Search Results (588)

This study explores the use of diatomite from West Kazakhstan as a silica-containing raw material for borosilicate glass production. Three glass batches, based on quartz sand, chalk, and diatomite, were synthesized with varying ratios of network-forming and modifying oxides. Partial replacement of quartz sand with diatomite enabled glass melting at 1150 °C, producing a homogeneous melt. Glasses with higher diatomite content showed improved chemical and water resistance; specifically, the sample containing 52% diatomite achieved hydrolytic class III and water resistance class IV (XA = 1.0 cm³·g⁻¹), whereas quartz-based control samples corresponded to classes IV–V. Heat resistance ranged from 120 to 160 °C depending on composition. These findings demonstrate that amorphous SiO₂ and active oxides in diatomite promote a stronger three-dimensional glass network, highlighting the potential of locally sourced diatomite as an alternative SiO₂ source for sustainable, energy-efficient borosilicate glass production. Full article

Calcium–silicate–hydrate (C-S-H), the primary binding phase governing cement paste cohesion, undergoes progressive physicochemical transformation upon carbonation—a process that critically dictates concrete durability in atmospheric environments. When CO₂ penetrates the porous cement matrix, it triggers a cascade of degradation mechanisms: calcium leaching decalcifies the C-S-H structure, inducing polymerization of silicate chains from dimeric to longer-chain configurations, while concurrent precipitation of calcium carbonate and amorphous silica gel fundamentally reconstitutes the nanoscale architecture. These nanoscale alterations propagate to macroscopic property evolution, manifesting as initial strength and stiffness gains due to pore-filling carbonation products followed by eventual deterioration as the cohesive binding network deteriorates. This review synthesizes current understanding of carbonation-induced structural evolution, examining the coupled influences of environmental parameters—CO₂ concentration, relative humidity, and temperature—alongside C-S-H intrinsic chemistry (Ca/Si ratio, aluminum substitution, and alkali content) on reaction kinetics and material performance. However, significant knowledge gaps persist: predictive models for in-service carbonation rates remain elusive due to the disconnect between idealized laboratory conditions and the heterogeneous, cracked reality of field concrete; the causal linkage between nanoscale C-S-H alteration and macroscale cracking patterns along with physical performance is poorly resolved, and most mechanistic studies rely on synthetic C-S-H, neglecting the compositional complexity of real Portland cement systems. We further propose emerging protection strategies, including surface barrier coatings and low-carbon alternative binders (geopolymers, calcium sulfoaluminate cements, carbon-negative materials such as recycled cement), which demonstrate enhanced carbonation resistance. Future research priorities include developing effective coating barriers for carbonation protection, developing operando characterization techniques for real-time reaction monitoring, deploying machine learning algorithms to bridge atomistic simulations with structural-scale predictions, and establishing long-term field performance databases to validate laboratory-derived degradation models. Full article

Second harmonic (SH) radiation can only be generated in non-centrosymmetric bulk crystals under electric dipole approximation. Nonlinear thin films made from bulk crystals are technologically challenging because of complex and high-temperature fabrication processes. In this work, heterostructures made of two distinct amorphous materials, namely SiO₂ and TiO₂, were prepared through plasma-enhanced atomic layer deposition (PEALD) with deposition temperature of 100 °C. By using the uniaxial dispersion model, we characterized the form birefringence of the deposited films, which can play a crucial role for the phase-matching condition in nonlinear waveguides or other nonlinear optical applications. By applying a fringe-based technique, we determined the largest diagonal component of the effective bulk second-order susceptibility, ${\chi }_{zzz}^{\left(2\right)}$ = 1.30 ± 0.13 pm/V, at a wavelength of 1032 nm. Noteworthy, we observed strong SHG signals from two-component nanolaminates, which are several orders of magnitude larger than those from single layers. The SHG signals from our samples only require the broken inversion symmetry at the interface. Here, optical properties of nanocomposites can be precisely engineered using the promising PEALD technology. Full article

The transition toward low-carbon and resource-efficient construction materials has intensified interest in geopolymer binders incorporating industrial and post-consumer wastes. Waste glass powder (WGP), a silica-rich component of the global glass waste stream, has emerged as a promising circular-economy precursor in alkali-activated systems; however, reported durability trends remain inconsistent and are often interpreted without mechanistic integration. This review synthesises current knowledge of WGP reactivity, gel chemistry, and long-term performance through an explicit reaction–transport–ageing (R–T–A) framework that links dissolution behaviour and phase assemblage development to pore connectivity, ion ingress, and time-dependent degradation. Under alkaline activation, the amorphous structure of WGP promotes silica release, modifying Si/Al ratios and governing the formation of N-A-S-H or hybrid N-A-S-H/C-(A)-S-H gels. These reaction products determine transport characteristics and ageing evolution, which collectively control chemical resistance, chloride ingress, alkali–silica reaction-type instability, and dimensional stability. Variability across studies is shown to arise from imbalances in particle fineness, replacement level, precursor chemistry, and activator design rather than intrinsic inconsistency in WGP behaviour. The R–T–A framework clarifies how reaction completeness, pore network architecture, and long-term phase stability interact to produce system-dependent durability outcomes. WGP demonstrates strong potential as a circular-economy precursor in alkali-activated binders; however, reliable structural application requires durability-informed mix design grounded in coupled reaction–transport–ageing mechanisms and supported by extended exposure testing under realistic service conditions. Full article

The accumulation of copper smelting slags generated by non-ferrous metallurgy represents both an environmental challenge and a potential source of technogenic raw materials for value-added products. In this study, the feasibility of producing magnesia–quartz proppants from secondary copper smelting slag formed after the pyrometallurgical extraction of iron and zinc was investigated. The slag, primarily composed of oxides of the SiO₂–CaO–Al₂O₃–MgO system, was processed by centrifugal melt granulation to obtain spherical granules suitable for proppant applications. The initial granules exhibited an amorphous glassy structure and insufficient mechanical strength, with up to 70% of particles destroyed under a pressure of 34.5 MPa. Controlled heat treatment within the temperature range of 300–1000 °C induced crystallization of silicate and aluminosilicate phases, leading to a significant improvement in mechanical performance. Optimal properties were achieved after holding at 800 °C for 60 min, where the fraction of crushed granules decreased to 10%, meeting the requirements of GOST R 54571-2011. The influence of MgO content on microstructure and strength was also examined. Increasing the MgO concentration from 5 to 16 wt.% resulted in grain refinement and improved crushing resistance, reducing the fraction of destroyed granules to 3%. To enhance chemical durability, a phenol–formaldehyde protective coating was applied, decreasing proppant solubility in a hydrochloric–hydrofluoric acid mixture from 19% to 2%. These results demonstrate that secondary copper smelting slag can serve as a promising raw material for producing standard-compliant proppants while contributing to the efficient utilization of metallurgical waste. Full article

This work investigates the potential of wollastonite-based brushite cement (WBC) for the stabilization and solidification of radioactive waste contaminated by ⁹⁰Sr. This phosphate binder was formed by the reaction of wollastonite (CaSiO₃) with a phosphoric acid solution containing borax and metallic cations (Al³⁺, Zn²⁺). Two cement pastes were investigated: a commercial binder (WBC-C) and an optimized formulation (WBC-O), produced using a zinc-free mixing solution with a higher aluminum content than that of WBC-C. Mineralogical characterizations using XRD, TGA, XRF, SEM-EDX, and Raman spectroscopy showed that both materials mainly contained amorphous hydrated silica and calcium aluminophosphate, along with crystalline brushite, residual wollastonite, and quartz. The stability of WBC-C under γ-irradiation was evaluated up to a dose of 1 MGy. The only observable effect was water radiolysis, leading to dihydrogen production at yields comparable to Portland cement matrices and geopolymers. Strontium leaching, assessed using the ANSI/ANS-16.1-2003 (R2008) procedure, followed a two-stage release mechanism combining surface wash-off and diffusion. The apparent diffusion coefficient D_a of Sr in WBC-C was markedly lower than typical values reported for Portland cement matrices. WBC-O exhibited enhanced Sr retention, possibly due to its higher aluminum content, which refines mesopores and reduces diffusion pathways accessible to Sr. WBC binders therefore appear to be promising candidates for strontium immobilization. Full article

Neural interfaces created using thin-film fabrication rely primarily on conductive metal traces for electrical interconnects. Here, we explore the use of tantalum (Ta) metal interconnects as a replacement for noble-metal interconnects such as Au, Pt or Ir. Ta has been investigated previously for interconnect metallization in flexible silicon ribbon cables, but the structure and properties of tantalum for neural device metallization have not been extensively reported. In the present work, Ta metal was sputter-deposited onto amorphous silicon carbide (a-SiC), with and without a base titanium (Ti) adhesion layer, and investigated as interconnect metallization. In the absence of a Ti adhesion layer, resistivity measurements revealed a factor of six difference between Ta resistivity depending on the presence of the Ti base layer, with direct deposition on a-SiC nucleating high resistivity β-Ta (ρ = 197 ± 31 µΩ·cm, mean ± standard deviation) and Ta deposited on Ti nucleating low resistivity α-Ta (ρ = 35 ± 6 µΩ·cm). X-ray diffraction confirmed the existence of the two crystal structures. Ta feature sizes of 2 µm were created using photolithography and reactive ion etching (RIE). Finally, planar microelectrode array test structures using α-Ta and Au trace metallization with low-impedance ruthenium oxide (RuO_x) electrodes were fabricated and investigated by cyclic voltammetry (CV) and current pulsing in saline. These devices underwent 500 CV cycles between −0.6 and +0.6 V without evidence of degradation. In response to charge-balanced, biphasic current pulses at 4 nC/phase, a 21 mV increase in access voltage was observed with α-Ta metallization compared to Au. These results warrant further investigation of Ta as thin-film metallization interconnects for neural interface devices. Full article

Iron ore tailings have been shown to promote the formation of soil aggregate cementing agents through weathering, thereby influencing soil aggregate formation in reclaimed land. However, their mechanism of action under different reclamation methods remains unclear. This study established a field station in the semi-arid region of Northern China to investigate three typical iron ore tailing reclamation methods, including topsoil blending type (DT), sublayer moisture conservation type (JT), and thick-layer tailings type (FT), with adjacent farmland as the control (CK). The analysis of soil organic carbon (SOC) components, soil inorganic carbon (SIC), iron/aluminum oxides, and aggregate composition and stability in the reclaimed soils revealed the evolution patterns of cementing materials and the potential mechanisms driving aggregate formation. The results indicate that the reclamation process promotes the weathering of tailings, with a significant increase in free iron oxide (Fed) content ranging from 19.09% to 41.93%. Iron oxides released from iron ore tailings influenced the reclaimed topsoil through plant litter return processes, resulting in a significantly higher amorphous iron oxide (Feo) content compared to CK. Additionally, the content of crystalline aluminum oxide (Alc) in the DT topsoil showed a significant increase, reaching 2.82 g/kg. The variation in organic and inorganic cementing agents significantly influences aggregate composition and stability, with soil particulate organic carbon (POC), crystalline iron oxide (Fec), Alc, and amorphous aluminum oxide (Alo) identified as the primary agents affecting aggregate formation (p < 0.05). After five years of reclamation, the proportion of DT macroaggregates (>0.25 mm) increased to 42.10%, and both the mean weight diameter (MWD) and the geometric mean diameter (GMD) increased significantly to 2.21 mm and 0.43 mm, respectively. In contrast, JT macroaggregates and microaggregates (0.053–0.25 mm) decreased to 26.88% and 29.01%, respectively, and aggregate stability significantly declined. FT macroaggregates and their stability showed no significant difference compared to CK. The study shows that after years of reclamation, both DT and FT reclamation methods have reached normal farmland levels in terms of aggregate formation and stability, making them practical and valuable reclamation solutions. Full article

This study investigates the deposition of amorphous silicon carbon nitride (a-SiCN) films using a microwave sheath–voltage combination plasma (MVP) source under duty-cycle-controlled deposition conditions. Duty ratios of 10, 30, 50, and 70% resulted in substrate temperatures of 180, 600, 980, and 1040 °C, respectively. The deposition rate reached a maximum of approximately 208 μm/h at a duty ratio of 30%. The atomic ratios of C, N, and Si remained nearly constant for duty ratios from 30% to 70%. X-ray diffraction confirmed that all films were amorphous. Raman spectra revealed features characteristic of amorphous carbon (a-C) for duty ratios of 30% or higher, suggesting the incorporation of a-C-like structures into the a-SiCN matrix. The film hardness increased as the duty-cycle-controlled deposition conditions shifted from 10% to 50% (180 to 980 °C), reaching a maximum of 22.65 ± 6.78 GPa at a duty ratio of 50%, and then decreased at 70% (1040 °C). These variations in hardness are suggested to be associated with coupled changes in hydrogen incorporation, C–N bonding, and the evolution of sp²-rich carbon clustering (graphite-like short-range ordering) under elevated temperature and ion-bombardment conditions. Full article

A microwave–hydrothermal (M-H) method was developed for synthesizing barium silicate from solutions of barium salts and sodium silicate. Advanced techniques (DTA, XRD, IR spectroscopy, SEM and TEM) were used to study the optical, granulometric, electrical and other functional characteristics of barium silicate. BaSiO₃ synthesized at 100 °C is an amorphous nano-sized powder (10–20 nm); however, the product synthesized at 240 °C has a crystalline structure (20–27 nm), whereas the crystalline phase of BaSiO₃ is typically obtained using known methods at temperatures above 400 °C (12–40 nm). During M-H synthesis, it was found that the structure formation mechanism and particle size of BaSiO₃ changed due to the peculiar features of microwave heating. The synthesized barium metasilicate exhibits a high diffuse reflectance coefficient of 92%. It is a wide-band-gap semiconductor with a band gap width of Eg = 4.1 eV. Both amorphous and crystalline phases of BaSiO₃ exhibit high photocatalytic activity in the UV range. This study shows that the developed M-H method enables the production of nano-sized powder and enhances the functional properties of barium silicate. Compared with conventional methods, the M-H method is more efficient due to reduced synthesis time and lower energy costs. Full article

The influence of Zn²⁺, Ca²⁺ and Co²⁺ doping on the thermal, structural, morphological, and magnetic characteristics of CdBi_0.1Fe_1.9O₄ nanoparticles synthetized via the sol–gel technique and calcined at 300, 600, 900 and 1200 °C was investigated. Thermal analysis revealed the initial formation of metallic glyoxylates up to 300 °C, followed by their decomposition into metal oxides and subsequent ferrite formation. X-ray diffraction revealed that the ferrites were poorly crystallized at lower temperatures, whereas at higher calcination temperatures all nanocomposites exhibited well-crystalized ferrites coexisting with the SiO₂ matrix, except for the Co_0.1Cd_0.9Bi_0.1Fe_1.9O₄@SiO₂ nanocomposite, which formed a single, well-defined crystalline phase. Atomic force microscopy images revealed spherical ferrite particles encapsulated within an amorphous layer, with particle size, surface area, and coating thickness influenced by both the type of dopant ion and the calcination temperature. The structural parameters estimated by X-ray diffraction, as well as the magnetic characteristics, were strongly influenced by the dopant type and thermal treatment. These results demonstrate that the structural and magnetic characteristics of CdBi₀.₁Fe₁.₉O₄ ferrites can be effectively tuned through controlled doping and calcination, providing insights for the design of tailored functional applications. Full article

In this study, we investigated the electrochemical properties and performance characteristics of Co_xS_y and silicon–carbon-based heterostructures synthesized on nickel foam substrates for energy storage applications. Cobalt sulfide films were successfully electrodeposited on nickel foam (NF) using cyclic voltammetry (CV) from the solutions with different Co²⁺ concentrations. The presence of a silicon–carbon sublayer promotes the deposition of cobalt sulfide material. The amorphous phase of α-CoS was observed by the X-ray diffraction technique. Raman spectroscopy confirmed the formation of CoS and CoS₂ phases. A significant increase in electrode areal capacitance is observed with the silicon–carbon film sublayer from 0.5 to 1.3 F·cm⁻² and from 1.6 to 2.3 F·cm⁻² at 3 mA·cm⁻² for samples prepared from solutions with CoCl₂·6H₂O concentrations of 0.005 M and 0.02 M, respectively. In the case of gravimetric capacitance, an increase is observed in the presence of a silicon–carbon sublayer for the SiC@CoS_0.005 sample, rising from 690 F·g⁻¹ to 748 F·g⁻¹ at 4 A·g⁻¹. Conversely, the SiC@CoS_0.02 sample shows a decrease from 1287 F·g⁻¹ to 6590 F·g⁻¹. It was shown that the capacitance of all the electrodes derives from the mix of diffusion-controlled and surface-controlled capacitance processes. The electrochemical impedance spectroscopy (EIS) analysis indicates that the formation of heterostructure materials significantly alters the electrochemical properties by reducing both R_f and R_s. Full article

Valorizing construction and demolition waste (CDW) via alkaline activation enables low-carbon binders. This study assesses binary geopolymers formulated with recycled brick powder (PLR) and recycled concrete powder (PCR) in seven precursor ratios (0–100% PCR), activated with a ternary NaOH/Na₂SiO₃/KOH solution (silicate modulus M_s ≈ 3.2) at L/B = 0.15, and cured for 7, 14, and 28 days. Compressive strength (fc), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS) were used to link microstructure–phases–properties. A local maximum in fc at ~30% PCR (16.2 MPa at 28 d) was observed versus 0% PCR (14.2 MPa) and ≥50% PCR (13.8 → 10.1 MPa at 28 d). XRD indicated a reduction in inherited crystalline phases and an increased amorphous fraction at ~30% PCR; FTIR (normalized peak position and FWHM of the T–O–Si band, not absolute intensity) suggested higher network extension; SEM-EDS (local/semiquantitative) showed a moderate rise in Ca that supports C-A-S-H domains bridging the N-A-S-H network. At a high PCR, excess Ca simplified mineralogy (quartz/portlandite dominance), promoted competitive routes (C-S-H/carbonation), reintroduced microdefects, and reduced fc. A theoretical oxide balance per mix identified a compositional window where Ca/(Si + Al) ≈ 0.35–0.45 coincides with the mechanical optimum and with XRD/FTIR tracers. Overall, a ~30% PCR window maximizes co-reticulation of N-A-S-H/C-A-S-H and densification without compromising aluminosilicate continuity, providing transferrable design and process-control criteria for CDW-based geopolymer binders. Full article

Fe-based metallic glasses are ideal candidates to be utilized in transformer cores owing to their outstanding soft magnetic properties. However, they are difficult to machine properly by conventional means due to their mechanical brittleness and poor thermal conductivity. Here, the cutting of Fe₉₁–Si_4.5–C_4.0–Al_0.5 amorphous alloy ribbons is reported with a sub-50 fs laser pulses. A systematic study is performed on local morphological and chemical composition changes to the machined edge in comparison to crystalline metals. It is shown that only the innermost 80 $\mu$m wide region of the cut edge shows any detectable modifications, which is much less than for continuous laser machining. Therefore, the proposed method is indeed a valuable approach to overcome the fine machining difficulties of metallic glasses. Full article

This study systematically examines the fluidity, setting time, mechanical properties, and microstructural evolution of metakaolin-based geopolymer grouting materials with a relatively high water-to-solid (W/S) ratio window. A four-factor, three-level orthogonal experimental design was employed to identify the dominant factors and main effect trends of W/S ratio, alkali dosage, water glass modulus (Ms, molar ratio of SiO₂ to Na₂O in alkali solution), and steel slag content on the material’s performance. The results indicated that the W/S ratio predominantly governed fluidity, while the alkali content was the primary controlling factor for setting time and early-age strength. An intermediate range of water glass modulus with a value of 1.6 provided balanced performance. The incorporation of steel slag with a range of 10–20% showed an age-dependent contribution: it not only tended to improve the rheology of the paste but also the later-age strength. XRD, FTIR, and SEM/EDS results suggested that the hardened binders were dominated by amorphous products, where alumimosilicate gel (N-A-S-H) and Ca-containing gel (C-S-H/C-A-S-H) may coexist depending on calcium availability and activator chemistry. The proposed parameter ranges are valid within the studied design space and provide guidance for the mix design of high-W/S geopolymer grout. Full article