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Reactors fluid bed

Fig. 13. Multistage spout-fluid-bed reactor. 1, spouted bed 2, perforated plate 3, spray no22le 4, air header 5, fluidi2ed bed. Fig. 13. Multistage spout-fluid-bed reactor. 1, spouted bed 2, perforated plate 3, spray no22le 4, air header 5, fluidi2ed bed.
Fig. 1. A typical process flowsheet for acrolein manufacture. A, Fixed-bed or fluid-bed reactor B, quench cooler C, absorber D, stripper E and F,... Fig. 1. A typical process flowsheet for acrolein manufacture. A, Fixed-bed or fluid-bed reactor B, quench cooler C, absorber D, stripper E and F,...
Fig. 24. Elements of a bubbleless turbulent fluid-bed reactor design where the internals create four stages. A represents the shrouded grid B, the first feed ... Fig. 24. Elements of a bubbleless turbulent fluid-bed reactor design where the internals create four stages. A represents the shrouded grid B, the first feed ...
Most A1F. and cryoHte producers have their own HF production faciUties. HF vapor is reacted with alumina trihydrate to form A1F. in a fluid-bed reactor. HF is reacted with sodium hydroxide to form sodium fluoride, which is then used to produce cryoHte. Producers who manufacture these products solely for use in the aluminum industry do not generally install Hquid HF storage and handling faciHties, and do not participate in the merchant HF market. [Pg.200]

More recently, Sasol commercialized a new type of fluidized-bed reactor and was also operating a higher pressure commercial fixed-bed reactor (38). In 1989, a commercial scale fixed fluid-bed reactor was commissioned having a capacity similar to existing commercial reactors at Sasol One (39). This effort is aimed at expanded production of higher value chemicals, in particular waxes (qv) and linear olefins. [Pg.81]

The MTO process employs a turbulent fluid-bed reactor system and typical conversions exceed 99.9%. The coked catalyst is continuously withdrawn from the reactor and burned in a regenerator. Coke yield and catalyst circulation are an order of magnitude lower than in fluid catalytic cracking (FCC). The MTO process was first scaled up in a 0.64 m /d (4 bbl/d) pilot plant and a successfiil 15.9 m /d (100 bbl/d) demonstration plant was operated in Germany with U.S. and German government support. [Pg.85]

The first of these reactions takes place at temperatures of about 150°C, the second reaction proceeds at about 550—660°C. Typical furnaces used to carry out the reaction include cast-iron retorts the Mannheim mechanical furnace, which consists of an enclosed stationary circular muffle having a concave bottom pan and a domed cover and the Laury furnace, which employs a horizontal two-chambered rotating cylinder for the reaction vessel. The most recent design is the Cannon fluid-bed reactor in which the sulfuric acid vapor is injected with the combustion gases into a fluidized bed of salts. The Mannaheim furnace has also been used with potassium chloride as the feed. [Pg.445]

The HF is fed into the bottom stage of a three-stage fluid bed reactor and Al(OH)2 is fed to the top stage where it is converted to activated alurnina at 300—400°C. In the middle stage, rising HF gas contacts downcorning alurnina and forms A1F. [Pg.137]

Sasol Fischer-Tropsch Process. 1-Propanol is one of the products from Sasol s Fischer-Tropsch process (7). Coal (qv) is gasified ia Lurgi reactors to produce synthesis gas (H2/CO). After separation from gas Hquids and purification, the synthesis gas is fed iato the Sasol Synthol plant where it is entrained with a powdered iron-based catalyst within the fluid-bed reactors. The exothermic Fischer-Tropsch reaction produces a mixture of hydrocarbons (qv) and oxygenates. The condensation products from the process consist of hydrocarbon Hquids and an aqueous stream that contains a mixture of ketones (qv) and alcohols. The ketones and alcohols are recovered and most of the alcohols are used for the blending of high octane gasoline. Some of the alcohol streams are further purified by distillation to yield pure 1-propanol and ethanol ia a multiunit plant, which has a total capacity of 25,000-30,000 t/yr (see Coal conversion processes, gasification). [Pg.119]

Cyanopyridines are usually manufactured from the corresponding picoline by catalytic, vapor-phase ammoxidation (eq. 7) in a fixed- or fluid-bed reactor (28). 3-Cyanopyridine (25) is the most important nitrile, as it undergoes partial or complete hydrolysis under basic conditions to give niacinamide... [Pg.326]

In one modification of this procedure, the starting material is pyroly2ed rice hulls in place of more conventional forms of sihcon dioxide (31). Another unique process involves chlorination of a combination of SiC and Si02 with carbon in a fluid-bed reactor (32). The advantages of this process are that it is less energy-intensive and substantially free of lower sihcon chlorides. [Pg.19]

Trichlorosilane. The primary production process for trichlorosilane is the direct reaction of hydrogen chloride gas and sihcon metal in a fluid-bed reactor. Although this process produces both trichlorosilane and sihcon tetrachloride, production of the latter can be minimi2ed by proper control of the reaction temperature (22). A significant amount of trichlorosilane is also produced by thermal rearrangement of sihcon tetrachloride in the presence of hydrogen gas and sihcon. [Pg.19]

Manufacture. Titanium chloride is manufactured by the chlorination of titanium compounds (1,134—138). The feedstocks usually used are mineral or synthetic mtile, beneficiated ilmenite, and leucoxenes. Because these are all oxygen-containing, it is necessary to add carbon as well as coke from either coal or fuel oil during chlorination to act as a reducing agent. The reaction is normally carried out as a continuous process in a fluid-bed reactor (139). The bed consists of a mixture of the feedstock and coke. These are fluidized by a stream of chlorine iatroduced at the base (see Fluidization). The amount of heat generated in the chlorination process depends on the relative proportions of CO2 or CO that are formed (eqs. 1 and 2), and the mechanism that... [Pg.131]

Qua.driva.Ient, Zirconium tetrafluoride is prepared by fluorination of zirconium metal, but this is hampered by the low volatility of the tetrafluoride which coats the surface of the metal. An effective method is the halogen exchange between flowing hydrogen fluoride gas and zirconium tetrachloride at 300°C. Large volumes are produced by the addition of concentrated hydrofluoric acid to a concentrated nitric acid solution of zirconium zirconium tetrafluoride monohydrate [14956-11-3] precipitates (69). The recovered crystals ate dried and treated with hydrogen fluoride gas at 450°C in a fluid-bed reactor. The thermal dissociation of fluorozirconates also yields zirconium tetrafluoride. [Pg.435]

Oxychlorination of Ethylene to Dichloroethane. Ethylene (qv) is converted to dichloroethane in very high yield in fixed-bed, multitubular reactors and fluid-bed reactors by reaction with oxygen and hydrogen chloride over potassium-promoted copper(II) chloride supported on high surface area, porous alumina (84) ... [Pg.203]

SASOLII a.ndIII. Two additional plants weie built and aie in operation in South Africa near Secunda. The combined annual coal consumption for SASOL II, commissioned in 1980, and SASOL III, in 1983, is 25 x 10 t, and these plants together produce approximately 1.3 x lO" m (80,000 barrels) per day of transportation fuels. A block flow diagram for these processes is shown in Figure 15. The product distribution for SASOL II and III is much narrower in comparison to SASOL I. The later plants use only fluid-bed reactor technology, and extensive use of secondary catalytic processing of intermediates (alkylation, polymerisation, etc) is practiced to maximise the production of transportation fuels. [Pg.292]

Catalyst Deactivation. Catalyst deactivation (45) by halogen degradation is a very difficult problem particularly for platinum (PGM) catalysts, which make up about 75% of the catalysts used for VOC destmction (10). The problem may weU He with the catalyst carrier or washcoat. Alumina, for example, a common washcoat, can react with a chlorinated hydrocarbon in a gas stream to form aluminum chloride which can then interact with the metal. Fluid-bed reactors have been used to offset catalyst deactivation but these are large and cosdy (45). [Pg.512]

Figure 2.2.1 shows the simplified sketch of the reactor used for the microactivity test. As can be seen, a fluid-bed catalyst is tested in a fixed bed reactor in the laboratory to predict its performance in a commercial fluid bed reactor. This can be done only because enormous empirical experience exists that has accumulated throughout several decades in several hundreds of reactors both in production and in laboratories. The standard states ... [Pg.33]

Fluid bed reactors became important to the petroleum industry with the development of fluid catalytic cracking (FCC) early in the Second World War. Today FCC is still widely used. The following section surveys the various fluid bed processes and examines the benefits of fluidization. The basic theories of fluidization phenomena are also reviewed. [Pg.26]

Many factors enter into the design of a fluid bed reactor which are unknown in more familiar reactor types. These can be illustrated with reference to fluid catalytic cracking. [Pg.43]

Permissible gas velocities are usually set by entrainment, and for a given throughput the vessel diameter is thus determined. The amount of catalyst or other bed particles is set by reaction kinetics and the bubble-solids contacting expected. Very often there is a scale-up debit involved in fluid bed reactors. As mentioned earlier, small reactors... [Pg.43]

Typical analysis of products from Fischer-Tropsch fixed and fluid-bed reactors... [Pg.126]

A slurry bed reactor is in a pilot stage investigation. This type is characterized by having the catalyst in the form of a slurry. The feed gas mixture is bubbled through the catalyst suspension. Temperature control is easier than the other two reactor types. An added advantage to slurry-bed reactor is that it can accept a synthesis gas with a lower H2/CO ratio than either the fixed-bed or the fluid-bed reactors. [Pg.126]

A fluid-bed reactor is used at moderate pressures at approximately 450°C. The reactor effluent, containing chlorinated organics, water, a small amount of HCl, carbon dioxide, and other impurities, is condensed in a water-cooled graphite exchanger, cooled in a refrigerated condenser, and then scrubbed. Separation of perchlor from the trichlor occurs by successive distillation. Figure 7-6 shows the PPG process. [Pg.204]

Both fixed and fluid-bed reactors are used to produce acrylonitrile, but most modern processes use fluid-bed systems. The Montedison-UOP process (Figure 8-2) uses a highly active catalyst that gives 95.6% propylene conversion and a selectivity above 80% for acrylonitrile. The catalysts used in ammoxidation are similar to those used in propylene oxidation to acrolein. Oxidation of propylene occurs readily at... [Pg.218]

High-density polyethylene (HDPE) is produced by a low-pressure process in a fluid-bed reactor. Catalysts used for HDPE are either of the Zieglar-type (a complex of A1(C2H5)3 and a-TiCl4) or silica-alumina impregnated with a metal oxide such as chromium oxide or molybdenum oxide. [Pg.327]

So far, consideration has been limited to chemistry physical constraints such as heat transfer may also dictate the way in which reactions are performed. Oxidation reactions are highly exothermic and effectively there are only two types of reactor in which selective oxidation can be achieved on a practical scale multitubular fixed bed reactors with fused salt cooling on the outside of the tubes and fluid bed reactors. Each has its own characteristics and constraints. Multitubular reactors have an effective upper size limit and if a plant is required which is too large to allow the use of a single reactor, two reactors must be used in parallel. [Pg.228]

Standifer, R. L. "Conversion of Plutonium Oxide to Plutonium Tetrafluoride with Fluorine in a Fluid Bed Reactor -Part I, Development Studies," U.S. AEC Rept. RFP-1889, Dow Chemical Company, Golden, Colorado, August 23, 1972. [Pg.375]


See other pages where Reactors fluid bed is mentioned: [Pg.182]    [Pg.84]    [Pg.246]    [Pg.456]    [Pg.399]    [Pg.415]    [Pg.517]    [Pg.518]    [Pg.527]    [Pg.528]    [Pg.19]    [Pg.484]    [Pg.119]    [Pg.291]    [Pg.291]    [Pg.461]    [Pg.1567]    [Pg.211]    [Pg.483]    [Pg.486]    [Pg.125]   
See also in sourсe #XX -- [ Pg.26 ]




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Bubbling Bed Reactor Simulations Using Two-Fluid Models

Catalyst Requirements for Gas-Phase Fluid-bed Reactor

FIXED-BED CATALYTIC REACTORS FOR FLUID-SOLID REACTIONS

FLUIDIZED-BED AND OTHER MOVING-PARTICLE REACTORS FOR FLUID-SOLID REACTIONS

Fixed-bed reactor design for solid catalyzed fluid-phase reactions

Fixed-fluid bed reactor

Fluid beds

High Spatial Resolution of Fluid Flow in Fixed-Bed Reactors

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