FE Chemical study materials
FE Chemical study resources

FE Chemical: Chemical Engineering

FE Chemical · Work through your exam, one topic at a time.

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Chemical Engineering

The Chemical Engineering domain of the FE Chemical exam tests integrated use of balances, thermodynamics, transport, reaction engineering, control, safety, and economics in short self-contained problems. Marks usually turn on a clear basis, consistent units, and the correct limiting assumption.

Balances and units

  • Select a basis (1 h, 100 mol feed, or 1 kg) and state steady state. Write total and component balances; inert components pass through unless purged.
  • Track mole versus mass units. For gases use partial pressure or molar flow; at standard conditions 1 lbmol ideal gas occupies 379 ft³ and 1 kmol occupies 22.414 m³.
  • Define conversion X, selectivity, and yield against the correct limiting reactant. Recycle raises overall conversion only when a purge or separation prevents inert buildup.

Thermodynamics and transport

  • For open steady systems, Q − W_s = Σ out n H − Σ in n H; use enthalpy paths and latent heats for phase change. Vapor-liquid equilibrium for ideal mixtures uses Raoult's law, y_i P = x_i P_i^sat.
  • Mechanical energy balance with friction: P1/ρ + v1²/2 + gz1 = P2/ρ + v2²/2 + gz2 + h_f. Reynolds number Re = ρvD/μ; Darcy-Weisbach h_f = f(L/D)(v²/2).
  • Heat exchanger duty Q = U A ΔT_lm F; add fouling resistances. Mass transfer uses Fick's law and two-film resistances; absorption columns often use NTU/HTU.

Reaction, control, and safety

  • Arrhenius k = A exp(−Ea/RT). For liquid constant-density first order: CSTR V = F_A0 X/[k C_A0(1−X)]; PFR V = (v0/k) ln[1/(1−X)].
  • PID controllers: proportional gain, integral eliminates offset, derivative anticipates; dead time destabilizes.
  • Check flammability limits, relief scenarios, and HAZOP deviations before accepting a design.

Worked example

A liquid feed of 100 L/min with C_A0 = 2 mol/L enters a CSTR where A → B is first order with k = 0.10 min⁻¹. Find V for 80% conversion. At the outlet, C_A = 2(1 − 0.80) = 0.40 mol/L, so −r_A = kC_A = 0.040 mol/(L·min). F_A0 = 100 × 2 = 200 mol/min. The CSTR design equation gives V = F_A0 X/(−r_A) = 200 × 0.80/0.040 = 4000 L. A PFR would need only (100/0.10) ln(1/0.20) ≈ 1609 L because its rate is not evaluated at the outlet.

Traps

  • Mixing gauge and absolute pressure, or mass and molar flow.
  • Using the CSTR rate at feed conditions instead of outlet conditions.
  • Assuming ΔT_lm applies without the correction factor F in multipass exchangers.
  • Forgetting inert accumulation in recycle loops and purge design.