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 1750 kg/h · 15% sugarStream 2ṁ₂ = ? · 30% sugarProduct20% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 20% sugar? Find ṁ2.

ṁ1 = 750 kg/hx1 = 15 %x2 = 30 %x3 = 20 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4800 kg/h · 14% saltProduct PP = ? · 35%Vapour W (pure water)0% salt

An evaporator concentrates a salt solution by boiling off pure water. Find the product flow P in kg/h.

F = 4800 kg/hxF = 14 %xP = 35 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 170 °C130 °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 = 2 kg/scp,h = 2.44 kJ/(kg·K)Th: 170 → 130 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 170 °C110 °Cwater · 15 °C55 °C · ṁ = ?10% lost

Hot ethanol 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 = 3 kg/scp,h = 2.44 kJ/(kg·K)Th: 170 → 110 °Ct: 15 → 55 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
190 g of CH₄V = 30 LT = 30 °CP = ?

A tank of 30 L contains 190 g of CH₄ at 30 °C. Treat it as an ideal gas and find the pressure P.

m = 190 gM = 16.04 g/molV = 30 LT = 30 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of CH₄ goes from 350 kPa, 5 L, 15 °C to 100 kPa and 50 °C. Find the new volume V2.

P1 = 350 kPaV1 = 5 LT1 = 15 °CP2 = 100 kPaT2 = 50 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 1/ν× M(CO2​)

20 g of CH4 and 20 g of O2 react according to CH4 + 2O2 → CO2 + 2H2O. What mass m of CO2 can form?

M(CH4) = 16.04M(O2) = 32M(CO2) = 44.01 g/mol
m = g
8.StoichiometryHard
m(C3​H8​)n(C3​H8​)n(H2​O)m(H2​O)÷ M(C3​H8​)× 4/1× M(H2​O)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 12 g of C3H8 reacts completely (the other reactants are in excess) and 17.26 g of H2O is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 17.26 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII110C−x−x+2xE1 − x1 − x2x

1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 36. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 36
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.1 mol/LKc = 0.1
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 100 gT = 140 °Cc = 0.449 J/(g·°C)Waterm = 300 gT = 25 °Cc = 4.18 J/(g·°C)

A 100 g block of iron (c = 0.449 J/(g·°C)) at 140 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.449 J/(g·°C)Tmetal = 140 °Cmwater = 300 gTwater = 25 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC3​H8​ + 5O₂reactants3CO₂ + 4H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C3H8 + 5O₂ → 3CO₂ + 4H₂O(l).

ΔH°f(C3H8) = −103.8 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 = ?80%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.1 L/(mol·min) and starts at 2 mol/L. How long does it take to reach 80% conversion? Find t.

k = 0.1 L/(mol·min)CA0 = 2 mol/LX = 80 %
t = min
14.Reaction kineticsHard
t (min)X (%)20 minX = ?

A first-order reaction has k = 0.002 min⁻¹ at 30 °C and an activation energy of 60 kJ/mol. The batch reactor is now run at 55 °C for 20 min. Find the conversion X reached.

k1 = 0.002 min⁻¹T1 = 30 °CEa = 60 kJ/molT2 = 55 °Ct = 20 minR = 8.314 J/(mol·K)
X = %
15.Reactor sizing (CSTR & PFR)Medium
QX = 90%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 90% conversion. How many times larger must a CSTR be than a PFR for the same feed rate, rate constant and conversion? Find the ratio VCSTR/VPFR.

X = 90%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
V = 500 LV = 500 LQ = 40 L/minX = ?

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in two equal CSTRs in series, each of 500 L. The feed rate is 40 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 500 L (×2)Q = 40 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT150 °C110 °C15 °C55 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 270 kW. The hot fluid cools from 150 to 110 °C and the cold fluid heats from 15 to 55 °C. The overall heat transfer coefficient is 1000 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 270 kWU = 1000 W/(m²·K)Th: 150 → 110 °CTc: 15 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT80 °C50 °C52.61 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.1 kJ/(kg·K)) cools from 80 to 50 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 800 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 80 → 50 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 800 W/(m²·K)
A = m²
19.Heat conductionMedium
Brick, k = 0.72100 mmGypsum board, k = 0.1775 mm18 °C6 °CQ̇ = ?

A wall is made of 100 mm of brick and 75 mm of gypsum board, with an area of 15 m². The outer faces are at 18 °C and 6 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.72 W/(m·K)L2 = 75 mm, k2 = 0.17 W/(m·K)A = 15 m²T1 = 18 °CT3 = 6 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.96100 mmWood, k = 0.1775 mmroom 22 °Coutside -8 °CQ̇ = ?

A wall of 100 mm glass and 75 mm wood separates a room at 22 °C from outside air at -8 °C. The convection coefficients are 8 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 20 m². Find the heat loss Q̇ through the wall.

L1 = 100 mm, k1 = 0.96 W/(m·K)L2 = 75 mm, k2 = 0.17 W/(m·K)A = 20 m²hi = 8 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = -8 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 2.1 m/sD = 75 mmL = 400 mf = 0.022

Water (ρ = 1000 kg/m³) flows at 2.1 m/s through a horizontal pipe, 400 m long, with an inside diameter of 75 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 = 400 mD = 75 mmf = 0.022ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 0.2Δz = ?L = 150 m, D = 200 mm, f = 0.0182× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.018. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 0.2) 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 60 L/s?

Q = 60 L/sL = 150 mD = 200 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 0.2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 60 L/sH = 36 m

A pump delivers 60 L/s of water (ρ = 1000 kg/m³) against a head of 36 m. The pump efficiency is 60% 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 = 60 L/sH = 36 mηpump = 60%ηmotor = 94%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 20 L/sΔz = 9 mL = 100 m, D = 100 mm, f = 0.015, ΣK = 2.5

A pump moves 20 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 9 m higher. The pipe is 100 m long with an inside diameter of 100 mm and a Darcy friction factor f = 0.015; the minor-loss coefficients add up to ΣK = 2.5 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 70%. Find the shaft power Pshaft in kW.

Q = 20 L/sΔz = 9 mL = 100 mD = 100 mmf = 0.015ΣK = 2.5η = 70%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 375 kg/h

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

Balances

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

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 750·(15 − 20)/(20 − 30) = 375 kg/h

Answer

ṁ2 = 375 kg/h
2.Mass balance

Answer: P = 1920 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 = 4800·14/35 = 1920 kg/h

Answer

P = 1920 kg/h
3.Energy balance

Answer: tout = 76.7 °C

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

Heat released by the hot stream

Q = 2·2.44·(170 − 130) = 195.2 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 195.2/(1·4.18) = 76.7 °C

Answer

tout = 76.7 °C
4.Energy balance

Answer: ṁc = 2.364 kg/s

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

Heat released

Qh = 3·2.44·(170 − 110) = 439.2 kW

Heat that reaches the water

Qc = (1 − 0.1)·439.2 = 395.3 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 395.3/(4.18·40) = 2.364 kg/s

Answer

ṁc = 2.364 kg/s
5.Ideal gas law

Answer: P = 995.2 kPa

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

Moles

n = m/M = 190/16.04 = 11.85 mol
T = 30 + 273.15 = 303.1 K

Pressure

P = nRT/V = 11.85·8.314·303.1/0.03 = 995.2 kPa

Answer

P = 995.2 kPa
6.Ideal gas law

Answer: V2 = 19.63 L

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

Absolute temperatures

T1 = 288.1 K, T2 = 323.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(350/100)·(323.1/288.1) = 19.63 L

Answer

V2 = 19.63 L
7.Stoichiometry

Answer: m = 13.75 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(CH4) = 20/16.04 = 1.247 mol
n(O2) = 20/32 = 0.625 mol

Limiting reactant

1.247/1 = 1.247, 0.625/2 = 0.3125 → O2

Mass of product

n(CO2) = 0.3125·1 = 0.3125 mol
m = 0.3125·44.01 = 13.75 g

Answer

m = 13.75 g
8.Stoichiometry

Answer: Y = 88 %

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 = 0.2721·4/1·18.02 = 19.61 g

Percent yield

Y = 17.26/19.61·100 = 88%

Answer

Y = 88%
9.Chemical equilibrium

Answer: [H2] = 0.25 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

36 = (2x)²/(1 − x)²

Take the square root

6 = 2x/(1 − x) → x = 1·6/(2 + 6) = 0.75 mol/L

Equilibrium concentration

[H₂] = 1 − x = 0.25 mol/L

Answer

[H2] = 0.25 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.0382 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

0.1 = x²/(0.1 − x) → x² + 0.1·x − 0.01 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.01))/2 = 0.0618 mol/L

Equilibrium concentration

[PCl₅] = 0.1 − 0.0618 = 0.0382 mol/L

Answer

[PCl5] = 0.0382 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 28.98 °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

100·0.449·(140 − Tf) = 300·4.18·(Tf − 25)

Solve for the final temperature

Tf = (44.9·140 + 1254·25)/(44.9 + 1254) = 28.98 °C

Answer

Tf = 28.98 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −2220 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

Answer

ΔH° = −2220 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 20 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).

Concentration at the end

CA = 2·(1 − 0.8) = 0.4 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (2.5 − 0.5)/0.1 = 20 min

Answer

t = 20 min
14.Reaction kinetics

Answer: X = 21.75 %

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 = 303.1 K, T2 = 328.1 K
k2 = 0.002·e−(60000/8.314)·(1/328.1 − 1/303.1) = 0.01227 min⁻¹

Conversion

X = 1 − e−0.01227·20 = 1 − 0.7825 = 21.75 %

Answer

X = 21.75 %
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 3.909

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.

k·τ for each reactor

CSTR: k·τ = X/(1 − X) = 0.9/0.1 = 9
PFR: k·τ = ln(1/(1 − X)) = ln(10) = 2.303

Ratio of volumes

VCSTR/VPFR = 9/2.303 = 3.909

Answer

VCSTR/VPFR = 3.909

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 80.25 %

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 = 500/40 = 12.5 min, kτ = 0.1·12.5 = 1.25

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 1.25) = 0.4444
C2/CA0 = 1/(1 + kτ)² = 0.1975
X = 1 − 0.1975 = 80.25%

Answer

X = 80.25%
17.Heat exchangers (LMTD)

Answer: A = 3.031 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 parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 150 − 15 = 135 K
ΔT₂ = Th,out − Tc,out = 110 − 55 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (135 − 55)/ln(135/55) = 89.09 K

Area

A = Q̇/(U·ΔTlm) = 270000/(1000·89.09) = 3.031 m²

Answer

A = 3.031 m²
18.Heat exchangers (LMTD)

Answer: A = 5.026 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) = 1.5·2.1·30 = 94.5 kW
Tc,out = 30 + 94.5/(1·4.18) = 52.61 °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 = 80 − 52.61 = 27.39 K
ΔT₂ = Th,out − Tc,in = 50 − 30 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (27.39 − 20)/ln(27.39/20) = 23.5 K

Area

A = Q̇/(U·ΔTlm) = 94500/(800·23.5) = 5.026 m²

Answer

A = 5.026 m²
19.Heat conduction

Answer: Q̇ = 310.3 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) = (100/1000)/(0.72·15) = 0.009259 K/W
R2 = L2/(k2A) = (75/1000)/(0.17·15) = 0.02941 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 12/0.03867 = 310.3 W

Answer

Q̇ = 310.3 W
20.Heat conduction

Answer: Q̇ = 832.9 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/(8·20) = 0.00625 K/W
R1 = L1/(k1A) = (100/1000)/(0.96·20) = 0.005208 K/W
R2 = L2/(k2A) = (75/1000)/(0.17·20) = 0.02206 K/W
Ro = 1/(hoA) = 1/(20·20) = 0.0025 K/W
ΣR = 0.03602 K/W

Heat loss

Q̇ = (22 − (-8))/0.03602 = 832.9 W

Answer

Q̇ = 832.9 W
21.Pipe friction & head loss

Answer: Δp = 258.7 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·(400/0.075)·2.1²/(2·9.81) = 26.37 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 = 1000·9.81·26.37 = 258720 Pa = 258.7 kPa

Answer

Δp = 258.7 kPa
22.Pipe friction & head loss

Answer: Δz = 2.937 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 = 0.06/0.03142 = 1.91 m/s
V²/(2g) = 0.1859 m

Loss coefficients

f·L/D = 0.018·150/0.2 = 13.5
ΣK = 0.5 + 2·0.3 + 0.2 + 1.0 = 2.3

Total head loss

hf = 13.5·0.1859 = 2.51 m
hm = 2.3·0.1859 = 0.4276 m
Δz = hf + hm = 2.937 m

Answer

Δz = 2.937 m
23.Pumps & pump power

Answer: Pel = 37.57 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 = 1000·9.81·0.06·36 = 21.19 kW

Shaft power

Pshaft = 21.19/0.6 = 35.32 kW

Electrical power

Pel = 35.32/0.94 = 37.57 kW

Answer

Pel = 37.57 kW
24.Pumps & pump power

Answer: Pshaft = 4.144 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 = 0.02/0.007854 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (15 + 2.5)·0.3305 = 5.784 m

Pump head

H = Δz + hL = 9 + 5.784 = 14.78 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.02·14.78/0.7 = 4.144 kW

Answer

Pshaft = 4.144 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