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 1950 kg/h · 20% 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 = 950 kg/hx1 = 20 %x2 = 30 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1900 kg/h · 15% NaOHProduct P30% 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 = 1900 kg/hxF = 15 %xP = 30 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 130 °C90 °Cwater · 15 °Ct = ? °C

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

ṁh = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 90 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 160 °C80 °Cwater · 15 °C55 °C · ṁ = ?5% lost

Hot ethanol 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 = 1.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 160 → 80 °Ct: 15 → 55 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
430 g of HeP = 600 kPaT = 25 °CV = ?

What volume V does 430 g of He occupy at 600 kPa and 25 °C? Treat it as an ideal gas.

m = 430 gM = 4.003 g/molP = 600 kPaT = 25 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 200 kPa, 10 L, 30 °C to 800 kPa and 220 °C. Find the new volume V2.

P1 = 200 kPaV1 = 10 LT1 = 30 °CP2 = 800 kPaT2 = 220 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(AlCl3​)m(AlCl3​)÷ M(X)× 2/ν× M(AlCl3​)

6 g of Al and 48 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(C3​H8​)n(C3​H8​)n(CO2​)m(CO2​)÷ M(C3​H8​)× 3/1× M(CO2​)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 12 g of C3H8 reacts completely (the other reactants are in excess) and 19.76 g of CO2 is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(CO2) = 44.01 g/molactual: 19.76 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.80.80C−x−x+2xE0.8 − x0.8 − x2x

0.8 mol/L of H₂ and 0.8 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 25. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 25
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.04 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.5 mol/LKc = 0.04
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 100 gT = 100 °Cc = 0.129 J/(g·°C)Waterm = 300 gT = 20 °Cc = 4.18 J/(g·°C)

A 100 g block of lead (c = 0.129 J/(g·°C)) at 100 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 20 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.129 J/(g·°C)Tmetal = 100 °Cmwater = 300 gTwater = 20 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2CH3OH + 3O₂ → 2CO₂ + 4H₂O(l).

ΔH°f(CH3OH) = −238.7 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
ΔH° = kJ
13.Reaction kineticsMedium
t (min)X (%)t = ?20%

A zero-order reaction has k = 0.005 mol/(L·min) and starts at 1.2 mol/L. How long does it take to reach 20% conversion? Find t.

k = 0.005 mol/(L·min)CA0 = 1.2 mol/LX = 20 %
t = min
14.Reaction kineticsHard
t (min)X (%)45 minX = ?

A first-order reaction has k = 0.01 min⁻¹ at 25 °C and an activation energy of 50 kJ/mol. The batch reactor is now run at 45 °C for 45 min. Find the conversion X reached.

k1 = 0.01 min⁻¹T1 = 25 °CEa = 50 kJ/molT2 = 45 °Ct = 45 minR = 8.314 J/(mol·K)
X = %
15.Reactor sizing (CSTR & PFR)Medium
Q = 5 L/minX = 80%V = ?, k = 0.4 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.4 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 5 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 80% conversion of A.

Q = 5 L/mink = 0.4 min⁻¹X = 80%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 50 L/minX = ?V = 800 L

A first-order liquid-phase reaction (k = 0.2 min⁻¹) runs in an 800 L plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 800 LQ = 50 L/mink = 0.2 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT140 °C125 °C55 °C25 °CΔT₁ΔT₂counter-flow

A shell-and-tube heat exchanger (one shell pass, two tube passes) must transfer 100 kW. The hot fluid cools from 140 to 125 °C and the cold fluid heats from 25 to 55 °C. The LMTD correction factor for this arrangement is F = 0.9, and U = 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 100 kWF = 0.9U = 800 W/(m²·K)Th: 140 → 125 °CTc: 25 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT95 °C55 °C?15 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.3 kg/s, cp = 2.3 kJ/(kg·K)) flows in the inner tube and cools from 95 to 55 °C. Water (0.5 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 15 °C. The inner tube has a diameter of 20 mm, and U = 300 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.3 kg/scp,h = 2.3 kJ/(kg·K)Th: 95 → 55 °Cṁc = 0.5 kg/sTc,in = 15 °CD = 20 mmU = 300 W/(m²·K)
L = m
19.Heat conductionMedium
Expanded polystyrene, k = 0.035150 mmConcrete, k = 1.425 mm20 °C10 °CTi​ = ?Q̇

A wall is made of 150 mm of expanded polystyrene and 25 mm of concrete, with an area of 12 m². The outer faces are at 20 °C and 10 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 0.035 W/(m·K)L2 = 25 mm, k2 = 1.4 W/(m·K)A = 12 m²T1 = 20 °CT3 = 10 °C
Ti = °C
20.Heat conductionHard
Gypsum board, k = 0.1750 mmMineral wool, k = 0.04100 mmroom 20 °Coutside 4 °CTs​ = ?Q̇

A wall of 50 mm gypsum board and 100 mm mineral wool separates a room at 20 °C from outside air at 4 °C. The convection coefficients are 10 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 4 m². Find the temperature Ts of the inside surface of the wall.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 100 mm, k2 = 0.04 W/(m·K)A = 4 m²hi = 10 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = 4 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.9 m/sD = 75 mmL = 50 mf = 0.028

Water (ρ = 1000 kg/m³) flows at 1.9 m/s through a horizontal pipe, 50 m long, with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.028 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.9 m/sL = 50 mD = 75 mmf = 0.028ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 5Δz = ?L = 300 m, D = 300 mm, f = 0.0183× 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 = 0.018. The minor losses are a square-edged entrance (K = 0.5), 3 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. What difference in water level Δz between the reservoirs gives a flow rate of 75 L/s?

Q = 75 L/sL = 300 mD = 300 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 5Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 12 m

In a test, a pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 12 m while its shaft takes 1.7 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 10 L/sH = 12 mPshaft = 1.7 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
200 kPa (gauge)PQ = 50 L/sΔz = 5 mL = 100 m, D = 200 mm, f = 0.022, ΣK = 6

A pump moves 50 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 5 m higher. The pipe is 100 m long with an inside diameter of 200 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 upper tank is closed and the air above its water is at a gauge pressure of 200 kPa. Find the head H the pump must add.

Q = 50 L/sΔz = 5 mL = 100 mD = 200 mmf = 0.022ΣK = 6ptank = 200 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 950 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) = 950·(20 − 25)/(25 − 30) = 950 kg/h

Answer

ṁ2 = 950 kg/h
2.Mass balance

Answer: W = 950 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 = 1900·15/30 = 950 kg/h

Total balance

W = F − P = 1900 − 950 = 950 kg/h

Answer

W = 950 kg/h
3.Energy balance

Answer: tout = 49.45 °C

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

Heat released by the hot stream

Q = 1.5·3.6·(130 − 90) = 216 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 216/(1.5·4.18) = 49.45 °C

Answer

tout = 49.45 °C
4.Energy balance

Answer: ṁc = 1.664 kg/s

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

Heat released

Qh = 1.5·2.44·(160 − 80) = 292.8 kW

Heat that reaches the water

Qc = (1 − 0.05)·292.8 = 278.2 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 278.2/(4.18·40) = 1.664 kg/s

Answer

ṁc = 1.664 kg/s
5.Ideal gas law

Answer: V = 443.8 L

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

Moles

n = 430/4.003 = 107.4 mol
T = 25 + 273.15 = 298.1 K

Volume

V = nRT/P = 107.4·8.314·298.1/600 = 443.8 L

Answer

V = 443.8 L
6.Ideal gas law

Answer: V2 = 4.067 L

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

Absolute temperatures

T1 = 303.1 K, T2 = 493.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(200/800)·(493.1/303.1) = 4.067 L

Answer

V2 = 4.067 L
7.Stoichiometry

Answer: m = 29.65 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) = 6/26.98 = 0.2224 mol
n(Cl2) = 48/70.9 = 0.677 mol

Limiting reactant

0.2224/2 = 0.1112, 0.677/3 = 0.2257 → Al

Mass of product

n(AlCl3) = 0.1112·2 = 0.2224 mol
m = 0.2224·133.33 = 29.65 g

Answer

m = 29.65 g
8.Stoichiometry

Answer: Y = 55 %

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(C3H8) = 12/44.1 = 0.2721 mol
m = 0.2721·3/1·44.01 = 35.93 g

Percent yield

Y = 19.76/35.93·100 = 55%

Answer

Y = 55%
9.Chemical equilibrium

Answer: [HI] = 1.143 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

25 = (2x)²/(0.8 − x)²

Take the square root

5 = 2x/(0.8 − x) → x = 0.8·5/(2 + 5) = 0.5714 mol/L

Equilibrium concentration

[HI] = 2x = 1.143 mol/L

Answer

[HI] = 1.143 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.3772 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

0.04 = x²/(0.5 − x) → x² + 0.04·x − 0.02 = 0

Solve the quadratic

x = (−0.04 + √(0.04² + 4·0.02))/2 = 0.1228 mol/L

Equilibrium concentration

[PCl₅] = 0.5 − 0.1228 = 0.3772 mol/L

Answer

[PCl5] = 0.3772 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 20.81 °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

100·0.129·(100 − Tf) = 300·4.18·(Tf − 20)

Solve for the final temperature

Tf = (12.9·100 + 1254·20)/(12.9 + 1254) = 20.81 °C

Answer

Tf = 20.81 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −1453 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° = [2·(−393.5) + 4·(−285.8)] − [2·(−238.7) + 3·0] = −1453 kJ

Answer

ΔH° = −1453 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 48 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).

Amount converted

CA0·X = 1.2·0.2 = 0.24 mol/L

Time

t = CA0·X/k = 0.24/0.005 = 48 min

Answer

t = 48 min
14.Reaction kinetics

Answer: X = 79.79 %

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).

Rate constant at the new temperature

T1 = 298.1 K, T2 = 318.1 K
k2 = 0.01·e−(50000/8.314)·(1/318.1 − 1/298.1) = 0.03554 min⁻¹

Conversion

X = 1 − e−0.03554·45 = 1 − 0.2021 = 79.79 %

Answer

X = 79.79 %
15.Reactor sizing (CSTR & PFR)

Answer: V = 20.12 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 − 0.8))/0.4 = 1.609/0.4 = 4.024 min

Volume

V = Q·τ = 5·4.024 = 20.12 L

Answer

V = 20.12 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 95.92 %

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 = 800/50 = 16 min, kτ = 0.2·16 = 3.2

Conversion

X = 1 − e−kτ = 1 − e−3.2 = 95.92%

Answer

X = 95.92%
17.Heat exchangers (LMTD)

Answer: A = 1.505 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 (counter-flow)

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

ΔT₁ = Th,in − Tc,out = 140 − 55 = 85 K
ΔT₂ = Th,out − Tc,in = 125 − 25 = 100 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (85 − 100)/ln(85/100) = 92.3 K

Area

A = Q̇/(U·F·ΔTlm,cf) = 100000/(800·0.9·92.3) = 1.505 m²

Answer

A = 1.505 m²
18.Heat exchangers (LMTD)

Answer: L = 28.02 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 = 0.3·2.3·(95 − 55) = 27.6 kW
Tc,out = 15 + 27.6/(0.5·4.18) = 28.21 °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 = 95 − 28.21 = 66.79 K
ΔT₂ = Th,out − Tc,in = 55 − 15 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (66.79 − 40)/ln(66.79/40) = 52.26 K

Area and length

A = 27600/(300·52.26) = 1.761 m²
L = A/(πD) = 1.761/(π·0.02) = 28.02 m

Answer

L = 28.02 m
19.Heat conduction

Answer: Ti = 10.04 °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) = (150/1000)/(0.035·12) = 0.3571 K/W
R2 = L2/(k2A) = (25/1000)/(1.4·12) = 0.001488 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 10/0.3586 = 27.88 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 20 − 27.88·0.3571 = 10.04 °C

Answer

Ti = 10.04 °C
20.Heat conduction

Answer: Ts = 19.45 °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.

Resistances in series

Ri = 1/(hiA) = 1/(10·4) = 0.025 K/W
R1 = L1/(k1A) = (50/1000)/(0.17·4) = 0.07353 K/W
R2 = L2/(k2A) = (100/1000)/(0.04·4) = 0.625 K/W
Ro = 1/(hoA) = 1/(30·4) = 0.008333 K/W
ΣR = 0.7319 K/W

Heat loss

Q̇ = (20 − (4))/0.7319 = 21.86 W
Ts = Troom − Q̇·Ri = 20 − 21.86·0.025 = 19.45 °C

Answer

Ts = 19.45 °C
21.Pipe friction & head loss

Answer: Δp = 33.69 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) = 0.028·(50/0.075)·1.9²/(2·9.81) = 3.435 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 = 1000·9.81·3.435 = 33693 Pa = 33.69 kPa

Answer

Δp = 33.69 kPa
22.Pipe friction & head loss

Answer: Δz = 1.457 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 = 0.075/0.07069 = 1.061 m/s
V²/(2g) = 0.05738 m

Loss coefficients

f·L/D = 0.018·300/0.3 = 18
ΣK = 0.5 + 3·0.3 + 5 + 1.0 = 7.4

Total head loss

hf = 18·0.05738 = 1.033 m
hm = 7.4·0.05738 = 0.4246 m
Δz = hf + hm = 1.457 m

Answer

Δz = 1.457 m
23.Pumps & pump power

Answer: η = 69.25 %

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 = 1000·9.81·0.01·12 = 1.177 kW

Efficiency

η = Ph/Pshaft = 1.177/1.7 = 69.25%

Answer

η = 69.25%
24.Pumps & pump power

Answer: H = 27.58 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 = 0.05/0.03142 = 1.592 m/s
V²/(2g) = 0.1291 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (11 + 6)·0.1291 = 2.195 m

Pressure head

p/(ρ·g) = 200000/(1000·9.81) = 20.39 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 5 + 20.39 + 2.195 = 27.58 m

Answer

H = 27.58 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