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A B,essentiallyirreversible reaction
n
rA = kc A
XA
(1 X A )2
= C A,0 k
c A,0 k
1 + c A,0 k
xA
(1 xA)2
= c A,0 k
xA = 1 ek
xA =
x A is independent of c A,0
x A independent of c A,0
k
1+k
x A = k for c A,0 k
c A,0
x A decreases with increasing c A,0
all reactors give same conversion at same
2k
for cA,0
xA = 1
2k
= 1 1
2
2
4k
1 4 2k
c A,0
for c A,0
4k
* Interesting to note that, with constant inlet concentration only, the variation of conversion
with space time for a second-order reaction in a PFR is the same as for a first-order reaction
in a CSTR.
Even though FRACTIONAL conversion doesnt change, a greater number of moles of A
are reacted to product per unit time or space time as the initial or inlet concentration of A
increases.
This is the behavior obtained in The Reactor Lab. This is an interesting case. This is a
quadratic equation with a + sign possible between the one-halves. There is a bifurcation
point at c A,0 = 4 k with the mathematical solution bifurcating, or splitting, as c A,0 is
increased past this point. The upper branch of the solution with the + sign is a locus of
unstable steady states: a infinitesimal increase in concentration would cause the conversion
to drop to the lower, stable steady state branch; an infinitesimal decrease in concentration
would cause the conversion to go to one with an infinite rate, however, see the next footnote.
To check for stability, look at the unsteady-state mole balance and see how the system
responds to small perturbations from steady-state.
No real reaction would stay zero or negative order all the way down to zero concentration,
i.e., x = 1; it would eventually change its kinetics at some point, e.g., to first order, so the full
range for these cases is hypothetical.
FOR A SECOND ORDER REACTION IN A CSTR:
1
1
1
XA = 1 +
+
2kC A0
4(kC A0
kC A0
)2
0.5
accum =
in
out
+ gen by rxn
0 = v0 C A0 (1 X i 1 ) v0 C A0 (1 X i ) kC 2A0 (1 X i )2 V
1
X
2
X i 2 + X i + 1 + i 1 = 0 where K = kC A0 (1 X i1 )
K
K
Xi = 1 +
1 1
1
X i 1
+
2
2K K 4K
K
0.5
and
V
v0