FE Chemical exam practice: cram pack

Formula sheets, the key method steps for every topic and 24 practice problems, with full solutions at the back.

New problemsBack to the course

In the print window, choose “Save as PDF” to keep a copy on your device.

1Formulas and methods

Mass balance

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

Energy balance

Sensible heat
Q = ṁ·cp·ΔT
Latent heat
Q = ṁ·hfg
Mixing
ΣṁcpTin = ΣṁcpTout
Water
cp ≈ 4.18 kJ/(kg·K)

Ideal gas law

Ideal gas law
pV = nRT
Gas constant
R = 8.314 J/(mol·K)
Combined gas law
p1V1/T1 = p2V2/T2
Moles
n = m/M
Temperature
T[K] = T[°C] + 273.15

Stoichiometry

Moles
n = m/M
Concentration
c = n/V
Mole ratio
use the coefficients of the balanced equation
Limiting reactant
the one that runs out first
Percent yield
actual / theoretical × 100%

Method

  1. Write and balance the chemical equation.
  2. Convert the given mass to moles: n = m/M.
  3. Use the coefficients as the mole ratio to find the moles of the substance you want.
  4. Convert back to mass with m = n·M. With two reactants, find the limiting reactant first.

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.

Calorimetry & enthalpy

Heat
q = m·c·ΔT
Water
c = 4.18 J/(g·°C)
Calorimeter
heat lost = heat gained
Enthalpy of reaction
ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants)

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

Heat exchangers (LMTD)

Heat duty
Q = U·A·ΔTlm
Log mean temperature difference
ΔTlm = (ΔT1 − ΔT2)/ln(ΔT1/ΔT2)
Stream balance
Q = ṁcp(Tin − Tout)

Heat conduction

Fourier’s law
Q̇ = kAΔT/L
Conduction resistance
R = L/(kA)
Convection resistance
R = 1/(hA)
Resistances in series
Q̇ = ΔTtotal/ΣR
U-value
U = 1/(ΣR·A)

Pipe friction & head loss

Reynolds number
Re = V·D/ν = ρ·V·D/μ
Flow regime
laminar below Re ≈ 2000, turbulent above Re ≈ 4000
Mean velocity
V = Q/A, A = π·D²/4
Darcy–Weisbach
hf = f·(L/D)·V²/(2g)
Minor losses
hm = ΣK·V²/(2g)
Typical K values
entrance 0.5, exit 1.0, 90° bend ≈ 0.3
Pressure drop
Δp = ρ·g·hf
Two open reservoirs
Δz = (f·L/D + ΣK)·V²/(2g)
Free outlet
H = (1 + f·L/D + ΣK)·V²/(2g)

Pumps & pump power

Hydraulic power
Ph = ρ·g·Q·H = Q·Δp
Shaft power
Pshaft = Ph/ηpump
Electrical power
Pel = Pshaft/ηmotor
Pump head
H = Δz + Δp/(ρ·g) + hL
System losses
hL = (f·L/D + ΣK)·V²/(2g)

2Practice problems

1.Mass balanceMedium
MixerStream 1550 kg/h · 30% NaOHStream 2ṁ₂ = ? · 10% NaOHProduct15% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 15% NaOH? Find ṁ2.

ṁ1 = 550 kg/hx1 = 30 %x2 = 10 %x3 = 15 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3500 kg/h · 19% NaOHProduct P50% 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 = 3500 kg/hxF = 19 %xP = 50 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 130 °C80 °Cwater · 30 °Ct = ? °C

Hot ethanol cools water in a counter-flow heat exchanger with no heat loss. Find the water outlet temperature tout.

ṁh = 1.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 130 → 80 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 130 °C80 °Cwater · 10 °C70 °C · ṁ = ?5% lost

Hot light oil heats water in an exchanger that loses 5% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 1 kg/scp,h = 2.1 kJ/(kg·K)Th: 130 → 80 °Ct: 10 → 70 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
450 g of HeP = 700 kPaT = 85 °CV = ?

What volume V does 450 g of He occupy at 700 kPa and 85 °C? Treat it as an ideal gas.

m = 450 gM = 4.003 g/molP = 700 kPaT = 85 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of CO₂ goes from 250 kPa, 5 L, 40 °C to 600 kPa and 150 °C. Find the new volume V2.

P1 = 250 kPaV1 = 5 LT1 = 40 °CP2 = 600 kPaT2 = 150 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

20 g of Na and 24 g of Cl2 react according to 2Na + Cl2 → 2NaCl. What mass m of NaCl can form?

M(Na) = 22.99M(Cl2) = 70.9M(NaCl) = 58.44 g/mol
m = g
8.StoichiometryHard
m(CH4​)n(CH4​)n(CO2​)m(CO2​)÷ M(CH4​)× 1/1× M(CO2​)

In the reaction CH4 + 2O2 → CO2 + 2H2O, 30 g of CH4 reacts completely (the other reactants are in excess) and 51.03 g of CO2 is collected. Find the percent yield Y.

M(CH4) = 16.04 g/molM(CO2) = 44.01 g/molactual: 51.03 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.50.50C−x−x+2xE0.5 − x0.5 − x2x

0.5 mol/L of H₂ and 0.5 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 50. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 50
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.400C−x+x+xE0.4 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.4 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.4 mol/LKc = 0.2
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 150 gT = 180 °Cc = 0.129 J/(g·°C)Waterm = 300 gT = 23 °Cc = 4.18 J/(g·°C)

A 150 g block of lead (c = 0.129 J/(g·°C)) at 180 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 23 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.129 J/(g·°C)Tmetal = 180 °Cmwater = 300 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H10 g C3​H8​C3​H8​ + 5O₂reactants3CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 10 g of C3H8 (M = 44.1 g/mol) burns completely: C3H8 + 5O₂ → 3CO₂ + 4H₂O(l). Give q as a positive number.

ΔH°f(C3H8) = −103.8 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = kJ
13.Reaction kineticsMedium
t (min)C (mol/L)5 min0.7

In a first-order reaction the concentration of A falls from 2 mol/L to 0.7 mol/L in 5 min. Find the rate constant k.

CA0 = 2 mol/LCA = 0.7 mol/Lt = 5 min
k = min⁻¹
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.20.012run 20.40.048n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.2 mol/L the rate is 0.012 mol/(L·s); with CA0 = 0.4 mol/L it is 0.048 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.2 mol/Lr1 = 0.012 mol/(L·s)CA0,2 = 0.4 mol/Lr2 = 0.048 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 5 L/minCA0​ = 2.5 mol/LCA​ = ?V = 100 L, k = 0.05 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.05 min⁻¹) runs in a 100 L plug-flow reactor (PFR). The feed enters at 5 L/min with CA0 = 2.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 100 LQ = 5 L/mink = 0.05 min⁻¹CA0 = 2.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
Q = 5 L/minX = ?V = 50 L

A first-order liquid-phase reaction (k = 0.15 min⁻¹) runs in a 50 L plug-flow reactor (PFR) fed at 5 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 50 LQ = 5 L/mink = 0.15 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT125 °C25 °C55 °C10 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 390 kW. The hot fluid cools from 125 to 25 °C and the cold fluid heats from 10 to 55 °C. The overall heat transfer coefficient is 500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 390 kWU = 500 W/(m²·K)Th: 125 → 25 °CTc: 10 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT95 °C55 °C15 °C?ΔT₁ΔT₂parallel flow

In a parallel-flow double-pipe heat exchanger, hot oil (0.2 kg/s, cp = 2.5 kJ/(kg·K)) flows in the inner tube and cools from 95 to 55 °C. Water (1 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 15 °C. The inner tube has a diameter of 25 mm, and U = 500 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.2 kg/scp,h = 2.5 kJ/(kg·K)Th: 95 → 55 °Cṁc = 1 kg/sTc,in = 15 °CD = 25 mmU = 500 W/(m²·K)
L = m
19.Heat conductionMedium
Brick, k = 0.72150 mmGypsum board, k = 0.1775 mm20 °C-1 °CQ̇ = ?

A wall is made of 150 mm of brick and 75 mm of gypsum board, with an area of 20 m². The outer faces are at 20 °C and -1 °C. Find the heat flow Q̇ through the wall.

L1 = 150 mm, k1 = 0.72 W/(m·K)L2 = 75 mm, k2 = 0.17 W/(m·K)A = 20 m²T1 = 20 °CT3 = -1 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.96150 mmWood, k = 0.1725 mmroom 22 °Coutside -9 °CQ̇ = ?

A wall of 150 mm glass and 25 mm wood separates a room at 22 °C from outside air at -9 °C. The convection coefficients are 6 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 6 m². Find the heat loss Q̇ through the wall.

L1 = 150 mm, k1 = 0.96 W/(m·K)L2 = 25 mm, k2 = 0.17 W/(m·K)A = 6 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = -9 °C
Q̇ = W
21.Pipe friction & head lossMedium
Q = 8 L/sD = 75 mmL = 500 mf = 0.02

Water flows at 8 L/s through a pipe 500 m long with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.02 and g = 9.81 m/s². Find the friction head loss hf.

Q = 8 L/sL = 500 mD = 75 mmf = 0.02g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 100 m, D = 200 mm, f = 0.022× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 200 mm (Darcy friction factor f = 0.02) runs from an open reservoir and discharges as a free jet into the air. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each) and a valve (K = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 80 L/s?

Q = 80 L/sL = 100 mD = 200 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 62 m

A pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 62 m. The pump efficiency is 80% and the electric motor driving it has an efficiency of 94%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 10 L/sH = 62 mηpump = 80%ηmotor = 94%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
300 kPa (gauge)PQ = 120 L/sΔz = 6 mL = 400 m, D = 250 mm, f = 0.02, ΣK = 5

A pump moves 120 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 6 m higher. The pipe is 400 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.02; the minor-loss coefficients add up to ΣK = 5 (entrance and exit included). Use g = 9.81 m/s². The upper tank is closed and the air above its water is at a gauge pressure of 300 kPa. Find the head H the pump must add.

Q = 120 L/sΔz = 6 mL = 400 mD = 250 mmf = 0.02ΣK = 5ptank = 300 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 1650 kg/h

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

Balances

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

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 550·(30 − 15)/(15 − 10) = 1650 kg/h

Answer

ṁ2 = 1650 kg/h
2.Mass balance

Answer: W = 2170 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 = 3500·19/50 = 1330 kg/h

Total balance

W = F − P = 3500 − 1330 = 2170 kg/h

Answer

W = 2170 kg/h
3.Energy balance

Answer: tout = 59.19 °C

Exchanger energy balance: with no losses, ṁhcp,h(Th,in − Th,out) = ṁccp,c(tout − tin).

Heat released by the hot stream

Q = 1.5·2.44·(130 − 80) = 183 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 183/(1.5·4.18) = 59.19 °C

Answer

tout = 59.19 °C
4.Energy balance

Answer: ṁc = 0.3977 kg/s

Energy balance with losses: heat released = heat absorbed + heat lost.

Heat released

Qh = 1·2.1·(130 − 80) = 105 kW

Heat that reaches the water

Qc = (1 − 0.05)·105 = 99.75 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 99.75/(4.18·60) = 0.3977 kg/s

Answer

ṁc = 0.3977 kg/s
5.Ideal gas law

Answer: V = 478.2 L

Ideal gas law: PV = nRT, with n = m/M.

Moles

n = 450/4.003 = 112.4 mol
T = 85 + 273.15 = 358.1 K

Volume

V = nRT/P = 112.4·8.314·358.1/700 = 478.2 L

Answer

V = 478.2 L
6.Ideal gas law

Answer: V2 = 2.815 L

Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.

Absolute temperatures

T1 = 313.1 K, T2 = 423.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(250/600)·(423.1/313.1) = 2.815 L

Answer

V2 = 2.815 L
7.Stoichiometry

Answer: m = 39.56 g

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Moles of each reactant

n(Na) = 20/22.99 = 0.8699 mol
n(Cl2) = 24/70.9 = 0.3385 mol

Limiting reactant

0.8699/2 = 0.435, 0.3385/1 = 0.3385 → Cl2

Mass of product

n(NaCl) = 0.3385·2 = 0.677 mol
m = 0.677·58.44 = 39.56 g

Answer

m = 39.56 g
8.Stoichiometry

Answer: Y = 62 %

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Theoretical yield

n(CH4) = 30/16.04 = 1.87 mol
m = 1.87·1/1·44.01 = 82.31 g

Percent yield

Y = 51.03/82.31·100 = 62%

Answer

Y = 62%
9.Chemical equilibrium

Answer: [H2] = 0.1102 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

50 = (2x)²/(0.5 − x)²

Take the square root

7.071 = 2x/(0.5 − x) → x = 0.5·7.071/(2 + 7.071) = 0.3898 mol/L

Equilibrium concentration

[H₂] = 0.5 − x = 0.1102 mol/L

Answer

[H2] = 0.1102 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.2 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

0.2 = x²/(0.4 − x) → x² + 0.2·x − 0.08 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.08))/2 = 0.2 mol/L

Equilibrium concentration

[Cl₂] = x = 0.2 mol/L

Answer

[Cl2] = 0.2 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 25.39 °C

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Heat balance

150·0.129·(180 − Tf) = 300·4.18·(Tf − 23)

Solve for the final temperature

Tf = (19.35·180 + 1254·23)/(19.35 + 1254) = 25.39 °C

Answer

Tf = 25.39 °C
12.Calorimetry & enthalpy

Answer: q = 503.4 kJ

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Enthalpy of reaction

ΔH° = [3·(−393.5) + 4·(−285.8)] − [1·(−103.8) + 5·0] = −2220 kJ

Heat for the given mass

n = 10/44.1 = 0.2268 mol
q = n·|ΔH°/1| = 0.2268·2220 = 503.4 kJ

Answer

q = 503.4 kJ
13.Reaction kinetics

Answer: k = 0.21 min⁻¹

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Integrated first-order law

k = ln(CA0/CA)/t = ln(2/0.7)/5 = 1.05/5 = 0.21 min⁻¹

Answer

k = 0.21 min⁻¹
14.Reaction kinetics

Answer: n = 2

Method of initial rates: for r = k·Cⁿ, comparing two runs that differ only in the starting concentration removes k: r₂/r₁ = (C₂/C₁)ⁿ. Doubling C doubles the rate for first order and quadruples it for second order.

Ratios

r2/r1 = 0.048/0.012 = 4
C2/C1 = 0.4/0.2 = 2

Order

n = ln(4)/ln(2) = 2

Answer

n = 2
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.9197 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.

Space time

τ = V/Q = 100/5 = 20 min

Outlet concentration

CA = 2.5·e−0.05·20 = 0.9197 mol/L

Answer

CA = 0.9197 mol/L

Conversion: X = 63.21%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 77.69 %

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 = 50/5 = 10 min, kτ = 0.15·10 = 1.5

Conversion

X = 1 − e−kτ = 1 − e−1.5 = 77.69%

Answer

X = 77.69%
17.Heat exchangers (LMTD)

Answer: A = 21.85 m²

LMTD method: the temperature difference between the streams changes along the exchanger, so the rate equation uses its logarithmic mean: Q̇ = U·A·ΔTlm, with ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂), where ΔT₁ and ΔT₂ are the differences at the two ends. Counter-flow gives a larger ΔTlm than parallel flow for the same inlet and outlet temperatures.

End temperature differences

In counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 125 − 55 = 70 K
ΔT₂ = Th,out − Tc,in = 25 − 10 = 15 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (70 − 15)/ln(70/15) = 35.7 K

Area

A = Q̇/(U·ΔTlm) = 390000/(500·35.7) = 21.85 m²

Answer

A = 21.85 m²
18.Heat exchangers (LMTD)

Answer: L = 9.331 m

LMTD method: the temperature difference between the streams changes along the exchanger, so the rate equation uses its logarithmic mean: Q̇ = U·A·ΔTlm, with ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂), where ΔT₁ and ΔT₂ are the differences at the two ends. Counter-flow gives a larger ΔTlm than parallel flow for the same inlet and outlet temperatures.

Heat duty and water outlet temperature

Q̇ = 0.2·2.5·(95 − 55) = 20 kW
Tc,out = 15 + 20/(1·4.18) = 19.78 °C

End temperature differences

In parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 95 − 15 = 80 K
ΔT₂ = Th,out − Tc,out = 55 − 19.78 = 35.22 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (80 − 35.22)/ln(80/35.22) = 54.58 K

Area and length

A = 20000/(500·54.58) = 0.7329 m²
L = A/(πD) = 0.7329/(π·0.025) = 9.331 m

Answer

L = 9.331 m
19.Heat conduction

Answer: Q̇ = 646.6 W

Thermal resistance: steady heat flow through layers in series behaves like current through resistors in series: Q̇ = ΔT/ΣR, with R = L/(kA) for a conducting layer and R = 1/(hA) for a convecting surface. The temperature drop across each layer is proportional to its resistance.

Layer resistances

R1 = L1/(k1A) = (150/1000)/(0.72·20) = 0.01042 K/W
R2 = L2/(k2A) = (75/1000)/(0.17·20) = 0.02206 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 21/0.03248 = 646.6 W

Answer

Q̇ = 646.6 W
20.Heat conduction

Answer: Q̇ = 357.7 W

Thermal resistance: steady heat flow through layers in series behaves like current through resistors in series: Q̇ = ΔT/ΣR, with R = L/(kA) for a conducting layer and R = 1/(hA) for a convecting surface. The temperature drop across each layer is proportional to its resistance.

Resistances in series

Ri = 1/(hiA) = 1/(6·6) = 0.02778 K/W
R1 = L1/(k1A) = (150/1000)/(0.96·6) = 0.02604 K/W
R2 = L2/(k2A) = (25/1000)/(0.17·6) = 0.02451 K/W
Ro = 1/(hoA) = 1/(20·6) = 0.008333 K/W
ΣR = 0.08666 K/W

Heat loss

Q̇ = (22 − (-9))/0.08666 = 357.7 W

Answer

Q̇ = 357.7 W
21.Pipe friction & head loss

Answer: hf = 22.28 m

Pipe flow: the Reynolds number Re = V·D/ν = ρ·V·D/μ tells laminar flow (Re below about 2000) from turbulent flow (above about 4000). Friction along a pipe costs the Darcy–Weisbach head loss hf = f·(L/D)·V²/(2g). Fittings, valves, the entrance and the exit add minor losses hm = ΣK·V²/(2g). Between two open reservoir surfaces the energy equation gives Δz = hf + hm, with the exit loss K = 1 included.

Mean velocity

A = π·0.075²/4 = 0.004418 m²
V = Q/A = 0.008/0.004418 = 1.811 m/s

Velocity head

V²/(2g) = 1.811²/(2·9.81) = 0.1671 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.02·(500/0.075)·1.811²/(2·9.81) = 22.28 m

Answer

hf = 22.28 m
22.Pipe friction & head loss

Answer: H = 4.66 m

Pipe flow: the Reynolds number Re = V·D/ν = ρ·V·D/μ tells laminar flow (Re below about 2000) from turbulent flow (above about 4000). Friction along a pipe costs the Darcy–Weisbach head loss hf = f·(L/D)·V²/(2g). Fittings, valves, the entrance and the exit add minor losses hm = ΣK·V²/(2g). Between two open reservoir surfaces the energy equation gives Δz = hf + hm, with the exit loss K = 1 included.

Velocity

V = Q/A = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Loss coefficients

f·L/D = 0.02·100/0.2 = 10
ΣK = 0.5 + 2·0.3 + 2 = 3.1

Energy equation

The outlet jet still carries its velocity head; it is not a loss but it has to be supplied.

H = (1 + 10 + 3.1)·0.3305 = 4.66 m

Answer

H = 4.66 m
23.Pumps & pump power

Answer: Pel = 8.088 kW

Pump power: the power given to the water is the hydraulic power Ph = ρ·g·Q·H = Q·Δp. The shaft must deliver more because the pump loses some: Pshaft = Ph/ηpump, and the motor draws Pel = Pshaft/ηmotor. The pump head H follows from the energy equation: static lift + pressure head + all friction and minor losses.

Hydraulic power

Ph = ρ·g·Q·H = 1000·9.81·0.01·62 = 6.082 kW

Shaft power

Pshaft = 6.082/0.8 = 7.603 kW

Electrical power

Pel = 7.603/0.94 = 8.088 kW

Answer

Pel = 8.088 kW
24.Pumps & pump power

Answer: H = 47.85 m

Pump power: the power given to the water is the hydraulic power Ph = ρ·g·Q·H = Q·Δp. The shaft must deliver more because the pump loses some: Pshaft = Ph/ηpump, and the motor draws Pel = Pshaft/ηmotor. The pump head H follows from the energy equation: static lift + pressure head + all friction and minor losses.

Velocity

V = Q/A = 0.12/0.04909 = 2.445 m/s
V²/(2g) = 0.3046 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (32 + 5)·0.3046 = 11.27 m

Pressure head

p/(ρ·g) = 300000/(1000·9.81) = 30.58 m

Pump head

Both surfaces are practically at rest, so there is no velocity head term.

H = Δz + p/(ρ·g) + hL = 6 + 30.58 + 11.27 = 47.85 m

Answer

H = 47.85 m

This is independent practice material. ExamProblems is not affiliated with or endorsed by the organisation that runs this exam, and the exam name is used only to describe the content. The FE exam is run by NCEES, which is not affiliated with ExamProblems and does not endorse it.

ExamProblems · examproblems.com/courses/fe-exam-chemical