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Constant stirred tank reactor

Perhaps the biggest oversight physical chemists make when discussing kinetics is the neglect of volume effects. To be sure any chemical engineer who would forget the influence of volume even in a constantly stirred tank reactor would not be long in the profession. The volume alone can affect the rate of the reaction. How many physical chemistry courses, or text books, point that out ... [Pg.22]

The simplest continuous reactor to consider is that of a constantly stirred tank reactor (CSTR) or precipitator, also called a mixed suspension, mixed product removal crystallizer (MSMPR) [98], shown in Figure 6.23. This tsrpe of precipitator has a constant volume, V, with an input flow rate equal to its output flow rate, Q. The population iJofR) in the precipitator is that which leaves as product. In this case, the population balance is used at steady state (i.e., drjfjdt — 0) ... [Pg.220]

Laboratory Fischer-Tropsch synthesis tests were performed in a slurry-phase Constant Stirred Tank Reactor. The pre-reduced catalyst (20-30 g) was suspended in ca 300 ml molten Fischer-Tropsch wax. Realistic Fischer-Tropsch conditions were employed, i.e. 220 °C 20 bar commercial synthesis gas feed 50 vol% H2, 25 vol% CO and 25 vol% inerts synthesis gas conversion levels in excess of 50%. Use was made of the ampoule sampling technique as the selected on-line synthesis performance monitoring method [23]. [Pg.57]

During the manufacturing process, if the grafting increases during early stages of the reaction, the phase volume will also increase, but the size of the particles will remain constant [146-148]. Furthermore, reactor choice plays a decisive role. If the continuous stirred tank reactor (CSTR) is used, little grafting takes place and the occlusion is poor and, consequently, the rubber efficiency is poor. However, in processes akin to the discontinuous system(e.g., tower/cascade reactors), the dispersed phase contains a large number of big inclusions. [Pg.658]

In Fig. 28, the abscissa kt is the product of the reaction rate constant and the reactor residence time, which is proportional to the reciprocal of the space velocity. The parameter k co is the product of the CO inhibition parameter and inlet concentration. Since k is approximately 5 at 600°F these three curves represent c = 1, 2, and 4%. The conversion for a first-order kinetics is independent of the inlet concentration, but the conversion for the kinetics of Eq. (48) is highly dependent on inlet concentration. As the space velocity increases, kt decreases in a reciprocal manner and the conversion for a first-order reaction gradually declines. For the kinetics of Eq. (48), the conversion is 100% at low space velocities, and does not vary as the space velocity is increased until a threshold is reached with precipitous conversion decline. The conversion for the same kinetics in a stirred tank reactor is shown in Fig. 29. For the kinetics of Eq. (48), multiple solutions may be encountered when the inlet concentration is sufficiently high. Given two reactors of the same volume, and given the same kinetics and inlet concentrations, the conversions are compared in Fig. 30. The piston flow reactor has an advantage over the stirred tank... [Pg.119]

In this work, the characteristic "living" polymer phenomenon was utilized by preparing a seed polymer in a batch reactor. The seed polymer and styrene were then fed to a constant flow stirred tank reactor. This procedure allowed use of the lumped parameter rate expression given by Equations (5) through (8) to describe the polymerization reaction, and eliminated complications involved in describing simultaneous initiation and propagation reactions. [Pg.297]

The concept of a well-stirred segregated reactor which also has an exponential residence time distribution function was introduced by Dankwerts (16, 17) and was elaborated upon by Zweitering (18). In a totally segregated, stirred tank reactor, the feed stream is envisioned to enter the reactor in the form of macro-molecular capsules which do not exchange their contents with other capsules in the feed stream or in the reactor volume. The capsules act as batch reactors with reaction times equal to their residence time in the reactor. The reactor product is thus found by calculating the weighted sum of a series of batch reactor products with reaction times from zero to infinity. The weighting factor is determined by the residence time distribution function of the constant flow stirred tank reactor. [Pg.297]

Stirred tank reactor. Suppose the tank is initially empty and is filled at a constant rate go with fluid having concentration A first-order reaction begins immediately. Find the concentration within the tank, a, as a function of time, t < tfiai-... [Pg.522]

Determine the fractional Ailing rate QflulQ that will All an isothermal, constant-density, stirred tank reactor while simultaneously achieving the steady-state conversion corresponding to flow rate Q. Assume a second-order reaction with aj kt = 1 and t = 5 h at the intended steady state. [Pg.534]

Consider a simple first-order exothermie reaction, A —> B, carried out in a single, constant-volume, continuous stirred-tank reactor (Fig. 3.12), with constant jacket coolant temperature, where r = - k Ca,. [Pg.151]

Thus it is possible for continuous stirred-tank reactor systems to be stable, or unstable, and also to form continuous oscillations in output, depending upon the system, constant and parameter, values. [Pg.156]

Continuous stirred-tank reactor. Dimensionless form Compare with TANK nth-order kinetics Constant V=1000 P = 10 CA0=100 n = 2 k=0.1 CINT=0.01,... [Pg.325]

It is important to understand that the time constant xp of a process, say, a stirred tank is not the same as the space time x. Review this point with the stirred-tank heater example in Chapter 2. Further, derive the time constant of a continuous flow stirred-tank reactor (CSTR) with a first-order chemical reaction... [Pg.61]

Since one is almost always concerned with liquid phase reactions when dealing with stirred tank reactors, the assumption of constant fluid density is usually appropriate. In this case equation 8.3.6 can be written as... [Pg.272]

Use the model based on a cascade of stirred tank reactors to predict the conversion that will be attained in the reactor of Illustration 11.1. Assume that the value of the first-order rate constant is 3.33 x 10 3sec-1. [Pg.416]


See other pages where Constant stirred tank reactor is mentioned: [Pg.535]    [Pg.648]    [Pg.135]    [Pg.275]    [Pg.275]    [Pg.616]    [Pg.648]    [Pg.535]    [Pg.648]    [Pg.135]    [Pg.275]    [Pg.275]    [Pg.616]    [Pg.648]    [Pg.279]    [Pg.280]    [Pg.501]    [Pg.135]    [Pg.555]    [Pg.295]    [Pg.298]    [Pg.324]    [Pg.23]    [Pg.568]    [Pg.172]    [Pg.345]    [Pg.454]    [Pg.536]    [Pg.347]    [Pg.347]    [Pg.108]    [Pg.128]    [Pg.83]    [Pg.247]    [Pg.329]    [Pg.397]    [Pg.208]    [Pg.32]    [Pg.244]   
See also in sourсe #XX -- [ Pg.275 ]

See also in sourсe #XX -- [ Pg.275 ]




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C Constant-Volume Continuous Stirred-Tank Reactor

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Reactor stirred

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Reactors stirring

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Tank reactor

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