The thermal degradation rate of organic carbon on fly ashes from different municipal solid waste incinerators, MSWIs, is studied in batch experiments in air. A global parameter, total organic carbon (TOC), is used to measure the decrease of reagent concentration in time. The TOC vs time data are well fitted by deconvolution treatment with a sum of two first-order reactions, Ri and Rj. To identify the limits of deconvolution, kinetics of the model systems dibenzofuran (DF)−biphenyl (BPh)−SiO 2 and DF−BPh−active carbon−SiO 2 are studied. Both Ri and Rj are carbon oxidation reactions to CO 2, the oxidized carbon being not from adsorbed organic compounds but from the native carbon matrix of MSWI fly ash. Large negative Δ S ⧧ values indicate that Ri and Rj transition states are more compact and stiffer than the reagent ones. Structural changes are more important than chemical transformations since the entropic term is predominant in determining the Δ G ⧧ values. The key experimental information for the formulation of a generalized kinetic model and a mechanism for carbon gasification (Part 2) is the temperature dependence of the preexponential parameters in the empirical rate equation.
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Lasagni et al. (1999) studied this question.
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