It is shown that the relationship between the catalyst/polymer structure, process conditions and final product properties needs to be addressed in more detail. From an industrial point of view, the interest starts from the need to control the growth of the catalyst/polymer particle during the polymerisation process. This first part of a two-part review discusses the different factors that can influence the physical properties of the nascent polymer, and how these can impact the evolution of particle morphology.
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ABSTRACT:In free radical polymerization diffusion-controlled processes take place simultaneously to the normal chemical reactions. Despite extensive efforts to model such processes a consistent model for the design of a polymerization reactor has not yet been established. In this article a semiempirical model describing the conversion, polymerization degree, and molecular weight distribution ( MWD ) for the free radical polymerization is developed for the entire course of the reaction. The model includes the change of termination, propagation, transfer, and initiation rate. By simultaneous parameter estimation from the conversion and degrees of polymerization data the model parameters have been determined for isothermal polymerizations of methyl methacrylate ( MMA ) and styrene ( ST ) . The simulation results for the conversion, degrees of polymerization, and MWD are in good accordance with experimental data for suspension and bulk polymerization of MMA and ST up to very high conversions. The influence of diffusion on the propagation rate in case of polymerization of MMA is negligible compared to the influence of the cage effect on the radical efficiency; in case of ST polymerization both effects must be included in the kinetic model. The model presented is also tested for polymerizations conducted in the presence of solvent and / or chain transfer agents.
ABSTRACT:Liquid propylene was polymerized in a 5-L autoclave batch reactor using a commercially available TiCl 4 /MgCl 2 /Al(ethyl) 3 /DCPDMS Ziegler-Natta catalyst, with a phthalate ester as internal electron donor. The powders from these polymerizations were characterized using laser diffraction particle size distribution (PSD) analysis, scanning electron microscopy (SEM), and bulk density measurements. These characteristics were analyzed as a function of the process conditions, including hydrogen and monomer concentration, polymerization temperature, and the prepolymerization method. It was shown that polymerization temperature influences the powder morphology to a large extent. At low temperatures, high-density particles were obtained, showing regular shaped particle surfaces and low porosities. With increasing temperature, the morphology gradually was transferred into a more open structure, with irregular surfaces and poor replication of the shape of the catalyst particle. When using a prepolymerization step at a relatively low temperature, the morphology obtained was determined by this prepolymerization step and was independent from conditions in main polymerization. The morphology obtained was the same as that observed after a full polymerization at temperature. Even when using a short polymerization at an increasing temperature, the morphology was strongly influenced by the initial conditions. The effect of variation in hydrogen concentration supported the conclusion that the initial polymerization rate determines the powder morphology. In the absence of hydrogen, high bulk densities, and regularly shaped particles were obtained, even at high temperatures. With increasing hydrogen concentration, the reaction rates increased rapidly, and with that changed the morphology.
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