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Process catalytic multiphase systems

Figure 1731. Fluidized bed reactor processes for the conversion of petroleum fractions, (a) Exxon Model IV fluid catalytic cracking (FCC) unit sketch and operating parameters. (Hetsroni, Handbook of Multiphase Systems, McGraw-Hill, New York, 1982). (b) A modem FCC unit utilizing active zeolite catalysts the reaction occurs primarily in the riser which can be as high as 45 m. (c) Fluidized bed hydroformer in which straight chain molecules are converted into branched ones in the presence of hydrogen at a pressure of 1500 atm. The process has been largely superseded by fixed bed units employing precious metal catalysts (Hetsroni, loc. cit.). (d) A fluidized bed coking process units have been built with capacities of 400-12,000 tons/day. Figure 1731. Fluidized bed reactor processes for the conversion of petroleum fractions, (a) Exxon Model IV fluid catalytic cracking (FCC) unit sketch and operating parameters. (Hetsroni, Handbook of Multiphase Systems, McGraw-Hill, New York, 1982). (b) A modem FCC unit utilizing active zeolite catalysts the reaction occurs primarily in the riser which can be as high as 45 m. (c) Fluidized bed hydroformer in which straight chain molecules are converted into branched ones in the presence of hydrogen at a pressure of 1500 atm. The process has been largely superseded by fixed bed units employing precious metal catalysts (Hetsroni, loc. cit.). (d) A fluidized bed coking process units have been built with capacities of 400-12,000 tons/day.
The most catalytic or noncatalytic processes involving reactions in multiphase systems. Such processes include heat and mass transfer and other diffusion phenomena. The applications of these processes are diverse and its reactors have their own characteristics, which depends on the type of process. For example, the hydrogenation of vegetable oils is conducted in a liquid phase slurry bed reactor, where the catalyst is in suspension, the flow of gaseous hydrogen keeps the particles in suspension. This type of reaction occurs in the gas-liquid-solid interface. [Pg.555]

Mass transfer with chemical reaction in multiphase systems" covers, indeed, a large area. Table 1 shows a general classification of the systems encountered. From the possible two-phase systems, solid-solid reactions, liquid-solid (reactive or catalytic) and gas-solid (reactive or catalytic) reactions are not discussed here. The first one was reviewed by Tamhankar and Doraiswamy (2) and gas-solid (reactive) systems, such as, coal gasification, calcination of limestone, reduction of ores, etc. have been treated in some detail in recent reviews (3-5). The industrially important fluid-solid catalytic processes were the topic of a previous Advanced Study Institute (6) and have been also discussed authoritatively elsewhere (5,7). Concerning solid (reactive)-liquid two-phase systems, only some interesting examples are presented in Table 2 (1). [Pg.4]

Flowever, information concerning the characteristics of these systems under the conditions of a continuous process is still very limited. From a practical point of view, the concept of ionic liquid multiphasic catalysis can be applicable only if the resultant catalytic lifetimes and the elution losses of catalytic components into the organic or extractant layer containing products are within commercially acceptable ranges. To illustrate these points, two examples of applications mn on continuous pilot operation are described (i) biphasic dimerization of olefins catalyzed by nickel complexes in chloroaluminates, and (ii) biphasic alkylation of aromatic hydrocarbons with olefins and light olefin alkylation with isobutane, catalyzed by acidic chloroaluminates. [Pg.271]

A recent proposal concerns mixed organic-aqueous tunable solvents (OATS) such as dimethyl ether-water, the solubility of which for substrates can be influenced by a third component such as carbon dioxide. CO2 acts as a antisolvent and as a switch to cause a phase separation and to decant the phases from each other (preferably under pressure). This behavior makes the operation of bi- or multiphase homogeneous catalytic processes easier and more economic the preferential dissolution at modest pressure of carbon dioxide causes phase separation which results in large distribution coefEcients of target molecules in biphasic organic-aqueous systems. This extraordinary behavior lead to a sophisticated flow scheme (Figure 6) [7]. [Pg.9]

Fluorous catalysis is now a weU-established area and provides a complementary approach to aqueous- or ionic-biphase catalysis and the other possibilities of multiphase homogeneous catalysis (not to mention combinations of the different processes). Since each catalytic chemical reaction could have its own perfectly designed catalyst (e.g., a chemzyme), the possibility of selecting from biphase systems ranging from fluorous to aqueous systems provides a powerful portfolio for catalyst designers. [Pg.405]


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See also in sourсe #XX -- [ Pg.246 , Pg.247 ]




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