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 · 40% NaOHStream 2ṁ₂ = ? · 10% 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 = 950 kg/hx1 = 40 %x2 = 10 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2600 kg/h · 19% sugarProduct P35% 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 = 2600 kg/hxF = 19 %xP = 35 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 120 °C70 °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: 120 → 70 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 170 °C70 °Cwater · 30 °C45 °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 = 2.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 170 → 70 °Ct: 30 → 45 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
70 g of O₂P = 450 kPaT = 45 °CV = ?

What volume V does 70 g of O₂ occupy at 450 kPa and 45 °C? Treat it as an ideal gas.

m = 70 gM = 32 g/molP = 450 kPaT = 45 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
He, M = 4.003 g/molP = 350 kPaT = 20 °Cρ = ?

Find the density ρ of He at 350 kPa and 20 °C, treating it as an ideal gas.

M = 4.003 g/molP = 350 kPaT = 20 °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​)

20 g of Al and 40 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(CaCO3​)n(CaCO3​)n(CaO)m(CaO)÷ M(CaCO3​)× 1/1× M(CaO)

In the reaction CaCO3 → CaO + CO2, 6 g of CaCO3 reacts completely (the other reactants are in excess) and 3.16 g of CaO is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CaO) = 56.08 g/molactual: 3.16 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.20.20C−x−x+2xE0.2 − x0.2 − x2x

0.2 mol/L of H₂ and 0.2 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 16
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.800C−x+x+xE0.8 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 at the reaction temperature. A container starts with 0.8 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.8 mol/LKc = 0.05
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 50 gT = 110 °Cc = 0.388 J/(g·°C)Waterm = 150 gT = 18 °Cc = 4.18 J/(g·°C)

A 50 g block of zinc (c = 0.388 J/(g·°C)) at 110 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 18 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.388 J/(g·°C)Tmetal = 110 °Cmwater = 150 gTwater = 18 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H50 g C6​H12​O6​C6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 g of C6H12O6 (M = 180.16 g/mol) burns completely: C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C6H12O6) = −1274 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)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.25 L/(mol·min) and an initial concentration of 1 mol/L. Find its first half-life t½.

k = 0.25 L/(mol·min)CA0 = 1 mol/L
t½ = min
14.Reaction kineticsHard
Tk20 °Ck1​?3·k1​

A reaction has an activation energy of 55 kJ/mol. At 20 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 3 times faster?

Ea = 55 kJ/molT1 = 20 °Ck2/k1 = 3R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 L/minX = 95%V = ?, k = 0.08 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.08 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 95% conversion of A.

Q = 80 L/mink = 0.08 min⁻¹X = 95%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 800 LQ = 40 L/minX = ?

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in an 800 L CSTR fed at 40 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 800 LQ = 40 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT125 °C95 °C20 °C60 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 230 kW. The hot fluid cools from 125 to 95 °C and the cold fluid heats from 20 to 60 °C. The overall heat transfer coefficient is 500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 230 kWU = 500 W/(m²·K)Th: 125 → 95 °CTc: 20 → 60 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT100 °C60 °C?25 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.2 kg/s, cp = 2.3 kJ/(kg·K)) flows in the inner tube and cools from 100 to 60 °C. Water (0.5 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 25 °C. The inner tube has a diameter of 40 mm, and U = 250 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.2 kg/scp,h = 2.3 kJ/(kg·K)Th: 100 → 60 °Cṁc = 0.5 kg/sTc,in = 25 °CD = 40 mmU = 250 W/(m²·K)
L = m
19.Heat conductionMedium
Glass, k = 0.9650 mmMineral wool, k = 0.0475 mm16 °C-5 °CTi​ = ?Q̇

A wall is made of 50 mm of glass and 75 mm of mineral wool, with an area of 20 m². The outer faces are at 16 °C and -5 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 0.96 W/(m·K)L2 = 75 mm, k2 = 0.04 W/(m·K)A = 20 m²T1 = 16 °CT3 = -5 °C
Ti = °C
20.Heat conductionHard
Expanded polystyrene, k = 0.035150 mmConcrete, k = 1.450 mmroom 21 °Coutside -11 °CTs​ = ?Q̇

A wall of 150 mm expanded polystyrene and 50 mm concrete separates a room at 21 °C from outside air at -11 °C. The convection coefficients are 7.7 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 4 m². Find the temperature Ts of the inside surface of the wall.

L1 = 150 mm, k1 = 0.035 W/(m·K)L2 = 50 mm, k2 = 1.4 W/(m·K)A = 4 m²hi = 7.7 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = -11 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 10 L/sD = 75 mmL = 800 mf = 0.025

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 = 0.025 and g = 9.81 m/s². Find the friction head loss hf.

Q = 10 L/sL = 800 mD = 75 mmf = 0.025g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10Δz = 30 mL = 200 m, D = 300 mm, f = 0.0253× bend (K = 0.3)

Two open reservoirs are joined by a pipe 200 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.025. The water surface of the upper reservoir is 30 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 3 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 = 30 mL = 200 mD = 300 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 10Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 150 L/sH = 56 m

A pump delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 56 m. The pump efficiency is 72% and the electric motor driving it has an efficiency of 92%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 150 L/sH = 56 mηpump = 72%ηmotor = 92%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 17 mL = 150 m, D = 200 mm, f = 0.018, ΣK = 6

A pump moves 75 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 17 m higher. The pipe is 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.018; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 75 L/sΔz = 17 mL = 150 mD = 200 mmf = 0.018ΣK = 6
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 475 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) = 950·(40 − 30)/(30 − 10) = 475 kg/h

Answer

ṁ2 = 475 kg/h
2.Mass balance

Answer: W = 1189 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 = 2600·19/35 = 1411 kg/h

Total balance

W = F − P = 2600 − 1411 = 1189 kg/h

Answer

W = 1189 kg/h
3.Energy balance

Answer: tout = 32.3 °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·(120 − 70) = 61 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 61/(2·4.18) = 32.3 °C

Answer

tout = 32.3 °C
4.Energy balance

Answer: ṁc = 13.64 kg/s

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

Heat released

Qh = 2.5·3.6·(170 − 70) = 900 kW

Heat that reaches the water

Qc = (1 − 0.05)·900 = 855 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 855/(4.18·15) = 13.64 kg/s

Answer

ṁc = 13.64 kg/s
5.Ideal gas law

Answer: V = 12.86 L

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

Moles

n = 70/32 = 2.188 mol
T = 45 + 273.15 = 318.1 K

Volume

V = nRT/P = 2.188·8.314·318.1/450 = 12.86 L

Answer

V = 12.86 L
6.Ideal gas law

Answer: ρ = 0.5748 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 = 350·4.003/(8.314·293.1) = 0.5748 kg/m³

Answer

ρ = 0.5748 kg/m³
7.Stoichiometry

Answer: m = 50.15 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) = 20/26.98 = 0.7413 mol
n(Cl2) = 40/70.9 = 0.5642 mol

Limiting reactant

0.7413/2 = 0.3706, 0.5642/3 = 0.1881 → Cl2

Mass of product

n(AlCl3) = 0.1881·2 = 0.3761 mol
m = 0.3761·133.33 = 50.15 g

Answer

m = 50.15 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(CaCO3) = 6/100.09 = 0.05995 mol
m = 0.05995·1/1·56.08 = 3.362 g

Percent yield

Y = 3.16/3.362·100 = 94%

Answer

Y = 94%
9.Chemical equilibrium

Answer: [H2] = 0.06667 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

16 = (2x)²/(0.2 − x)²

Take the square root

4 = 2x/(0.2 − x) → x = 0.2·4/(2 + 4) = 0.1333 mol/L

Equilibrium concentration

[H₂] = 0.2 − x = 0.06667 mol/L

Answer

[H2] = 0.06667 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.6234 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

0.05 = x²/(0.8 − x) → x² + 0.05·x − 0.04 = 0

Solve the quadratic

x = (−0.05 + √(0.05² + 4·0.04))/2 = 0.1766 mol/L

Equilibrium concentration

[PCl₅] = 0.8 − 0.1766 = 0.6234 mol/L

Answer

[PCl5] = 0.6234 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 20.76 °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

50·0.388·(110 − Tf) = 150·4.18·(Tf − 18)

Solve for the final temperature

Tf = (19.4·110 + 627·18)/(19.4 + 627) = 20.76 °C

Answer

Tf = 20.76 °C
12.Calorimetry & enthalpy

Answer: q = 777.6 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

Heat for the given mass

n = 50/180.16 = 0.2775 mol
q = n·|ΔH°/1| = 0.2775·2802 = 777.6 kJ

Answer

q = 777.6 kJ
13.Reaction kinetics

Answer: t½ = 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).

Second-order half-life

t½ = 1/(k·CA0) = 1/(0.25·1) = 4 min

Answer

t½ = 4 min

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

14.Reaction kinetics

Answer: T2 = 35 °C

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 temperature

T1 = 293.1 K

Solve Arrhenius for T₂

1/T2 = 1/293.1 − 8.314·ln(3)/55000 = 3.411 × 10⁻³ − 1.661 × 10⁻⁴ = 3.245 × 10⁻³ K⁻¹
T2 = 308.2 K = 35 °C

Answer

T2 = 35 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 2996 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))/0.08 = 2.996/0.08 = 37.45 min

Volume

V = Q·τ = 80·37.45 = 2996 L

Answer

V = 2996 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 66.67 %

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 = 800/40 = 20 min, kτ = 0.1·20 = 2

Conversion

X = kτ/(1 + kτ) = 2/(1 + 2) = 66.67%

Answer

X = 66.67%
17.Heat exchangers (LMTD)

Answer: A = 7.219 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 = 125 − 20 = 105 K
ΔT₂ = Th,out − Tc,out = 95 − 60 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (105 − 35)/ln(105/35) = 63.72 K

Area

A = Q̇/(U·ΔTlm) = 230000/(500·63.72) = 7.219 m²

Answer

A = 7.219 m²
18.Heat exchangers (LMTD)

Answer: L = 11.96 m

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 = 0.2·2.3·(100 − 60) = 18.4 kW
Tc,out = 25 + 18.4/(0.5·4.18) = 33.8 °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 = 100 − 33.8 = 66.2 K
ΔT₂ = Th,out − Tc,in = 60 − 25 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (66.2 − 35)/ln(66.2/35) = 48.95 K

Area and length

A = 18400/(250·48.95) = 1.503 m²
L = A/(πD) = 1.503/(π·0.04) = 11.96 m

Answer

L = 11.96 m
19.Heat conduction

Answer: Ti = 15.43 °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.

Layer resistances

R1 = L1/(k1A) = (50/1000)/(0.96·20) = 0.002604 K/W
R2 = L2/(k2A) = (75/1000)/(0.04·20) = 0.09375 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 21/0.09635 = 217.9 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 16 − 217.9·0.002604 = 15.43 °C

Answer

Ti = 15.43 °C
20.Heat conduction

Answer: Ts = 20.08 °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/(7.7·4) = 0.03247 K/W
R1 = L1/(k1A) = (150/1000)/(0.035·4) = 1.071 K/W
R2 = L2/(k2A) = (50/1000)/(1.4·4) = 0.008929 K/W
Ro = 1/(hoA) = 1/(20·4) = 0.0125 K/W
ΣR = 1.125 K/W

Heat loss

Q̇ = (21 − (-11))/1.125 = 28.44 W
Ts = Troom − Q̇·Ri = 21 − 28.44·0.03247 = 20.08 °C

Answer

Ts = 20.08 °C
21.Pipe friction & head loss

Answer: hf = 69.64 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) = 0.025·(800/0.075)·2.264²/(2·9.81) = 69.64 m

Answer

hf = 69.64 m
22.Pipe friction & head loss

Answer: Q = 318.1 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 = 0.025·200/0.3 = 16.67
ΣK = 0.5 + 3·0.3 + 10 + 1.0 = 12.4

Energy equation

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

30 = (16.67 + 12.4)·V²/(2·9.81)
V = √(2·9.81·30/29.07) = 4.5 m/s

Flow rate

Q = V·π·D²/4 = 4.5·0.07069 = 0.3181 m³/s = 318.1 L/s

Answer

Q = 318.1 L/s
23.Pumps & pump power

Answer: Pel = 124.4 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 = 1000·9.81·0.15·56 = 82.4 kW

Shaft power

Pshaft = 82.4/0.72 = 114.5 kW

Electrical power

Pel = 114.5/0.92 = 124.4 kW

Answer

Pel = 124.4 kW
24.Pumps & pump power

Answer: H = 22.66 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 = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (13.5 + 6)·0.2905 = 5.664 m

Pump head

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

H = Δz + hL = 17 + 5.664 = 22.66 m

Answer

H = 22.66 m

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