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Two-phase Reactors

Classification by Phase Despite the generic classification by operating mode, reactors are designed to accommodate the reactant phases and provide optimal conditions for reaction. Reactants may be fluid(s) or solid(s), and as such, several reactor types have been developed. Singlephase reactors are typically gas- (or plasma- ) or liquid-phase reactors. Two-phase reactors may be gas-liquid, liquid-liquid, gas-solid, or liquid-solid reactors. Multiphase reactors typically have more than two phases present. The most common type of multiphase reactor is a gas-liquid-solid reactor however, liquid-liquid-solid reactors are also used. The classification by phases will be used to develop the contents of this section. [Pg.7]

FIGURE 7A.10 Variation of power number with impeller speed for two-phase (gas-liquid) and three-phase (gas-liquid-solid) stirred reactors. Two phase (solid-liquid) system. A, fillet formation B, disappearance of fillets C, off-bottom suspension of solids D, recirculation of mixture. Three phase (gas-liquid-sohd). A, no dispersion of gas solid settled on bottom B, gas dispersed beginning of solid suspension C, gas dispersed off-bottom suspension of solids D, recirculation of mixture. (Reproduced from Rewatkar et al. 1991 with permission from American Chemical Society. 1991, American Chemical Society.)... [Pg.154]

A simultaneous flow of a gas and a liquid, a gas and a solid, two different liquids, or a liquid and a solid is described as a two-phase flow. Among these types of two-phase flow, gas-liquid flow is the most complex flow due to the deformability and the compressibility of the phases. The analysis of the two-phase flow is very important for liquid-cooled reactors. Two-phase flow occurs in the BWR core and in the steam generator of the PWRs. In order to analyze reactor systems with liquid-vapor mixtures, it is necessary to predict liquid-vapor density, pressure drop across a given channel length, flow stability, maximum flow rates, and heat transfer rates. As the liquid is vaporized, the mixture of vapor and liquid flow gives rise to interesting flow and heat transfer challenges. [Pg.754]

Fluidized Bed Reactor. Two-Phase Model with Ten Lump Reaction Scheme... [Pg.718]

Special consideration needs to be given to heterogeneous reactors, in which interaction of the phases is required for the reactions to proceed. In these situations, the rate of reaction may not be the deciding factor in the reactor design. The rate of transport of reactants and products from one phase to another can limit the rate at which products are obtained. For example, if reactants cannot get to the surface of a soHd catalyst faster than they would react at the surface, then the overall (observed) rate of the process is controlled by this mass transfer step. To improve the rate, the mass transfer must be increased. It would be useless to make changes that would affect only the surface reaction rate. Furthermore, if products do not leave the surface rapidly, they may block reaction sites and thus limit the overall rate. Efficient contacting patterns need to be utilized. Hence, fluidized bed reactors (two-phase backmixed emulator), trickle-bed systems (three-phase packed bed emulator), and slurry reactors (three-phase backmixed emulator) have... [Pg.70]

Catalyst recovery is a major operational problem because rhodium is a cosdy noble metal and every trace must be recovered for an economic process. Several methods have been patented (44—46). The catalyst is often reactivated by heating in the presence of an alcohol. In another technique, water is added to the homogeneous catalyst solution so that the rhodium compounds precipitate. Another way to separate rhodium involves a two-phase Hquid such as the immiscible mixture of octane or cyclohexane and aliphatic alcohols having 4—8 carbon atoms. In a typical instance, the carbonylation reactor is operated so the desired products and other low boiling materials are flash-distilled. The reacting mixture itself may be boiled, or a sidestream can be distilled, returning the heavy ends to the reactor. In either case, the heavier materials tend to accumulate. A part of these materials is separated, then concentrated to leave only the heaviest residues, and treated with the immiscible Hquid pair. The rhodium precipitates and is taken up in anhydride for recycling. [Pg.78]

Cyclohexane, produced from the partial hydrogenation of benzene [71-43-2] also can be used as the feedstock for A manufacture. Such a process involves selective hydrogenation of benzene to cyclohexene, separation of the cyclohexene from unreacted benzene and cyclohexane (produced from over-hydrogenation of the benzene), and hydration of the cyclohexane to A. Asahi has obtained numerous patents on such a process and is in the process of commercialization (85,86). Indicated reaction conditions for the partial hydrogenation are 100—200°C and 1—10 kPa (0.1—1.5 psi) with a Ru or zinc-promoted Ru catalyst (87—90). The hydration reaction uses zeotites as catalyst in a two-phase system. Cyclohexene diffuses into an aqueous phase containing the zeotites and there is hydrated to A. The A then is extracted back into the organic phase. Reaction temperature is 90—150°C and reactor residence time is 30 min (91—94). [Pg.242]

Fig. 3. Schematics of ahquid two-phase reactor system for 2-bromothiophene. Fig. 3. Schematics of ahquid two-phase reactor system for 2-bromothiophene.
Fig. 7. Process flow diagram for the two-phase hydroformylation of propylene where 1 = reactor 2 = separator 3 = phase separator ... Fig. 7. Process flow diagram for the two-phase hydroformylation of propylene where 1 = reactor 2 = separator 3 = phase separator ...
FIG. 23-25 Typ es of industrial gas/Hqiiid reactors, (a) Tray tower, (h) Packed, counter current, (c) Packed, parallel current, (d) Falling liquid film, (e) Spray tower, if) Bubble tower, (g) Venturi mixer, h) Static in line mixer, ( ) Tubular flow, (j) Stirred tank, (A,) Centrifugal pump, (/) Two-phase flow in horizontal tubes. [Pg.2105]

The effect of physical processes on reactor performance is more complex than for two-phase systems because both gas-liquid and liquid-solid interphase transport effects may be coupled with the intrinsic rate. The most common types of three-phase reactors are the slurry and trickle-bed reactors. These have found wide applications in the petroleum industry. A slurry reactor is a multi-phase flow reactor in which the reactant gas is bubbled through a solution containing solid catalyst particles. The reactor may operate continuously as a steady flow system with respect to both gas and liquid phases. Alternatively, a fixed charge of liquid is initially added to the stirred vessel, and the gas is continuously added such that the reactor is batch with respect to the liquid phase. This method is used in some hydrogenation reactions such as hydrogenation of oils in a slurry of nickel catalyst particles. Figure 4-15 shows a slurry-type reactor used for polymerization of ethylene in a sluiTy of solid catalyst particles in a solvent of cyclohexane. [Pg.240]

Measurements of the true reaction times are sometimes difficult to determine due to the two-phase nature of the fluid reactants in contact with the solid phase. Adsorption of reactants on the catalyst surface can result in catalyst-reactant contact times that are different from the fluid dynamic residence times. Additionally, different velocities between the vapor, liquid, and solid phases must be considered when measuring reaction times. Various laboratory reactors and their limitations for industrial use are reviewed below. [Pg.244]

Equation 6-108 is also a good approximation for a fluidized bed reactor up to the minimum fluidizing condition. However, beyond this range, fluid dynamic factors are more complex than for the packed bed reactor. Among the parameters that influence the AP in a fluidized bed reactor are the different types of two-phase flow, smooth fluidization, slugging or channeling, the particle size distribution, and the... [Pg.497]

A runaway reaction occurs when an exothermic system becomes uncontrollable. The reaction leads to a rapid increase in the temperature and pressure, which if not relieved can rupture the containing vessel. A runaway reaction occurs because the rate of reaction, and therefore the rate of heat generation, increases exponentially with temperature. In contrast, the rate of cooling increases only linearly with temperature. Once the rate of heat generation exceeds available cooling, the rate of temperature increase becomes progressively faster. Runaway reactions nearly always result in two-phase flow reliefs. In reactor venting, reactions essentially fall into three classifications ... [Pg.952]

Beaded polymeric supports are produced by a two-phase suspension polymerization in which microdrops of a monomer solution are directly converted to the corresponding microbeads. The size of a microdroplet is usually determined by a number of interrelated manufacturing parameters, which include the reactor design, the rate of stirring, the ratio of the monomer phase to water, the viscosity of both phases, and the type and concentration of the droplet stabilizer. [Pg.6]


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See also in sourсe #XX -- [ Pg.280 , Pg.310 ]




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Hydrodynamic Regimes in Two-Phase (Gas-Liquid) Stirred Tank Reactors

Reactor phase

Reactors with two well mixed phases

Two-Phase Catalytic Reactors

Two-Phase Fixed Bed Catalytic Reactors with

Two-Phase Flow in Fixed-Bed Reactors

Two-Phase Stirred Tank Reactors

Two-and three phase sparged reactors

Two-phase Flow in Trickle-Bed Reactors

Two-phase downflow fixed-bed reactors

Two-phase fluidized bed reactors

Two-phase reactor models

Two-phase semi-batch reactors

Two-phase upflow fixed-bed reactors

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