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Mix Reactors

Complete mix reactors Plug flow or complete mix reactors in series [Pg.122]

Bypass - A bypass is a parallel path taken by a portion of the fluid that skips the reactor altogether without any residence time. As with dead zones, a bypass is not very useful unless a plug flow or mixed tank reactor is placed into the bypass, resulting in a parallel-flow reactor system. [Pg.122]

Feedback - Feedback describes the removal of a portion of the fluid from the tail end or the middle of a system, moving it back toward the inflow. Feedback is often used in reactors that utilize bacterially mediated reactions to ensure a bacterial population. For example, activated sludge systems that are oriented in a channel-type of arrangement often need feedback to perform properly. [Pg.122]

Plug Flow with Dispersion - Plug flow with dispersion is a concept that is often used to describe one-dimensional flow systems. It is somewhat more flexible in computational models because the mixing within the system is not dependent on reactor size, as with complete mix tanks in series. Plug flow with dispersion will be described in the second half of this chapter because special techniques are needed for the analysis. [Pg.122]

The various systems that are modeled by complete mix reactors and plug flow reactors are given in Table 6.1. [Pg.122]


Multiple reactions in parallel producing byproducts. Consider again the system of parallel reactions from Eqs. (2.16) and (2.17). A batch or plug-flow reactor maintains higher average concentrations of feed (Cfeed) than a continuous well-mixed reactor, in which the incoming feed is instantly diluted by the PRODUCT and... [Pg.29]

In general terms, if the reaction to the desired product has a higher order than the byproduct reaction, use a batch or plug-flow reactor. If the reaction to the desired product has a lower order than the byproduct reaction, use a continuous well-mixed reactor. [Pg.30]

Keep both Cpeedi and Cfeed2 low (i.e., use a continuous well-mixed reactor). [Pg.30]

But what is the correct choice a byproduct reaction calls for a continuous well-mixed reactor. On the other hand, the byproduct series reaction calls for a plug-flow reactor. It would seem that, given this situation, some level of mixing between a plug-flow and a continuous well-mixed reactor will give the best... [Pg.31]

A series combination of plug-flow and continuous well-mixed reactors (Fig. 2.3c and d)... [Pg.33]

Polymerization reactions. Polymers are characterized by the distribution of molecular w eight about the mean as well as by the mean itself. The breadth of this distribution depends on whether a batch or plug-flow reactor is used on the one hand or a continuous well-mixed reactor on the other. The breadth has an important influence on the mechanical and other properties of the polymer, and this is an important factor in the choice of reactor. [Pg.33]

Solution We wish to avoid as much as possible the production of di- and triethanolamine, which are formed by series reactions with respect to monoethanolamine. In a continuous well-mixed reactor, part of the monoethanolamine formed in the primary reaction could stay for extended periods, thus increasing its chances of being converted to di- and triethanolamine. The ideal batch or plug-flow arrangement is preferred, to carefully control the residence time in the reactor. [Pg.50]

However, the laboratory data seem to indicate that a constant concentration in the reactor to maintain 63 percent sulfuric acid would be beneficial. Careful temperature control is also important. These two factors would suggest that a continuous well-mixed reactor is appropriate. There is a conflict. How can a well-defined residence time be maintained and simultaneously a constant concentration of sulfuric acid be maintained ... [Pg.52]

Continuous well-mixed reactors to plug-flow... [Pg.271]

The first distinction to be drawn, as far as heat transfer is concerned, is between the plug-flow and continuous well-mixed reactor. In the plug-flow reactor shown in Fig. 13.1, the heat transfer can take place over a range of temperatures. The shape of the profile depends on... [Pg.326]

Eigure 2 shows that even materials which are rather resistant to oxidation ( 2/ 1 0.1) are consumed to a noticeable degree at high conversions. Also the use of plug-flow or batch reactors can offer a measurable improvement in efficiencies in comparison with back-mixed reactors. Intermediates that cooxidize about as readily as the feed hydrocarbon (eg, ketones with similar stmcture) can be produced in perhaps reasonable efficiencies but, except at very low conversions, are subject to considerable loss through oxidation. They may be suitable coproducts if they are also precursors to more oxidation-resistant desirable materials. Intermediates which oxidize relatively rapidly (/ 2 / i — 3-50 eg, alcohols and aldehydes) are difficult to produce in appreciable amounts, even in batch or plug-flow reactors. Indeed, for = 50, to isolate 90% or more of the intermediate made, the conversion must... [Pg.337]

Eig. 3. Plot of maximum yield as a % of maximum (zero conversion) efficiency to a primary intermediate x axis is ratio of oxidation rate constants ( 2 / i) for primary intermediate vs feed ( ) plug-flow or batch reactor (B) back-mixed reactor (A) plug-flow advantage, %. [Pg.337]

Fig. 8. Combined flow reactor models (a) parallel flow reactors with longitudinal diffusion (diffusivities can differ), (b) internal recycle—cross-flow reactor (the recycle can be in either direction), comprising two countercurrent plug-flow reactors with intercormecting distributed flows, (c) plug-flow and weU-mixed reactors in series, and (d) 2ero-interniixing model, in which plug-flow reactors are parallel and a distribution of residence times dupHcates that... Fig. 8. Combined flow reactor models (a) parallel flow reactors with longitudinal diffusion (diffusivities can differ), (b) internal recycle—cross-flow reactor (the recycle can be in either direction), comprising two countercurrent plug-flow reactors with intercormecting distributed flows, (c) plug-flow and weU-mixed reactors in series, and (d) 2ero-interniixing model, in which plug-flow reactors are parallel and a distribution of residence times dupHcates that...
There are essentially three types of coal gasifiers moving-bed or countercurrent reactors fluidized-bed or back-mixed reactors and entrained-flow or plug-flow reactors. The three types are shown schematically in Eigure 2. [Pg.268]

Epichlorohydrin Elastomers without AGE. Polymerization on a commercial scale is done as either a solution or slurry process at 40—130°C in an aromatic, ahphatic, or ether solvent. Typical solvents are toluene, benzene, heptane, and diethyl ether. Trialkylaluniinum-water and triaLkylaluminum—water—acetylacetone catalysts are employed. A cationic, coordination mechanism is proposed for chain propagation. The product is isolated by steam coagulation. Polymerization is done as a continuous process in which the solvent, catalyst, and monomer are fed to a back-mixed reactor. Pinal product composition of ECH—EO is determined by careful control of the unreacted, or background, monomer in the reactor. In the manufacture of copolymers, the relative reactivity ratios must be considered. The reactivity ratio of EO to ECH has been estimated to be approximately 7 (35—37). [Pg.555]

Oxidants commonly used include ozone, permanganate, chlorine, chlorine dioxide, and ferrate, often in combination with catalysts. Standard-type mixed reactors are used with contact times of several minutes to an hour. Special reactors for use with ultraviolet light have been developed. [Pg.2227]

An anaerobic digester is a no-recycle complete mix reactor. Thus, its performance is independent of organic loading but is controlled by hydraulic retention time (HRT). Based on kinetic theoiy and values of the pseudo constants for methane bac teria, a minimum HRT of 3 to 4 days is required. To provide a safety factor and compensate for load variation as indicated earlier, HRT is kept in the range 10 to 30 days. Thickening of feed sludge is used to reduce the tank volume required... [Pg.2228]

The material balance for steady-state operation of a perfectly mixed reactor is ... [Pg.81]

Another classification refers to the shape of the vessel. In the case of the laboratory vessel installed with a stirrer, the composition and temperature of die reaction is homogeneous in all parts of die vessel. This type of vessel is classified as a stiiTcd tank or well mixed reactor. Where there is no mixing in the direction of flow as in the cylindrical vessel, it is classified as a plug flow or tubular flow reactor. [Pg.219]

Equation 9-15 gives the conversion expression for the second order reaction of a macrofluid in a mixed flow. An exponential integral, ei(a), which is a function of a, and its value can be found from tables of integrals. However, the conversion from Equation 9-15 is different from that of a perfectly mixed reactor without reference to RTD. An earlier analysis in Chapter 5 gives... [Pg.767]

The name continuous flow-stirred tank reactor is nicely descriptive of a type of reactor that frequently for both production and fundamental kinetic studies. Unfortunately, this name, abbreviated as CSTR, misses the essence of the idealization completely. The ideality arises from the assumption in the analysis that the reactor is perfectly mixed, and that it is homogeneous. A better name for this model might be continuous perfectly mixed reactor (CPMR). [Pg.383]

The reaction takes place at low temperature (40-60 °C), without any solvent, in two (or more, up to four) well-mixed reactors in series. The pressure is sufficient to maintain the reactants in the liquid phase (no gas phase). Mixing and heat removal are ensured by an external circulation loop. The two components of the catalytic system are injected separately into this reaction loop with precise flow control. The residence time could be between 5 and 10 hours. At the output of the reaction section, the effluent containing the catalyst is chemically neutralized and the catalyst residue is separated from the products by aqueous washing. The catalyst components are not recycled. Unconverted olefin and inert hydrocarbons are separated from the octenes by distillation columns. The catalytic system is sensitive to impurities that can coordinate strongly to the nickel metal center or can react with the alkylaluminium derivative (polyunsaturated hydrocarbons and polar compounds such as water). [Pg.272]

Fed-batch mixed reactor starting with a relatively dilute solution of substrate this provides control over the substrate concentration. High rates are avoided. Fed batch is used for baker s yeast to overcome catabolite repression and to control oxygen demand. It is also used routinely for production of Penicillin. [Pg.144]

Batch mixed reactor There are three principal modes of bioreactor operation (a) batch (b) fed batch (c) continuous. [Pg.144]

The performance data for plug versus mix reactor were obtained. The data were collected as the inverse of qx vs inverse of substrate concentration. Table E.1.1 shows the data based on obtained kinetic data. From the data plotted in Figure E.1.1, we can minimise the volume of the chemostat. A CSTR works better than a plug flow reactor for the production of biomass. Maximum qx is obtained with a substrate concentration in the leaving stream of 12g m 3. [Pg.300]

Fig. 1. Examples of the kinetic curves during ethylene polymerization by chromium oxide catalysts. Support—SiOs temperature—80°C polymerization at constant ethylene pressure in perfect mixing reactor. Curve 1—catalyst reduced by CO at 300°C. Curve 2— catalyst activated in vacuum (400°C) polymerization in the case of (1) and (2) in solvent (heptane) ethylene pressure 10 kg/cm2 02 content in ethylene 1 ppm, HsO 3 ppm. Curves 3, 4, 5, 6—catalyst activated in vacuum (400°C) polymerization without solvent ethylene pressure 19 (curve 3), 13 (curve 4), 4 (curve 5), and 2 (curve 6) kg/cm2 02 content in ethylene 1 ppm, HsO = 12 ppm. Fig. 1. Examples of the kinetic curves during ethylene polymerization by chromium oxide catalysts. Support—SiOs temperature—80°C polymerization at constant ethylene pressure in perfect mixing reactor. Curve 1—catalyst reduced by CO at 300°C. Curve 2— catalyst activated in vacuum (400°C) polymerization in the case of (1) and (2) in solvent (heptane) ethylene pressure 10 kg/cm2 02 content in ethylene 1 ppm, HsO 3 ppm. Curves 3, 4, 5, 6—catalyst activated in vacuum (400°C) polymerization without solvent ethylene pressure 19 (curve 3), 13 (curve 4), 4 (curve 5), and 2 (curve 6) kg/cm2 02 content in ethylene 1 ppm, HsO = 12 ppm.

See other pages where Mix Reactors is mentioned: [Pg.29]    [Pg.29]    [Pg.30]    [Pg.31]    [Pg.33]    [Pg.33]    [Pg.34]    [Pg.34]    [Pg.52]    [Pg.315]    [Pg.316]    [Pg.2701]    [Pg.511]    [Pg.512]    [Pg.517]    [Pg.38]    [Pg.376]    [Pg.1636]    [Pg.767]    [Pg.373]    [Pg.601]    [Pg.273]    [Pg.301]    [Pg.179]   


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