Search Results (1,999)

Granulated blast furnace slag is a commonly used supplementary cementitious material in cement-based materials. The raw materials for ironmaking and the cooling process affect its composition, thereby influencing its reactivity. Three types of slag were selected and incorporated at replacement ratios of 15%, 30%, and 50% to investigate the influence of chemical composition on the activity index of slag at different ages and the mechanisms. The results indicate that in the early hydration stage, slag primarily plays a mechanical filling and dilution role (inert volumetric occupation without significant heterogeneous nucleation), while the pozzolanic effect dominates at later stages. Al₂O₃ in the slag is activated at early ages to form ettringite; at replacement ratios of 30%, C-A-S-H gel is also formed at later ages; when the replacement ratio reaches 50%, the significant reduction in cement clinker content leads to dropping in system alkalinity—corresponding to a 50% reduction in cement-derived Ca(OH)₂, the activation of Al₂O₃ in the slag is not significant at early ages. The effects of glass content, alkali content, specific surface area, CaO + MgO content, quality coefficient, and basicity coefficient on the reactivity become prominent at longer ages. No additional crystalline phases beyond those present in pure cement paste were detected in the cement paste after slag incorporation. This study provides a theoretical basis and data support for the high-value utilization of industrial solid waste in green building materials. Full article

The rational configuration of electronic band structures through deep-seated structural disorder remains a formidable challenge in sustainable solar-to-fuel conversion. Herein, we report a transformative kinetic strategy to “freeze” an extraordinary density of non-equilibrium structural defects within an integrated Cu₄MgO₅/ZnO nanocomposite. Synthesized via a chitosan-assisted coordination-combustion route followed by rapid thermal quenching, the material preserves a record crystallographic dislocation density of 1.09 × 1015 m⁻² and significant lattice microstrain (1.04 × 10⁻³). This engineered structural disorder induces a profound reconfiguration of the electronic landscape, generating a continuous manifold of sub-bandgap “tail states” that narrow the optical bandgap to a remarkable 1.34 eV. Consequently, the defect-rich architecture facilitates unprecedented dual-channel photocatalytic performance under simulated solar irradiation in an aqueous solution containing 5 vol% triethanolamine (TEOA) as a sacrificial electron donor; the catalyst achieved a hydrogen evolution rate of 17,700.0 µmol g⁻¹ h⁻¹ and a methane production rate of 172.50 µmol g⁻¹ h⁻¹—representing a 36.3-fold and 43.1-fold enhancement over commercial ZnO, respectively. With an apparent quantum yield of 8.42% at 420 nm and robust photostability—maintaining 95.3% of its activity over five consecutive cycles (25 h total)—this noble-metal-free ternary system bypasses the limitations of traditional heterojunctions. Our findings establish a new benchmark for defect-engineered catalysts, providing a scalable blueprint for high-efficiency carbon neutrality and solar fuel production. Full article

Herbaceous biomass is a promising renewable energy resource, but its use in thermochemical systems is often limited by severe fouling and ash agglomeration resulting from alkali-rich ash chemistry. This study directly compares two practical fouling mitigation strategies, kaolin addition and acid washing, for alkali-rich torrefied kenaf biomass under identical experimental conditions. The study quantitatively distinguishes aluminosilicate-based alkali stabilization from pretreatment-based alkali removal as two distinct pathways for controlling ash transformation. Kenaf exhibited severe ash agglomeration and contained high levels of K₂O (17.38 wt.%), CaO (31.52 wt.%), MgO (14.98 wt.%), SO₃ (9.43 wt.%), and P₂O₅ (6.90 wt.%). Kaolin addition progressively shifted the ash composition toward a SiO₂–Al₂O₃-rich system. From KA-10 to KA-30, SiO₂ increased from 22.86 to 33.58 wt.%, while Al₂O₃ increased from 7.65 to 15.43 wt.%. X-ray diffraction (XRD) analysis further showed that increasing kaolin addition suppressed alkali-salt phases and promoted the formation of aluminum-silicate phases. In contrast, acid washing directly reduced alkali species, decreasing K₂O to 5.66–7.83 wt.% and eliminating detectable Na₂O. The acid-washed samples were characterized by calcium-rich sulfate and silicate phases, indicating a distinct ash transformation pathway. Kaolin addition primarily reduced fouling by promoting aluminosilicate-based alkali stabilization, whereas acid washing reduced alkali–metal contents before thermal treatment. This distinction clarifies the different roles of additive-based and pretreatment-based strategies for fouling control in alkali-rich herbaceous biomass. Full article

The Lower Carboniferous Um Bogma Formation in southwestern Sinai has sixteen paleokarst structures at Allouga, Abu Thor, and Abu Zarab. Each structure contains high uranium concentrations. These occur in a lateritic infill sequence formed along the southern Tethyan margin. Radiometric reconnaissance in this sector of the Arabian–Nubian Shield has been ongoing for decades. However, the mineralogical character of assemblages in the region was never systematically documented. This study uses multiple techniques to characterize both radioactive and non-radioactive mineral assemblages from paleokarst-fill materials at all sites. Geochemical analysis was used to clarify uranium fixation and ore genesis. Nine radioactive minerals were identified: carnotite, autunite, torbernite, uranophane, uranothorite, thorite, chalcophanite, natroboltwoodite, and soddyite. Eight nonradioactive accessory phases were also found: zircon, monazite, malachite, atacamite, jarosite, rutile, arsenopyrite, and paratacamite. Geochemical data indicate that iron oxide surface adsorption is the dominant mechanism of uranium fixation. A strong positive correlation between uranium and Fe₂O₃ (r = 0.98), together with negative correlations with carbonate-associated elements (CaO, MgO, Na₂O), supports this interpretation. Therefore, uranium is classified as a supergene, low-grade ore. It is concentrated during laterite maturation in paleokarst cavities. Its distribution is governed by ferruginous siltstone lithofacies, not the enclosing carbonate host. These findings offer a reference paragenetic framework for secondary uranium metallogenesis in Carboniferous carbonate terrains of the Arabian–Nubian Shield. They also provide a mineralogical template for exploration in similar paleokarst-hosted systems across the Arabian Platform. Full article

In alignment with global carbon neutrality goals, this study investigates the regulatory role of magnesium oxide (MgO) content on the macro–micro properties of carbonation-cured collapsible loess from the Hohhot region. While MgO carbonation is established for soil stabilization, the quantitative influence of MgO dosage on the specific phase evolution pathways and mechanical enhancement within the unique macro-porous fabric of aeolian loess remains poorly understood. Addressing this, we systematically examined loess specimens amended with varying MgO contents (10% to 30%) over carbonation periods up to 24 h. Unconfined compressive strength (UCS) tests, X-ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to correlate mechanical performance with mineralogical and microstructural evolution. Results indicate that MgO content acts as a primary regulator of the carbonation process. Higher MgO dosages substantially increased CO₂ uptake, resulting in a significant relative mass gain—up to more than a two-fold difference between the highest and lowest content samples—and culminated in a compressive strength of 10.48 MPa for the 30% MgO specimen. Microstructural analysis revealed a distinct temporal evolution interpreted to be governed by MgO-mediated supersaturation levels. Initially, Mg(OH)₂ agglomerates provided early strength, which was subsequently enhanced by the formation of a three-dimensional framework of nesquehonite, followed by the development of an interlocking skeletal network of hydromagnesite crystals. These carbonate phases enhanced loess strength via a combination of pore infilling, particle cementation, and the construction of a reinforcing micro-skeleton. This work elucidates the link between MgO content and the microstructural evolution of carbonated loess, providing new insights for the synergistic integration of soil stabilization and carbon sequestration in loess regions. The findings offer a valuable reference for engineering applications in collapsible soil environments under the context of sustainable development. Full article

A major challenge in wastewater treatment lies in developing cost-effective and sustainable adsorbent materials for efficient dye removal. In this study, a novel biochar functionalized with MgO nanoparticles derived from palm leaf waste (MgO/PLB nanoparticles) was synthesized and evaluated for the removal of Congo red (CR) from aqueous solutions. FTIR, SEM, BET, and TGA investigations were used to thoroughly analyze the produced nanocomposite’s physicochemical properties. FTIR analysis verified the successful incorporation of MgO nanoparticles, as evidenced by the presence of characteristic Mg–O vibrations and noticeable changes in surface functional groups. SEM analysis revealed a transformation from a compact structure to a rough, particle-decorated morphology, indicating increased surface heterogeneity. BET analysis indicated the development of mesoporous structures, accompanied by a substantial increase in specific surface area from 2 to 178 m²/g. TGA results further confirmed enhanced thermal stability, indicating the formation of a structurally robust adsorbent. Batch adsorption tests showed that CR removal depends on pH, dosage, concentration, and contact time, with maximum efficiency (~99%) achieved at pH 4 using 0.03 g of adsorbent. The adsorption followed pseudo second order kinetics and was best described by the Langmuir isotherm, with a maximum capacity of 23.4 mg/g. The regenerated nanomaterial retained more than 89% of its adsorption capacity after four successive cycles, demonstrating good reusability and stability. The developed MgO/PLB nanoparticles exhibit efficient adsorption performance, combined with low-cost synthesis and the utilization of abundant agricultural waste, making it an affordable and long-lasting adsorbent for applications involving wastewater treatment. Full article

This study addresses the corrosion problem of refractory materials during high-temperature molten treatment of pharmaceutical waste salt, and systematically investigates the interface behavior and corrosion mechanism of MgO-based refractory materials in simulated pharmaceutical waste salt (65 wt% NaCl-30 wt% Na₂SO₄-5 wt% CaCO₃). Through sessile drop wetting infiltration experiments, static corrosion tests (950 °C and 1150 °C/48 h), combined with SEM-EDS, XRD characterization, and FactSage thermodynamic calculations, the corrosion resistance of high-purity MgO phase (HM-97) refractory materials and magnesium–aluminum spinel composite phase (MA-85) refractory materials was compared and analyzed. The results show that due to the fine periclase grains and rich grain boundaries, the molten salt infiltration rate of HM-97 material in the 644–800 °C range is significantly higher than that of MA-85. After corrosion at 950 °C, HM-97 and MA-85 formed 47 μm and 53 μm transition layers respectively, and the HM-97 surface generated Ca₃Mg(SiO₄)₂ phase leading to uneven corrosion morphology. At 1150 °C, HM-97 produced long cracks and the transition layer thickness remained almost unchanged due to dissolution, while MA-85 formed an approximately 72 μm transition layer and a dense metamorphic layer. Phase analysis and thermodynamic calculations suggest that the MgAl₂O₄ phase in MA-85 is likely stable at high temperatures, which appears to effectively prevent molten salt infiltration and contribute to forming a protective metamorphic layer, thereby potentially enhancing the material’s corrosion resistance. The MgAl₂O₄ phase is proposed to improve the service performance of MgO-based refractory materials in the molten pharmaceutical waste salt environment. Full article

Given the increasing concern around greenhouse gas emissions and the decline in the availability of fossil fuels, there is increasing global demand to develop alternate fuels for maritime transportation that are sustainable and which have lower greenhouse gas emissions. Methanol is one such alternative fuel that has garnered considerable attention given its potential to be produced by more sustainable processes and its more favorable greenhouse gas emission profile in comparison with current fossil fuels. Understanding the physical and chemical properties of methanol under a range of conditions is essential for its development as a marine fuel. In this study, we seek to define physical and chemical properties of different methanol samples to simulate real-world storage conditions as these data are lacking in the literature. Several methanol samples were evaluated: nearly pure methanol; International Organization for Standardization (ISO) marine methanol (MM) grades A, B, and C; and methanol plus higher alcohols. We first evaluated all methanol samples for impurities, acetic acid content, density, and distillation range. We then characterized the effects of water absorption and found that methanol can easily absorb unacceptable water content from humid air within hours, necessitating storage conditions that prevent this process. In eight-week aging experiments at 20 °C and 40 °C in ambient air, we did not observe significant oxidation for any of the methanol samples; however, we did observe increases in acid number. We assessed the impact of contamination of methanol with water, marine gas oil (MGO), and an MGO–biodiesel mixture on density, viscosity, distillation range, and lubricity. Finally, we show that MGO contamination of methanol results in a slight increase in sooting tendency. In aggregate, our results provide an in-depth analysis of physical and chemical properties of methanol as well as the impacts of storage conditions and impurities on the properties of fuel methanol. Full article

The cohesion zone of a blast furnace is instrumental in determining the gas-dynamic regime and the efficiency of reducing gas utilization. The extent of this phenomenon is contingent upon the initial and final temperatures at which iron ore undergoes softening, which, in turn, are determined by the chemical and phase composition, as well as the degree of reduction of the charge. The present study investigated sinter with a basicity (CaO/SiO₂) ranging from 1.2 to 3.0 using a combination of methods. The experimental program involved the use of X-ray diffraction (XRD) with refinement using the Rietveld method, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), and load-dependent softening tests. It was established that as the basicity increased, the content of the calcium–aluminum silicoferrite (SFCA) binder phase increased from 6.2 to 17.5 wt.%, whilst the amount of hematite decreased from 12.6 to 2.3 wt.%. The softening onset temperature increases from 1185 to 1260 °C, the softening end temperature from 1345 to 1415 °C, and the softening interval narrows from 160 to 155 °C. The evolution of the phase composition of sinter during controlled reduction (0–95%) has been investigated for the first time. It has been demonstrated that the maximum accumulation of wustite (FeO) is attained at a reduction degree of 40–60%, irrespective of the basicity of the substance. It is precisely in this range that the minimum softening start (1040–1065 °C) and end (1170–1210 °C) temperatures are observed, which is associated with the formation of low-melting eutectics. The sinter belongs to the CaO–SiO₂–FeO–Al₂O₃–MgO system, and the softening behavior is governed by the FeO–CaO–SiO₂ system where low-melting eutectics form. When the reduction rate exceeds 60%, the metallic phase becomes dominant, leading to an increase in softening temperatures and a narrowing of the cohesion zone. It is evident from the data obtained that the optimal basicity range of the sinter is 2.0–2.5. Furthermore, it is recommended that a reduction degree of at least 60% is implemented in order to improve gas dynamics and increase blast furnace productivity. The findings can be utilized to enhance the efficiency of charge materials and refine mathematical models of the blast furnace process. Full article

The volcanic island of Fuerteventura (Canary Islands, Spain) offers the opportunity to investigate aqueous alteration in Mars-like environments. As on Mars, landscapes on Fuerteventura are typified by mafic volcanic landforms, minimal precipitation, strong winds, and minimal or absent vegetation. In this study, we perform reflectance spectral and geochemical analysis of near-surface basaltic materials from Fuerteventura’s Gairía caldera, as well as samples from a nearby arroyo. Tephra, outcrop rock, and soil-like material exhibit variations in color, spectral properties, mineralogy, and major oxides. Visible/near-infrared (VNIR) spectra of orange/light-brown materials have higher reflectance values and much stronger features attributed to phyllosilicates (including H₂O and Al-OH bands near 1.41–1.45, 1.91–1.92, 2.21, and 2.76 µm characteristic of montmorillonite in caldera and arroyo samples, plus shoulder features near 1.38 and 2.17 µm and a band at 2.70 µm indicative of kaolinite/halloysite in arroyo samples) compared to black/brown materials. Additionally, several of the highly altered samples contain spectral bands due to calcite at 2.33, 2.53, 3.36, 3.47, and 3.97 µm. Major oxide data reveal similar distinctions between lighter orange/tan (altered) versus darker (unaltered) samples. Lighter and orange-colored samples show elevated Al₂O₃ and depleted Fe₂O_3T, MgO, CaO, and Na₂O, as well as higher chemical index of alteration (CIA) values, overall characteristic of water-soluble cation release (and secondary clay formation) during incipient-to-intermediate chemical weathering of basalt. Gairía weathering trends inform phyllosilicate formation in arid volcanic settings broadly. Of particular interest is the chemical alteration of basalt to montmorillonite and kaolinite/halloysite taking place in warm but water-limited desert conditions, suggesting the potential for clay formation in analogous (warm but relatively dry) paleoenvironments on early Mars. Full article

The calcination kinetics of limestone and dolomite under conditions relevant to sorption-enhanced gasification (SEG) were investigated: mild temperature (775–850 °C), low CO₂ partial pressure (0.05–0.10 bar), and a steam-rich (H₂O balance) atmosphere. Experiments with two Ca-based sorbents (limestone and dolomite) were conducted in a fluidized bed reactor to assess both initial calcination kinetics and multicycle deactivation during 10 cycles under SEG carbonation conditions at 650 °C. Dolomite exhibited markedly higher calcination rates than limestone, which is consistent with the structural modifications induced by MgCO₃ decomposition and the presence of MgO, resulting in a slightly lower apparent activation energy (115.96 kJ mol⁻¹ for dolomite compared to 120.27 kJ mol⁻¹ for limestone). Both sorbents showed a strong sensitivity to the deviation from the equilibrium CO₂ partial pressure, with reaction orders near 2. The presence of steam was confirmed to have a significant catalytic effect, accelerating the first-cycle calcination rate compared to dry N₂ conditions. Sorbent deactivation caused by sintering was more pronounced at higher temperatures and CO₂ pressures. Dolomite showed significantly less deactivation, compared to limestone, which can be attributed to the increase in structural stability due to the presence of MgO. The kinetics obtained in this work contribute to the design of stable SEG based on dual fluidized bed reactors, particularly to assist in the selection of calcination operating conditions to minimize sorbent deactivation and in the development of stable CO₂-sorbents. Full article

This study focused on the inhibitory effects of wheat bran feruloyl oligosaccharides (FOs) on the formation of AGEs in three bovine serum albumin (BSA)-based non-enzymatic glycation models, namely BSA-fructose, BSA-methylglyoxal (MGO), and BSA-glyoxal (GO). In the BSA-fructose model, FOs at 0.25 mg/mL achieved a 62% inhibition rate of fructosamine, equivalent to approximately 78% of the activity of the positive control aminoguanidine (AG), and reduced fluorescent AGEs by over 50% on day 12. Additionally, FOs suppressed the accumulation of α-dicarbonyl compounds, key intermediates in the glycation pathway. In the BSA-MGO and BSA-GO system, the decreased fluorescence intensity of tryptophan residues indicated that FOs bound to BSA, inducing conformational changes in the protein microenvironment; this binding also inhibited protein carbonyl formation and the loss of thiol groups, thereby modulating the protein glycation process. Compared with their precursors (ferulic acid, FA; xylooligosaccharides, XOS), FOs exhibited comparable or even superior inhibitory activity against specific AGE subtypes, suggesting a synergistic effect between the feruloyl and oligosaccharide moieties. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed that FOs reduced the band intensity of 90 kDa AGEs in the glycation system, indicating the inhibition of protein-fructose cross-linking. Fluorescence spectroscopy confirmed that FOs dynamically quenched BSA with a single binding site, and thermodynamic calculations demonstrated that the binding was spontaneous (ΔG < 0), primarily driven by hydrogen bonds and van der Waals forces (ΔH < 0, ΔS < 0). This study systematically investigated the anti-glycation activities of FOs and their precursors. The findings demonstrate that FOs are promising natural glycation inhibitors and provide important theoretical and experimental support for related research. Furthermore, this study establish a basis for the green and high-value utilization of agricultural by-products like wheat bran. Full article

Fly ash (FA) from Zhundong coal combustion features high alkali/calcium content and a low Si/Al ratio, limiting its potential for conventional utilization. To enable its high-value application, six size-fractionated samples (FA1–FA6) were characterized via laser particle sizing, SEM-EDS, XRF, XRD, FT-IR, and TGA, to elucidate particle-size-dependent physicochemical and thermal properties. The results show that the size distribution centered at 48–150 μm (~71%). With decreasing size, the morphology shifted from irregular aggregates to smooth vitreous spheres. The chemical composition exhibits significant elemental segregation; the SiO₂ content decreases with decreasing particle size, while active components such as CaO, MgO, and Fe₂O₃ are significantly enriched in fine particles. The thermal conversion behavior is regulated by particle size: The combustion reaction under an air atmosphere conforms to the second-order kinetic model, with the activation energy decreasing from 192.73 kJ·mol⁻¹ for coarse particles (>150 μm) to 63.53 kJ·mol⁻¹ for fine particles (<43 μm); under a nitrogen atmosphere, the weight loss originates from the removal of structural water and the decomposition of carbonates, and fine particles exhibit a higher pyrolysis activation energy (504.15 kJ·mol⁻¹) in the high-temperature stage (850–940 °C) due to being rich in high-crystallinity carbonates. The results of this study elucidate the structure–activity relationship of “particle size-composition-activity” for Zhundong coal fly ash and propose a graded utilization scheme where coarse fractions are suitable for low-grade building fillers, while fine fractions can be used as feedstocks for coal pyrolysis catalysts and functional adsorbents, providing a theoretical basis for its targeted resource utilization based on particle size fractionation. Full article

To meet the stringent industrial service requirements of magnesia–chrome refractory bricks, this study adopts a technical approach that synergistically combines precise component ratio optimization with a vacuum-pressure MgSO₄ salt impregnation process to investigate the performance optimization of magnesia–chrome bricks. Samples were prepared by controlled formulation mixing, pressing at 250 MPa, drying at 110 °C, and firing at 1750 °C. Phase composition, microstructure, and physical–mechanical properties were characterized by XRD, SEM, and standard refractory test methods. The optimal additions of chromite powder and Cr₂O₃ micro-powder were determined to be 3 wt.% and 2 wt.%, respectively, which reacted with periclase to form a secondary composite spinel, creating a dense spinel bridge network that connected adjacent grains. Furthermore, when the proportion of sintered magnesia powder (MgO > 97 wt.%) was increased to 11 wt.%, the material achieved efficient densification facilitated by enhancing sintering performance. Based on this optimized formulation, and due to the high elemental compatibility between MgSO₄ and the magnesia–chrome brick matrix as well as the excellent permeability of the solution, the MgSO₄ vacuum-pressure salt impregnation process was subsequently applied. The salt solution filled the open pores and microcracks of the material, forming a crystalline salt micro-pillar reinforcing phase. Consequently, the apparent porosity of the material decreased to 10.98%, the bulk density increased to 3.23 g/cm³, and the cold compressive strength and cold modulus of rupture reached as high as 113.52 MPa and 24.91 MPa, respectively. This study innovatively establishes a new pathway for enhancing the mechanical properties of magnesia–chrome refractory bricks through the synergistic design of component ratio optimization and salt impregnation process. The prepared magnesia–chrome refractory bricks exhibit both excellent mechanical properties and volume stability. Full article

The dielectric response provides an integral description of polarization mechanisms across frequency ranges and constitutes a key physical basis for understanding ferroelectric behavior. Here, we systematically investigate the broadband dielectric response of Group-II metal oxide (BeO, MgO, CaO, ZnO, and CdO) monolayers using first-principles calculation. In the low-frequency regime, ionic polarization governs the dielectric response. A distinctive feature is the LO–TO degeneracy at the Γ point accompanied by a V-shaped nonanalytic LO phonon dispersion. d-state hybridization increases with the metal atomic number, resulting in higher Born effective charge, which works together with phonon softening, reduced mass and unit cell area to significantly strengthen the ionic dielectric contribution. The quasiparticle band gap decreases with the metal atomic number, driving redshifts of the dielectric function and wide band optical response from the deep-ultraviolet to the near-infrared. Particularly, CdO exhibits the strongest electronic polarization, with an optical dielectric constant of 2.68 and a static refractive index of 1.64. This work establishes a complete dielectric spectrum from ionic to electronic polarization, providing theoretical guidance for polarization engineering and design of two-dimensional ferroelectric devices. Full article