Search Results (11,837)

To systematically investigate the combined effects of moisture content, confining pressure, and loading rate on the mechanical properties of weakly cemented soft rock, this study focuses on the Jurassic coal measures from the Hoxtolgay coalfield in Xinjiang. A series of uniaxial and triaxial compression tests were conducted under varying moisture states, loading velocities, and confining pressures. Complementary X-ray diffraction (XRD), scanning electron microscopy (SEM), and Brazilian splitting tests were performed to analyze the microstructural evolution and tensile failure characteristics. The experimental results demonstrate that moisture content acts as the primary governing factor for mechanical degradation; increased hydration promotes clay mineral swelling and attenuates inter-granular cementation, leading to a continuous reduction in both compressive and tensile strengths, as well as the elastic modulus. Conversely, confining pressure consistently enhances these macroscopic mechanical parameters by restricting lateral deformation. While the loading rate alters the mechanical response, its impact is secondary compared to the definitive effects of moisture and stress constraints. Furthermore, by utilizing established stress–strain-based indices, the study quantitatively evaluates the brittleness characteristics, confirming that hydration fundamentally drives the rock mass from a brittle state toward ductility. This research elucidates the coupled degradation mechanisms of highly sensitive soft rock, providing a theoretical foundation for stability design and risk assessment in underground geotechnical engineering. Full article

To improve the adhesion and tribological performance of diamond-like carbon (DLC) coatings on steel substrate, a Ti-enhanced plasma nitriding (PNTi) layer was formed on the surface of 38CrMoAl steel, followed by deposition of a Cr-based interlayer (mainly CrN) and then a W interlayer. Finally, a DLC coating was deposited, resulting in a novel PNTi/DLC coating. For comparison, a conventional PN/DLC coating was prepared under the same processing conditions. Optical microscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy, hardness tests, and tribological experiments were performed to systematically investigate the effect of TiN-enriched PNTi supporting layer on the performances of the PNTi/DLC composite coating. The results show that comparing with PN/DLC composite coating, the critical load (Lc₂) of the PNTi/DLC coating was increased from 28.89 N to 43.25 N—about a 50% enhancement. The microhardness was increased from 2650 HV_0.05 to 4400 HV_0.05 (corresponding to 28.2 GPa to 44.1 GPa). The friction coefficient was decreased from 0.28 to 0.11, about a 60% reduction, and the wear rate declined more than 40%, from 4.81 × 10⁻⁶ to 2.90 × 10⁻⁶ mm³·N⁻¹·m⁻¹. The introduction of Ti promoted the in situ formation of TiN phase in the nitrided layer, which significantly improved the compactness of the nitrided layer and the adhesion at the film–substrate interface. Consequently, the PNTi/DLC composite coating exhibited excellent wear resistance and friction stability under high-load and severe tribological conditions. This study provides a promising perspective for engineering applications of steel-based DLC coatings in harsh service environments. Full article

This study systematically investigates the influence of CeO₂ content (0–0.6 wt.%) on the microstructure and mechanical properties of Stellite6/WC composite coatings fabricated by plasma spray welding. The phase composition and microstructure of the coatings were characterized using X-ray diffraction (XRD) and scanning electron microscopy (SEM), while microhardness and tribological performance were evaluated using a semi-automatic Vickers microhardness tester and a ball-on-disk tribometer. The results indicate that the coating with 0.4 wt.% CeO₂ exhibits the optimal combination of mechanical and tribological properties, achieving a maximum microhardness of 1107.62 HV_0.3—a 50.5% improvement over the unmodified coating—and a minimum wear mass loss of 1.4 mg, corresponding to a 78.1% reduction compared to the CeO₂-free counterpart. These findings demonstrate that appropriate CeO₂ addition significantly enhances both the microhardness and wear resistance of Stellite6/WC coatings, offering an effective strategy to mitigate surface degradation and extend the service life of 45 steel substrates under demanding operating conditions. Full article

The present study proposes a fractal-inspired multiscale framework to interpret the structural, thermal, mechanical and dielectric properties of polylactic acid (PLA). Experimental investigations were performed using tensile testing, TG-DTA thermal analysis, X-ray diffraction (XRD) and dielectric spectroscopy. The structural organization was analyzed using XRD data, where a scaling tendency compatible with power-law behavior was identified over a limited $\mathrm{q}$-range. The thermal degradation exhibited a sharp transition, while the mechanical and dielectric responses reflected the heterogenous behavior typical of semicrystalline polymers. Rather than claiming a fully validated fractal model, the present work introduces a conceptual multiscale interpretation, supported by experimental observations, and proposes a fractal integrity index (FII) as an exploratory descriptor integrating structural, thermal and mechanical information. The results suggest that fractal-based descriptors may provide a useful complementary framework for interpreting complex polymer behavior, although further validation across multiple materials and experimental conditions is required. 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

High-alkali coal can cause slagging and fouling and impact the operational lifespan of the boilers. Traditional single-indicator methods often yield inconsistent results when evaluating the slagging risk of high-alkali coal. In this study, six coal samples were selected and systematically analyzed for their slagging characteristics using scanning electron microscopy (SEM), X-ray fluorescence (XRF), X-ray diffraction (XRD), and ash morphology analysis. Furthermore, a comprehensive evaluation model was constructed by integrating the technique for order preference by similarity to ideal solution (TOPSIS) with the entropy weight method. Additionally, based on images of ash morphology, the fractal dimension (D) was introduced as a quantitative indicator to predict slagging tendency through crack characteristics. The results show that TF, ZD, and KB samples, which are rich in alkaline oxides (CaO, Fe₂O₃, Na₂O, K₂O), form low-melting-point eutectic silicates during combustion, resulting in significant melting and agglomeration with wide cracks between aggregates, indicating a strong slagging tendency. Their fractal dimensions (D) range from 1.81 to 1.92. In contrast, HM and WQ samples, dominated by SiO₂ and Al₂O₃, form high-melting-point mullite and quartz, showing loose ash morphology with uniformly distributed cracks and a weak slagging tendency, with D values of 1.68 and 1.75, respectively. A significant negative correlation was observed between D and the E-TOPSIS model (y = 3.54 − 1.72x). Therefore, fractal analysis allows for rapid assessment of slagging risk without the need for complex chemical testing. This study provides valuable insights for predicting the slagging tendency of high-alkali coal during combustion. Full article

This study investigates the effect of a 30 wt.% solid-content colloidal nano-silica (CNS) suspension, incorporated at 0–6 wt.% of cement, on the early-age (7 and 14 days) and later-age (28 and 56 days) compressive strength and microstructure of pumice aggregate lightweight concrete (PALC). The corresponding effective solid nano-silica content ranges from 0 to 1.8 wt.% of cement. Compressive strength increased with CNS dosage up to 5 wt.%, after which a plateau behavior was observed. At 7 days, compressive strength increased from 19.93 MPa to 26.81 MPa, corresponding to an improvement of approximately 34.5%. Although the 6 wt.% mixture showed slightly higher strength at early age, this trend was not sustained at later ages. The highest compressive strength at 56 days was obtained at 5 wt.% CNS (39.68 MPa), with a slight decrease at 6 wt.% CNS. X-ray diffraction (XRD) analysis indicated a reduction in calcium hydroxide (CH) peak intensity with increasing CNS content, suggesting the occurrence of pozzolanic reactions; however, this interpretation remains qualitative. Scanning electron microscopy (SEM) observations revealed a denser and more homogeneous matrix structure at 5 wt.% CNS, corresponding to improved mechanical performance. Slump values decreased from 9.0 cm to 6.6 cm with increasing CNS dosage, indicating reduced workability, while water absorption values slightly decreased from 18.51% to 17.20%. Full article

Background/Objectives: Fungal keratitis remains a vision-threatening infection, and current amphotericin B (AmphB) eye drops suffer from low corneal residence time, poor aqueous solubility, and the need for frequent dosing. This study develops electrospun nanofiber-based ophthalmic inserts combining polyvinyl alcohol (PVA), gamma-cyclodextrin (γ-CD), and sodium taurocholate (STC) to enhance AmphB solubility and provide a non-invasive, rapidly dissolving ophthalmic dosage form. Methods: γ-CD and STC-enhanced AmphB-loaded PVA nanofiber-based ophthalmic inserts with varying γ-CD and STC concentrations were prepared by electrospinning and characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). Drug content, in vitro release (Weibull modeling), antifungal activity against Candida albicans, Fusarium solani, and Aspergillus fumigatus, ocular cytocompatibility using the Hen’s Egg Test on Chorioallantoic Membrane (HET-CAM), and accelerated stability (40 ± 2 °C, 75 ± 5% relative humidity, 4 weeks) were evaluated. Results: Bead-free nanofibers with mean diameters between 216 ± 33 nm and 310 ± 35 nm were obtained, and XRD confirmed complete amorphization of AmphB within the PVA nanofiber matrix, forming an amorphous solid dispersion. All formulations showed rapid and nearly complete AmphB release (≈100% within 60 min), with Weibull β values < 0.75, indicating Fickian diffusion-controlled release. AmphB-loaded PVA nanofiber-based ophthalmic inserts produced inhibition zones and broth susceptibility profiles comparable to AmphB in dimethyl sulfoxide (DMSO), demonstrating preserved antifungal activity. HET-CAM scores (0–0.9) classified the inserts as practically non-irritant, and SEM/FTIR after accelerated storage showed no relevant morphological or physicochemical changes. Conclusions: These γ-CD and STC-enhanced AmphB-loaded PVA nanofiber-based ophthalmic inserts provide a non-invasive, rapidly dissolving ophthalmic dosage form that combines amorphous AmphB, immediate drug availability, and good ocular tolerance, supporting their further development as a patient-friendly treatment option for fungal keratitis. Full article

Fine migration is widely recognized as a primary cause of production decline in unconsolidated sandstone reservoirs. Migrated fines may accumulate within pore throats and obstruct flow channels, or they may be transported into the wellbore with the produced fluids, leading to operational issues such as wellbore plugging, pump sticking, and equipment abrasion. Despite extensive studies on fine migration, the role of particle wettability has received limited attention. In this study, the mineralogical composition of formation particles was first characterized using X-ray diffraction (XRD) and quantitative clay analysis. Surface modification experiments were then conducted to investigate the effect of hexadecylamine (HDA) on particle wettability and to determine the optimal reaction conditions. Surface characterization techniques were employed to elucidate the modification mechanism. Subsequently, sand-packed tube displacement experiments were performed to evaluate the influence of wettability alteration on fine migration behavior. The underlying mechanisms were further interpreted through interfacial thermodynamic analysis. Two potential field application schemes are proposed to facilitate practical implementation in oilfield operations. The results indicate that the water contact angle of formation particles increased from 0° to 150° when treated with 0.8 wt% HDA for 24 h. Surface characterization confirms that HDA molecules were physically adsorbed onto the particle surfaces. Displacement experiments demonstrate that the permeability reduction rate decreases significantly with increasing particle hydrophobicity. Thermodynamic analysis suggests that the work of adhesion on the modified particle surface was reduced by 93.3%, thereby weakening fluid–particle interfacial coupling and suppressing fine mobilization. This study provides a wettability-based approach for mitigating permeability damage caused by fine migration in unconsolidated sandstone reservoirs. Full article

This study investigates the influence of conventional textile pretreatment and periodate oxidation parameters on the structural modifications and functional properties of woven cotton fabrics. Unlike most studies focused on cellulose pulps or isolated textile fibers, the present work examines how the initial structural state of the textile substrate, determined by its pretreatment history, governs the oxidation pathways. Cotton fabrics were subjected to alkaline scouring (SC), hydrogen peroxide bleaching (BC), and combined scouring–bleaching (SBC), followed by sodium periodate oxidation under controlled conditions. Carbonyl species were quantified analytically and identified by ATR-FTIR spectroscopy, while structural changes were evaluated by X-ray diffraction (XRD). Mechanical properties were assessed using the normalized parameters (Fa/Fa₀ and E/E₀), hydrophilicity by water absorption capacity (WAC), and optical stability by the yellowness index (YI). The results demonstrated that the pretreatments influence the oxidant accessibility and the balance between carbonyl speciation. XRD analysis shows a moderate decrease in crystallinity, indicating partial preservation of the crystalline domains, whereas mechanical properties decrease significantly (35–65%), concomitant with a 25–45% reduction in WAC. These results suggest that the impairment in mechanical and hydrophilic properties is primarily governed by localized C2–C3 bond scission, secondary oxidative reactions, and supramolecular rearrangements, rather than by bulk crystalline loss. The oxidized SC series exhibits higher YI values associated with an increased free aldehyde content, while the BC and SBC fabrics show improved optical stability. Overall, these results demonstrate that pretreatment history governs periodate oxidation pathways and establishes clear structure–property relationship relevant for the controlled functionalization of woven cotton fabrics. Full article

The rational design of electrode materials with tailored composition and architecture is crucial for advancing high-capability electrochemical energy storage systems. This study reports that gadolinium-modified NiFe₂O₄ nanosheet electrodes were effectively synthesized on nickel foam via a hydrothermal approach followed by thermal treatment. A series of compositions (NiFe, NiFe–Gd1, NiFe–Gd2, and NiFe–Gd3) were prepared to systematically examine the effect of Gd incorporation on structural features and electrochemical properties. X-ray diffraction (XRD) analysis confirmed the formation of the cubic spinel NiFe₂O₄ phase without detectable secondary phases, indicating that the crystal structure remains intact after Gd introduction. X-ray photoelectron spectroscopy (XPS) further verified the presence of Ni²⁺, Fe³⁺, and Gd³⁺ species within the lattice environment. Morphological analysis using field-emission scanning electron microscopy (FESEM) revealed a nanosheet-based architecture, where the optimized NiFe–Gd2 electrode exhibited a porous and interconnected nanosheet framework with abundant exposed edges. This structural configuration improves electrolyte penetration and facilitates efficient ion transport during charge storage processes. Electrochemical measurements demonstrated that the NiFe–Gd2 electrode delivers an areal capacitance of 5235 mF cm⁻² at 10 mA cm⁻², along with improved reaction kinetics and low internal resistance. An asymmetric supercapacitor assembled using NiFe–Gd2 as the positive electrode and activated carbon as the negative electrode operated stably within a 0–1.5 V potential window, achieving an energy density of 0.136 mWh cm⁻² and a power density of 3.14 mW cm⁻², while retaining 86.55% of its initial capacitance after 7000 cycles. These results highlight the potential of rare-earth engineering as a viable strategy for designing advanced spinel ferrite electrodes and pave the way for the development of high-performance, durable, and scalable supercapacitor systems for practical energy storage applications. Full article

Copper functions as an exceptionally efficient conductor, garnering considerable interest in electrical and thermal applications; however, its relatively malleable nature and insufficient durability may hinder its structural effectiveness. This study focused on the development of copper-based nanocomposites by reinforcing a copper matrix with co-precipitated CuO/Al₂O₃ nanoparticles (varying from 0 to 10 wt% in increments of 2%). A thorough examination was conducted regarding the microstructural characteristics, mechanical properties, and the electrical and thermal conductivities of the composites. X-ray diffraction (XRD) and energy-dispersive spectroscopy (EDS) analysis validated the successful synthesis of nano-sized CuO and Al₂O₃ phases, with an estimated crystallite size of 33.2 ± 2.4 nm. Scanning electron microscopy revealed a relatively uniform distribution of nano-oxides within the copper matrix, albeit with signs of particle agglomeration at higher loading levels. The durability of the copper exhibited a significant enhancement attributed to the nano-oxide reinforcement, achieving an 180% increase relative to pure copper with a 10% reinforcement addition. Consequently, the tensile strength increased by approximately 68% (from around 154 MPa to nearly 260 MPa), while maintaining an exceptional level of ductility. The electrical conductivity of copper remained largely unchanged with the addition of nanoparticles; rather, a slight improvement in conductivity and a ~30% rise in thermal conductivity were observed at the maximum reinforcement level. This research work presents a copper-based nanocomposite that offers remarkable potential for applications requiring enhanced strength, wear resistance, and exceptional electrical and thermal conductivity. Full article

To develop a high-performance inorganic fireproof coating suitable for steel structures, this study utilized magnesium phosphate cement (MPC) as the matrix and introduced expanded perlite (EP) as a lightweight aggregate. The effects of EP content (40–55%) and magnesium-to-phosphorus ratio (M/P = 4:1–7:1) on the dry density, compressive strength, bond strength, and fire resistance of the coating were systematically investigated. X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA) were employed to reveal the phase evolution and microstructure evolution mechanisms at high temperatures. The results indicate that increasing EP content significantly reduces the dry density and thermal conductivity of the coating, enhancing thermal insulation performance. However, excessive incorporation leads to the deterioration of mechanical properties, with an optimal EP content of 45%. The M/P ratio influences the interfacial bond strength and high-temperature structural stability by regulating the proportion of the hydration product K-struvite (KMgPO₄·6H₂O) and residual MgO. Compressive strength peaked at M/P = 6:1 (0.80 MPa), while bond strength was optimal at M/P = 5:1 (0.097 MPa), corresponding to the best fire resistance (back-side temperature of 180.4 °C). At high temperatures, K-struvite dehydrates and transforms into anhydrous KMgPO₄, which, together with residual MgO and crystallized SiO₂ from EP, forms a dense ceramic skeleton, ensuring the structural integrity of the coating. Comprehensive performance evaluation determined the optimal mix ratio as M/P = 5:1 and EP content = 45%. The coating with this ratio exhibits a dry density of approximately 560 kg/m³, a 14-day compressive strength of 0.53 MPa, a bond strength of 0.097 MPa, and a back-side temperature of 180.4 °C under flame exposure, demonstrating a favorable balance of lightweight character, mechanical integrity, and thermal insulation performance suitable for steel structure fire protection applications. Full article

Biopolymer-based packaging films possess outstanding performances and are being developed as the alternatives to traditional petroleum-based plastic packaging films with many non-ignorable shortcomings. In this study, chitosan, succinylated pullulan (SP), and berberine (BBR) were combined to fabricate novel biopolymer-based composite films (CSSPB) via the layer-by-layer assembly method. The effects of the incorporation of BBR on the physicochemical properties of the film were investigated. It was found that after BBR was added, the tensile strength (TS), elongation at break (EAB), hydrophobicity, and antioxidant capacities of the film were enhanced. The chemical bonding, crystalline properties, elemental composition, and thermal stability of the films were also characterized by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA), respectively. The in vitro antifungal tests revealed the antifungal activities of the films with a relatively high BBR content against Colletotrichum gloeosporioides (CG). In the preservation experiments, the CSSPB films exhibited preservation effects on fresh-cut apples, which manifested as delaying browning, weight loss, an increase in the soluble solids content, and a decrease in hardness. The new CSSPB composite films were opined to hold application potential in the field of food packaging. Full article

The efficient recovery of coalbed methane (CBM) is critically constrained by the inherent low permeability of coal reservoirs, a challenge predominantly attributed to mineral blockages within the pore-fracture structure. In this study, the deashing efficacy of several acid solutions (HCl, HNO₃, HF, and CH₃COOH) on bituminous coals from the Yushuwan (YSW) and Jiangna (JN) mines was initially assessed to determine the optimal acidizing system. Subsequently, the multi-scale evolution of pore-fracture structures and the fractal characteristics of coal samples treated with the optimized acids were systematically investigated. A multi-analytical approach, integrating scanning electron microscopy (SEM), X-ray diffraction (XRD) with microcrystalline peak-fitting, and low-temperature nitrogen gas adsorption (LT-N₂GA), was employed to quantitatively elucidate the underlying transformation mechanisms. The experimental results indicate that HCl and HNO₃ emerged as the most effective agents for the YSW and JN coals, respectively. Optimized acidification achieved significant reductions in ash content (specifically, an ash removal efficiency of 83.99% for HCl-treated YSW coal) through the selective dissolution of carbonate and clay minerals, thereby facilitating the exposure of the organic matrix and the induction of extensive dissolution pits and secondary fractures. Although the dissolution-induced collapse of mineral-supported fine pores led to a reduction in both total pore volume and BET specific surface area, the average pore diameter undergoes a substantial increase (e.g., nearly doubling from 9.0068 nm to 16.5126 nm for the JN coal). Furthermore, the reduction in Frenkel–Halsey–Hill (FHH) fractal dimensions (D₁ and D₂) indicates a decrease in pore-surface complexity and structural heterogeneity. These findings reveal that optimized acidification induces significant alterations in pore structure and mineral composition. The treatment facilitates the conversion of isolated pores into interconnected networks, accompanied by an increase in pore volume and a shift in pore size distribution toward larger dimensions. This research elucidates the mechanisms of mineral dissolution and pore expansion, providing a fundamental characterization of the microstructural evolution of coal in response to acid treatment. Full article