Search Results (397)

Humic substances (HS), derived from the degradation of organic matter in terrestrial and aquatic systems, play critical roles in nutrient cycling, metal complexation, and soil fertility. This study investigates whether HS derived from Greek peaty lignite (leonardite) can bind Mo(VI), an essential micronutrient for nitrogen fixation and assimilation processes. Titration experiments showed that the addition of Mo(VI) to HS solutions decreased pH, indicating Mo(VI)–HS complexation via proton-release reactions. UV-Vis spectra revealed charge-transfer interactions without evidence of Mo reduction, while FTIR analysis confirmed that carboxylic, phenolic, and alcoholic groups participate in Mo(VI)–HS association as indicated by shifts in COO–, C=O, and O–H vibrations. The results demonstrate that HS can effectively complex Mo(VI), increasing its solubility and potentially enhancing its bioavailability in soils. These findings highlight the value of humic-rich materials such as leonardite in sustainable crop nutrition. Full article

Electronics evolution drives SMMs as a frontier, overcoming conventional magnetic material limits via molecular spin coupling. Two relevant Co(II) mononuclear complexes, [Co(MOP)₄(N₃)₂] (1) and [Co(MSP)₄(N₃)₂] (2) (MOP = 4-methoxypridine and MSP = 4-methylthiopyridine) were synthesized through changing the substituents of ligands. The Co(II) ions in the two complexes show octahedron coordination geometries. The replacement of the O to S in the equatorial plane leads to different Jahn–Teller effect because of the shorter Co(II)-N in the equatorial plane, resulting in the significantly different slow relaxation process confirmed by ab initio calculation. The results confirm the Co(II) ion is sensitive to ligand field. Full article

The present study demonstrates that the corrosion behavior of dental cobalt–chromium (Co–Cr) alloys is strongly influenced by the interaction between microstructure, manufacturing technique, and oral chemical environment. A comparative investigation was conducted on Co–Cr specimens fabricated using four technological routes: conventional casting, CAD/CAM machining, Selective Laser Melting (SLM), and Direct Metal Laser Sintering (DMLS). The study included microstructural characterization, evaluation of generalized corrosion behavior using the rotating electrode technique, assessment of localized crevice corrosion, and quantitative analysis of the release of twenty metallic cations. Extraction tests were performed for 168 h in two media simulating aggressive oral environments: 0.07 N HCl (acidic medium) and a fluoride-containing electrolyte (0.1% NaF + 0.1% KF). Electrochemical measurements were recorded in the current density range of 10⁻¹⁰ to 10⁻⁷ A/cm², while released cation concentrations were quantified at the µg/L level. All alloys exhibited very low corrosion current densities (icorr in the 10⁻⁸ to 10⁻⁹ A·cm⁻² range), confirming overall good corrosion resistance. Among all manufacturing routes, CAD/CAM specimens demonstrated the highest electrochemical performance, with a wide passivity domain extending up to approximately 740 mV/SCE. A statistical interaction analysis between extraction media and manufacturing techniques was performed using the non-parametric Mann–Whitney (MW) U test. Among the analyzed elements, only chromium showed a statistically significant difference between media (p < 0.05), with an approximately 25-fold-higher release in acidic conditions compared with the fluoride medium, confirming the predominant role of proton-induced destabilization of the protective Cr₂O₃ passive film. In contrast, fluoride-containing media induced selective release of elements such as Cu (3× higher), W (2.5× higher), and Mo (1.4× higher), associated with complexation phenomena. The manufacturing route significantly influences corrosion behavior. Although additive manufacturing technologies (SLM/DMLS) enable highly accurate and customized prosthetic designs, rapid solidification and microstructural heterogeneities may increase susceptibility to localized corrosion compared with more homogeneous CAD/CAM materials. Clinically, these findings suggest that future restorative strategies should incorporate corrosion-aware material selection within digital workflows. As digital dentistry evolves, predictive models integrating patient-specific oral conditions may assist clinicians in selecting the most appropriate material system for long-term performance. In conclusion, the long-term success of dental Co–Cr prosthetic devices depends not only on mechanical strength and precision of fit, but also on sustained electrochemical stability in the complex oral environment. Full article

This work describes the fabrication of an eco-friendly sponge for the removal of dyes from aqueous solutions. For this purpose, a reused cellulose sponge (CS) that is commercially sold for makeup was covered with polyaniline (PANI), a conductive polymer that allows the addition of functional groups that are compatible with dyes present in aqueous solutions. An SEM analysis showed the successful deposition of PANI over CS fibers and confirmed that the porosity of the sponge remained after the polymerization step. The adsorption performance of the PANI-CS was evaluated in batch mode using methyl orange (MO). The adsorption capacity was 308 mg/g at pH 4.0 and after 110 min. PANI-CS achieved an adsorption percentage of 84% (C_o = 25 mg/L MO) after only 20 min. The experimental data were adjusted to different isotherm adsorption models; the best fit was obtained using the Halsey model. Furthermore, the adsorption performance of PANI-CS was studied in continuous mode using a bespoke adsorption column with recirculation. The results indicated that after 5 min of interaction time, 59% of the initial MO concentration (25 mg/L) was adsorbed. These results show the potential of PANI-CS as an inexpensive adsorbent for large-scale adsorption of dyes from aqueous media. Full article

In this work, a comprehensive first-principles investigation of the electronic, magnetic, and optical properties of pristine and Fe-, Co-, and Ni-doped MoS₂ monolayers is presented within the framework of density functional theory. Substitutional transition-metal doping at the Mo site is shown to induce spin-polarized impurity states within the pristine band gap, leading to significant modifications of the electronic structure, including metallic, semimetallic, or half-metallic behavior depending on the dopant species. The calculated spin-resolved band structures and projected density of states reveal a strong hybridization between the dopant $3d$ orbitals and the Mo-$4d$/S-$3p$ states, giving rise to sizable magnetic moments and dopant-dependent exchange splitting. When spin–orbit coupling is included, the combined effect of exchange interactions and relativistic effects leads to an effective valley splitting at the K and $K^{\prime }$ points, whose magnitude and sign depend sensitively on the chemical nature of the dopant. Optical properties are analyzed within a linear-response framework, showing pronounced dopant-induced modifications of the optical spectra. While the pristine monolayer exhibits well-defined excitonic features, transition-metal substitution introduces low-energy optical transitions associated with impurity-related states. Consequently, the exciton binding energies estimated from the difference between the electronic and optical gaps are interpreted as effective measures of dopant-induced perturbations to optical transitions, rather than as quantitative many-body excitonic binding energies in the strict sense. These results provide microscopic insight into the interplay between magnetism, spin–orbit coupling, and optical response in doped MoS₂ monolayers, highlighting the potential of transition-metal substitution as a route to engineer spin- and valley-dependent phenomena in two-dimensional materials. Full article

This study assessed trace mineral levels (Co, Cr, Cu, Fe, Mn, Mo, Se, and Zn) in paired serum samples from multiparous Holstein Friesian cows and their calves after colostrum intake, to explore potential relationships between maternal and neonatal mineral status. The acid-digested samples were analyzed by inductively coupled plasma mass spectrometry. Serum levels of Co, Cu, Fe, and Se were significantly higher in cows than in calves (p < 0.001), while Zn levels were higher in calves. The levels of Cr, Mn, and Mo were similar in both groups. Overall, mineral deficiencies were more prevalent in cows, with Se being the most deficient element, followed by Zn, Cu, and Co. Calves were more deficient in Co and Mn than their mothers but were not generally deficient in Se. Serum levels of Cr, Cu, Mn, Mo, and Se were positively correlated in cows and their calves, suggesting that maternal mineral status influences neonatal mineral levels. Overall, these results provide insights into trace mineral dynamics in cow–calf pairs. Further studies are needed to clarify the relative contribution of placental and colostral mineral transfer. Full article

This study investigates pure and Ag-doped SrMoO₄ powders (Sr_1−xAg_xMoO₄, x = 0, 0.01, 0.07), focusing on structural, optical, and functional properties. We evaluate its photocatalytic performance, capacitance response in lactate solution and water, and antimicrobial activity in textiles. The diffraction patterns could be indexed to the pure tetragonal phase SrMoO₄. The doping of SrMoO₄ with Ag⁺ ions affects the morphology and particle size of the samples designed by co-precipitation. SrMoO₄ pure and Ag⁺-doped samples exhibited promising results in detecting water and lactate solutions, as well as photocatalysis. Pure SrMoO₄ was more efficient in the photodegradation of methylene blue (MB) than the sample doped with Ag⁺. Among the bactericidal test results, sample SMO:0.01-P4, without light, in S. aureus, and SMO:0.07-P3, with light in E. coli, showed a slight distance from the inhibition halo. These results suggest that the treated textile may possess a characteristic bactericidal capacity that deserves further exploration. This comprehensive analysis offers insights into the structure–function relationship of SrMoO₄:Ag and advances the development of multifunctional materials. Full article

Background/Objectives: Chronic low-grade inflammation underlies persistent pain, sleep disturbance, fatigue, and reduced perceived well-being. ACT (anti-inflammatory cellular treatment), CO (circulatory optimization), and MO (metabolic optimization) are non-invasive REAC-based biomodulation protocols within the Inside Blue Zone (IBZ) framework, yet real-world evidence on patient-reported outcomes remains limited. The aim of this study was to evaluate pain intensity and symptom burden (sleep disturbance, fatigue, perceived well-being) in subjects undergoing ACT, CO, and MO within a Post-Market Clinical Follow-Up (PMCF) framework. Methods: This prospective observational PMCF study enrolled 50 subjects receiving sequential ACT, CO, and MO in routine practice. Pain was assessed at baseline (T0), end of treatment (T1), and follow-up (T2) using a Visual Analog Scale (VAS). Secondary outcomes were analyzed through clinically meaningful severity categories. Results: VAS scores decreased significantly from T0 to T1 (t(49) = 21.37, p < 0.001, Cohen’s d = 3.02) and remained reduced at T2. Seventy-eight percent met responder criteria. Secondary outcomes shifted toward lower severity categories at both timepoints. No adverse events occurred. Conclusions: Sequential ACT, CO, and MO produced clinically meaningful pain reductions and favorable symptom severity shifts with good tolerability, supporting clinical performance of this REAC-based approach in chronic low-grade inflammatory conditions. Full article

Maize silage can play a key role in policies aimed at stabilising local energy systems, as it constitutes a critical renewable feedstock for European biogas plants. By providing a dense and predictable source of chemical energy, it supports balance and reliability in the agricultural energy sector. To convert this potential into stable energy production, operators require kinetic models that translate routine silage quality indicators into concrete guidance for digester operation and control. Therefore, the aim of this article was to evaluate the batch kinetics of anaerobic digestion (AD) of maize silage and to select an adequate model for describing biochemical methane potential (BMP) profiles and associated energy recovery in the context of start-up, organic loading rate (OLR), hydraulic retention time (HRT) and feedstock preparation. Ten batches of silage (A–J) were examined, covering a realistic range of pH, electrical conductivity (EC), dry and volatile solids, ash, protein–fat–fibre fractions, fibre composition (NDF, ADF and ADL), derived fractions (hemicellulose, cellulose, and residual organic matter (OM)), C/N ratio and macro-/micronutrient profiles, including trace elements relevant to methanogenesis (Ni, Co, Mo, and Se). BMP tests were carried out in batch mode, and the resulting curves were fitted using the modified Gompertz and a first-order kinetic model. Methane yields of approx. 100–120 m³ CH₄/Mg fresh matter (FM) and 336–402 m³ CH₄/Mg volatile solids (VS), with CH₄ contents of 52–57% v/v, were typical for energy-grade maize silage. Kinetic and energetic behaviours were governed mainly by residual OM and hemicellulose (shortening the lag phase and increasing the maximum methane production rate), the ADL/cellulose ratio (controlling the slower hydrolytic tail), EC and Na/Cl/S (extending the lag phase), and C/N together with Ni/Co/Mo/Se (stabilising methanogenesis). The modified Gompertz model reproduced BMP curves with a pronounced lag phase and asymmetry more accurately (lower error and better information criterion values), and its parameters directly support start-up design, OLR ramp-up and energetic performance optimisation in bioenergy reactors. The novelty of this work lies in combining batch BMP tests, comparative kinetic modelling and detailed silage characterisation to establish quantitative links between kinetic parameters and routine maize silage quality indicators that are directly relevant for biogas plant operation and renewable energy production. Full article

Clementine, mandarin, and orange peels, which are usually discarded, can serve as promising, sustainable dietary supplements with beneficial compositions, as demonstrated in this study. Citrus peels are low in ash, fat, and protein, but high in moisture, fibre, sugar, and polyunsaturated fatty acids (PUFAs) (up to 60%). They contain high levels of omega-3 and omega-6 fatty acids, up to 30% each, making them a good health-promoting source, as shown by the values of nutritional indices as follows: PUFA/saturated fatty acid (SFA) (1.94 to 2.30), monounsaturated fatty acid (MUFA)/SFA (0.39 to 0.84), and PUFA/MUFA (2.37 to 5.82). Essential macro elements (K > Ca > Mg > S > P > Na) and trace elements (Fe > Zn > Mn > Cu > Cr > Mo > Co > Se) are unevenly distributed among the peels, along with non-essential elements, with Al (37 to 51 mg/kg) and Sr (17 to 30 mg/kg) predominating. Rare elements in food, such as V and W, are found up to 41 and 79 µg/kg respectively, followed by Nb > Ga > Y > Ge (5 to 11 µg/kg). Although citrus peels have a nutrient-dense composition, their monitoring must be ensured before inclusion in the common diet, particularly regarding non-essential elements, as for most of them the reference doses are not established and they could be harmful to human health. Full article

This study aimed to determine the exposure levels of young individuals living in Istanbul, a region in Turkey with a high population density and significant environmental pollution, by measuring the levels of heavy metals and trace elements in blood, serum, and urine. A total of 95 young people aged 18–24 participated in the study. Toxic heavy metals (Pb, As, Hg, Cd, and Cr) and physiological trace elements (Cu, Zn, Se, Mo, Mn, and Co) were measured in participants’ whole blood, serum, and urine samples using the ICP-MS technique. Participants were stratified by gender, as differences in body surface area may affect the absorption and metabolism of trace elements, and by smoking status, since smoking is a recognized source of heavy metal exposure. Gender differences revealed that blood lead levels were higher in males (p < 0.05), while manganese levels were higher in females (p < 0.05). When serum samples were analyzed, males had significantly higher zinc (p < 0.05) and selenium (p < 0.05) levels compared to females, whereas females had significantly higher levels of copper (p < 0.05) and cobalt (p < 0.05). Similar differences for copper (p < 0.05) and cobalt (p < 0.05) were observed in urine samples, with higher levels found in females. Blood cadmium levels were found to be significantly higher in smokers (p < 0.05). This biomonitoring study is one of the rare studies conducted in this region to assess heavy metal exposure among young adults. Full article

Naproxen (NPX) is a widely occurring, refractory organic contaminant that cannot be removed by conventional water treatment processes. In response to the growing environmental pollution caused by NPX, an innovative and highly efficient green degradation method has been developed, designed on the principles of sustainability to promote long-term ecosystem health and advance a circular economy. In this study, using zero-valent molybdenum as a catalyst in combination with trivalent iron (Fe³⁺) and hydrogen peroxide (H₂O₂), we constructed a Mo/Fe³⁺/H₂O₂ system to treat NPX-contaminated water. The effects of solution pH, H₂O₂ concentration, Fe³⁺ concentration, Mo dosage, and co-existing water-matrix constituents (Cl⁻, HCO₃⁻, PO₄³⁻, NO₃⁻, and humic acid (HA)) on NPX removal were investigated; reactive species were identified; and the reusability of Mo as well as its performance under the continuous-flow condition were evaluated. The results showed that the optimal pH was 3 and the appropriate Fe³⁺ dosage is 100 µM. With 500 µM H₂O₂, 87.9% of NPX was removed within 7 min, and a moderate increase in Fe³⁺ concentration, together with a suitable H₂O₂ level, enhanced the removal efficiency. HCO₃⁻, Cl⁻, and HA exerted slight inhibition, whereas PO₄³⁻ markedly suppressed NPX degradation. Recycling tests and the 6 h continuous-flow treatment demonstrated excellent reusability and stability of Mo. Quenching experiments revealed that HO^• and Fe(IV) were the dominant reactive species responsible for NPX degradation. Full article

The manufacturing systems face growing demands due to the instability of the market, the demanding sustainability policies, and the high rate of old equipment, but traditional planning structures are mostly fixed and deterministic, leading to the inefficiency of joint optimization of operational stability and environmental sustainability in unpredictable situations. This research proposed and empirically tested an artificial-intelligence-based adaptive planning platform, which combines a physics-based Digital Twin (DT) and a Pareto-conditioned Multi-Objective Proximal Policy Optimization (MO-PPO) algorithm to be able to co-optimize reliability and sustainability indicators in real-time. The platform reinvents manufacturing planning as a Constrained Multi-Objective Markov Decision Process (CMDP), optimizing an Overall Equipment Effectiveness (OEE) and energy carbon intensity as well as material waste, and strongly adhering to operational restrictions. The study utilizes a four-layer cyber–physical architecture, which includes an edge-based data acquisition layer, a high-fidelity stochastic simulation engine that is calibrated via Bayesian inference, a graph attention network-based state-encoding layer, and a closed-loop execution loop that runs with 60 s long planning cycles. In this study, a statistically significant enhancement was shown in 10,000 stochastic simulation experiments and a 12-week industrial pilot deployment: 96.8% schedule performance, 84.7% OEE, 16.5% cut in specific energy usage (2.38 kWh/kg), 17.1% reduction in material-waste rate (6.8%), and 21.4% enhancement in carbon effectiveness, outperforming all baseline strategies (p = 0.001). The analysis showed that there was a surprising synergistic correlation between waste minimization and OEE enhancement (r = −0.73), and 34.1% of overall OEE improvement could be explained by sustainability strategies. This study provides a robust framework for adaptive, resilient, and eco-friendly manufacturing processes in line with Industry 5.0 ideologies. Full article

Herein, a cobalt–molybdenum bimetallic oxide precursor was synthesized via a hydrothermal route, followed by a phosphidation strategy in a tube furnace to produce a CoMoP cocatalyst. Subsequently, a CoMoP/BiVO₄ composite photoanode was successfully constructed by loading the CoMoP cocatalyst onto the surface of an electrodeposited BiVO₄ film using a drop-casting method. A suite of analytical tools such as TEM, XRD, and XPS was utilized to comprehensively examine the material morphology and crystalline features, verifying that CoMoP was effectively anchored on the BiVO₄ surface with intimate interfacial contact. Photoelectrochemical (PEC) performance testing indicated that the composite photoanode achieved optimal performance with a 200 µL loading of the CoMoP dispersion (2 mg/mL). Under front-side illumination, the photocurrent density of the CoMoP/BiVO₄ composite photoelectrode reached a photocurrent density of 2.8 mA/cm² at 1.23 V (vs. RHE), which is approximately 3.1 times higher than that of unmodified BiVO₄ (0.9 mA/cm²). Under back-side illumination, the composite photoanode generated 3.5 mA/cm², representing a 2.3-fold improvement over the 1.5 mA/cm² recorded for bare BiVO₄. The bandgap energy of BiVO₄ was determined to be approximately 2.44 eV based on UV–vis absorption spectra and the corresponding Tauc plot. Owing to its metallic nature, CoMoP exhibits strong broadband absorption in the visible-light region and does not display an intrinsic semiconductor bandgap behavior. Combined with photoluminescence (PL) spectroscopy and PEC results, it was demonstrated that the CoMoP loading effectively promoted interfacial charge separation and transport while accelerating water oxidation kinetics. These results demonstrate that the CoMoP/BiVO₄ system serves as an advanced semiconductor material with excellent performance for photoelectrocatalytic water splitting. Full article

This study assesses the distribution of nutrients, trace elements, and heavy metals across different granulometric fractions of municipal solid waste (MSW) compost from three regions: Kaunas and Alytus (Lithuania) and Daugavpils (Latvia). Samples were collected from mechanical biological treatment plants (MBTPs) and fractionated into six different granulometric fractions (>5 mm, 5–2.5 mm, 2.5–1 mm, 1–0.5 mm, 0.5–0.2 mm, and <0.2 mm). Each fraction was subjected to physicochemical characterization. Macronutrients (Ca, K, Mg, P), trace elements (Al, As, Co, Fe, Mn, Mo), and heavy metals (Cd, Cr, Cu, Ni, Pb, Zn) were analyzed using ICP-OES in triplicate. Results showed that essential nutrients and toxic metals were retained more in the finer fractions (<1 mm). In contrast, undesirable impurities, mainly glass, were retained in the coarse fractions across all the studied areas. All fractions in the compost samples of Kaunas, and coarse fractions (>5 mm, and 5–2.5 mm) of Alytus and Daugavpils are suitable to use as a soil amendment only if the undesirable impurities are removed to the acceptable limits in the coarse fractions. The fine fractions of Alytus have higher levels of heavy metals (Cd, Cr, Cu, Ni, Pb, Zn), while Daugavpils showed higher levels of Cd, Cu, Ni, and Zn, exceeding the EU limits. Regarding physical fractionation, results showed that nutrients and heavy metals increased in the compost as particle size decreased. Our findings suggest that removing particle sizes < 1 mm and large impurities from the coarse fractions can enhance compost quality. Overall, particle-size fractionation can improve the consistency and safety of MBT-derived MSW compost for reuse in circular waste management systems. Full article