Search Results (25,605)

The global demand for biodiesel production is steadily increasing. Conventional homogeneous basic catalysts, while widely used in the industry, face significant drawbacks, such as the requirement for high-quality feedstock, excessive waste generation, and multiple purification steps. In this study, an acidic silane (IM-CPTMS-BS-H₂SO₄) containing imidazolium and sulfonic groups was synthesized. Heterogeneous catalysts were then prepared by anchoring varying proportions of the silane onto SBA-15 mesoporous solids. These materials were characterized by FTIR, ¹³C and ²⁹Si NMR, TGA, XRD, CHNS and acidity measurements. The catalysts were evaluated in the transesterification of methyl acetate with ethanol, with increasing catalytic conversions with the amount of grafted IM-CPTMS-BS-H₂SO₄. Furthermore, increasing the catalyst loading (from 2% to 5% wt.) and the reaction temperature (from 50 °C to 65 °C) led to higher methyl acetate conversion rates. Full article

The influence of zirconia incorporation and template type on the physicochemical properties of NiMo/Al₂O₃-ZrO₂ catalysts was investigated for the hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DMDBT) and the hydrogenation (HYD) of naphthalene (N). Catalysts were prepared by co-impregnation on supports synthesized via a sol-gel method using starch (A) and activated carbon (C) as structure-directing templates, followed by zirconium incorporation through a grafting procedure. The resulting materials were characterized by SEM–EDX, N₂ physisorption, H₂-TPR, XPS, HRTEM, and pyridine-FTIR. SEM-EDX confirmed homogeneous metal distributions and compositions close to nominal values (Mo = 20 wt%, Ni = 5 wt%, Zr = 11 wt%) with Ni/(Ni + Mo) = 0.30. N₂ adsorption–desorption isotherms correspond to type IV(a) with H3-H4 hysteresis loops, characteristic of mesoporous structures. After metal incorporation, surface areas decreased to 96 m² g⁻¹ for NiMo/Al₂O₃ and 81 m² g⁻¹ for Zr-modified catalysts, while the activated carbon-templated sample preserved a larger mesoporous volume (0.335 cm³ g⁻¹) and higher macroporosity (72%). H₂-TPR profiles indicated improved reducibility for Zr-containing catalysts. XPS revealed an increase of MoS₂ species from 45% in NiMo/Al₂O₃ to 75% in NiMo/Al₂O₃-ZrO₂(C), accompanied by a higher degree of sulfidation index (DSI) from 47.1% to 73.9%. HRTEM analysis of Zr-modified catalysts revealed longer MoS₂ slabs (11.8–12.1 nm) and higher edge-to-corner ratios (17–17.4) compared with NiMo/Al₂O₃ (6.2 nm; fe/fc = 8.2). Pyridine-FTIR showed a substantial increase in total acidity from 91 to 421 μmol g⁻¹ upon Zr addition. Catalytically, NiMo/Al₂O₃-ZrO₂(C) exhibited the highest HDS conversion (40%), reaction rate (10.5 × 10⁻⁹ mol s⁻¹ g⁻¹), and TOF (4.69 × 10⁻⁵ s⁻¹), whereas NiMo/Al₂O₃-ZrO₂(A) reached the highest naphthalene conversion (97.18%), with a reaction rate of 27.4 × 10⁻⁷ mol s⁻¹ g⁻¹ and TOF of 12.9 × 10⁻³ s⁻¹. These results demonstrate that Zr incorporation and the activated carbon template favored hydrodesulfurization, whereas the starch template promoted hydrogenation performance. Full article

Cinnamomum zeylanicum (C. zeylanicum) is rich in bioactives, such as cinnamaldehyde and phenols, which are susceptible to thermal degradation, volatilisation, and oxidative deterioration during processing and storage, thereby reducing chemical stability and limiting bioavailability. Encapsulation using lecithin and chitosan-based systems mitigates these instabilities by forming a protective barrier against oxygen, light, and heat while enhancing structural stability. In this study, freeze-dried extracts of C. zeylanicum were encapsulated into lecithin-based primary liposomes (PL) and chitosan-coated secondary liposomes (CH/L). The coating of liposomes with chitosan improves the liposome stability, mucoadhesion, and provides protection in the gastric pH while facilitating electrostatic bonding with the biological membrane. The high compatibility and low toxicity of chitosan also make it a suitable carrier in food and nutraceutical applications. The formed liposomes were characterised for particle size, polydispersity index, zeta potential, encapsulation efficiency (EE), and storage stability over 8 weeks. CH/L showed superior EE (89.027%) compared to the PL (84.154%; p < 0.05). The particle size, polydispersity index, and zeta potential of the cinnamon-loaded lecithin-based primary liposome (CZ-PL) upon formation were 161.93 nm, 0.13, and −37.597 mV. In comparison, those of the cinnamon-loaded chitosan-coated liposomes (CZ-CH/L) were 591.7 nm, 0.27, and +28.17 mV. The particle size of CZ-PL and CZ-CH/L was 175.90 and 588.60 nm after 8 weeks of storage. The TEM confirmed the spherical morphology of the liposomes. The differential scanning calorimetry analysis demonstrated the disappearance of the characteristic cinnamon melting peak and shifts in liposomal transition temperatures, confirming successful encapsulation. FTIR analysis showed reduction or disappearance of characteristic cinnamon fingerprint peaks and slight band shifts, indicating successful encapsulation and non-covalent interactions, including hydrogen bonding and electrostatic effects, within the liposomal systems. These findings imply that lecithin-based and chitosan-coated liposomes could be employed to successfully carry C. zeylanicum bioactives. Full article

To address heavy metal contamination in wastewater, this study developed a novel chelating resin (PS-2-AB) by grafting 2-aminobenzimidazole onto chloromethylated polystyrene. The resin was characterized using SEM, BET, FTIR, and XPS to confirm successful modification and analyze its structural properties. Batch adsorption tests were conducted to evaluate its removal performance for Cu(II) and Ni(II) ions. Under optimal conditions (pH 5.0–7.0, dosage: 1.0 g/L), PS-2-AB achieved maximum adsorption capacities of 125.04 mg/g for Cu(II) and 157.44 mg/g for Ni(II), which are significantly higher than those of the commercial resin D113 (44.68 mg/g for Cu(II) and 25.17 mg/g for Ni(II)) under the same conditions. Adsorption kinetics followed the pseudo-second-order model, indicating chemisorption-dominated behavior, while equilibrium data fit the Langmuir model, suggesting monolayer adsorption. Thermodynamic parameters confirmed a spontaneous and endothermic process. After five regeneration cycles, PS-2-AB retained approximately 87% (Cu) and 89% (Ni) of its original capacity, demonstrating good reusability. These results indicate that PS-2-AB exhibits markedly better adsorption performance than D113, making it a promising and cost-effective adsorbent for the efficient removal of Cu(II) and Ni(II) from aqueous media. Full article

The textile industry wastewater contaminated by azo dyes usually contains a certain amount of salinity. Therefore, screening for microorganisms capable of degrading azo dyes in saline environments is of great significance. In this study, the decolorizing activity of azo dye methyl red (MR) by Klebsiella aerogenes WH2 (WH2), newly isolated from soil, was evaluated. WH2 was able to decolorize 92.4% and 86.0% of MR at concentrations of 200 mg/L and 300 mg/L within 24 h, respectively. Given that WH2 exhibited enhanced growth and superior degradation capacity in the presence of 2.5% NaCl compared to salt-free conditions, it can be classified as a slight halophile. Approximately 87.7% of MR was removed by WH2 in the presence of 10.0% NaCl within 24 h. Azoreductase activity assays indicated that WH2 retained higher enzyme activity in the presence of NaCl concentrations not exceeding 7.5%. The degradation products and putative metabolic pathways for MR degradation by WH2 were analyzed using FTIR and LC-MS. Phytotoxicity analysis based on seed germination of Vigna radiata indicated that the degradation products of MR exhibited less toxicity than the parent compound. The high degradation efficiency of MR under high salt concentrations makes WH2 a promising candidate for the treatment of saline textile wastewater. Full article

Historic structures that possess cultural heritage value are important documents that convey the architectural understanding, material technology, and construction techniques of past civilizations to the present day. However, these structures are exposed over time to physical, chemical, and mechanical deterioration due to environmental effects, climatic conditions, the natural aging processes of materials, and human interventions. The conservation and faithful restoration of historic structures necessitate the scientific determination of the properties of original building materials. In this study, we aimed to determine the physical, chemical, mineralogical, thermal, and mechanical properties of the original building materials used in the Old Armenian Church located in the city of Çanakkale. In order to reveal the chemical and mineralogical compositions of the samples, XRD, SEM, Raman, and FTIR analyses were applied. The thermal behaviors of the materials were examined through TGA. To determine the physical properties, tests for unit volume weight, specific gravity, compactness, porosity, and water absorption capacity were carried out. For the determination of mechanical properties, compressive strength tests—as well as non-destructive testing methods such as the Schmidt hammer and UPV measurements—were employed. The analysis results indicate that the materials used in the structure have a carbonate-based mineralogical composition and that calcite-bonded systems are dominant. While the physical and mechanical data reveal that the materials possess a compact internal structure, they also indicate that microcracks and weathering processes may be effective in certain areas. These findings emphasize the importance of using lime-based mortars and stones compatible with the original materials in restoration works. Full article

Background/Objectives: Enteric drug forms are developed to delay drug release to avoid drug degradation in the acidic environment of the stomach or to prevent irritation of the stomach mucosa. The bioavailability of posaconazole (POS) after oral administration depends on stomach pH and food intake. Delayed-release tablets and unmodified oral suspension are the POS formulations currently available on the market. The oral suspension formulation is characterized by highly variable bioavailability, which may significantly affect therapy effectiveness. Methods: In this study, multi-unit drug forms with delayed and sustained POS release were designed. Polymeric microparticles consisting of sodium alginate (ALG), methacrylic acid–ethyl acrylate copolymer (EUD), or both, were prepared using the spray-drying technique. The formulations that met the pharmacopoeia enteric release standards in the in vitro dissolution test were subjected to further in vitro evaluation via swelling and mucoadhesion assays, an antifungal activity test, attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR), and thermal analysis. Results: It was shown that EUD formulations at concentrations of 5% and 6% provided enteric release, whereas ALG at 1.5% concentration exhibited a sustained, although not delayed, POS release profile. The optimal blended formulations (EAP15–EAP18), comprising 4% EUD with 1.5–2.0% ALG and either 1% or 4% POS, met the pharmacopoeia criteria for enteric dosage forms. Furthermore, these blends demonstrated the most favorable sustained-release profiles in the buffer phase, ranging from 2 to 3 h. The microparticles exhibited beneficial swelling and mucoadhesive properties, which are essential for prolonging contact with the intestinal mucosa; combined with antifungal properties. Conclusions: Obtained carrier may provide a promising preliminary basis for developing a multi-unit, sustained-release enteric dosage form for POS and future in vivo investigations. Full article

Thermoplastic polyurethane properties are governed by the interplay between soft-segment mobility, hard-segment interactions, and segmented morphology, yet the extent to which atomistic predictions of their thermal and mechanical behavior depend on force-field choice remains insufficiently benchmarked. Here, we combine FTIR, DSC, TGA, and tensile testing with all-atom molecular dynamics simulations to investigate HDI–PEG polyurethane systems across a controlled soft-segment series. Experimentally, films with PEG molecular weights of 400, 1000, and 1500 g/mol were characterized, while simulations were extended to 400–2000 g/mol to compare two complementary force-field frameworks under a consistent protocol: OPLS-AA, a conventional atom-type-based force field, and OpenFF/Sage, a direct-chemical-perception framework augmented here with bespoke torsional refinements. Both force fields reproduce the composition-driven decrease in Tg and density with increasing PEG length, but differ systematically in absolute values, with OPLS-AA predicting higher densities and Tg values than OpenFF. Tensile experiments show the highest elastic modulus for PEG400, a marked decrease at PEG1000, and a partial recovery at PEG1500. Although nanosecond-scale deformation simulations overestimate absolute moduli because they probe high-rate elastic response, they recover composition-dependent stiffness differences, with OpenFF yielding a more pronounced non-monotonic trend than OPLS-AA. Overall, this work provides an experimentally anchored benchmark for assessing which composition-driven trends in HDI–PEG polyurethanes are robust across force-field families, and which observables remain sensitive to model assumptions and simulation scale. Full article

In this study, TiO₂ nanoparticles (NPs), CdS NPs and TiO₂/CdS nanocomposite were synthesized via the sol–gel, hydrothermal and ex situ method, respectively. The synthesized materials were characterized using XRD, UV–vis DRS, FTIR, SEM, and EDX analysis. XRD analysis confirmed the crystalline structure of the as-prepared samples, while the bandgap energy of TiO₂ NPs, CdS NPs, and TiO₂/CdS nanocomposite were determined to be 2.98, 1.94, and 2.27 eV, respectively. Photocatalytic efficiency of TiO₂ NPs, CdS NPs, and TiO₂/CdS nanocomposite was systematically evaluated by photocatalytic degradation of crystal violet (CV) dye under visible-light irradiation. Under optimized reaction conditions of [CV concentration] = 20 mg/L, [catalyst dosage] = 0.25 g/L, and pH = 6, TiO₂/CdS nanocomposite achieved 86.3% removal of CV within 180 min, outperforming pure TiO₂ NPs (16.4%) and CdS NPs (66.9%). The enhanced performance of TiO₂/CdS nanocomposite as compared to CdS NPs is attributed to improved charge separation via heterojunction formation, while significantly superior performance over TiO₂ demonstrates successful visible-light activation. Further optimization study revealed that maximum removal efficiency of CV (97.1%) was achieved at lower dye concentration (10 mg/L). Photocatalytic degradation of CV followed pseudo-first-order kinetics. Moreover, scavenger experiments confirmed hydroxyl radicals (^•OH) as dominant reactive species. Furthermore, the TiO₂/CdS nanocomposite demonstrated good reusability with minimal activity loss after five runs. Additionally, the as-prepared nanocomposites showed significant antibacterial activity against Pseudomonas aeruginosa (P. aeruginosa). The present study indicated that TiO₂/CdS nanocomposite could be simultaneously used for degradation of organic pollutants as well as for removal of microorganisms while targeting environmental sustainability and water purification. Full article

Activated carbons are usually prepared from natural precursors (e.g., fruit stones or nutshells) by carbonization and activation processes carried out at 400–1000 °C. They exhibit well-developed porosity, and chemical activation introduces hydrophilic functional groups on their surface, providing excellent sorption properties. However, the high temperatures required during thermal treatment increase production costs. In this work, cost-reducing methods for preparing carbon sorbents are proposed. Carbonization of H₃PO₄ activated waste pistachio nutshells was performed using classical pyrolysis (500 or 550 °C, 30 min, N₂ atmosphere) and microwave treatment (power 1000 W, 20 min). The properties of the synthesized carbons were characterized using thermogravimetry and spectroscopic techniques including infrared (ATR), Raman, photoelectron (XPS) spectroscopies, and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). Porous structure parameters were determined using nitrogen adsorption experiments. The efficiency of Pb²⁺ removal from spiked ultrapure, tap and river water was evaluated by batch sorption experiments and inductively coupled plasma–mass spectrometry. The most porous carbons were those prepared at 500 and 550 °C, with specific surface areas of 910 and 256 m²/g, respectively. Surface phosphates increased the Pb²⁺ sorption efficiency to 99% from ultrapure water, at an initial concentration of 300 µg Pb²⁺/L. The material obtained with the microwave method was not fully carbonized and remained nonporous, but it also exhibited 99% Pb²⁺ uptake from ultrapure water due to the presence of oxygen-containing surface groups. The Pb²⁺ removal from spiked tap and river water reached up to 84% and 94%, respectively, at the spiking level of 300 µg Pb²⁺/L. Full article

This study investigates the potential of Fischer–Tropsch (FT) waxes, synthesized from natural gas, as high-performance and sustainable alternatives to conventional ester waxes in cosmetic applications. To evaluate their technical viability, a series of FT waxes with varying hydrocarbon chain lengths were synthesized and characterized. Safety was rigorously assessed through human patch tests and irritation surveys, while sensory attributes, including gloss and transparency, were compared against beeswax and carnauba wax. Furthermore, the impact on the skin barrier was analyzed using Attenuated Total Reflection Fourier Transform Infrared (ATR-FTIR) spectroscopy to determine lipid packing characteristics. The results demonstrated that FT waxes possess an excellent safety profile with irritation levels comparable to traditional waxes. Sensory evaluations revealed that adjusting the hydrocarbon chain length allows for precise control over melting points and texture, offering significant formulation flexibility. Crucially, lipid packing analysis indicated that FT waxes promote an orthorhombic organization, effectively mimicking and reinforcing the native crystalline structure of the human skin barrier. These findings conclude that FT waxes provide both superior sensory properties and functional skin-barrier benefits, positioning them as versatile and innovative ingredients for advanced dermo-cosmetic formulations. Full article

Selenium nanoparticles (SeNPs) represent promising bioactive agents due to their reduced toxicity and multifunctional biological properties. In this study, SeNPs were synthesized via an eco-friendly phytosynthesis approach using Curcuma longa extract, yielding curcumin-functionalized selenium nanoparticles (cur–SeNPs). The composites (cur–SeNPs), either in native extract form or isolated, were incorporated into siloxane hybrid matrices prepared by the sol–gel method from tetraethyl orthosilicate: dimethyldimethoxysilane precursors, with polyvinylpyrrolidone (PVP) as a structural modifier. The host matrices were differentiated by the ratios between the precursors of the siloxane network, 3:1 for CS0–CS4, respectively, 1:1 for CS5, modified with PVP in the case of CS2 and CS3. These were loaded with cur–SeNPs–T in the cases of CS1, CS2, CS5 or with cur–SeNPs for CS3 and CS4. FTIR, XRD, SEM, and EDX analyses confirmed the formation of amorphous siloxane networks with well-dispersed SeNPs (up to ~12 wt%). PVP incorporation generated ordered mesoporous structures, increasing total pore volume sixfold and enlarging the average pore diameter to 9.26 nm. Studies about selenium ion release demonstrate that mesoporosity significantly enhances diffusion-controlled release. Antimicrobial assays against Staphylococcus aureus, Escherichia coli, and Candida albicans reveal a synergistic effect between curcuminoids and SeNPs, particularly in matrices with higher nanoparticle loading. The sol–gel technique for obtaining hybrid materials is very versatile regarding the supports on which the resulting materials or the compounds hosted in these host networks can be deposited. The dynamics of the development of hybrid materials is also reflected in the multitude of applications in various fields such as bio-medical, electronics, agriculture or food. Results obtained in this work highlight the potential of the developed systems for antimicrobial coatings on glass substrates and targeted delivery applications. Full article

This study presents a source-specific experimental evaluation of particle board waste sludge (PBWS), a sludge-type industrial by-product from the wood-based panel industry, as a partial cement replacement in Portland cement paste systems. The hydration-related behavior of cement pastes containing 0%, 5%, 10%, and 20% PBWS at 7, 28, and 90 days was investigated using Fourier Transform Infrared Spectroscopy (FT-IR), X-Ray Diffraction (XRD), and Thermogravimetry/Derivative Thermogravimetry (TG/DTG). The results showed that PBWS affected phase development and thermal decomposition behavior depending on replacement level and curing age. In the TG/DTG analysis, mass losses in the 30–230 °C region were generally higher in the PBWS-containing mixtures than in the reference paste, particularly at 28 and 90 days, suggesting differences in dehydration-related phase development. FT-IR and XRD results further showed that PBWS modified the evolution of hydration-related phases in the blended systems. From an environmental perspective, increasing PBWS replacement reduced the calculated energy intensity, CO₂ emissions, and production cost; at 20% replacement, these values decreased from 3300 to 2654 MJ/t, from 830 to 706.77 kg/t, and from 3400 to 2867.16 TL/t, respectively. Overall, the results indicate that PBWS has the potential to improve the environmental profile of cement-based production while influencing hydration-related phase evolution in blended paste systems. Full article

The persistence of azo dyes in industrial effluents poses significant environmental risks; therefore, there is a need to develop effective adsorbents. This study investigates the efficiency of a Cu₂O/CuO nanocomposite as an adsorbent for the removal of a model dye, methyl orange (MO), from aqueous solutions. The material was characterized by XRD, SEM and BET analyses, revealing a dominant Cu₂O phase (96 wt%) with CuO fractions, and an average particle size of ~18 nm paired with a specific surface area of 19.54 m² g⁻¹. FTIR and TOC assays revealed the adsorption and degradation of MO by action of the nanocomposite. Operational parameters such as adsorbent dosage, initial dye concentration, pH, and the point of zero charge (PZC) were investigated. Under the optimized conditions, the nanocomposite achieved a dye removal efficiency of 97.0%. The kinetic results showed a strong correlation with the pseudo-second-order model. Furthermore, isotherm analysis revealed that the adsorption process is best described by the Langmuir–Freundlich model, demonstrating an outstanding maximum theoretical adsorption capacity (q_max) of 254.76 mg g⁻¹, which closely aligns with the experimental value (249.48 mg g⁻¹). The findings demonstrated that the synthesized Cu₂O/CuO nanocomposite acts as an efficient and promising adsorbent for the remediation of dye-contaminated waters. Full article

The generation of agro-industrial residues represents an environmental challenge and an opportunity for their valorization within a circular economy framework. In this study, Agave salmiana bagasse residues were evaluated as a reinforcing material for developing bioplastics made from maize starch (polymer matrix). Maguey bagasse was collected, ground and sieved to particle sizes below 200 μm and incorporated into bioplastic formulations at different content levels. Five bioplastic films (M1–M5) were obtained and characterized regarding their physical, chemical, mechanical, thermal, and morphological properties. The evaluated parameters included density, color (CIE Lab*), moisture content, water absorption, FTIR analysis, tensile properties, thermal behavior, and surface morphology via SEM. The results showed significant differences among the bioplastic formulations. The moisture content ranged from 7.15% to 10.57%, while water absorption after 24 h reached values of up to 65% for the formulation with the highest bagasse content. Mechanical and thermal analyses indicated that the incorporation of maguey bagasse influenced the structural performance of the bioplastics, while SEM observations revealed changes in surface morphology associated with fiber incorporation. These findings demonstrate the potential of A. salmiana bagasse as a reinforcing agent in starch-based bioplastics, contributing to the development of sustainable materials. The results support their potential as a biodegradable material with exploratory application in an agricultural system. Full article