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 1950 kg/h · 5% sugarStream 2ṁ₂ = ? · 35% sugarProduct25% sugar

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

ṁ1 = 950 kg/hx1 = 5 %x2 = 35 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4400 kg/h · 14% sugarProduct P30% sugarVapour W (pure water)W = ? kg/h

An evaporator concentrates a sugar solution by boiling off pure water. Find the water evaporated W in kg/h.

F = 4400 kg/hxF = 14 %xP = 30 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 150 °C120 °Cwater · 25 °Ct = ? °C

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

ṁh = 0.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 150 → 120 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 120 °C70 °Cwater · 30 °C45 °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: 120 → 70 °Ct: 30 → 45 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
190 g of N₂P = 550 kPaT = 35 °CV = ?

What volume V does 190 g of N₂ occupy at 550 kPa and 35 °C? Treat it as an ideal gas.

m = 190 gM = 28.01 g/molP = 550 kPaT = 35 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
He, M = 4.003 g/molP = 600 kPaT = 10 °Cρ = ?

Find the density ρ of He at 600 kPa and 10 °C, treating it as an ideal gas.

M = 4.003 g/molP = 600 kPaT = 10 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(AlCl3​)m(AlCl3​)÷ M(X)× 2/ν× M(AlCl3​)

30 g of Al and 24 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(Fe2​O3​)n(Fe2​O3​)n(CO2​)m(CO2​)÷ M(Fe2​O3​)× 3/1× M(CO2​)

In the reaction Fe2O3 + 3CO → 2Fe + 3CO2, 12 g of Fe2O3 reacts completely (the other reactants are in excess) and 7.44 g of CO2 is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(CO2) = 44.01 g/molactual: 7.44 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.40.40C−x−x+2xE0.4 − x0.4 − x2x

0.4 mol/L of H₂ and 0.4 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 50. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 50
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I100C−x+x+xE1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 1 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 1 mol/LKc = 0.2
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 50 gT = 170 °Cc = 0.449 J/(g·°C)Waterm = 150 gT = 16 °Cc = 4.18 J/(g·°C)

A 50 g block of iron (c = 0.449 J/(g·°C)) at 170 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 16 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.449 J/(g·°C)Tmetal = 170 °Cmwater = 150 gTwater = 16 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l).

ΔH°f(C6H12O6) = −1274 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)40 min0.3

In a first-order reaction the concentration of A falls from 1.5 mol/L to 0.3 mol/L in 40 min. Find the rate constant k.

CA0 = 1.5 mol/LCA = 0.3 mol/Lt = 40 min
k = min⁻¹
14.Reaction kineticsHard
Tk20 °C0.00260 °C0.0805

The rate constant of a reaction is 0.002 min⁻¹ at 20 °C and 0.0805 min⁻¹ at 60 °C. Find the activation energy Ea.

k1 = 0.002 min⁻¹T1 = 20 °Ck2 = 0.0805 min⁻¹T2 = 60 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 10 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 10 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 = 10 L/mink = 0.4 min⁻¹X = 80%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 250 LQ = 50 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 250 L CSTR fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 250 LQ = 50 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT115 °C100 °C25 °C40 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 500 kW. The hot fluid cools from 115 to 100 °C and the cold fluid heats from 25 to 40 °C. The overall heat transfer coefficient is 300 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 500 kWU = 300 W/(m²·K)Th: 115 → 100 °CTc: 25 → 40 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT120 °C??25 °CΔT₁ΔT₂counter-flow

In a counter-flow heat exchanger both streams have the same heat capacity rate, ṁ·cp = 2 kW/K. The hot stream enters at 120 °C and the cold stream at 25 °C. The exchanger has A = 6 m² and U = 800 W/(m²·K). Find the hot outlet temperature Th,out.

Ch = Cc = 2 kW/KTh,in = 120 °CTc,in = 25 °CA = 6 m²U = 800 W/(m²·K)
Th,out = °C
19.Heat conductionMedium
Gypsum board, k = 0.17150 mmWood, k = 0.1750 mm20 °C7 °CTi​ = ?Q̇

A wall is made of 150 mm of gypsum board and 50 mm of wood, with an area of 20 m². The outer faces are at 20 °C and 7 °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 = 0.17 W/(m·K)A = 20 m²T1 = 20 °CT3 = 7 °C
Ti = °C
20.Heat conductionHard
Brick, k = 0.72250 mmConcrete, k = 1.425 mmroom 22 °Coutside -12 °CQ̇

A wall of 250 mm brick and 25 mm concrete separates a room at 22 °C from outside air at -12 °C. The convection coefficients are 10 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 20 m². Find the overall heat transfer coefficient U of the wall.

L1 = 250 mm, k1 = 0.72 W/(m·K)L2 = 25 mm, k2 = 1.4 W/(m·K)A = 20 m²hi = 10 W/(m²·K)ho = 25 W/(m²·K)Troom = 22 °CTout = -12 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 1.3 m/sD = 250 mmL = 100 mf = 0.015

Water flows at a mean velocity of 1.3 m/s through a pipe 100 m long with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the friction head loss hf.

V = 1.3 m/sL = 100 mD = 250 mmf = 0.015g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10Δz = 28 mL = 500 m, D = 300 mm, f = 0.0154× bend (K = 0.3)

Two open reservoirs are joined by a pipe 500 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.015. The water surface of the upper reservoir is 28 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 4 bends (K = 0.3 each), a valve (K = 10) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². Find the flow rate Q in L/s.

Δz = 28 mL = 500 mD = 300 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 10Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 100 L/sH = 20 m

In a test, a pump delivers 100 L/s of water (ρ = 1000 kg/m³) against a head of 20 m while its shaft takes 23.9 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 100 L/sH = 20 mPshaft = 23.9 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 29 mL = 150 m, D = 150 mm, f = 0.02, ΣK = 5

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 29 m higher. The pipe is 150 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.02; the minor-loss coefficients add up to ΣK = 5 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 50 L/sΔz = 29 mL = 150 mD = 150 mmf = 0.02ΣK = 5
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 1900 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) = 950·(5 − 25)/(25 − 35) = 1900 kg/h

Answer

ṁ2 = 1900 kg/h
2.Mass balance

Answer: W = 2347 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 = 4400·14/30 = 2053 kg/h

Total balance

W = F − P = 4400 − 2053 = 2347 kg/h

Answer

W = 2347 kg/h
3.Energy balance

Answer: tout = 33.76 °C

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

Heat released by the hot stream

Q = 0.5·2.44·(150 − 120) = 36.6 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 36.6/(1·4.18) = 33.76 °C

Answer

tout = 33.76 °C
4.Energy balance

Answer: ṁc = 1.22 kg/s

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

Heat released

Qh = 0.5·3.6·(120 − 70) = 90 kW

Heat that reaches the water

Qc = (1 − 0.15)·90 = 76.5 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 76.5/(4.18·15) = 1.22 kg/s

Answer

ṁc = 1.22 kg/s
5.Ideal gas law

Answer: V = 31.6 L

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

Moles

n = 190/28.01 = 6.783 mol
T = 35 + 273.15 = 308.1 K

Volume

V = nRT/P = 6.783·8.314·308.1/550 = 31.6 L

Answer

V = 31.6 L
6.Ideal gas law

Answer: ρ = 1.02 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

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

Density

ρ = 600·4.003/(8.314·283.1) = 1.02 kg/m³

Answer

ρ = 1.02 kg/m³
7.Stoichiometry

Answer: m = 30.09 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) = 30/26.98 = 1.112 mol
n(Cl2) = 24/70.9 = 0.3385 mol

Limiting reactant

1.112/2 = 0.556, 0.3385/3 = 0.1128 → Cl2

Mass of product

n(AlCl3) = 0.1128·2 = 0.2257 mol
m = 0.2257·133.33 = 30.09 g

Answer

m = 30.09 g
8.Stoichiometry

Answer: Y = 74.99 %

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) = 12/159.69 = 0.07515 mol
m = 0.07515·3/1·44.01 = 9.921 g

Percent yield

Y = 7.44/9.921·100 = 74.99%

Answer

Y = 74.99%
9.Chemical equilibrium

Answer: [H2] = 0.08819 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

50 = (2x)²/(0.4 − x)²

Take the square root

7.071 = 2x/(0.4 − x) → x = 0.4·7.071/(2 + 7.071) = 0.3118 mol/L

Equilibrium concentration

[H₂] = 0.4 − x = 0.08819 mol/L

Answer

[H2] = 0.08819 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.3583 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

0.2 = x²/(1 − x) → x² + 0.2·x − 0.2 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.2))/2 = 0.3583 mol/L

Equilibrium concentration

[Cl₂] = x = 0.3583 mol/L

Answer

[Cl2] = 0.3583 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 21.32 °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

50·0.449·(170 − Tf) = 150·4.18·(Tf − 16)

Solve for the final temperature

Tf = (22.45·170 + 627·16)/(22.45 + 627) = 21.32 °C

Answer

Tf = 21.32 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −2802 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° = [6·(−393.5) + 6·(−285.8)] − [1·(−1274) + 6·0] = −2802 kJ

Answer

ΔH° = −2802 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.04024 min⁻¹

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).

Integrated first-order law

k = ln(CA0/CA)/t = ln(1.5/0.3)/40 = 1.609/40 = 0.04024 min⁻¹

Answer

k = 0.04024 min⁻¹
14.Reaction kinetics

Answer: Ea = 75.01 kJ/mol

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 temperatures

T1 = 293.1 K, T2 = 333.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·3.695/(-4.096e-4) = 75008 J/mol
Ea = 75.01 kJ/mol

Answer

Ea = 75.01 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: V = 40.24 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 = 10·4.024 = 40.24 L

Answer

V = 40.24 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 55.56 %

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 = 250/50 = 5 min, kτ = 0.25·5 = 1.25

Conversion

X = kτ/(1 + kτ) = 1.25/(1 + 1.25) = 55.56%

Answer

X = 55.56%
17.Heat exchangers (LMTD)

Answer: A = 22.53 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 = 115 − 25 = 90 K
ΔT₂ = Th,out − Tc,out = 100 − 40 = 60 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (90 − 60)/ln(90/60) = 73.99 K

Area

A = Q̇/(U·ΔTlm) = 500000/(300·73.99) = 22.53 m²

Answer

A = 22.53 m²
18.Heat exchangers (LMTD)

Answer: Th,out = 52.94 °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

2·(120 − Th,out) = 4.8·(Th,out − 25)
Th,out = (2·120 + 4.8·25)/(2 + 4.8) = 52.94 °C

Answer

Th,out = 52.94 °C

Heat transferred: Q̇ = 134.1 kW; the cold stream leaves at 92.06 °C.

19.Heat conduction

Answer: Ti = 10.25 °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)/(0.17·20) = 0.04412 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·20) = 0.01471 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 13/0.05882 = 221 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 20 − 221·0.04412 = 10.25 °C

Answer

Ti = 10.25 °C
20.Heat conduction

Answer: U = 1.98 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/(10·20) = 0.005 K/W
R1 = L1/(k1A) = (250/1000)/(0.72·20) = 0.01736 K/W
R2 = L2/(k2A) = (25/1000)/(1.4·20) = 0.0008929 K/W
Ro = 1/(hoA) = 1/(25·20) = 0.002 K/W
ΣR = 0.02525 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(20·0.02525) = 1.98 W/(m²·K)

Answer

U = 1.98 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 0.5168 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) = 1.3²/(2·9.81) = 0.08614 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.015·(100/0.25)·1.3²/(2·9.81) = 0.5168 m

Answer

hf = 0.5168 m
22.Pipe friction & head loss

Answer: Q = 269.8 L/s

Pipe flow: the Reynolds number Re = V·D/ν = ρ·V·D/μ tells laminar flow (Re below about 2000) from turbulent flow (above about 4000). Friction along a pipe costs the Darcy–Weisbach head loss hf = f·(L/D)·V²/(2g). Fittings, valves, the entrance and the exit add minor losses hm = ΣK·V²/(2g). Between two open reservoir surfaces the energy equation gives Δz = hf + hm, with the exit loss K = 1 included.

Loss coefficients

f·L/D = 0.015·500/0.3 = 25
ΣK = 0.5 + 4·0.3 + 10 + 1.0 = 12.7

Energy equation

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

28 = (25 + 12.7)·V²/(2·9.81)
V = √(2·9.81·28/37.7) = 3.817 m/s

Flow rate

Q = V·π·D²/4 = 3.817·0.07069 = 0.2698 m³/s = 269.8 L/s

Answer

Q = 269.8 L/s
23.Pumps & pump power

Answer: η = 82.09 %

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 = 1000·9.81·0.1·20 = 19.62 kW

Efficiency

η = Ph/Pshaft = 19.62/23.9 = 82.09%

Answer

η = 82.09%
24.Pumps & pump power

Answer: H = 39.2 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 = 0.05/0.01767 = 2.829 m/s
V²/(2g) = 0.408 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (20 + 5)·0.408 = 10.2 m

Pump head

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

H = Δz + hL = 29 + 10.2 = 39.2 m

Answer

H = 39.2 m

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