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 1900 kg/h · 50% NaOHStream 2ṁ₂ = ? · 20% 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 = 900 kg/hx1 = 50 %x2 = 20 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2400 kg/h · 8% sugarProduct P40% 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 = 2400 kg/hxF = 8 %xP = 40 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 140 °C100 °Cwater · 15 °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 → 100 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 130 °C60 °Cwater · 25 °C60 °C · ṁ = ?5% lost

Hot glycol mix heats water in an exchanger that loses 5% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 0.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 60 °Ct: 25 → 60 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
90 g of CH₄P = 150 kPaT = 30 °CV = ?

What volume V does 90 g of CH₄ occupy at 150 kPa and 30 °C? Treat it as an ideal gas.

m = 90 gM = 16.04 g/molP = 150 kPaT = 30 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 300 kPa, 5 L, 15 °C to 250 kPa and 70 °C. Find the new volume V2.

P1 = 300 kPaV1 = 5 LT1 = 15 °CP2 = 250 kPaT2 = 70 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

20 g of H2 and 8 g of O2 react according to 2H2 + O2 → 2H2O. What mass m of H2O can form?

M(H2) = 2.016M(O2) = 32M(H2O) = 18.02 g/mol
m = g
8.StoichiometryHard
m(CaCO3​)n(CaCO3​)n(CO2​)m(CO2​)÷ M(CaCO3​)× 1/1× M(CO2​)

In the reaction CaCO3 → CaO + CO2, 16 g of CaCO3 reacts completely (the other reactants are in excess) and 4.36 g of CO2 is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CO2) = 44.01 g/molactual: 4.36 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.20.20C−x−x+2xE0.2 − x0.2 − x2x

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

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 16
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I1.500C−x+x+xE1.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 1.5 mol/LKc = 0.02
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 150 gT = 130 °Cc = 0.385 J/(g·°C)Waterm = 300 gT = 20 °Cc = 4.18 J/(g·°C)

A 150 g block of copper (c = 0.385 J/(g·°C)) at 130 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 20 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.385 J/(g·°C)Tmetal = 130 °Cmwater = 300 gTwater = 20 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l).

ΔH°f(C2H6) = −84.7 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
ΔH° = kJ
13.Reaction kineticsMedium
t (min)X (%)t = ?50%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.25 L/(mol·min) and starts at 1.5 mol/L. How long does it take to reach 50% conversion? Find t.

k = 0.25 L/(mol·min)CA0 = 1.5 mol/LX = 50 %
t = min
14.Reaction kineticsHard
Tk20 °C0.0145 °C?

A reaction has a rate constant of 0.01 min⁻¹ at 20 °C and an activation energy of 50 kJ/mol. Find the rate constant k2 at 45 °C.

k1 = 0.01 min⁻¹T1 = 20 °CT2 = 45 °CEa = 50 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 40 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 40 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 = 40 L/mink = 0.15 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 50 LQ = 20 L/minX = ?

A first-order liquid-phase reaction (k = 0.4 min⁻¹) runs in a 50 L CSTR fed at 20 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 50 LQ = 20 L/mink = 0.4 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT100 °C60 °C20 °C55 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 310 kW. The hot fluid cools from 100 to 60 °C and the cold fluid heats from 20 to 55 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 310 kWU = 800 W/(m²·K)Th: 100 → 60 °CTc: 20 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT165 °C75 °C45.14 °C15 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.1 kJ/(kg·K)) cools from 165 to 75 °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 = 200 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.1 kJ/(kg·K)Th: 165 → 75 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 15 °CU = 200 W/(m²·K)
A = m²
19.Heat conductionMedium
Concrete, k = 1.450 mmExpanded polystyrene, k = 0.03575 mm21 °C-7 °CTi​ = ?Q̇

A wall is made of 50 mm of concrete and 75 mm of expanded polystyrene, with an area of 15 m². The outer faces are at 21 °C and -7 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 1.4 W/(m·K)L2 = 75 mm, k2 = 0.035 W/(m·K)A = 15 m²T1 = 21 °CT3 = -7 °C
Ti = °C
20.Heat conductionHard
Expanded polystyrene, k = 0.03550 mmWood, k = 0.1725 mmroom 20 °Coutside 4 °CQ̇ = ?

A wall of 50 mm expanded polystyrene and 25 mm wood separates a room at 20 °C from outside air at 4 °C. The convection coefficients are 8 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 6 m². Find the heat loss Q̇ through the wall.

L1 = 50 mm, k1 = 0.035 W/(m·K)L2 = 25 mm, k2 = 0.17 W/(m·K)A = 6 m²hi = 8 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = 4 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 1.6 m/sD = 150 mmL = 800 mf = 0.015

Water (ρ = 1000 kg/m³) flows at 1.6 m/s through a horizontal pipe, 800 m long, with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.6 m/sL = 800 mD = 150 mmf = 0.015ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 10Δz = ?L = 100 m, D = 300 mm, f = 0.0224× bend (K = 0.3)

Two open reservoirs are joined by a pipe 100 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.022. The minor losses are a square-edged entrance (K = 0.5), 4 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. What difference in water level Δz between the reservoirs gives a flow rate of 200 L/s?

Q = 200 L/sL = 100 mD = 300 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 10Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 100 L/sH = 78 m

A pump with an efficiency of 75% delivers 100 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 = 100 L/sH = 78 mη = 75%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 10 mL = 500 m, D = 200 mm, f = 0.025, ΣK = 8

A pump moves 50 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 10 m higher. The pipe is 500 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 = 8 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 72%. Find the shaft power Pshaft in kW.

Q = 50 L/sΔz = 10 mL = 500 mD = 200 mmf = 0.025ΣK = 8η = 72%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 4500 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) = 900·(50 − 25)/(25 − 20) = 4500 kg/h

Answer

ṁ2 = 4500 kg/h
2.Mass balance

Answer: W = 1920 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 = 2400·8/40 = 480 kg/h

Total balance

W = F − P = 2400 − 480 = 1920 kg/h

Answer

W = 1920 kg/h
3.Energy balance

Answer: tout = 65.24 °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·(140 − 100) = 210 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 210/(1·4.18) = 65.24 °C

Answer

tout = 65.24 °C
4.Energy balance

Answer: ṁc = 0.8182 kg/s

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

Heat released

Qh = 0.5·3.6·(130 − 60) = 126 kW

Heat that reaches the water

Qc = (1 − 0.05)·126 = 119.7 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 119.7/(4.18·35) = 0.8182 kg/s

Answer

ṁc = 0.8182 kg/s
5.Ideal gas law

Answer: V = 94.28 L

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

Moles

n = 90/16.04 = 5.611 mol
T = 30 + 273.15 = 303.1 K

Volume

V = nRT/P = 5.611·8.314·303.1/150 = 94.28 L

Answer

V = 94.28 L
6.Ideal gas law

Answer: V2 = 7.145 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) = 5·(300/250)·(343.1/288.1) = 7.145 L

Answer

V2 = 7.145 L
7.Stoichiometry

Answer: m = 9.01 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(H2) = 20/2.016 = 9.921 mol
n(O2) = 8/32 = 0.25 mol

Limiting reactant

9.921/2 = 4.96, 0.25/1 = 0.25 → O2

Mass of product

n(H2O) = 0.25·2 = 0.5 mol
m = 0.5·18.02 = 9.01 g

Answer

m = 9.01 g
8.Stoichiometry

Answer: Y = 61.97 %

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Theoretical yield

n(CaCO3) = 16/100.09 = 0.1599 mol
m = 0.1599·1/1·44.01 = 7.035 g

Percent yield

Y = 4.36/7.035·100 = 61.97%

Answer

Y = 61.97%
9.Chemical equilibrium

Answer: [HI] = 0.2667 mol/L

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

Equilibrium expression

16 = (2x)²/(0.2 − x)²

Take the square root

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

Equilibrium concentration

[HI] = 2x = 0.2667 mol/L

Answer

[HI] = 0.2667 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 1.337 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

0.02 = x²/(1.5 − x) → x² + 0.02·x − 0.03 = 0

Solve the quadratic

x = (−0.02 + √(0.02² + 4·0.03))/2 = 0.1635 mol/L

Equilibrium concentration

[PCl₅] = 1.5 − 0.1635 = 1.337 mol/L

Answer

[PCl5] = 1.337 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 24.84 °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

150·0.385·(130 − Tf) = 300·4.18·(Tf − 20)

Solve for the final temperature

Tf = (57.75·130 + 1254·20)/(57.75 + 1254) = 24.84 °C

Answer

Tf = 24.84 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −3119 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° = [4·(−393.5) + 6·(−285.8)] − [2·(−84.7) + 7·0] = −3119 kJ

Answer

ΔH° = −3119 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 2.667 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).

Concentration at the end

CA = 1.5·(1 − 0.5) = 0.75 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (1.333 − 0.6667)/0.25 = 2.667 min

Answer

t = 2.667 min
14.Reaction kinetics

Answer: k2 = 0.05013 min⁻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 temperatures

T1 = 293.1 K, T2 = 318.1 K

Arrhenius ratio

ln(k2/k1) = −(50000/8.314)·(1/318.1 − 1/293.1) = 1.612
k2 = 0.01·e1.612 = 0.05013 min⁻¹

Answer

k2 = 0.05013 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 614 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 = 40·15.35 = 614 L

Answer

V = 614 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 50 %

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 = 50/20 = 2.5 min, kτ = 0.4·2.5 = 1

Conversion

X = kτ/(1 + kτ) = 1/(1 + 1) = 50%

Answer

X = 50%
17.Heat exchangers (LMTD)

Answer: A = 14.33 m²

LMTD method: the temperature difference between the streams changes along the exchanger, so the rate equation uses its logarithmic mean: Q̇ = U·A·ΔTlm, with ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂), where ΔT₁ and ΔT₂ are the differences at the two ends. Counter-flow gives a larger ΔTlm than parallel flow for the same inlet and outlet temperatures.

End temperature differences

In parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 100 − 20 = 80 K
ΔT₂ = Th,out − Tc,out = 60 − 55 = 5 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (80 − 5)/ln(80/5) = 27.05 K

Area

A = Q̇/(U·ΔTlm) = 310000/(800·27.05) = 14.33 m²

Answer

A = 14.33 m²
18.Heat exchangers (LMTD)

Answer: A = 10.92 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.

Heat duty and water outlet temperature

Q̇ = ṁhcp,h(Th,in − Th,out) = 1·2.1·90 = 189 kW
Tc,out = 15 + 189/(1.5·4.18) = 45.14 °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 = 165 − 45.14 = 119.9 K
ΔT₂ = Th,out − Tc,in = 75 − 15 = 60 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (119.9 − 60)/ln(119.9/60) = 86.5 K

Area

A = Q̇/(U·ΔTlm) = 189000/(200·86.5) = 10.92 m²

Answer

A = 10.92 m²
19.Heat conduction

Answer: Ti = 20.54 °C

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

Layer resistances

R1 = L1/(k1A) = (50/1000)/(1.4·15) = 0.002381 K/W
R2 = L2/(k2A) = (75/1000)/(0.035·15) = 0.1429 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 28/0.1452 = 192.8 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 21 − 192.8·0.002381 = 20.54 °C

Answer

Ti = 20.54 °C
20.Heat conduction

Answer: Q̇ = 55.36 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/(8·6) = 0.02083 K/W
R1 = L1/(k1A) = (50/1000)/(0.035·6) = 0.2381 K/W
R2 = L2/(k2A) = (25/1000)/(0.17·6) = 0.02451 K/W
Ro = 1/(hoA) = 1/(30·6) = 0.005556 K/W
ΣR = 0.289 K/W

Heat loss

Q̇ = (20 − (4))/0.289 = 55.36 W

Answer

Q̇ = 55.36 W
21.Pipe friction & head loss

Answer: Δp = 102.4 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) = 0.015·(800/0.15)·1.6²/(2·9.81) = 10.44 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 = 1000·9.81·10.44 = 102400 Pa = 102.4 kPa

Answer

Δp = 102.4 kPa
22.Pipe friction & head loss

Answer: Δz = 8.174 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 = 0.2/0.07069 = 2.829 m/s
V²/(2g) = 0.408 m

Loss coefficients

f·L/D = 0.022·100/0.3 = 7.333
ΣK = 0.5 + 4·0.3 + 10 + 1.0 = 12.7

Total head loss

hf = 7.333·0.408 = 2.992 m
hm = 12.7·0.408 = 5.182 m
Δz = hf + hm = 8.174 m

Answer

Δz = 8.174 m
23.Pumps & pump power

Answer: Pshaft = 102 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 = 1000·9.81·0.1·78 = 76.52 kW

Shaft power

Pshaft = Ph/η = 76.52/0.75 = 102 kW

Answer

Pshaft = 102 kW
24.Pumps & pump power

Answer: Pshaft = 13.01 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.

Velocity

V = Q/A = 0.05/0.03142 = 1.592 m/s
V²/(2g) = 0.1291 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (62.5 + 8)·0.1291 = 9.102 m

Pump head

H = Δz + hL = 10 + 9.102 = 19.1 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.05·19.1/0.72 = 13.01 kW

Answer

Pshaft = 13.01 kW

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