Search Results (1,743)

Objective: To determine whether contrast therapy improves recovery after climbing-specific forearm fatigue in amateur climbers. Methods: In a randomized repeated-measures trial, 40 climbers were allocated to passive recovery (n = 20) or Game Ready contrast therapy (n = 20). Both groups completed a fixed-task intermittent fingerboard protocol on a 20 mm edge using a half-crimp grip, with 7 s of work and 3 s of rest for five sets; the load was not individualized to climbing-specific maximal finger-flexor force. The intervention group received bilateral forearm treatment consisting of alternating 1 min cold (3 °C) and heat (45 °C) phases combined with pneumatic compression ranging from 15 to 75 mmHg. Sessions lasted 20 min and were administered immediately after post-fatigue testing, at 24 h and 48 h, and then three times weekly on alternate days for 8 weeks, for a total of 27 sessions. Outcomes were assessed at baseline, immediately after fatigue, at 24 h and 48 h, and after 8 weeks. Outcomes included perfusion, reactive hyperemia, stiffness, pressure pain threshold, grip strength, perceived recovery, creatine kinase, and interleukin-6. Results: Immediate post-fatigue responses were comparable. Contrast therapy produced greater 24 h and 48 h resting perfusion responses (+7.28 percentage points, 95% CI 6.58 to 7.98; +7.62, 95% CI 6.94 to 8.31; both adjusted p < 0.001). At week 8, peak hyperemic perfusion improved more with contrast therapy (+6.21 PU, 95% CI 5.62 to 6.79; p < 0.001). Recovery favored contrast therapy for stiffness at 48 h (−71.7 N/m, 95% CI −75.6 to −67.8), pressure pain threshold at week 8 (+8.1 N/cm², 95% CI 7.3 to 8.8), and grip strength at 48 h (+7.8 kgf, 95% CI 7.3 to 8.3; all p < 0.001). CK and IL-6 differences were transient, and no serious adverse events or intervention-related discontinuations were recorded. Conclusions: Contrast therapy was associated with more favorable cutaneous perfusion, post-occlusive reactive hyperemia-derived, and neuromechanical recovery outcomes, whereas biochemical differences were limited and time-dependent. The vascular findings do not establish improved endothelial function or nitric-oxide-mediated vasodilation because these mechanisms were not directly assessed. Trial registration: ISRCTN49499065 on 23 June 2025. Full article

Background/Objectives: α-lipoic acid (ALA) shows therapeutic potential but faces poor aqueous solubility (BCS Class II), gastric instability, and low oral bioavailability (~30%). This work investigated the formulation of cyclodextrin (CD) inclusion complexes of ALA to overcome the aforementioned limitations and improve nutraceutical applications. Methods: Phase solubility studies in simulated gastric and intestinal fluids screened for optimal CD, followed by molecular dynamics simulations and MM-PBSA binding free energy calculations. Inclusion complexes of choice were prepared by grinding, spray-drying, and lyophilization, followed by solid-state characterization (DSC/XRPD/FTIR). Further analysis was performed using pH-shift dissolution (USP II), permeability (PermeaPad^®, Caco-2), and (photo)stability according to ICH. Results: Hydroxypropyl-β-cyclodextrin (HPβCD) emerged as the optimal host due to favorable complexation, as confirmed by phase solubility studies and supported by molecular modeling, which revealed a favorable balance between inclusion complex stability and pH-triggered drug release. Formulations based on spray-dried and lyophilized HPβCD–ALA complexes (HPβALA-sd and HPβALA-lyo), in which ALA was fully amorphized, achieved near-complete dissolution within five minutes under biorelevant pH-shift conditions. This performance markedly exceeded that of free ALA (approximately 66% dissolution at pH 7.4) while maintaining moderate permeability (Papp 8–9 × 10⁻⁶ cm/s). Storage stability was enhanced markedly (88–90% ALA retention after 6 months at 40 °C/75% RH vs. 36% for free ALA) while UV stability was not improved through CD-complexation, probably due to interaction of UV-VIS light with the exposed portion of ALA. Conclusions: Even though the permeability of ALA–CD inclusion complexes remained medium (Papp ~ 8–9 × 10⁻⁶ cm/s) and unaffected by complexation, a significantly improved dissolution profile indicates better expected bioavailability compared to pure ALA. Full article

To investigate the rutting resistance of Large Stone Asphalt Mixture (nominal maximum aggregate size of 53 mm, abbreviated as LSAM-50), this study evaluated the effects of temperature, load, and their interaction on the rutting performance of LSAM-50 through large-thickness rutting tests. It analyzed the characteristics of rutting deformation under varying thermal and loading conditions, established a permanent deformation-temperature-load dependency model, and explored the correlations between permanent deformation and high-temperature evaluation indicators. The findings indicate that the temperature-load interaction fundamentally alters the load-transfer mechanism between the viscoelastic matrix and coarse aggregates within LSAM-50, thereby activating the interlocking effect of its thick structural skeleton. The dynamic stability undergoes a pronounced reduction as temperature or load increases, peaking at a degradation rate of 40–57% within the 40–50 °C interval. Furthermore, the rutting deformation of the LSAM-50 mixture demonstrates significant temperature and load dependency; as the number of loading cycles increases, the deformation exhibits an initial rapid escalation before reaching a plateau. During temperature elevation and load escalation, the rutting deformation increases in a step-wise manner. Notably, the preliminary application of low temperatures and light loads imparts a substantial “training” effect on the material’s rutting resistance. Once the mixture is wheel-tracked to densification under high temperatures or heavy loads, negligible new deformation is generated during the subsequent cooling or unloading phases. Specifically, upon the initial unloading from 1.1 MPa to 0.9 MPa, the incremental deformation is merely 0.04 mm; upon further unloading to 0.7 MPa, the additional deformation approaches 0 mm. The established permanent deformation-temperature-load dependency model for LSAM-50 yields a high predictive correlation of 96%. Moreover, the permanent deformation exhibits robust linear relationships with 1-h rutting depth (R² = 0.95), compressive strength (R² = 0.91), and shear strength (R² = 0.97). These indicators can thus facilitate the rapid and precise estimation of permanent pavement deformation. Full article

The transient heat-transfer behavior of hybrid natural-fiber-reinforced epoxy composites containing 0–5 wt% conch shell filler and 20–35 wt% combined banana–bagasse fiber reinforcement was evaluated using active infrared thermography. A standardized protocol comprising 30 s of convective heating with 100 °C hot air followed by 60 s of natural cooling was applied to seven composite configurations tested in triplicate. The transient response was analyzed in three phases: active heating (0–30 s), thermal lag (30–57 s), and natural cooling (57–90 s). Maximum temperature ($T_{max}$), heating rate ($R_h$), cooling rate ($R_c$), and a thermal retention ratio ($TR$) were extracted and statistically validated by one-way ANOVA with Bonferroni correction. For specimens exhibiting zero within-group variance at the camera display resolution, significance was confirmed using exact permutation tests. Filler incorporation (3–5 wt%) was the dominant factor governing peak-temperature reduction; F5B15S10 (5 wt% filler, 25 wt% total fiber) achieved the lowest $T_{max}$ (33.80 °C, 4.57 °C below neat epoxy). Cooling efficiency was primarily governed by fiber content; F3B15S20 (3 wt% filler, 35 wt% total fiber) demonstrated the most efficient heat dissipation ($TR=0.721$). These findings demonstrate that heating resistance and cooling efficiency are governed by partially independent mechanisms, enabling tailored material design. This study indicates that the proposed transient thermographic protocol provides a valuable reference to thermal management design of hybrid biocomposites in automotive interior and building envelope applications. Full article

Asymmetric quantum codes are useful for quantum channels in which phase and bit errors occur with different probabilities, since the two distances, $d_z$ and $d_x$, can be controlled separately. We develop a permutation-paired matrix-product construction for such codes over ${\mathbb{F}}_q$. The main task is to build classical code pairs $\mathcal{C},\mathcal{D}\subseteq {\mathbb{F}}_{q^2}^{kn}$ satisfying the Hermitian inclusion ${\mathcal{D}}^{{\perp }_{\mathrm{H}}}\subseteq \mathcal{C}$, while keeping explicit dimension and distance bounds. Let $A\in {\mathbb{F}}_{q^2}^{k\times k}$ be a non-singular-by-columns (NSC) matrix with $A{A}^{†}=D{P}_{\tau }$, where D is an invertible diagonal and $P_{\tau }$ corresponds to an involution $\tau$. For $\mathcal{C}=[C_1,\dots ,C_k]A$ and $\mathcal{D}=[D_1,\dots ,D_k]A$, we prove ${\mathcal{D}}^{{\perp }_{\mathrm{H}}}=[D_{\tau \left(1\right)}^{{\perp }_{\mathrm{H}}},\dots ,D_{\tau \left(k\right)}^{{\perp }_{\mathrm{H}}}]A$. Thus, the global inclusion ${\mathcal{D}}^{{\perp }_{\mathrm{H}}}\subseteq \mathcal{C}$ is equivalent to the shorter paired inclusions $D_{\tau \left(i\right)}^{{\perp }_{\mathrm{H}}}\subseteq C_i$. This yields asymmetric quantum codes with parameters ${\left[[kn,{\sum }_{i=1}^k(r_i+s_i)-kn,d_z/d_x]\right]}_q$, where the bounds for $d_z$ and $d_x$ follow from NSC matrix-product distance estimates. For nested maximum distance separable (MDS) constituents, the paired conditions reduce to $r_i+s_{\tau \left(i\right)}\ge n$, giving explicit infinite families. Concrete $\tau$-OD matrices and numerical examples show that nontrivial permutations can increase the quantum dimension while preserving prescribed lower bounds for $d_z$ and $d_x$. Full article

Transition-metal sulfides are promising electrode materials for high-performance supercapacitors but are often limited by poor conductivity, particle agglomeration, and insufficient active sites. Herein, Co-doped NiS₂ with tunable sulfur vacancies was directly grown on flexible carbon cloth via a facile one-step solvothermal method by systematically controlling sulfur source ratio, Ni:Co ratio, temperature, and reaction time. Structural analyses reveal that the optimized conditions of S:(Ni + Co) = 3:1, Ni:Co = 2:1, 160 °C, and 15 h promote the formation of phase-pure Co-doped NiS₂ hierarchical microspheres with enhanced crystallinity and abundant active sites from the synergistic interaction between Ni and Co. Consequently, the optimized electrode delivers an impressive capacitance of 1296 F g⁻¹ at a current density of 1 A g⁻¹, along with excellent rate performance, retaining more than 88% of its capacitance after 1500 charge/discharge cycles at current densities ranging from 2 to 20 A g⁻¹. This work highlights the critical role of synthesis parameter engineering in regulating defect chemistry, structure, and electrochemical performance in advanced energy storage applications. Full article

Magnesium–rich environments are frequently encountered in cementitious systems, including the use of high–Mg raw materials in clinker production, cement–clay interfaces relevant to nuclear waste disposal, and exposure of cement–based materials to seawater, where progressive decalcification can substantially alter the structure and durability of calcium aluminosilicate hydrate (C–A–S–H) phases. In this study, density functional theory (DFT) calculations were employed to investigate the combined effects of interlayer and intralayer partial decalcification, Mg²⁺ substitution, and reinforcement with epoxy– and hydroxyl–functionalized reduced graphene oxide (rGO) on the structural stability and elastic properties of alkali charge–balanced C–A–S–H under dry and hydrated conditions. Adsorption–energy calculations reveal thermodynamically favorable interactions between functionalized rGO and silicate hydrate species in the presence of Mg²⁺, with hydroxyl/rGO promoting stronger interfacial stabilization and epoxy/rGO preserving greater graphene lattice integrity. The results demonstrate that Mg²⁺ substitution together with rGO intercalation generally enhances the mechanical response of partially decalcified structures through structural densification and interfacial cohesion. Relative to dry systems, hydration further improves elastic performance, increasing Young’s modulus and bulk modulus by 1–11% and 4–19%, respectively, for interlayer decalcified nanocomposites, while intralayer configurations exhibit stronger but model–dependent enhancements of up to ≈22% and ≈33%. Compared with untreated systems, rGO–treated nan–composites exhibit enhanced stiffness, with Young’s modulus and bulk modulus increasing by up to ≈22% and ≈15%, respectively. Overall, these findings provide atomistic insights into stabilization mechanisms in partially decalcified alkali charge–balanced C–A–S–H systems and identify Mg²⁺–rGO incorporation as a promising strategy for mitigating decalcification–induced degradation in durable low–carbon cementitious nanocomposites. Full article

Background/Objectives: Ursodeoxycholic acid (UDCA) is a bile acid widely used for the treatment of cholestatic liver diseases; however, its poor aqueous solubility represents a major limitation for the development of oral liquid formulations, particularly in pediatric patients requiring accurate and flexible dosing. This study aimed to develop and characterize a fully solubilized extemporaneous UDCA oral formulation using the ready-to-use vehicle Wagner, with particular emphasis on the role of hydroxypropyl-β-cyclodextrin (HP-β-CD) as a solubilizing excipient. Methods: Phase-solubility studies, Job’s plot analysis, and ¹H NMR spectroscopy were performed to investigate the host–guest interaction between UDCA and HP-β-CD, confirming the formation of a stable 1:1 inclusion complex responsible for a marked increase in drug solubility. The aqueous solubility of UDCA increased from approximately 0.02 mg/mL in water to 31 ± 1 mg/mL in the Wagner base containing HP-β-CD, compared to ~10 mg/mL in the corresponding cyclodextrin-free vehicle. Chemical stability was evaluated using an HPLC method adapted from the European Pharmacopoeia, employing dual detection (refractive index and photodiode array detector) to ensure specificity and stability-indicating capability. Results: The UDCA solution (20 mg/mL) remained chemically stable for at least 4 months under refrigerated (4–8 °C) and room temperature (25 °C) conditions, with only moderate degradation observed at 40 °C. Physical stability studies confirmed the absence of precipitation, phase separation, or significant pH variations under all storage conditions. Conclusions: Wagner-based formulation enabled the development of a stable and homogeneous UDCA oral solution, providing a complementary formulation strategy to conventional suspension-based preparations. This approach represents a robust and patient-oriented strategy for extemporaneous compounding, particularly suitable for pediatric use. Full article

Aiming at the characteristics of high viscosity and poor fluidity of high waxy ordinary heavy oil, a Janus silica-based nanosheet composite viscosity reducer was designed and prepared in this paper. The viscosity reducer was assembled by asymmetric Gemini viscosity reducer and silica nanosheets through dehydration condensation reaction, and its structure was verified by FT-IR, ¹HNMR, XPS and DLS. The viscosity reduction performance, emulsion stability, interfacial tension and flow performance of the viscosity reducer were systematically evaluated by taking heavy oil with wax content of 35.7% and viscosity of 237 mPa·s at 30 °C as the research object. The results showed that, at an oil-to-viscosity-reducer-solution volume ratio of 3:7 and a viscosity reducer mass fraction of 0.3%, the maximum viscosity reduction rate reached 94.5% at 30 °C, calculated relative to the viscosity of the dehydrated original heavy oil. The oil–water interfacial tension was significantly reduced, and the 24 h bleeding ratio, defined as the volume percentage of separated water relative to the initial aqueous phase volume, was only 7.3%, indicating good emulsion stability. The core flow experiment shows that the resistance coefficient is reduced to the lowest at 0.3% concentration, and the seepage capacity is significantly improved. The analysis of total hydrocarbon gas chromatography showed that the content of high-carbon wax components in the C₂₃-C₃₀ range decreased by 4.79 percentage points after treatment, indicating that the viscosity reducer preferentially interacted with high-carbon wax molecules and promoted wax-crystal dispersion, thereby weakening the three-dimensional wax-crystal network. The viscosity reducer has the synergistic effect of dispersing wax crystals, reducing interfacial tension and stabilizing emulsification, which provides a low-cost and high-performance technical approach for the efficient exploitation of high waxy ordinary heavy oil. Full article

To address the common drawbacks of polyamine-based CO₂ absorbents, such as high viscosity and precipitation at high CO₂ loading, a novel liquid–liquid biphasic absorbent composed of triethylenetetramine (TETA), 1-(2-aminoethyl)piperazine (AEP), N,N-dimethylacetamide (DMAC), and H₂O was developed in this study. By comprehensively evaluating CO₂ saturation loading, phase separation behavior, rheological properties of the CO₂-rich phase, precipitation suppression, and desorption–regeneration performance, the optimal absorbent formulation was identified as 20 wt% TETA + 10 wt% AEP + 40 wt% DMAC + 30 wt% H₂O. The optimized system enabled more than 98% of the CO₂ absorption products to be concentrated in the lower phase, which accounted for only 56% of the total liquid volume. Compared with the AEP-free TETA/DMAC/H₂O system, the optimized AEP-modified absorbent effectively eliminated precipitation and reduced the viscosity of the CO₂-rich phase to 62.3 mPa·s, while also improving the desorption behavior and cyclic stability of the system. In addition, ¹³C NMR analysis suggested that the salting-out effect is the main driving force for phase separation, with ionic products preferentially enriched in the aqueous phase to form the CO₂-rich lower phase. AEP contributes to viscosity reduction, precipitation suppression, and enhanced regeneration by weakening carbamate aggregation through steric hindrance and promoting bicarbonate formation. Full article

The selective conversion of syngas (CO + H₂) to higher alcohols (C₂₊OH) via Fischer–Tropsch synthesis (FTS) is a strategically important but challenging process, requiring catalysts that can simultaneously sustain C–C chain growth and preserve C–O bonds in reactive intermediates. Over the past decade (2015–2025), perovskite-type complex oxides with the formula ABO₃ have emerged as powerful precatalysts for this application, with LaCoO₃ attracting particular attention due to its structural flexibility, controllable reducibility, and the unique catalytic role of the La₂O₃ phase formed upon reduction. This review systematically covers recent advances in synthesis strategies for LaCoO₃ and substituted perovskites, including sol–gel, co-precipitation, mechanochemical, and template-assisted (KIT-6, SBA-15) methods; effects of A-site (Sr) and B-site (Cu, Ga, Ni, Mn) substitution on reducibility, active phase dispersion, and product selectivity; alkali promotion and its interaction with the perovskite-derived active phase; mechanistic understanding of the alcohol-forming pathway, including the Co⁰/Co³⁺ bifunctional site concept, CO insertion mechanism, and the role of La₂O₃ in suppressing the Boudouard reaction; and catalyst stability and deactivation pathways under FTS conditions. Original data from LaCoO₃ catalysts prepared by co-precipitation with ethylene glycol (LCO-1: S_KOH = 90%, Y_KOH = 57 mg·g⁻¹·h⁻¹) and via citrate/KIT-6 template synthesis (LCO/KIT-6: Y_KOH = 80 mg·g⁻¹·h⁻¹, S_BET = 220 m²/g) at 240 °C and 2 MPa serve as the primary experimental reference throughout. Key challenges, including the surface area–selectivity trade-off, long-term stability under industrial conditions, and opportunities in CO₂ hydrogenation, are critically discussed. Full article

This study investigates the effects and mechanisms of three mineral admixtures—fly ash (FA), silica fume (SF), and metakaolin (MK)—on the fresh, mechanical, and microstructural properties of Yellow River sediment (YRS)-based shotcrete. A comprehensive experimental program was conducted, including setting time determination, workability assessment, and mechanical strength evaluation, complemented by microstructural characterization using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The results indicate that the incorporation of FA prolonged initial and final setting times and improved pumpability but reduced build-up thickness and compressive strength; splitting tensile strength at later ages remained comparable to the control. SF shortened the final setting time and reduced flowability but enhanced shootability, layer build-up, and medium- to later-age compressive and tensile strengths, with an optimal dosage of 5%. MK accelerated the final setting time, slightly reduced early-age compressive strength, but improved early-age splitting tensile strength and achieved 28-day compressive strength comparable to the control. Microstructural analyses revealed that FA participates in pozzolanic reactions forming C–(A)–S–H gel, while SF and MK promote the formation of dense C–S–H and carboalumination phases, enhancing matrix densification. Based on performance evaluation, the recommended dosages are FA ≤ 20%, SF ≤ 15%, and MK ≤ 15%. These results establish clear links between macroscopic performance and microstructural evolution, providing experimental guidance for the sustainable development of YRS-based shotcrete. Full article

The scarcity of natural aggregates and the accumulation of oil sludge in desert regions pose critical challenges for highway construction. Although aeolian sand and oil sludge pyrolysis residue have been studied individually as construction materials, their combined use in foamed lightweight soil remains unexplored. This study addresses this gap by developing a novel foamed lightweight soil termed SOFS, which is created through the synergistic modification of aeolian sand and oil sludge pyrolysis residue. A six-factor, five-level orthogonal array (L25) was employed to systematically investigate the effects of residue content, sand content, foam-to-slurry ratio, foaming agent dilution, water-to-solid ratio, and mixing time. The evaluated properties included physical properties (fluidity and wet density), mechanical properties (compressive, splitting tensile, and flexural strength), and durability (wet–dry and freeze–thaw resistance). Scanning electron microscopy was used to examine the microstructural mechanisms. Variance and range analysis identified the optimal mixture, designated H14, which achieved 28-day compressive, splitting tensile, and flexural strengths of 3.75 MPa, 2.21 MPa, and 0.9 MPa, respectively, thereby meeting desert roadbed requirements. Compared with conventional materials, H14 exhibited superior durability, with strength losses of only 16.3% in compressive strength and 19.1% in splitting tensile strength after 25 cycles. Microstructural analysis revealed a dense C-S-H gel network encapsulating the solid waste particles, with nanoscale Al- and Cl-rich crystalline phases observed at interfacial pores—a phenomenon that has rarely been documented in previous studies. These findings provide a theoretical and technical foundation for solid waste valorization and the development of sustainable desert infrastructure. Full article

The catalytic removal of refractory VOCs in gas–solid reactions usually suffers from the formation of toxic byproducts and catalyst deactivation. The advanced oxidation process (AOP) wet scrubber has recently attracted interest in VOCs purification due to its high efficiency and inhibited gaseous byproducts emission. MOFs/metal sulfides (termed M50C50) were designed to activate peroxymonosulfate (PMS) for toluene removal in a wet scrubber. The heterojunction interface synergistically couples MIL-100(Fe) and CoS for dual functions, the M50C50 enabled the rapid transfer the toluene from the gas phase to the aqueous phase, where they were subsequently mineralized by SO₄^•− and •OH radicals. The primary active sites responsible for PMS activation were identified as reducing sulfur species, along with low-valence cobalt and iron species. Over 90% of toluene were removed with a wide pH range, while •OH and SO₄^•− were involved in the mineralization of intermediates. The process showed high mineralization efficiency (75% CO₂ evolution) and effectively reduced the formation of toxic byproducts, underscoring its potential for minimizing secondary pollution risks. This work provides a novel route to designing composite catalysts for deep VOC oxidation via AOP wet scrubbers, greatly facilitating their use in environmental remediation. Full article

This study aimed to optimize the nitriding parameters for Plasma Immersion Ion Implantation (PIII) of stainless steels. UNS S32750 super duplex stainless steel, widely employed in the petrochemical industry, was subjected to PIII under varying nitriding atmospheres (mixtures of H₂ and N₂) and treatment pressures. The fixed PIII nitriding parameters included a temperature of 300 °C, a duration of 3 h, a bias voltage of approximately −10 kV, a frequency of 500 Hz, and a pulse width of 30 μs. Following the treatments, the phases were characterized by X-ray diffraction (XRD), while the hardness and elastic modulus of the modified surfaces were evaluated via nanoindentation. Regarding the nitriding atmosphere, gas mixtures approaching a 60% N₂/40% H₂ (vol.) ratio yielded a higher volume fraction of nitrogen-rich expanded phases in solid solution. Furthermore, higher treatment pressures promoted the formation of these expanded phases, consequently enhancing the surface hardness up to 2.7 times the hardness value of the untreated sample. These findings stand in contrast to those found for low-energy plasma nitriding (PN) processes. Full article