Chemical Reaction Engineering: cram pack

Formula sheets, the key method steps for every topic and 8 practice problems, with full solutions at the back.

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1Formulas and methods

Reaction kinetics

First order
ln(CA/CA0) = −kt
Half-life (first order)
t½ = ln 2/k
Second order
1/CA = 1/CA0 + kt
Arrhenius
k = A·e−Ea/(RT)
Two temperatures
ln(k2/k1) = (Ea/R)(1/T1 − 1/T2)

Reactor sizing (CSTR & PFR)

Space time
τ = V/Q
CSTR, first order
τ = X/(k·(1 − X)), CA = CA0/(1 + kτ)
PFR, first order
τ = ln(1/(1 − X))/k, CA = CA0·e−kτ
Conversion from volume
CSTR: X = kτ/(1 + kτ), PFR: X = 1 − e−kτ
N equal CSTRs in series
X = 1 − 1/(1 + kτi)N

Chemical equilibrium

Equilibrium constant
Kc = [C]c[D]d/([A]a[B]b)
ICE table
Initial, Change (×coefficient), Equilibrium
Quadratic
x = (−b + √(b² − 4ac))/(2a)

Method

  1. Write Kc with products over reactants, each raised to the power of its coefficient.
  2. Set up an ICE table: Initial, Change (in steps of x times the coefficients), Equilibrium.
  3. Put the equilibrium expressions into Kc and solve for x.
  4. Check whether x is small enough for an approximation; otherwise solve the quadratic.

Mass balance

Steady state
in = out
Total balance
ṁ1 + ṁ2 = ṁ3
Component balance
ṁ1x1 + ṁ2x2 = ṁ3x3
Evaporator
F·xF = P·xP, W = F − P

2Practice problems

1.Reaction kineticsMedium
t (min)X (%)t = ?50%

A first-order reaction in a batch reactor has k = 0.1 min⁻¹. How long does it take to reach 50% conversion? Find t.

k = 0.1 min⁻¹X = 50 %
t = min
2.Reaction kineticsHard
Tk30 °C0.0240 °C0.0551

The rate constant of a reaction is 0.02 min⁻¹ at 30 °C and 0.0551 min⁻¹ at 40 °C. Find the activation energy Ea.

k1 = 0.02 min⁻¹T1 = 30 °Ck2 = 0.0551 min⁻¹T2 = 40 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
3.Reactor sizing (CSTR & PFR)Medium
Q = 20 L/minX = 70%V = ?, k = 0.1 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.1 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 20 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 70% conversion of A.

Q = 20 L/mink = 0.1 min⁻¹X = 70%
V = L
4.Reactor sizing (CSTR & PFR)Hard
V = 800 LQ = 5 L/minX = ?

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in an 800 L CSTR fed at 5 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 800 LQ = 5 L/mink = 0.12 min⁻¹
X = %
5.Chemical equilibriumMedium
H2​I2​HII110C−x−x+2xE1 − x1 − x2x

1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 49. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 49
[H2] = mol/L
6.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.5 mol/LKc = 0.1
[Cl2] = mol/L
7.Mass balanceMedium
MixerStream 1850 kg/h · 5% sugarStream 2ṁ₂ = ? · 45% sugarProduct40% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 40% sugar? Find ṁ2.

ṁ1 = 850 kg/hx1 = 5 %x2 = 45 %x3 = 40 %
ṁ2 = kg/h
8.Mass balanceHard
EvaporatorFeed F1200 kg/h · 14% NaOHProduct P45% NaOHVapour W (pure water)W = ? kg/h

An evaporator concentrates a NaOH solution by boiling off pure water. Find the water evaporated W in kg/h.

F = 1200 kg/hxF = 14 %xP = 45 %
W = kg/h

3Solutions

1.Reaction kinetics

Answer: t = 6.931 min

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Conversion and concentration

C/C0 = 1 − X = 0.5

Solve for the time

t = −ln(1 − X)/k = −ln(0.5)/0.1 = 6.931 min

Answer

t = 6.931 min
2.Reaction kinetics

Answer: Ea = 79.98 kJ/mol

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Absolute temperatures

T1 = 303.1 K, T2 = 313.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·1.013/(-1.053e-4) = 79985 J/mol
Ea = 79.98 kJ/mol

Answer

Ea = 79.98 kJ/mol
3.Reactor sizing (CSTR & PFR)

Answer: V = 240.8 L

Ideal reactors, first-order reaction (−rA = k·CA) at steady state, with space time τ = V/Q. A CSTR is perfectly mixed, so the whole volume reacts at the low outlet concentration: τ = X/(k·(1 − X)) and CA = CA0/(1 + k·τ). In a PFR each slice of fluid reacts like a small batch reactor: τ = ln(1/(1 − X))/k and CA = CA0·e−k·τ. For the same conversion a CSTR always needs more volume than a PFR.

Space time

τ = ln(1/(1 − 0.7))/0.1 = 1.204/0.1 = 12.04 min

Volume

V = Q·τ = 20·12.04 = 240.8 L

Answer

V = 240.8 L
4.Reactor sizing (CSTR & PFR)

Answer: X = 95.05 %

Ideal reactors, first-order reaction (−rA = k·CA) at steady state, with space time τ = V/Q. A CSTR is perfectly mixed, so the whole volume reacts at the low outlet concentration: τ = X/(k·(1 − X)) and CA = CA0/(1 + k·τ). In a PFR each slice of fluid reacts like a small batch reactor: τ = ln(1/(1 − X))/k and CA = CA0·e−k·τ. For the same conversion a CSTR always needs more volume than a PFR.

Space time

τ = V/Q = 800/5 = 160 min, kτ = 0.12·160 = 19.2

Conversion

X = kτ/(1 + kτ) = 19.2/(1 + 19.2) = 95.05%

Answer

X = 95.05%
5.Chemical equilibrium

Answer: [H2] = 0.2222 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

49 = (2x)²/(1 − x)²

Take the square root

7 = 2x/(1 − x) → x = 1·7/(2 + 7) = 0.7778 mol/L

Equilibrium concentration

[H₂] = 1 − x = 0.2222 mol/L

Answer

[H2] = 0.2222 mol/L
6.Chemical equilibrium

Answer: [Cl2] = 0.1791 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

0.1 = x²/(0.5 − x) → x² + 0.1·x − 0.05 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.05))/2 = 0.1791 mol/L

Equilibrium concentration

[Cl₂] = x = 0.1791 mol/L

Answer

[Cl2] = 0.1791 mol/L
7.Mass balance

Answer: ṁ2 = 5950 kg/h

Steady-state mass balance: in = out for the total and for each component. Blending problems combine both.

Balances

Total: ṁ3 = ṁ1 + ṁ2
sugar: ṁ1x1 + ṁ2x2 = (ṁ1 + ṁ2)x3

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 850·(5 − 40)/(40 − 45) = 5950 kg/h

Answer

ṁ2 = 5950 kg/h
8.Mass balance

Answer: W = 826.7 kg/h

Tie component: a component that passes through unchanged in one stream (here the solute) links the flows directly. Then the total balance gives the rest.

Solute balance

F·xF = P·xP → P = 1200·14/45 = 373.3 kg/h

Total balance

W = F − P = 1200 − 373.3 = 826.7 kg/h

Answer

W = 826.7 kg/h

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