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.

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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 · 35% NaOHStream 2ṁ₂ = ? · 5% NaOHProduct30% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 30% NaOH? Find ṁ2.

ṁ1 = 650 kg/hx1 = 35 %x2 = 5 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4800 kg/h · 5% 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 = 4800 kg/hxF = 5 %xP = 50 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 130 °C100 °Cwater · 10 °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 → 100 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 170 °C70 °Cwater · 20 °C50 °C · ṁ = ?15% lost

Hot ethanol heats water in an exchanger that loses 15% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 2 kg/scp,h = 2.44 kJ/(kg·K)Th: 170 → 70 °Ct: 20 → 50 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
120 g of CO₂P = 650 kPaT = 45 °CV = ?

What volume V does 120 g of CO₂ occupy at 650 kPa and 45 °C? Treat it as an ideal gas.

m = 120 gM = 44.01 g/molP = 650 kPaT = 45 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
N₂, M = 28.01 g/molP = 200 kPaT = 150 °Cρ = ?

Find the density ρ of N₂ at 200 kPa and 150 °C, treating it as an ideal gas.

M = 28.01 g/molP = 200 kPaT = 150 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 4/ν× M(H2​O)

30 g of C3H8 and 20 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of H2O can form?

M(C3H8) = 44.1M(O2) = 32M(H2O) = 18.02 g/mol
m = g
8.StoichiometryHard
m(Fe2​O3​)n(Fe2​O3​)n(CO2​)m(CO2​)÷ M(Fe2​O3​)× 3/1× M(CO2​)

In the reaction Fe2O3 + 3CO → 2Fe + 3CO2, 6 g of Fe2O3 reacts completely (the other reactants are in excess) and 3.87 g of CO2 is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(CO2) = 44.01 g/molactual: 3.87 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 = 9. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 9
[H2] = 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 [Cl2].

[PCl₅]₀ = 0.5 mol/LKc = 0.04
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 250 gT = 130 °Cc = 0.388 J/(g·°C)Waterm = 100 gT = 21 °Cc = 4.18 J/(g·°C)

A 250 g block of zinc (c = 0.388 J/(g·°C)) at 130 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 21 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.388 J/(g·°C)Tmetal = 130 °Cmwater = 100 gTwater = 21 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC2​H5​OH + 3O₂reactants2CO₂ + 3H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C2H5OH + 3O₂ → 2CO₂ + 3H₂O(l).

ΔH°f(C2H5OH) = −277.7 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 = ?50%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.5 L/(mol·min) and starts at 1.5 mol/L. How long does it take to reach 50% conversion? Find t.

k = 0.5 L/(mol·min)CA0 = 1.5 mol/LX = 50 %
t = min
14.Reaction kineticsHard
Tk20 °Ck1​?10·k1​

A reaction has an activation energy of 80 kJ/mol. At 20 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 10 times faster?

Ea = 80 kJ/molT1 = 20 °Ck2/k1 = 10R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minX = 90%V = ?, k = 0.3 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.3 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 25 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 90% conversion of A.

Q = 25 L/mink = 0.3 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 1000 LQ = 80 L/minX = ?

A first-order liquid-phase reaction (k = 0.4 min⁻¹) runs in a 1000 L CSTR fed at 80 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 1000 LQ = 80 L/mink = 0.4 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT150 °C115 °C125 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 30 kW. The hot fluid cools from 150 to 115 °C and the cold fluid heats from 25 to 125 °C. The overall heat transfer coefficient is 1000 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 30 kWU = 1000 W/(m²·K)Th: 150 → 115 °CTc: 25 → 125 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT135 °C85 °C38.76 °C25 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.3 kJ/(kg·K)) cools from 135 to 85 °C in a counter-flow exchanger. It heats 3 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 25 °C. With U = 500 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.3 kJ/(kg·K)Th: 135 → 85 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 25 °CU = 500 W/(m²·K)
A = m²
19.Heat conductionMedium
Brick, k = 0.72250 mmGypsum board, k = 0.17100 mm23 °C-4 °CTi​ = ?Q̇

A wall is made of 250 mm of brick and 100 mm of gypsum board, with an area of 10 m². The outer faces are at 23 °C and -4 °C. Find the temperature Ti at the interface between the two layers.

L1 = 250 mm, k1 = 0.72 W/(m·K)L2 = 100 mm, k2 = 0.17 W/(m·K)A = 10 m²T1 = 23 °CT3 = -4 °C
Ti = °C
20.Heat conductionHard
Wood, k = 0.17250 mmBrick, k = 0.72150 mmroom 22 °Coutside -1 °CTs​ = ?Q̇

A wall of 250 mm wood and 150 mm brick separates a room at 22 °C from outside air at -1 °C. The convection coefficients are 10 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 12 m². Find the temperature Ts of the inside surface of the wall.

L1 = 250 mm, k1 = 0.17 W/(m·K)L2 = 150 mm, k2 = 0.72 W/(m·K)A = 12 m²hi = 10 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = -1 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.7 m/sD = 150 mmL = 500 mf = 0.015

Water (ρ = 1000 kg/m³) flows at 1.7 m/s through a horizontal pipe, 500 m long, with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.7 m/sL = 500 mD = 150 mmf = 0.015ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 5free outletH = ?L = 100 m, D = 250 mm, f = 0.024× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 250 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), 4 bends (K = 0.3 each) and a valve (K = 5). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 60 L/s?

Q = 60 L/sL = 100 mD = 250 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 5
H = m
23.Pumps & pump powerMedium
PQ = 60 L/sH = 70 m

A pump with an efficiency of 72% delivers 60 L/s of water (ρ = 1000 kg/m³) against a head of 70 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 60 L/sH = 70 mη = 72%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 14 mL = 200 m, D = 250 mm, f = 0.015, ΣK = 8

A pump moves 75 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 200 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.015; the minor-loss coefficients add up to ΣK = 8 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 75 L/sΔz = 14 mL = 200 mD = 250 mmf = 0.015ΣK = 8
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 130 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) = 650·(35 − 30)/(30 − 5) = 130 kg/h

Answer

ṁ2 = 130 kg/h
2.Mass balance

Answer: W = 4320 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 = 4800·5/50 = 480 kg/h

Total balance

W = F − P = 4800 − 480 = 4320 kg/h

Answer

W = 4320 kg/h
3.Energy balance

Answer: tout = 22.92 °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 − 100) = 162 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 162/(3·4.18) = 22.92 °C

Answer

tout = 22.92 °C
4.Energy balance

Answer: ṁc = 3.308 kg/s

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

Heat released

Qh = 2·2.44·(170 − 70) = 488 kW

Heat that reaches the water

Qc = (1 − 0.15)·488 = 414.8 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 414.8/(4.18·30) = 3.308 kg/s

Answer

ṁc = 3.308 kg/s
5.Ideal gas law

Answer: V = 11.1 L

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

Moles

n = 120/44.01 = 2.727 mol
T = 45 + 273.15 = 318.1 K

Volume

V = nRT/P = 2.727·8.314·318.1/650 = 11.1 L

Answer

V = 11.1 L
6.Ideal gas law

Answer: ρ = 1.592 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 150 + 273.15 = 423.1 K

Density

ρ = 200·28.01/(8.314·423.1) = 1.592 kg/m³

Answer

ρ = 1.592 kg/m³
7.Stoichiometry

Answer: m = 9.01 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(C3H8) = 30/44.1 = 0.6803 mol
n(O2) = 20/32 = 0.625 mol

Limiting reactant

0.6803/1 = 0.6803, 0.625/5 = 0.125 → O2

Mass of product

n(H2O) = 0.125·4 = 0.5 mol
m = 0.5·18.02 = 9.01 g

Answer

m = 9.01 g
8.Stoichiometry

Answer: Y = 78.01 %

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(Fe2O3) = 6/159.69 = 0.03757 mol
m = 0.03757·3/1·44.01 = 4.961 g

Percent yield

Y = 3.87/4.961·100 = 78.01%

Answer

Y = 78.01%
9.Chemical equilibrium

Answer: [H2] = 0.4 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/(1 − x)²

Take the square root

3 = 2x/(1 − x) → x = 1·3/(2 + 3) = 0.6 mol/L

Equilibrium concentration

[H₂] = 1 − x = 0.4 mol/L

Answer

[H2] = 0.4 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.1228 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

[Cl₂] = x = 0.1228 mol/L

Answer

[Cl2] = 0.1228 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 41.53 °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

250·0.388·(130 − Tf) = 100·4.18·(Tf − 21)

Solve for the final temperature

Tf = (97·130 + 418·21)/(97 + 418) = 41.53 °C

Answer

Tf = 41.53 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −1367 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) + 3·(−285.8)] − [1·(−277.7) + 3·0] = −1367 kJ

Answer

ΔH° = −1367 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 1.333 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 = 1.5·(1 − 0.5) = 0.75 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (1.333 − 0.6667)/0.5 = 1.333 min

Answer

t = 1.333 min
14.Reaction kinetics

Answer: T2 = 42.12 °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 = 293.1 K

Solve Arrhenius for T₂

1/T2 = 1/293.1 − 8.314·ln(10)/80000 = 3.411 × 10⁻³ − 2.393 × 10⁻⁴ = 3.172 × 10⁻³ K⁻¹
T2 = 315.3 K = 42.12 °C

Answer

T2 = 42.12 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 191.9 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 − 0.9))/0.3 = 2.303/0.3 = 7.675 min

Volume

V = Q·τ = 25·7.675 = 191.9 L

Answer

V = 191.9 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 83.33 %

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 = 1000/80 = 12.5 min, kτ = 0.4·12.5 = 5

Conversion

X = kτ/(1 + kτ) = 5/(1 + 5) = 83.33%

Answer

X = 83.33%
17.Heat exchangers (LMTD)

Answer: A = 0.5912 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 = 150 − 125 = 25 K
ΔT₂ = Th,out − Tc,in = 115 − 25 = 90 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (25 − 90)/ln(25/90) = 50.74 K

Area

A = Q̇/(U·ΔTlm) = 30000/(1000·50.74) = 0.5912 m²

Answer

A = 0.5912 m²
18.Heat exchangers (LMTD)

Answer: A = 4.498 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) = 1.5·2.3·50 = 172.5 kW
Tc,out = 25 + 172.5/(3·4.18) = 38.76 °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 = 135 − 38.76 = 96.24 K
ΔT₂ = Th,out − Tc,in = 85 − 25 = 60 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (96.24 − 60)/ln(96.24/60) = 76.7 K

Area

A = Q̇/(U·ΔTlm) = 172500/(500·76.7) = 4.498 m²

Answer

A = 4.498 m²
19.Heat conduction

Answer: Ti = 12.98 °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) = (250/1000)/(0.72·10) = 0.03472 K/W
R2 = L2/(k2A) = (100/1000)/(0.17·10) = 0.05882 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 27/0.09355 = 288.6 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 23 − 288.6·0.03472 = 12.98 °C

Answer

Ti = 12.98 °C
20.Heat conduction

Answer: Ts = 20.74 °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/(10·12) = 0.008333 K/W
R1 = L1/(k1A) = (250/1000)/(0.17·12) = 0.1225 K/W
R2 = L2/(k2A) = (150/1000)/(0.72·12) = 0.01736 K/W
Ro = 1/(hoA) = 1/(20·12) = 0.004167 K/W
ΣR = 0.1524 K/W

Heat loss

Q̇ = (22 − (-1))/0.1524 = 150.9 W
Ts = Troom − Q̇·Ri = 22 − 150.9·0.008333 = 20.74 °C

Answer

Ts = 20.74 °C
21.Pipe friction & head loss

Answer: Δp = 72.25 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) = 0.015·(500/0.15)·1.7²/(2·9.81) = 7.365 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 = 1000·9.81·7.365 = 72250 Pa = 72.25 kPa

Answer

Δp = 72.25 kPa
22.Pipe friction & head loss

Answer: H = 1.196 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 = 0.06/0.04909 = 1.222 m/s
V²/(2g) = 0.07615 m

Loss coefficients

f·L/D = 0.02·100/0.25 = 8
ΣK = 0.5 + 4·0.3 + 5 = 6.7

Energy equation

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

H = (1 + 8 + 6.7)·0.07615 = 1.196 m

Answer

H = 1.196 m
23.Pumps & pump power

Answer: Pshaft = 57.23 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 = 1000·9.81·0.06·70 = 41.2 kW

Shaft power

Pshaft = Ph/η = 41.2/0.72 = 57.23 kW

Answer

Pshaft = 57.23 kW
24.Pumps & pump power

Answer: H = 16.38 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 = 0.075/0.04909 = 1.528 m/s
V²/(2g) = 0.119 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (12 + 8)·0.119 = 2.38 m

Pump head

Both surfaces are open and practically at rest, so pressure and velocity terms drop out.

H = Δz + hL = 14 + 2.38 = 16.38 m

Answer

H = 16.38 m

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