Search Results (22,611)

A previously unexplored magnetic biocomposite (CMC-HSDs/Fe₃O₄) was developed through the valorization of hydrophobic scleroprotein discards (HSDs). The synthesized material was evaluated for its efficacy in the adsorption of Cr(VI) and Hg(II) ions from contaminated aqueous systems. The physicochemical properties of the synthesized CMC-HSDs/Fe₃O₄ nanocomposite were characterized using XRD, FTIR, BET, TG/DTG, FESEM, EDX, and elemental mapping. Subsequently, a Box–Behnken experimental design was employed to model and optimize the adsorption process for Cr(VI) and Hg(II), focusing on the critical parameters of solution pH, adsorbent dosage, and interaction time. Kinetic data were best fitted to the pseudo-first-order (PFO) model. Equilibrium isotherm analysis revealed that Cr(VI) adsorption followed the Langmuir model, while Hg(II) adsorption was better fitted by the Freundlich model. Advanced ionic calculations elucidated a consistent multimolecular adsorption mechanism for both ions, characterized by temperature invariance and a preferential vertical geometry of the adsorbed species. Through a production cost of 25.56 USD/kg, the biosorbent demonstrates excellent reusability, retaining 88.60% efficiency for Cr(VI) and 85.69% for Hg(II) after five adsorption–desorption cycles. Based on a 50 mg/L influent concentration, projected treatment costs are ~$3.50/100 L for Cr(VI) and ~$1.22/100 L for Hg(II), underscoring the nanocomposite’s economic feasibility for industrial deployment in advanced tertiary wastewater remediation. Full article

Native cellulose I can be converted into crystalline polymorphs II and III_I, while cellulose II can be further converted into III_II through chemical treatments that induce significant structural, physical, and chemical changes. Accurate identification and differentiation of these polymorphs is essential for predicting fiber reactivity and processing behavior, but current methods are time-consuming. This study demonstrates the potential of near-infrared hyperspectral imaging (HSI-NIR) combined with linear discriminant analysis as a rapid, non-destructive tool for polymorph discrimination. Cellulose I, II, III_I, and III_II were produced from bleached kraft pulps of eucalyptus and pine and from cotton linters using NaOH (20% w/v) and ethylenediamine treatments. HSI-NIR successfully differentiated polymorphs based on spectral signatures in the 1480–1600 nm range, regardless of botanical source. Complementary characterization by XRD confirmed polymorph conversions, showing crystallinity reductions of 10–15% for cellulose I→II and I→III_I conversions, with crystallite size decreasing from 7.2 nm (cotton CI) to 3.2–3.4 nm in all CIII_II samples. XPS analysis revealed increased C-O surface accessibility in cellulose II and III, with complete disappearance of COOH groups in cellulose III samples. These results establish HSI as a promising screening tool for cellulose polymorph identification (>95% classification accuracy) and provide comprehensive baseline data on structural and chemical transformations that govern fiber reactivity in chemical and enzymatic processes. Full article

Wear remains a dominant cause of performance loss and premature failure in mechanical components, motivating the development of environmentally benign surface-engineering solutions. Among thermal spray systems, high-velocity oxy-fuel (HVOF)-sprayed WC-Co coatings are widely applied under severe wear conditions. The development of nanophase coatings offers the potential for enhanced mechanical performance. However, retaining the nanostructure and limiting decarburization during deposition remain key challenges. In this study, nanophase WC-12Co feedstocks with two particle size ranges, together with Al-modified nanophase powders, were used to deposit coatings under optimized HVOF spraying conditions (spray distance 200 mm, reduced O₂/fuel ratio, and high particle velocity) and were benchmarked against a conventional WC-12Co (12 wt.% Co) coating. The coatings were characterized in terms of microstructure and phase constitution (OM, SEM/EDS, XRD) as well as thickness, porosity (0.5–3.6%), adhesion strength (up to 65 MPa), and microhardness (~1040–1210 HV). Tribological behavior was assessed by ASTM G99 pin-on-disk testing and counterbody wear was quantified via geometric volume loss estimations. The use of larger nanophase particles enabled effective nanostructure retention with limited decarburization, whereas reducing particle size intensified decarburization, promoting increased W₂C formation, and markedly reduced coating cohesion, despite lower porosity and higher hardness. Aluminum additions enhanced coating microhardness and suppressed Co₃W₃C formation, indicating improved phase stability with minimal additional decarburization. Although coating wear remained negligible for all systems, Al-containing coatings exhibited increased friction (up to 35%) and significantly higher counterbody wear (up to sevenfold) compared to the Al-free nanophase coating, which was found to correlate with coating microhardness. Overall, the results demonstrate that optimizing nanophase WC-Co coatings requires balancing competing mechanisms between microstructural stability, cohesive integrity, and tribological response, highlighting the critical role of feedstock design in tailoring coating performance. Full article

This work presents the first in-depth investigation of Theodor Aman’s paintings that focuses on three of his heritage artworks: “Hora de peste Olt” (1866), “Teleleice în Harem” (1879), and “Regimul vechi” (1881), and that relies on both elemental and spectroscopic analytical techniques. Non-destructive Raman spectroscopy was employed on all three works of art to identify the pigments used by the Romanian master. In addition, micro-samples were available from “Hora de peste Olt” and “Teleleice în Harem”, which were further analyzed using XRD, micro-Raman, ATR-FTIR, and SEM-EDS techniques to provide complementary information on the pigments. SEM-EDS was also applied to study the structure of the preparation layers. The analyses revealed significant differences between the artworks in terms of both the pigments employed and the preparation of the canvas, suggesting that the earlier artwork belongs to one creative phase, while the newer pieces can be attributed to a later phase in the artist’s career. Full article

Recently, polyhydroxyalkanoates (PHAs) have gained significant attention as a bioactive material for replacing petrochemical plastics. PHAs can be produced by microorganisms growing on sludge substrates. In this study, fish-processing wastewater was investigated as an alternative substrate for PHA production using Bacillus cereus. Wastewater dilution, carbon-to-nitrogen ratio modification, and the addition of fish oil as a lipidic substrate were examined, and bacterial growth and biopolymer production were optimized. First, wastewater was diluted (25–100%) and examined. The 50% dilution treatment was selected, yielding a CDM of 0.426 g/L and a PHA content of 6.69%. In subsequent steps, the effects of wastewater fermentation and bacterial adaptation prior to the main production processes were investigated. According to the results, the 50% and 100% fermented treatments exhibited higher CDM values (0.970–1.022 g/L) compared to the non-fermented treatments. Cultures inoculated with adapted bacteria showed superior performance (CDM: 1.455 g/L, PHA: 0.499 g/L, PHA content: 34.63%) relative to non-adapted treatments. The effect of the carbon-to-nitrogen (C/N) ratio was also optimized by supplementing two carbon sources: glucose and crude fish oil. The optimal treatment T1 (effluent + 0.6 g/L glucose) had a CDM of 1.32 g/L and a PHA content of 0.215 g/L. Treatment 1, which consisted solely of effluent and fish oil, exhibited higher values (CDM: 1.12 g/L, PHA: 0.65 g/L) and was therefore considered the cost-effective treatment. Subsequently, a scale-up process was conducted in a 4 L bioreactor over 300 h under semi-continuous, long-term cultivation. The optimal harvesting time for the biopolymer was achieved during the fourth cycle (180–240 h). The produced biopolymer was characterized using FTIR, NMR, TGA, DSC, SEM, and XRD analyses, confirming the production of a copolymer, specifically poly(3-hydroxybutyrate-co-3-hydroxyvalerate). This study used wastewater from the fish industry for the production of biodegradable polyhydroxyalkanoates. Full article

The disposal of waste tyres presents a significant environmental challenge, necessitating sustainable, high-value recycling solutions. This study explores the incorporation of waste tyre metal fibre (WTMF) into hot mix asphalt (HMA) to enhance mechanical performance while reducing its electrical resistivity as well as the landfill burden. The primary goal of this research is to apply response surface methodology (RSM) to experimental data for modelling and optimizing WTMF-modified HMA mixes by capturing the coupled effects of fibre reinforcement and binder content on mechanical and functional performance. The microstructural characteristics of WTMF were examined using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). WTMF-modified mixes containing five WTMF dosages (from 0% to 1.50%) and bitumen contents from 4% to 6% were prepared and tested in the laboratory. The resulting dataset was used for RSM modelling, with WTMF and bitumen contents as input factors and Marshall stability, flow, porosity, and electrical resistivity as response variables. The central composite design (CCD) technique was employed to quantify interaction effects and to identify statistically significant trends. The developed models were validated using statistical indicators, and optimal mixture compositions were determined and experimentally verified. Microstructural analysis revealed WTMF’s irregular, rough surface with microcracks and pits, aiding crack-bridging and stress transfer. RSM results indicated 0.71% WTMF and 5.1% bitumen as an optimal combination of factors. Furthermore, high R² (>0.80) and adequate precision (>4.0) values from analysis of variance (ANOVA) underscore the significance of the proposed models, revealing a robust correlation between experimental and predicted data. This study demonstrated WTMF’s potential to be used in conventional HMA mixes, offering a sustainable recycling pathway for waste tyres. Full article

This study investigated the influence of Mn content (70 wt.%, 75 wt.%, and 80 wt.%) on the microstructure, mechanical properties and damping capacity of Mn-Cu alloys using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), mechanical testing and dynamic mechanical analysis (DMA). The results indicate that during cooling after aging, the Mn-Cu alloy undergoes martensitic transformation, resulting in a dual-phase structure of fcc and fct. The 70 wt.% Mn alloy exhibits a mixed-grain structure with mostly long, straight twin bands, while the 75 wt.% and 80 wt.% Mn alloys consist of fine equiaxed grains with mostly intersecting twin bands. The microstructure determines the properties of the alloy. As the Mn content increases, the mechanical properties initially increase and then decrease, and the 75 wt.% Mn alloy has the best mechanical performance (UTS = 534 MPa, YS = 263 MPa). In contrast, the damping capacity shows a decreasing trend, and the 70 wt.% Mn alloy exhibits the best damping capacity (tanδ = 0.064). The main damping peak of tanδ in Mn-Cu alloys is derived from the relaxation of the twin boundaries, and the less obvious secondary peak is the internal friction peak of martensitic transformation. Full article

Polyester resin biocomposites containing biochar have attracted attention for improving mechanical strength and thermal stability while promoting sustainability. The pyrolysis temperature of biochar and its proportion in the polymer matrix are key factors affecting biocomposite performance. This study examined how biochar pyrolysis temperatures (400, 600, 800 °C) and incorporation levels (10, 20, 30 wt.%) influence the physical, chemical, mechanical, flammability, and morphological properties of polyester-based biocomposites. The samples were analyzed for density, water absorption, FTIR, XRD, flexural and tensile strength, ignition time, structural degradation, volumetric loss, and SEM microstructure. Biocomposites with 30 wt.% biochar produced at 800 °C showed the best mechanical properties, with a flexural strength of 95.3 MPa and an elastic modulus of 4417.4 MPa, representing increases of 14.5% and 45.7%, respectively, over the control. FTIR and XRD results revealed decreased aliphatic groups and increased aromaticity at higher pyrolysis temperatures, improving interactions between the matrix and biochar. These biocomposites also demonstrated enhanced thermal stability, with an ignition time of approximately 963 s, delayed structural degradation, and reduced volumetric loss (~19.3%). Overall, pyrolysis temperature and biochar content significantly influence the structural, mechanical, and thermal properties of polyester biocomposites, showing that biochar serves as a sustainable, performance-enhancing component in thermoset polymer matrices. Full article

This study proposes a sustainable, integrated biorefinery approach to valorize mussel shell waste into high-value products, including chitin, chitosan, and calcium formate. Formic acid was employed as an effective demineralizing agent, enabling not only efficient mineral removal but also the direct conversion of the demineralization effluent into value-added calcium formate. The sequential extraction processes, demineralization, deproteinization, and decolorization, successfully yielded purified chitin (PCH), which was subsequently deacetylated to produce chitosan (CTS) with a degree of deacetylation of 85% and a molecular weight of 75 kDa. The physicochemical properties of all products were characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). FTIR and XRD analyses confirmed the successful extraction of chitin and chitosan, demonstrating the feasibility of mussel shells as an alternative biopolymer source. In parallel, calcium formate (CCF) was obtained from the demineralization effluent with a yield of 94.19%, and its formation was verified by FTIR and XRD. Elemental analysis by XRF exhibited 98.3% CaO with minimal non-toxic impurities. The TGA/DTG profiles of CCF exhibited a well-defined two-step thermal decomposition, confirming its anhydrous form. Overall, this environmentally benign process enables the simultaneous production of multiple value-added products while significantly improving resource utilization and reducing waste generation. The proposed integrated biorefinery model offers a promising, economically viable pathway for marine biomass valorization, aligned with the Bio-Circular-Green (BCG) economy concept. Full article

Juglone (5-hydroxy-1,4-naphthalenedione), a natural compound derived from walnut husks, was investigated as a sustainable dual-function antibacterial agent and corrosion inhibitor for Q235 steel in sulfate-reducing bacteria (SRB)-containing seawater. Juglone was synthesized via an improved one-pot method, and its performance was evaluated through antibacterial assays, weight loss measurements, surface characterization (SEM, XPS, XRD), and electrochemical techniques (EIS, PDP). Juglone exhibited potent antibacterial activity against Desulfovibrio sp., with a minimum inhibitory concentration (MIC) of 40 mg/L. At 20 mg/L (0.5 MIC) and 40 mg/L (1 MIC), it effectively suppressed bacterial growth and metabolism, mitigating corrosion. At 80 mg/L (2 MIC), a dual-action mechanism was observed: strong antibacterial effect combined with chemical reaction with H₂S, a corrosive SRB metabolite, forming a protective thiol-containing film on the steel surface. This reduced the corrosion current density from 3.16 × 10⁻⁵ A/cm² to 7.94 × 10⁻⁷ A/cm², achieving an inhibition efficiency of 97.5%. Juglone represents a promising green alternative to conventional toxic antibacterial agents, aligning with circular economy principles. Full article

The hornblende gabbro investigated in this study crops out in northwestern Elazığ, eastern Türkiye, within the Southeastern Anatolian Orogenic Belt (SAOB), where Late Cretaceous ophiolitic, volcanic, plutonic, and metamorphic units are widely exposed. This study examines the petrology, whole-rock geochemistry, Sr–Nd isotopic composition, mineral chemistry, and crystallisation conditions of these gabbroic bodies to constrain their petrogenesis and tectonomagmatic significance. Field observations show that the rock occurs as rounded to sub-rounded blocks with fresh inner cores and altered outer rims. Petrographic and XRD data indicate that the fresh gabbro mainly consists of plagioclase and amphibole, whereas the altered outer rims contain quartz and minor secondary phases. Whole-rock geochemical data classify the samples as low- to medium-K, tholeiitic, and predominantly metaluminous gabbro. Primitive mantle-normalised trace-element patterns display enrichment in large-ion lithophile elements and depletion in high-field-strength elements, whereas chondrite-normalised REE patterns show slight LREE enrichment, relatively flat HREE patterns, and weak Eu anomalies. Sr–Nd isotopic compositions are characterised by positive εNd_(T) values (+4.4 to +5.3) and moderately radiogenic initial ⁸⁷Sr/⁸⁶Sr ratios (0.704792–0.705344), indicating a predominantly mantle-derived magma source affected by subduction-related modification, with limited crustal contribution. Mineral chemistry data show that amphiboles belong to the calcic amphibole group and plot in the magnesio-hornblende field. Amphibole thermobarometric calculations yielded temperatures of 873–991 °C and pressures of 1.49–3.26 kbar, corresponding to crystallisation depths of 5.1–15.3 km. Overall, the results indicate that the hornblende gabbro was derived from a mafic magma generated from a spinel lherzolite mantle source and crystallised in a subduction-related tectonomagmatic setting. Full article

High-entropy alloys (HEAs) are typically produced using high-temperature metallurgical routes; however, alternative synthesis approaches based on wet-chemical processing remain relatively unexplored. In this study, a compositionally complex two-phase AgCuCoNiFe high-entropy alloy was synthesized using a precipitation–reduction strategy involving co-precipitation of mixed metal carbonates followed by thermal reduction in a reducing atmosphere. The objective of the work was to evaluate the feasibility of this hydrometallurgical route for preparing compositionally complex alloys and to investigate the structural evolution of the material as a function of reduction time. Quantitative MP-AES analysis confirmed efficient co-precipitation of all five elements, enabling the preparation of a precursor with near-equimolar metal composition. Structural characterization using SEM, EDS, and XRD revealed the presence of surface compositional heterogeneity in the as-reduced state, characterized by Ag-enriched domains. After controlled surface abrasion, the internal material exhibited significantly more uniform elemental distribution, although the obtained composition was not equimolar. X-ray diffraction patterns showed a transition from multiple sharp reflections at the surface to broadened peaks in the bulk, consistent with enhanced alloying within the bulk compared to the surface, while still revealing a two-phase character. Microhardness measurements indicated moderate hardness with mean values in the range of 187–221 HV with no significant dependence on reduction time, while wettability analysis revealed moderately hydrophilic behavior with contact angles in the range of approximately 75–83°. The results suggest that precipitation–reduction can be a viable alternative route for the synthesis of multicomponent HEAs, enabling the formation of chemically mixed alloy structures without the use of conventional melting-based processing. However, the obtained alloy exhibits incomplete chemical homogeneity, indicating that further optimization of the synthesis conditions is required to achieve a fully uniform composition. Full article

In this work, Ce-doped ZnO thin films at various contents of cerium were deposited on glass substrates by thermal vacuum evaporation to study the influence of Ce concentration on their optical, structural, morphological, and photocatalytic behavior. Pure ZnO and Ce-doped ZnO films doped with 2% and 5% Ce were characterized by SEM, XRD, AFM, UV–VIS spectroscopy, and ellipsometry. The XRD analysis confirmed that all the films retained the hexagonal wurtzite structure, while Ce incorporation induced lattice strain and reduced crystallite size, particularly at higher doping levels. SEM and AFM studies showed that films with 2% Ce exhibited smaller grain size and lower roughness, whereas 5% Ce-doped films showed grain growth and increased roughness. Pure ZnO films displayed high transparency (>90%), whereas Ce incorporation caused a red shift in the absorption edge and narrowing of the optical band gap due to defect-related states and lattice distortion. Photocatalytic experiments revealed that Ce doping improved charge carrier separation and increased the number of oxygen vacancies. Among all samples, the 2% Ce-doped ZnO film demonstrated the highest photocatalytic efficiency. These findings highlight the importance of controlled Ce doping in tuning the microstructure, optical properties, and photocatalytic performance of ZnO thin films, making them suitable for environmental remediation and optoelectronic applications. Full article

Mechanically activated pyrite plays an important role in gold extraction and coal utilization, but its reactivity may change markedly during storage. This study investigates how air deactivation during storage affects the crystal structure and subsequent thermal decomposition behavior of mechanically activated pyrite. Pyrite was mechanically activated and then stored in air for 0, 7 and 180 days. X-ray diffraction (XRD) combined with Rietveld refinement was used to characterize variations in lattice parameters and unit-cell-related structural features, while non-isothermal thermogravimetric–differential scanning calorimetry (TG-DSC) under an argon atmosphere, together with the Flynn–Wall–Ozawa (FWO) method, was applied to evaluate the decomposition kinetics. Air deactivation induced a non-monotonic evolution of lattice parameters and unit-cell volume, which is attributed to combined effects of residual stress relaxation and air-induced surface-related modification during storage. All samples exhibited two mass-loss stages during heating, reflecting stepwise thermal decomposition, and their decomposition behavior varied systematically with deactivation time. The apparent activation energy depended on both conversion fraction and deactivation degree, and nucleation-and-growth-type mechanisms were found to dominate the decomposition process, with their relative contributions evolving with storage time. These results clarify how prior air-deactivation history influences the structural evolution and subsequent thermal decomposition behavior of mechanically activated pyrite and provide useful insight for its storage and utilization in related processes. Full article

This study investigated the impact of incorporating calcined eggshell and carbon nanotube (CNT) on the properties of polyvinyl alcohol (PVOH) blends. Prior to solution casting, eggshell waste underwent a calcination process and then the samples were prepared via solution cast method. Mechanical properties study revealed a significant enhancement in tensile strength and elongation at break with increasing loads of calcined eggshell and CNT. Higher tensile strength was observed with increasing CNT loading for PVOH blends added with 1 phr and 3 phr calcined eggshell, owing to the reinforcing role of CNT in the composite matrix. In contrast, the tensile strength at 0.3 phr CNT is lower than at 0.2 phr CNT due to CNT agglomeration, which weakens the interfacial adhesion with the PVOH matrix and hinders effective stress transfer during deformation. SEM images depicted well-dispersion and interaction effect of calcined eggshell particles and CNT particles at low loading levels. The good interaction effect between calcined eggshell and PVOH matrix (which both exhibit hydrophilic behaviour) is mainly attributed to the presence of hydrogen bonding in the polymer matrix, as proven in FTIR analysis. XRD analysis revealed significant peaks in the 2θ range of 19° to 21°, suggesting that increased amounts of calcined eggshells influenced the crystallite size of the original PVOH matrix. In summary, the addition of calcined eggshell and CNT at low loading levels markedly enhanced the mechanical, physical, and thermal properties of the composite material. Full article