Addition Of SiO2 Research Articles

Structural Features Investigation of a Highly Dispersed NiO–SiO<sub>2</sub> Catalyst by X-Ray Analysis of the Atomic Pair Distribution Function

In the present work NiO and NiO–SiO2 were investigated by X-ray diffraction and radial atomic pair distribution methods. By X-ray diffraction method, it was determined that the NiO particle sizes have coherent scattering region of more than 100 nm, while the NiO–SiO2 sample has a particle size of about 2–3 nm. At the same time, full-profile Rietveld simulation does not describe the effects observed on diffraction: the asymmetry of peaks, the appearance of an additional shoulder of peak 111 in the area of small angles, so the radial atomic pair distribution method was used to analyze the structure. During the simulation of the experimental atomic pair distribution curve, 3 different models were used: pure NiO, a mixture of NiO and Ni2SiO4, and a modified NiO model with Si embedded in the lattice. The latter model was created based on the assumption of silicon incorporation into the NiO structure, which can be evidenced by X-ray diffraction data. According to the results of radial atomic pair distribution modeling it is the latter model that gives the best description of the observed effects: significantly increased unit cell parameter, compared to the sample without SiO2 addition, as well as decreased metal cation–oxygen distances in the structure, while cation–cation distances are increased.

Preparation and properties of bio-based PA56/SiO2–NH2 composite nanofiber membranes for high efficiency oil-water separation

With the continuous development of environmental protection and resource recycling demands, the development of bio-based separation membrane materials has increasingly attracted attention. Bio-based polyamide 56 (PA56), exhibiting excellent hydrophilicity, spinnability, and mechanical properties, is expected to complement and replace traditional separation membrane materials. In this study, the electrospinning preparation and structural control of PA56 nanofiber membranes were achieved through the optimization of PA56 content and mixed solvent ratios. The study found that when the PA56 content was 16 wt% and the formic acid to acetone ratio in the mixed solvent was 8:2, the nanofiber diameter distribution was the most uniform. Building on this, amino-functionalized modified silica (SiO2–NH2) nanoparticles were introduced to prepare PA56/SiO2–NH2 composite nanofiber membranes featuring a cobweb-like nanofiber network and micro-nodule structure. The effects of the addition of SiO2–NH2 nanoparticles on the morphology, structure, and properties of the fiber membranes were studied. The results indicate that the control of the mixed solvent ratio and the addition of SiO2–NH2 nanoparticles led to the formation of a cobweb-like nanofiber network and micro-nano nodular structure on the nanofiber surface, enhancing the hydrophilicity of PA56 nanofiber membranes. The M − 3 membrane with a nanoparticle addition amount of 0.8 wt% exhibited high hydrophilicity and underwater superoleophobic properties, achieving efficient separation of stable oil-in-water emulsions with a separation efficiency of 99.8 %. This work provides a new bio-based membrane material and its preparation method for treating oily wastewater using the membrane separation method.

Study on the mechanism of vacuum carbothermal reduction of Ca3(PO4)2 enhanced by SiO2

Vacuum carbothermal reduction mechanism of Ca3(PO4)2 with addition SiO2 was studied by combining FactSage 8.1 thermodynamic theoretical calculations with experiments. The theoretical calculations showed that adding SiO2 effectively reduced the initial reaction temperature. The experimental results showed that the addition of SiO2 significantly improved weight loss and volatilization rates of phosphorus. Ca2SiO4 and CaSiO3 were generated during the reaction. When the SiO2/CaO ratio was 1.25 at 1300 °C, the reduction effect of Ca3(PO4)2 and the volatilization rate of phosphorus was optimal, with a volatilization rate of 91.98 %. Excessive SiO2 led to insufficient contact between the reactants and reducing agent C, thereby hindering the reaction. Simultaneously, a large amount of liquid phase was produced, which deteriorated the kinetic conditions of gas diffusion and affected the reaction. In the reduction process, Ca3(PO4)2 reacted with reducing agent C to generate CaO, then reacted with external SiO2 to generate low melting point CaSiO3, which wrapped the unreacted core. With an increase in the low melting point CaSiO3, the mass transfer in the reaction changed from diffusion mass transfer to flow mass transfer, which promoted the inward diffusion of reducing agent C to contact the unreacted core until the reduction reaction was completed.

Study on the effect of particles in oilfield produced water on the deposition process of CaCO3

In crude oil production, scale deposition significantly reduces production output and elevates operational costs, posing a severe threat to production safety. While chemical methods have been extensively explored for the scaling and inhibition of inorganic salts, the inorganic scaling triggered by solid particle scaling in complex oilfield water has largely been overlooked. This study involves the introduction of particles into a supersaturated CaCO3 solution, utilizing static scale inhibition and conductivity techniques to examine their influence on the scaling process and crystallization rate. It is evident that solid particles expedite the deposition process of CaCO3. Moreover, the deposition rate of CaCO3 is influenced by factors such as the solid particle content, particle size, and stirring speed. It is noteworthy that the presence of solid particles solely impacts the formation rate of CaCO3 crystals, without altering the total deposition. Specifically, under conditions of 70°C, 250/min stirring speed, and 0.08% SiO2 addition, the deposition rate of CaCO3 is enhanced by 13.5%. The nucleus growth rate constant increases from 11.10 × 10-3min-1 to 14.52 × 10-3min-1 and the crystal growth rate constant increases from 3.02 × 10-3min-1 to 3.36 × 10-3min-1 at most. Observations made through scanning electron microscopy (SEM) and polarized light microscopy reveal that scaling occurs predominantly on the added solid particles in later stages, indicating that solid particles in supersaturated solutions serve as crystal nuclei, inducing the growth of CaCO3 crystals and thus accelerating scaling. This research provides valuable insights for the study of scaling in complex water environments.

Engineering the meta-phosphate BaO–Al2O3–P2O5 glass network for high average power (HAP) laser applications: Systematic composition modifications and SiO2 integration

The metaphosphate glasses are the preferred gain media for high-power solid-state laser applications. In the context of solid-state glass lasers, the main challenge to attain high average power (HAP) is to govern excessive thermal loading during operation. This work focuses on addressing thermal loading issues through improving thermal and mechanical properties of the meta-phosphate BaO–Al2O3–P2O5 laser glass system by engineering its molecular structure through systematic composition modifications with SiO2 incorporation. FTIR, Raman and 27Al MAS-NMR spectroscopy indicate stronger P–O–P bridges with decreasing glass basicity and increasing [AlO4] formations beyond 12.5 mol% Al2O3. The O/P ratio increases from 3.05 to 3.43 with up to 20 mol% SiO2 in Series-A and from 3.13 to 3.49 with up to 15 mol% SiO2 in Series-B, altering the Al coordination number from 6 to 4 to maintain the glass network charge balance. Increased [AlO4] formation raises Young's modulus from 61 GPa to 73 GPa and decreases Poisson's ratio from 0.30 to 0.24. These changes enhance fracture toughness and reduce CTE. Further, SiO2 inclusion enhances thermal conductivity by increasing glass network compactness and rigidity. These modifications highlight the improved thermo-mechanical properties of the SiO2-modified Series-B glasses. Yb3+ emission cross-section rises from 0.495 × 10−20 cm2 in ABSP-A1 glass to 0.502 × 10−20 cm2 in ABSP-B1 with increased [AlO4] formation. More AlPO4-like units in ABSP-B1 increase average glass phonon energy, reducing Yb3+ fluorescence lifetime from 1062 μs to 945 μs, whereas SiO2 addition boosts Yb3+ fluorescence lifetime again. Lower OH− content further extends Yb3+ fluorescence lifetime in Series-B glasses with higher SiO2 content. This study underscores the intricate relationship between glass molecular structure and thermal, mechanical, and spectroscopic properties, advancing high-power silico-phosphate laser glass development.

The Influence of Ag Addition and Different SiO2 Precursors on the Structure of Silica Thin Films Synthesized by the Sol-Gel Method.

In this work, the structure of silica thin films synthesized with three different SiO2 precursors and obtained by the sol-gel method and dip coating technique was studied. Additionally, the influence of Ag addition on the obtained silica sols and then gel structure was investigated. Silica coatings show antireflective properties and high thermal resistance, as well as hydrophobic or hydrophilic properties. Three different silica precursors, TEOS (tetraethylorthosilicate), DDS (dimethyldietoxysilane) and AerosilTM, were selected for the synthesis. DDS added to silica sol act as a pore size modifier, while Ag atoms are known for their antibacterial activity. Coatings were deposited on two different substrates: steel and titanium, dried and annealed at 500 °C in air (steel substrate) and in argon (titanium substrate). For all synthesized films, IR (infrared) spectroscopic studies were performed together with GID and XRD (Grazing Incidence Diffraction, X-ray Diffraction) measurements. The topography and morphology of the surface were traced by SEM and AFM microscopic methods, providing information on the samples' roughness, particle sizes and thickness of the particular layers. The wetting angle values were also measured. GID and XRD measurements pointed to the distinct contribution of an amorphous phase in the samples, allowing us to recognize the crystalline phases and calculate the silver crystallite sizes. The FTIR spectra gave information on the first coordination sphere of the studied samples.

Preparation and Photocatalytic Properties of Al2O3-SiO2-TiO2 Porous Composite Semiconductor Ceramics.

Titanium dioxide (TiO2) is widely employed in the catalytic degradation of wastewater, owing to its robust stability, superior photocatalytic efficiency, and cost-effectiveness. Nonetheless, isolating the fine particulate photocatalysts from the solution post-reaction poses a significant challenge in practical photocatalytic processes. Furthermore, these particles have a tendency to agglomerate into larger clusters, which diminishes their stability. To address this issue, the present study has developed Al2O3-SiO2-TiO2 composite semiconductor porous ceramics and has systematically explored the influence of Al2O3 and SiO2 on the structure and properties of TiO2 porous ceramics. The findings reveal that the incorporation of Al2O3 augments the open porosity of the ceramics and inhibits the aggregation of TiO2, thereby increasing the catalytic site and improving the light absorption capacity. On the other hand, the addition of SiO2 enhances the bending strength of the ceramics and inhibits the conversion of anatase to rutile, thereby further enhancing its photocatalytic activity. Consequently, at an optimal composition of 55 wt.% Al2O3, 40 wt.% TiO2, and 5 wt.% SiO2, the resulting porous ceramics exhibit a methylene blue removal rate of 91.50%, and even after undergoing five cycles of testing, their catalytic efficiency remains approximately 83.82%. These outcomes underscore the exceptional photocatalytic degradation efficiency, recyclability, and reusability of the Al2O3-SiO2-TiO2 porous ceramics, suggesting their substantial potential for application in the treatment of dye wastewater, especially for the removal of methylene blue.

Fabrication of Hybrid Epoxy Composites (Joint Compound Adhesive) for Aluminum Substrate Applications and Their Evaluation for Mechanical Properties.

This research endeavor deals with the development of an epoxy hybrid nanocomposite using aliphatic diglycidyl ether of a bisphenol A (DGEBA) epoxy matrix. The formulation used the stoichiometric ratio of the curing agent and incorporated nanopigments such as zirconium and silica, along with other microfillers. We incorporated Zr and SiO2 nanoparticles and various other additives in the epoxy matrix and ensured homogeneous dispersion by using sonication methodology along with silane as a coupling agent. Aluminum molds were utilized to fabricate dumbbell-shaped ASTM standard samples for the testing of mechanical properties. The adhesive properties were evaluated through standard lap shear tests. Fourier transform infrared spectroscopy was utilized to analyze the cross-linking reaction of the epoxy moiety and the polyamidoamine adduct curing agent. Further characterization using field emission scanning electron microscopy, energy-dispersive spectroscopy, and high-resolution transmission electron microscopy confirmed the presence and uniform dispersion of the fillers and nanopigments. The results showed good enhancements in ultimate tensile strength, yield strength, and elastic modulus of 95.3, 162.1, and 425.4%, respectively, compared to formulations using only SiO2. The addition of ZrO2 and SiO2, along with various microfillers, such as talc and aluminum silicate, led to significant improvements in the mechanical properties. This study demonstrates the synergistic efficiency of combining SiO2 and ZrO2 along with microfillers, such as talc and aluminum silicate, in epoxy resin for diverse applications in the construction industry, where mechanical strength and substrate adhesion are crucial.

Immobilization of heavy metals with chlorine and liquid phase formation during thermal treatment of MSWI fly ash

Due to effective detoxification, thermal treatment is a preferred treatment technology of municipal solid waste incineration (MSWI) fly ash. However, immobilization behavior of heavy metals during thermal treatment is unclear. In this work, a circulated fluidized bed fly ash with SiO2 addition and a grate furnace fly ash with high silica-aluminum coal ash addition were used to investigate combined effect of active chlorine content, liquid polymerization degree, temperature of initial liquid phase formation and liquid phase formation rate on the immobilization ratios of Zn, Pb and Cd by principle component analysis (PCA). The results show that the decrease in active chlorine content favors the immobilization of Zn, Pb and Cd because chlorination volatilization is reduced. Both the increase in liquid polymerization degree and the formation of initial liquid phase at low temperature promote the immobilization of Zn, Pb and Cd for physical encapsulation. However, a rapid formation of liquid phase is not favorable for the immobilization of Zn, Pb and Cd, because transfer of heavy metals between crystals and liquid phase is impeded by high viscosity of liquid phase during fusion. The results can provide a reference for how to achieve the immobilization of heavy metals by adjusting the chemical composition of MSWI fly ash during thermal treatment.

Investigation on the radiative characteristics of ZnO-SiO2 nanofluids in spectral splitting photovoltaic/thermal systems

The application of nanofluid spectral splitting technology in photovoltaic/thermal (PV/T) systems has attracted more attention. In this study, zinc oxide and silica nanoparticles were selected to prepare ZnO-SiO2-H2O mixed nanofluids with different concentrations to investigate the radiative characteristics and their effect on PV/T system. An experimental system was established to measure nanofluids transmission properties in 0.36–2.5 μm, and the radiation characteristics were further analyzed using Mie scattering theoretical model. Besides, thermodynamic model was established to investigate the influence of mixed nanofluids on PV/T system performance. Results indicate that Mie theory can predict the radiative properties of mixed nanofluids well. The ZnO-SiO2-H2O nanofluids have better filtering performance than that of ZnO-H2O nanofluids under same particle concentration. When the mass ratio of ZnO/SiO2 is 0.01 %/0.05 %, the filtering efficiency of the nanofluid achieves 46.18 %. Increasing the concentration of SiO2 can regulate the transmittance of the ZnO-SiO2-H2O nanofluids and improve the PV/T system efficiency by 5 %. Based on ZnO nanofluids, the addition of SiO2 further optimizes PV/T system performance, increasing the system merit function (MF) value The nanofluid spectral splitting PV/T system for Si cells with a ZnO/SiO2 mass ratio of 0.003 %/0.056 % can reach a MF value of 1.342.

Recycling devulcanized EPDM to improve engineering properties of SBR rubber compounds

Ethylene propylene diene rubbers (EPDM) have gained substantial attention in automotive and industrial applications owing to their exceptional resistance against weathering and heat. Despite their advantages, the elastomeric nature of EPDM poses challenges in its recycling due to the presence of crosslinks in their chemical structure, preventing them from melting. To overcome this issue, devulcanized EPDM (EPDMd) has been developed, characterized by the effective breaking of these crosslinks. Our study focuses on common composites that include Styrene Butadiene Rubber (SBR), EPDM and silica, but with the incorporation of devulcanized EPDM (EPDMd).We have studied the mechanical, thermal, structural and dielectric properties of SBR composites containing EPDMd at variable compositions (0, 20, 40, 50, 60 phr). Employing techniques such as Thermogravimetric Analysis (TGA), Fourier Transform Infrared Spectropy (FTIR), and Scanning Electronic Microscopy (SEM), we have explored the microstructural changes driving the macroscopic effects on the measured properties.The results show that incorporating EPDMd improves the crosslinking degree and, at optimal 40 phr loading, significantly increases the mechanical properties of SBR matrix. The addition of SiO2, in general, reduce tensile strength and elongation, while increasing the Young's modulus, except for compositions around 40 phr EPDMd. The dielectric measurements are in concordance with the previous data, showing a moderation of the Maxwell–Wagner–Sillars (MWS) effect due to SiO2 in highly filled EPDMd composites at 40 phr EPDMd.

Molecular dynamics simulation on the variations in characteristics of aqueous solution with diverse additives: Inspirations for binary ice preparation

Ice slurry, as a novel energy storage medium, possesses the superiority of high energy storage density. The freezing point inhibitors are employed to regulate the supercooling phenomenon of water, while the macroscopic experiments are complicated to elucidate the action mechanism. Consequently, this paper adopts molecular dynamic simulation method to investigate the mean square displacement, radial distribution function, hydrogen bonds types, hydrogen bonds number and length of water at various concentrations of ethanol, NaCl, and SiO2 additives. The results indicate that the average number of hydrogen bonds of the system composed with 600 pure water molecules is 1127.24, and the average length of hydrogen bonds is 2.33 Å. Moreover, the addition of alcoholics and chlorides inhibits the hydrogen bonds between water and water molecules, and promotes the generation of hydrogen bonds, thus weakening the diffusion motion of water molecules. Whereas, it is observed that the addition of nanoparticles leads to agglomeration in pure water system, resulting an increase in the viscosity and a decrease in the diffusion rate of the system. The proposed microscopic model can effectively depict the potential interaction mechanisms of additives and water, which is contributing to develop effective freezing point inhibitors and improve the energy utilization efficiency.

Influence of SiO2 Nanoparticles Extracted from Biomass on the Properties of Electrodeposited Ni Matrix Composite Films on Si(100) Substrate.

Lab-made biosilica (SiO2) nanoparticles were obtained from waste biomass (rice husks) and used as eco-friendly fillers in the production of nickel matrix composite films via the co-electrodeposition technique. The produced biosilica nanoparticles were characterized using XRD, FTIR, and FE-SEM/EDS. Amorphous nano-sized biosilica particles with a high SiO2 content were obtained. Various current regimes of electrodeposition, such as direct current (DC), pulsating current (PC), and reversing current (RC) regimes, were applied for the fabrication of Ni and Ni/SiO2 films from a sulfamate electrolyte. Ni films electrodeposited with or without 1.0 wt.% biosilica nanoparticles in the electrolyte were characterized using FE-SEM/EDS (morphology/elemental analyses, roundness), AFM (roughness), Vickers microindentation (microhardness), and sheet resistance. Due to the incorporation of SiO2 nanoparticles, the Ni/SiO2 films were coarser than those obtained from the pure sulfamate electrolyte. The addition of SiO2 to the sulfamate electrolyte also caused an increase in the roughness and electrical conductivity of the Ni films. The surface roughness values of the Ni/SiO2 films were approximately 44.0%, 48.8%, and 68.3% larger than those obtained for the pure Ni films produced using the DC, PC, and RC regimes, respectively. The microhardness of the Ni and Ni/SiO2 films was assessed using the Chen-Gao (C-G) composite hardness model, and it was shown that the obtained Ni/SiO2 films had a higher hardness than the pure Ni films. Depending on the applied electrodeposition regime, the hardness of the Ni films increased from 29.1% for the Ni/SiO2 films obtained using the PC regime to 95.5% for those obtained using the RC regime, reaching the maximal value of 6.880 GPa for the Ni/SiO2 films produced using the RC regime.

Stabilization of δ-like Bi2O3 Phase at Room Temperature in Binary and Ternary Bismuthate Glass Systems with Al2O3, SiO2, GeO2, and B2O3.

Recently, it was shown that the nanocrystallization of Bi2O3 glasses with the addition of SiO2 and Al2O3 leads to the stabilization of the δ-like Bi2O3 phase at least down to room temperature, which is significantly below its stability range in bulk form. In this research, we investigated the properties of bismuthate glasses synthesized with various glass-forming agents such as SiO2, GeO2, B2O3, and Al2O3. It was demonstrated that vitrification of all these systems is possible using a standard melt quenching route. Furthermore, we investigated the crystallization processes in pristine glasses upon increasing the temperature and the thermal stability of arising phases using thermal analysis and high-temperature XRD in situ experiments. It was shown that it is possible to stabilize crystallites' isostructures with δ-Bi2O3 embedded in a residual glassy matrix down to room temperature. The temperature range of the appearance of the δ-like phase strongly depended on the nominal composition of the glasses. We postulate that the confinement effect depends on the local properties of the residual glassy matrix and its ability to introduce sufficient force to stretch the structure of the δ-like Bi2O3 phase in the nanocrystallites.

Polymorphic Localized Heterostructure Design for High-Performance Amorphous/Nanocrystalline Composite Film.

Analogous to linear dielectric, amorphous perovskite dielectrics characterized of high breakdown strength and low remanent polarization possess in-depth application in the sea, land, and air fields. Amorphous engineering is a common approach to balance the inverse relationship between polarization and breakdown strength in dielectric ceramic capacitor, however, the low polarization is the major barrier limiting the improvement of energy storage density. To address this concern, the polymorphic localized heterostructure confirmed by high-resolution transmission electron microscope (HR-TEM) and HADDF images is constructed in BaTiO3-Bi(Ni0.5Zr0.5)O3 amorphous/nanocrystalline composite film with SiO2 addition (BT-BNZ-xS, x = 3, 5, 7, 10 mol%). The stability of nanocrystalline region achieved by Si-rich transition region and the enhancive ultra-short-range ordering in the amorphous region synergistically result in large breakdown strength and nonhysteretic polarized response. This polymorphic localized heterostructure optimizes the thermal stability in a wide temperature range and contributes ultrahigh energy storage density of 149.9 J cm-3 with markedly enhanced efficiency of 79.0%. This study provides a universal strategy to design the polarization behavior in other amorphous perovskite-based dielectrics.

The study on the magnetic interaction between the duel magnetic layers and the FINEMET ribbon

Due to the sensitive magnetic field response of the GMI effect, the peak field in magneto impedance curves obtained from the composite magnetic ribbons shows great dependence on the magnetic interaction, which has gained intensive attention in the study of the diversity and the mechanism of magnetic interaction. In this work, FINEMET/Fe20Ni80/SiO2/Fe20Ni80 composite ribbons with a fixed thickness of outer Fe20Ni80 layer (200 nm) and variable thickness ratio of the inner Fe20Ni80 and SiO2 layers, ranging from the 1:4 to 4:1 were prepared. Then the GMI response was utilized to investigate the influence of the exchange couple and the dipole interaction to magnetic properties of the base ribbon. The experimental results indicated that additional SiO2 layer can successfully induce slight magnetic differences of the two Fe20Ni80 layers, which results in the emergence of four-peak GMI profiles. Besides, the frequency-dependent nature of the peaks was explored, revealing that both dipole interaction and exchange couple influence the magnetic properties, contributing to the occurrence of four-peak GMI curves. Thus, the insights presented in this work are thought to be valuable for understanding the mechanisms of multilayer composite ribbons in future sensing applications.

Influence of SiO2@CaAl-LDH core-shell nanocomposite on rheology and hydration of cement

Nano-SiO2@ Layered double hydroxide (LDH) core-shell nanocomposite shows a promising application as high-efficiency chloride adsorbent in cement-based materials. However, its effect on rheology and hydration of cement is not yet known. In this study, the SiO2@CaAl- LDH core-shell nanocomposite by growing the LDH on nano-SiO2 surface was firstly created using in-situ co-precipitation method. The influence of as-synthesized nanocomposite on the rheology and hydration of cement was systematacially researched through contrasting experiments. Besides, microstructures of SiO2@LDH and its cement paste were characterized. The results show that the LDH with petal-like shape on the nano-SiO2 surface exhibits a higher specific area than pure nano-SiO2 and LDH alone. The addition of SiO2@CaAl-LDH core-shell material significantly shortens the initial and final setting time of cement and increases cement hydration heat generation rate and the total exothermic amount for 72 h. Contrary to the mixture of LDH, the additions of nano-SiO2 and SiO2@LDH increases the yield stress and plastic viscosity of cement paste. Compared to the additions of LDH and SiO2, the addition of SiO2@LDH more significantly enhances the strength of cement, of which the highest increasing level reaches 66 % at the early age of 1 d. In addition, SiO2@LDH exhibits the best refinement effect on the pore structure of cement because of the synergetic effect between the LDH and nano-SiO2.

Exploring the influence of native minerals in coal gangue on CG/PE composite manufacturing and performance: Examining SiO2's role in interfacial compatibility

AbstractThis study delves into the influence of inherent minerals within coal gangue (CG) on the preparation and performance of coal gangue /polyethylene (CG/PE) composites, focusing on the role of SiO2 in interfacial compatibility. A systematic examination unveils the consequences of varying SiO2 content on physical, mechanical, thermal, and microstructural attributes of the composites. SiO2 incorporation significantly improves physical properties, boosting density and hardness but impacting tensile strength negatively. It enhances bending strength and modulus while diminishing tensile strength. Judicious SiO2 addition enhances thermal stability, but excess SiO2 may compromise thermal decomposition. Microstructural analysis, including SEM and FTIR, elucidates SiO2‐PE interactions, primarily through physical entanglement. SiO2 introduction promotes more ordered PE molecular chain arrangements, elevating composite crystallinity. In summary, this study provides in‐depth insights into SiO2's mechanistic impact on CG/PE composite properties, laying a robust foundation for designing environmentally friendly composites. These findings hold promise for advancing sustainable materials science and engineering. Future research may explore SiO2 optimization for specific applications and synergistic effects with other fillers in composites.Highlights SiO2 greatly improves the properties of CG/PE composites with detailed exploration. Reveals the specific SiO2‐PE interaction mechanism for a better comprehension. Performs structural analysis via XRD with valuable findings presented. Promotes pioneering advancements in eco‐friendly materials with broad significance.

Controllable decomposition/recrystallization of water-sensitive CsPbBr3 glass ceramics for dynamic anti‐counterfeiting with high security

Due to the sensitivity to water, the all-inorganic CsPbBr3 nanocrystals have been widely applied in information encryption with spatial dimensions. However, the absence of time-dimension information limits the information capacity for the application of CsPbBr3. In this work, the CsPbBr3 nanocrystal was combined with water-sensitive borophosphate glass, achieving decomposing/recrystallization of CsPbBr3 nanocrystal with multi-dimension. The addition of SiO2 confirms that the collapse of the borophosphate glass network structure causes the exposure of the CsPbBr3 nanocrystals. The decomposition and recrystallization mechanism of CsPbBr3 nanocrystals in glass-ceramics upon encountering water has been verified. Finally, an information encryption strategy, using the mixture of CsPbBr3 glass ceramic and sodium carboxymethylcellulose as ink, is designed via adopting screen-printing technology, which not only provides a new idea for the preparation of CsPbBr3 nanocrystals, but also establish a new avenue for the information encryption technology.

SiO2-bearing Fluxes Induced Evolution of γ Columnar Grain Size

Understanding the controlling mechanisms of γ columnar grain size in the weld metal of low-carbon, low-alloy steel is critical for optimizing resultant microstructures and the weld metal’s ensuing properties. Here, we investigate the role of welding flux composition upon the γ columnar grain size by submerged arc welding of EH36 shipbuilding steel with designed CaF2-SiO2 fluxes. We found that the addition of SiO2 from 5 to 40 mass-% increases average columnar grain size by a factor of nearly 2.5, which results from the change of the weld pool solidification mode from peritectic to primary δ solidification. Such a change is directly related to element transfer behaviors between the flux and the weld metal. Furthermore, we offer compelling evidence that alterations in γ columnar grain size are not primarily governed by significantly populated inclusions and/or weld metal macro-morphological changes. Our findings may largely serve as a viable strategy toward designing welding consumables to match base metals to ensure the soundness of the weldment.