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 1650 kg/h · 15% saltStream 2ṁ₂ = ? · 30% saltProduct25% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 25% salt? Find ṁ2.

ṁ1 = 650 kg/hx1 = 15 %x2 = 30 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1700 kg/h · 11% 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 = 1700 kg/hxF = 11 %xP = 45 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 180 °C130 °Cwater · 20 °Ct = ? °C

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

ṁh = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 180 → 130 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 160 °C60 °Cwater · 15 °C35 °C · ṁ = ?10% lost

Hot glycol mix heats water in an exchanger that loses 10% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 2 kg/scp,h = 3.6 kJ/(kg·K)Th: 160 → 60 °Ct: 15 → 35 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
430 g of O₂P = 350 kPaT = 40 °CV = ?

What volume V does 430 g of O₂ occupy at 350 kPa and 40 °C? Treat it as an ideal gas.

m = 430 gM = 32 g/molP = 350 kPaT = 40 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
O₂, M = 32 g/molP = 800 kPaT = 10 °Cρ = ?

Find the density ρ of O₂ at 800 kPa and 10 °C, treating it as an ideal gas.

M = 32 g/molP = 800 kPaT = 10 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(AlCl3​)m(AlCl3​)÷ M(X)× 2/ν× M(AlCl3​)

24 g of Al and 64 g of Cl2 react according to 2Al + 3Cl2 → 2AlCl3. What mass m of AlCl3 can form?

M(Al) = 26.98M(Cl2) = 70.9M(AlCl3) = 133.33 g/mol
m = g
8.StoichiometryHard
m(Al)n(Al)n(AlCl3​)m(AlCl3​)÷ M(Al)× 2/2× M(AlCl3​)

In the reaction 2Al + 3Cl2 → 2AlCl3, 12 g of Al reacts completely (the other reactants are in excess) and 36.77 g of AlCl3 is collected. Find the percent yield Y.

M(Al) = 26.98 g/molM(AlCl3) = 133.33 g/molactual: 36.77 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.20.20C−x−x+2xE0.2 − x0.2 − x2x

0.2 mol/L of H₂ and 0.2 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 9. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.2500C−x+x+xE0.25 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 at the reaction temperature. A container starts with 0.25 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.25 mol/LKc = 0.08
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 200 gT = 200 °Cc = 0.385 J/(g·°C)Waterm = 200 gT = 17 °Cc = 4.18 J/(g·°C)

A 200 g block of copper (c = 0.385 J/(g·°C)) at 200 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 17 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.385 J/(g·°C)Tmetal = 200 °Cmwater = 200 gTwater = 17 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H20 g CH4​CH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 20 g of CH4 (M = 16.04 g/mol) burns completely: CH4 + 2O₂ → CO₂ + 2H₂O(l). Give q as a positive number.

ΔH°f(CH4) = −74.8 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)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.05 L/(mol·min) and an initial concentration of 0.5 mol/L. Find its first half-life t½.

k = 0.05 L/(mol·min)CA0 = 0.5 mol/L
t½ = min
14.Reaction kineticsHard
Tk50 °Ck1​?10·k1​

A reaction has an activation energy of 40 kJ/mol. At 50 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 10 times faster?

Ea = 40 kJ/molT1 = 50 °Ck2/k1 = 10R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 20 L/minX = 75%V = ?, k = 0.5 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.5 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 75% conversion of A.

Q = 20 L/mink = 0.5 min⁻¹X = 75%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 200 LQ = 40 L/minX = ?

A first-order liquid-phase reaction (k = 0.4 min⁻¹) runs in a 200 L CSTR fed at 40 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 40 L/mink = 0.4 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT165 °C60 °C100 °C20 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 320 kW. Its heat transfer area is 5 m². The hot fluid cools from 165 to 60 °C and the cold fluid heats from 20 to 100 °C. Find the overall heat transfer coefficient U.

Q̇ = 320 kWA = 5 m²Th: 165 → 60 °CTc: 20 → 100 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT100 °C50 °C52.68 °C15 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.1 kJ/(kg·K)) cools from 100 to 50 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 15 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 100 → 50 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 15 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Wood, k = 0.1750 mmConcrete, k = 1.425 mm16 °C10 °CTi​ = ?Q̇

A wall is made of 50 mm of wood and 25 mm of concrete, with an area of 10 m². The outer faces are at 16 °C and 10 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 25 mm, k2 = 1.4 W/(m·K)A = 10 m²T1 = 16 °CT3 = 10 °C
Ti = °C
20.Heat conductionHard
Concrete, k = 1.4100 mmWood, k = 0.17100 mmroom 21 °Coutside 5 °CQ̇ = ?

A wall of 100 mm concrete and 100 mm wood separates a room at 21 °C from outside air at 5 °C. The convection coefficients are 8 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 15 m². Find the heat loss Q̇ through the wall.

L1 = 100 mm, k1 = 1.4 W/(m·K)L2 = 100 mm, k2 = 0.17 W/(m·K)A = 15 m²hi = 8 W/(m²·K)ho = 25 W/(m²·K)Troom = 21 °CTout = 5 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 2.1 m/sD = 200 mmL = 100 mf = 0.022

Water (ρ = 1000 kg/m³) flows at 2.1 m/s through a horizontal pipe, 100 m long, with an inside diameter of 200 mm. Use the Darcy friction factor f = 0.022 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2.1 m/sL = 100 mD = 200 mmf = 0.022ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 5Δz = 24 mL = 300 m, D = 300 mm, f = 0.0252× bend (K = 0.3)

Two open reservoirs are joined by a pipe 300 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.025. The water surface of the upper reservoir is 24 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 5) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². Find the flow rate Q in L/s.

Δz = 24 mL = 300 mD = 300 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 5Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 15 L/sH = 36 m

A pump with an efficiency of 85% delivers 15 L/s of water (ρ = 1000 kg/m³) against a head of 36 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 15 L/sH = 36 mη = 85%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 30 L/sΔz = 14 mL = 100 m, D = 150 mm, f = 0.022, ΣK = 6

A pump moves 30 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 14 m higher. The pipe is 100 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.022; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 65%. Find the shaft power Pshaft in kW.

Q = 30 L/sΔz = 14 mL = 100 mD = 150 mmf = 0.022ΣK = 6η = 65%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 1300 kg/h

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

Balances

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

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 650·(15 − 25)/(25 − 30) = 1300 kg/h

Answer

ṁ2 = 1300 kg/h
2.Mass balance

Answer: W = 1284 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 = 1700·11/45 = 415.6 kg/h

Total balance

W = F − P = 1700 − 415.6 = 1284 kg/h

Answer

W = 1284 kg/h
3.Energy balance

Answer: tout = 95.36 °C

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

Heat released by the hot stream

Q = 1.5·2.1·(180 − 130) = 157.5 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 157.5/(0.5·4.18) = 95.36 °C

Answer

tout = 95.36 °C
4.Energy balance

Answer: ṁc = 7.751 kg/s

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

Heat released

Qh = 2·3.6·(160 − 60) = 720 kW

Heat that reaches the water

Qc = (1 − 0.1)·720 = 648 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 648/(4.18·20) = 7.751 kg/s

Answer

ṁc = 7.751 kg/s
5.Ideal gas law

Answer: V = 99.96 L

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

Moles

n = 430/32 = 13.44 mol
T = 40 + 273.15 = 313.1 K

Volume

V = nRT/P = 13.44·8.314·313.1/350 = 99.96 L

Answer

V = 99.96 L
6.Ideal gas law

Answer: ρ = 10.87 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 10 + 273.15 = 283.1 K

Density

ρ = 800·32/(8.314·283.1) = 10.87 kg/m³

Answer

ρ = 10.87 kg/m³
7.Stoichiometry

Answer: m = 80.24 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(Al) = 24/26.98 = 0.8895 mol
n(Cl2) = 64/70.9 = 0.9027 mol

Limiting reactant

0.8895/2 = 0.4448, 0.9027/3 = 0.3009 → Cl2

Mass of product

n(AlCl3) = 0.3009·2 = 0.6018 mol
m = 0.6018·133.33 = 80.24 g

Answer

m = 80.24 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(Al) = 12/26.98 = 0.4448 mol
m = 0.4448·2/2·133.33 = 59.3 g

Percent yield

Y = 36.77/59.3·100 = 62%

Answer

Y = 62%
9.Chemical equilibrium

Answer: [H2] = 0.08 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

9 = (2x)²/(0.2 − x)²

Take the square root

3 = 2x/(0.2 − x) → x = 0.2·3/(2 + 3) = 0.12 mol/L

Equilibrium concentration

[H₂] = 0.2 − x = 0.08 mol/L

Answer

[H2] = 0.08 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.107 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

0.08 = x²/(0.25 − x) → x² + 0.08·x − 0.02 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.02))/2 = 0.107 mol/L

Equilibrium concentration

[Cl₂] = x = 0.107 mol/L

Answer

[Cl2] = 0.107 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 32.43 °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

200·0.385·(200 − Tf) = 200·4.18·(Tf − 17)

Solve for the final temperature

Tf = (77·200 + 836·17)/(77 + 836) = 32.43 °C

Answer

Tf = 32.43 °C
12.Calorimetry & enthalpy

Answer: q = 1110 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° = [1·(−393.5) + 2·(−285.8)] − [1·(−74.8) + 2·0] = −890.3 kJ

Heat for the given mass

n = 20/16.04 = 1.247 mol
q = n·|ΔH°/1| = 1.247·890.3 = 1110 kJ

Answer

q = 1110 kJ
13.Reaction kinetics

Answer: t½ = 40 min

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).

Second-order half-life

t½ = 1/(k·CA0) = 1/(0.05·0.5) = 40 min

Answer

t½ = 40 min

Each later half-life is twice as long, because C₀ has halved.

14.Reaction kinetics

Answer: T2 = 109.1 °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).

Absolute temperature

T1 = 323.1 K

Solve Arrhenius for T₂

1/T2 = 1/323.1 − 8.314·ln(10)/40000 = 3.095 × 10⁻³ − 4.786 × 10⁻⁴ = 2.616 × 10⁻³ K⁻¹
T2 = 382.3 K = 109.1 °C

Answer

T2 = 109.1 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 55.45 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 − 0.75))/0.5 = 1.386/0.5 = 2.773 min

Volume

V = Q·τ = 20·2.773 = 55.45 L

Answer

V = 55.45 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 66.67 %

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 = 200/40 = 5 min, kτ = 0.4·5 = 2

Conversion

X = kτ/(1 + kτ) = 2/(1 + 2) = 66.67%

Answer

X = 66.67%
17.Heat exchangers (LMTD)

Answer: U = 1243 W/(m²·K)

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 = 165 − 100 = 65 K
ΔT₂ = Th,out − Tc,in = 60 − 20 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (65 − 40)/ln(65/40) = 51.49 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 320000/(5·51.49) = 1243 W/(m²·K)

Answer

U = 1243 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: A = 2.57 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.

Heat duty and water outlet temperature

Q̇ = ṁhcp,h(Th,in − Th,out) = 1.5·2.1·50 = 157.5 kW
Tc,out = 15 + 157.5/(1·4.18) = 52.68 °C

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 = 100 − 52.68 = 47.32 K
ΔT₂ = Th,out − Tc,in = 50 − 15 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (47.32 − 35)/ln(47.32/35) = 40.85 K

Area

A = Q̇/(U·ΔTlm) = 157500/(1500·40.85) = 2.57 m²

Answer

A = 2.57 m²
19.Heat conduction

Answer: Ti = 10.34 °C

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) = (50/1000)/(0.17·10) = 0.02941 K/W
R2 = L2/(k2A) = (25/1000)/(1.4·10) = 0.001786 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 6/0.0312 = 192.3 W

Interface temperature

The temperature drops across the first layer by Q̇·R₁.

Ti = T1 − Q̇·R1 = 16 − 192.3·0.02941 = 10.34 °C

Answer

Ti = 10.34 °C
20.Heat conduction

Answer: Q̇ = 291 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/(8·15) = 0.008333 K/W
R1 = L1/(k1A) = (100/1000)/(1.4·15) = 0.004762 K/W
R2 = L2/(k2A) = (100/1000)/(0.17·15) = 0.03922 K/W
Ro = 1/(hoA) = 1/(25·15) = 0.002667 K/W
ΣR = 0.05498 K/W

Heat loss

Q̇ = (21 − (5))/0.05498 = 291 W

Answer

Q̇ = 291 W
21.Pipe friction & head loss

Answer: Δp = 24.25 kPa

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.

Head loss

hf = f·(L/D)·V²/(2g) = 0.022·(100/0.2)·2.1²/(2·9.81) = 2.472 m

Pressure drop

The pipe is horizontal and the velocity does not change, so the energy equation reduces to Δp = ρ·g·hf.

Δp = ρ·g·hf = 1000·9.81·2.472 = 24255 Pa = 24.25 kPa

Answer

Δp = 24.25 kPa
22.Pipe friction & head loss

Answer: Q = 270.7 L/s

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.

Loss coefficients

f·L/D = 0.025·300/0.3 = 25
ΣK = 0.5 + 2·0.3 + 5 + 1.0 = 7.1

Energy equation

Both surfaces are open to the air and practically at rest, so all of Δz is lost in the pipe.

24 = (25 + 7.1)·V²/(2·9.81)
V = √(2·9.81·24/32.1) = 3.83 m/s

Flow rate

Q = V·π·D²/4 = 3.83·0.07069 = 0.2707 m³/s = 270.7 L/s

Answer

Q = 270.7 L/s
23.Pumps & pump power

Answer: Pshaft = 6.232 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 = 1000·9.81·0.015·36 = 5.297 kW

Shaft power

Pshaft = Ph/η = 5.297/0.85 = 6.232 kW

Answer

Pshaft = 6.232 kW
24.Pumps & pump power

Answer: Pshaft = 7.713 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.

Velocity

V = Q/A = 0.03/0.01767 = 1.698 m/s
V²/(2g) = 0.1469 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (14.67 + 6)·0.1469 = 3.036 m

Pump head

H = Δz + hL = 14 + 3.036 = 17.04 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.03·17.04/0.65 = 7.713 kW

Answer

Pshaft = 7.713 kW

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