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 1850 kg/h · 15% saltStream 2ṁ₂ = ? · 50% 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 = 850 kg/hx1 = 15 %x2 = 50 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1000 kg/h · 13% sugarProduct P60% 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 = 1000 kg/hxF = 13 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 140 °C60 °Cwater · 15 °Ct = ? °C

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

ṁh = 2.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 140 → 60 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 120 °C90 °Cwater · 15 °C50 °C · ṁ = ?10% lost

Hot glycol mix heats water in an exchanger that loses 10% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 120 → 90 °Ct: 15 → 50 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
60 g of HeV = 20 LT = 85 °CP = ?

A tank of 20 L contains 60 g of He at 85 °C. Treat it as an ideal gas and find the pressure P.

m = 60 gM = 4.003 g/molV = 20 LT = 85 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
Ar, M = 39.95 g/molP = 850 kPaT = 20 °Cρ = ?

Find the density ρ of Ar at 850 kPa and 20 °C, treating it as an ideal gas.

M = 39.95 g/molP = 850 kPaT = 20 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

8 g of H2 and 20 g of O2 react according to 2H2 + O2 → 2H2O. What mass m of H2O can form?

M(H2) = 2.016M(O2) = 32M(H2O) = 18.02 g/mol
m = g
8.StoichiometryHard
m(H2​)n(H2​)n(H2​O)m(H2​O)÷ M(H2​)× 2/2× M(H2​O)

In the reaction 2H2 + O2 → 2H2O, 30 g of H2 reacts completely (the other reactants are in excess) and 252.1 g of H2O is collected. Find the percent yield Y.

M(H2) = 2.016 g/molM(H2O) = 18.02 g/molactual: 252.1 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 = 36. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 36
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.5 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.5 mol/LKc = 0.5
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 150 gT = 190 °Cc = 0.388 J/(g·°C)Waterm = 300 gT = 22 °Cc = 4.18 J/(g·°C)

A 150 g block of zinc (c = 0.388 J/(g·°C)) at 190 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 22 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.388 J/(g·°C)Tmetal = 190 °Cmwater = 300 gTwater = 22 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l).

ΔH°f(C2H6) = −84.7 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 = ?90%

A zero-order reaction has k = 0.05 mol/(L·min) and starts at 0.8 mol/L. How long does it take to reach 90% conversion? Find t.

k = 0.05 mol/(L·min)CA0 = 0.8 mol/LX = 90 %
t = min
14.Reaction kineticsHard
Tk35 °C0.00575 °C0.144

The rate constant of a reaction is 0.005 min⁻¹ at 35 °C and 0.144 min⁻¹ at 75 °C. Find the activation energy Ea.

k1 = 0.005 min⁻¹T1 = 35 °Ck2 = 0.144 min⁻¹T2 = 75 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minCA0​ = 1 mol/LCA​ = ?V = 200 L, k = 0.15 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.15 min⁻¹) runs in a 200 L plug-flow reactor (PFR). The feed enters at 25 L/min with CA0 = 1 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 200 LQ = 25 L/mink = 0.15 min⁻¹CA0 = 1 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
V = 100 LV = 100 LQ = 25 L/minX = ?

A first-order liquid-phase reaction (k = 0.15 min⁻¹) runs in two equal CSTRs in series, each of 100 L. The feed rate is 25 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 100 L (×2)Q = 25 L/mink = 0.15 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT145 °C95 °C50 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 100 kW. Its heat transfer area is 2.5 m². The hot fluid cools from 145 to 95 °C and the cold fluid heats from 25 to 50 °C. Find the overall heat transfer coefficient U.

Q̇ = 100 kWA = 2.5 m²Th: 145 → 95 °CTc: 25 → 50 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT150 °C95 °C43.82 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.1 kJ/(kg·K)) cools from 150 to 95 °C in a counter-flow exchanger. It heats 3 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 300 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 150 → 95 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 300 W/(m²·K)
A = m²
19.Heat conductionMedium
Glass, k = 0.96200 mmExpanded polystyrene, k = 0.035100 mm24 °C1 °CTi​ = ?Q̇

A wall is made of 200 mm of glass and 100 mm of expanded polystyrene, with an area of 20 m². The outer faces are at 24 °C and 1 °C. Find the temperature Ti at the interface between the two layers.

L1 = 200 mm, k1 = 0.96 W/(m·K)L2 = 100 mm, k2 = 0.035 W/(m·K)A = 20 m²T1 = 24 °CT3 = 1 °C
Ti = °C
20.Heat conductionHard
Concrete, k = 1.4200 mmGlass, k = 0.9650 mmroom 21 °Coutside -12 °CTs​ = ?Q̇

A wall of 200 mm concrete and 50 mm glass separates a room at 21 °C from outside air at -12 °C. The convection coefficients are 10 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 12 m². Find the temperature Ts of the inside surface of the wall.

L1 = 200 mm, k1 = 1.4 W/(m·K)L2 = 50 mm, k2 = 0.96 W/(m·K)A = 12 m²hi = 10 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = -12 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 10 L/sD = 75 mmL = 800 mf = 0.02

Water flows at 10 L/s through a pipe 800 m long with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.02 and g = 9.81 m/s². Find the friction head loss hf.

Q = 10 L/sL = 800 mD = 75 mmf = 0.02g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2Δz = 23 mL = 300 m, D = 300 mm, f = 0.0222× bend (K = 0.3)

Two open reservoirs are joined by a pipe 300 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.022. The water surface of the upper reservoir is 23 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 2) 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 = 23 mL = 300 mD = 300 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 60 L/sH = 80 m

A pump with an efficiency of 85% delivers 60 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 = 60 L/sH = 80 mη = 85%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
300 kPa (gauge)PQ = 120 L/sΔz = 24 mL = 200 m, D = 250 mm, f = 0.02, ΣK = 8

A pump moves 120 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 24 m higher. The pipe is 200 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.02; the minor-loss coefficients add up to ΣK = 8 (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 300 kPa. Find the head H the pump must add.

Q = 120 L/sΔz = 24 mL = 200 mD = 250 mmf = 0.02ΣK = 8ptank = 300 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 340 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) = 850·(15 − 25)/(25 − 50) = 340 kg/h

Answer

ṁ2 = 340 kg/h
2.Mass balance

Answer: W = 783.3 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 = 1000·13/60 = 216.7 kg/h

Total balance

W = F − P = 1000 − 216.7 = 783.3 kg/h

Answer

W = 783.3 kg/h
3.Energy balance

Answer: tout = 115.5 °C

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

Heat released by the hot stream

Q = 2.5·2.1·(140 − 60) = 420 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 420/(1·4.18) = 115.5 °C

Answer

tout = 115.5 °C
4.Energy balance

Answer: ṁc = 0.9966 kg/s

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

Heat released

Qh = 1.5·3.6·(120 − 90) = 162 kW

Heat that reaches the water

Qc = (1 − 0.1)·162 = 145.8 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 145.8/(4.18·35) = 0.9966 kg/s

Answer

ṁc = 0.9966 kg/s
5.Ideal gas law

Answer: P = 2232 kPa

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

Moles

n = m/M = 60/4.003 = 14.99 mol
T = 85 + 273.15 = 358.1 K

Pressure

P = nRT/V = 14.99·8.314·358.1/0.02 = 2232 kPa

Answer

P = 2232 kPa
6.Ideal gas law

Answer: ρ = 13.93 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 20 + 273.15 = 293.1 K

Density

ρ = 850·39.95/(8.314·293.1) = 13.93 kg/m³

Answer

ρ = 13.93 kg/m³
7.Stoichiometry

Answer: m = 22.52 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(H2) = 8/2.016 = 3.968 mol
n(O2) = 20/32 = 0.625 mol

Limiting reactant

3.968/2 = 1.984, 0.625/1 = 0.625 → O2

Mass of product

n(H2O) = 0.625·2 = 1.25 mol
m = 1.25·18.02 = 22.52 g

Answer

m = 22.52 g
8.Stoichiometry

Answer: Y = 94 %

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(H2) = 30/2.016 = 14.88 mol
m = 14.88·2/2·18.02 = 268.2 g

Percent yield

Y = 252.1/268.2·100 = 94%

Answer

Y = 94%
9.Chemical equilibrium

Answer: [H2] = 0.1 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/(0.4 − x)²

Take the square root

6 = 2x/(0.4 − x) → x = 0.4·6/(2 + 6) = 0.3 mol/L

Equilibrium concentration

[H₂] = 0.4 − x = 0.1 mol/L

Answer

[H2] = 0.1 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.309 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

0.5 = x²/(0.5 − x) → x² + 0.5·x − 0.25 = 0

Solve the quadratic

x = (−0.5 + √(0.5² + 4·0.25))/2 = 0.309 mol/L

Equilibrium concentration

[Cl₂] = x = 0.309 mol/L

Answer

[Cl2] = 0.309 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 29.45 °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

150·0.388·(190 − Tf) = 300·4.18·(Tf − 22)

Solve for the final temperature

Tf = (58.2·190 + 1254·22)/(58.2 + 1254) = 29.45 °C

Answer

Tf = 29.45 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −3119 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° = [4·(−393.5) + 6·(−285.8)] − [2·(−84.7) + 7·0] = −3119 kJ

Answer

ΔH° = −3119 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 14.4 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 = 0.8·0.9 = 0.72 mol/L

Time

t = CA0·X/k = 0.72/0.05 = 14.4 min

Answer

t = 14.4 min
14.Reaction kinetics

Answer: Ea = 74.93 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 = 308.1 K, T2 = 348.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·3.36/(-3.728e-4) = 74932 J/mol
Ea = 74.93 kJ/mol

Answer

Ea = 74.93 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.3012 mol/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 = V/Q = 200/25 = 8 min

Outlet concentration

CA = 1·e−0.15·8 = 0.3012 mol/L

Answer

CA = 0.3012 mol/L

Conversion: X = 69.88%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 60.94 %

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 = 100/25 = 4 min, kτ = 0.15·4 = 0.6

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 0.6) = 0.625
C2/CA0 = 1/(1 + kτ)² = 0.3906
X = 1 − 0.3906 = 60.94%

Answer

X = 60.94%
17.Heat exchangers (LMTD)

Answer: U = 488.6 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 counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 145 − 50 = 95 K
ΔT₂ = Th,out − Tc,in = 95 − 25 = 70 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (95 − 70)/ln(95/70) = 81.86 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 100000/(2.5·81.86) = 488.6 W/(m²·K)

Answer

U = 488.6 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: A = 6.882 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) = 1.5·2.1·55 = 173.3 kW
Tc,out = 30 + 173.3/(3·4.18) = 43.82 °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 = 150 − 43.82 = 106.2 K
ΔT₂ = Th,out − Tc,in = 95 − 30 = 65 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (106.2 − 65)/ln(106.2/65) = 83.91 K

Area

A = Q̇/(U·ΔTlm) = 173250/(300·83.91) = 6.882 m²

Answer

A = 6.882 m²
19.Heat conduction

Answer: Ti = 22.44 °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) = (200/1000)/(0.96·20) = 0.01042 K/W
R2 = L2/(k2A) = (100/1000)/(0.035·20) = 0.1429 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 23/0.1533 = 150.1 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 24 − 150.1·0.01042 = 22.44 °C

Answer

Ti = 22.44 °C
20.Heat conduction

Answer: Ts = 11.43 °C

Thermal resistance: steady heat flow through layers in series behaves like current through resistors in series: Q̇ = ΔT/ΣR, with R = L/(kA) for a conducting layer and R = 1/(hA) for a convecting surface. The temperature drop across each layer is proportional to its resistance.

Resistances in series

Ri = 1/(hiA) = 1/(10·12) = 0.008333 K/W
R1 = L1/(k1A) = (200/1000)/(1.4·12) = 0.0119 K/W
R2 = L2/(k2A) = (50/1000)/(0.96·12) = 0.00434 K/W
Ro = 1/(hoA) = 1/(20·12) = 0.004167 K/W
ΣR = 0.02875 K/W

Heat loss

Q̇ = (21 − (-12))/0.02875 = 1148 W
Ts = Troom − Q̇·Ri = 21 − 1148·0.008333 = 11.43 °C

Answer

Ts = 11.43 °C
21.Pipe friction & head loss

Answer: hf = 55.71 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·0.075²/4 = 0.004418 m²
V = Q/A = 0.01/0.004418 = 2.264 m/s

Velocity head

V²/(2g) = 2.264²/(2·9.81) = 0.2611 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.02·(800/0.075)·2.264²/(2·9.81) = 55.71 m

Answer

hf = 55.71 m
22.Pipe friction & head loss

Answer: Q = 293.9 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 = 0.022·300/0.3 = 22
ΣK = 0.5 + 2·0.3 + 2 + 1.0 = 4.1

Energy equation

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

23 = (22 + 4.1)·V²/(2·9.81)
V = √(2·9.81·23/26.1) = 4.158 m/s

Flow rate

Q = V·π·D²/4 = 4.158·0.07069 = 0.2939 m³/s = 293.9 L/s

Answer

Q = 293.9 L/s
23.Pumps & pump power

Answer: Pshaft = 55.4 kW

Pump power: the power given to the water is the hydraulic power Ph = ρ·g·Q·H = Q·Δp. The shaft must deliver more because the pump loses some: Pshaft = Ph/ηpump, and the motor draws Pel = Pshaft/ηmotor. The pump head H follows from the energy equation: static lift + pressure head + all friction and minor losses.

Hydraulic power

Ph = ρ·g·Q·H = 1000·9.81·0.06·80 = 47.09 kW

Shaft power

Pshaft = Ph/η = 47.09/0.85 = 55.4 kW

Answer

Pshaft = 55.4 kW
24.Pumps & pump power

Answer: H = 61.89 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 = 0.12/0.04909 = 2.445 m/s
V²/(2g) = 0.3046 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (16 + 8)·0.3046 = 7.31 m

Pressure head

p/(ρ·g) = 300000/(1000·9.81) = 30.58 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 24 + 30.58 + 7.31 = 61.89 m

Answer

H = 61.89 m

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