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 1500 kg/h · 10% 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 = 500 kg/hx1 = 10 %x2 = 30 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1200 kg/h · 12% NaOHProduct P55% 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 = 1200 kg/hxF = 12 %xP = 55 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 150 °C110 °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: 150 → 110 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 180 °C110 °Cwater · 25 °C40 °C · ṁ = ?15% lost

Hot glycol mix 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 = 0.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 180 → 110 °Ct: 25 → 40 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
400 g of HeP = 400 kPaT = 45 °CV = ?

What volume V does 400 g of He occupy at 400 kPa and 45 °C? Treat it as an ideal gas.

m = 400 gM = 4.003 g/molP = 400 kPaT = 45 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
Ar, M = 39.95 g/molP = 450 kPaT = 90 °Cρ = ?

Find the density ρ of Ar at 450 kPa and 90 °C, treating it as an ideal gas.

M = 39.95 g/molP = 450 kPaT = 90 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

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

M(Na) = 22.99M(Cl2) = 70.9M(NaCl) = 58.44 g/mol
m = g
8.StoichiometryHard
m(Fe2​O3​)n(Fe2​O3​)n(CO2​)m(CO2​)÷ M(Fe2​O3​)× 3/1× M(CO2​)

In the reaction Fe2O3 + 3CO → 2Fe + 3CO2, 4 g of Fe2O3 reacts completely (the other reactants are in excess) and 2.81 g of CO2 is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(CO2) = 44.01 g/molactual: 2.81 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.250.250C−x−x+2xE0.25 − x0.25 − x2x

0.25 mol/L of H₂ and 0.25 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 49. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 49
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.200C−x+x+xE0.2 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.2 mol/LKc = 0.05
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 250 gT = 120 °Cc = 0.897 J/(g·°C)Waterm = 300 gT = 23 °Cc = 4.18 J/(g·°C)

A 250 g block of aluminium (c = 0.897 J/(g·°C)) at 120 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 23 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.897 J/(g·°C)Tmetal = 120 °Cmwater = 300 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HCH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction CH4 + 2O₂ → CO₂ + 2H₂O(l).

ΔH°f(CH4) = −74.8 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)C (mol/L)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.02 L/(mol·min) and an initial concentration of 0.2 mol/L. Find its first half-life t½.

k = 0.02 L/(mol·min)CA0 = 0.2 mol/L
t½ = min
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.20.012run 20.40.024n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.2 mol/L the rate is 0.012 mol/(L·s); with CA0 = 0.4 mol/L it is 0.024 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.2 mol/Lr1 = 0.012 mol/(L·s)CA0,2 = 0.4 mol/Lr2 = 0.024 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minX = 60%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 25 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 60% conversion of A.

Q = 25 L/mink = 0.5 min⁻¹X = 60%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 2000 LQ = 80 L/minX = ?

A first-order liquid-phase reaction (k = 0.5 min⁻¹) runs in a 2000 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 = 2000 LQ = 80 L/mink = 0.5 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT170 °C145 °C10 °C55 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 350 kW. Its heat transfer area is 2 m². The hot fluid cools from 170 to 145 °C and the cold fluid heats from 10 to 55 °C. Find the overall heat transfer coefficient U.

Q̇ = 350 kWA = 2 m²Th: 170 → 145 °CTc: 10 → 55 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT150 °C??25 °CΔT₁ΔT₂counter-flow

In a counter-flow heat exchanger both streams have the same heat capacity rate, ṁ·cp = 1.5 kW/K. The hot stream enters at 150 °C and the cold stream at 25 °C. The exchanger has A = 4 m² and U = 300 W/(m²·K). Find the hot outlet temperature Th,out.

Ch = Cc = 1.5 kW/KTh,in = 150 °CTc,in = 25 °CA = 4 m²U = 300 W/(m²·K)
Th,out = °C
19.Heat conductionMedium
Gypsum board, k = 0.17150 mmConcrete, k = 1.450 mm18 °C-15 °CTi​ = ?Q̇

A wall is made of 150 mm of gypsum board and 50 mm of concrete, with an area of 6 m². The outer faces are at 18 °C and -15 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 0.17 W/(m·K)L2 = 50 mm, k2 = 1.4 W/(m·K)A = 6 m²T1 = 18 °CT3 = -15 °C
Ti = °C
20.Heat conductionHard
Wood, k = 0.17200 mmMineral wool, k = 0.04100 mmroom 21 °Coutside -2 °CQ̇

A wall of 200 mm wood and 100 mm mineral wool separates a room at 21 °C from outside air at -2 °C. The convection coefficients are 8 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 4 m². Find the overall heat transfer coefficient U of the wall.

L1 = 200 mm, k1 = 0.17 W/(m·K)L2 = 100 mm, k2 = 0.04 W/(m·K)A = 4 m²hi = 8 W/(m²·K)ho = 25 W/(m²·K)Troom = 21 °CTout = -2 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 1.7 m/sD = 100 mmL = 200 mf = 0.03

Water flows at a mean velocity of 1.7 m/s through a pipe 200 m long with an inside diameter of 100 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the friction head loss hf.

V = 1.7 m/sL = 200 mD = 100 mmf = 0.03g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10free outletH = ?L = 300 m, D = 300 mm, f = 0.0183× bend (K = 0.3)

A pipe 300 m long with an inside diameter of 300 mm (Darcy friction factor f = 0.018) 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), 3 bends (K = 0.3 each) and a valve (K = 10). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 150 L/s?

Q = 150 L/sL = 300 mD = 300 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 10
H = m
23.Pumps & pump powerMedium
PQ = 25 L/sH = 18 m

A pump with an efficiency of 85% delivers 25 L/s of water (ρ = 1000 kg/m³) against a head of 18 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 25 L/sH = 18 mη = 85%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 80 L/sΔz = 30 mL = 150 m, D = 200 mm, f = 0.018, ΣK = 6

A pump moves 80 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 30 m higher. The pipe is 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.018; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 80 L/sΔz = 30 mL = 150 mD = 200 mmf = 0.018ΣK = 6
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 1500 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) = 500·(10 − 25)/(25 − 30) = 1500 kg/h

Answer

ṁ2 = 1500 kg/h
2.Mass balance

Answer: W = 938.2 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 = 1200·12/55 = 261.8 kg/h

Total balance

W = F − P = 1200 − 261.8 = 938.2 kg/h

Answer

W = 938.2 kg/h
3.Energy balance

Answer: tout = 61.13 °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·(150 − 110) = 195.2 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 195.2/(1.5·4.18) = 61.13 °C

Answer

tout = 61.13 °C
4.Energy balance

Answer: ṁc = 1.708 kg/s

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

Heat released

Qh = 0.5·3.6·(180 − 110) = 126 kW

Heat that reaches the water

Qc = (1 − 0.15)·126 = 107.1 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 107.1/(4.18·15) = 1.708 kg/s

Answer

ṁc = 1.708 kg/s
5.Ideal gas law

Answer: V = 660.8 L

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

Moles

n = 400/4.003 = 99.93 mol
T = 45 + 273.15 = 318.1 K

Volume

V = nRT/P = 99.93·8.314·318.1/400 = 660.8 L

Answer

V = 660.8 L
6.Ideal gas law

Answer: ρ = 5.954 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 90 + 273.15 = 363.1 K

Density

ρ = 450·39.95/(8.314·363.1) = 5.954 kg/m³

Answer

ρ = 5.954 kg/m³
7.Stoichiometry

Answer: m = 30.5 g

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

Moles of each reactant

n(Na) = 12/22.99 = 0.522 mol
n(Cl2) = 24/70.9 = 0.3385 mol

Limiting reactant

0.522/2 = 0.261, 0.3385/1 = 0.3385 → Na

Mass of product

n(NaCl) = 0.261·2 = 0.522 mol
m = 0.522·58.44 = 30.5 g

Answer

m = 30.5 g
8.Stoichiometry

Answer: Y = 84.97 %

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) = 4/159.69 = 0.02505 mol
m = 0.02505·3/1·44.01 = 3.307 g

Percent yield

Y = 2.81/3.307·100 = 84.97%

Answer

Y = 84.97%
9.Chemical equilibrium

Answer: [H2] = 0.05556 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

49 = (2x)²/(0.25 − x)²

Take the square root

7 = 2x/(0.25 − x) → x = 0.25·7/(2 + 7) = 0.1944 mol/L

Equilibrium concentration

[H₂] = 0.25 − x = 0.05556 mol/L

Answer

[H2] = 0.05556 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.1219 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

0.05 = x²/(0.2 − x) → x² + 0.05·x − 0.01 = 0

Solve the quadratic

x = (−0.05 + √(0.05² + 4·0.01))/2 = 0.07808 mol/L

Equilibrium concentration

[PCl₅] = 0.2 − 0.07808 = 0.1219 mol/L

Answer

[PCl5] = 0.1219 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 37.71 °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

250·0.897·(120 − Tf) = 300·4.18·(Tf − 23)

Solve for the final temperature

Tf = (224.3·120 + 1254·23)/(224.3 + 1254) = 37.71 °C

Answer

Tf = 37.71 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −890.3 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

Answer

ΔH° = −890.3 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t½ = 250 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/(0.02·0.2) = 250 min

Answer

t½ = 250 min

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

14.Reaction kinetics

Answer: n = 1

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

Ratios

r2/r1 = 0.024/0.012 = 2
C2/C1 = 0.4/0.2 = 2

Order

n = ln(2)/ln(2) = 1

Answer

n = 1
15.Reactor sizing (CSTR & PFR)

Answer: V = 45.81 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 − 0.6))/0.5 = 0.9163/0.5 = 1.833 min

Volume

V = Q·τ = 25·1.833 = 45.81 L

Answer

V = 45.81 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 92.59 %

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 = 2000/80 = 25 min, kτ = 0.5·25 = 12.5

Conversion

X = kτ/(1 + kτ) = 12.5/(1 + 12.5) = 92.59%

Answer

X = 92.59%
17.Heat exchangers (LMTD)

Answer: U = 1438 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 parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 170 − 10 = 160 K
ΔT₂ = Th,out − Tc,out = 145 − 55 = 90 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (160 − 90)/ln(160/90) = 121.7 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 350000/(2·121.7) = 1438 W/(m²·K)

Answer

U = 1438 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: Th,out = 94.44 °C

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.

Constant temperature difference

The cold outlet sits opposite the hot inlet: Tc,out = Tc,in + (Th,in − Th,out), so ΔT₁ = Th,in − Tc,out = Th,out − Tc,in = ΔT₂.

ΔTlm = Th,out − Tc,in

Energy balance equals rate equation

1.5·(150 − Th,out) = 1.2·(Th,out − 25)
Th,out = (1.5·150 + 1.2·25)/(1.5 + 1.2) = 94.44 °C

Answer

Th,out = 94.44 °C

Heat transferred: Q̇ = 83.33 kW; the cold stream leaves at 80.56 °C.

19.Heat conduction

Answer: Ti = −13.72 °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)/(0.17·6) = 0.1471 K/W
R2 = L2/(k2A) = (50/1000)/(1.4·6) = 0.005952 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 33/0.153 = 215.7 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 18 − 215.7·0.1471 = −13.72 °C

Answer

Ti = −13.72 °C
20.Heat conduction

Answer: U = 0.2603 W/(m²·K)

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/(8·4) = 0.03125 K/W
R1 = L1/(k1A) = (200/1000)/(0.17·4) = 0.2941 K/W
R2 = L2/(k2A) = (100/1000)/(0.04·4) = 0.625 K/W
Ro = 1/(hoA) = 1/(25·4) = 0.01 K/W
ΣR = 0.9604 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(4·0.9604) = 0.2603 W/(m²·K)

Answer

U = 0.2603 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 8.838 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 head

V²/(2g) = 1.7²/(2·9.81) = 0.1473 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.03·(200/0.1)·1.7²/(2·9.81) = 8.838 m

Answer

hf = 8.838 m
22.Pipe friction & head loss

Answer: H = 6.977 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 = 0.15/0.07069 = 2.122 m/s
V²/(2g) = 0.2295 m

Loss coefficients

f·L/D = 0.018·300/0.3 = 18
ΣK = 0.5 + 3·0.3 + 10 = 11.4

Energy equation

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

H = (1 + 18 + 11.4)·0.2295 = 6.977 m

Answer

H = 6.977 m
23.Pumps & pump power

Answer: Pshaft = 5.194 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 = 1000·9.81·0.025·18 = 4.415 kW

Shaft power

Pshaft = Ph/η = 4.415/0.85 = 5.194 kW

Answer

Pshaft = 5.194 kW
24.Pumps & pump power

Answer: H = 36.44 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 = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (13.5 + 6)·0.3305 = 6.445 m

Pump head

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

H = Δz + hL = 30 + 6.445 = 36.44 m

Answer

H = 36.44 m

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