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 1250 kg/h · 35% NaOHStream 2ṁ₂ = ? · 20% 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 = 250 kg/hx1 = 35 %x2 = 20 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4100 kg/h · 10% sugarProduct P65% 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 = 4100 kg/hxF = 10 %xP = 65 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 140 °C110 °Cwater · 25 °Ct = ? °C

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

ṁh = 2.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 140 → 110 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 160 °C110 °Cwater · 30 °C75 °C · ṁ = ?15% lost

Hot glycol mix 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 = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 160 → 110 °Ct: 30 → 75 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
210 g of CH₄V = 10 LT = 45 °CP = ?

A tank of 10 L contains 210 g of CH₄ at 45 °C. Treat it as an ideal gas and find the pressure P.

m = 210 gM = 16.04 g/molV = 10 LT = 45 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
He, M = 4.003 g/molP = 200 kPaT = 140 °Cρ = ?

Find the density ρ of He at 200 kPa and 140 °C, treating it as an ideal gas.

M = 4.003 g/molP = 200 kPaT = 140 °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​)

24 g of Al and 24 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(Al)n(Al)n(AlCl3​)m(AlCl3​)÷ M(Al)× 2/2× M(AlCl3​)

In the reaction 2Al + 3Cl2 → 2AlCl3, 6 g of Al reacts completely (the other reactants are in excess) and 26.98 g of AlCl3 is collected. Find the percent yield Y.

M(Al) = 26.98 g/molM(AlCl3) = 133.33 g/molactual: 26.98 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII110C−x−x+2xE1 − x1 − x2x

1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 4. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 4
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.2500C−x+x+xE0.25 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.01 at the reaction temperature. A container starts with 0.25 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.25 mol/LKc = 0.01
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 100 gT = 150 °Cc = 0.897 J/(g·°C)Waterm = 200 gT = 23 °Cc = 4.18 J/(g·°C)

A 100 g block of aluminium (c = 0.897 J/(g·°C)) at 150 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 23 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.897 J/(g·°C)Tmetal = 150 °Cmwater = 200 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H50 g C2​H5​OHC2​H5​OH + 3O₂reactants2CO₂ + 3H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 g of C2H5OH (M = 46.07 g/mol) burns completely: C2H5OH + 3O₂ → 2CO₂ + 3H₂O(l). Give q as a positive number.

ΔH°f(C2H5OH) = −277.7 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)X (%)t = ?75%

A zero-order reaction has k = 0.025 mol/(L·min) and starts at 2 mol/L. How long does it take to reach 75% conversion? Find t.

k = 0.025 mol/(L·min)CA0 = 2 mol/LX = 75 %
t = min
14.Reaction kineticsHard
Tk40 °C0.155 °C0.202

The rate constant of a reaction is 0.1 min⁻¹ at 40 °C and 0.202 min⁻¹ at 55 °C. Find the activation energy Ea.

k1 = 0.1 min⁻¹T1 = 40 °Ck2 = 0.202 min⁻¹T2 = 55 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 40 L/minCA0​ = 1.5 mol/LCA​ = ?V = 1000 L, k = 0.1 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.1 min⁻¹) runs in a 1000 L plug-flow reactor (PFR). The feed enters at 40 L/min with CA0 = 1.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 1000 LQ = 40 L/mink = 0.1 min⁻¹CA0 = 1.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
V = 250 LV = 250 LQ = 20 L/minX = ?

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in two equal CSTRs in series, each of 250 L. The feed rate is 20 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 250 L (×2)Q = 20 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT110 °C20 °C90 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 110 °C on the outside of the tubes. Cooling water (1.5 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 20 to 90 °C. The overall heat transfer coefficient is 3500 W/(m²·K). Find the heat transfer area A needed.

Ts = 110 °Cṁ = 1.5 kg/scp = 4.18 kJ/(kg·K)Tc: 20 → 90 °CU = 3500 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT140 °C10 °C?ΔT₁ΔT₂condensing steam

Steam condenses at a constant 140 °C on the outside of the tubes of a condenser with a heat transfer area of 2 m² and U = 1500 W/(m²·K). Cooling water (1 kg/s, cp = 4.18 kJ/(kg·K)) enters the tubes at 10 °C. Find the water outlet temperature Tc,out.

Ts = 140 °CA = 2 m²U = 1500 W/(m²·K)ṁ = 1 kg/scp = 4.18 kJ/(kg·K)Tc,in = 10 °C
Tc,out = °C
19.Heat conductionMedium
Mineral wool, k = 0.04250 mmExpanded polystyrene, k = 0.035100 mm19 °C1 °CTi​ = ?Q̇

A wall is made of 250 mm of mineral wool and 100 mm of expanded polystyrene, with an area of 4 m². The outer faces are at 19 °C and 1 °C. Find the temperature Ti at the interface between the two layers.

L1 = 250 mm, k1 = 0.04 W/(m·K)L2 = 100 mm, k2 = 0.035 W/(m·K)A = 4 m²T1 = 19 °CT3 = 1 °C
Ti = °C
20.Heat conductionHard
Glass, k = 0.96250 mmWood, k = 0.1750 mmroom 21 °Coutside 1 °CQ̇ = ?

A wall of 250 mm glass and 50 mm wood separates a room at 21 °C from outside air at 1 °C. The convection coefficients are 10 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 4 m². Find the heat loss Q̇ through the wall.

L1 = 250 mm, k1 = 0.96 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 4 m²hi = 10 W/(m²·K)ho = 30 W/(m²·K)Troom = 21 °CTout = 1 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 2.4 m/sD = 200 mmL = 500 mf = 0.018

Water flows at a mean velocity of 2.4 m/s through a pipe 500 m long with an inside diameter of 200 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the friction head loss hf.

V = 2.4 m/sL = 500 mD = 200 mmf = 0.018g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5free outletH = ?L = 200 m, D = 250 mm, f = 0.0152× bend (K = 0.3)

A pipe 200 m long with an inside diameter of 250 mm (Darcy friction factor f = 0.015) runs from an open reservoir and discharges as a free jet into the air. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each) and a valve (K = 5). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 50 L/s?

Q = 50 L/sL = 200 mD = 250 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 5
H = m
23.Pumps & pump powerMedium
PQ = 40 L/sH = 34 m

A pump with an efficiency of 85% delivers 40 L/s of water (ρ = 1000 kg/m³) against a head of 34 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 40 L/sH = 34 mη = 85%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 9 mL = 150 m, D = 200 mm, f = 0.025, 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 9 m higher. The pipe is 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.025; 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 = 9 mL = 150 mD = 200 mmf = 0.025ΣK = 6
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 125 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) = 250·(35 − 30)/(30 − 20) = 125 kg/h

Answer

ṁ2 = 125 kg/h
2.Mass balance

Answer: W = 3469 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 = 4100·10/65 = 630.8 kg/h

Total balance

W = F − P = 4100 − 630.8 = 3469 kg/h

Answer

W = 3469 kg/h
3.Energy balance

Answer: tout = 62.68 °C

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

Heat released by the hot stream

Q = 2.5·2.1·(140 − 110) = 157.5 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 157.5/(1·4.18) = 62.68 °C

Answer

tout = 62.68 °C
4.Energy balance

Answer: ṁc = 1.22 kg/s

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

Heat released

Qh = 1.5·3.6·(160 − 110) = 270 kW

Heat that reaches the water

Qc = (1 − 0.15)·270 = 229.5 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 229.5/(4.18·45) = 1.22 kg/s

Answer

ṁc = 1.22 kg/s
5.Ideal gas law

Answer: P = 3463 kPa

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

Moles

n = m/M = 210/16.04 = 13.09 mol
T = 45 + 273.15 = 318.1 K

Pressure

P = nRT/V = 13.09·8.314·318.1/0.01 = 3463 kPa

Answer

P = 3463 kPa
6.Ideal gas law

Answer: ρ = 0.2331 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 140 + 273.15 = 413.1 K

Density

ρ = 200·4.003/(8.314·413.1) = 0.2331 kg/m³

Answer

ρ = 0.2331 kg/m³
7.Stoichiometry

Answer: m = 30.09 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) = 24/26.98 = 0.8895 mol
n(Cl2) = 24/70.9 = 0.3385 mol

Limiting reactant

0.8895/2 = 0.4448, 0.3385/3 = 0.1128 → Cl2

Mass of product

n(AlCl3) = 0.1128·2 = 0.2257 mol
m = 0.2257·133.33 = 30.09 g

Answer

m = 30.09 g
8.Stoichiometry

Answer: Y = 90.99 %

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(Al) = 6/26.98 = 0.2224 mol
m = 0.2224·2/2·133.33 = 29.65 g

Percent yield

Y = 26.98/29.65·100 = 90.99%

Answer

Y = 90.99%
9.Chemical equilibrium

Answer: [HI] = 1 mol/L

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

Equilibrium expression

4 = (2x)²/(1 − x)²

Take the square root

2 = 2x/(1 − x) → x = 1·2/(2 + 2) = 0.5 mol/L

Equilibrium concentration

[HI] = 2x = 1 mol/L

Answer

[HI] = 1 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.2048 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

0.01 = x²/(0.25 − x) → x² + 0.01·x − 0.0025 = 0

Solve the quadratic

x = (−0.01 + √(0.01² + 4·0.0025))/2 = 0.04525 mol/L

Equilibrium concentration

[PCl₅] = 0.25 − 0.04525 = 0.2048 mol/L

Answer

[PCl5] = 0.2048 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 35.31 °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

100·0.897·(150 − Tf) = 200·4.18·(Tf − 23)

Solve for the final temperature

Tf = (89.7·150 + 836·23)/(89.7 + 836) = 35.31 °C

Answer

Tf = 35.31 °C
12.Calorimetry & enthalpy

Answer: q = 1483 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° = [2·(−393.5) + 3·(−285.8)] − [1·(−277.7) + 3·0] = −1367 kJ

Heat for the given mass

n = 50/46.07 = 1.085 mol
q = n·|ΔH°/1| = 1.085·1367 = 1483 kJ

Answer

q = 1483 kJ
13.Reaction kinetics

Answer: t = 60 min

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Amount converted

CA0·X = 2·0.75 = 1.5 mol/L

Time

t = CA0·X/k = 1.5/0.025 = 60 min

Answer

t = 60 min
14.Reaction kinetics

Answer: Ea = 40.05 kJ/mol

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Absolute temperatures

T1 = 313.1 K, T2 = 328.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·0.7031/(-1.460e-4) = 40046 J/mol
Ea = 40.05 kJ/mol

Answer

Ea = 40.05 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.1231 mol/L

Ideal reactors, first-order reaction (−rA = k·CA) at steady state, with space time τ = V/Q. A CSTR is perfectly mixed, so the whole volume reacts at the low outlet concentration: τ = X/(k·(1 − X)) and CA = CA0/(1 + k·τ). In a PFR each slice of fluid reacts like a small batch reactor: τ = ln(1/(1 − X))/k and CA = CA0·e−k·τ. For the same conversion a CSTR always needs more volume than a PFR.

Space time

τ = V/Q = 1000/40 = 25 min

Outlet concentration

CA = 1.5·e−0.1·25 = 0.1231 mol/L

Answer

CA = 0.1231 mol/L

Conversion: X = 91.79%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 84 %

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 = 250/20 = 12.5 min, kτ = 0.12·12.5 = 1.5

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 1.5) = 0.4
C2/CA0 = 1/(1 + kτ)² = 0.16
X = 1 − 0.16 = 84%

Answer

X = 84%
17.Heat exchangers (LMTD)

Answer: A = 2.694 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 = 1.5·4.18·(90 − 20) = 438.9 kW

End temperature differences

ΔT₁ = 110 − 20 = 90 K
ΔT₂ = 110 − 90 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (90 − 20)/ln(90/20) = 46.54 K

Area

A = Q̇/(U·ΔTlm) = 438900/(3500·46.54) = 2.694 m²

Answer

A = 2.694 m²
18.Heat exchangers (LMTD)

Answer: Tc,out = 76.58 °C

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.

Combine the energy balance and the rate equation

With ΔT₁ = Ts − Tc,in and ΔT₂ = Ts − Tc,out, the difference ΔT₁ − ΔT₂ equals the water temperature rise, so the rise cancels.

ṁcp(ΔT₁ − ΔT₂) = U·A·(ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂)
ln(ΔT₁/ΔT₂) = U·A/(ṁcp) = 1500·2/(1·4180) = 0.7177

Outlet temperature

ΔT₂ = ΔT₁·e−0.7177 = 130·0.4879 = 63.42 K
Tc,out = 140 − 63.42 = 76.58 °C

Answer

Tc,out = 76.58 °C

Heat transferred: Q̇ = 278.3 kW.

19.Heat conduction

Answer: Ti = 6.647 °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) = (250/1000)/(0.04·4) = 1.563 K/W
R2 = L2/(k2A) = (100/1000)/(0.035·4) = 0.7143 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 18/2.277 = 7.906 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 19 − 7.906·1.563 = 6.647 °C

Answer

Ti = 6.647 °C
20.Heat conduction

Answer: Q̇ = 116.3 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.

Resistances in series

Ri = 1/(hiA) = 1/(10·4) = 0.025 K/W
R1 = L1/(k1A) = (250/1000)/(0.96·4) = 0.0651 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·4) = 0.07353 K/W
Ro = 1/(hoA) = 1/(30·4) = 0.008333 K/W
ΣR = 0.172 K/W

Heat loss

Q̇ = (21 − (1))/0.172 = 116.3 W

Answer

Q̇ = 116.3 W
21.Pipe friction & head loss

Answer: hf = 13.21 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 head

V²/(2g) = 2.4²/(2·9.81) = 0.2936 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.018·(500/0.2)·2.4²/(2·9.81) = 13.21 m

Answer

hf = 13.21 m
22.Pipe friction & head loss

Answer: H = 1.01 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 = 0.05/0.04909 = 1.019 m/s
V²/(2g) = 0.05288 m

Loss coefficients

f·L/D = 0.015·200/0.25 = 12
ΣK = 0.5 + 2·0.3 + 5 = 6.1

Energy equation

The outlet jet still carries its velocity head; it is not a loss but it has to be supplied.

H = (1 + 12 + 6.1)·0.05288 = 1.01 m

Answer

H = 1.01 m
23.Pumps & pump power

Answer: Pshaft = 15.7 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 = 1000·9.81·0.04·34 = 13.34 kW

Shaft power

Pshaft = Ph/η = 13.34/0.85 = 15.7 kW

Answer

Pshaft = 15.7 kW
24.Pumps & pump power

Answer: H = 16.19 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) = (18.75 + 6)·0.2905 = 7.19 m

Pump head

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

H = Δz + hL = 9 + 7.19 = 16.19 m

Answer

H = 16.19 m

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