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This study systematically investigates the crystallization behavior, phase evolution, and dielectric properties of a BaO-Al₂O₃-SiO₂ glass system modified with 10 wt% TiO₂. Thermal characterization revealed that TiO₂ addition notably reduced the glass transition temperature (from 781.6°C to 779.4°C) and softening point (from 838°C to 824.8°C) compared to the TiO₂-free glass, consequently decreasing the calculated nucleation temperature (from 810°C to 800°C). While differential thermal analysis indicated sluggish crystallization kinetics, isothermal heat treatments identified 1000°C as the optimal processing temperature, leading to the development of a multiphase crystalline assemblage that beneficially included the target monoclinic Ba3.75Al7.5Si8.5O32 phase, which was absent in the TiO₂-free glass. X-ray diffraction identified this phase, along with celsian (BaAl₂Si₂O8) polymorphs and barium titanate crystallites, as the dominant crystalline phases. SEM revealed anisotropic crystal growth (1.14-1.52 μm length). Dielectric characterization in the Ku-band (12.4-18 GHz) demonstrated significant property enhancements, with the relative permittivity decreasing from 10.40 to 6.38 and loss tangent improving from 0.3 to 0.2 after crystallization. These improvements, attributed to the specifically tailored crystalline phase assemblage facilitated by TiO₂, make this glass-ceramic system particularly suitable for advanced microwave applications requiring low dielectric loss and high-frequency stability. The effectiveness of TiO₂ as a crystallization modifier for achieving optimized dielectric properties through controlled devitrification and targeted phase formation is underscored.
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1- The addition of 10 wt% TiO₂ to the BaO-Al₂O₃-SiO₂ glass system resulted in a notable reduction in the glass transition temperature (from 781.6°C to 779.4°C) and softening point (from 838°C to 824.8°C), consequently decreasing the calculated nucleation temperature (from 810°C to 800°C).
2- Isothermal heat treatments at 1000°C led to the development of a multiphase crystalline assemblage in the TiO₂-containing glass that beneficially included the target monoclinic Ba3.75Al7.5Si8.5O32 phase, which was absent in the TiO₂-free glass. X-ray diffraction analysis confirmed the presence of this phase, along with celsian (BaAl₂Si₂O8) polymorphs and barium titanate crystallites.
3-Dielectric characterization in the Ku-band (12.4-18 GHz) demonstrated significant property enhancements, with the relative permittivity decreasing from 10.40 to 6.38 and the loss tangent improving from 0.3 to 0.2 after crystallization.
4- These improvements in dielectric properties are attributed to the formation of the specifically tailored crystalline phase assemblage, including the desired Ba3.75Al7.5Si8.5O32 phase, and the controlled microstructure facilitated by TiO₂ addition.