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 1450 kg/h · 35% saltStream 2ṁ₂ = ? · 10% saltProduct20% salt

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

ṁ1 = 450 kg/hx1 = 35 %x2 = 10 %x3 = 20 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3700 kg/h · 11% saltProduct PP = ? · 30%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 = 3700 kg/hxF = 11 %xP = 30 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 140 °C70 °Cwater · 25 °Ct = ? °C

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

ṁh = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 140 → 70 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 160 °C80 °Cwater · 25 °C60 °C · ṁ = ?10% lost

Hot light oil 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 = 2.1 kJ/(kg·K)Th: 160 → 80 °Ct: 25 → 60 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
430 g of CO₂V = 50 LT = 45 °CP = ?

A tank of 50 L contains 430 g of CO₂ at 45 °C. Treat it as an ideal gas and find the pressure P.

m = 430 gM = 44.01 g/molV = 50 LT = 45 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
O₂, M = 32 g/molP = 650 kPaT = 160 °Cρ = ?

Find the density ρ of O₂ at 650 kPa and 160 °C, treating it as an ideal gas.

M = 32 g/molP = 650 kPaT = 160 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(Fe)m(Fe)÷ M(X)× 2/ν× M(Fe)

8 g of Fe2O3 and 80 g of CO react according to Fe2O3 + 3CO → 2Fe + 3CO2. What mass m of Fe can form?

M(Fe2O3) = 159.69M(CO) = 28.01M(Fe) = 55.85 g/mol
m = g
8.StoichiometryHard
m(C3​H8​)n(C3​H8​)n(H2​O)m(H2​O)÷ M(C3​H8​)× 4/1× M(H2​O)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 4 g of C3H8 reacts completely (the other reactants are in excess) and 5.56 g of H2O is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 5.56 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 = 25. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 25
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.1 mol/LKc = 0.2
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 50 gT = 100 °Cc = 0.385 J/(g·°C)Waterm = 200 gT = 15 °Cc = 4.18 J/(g·°C)

A 50 g block of copper (c = 0.385 J/(g·°C)) at 100 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 15 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.385 J/(g·°C)Tmetal = 100 °Cmwater = 200 gTwater = 15 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H50 g C4​H10​2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 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)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.1 L/(mol·min) and an initial concentration of 0.5 mol/L. Find its first half-life t½.

k = 0.1 L/(mol·min)CA0 = 0.5 mol/L
t½ = min
14.Reaction kineticsHard
1/Tln kT = 40 °Cln 0.02ln A = ?Ea​ = 75 kJ/mol

A first-order reaction has a rate constant of 0.02 s⁻¹ at 40 °C and an activation energy of 75 kJ/mol. Find the pre-exponential factor A in the Arrhenius equation.

k = 0.02 s⁻¹T = 40 °CEa = 75 kJ/molR = 8.314 J/(mol·K)
A = s⁻¹
15.Reactor sizing (CSTR & PFR)Medium
QX = 50%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 50% conversion. How many times larger must a CSTR be than a PFR for the same feed rate, rate constant and conversion? Find the ratio VCSTR/VPFR.

X = 50%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
V = 800 LQ = 100 L/minX = ?

A first-order liquid-phase reaction (k = 0.5 min⁻¹) runs in an 800 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 = 800 LQ = 100 L/mink = 0.5 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT170 °C35 °C55 °C15 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 320 kW. The hot fluid cools from 170 to 35 °C and the cold fluid heats from 15 to 55 °C. The overall heat transfer coefficient is 1500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 320 kWU = 1500 W/(m²·K)Th: 170 → 35 °CTc: 15 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT100 °C40 °C55.89 °C20 °CΔT₁ΔT₂counter-flow

Hot oil (2 kg/s, cp = 2.5 kJ/(kg·K)) cools from 100 to 40 °C in a counter-flow exchanger. It heats 2 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 20 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 2 kg/scp,h = 2.5 kJ/(kg·K)Th: 100 → 40 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 20 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Mineral wool, k = 0.04100 mmExpanded polystyrene, k = 0.03575 mm22 °C-5 °CQ̇ = ?

A wall is made of 100 mm of mineral wool and 75 mm of expanded polystyrene, with an area of 15 m². The outer faces are at 22 °C and -5 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.04 W/(m·K)L2 = 75 mm, k2 = 0.035 W/(m·K)A = 15 m²T1 = 22 °CT3 = -5 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.035150 mmGlass, k = 0.96150 mmroom 21 °Coutside -9 °CTs​ = ?Q̇

A wall of 150 mm expanded polystyrene and 150 mm glass separates a room at 21 °C from outside air at -9 °C. The convection coefficients are 8 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 6 m². Find the temperature Ts of the inside surface of the wall.

L1 = 150 mm, k1 = 0.035 W/(m·K)L2 = 150 mm, k2 = 0.96 W/(m·K)A = 6 m²hi = 8 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = -9 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 40 L/sD = 200 mmL = 100 mf = 0.015

Water flows at 40 L/s through a pipe 100 m long with an inside diameter of 200 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the friction head loss hf.

Q = 40 L/sL = 100 mD = 200 mmf = 0.015g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10Δz = 26 mL = 150 m, D = 150 mm, f = 0.0222× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.022. The water surface of the upper reservoir is 26 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 = 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 = 26 mL = 150 mD = 150 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 10Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 150 L/sH = 32 m

A pump with an efficiency of 80% delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 32 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 150 L/sH = 32 mη = 80%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
100 kPa (gauge)PQ = 120 L/sΔz = 7 mL = 100 m, D = 250 mm, f = 0.022, ΣK = 5

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 7 m higher. The pipe is 100 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.022; the minor-loss coefficients add up to ΣK = 5 (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 100 kPa. Find the head H the pump must add.

Q = 120 L/sΔz = 7 mL = 100 mD = 250 mmf = 0.022ΣK = 5ptank = 100 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 675 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) = 450·(35 − 20)/(20 − 10) = 675 kg/h

Answer

ṁ2 = 675 kg/h
2.Mass balance

Answer: P = 1357 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 = 3700·11/30 = 1357 kg/h

Answer

P = 1357 kg/h
3.Energy balance

Answer: tout = 55.14 °C

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

Heat released by the hot stream

Q = 1.5·3.6·(140 − 70) = 378 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 378/(3·4.18) = 55.14 °C

Answer

tout = 55.14 °C
4.Energy balance

Answer: ṁc = 1.55 kg/s

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

Heat released

Qh = 1.5·2.1·(160 − 80) = 252 kW

Heat that reaches the water

Qc = (1 − 0.1)·252 = 226.8 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 226.8/(4.18·35) = 1.55 kg/s

Answer

ṁc = 1.55 kg/s
5.Ideal gas law

Answer: P = 516.9 kPa

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

Moles

n = m/M = 430/44.01 = 9.771 mol
T = 45 + 273.15 = 318.1 K

Pressure

P = nRT/V = 9.771·8.314·318.1/0.05 = 516.9 kPa

Answer

P = 516.9 kPa
6.Ideal gas law

Answer: ρ = 5.776 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 160 + 273.15 = 433.1 K

Density

ρ = 650·32/(8.314·433.1) = 5.776 kg/m³

Answer

ρ = 5.776 kg/m³
7.Stoichiometry

Answer: m = 5.596 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(Fe2O3) = 8/159.69 = 0.0501 mol
n(CO) = 80/28.01 = 2.856 mol

Limiting reactant

0.0501/1 = 0.0501, 2.856/3 = 0.952 → Fe2O3

Mass of product

n(Fe) = 0.0501·2 = 0.1002 mol
m = 0.1002·55.85 = 5.596 g

Answer

m = 5.596 g
8.Stoichiometry

Answer: Y = 85.04 %

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(C3H8) = 4/44.1 = 0.0907 mol
m = 0.0907·4/1·18.02 = 6.538 g

Percent yield

Y = 5.56/6.538·100 = 85.04%

Answer

Y = 85.04%
9.Chemical equilibrium

Answer: [HI] = 0.5714 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

25 = (2x)²/(0.4 − x)²

Take the square root

5 = 2x/(0.4 − x) → x = 0.4·5/(2 + 5) = 0.2857 mol/L

Equilibrium concentration

[HI] = 2x = 0.5714 mol/L

Answer

[HI] = 0.5714 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.02679 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/(0.1 − x) → x² + 0.2·x − 0.02 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.02))/2 = 0.07321 mol/L

Equilibrium concentration

[PCl₅] = 0.1 − 0.07321 = 0.02679 mol/L

Answer

[PCl5] = 0.02679 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 16.91 °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

50·0.385·(100 − Tf) = 200·4.18·(Tf − 15)

Solve for the final temperature

Tf = (19.25·100 + 836·15)/(19.25 + 836) = 16.91 °C

Answer

Tf = 16.91 °C
12.Calorimetry & enthalpy

Answer: q = 2475 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 = 50/58.12 = 0.8603 mol
q = n·|ΔH°/2| = 0.8603·2877 = 2475 kJ

Answer

q = 2475 kJ
13.Reaction kinetics

Answer: t½ = 20 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/(0.1·0.5) = 20 min

Answer

t½ = 20 min

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

14.Reaction kinetics

Answer: A = 6.483 × 10¹⁰ s⁻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 temperature

T = 40 + 273.15 = 313.1 K

Solve Arrhenius for A

Ea/(RT) = 75000/(8.314·313.1) = 28.81
A = k·e28.81 = 0.02·3.241 × 10¹² = 6.483 × 10¹⁰ s⁻¹

Answer

A = 6.483 × 10¹⁰ s⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 1.443

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.

k·τ for each reactor

CSTR: k·τ = X/(1 − X) = 0.5/0.5 = 1
PFR: k·τ = ln(1/(1 − X)) = ln(2) = 0.6931

Ratio of volumes

VCSTR/VPFR = 1/0.6931 = 1.443

Answer

VCSTR/VPFR = 1.443

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 80 %

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 = 800/100 = 8 min, kτ = 0.5·8 = 4

Conversion

X = kτ/(1 + kτ) = 4/(1 + 4) = 80%

Answer

X = 80%
17.Heat exchangers (LMTD)

Answer: A = 3.928 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 = 170 − 55 = 115 K
ΔT₂ = Th,out − Tc,in = 35 − 15 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (115 − 20)/ln(115/20) = 54.31 K

Area

A = Q̇/(U·ΔTlm) = 320000/(1500·54.31) = 3.928 m²

Answer

A = 3.928 m²
18.Heat exchangers (LMTD)

Answer: A = 6.561 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) = 2·2.5·60 = 300 kW
Tc,out = 20 + 300/(2·4.18) = 55.89 °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 − 55.89 = 44.11 K
ΔT₂ = Th,out − Tc,in = 40 − 20 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (44.11 − 20)/ln(44.11/20) = 30.48 K

Area

A = Q̇/(U·ΔTlm) = 300000/(1500·30.48) = 6.561 m²

Answer

A = 6.561 m²
19.Heat conduction

Answer: Q̇ = 87.23 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) = (100/1000)/(0.04·15) = 0.1667 K/W
R2 = L2/(k2A) = (75/1000)/(0.035·15) = 0.1429 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 27/0.3095 = 87.23 W

Answer

Q̇ = 87.23 W
20.Heat conduction

Answer: Ts = 20.19 °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/(8·6) = 0.02083 K/W
R1 = L1/(k1A) = (150/1000)/(0.035·6) = 0.7143 K/W
R2 = L2/(k2A) = (150/1000)/(0.96·6) = 0.02604 K/W
Ro = 1/(hoA) = 1/(20·6) = 0.008333 K/W
ΣR = 0.7695 K/W

Heat loss

Q̇ = (21 − (-9))/0.7695 = 38.99 W
Ts = Troom − Q̇·Ri = 21 − 38.99·0.02083 = 20.19 °C

Answer

Ts = 20.19 °C
21.Pipe friction & head loss

Answer: hf = 0.6197 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·0.2²/4 = 0.03142 m²
V = Q/A = 0.04/0.03142 = 1.273 m/s

Velocity head

V²/(2g) = 1.273²/(2·9.81) = 0.08263 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.015·(100/0.2)·1.273²/(2·9.81) = 0.6197 m

Answer

hf = 0.6197 m
22.Pipe friction & head loss

Answer: Q = 68.35 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 = 0.022·150/0.15 = 22
ΣK = 0.5 + 2·0.3 + 10 + 1.0 = 12.1

Energy equation

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

26 = (22 + 12.1)·V²/(2·9.81)
V = √(2·9.81·26/34.1) = 3.868 m/s

Flow rate

Q = V·π·D²/4 = 3.868·0.01767 = 0.06835 m³/s = 68.35 L/s

Answer

Q = 68.35 L/s
23.Pumps & pump power

Answer: Pshaft = 58.86 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 = 1000·9.81·0.15·32 = 47.09 kW

Shaft power

Pshaft = Ph/η = 47.09/0.8 = 58.86 kW

Answer

Pshaft = 58.86 kW
24.Pumps & pump power

Answer: H = 21.4 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) = (8.8 + 5)·0.3046 = 4.203 m

Pressure head

p/(ρ·g) = 100000/(1000·9.81) = 10.19 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 7 + 10.19 + 4.203 = 21.4 m

Answer

H = 21.4 m

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