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Adiabatic stirred flow reactor

Example 12.12 Adiabatic stirred flow reactor Consider the following reaction  [Pg.627]

The reaction occurs in an adiabatic stirred flow reactor with feed flow rate F, transient compositions cA, and cB and reaction rate JT, and total mass of reacting mixtures M. For small perturbations around the stationary state(s), the following expansions are used  [Pg.627]

In stable systems, such disturbances vanish in time and the stationary values are restored. For very small perturbations, the reaction rate disturbance may be expanded with negligible second order and higher terms as follows  [Pg.628]

This expansion may lead to the linearization of differential equations above. [Pg.628]

1 Using the truncated virial equation of state with the second virial coefficient B T) [Pg.628]


Keairns and Manning AIChE J., 15 (660), 1969] have used the reaction between sodium thiosulfate and hydrogen peroxide in a well-stirred flow reactor to check a computer simulation of adiabatic CSTR operation. Data on their experimental conditions and the reaction parameters are listed below. The reaction may be considered second-order in sodium thiosulfate. [Pg.386]

Continuous adiabatic perfectly stirred flow reactor. [Pg.220]

Fig ure 6-22. Temperature versus conversion for a first order irreversible reaction in an adiabatic continuous flow stirred tank reactor. [Pg.506]

There are a variety of limiting forms of equation 8.0.3 that are appropriate for use with different types of reactors and different modes of operation. For stirred tanks the reactor contents are uniform in temperature and composition throughout, and it is possible to write the energy balance over the entire reactor. In the case of a batch reactor, only the first two terms need be retained. For continuous flow systems operating at steady state, the accumulation term disappears. For adiabatic operation in the absence of shaft work effects the energy transfer term is omitted. For the case of semibatch operation it may be necessary to retain all four terms. For tubular flow reactors neither the composition nor the temperature need be independent of position, and the energy balance must be written on a differential element of reactor volume. The resultant differential equation must then be solved in conjunction with the differential equation describing the material balance on the differential element. [Pg.254]

The stirred reactor may be compared to a plug flow reactor in which premixed fuel-air mixtures flow through the reaction tube. In this case, the unbumed gases enter at temperature T0 and leave the reactor at the flame temperature T. The system is assumed to be adiabatic. Only completely burned products leave the reactor. This reactor is depicted in Fig. 4.50. [Pg.236]

The reactor system may consist of a number of reactors which can be continuous stirred tank reactors, plug flow reactors, or any representation between the two above extremes, and they may operate isothermally, adiabatically or nonisothermally. The separation system depending on the reactor system effluent may involve only liquid separation, only vapor separation or both liquid and vapor separation schemes. The liquid separation scheme may include flash units, distillation columns or trains of distillation columns, extraction units, or crystallization units. If distillation is employed, then we may have simple sharp columns, nonsharp columns, or even single complex distillation columns and complex column sequences. Also, depending on the reactor effluent characteristics, extractive distillation, azeotropic distillation, or reactive distillation may be employed. The vapor separation scheme may involve absorption columns, adsorption units,... [Pg.226]

Knowledge of these types of reactors is important because some industrial reactors approach the idealized types or may be simulated by a number of ideal reactors. In this chapter, we will review the above reactors and their applications in the chemical process industries. Additionally, multiphase reactors such as the fixed and fluidized beds are reviewed. In Chapter 5, the numerical method of analysis will be used to model the concentration-time profiles of various reactions in a batch reactor, and provide sizing of the batch, semi-batch, continuous flow stirred tank, and plug flow reactors for both isothermal and adiabatic conditions. [Pg.220]

Consider an exothermic irreversible reaction with first order kinetics in an adiabatic continuous flow stirred tank reactor. It is possible to determine the stable operating temperatures and conversions by combining both the mass and energy balance equations. For the mass balance equation at constant density and steady state condition,... [Pg.504]

FINDING REQUIRED VOLUME FOR AN ADIABATIC CONTINUOUS-FLOW STIRRED-TANK REACTOR 5.6... [Pg.142]

We have a first-order homogeneous reaction, taking place in an ideal stirred tank reactor. The volume of the reactor is 20 X 10 3 m3. The reaction takes place in the liquid phase. The concentration of the reactant in the feed flow is 3.1 kmol/m3 and the volumetric flow rate of the feed is 58 X 10 m3/s. The density and specific heat of the reaction mixture are constant at 1000 kg/m3 and 4.184kJ/(kg K). The reactor operates at adiabatic conditions. If the feed flow is at 298 K, investigate the possibility of multiple solutions for conversion at various temperatures in the product stream. The heat of reaction and the rate of reaction are... [Pg.629]

While the adiabatic batch reactor is important and presents many control issues in its own right, we are concerned here primarily with continuous systems. We consider in detail two distinct reactor types the continuous stirred tank reactor (CSTRj and the plug-flow reactor. They differ fundamentally in the way the reactants and the products... [Pg.81]

Even adiabatic operation results in the formation of considerable amounts of the undesirable dichloropropane. This occurs in the first part of the reactor, where the temperature of the flowing mixture is low. This is an illustration of the discussion at the beginning of the chapter with respect to Fig. 5-la and b. The conditions correspond to the low-conversion range of Fig. 5-lb before the maximum rate is reached. A tubular-flow reactor is less desirable for these conditions than a stirred-tank unit. The same reaction system is illustrated in Example 5-3 for a stirred-tank unit. [Pg.223]

Adiabatic or nonisothermal operation of a stirred tank reactor presents a different physical situation from that for plug flow, since spatial variations of concentration and temperature do not exist. Rather, reaction heat effects manifest themselves by establishing a temperature level within the CSTR that differs from that of the feed. Thus, when we use the terms adiabatic or nonisothermal in reference to CSTR systems, it will be understood to imply analysis where thermal effects are included in the conservation equations but not to imply the existence of thermal gradients. [Pg.295]

ILLUSTRATION 10.3 Adiabatic Operation of a Cascade of Continuous Flow Stirred-Tank Reactors... [Pg.313]

Two types of reactors are used for the production of LDPE either a stirred vessel (autoclave) or a tubular reactor. The autoclave reactor operates adiabatically. The tubular reactor is cooled with a jacket. The autoclave reactor has a length to diameter ratio (L/D) between 4 and 16. Tubular reactors have L/D ratios above 10000. The inner diameter of the high pressure tubes used for the tubular reactors range between 25 and 100 mm. The operating pressure ranges between 100 and 250 MPa (1000-2500 bars) for the autoclave reactor and between 200 - 350 MPa (2000 - 3500 bar) for the tubular reactor. A basic flow diagram for LDPE processes is shown in Figure 3.7. [Pg.38]


See other pages where Adiabatic stirred flow reactor is mentioned: [Pg.583]    [Pg.583]    [Pg.230]    [Pg.365]    [Pg.328]    [Pg.108]    [Pg.79]    [Pg.409]    [Pg.41]    [Pg.98]    [Pg.59]    [Pg.130]    [Pg.902]    [Pg.76]    [Pg.549]    [Pg.341]    [Pg.189]    [Pg.753]    [Pg.170]    [Pg.613]   


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