Search Results (9,848)

Threaded fasteners and tapping joints are essential for the structural integrity and leak-proof performance of subsea systems subjected to high external pressure, aggressive corrosion, and complex cyclic loading. This study presents a comprehensive, systematically structured review of experimental, analytical, and numerical investigations of nut–bolt and threaded connections used in deep- and ultra-deepwater applications. The literature is classified based on governing performance parameters, including thread engagement mechanics, preload retention, fracture behavior, corrosion–fatigue interaction, material evolution, and environmental effects such as hydrostatic pressure and thermal gradients. Experimental observations are critically synthesized with finite element modeling to interpret stress distributions, failure mode transitions, and sealing reliability. A comparative material selection framework is developed by linking conventional carbon steels with advanced alloys such as duplex stainless steels, titanium, and nickel-based materials for long-term subsea service. The novelty of this review lies in the development of an integrated, design-oriented framework that unifies engagement optimization, preload control, fracture modeling strategies, material selection, and environmental coupling into a single engineering interpretation for subsea fastening systems, which has not been collectively addressed in previous studies. The presented synthesis provides direct application guidelines for improving the design, analysis, and operational reliability of subsea bolted joints. Full article

Current strategies for treating organic dye wastewater are shifting from single-function removal processes and catalytic degradation methods toward more integrated treatment approaches. This study proposes a multifunctional composite integrating adsorption–photodegradation–intelligent recovery for photodegradation and recovery of methylene blue-contaminated wastewater. By optimizing the preparation process to precisely control the pore size and arrangement of the aerogel, a hierarchical porous framework with a high specific surface area is formed, featuring efficient mass transfer and ultra-multiple loading sites. The graphene framework enhances visible-light absorption by optimizing TiO₂ loading, agglomeration behavior and addressing detachable defects through a metal–polyphenol network. After 60 min of illumination, the degradation efficiency exceeds 99.5%, demonstrating superior cycling stability. After 100 cycles, the photocatalytic efficiency remains above 97%, showcasing excellent durability. Furthermore, the in situ polymerized thermoresponsive poly (N-isopropylacrylamide) (PNIPAm) composite exhibits smart responsiveness, enabling reversible temperature-responsive adsorption–desorption behavior within PNIPAm’s LCST range. with an adsorption capacity of 28,000 mg/g at LCST. Heating above LCST desorbs 90.2% of the wastewater, and adsorption stability remains above 98% after 100 thermal cycles, resolving operational challenges in mechanical wastewater recovery. The synergistic integration of an anisotropic porous structure, stable TiO₂ loading, and thermal responsiveness provides an efficient platform for integrated adsorption and recovery. Full article

Mathematical and numerical models for Packed Bed Thermal Energy Storage (PBTES) systems are essential to predict the different parameters that influence their thermodynamic behavior and then optimize their performance and efficiency. In this research paper, an industrial-scale sensible thermocline Packed Bed Thermal Energy Storage system (9.17 m high and 4.72 m in diameter) was modeled and simulated during the heat charging process, based on FEM, CFD one-dimensional, and two-phase analysis. The model rigorously couples the Local Thermal Non-Equilibrium (LTNE) energy formulation with Darcy–Forchheimer hydrodynamics. The developed model was verified and validated using experimental data from the literature. The model was in close agreement with the experiment, with a global mean relative error of 3.62%. The two-dimensional velocity and temperature fields were presented to describe flow and temperature distributions in the hybrid medium (free and porous). The effect of varying flow rates (8–15 kg/s), porosities (0.35–0.55), and particle diameters (5–20 cm) on the thermal behavior of the heat storage system, temperature fields for solid and fluid, thermocline behavior, and charge efficiency were evaluated and presented. The simulation results demonstrate that the system achieves a high charge efficiency of 92.3% at a nominal charging rate of 15 kg/s. Increasing mass flow rate accelerates charging but widens the thermocline thickness and thermal stratification. Furthermore, increasing the porosity from 0.35 to 0.55 reduced charging time, decreased the temperature difference between the HTF and the storage medium by 10 °C, and increased the final heat charging efficiency by 8%. On the contrary, an increase in particle size from 5 to 20 cm leads to a slower rise in temperature within the solid phase, creating an important LTNE lag of ≈34 °C, thereby reducing the final heat charge efficiency by 16%, and prolonging the time required to charge the tank. Full article

Nd₂NiO_4+δ was investigated as a Ruddlesden–Popper (RP) cathode material for intermediate-temperature solid oxide fuel cells (IT-SOFCs), with particular emphasis on its electrochemical performance and oxygen reduction reaction mechanism. The material was synthesized via a polymeric sol–gel route derived from Pechini’s method and evaluated in symmetric cells using Ce_0.9Gd_0.1O_2−δ (GDC) as the electrolyte. X-ray diffraction confirmed the formation of a single RP phase and good chemical compatibility with GDC after thermal treatments at 800 °C. Cathode layers with thicknesses of 8–12 µm were deposited by dip-coating. Electrical conductivity measurements revealed a thermally activated semiconducting behavior governed by Ni²⁺/Ni³⁺ small-polaron hopping, with an activation energy of ~1.08 eV. Electrochemical impedance spectroscopy showed a strong temperature dependence of the area-specific resistance, decreasing from 9.18 Ω·cm² at 600 °C to 0.39 Ω·cm² at 800 °C. Distribution of relaxation times (DRT) analysis enabled the identification of the dominant electrochemical processes, indicating that oxygen surface exchange reactions are more favorable than charge transfer at the cathode–electrolyte interface, which remains the main limiting step. These results demonstrate that Nd₂NiO_4+δ is a promising cathode for IT-SOFC operation, while further optimization of the electrode–electrolyte interface is required to enhance its oxygen reduction kinetics. Full article

Expanded polystyrene (EPS) waste poses a major environmental concern due to its high volume, low density, and resistance to biodegradation. In this study, post-consumer EPS was reprocessed into continuous microfibers by Air Jet Spinning (AJS) using chloroform and chloroform/D-limonene as solvent systems. The effects of polymer concentration, air pressure, and solvent ratio on fiber formation were systematically investigated through rheological and surface tension analyses. The incorporation of 10 vol. % D-limonene improved jet stability and reduced bead formation, attributed to its lower volatility and favorable solubility with EPS, as supported by Hansen solubility parameters. SEM analysis confirmed uniform microfiber formation within a defined processing window. FTIR spectra indicated preservation of the polystyrene chemical structure, while TGA and DSC analyses were used to evaluate thermal behavior and assess potential residual solvent retention, particularly related to D-limonene. The results elucidate the interplay between solvent volatility, solution properties, and fiber morphology, establishing a sustainable processing framework for converting EPS waste into value-added fibrous materials via AJS. This work contributes to the United National Sustainable Development Goals, particularly SDG 12 (Responsible Consumption and Production) by promoting EPS waste valorization, and SDG 13 (Climate Action) through the partial replacement of conventional solvents with sustainable alternative. Full article

Calcium carbonate is a widely used filler in polymer composites due to its low cost and ability to improve stiffness, dimensional stability, and impact resistance. However, its hydrophilic surface limits compatibility with nonpolar polymer matrices, making surface modification essential to improve filler dispersion and interfacial adhesion. Stearic acid is commonly applied as a surface modifier for calcium carbonate because it readily chemisorbs onto the mineral surface and forms densely packed self-assembled monolayers that improve hydrophobic character. Despite its widespread use, stearic acid exhibits limited thermal and interfacial stability under polymer processing conditions, motivating the development of stabilization strategies. In this work, gamma and electron-beam irradiation were applied to stearic-acid-modified calcium carbonate to modify the surface-bound stearic acid layer with the aim of enhancing its interfacial stability, surface resistance, and hydrophobic performance, and to evaluate the influence of irradiation atmosphere on these effects. The modified materials were characterized in terms of structural integrity, surface wettability, surface free energy, thermal stability, and optical properties. The results demonstrate that ionizing radiation enhances surface hydrophobicity and coating durability while preserving the crystal structure of the CaCO₃ substrate. Gamma irradiation of stearic-acid-modified vaterite exhibited strong atmosphere dependence, with improved hydrophobicity under oxygen-free conditions, whereas electron-beam irradiation showed more robust and oxygen-insensitive behavior. Based on the observed improvements in hydrophobicity, surface free energy, and thermal stability, electron-beam irradiation emerges as a promising and less atmosphere-sensitive approach for producing durable stearic-acid-modified CaCO₃ fillers suitable for polymer composite applications. Full article

To facilitate the development of low-cost LTCC substrate materials and the high-value utilization of industrial tailings, α-cordierite glass-ceramics with varying Na₂O additions were prepared from perlite tailings as the main raw material via the melt-quenching method followed by sintering-induced crystallization. The synergistic effects of sintering temperature and Na₂O addition on the parent glass structure, crystallization behavior, and properties were systematically investigated. The results demonstrated that the addition of Na₂O effectively depolymerized the degree of network polymerization of the parent glass, altered the crystallization pathway of cordierite crystal, and promoted the densification of glass-ceramics at lower sintering temperature. The calculations of crystallization kinetics revealed that the crystallization process of α-cordierite was mainly dominated by three-dimensional bulk growth, and its nucleation mechanism changed from “site saturation” to “continuous nucleation” with the increase of Na₂O addition. The α-cordierite glass-ceramics sintered at 850 °C with 0.6 wt.% Na₂O addition exhibited the optimal comprehensive properties, including low dielectric constant (5.82 @ 10 MHz) and dielectric loss (1.80 × 10⁻² @ 10 MHz), high flexural strength (147.3 MPa), a Vickers hardness (9.01 GPa), and suitable coefficient of thermal expansion (2.96 × 10⁻⁶ K⁻¹, close to Si). The glass-ceramics are expected to be an ideal candidate for low-cost LTCC substrate materials. Full article

This study presents a comprehensive comparative analysis of the performance, combustion, and emission characteristics of a single-cylinder, four-stroke spark-ignition engine fueled by commercial gasoline and raw biogas enhanced with cerium oxide (CeO₂) nanoparticles. Raw biogas containing 58% methane was tested without carbon dioxide removal to reflect practical rural applications, while CeO₂ nanoparticles were ultrasonically dispersed in the fuel to promote homogeneous suspension and catalytic activity. Experiments were conducted under wide-open and part-throttle conditions across a range of engine speeds, with simultaneous measurement of brake thermal efficiency, brake-specific fuel consumption, volumetric efficiency, in-cylinder pressure, heat release rate, combustion phasing, and regulated emissions. The results showed that while gasoline consistently outperformed biogas in torque and power due to its higher heating value and flame speed, the addition of CeO₂ significantly reduced the performance gap. For the biogas mode, CeO₂ addition increased brake thermal efficiency by up to 5%, lowered brake-specific fuel consumption by up to 8%, and shifted the start of main combustion to earlier crank angles, indicating faster and more complete combustion, particularly at high loads where higher temperatures activate CeO₂’s catalytic behavior. Emission analysis revealed that CeO₂-blended biogas reduced carbon monoxide emissions by approximately 25% and unburned hydrocarbons by up to 55% compared with gasoline, while nitrogen oxide emissions were consistently 15–22% lower. These reductions were observed across both wide-open and part-throttle conditions, confirming improved combustion completeness and lower peak flame temperatures. These improvements are attributed to CeO₂’s oxygen-storage capability, catalytic oxidation activity, and enhanced thermal conductivity, which collectively strengthen combustion completeness and cyclic stability. The findings demonstrate that nanoparticle-enhanced biogas can substantially improve the environmental and operational viability of spark-ignition engines, offering a practical pathway for integrating renewable gaseous fuels into existing transportation systems. Full article

Cellulose paper, a natural polymeric dielectric, determines the lifetime of oil–paper insulation systems in transformers, yet its molecular degradation behavior in ester-based insulating media remains insufficiently clarified. This study investigates the electro–thermal aging of cellulose polymer immersed in soybean-based natural ester (SBNE) and palm fatty acid ester (PFAE), with emphasis on depolymerization and its relationship with partial discharge (PD) activity. Accelerated aging experiments were conducted under combined electrical and thermal stress, and the evolution of the degree of polymerization (DP) was measured to quantify polymer chain scission. Phase-resolved PD (PRPD) patterns were recorded during aging, and multi-dimensional statistical features were extracted and reduced using principal component analysis to characterize degradation-sensitive electrical responses. The results show a progressive decrease in DP with aging time in both ester media, accompanied by distinct PD evolution characteristics, indicating different influences of the two esters on cellulose polymer stability. An ensemble learning model integrating multiple classifiers was further employed to identify aging stages based on PD features, achieving reliable discrimination performance. These findings establish a correlation between cellulose depolymerization and dielectric discharge behavior, providing a polymer-centered interpretation of aging mechanisms in ester-based oil–paper insulation systems. Full article

Microstructural and morphological effects of cobalt (Co), nickel (Ni), and cerium (Ce) microalloying on the SAC305 lead-free solder alloy were investigated, with emphasis on the solidification behavior under slow cooling conditions. Although the individual effects of these elements have been previously reported, their combined influence remains scarcely addressed. Thermal behavior, elemental composition, and surface integrity of the solder joints were analyzed. The addition of Co, Ni, and Ce resulted in a significant shift of the onset temperature during cooling, indicating reduced undercooling. Microalloying led to a transformation of the intermetallic layer (IML) morphology from scalloped to planar, and a 60% reduction in the number of shrinkage voids. The average β-Sn grain size decreased by 37.5%, while the eutectic area increased from 32% to 38%. The substitution of Cu atoms by Co and Ni within the Cu₆Sn₅ lattice formed thermodynamically stable (Cu,Co,Ni)₆Sn₅ phases. These findings demonstrate that the synergistic effect of Co, Ni, and Ce microadditives effectively refines the microstructure, suppresses undercooling, and enhances the overall reliability of SAC305 solder joints. Full article

Extended-solvent steam-assisted gravity drainage (ES-SAGD) has emerged as a promising advancement over conventional SAGD for improving the efficiency and sustainability of in situ heavy oil and bitumen recovery. By co-injecting light hydrocarbon or alternative solvents with steam, ES-SAGD integrates thermal and compositional mechanisms to reduce viscosity, accelerate chamber development, and reduce steam–oil ratios. This review synthesizes the current state of knowledge on ES-SAGD, encompassing fundamental transport mechanisms, solvent selection and phase behavior, mass transfer dynamics, laboratory and physical modeling studies, numerical simulation approaches, and field-scale operational experiences. Experimental evidence consistently demonstrates substantial mobility enhancement through solvent-induced dilution, while compositional thermal simulations highlight an improved sweep efficiency and reduced energy intensity relative to steam-only processes. Field pilots further validate accelerated early-time production and significant steam savings, though challenges related to solvent retention, asphaltene stability, and reservoir heterogeneity persist. Key research gaps are identified in solvent transport prediction, formation damage risk, long-term solvent recovery, and integrated economic–environmental optimization. Overall, ES-SAGD offers a viable pathway toward lower-emission, higher-efficiency bitumen production, provided that solvent chemistry, reservoir complexity, and operational controls are carefully managed through continued research and targeted field deployment. Full article

Functionally graded porous beams are increasingly used in lightweight engineering structures, where thermal effects and material inhomogeneity significantly influence vibration behavior. In this study, the thermoelastic free vibration of functionally graded porous Euler–Bernoulli beams with temperature-dependent material properties is investigated by considering uniform and symmetric porosity distributions, together with uniform, linear, and nonlinear temperature fields. The governing equations are derived based on classical Euler–Bernoulli beam theory and solved using the Differential Transformation Method, while the accuracy of the semi-analytical formulation is verified through a Hermite-based finite element model. The results show that increasing temperature reduces the bending stiffness due to thermal axial forces and leads to a rapid decrease in natural frequency as the critical buckling temperature is approached. Increasing porosity generally decreases the natural frequency, although a slight increase may occur in symmetric distributions because of the accompanying reduction in mass density. The present study provides a computational framework for the thermo-vibration analysis of functionally graded porous beams in lightweight structural applications. Full article

This study reports the synthesis, spectroscopic characterization, and biological evaluation of a novel moxifloxacin hydrazide derivative (MOX-H) and its metal complexes with Co(II), Ni(II), Cu(II), VO(IV), and Gd(III). The ligand was synthesized by hydrazinolysis of moxifloxacin hydrochloride, and the resulting hydrazide was subsequently complexed with the respective metal salts. The interaction between MOX-H and the metal ions yielded the corresponding complexes, formulated as [Co(H₂O)Cl(MOX-H)₂]Cl·2.5H₂O, [Ni(H₂O)Cl(MOX-H)₂]Cl.4.5H₂O, [VO(MOX-H)₂]SO₄.3.5H₂O, [Gd (H₂O)(MOX-H)₂(NO₃)₂]NO₃.2H₂O, and [Cu(MOX-H)₂(H₂O)Cl]Cl·xH₂O (where x = 2, 2.5, 0.5, for products synthesized via template, microwave-assisted, and hydrothermal methods, respectively). The synthesized analogues were characterized by elemental analysis (CHN), FT-IR, UV-visible, and ¹H NMR spectroscopy, and mass spectrometry, as well as thermogravimetric (TG/DTG) and magnetic measurements. FT-IR spectra confirmed coordination through the hydrazide carbonyl and amine groups, while UV–visible and magnetic data indicated predominantly octahedral geometries. The thermal behavior exhibited multistep decomposition with activation parameters supporting exothermic processes. When compared to the free ligand, the metal complexes showed increased antimicrobial activity against both Gram-positive and Gram-negative bacteria and fungus species, particularly for the Co(II) and Cu(II) complexes, which showed the largest inhibition zones. The Cu(II)–MOX-H complex exhibited the lowest MIC values (4.88–9.76 µg/mL) among all tested compounds, confirming its outstanding antibacterial potency and high sensitivity compared to the free ligand and standard drug. Cytotoxicity assays demonstrated selective anticancer activity, with the Cu(II)–MOX-H complex showing the highest potency (IC₅₀ ≈ 2.95 µM against MCF-7 and IC₅₀ ≈ 0.98 µM against HepG-2), while maintaining minimal toxicity toward normal cells. These findings were corroborated by molecular docking investigations, which showed that the MOX-H complexes had substantial binding affinities (−9 to −10 kcal/mol) toward DNA topoisomerase II, consistent with their observed biological effects. Full article

During fires, the temperature difference between indoor and outdoor environments induces out-of-plane deformation in steel studs. Due to the differential coefficients of thermal expansion between panels and steel, the panels exert a restraining effect on the studs. However, there remains a lack of systematic experimental and theoretical models addressing the failure modes, restraining mechanisms, and synergistic effects of various panels on steel studs. This study conducted high-temperature bending tests to compare the failure modes, load–displacement curves, and key mechanical parameters (peak load, elastic stiffness) of connections combining steel studs with three types of panels: autoclaved lightweight concrete (ALC) panels, fire-resistant gypsum boards, and medium-density calcium silicate board. The research clarifies the constraining effect and temperature sensitivity of different panels. Based on experimental data, a bending constitutive model was developed to quantify the attenuation of the out-of-plane constraining effect at elevated temperatures. The results indicate that the load–displacement curves exhibit three distinct stages: Elastic Ascending Stage, Elastoplastic Ascending Stage, and Post-Peak Stage. A two-stage bending constitutive model was proposed and formulated. Comparison between numerical simulations and experimental specimens in terms of failure modes and characteristic parameters demonstrated that simplifying the panels as spring elements, with stiffness defined by the proposed bending constitutive model, yields errors within 15%, confirming the accuracy of the model. This study systematically investigates the influence of sheathing panels on the high-temperature out-of-plane mechanical behavior of cold-formed steel studs, innovatively proposes a two-stage bending constitutive model, provides theoretical and data support for cold-formed steel structural fire-resistant design, and offers new perspectives and methodologies for future research. Full article

To mitigate the issue of brittleness and cracking in epoxy resin (EP) anti-skid systems, this study investigates four key aspects tailored to application scenarios: toughening, low shrinkage, strong adhesion, and rapid curing at ambient temperature. 1,4-Butanediol diglycidyl ether (BDDE) was used to extend the chain of triethylenetetramine (TETA), followed by a Mannich reaction with formaldehyde (F) and cardanol to prepare a flexible aliphatic amine Mannich base curing agent containing flexible segments (Curing Agent B). The influence of composition ratios on the mechanical properties of the cured product was studied. The curing performance of the epoxy system under various temperature conditions and its adhesion to asphalt substrates were characterized. The thermal shrinkage behavior of the epoxy system under temperature-variable environments was also investigated. The results indicated that the elongation at break of the epoxy curing system, after chain extension and toughening, increased from 28.7% to 40.4%, representing a 28.9% increase. When n (Cardanol):n (TETA):n (F):n (BDDE) = 1:1.4:0.8:0.7 (molar ratio of reactants), m (EP):m (Curing Agent B) = 1:1 (mass ratio), and epoxy-terminated polyurethane (EPU) prepolymer constituted 10% of the epoxy resin mass; the epoxy curing system exhibited an elongation at break of 44.3%, a tensile strength of 7.0 MPa, a bond strength of 6.9 MPa, and an impact toughness of 1.77 J/cm². Furthermore, it exhibited rapid curing at a low temperature (0~5 °C) and at room temperature (25 °C). Additionally, when bisphenol F epoxy resin was used, the system demonstrated optimal thermal expansion properties. Full article