Reactor a batch

Figure 4.1. Progression of concentration in reactors, (a) Batch (b) batch with preloading (c) staged (d) tubular flow. 

Ujhidy and co-workers studied the thermal ring closure of )V-(3-chloro-phenyl)aminomethylenemalonate (250) to 7-chloro-4-hydroxyquinoline-3-carboxylate (759, R = Cl, R1 = H) in Dowtherm A containing 5% or 10% of paraffin oil at 230°C, 235°C, 240°C, 245°C, 250°C, and 255°C in different reactors (a continuous tank reactor, a batch tank reactor, a cascade of... 

Fig. 1. Types of reactor, (a) Batch reactor. All the reactants are added at the beginning of the reaction and the products are removed at the end. (b) Continuous stirred tank. Reactants are fed to the reactor and products removed continuously, (c) Tubular reactor. Products are fed to the inlet, reaction occurs as the stream flows down the tube and products emerge at the exit.

Figure 5.1 The three types of ideal reactors (a) batch reactor, or BR (b) plug flow reactor, or PFR and (c) mixed flow reactor, or MFR.

Fig. 15.1. Types of electrochemical reactor (a) Batch reactor (b) Plug flow reactor (c) Backmix flow reactor.

FIG. 7-1 Types of ideal reactors (a) Batch or semibatch. (b) CSTR or series of CSTRs. (c) Plug flow. 

We also discussed the choice of the reactor. A batch reactor has a much larger volume per unit of reaction product and tank like pressure vessels are much more expensive than cylindrical vessels. This combined with the difficulties of handling catalyst slurries and above all of preventing losses of the often rather expensive catalysts made us consider continuously operating reactors with fixed catalyst beds too. We eventually chose for the packed bubble column as a well suited reactor. 

A plug flow reactor may be realized using immobilized enzymes within a column reactor or using soluble enzymes within a cascade of membrane reactors. A batch or a repetitive batch process with soluble enzymes (see below) has the same productivity as the plug flow reactor. 

Figure 17.1 Some types of srtlid/liquid reactors (a) batch (b) Uquid continuous ...

Fig. 9.3 Schematic images of examples of photoelectrochemical reactors (a) Batch reactor, (b) Flow reactor, c Recirculating batch reactor (evacuation is optional)...

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... 

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. 

Keep both Cpeedi and Cpeed2 high (i.e., use a batch or plug-flow reactor). 

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. 

Using a batch reactor, a constant concentration of sulfuric acid can be maintained by adding concentrated sulfuric acid as the reaction progresses, i.e., semi-batch operation. Good temperature control of such systems can be maintained, as we shall discuss later. 

Fixing the rate of heat transfer in a batch reactor is often not the best way to control the reaction. The heating or cooling characteristics can be varied with time to suit the characteristics of the reaction. Because of the complexity of hatch operation and the fact that operation is usually small scale, it is rare for any attempt to be made... 

With a batch process, such as hot isostatic compaction (HIP), heat exchange as used in a continuous reactor is not possible, and it is common practice to provide a furnace within the pressure vessel which is thermally insulated to ensure that the temperature of the vessel does not rise above 300°C. Most HIP operations involve gas pressures in the range 70—200 MPa (10—29,000 psi) and temperatures of 1250—2000°C, occasionally 2250°C (74). The pressure vessel may have a bore diameter from 27 to 1524 mm (75) and is nearly always provided with threaded closures sealed with O-rings made of elastomer provided the temperature is low enough. 

Efficiency of Intermediate Formation. The variation of the efficiency of a primary intermediate with conversion of the feed hydrocarbon can be calculated (22). Ratios of the propagation rate constants ( 2 / i) reactor type (batch or plug-flow vs back-mixed) are important parameters. 

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, %. 

The typical SEA process uses a manganese catalyst with a potassium promoter (for solubilization) in a batch reactor. A manganese catalyst increases the relative rate of attack on carbonyl intermediates. Low conversions are followed by recovery and recycle of complex intermediate streams. Acid recovery and purification involve extraction with caustic and heat treatment to further decrease small amounts of impurities (particularly carbonyls). The fatty acids are recovered by freeing with sulfuric acid and, hence, sodium sulfate is a by-product. 

The polymerization of monomers to form hydrocarbon resins is typically carried out by either the direct addition of catalyst to a hydrocarbon fraction or by the addition of feed to a solvent—catalyst slurry or solution. Most commercial manufacturers use a continuous polymerization process as opposed to a batch process. Reactor temperatures are typically in the range of 0—120°C. 

The majority of thermal polymerizations are carried out as a batch process, which requires a heat-up and a cool down stage. Typical conditions are 250—300°C for 0.5—4 h in an oxygen-free atmosphere (typically nitrogen) at approximately 1.4 MPa (200 psi). A continuous thermal polymerization has been reported which utilizes a tubular flow reactor having three temperature zones and recycle capabiHty (62). The advantages of this process are reduced residence time, increased production, and improved molecular weight control. Molecular weight may be controlled with temperature, residence time, feed composition, and polymerizate recycle. 

Reaction conditions depend on the composition of the bauxite ore, and particularly on whether it contains primarily gibbsite, Al(OH)2, or boehmite [1318-23-6] AlOOH. The dissolution process is conducted in large, stirred vessels or alternatively in a tubular reactor. The process originated as a batch process, but has been converted to a continuous one, using a series of stirred tank reactors or a tubular reactor. 

In the most common production method, the semibatch process, about 10% of the preemulsified monomer is added to the deionised water in the reactor. A shot of initiator is added to the reactor to create the seed. Some manufacturers use master batches of seed to avoid variation in this step. Having set the number of particles in the pot, the remaining monomer and, in some cases, additional initiator are added over time. Typical feed times ate 1—4 h. Lengthening the feeds tempers heat generation and provides for uniform comonomer sequence distributions (67). Sometimes skewed monomer feeds are used to offset differences in monomer reactivity ratios. In some cases a second monomer charge is made to produce core—shell latices. At the end of the process pH adjustments are often made. The product is then pumped to a prefilter tank, filtered, and pumped to a post-filter tank where additional processing can occur. When the feed rate of monomer during semibatch production is very low, the reactor is said to be monomer starved. Under these... 

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