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Che341 Examples Batchr

1) The document provides 5 examples of chemical reaction engineering problems. The examples include deriving rate equations and calculating rate constants for first-order and second-order reactions. Reaction conditions like temperature, initial concentrations, and mechanisms are provided. 2) The examples require applying concepts like integrated rate laws, determining rate orders, and establishing relationships between reactants and products to derive rate equations. 3) Rate constants are calculated by fitting integrated rate equations to experimental data relating extent of reaction to time under different conditions.

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0% found this document useful (0 votes)
607 views9 pages

Che341 Examples Batchr

1) The document provides 5 examples of chemical reaction engineering problems. The examples include deriving rate equations and calculating rate constants for first-order and second-order reactions. Reaction conditions like temperature, initial concentrations, and mechanisms are provided. 2) The examples require applying concepts like integrated rate laws, determining rate orders, and establishing relationships between reactants and products to derive rate equations. 3) Rate constants are calculated by fitting integrated rate equations to experimental data relating extent of reaction to time under different conditions.

Uploaded by

Aybike Taşdemir
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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GAZI UNIVERSITY

CHEMICAL ENGINEERING
ChE341 CHEMICAL REACTION ENGINEERING

EXAMPLES

1) The first order reaction A B is carried out in a constant-volume batch reactor (k=0.31 min-1).
Derive an equation for time as a function of reactant concentration and calculate the time
necessary to reduce the number of moles of A to 1% of its initial value.

CA = 0.01CA0 k=0.31 min-1 t= 15 min

2) Find the first-order rate constant for the disappearance of A in the gas reaction 2A  R if, on
holding the pressure constant, the volume of the reaction mixture, starting with 80% A,
decreases by 20% in 3 min.

3 min

V V= 0.8 V

2A R
0.8 A 0.4 R
0.2 inert 0.2 inert

1 0.6
When 𝑥 =0 𝑥 =1

.
𝜀 = = - 0.4
∆𝑉 = 0.8 V − V = -0.2 V

.
-ln (1- .
) = k (3 min)

k= 0.231 min-1
3) The following reaction takes place in the gas phase at 400oC.

A+ B → C

The initial composition is as follows (mole percents).

A : 0.40 B: 0.40 C: 0.11 Inerts: 0.09

The reaction takes place in an isothermal reactor that is maintained at a constant pressure of 1 atm.

If the reaction is first-order in A and first-order in B, and if the value of k is 2 liters/mole min, how

long will it take for the mole fraction C to reach 0.15?

NC = NC0 + NA0 XA NA = NA0- NA0 XA NB = NB0 - NB0XB


NA0 XA = NB0XB also NA0 = NB0 that’s why NA = NB

Suppose initially 100 moles mixture


Mole fraction of C yC = 0.15 =

0.15 = XA = 0.086
( )

-rA = - = = k CA C B

CA = CB so

- = = k CA 2

CA0 2 (1−𝑋𝐴) 2
=k( )

( )
= k𝐶 ∫ 𝑑𝑡= k𝐶 𝑡
( )

.
.
𝑋𝐴
𝜀 ln (1 − 𝑋 ) + (1+ 𝜀 ) k𝐶 𝑡
(1−𝑋𝐴 ) =

A + B → C

40 A
40 B
11 C (11+40) = 51 C
9 inert 9 inert

100 60

( . )
𝜀 = = -0.4 = = 7.248x 10-3 mol/L
. ( )

0.086
−0.4ln (1 − 0.086 ) + (1- 0.4) (2) (7.248x 10 )𝑡
(1−0.086) =

t = 6.33 min
4) Pure gaseous A is prepared under refrigeration and is introduced into a thin-walled capillary
which acts as reaction vessel as shown in Figure. No appreciable reaction occurs during
handling. The reaction vessel is rapidly plunged into a bath of boiling point water, reactant A
decomposes to completion according to the reaction A→R+S, and the following data are
obtained:
Time, min 0.5 1 1.5 2 3 4 6 10 ∞
Length of capillary occupied by reaction 6.1 6.8 7.2 7.5 7.85 8.1 8.4 8.7 9.4
mixture, cm
Find the rate equation in units of moles, liters and minutes.

V= V0(1 + 𝜀𝐴 𝑋𝐴 )
L : Length of capillary occupied by reaction mixture
S : Cross sectional area of capillary tube

L . S = L0 S (1 + 𝜀𝐴 𝑋𝐴 )

L / L0 = ( 1 + 𝜀 𝑋 )

A→R+S
1A 1R,1S

1 2

2−1
𝜀 = =1
1

At any t L / L0 = ( 1 + 𝑋 ) 𝑋 = ( L / L0) -1

𝑋 = ( L / L0) -1

At t =∞ 𝑋 = 1 𝑠𝑜 2 = L∞ / L0 L0 = L∞ / 2 , L0 = 9.4 / 2 =4.7 cm
- = = k CA 2

CA0 2 (1−𝑋𝐴) 2
=k( )
.
.

𝑋𝐴
𝜀 ln (1 − 𝑋 ) + (1+ 𝜀 ) k𝐶 𝑡
(1−𝑋𝐴 ) =

𝜀 = 1,

ln(1 − 𝑋 ) + 2 = k𝐶 𝑡
( )

.
Time, min 0.5 1 1.5 2 3 4 6 10 ∞
L, cm 6.1 6.8 7.2 7.5 7.85 8.1 8.4 8.7 9.4
𝑋 = ( L / 4.7) -1 0.297 0.446 0.53 0.6 0.67 0.72 0.79 0.85 1

ln(1 − 𝑋 ) + 2 0.5 1.04 1.5 2.08 2.9 3.88 5.94 9.47


( )

Slope = 0.79 = k𝐶
5) The data in table is about the reaction of sulfuric acid with diethylsulfate in aqueous solution
at 22.9OC.
H2S04 + (C2H5)2SO4  2C2H5SO4H
Initial concentrations of H2S04 and (C2H5)2SO4 are each 5.5 mol/liter. Find a rate equation for this
reaction.

A+B ↔ 2R

Assume second order reversible reaction

(Since CR at ∞ time < 2 𝐶 it is reversible )

− = k1 CACB – k2 CR2

since 𝐶 = 𝐶 = 5.5 and 𝐶 𝑥 =𝐶 𝑥 CA = CB

𝑎𝑛𝑑 − = k 1 CA 2 – k 2 CR 2

CA= CA0 − 𝐶 𝑥 CR = 2 𝐶 𝑥

At equilibrium since − =0, k2 CRe 2 = k1 CAe2

k2 (2𝐶 𝑥 e)2 = k1 (CA0 --- 𝐶 𝑥 e)2

( )
k2 =

Inserting k2 to the main equation,


( )
− = CA0 =k1 CA02(1 − 𝑥 )2– ( ) (2 𝐶 𝑥 )2

integration of rate equation gives

CR= CR0 + 2 𝐶 𝑥 and 𝑥 =

t(min) CR XA
mol/L

0 0 0 0
48 1.38 0.125 0.259
75 2.24 0.2036 0.466
96 2.75 0.25 0.616
127 3.31 0.3 0.813
162 3.81 0.346 1.033
180 4.11 0.37 1.193
267 4.86 0.442 1.77
410 5.42 0.49 2.67
∞ 5.80 0.527

CRe 𝑥 e
Slope =0.00675 =2 k1 ( -1) 5.5
.

k1, k2 can be calculated seperately


( )
k2 =

k1=1.3 x 10-4
k2=2.6 x 10-5

r=1.3 x 10-4 CACB – 2.6 x 10-5 CC2

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