Search Results (641)

Background: Precision medicine refers to the formulation of personalized drug regimens according to the individual characteristics of patients to achieve optimal efficacy and minimize adverse reactions. Additive manufacturing (AM), also known as three-dimensional (3D) printing, has emerged as an optimal solution for precision drug delivery, enabling customizable and the fabrication of multifunctional structures with precise control over morphology and release behavior in pharmaceutics. However, the influence of 3D printing parameters on the printed tablets, especially regarding in vitro and in vivo performance, remains poorly understood, limiting the optimization of manufacturing processes for controlled-release profiles. Objective: To establish the fabrication process of 3D-printed controlled-release tablets via comprehensively understanding the printing parameters using fused deposition modeling (FDM) combined with hot-melt extrusion (HME) technologies. HPMC-AS/HPC-EF was used as the drug delivery matrix and carbamazepine (CBZ) was used as a model drug to investigate the in vitro drug delivery performance of the printed tablets. Methodology: Thermogravimetric analysis (TGA) was employed to assess the thermal compatibility of CBZ with HPMC-AS/HPC-EF excipients up to 230 °C, surpassing typical processing temperatures (160–200 °C). The formation of stable amorphous solid dispersions (ASDs) was validated using differential scanning calorimetry (DSC), hot-stage polarized light microscopy (PLM), and powder X-ray diffraction (PXRD). A 15-group full factorial design was then used to evaluate the effects of the fan speed (20–100%), platform temperature (40–80 °C), and printing speed (20–100 mm/s) on the tablet properties. Response surface modeling (RSM) with inverse square-root transformation was applied to analyze the dissolution kinetics, specifically t_50% (time for 50% drug release) and Q_4h (drug released at 4 h). Results: TGA confirmed the thermal compatibility of CBZ with HPMC-AS/HPC-EF, enabling stable ASD formation validated by DSC, PLM, and PXRD. The full factorial design revealed that printing speed was the dominant parameter governing dissolution behavior, with high speeds accelerating release and low speeds prolonging release through porosity-modulated diffusion control. RSM quadratic models showed optimal fits for t_50% (R² = 0.9936) and Q_4h (R² = 0.9019), highlighting the predictability of release kinetics via process parameter tuning. This work demonstrates the adaptability of polymer composite AM for tailoring drug release profiles, balancing mechanical integrity, release kinetics, and manufacturing scalability to advance multifunctional 3D-printed drug delivery devices in pharmaceutics. Full article

The discharge of oily wastewater threatens the ecosystem and human health, and the efficient treatment of oily wastewater is confronted with problems of high mass transfer resistance at the oil-water-solid multiphase interface, significant light shielding effect, and easy deactivation of photocatalysts. Although traditional physical separation methods avoid secondary pollution by chemicals and can effectively separate floating oil and dispersed oil, they are ineffective in removing emulsified oil with small particle sizes. To address these complex challenges, photocatalytic technology and photocatalysis-based improved technologies have emerged, offering significant application prospects in degrading organic pollutants in oily wastewater as an environmentally friendly oxidation technology. In this paper, the degradation mechanism, kinetic mechanism, and limitations of conventional photocatalysis technology are briefly discussed. Subsequently, the surface interface modulation functions of metal doping and heterojunction energy band engineering, along with their applications in enhancing the light absorption range and carrier separation efficiency, are reviewed. Focus on typical studies on the separation and degradation of aqueous and oily phases using photocatalytic membrane technology, and illustrate the advantages and mechanisms of photocatalysts loaded on the membranes. Finally, other new approaches and converging technologies in the field are outlined, and the challenges and prospects for the future treatment of oily wastewater are presented. Full article

This study presents the structural and compositional characterisation of a newly developed Ti55Al27Mo13 alloy synthesised via aluminothermic reaction. The alloy was designed to overcome the limitations of conventional processing routes for high–melting–point elements such as Ti and Mo, enabling the formation of a complex, multi–phase microstructure in a single high–temperature step. The aim was to develop and characterise a material with microstructural features expected to enhance wear resistance, oxidation behaviour, and thermal stability in future applications. The alloy is intended as a precursor for composite nanopowders and surface coatings applied to aluminium–, magnesium–, and iron–based substrates subjected to mechanical and thermal loading. Elemental analysis (XRF, EDS) confirmed the presence of Ti, Al, Mo, and minor elements such as Si, Fe, and C. Microstructural investigations using laser confocal and scanning electron microscopy revealed a heterogeneous structure comprising solid solutions, eutectic regions, and dispersed oxide and carbide phases. Notably, the alloy exhibits high hardness values, reaching >2400 HV in Al₂O₃ regions and ~1300 HV in Mo– and Si–enriched solid solutions. These results suggest the material’s substantial potential for protective surface engineering. Further tribological, thermal, and corrosion testing, conducted with meticulous attention to detail, will follow to validate its functional performance in target applications. Full article

Magnetic nanoparticles (MNPs), especially iron oxide (Fe₃O₄), display distinctive superparamagnetic characteristics and elevated surface-area-to-volume ratios, facilitating improved physicochemical interactions with solutes and pollutants. These characteristics make MNPs strong contenders for use in water treatment applications. This research investigates the application of iron oxide MNPs synthesized via co-precipitation as innovative draw solutes in forward osmosis (FO) for treating synthetic produced water (SPW). The FO membrane underwent surface modification with sulfobetaine methacrylate (SBMA), a zwitterionic polymer, to increase hydrophilicity, minimize fouling, and elevate water flux. The SBMA functional groups aid in electrostatic repulsion of organic and inorganic contaminants, simultaneously encouraging robust hydration layers that improve water permeability. This adjustment is vital for sustaining consistent flux performance while functioning with MNP-based draw solutions. Material analysis through thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR) verified the MNPs’ thermal stability, consistent morphology, and modified surface chemistry. The FO experiments showed a distinct relationship between MNP concentration and osmotic efficiency. At an MNP dosage of 10 g/L, the peak real-time flux was observed at around 3.5–4.0 L/m²·h. After magnetic regeneration, 7.8 g of retrieved MNPs generated a steady flow of ~2.8 L/m²·h, whereas a subsequent regeneration (4.06 g) resulted in ~1.5 L/m²·h, demonstrating partial preservation of osmotic driving capability. Post-FO draw solutions, after filtration, exhibited total dissolved solids (TDS) measurements that varied from 2.5 mg/L (0 g/L MNP) to 227.1 mg/L (10 g/L MNP), further validating the effective dispersion and solute contribution of MNPs. The TDS of regenerated MNP solutions stayed similar to that of their fresh versions, indicating minimal loss of solute activity during the recycling process. The combined synergistic application of SBMA-modified FO membranes and regenerable MNP draw solutes showcases an effective and sustainable method for treating produced water, providing excellent water recovery, consistent operational stability, and opportunities for cyclic reuse. Full article

Occupied and unoccupied electronic states of altermagnetic MnTe(0001) single crystals were studied by photoemission and inverse-photoemission spectroscopies after establishing a reproducible surface cleaning procedure involving repeated sputtering and annealing cycles. The angle-resolved photoemission spectroscopy (ARPES) exhibited a hole-like band dispersion centered at the $\overline{\mathsf{\Gamma }}$ point, which was consistent with the reported ARPES results and our density functional theory (DFT) calculations with the on-site Coulomb interaction U. The observed Mn 3d↑-derived peak at −3.5 eV, however, significantly deviated from the DFT + U calculations. Meanwhile, the Mn 3d↓-derived peak at +3.0 eV observed by inverse-photoemission spectroscopy agreed well with the DFT + U results. Based on simulations of the spectral function employing an w-dependent model self-energy, we found significant relaxation effects in the electron-removal process, while such effects were negligible in the electron-addition process. Our study provides a comprehensive picture of electronic states, forming a solid foundation for understanding the magnetic and transport properties of MnTe. Full article

Background/Objectives: Thymol, one of the main compounds of thyme essential oil, has shown promising effects in treating various skin disorders owing to its anti-inflammatory, antimicrobial and antioxidative activities. Due to its limited solubility in water, thymol is commonly used in higher concentrations to achieve a suitable therapeutic effect, which can consequently lead to skin irritation. To overcome these limitations, we incorporated thymol into a vesicular phospholipid gel (VPG), a novel semisolid dermal vehicle consisting of highly concentrated dispersion of phospholipid vesicles (liposomes). Methods: Thymol was successfully loaded into two VPGs differing in bilayer fluidity, which were characterized for the physicochemical and rheological properties, storage stability, in vitro release, ex vivo skin permeability, in vitro compatibility with epidermal cells, wound healing potential, and antibacterial activity against skin-relevant bacterial strains. Results: High pressure homogenization method enabled preparation of VPG-liposomes of neutral surface charge in the size range 140–150 nm with polydispersity indexes below 0.5. Both types of VPGs exhibited viscoelastic solid-like structures appropriate for skin administration and ensured skin localization of thymol. Although both types of VPGs enabled prolonged release of thymol, the presence of cholesterol in the VPG increased the rigidity of the corresponding liposomes and further slowed down thymol release. Conclusions: Loading of thymol into VPGs significantly reduced its cytotoxicity toward human keratinocytes in vitro even at very high concentrations, compared to free thymol. Moreover, it facilitated in vitro wound healing activity, proving its potential as a vehicle for herbal-based medicines. However, the antibacterial activity of thymol against Staphylococcus aureus and methicillin-resistant S. aureus was hindered by VPGs, which represents a challenge in their development. Full article

This research aims to synthesize a novel hydrogel bio-composite based on natural clay, sodium alginate (Na-AL), and iota-carrageenan as adsorbents to remove phosphate ions from aqueous solutions. The adsorbents were characterized by a variety of techniques, such as Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy coupled with energy dispersive X-rays (SEM-EDX), and the determination of point zero charge (PZC). This research investigated how the adsorption process is influenced by parameters such as adsorbent dose, contact time, solution pH, and temperature. In this study, we used four isotherms and four kinetic models to investigate phosphate ion removal on the prepared bio-composite. The results showed that the second-order kinetic (PSO) model is the best model for describing the adsorption process. The findings demonstrate that the R² values are highly significant in both the Langmuir and Freundlich models (very close to 1). This suggests that Langmuir and Freundlich models, with a diversity of adsorption sites, promote the adsorption of phosphate ions. The maximum adsorbed amounts of phosphate ions by the bio-composite used were 140.84 mg/g for H₂PO₄⁻ ions and 105.26 mg/g for HPO₄²⁻ ions from the batch system. The positive ∆H° confirms the endothermic and physical nature of adsorption, in agreement with experimental results. Negative ∆G° values indicate spontaneity, while the positive ∆S° reflects increased disorder at the solid–liquid interface during phosphate uptake. The main parameters, including adsorbent dosage (mg), contact time (min), and initial concentration (mg/L), were tuned using the Box–Behnken design of the response surface methodology (BBD-RSM) to achieve the optimum conditions. The reliability of the constructed models is demonstrated by their high correlation coefficients (R²). An R² value of 0.9714 suggests that the model explains 97.14% of the variability in adsorption efficiency (%), which reflects its strong predictive capability and reliability. Finally, the adsorption behavior of phosphate ions on the prepared bio-composite beads was analyzed using an artificial neural network (ANN) to predict the process efficiency. The ANN model accurately predicted the adsorption of phosphate ions onto the bio-composite, with a strong correlation (R² = 0.974) between the predicted and experimental results. Full article

To improve the combustion performance of boron powder, a method was developed for synthesizing boron–magnesium–titanium (B-Mg-Ti) ternary composite powders with controlled metal content. Boron–magnesium (B-Mg) base materials were first prepared via electrical explosion, followed by the incorporation of titanium powder at varying mass fractions (1 wt.%, 3 wt.%, 5 wt.%, and 7 wt.%) through mechanical ball milling. Field emission scanning electron microscopy (FE-SEM) revealed that the addition of titanium promoted a more uniform dispersion of magnesium within the boron agglomerates. Moreover, nanoscale titanium particles were observed to be embedded on the particle surfaces, confirming successful microscale composite formation. Particle size distribution was measured using a Malvern 3000 laser particle size analyzer, and results showed that the particle size of the ternary composites decreased gradually with increasing titanium content. Specific surface area was determined via the Brunauer–Emmett–Teller (BET) method, with all samples exhibiting values greater than 15 m²/g, indicating good surface reactivity. Furthermore, the rheological behavior of the B-Mg-Ti composite powders, when combined with terminal hydroxyl polybutadiene (HTPB)—a typical binder in solid propellants—was evaluated. Viscosity measurements were conducted using a rotational rheometer at constant temperatures of 20 °C and 70 °C. The results demonstrated a marked decrease in viscosity with increasing titanium content, suggesting that titanium incorporation enhances the flowability of the composite powders. This study systematically evaluated the influence of titanium content on the structural and physicochemical properties of B-Mg-Ti composite powders, thereby providing a valuable experimental foundation for the optimized design of boron-based combustion systems and the enhancement of their processing and application performance. Full article

This study investigates the influence of specific surface area (SSA) and aluminum hydroxide particle size on sodium aluminate’s purification efficiency in the Bayer process. This research examines how variations in SSA affect the adsorption and incorporation of contaminants such as Cu, Fe, and Zn, as well as the optimal balance between effective purification and excessive Al₂O₃ loss. Different SSA values and purification durations are analyzed to optimize the purification process and determine conditions that maximize impurity removal while maintaining system stability. Additionally, solid residue characterization using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS) provides insights into impurity incorporation mechanisms, including isomorphic replacement, surface adsorption, and co-crystallization. This study highlights key process parameters that influence impurity behavior and crystallization dynamics, offering valuable guidance for refining industrial purification strategies and improving aluminum hydroxide quality. Full article

Underground mine surveys present unique challenges, including the logistics of deploying an energy source, placing geophones in solid rock, managing reverberation from the adit, and ensuring safety. We present the results of seismic surveying at the historic Deer Trail Mine in south-central Utah (USA). The mine is located along the eastern side of the Tushar Range. The surveys utilised a narrow, mostly horizontal adit, 120–510 m below the ground surface. The country rock consists of highly fractured and mineralised Permian to Pennsylvanian quartzites, shales, and limestones. A short test of a 96-channel common midpoint (CMP) P-wave profile was conducted using an accelerated weight-dropper source. We supplemented the P-wave survey with tests of surface-wave dispersion and horizontal-vertical spectral ratio modelling for shallow S-wave structure. These tests confirmed the capability to map shallow, small-scale structure. A conventional CMP 264-channel survey with an explosive source covered 1728 m. A static recording array was used for both surveys with 4.5-Hz vertical geophones. The conventional CMP profile imaged horizontal and dipping reflectors down to about 2000 m, interpreted as lithologic variations in the bedrock. Our study demonstrates the potential for high-resolution seismic exploration in an unconventional and challenging setting to guide the exploitation of deeply buried mineral resources. Full article

In this study, a polycarboxylate coal–water slurry dispersant (SSPA) containing benzenesulfonic acid groups was synthesized using allyl alcohol polyoxyethylene ether 500, sodium styrenesulfonate, and acrylic acid as raw materials. The effects of SSPA and a commercially available naphthalene-based dispersant (MF) on the slurry characteristics of low-rank coal were compared, and the maximum solid content of CWS prepared with SSPA reached 65.2%, which was 4% higher than that achieved with MF (61.2%). Unlike the more electronegative MF dispersant, SSPA features long polyether side chains that exert a robust steric hindrance effect, significantly enhancing coal particle dispersion. This results in a decrease in apparent viscosity and an increase in the stability of the CWS formulated with SSPA. Furthermore, adsorption experiments revealed that the adsorption kinetics of both SSPA and MF on coal conformed to the pseudo-second-order kinetic model. SSPA’s adsorption on coal particles followed the Langmuir isothermal adsorption model, and the K_L value of 0.0094 for SSPA was greater than that of MF (0.0086). This indicates that SSPA has a stronger affinity for the coal surface. Overall, the superior adsorption efficacy of SSPA is attributed to the benzene ring in its nonpolar group, which facilitates steric hindrance with aromatic structures in coal. Additionally, SSPA improves slurry stability, achieving a penetration rate of 96.7%. Finally, the carboxylic acid groups in SSPA likely engage in electrostatic attraction with cations on the coal surface, enhancing adsorption. Full article

This study investigates the effects of B₄C content (2.5, 5, 7.5, and 10 wt.%) on the microstructure and wear resistance of laser cladding 316 stainless steel coatings on a 2Cr12MoV steel substrate. The coating was prepared by laser cladding technology. The phase composition, microstructure evolution, microhardness, and tribological properties of the coating were analyzed. The results show that the decomposition of B₄C particles is complete, and the phase composition of the coating includes Austenite, Fe₂₃ (B₃C₃), Cr₂₃ (B_1.5C_4.5), and a Fe-Ni solid solution. The increase in B₄C content significantly increased the microhardness of the material from 206 HV_0.2 (substrate) to 829 HV_0.2 (10 wt.% B₄C) by 4.02 times. Wear resistance also improved, with the 10 wt.% coating exhibiting the lowest wear rate (10 × 10⁻⁸ mm³/N·m) due to fine-grained and dispersion strengthening mechanisms. However, excessive B₄C (10 wt.%) induced cracks from increased brittleness, resulting in higher friction coefficients. The wear mechanism consists of fatigue wear, adhesive wear, and oxidative wear, and the degree of wear decreases with the increase in B₄C content. This work demonstrates that the addition of B₄C effectively improves the hardness and wear resistance of 316 stainless steel coatings, providing practical insights into surface engineering in high wear applications. Full article

h-BN spherical nanoparticles, known as white graphene, have good anti-wear properties, long service life, chemical inertness, and stability, which provide superior lubricating performance as a solid additive item to nanofluids. However, the poor dispersion stability of h-BN nanoparticles in nanofluids is a bottleneck that restricts their application. Currently, to prepare h-BN nanofluids with good dispersion stability, a cold plasma (CP) modification of h-BN nanoparticles is proposed in this study. In this research, h-BN nanofluid with added surfactant (SNL), CP-modified h-BN nanofluid with N₂ as the working gas (CP(N₂)NL), and CP-modified h-BN nanofluid with O₂ as the working gas (CP(O₂)NL) were prepared, separately. The mechanism of the dispersion stability of CP-modified h-BN nanofluid was analyzed using X-ray photoelectron spectroscopy (XPS), and the performance of CP-modified nanofluid was analyzed based on static observation of nanofluid, kinematic viscosity, and heat transfer properties. Finally, friction and wear experiments were conducted to further analyze the tribological performance of h-BN nanofluids based on the coefficient of friction, 3D surface morphology, surface roughness (Sa), scratches, and micro-morphology. The results show that CP-modified h-BN nanofluid has excellent dispersed suspension stability and can be statically placed for more than 336 h. The CP-modified h-BN nanofluid showed stable friction-reducing, anti-wear, and heat transfer performance, in which the coefficient of friction of h-BN nanofluid was about 0.66 before and after 24 h of settling. The Sa value of the sample was reduced by 31.6–49.2% in comparison with pure cottonseed oil (CO). Full article

Background/Objectives: Difenoconazole (DFC) is a broad-spectrum fungicide. However, its application is limited due to poor aqueous solubility. Drugs with low solubility can be better absorbed using nanostructured lipid carriers (NLCs). Hence, the application of DFC in an NLC delivery system is proposed. Methods: Difenoconazole-loaded nanostructured lipid carriers (DFC-NLCs) with different solid–liquid lipid ratios were prepared by solvent diffusion method. Key physicochemical parameters, including particle diameter, surface charge (zeta potential), drug encapsulation efficiency, and morphological characteristics, were systematically characterized. Using Rhizoctonia solani (R. solani) as the model strain, inhibitory efficiency of DFC-NLC dispersion was compared with that of commercial dosage forms, such as 25% DFC emulsifiable concentrate (DFC-EC) and 40% DFC suspension concentrate (DFC-SC). Additionally, uptakes of DFC-NLC dispersions in R. solani were further observed by fluorescence probe technology. The safety profiles of DFC-NLCs and commercial dosage forms were evaluated using zebrafish as the model organism. Acute toxicity studies were conducted to determine the maximum non-lethal concentration (MNLC) and 10% lethal concentration (LC₁₀). Developmental toxicity studies were performed to observe toxic phenotypes. Results: DFC-NLC dispersions were in the nanometer range (≈200 nm) with high zeta potential, spherical in shape with encapsulation efficiency 69.1 ± 1.8%~95.0 ± 2.6%, and drug loading 7.1 ± 0.3%~9.7 ± 0.6% determined by high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). Compared with commercial dosage forms, the antifungal effect of the DFC-NLC on R. solani was significantly improved in in vitro antibacterial experiments (p < 0.05). The 50% effective concentration (EC₅₀) values were 0.107 mg·L⁻¹ (DFC-NLC), 0.211 mg·L⁻¹ (DFC-EC), and 0.321 mg·L⁻¹ (DFC-SC), respectively. The uptakes of FITC-labeled DFC-NLC demonstrated that an NLC was appropriate to deliver DFC into pathogen to enhance the target effect. In safety assessment studies, DFC-NLCs exhibited a superior safety profile compared with commercial formulations (p < 0.05). Conclusions: This study investigates the feasibility of NLCs as delivery systems for poorly water-soluble fungicides, demonstrating their ability to enhance antifungal efficacy and reduce environmental risks. Full article

In previous studies, a new methodology was developed to determine the free dispersive and polar energies, the surface energies, and Lewis acid–base parameters of a polystyrene–divinylbenzene (S-DVB) copolymer modified by melamine, 5-Hydroxy-6-methyluracil, and 5-fluouracil. In this paper, we were interested in the determination of the work of the adhesion of solvents on the modified copolymer as a function of temperature and for the different modifiers with the help of inverse gas chromatography at infinite dilution. The variations in the London dispersive and polar surface properties of copolymers against the temperature led to the determination of the different acid–base components of their surface energies. Using Fowkes’s equation, van Oss’s relation, and Owens’s concept, we obtained the variations in the dispersive and polar works of the adhesion of the different solid surfaces, and the corresponding forces of interaction between the organic solvents and the modified copolymer. It was shown that the work of adhesion is a function of two thermodynamic variables: the temperature and the modifier percentage. Full article