Faculty Publications

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    Optical, dielectric and mechanical properties of silver nanoparticle embedded calcium phosphate glass
    (Elsevier, 2014) Venkateswara Rao, G.V.; Shashikala, H.D.
    Silver nanoparticles have been embedded in 50 mol% CaO-50 mol% P 2O5 glass using melt quenching technique. The quenched glasses were heat treated at 550 °C for different durations between 10 and 50 h. The growth of silver nanoparticles in glass matrix appeared to be time dependent. FTIR spectra revealed that silver nanocluster formation had not affected the position of vibration bands of basic phosphate tetrahedral network. The Ag nanoparticle embedded glass matrix showed the red shift and broadening of the surface plasmon resonance (SPR) peak in the visible region with the increase in the duration of the heat treatment. Results showed the increase in size of the nanoparticles in glass matrix with heat treatment which was further confirmed using transmission electron microscopy and XRD. X-ray diffraction studies indicated the presence of Ag crystalline peaks along with amorphous structure on heat treatment at 550 °C for 50 h. The dielectric constant of these glasses increased as the duration of the heat treatment increased. Increase in both Vickers hardness and fracture toughness, and decrease in brittleness were observed which can be attributed to the increase in size of the nanoparticles in glass matrix. © 2014 Elsevier B.V.
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    Effect of heat treatment on optical, dielectric and mechanical properties of silver nanoparticle embedded CaOCaF2P2O5 glass
    (Elsevier Ltd, 2015) Venkateswara Rao, G.; Shashikala, H.D.
    Silver nanoparticle have been embedded in CaOCaF2P2O5 glass using melt quenching technique. The quenched glasses were heat treated at 550 °C for 10, 20, 30, 40 and 50 h. The growth of silver nanoparticle in the glass matrix appeared to be time dependent. FTIR spectra show that silver nanoparticle formation has not affected the vibration bands of basic phosphate tetrahedral network. The increase in compactness of the glass structure is confirmed by increase in measured density of the glasses with increase in the duration of the heat treatment. Glass containing spherical silver nanoparticle shows the red shift and increase in the full width half maxima (FWHM) of the surface plasmon resonance (SPR) in the visible region with increase in the duration of the heat treatment. X-ray diffraction pattern indicated the presence of Ag crystalline peaks along with amorphous structure on heat treating at 550°C for 50 h. For the glass samples, the increase in dielectric constant and low dielectric loss around 0.005 were observed with increase in duration of the heat treatment. Both Vickers hardness and fracture toughness increased while the brittleness decreased which can be attributed to the increase in size of the nanoparticles in glass matrix. © 2014 Elsevier B.V. All rights reserved.
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    Optical absorption, mechanical properties and FTIR studies of silver-doped barium phosphate glasses
    (Society of Glass Technology christine@glass.demon.co.uk, 2016) Narayanan, M.K.; Shashikala, H.D.
    Silver-doped barium phosphate glasses, of composition 50BaO-50P2O5-4Ag2O-4SnO, were prepared by conventional melt quenching and subsequent heat treatment. Prepared glasses were heat treated for a fixed duration of 10 h at different temperatures 400, 450 and 500°C to develop silver nanoparticles of different sizes. Formation and the size of the silver nanoparticles were evaluated using the surface plasmon resonance (SPR) band of the optical absorption spectrum, which revealed that both of them were temperature dependent. Spectral positions of the SPR peaks of the glass samples heat treated at 450 and 500°C were observed around 3.0 eV. Absence of significant size dependent shift in SPR peaks of these samples from 3.0 eV indicates the formation of spherical silver nanoparticles smaller than 20 nm inside the glass matrix, which falls in the quasi-static regime of Mie theory. The effect of heat treatment on the local network structure of the phosphate glass matrix assessed using FTIR spectra shows that formation and growth of silver nanoclusters do not affect the basic metaphosphate network structure. A slight improvement is observed in density as well as in the mechanical properties of the heat treated samples due to densification of the glass matrix by dispersed silver nanoparticles.
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    Optical and structural properties of BCBS glass system with and without alumina
    (Elsevier B.V., 2018) Bhattacharya, S.; Shashikala, H.D.
    BaO–CaO–Al2O3–SiO2 (BCAS) glass and their derivatives have gained extreme importance for their high endurance to elevated temperatures and being suitable for various electrochemical applications. Two glass systems, one being 50mol% [SiO2–B2O3]-xBaO-(45-x)CaO–5Al2O3 called as BCBSA and another without Al2O3 termed as BCBS were synthesized using melt quenching technique in the present work. Addition of ZnO and MgO as flux helped in melting them at 1300 °C which is much lower than the usual melting temperature of these glasses [1–4]. Density of the quenched glasses was measured by Archimedes method and structural bond vibrations were confirmed through FTIR. UV Visible spectroscopy was used to determine band gap energy and confirm the insulating nature of the synthesized glasses. The samples were isothermally heated at 700 °C, 800 °C for 50 h and at 900 °C for 50 and 100 h duration in air to allow the devitrification process to take place. The heat treated samples were analyzed by X-ray diffraction to identify the developed phases. Five Al2O3 free samples synthesized at 1300 °C by regular melt quenching technique were found to be devoid of the monocelsian phase. This is a detrimental phase for high temperature sealant applications as it has a very low coefficient of thermal expansion (CTE). Al2O3 free BCBS glasses, properties of which are being reported for the first time and glasses with low BaO concentrations are found to meet the requirements for high temperature applications as sealants in Solid Oxide Fuel Cell (SOFC). © 2018 Elsevier B.V.