A Model-Fitting Approach to Characterizing Polymer Decomposition Kinetics

The use of isoconversional, sometimes called model-free, kinetic analysis methods have recently gained favor in the thermal analysis community. Although these methods are very useful and instructive, the conclusion that model fitting is a poor approach is largely due to improper use of the model fitting approach, such as fitting each heating rate separately. The current paper shows the ability of model fitting to correlate reaction data over very wide time-temperature regimes, including simultaneous fitting of isothermal and constant heating rate data. Recently published data on cellulose pyrolysis by Capart et al. (TCA, 2004) with a combination of an autocatalytic primary reaction and an nth-order char pyrolysis reaction is given as one example. Fits for thermal decomposition of Estane, Viton-A, and Kel-F over very wide ranges of heating rates is also presented. The Kel-F required two parallel reactions--one describing a small, early decomposition process, and a second autocatalytic reaction describing the bulk of pyrolysis. Viton-A and Estane also required two parallel reactions for primary pyrolysis, with the first Viton-A reaction also being a minor, early process. In addition, the yield of residue from these two polymers depends on the heating rate. This is an example of a competitive reaction between volatilization and char formation, which violates the basic tenet of the isoconversional approach and is an example of why it has limitations. Although more complicated models have been used in the literature for this type of process, we described our data well with a simple addition to the standard model in which the char yield is a function of the logarithm of the heating rate