Fluidized beds 3 phase

The performance of fluidized-bed reactors is not approximated by either the well-stirred or plug-flow idealized models. The solid phase tends to be well-mixed, but the bubbles lead to the gas phase having a poorer performance than well mixed. Overall, the performance of a fluidized-bed reactor often lies somewhere between the well-stirred and plug-flow models. 

By contrast, if the reactor is continuous well-mixed, then the reactor is isothermal. This behavior is typical of stirred tanks used for liquid-phase reactions or fluidized-bed reactors used for gas-phase reactions. The mixing causes the temperature in the reactor to be effectively uniform. 

Pressure Drop. The pressure drop across a two-phase suspension is composed of various terms, such as static head, acceleration, and friction losses for both gas and soflds. For most dense fluid-bed appHcations, outside of entrance or exit regimes where the acceleration pressure drop is appreciable, the pressure drop simply results from the static head of soflds. Therefore, the weight of soflds ia the bed divided by the height of soflds gives the apparent density of the fluidized bed, ie... 

Bubbles and Fluidized Beds. Bubbles, or gas voids, exist in most fluidized beds and their role can be important because of the impact on the rate of exchange of mass or energy between the gas and soflds in the bed. Bubbles are formed in fluidized beds from the inherent instabiUty of two-phase systems. They are formed for Group A powders when the gas velocity is sufficient to start breaking iaterparticle forces at For Group B powders, where iaterparticle forces are usually negligible, and bubbles form immediately upon fluidization. Bubbles, which are inherently... 

M ass Transfer. Mass transfer in a fluidized bed can occur in several ways. Bed-to-surface mass transfer is important in plating appHcations. Transfer from the soHd surface to the gas phase is important in drying, sublimation, and desorption processes. Mass transfer can be the limiting step in a chemical reaction system. In most instances, gas from bubbles, gas voids, or the conveying gas reacts with a soHd reactant or catalyst. In catalytic systems, the surface area of a catalyst can be enormous. Eor Group A particles, surface areas of 5 to over 1000 m /g are possible. 

Polymerization in the Gas Phase. Many polymerization catalysts can be adapted for use in the gas phase. A gas-phase reactor contains a bed of small PE particles that is agitated either by a mechanical stirrer or by employing the fluidized-bed technique. These processes are economical because they do not requite solvent tecitculation streams. 

Heterogeneous hydrogenation catalysts can be used in either a supported or an unsupported form. The most common supports are based on alurnina, carbon, and siUca. Supports are usually used with the more expensive metals and serve several purposes. Most importandy, they increase the efficiency of the catalyst based on the weight of metal used and they aid in the recovery of the catalyst, both of which help to keep costs low. When supported catalysts are employed, they can be used as a fixed bed or as a slurry (Uquid phase) or a fluidized bed (vapor phase). In a fixed-bed process, the amine or amine solution flows over the immobile catalyst. This eliminates the need for an elaborate catalyst recovery system and minimizes catalyst loss. When a slurry or fluidized bed is used, the catalyst must be separated from the amine by gravity (settling), filtration, or other means. 

Fig. 3. Continuous fluidized-bed vapor phase reduction of nitrobenzene.

Suspended Particle Techniques. In these methods of size enlargement, granular soHds are produced direcdy from a Hquid or semiliquid phase by dispersion in a gas to allow solidification through heat and/or mass transfer. The feed Hquid, which may be a solution, gel, paste, emulsion, slurry, or melt, must be pumpable and dispersible. Equipment used includes spray dryers, prilling towers, spouted and fluidized beds, and pneumatic conveying dryers, all of which are amenable to continuous, automated, large-scale operation. Because attrition and fines carryover are common problems with this technique, provision must be made for recovery and recycling. 

Fluidized-Bed Vinegar Reactors. Intimate contact of air A.cetohacter is achieved in fluidized-bed or tower-type systems. Air introduced through perforations in the bottom of each unit suspends the mixture of Hquid and microorganisms within the unit. Air bubbles penetrating the bottom plate keep Jicetobacter m. suspension and active for the ethanol oxidation in the Hquid phase. Addition of a carrier for the bacterial ceUs to the Hquid suspension is reported to improve the performance (58—60). 

In oxychlorination, ethylene reacts with dry HCl and either air or pure oxygen to produce EDC and water. Various commercial oxychlorination processes differ from one another to some extent because they were developed independentiy by several different vinyl chloride producers (78,83), but in each case the reaction is carried out in the vapor phase in either a fixed- or fluidized-bed reactor containing a modified Deacon catalyst. Unlike the Deacon process for chlorine production, oxychlorination of ethylene occurs readily at temperatures weU below those requited for HCl oxidation. 

The use of a fluidized-bed reactor is possible only when the reactants are essentiaUy in the gaseous phase. Eluidized-beds are not suitable for middle distiUate synthesis, where a heavy wax is formed. Eor gasoline synthesis processes like the MobU MTG process and the Synthol process, such reactors are especiaUy suitable when frequent or continuous regeneration of the catalyst is required. Slurry reactors and ebuUiating-bed reactors comprising a three-phase system with very fine catalyst are, in principle, suitable for middle distiUate and wax synthesis, but have not been appHed on a commercial scale. 

Halogenation—Hydrohalogenation. The most important iatermediate is ethylene dichloride [107-06-2] (EDC) which is produced from ethylene either by direct chlorination or by oxychloriaation. Direct chlorination is carried out ia the Hquid or vapor phase over catalysts of iron, alumiaum, copper, or antimony chlorides, and at conditions of 60°C. Oxychloriaation is carried out ia a fixed or fluidized bed at 220°C with a suitable soHd chloride catalyst. 

Contactive (Direct) Heat Transfer Contactive heat-transfer equipment is so constructed that the particulate burden in solid phase is directly exposed to and permeated by the heating or cooling medium (Sec. 20). The carrier may either heat or cool the solids. A large amount of the industrial heat processing of sohds is effected by this mechanism. Physically, these can be classified into packed beds and various degrees of agitated beds from dilute to dense fluidized beds. 

Entrained Sohds Bubble Columns with the Sohd Fluidized by Bubble Action The three-phase mixture flows through the vessel and is separated downstream. Used in preference to fluidized beds when catalyst particles are veiy fine or subject to disintegration in process. 

Three-phase fluidized bed reactors are used for the treatment of heavy petroleum fractions at 350 to 600°C (662 to 1,112°F) and 200 atm (2,940 psi). A biological treatment process (Dorr-Oliver Hy-Flo) employs a vertical column filled with sand on which bacderial growth takes place while waste liquid and air are charged. A large interfacial area for reaction is provided, about 33 cmVcm (84 inVirr), so that an 85 to 90 percent BOD removal in 15 min is claimed compared with 6 to 8 h in conventional units. 

As an example of the chemical signihcance of the process technology, the products of die Fischer-Tropsch synthesis, in which a signihcant amount of gas phase polymerization occurs vary markedly from hxed bed operation to the fluidized bed. The hxed bed product contains a higher proportion of straight chain hydrocarbons, and the huidized bed produces a larger proportion of branched chain compounds. 

This reaction is carried out in tall fluidized beds of high L/dt ratio. Pressures up to 200 kPa are used at temperatures around 300°C. The copper catalyst is deposited onto the surface of the silicon metal particles. The product is a vapor-phase material and the particulate silicon is gradually consumed. As the particle diameter decreases the minimum fluidization velocity decreases also. While the linear velocity decreases, the mass velocity of the fluid increases with conversion. Therefore, the leftover small particles with the copper catalyst and some debris leave the reactor at the top exit. 

Fluidized-bed adsorbers have several disadvantages. The continuous handling and transport of solids is expensive from an equipment standpoint fluidized-bed systems must be large to be economical. Solids handling also presents a potential for mechanical problems. Careful control is required to keep the adsorbent fluidized, while minimizing adsorbent loss with the gas-phase attrition of the adsorbent can be high, requiring substantial makeup. 

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