The kinetics of the pyrolysis of n‐hexane was studied in a conventional static reactor over a temperature range of 650–840 K. The overall reaction is essentially first order with the kinetic parameters A = 1013.92 s−1 and EA = 260.3 kJ/mol. The distributions of the main products were analyzed by gas chromatography. A reaction model involving 240 elementary reactions was developed to describe the experimental rate data. The agreement of the model with experimental data was surprisingly good over a wide range of temperatures and pressures and up to medium extents of conversion. Methods for sensitivity studies based upon the quasi‐stationary‐state assumption (QSSA) were developed, and for a number of more detailed effects, such as self‐inhibition, explanations could be given. It was also shown that the hexyl isomerization reactions influence strongly the product distribution. The outstanding capability of kinetic modeling with computer simulations in handling complex kinetic systems is demonstrated.
The thermal degradation of polydisperse polystyrene samples with mol. wts. (3,) between 6OOOO and 220000 has been investigated at different temperatures under oxygen free conditions. Product analysis has been carried out by GPC. The experimental degradation could be simulated by a model consisting of scission and depolymerization. The dynamical behaviour of this model is expressed in a matrix form. The ratio of scission and depolymerization is constant for all polymers and different temperatures during degradation. Therefore, a master curve could be evaluated, which gives a general relation between the decrease of mol. wt. and the mass of volatiles. Finally a radical chain mechanism has been proposed in a lumped form which is consistent with the kinetic model and the experimental results. 0025-1 16X/82/05 1207-12/%03.00
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