Impact of TeO2–B2O3 manipulation on physical,structural, optical and radiation shielding properties of Ho/Yb codoped mixed glass former borotellurite glass

In this work, (75-x)B₂O₃-xTeO₂-11Bi₂O₃–10Li₂O-1Ho₂O₃-3Yb₂O₃ (x = 10–60 mol%) mixed glass former (MGF) glasses were prepared by using the melt-quenching method to investigate the effect of mixed glass former between B₂O₃ and TeO₂ on the structural, optical and radiation shielding properties of glass. The amorphous nature of the glass samples was confirmed through XRD measurement. Optical ultraviolet–visible light (UV–Vis) spectroscopy revealed that the direct and indirect optical band gap (E_opt) decreased as TeO₂ content increased except for the anomaly at x = 30 mol% due to the interchanging dominance of bridging oxygen (BO) and non-bridging oxygen (NBO) in the glass network. Both direct and indirect refractive indices, n posted an increment except for x = 30 mol% due to polarizability influence of BO and NBO. Urbach energy, E_u declined thus indicating lesser disorder and less defects on the glass structure. The radiation shielding properties of the glass samples were determined for 15 keV–15 MeV photon energy range by using Phy-X/PSD software. Atomic number-dependent parameters such as mass attenuation coefficient (MAC) and effective atomic number (Z_eff) demonstrated an enhanced performances caused by higher Z of Te over B. Meanwhile, density-dependent parameters such as linear attenuation coefficient (LAC), mean-free path (MFP), half-value layer (HVL) and tenth-value layer (TVL) all exhibited an improvement over TeO₂ concentration due to higher density data obtained.     

Effect of MgO addition on the properties of PbO –TiO2–B2O3 glass and glass–ceramics

Glass samples with composition of (50?X) PbO–X MgO–25 TiO₂–25B₂O₃ (where X=0, 5, 10 and 15 mol%) were prepared using conventional quenching technique. The amorphous nature of glass samples were confirmed by XRD. The glass transition temperature, T_g and crystallization temperature T_c were determined from the DTA. It has been observed that the addition of MgO enhances the T_g. The rise in T_g with MgO content may be attributed to the greater field strength of Mg²⁺ cation (as compared to Pb²⁺) which leads to the formation of stronger bonds. These glass samples were converted to glass–ceramics by following a two-stage heat treatment schedule. It was observed that there was good correlation between the density and CTE results of the glass–ceramics. The XRD results revealed the formation of tetragonal lead titanate as a major crystalline phase in the glass–ceramics. The addition of MgO to the glass contributes to the formation of MgB₄O₇. The dielectric constant for all the glass–ceramic samples was observed to be higher than that of corresponding glass samples. Further, with addition of MgO the room temperature dielectric constant for glass–ceramic samples increases up to 10 mol% of MgO and then decreases for 15 mol%. It has been further observed that the variation of dielectric constant of glass–ceramic samples with MgO content is exactly opposite to the variation of crystallite size of PbTiO₃ embedded in the glass ceramic-samples.     

Influence of the glass–calcium carbonate mixture's characteristics on the foaming process and the properties of the foam glass

We prepared foam glasses from cathode-ray-tube panel glass and CaCO₃ as a foaming agent. We investigated the influences of powder preparation, CaCO₃ concentration and foaming temperature and time on the density, porosity and homogeneity of the foam glasses. The results show that the decomposition kinetics of CaCO₃ has a strong influence on the foaming process. The decomposition temperature can be modified by varying the milling time of the glass–CaCO₃ mixture and thus for a specific CaCO₃ concentration an optimum milling time exists, at which a minimum in density and a homogeneous closed porosity are obtained. Under the optimum preparation conditions the samples exhibit a density of 260 kg/m³. The thermal conductivity of the foam glass was measured to be 50–53 mW/(m K). The observed dependence of the foaming process on the decomposition kinetics of the foaming agent can be applied as a universal rule for foaming processes based on thermal decomposition.     

Effects of Sr and Mg dopants on biological and mechanical properties of SiO2–CaO–P2O5 bioactive glass

In the present study, the effects of Sr and Mg were investigated on mechanical and biological properties of 58S bioactive glass (BG). SiO₂-P₂O₅-CaO BG with different contents of Sr and Mg were synthesized via the sol-gel method and immersed in simulated body fluid (SBF) for several days to explore their biocompatibility. Precise analyses of the BG using X-ray powder diffraction, scanning electron microscopy, and transmission electron microscopy showed that the Mg-doped BG containing 8 wt % MgO possessed better biocompatibility. It was also found that mechanical properties of the BG could be improved by increasing the amounts of MgO and SrO. Both 5Sr-BG and 8Mg-BG samples did not exhibit any cytotoxicity while showing high alkaline phosphatase activity in comparison with control specimens. However, the Sr-doped BG sample including 5 wt % SrO demonstrated enhanced bioactivity and biocompatibility.     

Effect of heat treatment on the optical properties of sol–gel-derived,fully dielectric solar control coatings on glass

TiO₂ and zeolite were used as high index and low index dielectric materials respectively to generate fully dielectric solar control coatings on glass. TiO₂|Zeolite|TiO₂ trilayer stacks as well as single layer TiO₂ and zeolite coatings were generated on soda lime glass substrates using dip-coating technique. The coatings were densified at 450°C in air using a conventional muffle furnace and a conveyorized belt furnace with a total cycle time of 330 and 30 min, respectively, per layer. The effect of heat-treatment time on the optical properties of multilayered and single-layered coatings was studied. Spectroscopic ellipsometric analysis was carried out on individual layers of the stack to elucidate thickness, roughness, and refractive index data. The ellipsometry data were subsequently used as inputs to simulate the UV–Vis–NIR transmittance spectra of the trilayer stacks generated by TFCalc^® software, for comparison with experimentally obtained data. The morphology and phase compositions of the coatings were studied using scanning electron microscopy and grazing angle incidence X-ray diffraction analysis. Different heat treatment schedules were found to result in different optical properties. The results from the present study could be used to recommend suitable heat treatment schedules for generating solar control coatings that could be used for either architectural or automotive applications.     

Effects of the ionizing irradiation of γ-rays,X-rays,and UV-rays on the optical properties of Ag-contained/Ag-free photo-thermo-refractive glass

To simulate the effects of ionizing irradiation on photo-thermo-refractive (PTR) glass in a cosmic environment, the optical properties changes under ionizing irradiation (γ-, X- and UV-ray) were investigated on PTR-glass with and without Ag doped (named as PTR-S and PTR-F, respectively) samples. Thermoluminescence (TL), transmission electron microscopy (TEM) measurements, UV-VIS absorption spectroscopy analysis, Gaussian peak fitting, and continuous wave electron paramagnetic resonance (CW-EPR) were used to determine the species of the irradiation-induced color centers. The radiation resistance properties of the Ag-species on the PTR-S glass were evaluated by comparing the defect center concentrations in the irradiated PTR-S and PTR-F glasses. The results showed that absorption in PTR-F and PTR-S glass increased significantly with increasing γ-irradiation dose, which was related to HC₁, HC₂, E′, L, ETC defect centers and Ag-species, and the formation of HC₁, HC₂, E’, and L-centers was reduced by the doping of Ag into the PTR-S glass matrix. Compared with the γ-irradiation, X-irradiation showed a similar effect. In comparison, UV-irradiation induced fewer defect centers and smaller Ag (NPs). This discrepancy could be caused by variations in photon energies.     

Effect of CaO doping on the properties and crystallization behavior of Y2O3–Al2O3–SiO2 glass

Nowadays, Y₂O₃–Al₂O₃–SiO₂ (YAS) glass joining is considered to be a promising scheme for nuclear-grade continuous silicon carbide (SiC) fiber reinforced SiC matrix composites (SiC/SiC). CaO has great potential for nuclear applications since it has low reactivity and low decay rate under nuclear irradiation. In this paper, the effect of CaO doping on the structure, thermophysical properties, and crystallization behavior of YAS glass was systematically studied. As the CaO doping content increased, the number of bridge oxygens and the viscosity at high temperatures reduced gradually. After heat treatment at 1400 °C, the main phases in YAS glass were β-Y₂Si₂O₇, mullite, and SiO₂ (coexistence of crystalline and glass phases), while that with 3.0% CaO doping turned into a single glassy phase under the same treatment conditions. Moreover, a structural model and the modification mechanism were proposed, which provided a theoretical basis for the subsequent component design and optimization.     

Effects of CaO–B2O3–SiO2 glass additive on the microstructure and electrical properties of BCZT lead-free ceramic

Addition of CaO–B₂O₃–SiO₂ (CBS) glass was performed to lower the sintering temperature of lead-free Ba_0.85Ca_0.15Zr_0.1Ti_0.9O₃ (BCZT) ceramics. Orthorhombic and tetragonal phases coexisted in CBS-free BCZT ceramics. The BCZT ceramics transformed into a pseudo-cubic phase when sintered at 1300 °C with increasing CBS glass content. Additionally, the secondary phase, Ba₂TiSi₂O₈, was observed when CBS glass was added. The density initially increased, reached a maximum value with 2 wt% CBS glass, and then decreased rapidly with further increase in CBS glass content, which was consistent with the microstructure. The ɛ, T_c, P_r, and d₃₃ depend on microstructure, and the results agree with the density. Evident relaxation behavior was observed. Observed results were inferred to be dependent on the microstructure, phase structure, lattice distortion, and secondary phase. The sample with 2 wt% CBS glass showed the excellent performance, which could be a promising substitute to lead-free piezoelectric ceramics for lead-based materials.     

Effect of properties and crystallization behavior of BaO–ZnO–B2O3–SiO2 glass on the electrical conductivity of Cu paste

The extensive application of multilayer ceramic capacitors provides an attractive development for terminal electrode pastes. However, the growing requirement for advanced glass materials used in terminal electrode pastes is substantiated. Therefore, to advance the development of electrode pastes, better development and deeper exploration of glass powder are required. Here, a series of BaO–ZnO–B₂O₃–SiO₂ (BZBS) glasses were prepared by melt-quenching technique, which are used to investigate the effect of the introduction of BaO on structure and properties of the ZnO–B₂O₃–SiO₂ (ZBS) glass. With the introduction of BaO, the relative amount of [BO₄] was much less, which made the glass network structure loosen, decreased the glass transition temperature (T_g) and increased the coefficient of thermal expansion of the glass. The decreasing contact angle was observed on the surface of a barium titanate (BaTiO₃) substrate. When the BaO content was around 3–7 mol%, the stability of ZBS glass frit could be strengthened by inhibiting the precipitation of Zn₂SiO₄ crystal. In addition, to further characterize the effect of glass on terminal electrode paste, BZBS glass powder was adopted to prepare copper electrode paste, which was printed on the BaTiO₃ substrate and subsequently fired at 800°C for 10 min. With the related copper paste containing ZBS glass doped with 7 mol% BaO, the optimum value of acid resistance and sheet resistance (1.99 mΩ) were exhibited, at which the coated copper paste formed a dense conducting layer.     

Effects of hafnium sources and hafnium content on the structures and properties of SiBNC–Hf ceramic precursors

The synthesis of SiBNC–M (M is metal element) multinary ceramic precursors has mainly been through chemical modification of the SiBNC ceramic precursors with the introduction of the metal element/compound. This misses the simplicity, efficiency, and combined benefits of single reactor synthesis routes. We herein adopt a one-pot method to synthesize SiBNC–Hf ceramic precursors (PBSHZ) from different Hf sources, and with varying Hf content. The starting materials include hafnium tetrachloride, hafnium dichloride, trichlorosilane, hexamethyldisilazane, and boron trichloride. Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis are employed to characterize the structures and properties of the PBSHZ. The results reveal the successful incorporation of Hf into the precursors. Compared to the hafnium tetrachloride source, the precursor synthesized from hafnium dichloride yields more ceramics and shows better solubility, due to fewer Hf–Cl bonds available for reaction. Meanwhile, there is a positive correlation between the rise in the Hf content of PBSHZ and the ceramic yield. However, the solubility and processability of the precursors decline, due to the multiplication of the cross-linking degree in the molecular structure. Further FT-IR, NMR, XPS, and thermogravimetry–mass spectrometry (TG–MS) analysis indicate a full polymer-to-ceramic transformation at 1000°C pyrolysis temperature. At this point, the SiBNC–Hf ceramics mainly consist of an Si–B–N skeleton, HfN, and free carbon.     

Effect of BaO ratio on the structure of glass–ceramic composite materials from the SiO2–Al2O3–Na2O–K2O–CaO system

This article focused on effect of the content of barium oxide on microstructure of the glass–ceramic materials based on the system SiO₂–Al₂O₃–Na₂O–K₂O–CaO. The following characterisation techniques have been used: X-ray diffraction (XRD), scanning electron microscopy with micro-analyser (SEM–EDS), mid-infrared analysis (MIR), far-infrared analysis (FIR) and Raman Spectroscopy. Significant differences were observed in microstructure of silica–alumina network of glassy phase and phase composition related to changes in the amount of the barium oxide additive. Discussed results are part of a larger project implemented under the PBS Applied Research Programme, in order to determine the compositions of glass–ceramic materials with potential application as a chemically resistant hard coatings or/and resistant to thermal shock or as construction materials.     

The role of MgO on the structural properties of CaO–Na2O(MgO)–P2O5–CaF2–SiO2 derived glass ceramics

The effect of increasing MgO/Na₂O replacements (on mole basis) on the crystallization characteristics of glasses based on the CaO–Na₂O(MgO)–P₂O₅–CaF₂–SiO₂ system were studied by using DTA, XRD, and SEM. The crystallization characteristics of the glasses, the type of crystalline phases formed and the resulting microstructure were investigated. The main crystalline phases formed after controlled heat-treatment of the base glass were diopside, wollastonite solid solution, fluoroapatite and sodium calcium silicate phases. The increase of MgO at the expense of Na₂O led to decrease the amount of sodium calcium silicate phase. The Vicker's microhardness values (5837–3362 MPa) of the resulting glass–ceramics were markedly improved by increasing the MgO-content in the glasses. The obtained data were correlated to the nature and concentration of the crystalline phases formed and the resulting microstructure.     

Effect of powder–liquid ratio and admixture on properties of metakaolin-based geopolymer coating

Protective coating is one of the effective ways to help concrete structures resist environmental erosion. However, most of the existing coating materials are organic compounds, which have the disadvantages of poor durability and high energy consumption. In this study, metakaolin with excellent durability was used as the main raw material, and a flexible and waterproof ethylene-vinyl acetate emulsion was added to improve the high brittleness characteristics of metakaolin, resulting in a metakaolin-based geopolymer coating material. Through tests such as water absorption, hardness, gloss, and tensile properties, we investigated the effects of the powder–liquid ratio and the type and amount of admixture on the properties of the coating. The results show that the coating exhibits better performance when the powder-to-liquid ratio is 0.6. Based on this, it was found that the optimal dosage of water-reducing agent, coupling agent, and defoamer was 0.7%, 0.3%, and 0.3%, respectively.     

Growth and optical properties of ZnO–In2O3 heterostructure nanowires

ZnO–In₂O₃ heterostructure nanowires were grown on a Si (111) substrate using the thermal evaporation method. Scanning electron microscopy results showed that the ZnO nanowires had spherical caps. The X-ray diffraction (XRD) pattern and energy-dispersive X-ray (EDX) spectrum indicated that these caps were In₂O₃. An analysis of the early growth process revealed that indium oxide might have played a self-catalytic role. Therefore, it was plausible that the vapor–liquid–solid mechanism (VLS) was responsible for the growth of the ZnO–In₂O₃ heterostructure nanowires. The optical properties of the products were characterized using a photoluminescence (PL) technique. The PL results for the ZnO–In₂O₃ heterostructure nanowires showed a strong peak in the ultraviolet region as a result of the near band emission and a negligible peak for the visible emissions that occurred as a result of the defects. Based on these PL results, it was found that the In₂O₃ nanostructures not only introduced the caps at the tips of the ZnO nanowires but also partially passivated the nanowire surfaces, leading to an improved near band edge emission and the suppression of the defect luminescence.     

Clarifying the effect of sintering conditions on the microstructure and mechanical properties of β-tricalcium phosphate

The effect of the sintering conditions (temperature and time) on the microstructure (density and grain size) and mechanical properties (hardness, elastic modulus, and strength) of β-tricalcium phosphate (β-TCP) bioceramics fabricated from Ca-deficient commercial powders is analyzed. Contrary to current general opinion, it is demonstrated that the optimal sintering temperature to maximize the mechanical performance of this β-TCP material is not necessarily below the β ? α transformation temperature (1125 °C). In particular, optimal performance was achieved in samples sintered at 1200 °C for 3 h, since it was not until higher temperatures or longer sintering times that microcracking develops and mechanical properties are degraded. It is argued that the residual stresses developed during this reversible transformation do not lead to microcrack propagation until sufficiently large starting flaws develop in the microstructure as a consequence of grain growth. Implications of these findings for the processing routes to improve sintering of this important bioceramic are discussed.     

The effect of glass composition and structure on photochromic properties of LiF–Al2O3–B2O3 glassy materials

Theoretical Foundations of Chemical Engineering - The glass-forming region of the LiF–Al2O3–B2O3 system and the phase diagram of this region have been studied. Properties of glasses and...     

Preparation and properties of ferrimagnetic glass–ceramic foams based on pyrite slag

By employing a melt-sintering method, we prepared a new type of ferrimagnetic glass–ceramic foam (FGCF) using ferrimagnetic glass–ceramic and foaming agent SrCO₃. The ferrimagnetic glass–ceramics were fabricated based on pyrite slag by a melt-quenching method. The effects of foaming agent content, sintering temperature and time on microstructure, magnetic properties, microwave absorption performance, compressive strength, and thermal conductivity of the as-obtained FGCF were analyzed. This foaming process at 1100°C for 40 min with 3-wt% SrCO₃ provided an FGCF with a bulk density of .693 g/cm³, a porosity of 63.60%, a specific saturation magnetic moment of 5.2 A m²/kg, a compressive strength of 2.61 MPa, a thermal conductivity of .241 W/(m K), and the calculated reflection loss of −12.1 dB for a layer thickness of 9 mm.