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Polymerization reactions flow stirred tank

In this short initial communication we wish to describe a general purpose continuous-flow stirred-tank reactor (CSTR) system which incorporates a digital computer for supervisory control purposes and which has been constructed for use with radical and other polymerization processes. The performance of the system has been tested by attempting to control the MWD of the product from free-radically initiated solution polymerizations of methyl methacrylate (MMA) using oscillatory feed-forward control strategies for the reagent feeds. This reaction has been selected for study because of the ease of experimentation which it affords and because the theoretical aspects of the control of MWD in radical polymerizations has attracted much attention in the scientific literature. [Pg.253]

In this work, the characteristic "living" polymer phenomenon was utilized by preparing a seed polymer in a batch reactor. The seed polymer and styrene were then fed to a constant flow stirred tank reactor. This procedure allowed use of the lumped parameter rate expression given by Equations (5) through (8) to describe the polymerization reaction, and eliminated complications involved in describing simultaneous initiation and propagation reactions. [Pg.297]

Continuous-flow stirred-tank reactors (CSTRs) can be cooled in three ways. The most elegant method is to allow boiling of the monomer or solvent so that the heat of reaction is removed in an overhead condenser. The pressure in the vessel is set to give the desired temperature. The condensate can be returned to the vessel or recycled back to the feed. This process is commonly used for polystyrene. Chilling the feed is another means for managing the exotherm in a CSTR. Refrigeration to -40°C has been used for the bulk, continuous polymerization of PMMA. Laboratory reactors and small-scale industrial reactors can be cooled using jackets or internal coils, but this method scales up poorly. [Pg.852]

Temperature and free-radical concentration are important features that vary along the length of the plug-flow tubular reactor model of the polymerization of ethylene/ Stirred-tank reactor models of the anionic polymerization of styrene and of butadiene have been described and tested against experiments. Mathematical modelling of polymerization reactions receives some attention in the book by Froment and Bischoff. ... [Pg.364]

Polystyrene can be easily prepared by emulsion or suspension techniques. Harkins (1 ), Smith and Ewart(2) and Garden ( ) have described the mechanisms of emulsTon polymerization in batch reactors, and the results have been extended to a series of continuous stirred tank reactors (CSTR)( o Much information on continuous emulsion reactors Ts documented in the patent literature, with such innovations as use of a seed latex (5), use of pulsatile flow to reduce plugging of the tube ( ), and turbulent flow to reduce plugging (7 ). Feldon (8) discusses the tubular polymerization of SBR rubber wTth laminar flow (at Reynolds numbers of 660). There have been recent studies on continuous stirred tank reactors utilizing Smith-Ewart kinetics in a single CSTR ( ) as well as predictions of particle size distribution (10). Continuous tubular reactors have been examined for non-polymeric reactions (1 1 ) and polymeric reactions (12.1 31 The objective of this study was to develop a model for the continuous emulsion polymerization of styrene in a tubular reactor, and to verify the model with experimental data. [Pg.367]

Example 4-8 An ideal continuous stirred-tank reactor is used for the homogeneous polymerization of monomer M. The volumetric flow rate is O, the volume of the reactor is V, and the density of the reaction solution is invariant with composition. The concentration of monomer in the feed is [M]o. The polymer product is produced by an initiation step and a consecutive series of propagation reactions. The reaction mechanism and rate equations may be described as follows, where is the activated monomer and P2, . . , P are polymer molecules containing n monomer units ... [Pg.169]


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