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Stirred polymerization reactor

Some slurry processes use continuous stirred tank reactors and relatively heavy solvents (57) these ate employed by such companies as Hoechst, Montedison, Mitsubishi, Dow, and Nissan. In the Hoechst process (Eig. 4), hexane is used as the diluent. Reactors usually operate at 80—90°C and a total pressure of 1—3 MPa (10—30 psi). The solvent, ethylene, catalyst components, and hydrogen are all continuously fed into the reactor. The residence time of catalyst particles in the reactor is two to three hours. The polymer slurry may be transferred into a smaller reactor for post-polymerization. In most cases, molecular weight of polymer is controlled by the addition of hydrogen to both reactors. After the slurry exits the second reactor, the total charge is separated by a centrifuge into a Hquid stream and soHd polymer. The solvent is then steam-stripped from wet polymer, purified, and returned to the main reactor the wet polymer is dried and pelletized. Variations of this process are widely used throughout the world. [Pg.384]

Gas-phase polymerization of propylene was pioneered by BASF, who developed the Novolen process which uses stirred-bed reactors (Fig. 8) (125). Unreacted monomer is condensed and recycled to the polymerizer, providing additional removal of the heat of reaction. As in the early Hquid-phase systems, post-reactor treatment of the polymer is required to remove catalyst residues (126). The high content of atactic polymer in the final product limits its usefiilness in many markets. [Pg.414]

Third-generation high yield supported catalysts are also used in processes in which Hquid monomer is polymerized in continuous stirred tank reactors. The Hypol process (Mitsui Petrochemical), utilizes the same supported catalyst technology as the Spheripol process (133). Rexene has converted the hquid monomer process to the newer high yield catalysts. Shell uses its high yield (SHAC) catalysts to produce homopolymers and random copolymers in the Lippshac process (130). [Pg.416]

Tosun, G., 1992. A mathematical model of mixing and polymerization in a semibatch stirred tank reactor. American Institution of Chemical Engineers Journal, 38, 425 37. [Pg.325]

Polymerizing ethylene can occur either in a tubular or in a stirred autoclave reactor. In the stirred autoclave, the heat of the reaction is absorbed by the cold ethylene feed. Stirring keeps a uniform temperature throughout the reaction vessel and prevents agglomeration of the polymer. [Pg.326]

The polymeric material produced in a single stirred-tank reactor will, except for stochastic variations, be of uniform composition. This polymer composition can be significantly different from the composition in the monomer feed mixture unless the conversion is high. If several tanks are connected in series the composition of the polymer produced in each reactor can be quite different. Since most particles are formed in the first reactor this change in composition in the following reactors can yield polymer particles in which composition varies with radius within the particles. [Pg.8]

Continuous stirred-tank reactors can behave very differently from batch reactors with regard to the number of particles formed and polymerization rate. These differences are probably most extreme for styrene, a monomer which closely follows Smith-Ewart Case 2 kinetics. Rate and number of particles in a batch reactor follows the relationship expressed by Equation 13. [Pg.9]

IT Duerksen, J.H., "Free Radical Polymerization of Styrene in Continuous Stirred Tank Reactors", Ph.D. Thesis, McMaster University, Hamilton, Ontario (1968). [Pg.70]

Various reactor combinations are used. For example, the product from a relatively low solids batch-mass reactor may be transferred to a suspension reactor (for HIPS), press (for PS), or unagitated batch tower (for PS) for finishing. In a similar fashion, the effluent from a continuous stirred tank reactor (CSTR) may be transferred to a tubular reactor or an unagitated or agitated tower for further polymerization before devolatilization. [Pg.72]

Peaking and Non-isothermal Polymerizations. Biesenberger a (3) have studied the theory of "thermal ignition" applied to chain addition polymerization and worked out computational and experimental cases for batch styrene polymerization with various catalysts. They define thermal ignition as the condition where the reaction temperature increases rapidly with time and the rate of increase in temperature also increases with time (concave upward curve). Their theory, computations, and experiments were for well stirred batch reactors with constant heat transfer coefficients. Their work is of interest for understanding the boundaries of stability for abnormal situations like catalyst mischarge or control malfunctions. In practice, however, the criterion for stability in low conversion... [Pg.75]

The advantages of continuous tubular reactors are well known. They include the elimination of batch to batch variations, a large heat transfer area and minimal handling of chemical products. Despite these advantages there are no reported commercial instances of emulsion polymerizations done in a tubular reactor instead the continuous emulsion process has been realized in series-connected stirred tank reactors (1, . ... [Pg.113]

An Experimental Study Using Feed Perturbations for a Free-Radically Initiated Homogeneous Polymerization in a Continuous-Flow Stirred-Tank Reactor... [Pg.253]

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]

The research programme into n-butyl lithium initiated, anionic polymerization started at Leeds in 1972 and involved the construction of a pilot scale, continuous stirred tank reactor. This was operated isothermally, to obtain data under a typical range of industrial operating conditions. [Pg.281]

A pilot scale plant, incorporating a three litre continuous stirred tank reactor, was used for an investigation into the n-butyl lithium initiated, anionic polymerization of butadiene in n-hexane solvent. The rig was capable of being operated at elevated temperatures and pressures, comparable with industrial operating conditions. [Pg.294]

Anionic Styrene Polymerization in a Continuous Stirred-Tank Reactor... [Pg.295]

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]

Reactor Conditions for Experimental Runs. Operating conditions for the continuous, stirred tank reactor runs were chosen to study the effects of mixing speed on the monomer conversion and molecular weight distribution at different values for the number average degree of polymerization of the product polymer. [Pg.309]

Continuous-flow stirred tank reactors are widely used for free-radical polymerizations. They have two main advantages the solvent or monomer can be boiled to remove the heat of polymerization, and fairly narrow molecular weight and copolymer composition distributions can be achieved. Stirred tanks or... [Pg.492]

Ease of access to the interior surface of stirred tanks is an additional advantage of this type of reactor. This consideration is particularly significant in polymerization reactors, where one needs to worry about periodic cleaning of internal surfaces. [Pg.250]

Continuous-stirred tank reactor anionic polymerization, 23 385, 394-395, 396 Continuous-stirred-tank-reactor processes, 23 366, 367... [Pg.214]

CSTR reactor system, 23 396. See also Continuous- stirred tank reactor (CSTR) anionic polymerization C-toxiferine, 2 74, 99 C-type inks, 14 324, 326 C-type natriuretic peptide (CNP), 5 186-187... [Pg.237]


See other pages where Stirred polymerization reactor is mentioned: [Pg.204]    [Pg.204]    [Pg.280]    [Pg.384]    [Pg.386]    [Pg.386]    [Pg.413]    [Pg.521]    [Pg.2102]    [Pg.254]    [Pg.31]    [Pg.32]    [Pg.76]    [Pg.76]    [Pg.295]    [Pg.295]    [Pg.297]    [Pg.298]    [Pg.322]    [Pg.323]    [Pg.413]    [Pg.505]    [Pg.567]    [Pg.288]    [Pg.329]    [Pg.336]    [Pg.139]    [Pg.1518]   
See also in sourсe #XX -- [ Pg.204 ]




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