Search Results (14,361)

Sodium sulfate-activated slag cement is considered a highly promising low-carbon cementitious material; however, its application is limited by low early-age activation efficiency and slow strength development. This study aims to systematically elucidate the coupled regulatory mechanism of alkalinity (2% and 4% Na₂O equivalent) and sodium sulfate dosage on the performance of alkali-activated slag (AAS). Under standard curing conditions (20 ± 2 °C, relative humidity ≥ 95%), the macroscopic properties of the samples (workability, setting time, and compressive strength) and the evolution of their microstructure (analyzed by XRD, FTIR, and SEM-EDS) were evaluated. The results indicate that the effect of sodium sulfate on alkali-activated slag (AAS) strongly depends on the alkalinity. Under low-alkalinity conditions (2% Na₂O), sodium sulfate exhibits a synergistic activation effect by increasing the ionic concentration, promoting slag depolymerization and the nucleation of ettringite (AFt). Specifically, compared with the control, incorporating 6 wt% sodium sulfate (N2S6 mix) increased compressive strength by approximately 82% at 3 days and 21% at 28 days. In contrast, under high-alkalinity conditions (4% Na₂O), excessive sodium sulfate (≥2 wt%) shows an inhibitory effect. This is likely because an excess of sodium sulfate interferes with the normal polymerization pathways of the aluminosilicate network, suppressing the formation of the primary C-(A)-S-H gel and thus significantly reducing later-age strength. Microstructural analysis revealed that the hydration products in the composite-activated system mainly consist of C-(A)-S-H gel, ettringite (AFt), monosulfate (AFm), and hydrotalcite. This study investigates the observed kinetic trends of anion-competitive hydration under different alkalinity conditions, providing a theoretical basis for the mix design of low-carbon alkali-activated materials and the valorization of coal chemical industrial salts. Full article

The selective oxidative transformation of 5-hydroxymethylfurfural (HMF) is a key route toward producing a wide variety of chemicals in the biorefinery industry. Herein, we report a NiAl layered double hydroxide (NiAl-LDH) catalyst as a highly effective electrocatalytic oxidation catalyst for the transformation of HMF into 2,5-diformylfuran (DFF), a valuable furan-based chemical, with about 75.53% DFF selectivity under neutral conditions. It demonstrated good stability without deactivation after 9 cycles of repeated electrolysis. The NiAl-LDH electrocatalyst was deposited on a nickel foam support via a hydrothermal method, and its structural properties and surface morphology were extensively investigated. Systematic studies of reaction temperature, current intensity, and electrolyte concentration revealed that the neutral electrolyte plays a critical role in achieving high DFF selectivity by suppressing aldehyde over-oxidation. Mechanistic investigations with electrochemically active surface area (ECSA), electrochemical impedance spectroscopy (EIS), Tafel slope and density functional theory (DFT) calculations revealed that the reversible transformation between Ni(OH)₂ and active NiOOH species in the NiAl-LDH electrocatalyst was the main reason for the oxidation of HMF, while the incorporation of Al provided structural support to the electrode, enabling the catalyst to exhibit excellent stability during electrolysis. Overall, this work demonstrates an active, earth-abundant metal electrocatalyst for the valorization of biomass-derived 5-HMF to DFF. Full article

Stabilizing weak soils is a well-known pavement and geotechnical engineering technique. This technique involves introducing minimal cementitious materials to improve the soil’s geotechnical characteristics. This paper investigates the use of recycled industrial polymer waste (IPW) as a reinforcement material in the presence of cementitious binders to stabilize weak silty sand soil (SM), supporting sustainable engineering practices. The randomly distributed IPW were added as percentages of 0%, 5%, and 10% to a mixture of lime soil and cement soil, with varying amounts of 0% to 6% of lime (L) and 0% to 6% of ordinary Portland cement (OPC), respectively. The laboratory experiments were conducted on natural and stabilized samples in wet (unsoaked) and submerged (soaked) conditions. The experimental program included Proctor compaction, California bearing ratio (CBR), unconfined compressive strength (UCS), durability tests, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction analyses. The resilient modulus (Mr) was estimated using an empirical equation. The outcomes of this experimental study show that adding a combination of IPW shreds with a small amount of L and/or OPC to the SM soil provides a significant increase in the UCS, CBR, durability and Mr values compared with case of SM with only L, which allows for superior characteristics and increases strength and stiffness parameters throughout any phase of earthwork construction design, resulting in stronger and stiffer subgrades. These results were reinforced by microstructural observations from SEM, EDS, and DRX, confirming the formation of cementitious gels and chemical compounds, consistent with the macro-scale mechanical improvements. The expected practical outcomes include potential reductions in pavement thickness, which can help lower pavement stabilization costs and extend its service life. Additionally, the use of waste materials to replace raw materials contributes to decreased energy consumption and emissions, although detailed assessments are needed to quantify these effects. Full article

Recyclers worldwide face a common bottleneck: incoming mixed plastic bales are chemically opaque, yet the choice between mechanical recycling, chemical recycling, and energy recovery hinges on contaminant levels that cannot be judged by visual inspection alone. This study develops and validates a tiered analytical decision-support framework that translates standard laboratory measurements into explicit, actionable go/no-go routing criteria for any mixed polyolefin waste stream. The framework is organized into three successive analytical tiers of increasing specificity: Tier 1 uses FTIR and DSC for rapid polymer identification and thermal subclass confirmation; Tier 2 applies TGA/DTG for thermal stability assessment and filler quantification; and Tier 3 deploys ICP-OES, WD-XRF, CIC, and TG–MS for targeted heavy metal, halogen, and evolved gas profiling, triggered only when Tier 1/2 flags are raised. This staged logic minimizes unnecessary testing while ensuring that contaminant-relevant information is captured where it matters. The framework is demonstrated on nine blind mixed plastic waste streams (P1–P9) supplied by an industrial recycling facility without prior disclosure of polymer identity, filler content, or additive history—conditions that replicate the uncertainty encountered at any sorting plant globally. Application of the tiered protocol identified dominant polymers (HDPE, LDPE, PP), quantified inorganic fillers (CaCO₃ up to ~38 wt%), and detected hazardous contaminants, including chlorine (up to ~1900 ppm), lead, chromium, and titanium, enabling each stream to be assigned to a specific recycling route with defined contaminant thresholds. Because the method relies exclusively on commercially available, vendor-independent instrumentation and follows a reproducible, rule-based decision logic, it is directly transferable to recycling facilities in any geographic context without site-specific calibration. The proposed framework thus provides a practical, scalable decision-support tool for feedstock-level quality control under emerging regulations such as the UNEP Global Plastics Treaty. Full article

Starches from various botanical sources are extensively utilized across food applications due to their functional and technological properties. However, native starches exhibit limitations under processing conditions involving heat, pH shifts, or mechanical stress, which restrict their application. In response, the demand for “clean-label” products has driven interest in sustainable and non-chemical modification strategies. This review aims to provide a critical overview of the effects of unconventional technologies—including ozone, ultrasound, high-pressure processing, high-pressure homogenization, pulsed electric fields, and cold plasma—on starch granule structure and the resulting pasting properties. A bibliometric analysis based on 1679 documents from Scopus and Web of Science^® highlighted a lack of previous studies integrating quantitative trends with in-depth technical discussion. The selected technologies demonstrate potential to enhance starch functionality through distinct modification mechanisms, although their effects are highly dependent on starch source, structure, and processing parameters. Despite promising advances, most applications remain restricted to laboratory scale, and further research is required to optimize conditions and promote industrial feasibility. Full article

Optical fiber sensors deployed in harsh industrial fields, e.g., high-temperature wet-oxygen, face severe challenges in signal attenuation and mechanical degradation. While amorphous silicon oxycarbide (a-SiOC) coatings offer a promising solution due to their adjustable thermo-mechanical properties, balancing their structural density with environmental stability remains a critical technical bottleneck. In this study, a-SiOC coatings were deposited on optical fibers using hexamethyldisilane (HMDS) and trace oxygen via radio-frequency capacitively coupled plasma-enhanced chemical vapor deposition (PECVD). A systematic investigation was conducted to determine the impact of deposition temperature (70–420 °C) on the precursor dissociation kinetics, microstructural evolution, and corrosion resistance of the coatings. An elevation in temperature promotes the elimination of organic terminal groups (–CH₃, –H) and enhances surface diffusion, driving the coating from a loose, carbon-rich “polymer-like” structure (dominated by Si–C bonds) to a dense, inorganic “silica-like” skeleton (dominated by Si–O–Si bonds). High-temperature corrosion tests in a wet-oxygen environment (500–900 °C) demonstrate that the failure mechanism is highly dependent on deposition temperature. Coatings deposited at low temperatures suffer catastrophic cracking due to pronounced oxidative shrinkage and the release of volatile species, whereas coatings deposited at 420 °C exhibit microcracking caused by severe carbon phase separation and stress concentration within the rigid inorganic network. In the present system, 350 °C is identified as the optimal deposition temperature, as it achieves the best balance of network densification and structural flexibility, while exhibiting the best mechanical performance. Full article

Coffee is among the most widely consumed beverages globally being cultivated in nearly 80 countries. Its processing generates large quantities of by-products, including mucilage, pulp/husks, silverskin, parchment, and spent coffee grounds. Although traditionally treated as waste, these residues are increasingly recognized as valuable resources rich in bioactive compounds exhibiting antioxidant, antimicrobial, and health-promoting properties. This review explores the antimicrobial potential of coffee by-products, with particular emphasis on their chemical composition and mechanisms of action. Compounds such as caffeine, chlorogenic acids, polyphenols, and melanoidins have demonstrated inhibitory effects against a broad spectrum of bacteria, including both Gram-positive and Gram-negative bacteria. Many of these compounds, which originate from plant’s defensive system or result from Maillard reactions, are known to disrupt microbial membranes, inhibit DNA repair, and interfere with pathogen metabolism. However, the available literature on their antimicrobial effectiveness remains limited. In the context of the rising worldwide concern over antimicrobial resistance, coffee by-products represent a sustainable and promising source of novel antimicrobial agents. Their valorization may support advances in food preservation, pharmaceutical innovation, and waste management practices, contributing to the implementation of a circular economy framework in the coffee industry while promoting environmental, economic, and social sustainability. Full article

p-Methoxy-m-nitrobenzoic acid (MNBA) serves as a valuable chemical intermediate across numerous domains. Nevertheless, the synthesis of MNBA through non-catalytic oxidation processes invariably results in the production of environmentally polluting substances. In this study, we report an environmentally benign catalytic oxidation system for the synthesis of MNBA using water as a solvent. Based on the two-step TEMPO/KBr/NaOCl/NaClO₂ system, which achieved a 91.4% yield at 70 °C, we have devised a simplified one-step procedure employing the TEMPO/KBr/NaClO₂ system. This less energy-intensive input method yields 90.1% MNBA at 60 °C. Systematic optimization has revealed that temperature, time, and oxidant quantity are critical parameters. Furthermore, acidic conditions have been found to reduce yields due to the decomposition of NaClO₂. The aqueous-phase approach completely avoids organic solvents and facilitates product isolation. A synergistic catalytic mechanism involving N-oxoammonium intermediates is proposed. This work establishes a sustainable strategy for preparing multifunctional aromatic carboxylic acids, addressing key challenges in both ecological impact and industrial scalability for fine chemical production. Full article

Electrocatalytic CO₂ reduction reaction (CO₂RR) to ethylene (C₂H₄) has emerged as a promising approach for converting CO₂ into valuable chemicals while utilizing renewable electricity. To facilitate the commercialization of this technology, a process-level techno-economic assessment (TEA) is constructed for a plant producing 100 tons/day of C₂H₄ from coal-power flue gas CO₂ using a membrane electrode assembly (MEA) electrolyzer and downstream gas separations. The model integrates (i) flue gas CO₂ capture by chemical absorption, (ii) CO₂RR to C₂H₄ with H₂ as the only co-product, and (iii) cathode off-gas separation by pressure swing adsorption (PSA) plus anode off-gas CO₂ recovery and recycle. A Cu₁₀–Sn catalyst measured in an H-cell is projected to MEA operation by scaling current density by 10×, yielding a “Case Study in This Article” scenario of j = 246 mA·cm⁻² and FE(C₂H₄) = 48.74%. Under this scenario, the total cost is 592.61 thousand USD/day (5926 USD/ton), dominated by electricity (39.8%). Scenario analysis shows that the total cost can decrease to 76,755.0 USD/day (767.6 USD/ton) under a future-outlook case with improved electrolyzer performance and low-cost power, enabling a net profit of 19,945.0 USD/day at an ethylene selling price of 967 USD/ton. Sensitivity analysis identifies FE(C₂H₄), full-cell voltage, and electricity price as the most influential variables. The results translate laboratory catalyst metrics into industrial cost drivers and clarify quantitative performance targets for commercialization. Full article

This study presents a rapid, eukaryotic impedimetric biosensor that applies the yeast Saccharomyces cerevisiae as a robust, cost-effective biorecognition element for monitoring the acute toxicity of two representative pharmaceuticals, naproxen and isoniazid, in aquatic systems. The biosensor utilizes a previously developed three-electrode system made from type 316 stainless steel. Yeast cells seeded onto these electrodes serve as the biosensing element. By monitoring changes in electrical impedance, the system quantifies the cellular stress induced by pharmaceutical exposure. Electrochemical Impedance Spectroscopy (EIS) revealed a concentration-dependent decrease in both resistance and capacitance, attributed to cell death and subsequent desorption from the working electrode surface. These findings were validated through optical density at 600 nm (OD₆₀₀) growth curve analysis and methylene blue viability staining, which confirmed metabolic inhibition and membrane damage. Results indicate a linear response for naproxen within the 2.5 mM to 20 mM range, with a LOD of 0.509 mM, and for isoniazid within the 10 mM to 100 mM range, with a LOD of 0.684 mM. Naproxen demonstrated a more pronounced cytotoxic effect, with cell viability dropping to 41.08% at 10 mM compared to 68.79% for isoniazid. While conventional analytical methods focus on chemical quantification, this proof-of-concept biosensor provides a rapid toxic/non-toxic signal, offering a biologically relevant tool for real-time monitoring of industrial waste streams and acute environmental contamination. Full article

The accelerating generation of waste streams is observed globally. Spanning lignocellulosic biomass, plastic waste, sewage sludge, and industrial residues, this review presents both an urgent management challenge and a compelling materials opportunity. Carbon materials derived from these waste streams offer a sustainable route to functional carbons applicable in electrochemical energy storage, adsorption, heterogeneous catalysis, and high-temperature applications. Yet their rational design remains constrained by incomplete understanding of the relationships between feedstock composition, processing pathway, structural characteristics, and functional performance. This review provides an integrated analysis of waste-derived carbon materials from processing pathways to structure–property–function relationships. The principal feedstock categories are examined for their compositional characteristics and implications for carbon yield and structure. Five primary processing routes are assessed. The five routes examined are pyrolysis, hydrothermal carbonisation, physical and chemical activation, and microwave-assisted processing. They are assessed comparatively with emphasis on structural outcomes and governing parameters. The resulting structural characteristics are discussed. These are morphology, hierarchical pore architecture, surface chemistry, heteroatom doping, and crystallinity. They are discussed alongside their characterisation methods and known limitations as performance predictors. Structure–property relationships are examined quantitatively. Heteroatom-doped hierarchical porous carbons achieve 612 F/g specific capacitance. Turbostratic hard carbons deliver 450 mAh/g sodium storage with over 90% retention. Hierarchical porous carbons demonstrate CO₂ uptake of 5.0 mmol/g and dye adsorption exceeding 9000 mg/g under optimised laboratory conditions; these values reflect individual studies and are not directly comparable across systems. Biomass-derived sulfonated carbon catalysts sustain biodiesel yields above 90% over multiple cycles. Challenges of feedstock variability, process scalability, environmental compliance, and economic feasibility are addressed, and machine learning-guided design, standardised characterisation methodology, and circular economy policy frameworks are identified as key enablers for translating laboratory performance into industrial reality. Full article

Conventional wastewater treatment systems cannot effectively eliminate micropollutants such as contaminants of emerging concern (CECs). These compounds, even at trace levels, are persistent or pseudo-persistent, bioaccumulative, and potentially harmful to ecosystems and human health. Advanced oxidation processes (AOPs), based on the in situ generation of highly reactive oxygen species, have emerged as promising solutions. Peroxyacetic acid (PAA) has gained attention due to its strong oxidizing capacity, broad antimicrobial activity, environmentally benign by-products, and compatibility with different activation methods. This review provides an updated and integrated synthesis of recent advances in PAA-based AOPs for the degradation of major CEC groups, including pharmaceuticals, personal care products, pesticides, and industrial chemicals, as well as for the oxidative modification of microplastics (MPs). The review discusses several strategies for PAA activation and critically discusses removal efficiency, underlying mechanisms, and current limitations, emphasizing the gap between pollutant transformation and complete mineralization. Furthermore, the article highlights a key research need, which is the assessment of the toxicity of transformation products and their validation under realistic conditions. Overall, this review provides insight into the potential and challenges of PAA-based AOPs for sustainable water treatment. Full article

Background/Objectives: The increased prevalence of multidrug-resistant Escherichia coli and carbapenemase-producing Enterobacteriaceae poses a critical threat to global health and food safety. Antimicrobial Blue Light (aBL) in the 400–470 nm spectrum has emerged as a promising, chemical-free disinfection strategy that targets intracellular porphyrins and flavins to induce oxidative stress. However, the influence of wavelength, dosimetry, and environmental stressors on endogenous photoinactivation remains poorly standardized regarding optical parameters and biological exposure protocols. This systematic review aimed to evaluate the antimicrobial efficacy of pure blue light (400–470 nm) against E. coli across various phenotypes and environmental conditions, excluding the use of exogenous photosensitizers. Methods: PubMed, Scopus, and Web of Science were searched for studies that utilized 400–470 nm light as an antimicrobial agent against E. coli. Data extraction focused on spectral efficiency, total fluence (J/cm²), and log₁₀ reduction. The Risk of Bias was assessed using an adapted Office of Health Assessment and Translation tool for in vitro studies. Results: Synthesis of 11 high-quality studies indicated that wavelengths near 405 nm have the highest germicidal efficiency due to the Soret band absorption of endogenous porphyrins. Efficacy is highly dose-dependent: significant log₁₀ reductions were achieved in planktonic cells, although biofilms required substantially higher fluences. Sub-lethal environmental stressors such as acidic pH, high salinity, and thermal fluctuations demonstrated a synergistic effect, which significantly enhanced the rate of photoinactivation. Multidrug-resistant and carbapenemase-producing Enterobacteriaceae strains showed similar susceptibility to aBL relative to antibiotic-sensitive strains, suggesting no cross-resistance between light and traditional drugs. Conclusions: Endogenous blue light is a highly effective, non-thermal technology for E. coli decontamination. Its efficacy is modulated by the interplay between optical parameters and environmental conditions. These findings provide a framework for the development of standardized protocols for applying aBL to clinical wound care and food industry use cases. They also highlight the potential of aBL as a critical tool in the post-antibiotic era. This systematic review was registered in the International prospective register of systematic reviews (PROSPERO) under protocol CRD420261331871. Full article

This study investigates the agglomeration of chromium-containing dust from ferroalloy production using rigid vacuum extrusion. Direct utilization of fine technogenic materials in submerged arc furnaces is limited due to poor gas permeability, increased dust generation, and unstable smelting conditions. The aim of this work was to compare bentonite and polymer binders in brex production and evaluate their metallurgical applicability. Chromium-containing dust from the gas-cleaning system of the Aktobe Ferroalloy Plant (TNC Kazchrome JSC, ERG) was characterized using chemical analysis and SEM/EDS methods. The material exhibited a heterogeneous structure composed mainly of chromium-containing spinel, silicate, and oxide phases. Pilot-industrial extrusion tests were performed using J.C. Steele & Sons equipment with bentonite (10 wt.%) and polymer binder TD 021.005.BS (2.5 wt.%). The polymer binder provided improved brex geometry and significantly higher mechanical strength, achieving impact strength values up to 89.5% after curing. SEM/EDS analysis of the obtained brexes confirmed the formation of a dense agglomerated structure with uniform distribution of chromium-containing phases. Thermodynamic modeling using FactSage 8.4 showed that brex addition does not significantly affect slag composition, phase equilibria, or metal quality during high-carbon ferrochrome smelting. The results demonstrate the feasibility of polymer binders for efficient recycling of chromium-containing technogenic wastes by rigid vacuum extrusion. Full article

Galactooligosaccharides (GOS) are one of the internationally recognized prebiotic products, which have become a hot research focus in the field of biofoods because of their strong prebiotic, sugar substitution and inflammation alleviation functions. β-galactosidase (Bgal) of different microorganisms is utilized industrially in order to achieve the biosynthesis of GOS. Although the biosynthesis of GOS has been supported by certain technologies, there is still room for further improvement of its synthetic yield. This paper mainly introduces the function and biosynthesis of GOS and its research progress in recent years to enhance the yield of biosynthesis. This paper also combines the research progress in related fields in recent years, based on the basic theories of molecular biology and bioinformatics, discusses the research progress of green, innovative approaches including enzyme engineering, enzyme immobilization, surface display, and microbial fermentation on the synthesis of GOS. Full article