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 1250 kg/h · 35% NaOHStream 2ṁ₂ = ? · 15% 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 = 250 kg/hx1 = 35 %x2 = 15 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4000 kg/h · 13% sugarProduct PP = ? · 40%Vapour W (pure water)0% sugar

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

F = 4000 kg/hxF = 13 %xP = 40 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 150 °C80 °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 = 2.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 150 → 80 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 140 °C60 °Cwater · 25 °C45 °C · ṁ = ?5% lost

Hot ethanol heats water in an exchanger that loses 5% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 2.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 140 → 60 °Ct: 25 → 45 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
480 g of ArV = 5 LT = 5 °CP = ?

A tank of 5 L contains 480 g of Ar at 5 °C. Treat it as an ideal gas and find the pressure P.

m = 480 gM = 39.95 g/molV = 5 LT = 5 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of CH₄ goes from 150 kPa, 5 L, 20 °C to 700 kPa and 170 °C. Find the new volume V2.

P1 = 150 kPaV1 = 5 LT1 = 20 °CP2 = 700 kPaT2 = 170 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(MgO)m(MgO)÷ M(X)× 2/ν× M(MgO)

30 g of Mg and 40 g of O2 react according to 2Mg + O2 → 2MgO. What mass m of MgO can form?

M(Mg) = 24.31M(O2) = 32M(MgO) = 40.3 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, 30 g of Fe2O3 reacts completely (the other reactants are in excess) and 23.32 g of CO2 is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(CO2) = 44.01 g/molactual: 23.32 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 [HI].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 36
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.400C−x+x+xE0.4 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.4 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.4 mol/LKc = 0.2
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 200 gT = 90 °Cc = 0.449 J/(g·°C)Waterm = 400 gT = 16 °Cc = 4.18 J/(g·°C)

A 200 g block of iron (c = 0.449 J/(g·°C)) at 90 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 16 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.449 J/(g·°C)Tmetal = 90 °Cmwater = 400 gTwater = 16 °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 = ?40%

A zero-order reaction has k = 0.02 mol/(L·min) and starts at 0.5 mol/L. How long does it take to reach 40% conversion? Find t.

k = 0.02 mol/(L·min)CA0 = 0.5 mol/LX = 40 %
t = min
14.Reaction kineticsHard
Tk30 °C0.150 °C?

A reaction has a rate constant of 0.1 min⁻¹ at 30 °C and an activation energy of 75 kJ/mol. Find the rate constant k2 at 50 °C.

k1 = 0.1 min⁻¹T1 = 30 °CT2 = 50 °CEa = 75 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 40 L/minX = 95%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 40 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 95% conversion of A.

Q = 40 L/mink = 0.4 min⁻¹X = 95%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 1000 LQ = 20 L/minX = ?

A first-order liquid-phase reaction (k = 0.4 min⁻¹) runs in a 1000 L CSTR fed at 20 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 1000 LQ = 20 L/mink = 0.4 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT150 °C135 °C95 °C30 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 300 kW. The hot fluid cools from 150 to 135 °C and the cold fluid heats from 30 to 95 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 300 kWU = 800 W/(m²·K)Th: 150 → 135 °CTc: 30 → 95 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT80 °C50 °C63.83 °C10 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.5 kJ/(kg·K)) cools from 80 to 50 °C in a counter-flow exchanger. It heats 0.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 10 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.5 kJ/(kg·K)Th: 80 → 50 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 10 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Wood, k = 0.17150 mmGypsum board, k = 0.17150 mm22 °C-9 °CQ̇ = ?

A wall is made of 150 mm of wood and 150 mm of gypsum board, with an area of 12 m². The outer faces are at 22 °C and -9 °C. Find the heat flow Q̇ through the wall.

L1 = 150 mm, k1 = 0.17 W/(m·K)L2 = 150 mm, k2 = 0.17 W/(m·K)A = 12 m²T1 = 22 °CT3 = -9 °C
Q̇ = W
20.Heat conductionHard
Concrete, k = 1.4100 mmMineral wool, k = 0.0425 mmroom 22 °Coutside -4 °CQ̇ = ?

A wall of 100 mm concrete and 25 mm mineral wool separates a room at 22 °C from outside air at -4 °C. The convection coefficients are 6 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 8 m². Find the heat loss Q̇ through the wall.

L1 = 100 mm, k1 = 1.4 W/(m·K)L2 = 25 mm, k2 = 0.04 W/(m·K)A = 8 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = -4 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 1.2 m/sD = 150 mmL = 100 mf = 0.03

Water flows at a mean velocity of 1.2 m/s through a pipe 100 m long with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the friction head loss hf.

V = 1.2 m/sL = 100 mD = 150 mmf = 0.03g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 0.2Δz = ?L = 150 m, D = 250 mm, f = 0.022× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.02. 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 80 L/s?

Q = 80 L/sL = 150 mD = 250 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 0.2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 50 L/sH = 80 m

A pump with an efficiency of 70% delivers 50 L/s of water (ρ = 1000 kg/m³) against a head of 80 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 50 L/sH = 80 mη = 70%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 16 mL = 150 m, D = 150 mm, f = 0.02, ΣK = 6

A pump moves 50 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 16 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 = 6 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 65%. Find the shaft power Pshaft in kW.

Q = 50 L/sΔz = 16 mL = 150 mD = 150 mmf = 0.02ΣK = 6η = 65%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 83.33 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) = 250·(35 − 30)/(30 − 15) = 83.33 kg/h

Answer

ṁ2 = 83.33 kg/h
2.Mass balance

Answer: P = 1300 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 = 4000·13/40 = 1300 kg/h

Answer

P = 1300 kg/h
3.Energy balance

Answer: tout = 98.1 °C

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

Heat released by the hot stream

Q = 2.5·2.44·(150 − 80) = 427 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 427/(1.5·4.18) = 98.1 °C

Answer

tout = 98.1 °C
4.Energy balance

Answer: ṁc = 5.545 kg/s

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

Heat released

Qh = 2.5·2.44·(140 − 60) = 488 kW

Heat that reaches the water

Qc = (1 − 0.05)·488 = 463.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 463.6/(4.18·20) = 5.545 kg/s

Answer

ṁc = 5.545 kg/s
5.Ideal gas law

Answer: P = 5557 kPa

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

Moles

n = m/M = 480/39.95 = 12.02 mol
T = 5 + 273.15 = 278.1 K

Pressure

P = nRT/V = 12.02·8.314·278.1/0.005 = 5557 kPa

Answer

P = 5557 kPa
6.Ideal gas law

Answer: V2 = 1.62 L

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

Absolute temperatures

T1 = 293.1 K, T2 = 443.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(150/700)·(443.1/293.1) = 1.62 L

Answer

V2 = 1.62 L
7.Stoichiometry

Answer: m = 49.73 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(Mg) = 30/24.31 = 1.234 mol
n(O2) = 40/32 = 1.25 mol

Limiting reactant

1.234/2 = 0.617, 1.25/1 = 1.25 → Mg

Mass of product

n(MgO) = 0.617·2 = 1.234 mol
m = 1.234·40.3 = 49.73 g

Answer

m = 49.73 g
8.Stoichiometry

Answer: Y = 94.02 %

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) = 30/159.69 = 0.1879 mol
m = 0.1879·3/1·44.01 = 24.8 g

Percent yield

Y = 23.32/24.8·100 = 94.02%

Answer

Y = 94.02%
9.Chemical equilibrium

Answer: [HI] = 1.5 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

[HI] = 2x = 1.5 mol/L

Answer

[HI] = 1.5 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.2 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/(0.4 − x) → x² + 0.2·x − 0.08 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.08))/2 = 0.2 mol/L

Equilibrium concentration

[PCl₅] = 0.4 − 0.2 = 0.2 mol/L

Answer

[PCl5] = 0.2 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 19.77 °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

200·0.449·(90 − Tf) = 400·4.18·(Tf − 16)

Solve for the final temperature

Tf = (89.8·90 + 1672·16)/(89.8 + 1672) = 19.77 °C

Answer

Tf = 19.77 °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 = 10 min

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Amount converted

CA0·X = 0.5·0.4 = 0.2 mol/L

Time

t = CA0·X/k = 0.2/0.02 = 10 min

Answer

t = 10 min
14.Reaction kinetics

Answer: k2 = 0.6307 min⁻¹

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 = 303.1 K, T2 = 323.1 K

Arrhenius ratio

ln(k2/k1) = −(75000/8.314)·(1/323.1 − 1/303.1) = 1.842
k2 = 0.1·e1.842 = 0.6307 min⁻¹

Answer

k2 = 0.6307 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 299.6 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 − 0.95))/0.4 = 2.996/0.4 = 7.489 min

Volume

V = Q·τ = 40·7.489 = 299.6 L

Answer

V = 299.6 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 95.24 %

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 = 1000/20 = 50 min, kτ = 0.4·50 = 20

Conversion

X = kτ/(1 + kτ) = 20/(1 + 20) = 95.24%

Answer

X = 95.24%
17.Heat exchangers (LMTD)

Answer: A = 4.85 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 − 95 = 55 K
ΔT₂ = Th,out − Tc,in = 135 − 30 = 105 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (55 − 105)/ln(55/105) = 77.32 K

Area

A = Q̇/(U·ΔTlm) = 300000/(800·77.32) = 4.85 m²

Answer

A = 4.85 m²
18.Heat exchangers (LMTD)

Answer: A = 2.85 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) = 1.5·2.5·30 = 112.5 kW
Tc,out = 10 + 112.5/(0.5·4.18) = 63.83 °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 − 63.83 = 16.17 K
ΔT₂ = Th,out − Tc,in = 50 − 10 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (16.17 − 40)/ln(16.17/40) = 26.31 K

Area

A = Q̇/(U·ΔTlm) = 112500/(1500·26.31) = 2.85 m²

Answer

A = 2.85 m²
19.Heat conduction

Answer: Q̇ = 210.8 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) = (150/1000)/(0.17·12) = 0.07353 K/W
R2 = L2/(k2A) = (150/1000)/(0.17·12) = 0.07353 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 31/0.1471 = 210.8 W

Answer

Q̇ = 210.8 W
20.Heat conduction

Answer: Q̇ = 227.8 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/(6·8) = 0.02083 K/W
R1 = L1/(k1A) = (100/1000)/(1.4·8) = 0.008929 K/W
R2 = L2/(k2A) = (25/1000)/(0.04·8) = 0.07813 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.1141 K/W

Heat loss

Q̇ = (22 − (-4))/0.1141 = 227.8 W

Answer

Q̇ = 227.8 W
21.Pipe friction & head loss

Answer: hf = 1.468 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) = 1.2²/(2·9.81) = 0.07339 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.03·(100/0.15)·1.2²/(2·9.81) = 1.468 m

Answer

hf = 1.468 m
22.Pipe friction & head loss

Answer: Δz = 1.936 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 = 0.08/0.04909 = 1.63 m/s
V²/(2g) = 0.1354 m

Loss coefficients

f·L/D = 0.02·150/0.25 = 12
ΣK = 0.5 + 2·0.3 + 0.2 + 1.0 = 2.3

Total head loss

hf = 12·0.1354 = 1.625 m
hm = 2.3·0.1354 = 0.3114 m
Δz = hf + hm = 1.936 m

Answer

Δz = 1.936 m
23.Pumps & pump power

Answer: Pshaft = 56.06 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 = 1000·9.81·0.05·80 = 39.24 kW

Shaft power

Pshaft = Ph/η = 39.24/0.7 = 56.06 kW

Answer

Pshaft = 56.06 kW
24.Pumps & pump power

Answer: Pshaft = 20.08 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 = 0.05/0.01767 = 2.829 m/s
V²/(2g) = 0.408 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (20 + 6)·0.408 = 10.61 m

Pump head

H = Δz + hL = 16 + 10.61 = 26.61 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.05·26.61/0.65 = 20.08 kW

Answer

Pshaft = 20.08 kW

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