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 1800 kg/h · 10% sugarStream 2ṁ₂ = ? · 50% sugarProduct25% sugar

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

ṁ1 = 800 kg/hx1 = 10 %x2 = 50 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1400 kg/h · 6% sugarProduct P60% 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 = 1400 kg/hxF = 6 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 170 °C110 °Cwater · 10 °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: 170 → 110 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 180 °C140 °Cwater · 25 °C65 °C · ṁ = ?10% lost

Hot light oil heats water in an exchanger that loses 10% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 2 kg/scp,h = 2.1 kJ/(kg·K)Th: 180 → 140 °Ct: 25 → 65 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
50 g of ArV = 30 LT = 95 °CP = ?

A tank of 30 L contains 50 g of Ar at 95 °C. Treat it as an ideal gas and find the pressure P.

m = 50 gM = 39.95 g/molV = 30 LT = 95 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 300 kPa, 5 L, 10 °C to 350 kPa and 90 °C. Find the new volume V2.

P1 = 300 kPaV1 = 5 LT1 = 10 °CP2 = 350 kPaT2 = 90 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

12 g of H2 and 64 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(Fe2​O3​)n(Fe2​O3​)n(Fe)m(Fe)÷ M(Fe2​O3​)× 2/1× M(Fe)

In the reaction Fe2O3 + 3CO → 2Fe + 3CO2, 24 g of Fe2O3 reacts completely (the other reactants are in excess) and 12.59 g of Fe is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(Fe) = 55.85 g/molactual: 12.59 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 = 25. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.5 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 = 0.2 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.1 mol/LKc = 0.2
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 200 gT = 130 °Cc = 0.129 J/(g·°C)Waterm = 100 gT = 19 °Cc = 4.18 J/(g·°C)

A 200 g block of lead (c = 0.129 J/(g·°C)) at 130 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 19 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.129 J/(g·°C)Tmetal = 130 °Cmwater = 100 gTwater = 19 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H10 g C6​H12​O6​C6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 10 g of C6H12O6 (M = 180.16 g/mol) burns completely: C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C6H12O6) = −1274 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)60 min0.25

In a first-order reaction the concentration of A falls from 0.5 mol/L to 0.25 mol/L in 60 min. Find the rate constant k.

CA0 = 0.5 mol/LCA = 0.25 mol/Lt = 60 min
k = min⁻¹
14.Reaction kineticsHard
Tk30 °C0.0560 °C3.64

The rate constant of a reaction is 0.05 min⁻¹ at 30 °C and 3.64 min⁻¹ at 60 °C. Find the activation energy Ea.

k1 = 0.05 min⁻¹T1 = 30 °Ck2 = 3.64 min⁻¹T2 = 60 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 40 L/minX = 85%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 85% conversion of A.

Q = 40 L/mink = 0.15 min⁻¹X = 85%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 200 LV = 200 LQ = 40 L/minX = ?

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in two equal CSTRs in series, each of 200 L. The feed rate is 40 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 200 L (×2)Q = 40 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT100 °C20 °C75 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 100 °C on the outside of the tubes. Cooling water (3 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 20 to 75 °C. The overall heat transfer coefficient is 3500 W/(m²·K). Find the heat transfer area A needed.

Ts = 100 °Cṁ = 3 kg/scp = 4.18 kJ/(kg·K)Tc: 20 → 75 °CU = 3500 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT165 °C??30 °CΔT₁ΔT₂counter-flow

In a counter-flow heat exchanger both streams have the same heat capacity rate, ṁ·cp = 1.5 kW/K. The hot stream enters at 165 °C and the cold stream at 30 °C. The exchanger has A = 2 m² and U = 800 W/(m²·K). Find the hot outlet temperature Th,out.

Ch = Cc = 1.5 kW/KTh,in = 165 °CTc,in = 30 °CA = 2 m²U = 800 W/(m²·K)
Th,out = °C
19.Heat conductionMedium
Glass, k = 0.96150 mmConcrete, k = 1.4100 mm18 °C-8 °CTi​ = ?Q̇

A wall is made of 150 mm of glass and 100 mm of concrete, with an area of 20 m². The outer faces are at 18 °C and -8 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 0.96 W/(m·K)L2 = 100 mm, k2 = 1.4 W/(m·K)A = 20 m²T1 = 18 °CT3 = -8 °C
Ti = °C
20.Heat conductionHard
Expanded polystyrene, k = 0.035200 mmBrick, k = 0.72150 mmroom 20 °Coutside 5 °CTs​ = ?Q̇

A wall of 200 mm expanded polystyrene and 150 mm brick separates a room at 20 °C from outside air at 5 °C. The convection coefficients are 6 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 12 m². Find the temperature Ts of the inside surface of the wall.

L1 = 200 mm, k1 = 0.035 W/(m·K)L2 = 150 mm, k2 = 0.72 W/(m·K)A = 12 m²hi = 6 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = 5 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.2 m/sD = 150 mmL = 800 mf = 0.018

Water (ρ = 1000 kg/m³) flows at 1.2 m/s through a horizontal pipe, 800 m long, with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.2 m/sL = 800 mD = 150 mmf = 0.018ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 100 m, D = 250 mm, f = 0.0224× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 250 mm (Darcy friction factor f = 0.022) 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), 4 bends (K = 0.3 each) and a valve (K = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 150 L/s?

Q = 150 L/sL = 100 mD = 250 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 150 L/sH = 64 m

A pump with an efficiency of 80% delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 64 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 150 L/sH = 64 mη = 80%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 80 L/sΔz = 25 mL = 300 m, D = 200 mm, f = 0.015, ΣK = 6

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 25 m higher. The pipe is 300 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 = 6 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 78%. Find the shaft power Pshaft in kW.

Q = 80 L/sΔz = 25 mL = 300 mD = 200 mmf = 0.015ΣK = 6η = 78%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 480 kg/h

Steady-state mass balance: in = out for the total and for each component. Blending problems combine both.

Balances

Total: ṁ3 = ṁ1 + ṁ2
sugar: ṁ1x1 + ṁ2x2 = (ṁ1 + ṁ2)x3

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 800·(10 − 25)/(25 − 50) = 480 kg/h

Answer

ṁ2 = 480 kg/h
2.Mass balance

Answer: W = 1260 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 = 1400·6/60 = 140 kg/h

Total balance

W = F − P = 1400 − 140 = 1260 kg/h

Answer

W = 1260 kg/h
3.Energy balance

Answer: tout = 85.36 °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·(170 − 110) = 315 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 315/(1·4.18) = 85.36 °C

Answer

tout = 85.36 °C
4.Energy balance

Answer: ṁc = 0.9043 kg/s

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

Heat released

Qh = 2·2.1·(180 − 140) = 168 kW

Heat that reaches the water

Qc = (1 − 0.1)·168 = 151.2 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 151.2/(4.18·40) = 0.9043 kg/s

Answer

ṁc = 0.9043 kg/s
5.Ideal gas law

Answer: P = 127.7 kPa

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

Moles

n = m/M = 50/39.95 = 1.252 mol
T = 95 + 273.15 = 368.1 K

Pressure

P = nRT/V = 1.252·8.314·368.1/0.03 = 127.7 kPa

Answer

P = 127.7 kPa
6.Ideal gas law

Answer: V2 = 5.497 L

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

Absolute temperatures

T1 = 283.1 K, T2 = 363.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(300/350)·(363.1/283.1) = 5.497 L

Answer

V2 = 5.497 L
7.Stoichiometry

Answer: m = 72.08 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) = 12/2.016 = 5.952 mol
n(O2) = 64/32 = 2 mol

Limiting reactant

5.952/2 = 2.976, 2/1 = 2 → O2

Mass of product

n(H2O) = 2·2 = 4 mol
m = 4·18.02 = 72.08 g

Answer

m = 72.08 g
8.Stoichiometry

Answer: Y = 75 %

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(Fe2O3) = 24/159.69 = 0.1503 mol
m = 0.1503·2/1·55.85 = 16.79 g

Percent yield

Y = 12.59/16.79·100 = 75%

Answer

Y = 75%
9.Chemical equilibrium

Answer: [H2] = 0.1429 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/(0.5 − x)²

Take the square root

5 = 2x/(0.5 − x) → x = 0.5·5/(2 + 5) = 0.3571 mol/L

Equilibrium concentration

[H₂] = 0.5 − x = 0.1429 mol/L

Answer

[H2] = 0.1429 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.02679 mol/L

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

Equilibrium expression

0.2 = x²/(0.1 − x) → x² + 0.2·x − 0.02 = 0

Solve the quadratic

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

Equilibrium concentration

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

Answer

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

Answer: Tf = 25.45 °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

200·0.129·(130 − Tf) = 100·4.18·(Tf − 19)

Solve for the final temperature

Tf = (25.8·130 + 418·19)/(25.8 + 418) = 25.45 °C

Answer

Tf = 25.45 °C
12.Calorimetry & enthalpy

Answer: q = 155.5 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° = [6·(−393.5) + 6·(−285.8)] − [1·(−1274) + 6·0] = −2802 kJ

Heat for the given mass

n = 10/180.16 = 0.05551 mol
q = n·|ΔH°/1| = 0.05551·2802 = 155.5 kJ

Answer

q = 155.5 kJ
13.Reaction kinetics

Answer: k = 0.01155 min⁻¹

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).

Integrated first-order law

k = ln(CA0/CA)/t = ln(0.5/0.25)/60 = 0.6931/60 = 0.01155 min⁻¹

Answer

k = 0.01155 min⁻¹
14.Reaction kinetics

Answer: Ea = 120 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 = 303.1 K, T2 = 333.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·4.288/(-2.970e-4) = 120009 J/mol
Ea = 120 kJ/mol

Answer

Ea = 120 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: V = 505.9 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 − 0.85))/0.15 = 1.897/0.15 = 12.65 min

Volume

V = Q·τ = 40·12.65 = 505.9 L

Answer

V = 505.9 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 60.94 %

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 = 200/40 = 5 min, kτ = 0.12·5 = 0.6

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 0.6) = 0.625
C2/CA0 = 1/(1 + kτ)² = 0.3906
X = 1 − 0.3906 = 60.94%

Answer

X = 60.94%
17.Heat exchangers (LMTD)

Answer: A = 4.167 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 = 3·4.18·(75 − 20) = 689.7 kW

End temperature differences

ΔT₁ = 100 − 20 = 80 K
ΔT₂ = 100 − 75 = 25 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (80 − 25)/ln(80/25) = 47.29 K

Area

A = Q̇/(U·ΔTlm) = 689700/(3500·47.29) = 4.167 m²

Answer

A = 4.167 m²
18.Heat exchangers (LMTD)

Answer: Th,out = 95.32 °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.

Constant temperature difference

The cold outlet sits opposite the hot inlet: Tc,out = Tc,in + (Th,in − Th,out), so ΔT₁ = Th,in − Tc,out = Th,out − Tc,in = ΔT₂.

ΔTlm = Th,out − Tc,in

Energy balance equals rate equation

1.5·(165 − Th,out) = 1.6·(Th,out − 30)
Th,out = (1.5·165 + 1.6·30)/(1.5 + 1.6) = 95.32 °C

Answer

Th,out = 95.32 °C

Heat transferred: Q̇ = 104.5 kW; the cold stream leaves at 99.68 °C.

19.Heat conduction

Answer: Ti = 0.1569 °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)/(0.96·20) = 0.007813 K/W
R2 = L2/(k2A) = (100/1000)/(1.4·20) = 0.003571 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 26/0.01138 = 2284 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 18 − 2284·0.007813 = 0.1569 °C

Answer

Ti = 0.1569 °C
20.Heat conduction

Answer: Ts = 19.59 °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/(6·12) = 0.01389 K/W
R1 = L1/(k1A) = (200/1000)/(0.035·12) = 0.4762 K/W
R2 = L2/(k2A) = (150/1000)/(0.72·12) = 0.01736 K/W
Ro = 1/(hoA) = 1/(30·12) = 0.002778 K/W
ΣR = 0.5102 K/W

Heat loss

Q̇ = (20 − (5))/0.5102 = 29.4 W
Ts = Troom − Q̇·Ri = 20 − 29.4·0.01389 = 19.59 °C

Answer

Ts = 19.59 °C
21.Pipe friction & head loss

Answer: Δp = 69.12 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) = 0.018·(800/0.15)·1.2²/(2·9.81) = 7.046 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 = 1000·9.81·7.046 = 69120 Pa = 69.12 kPa

Answer

Δp = 69.12 kPa
22.Pipe friction & head loss

Answer: H = 6.425 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 = 0.15/0.04909 = 3.056 m/s
V²/(2g) = 0.4759 m

Loss coefficients

f·L/D = 0.022·100/0.25 = 8.8
ΣK = 0.5 + 4·0.3 + 2 = 3.7

Energy equation

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

H = (1 + 8.8 + 3.7)·0.4759 = 6.425 m

Answer

H = 6.425 m
23.Pumps & pump power

Answer: Pshaft = 117.7 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 = 1000·9.81·0.15·64 = 94.18 kW

Shaft power

Pshaft = Ph/η = 94.18/0.8 = 117.7 kW

Answer

Pshaft = 117.7 kW
24.Pumps & pump power

Answer: Pshaft = 34.63 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 = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (22.5 + 6)·0.3305 = 9.419 m

Pump head

H = Δz + hL = 25 + 9.419 = 34.42 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.08·34.42/0.78 = 34.63 kW

Answer

Pshaft = 34.63 kW

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