Densification effects on the fracture in fused silica under Vickers indentation

This study investigates the effects of densification on the deformation and fracture in fused silica under Vickers indentation by both the finite element analysis (FEA) and experimental tests. A refined elliptical constitutive model was used, which enables us to investigate the effects of the evolution of yield stress under pure shear and elastic properties with densification. The densification distribution was predicted and compared with experiments. The plastic deformation and indentation stress fields were used to analyze the initiation and morphology of various crack types. The formation mechanism of borderline cracks was revealed for the first time. This study reveals that the asymmetry of the densification distribution and elastic-plastic boundary significantly influences the cracking behavior. Under the Vickers indentation, conical cracks have the largest penetration depth. When these cracks emerge from a region far from the impression, they extend with constant radii to form circles on the sample surface. Otherwise, they tend to be initiated at the centers of the indenter-material contact edges before propagating towards the impression corners with increasing radii. Therefore, the borderline cracks consisting of successive partial conical cracks can form at a low load and makes them the first type of crack to appear.     

Differences in indentation and wear behaviors between the two sides of thermally tempered soda lime silica glass

Thermal tempering is an industrial process widely used to make soda lime silica (SLS) glass panels stronger and tougher. During the tempering process, the upper and bottom sides of the glass may experience different cooling rates, and thus, their properties could be different. This study characterized changes in surface composition and subsurface glass network structures as well as indentation and wear resistance properties of the air- and tin-sides of 6-mm-thick SLS window panels faced toward the upper and sliding roller sides during thermal tempering. The results showed that although the chemical and structural differences detected with X-ray photoelectron spectroscopy and specular reflection infrared spectroscopy are subtle, there are large differences in nanoindentation behaviors and mechanochemical wear properties of the SLS glass surface. The findings of this study provide further insights into the performance difference between the air- and tin-sides of the SLS glass panel treated with thermal tempering.     

Ultra-low energy joining: An invisible strong bond at room temperature

We developed Cold Isostatic Joining (CIJ) which is an environmental friendly room temperature joining method. This technique extends cold sintering process to joining of glasses. By optimizing the CIJ conditions a shear stress (18 MPa) comparable to bulk fused silica was achieved. The technique surpasses other joining methods (e.g. adhesive bonding and brazing), because it is insensitive to thermal degradation. Unlike pressure-less silicate bonding, pressure assisted CIJ resulted in a thin joining interlayer (≈27 nm) which maintained its integrity after being heated up to 1000 °C. The in-line transmittance (92%) was identical to un-joined material over the full spectrum making the joining nearly undetectable. The mechanism of CIJ formation and joining were clarified using X-ray diffraction (XRD and pole figure), scanning electron microscopy (SEM) and in line transmittance measurements. The cold joining method could find applications in the field of optics and semiconductors for wafer and lens bonding.     

玻璃棉/SiO2气凝胶复合板的改性研究

通过选取无水乙醇为溶剂，以SiO₂气凝胶为溶质，制备SiO₂气凝胶改性溶液，并将其应用于改善玻璃棉的保温性能。通过浸润及常压干燥的方法制取玻璃棉/SiO₂气凝胶复合板，研究SiO₂气凝胶的质量分数和浸润时间对其性能的影响，并与溶胶-凝胶法制备的玻璃棉/SiO₂气凝胶复合板相比。研究表明SiO₂气凝胶的质量分数和浸润时间对玻璃棉/SiO₂气凝胶复合板的性能有显著影响。当SiO₂气凝胶质量分数达到8%且浸润时间为20 min时，玻璃棉/SiO₂气凝胶复合板的短期吸水率、热导率分别下降了38.09%、18.32%，抗压强度上升了102.89%。与溶胶-凝胶法相比，本方法具有制备周期短、工艺较为简洁、成本低等优点，更适宜于大规模生产应用。     

配加蒙古精矿对球团矿性能的影响

对蒙古精矿在包钢624 m2带式球团的合理利用进行了全面研究。研究表明，随着蒙古精矿配比增加，球团矿品位提高，还原膨胀率增加，当配比小于20%时，还原膨胀率小于20.0%，主要是由于还原后球团矿矿物组成中析出大量金属铁，在浮氏体(FexO)转变为铁的阶段，铁晶粒自浮士体表面向外长出晶须，晶须的生长让晶粒产生位移或晶粒开裂，导致球团结构疏松发生膨胀。通过添加适量矽石，可显著降低球团还原膨胀率，当配加30%～50%的蒙古精矿时，可通过添加1.0%～2.0%的矽石，将球团还原膨胀率降低至20%以内，球团矿质量满足高炉冶炼生产要求。     

Solution‐Processable Photonic Inks of Mie‐Resonant Hollow Carbon–Silica Nanospheres

Hollow carbon–silica nanospheres that exhibit angle‐independent structural color with high saturation and minimal absorption are made. Through scattering calculations, it is shown that the structural color arises from Mie resonances that are tuned precisely by varying the thickness of the shells. Since the color does not depend on the spatial arrangement of the particles, the coloration is angle independent and vibrant in powders and liquid suspensions. These properties make hollow carbon–silica nanospheres ideal for applications, and their potential in making flexible, angle‐independent films and 3D printed films is explored.     

Effect of silica on the ZnS nanoparticles for stable and sustainable antibacterial application

Silica-capped Zinc Sulfide (ZnS) nanoparticles were synthesized for the use as stable and long-term antibacterial agents because silica is a very important component in food packaging applications for moisture absorption in tune with its property of biocompatibility and water solubility. The variation in morphological and optical properties of core-shell nanostructures was studied by changing the concentration of silica in a core-shell combination. The structural and morphological properties of silica-capped ZnS have been observed by powder X-ray diffraction (PXRD) and transmission electron microscopic (TEM) studies, respectively. Uncapped ZnS nanoparticles with particle size of 2-4 nm in a highly agglomerated state have been observed from TEM, which shows that they can be used only for short-term antibacterial action despite its excellent zone of inhibition (antibiotic sensitivity). However, ZnS/SiO₂ core-shell nanostructures are highly monodisperse in nature and the particle size increases up to 5-8 nm with increase in silica concentration. Fourier-transform infrared spectroscopy (FTIR) analysis confirms the formation of silica capping on the ZnS surface. The inhibition of defect-related emission by silica capping in energy-resolved photoluminescence studies also shows the formation of very stable ZnS nanoparticles. To study the antibacterial properties of the pure and silica-capped ZnS nanostructure the agar-well diffusion method was employed against both gram-positive and gram-negative bacteria. The obtained results indicate that pure ZnS shows excellent antibacterial action but it can last only for few days.     

Poly(L-lysine)-poly(ethylene glycol) layers with different structure and their influence on silica suspension stability

The effects of the structure of di- and triblock copolymers of poly(L-lysine) – LYS with poly(ethylene glycol) – PEG as well as the length of nonionic fragment in the LYS-PEG macromolecule on the copolymer chains conformation in the adsorption layer formed on the colloidal silica (SiO2) surface were examined. Spectrophotometry and turbidimetry were applied for the determination of copolymer adsorbed amounts and stability coefficients of silica aqueous suspensions. The electrokinetic parameters such as solid surface charge density and zeta potential were also estimated. The adsorption of LYS-PEG was proved to be the highest at pH 10 whereas the lowest adsorption on the solid surface was found for the triblock copolymer with long fragments of LYS at the same pH value.     

Adsorption performance of mesoporous silicas towards a cationic dye. Influence of mesostructure on adsorption capacity

The dye adsorption performance of four mesoporous silicas with different structure and textural properties, MCM-41, MCM-48, SBA-15 and mesocellular silica foam (MCF), was studied and compared by using toluidine blue O (TBO) as dye model in aqueous solution. These materials were characterized by X-ray diffraction (XRD), small-angle X-ray scattering, nitrogen adsorption-desorption analyses, and transmission electron microscopy (TEM). The effect of some parameters such as adsorbent dosage, contact time, temperature, and pH on the TBO removal in aqueous solution was studied. Results showed that adsorption capacity raised when adsorbent dosage, contact time and pH solution were increased while an increase in temperature decreased the adsorption of TBO. Langmuir, Freundlich and Temkin isotherm models were employed to elucidate the adsorption mechanism while the adsorption rate data were analyzed according to the pseudo-first and second-order kinetic models. Results showed that adsorption of TBO onto MCM-48, SBA-15, and MCF fitted well the Freundlich isotherm model while the kinetic studies showed that adsorption process could be better described by the pseudo-second-order model for all mesoporous silicas. Finally, some solvents were evaluated to carried out dye desorption from the TBO-loaded mesoporous silicas founding that acetic acid was the most efficient.     

棉织物的硅溶胶疏水整理

为实现超疏水织物的绿色加工,采用正硅酸乙酯(TEOS)为前驱体,乙醇和水为溶剂制备硅溶胶预缩体对棉织物进行疏水整理,研究各工艺因素对棉织物疏水性能的影响,重点分析预缩体的制备、硅烷偶联剂的添加、低温烘干工艺与提高整理织物疏水性的相关性。结果表明:棉织物表面的SiO₂纳米粒子形成的粗糙表面与织物表面结合的疏水脂肪烃链可赋予织物良好的疏水性;在TEOS量为0.1 mol,乙醇量为0.9 mol,水的量为0.8 mol,先二浸二轧硅溶胶,再浸轧十六烷基三甲氧基硅烷醇溶剂优化工艺条件下,整理棉织物的水接触角可达152.1°,棉织物的力学性能得到提高。