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Difficulties in Scaling Up The Fluidized Bed Reactor
Difficulties in Scaling Up The Fluidized Bed Reactor
Difficulties in Scaling Up The Fluidized Bed Reactor
Reactor
The purpose of running experiments in the laboratory is to
obtain information to help the engineer in his design of large-
scale operating units. However, the scaleup and design of
bubbling fluidized bed (BFB) reactors is uncertain, for several
reasons. Primarily, it is because the size of bubbles in the larger
unit strongly influences the conversion of reactant, and this
factor cannot be reliably estimated from small-scale laboratory
experiments. We discuss this problem.
During the second world war, the United States had an urgent
need to produce enormous quantities of aviation gasoline. Fine
particle fluidization (the fluidized catalytic cracking (FCC)
process) was proposed and chosen; commercial plants were built
chop-chop and were wildly successful. Interestingly, all were
built without any basic information on flow behavior, heat and
mass transfer, reaction behavior, and other contacting phenom-
ena in these units. After the war, news of this new gas-solid
(G/S) contacting method was made public, and this spurred the
research community to explore its properties and its unique
features.
The first phenomenon studied was the very simplest: the heat-
transfer rate between particles and the fluidizing gas. Until 1965,
there were at least 14 such studies. These came from all over
the worldsfrom countries such as the United States, Europe,
Russia, and Japan. These researchers measured the temperatures
of gases entering and leaving a reactor and, assuming plug flow
or mixed flow of gas in the bed, calculated values for the kinetic Figure 1. Reported result for nine experimental studies of gas-solid (G/
factor (h). Figure 1 shows some of their results on a plot of S) heat transfer in fluidized beds (see Kunii and Levenspiel1).
Nusselt number versus Reynolds number (Nu vs Re). This figure same mistake, and that all their results were wrong. What is
shows the values for h for the heating of a single particle falling the explanation for this? Let us see.
through a gas and also for particles mixing in bubbling fluidized Now, for any process, there are four inter-related quantities:
bed (BFB) reactors. The experimental values in BFB reactors (1) the inlet gas to the BFB reactor; (2) the outlet gas to the
all lie well below the single particle correlationssome by a BFB reactor; (3) the kinetics, including the heat- and mass-
factor of 1000 or more. transfer coefficients between the heating particle and the bed
It is hard to understand why none of the 14 groups of solids; and (4) the flow pattern of solids in the vessel. If you
experimenters questioned this low result. Would the researcher measure quantities 1 and 2, then 3 and 4 are related. Therefore,
not suspect that, in an environment that contains many buffeting if you make an error in quantity 3, then quantity 4 is also wrong.
and colliding particles and much turbulence, the h value between Here, in these experiments, because the kinetic factor (h) is way
a particle and a gas would be greater than for a single falling off, this means that the flow model chosen (plug or mixed flow)
particle? Why was it actually lower? Why wasn’t the researcher is also wrong. But what is it? That is our problem.
suspicious? What kind of a researcher was he?
Any of the researchers could have conducted a theoretical Chemical Reactor: Plug Flow or Mixed Flow Model?
experiment to determine whether the reported results were Numerous investigators have studied the behavior of solid
reasonable and made sense. Let us do that now. catalyzed BFB reactors. They measured the fluid compositions
Let us introduce a single particle into a fluidized bed at 0 °C entering and leaving the reactor, and they knew the reaction
and ask how long it takes for the particle to heat up to 90 °C. rate constant (the kinetics), so they could check the fit of this
(See Figure 2.) Eight minutes or a quarter of a second: which flow model or that flow model.
sounds more reasonable? Certainly not the 8 min. This example Thirty-nine flow experiments were conducted by five different
suggests that all nine groups of experimenters had made the reactor groups in various flow reactors, and the extent of the
10.1021/ie071355v CCC: $40.75 © xxxx American Chemical Society
Published on Web 12/22/2007 PAGE EST: 4.7
B
Figure 2. Depiction of the time needed to heat a single, very tiny, particle
in a fluidized bed; plots from theory and from experiment are shown.
Figure 6. Fitting the five data points with a first-, second-, and third-
degree polynomial.
Figure 14. Sketch showing the decrease in conversion, using the three-
region model, with increasing bubble size.
Figure 11. Depiction of the three-region flow model for fine particle
bubbling fluidized beds (BFBs).
Figure 12. Sketch showing the chemical conversion for the three-region
model. Five factors are involved.
“Keep things as simple as possible, but not simpler” But does this represent an engineering model? The definitive
answer to this question requires that experiments be performed
With this in mind, we choose the three-region flow model of using different bubble sizes and how the conversion changes
Kunii and Levenspiel,1,4 which contains just one size of bubble with bubble size be monitored. No one has done this yet;
(shown in Figure 11). Only one parameter of this model can be therefore, one must turn to the theoretical estimate.
observed and measured: it is the bubble size. For this estimation, consider the example of Figure 13, which
The chemical conversion for this model involves five represents a bed 2 m in diameter and 2 m high, containing 7
factors: the two transfer rates and the three reaction rates. This tons of catalyst with the rate constant shown.
is shown in Figure 12. One should also note that these rate Let us see what conversion this model predicts for different
factors can be determined without computer calculations. bubble sizes, and let us see if the predictions are reasonable.
PAGE EST: 4.7 E
Octave Levenspiel
Emeritus Professor,
Chemical Engineering Department,
Oregon State UniVersity,
CorVallis, Oregon 97331-2702
IE071355V