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Montedison slurry process

Figure 17.1 Comparison of low and high yield Montedison slurry processes. Figure 17.1 Comparison of low and high yield Montedison slurry processes.
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]

Montedison and Mitsui Petrochemical iatroduced MgCl2-supported high yield catalysts ia 1975 (7). These third-generation catalyst systems reduced the level of corrosive catalyst residues to the extent that neutralization or removal from the polymer was not required. Stereospecificity, however, was iasufficient to eliminate the requirement for removal of the atactic polymer fraction. These catalysts are used ia the Montedison high yield slurry process (Fig. 9), which demonstrates the process simplification achieved when the sections for polymer de-ashing and separation and purification of the hydrocarbon diluent and alcohol are eliminated (121). These catalysts have also been used ia retrofitted RexaH (El Paso) Hquid monomer processes, eliminating the de-ashing sections of the plant (Fig. 10) (129). [Pg.415]

Most commercial processes produce polypropylene by a Hquid-phase slurry process. Hexane or heptane are the most commonly used diluents. However, there are a few examples in which Hquid propylene is used as the diluent. The leading companies involved in propylene processes are Amoco Chemicals (Standard OH, Indiana), El Paso (formerly Dart Industries), Exxon Chemical, Hercules, Hoechst, ICl, Mitsubishi Chemical Industries, Mitsubishi Petrochemical, Mitsui Petrochemical, Mitsui Toatsu, Montedison, Phillips Petroleum, SheU, Solvay, and Sumimoto Chemical. Eastman Kodak has developed and commercialized a Hquid-phase solution process. BASE has developed and commercialized a gas-phase process, and Amoco has developed a vapor-phase polymerization process that has been in commercial operation since early 1980. [Pg.128]

The initial development of a slurry process for Ziegler-based catalysts did not face the same problems as scientists at Phillips. Since Ziegler catalysts are much more sensitive to hydrogen, molecular weight control does not rely on precise control of high reactor temperatures, as it did for the chromium oxide based loop slurry process. Therefore, lower reactor temperatures and heavier hydrocarbons were possible, and there was no need to go beyond a stirred tank. Hoechst developed the first such process, but Montedison, Mitsui, Solvay, and others have also developed similar processes. [Pg.2861]

The first commercial production of crystalline PP was done by the Montedison company at Ferrara, Italy in 1957 using the MOPLEN batch slurry process. [Pg.1]

The Unipol process employs a fluidized bed reactor (see Section 3.1.2) for the preparation of polyethylene and polypropylene. A gas-liquid fluid solid reactor, where both liquid and gas fluidize the solids, is used for Ziegler-Natta catalyzed ethylene polymerization. Hoechst, Mitsui, Montedison, Solvay et Cie, and a number of other producers use a Ziegler-type catalyst for the manufacture of LLDPE by slurry polymerization in hexane solvent (Fig. 6.11). The system consists of a series of continuous stirred tank reactors to achieve the desired residence time. 1-Butene is used a comonomer, and hydrogen is used for controlling molecular weight. The polymer beads are separated from the liquid by centrifugation followed by steam stripping. [Pg.125]

Montedison, Mitsui Monomer slurry reactor Relatively simple process with high product yield... [Pg.127]

Fig. 49. Montedison high-yield slurry polypropylene process 173). By permission of Gulf Publ. Co. Fig. 49. Montedison high-yield slurry polypropylene process 173). By permission of Gulf Publ. Co.

See other pages where Montedison slurry process is mentioned: [Pg.771]    [Pg.772]    [Pg.1147]    [Pg.37]    [Pg.43]    [Pg.6804]    [Pg.53]    [Pg.399]    [Pg.413]    [Pg.6803]   
See also in sourсe #XX -- [ Pg.566 ]




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