2014
DOI: 10.1016/j.ceramint.2014.04.089
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Non-isothermal free-models kinetic analysis on crystallization of europium-doped phosphate glasses

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Cited by 10 publications
(2 citation statements)
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“…The activation energies increases with increase in conversion in the range 0.05 < α < 0.80, with the maximum value at 532 kJ mol −1 and demonstrates the complex nature of thermal decomposition of the poly(1‐octene‐ co ‐BMA) copolymer . Subsequent to the initial decomposition of weak linkages the activation energy increases at the later stages of decomposition …”
Section: Resultsmentioning
confidence: 99%
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“…The activation energies increases with increase in conversion in the range 0.05 < α < 0.80, with the maximum value at 532 kJ mol −1 and demonstrates the complex nature of thermal decomposition of the poly(1‐octene‐ co ‐BMA) copolymer . Subsequent to the initial decomposition of weak linkages the activation energy increases at the later stages of decomposition …”
Section: Resultsmentioning
confidence: 99%
“…This analysis is based on F ‐test on fit quality for thermogravimetric curves, and the principle of selection is based on the best possible process mechanism corresponding to the best agreement between E FR = E FR ( α ) (where, E FR is the activation energy calculated from isoconversional method of FR, α is the degree of conversion). The best fit data was obtained from nonisothermal experimental data and actual activation energy values obtained by applying the differential methods of isothermal data simulated by the software using nonisothermal kinetic parameters . After simulation of the experimental data for 0.05 ≤ α ≤ 0.80, the selection of the best fit model was done by the Netzsch software programme.…”
Section: Resultsmentioning
confidence: 99%