12 research outputs found

    Enhanced general analytical equation for the kinetics of the thermal degradation of poly(lactic acid)/montmorillonite nanocomposites driven by random scission

    No full text
    An enhanced general analytical equation has been developed in order to evaluate the kinetic parameters of the thermal degradation of nanocomposites, composed of poly(lactic acid) (PLA) and organo-modified montmorillonite (OMMT) nanoparticles. This improvement has consisted of replacing the n-order conversion function by a modified form of the Sestak-Berggren equation f(a) = c (1 - a)nam that led to a better adjustment of experimental data and also adequately represented the conventional mechanisms for solid-state processes. The kinetic parameters so obtained have been compared to those determined by conventional differential and isoconversional methods. Given that the thermal degradation of PLA has been argued to be caused by random chain scission reactions of ester groups, the conversion function f(a) = L (L - 1)x(1 - x)L-1, corresponding to a random scission mechanism, has been tested. Once optimized the kinetic model, the thermal degradation kinetics of nanocomposites (0.5 and 2.5% of OMMT) was compared to that of the polymer matrix. Moreover, the thermal stability of nanocomposites was tested and compared to that of the polymer matrix.Postprint (published version

    Enhanced general analytical equation for the kinetics of the thermal degradation of poly(lactic acid)/montmorillonite nanocomposites driven by random scission

    No full text
    An enhanced general analytical equation has been developed in order to evaluate the kinetic parameters of the thermal degradation of nanocomposites, composed of poly(lactic acid) (PLA) and organo-modified montmorillonite (OMMT) nanoparticles. This improvement has consisted of replacing the n-order conversion function by a modified form of the Sestak-Berggren equation f(a) = c (1 - a)nam that led to a better adjustment of experimental data and also adequately represented the conventional mechanisms for solid-state processes. The kinetic parameters so obtained have been compared to those determined by conventional differential and isoconversional methods. Given that the thermal degradation of PLA has been argued to be caused by random chain scission reactions of ester groups, the conversion function f(a) = L (L - 1)x(1 - x)L-1, corresponding to a random scission mechanism, has been tested. Once optimized the kinetic model, the thermal degradation kinetics of nanocomposites (0.5 and 2.5% of OMMT) was compared to that of the polymer matrix. Moreover, the thermal stability of nanocomposites was tested and compared to that of the polymer matrix

    Enhanced general analytical equation for the kinetics of the thermal degradation of poly(lactic acid) driven by random scission

    No full text
    An enhanced general analytical equation has been developed in order to evaluate the kinetic parameters of the thermal degradation of poly(lactic acid) (PLA) at various linear heating rates and at constant rate conditions. This improvement consisted of replacing the n-order conversion function by a modified form of the Sestak-Berggren equation f(α) = c(1−α)nαm, which led to better adjustment of experimental data, and also adequately represented the conventional mechanisms for solid-state processes. The kinetic parameters so obtained have been compared to those determined by conventional differential and isoconversional methods. Given that the thermal degradation of PLA has been argued to be caused by random chain scission reactions of ester groups, the conversion function (α) = 2(α1/2−α), corresponding to a random scission mechanism, has been tested.Peer Reviewe

    Enhanced general analytical equation for the kinetics of the thermal degradation of poly(lactic acid) driven by random scission

    No full text
    An enhanced general analytical equation has been developed in order to evaluate the kinetic parameters of the thermal degradation of poly(lactic acid) (PLA) at various linear heating rates and at constant rate conditions. This improvement consisted of replacing the n-order conversion function by a modified form of the Sestak-Berggren equation f(α) = c(1−α)nαm, which led to better adjustment of experimental data, and also adequately represented the conventional mechanisms for solid-state processes. The kinetic parameters so obtained have been compared to those determined by conventional differential and isoconversional methods. Given that the thermal degradation of PLA has been argued to be caused by random chain scission reactions of ester groups, the conversion function (α) = 2(α1/2−α), corresponding to a random scission mechanism, has been tested.Peer Reviewe
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