mechanism linking a microRNA to neuromodulator-dependent behavioral plasticity, providing insight into the control of grooming intensity in honeybees. Full article

Skin temperature measurement is a complex issue. Skin tissue is one of the main thermoregulatory organs and takes major responsibility for heat exchange in the organism. Accurate skin temperature measurement may contribute to better estimation of deep core temperature, which is why enhancing possibilities of skin temperature measurement is considered substantial. However, the real value of the skin temperature can be influenced by many biological and non-biological factors. Some of the external factors such as extensive wind or extreme ambient temperature may significantly influence the raw value of the skin temperature regardless of the choice of the measuring point. Despite that, abnormal thermoregulatory behaviour can occur due to internal body stresses and reactions. Whilst internal influence is even more difficult to track than external factors, it is crucial to monitor and identify the thermal stresses in a correct way. The paper proposes a wrist temperature measurement system. The system consists of a sensory part placed in a housing adapted to the shape of the wrist. The sensory component enables contact measurement of wrist skin temperature under the assumed experimental conditions. The housing is designed to provide stable positioning of the sensory component relative to the wrist while simultaneously isolating it from external conditions. The paper presents the results of a case study concerning human thermoregulation, quantifying the thermal response of the hand under low-temperature exposure in temperature chamber and during the subsequent rewarming phase after removal. During the experiment, temperature measurements of both hands were recorded. One of the co-authors participated in this case experiment. The temperature measurement results were compared between the hand subjected to thermal stress and the hand not exposed to low temperatures. Differences in the participant response to repeated thermal stress are demonstrated. The results highlight the complexity of the human body’s thermoregulation process in extremely cold environments. Full article

Anaerobic co-digestion of substrates offers synergistic benefits, enhancing methane production and improving the operational stability of wastewater treatment. The present study, for the first time, evaluated the biochemical methane potential and kinetics modeling performance of two regional wastewater streams—swine wastewater (SW) and nejayote wastewater (NW)—under mesophilic batch conditions. Five substrate ratios (SW/NW: 100/0 to 0/100) were tested, and interaction effects were measured using the co-digestion performance index (CPI). All mixtures demonstrated synergistic effects, with CPI values ranging from 1.12 to 1.26. NW exhibited the highest methane yield (438 ± 25 NL-CH₄/kgCOD_T-removed), nearly twice that obtained for SW (227 ± 18 NL-CH₄/kgCOD_T-removed). In addition, co-digestion improved the methane yield of SW as mono-digestion, with production increasing from 281.8 ± 12.4 to 304.7 ± 27.8 NL-CH₄/kgCOD_T-removed in all mixtures. The methane production kinetics were analyzed using six mathematical models. The multi-phase Gompertz model provided the best fit (R² > 0.99), while the two-phase model offered the best balance of accuracy and simplicity according to Akaike’s criterion. The present model effectively described the diauxic patterns of methane production resulting from substrate heterogeneity with an error of <8% for all experimental assays. Full article

The aim of this research was to quantify the capacity of different shrub species to remove atmospheric CO₂, to adsorb particulate matter and to dissipate latent heat through transpiration. A total of 308 established plants comprising Deutzia scabra, Elaeagnus × ebbingei, Euonymus japonicus, Forsythia × intermedia, Laurus nobilis, Ligustrum vulgare, Pittosporum tobira, Prunus laurocerasus and Viburnum tinus were selected in Lugano (Switzerland) and Bolzano (Italy). Stem diameter, crown radius, Leaf Area Index, net CO₂ assimilation per unit leaf area (A_leaf), transpiration, and stomatal conductance (g_s) were measured during spring, summer, and fall. The net CO₂ assimilation per unit of crown projection area and per plant were calculated by upscaling A_leaf using a multilayer model. Latent heat dissipation was calculated using the Penman–Monteith equation. The amount of PM trapped on leaves was measured using a gravimetric method. Differences in leaf area and leaf gas exchange among species affected their capacity to deliver specific ecosystem services. Forsythia, Pittosporum, Elaeagnus and Deutzia removed about 40% more CO₂ per unit crown projection area than Laurus, Ligustrum, and Euonymus. Latent heat dissipation by shrubs was, on average, 130 W m⁻², which is comparable to that of tree species. PM removal per unit leaf area was higher in species with sparse canopies and rough leaf surfaces. Full article

The uncontrolled discharge of synthetic azo dyes such as methyl orange (MO) into water bodies has become a major environmental concern because of their strong chemical stability, limited biodegradability, and harmful effects on aquatic ecosystems. In this study, MgNiFe layered double hydroxides (LDHs) were synthesized through a co-precipitation route using a molar ratio of (Mg + Ni)/Fe equal to 3, and their adsorption ability toward MO in aqueous media was investigated. The prepared materials were characterized by X-ray diffraction (XRD), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDX), Fourier-transform infrared spectroscopy (FTIR), and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The characterization results revealed the successful formation of a hydrotalcite-like layered structure with good crystallinity, a relatively uniform distribution of metallic species, and the incorporation of carbonate anions within the interlayer galleries. In addition, the adsorption performance was evaluated by studying the effects of several operational factors, namely adsorbent dosage, initial pH, and contact time. To better understand the interaction between these parameters and identify the optimum operating conditions, a Box–Behnken response surface design was applied. The results indicate solution pH is the most influential parameter in the adsorption process. Under optimized conditions, a maximum removal efficiency of 86.86% was obtained, corresponding to an adsorption capacity of approximately ~86.86 mg·g⁻¹ (based on 100 mL solution volume). The enhanced adsorption performance may be attributed to the combined effect of the multivalent metal cations (Mg²⁺, Ni²⁺, and Fe³⁺), likely increases the surface positive charge density of the LDH and promotes interactions with anionic dye molecules. These interactions are suggested to involve electrostatic attraction and possible surface adsorption processes. However, in the absence of post-adsorption characterization, the exact adsorption mechanism remains hypothetical. Overall, the results demonstrate the promising potential of MgNiFe LDHs as efficient adsorbent materials for the treatment of dye-contaminated wastewater. Full article

Polycyclic aromatic hydrocarbons (PAHs) are highly toxic pollutants in marine ecosystems, necessitating efficient remediation. This study synthesized magnesium phthalocyanine (MgPc) and its modified derivatives, magnesium azaphthalocyanine (NMgPc) and methyl-substituted magnesium azaphthalocyanine (MeNMgPc), as visible-light-driven photocatalysts for PAH degradation. To enhance efficiency and recoverability, these photosensitizers were immobilized onto coconut shell activated carbon (AC) via multiple ultrasonic impregnation. Characterizations (UV-Vis, SEM, EDAX, BET) confirmed successful active component deposition; nitrogen substitution and peripheral methyl groups synergistically tuned the electronic structure and suppressed aggregation. Under xenon lamp irradiation, the MeNMgPc/C composite exhibited superior activity, degrading 90.55% of naphthalene. Box-Behnken response surface optimization identified optimal conditions (13.18 g/L dosage, 20 A, 2.28 h), yielding 96.67% experimental removal and adhering to pseudo-first-order kinetics. Mechanistic studies via electron spin resonance identified hydroxyl (•OH) and superoxide radicals (O₂^•−) as primary reactive species. GC-MS analysis elucidated a sequential phenanthrene ring-opening pathway, progressing to ultimate mineralization into CO₂. Consequently, MeNMgPc/C presents a highly efficient, recoverable photocatalytic platform for marine PAH remediation. Full article

Antimicrobial resistance genes threaten the effective treatment of infectious diseases, underscoring the importance of their control in line with the EU One Health policy. Wastewater treatment plants are recognized hotspots for antimicrobial resistance. We assessed whether multi-channel mixed-matrix membranes (MCMMMs)—polyethersulfone (PES)/polyvinylpyrrolidone (PVP) ultrafiltration membranes with embedded activated carbon—can concurrently reduce microorganisms and extracellular DNA in wastewater effluent, building on prior reports of micropollutant removal. We evaluated the performance of MCMMMs in removing Escherichia coli and Saccharomyces cerevisiae as model organisms, as well as colony-forming units (CFUs) from wastewater effluent at a transmembrane pressure of 1 bar with a filtration area of 66 cm² over 1 h. DNA was extracted from wastewater effluent following filtration and analyzed to assess changes in microbial community composition. MCMMMs achieved log₁₀ reductions of 5.47 ± 0.42 (Escherichia coli), 5.99 ± 0.46 (Saccharomyces cerevisiae), and 2.79 ± 0.31 (wastewater CFU); reductions by pure PES/PVP membranes were comparable: higher for Escherichia coli and wastewater CFUs, lower for Saccharomyces cerevisiae. Amplicon sequencing showed altered relative abundances in wastewater effluent. Collectively, these findings demonstrate the potential of MCMMMs to simultaneously remove microorganisms, extracellular DNA, and micropollutants, highlighting their suitability for water treatment applications within the One Health framework. Full article