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)
Formula sheets, the key method steps for every topic and 8 practice problems, with full solutions at the back.
A first-order reaction in a batch reactor has k = 0.01 min⁻¹. How long does it take to reach 50% conversion? Find t.
A reaction has an activation energy of 80 kJ/mol. At 30 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 10 times faster?
A liquid-phase first-order reaction A → B (k = 0.05 min⁻¹) runs in a 150 L plug-flow reactor (PFR). The feed enters at 5 L/min with CA0 = 2 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.
A first-order liquid-phase reaction (k = 0.2 min⁻¹) runs in a 250 L CSTR fed at 5 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.
0.4 mol/L of H₂ and 0.4 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 50. Find the equilibrium concentration [HI].
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 0.25 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].
How much of stream 2 must be added each hour to stream 1 so that the blended product contains 20% salt? Find ṁ2.
An evaporator concentrates a NaOH solution by boiling off pure water. Find the product flow P in kg/h.
Answer: t = 69.31 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).
Answer: T2 = 53.71 °C
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).
Answer: CA = 0.4463 mol/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.
Conversion: X = 77.69%.
Answer: X = 90.91 %
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.
Answer: [HI] = 0.6236 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.
Answer: [Cl2] = 0.06141 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.
Answer: ṁ2 = 1400 kg/h
Steady-state mass balance: in = out for the total and for each component. Blending problems combine both.
Answer: P = 387.5 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.
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