Non-isothermal sinter-crystallisation of satin glazes: A kinetic model
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Altres documents de l'autoria: José Luis, Amorós Albaro; Blasco Roca, Encarna; Moreno Berto, Arnaldo Vicente; Gómez-Tena, Maria Pilar; Feliu Mingarro, Carlos
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Mostra el registre complet de l'elementcomunitat-uji-handle:10234/9
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comunitat-uji-handle3:10234/8618
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INVESTIGACIONMetadades
Títol
Non-isothermal sinter-crystallisation of satin glazes: A kinetic modelAutoria
Data de publicació
2018-05Editor
ElsevierISSN
0272-8842; 1873-3956Cita bibliogràfica
AMORÓS, J. L., et al. Non-isothermal sinter-crystallisation of satin glazes: A kinetic model. Ceramics International, 2018, vol. 44, no 7, p. 7780-7787Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
https://www.sciencedirect.com/science/article/pii/S0272884218302244Versió
info:eu-repo/semantics/submittedVersionParaules clau / Matèries
Resum
Many materials of a glass-ceramic nature are obtained by glass particle sinter-crystallisation, whose process kinetics have been studied very little. The present study analyses the physico-chemical transformations ... [+]
Many materials of a glass-ceramic nature are obtained by glass particle sinter-crystallisation, whose process kinetics have been studied very little. The present study analyses the physico-chemical transformations that develop during the firing of a complex commercial satin glaze (containing more than five phases), with high frit content, particularly focusing on sinter-crystallisation kinetics. Glaze sintering and phase evolution were studied by hot stage microscopy (HSM) and X-ray diffraction (XRD). The glaze melting and crystallisation ranges and the kinetic parameters of the crystallisation process were determined by differential thermal analysis (DTA). Glaze sinter-crystallisation behaviour and the development of the crystal mass fractions, residual glass compositions, and effective viscosity, ηeff, during heating are discussed, based on Rietveld analysis of the XRD data. A new kinetic model was developed that describes the non-isothermal sinter-crystallisation of materials exhibiting three-stage sintering. A two-step kinetic model is involved: sintering with concurrent surface crystallisation (corresponding to sintering stages I and II) and sintering with simultaneous partial melting of crystalline phases (sintering stage III). The experimental data obtained by hot stage microscopy (HSM) at different heating rates were compared with those estimated by the model. The results obtained by the two methods exhibited very good agreement. The crystallisation kinetic parameters (activation energy, Ecr, and Avrami index, n, obtained by DTA, were consistent with the viscous flow activation energy, Q2, corresponding to the first sintering step (sintering stages I and II). The model was used to calculate the values of the effective sintering viscosity, ηs, of the glaze melt. These values were compared with the experimental effective viscosity, ηeff, data obtained by hot stage microscopy (HSM). Both sets of results exhibited good agreement. Effective sintering viscosity, ηs, which is readily measurable, helps better understand the role played by the different glaze constituents and by the firing conditions in sintering, enabling more rational design of these materials. [-]
Publicat a
Ceramics International, 2018, vol. 44, no 7Drets d'accés
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info:eu-repo/semantics/openAccess
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