Let the reaction be
A = B
Conversion = 90%
Temperature T1 = 40°C + 273 = 313 K
Time t1 = 10.0 min
Temperature T2 = 50°C + 273 = 323 K
Time t2 = 3.0 min
For Batch reactor
dNA/dt = rA * V
d(NA/V)/dt = kCA
dCA/dt = kCA
Integrate the above equation
CA = CA0 exp(-kt)
CA0(1-X) = CA0 exp(-kt)
ln (1-X) = - kt
At X = 0.90
t1 = 10 min
ln (1-0.9) = - k * 10
k1 = 0.2303 min-1
At X = 0.90
t2 = 3 min
ln (1-0.9) = - k * 3
k2 = 0.7675 min-1
From the Arrhenius equation
ln (k2/k1) = (Ea/R) (1/T1 - 1/T2)
ln (0.7675/0.2303) = (Ea/8.314) (1/313 - 1/323)
Ea = 101180.13 J/mol
Part a
Temperature T =?
Time t = 1.0 min
At X = 0.90
t = 1 min
ln (1-X) = - kt
ln (1-0.9) = - k * 1
k = 2.303 min-1
From the Arrhenius equation
ln (k/k1) = (Ea/R) (1/T1 - 1/T)
ln (2.303/0.2303) = (101180.13/8.314) (1/313 - 1/T)
2.303 = 12169.85 (1/313 - 1/T)
(1/313 - 1/T) = 0.00018924
T = 332.71 K
T = 59.71 °C
At 59.71 °C, conversion will be 90% in 1 min.
Part b
First order reaction
T1 = 40 + 273 = 313 K
Rate constant k1 = 0.2303 min-1
X3 = 0.99
Time t3 =?
ln (1-X) = - k1*t3
ln (1-0.99) = - 0.2303 * t3
t3 = 20 min
T2 = 50 + 273 = 323 K
Rate constant k2 = 0.7675 min-1
X3 = 0.99
Time t4 =?
ln (1-X) = - k2*t4
ln (1-0.99) = - 0.7675 * t4
t4 = 6 min
Part c
For 2nd order reaction
1/CA = (1/CA0) + kt
CA0 = 10 mol/L
X = 0.99
CA = CA0(1-X) = 10*(1-0.99) = 0.10 mol/L
T1 = 313 K
Rate constant k1 = 0.2303 min-1
1/CA = (1/CA0) + k1*t
1/0.10 = (1/10) + 0.2303*t
t = 43 min
T2 = 323 K
Rate constant k2 = 0.7675 min-1
1/CA = (1/CA0) + k1*t
1/0.10 = (1/10) + 0.7675*t
t = 13 min
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