Search Results (2,629)

The physicochemical characteristics of hydrochars produced from tobacco stems through hydrothermal carbonization (HTC) at different temperatures were investigated, along with the variation in contents of nicotine, niacin, and chlorogenic acid in both the hydrochars and the liquid phase. The results indicated that dehydration was the predominant reaction during HTC of wet tobacco stems (WTS), leading to a decrease in the H/C and O/C atomic ratios of the hydrochars. As temperature increased, polycondensation and aromatization reactions became more pronounced, which corresponded with a reduction in the intensity of functional group vibrations such as C–N and N–O in FT-IR spectra. XPS analysis revealed a gradual increase in C=O content, whereas the proportions of C–OH and C–O bonds declined from 51.74% and 35.13% to 36.95% and 20.84%, respectively. Furthermore, the content of pyridine-N rose from 31.08% to 41.30%, while pyrrole-N and quaternary-N contents decreased to varying degrees. Both nicotine and niacin levels in the hydrochars and carbonization liquids exhibited an initial increase followed by a decline, whereas chlorogenic acid content consistently decreased. The underlying mechanisms for the observed changes in nicotine, niacin, and chlorogenic acid contents during HTC are discussed in detail. Full article

The magmatic Ni-Co-Cu mineralization in the Iken deposit in the central part of the Kun-Manie complex, Amur Oblast, Russia, hosted by an olivine-bearing websterite, is of a low-sulfide type. The fine-grained disseminations of base metal sulfides (BMS), dominantly pyrrhotite, pentlandite (a major source of Ni of industrial importance), and chalcopyrite, are followed by a scarce Pd-Pt-Ag mineralization. Elevated contents of Al in orthopyroxene (mean 2.78 wt.% Al₂O₃) along with Al–Na enrichment in clinopyroxene (diopside; mean 5.10 wt.% Al₂O₃) are associated with highly aluminous compositions of low-chromium members of the spinel–hercynite series. High levels of TiO₂ in kaersutite and titanian phlogopite also reflect a pronounced degree of fractionation of the ore-forming melt. Minor portions of sulfide melt are distributed evenly as a result of immiscibility at advanced stages of orthopyroxene crystallization, after the formation of olivine. Differentiated grains of droplet-like BMS largely settled in situ close to grain boundaries of orthopyroxene or occupied interstitial spaces of pyroxenes and olivine in association with spinel–hercynite and fluorapatite. A combination of late saturation in S with relatively quick cooling rates of the hypabyssal body prevented the effective settlement and accumulation of sulfide droplets in the ore zone. The well-developed lamellae of troilite (Fe₅₀S₅₀) exsolved from the host pyrrhotite Fe₄₈S₅₂ during subsolidus cooling, as a consequence of a low-temperature reaction triggered by a sudden drop in fO₂. An influx of mantle-derived fluid bearing CO₂, CO, and CH₄ with the rising magma could be the primary cause of the fO₂ reduction. Also, graphite-bearing metasedimentary rocks could have been assimilated. Tiny grains of minerals of noble metals (moncheite and merenskyite with essential amounts of melonite component, sperrylite, hessite, alloy Au_63.2Ag_36.8, and argentopentlandite) deposited late in a fluid-enriched medium under submagmatic conditions. Full article

Bisphenol A type epoxy resin has the problem of relatively high brittleness after curing. Although traditional polysiloxane toughening methods can improve toughness, they often come at the expense of strength. In this paper, methylphenyl dimethoxysilane (MPS) was used as a monomer to synthesize end-hydroxyl poly(methylphenyl)siloxane (PMPS), which was then used to modify E51 epoxy resin. The structure and reaction degree were characterized by infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry and viscosity tests. The mechanical test results show that when the PMPS content is 20 wt%, the tensile, flexural, compressive and impact strengths of the modified resin increase by 31.26%, 26.16%, 18.53% and 98.66%, respectively, compared with the unmodified resin, and the tensile and flexural elastic moduli increase by 38.36% and 32.25%, respectively. The fracture toughness increases by 60.29%, indicating that the strength, stiffness and toughness of the material have all been improved. Dynamic mechanical analysis shows that the glass transition temperature and crosslinking density of the system gradually decrease with increasing PMPS content. Thermogravimetric analysis shows that the introduction of PMPS increases the char yield and decreases the maximum thermal decomposition rate, thereby enhancing the thermal stability of the system. Microscopic morphology analysis by optical microscopy, scanning electron microscopy and atomic force microscopy shows that the system has good compatibility, and the internal different modulus phases are distributed in a network-like manner, forming a uniform co-continuous or bicontinuous phase structure. This structure effectively promotes stress transfer and energy dissipation, alleviates local stress concentration, and thus comprehensively improves the mechanical properties of the resin system. Full article

During the continuous casting of high-titanium steel, traditional fluorine-containing mold fluxes are prone to causing fluoride contamination, equipment corrosion, and intensified slag–metal interface reactions. There is an urgent need to develop highly adaptable fluorine-free mold flux systems. In this study, titanium-containing blast furnace slag was used as the primary base material, while borax, soda ash, and witherite were selected as fluoride-substituting mineral raw materials. The effects of these mineral raw materials on the melting properties, crystallization behavior, crystalline phases, and microstructure of fluorine-free mold fluxes were systematically investigated, and an optimized mold flux design suitable for continuous casting of high-titanium steel was further developed. The results indicate that borax significantly reduces the melting temperature and viscosity and markedly suppresses the growth of crystalline phases such as calcium borosilicate, nepheline, and perovskite by weakening the polymerization degree of the silicate network, thereby substantially decreasing the crystallization ability of the mold flux. Soda ash primarily acts as a strong fluxing and network-depolymerizing agent, promoting the formation of low-polymerized structural units. It also enhances the tendency toward ordered atomic arrangement, thereby markedly increasing nepheline precipitation and the overall crystallization ratio. Witherite exerts a relatively mild effect on slag structure and phase evolution; its moderate addition helps synergistically reduce the melting point, viscosity, and crystallization ratio, thereby supporting performance stability. The optimized fluorine-free mold flux, designed on the basis of these findings, maintains a suitable initial crystallization temperature and critical crystallization cooling rate while exhibiting lower melting temperature, viscosity, and crystallization ratio than conventional fluorine-bearing flux. The findings establish a theoretical basis for designing eco-friendly mold fluxes suitable for high-titanium steel and for enhancing billet quality. Full article

Accelerated carbonation of cement-based materials offers a promising route for CO₂ sequestration driven by waste heat co-emitted from cement and power plants; however, existing kinetic models typically describe the low-temperature gas–liquid–solid regime near 100 °C and the high-temperature gas–solid regime near 600 °C in isolation, limiting their applicability to plant-scale reactor design. This study proposes a unified dual-regime kinetic framework spanning 20–700 °C. The low-temperature branch couples Henry’s-law CO₂ solubility, a sigmoidal water-film stability function, and an Arrhenius ionic reaction term, whereas the high-temperature branch integrates shrinking-core surface reaction and product-layer diffusion with an attenuation term near the CaCO₃ decomposition onset. Seven parameters were calibrated by bounded least squares against a 51-point temperature dataset compiled from the author’s previously published carbonation experiments. The calibrated model reproduced the bimodal temperature dependence of the carbonation degree (R² = 0.62; RMSE = 0.083), with peaks near 100 °C and 640 °C, and predicted reactor volumes of order-of-magnitude 150–200 m³ for a 1 Mt/y cement plant under three waste-heat operating points. The framework bridges particle-scale kinetic and plant-scale design, and identifies mixing as the dominant operational sensitivity at the clinker-cooler condition. Full article

The increasing accumulation of mine waste and the associated release of toxic elements represent a major environmental challenge, particularly in regions impacted by Pb–Zn mining activities. In this context, this study aims to investigate the valorization of mine waste from Lakhouat, an abandoned Pb–Zn site in Northern Tunisia, as a sustainable additive in metakaolin-based geopolymers. This approach contributes to circular economy strategies by transforming hazardous waste into value-added materials for environmental and construction applications. Geopolymer formulations were synthesized by incorporating mine waste at different proportions (0, 5, 10, 20, and 30 wt.%) with metakaolin, while maintaining constant SiO₂/Al₂O₃ and Na₂O/Al₂O₃ molar ratios. The materials were prepared through alkali activation using sodium silicate and sodium hydroxide, followed by curing. Comprehensive characterization was carried out using X-ray fluorescence (XRF), X-ray diffraction (XRD), and scanning electron microscopy (SEM). In addition, adsorption experiments using methylene blue (MB) were conducted to evaluate the environmental performance of the synthesized geopolymers. The results revealed that the mine waste contains high concentrations of potentially toxic elements (up to 2.23 wt.% Pb and 8.2 wt.% Zn), highlighting the need for effective stabilization. Microstructural analysis confirmed the formation of predominantly amorphous geopolymer matrices with varying degrees of reaction depending on MW content. The highest compressive strengths (25–30 MPa) were achieved for formulations containing 5–10 wt.% MW after 28 days of curing. Furthermore, the geopolymers demonstrated efficient methylene blue removal, following pseudo-second-order kinetics and fitting the Langmuir isotherm model, with enhanced adsorption performance observed at higher MW contents. These findings indicate that MW-based geopolymers are promising materials for mine waste valorization and methylene blue removal. However, standardized leaching tests are required to confirm the long-term immobilization of Pb, Zn, Cd, As, and other potentially toxic elements within the geopolymer matrix. The study highlights their potential as sustainable, low-impact materials, supporting waste valorization and contributing to the development of environmentally resilient systems within a circular economy framework. Full article

In this study, a novel protein glutaminase derived from Chryseobacterium lactis CGMCC 33780 (CLPG) was successfully purified via a one-step cell surface display approach, yielding its mature form. Subsequently, the enzymatic properties of CLPG were characterized. It exhibited optimal activity at a pH of 5 and a reaction temperature of 50 °C, and retained over 70% of its activity after a 12 h incubation at 50 °C. The study further investigated the impact of CLPG-mediated deamidation on the structural and functional attributes of krill protein isolate (KPI). A comprehensive analysis was conducted on the deamidation extent, conformational alterations, and microstructural morphology of KPI, employing techniques such as FTIR, CD, DSC, and SEM. After deamidation treatment with CLPG, the foaming and emulsifying properties of KPI were moderately shifted. When the CLPG dosage was 1.0 U/g with a corresponding deamidation degree of 15.18%, the emulsifying property of KPI reached the maximum value of 23%. These property enhancements were possibly primarily attributed to the increased electrostatic repulsion and hydrophobicity induced during the deamidation process. This work not only pioneers a novel method for the expression and purification of protein glutaminase but also applies it to the modification of krill protein, offering fresh insights for the development and application of protein glutaminases. Full article

Lithium-ion batteries have become crucial energy carriers in multiple core fields owing to their excellent comprehensive performance. Nevertheless, as battery energy and power densities continue to rise and operating conditions grow increasingly complex, thermal safety issues have become increasingly prominent. Immersion liquid cooling technology has attracted widespread attention in academic and engineering fields for its outstanding heat transfer and temperature uniformity performance. As a core component of this technology, the selection of liquid coolants is of vital importance. Various coolants investigated in existing studies generally suffer from limitations to varying degrees. Against this backdrop, intrinsically safe fluorocarbon C₇H₄F₁₂O (3F-135) serves as an ideal liquid cooling medium for lithium-ion batteries, thanks to its high thermal stability, superior electrical insulation and environmental friendliness (zero ODP, extremely low GWP). However, its decomposition mechanism and reaction pathways under extreme thermal runaway conditions of batteries remain unclear. In this study, a tube furnace was adopted to simulate high-temperature environments induced by thermal runaway, and gas chromatography–mass spectrometry (GC-MS) was employed to analyze decomposition products and decomposition ratios of 3F-135. Subsequently, density functional theory (DFT) calculations were utilized to construct the pyrolysis reaction network of 3F-135. Ultimately, the dominant pyrolysis pathways in different temperature ranges were clarified, providing theoretical support for the application and selection of intrinsically safe liquid coolants. Full article

Penaeus sp. shells (shrimp) were used to extract chitosan using acid and basic treatments, which were characterized by IR spectroscopy, Raman spectroscopy, potentiometric titration, and elemental analysis. The degrees of deacetylation were determined to be 71.8%, 75.6%, 53.4%, and 68.6%, respectively. Likewise, viscosimetry measurements were carried out, determining an average molecular weight of chitosan 1 of 1521467.919 (g/mol). The obtained chitosan was used as a substrate in condensation reactions with 10 para-substituted benzaldehydes. The products obtained were characterized by IR, Raman, and ¹H-NMR spectroscopy, AE (Elemental Analysis), TGA (Thermogravimetric Analysis), and DSC (Differential Scanning Calorimetry). For the obtained polymers, biological assays of cytotoxicity using RAW macrophage cells and leishmanicidal activity on promastigotes of Leishmania mexicana were performed. The results show that the synthesized products do not present in vitro cytotoxicity, and that 1 (Chitosan) and 3i (Schiff Base) present leishmanicidal activity. Selected derivatives were incorporated into polyvinyl alcohol-based films and evaluated for surface topography and gas permeability. AFM revealed nanometric roughness patterns, while gas exchange studies demonstrated selective CO₂/O₂ permeability, supporting passive modified atmosphere formation in packaged carrots. Mechanical characterization revealed that the incorporation of Schiff base derivatives significantly influences tensile strength and flexibility, with certain films exhibiting enhanced elongation and mechanical performance compared to pure PVA, highlighting their potential for packaging applications. These findings confirm that chemical functionalization enhances the versatility of chitosan, allowing the design of tailored biopolymers. The synthesized derivatives show promising characteristics for the development of biodegradable films with potential applications in food packaging and antiparasitic material development. Full article

The Atlantic blue crab (Callinectes sapidus) is an invasive species widely distributed in the Mediterranean Sea, causing significant ecological and economic impacts. Despite its low commercial value and the limited utilization of undersized and non-marketable specimens, whole blue crab biomass represents a promising resource for the production of value-added compounds within a circular bioeconomy framework. In this study, whole blue crab biomass, including undersized individuals and non-marketable fractions, was directly valorized through enzymatic hydrolysis for the production of protein hydrolysates. Three commercial proteases (Alcalase, Neutrase, and Papain) were comparatively evaluated for protein hydrolysate production, and the hydrolysis conditions were assessed based on soluble matter yield. The evaluation of hydrolysis conditions identified pH 8, 50 °C, enzyme-to-substrate ratio of 2500 U g⁻¹, a solid-to-liquid ratio of 1:4, and a reaction time of 8 h as the most effective conditions for protein solubilization. Under these conditions, maximum soluble matter yields of 57.69% for Alcalase, 51.64% for Neutrase, and 48.44% for Papain were obtained. The obtained hydrolysates were subsequently characterized in terms of protein content and degree of hydrolysis (DH), both of which were significantly affected by enzyme type, following the order Alcalase (64.59 ± 0.75%) > Neutrase (62.29 ± 0.82%) > Papain (58.88 ± 0.65%). A similar trend was observed for degrees of hydrolysis (DH) of the products (43.20 ± 1.24%, 40.29 ± 1.05%, 37.26 ± 1.13%) respectively. Techno-functional properties of the hydrolysates were also enzyme-dependent and closely related to the extent of hydrolysis. Alcalase produced hydrolysates with higher DH, favoring the formation of smaller and more hydrophilic peptides, which enhanced water solubility (98.18 ± 0.51%) and antioxidant activity (77.08 ± 1.06%). In contrast, Papain-derived hydrolysates showed lower hydrolysis extent, likely preserving larger peptide structures and hydrophobic domains associated with higher emulsifying activity (16.10 ± 0.46 m² g⁻¹) and foaming capacity (30.47 ± 1.40%). Neutrase displayed intermediate behavior across most parameters. Overall, the results demonstrate that enzymatic hydrolysis of whole blue crab biomass is an effective valorization strategy, and that enzyme selection plays a key role in modulating hydrolysis efficiency and techno-functional properties. This approach provides a sustainable pathway for the management of invasive species while generating functional ingredients for food and nutraceutical applications. Full article

This study focuses on a group of scanning electrochemical probe microscopies used to reveal the early stages of galvanic coupling corrosion reactions, based on the use of microelectrochemical sensors for measuring local potentials and currents associated with chemical reactions occurring at anodic and cathodic sites, and their correlation with results obtained with conventional electrochemical techniques. Although galvanic corrosion between dissimilar metals is generally analyzed by assuming that the anodic and cathodic half-cell processes occur in different metals, the use of microelectrochemical techniques reveals that the corrosion process is actually more heterogeneous. Cathodic activity is present in both metals, but to very different degrees. Anodic activity is also localized, as the surface of the more reactive metal is not fully available to undergo anodic dissolution. Because galvanic corrosion processes are heterogeneously distributed over the surface of the coupled materials, even in model systems, the identification of cathodic sites and reactions is often insufficient when monitored by conventional electrochemical methods. These observations are particularly relevant when corrosion protection measures aim to minimize or eliminate the activity of cathodic reaction sites. Full article

As lithium demand surges and primary resources face depletion, lithium-bearing wastewater from urban mines has become a crucial secondary resource. For highly alkaline (pH 9–12), low-lithium (Li⁺ 0.5–5 g/L), high-sodium (Na/Li mass ratio > 30) wastewater generated from the alkaline leaching-washing of spent lithium-ion batteries in urban mining, a single-component, synergist-free extraction process employing HBL121 in sulfonated kerosene was developed, and its extraction stoichiometry, reaction mechanism, and industrial feasibility were elucidated. Saponification significantly enhanced extraction under moderate alkalinity: the saponified system achieved over 99% extraction efficiency at pH 11.0, whereas the non-saponified system required pH > 13.5 for comparable performance, thereby lowering alkali consumption by 81%. Under optimal conditions (saponification degree 40%, 30% (v/v) HBL121 and 70% (v/v) sulfonated kerosene, organic-to-aqueous phase ratio O/A = 1:1, extraction time 5 min), single-stage extraction efficiency exceeded 99%. A McCabe-Thiele diagram was used to determine the theoretical stage number for lithium stripping, showing that essentially all lithium ions can be stripped via a three-stage countercurrent process. Using 3.0 mol/L H₂SO₄ at an aqueous-to-organic phase ratio of 1:4, the stripping efficiency exceeded 99% from the loaded organic. Slope analysis, FT-IR, and ESI-MS confirmed a coordination mechanism between HBL121 and metal ions, forming a stable anionic bisphosphonate complex [LiNa₂(C₂₈H₄₄O₇P₂)]⁻, whose neutral parent form is HLiNa₂(C₂₈H₄₄O₇P₂). Full article

This study investigated the optimization of the physicochemical properties of normal maize starch (NMS) by esterification with octenyl succinic anhydride (OSA). The synergistic effects of OSA addition time, temperature, and total reaction time on the degree of substitution (DS) and the physicochemical properties of starch were evaluated using a combination of single-factor experiments and Response Surface Methodology (RSM). FT-IR spectroscopy confirmed the successful incorporation of OSA groups into starch molecules, with the appearance of two characteristic absorption peaks at 1724 and 1572 cm⁻¹. Single-factor experiments revealed that a temperature of 40 °C, an OSA addition time of 2 h, and a total reaction time of 6 h effectively maximized the DS. These conditions balanced efficient esterification with the suppression of OSA hydrolysis and droplet aggregation. The resulting optimized OSA starch displayed lower gelatinization temperature and enthalpy, higher viscosity, more pronounced shear-thinning behavior, and greater resistance to retrogradation. Pearson correlation and simple linear regression analyses demonstrated that DS was negatively correlated with both ΔH and G′_max. The RSM model accurately predicted the optimal synthesis parameters (41.96 °C, 2.25 h OSA addition time, 6.9 h total reaction time), achieving a validated DS of 0.0258. This study provides valuable insights for producing starch-based additives in complex food systems. Full article

As thermal power units in China shift toward serving as flexible regulation sources in new-type power systems, accurately assessing the axial thrust of steam turbine regulating stages under off-design conditions has become critical. This paper employs numerical methods to investigate the axial thrust characteristics and nozzle structural optimization of the regulating stage under off-design conditions (VWO, THA, 75% THA, 50% THA). Steady-state results reveal significant deviations in the interstage hub forces predicted by 3D simulations compared with those from the conventional 1D formula under partial admission, prompting a correction. Unsteady results show that reducing the partial admission degree intensifies flow unsteadiness, increasing rotor blade axial force fluctuation from 1175 N (VWO) to 2057 N (50% THA). In terms of structural optimization, compared with not increasing the nozzle angle, increasing the nozzle angle by 2° reduces the total axial force on the regulating stage by 7.3%; compared with not extending the inlet guide arc segment, extending its length by 40 mm increases the axial force on the rotor blade by 1.6%, but decreases the maximum amplitude from 323.9 to 249.9. Based on these findings, the optimization direction for the nozzle structure is proposed. Full article

A novel water treatment agent, ethylenediamine–benzenesulfonic acid-modified polyaspartic acid (PASP-S), was controllably synthesized using an amino ring-opening reaction. The controllable synthesis methods, conditions for polymerization degree, and the molecular weight of the new polymer were explored. The structure was characterized using Fourier-transform infrared spectroscopy (FT-IR), ¹H nuclear magnetic resonance (¹H-NMR), and gel permeation chromatography (GPC). The scale inhibition, corrosion inhibition, and fluorescence properties of the new polymer, as well as the corresponding mechanisms, were investigated using static scale inhibition tests, electrochemical measurements, X-ray photoelectron spectroscopy (XPS), density functional theory (DFT), and frontier molecular orbital (FMO) theory. The results indicate that PASP-S exhibits strong Ca²⁺ chelation ability and can effectively inhibit CaCO₃ and CaSO₄ scaling. At 50 mg/L, the scale inhibition efficiency for Ca₃(PO₄)₂ reaches 99.50%. At 30 mg/L, its corrosion inhibition efficiency is 33.19% higher than that of PASP. Unexpectedly, the polymer shows remarkable selective antibacterial activity. At 100 mg/mL, the inhibition rate against Escherichia coli (E. coli) is 71%, while no obvious inhibition is observed for Bacillus cereus. A good linear relationship is found between fluorescence intensity and concentration. Mechanistic studies demonstrate that PASP-S adsorbs on the scale surface, suppressing crystal growth and distorting crystal morphology. Meanwhile, it forms a protective film on the electrode surface, thus reducing the dissolution and corrosion of carbon steel. Full article