Search Results (475)

Background/Objectives: Overweight and obesity affect a majority of adults, contributing to metabolic disorders. Caloric restriction often leads to undesirable lean mass loss alongside fat reduction. This study investigated whether exogenous β-hydroxybutyrate (BHB) supplementation, as an adjunct to a hypocaloric diet, improves body composition and metabolic markers in overweight and obese adults by preferentially reducing fat mass while preserving lean mass. Methods: In this 8-week randomized, double-blind, placebo-controlled trial, 51 adults were assigned to receive either racemic BHB mineral salts or placebo (maltodextrin) twice daily, alongside modest caloric restriction. Assessments at baseline and week 8 included dual-energy X-ray absorptiometry for body composition, indirect calorimetry for resting metabolic rate (RMR), and venous blood analyses for cardiometabolic biomarkers (e.g., lipids, HOMA-IR, uric acid, liver enzymes). Results: Body mass decreased in both groups over the intervention (p < 0.01 within placebo and p < 0.001 within BHB). Within the BHB group, fat mass decreased significantly (−2 kg; p < 0.05 vs. baseline), body fat percentage improved (p < 0.01 vs. baseline), and lean-to-fat mass ratio increased (p < 0.05 vs. baseline); no such significant changes were observed within the placebo group. Group × time interactions were not significant for these body composition variables (p > 0.05). Furthermore, lean mass was largely preserved, with no declines in RMR. Within the BHB group, LDL cholesterol was reduced (p < 0.05 vs. baseline), while other lipids, HOMA-IR, and uric acid remained stable, with liver enzymes showing a positive change. Conclusions: Exogenous BHB supplementation may enhance the quality of diet-induced weight loss through within-group improvements in fat mass reduction and lean mass preservation, with no adverse metabolic impacts. Full article

For complexation of mRNA into polyplexes, double-pH-responsive lipo-xenopeptides (XP), comprising tetraethylene pentamino succinic acid (Stp) and lipoamino fatty acids (LAFs), were combined with PEGylated lipids, either DMG-PEG 2 kDa (DMG-PEG) or azido-group-containing DSPE-PEG 2 kDa (DSPE-PEG-N3), to increase colloidal stability and to facilitate ligand-mediated targeted mRNA delivery. LAF-XPs mixed with DMG-PEG at low (1.5% and 3%) molar ratios improved colloidal stability and retained transfection efficiency. PEGylation also enabled the formulation of otherwise unstable carrier complexes and prevented aggregation induced by salt, proteins, and serum. PEGylation of more positively charged Stp-LAF₂ mRNA polyplexes decreased fibrinogen adsorption. More neutral, LAF-rich Stp-LAF₄ polyplexes exhibited low fibrinogen binding without PEGylation. Intravenous administration of these stabilized mRNA complexes demonstrated enhanced biosafety while preserving transfection efficiency. DSPE-PEG-N3 was selected for cell targeting after strain-promoted azide-alkyne cycloaddition (SPAAC)-mediated click-coupling of DBCO-modified ligands. Higher PEG ratios (10% and 20%) provided effective shielding but reduced transfection efficiency, a drawback known as the “PEG dilemma”. Functionalization with an EGFR-targeting ligand restored transfection in EGFR-positive cell lines in a ligand-specific manner. High transfection efficiency is consistent with a lipophilic-to-hydrophilic polarity switch of LAF-XP carriers upon endosomal protonation, triggering dissociation of the PEG lipids and deshielding of the polyplex. Full article

Complex compounds are under close scrutiny by scientists as precursors, which are needed to produce functional materials. When the thermolysis method of double complex salts is used on an industrial scale, the most detailed information on the thermal decomposition, including the kinetics of decomposition, is required. The kinetics of pyrolysis, solid, and gaseous products of [Co(NH₃)₆][Fe(C₂O₄)₃]∙2H₂O (I) and [Co(en)₃][Fe(C₂O₄)₃] (II) (en—ethylenediamine) thermolysis were studied in this work. The solid products of thermal decomposition were studied using scanning electron microscopy and elemental analysis, and the specific surface area (8 and 71 m²/g, respectively) was measured. It was determined that a double complex salt (DCS) with a coordinated en has a higher thermal stability than with NH₃ due to the chelation effect. Full article

Background/Objectives: Osteopenia is common in postmenopausal women and predisposes to osteoporosis and fracture, representing a population at risk of bone loss but without indication for pharmacologic therapy. Conventional calcium salts offer modest, often transient gains in bone mineral density (BMD). We evaluated whether CalGo^®, a salmon bone complex containing microcrystalline hydroxyapatite within a collagen-rich matrix, preserves BMD versus placebo in post-menopausal women with osteopenia. Methods: In a 24-month, randomized, double-blind, placebo-controlled trial, 80 women (50–80 years) with dual-energy X-ray absorptiometry (DXA)-confirmed femoral-neck osteopenia were assigned to CalGo^® (2 g/day) or placebo. The prespecified primary endpoint was 24-month change in femoral-neck BMD (g/cm²) analyzed by linear regression (unadjusted and baseline-adjusted). Secondary endpoints included lumbar spine and distal radius BMD, serum P1NP and β-CTX-I, health-related quality of life, and safety. Results: The primary analysis included participants with 24-month DXA (CalGo^® n = 29; placebo n = 30). Femoral-neck BMD was maintained with CalGo^® (+0.003 g/cm²; +0.4%) but declined with placebo (−0.017 g/cm²; −2.4%), yielding a significant baseline-adjusted between-group difference of +0.019 g/cm² (95% confidence interval (CI) 0.001–0.038; p = 0.044). Lumbar-spine loss was attenuated with CalGo^® (−0.005 g/cm²; −0.3%) versus placebo (−0.028 g/cm²; −3.4%); the adjusted difference favored CalGo^® (+0.026 g/cm²; p = 0.058). In exploratory responder analysis, ≥1% lumbar-spine gain was more likely with CalGo^® (32.5% vs. 11.4%; OR 3.61; p = 0.043). No treatment effects were observed at the distal radius, in P1NP or β-CTX-I, or in EQ-5D-3L/EQ-VAS. CalGo^® was well tolerated with no hepatic or renal safety signals. Conclusions: CalGo^® maintained femoral-neck bone mineral density and reduced lumbar-spine loss over 24 months in osteopenic women, with good tolerability. These findings support its potential role as a nutritional approach for maintaining bone health. Full article

Salinity is a major abiotic stress that limits plant growth and survival. Colobanthus quitensis, the only native dicotyledon in the Antarctic Peninsula and southern South America, naturally inhabits environments with contrasting salinity regimes. This study compared the salt stress responses of three geographically distinct populations—Antarctic (pA), Magellanic coastal (pPA), and Andean inland (pC)—exposed to 0, 50, and 150 mM NaCl under controlled conditions. Morpho-physiological traits, photosynthetic parameters, osmolyte accumulation, oxidative damage markers, and antioxidant responses were evaluated. Population-specific strategies were observed. In pA, salinity reduced shoot biomass by 58% and doubled lipid peroxidation levels at 50 mM, indicating high oxidative stress. In pPA, shoot growth was maintained even at 150 mM, although chlorophyll and carotenoid contents decreased by approximately 20%, along with a reduction in total antioxidant capacity. In contrast, pC showed a coordinated tolerance response, maintaining biomass while accumulating the highest proline levels (742 µmol g⁻¹ FW at 150 mM) and enhancing total antioxidant capacity by 35% compared to the control. Multivariate analyses supported the contrasting strategies among populations. These results provide novel evidence of local adaptation and ecological plasticity in C. quitensis, particularly highlighting the hidden resilience of non-coastal populations. The findings support the potential of this extremophile species as a model system for investigating salinity tolerance and as a promising genetic resource for developing biotechnological strategies aimed at improving crop resilience under saline conditions. Full article

To meet gas turbines’ growing demand for high-performance thermal barrier coatings (TBCs), this study addresses the limitations of traditional single-layer 8% Y₂O₃-stabilized ZrO₂ (YSZ) coatings in high-temperature corrosive environments. Atmospheric plasma spraying (APS) was used to fabricate the double-ceramic TBCs with (Sm_0.2Gd_0.2Dy_0.2Er_0.2Yb_0.2)₂(Zr_0.7Hf_0.3)₂O₇ (RHZ) as the outer layer and YSZ as the inner layer; thermal cycling corrosion tests (1000 °C, Na₂SO₄ + V₂O₅ molten salt) were conducted to compare its performance with traditional single-layer YSZ. The results showed that the YSZ corrosion products were m-ZrO₂ and YVO₄, while RHZ/YSZ produced rare-earth vanadates, m-(Zr,Hf)O₂, and t′-(Zr,Hf)O₂, and corrosion degree was positively correlated with salt concentration (which was more impactful) and the number of cycles. Both coatings failed via molten salt penetration, thermochemical reaction, and crack-induced spallation. The corrosion mechanism between the RHZ/YSZ coating and the mixed salt can be explained based on the Lewis acid–base theory and the optical basicity. The RHZ layer on the surface of RHZ/YSZ coatings indeed hinders the penetration of corrosive molten salts into the underlying YSZ layer to some extent. Full article

MXenes, a rapidly emerging family of two-dimensional transition metal carbides and nitrides, have attracted considerable attention in recent years for their potential in next-generation energy storage technologies. In solid-state batteries (SSBs), they combine metallic-level conductivity (>10³ S cm⁻¹), adjustable surface terminations, and mechanical resilience, which makes them suitable for diverse functions within the cell architecture. Current studies have shown that MXene-based anodes can deliver reversible lithium storage with Coulombic efficiencies approaching ~98% over 500 cycles, while their use as conductive additives in cathodes significantly improves electron transport and rate capability. As interfacial layers or structural scaffolds, MXenes effectively buffer volume fluctuations and suppress lithium dendrite growth, contributing to extended cycle life. In solid polymer and composite electrolytes, MXene fillers have been reported to increase Li⁺ conductivity to the 10⁻³–10⁻² S cm⁻¹ range and enhance Li⁺ transference numbers (up to ~0.76), thereby improving both ionic transport and mechanical stability. Beyond established Ti-based systems, double transition metal MXenes (e.g., Mo₂TiC₂, Mo₂Ti₂C₃) and hybrid heterostructures offer expanded opportunities for tailoring interfacial chemistry and optimizing energy density. Despite these advances, large-scale deployment remains constrained by high synthesis costs (often exceeding USD 200–400 kg⁻¹ for Ti₃C₂T_x at lab scale), restacking effects, and stability concerns, highlighting the need for greener etching processes, robust quality control, and integration with existing gigafactory production lines. Addressing these challenges will be crucial for enabling MXene-based SSBs to transition from laboratory prototypes to commercially viable, safe, and high-performance energy storage systems. Beyond summarizing performance, this review elucidates the mechanistic roles of MXenes in SSBs—linking lithiophilicity, field homogenization, and interphase formation to dendrite suppression at Li|SSE interfaces, and termination-assisted salt dissociation, segmental-motion facilitation, and MWS polarization to enhanced electrolyte conductivity—thereby providing a clear design rationale for practical implementation. Full article

The application of organic amendments and humic acids (HA) often ameliorates saline soils, but the mechanisms responsible for their positive action have never been fully clarified. HA from four different origins (Elliott soil—EHA, peat—PHA, leonardite—LHA and compost—CHA) and polyacrylic acid (PAA) were characterized by acid–base titrations and ¹H-NMR spectroscopy and tested in laboratory experiments by measuring changes in electric conductivity (EC) and pH following micro-additions of Na₂CO₃ or NaCl. The effective salinity amelioration potential (SAP_eff) of HA, which expresses the amount of Na₂CO₃ neutralized per unit weight of HA at a given pH, was calculated. PAA had the highest capacity of mitigation, corresponding to 49.9 mg Na₂CO₃ g⁻¹, followed by LHA, EHA and PHA, whose SAP_eff values were similar and only slightly lower, and with CHA having the lowest value (25.1 mg Na₂CO₃ g⁻¹ HA). All substances failed to display any effect at constant pH when NaCl was the only salt present. The dissociation of acid groups, when HA become exposed to a more alkaline pH, produces an excess of negative charges that attracts more cations within the diffuse double layer. Because of the slower diffusion of HA and their tendency to aggregate at high ionic strengths, this action reduces the osmolarity of the soil solution and therefore mitigates salinity stress. Full article

Nano-silica is widely used to enhance gel properties, but its size, concentrations, and aggregation behaviors all matter. The influencing rules of these factors remain unclear especially in harsh reservoir conditions. This study presented a comprehensive investigation into the gelation, rheological, and plugging properties of phenolic polymer gels reinforced by modified nano-silica (GSNP) of different sizes and concentrations in harsh reservoir conditions. Specifically, the nano-silica was modified with a highly soluble silane, and gel properties were evaluated through rheological, differential scanning calorimetry (DSC), and sandpack flooding tests. The results showed that the incorporation of GSNP prolonged the gelation time, enhanced gel strength, and improved stability, allowing the gelation solution to enter deeper into the formation while maintaining long-time effectiveness. The optimal gel system was obtained with 0.4 wt.% GSNP-30, under which condition the storage modulus increased by approximately 14 times, and the content of non-freezable bound water more than doubled. This system exhibited plugging efficiency exceeding 80% in formations with permeabilities ranging from 1000 to 6000 millidarcy and enhanced the oil recovery factor by over 25%. The reinforcement mechanisms were attributed to the adsorption of GSNP onto polymer chains and its role in filling the gel matrix, which enhanced polymer hydrophilicity, suppressed polymer aggregation/curling, prevented ion penetration, and promoted the formation of a more uniform gel network. Careful optimization of nanoparticle size and concentration was essential to avoid the detrimental effects due to nanoparticle overfilling and aggregation. The novelty of this study lies in the practicable formulation of thermal and salt-tolerant gel systems with facile modified nano-silica of varying sizes and the systematic study of size and concentration effects. These findings offer practical guidance for tailoring nanoparticle parameters to cater for high-temperature and high-salinity reservoir conditions. Full article

The method of obtaining functional materials almost always influences the physicochemical properties of the resulting substances. The plasma treatment of solid materials is considered to be a more energy efficient method when compared with thermal destruction. Our work is the first to treat double complex salt (DCS) [Co(NH₃)₆][Fe(CN)₆] with different plasma discharge modes. We have demonstrated the possibility of obtaining a single-phase spinel with a CoFe₂O₄ structure as a result of the calcination in air of the plasma destruction product. The crystallite sizes of the obtained spinel are 40 nm, with a lattice constant 8.38 Å. Full article

This work describes the synthesis and characterization of novel organometallic polymeric frameworks derived from lactone-based poly(benzofuran-co-arylacetic acid) (PBAAA) ligands complexed with 3d transition metal salts (Co²⁺, Cu²⁺, Zn²⁺). Two distinct synthetic approaches were investigated: conventional solution-based methods and mechanochemical ball milling. A comprehensive spectroscopic evaluation was performed utilizing FTIR, XRD, UV-Vis, and XPS techniques to detail the structural characteristics of the synthesized materials. The thermal assessments were conducted using TGA and thermal conductivity, demonstrating that the chosen synthesis method has a significant impact on the crystallinity, coordination environment, and thermal transport characteristics of the resultant complexes. Remarkably, using the mechanosynthesis, the resulting organometallic polymer materials exhibited enhanced chain ordering and improved thermal conductivity, with a value of 0.32 W/mK, almost double that of the starting polymer. A correlation was identified among thermal conductivity, metal ionic radius, coordination number, and the synthesis method utilized. XPS analysis revealed the presence of multiple oxidation states and varied electronic environments, particularly in copper complexes. These had a direct effect on how they behaved when heated. These results show that mechanochemical synthesis is a useful and long-lasting method to make complex organometallic polymers with thermal properties that can be changed. Full article

Polymer gel-based triboelectric nanogenerators (TENGs) have emerged as versatile platforms for self-powered sensing due to their inherent softness, stretchability, and tunable conductivity. This review comprehensively explores the roles of polymer gels in TENG architecture, including their function as triboelectric layers, electrodes, and conductive matrices. We analyze four operational modes—vertical contact-separation, lateral-sliding, single-electrode, and freestanding configurations—alongside key performance metrics. Recent studies have reported output voltages of up to 545 V, short-circuit currents of 48.7 μA, and power densities exceeding 120 mW/m², demonstrating the high efficiency of gel-based TENGs. Gel materials are classified by network structure (single-, double-, and multi-network), matrix composition (hydrogels, aerogels, and ionic gels), and dielectric medium. Strategies to enhance conductivity using ionic salts, conductive polymers, and nanomaterials are discussed in relation to triboelectric output and sensing sensitivity. Morphological features such as surface roughness, porosity, and micro/nano-patterning are examined for their impact on charge generation. Application-focused sections detail the integration of gel-based TENGs in health monitoring (e.g., sweat, glucose, respiratory, and tremor sensing), environmental sensing (e.g., humidity, fire, marine, and gas detection), and tactile interfaces (e.g., e-skin and wearable electronics). Finally, we address current challenges, including mechanical durability, dehydration, and system integration, and outline future directions involving self-healing gels, hybrid architectures, and AI-assisted sensing. This review expands the subject area by synthesizing recent advances and offering a strategic roadmap for developing intelligent, sustainable, and multifunctional TENG-based sensing technologies. Full article

This study introduces a two-step treatment method for synthetic and real electric arc furnace dust (EAFD) wastewater, integrating sorption with Mg–Al layered double hydroxides (LDHs) and electrodialysis (ED). The hydrotalcite (LDH), mainly Mg₆Al₂(CO₃)OH₁₆·4H₂O (hydrotalcite-2H), was characterized by XRD, FTIR, SEM, and EDX, confirming its layered structure and ion-exchange capacity. Calcination at 550 °C was identified as optimal, enhancing sorption efficiency while retaining rehydration potential. Sorption tests demonstrated high effectiveness in removing multivalent ions, achieving over 99% elimination of Ca²⁺, SO₄²⁻, and Pb²⁺ ions and Cr from both synthetic and real wastewater. In contrast, monovalent ions such as Na⁺ and K⁺ were not effectively removed, except for partial removal of Cl⁻. To overcome this limitation, electrodialysis was applied in the second step, successfully targeting the remaining monovalent ions and achieving more than 95% conductivity reduction. A key challenge of ED, salt precipitation caused by calcium and sulphate in the concentrate, was effectively mitigated by the prior LDH treatment. The combined process minimized scaling risks, improved overall ion removal (above 97% for Na⁺ and K⁺), and produced low-salinity effluents (0.84 mS cm⁻¹), suitable for reuse in hydrometallurgical operations. These findings demonstrate that coupling LDH sorption with electrodialysis provides a sustainable and efficient strategy for treating high-salinity industrial wastewaters, particularly those originating from EAFD processes. Full article

In coastal countries facing a shortage of drinking water, seawater desalination is essential for the production of potable water. During desalination, a large volume of waste stream, known as brine, is generated. This stream contains high concentrations of salts, particularly those of economic importance to the European Union, such as magnesium and calcium. By further processing this stream, these materials can be recovered. One method studied for separating magnesium from wastewater is membrane crystallization (MCr). The MCr process developed in this work utilizes ion-exchange membranes that separate the model brine solution from a precipitating agent, which is a solution of sodium hydroxide. During the process, the membrane allows the transport of anions between the two solutions, enabling the reaction between OH⁻ anions and Mg²⁺ cations, which leads to the formation of a magnesium hydroxide precipitate. The formed precipitate can then be filtered out of the brine solution, which now has decreased salinity due to crystallization facilitated by the ion-exchange membrane. However, precipitation occurs near the membrane surface, resulting in the deposition of magnesium hydroxide onto the outer surface of the membrane. The aim of this study is to investigate methods for effectively removing magnesium hydroxide from the membrane surface, with a primary focus on maximizing the yield of magnesium hydroxide crystals in suspension. Crystal removal was induced by circulation of hydrochloric acid, followed by circulation of demineralized water through the membrane module after crystallization. In this study, a membrane module made of hollow-fiber anion-exchange membranes was employed. The production cost of these membranes is approximately 50% lower per square meter compared to flat-sheet membranes commonly used in electrodialysis, demonstrating strong potential for commercial application. More than 85% magnesium conversion was achieved during the process, yet the majority of the crystals remained attached to the membrane. Circulation of hydrochloric acid and demineralized water after the crystallization process caused detachment of the crystals into suspension, nearly doubling their yield. Full article

Zinc-aluminum-magnesium (ZAM) steel, with its superior corrosion resistance and mechanical properties, is progressively supplanting traditional galvanized steel and zinc-aluminum steel. In this study, a solution containing sodium carbonate-only was employed as the treatment medium to form a vertically grown layered double hydroxide (LDH) pretreatment layer on the surface of ZAM steel via a simple immersion process at 50 °C. The temperature and salt solution not only provide the conditions for the dissolution of metal ions but also facilitate the formation of LDH products. The resulting LDH pretreatment layer exhibits excellent adhesion to the metal surface and enhances the adhesion of the top epoxy coatings. Furthermore, the “LDH/corrosion inhibitor/epoxy” coating system ensures ZAM steel remains rust-free in a 3.5 wt.% NaCl solution for a minimum of 120 days. This innovative approach offers a promising avenue for extending the durability and service life of ZAM steel in corrosive environments. Full article