Search Results (1,129)

This study experimentally investigated the movement, combustion, and potassium (K) and chlorine (Cl) migration behaviors of three biomass types: densified wood pellets (heavy), corn straw (lightweight), and wheat straw (lightweight, friable). The experiments were conducted under conditions representative of industrial coal-fired circulating fluidized bed (CFB) boilers, with a temperature range of 850–950 °C and a fluidization velocity of 6–8 m/s. Results show that densified wood pellets sink into the dense-phase zone and release volatiles slowly, in about 50 s. As the volatiles are nearly fully released, the pellets fracture multiple times along their length, eventually forming nearly spherical particles. Their movement and combustion processes closely resemble those of coal, making them suitable for direct co-firing in coal-fired CFB boilers. Conversely, corn straw and wheat straw exhibit low density, high volatile release rates (2 and 10 times that of wood pellets, respectively), rapid char fragmentation and abrasion, and high inherent K and Cl content (with >50% of K and >90% of Cl released). These properties lead to particle segregation, shortened gas-phase combustion time, an upward shift in heat release distribution, and potential risks such as high-temperature KCl corrosion, HCl dew point corrosion, ash slagging, and bed agglomeration. Therefore, untreated corn straw and wheat straw are unsuitable for co-firing in conventional coal-fired CFB boilers. This study provides essential data and engineering guidance: strict quality control is necessary for wood pellets to prevent Cl contamination, while pretreatment is mandatory for straw fuels. These findings offer practical insights for implementing diverse biomass co-firing strategies in coal-fired CFB boilers. Full article

This study addresses the challenges posed by weakly cemented strata in mine tunnels, where surrounding rock softens and deforms upon water exposure, which promotes the development of seepage pathways, and exhibits insufficient stability in bolt (cable) support systems. This study conducts laboratory grouting tests using silica sol on typical weakly cemented sandstone from Xinjiang mining areas. The mineral composition and pore structure were characterized using XRD, SEM, and mercury porosimetry. The injectable mixing ratio parameters for silica sol and the catalyst were determined through viscosity-time evolution tests. Grouting was performed using a custom-built constant-pressure grouting apparatus. After curing, unconfined compressive strength (UCS) and porosity-permeability tests were conducted to evaluate the micro-mechanism of grouting effects on the mechanical and permeability properties of weakly cemented sandstone. The results indicate: (1) The sandstone exhibits a high clay mineral content of 39.8%, dominated by illite. Its pores are primarily small-scale (10–100 nm), accounting for 79.31% of the total pore volume. This scale matches that of silica sol nanoparticles (approximately 9–20 nm), facilitating slurry penetration into micro-pores; (2) microscopic analyses reveal that silica sol effectively reconstructs pore structures through permeation filling and surface coating. Compared to KCl-induced gelation (with approximately 8% gel coverage), NaCl-induced gelation forms a more continuous gel film with more complete pore filling, achieving coverage of around 22%. Furthermore, the larger surface area of the gel aggregates indicates a more thorough filling of micro- and nano-pores, effectively enhancing rock mass compactness. (3) Permeability decreased from 6.91 mD to 3.55 mD, a reduction of 48.6%, while porosity decreased from 16.94% to 13.55%, showing a phased reduction during the grouting process; (4) following pressure grouting stabilization, the uniaxial compressive strength of sandstone increased appropriately by approximately 7–14%, while the elastic modulus rose by about 18–28%. The failure mechanism shifted from shear brittleness to a shear-tension composite state, with enhanced post-peak bearing capacity. These findings provide support for optimizing silica sol grouting parameters in weakly cemented strata tunnels and for the synergistic reinforcement of rock mass permeability and strength. Full article

Bacterial poly(A) polymerases (PAPs) play an important role in RNA metabolism but remain poorly characterized outside Gammaproteobacteria. Here, we cloned and biochemically characterized the first PAP from Alphaproteobacteria, specifically from Marinobacter lipolyticus (Mli PAP). Using homology-based screening against E. coli PAP-1, we identified Mli PAP, sharing 54.8% sequence identity with its E. coli counterpart. The enzyme was expressed in E. coli but formed insoluble inclusion bodies; the active enzyme was purified as a fusion protein with the DsbA protein and used for functional assays. Mli PAP exhibited optimal activity at 30 °C and similar thermostability to E. coli PAP-1. ATP was the preferred substrate, with K_m comparable to E. coli PAP-1 (1.61 mM and 1.70 mM, respectively), and Mg²⁺ (10 mM) was identified as the optimal cofactor. Mli PAP displayed salt-dependent activity, with the most effective polyadenylation in KCl and inhibition by NaCl and ammonium salts, contrasting with the halophilic nature of its host. This study provides the first functional insights into PAPs from Alphaproteobacteria, broadening the understanding of PAP diversity and biochemical properties, as well as the potential applications of PAPs in biotechnology. Full article

Background: Early detection of modifiable risk factors for long-term care certification with dementia is essential. This study aimed to develop a risk-scoring tool using data from the Kihon Checklist and Questionnaire for the Late-Stage Elderly over a 2-year period to predict long-term care certification with dementia under Japan’s Long-Term Care Insurance system. Methods: Participants included 2041 functionally independent, community-dwelling older adults in Kure City, Japan, as of March 2021. A retrospective cohort study was conducted. Associations between KCL and LSEQ domains and certification for long-term care with dementia were examined using logistic regression. To improve practical use, a score chart was developed to predict certification for long-term care with dementia. Results: Two years after completing the Kihon Checklist and Questionnaire, 143 participants (7.0%) were certified for long-term care with dementia. Factors independently associated with certification for long-term care with to dementia included age, homebound status, cognitive decline, and locomotor decline. The prediction model, developed using these variables, showed excellent discriminatory ability, with an area under the curve of 0.790 (95% confidence interval: 0.754–0.827). Conclusions: We developed an effective predictive model for future long-term care certification with dementia using routinely collected administrative data. This tool may help healthcare providers and health planners identify older adults at increased risk of long-term care certification with dementia. Full article

The depletion of natural resources remains an acute global problem, highlighting the importance of developing sustainable technologies that enable the simultaneous extraction of metals and recycling of waste. This paper describes a study of a technology for recycling aluminum slag from foundries to produce secondary aluminum alloy and regenerated flux. Research and processing methods include X-ray phase and spectral analysis of slag composition, multi-stage grinding in a jaw crusher and planetary mill, screening for fraction separation, and selective dissolution of the oxide–salt phase in water or hydrochloric acid followed by filtration and evaporation; obtaining regenerated flux based on phase diagrams of chloride systems; and briquetting and remelting of the extracted aluminum. The technology ensures the extraction of up to 85% of the metallic aluminum from slag and the production of regenerated flux based on the NaCl–KCl–MgCl₂ system with a low melting point. Full article

With the increasingly stringent environmental regulations, the development of high-performance and eco-friendly shale inhibitors for water-sensitive formations has become an urgent priority. Chitosan, a renewable biopolymer derived from chitin, has inherent potential as a shale inhibitor but is limited by low water solubility and suboptimal inhibition efficiency. To overcome these limitations, cationic quaternary ammonium groups were grafted onto chitosan through etherification with 3-chloro-2-hydroxypropyltrimethylammonium chloride (CHA), yielding chitosan quaternary ammonium chloride (QASC). Systematic evaluation through linear swelling, rolling recovery, and bentonite inhibition tests revealed QASC’s superior performance. Notably, 1% QASC reduced bentonite swelling to 28.1% after 16 h, outperforming 5% KCl (48.2%) and 1% polyetheramine (41.1%). Remarkably, QASC achieved 88.4% shale recovery at 150 °C significantly exceeding the values for polyetheramine (52%) and pure water (13.2%). Mechanistic analysis revealed that QASC inhibits clay hydration through dual mechanisms: (1) electrostatic and hydrogen-bond mediated adsorption on clay surfaces, effectively neutralizing surface charges and diminishing hydration films; (2) intercalation into clay interlayers to create a physical barrier against water invasion. This synergistic combination ensures stable inhibitory performance under elevated temperatures. Given its enhanced biodegradability, QASC emerges as a sustainable alternative to conventional inhibitors, effectively addressing the dual challenges of technical performance and environmental compatibility in shale gas drilling operations. Full article

Iodine is produced through nuclear fission reactions in nuclear reactors. Understanding the electrochemistry of iodine species is crucial for reprocessing used nuclear fuels via molten salt electrolysis, deploying next-generation molten salt nuclear reactors, and developing iodide-based molten salt batteries. Cyclic voltammetry (CV) was conducted in LiCl-KCl eutectic molten salts at 450, 500, and 550 °C, both with and without the addition of KI as an iodine source. Based on the CV results, the diffusivities of iodide and triiodide species, as well as the activation energies for diffusion, were determined. Additionally, formal potentials of various iodide and interhalogen complexes were derived, allowing for the calculation of the stability constants for halide exchange reactions. The diffusivities of iodide ranged from 0.14 to 6.9 × 10⁻⁷ cm²/s, while those of triiodide were roughly an order of magnitude lower. Increasing the KI content from 1 wt% to 5 wt% reduced the diffusion coefficient, whereas increasing temperature, as expected, boosted diffusivity. The activation energy for iodide diffusion in LiCl-KCl increased from 46.5 kJ/mol to 112 kJ/mol as KI concentration rose from 1 wt% to 5 wt%. Full article

Background/objectives: Potassium-enriched lower-sodium salt substitutes (LSSS) offer consumers a practical way to increase potassium intake and decrease sodium intake, thereby reducing their risk of high blood pressure and cardiovascular disease. This risk reduction, however, depends on whether consumers can access affordable, evidence-based LSSS products. This study investigated the availability, formulation and price of LSSS in China. Methods: A cross-sectional salt survey was conducted across 195 supermarkets in 15 cities from 2023 to 2025 in China. Results: LSSS availability varied substantially by supermarket size: 90.9% of large (33), 88.9% of middle-sized (45), and only 53.0% of small supermarkets (117) stocked LSSS. Of 1861 total salt products surveyed, 310 were LSSS and 1551 were regular salt. A critical evidence–practice gap exists in product formulation: the mean potassium chloride (KCl) content among unique LSSS products was only 16.6%, with 53.4% of LSSS containing <15% KCl. LSSS products are also consistently more expensive than regular salt. The median LSSS price (11.7 yuan/kg) was significantly higher than regular salt (9.8 yuan/kg, p < 0.001). Price disparities were most pronounced at lower price points. Within-brand and within-supermarket comparisons revealed that the lowest-priced LSSS cost 2.0-fold and 2.2-fold more than the lowest-priced regular salt, respectively. Multiple regression analysis identified that LSSS price was significantly associated with KCl content, salt source, supermarket size and geographic region. Conclusions: Consumer access to affordable, effective LSSS products can be increased by expanding LSSS availability in small supermarkets, incentivizing higher-KCl formulations, and reducing price barriers to consumer adoption, which could substantially contribute to salt reduction at the population level. Full article

Tight conglomerate reservoirs exhibit strong pore-scale heterogeneity and extremely low permeability, in which spontaneous imbibition is primarily governed by capillary and viscoelastic effects. In this study, the imbibition dynamics of four representative fracturing fluid systems, including slickwater, 3% potassium chloride (KCl) brine, hydrolyzed polyacrylamide (HPAM) viscoelastic fluid, and a nanoemulsion (NE), were investigated using a temperature-controlled nuclear magnetic resonance (NMR) monitoring system. This approach enables real-time quantification of fluid uptake and pore-scale redistribution through time-resolved T₂ spectral analysis. The experimental results reveal a three-stage imbibition process consisting of rapid capillary-driven uptake, viscoelastic-retarded transition, and final equilibrium. Among the four fracturing fluid systems, the nanoemulsion exhibits the lowest interfacial tension (1.72 mN/m), the strongest wettability alteration, and the highest equilibrium recovery (0.76), which is nearly 80% greater than that of slickwater. Based on these observations, a multiscale capillary–viscoelastic coupling model was developed by extending the Lucas–Washburn framework to incorporate pore-size distribution, time-dependent wettability evolution, and viscoelastic damping. The model fits the experimental data well (R² > 0.90) and identifies viscosity as the most influential parameter controlling the imbibition rate (sensitivity = 0.78). Energy analysis further indicates that capillary energy dominates the early stage, whereas viscoelastic energy storage sustains fluid transport during the later stage. SEM observations were further used to qualitatively corroborate pore heterogeneity and pore–mineral associations, supporting the NMR-based pore-scale interpretation. This study provides a quantitative framework for describing non-Newtonian capillary flow in tight conglomerate rocks and enhances the understanding of capillary–viscoelastic interactions relevant to multiphase fluid migration. Full article

Orange peel is an abundant by-product of the citrus industry and a significant source of phenolic compounds with potential applications in the food, nutraceutical, and pharmaceutical industries. However, many of these compounds are bound or glycosylated, with low bioavailability. The objective of this study was to release and biotransform polyphenols from orange peels through solid-state fermentation using Aspergillus niger. A Box–Hunter and Hunter experimental design was employed in which the inoculum size (1 × 10⁶–1 × 10⁸ spores/g) and the concentrations of KCl and MgSO₄ (0.76–1.56 g/L) were evaluated as independent factors to assess their effects on the release of hydrolyzable and condensed tannins. After 12 days of fermentation at 28 °C, the resulting extracts were analyzed using colorimetric methods and HPLC-ESI-MS analysis. The results showed significant increases in tannin release, reaching up to 220.63 mg CE/g of condensed tannins, and compounds such as ferulic acid, epicatechin, and quercetin derivatives were identified in the extracts. In conclusion, solid-state fermentation is a strategy for valorizing citrus waste and generating polyphenolic extracts with potential functional and industrial value. Full article

Heparan sulfates (HS) are polysaccharides abundantly expressed in the extracellular matrix and the glycocalyx of endothelial cells, having a putative role in vascular function. The role of HS in vascular reactivity remains unclear. Herein, we sought to determine whether HS regulate the vascular tone in physiological conditions. Using male, 6–8-weeks-old, CD1, C57BL/6, syndecan 1 (Sdc1^−/−) and glypican 1 (Gpc1^−/−) knockout mice, we investigated if the degradation of HS with heparinase III altered vascular reactivity to norepinephrine (NE), acetylcholine (ACh) and potassium chloride (KCl). Our findings indicate that HS are crucial players in the vascular response to NE and ACh in CD1, C57BL/6, and Sdc1^−/− but not in Gpc1^−/− mice. Both Sdc1^−/− and Gpc1^−/− showed increased compensatory expression of syndecan 2 and syndecan 4. However, while Sdc1^−/− showed decreased expression of glypican 1, Gpc1^−/− showed increased expression of syndecan 1 in aortic homogenates. The lack of response to the vascular reactivity effects of heparinase III in Gpc1^−/− suggests a differential role of HS to proteoglycan function in the regulation of the vascular tone. Our data demonstrate a physiological role for HS in the regulation of the vascular tone in physiological conditions. Full article

The rate constant k_OH for the reaction of 1,1,1,3,3,3-hexafluoroprop-2-imine with OH radicals was measured relative to two reference compounds, CH₃F and CH₃CHF₂, to be k_OH = (4.2 ± 1.1) × 10⁻¹⁴ cm³ molecule⁻¹ s⁻¹ at 295 K. This implies an atmospheric lifetime with respect to consumption by OH of 0.75 years. Reaction with Cl atoms yielded k_Cl = (7.9 ± 1.7) × 10⁻¹⁶ cm³ molecule⁻¹ s⁻¹ at 295 K, and reaction with O₃ has an upper limit of k_O3 < 4 × 10⁻²³ cm³ molecule⁻¹ s⁻¹, so that the atmospheric consumption by Cl and O₃ is negligibly slow. Absolute infrared cross sections of the imine yield a radiative efficiency of 0.34 W m⁻² ppb⁻¹, which is corrected to 0.23 W m⁻² ppb⁻¹ for the effects of atmospheric lifetime. The imine’s corresponding 100-year global warming potential is 64 ± 19. This value is an upper limit, given that heterogenous atmospheric removal paths, such as hydrolysis in water droplets, are not included. Full article

Li₃PO₄ is a promising raw material for the low-cost synthesis of high-performance LiFePO₄. Reactive crystallization from low-concentration lithium-rich brine is a key process for the efficient preparation of high-quality Li₃PO₄ products. The effect of operating conditions (temperature/supersaturation/impurities/ultrasonic) on the induction time was investigated using a focused beam reflectance measurement. The evaluation of the primary nucleation, growth kinetics, and parameters for the extraction of Li₃PO₄ from low-concentration lithium-rich brine was conducted using an induction time method. The dominant mechanisms at different stages were inferred through online monitoring of the particle size distribution during the Li₃PO₄ crystallization process. Results show that induction time decreases with increasing operating conditions (temperature/supersaturation/ultrasonic frequency), indicating that their increases all promote nucleation. Impurities (NaCl/KCl) did not significantly affect the induction time, whereas Na₂SO₄ and Na₂B₄O₇ significantly increased it, with Na₂B₄O₇ showing the most notable effect. Classical nucleation theory was applied to determine kinetic parameters (nucleation activation energy/interfacial tension/contact angle/critical nucleus size/surface entropy factor). Results indicate that Li₃PO₄ mainly nucleates through heterogeneous nucleation, with a temperature increase weakening the role of heterogeneous nucleation. Fitted models indicate that Li₃PO₄ predominantly follows the secondary nucleation and spiral growth mechanism. Our findings are crucial for crystallization design and control in producing high-quality Li₃PO₄ from lithium-rich brines. Full article

This work demonstrates laser-induced breakdown spectroscopy (LIBS) applied to a stream of aerosolized salt from molten eutectic LiCl-KCl. We demonstrate analytical capabilities to track fission-product surrogates of Cs, Sr, Pr, and Nd simultaneously, with application to monitor salts in pyroprocessing schemes and molten salt reactors. This work demonstrates limits of detection using LIBS on the order of 100 $\mathsf{\mu }$g/g, which proves potentially applicable to monitoring fission-product concentrations in pyroprocessing applications. Additionally, this work explores fundamental aspects of plasma temperature and plasma electron density of the aerosolized species during LIBS with a specific focus on potential non-uniform plasma conditions in the aerosol. Full article

This review examines the feasibility of electrochemical synthesis of poly-L-arginine (PArg) using repetitive cyclic voltammetry in neutral aqueous phosphate-buffered saline. Previous studies on electrochemical deposition of PArg onto different carbonaceous electrode materials are discussed with respect to the already reported mechanistic models. Some controversial interpretations are of interest, predominantly the formation of peptide bonds during the electropolymerisation of L-arginine. Several alternative anodic pathways are considered via the possibilities and limitations of ways of attaching L-arginine molecules to the electrode surface. Furthermore, the role of oxygen-containing surface groups is discussed, as this aspect has been largely overlooked in the context of L-arginine deposition, despite the O-terminating character of the electrode surface and its effect on the reactivity of the nucleophilic guanidine group in L-arginine. Also, the application of extremely high potentials around +2 V vs. Ag/AgCl/3 mol L⁻¹ KCl is considered, as it can lead to the generation of reactive oxygen species that may interfere with or even govern the entire deposition process. Thus, the absence of such considerations may raise doubts about the peptide nature of the electrochemically assisted polymerisation of this basic amino acid. Finally, it seems that the identity of the electrochemically synthesised PArg does not correspond to that of this polymer prepared by conventional methods, such as solid-phase peptide synthesis, solution-phase synthesis, or N-carboxy-anhydride polymerisation, and therefore the whole process remains unproved. Full article