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 1200 kg/h · 50% sugarStream 2ṁ₂ = ? · 15% sugarProduct20% sugar

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

ṁ1 = 200 kg/hx1 = 50 %x2 = 15 %x3 = 20 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3800 kg/h · 9% saltProduct PP = ? · 60%Vapour W (pure water)0% salt

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

F = 3800 kg/hxF = 9 %xP = 60 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 130 °C80 °Cwater · 20 °Ct = ? °C

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

ṁh = 3 kg/scp,h = 2.44 kJ/(kg·K)Th: 130 → 80 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 130 °C60 °Cwater · 10 °C65 °C · ṁ = ?5% lost

Hot glycol mix 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 = 1 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 60 °Ct: 10 → 65 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
430 g of ArV = 50 LT = 35 °CP = ?

A tank of 50 L contains 430 g of Ar at 35 °C. Treat it as an ideal gas and find the pressure P.

m = 430 gM = 39.95 g/molV = 50 LT = 35 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 100 kPa, 20 L, 10 °C to 750 kPa and 190 °C. Find the new volume V2.

P1 = 100 kPaV1 = 20 LT1 = 10 °CP2 = 750 kPaT2 = 190 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(AlCl3​)m(AlCl3​)÷ M(X)× 2/ν× M(AlCl3​)

8 g of Al and 8 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(N2​)n(N2​)n(NH3​)m(NH3​)÷ M(N2​)× 2/1× M(NH3​)

In the reaction N2 + 3H2 → 2NH3, 24 g of N2 reacts completely (the other reactants are in excess) and 18.09 g of NH3 is collected. Find the percent yield Y.

M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 18.09 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.80.80C−x−x+2xE0.8 − x0.8 − x2x

0.8 mol/L of H₂ and 0.8 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 = 0.8 mol/LKc = 50
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.200C−x+x+xE0.2 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.01 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.2 mol/LKc = 0.01
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 150 gT = 200 °Cc = 0.897 J/(g·°C)Waterm = 250 gT = 16 °Cc = 4.18 J/(g·°C)

A 150 g block of aluminium (c = 0.897 J/(g·°C)) at 200 °C is dropped into 250 g of water (c = 4.18 J/(g·°C)) at 16 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.897 J/(g·°C)Tmetal = 200 °Cmwater = 250 gTwater = 16 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H100 g C4​H10​2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 100 g of C4H10 (M = 58.12 g/mol) burns completely: 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l). Give q as a positive number.

ΔH°f(C4H10) = −125.6 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = kJ
13.Reaction kineticsMedium
t (min)C (mol/L)30 min0.6

In a first-order reaction the concentration of A falls from 1.2 mol/L to 0.6 mol/L in 30 min. Find the rate constant k.

CA0 = 1.2 mol/LCA = 0.6 mol/Lt = 30 min
k = min⁻¹
14.Reaction kineticsHard
t (min)X (%)60 minX = ?

A first-order reaction has k = 0.01 min⁻¹ at 30 °C and an activation energy of 50 kJ/mol. The batch reactor is now run at 60 °C for 60 min. Find the conversion X reached.

k1 = 0.01 min⁻¹T1 = 30 °CEa = 50 kJ/molT2 = 60 °Ct = 60 minR = 8.314 J/(mol·K)
X = %
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 L/minX = 70%V = ?, k = 0.05 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.05 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 80 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 70% conversion of A.

Q = 80 L/mink = 0.05 min⁻¹X = 70%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 100 LQ = 100 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 100 L CSTR fed at 100 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 100 LQ = 100 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT155 °C90 °C20 °C70 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 450 kW. The hot fluid cools from 155 to 90 °C and the cold fluid heats from 20 to 70 °C. The overall heat transfer coefficient is 300 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 450 kWU = 300 W/(m²·K)Th: 155 → 90 °CTc: 20 → 70 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT165 °C125 °C37.01 °C15 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.3 kJ/(kg·K)) cools from 165 to 125 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 15 °C. With U = 500 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.3 kJ/(kg·K)Th: 165 → 125 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 15 °CU = 500 W/(m²·K)
A = m²
19.Heat conductionMedium
Brick, k = 0.72150 mmGlass, k = 0.9675 mm23 °C-5 °CTi​ = ?Q̇

A wall is made of 150 mm of brick and 75 mm of glass, with an area of 6 m². The outer faces are at 23 °C and -5 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 0.72 W/(m·K)L2 = 75 mm, k2 = 0.96 W/(m·K)A = 6 m²T1 = 23 °CT3 = -5 °C
Ti = °C
20.Heat conductionHard
Wood, k = 0.17150 mmMineral wool, k = 0.0425 mmroom 20 °Coutside 0 °CQ̇ = ?

A wall of 150 mm wood and 25 mm mineral wool separates a room at 20 °C from outside air at 0 °C. The convection coefficients are 6 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 20 m². Find the heat loss Q̇ through the wall.

L1 = 150 mm, k1 = 0.17 W/(m·K)L2 = 25 mm, k2 = 0.04 W/(m·K)A = 20 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 20 °CTout = 0 °C
Q̇ = W
21.Pipe friction & head lossMedium
Q = 6 L/sD = 50 mmL = 50 mf = 0.022

Water flows at 6 L/s through a pipe 50 m long with an inside diameter of 50 mm. Use the Darcy friction factor f = 0.022 and g = 9.81 m/s². Find the friction head loss hf.

Q = 6 L/sL = 50 mD = 50 mmf = 0.022g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 100 m, D = 200 mm, f = 0.0254× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 200 mm (Darcy friction factor f = 0.025) 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 = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 40 L/s?

Q = 40 L/sL = 100 mD = 200 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 14 m

In a test, a pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 14 m while its shaft takes 1.6 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 10 L/sH = 14 mPshaft = 1.6 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
200 kPa (gauge)PQ = 20 L/sΔz = 7 mL = 100 m, D = 100 mm, f = 0.022, ΣK = 4

A pump moves 20 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 7 m higher. The pipe is 100 m long with an inside diameter of 100 mm and a Darcy friction factor f = 0.022; the minor-loss coefficients add up to ΣK = 4 (entrance and exit included). Use g = 9.81 m/s². The upper tank is closed and the air above its water is at a gauge pressure of 200 kPa. Find the head H the pump must add.

Q = 20 L/sΔz = 7 mL = 100 mD = 100 mmf = 0.022ΣK = 4ptank = 200 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 1200 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) = 200·(50 − 20)/(20 − 15) = 1200 kg/h

Answer

ṁ2 = 1200 kg/h
2.Mass balance

Answer: P = 570 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 = 3800·9/60 = 570 kg/h

Answer

P = 570 kg/h
3.Energy balance

Answer: tout = 78.37 °C

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

Heat released by the hot stream

Q = 3·2.44·(130 − 80) = 366 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 366/(1.5·4.18) = 78.37 °C

Answer

tout = 78.37 °C
4.Energy balance

Answer: ṁc = 1.041 kg/s

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

Heat released

Qh = 1·3.6·(130 − 60) = 252 kW

Heat that reaches the water

Qc = (1 − 0.05)·252 = 239.4 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 239.4/(4.18·55) = 1.041 kg/s

Answer

ṁc = 1.041 kg/s
5.Ideal gas law

Answer: P = 551.5 kPa

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

Moles

n = m/M = 430/39.95 = 10.76 mol
T = 35 + 273.15 = 308.1 K

Pressure

P = nRT/V = 10.76·8.314·308.1/0.05 = 551.5 kPa

Answer

P = 551.5 kPa
6.Ideal gas law

Answer: V2 = 4.362 L

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

Absolute temperatures

T1 = 283.1 K, T2 = 463.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 20·(100/750)·(463.1/283.1) = 4.362 L

Answer

V2 = 4.362 L
7.Stoichiometry

Answer: m = 10.03 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) = 8/26.98 = 0.2965 mol
n(Cl2) = 8/70.9 = 0.1128 mol

Limiting reactant

0.2965/2 = 0.1483, 0.1128/3 = 0.03761 → Cl2

Mass of product

n(AlCl3) = 0.03761·2 = 0.07522 mol
m = 0.07522·133.33 = 10.03 g

Answer

m = 10.03 g
8.Stoichiometry

Answer: Y = 62.01 %

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(N2) = 24/28.02 = 0.8565 mol
m = 0.8565·2/1·17.03 = 29.17 g

Percent yield

Y = 18.09/29.17·100 = 62.01%

Answer

Y = 62.01%
9.Chemical equilibrium

Answer: [H2] = 0.1764 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/(0.8 − x)²

Take the square root

7.071 = 2x/(0.8 − x) → x = 0.8·7.071/(2 + 7.071) = 0.6236 mol/L

Equilibrium concentration

[H₂] = 0.8 − x = 0.1764 mol/L

Answer

[H2] = 0.1764 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.04 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

0.01 = x²/(0.2 − x) → x² + 0.01·x − 0.002 = 0

Solve the quadratic

x = (−0.01 + √(0.01² + 4·0.002))/2 = 0.04 mol/L

Equilibrium concentration

[Cl₂] = x = 0.04 mol/L

Answer

[Cl2] = 0.04 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 36.99 °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

150·0.897·(200 − Tf) = 250·4.18·(Tf − 16)

Solve for the final temperature

Tf = (134.6·200 + 1045·16)/(134.6 + 1045) = 36.99 °C

Answer

Tf = 36.99 °C
12.Calorimetry & enthalpy

Answer: q = 4951 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° = [8·(−393.5) + 10·(−285.8)] − [2·(−125.6) + 13·0] = −5755 kJ

Heat for the given mass

n = 100/58.12 = 1.721 mol
q = n·|ΔH°/2| = 1.721·2877 = 4951 kJ

Answer

q = 4951 kJ
13.Reaction kinetics

Answer: k = 0.0231 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(1.2/0.6)/30 = 0.6931/30 = 0.0231 min⁻¹

Answer

k = 0.0231 min⁻¹
14.Reaction kinetics

Answer: X = 97.21 %

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Rate constant at the new temperature

T1 = 303.1 K, T2 = 333.1 K
k2 = 0.01·e−(50000/8.314)·(1/333.1 − 1/303.1) = 0.05968 min⁻¹

Conversion

X = 1 − e−0.05968·60 = 1 − 0.02785 = 97.21 %

Answer

X = 97.21 %
15.Reactor sizing (CSTR & PFR)

Answer: V = 1926 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 − 0.7))/0.05 = 1.204/0.05 = 24.08 min

Volume

V = Q·τ = 80·24.08 = 1926 L

Answer

V = 1926 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 20 %

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 = 100/100 = 1 min, kτ = 0.25·1 = 0.25

Conversion

X = kτ/(1 + kτ) = 0.25/(1 + 0.25) = 20%

Answer

X = 20%
17.Heat exchangers (LMTD)

Answer: A = 24.91 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 = 155 − 20 = 135 K
ΔT₂ = Th,out − Tc,out = 90 − 70 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (135 − 20)/ln(135/20) = 60.22 K

Area

A = Q̇/(U·ΔTlm) = 450000/(300·60.22) = 24.91 m²

Answer

A = 24.91 m²
18.Heat exchangers (LMTD)

Answer: A = 1.549 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) = 1·2.3·40 = 92 kW
Tc,out = 15 + 92/(1·4.18) = 37.01 °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 = 165 − 37.01 = 128 K
ΔT₂ = Th,out − Tc,in = 125 − 15 = 110 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (128 − 110)/ln(128/110) = 118.8 K

Area

A = Q̇/(U·ΔTlm) = 92000/(500·118.8) = 1.549 m²

Answer

A = 1.549 m²
19.Heat conduction

Answer: Ti = 2.636 °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)/(0.72·6) = 0.03472 K/W
R2 = L2/(k2A) = (75/1000)/(0.96·6) = 0.01302 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 28/0.04774 = 586.5 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 23 − 586.5·0.03472 = 2.636 °C

Answer

Ti = 2.636 °C
20.Heat conduction

Answer: Q̇ = 232 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/(6·20) = 0.008333 K/W
R1 = L1/(k1A) = (150/1000)/(0.17·20) = 0.04412 K/W
R2 = L2/(k2A) = (25/1000)/(0.04·20) = 0.03125 K/W
Ro = 1/(hoA) = 1/(20·20) = 0.0025 K/W
ΣR = 0.0862 K/W

Heat loss

Q̇ = (20 − (0))/0.0862 = 232 W

Answer

Q̇ = 232 W
21.Pipe friction & head loss

Answer: hf = 10.47 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.

Mean velocity

A = π·0.05²/4 = 0.001963 m²
V = Q/A = 0.006/0.001963 = 3.056 m/s

Velocity head

V²/(2g) = 3.056²/(2·9.81) = 0.4759 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.022·(50/0.05)·3.056²/(2·9.81) = 10.47 m

Answer

hf = 10.47 m
22.Pipe friction & head loss

Answer: H = 1.421 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 = 0.04/0.03142 = 1.273 m/s
V²/(2g) = 0.08263 m

Loss coefficients

f·L/D = 0.025·100/0.2 = 12.5
ΣK = 0.5 + 4·0.3 + 2 = 3.7

Energy equation

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

H = (1 + 12.5 + 3.7)·0.08263 = 1.421 m

Answer

H = 1.421 m
23.Pumps & pump power

Answer: η = 85.84 %

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 = 1000·9.81·0.01·14 = 1.373 kW

Efficiency

η = Ph/Pshaft = 1.373/1.6 = 85.84%

Answer

η = 85.84%
24.Pumps & pump power

Answer: H = 35.98 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 = 0.02/0.007854 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (22 + 4)·0.3305 = 8.593 m

Pressure head

p/(ρ·g) = 200000/(1000·9.81) = 20.39 m

Pump head

Both surfaces are practically at rest, so there is no velocity head term.

H = Δz + p/(ρ·g) + hL = 7 + 20.39 + 8.593 = 35.98 m

Answer

H = 35.98 m

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