Search Results (376)

Objectives: This study characterised the bioactive properties (i.e., ion release, pH rise, and apatite formation) of a newly developed Voco Profluorid + BioMin F varnish. Three additional varnishes were investigated for comparison: Clinpro™ White Varnish (3M™, St. Paul, MN, USA), MI Varnish (GC, Tokyo, Japan), and Profluorid varnish (VOCO GmbH, Cuxhaven, Germany). The Clinpro™ White and MI varnishes were chosen for comparison due to their similar composition of active ingredients. Profluorid served as a standard fluoride-only varnish reference. Methods: Dental varnish ingredients were characterised using ATR-FTIR, XRD, and ¹⁹F and ³¹P MAS-NMR. Coated coverslips were immersed in Tris buffer and artificial saliva (pH 4.0 and 7.0) for 2–24 h. Ion release was analysed using ICP-OES and a fluoride ion-selective electrode whilst monitoring pH changes. Post-immersion, coverslips were analysed by XRD and MAS-NMR to assess possible apatite formation. Results: XRD and ¹⁹F MAS-NMR detected NaF in all four varnishes. BioMin F varnish showed a ³¹P peak matching BioMin F glass, with an additional brushite peak, indicating partial reaction of the bioactive glass (BAG) with rosin resin water. All varnishes released fluoride and calcium, but only BioMin F and MI varnishes released phosphate, which is essential for the formation of calcium fluorapatite. Post-immersion analysis confirmed fluorapatite formation in BioMin F and, to a lesser extent, the Profluorid varnish. No apatite formation was observed in the other two varnishes. MI varnish exhibited calcium fluoride formation before and after immersion, as evidenced by XRD and ¹⁹F MAS-NMR analysis. Conclusions: The novel BioMin F varnish potentially promotes remineralisation by providing a sustained and slow release of therapeutic ions that are essential for the formation of fluorapatite. 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

This study investigates the feasibility of utilising alkali-activated slag (AAS) and construction demolition waste (CDW) as cemented paste backfill materials. The fluidity, unconfined compressive strength, bleeding rate, and sulfate resistance of AAS-CDW backfill systems were systematically analysed. Hydration mechanisms were characterised using SEM-EDS and XRD. A novel backfill system and application process were developed and implemented in Jining Coal Mine, Shandong Province. Results indicate that a 30% waste red brick addition enhances 28-day compressive strength by 9.3% and reduces the bleeding rate by 32%, while a 10% fly ash addition optimises slurry fluidity. Notably, the AAS-based backfill exhibits superior mechanical properties and sulfate resistance compared to ordinary Portland cement (OPC)-based systems. The 28-day compressive strength of the AAS backfill reached 5.31 MPa, which is 53.4% higher than that of the OPC backfill, and its strength loss rate after sulfate attack was reduced by 13%. The solid waste utilisation rate of the AAS backfill approaches 100%. Hydration products primarily comprise ettringite (Aft), C-A-S-H gel, and hydrotalcite (HT), resulting in higher compactness than OPC-RA mixtures. Full article

In this work, sodium alginate (NaAlg) membranes were enhanced with synthesized zinc oxide (ZnO) nanoplates to enable efficient pervaporation dehydration of isopropyl alcohol (IPA). A comprehensive suite of characterisation techniques—scanning electron (SEM) and atomic force (AFM) microscopy, Fourier-transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), contact angle and liquid uptake measurements—along with density functional theory (DFT) calculations, was employed to establish robust structure–property relationships and to elucidate filler–polymer interactions. Membranes with different ZnO contents were prepared, and membranes based on the optimal NaAlg-ZnO(5%) composite were cross-linked with CaCl₂ to improve stability in aqueous solutions, and supported membranes were developed for prospective applications by applying this composite onto the prepared porous cellulose acetate (CA) substrate. This developed cross-linked supported NaAlg-ZnO(5%)/CA membrane had a permeation flux increased by 2 times or more compared to a dense NaAlg membrane during dehydration of IPA (12–30 wt.% water) with a permeate water content above 99 wt.%. The integrated experimental–theoretical approach provides mechanistic insight into ZnO–NaAlg interactions and demonstrates the strong potential of these mixed matrix membranes for high-efficiency alcohol dehydration, offering a rational design paradigm for next-generation pervaporation membranes. Full article

Quench–polish–quench (QPQ) of 40Cr steel was performed to improve its tribological properties and corrosion resistance, thereby enhancing the service performance of components such as gears and bearings. The 40Cr steel was treated by QPQ at 580 °C and 620 °C for 90 or 120 min. Optical microscopy (OM, Sunny Group, Ningbo, China), scanning electron microscopy (SEM, Hitachi, Tokyo, Japan), and X-ray diffraction (XRD Rigaku Corporation, Tokyo, Japan) were used to characterise the microstructure and phase constitution. Ball-on-disk tribometry, electrochemical tests, and salt spray tests in 3.5 wt.% NaCl evaluated surface performance. At 580 °C, a composite structure of Fe₃O₄ and ε-Fe₂₋₃N formed on the surface. When the temperature rose to 620 °C, ε-Fe_2–3N gradually transformed into γ′-Fe₄N. Within the scope of this study, the diffusion layer depth exhibits an approximately linear relationship with increasing processing temperature and holding time, and the surface hardness is 67–112% higher than that of the untreated sample. After QPQ treatment, the wear mechanism changed from adhesive wear to abrasive wear. However, under the treatment conditions of 620 °C × 120 min, brittle surface spalling increased roughness, thereby increasing the coefficient of friction. As treatment time increases, nitrogen atoms continue to diffuse outward as Fe₂N transforms to the γ′ phase. This increases the composite layer’s porosity and decreases its corrosion resistance. The best corrosion resistance was observed at 580 °C for 120 min, with a corrosion potential of −0.4325 V, corrosion current density of 1.80 × 10⁻⁶ A·cm⁻², and polarisation resistance of 24,500 Ω. Corrosion performance depends on overall surface integrity. Porosity morphology strongly influences this property. For 40Cr steel, the results show that surface properties are primarily determined by the quality of the compound layer’s microstructure. Specifically, density, phase-composition stability, and defect control are more important than the commonly held view of layer thickness. Full article

By examining a novel nanomaterial that has been modified for use in sustainable construction, this study primarily responds to the growing need for environmentally acceptable materials. The primary goal was to improve the functional and aesthetic qualities of building materials by synthesizing and characterizing environmentally friendly clay-based nanomaterials doped with cobalt pyrophosphate (Co₂P₂O₄). The authors employed contemporary experimental methods, such as scanning electron microscopy (SEM) for morphological characterisation, Fourier transform infrared spectroscopy (FT-IR) for molecular bonding assessment, and X-ray diffraction (XRD) for crystal structure research. The published findings show the doped nanomaterials’ potential durability as well as their structural integrity. An economic assessment is part of the investigation. The study is noteworthy for emphasizing the potential of cobalt-doped pyrophosphate nanoparticles as eco-friendly colour pigments for construction materials made of clay. Full article

The management of hazardous municipal solid waste incineration (MSWI) residues represents a critical challenge for sustainable development due to their increasing generation and environmental risk. At the same time, the cement industry faces urgent pressure to reduce CO₂ emissions associated with clinker production, creating a demand for alternative supplementary cementitious materials. The aim of this study was to evaluate the feasibility of valorising hazardous municipal solid waste incineration (MSWI) air pollution control fly ash (EWC 19 01 07*) as a constituent of Portland composite cement, in line with circular economy principles and the need to reduce CO₂ emissions associated with clinker production. The investigated fly ash, originating from flue gas cleaning processes, is characterised by high alkalinity and elevated concentrations of heavy metals, which currently necessitate controlled landfilling. To enable its safe reuse, the ash was subjected to high-temperature thermal treatment following granulation and subsequently incorporated into cement formulations under semi-industrial conditions. Two Portland composite cements were produced with different ash contents, corresponding to CEM II/A-07 and CEM II/B-07, while a Portland cement manufactured from the same clinker was used as a reference material. The chemical and phase composition of the ash before and after thermal treatment was analysed using XRF and XRD, supported by SEM/EDS observations. The results demonstrate that thermal treatment at 1150 °C induces partial phase stabilisation of APC fly ash without full vitrification, allowing its integration into cement systems under semi-industrial conditions. The incorporation of ash significantly alters hydration behaviour through increased water demand governed by particle porosity, CaO-rich phase composition, and early ionic interactions in the pore solution, leading to reduced workability and mechanical performance. While immobilisation efficiencies exceeding 99.5% were achieved for most heavy metals due to precipitation and incorporation into hydration products, barium exhibited persistent leaching controlled by its solubility under highly alkaline conditions and limited incorporation into C–S–H phases. These findings define both the technological feasibility and the key environmental constraints of APC fly ash utilisation in Portland composite cement. From a sustainability perspective, the proposed approach contributes to the reduction in hazardous waste landfilling and supports clinker substitution in cement production. The results demonstrate the potential of integrating waste management and low-carbon material design within a circular economy framework while highlighting current environmental limitations related to barium leaching. Full article

Flexible and biocompatible sensors are vital for a wide range of biomedical applications, including real-time health monitoring, intracranial pressure monitoring, knee replacement surgeries, wearables, and smart prosthetics. While various highly sensitive and stable pressure sensors have been demonstrated, they often lack the conformability and biocompatibility crucial for their wider application in various bio-integrated electronic systems. Herein, a piezoelectric pressure sensor is proposed using a hybrid polymer composite by leveraging the unique properties of Chitosan and Parylene C. Various material characterisations, such as XRD and FTIR, were performed to reveal structural and chemical characteristics of the novel composite material. Next, electromechanical characterisations of the pressure sensor were performed to reveal its dynamic sensing properties. The pressure sensor exhibits excellent sensitivity for both pressure and frequency, as well as cyclic stability (10³ cycles), wide pressure range (20–70 kPa), and biocompatibility. Full article

This study evaluated the influence of four thermal pretreatment techniques—autoclaving, hot-air oven treatment, hot-water immersion, and microwave irradiation—on Parthenium hysterophorus biomass to improve its biodegradability and biogas generation potential under batch anaerobic digestion. Among the investigated methods, hot-air oven pretreatment at 110 °C for 90 min exhibited the most significant enhancement in biomass solubilization, as indicated by a 51.5% rise in soluble chemical oxygen demand (sCOD) and an increase in volatile fatty acids (VFAs) compared with the untreated control. These compositional improvements facilitated faster hydrolysis and led to a 25.73% higher cumulative methane yield in biochemical methane potential (BMP) assays. Structural analysis revealed pronounced alterations in the lignocellulosic matrix, with reductions in hemicellulose and partial delignification improving substrate accessibility. Complementary characterisation using field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) confirmed the disruption of crystalline cellulose regions and modification of functional groups, supporting the observed biochemical improvements. Collectively, the results demonstrate that hot-air oven pretreatment is a practical and energy-efficient approach for enhancing the digestibility of P. hysterophorus biomass, promoting its utilisation as a sustainable feedstock for renewable biogas production and environmental management of this invasive weed. Full article

This study analyses the effect of electrolytic plasma treatment on improving the wear resistance of 30CrMnSi steel used under conditions of high abrasive and impact-abrasive loads. The samples were processed using various technological regimes, namely electrolytic plasma quenching, nitriding, nitrocarburising, and carburising. A range of analytical methods were employed to comprehensively characterise the structure, phase composition, and mechanical properties, including SEM/EDS, XRD, and microhardness testing. The tribological properties of the materials were evaluated using a TRB³ tribometer, and abrasive and impact-abrasive wear tests were performed in accordance with GOST 23.208–79 and GOST 23.207–79 standards. The results show that electrolytic plasma treatment leads to the formation of diffusion layers with a thickness of 50–150 μm, accompanied by the formation of carbide, nitride, and carbonitride phases (Fe₄C, Fe₇C₃, Fe₄N, Fe₂N, Fe₃(CN)). This process results in a significant increase in surface hardness (up to 610–930 HV) and improved wear resistance. The study indicates that electrolytic plasma nitrocarburising provides a favourable combination of hardness and tribological behaviour, leading to a low friction coefficient (0.25–0.35) and enhanced resistance to abrasive and impact-abrasive wear. The obtained results demonstrate the potential of this technology for improving the performance of components made of 30CrMnSi steel operating under severe wear conditions. Full article

Lignocellulose biomass (LB) has gained interest as a second-generation renewable feedstock for producing bio-based products within a circular economy framework. Hemp hurds, a byproduct of industrial hemp processing, are one of the LB feedstocks that have gained attraction. This study examines the physicochemical properties of hemp hurds to evaluate their suitability as substrates for bioproduct synthesis. The chemical analysis of hemp hurds showed that the polysaccharide content is 53.4%, lignin is 20.8%, extractives are 15%, and ash is 4.35%. The moisture content is 6.34%, and the density is 1.0016 g/mL, indicating low porosity and a small surface area, which limits enzyme access to cellulose. Structural analysis using X-ray diffraction (XRD) indicated a crystallinity index of 40.20%, and the Fourier Transform Infrared Spectrophotometer (FTIR) confirmed the characteristic peaks representing cellulose, hemicellulose, and lignin at 3332 cm⁻¹, 1734 cm⁻¹, and 1510 cm⁻¹, respectively. The Scanning Electron Microscope (SEM) revealed a tightly packed surface with smooth, low porosity, whereas the Thermogravimetric Analyser (TGA) indicated decomposition in phases for hemicellulose, cellulose, and lignin. The structural and chemical findings of hemp hurds characterisation suggest that they are a suitable raw material for producing various bio-based materials. Full article

Cellulose has received significant attention, given its high demand for the transition to sustainable fuels and renewable energy, addressing the environmental challenges of fossil fuels. Fast pyrolysis is a process that can transform cellulose into bio-oil. Although the bio-oils produced contain considerable amounts of oxygen and water, they are highly corrosive and highly viscous, which limits their utility as biofuels. Pyrolysis bio-oils require upgrading to remove oxygen and corrosive components, thereby enhancing their stability for use as biofuels and their environmental sustainability. This study investigates the catalytic pyrolysis of cellulose without a catalyst and with Ga/HZSM-5 catalysts with various gallium loadings (0.3, 3 and 9 wt%) and bulk Ga₂O₃ catalysts using pyrolysis/gas chromatography–mass spectrometry (Py/GC-MS). The catalytic influence of different gallium loadings on HZSM-5 in cellulose pyrolysis reactions is discussed using a range of characterisation techniques, including ICP, XRD, N₂ porosimetry, DRIFTS, and TPRS. The main production of oxygenated compounds (furan, sugar, ketone and phenol) and hydrocarbon products, including total aromatic and monocyclic and polycyclic aromatics, as well as benzene, toluene, xylene (BTX) and naphthalene compounds, using a family of Ga-doped HZSM-5 catalysts for cellulose pyrolysis is investigated for making sustainable cellulose-derived fuel. Ga(3)/HZSM-5 formed the highest amount of aromatics, displaying that aromatic yield depends on the Brønsted-to-Lewis acid balance (2.3 ratio) and total acidity (1.03 mmol·g⁻¹), rather than on gallium loading alone. Full article

The development of sustainable pigments from natural sources is gaining interest due to environmental concerns and the need for bio-based alternatives to synthetic dyes. This study investigates the synthesis of hybrid pigments by adsorbing anthocyanins—extracted from pomegranate agro-waste—onto halloysite (HA) nanotubes. A full factorial design was applied to evaluate the influence of pH and surfactant type (cetylpyridinium bromide and sodium dodecyl sulfate) on pigment colour and the thermal and structural stability of the hybrids. Adsorption was carried out in 400 mL dispersion baths containing 10 g of HA and 5% w/w anthocyanins. Surfactants (2% w/w) were added before the pigment, followed by 200 µL of silane. Dispersions were stirred at high speed for 1 h and then at 500 rpm for 23 h to ensure adsorption without premature desorption. Characterisation (TGA, XRD, FTIR, UV-Vis/NIR, SEM, EDX, BET) confirmed the preservation of HA structure and minimal changes in thermal behaviour. Pigment colour varied with synthesis conditions, especially pH: a higher pH increased brightness and yielded yellowish tones, while a lower pH resulted in reddish-blue hues with greater variability. The results confirm halloysite’s potential as a stable carrier for natural dyes and demonstrate that pH effectively tunes hybrid pigment colour. Full article

This study systematically investigates the role of Ni in Co₂SiO₄ in a bimetallic (Co²⁺,Ni²⁺)₂SiO₄ olivine-type system and the materials’ catalytic efficiency in a model Heck–Mizoroki coupling reaction. Thus, a series of olivines with varying (Co²⁺,Ni²⁺)₂SiO₄ compositions (0–100% Ni) was synthesised and characterised by ICP-OES, FTIR/Raman, P-XRD and XPS analysis. Ideal mixing of metals was achieved with (49:51) Co:Ni. Catalytic testing revealed distinct conversion vs. time profiles, with the (69:31) Co:Ni olivine exhibiting the best overall performance, combining good reactivity with near-perfect selectivity (>99%) and improved stability. Mechanistic pathways were probed through product scope analysis, reactant–product temporal profiling, leaching and radical scavenging experiments. Results suggest a radical-assisted Heck–Mizoroki mechanism. Spectroscopic data correlated Co²⁺ and Ni²⁺ incorporation with M1 and M2 site occupancy, where Ni²⁺ M2 sites enhanced reactant activation and intermediate stability and Co²⁺ in the M1 site enhanced product release, though also homocoupling in Co₂SiO₄. Minimal leaching was observed for all bimetallic catalysts. These findings highlight the tunability of bimetallic olivines for C–C coupling reactions via controlled cation distribution. Full article

This study investigates the valorisation of lemon industry by-products as carbon sources to produce poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) using the halophilic archaeon Haloferax mediterranei. The resulting polymer (HFX PHBV) was supplemented with nucleating agents (orotic acid, boron nitride, and theobromine) and compared with a commercial PHBV grade (Enmat Y1000) under identical conditions. Fermentation strategies were optimised by varying the lemon by-product concentration, inoculum size, and nutrient stoichiometry (C:N:P ratios), followed by scaleup in a 2 L bioreactor. A 11% (v/v) lemon by-product combined with a 5% (v/v) inoculum yielded the highest productivity under minimal medium conditions (2.127 g/L PHBV), while enriched media further enhanced the polymer accumulation (up to 3.250 g/L PHBV). A comparative characterisation of HFX PHBV and Enmat Y1000, using NMR, TGA, MFR, DSC, Raman spectroscopy, XRD, and DMA, revealed that HFX PHBV exhibited lower crystallinity, increased flexibility, and a high hydroxyvalerate content (27.4%), which conferred improved ductility. Investigation of nucleating agents demonstrated that orotic acid was the most effective at enhancing the crystallisation kinetics. Overall, this study demonstrates an efficient PHBV production process based on waste valorisation, yielding a biopolymer with competitive physicochemical properties relative to a commercial standard, and provides integrated solutions to the global challenges of plastic pollution and food waste. Full article