Controlled stirred tank reactor

Wet Oxidation Reactor Design. Several types of reactor designs have been employed for wet oxidation processes. Zimpro, the largest manufacturer of wet oxidation systems, typically uses a tower reactor system. The reactor is a bubble tower where air is introduced at the bottom to achieve plug flow with controlled back-mixing. Residence time is typically under one hour. A horizontal, stirred tank reactor system, known as the Wetox process, was initially developed by Barber-Cohnan, and is also offered by Zimpro. 

Some slurry processes use continuous stirred tank reactors and relatively heavy solvents (57) these ate employed by such companies as Hoechst, Montedison, Mitsubishi, Dow, and Nissan. In the Hoechst process (Eig. 4), hexane is used as the diluent. Reactors usually operate at 80—90°C and a total pressure of 1—3 MPa (10—30 psi). The solvent, ethylene, catalyst components, and hydrogen are all continuously fed into the reactor. The residence time of catalyst particles in the reactor is two to three hours. The polymer slurry may be transferred into a smaller reactor for post-polymerization. In most cases, molecular weight of polymer is controlled by the addition of hydrogen to both reactors. After the slurry exits the second reactor, the total charge is separated by a centrifuge into a Hquid stream and soHd polymer. The solvent is then steam-stripped from wet polymer, purified, and returned to the main reactor the wet polymer is dried and pelletized. Variations of this process are widely used throughout the world. 

Continuous-flow stirred-tank reactors ia series are simpler and easier to design for isothermal operation than are tubular reactors. Reactions with narrow operating temperature ranges or those requiring close control of reactant concentrations for optimum selectivity benefit from series arrangements. 

Over 25 years ago the coking factor of the radiant coil was empirically correlated to operating conditions (48). It has been assumed that the mass transfer of coke precursors from the bulk of the gas to the walls was controlling the rate of deposition (39). Kinetic models (24,49,50) were developed based on the chemical reaction at the wall as a controlling step. Bench-scale data (51—53) appear to indicate that a chemical reaction controls. However, flow regimes of bench-scale reactors are so different from the commercial furnaces that scale-up of bench-scale results caimot be confidently appHed to commercial furnaces. For example. Figure 3 shows the coke deposited on a controlled cylindrical specimen in a continuous stirred tank reactor (CSTR) and the rate of coke deposition. The deposition rate decreases with time and attains a pseudo steady value. Though this is achieved in a matter of rninutes in bench-scale reactors, it takes a few days in a commercial furnace. 

A differential equation for a function that depends on only one variable, often time, is called an ordinary differential equation. The general solution to the differential equation includes many possibilities the boundaiy or initial conditions are needed to specify which of those are desired. If all conditions are at one point, then the problem is an initial valueproblem and can be integrated from that point on. If some of the conditions are available at one point and others at another point, then the ordinaiy differential equations become two-point boundaiy value problems, which are treated in the next section. Initial value problems as ordinary differential equations arise in control of lumped parameter models, transient models of stirred tank reactors, and in all models where there are no spatial gradients in the unknowns. 

In this short initial communication we wish to describe a general purpose continuous-flow stirred-tank reactor (CSTR) system which incorporates a digital computer for supervisory control purposes and which has been constructed for use with radical and other polymerization processes. The performance of the system has been tested by attempting to control the MWD of the product from free-radically initiated solution polymerizations of methyl methacrylate (MMA) using oscillatory feed-forward control strategies for the reagent feeds. This reaction has been selected for study because of the ease of experimentation which it affords and because the theoretical aspects of the control of MWD in radical polymerizations has attracted much attention in the scientific literature. 

This set of first-order ODEs is easier to solve than the algebraic equations where all the time derivatives are zero. The initial conditions are that a ut = no, bout = bo,... at t = 0. The long-time solution to these ODEs will satisfy Equations (4.1) provided that a steady-state solution exists and is accessible from the assumed initial conditions. There may be no steady state. Recall the chemical oscillators of Chapter 2. Stirred tank reactors can also exhibit oscillations or more complex behavior known as chaos. It is also possible that the reactor has multiple steady states, some of which are unstable. Multiple steady states are fairly common in stirred tank reactors when the reaction exotherm is large. The method of false transients will go to a steady state that is stable but may not be desirable. Stirred tank reactors sometimes have one steady state where there is no reaction and another steady state where the reaction runs away. Think of the reaction A B —> C. The stable steady states may give all A or all C, and a control system is needed to stabilize operation at a middle steady state that gives reasonable amounts of B. This situation arises mainly in nonisothermal systems and is discussed in Chapter 5. 

P 11] Reactions were performed in a completely stirred tank reactor of 10 ml volume [84]. The stirrer was set to 700 rpm. The reactor was immersed in a water bath. Owing to the small size of the reactor, special precautions had to be taken for stirring and for temperature control of the bath [84]. 

Influence of the mode of operation on process performance. The mode of operation of stirred-tank reactors can also significantly affect reactor performance. The history of concentrations will be changed by the time policy of reactant(s) addition to the reaction mixture. In view of our very limited possibility of controlling of temperature in stirred-tank reactors, the temperature-time dependencies for different policies of dosing will also be different. For example, the result of nitration depends upon the method of addition of nitric acid to aromatics, and the choice which phase is dispersed and which is continuous. Consequently, if the reaction is concentration- or temperature-sensitive the result will be dependent on the mode of operation (see Example 5.3.1.5). 

Fig. 5.4-23 shows a sketch drawing of a BSC (Brogli et al., 1981). The stirred-tank reactor made of glass (a metal version is also available) is surrounded by a jacket through which a heat-transfer fluid flows at a very high rate the jacket is not insulated. The temperature of the circulation loop is regulated by a cascaded controller so that the heat evolution in the reactor is equilibrated by heat transfer through the reactor wall. The temperature in the loop is adjusted by injection of thermostatted hot or cold fluid. 

Although continuous stirred-tank reactors (Fig. 3.12) normally operate at steady-state conditions, a derivation of the full dynamic equation for the system, is necessary to cover the instances of plant start up, shut down and the application of reactor control. 

A cascade of three continuous stirred-tank reactors arranged in series, is used to carry out an exothermic, first-order chemical reaction. The reactors are jacketed for cooling water, and the flow of water through the cooling jackets is countercurrent to that of the reaction. A variety of control schemes can be employed and are of great importance, since the reactor scheme shows a multiplicity of possible stable operating points. This example is taken from the paper of Mukesh and Rao (1977). 

Figure 5.23. A typical stirred tank reactor control scheme, temperature cascade control, and reagent ...

Continuous flow stirred tank reactors are normally just what the name implies—tanks into which reactants flow and from which a product stream is removed on a continuous basis. CFSTR, CSTR, C-star, and back-mix reactor are only a few of the names applied to the idealized stirred tank flow reactor. We will use the letters CSTR as a shorthand notation in this textbook. The virtues of a stirred tank reactor lie in its simplicity of construction and the relative ease with which it may be controlled. These reactors are used primarily for carrying out liquid phase reactions in the organic chemicals... 

The responses of a single ideal stirred tank reactor to ideal step and pulse inputs are shown in Figure 11.4. Note that any change in the reactor inlet stream shows up immediately at the reactor outlet in these systems. This fact is used to advantage in the design of automatic control systems for stirred tank reactors. 

The first application of a rhodium-ligand system was realized in the LPO-process (low pressure oxo Fig. 18). Huge stirred tank reactors are used, equipped with internal heat exchangers to control the heat of reaction. The solution of the catalyst recycle is simple but efficient. The catalyst remains in the reactor, products and unconverted propene are stripped by a huge excess of synthesis gas. Because of strong foaming, only a part of the reaction volume is used. After the gas has left the reactor, the products are removed by condensing, the big part of synthesis gas is separated from the liquid products and recycled via compressors. The liquid effluent of the gas-liquid separator... 

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