Search Results (994)

Hydrogels comprise three-dimensional networks of hydrophilic polymers and have attracted considerable interest in various sectors, including the biomedical, pharmaceutical, agricultural, and food industries. These materials offer significant benefits for food packaging applications, such as high mechanical strength and excellent water absorption capacity, thereby contributing to the extension of product shelf life. Therefore, the aim of this study is to compare the performance of citric acid and glutaraldehyde as crosslinking agents in gelatine-based hydrogels reinforced with cellulose nanocrystals (CNC), contributing to the development of safe and environmentally responsible materials. The hydrogels were prepared using the casting method and characterised in terms of their physical, mechanical, and structural properties. The results indicated that hydrogels crosslinked with glutaraldehyde exhibited higher opacity, lower transparency, and greater mechanical strength, whereas those crosslinked with citric acid demonstrated improved clarity, reduced water permeability, and enhanced swelling capacity. The incorporation of CNC further improved mechanical strength, reduced weight loss, and altered both surface homogeneity and optical properties. Microstructural results obtained by SEM were consistent with the mechanical properties evaluated (TS, %E, and EM). The Gel-ca hydrogel displayed the highest elongation value (98%), reflecting better cohesion within the polymeric matrix. In contrast, films incorporating CNC exhibited greater roughness and cracking, which correlated with increased rigidity and mechanical strength, as evidenced by the high Young’s modulus (420 MPa in Gel-ga-CNC2). These findings suggest that the heterogeneity and porosity induced by CNC limit the mobility of polymer chains, resulting in less flexible and more rigid structures. Additionally, the DSC analysis revealed that gelatine hydrogels did not exhibit a well-defined Tg, due to the predominance of crystalline domains. Systems crosslinked with citric acid showed greater thermal stability (higher Tm and ΔH_m values), while those crosslinked with glutaraldehyde, although mechanically stronger, exhibited lower thermal stability. These results confirm the decisive effect of the crosslinking agent and CNC incorporation on the structural and thermal behaviour of hydrogels. In this context, the application of hydrogels in packaged products represents an eco-friendly alternative that enhances product presentation. This research supports the reduction in plastic consumption whilst promoting the principles of a circular economy and facilitating the development of materials with lower environmental impact. Full article

The study presents the results of investigations into various types of anhydrous pyrolysis aimed at determining the kinetic parameters of hydrocarbon generation processes from source rocks. Surface outcrop samples from the Silesian, Dukla, and Skole units, characterized by a low level of thermal maturity, were used as experimental material. The samples predominantly represented the Menilite Beds from the aforementioned three units, but also included Istebna, Lgota, Verovice, and Spas beds, which exhibit significantly lower parameters that describe generation properties. The anhydrous pyrolysis experiments provided information on the rate of organic matter decomposition (TG/DSC), the degree of conversion (Rock-Eval), the quality of the obtained products (Py/GC), and the isotopic composition of the gaseous products (Py/GC/IRMS). Chromatographic analyses confirmed the oil-prone nature of kerogen contained in the Menilites from the Dukla Unit (Tylawa area), the Silesian Unit (Iwonicz fold), and the Skole Unit, revealing an equal share of all hydrocarbon fractions: C₁–C₉, C₁₀–C₁₅, and C₁₅₊. Through the integration of pyrolytic studies conducted on potential source rocks in the polish Outer Carpathians, a new type of information was obtained regarding the rate of organic matter decomposition, as well as the fractional and isotopic composition of the pyrolysis products. The set of obtained results was used to estimate the activation energy and characterize the potential source levels. The innovative aspect of this approach involved the isotopic characterization of gaseous products generated during thermal degradation of the source rocks. These data were subsequently used to establish genetic correlations with natural gases accumulated in hydrocarbon reservoirs of the Carpathian region. It has been demonstrated that pyrolysis using PY-GC-IRMS can yield results comparable to those obtained through generation in natural geological conditions. Full article

Cu₂S has wide-ranging applications in the energy field, particularly as electrode materials and components of energy storage devices. However, the migration of copper ions is prone to component segregation and copper precipitation, impairing long-term thermal stability and service performance. Ce₂S₃ not only possesses the unique 4f electron layer structure of Ce but also has high thermal stability and chemical inertness. Here, we report for the first time that the thermal stability and mechanical properties of Cu₂S can be significantly enhanced by introducing the dispersed phase Ce₂S₃. Thermogravimetry—differential scanning calorimetry (TG-DSC) results show that the addition of 6 wt% Ce₂S₃ improves the thermal stability of Cu₂S sintered at 400 °C. X-ray diffraction (XRD) results indicate that the crystal structure of Cu₂S gradually transforms to tetragonal Cu_1.96S and orthorhombic Cu_1.8S phase at 400 °C with the increase of Ce₂S₃ addition. Scanning electron microscopy (SEM) results show that the particle size gradually decreased with the increase of Ce₂S₃ amount, indicating that the Ce₂S₃ addition increased the reactivity. The Ce content in Cu₂S increased gradually with the increase of Ce₂S₃ amount at 400–600 °C. The 7 wt% Ce₂S₃-Cu₂S exhibits paramagnetic behavior with a saturation magnetization of 1.2 µ_B/Ce. UV-Vis analysis indicates that the addition of Ce₂S₃ can reduce the optical energy gap and enrich the band structure of Cu₂S. With increasing addition of Ce₂S₃ and rising sintering temperature, the density of Ce₂S₃-Cu₂S gradually increases, and the hardness of Ce₂S₃-Cu₂S increases by 52.5% at 400 °C and by 34.2% at 600 °C. The friction test results show that an appropriate addition amount of Ce₂S₃ can increase the friction coefficients of Cu₂S. Ce₂S₃ modification offers a novel strategy to simultaneously enhance the structural and service stability of Cu₂S by regulating Cu ion diffusion and suppressing compositional fluctuations. Full article

Aluminum hydride (AlH₃) is a promising candidate for enhancing the combustion performance of liquid fuels due to its high energy density and exceptional hydrogen storage capacity. This study investigated the ignition and combustion characteristics of μ-AlH₃ particles in kerosene droplets using TG-DSC analysis, high-speed imaging, laser ignition, and combustion product characterization, with comparisons to micron- and nano-aluminum powders. Results showed that the exothermic combustion of hydrogen released from AlH₃ decomposition lowered the primary oxidation temperature of aluminum, leading to more intense combustion with smaller ejected particles. The particle size of kerosene droplets containing AlH₃ rapidly decreases due to the escape of hydrogen. The heat released by the combustion of hydrogen significantly accelerates the combustion of droplets, and the fastest combustion rate is observed at a concentration of 1% AlH₃. The combustion products of kerosene droplets containing AlH₃ are smaller than those of kerosene droplets containing aluminum, indicating that their combustion efficiency is higher. A combustion model for AlH₃-based kerosene droplets was developed, demonstrating less than 10% error in predicting ignition delay and burning rates. These findings provide valuable insights for the application of AlH₃ in liquid fuels. Full article

The control of crystal form in chiral active pharmaceutical ingredients (APIs) is a critical challenge in pharmaceutical development, as differences in solid-state structure can significantly influence physical properties and manufacturing performance. Troglitazone, a molecule with two chiral centers, exists as four stereoisomers (RR, SS, RS, SR) that crystallize as two enantiomeric pairs: RR/SS and RS/SR. This study aims to elucidate the relationship between solution-state molecular interactions and crystallization behavior of these diastereomeric pairs. Antisolvent crystallization experiments were conducted for both mixed solutions containing all four isomers and solutions of individual pairs. Crystallization kinetics were monitored by HPLC, and the resulting solids were characterized by PXRD, DSC, TG, and microscopic observation. Nucleation induction times were determined over a range of supersaturation levels. To probe intermolecular interactions in solution, NOESY and targeted NOE NMR experiments were performed, and the results were compared with crystallographic data. The RS/SR crystals(H-form) consistently exhibited shorter induction times and faster crystallization rates than the RR/SS crystals (L-form), even under conditions where RR/SS solutions were more supersaturated. In mixed solutions, H-form crystallized preferentially, with L-form either remaining in solution or being incorporated into H-form crystals as a solid solution. NOESY and NOE analyses revealed intermolecular proximities between protons that are distant in the molecular structure, indicating the presence of ordered aggregates in solution. These aggregates were more structurally compatible with the H-form than with the L-form crystal lattice, as supported by crystallographic distance analysis. The results demonstrate that differences in nucleation kinetics between troglitazone diastereomers are closely linked to solution-state molecular arrangements. Understanding these relationships provides a molecular-level basis for the rational design of selective crystallization processes for chiral APIs. Full article

Mortars taken from the 16th century Venetian Fortress of Bergamo (Italy) were characterized (binder-concentrated fractions and aggregate fractions as well as bulk samples) with a multi-analytical approach using X-ray diffraction (XRD), inductively coupled plasma optical emission spectrophotometry (ICP-OES), optical microscopy (OM), differential scanning calorimetry (DSC) and thermogravimetric analysis (TG). The results showed the presence of calcite, hydrocalumite and hydrotalcite-type compounds, brucite, aragonite, plombierite and a large fraction of amorphous phases (ranging between 14 and 27 wt%) in the binder. Quartz and carbonate-rich sands were used as aggregates. The mortar is a Mg-rich material containing 4–5 wt% brucite. No evidence of magnesite or hydromagnesite was found in any sample, although these phases are frequently detected in the binder of buildings from the Renaissance period that are located in Northern Italy. The large average amount (12–13 wt%) of reactive silicate, such as Mg-containing phyllosilicates that can react with lime, and the presence of carbonate-containing hydrocalumite and hydrotalcite indicate hydraulic interactions between lime and reactive silicate aggregates. The CO₂/H₂O_bound ratio, evaluated from the weight loss referred to the finer fraction (<63 μm), ranges from 1.99 to 2.55, which suggests that the walls of Bergamo were constructed using lime-based mortar with hydraulic properties. Full article

A novel quinoline-containing benzoxazine resin, 8HQ-fa, has been successfully synthesized at room temperature using sustainable raw materials, such as 8-hydroxyquinoline and furfurylamine as the phenol and amine source, respectively. The chemical structure of the hereinafter referred to as quinolinoxazine is fully characterized by Fourier transform infrared spectroscopy (FT-IR), ¹H and ¹³C nuclear magnetic resonance spectroscopy (NMR), as well as by 2D ¹H–¹H nuclear Overhauser effect spectroscopy (NOESY) and ¹H–¹³C heteronuclear multiple quantum correlation (HMQC) NMR. Thermal properties and polymerization behavior of the monomer are studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The resulting polymer is also characterized in terms of its thermal and fire-related properties by DSC, TGA, and microscale combustion calorimetry (MCC). The resulting thermoset, poly(8HQ-fa), presents good thermal stability as evidenced by its T_g (201 °C), T_d5 and T_d10 (307 and 351 °C, respectively), and char yield (42%), and low flammability as determined by the LOI, heat release capacity, and total heat released values (34.3, 143 J/gK, and 10.8 kJ/g, respectively), making it a self-extinguishing thermoset. The combination of properties and advantages in the synthesis of 8HQ-fa, accompanied by a low polymerization temperature, suggests its great potential in the field of high-performance polymers. Full article

River sediments have attracted increasing attention as alternative raw materials for sustainable cementitious materials due to their abundant availability and silica–alumina-rich composition. In this study, a systematic literature search was conducted in Web of Science and Google Scholar using combinations of the keywords “river sediment,” “cementitious materials,” “activation,” and “pozzolanic activity,” covering publications up to July 2025. In addition, a citation network tool (Connected Papers) was employed to trace related works and ensure comprehensive coverage of emerging studies. This review systematically examines the properties of river sediments from diverse regions, along with activation and modification techniques such as alkali/acid activation, thermal calcination, and mechanical milling. Their applications in various cementitious systems are analyzed, with mix design models compared to elucidate the effects of replacing fine aggregates, coarse aggregates, and cement on workability, strength, and durability. Multi-scale characterization via XRD, FTIR, and TG-DSC reveals the mechanisms of C–S–H and C–A–S–H gel formation, pore refinement, and interfacial transition zone densification. The review highlights three key findings: (1) moderate sediment replacement (20–30%) improves strength without compromising flowability; (2) alkali–water glass activation and calcination at 600–850 °C effectively enhance pozzolanic activity; and (3) combining the minimum paste thickness theory with additives such as water reducers, fibers, or biochar enables high-performance and low-carbon concrete design. This review provides a comprehensive theoretical foundation and technical pathway for the high-value utilization of river sediments, carbon reduction in concrete, and sustainable resource recycling. Full article

In recent years, membrane separation technology has undergone continuous advancements. Microfiltration (MF) membranes, as an important type, are usually prepared by electrospinning—a simple and efficient method. This study reports the development of crosslinked polyvinyl alcohol/polyethylene glycol (cPVA/PEG) nanofiber membranes through a combination of electrospinning and chemical crosslinking, investigating the effects of different crosslinking concentrations on the membrane morphology, surface wettability, and tensile properties. Comprehensive characterization was carried out by using scanning electron microscopy (SEM), a Fourier-transform infrared spectrometer (FTIR), an X-ray diffractometer (XRD), a thermogravimetric (TG) analyzer, differential scanning calorimetry (DSC), a contact angle tester, a universal testing machine, etc. The results showed that at the crosslinking concentration of 15%, the cPVA/PEG fiber membrane achieved a breaking stress of 29.07 ± 2.60 MPa, a breaking strain of 77.60 ± 6.02%, and a porosity exceeding 43%. SEM, FTIR, XRD, TG, and DSC analyses collectively confirmed the occurrence of chemical crosslinking within the membrane structure. The cPVA/PEG-15 membrane exhibited no observable shrinkage or curling upon water contact, combined with excellent hydrophilicity and lipophilicity in the air. These properties indicate that the membrane can serve as a novel functional membrane substrate (e.g., as hydrophilic separation layers) and is expected to play an important role in fields such as seawater desalination and wastewater treatment, demonstrating significant application potential. Full article

The decomposition of high-energy materials often releases large volumes of toxic fumes, contributing to environmental pollution. To reduce these emissions, eco-friendly formulations are being developed by modifying chemical composition or adding functional additives that enhance combustion and reduce toxic byproducts. Hydrogen peroxide (H₂O₂), acting as both an oxidizer and potential fuel, shows promise in lowering NO_x emissions. However, its impact on formulation stability must be assessed. This study examines the morphological and thermal behavior of an ammonium nitrate, fuel oil, and hydrogen peroxide (ANFOHP) formulation using scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and thermal analysis based on thermogravimetry (TG) connected with differential scanning calorimetry (DSC) techniques. SEM showed that the fuel oil–hydrogen peroxide (FOHP) blend formed a thin film on ammonium nitrate prills without structural damage. XRD patterns indicated an intact crystalline structure. Moreover, FT-IR analysis performed both for fresh and 24-h stored samples evidenced no structural changes. In turn, TG/DSC revealed altered thermal behavior, with a new endothermic peak near 80 °C corresponding to the simultaneous evaporation of water and hydrogen peroxide from the ANFO surface, and reduced intensity of the main ANFO decomposition peak, indicating a shift in the thermal behavior induced by the FOHP blend. Full article

This study focused on the development and characterization of polyvinyl alcohol (PVA)- and konjac glucomannan (KGM)-based composite films enriched with natural bioactive additives. A PK (PVA/KGM) matrix with the optimum tensile strength was selected, and five film formulations were prepared by incorporating Aronia melanocarpa extract (AME), red dragon fruit extract (DFE), and thyme essential oil (TEO). TEO was also introduced via a Pickering emulsion (PE) technique. The total phenolic content (TPC) and free radical scavenging activity (FRSA) of extracts and films were determined, where AME exhibited the highest antioxidant activity (TPC: 243 mg GAE/g; FRSA: 81.7%). The additive-free PK film displayed limited antioxidant activity (18%), while antioxidant capacity significantly improved with extract and EO incorporation. The PK-A film (AME-added) demonstrated the highest tensile strength and lowest water vapor permeability, supported by increased local crystallinity detected in XRD. Color analysis indicated dominant red-violet tones in AME films and greenish-yellow tones in DFE films. FTIR confirmed that no new chemical bonds were formed between active compounds and the polymer matrix. DSC thermograms revealed consistent melting peaks (~150 °C) for all films, while Tg varied from 37 to 73 °C depending on additive type, reflecting plasticization effects of extracts and the counterbalancing effect of essential oil. The most hydrophobic (76.8°) and opaque sample was PK-ADO, prepared via the PE technique. Overall, natural extracts improved the structural, thermal, barrier, and antioxidant properties of PK films. Full article

This study prepared alkali-activated cementitious composites using high-whiteness kaolin, sodium water glass, and NaOH as the main raw materials. Multiple methods, including FE-SEM, XRD, whiteness/light transmittance tests, shrinkage rate measurements, DSC-TG, flexural strength testing, and hydrolysis resistance testing, were used to investigate the effects of curing temperature and time on material properties. The optimal parameters were determined as kaolin calcined at 1100 °C, activator modulus 1.25, calcined kaolin-to-activator ratio 1:1, and 2.5% deionized water added for molding. The optimal sample achieved a flexural strength of 23.81 MPa, with the bonding strength to porcelain 60.17 times that of gypsum and 1.90 times that of kaolin-bonded materials. Curing below 100 °C slowed polymerization, while temperatures exceeding 100 °C accelerated it, with violent reaction at 120 °C. Curing beyond 10 h reduced flexural strength. A large number of cage-like, ‘zeolite-like’ structures formed, closely relating to material properties. This study provides references for ceramic restoration materials. Full article

Rapeseed is a valuable oilseed crop, and efficient drying plays a crucial role in preserving its quality. Because of the high moisture content in rapeseed, drying using the conventional methods may cause it to overheat. The benefit of energy-efficient sorption drying is that it allows one to carefully remove moisture from seeds without using heat, thus ensuring better quality. This study focuses on the characteristics of rapeseed drying using fine crystalline magnesium sulfate MgSO₄·nH₂O as a desiccant. The properties of the desiccant were analyzed using the SEM–EDS, XRD, ATR–MIR, and DSC-TG techniques before and after contacting rapeseed. The findings demonstrate that the desired moisture content of 7–8% can be achieved within 60–240 min, depending on the initial moisture content of rapeseed (ranging from 12% to 16%) and the desiccant-to-rapeseed ratio (1:2, 1:4, or 1:6). An analysis of crystalline hydrates after sorption drying indicates that the desiccant can be reused without intermediate regeneration during multi-stage drying of two to three rapeseed batches. The germination capacity of the seeds after sorption drying was as high as 90%, meeting the standards for elite rapeseed categories. This research demonstrates that sorption drying using magnesium sulfate is an efficient method for reducing moisture content in oilseeds, while maintaining their quality. Full article

Bio-based polymeric composites were prepared by dispersing different amounts of olive pit (OP) powder within an acrylate epoxidized soybean oil (AESO) photocurable resin using tetrahydrofurfuryl acrylate (THFA) as diluent and (2,4,6-trimethylbenzoyl), phosphine oxide (BAPO) as photo-initiator, and they were photocured by Vat Photopolymerization (VP) using a Liquid Crystal Display (LCD) 3D printer. Formulation viscosity was studied because of its important role in a VP process able to influence the printability of the final parts. Different 3D printed architectures were successfully realized with good resolution and accuracy, high level of detail, and flexibility. The effect of OP addition was investigated by thermal (TGA and DSC), morphological (SEM and PSD), viscoelastic (DMA), and mechanical (tensile testing) characterization. The filler led to an increase in the T_g, storage modulus, and tensile properties, underlining the stiffening effect induced by the OP particles onto the polymeric starting resin. This underlines the possibility to apply these bio-based composites in many application fields by valorizing agro-wastes, developing more sustainable materials, and taking advantages of VP 3D printing, such as low costs, minimal wastage, and customized geometry. Biocompatibility tests were also successfully carried out. The results clearly indicate that the AESO-based composites promote cell adhesion and viability. Full article

This work evaluates the CO₂-adsorption relevance and cycling stability of graphene oxide–silica (GO-SiO₂) and reduced graphene oxide–silica (rGO-SiO₂) gels after amine functionalization, demonstrating high-capacity retention under repeated adsorption–desorption cycles: rGO-SiO₂-APTMS retains ≈96.3% of its initial uptake after 50 cycles, while GO-SiO₂-APTMS retains ≈90.0%. The use of surfactants to control the organization of inorganic and organic molecules has enabled the development of ordered mesostructures, such as mesoporous silica and organic/inorganic nanocomposites. Owing to the outstanding properties of graphene and its derivatives, synthesizing mesostructures intercalated between graphene sheets offers nanocomposites with novel morphologies and enhanced functionalities. In this study, GO-SiO₂ and rGO-SiO₂ gels were synthesized and characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TG), mass spectrometry (MS), N₂ adsorption–desorption isotherms, and transmission electron microscopy (TEM). The resulting materials exhibit a laminar architecture, with mesoporous silica domains grown between graphene-based layers; the silica contents are 83.6% and 87.6%, and the specific surface areas reach 446 and 710 m²·g⁻¹, respectively. The laminar architecture is retained regardless of the surfactant-removal route; however, in GO-SiO₂ obtained by solvent extraction, a fraction of the surfactant remains partially trapped. Together with their high surface area, hierarchical porosity, and amenability to surface functionalization, these features establish amine-grafted graphene–silica gels, particularly rGO-SiO₂-APTMS, as promising CO₂-capture adsorbents. Full article