成分对 Bi2O3-B2O3-ZnO-SiO2 玻璃的结构、热特性和某些物理特性的影响

Pub Date : 2024-05-14 DOI:10.15251/jor.2024.203.273
Y. Hordieiev, A. Zaichuk
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引用次数: 0

摘要

研究了成分对 55Bi2O3-(35-x-y)B2O3-(5+x)ZnO-(5+y)SiO2 (其中 0 ≤ x,y ≤ 15 mol%)硼酸铋玻璃的结构、热和一些物理特性的影响。利用 X 射线衍射 (XRD)、扫描电子显微镜 (SEM)、傅立叶变换红外光谱 (FTIR)、差热分析 (DTA) 和稀释测定法等技术进行了综合分析。XRD 证实了玻璃样品的无定形性质,而傅立叶变换红外光谱则显示玻璃主要由 BO4、BO3、BiO6、BiO3、ZnO4 和 SiO4 结构单元组成。DTA 进一步证明了样品的玻璃态,并揭示了玻璃转化(Tg)、结晶(Tc)和熔化(Tm)等关键温度。研究发现,用二氧化硅代替 B2O3 会提高所有特征温度,而用氧化锌代替则会降低 Tg 和 Tc,但会提高 Tm。55Bi2O3-20B2O3-20ZnO-5SiO2 成分的玻璃具有最高的热稳定性,ΔT 为 99°C。稀释测量结果表明,所研究的玻璃具有较高的热膨胀系数(10.0-10.7 ppm/°C)值、较低的玻璃转变温度(345-376°C)和较低的稀释软化温度(364-392°C)。此外,还准确测定了样品的密度和摩尔体积。
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Effects of composition on the structure, thermal and some physical characteristics of Bi2O3-B2O3-ZnO-SiO2 glasse
The influence of composition on the structure, thermal, and some physical characteristics of bismuth borate glasses, formulated as 55Bi2O3–(35-x-y)B2O3–(5+x)ZnO–(5+y)SiO2 (where 0 ≤ x, y ≤ 15 mol%), was investigated. Comprehensive analyses were conducted using techniques such as X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier-Transform Infrared Spectroscopy (FTIR), Differential Thermal Analysis (DTA), and Dilatometry. XRD confirmed the amorphous nature of the glass samples, while FTIR spectroscopy revealed that the glasses are primarily composed of BO4, BO3, BiO6, BiO3, ZnO4, and SiO4 structural units. DTA provided further evidence of the samples' glassy state and insights into key temperatures like glass transition (Tg), crystallization (Tc), and melting (Tm). The study finds that substituting B2O3 with SiO2 increases all characteristic temperatures, whereas replacing it with ZnO decreases Tg and Tc but increases Tm. The maximum thermal stability, indicated by a ΔT of 99°C, was observed in the glass with a 55Bi2O3–20B2O3–20ZnO–5SiO2 composition. Dilatometric measurements showed that the investigated glasses have a high coefficient of thermal expansion (10.0–10.7 ppm/°C) values, a low glass transition temperature (345–376°C), and a low dilatometric softening temperature (364–392°C). Additionally, the density and molar volume of the samples were accurately determined.
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