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 1350 kg/h · 20% NaOHStream 2ṁ₂ = ? · 35% NaOHProduct25% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 25% NaOH? Find ṁ2.

ṁ1 = 350 kg/hx1 = 20 %x2 = 35 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3300 kg/h · 16% 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 = 3300 kg/hxF = 16 %xP = 35 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 180 °C120 °Cwater · 20 °Ct = ? °C

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

ṁh = 0.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 180 → 120 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 120 °C70 °Cwater · 10 °C75 °C · ṁ = ?15% lost

Hot ethanol 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 = 2.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 120 → 70 °Ct: 10 → 75 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
60 g of O₂V = 30 LT = 50 °CP = ?

A tank of 30 L contains 60 g of O₂ at 50 °C. Treat it as an ideal gas and find the pressure P.

m = 60 gM = 32 g/molV = 30 LT = 50 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
CO₂, M = 44.01 g/molP = 750 kPaT = 170 °Cρ = ?

Find the density ρ of CO₂ at 750 kPa and 170 °C, treating it as an ideal gas.

M = 44.01 g/molP = 750 kPaT = 170 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

16 g of Na and 16 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, 4 g of CH4 reacts completely (the other reactants are in excess) and 7.01 g of H2O is collected. Find the percent yield Y.

M(CH4) = 16.04 g/molM(H2O) = 18.02 g/molactual: 7.01 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.250.250C−x−x+2xE0.25 − x0.25 − x2x

0.25 mol/L of H₂ and 0.25 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 25. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 25
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 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 = 0.08
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 250 gT = 180 °Cc = 0.449 J/(g·°C)Waterm = 400 gT = 21 °Cc = 4.18 J/(g·°C)

A 250 g block of iron (c = 0.449 J/(g·°C)) at 180 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 21 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.449 J/(g·°C)Tmetal = 180 °Cmwater = 400 gTwater = 21 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H250 g C4​H10​2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 250 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 0.8 mol/L. Find its first half-life t½.

k = 0.1 L/(mol·min)CA0 = 0.8 mol/L
t½ = min
14.Reaction kineticsHard
1/Tln kT = 30 °Cln 0.002ln A = ?Ea​ = 75 kJ/mol

A first-order reaction has a rate constant of 0.002 s⁻¹ at 30 °C and an activation energy of 75 kJ/mol. Find the pre-exponential factor A in the Arrhenius equation.

k = 0.002 s⁻¹T = 30 °CEa = 75 kJ/molR = 8.314 J/(mol·K)
A = s⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minX = 60%V = ?, k = 0.25 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.25 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 25 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 60% conversion of A.

Q = 25 L/mink = 0.25 min⁻¹X = 60%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 50 L/minX = ?V = 200 L

A first-order liquid-phase reaction (k = 0.4 min⁻¹) runs in a 200 L plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 50 L/mink = 0.4 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT115 °C35 °C55 °C15 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 490 kW. The hot fluid cools from 115 to 35 °C and the cold fluid heats from 15 to 55 °C. The overall heat transfer coefficient is 500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 490 kWU = 500 W/(m²·K)Th: 115 → 35 °CTc: 15 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT120 °C85 °C49.26 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (2 kg/s, cp = 2.3 kJ/(kg·K)) cools from 120 to 85 °C in a counter-flow exchanger. It heats 2 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 2 kg/scp,h = 2.3 kJ/(kg·K)Th: 120 → 85 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Gypsum board, k = 0.17150 mmGlass, k = 0.9675 mm23 °C-5 °CTi​ = ?Q̇

A wall is made of 150 mm of gypsum board and 75 mm of glass, with an area of 12 m². The outer faces are at 23 °C and -5 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 0.17 W/(m·K)L2 = 75 mm, k2 = 0.96 W/(m·K)A = 12 m²T1 = 23 °CT3 = -5 °C
Ti = °C
20.Heat conductionHard
Expanded polystyrene, k = 0.035100 mmBrick, k = 0.7225 mmroom 21 °Coutside -11 °CTs​ = ?Q̇

A wall of 100 mm expanded polystyrene and 25 mm brick separates a room at 21 °C from outside air at -11 °C. The convection coefficients are 6 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 20 m². Find the temperature Ts of the inside surface of the wall.

L1 = 100 mm, k1 = 0.035 W/(m·K)L2 = 25 mm, k2 = 0.72 W/(m·K)A = 20 m²hi = 6 W/(m²·K)ho = 25 W/(m²·K)Troom = 21 °CTout = -11 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 50 L/sD = 250 mmL = 300 mf = 0.018

Water flows at 50 L/s through a pipe 300 m long with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the friction head loss hf.

Q = 50 L/sL = 300 mD = 250 mmf = 0.018g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2Δz = ?L = 400 m, D = 300 mm, f = 0.0153× bend (K = 0.3)

Two open reservoirs are joined by a pipe 400 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.015. The minor losses are a square-edged entrance (K = 0.5), 3 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. What difference in water level Δz between the reservoirs gives a flow rate of 150 L/s?

Q = 150 L/sL = 400 mD = 300 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 30 L/sH = 30 m

A pump delivers 30 L/s of water (ρ = 1000 kg/m³) against a head of 30 m. The pump efficiency is 85% 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 = 30 L/sH = 30 mηpump = 85%ηmotor = 92%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
350 kPa (gauge)PQ = 75 L/sΔz = 22 mL = 200 m, D = 200 mm, f = 0.018, ΣK = 8

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 22 m higher. The pipe is 200 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 = 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 350 kPa. Find the head H the pump must add.

Q = 75 L/sΔz = 22 mL = 200 mD = 200 mmf = 0.018ΣK = 8ptank = 350 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 175 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) = 350·(20 − 25)/(25 − 35) = 175 kg/h

Answer

ṁ2 = 175 kg/h
2.Mass balance

Answer: W = 1791 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 = 3300·16/35 = 1509 kg/h

Total balance

W = F − P = 3300 − 1509 = 1791 kg/h

Answer

W = 1791 kg/h
3.Energy balance

Answer: tout = 27.54 °C

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

Heat released by the hot stream

Q = 0.5·2.1·(180 − 120) = 63 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 63/(2·4.18) = 27.54 °C

Answer

tout = 27.54 °C
4.Energy balance

Answer: ṁc = 0.9542 kg/s

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

Heat released

Qh = 2.5·2.44·(120 − 70) = 305 kW

Heat that reaches the water

Qc = (1 − 0.15)·305 = 259.3 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 259.3/(4.18·65) = 0.9542 kg/s

Answer

ṁc = 0.9542 kg/s
5.Ideal gas law

Answer: P = 167.9 kPa

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

Moles

n = m/M = 60/32 = 1.875 mol
T = 50 + 273.15 = 323.1 K

Pressure

P = nRT/V = 1.875·8.314·323.1/0.03 = 167.9 kPa

Answer

P = 167.9 kPa
6.Ideal gas law

Answer: ρ = 8.959 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 170 + 273.15 = 443.1 K

Density

ρ = 750·44.01/(8.314·443.1) = 8.959 kg/m³

Answer

ρ = 8.959 kg/m³
7.Stoichiometry

Answer: m = 26.38 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) = 16/22.99 = 0.696 mol
n(Cl2) = 16/70.9 = 0.2257 mol

Limiting reactant

0.696/2 = 0.348, 0.2257/1 = 0.2257 → Cl2

Mass of product

n(NaCl) = 0.2257·2 = 0.4513 mol
m = 0.4513·58.44 = 26.38 g

Answer

m = 26.38 g
8.Stoichiometry

Answer: Y = 78 %

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) = 4/16.04 = 0.2494 mol
m = 0.2494·2/1·18.02 = 8.988 g

Percent yield

Y = 7.01/8.988·100 = 78%

Answer

Y = 78%
9.Chemical equilibrium

Answer: [H2] = 0.07143 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/(0.25 − x)²

Take the square root

5 = 2x/(0.25 − x) → x = 0.25·5/(2 + 5) = 0.1786 mol/L

Equilibrium concentration

[H₂] = 0.25 − x = 0.07143 mol/L

Answer

[H2] = 0.07143 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.04202 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

0.08 = x²/(0.1 − x) → x² + 0.08·x − 0.008 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.008))/2 = 0.05798 mol/L

Equilibrium concentration

[PCl₅] = 0.1 − 0.05798 = 0.04202 mol/L

Answer

[PCl5] = 0.04202 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 31 °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

250·0.449·(180 − Tf) = 400·4.18·(Tf − 21)

Solve for the final temperature

Tf = (112.3·180 + 1672·21)/(112.3 + 1672) = 31 °C

Answer

Tf = 31 °C
12.Calorimetry & enthalpy

Answer: q = 12377 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 = 250/58.12 = 4.301 mol
q = n·|ΔH°/2| = 4.301·2877 = 12377 kJ

Answer

q = 12377 kJ
13.Reaction kinetics

Answer: t½ = 12.5 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/(0.1·0.8) = 12.5 min

Answer

t½ = 12.5 min

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

14.Reaction kinetics

Answer: A = 1.677 × 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 = 30 + 273.15 = 303.1 K

Solve Arrhenius for A

Ea/(RT) = 75000/(8.314·303.1) = 29.76
A = k·e29.76 = 0.002·8.384 × 10¹² = 1.677 × 10¹⁰ s⁻¹

Answer

A = 1.677 × 10¹⁰ s⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 91.63 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 − 0.6))/0.25 = 0.9163/0.25 = 3.665 min

Volume

V = Q·τ = 25·3.665 = 91.63 L

Answer

V = 91.63 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 79.81 %

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 = 200/50 = 4 min, kτ = 0.4·4 = 1.6

Conversion

X = 1 − e−kτ = 1 − e−1.6 = 79.81%

Answer

X = 79.81%
17.Heat exchangers (LMTD)

Answer: A = 26.92 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 = 115 − 55 = 60 K
ΔT₂ = Th,out − Tc,in = 35 − 15 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (60 − 20)/ln(60/20) = 36.41 K

Area

A = Q̇/(U·ΔTlm) = 490000/(500·36.41) = 26.92 m²

Answer

A = 26.92 m²
18.Heat exchangers (LMTD)

Answer: A = 1.716 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) = 2·2.3·35 = 161 kW
Tc,out = 30 + 161/(2·4.18) = 49.26 °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 = 120 − 49.26 = 70.74 K
ΔT₂ = Th,out − Tc,in = 85 − 30 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (70.74 − 55)/ln(70.74/55) = 62.54 K

Area

A = Q̇/(U·ΔTlm) = 161000/(1500·62.54) = 1.716 m²

Answer

A = 1.716 m²
19.Heat conduction

Answer: Ti = −2.722 °C

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

Layer resistances

R1 = L1/(k1A) = (150/1000)/(0.17·12) = 0.07353 K/W
R2 = L2/(k2A) = (75/1000)/(0.96·12) = 0.00651 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 28/0.08004 = 349.8 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 23 − 349.8·0.07353 = −2.722 °C

Answer

Ti = −2.722 °C
20.Heat conduction

Answer: Ts = 19.28 °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/(6·20) = 0.008333 K/W
R1 = L1/(k1A) = (100/1000)/(0.035·20) = 0.1429 K/W
R2 = L2/(k2A) = (25/1000)/(0.72·20) = 0.001736 K/W
Ro = 1/(hoA) = 1/(25·20) = 0.002 K/W
ΣR = 0.1549 K/W

Heat loss

Q̇ = (21 − (-11))/0.1549 = 206.5 W
Ts = Troom − Q̇·Ri = 21 − 206.5·0.008333 = 19.28 °C

Answer

Ts = 19.28 °C
21.Pipe friction & head loss

Answer: hf = 1.142 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·0.25²/4 = 0.04909 m²
V = Q/A = 0.05/0.04909 = 1.019 m/s

Velocity head

V²/(2g) = 1.019²/(2·9.81) = 0.05288 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.018·(300/0.25)·1.019²/(2·9.81) = 1.142 m

Answer

hf = 1.142 m
22.Pipe friction & head loss

Answer: Δz = 5.6 m

Pipe flow: the Reynolds number Re = V·D/ν = ρ·V·D/μ tells laminar flow (Re below about 2000) from turbulent flow (above about 4000). Friction along a pipe costs the Darcy–Weisbach head loss hf = f·(L/D)·V²/(2g). Fittings, valves, the entrance and the exit add minor losses hm = ΣK·V²/(2g). Between two open reservoir surfaces the energy equation gives Δz = hf + hm, with the exit loss K = 1 included.

Velocity

V = Q/A = 0.15/0.07069 = 2.122 m/s
V²/(2g) = 0.2295 m

Loss coefficients

f·L/D = 0.015·400/0.3 = 20
ΣK = 0.5 + 3·0.3 + 2 + 1.0 = 4.4

Total head loss

hf = 20·0.2295 = 4.59 m
hm = 4.4·0.2295 = 1.01 m
Δz = hf + hm = 5.6 m

Answer

Δz = 5.6 m
23.Pumps & pump power

Answer: Pel = 11.29 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 = 1000·9.81·0.03·30 = 8.829 kW

Shaft power

Pshaft = 8.829/0.85 = 10.39 kW

Electrical power

Pel = 10.39/0.92 = 11.29 kW

Answer

Pel = 11.29 kW
24.Pumps & pump power

Answer: H = 65.23 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) = (18 + 8)·0.2905 = 7.553 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 = 22 + 35.68 + 7.553 = 65.23 m

Answer

H = 65.23 m

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