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 1650 kg/h · 15% saltStream 2ṁ₂ = ? · 35% 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 = 650 kg/hx1 = 15 %x2 = 35 %x3 = 20 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4900 kg/h · 8% saltProduct P45% saltVapour W (pure water)W = ? kg/h

An evaporator concentrates a salt solution by boiling off pure water. Find the water evaporated W in kg/h.

F = 4900 kg/hxF = 8 %xP = 45 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 180 °C60 °Cwater · 30 °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: 180 → 60 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 170 °C60 °Cwater · 20 °C80 °C · ṁ = ?15% lost

Hot light oil heats water in an exchanger that loses 15% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 1 kg/scp,h = 2.1 kJ/(kg·K)Th: 170 → 60 °Ct: 20 → 80 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
100 g of ArV = 30 LT = 0 °CP = ?

A tank of 30 L contains 100 g of Ar at 0 °C. Treat it as an ideal gas and find the pressure P.

m = 100 gM = 39.95 g/molV = 30 LT = 0 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 400 kPa, 20 L, 15 °C to 100 kPa and 70 °C. Find the new volume V2.

P1 = 400 kPaV1 = 20 LT1 = 15 °CP2 = 100 kPaT2 = 70 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

12 g of Na and 10 g of Cl2 react according to 2Na + Cl2 → 2NaCl. What mass m of NaCl can form?

M(Na) = 22.99M(Cl2) = 70.9M(NaCl) = 58.44 g/mol
m = g
8.StoichiometryHard
m(CH4​)n(CH4​)n(H2​O)m(H2​O)÷ M(CH4​)× 2/1× M(H2​O)

In the reaction CH4 + 2O2 → CO2 + 2H2O, 16 g of CH4 reacts completely (the other reactants are in excess) and 31.64 g of H2O is collected. Find the percent yield Y.

M(CH4) = 16.04 g/molM(H2O) = 18.02 g/molactual: 31.64 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.50.50C−x−x+2xE0.5 − x0.5 − x2x

0.5 mol/L of H₂ and 0.5 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 49. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 49
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.5 mol/LKc = 0.2
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 50 gT = 100 °Cc = 0.385 J/(g·°C)Waterm = 400 gT = 16 °Cc = 4.18 J/(g·°C)

A 50 g block of copper (c = 0.385 J/(g·°C)) at 100 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 16 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.385 J/(g·°C)Tmetal = 100 °Cmwater = 400 gTwater = 16 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H25 g CH4​CH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 25 g of CH4 (M = 16.04 g/mol) burns completely: CH4 + 2O₂ → CO₂ + 2H₂O(l). Give q as a positive number.

ΔH°f(CH4) = −74.8 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 = 0.05 L/(mol·min) and an initial concentration of 1.5 mol/L. Find its first half-life t½.

k = 0.05 L/(mol·min)CA0 = 1.5 mol/L
t½ = min
14.Reaction kineticsHard
Tk20 °Ck1​?10·k1​

A reaction has an activation energy of 90 kJ/mol. At 20 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 10 times faster?

Ea = 90 kJ/molT1 = 20 °Ck2/k1 = 10R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minX = 90%V = ?, k = 0.15 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.15 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 90% conversion of A.

Q = 50 L/mink = 0.15 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 1500 LV = 1500 LQ = 50 L/minX = ?

A first-order liquid-phase reaction (k = 0.2 min⁻¹) runs in two equal CSTRs in series, each of 1500 L. The feed rate is 50 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 1500 L (×2)Q = 50 L/mink = 0.2 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT120 °C30 °C85 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 120 °C on the outside of the tubes. Cooling water (4 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 30 to 85 °C. The overall heat transfer coefficient is 2000 W/(m²·K). Find the heat transfer area A needed.

Ts = 120 °Cṁ = 4 kg/scp = 4.18 kJ/(kg·K)Tc: 30 → 85 °CU = 2000 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT95 °C45 °C33.34 °C15 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.3 kJ/(kg·K)) cools from 95 to 45 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 15 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.3 kJ/(kg·K)Th: 95 → 45 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 15 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Expanded polystyrene, k = 0.03550 mmMineral wool, k = 0.0450 mm24 °C-8 °CQ̇ = ?

A wall is made of 50 mm of expanded polystyrene and 50 mm of mineral wool, with an area of 15 m². The outer faces are at 24 °C and -8 °C. Find the heat flow Q̇ through the wall.

L1 = 50 mm, k1 = 0.035 W/(m·K)L2 = 50 mm, k2 = 0.04 W/(m·K)A = 15 m²T1 = 24 °CT3 = -8 °C
Q̇ = W
20.Heat conductionHard
Mineral wool, k = 0.0450 mmGlass, k = 0.96100 mmroom 22 °Coutside 1 °CQ̇

A wall of 50 mm mineral wool and 100 mm glass separates a room at 22 °C from outside air at 1 °C. The convection coefficients are 10 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 8 m². Find the overall heat transfer coefficient U of the wall.

L1 = 50 mm, k1 = 0.04 W/(m·K)L2 = 100 mm, k2 = 0.96 W/(m·K)A = 8 m²hi = 10 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = 1 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 3 m/sD = 150 mmL = 150 mf = 0.03

Water (ρ = 1000 kg/m³) flows at 3 m/s through a horizontal pipe, 150 m long, with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 3 m/sL = 150 mD = 150 mmf = 0.03ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 0.2Δz = 23 mL = 300 m, D = 250 mm, f = 0.0153× bend (K = 0.3)

Two open reservoirs are joined by a pipe 300 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.015. 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), 3 bends (K = 0.3 each), a valve (K = 0.2) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². Find the flow rate Q in L/s.

Δz = 23 mL = 300 mD = 250 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 0.2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 30 L/sH = 78 m

A pump with an efficiency of 65% delivers 30 L/s of water (ρ = 1000 kg/m³) against a head of 78 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 30 L/sH = 78 mη = 65%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
350 kPa (gauge)PQ = 80 L/sΔz = 13 mL = 150 m, D = 200 mm, f = 0.015, ΣK = 5

A pump moves 80 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 13 m higher. The pipe is 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.015; 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 350 kPa. Find the head H the pump must add.

Q = 80 L/sΔz = 13 mL = 150 mD = 200 mmf = 0.015ΣK = 5ptank = 350 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 216.7 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) = 650·(15 − 20)/(20 − 35) = 216.7 kg/h

Answer

ṁ2 = 216.7 kg/h
2.Mass balance

Answer: W = 4029 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 = 4900·8/45 = 871.1 kg/h

Total balance

W = F − P = 4900 − 871.1 = 4029 kg/h

Answer

W = 4029 kg/h
3.Energy balance

Answer: tout = 80.24 °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·(180 − 60) = 630 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 630/(3·4.18) = 80.24 °C

Answer

tout = 80.24 °C
4.Energy balance

Answer: ṁc = 0.7829 kg/s

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

Heat released

Qh = 1·2.1·(170 − 60) = 231 kW

Heat that reaches the water

Qc = (1 − 0.15)·231 = 196.3 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 196.3/(4.18·60) = 0.7829 kg/s

Answer

ṁc = 0.7829 kg/s
5.Ideal gas law

Answer: P = 189.5 kPa

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

Moles

n = m/M = 100/39.95 = 2.503 mol
T = 0 + 273.15 = 273.1 K

Pressure

P = nRT/V = 2.503·8.314·273.1/0.03 = 189.5 kPa

Answer

P = 189.5 kPa
6.Ideal gas law

Answer: V2 = 95.27 L

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

Absolute temperatures

T1 = 288.1 K, T2 = 343.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 20·(400/100)·(343.1/288.1) = 95.27 L

Answer

V2 = 95.27 L
7.Stoichiometry

Answer: m = 16.49 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(Na) = 12/22.99 = 0.522 mol
n(Cl2) = 10/70.9 = 0.141 mol

Limiting reactant

0.522/2 = 0.261, 0.141/1 = 0.141 → Cl2

Mass of product

n(NaCl) = 0.141·2 = 0.2821 mol
m = 0.2821·58.44 = 16.49 g

Answer

m = 16.49 g
8.Stoichiometry

Answer: Y = 88.01 %

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(CH4) = 16/16.04 = 0.9975 mol
m = 0.9975·2/1·18.02 = 35.95 g

Percent yield

Y = 31.64/35.95·100 = 88.01%

Answer

Y = 88.01%
9.Chemical equilibrium

Answer: [HI] = 0.7778 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

49 = (2x)²/(0.5 − x)²

Take the square root

7 = 2x/(0.5 − x) → x = 0.5·7/(2 + 7) = 0.3889 mol/L

Equilibrium concentration

[HI] = 2x = 0.7778 mol/L

Answer

[HI] = 0.7778 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.2683 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/(0.5 − x) → x² + 0.2·x − 0.1 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.1))/2 = 0.2317 mol/L

Equilibrium concentration

[PCl₅] = 0.5 − 0.2317 = 0.2683 mol/L

Answer

[PCl5] = 0.2683 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 16.96 °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) = 400·4.18·(Tf − 16)

Solve for the final temperature

Tf = (19.25·100 + 1672·16)/(19.25 + 1672) = 16.96 °C

Answer

Tf = 16.96 °C
12.Calorimetry & enthalpy

Answer: q = 1388 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° = [1·(−393.5) + 2·(−285.8)] − [1·(−74.8) + 2·0] = −890.3 kJ

Heat for the given mass

n = 25/16.04 = 1.559 mol
q = n·|ΔH°/1| = 1.559·890.3 = 1388 kJ

Answer

q = 1388 kJ
13.Reaction kinetics

Answer: t½ = 13.33 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/(0.05·1.5) = 13.33 min

Answer

t½ = 13.33 min

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

14.Reaction kinetics

Answer: T2 = 39.5 °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(10)/90000 = 3.411 × 10⁻³ − 2.127 × 10⁻⁴ = 3.199 × 10⁻³ K⁻¹
T2 = 312.6 K = 39.5 °C

Answer

T2 = 39.5 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 767.5 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 − 0.9))/0.15 = 2.303/0.15 = 15.35 min

Volume

V = Q·τ = 50·15.35 = 767.5 L

Answer

V = 767.5 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 97.96 %

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 = 1500/50 = 30 min, kτ = 0.2·30 = 6

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 6) = 0.1429
C2/CA0 = 1/(1 + kτ)² = 0.02041
X = 1 − 0.02041 = 97.96%

Answer

X = 97.96%
17.Heat exchangers (LMTD)

Answer: A = 7.896 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 from the water side

Q̇ = 4·4.18·(85 − 30) = 919.6 kW

End temperature differences

ΔT₁ = 120 − 30 = 90 K
ΔT₂ = 120 − 85 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (90 − 35)/ln(90/35) = 58.23 K

Area

A = Q̇/(U·ΔTlm) = 919600/(2000·58.23) = 7.896 m²

Answer

A = 7.896 m²
18.Heat exchangers (LMTD)

Answer: A = 1.745 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) = 1·2.3·50 = 115 kW
Tc,out = 15 + 115/(1.5·4.18) = 33.34 °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 = 95 − 33.34 = 61.66 K
ΔT₂ = Th,out − Tc,in = 45 − 15 = 30 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (61.66 − 30)/ln(61.66/30) = 43.94 K

Area

A = Q̇/(U·ΔTlm) = 115000/(1500·43.94) = 1.745 m²

Answer

A = 1.745 m²
19.Heat conduction

Answer: Q̇ = 179.2 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) = (50/1000)/(0.035·15) = 0.09524 K/W
R2 = L2/(k2A) = (50/1000)/(0.04·15) = 0.08333 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 32/0.1786 = 179.2 W

Answer

Q̇ = 179.2 W
20.Heat conduction

Answer: U = 0.6648 W/(m²·K)

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/(10·8) = 0.0125 K/W
R1 = L1/(k1A) = (50/1000)/(0.04·8) = 0.1563 K/W
R2 = L2/(k2A) = (100/1000)/(0.96·8) = 0.01302 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.188 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(8·0.188) = 0.6648 W/(m²·K)

Answer

U = 0.6648 W/(m²·K)
21.Pipe friction & head loss

Answer: Δp = 135 kPa

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.

Head loss

hf = f·(L/D)·V²/(2g) = 0.03·(150/0.15)·3²/(2·9.81) = 13.76 m

Pressure drop

The pipe is horizontal and the velocity does not change, so the energy equation reduces to Δp = ρ·g·hf.

Δp = ρ·g·hf = 1000·9.81·13.76 = 135000 Pa = 135 kPa

Answer

Δp = 135 kPa
22.Pipe friction & head loss

Answer: Q = 229.7 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 = 0.015·300/0.25 = 18
ΣK = 0.5 + 3·0.3 + 0.2 + 1.0 = 2.6

Energy equation

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

23 = (18 + 2.6)·V²/(2·9.81)
V = √(2·9.81·23/20.6) = 4.68 m/s

Flow rate

Q = V·π·D²/4 = 4.68·0.04909 = 0.2297 m³/s = 229.7 L/s

Answer

Q = 229.7 L/s
23.Pumps & pump power

Answer: Pshaft = 35.32 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 = 1000·9.81·0.03·78 = 22.96 kW

Shaft power

Pshaft = Ph/η = 22.96/0.65 = 35.32 kW

Answer

Pshaft = 35.32 kW
24.Pumps & pump power

Answer: H = 54.05 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 = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (11.25 + 5)·0.3305 = 5.371 m

Pressure head

p/(ρ·g) = 350000/(1000·9.81) = 35.68 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 13 + 35.68 + 5.371 = 54.05 m

Answer

H = 54.05 m

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