This article describes a mathematical model for the finishing stage of nylon-6,6 polycondensation in a twin-screw extruder reactor. In the model, the extruder is conceptually divided into two regions. The first one is the partially filled degassing zone, which is operated under low pressure and where the evaporation of water from the polymer takes place. The rate of evaporation is considered to depend on an overall mass transfer coefficient and is limited by the water-polymer physical equilibrium. In the second region, which is fully filled, the polymer flow is assumed to be plug-flow and, in this region, the reversible polycondensation reaction occurs, as well as degradation reactions. A comparison with experimental data obtained in an industrial plant shows fairly good agreement with model predictions after optimal fitting of the rate coefficients.

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The determination of conversion during suspension polymerization reactions is not an easy task due to the heterogeneity of the reaction medium and the tendency of particles to agglomerate rapidly when stirring is stopped. Usually, bulk polymerization in ampoules is employed to study the kinetics of suspension polymerization reactions. In this work, a comparison of different techniques for the determination of conversion during suspension polymerization reactions is presented. Results showed a good agreement between the conversion obtained by gravimetry during styrene suspension polymerization and on-line conversion monitoring data using fiber-optic based Raman Spectroscopy. Nevertheless, the polymerization rate of styrene bulk polymerization carried out in ampoules was higher than the real reaction rate of styrene suspension polymerization due to slightly higher reaction temperatures. Simulation results using the experimental temperature data in a mathematical model confirmed these results

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