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 1600 kg/h · 10% saltStream 2ṁ₂ = ? · 35% saltProduct30% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 30% salt? Find ṁ2.

ṁ1 = 600 kg/hx1 = 10 %x2 = 35 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1100 kg/h · 8% NaOHProduct P60% NaOHVapour W (pure water)W = ? kg/h

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

F = 1100 kg/hxF = 8 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 160 °C110 °Cwater · 30 °Ct = ? °C

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

ṁh = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 160 → 110 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 150 °C90 °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 kg/scp,h = 2.44 kJ/(kg·K)Th: 150 → 90 °Ct: 10 → 75 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
400 g of HeP = 250 kPaT = 90 °CV = ?

What volume V does 400 g of He occupy at 250 kPa and 90 °C? Treat it as an ideal gas.

m = 400 gM = 4.003 g/molP = 250 kPaT = 90 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of CO₂ goes from 250 kPa, 20 L, 20 °C to 300 kPa and 60 °C. Find the new volume V2.

P1 = 250 kPaV1 = 20 LT1 = 20 °CP2 = 300 kPaT2 = 60 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 3/ν× M(CO2​)

12 g of C3H8 and 48 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of CO2 can form?

M(C3H8) = 44.1M(O2) = 32M(CO2) = 44.01 g/mol
m = g
8.StoichiometryHard
m(N2​)n(N2​)n(NH3​)m(NH3​)÷ M(N2​)× 2/1× M(NH3​)

In the reaction N2 + 3H2 → 2NH3, 20 g of N2 reacts completely (the other reactants are in excess) and 21.39 g of NH3 is collected. Find the percent yield Y.

M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 21.39 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.10.10C−x−x+2xE0.1 − x0.1 − x2x

0.1 mol/L of H₂ and 0.1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 9. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.1 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.400C−x+x+xE0.4 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.4 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.4 mol/LKc = 0.1
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 100 gT = 200 °Cc = 0.897 J/(g·°C)Waterm = 150 gT = 23 °Cc = 4.18 J/(g·°C)

A 100 g block of aluminium (c = 0.897 J/(g·°C)) at 200 °C is dropped into 150 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 = 200 °Cmwater = 150 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HCH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction CH4 + 2O₂ → CO₂ + 2H₂O(l).

ΔH°f(CH4) = −74.8 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)C (mol/L)5 min0.45

In a first-order reaction the concentration of A falls from 1.5 mol/L to 0.45 mol/L in 5 min. Find the rate constant k.

CA0 = 1.5 mol/LCA = 0.45 mol/Lt = 5 min
k = min⁻¹
14.Reaction kineticsHard
Tk40 °Ck1​?2·k1​

A reaction has an activation energy of 70 kJ/mol. At 40 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 2 times faster?

Ea = 70 kJ/molT1 = 40 °Ck2/k1 = 2R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minX = 90%V = ?, k = 0.12 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.12 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 90% conversion of A.

Q = 50 L/mink = 0.12 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 100 LQ = 25 L/minX = ?

A first-order liquid-phase reaction (k = 0.5 min⁻¹) runs in a 100 L CSTR fed at 25 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 100 LQ = 25 L/mink = 0.5 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT130 °C10 °C75 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 130 °C on the outside of the tubes. Cooling water (2 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 10 to 75 °C. The overall heat transfer coefficient is 2500 W/(m²·K). Find the heat transfer area A needed.

Ts = 130 °Cṁ = 2 kg/scp = 4.18 kJ/(kg·K)Tc: 10 → 75 °CU = 2500 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT115 °C60 °C41.45 °C25 °CΔT₁ΔT₂counter-flow

Hot oil (0.5 kg/s, cp = 2.5 kJ/(kg·K)) cools from 115 to 60 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 25 °C. With U = 500 W/(m²·K), find the heat transfer area A needed.

ṁh = 0.5 kg/scp,h = 2.5 kJ/(kg·K)Th: 115 → 60 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 25 °CU = 500 W/(m²·K)
A = m²
19.Heat conductionMedium
Concrete, k = 1.4250 mmBrick, k = 0.7250 mm18 °C2 °CTi​ = ?Q̇

A wall is made of 250 mm of concrete and 50 mm of brick, with an area of 12 m². The outer faces are at 18 °C and 2 °C. Find the temperature Ti at the interface between the two layers.

L1 = 250 mm, k1 = 1.4 W/(m·K)L2 = 50 mm, k2 = 0.72 W/(m·K)A = 12 m²T1 = 18 °CT3 = 2 °C
Ti = °C
20.Heat conductionHard
Brick, k = 0.72250 mmGypsum board, k = 0.1725 mmroom 22 °Coutside -7 °CTs​ = ?Q̇

A wall of 250 mm brick and 25 mm gypsum board separates a room at 22 °C from outside air at -7 °C. The convection coefficients are 6 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 20 m². Find the temperature Ts of the inside surface of the wall.

L1 = 250 mm, k1 = 0.72 W/(m·K)L2 = 25 mm, k2 = 0.17 W/(m·K)A = 20 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = -7 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 5 L/sD = 50 mmL = 800 mf = 0.03

Water flows at 5 L/s through a pipe 800 m long with an inside diameter of 50 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the friction head loss hf.

Q = 5 L/sL = 800 mD = 50 mmf = 0.03g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 0.2free outletH = ?L = 100 m, D = 250 mm, f = 0.0223× 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), 3 bends (K = 0.3 each) and a valve (K = 0.2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 60 L/s?

Q = 60 L/sL = 100 mD = 250 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 0.2
H = m
23.Pumps & pump powerMedium
PQ = 150 L/sH = 12 m

In a test, a pump delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 12 m while its shaft takes 21.5 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 150 L/sH = 12 mPshaft = 21.5 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 120 L/sΔz = 10 mL = 500 m, D = 250 mm, f = 0.02, ΣK = 6

A pump moves 120 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 250 mm and a Darcy friction factor f = 0.02; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 70%. Find the shaft power Pshaft in kW.

Q = 120 L/sΔz = 10 mL = 500 mD = 250 mmf = 0.02ΣK = 6η = 70%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 2400 kg/h

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

Balances

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

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 600·(10 − 30)/(30 − 35) = 2400 kg/h

Answer

ṁ2 = 2400 kg/h
2.Mass balance

Answer: W = 953.3 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 = 1100·8/60 = 146.7 kg/h

Total balance

W = F − P = 1100 − 146.7 = 953.3 kg/h

Answer

W = 953.3 kg/h
3.Energy balance

Answer: tout = 94.59 °C

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

Heat released by the hot stream

Q = 1.5·3.6·(160 − 110) = 270 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 270/(1·4.18) = 94.59 °C

Answer

tout = 94.59 °C
4.Energy balance

Answer: ṁc = 0.916 kg/s

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

Heat released

Qh = 2·2.44·(150 − 90) = 292.8 kW

Heat that reaches the water

Qc = (1 − 0.15)·292.8 = 248.9 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 248.9/(4.18·65) = 0.916 kg/s

Answer

ṁc = 0.916 kg/s
5.Ideal gas law

Answer: V = 1207 L

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

Moles

n = 400/4.003 = 99.93 mol
T = 90 + 273.15 = 363.1 K

Volume

V = nRT/P = 99.93·8.314·363.1/250 = 1207 L

Answer

V = 1207 L
6.Ideal gas law

Answer: V2 = 18.94 L

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

Absolute temperatures

T1 = 293.1 K, T2 = 333.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 20·(250/300)·(333.1/293.1) = 18.94 L

Answer

V2 = 18.94 L
7.Stoichiometry

Answer: m = 35.93 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(C3H8) = 12/44.1 = 0.2721 mol
n(O2) = 48/32 = 1.5 mol

Limiting reactant

0.2721/1 = 0.2721, 1.5/5 = 0.3 → C3H8

Mass of product

n(CO2) = 0.2721·3 = 0.8163 mol
m = 0.8163·44.01 = 35.93 g

Answer

m = 35.93 g
8.Stoichiometry

Answer: Y = 87.98 %

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(N2) = 20/28.02 = 0.7138 mol
m = 0.7138·2/1·17.03 = 24.31 g

Percent yield

Y = 21.39/24.31·100 = 87.98%

Answer

Y = 87.98%
9.Chemical equilibrium

Answer: [H2] = 0.04 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

9 = (2x)²/(0.1 − x)²

Take the square root

3 = 2x/(0.1 − x) → x = 0.1·3/(2 + 3) = 0.06 mol/L

Equilibrium concentration

[H₂] = 0.1 − x = 0.04 mol/L

Answer

[H2] = 0.04 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.1562 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

0.1 = x²/(0.4 − x) → x² + 0.1·x − 0.04 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.04))/2 = 0.1562 mol/L

Equilibrium concentration

[Cl₂] = x = 0.1562 mol/L

Answer

[Cl2] = 0.1562 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 45.15 °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·(200 − Tf) = 150·4.18·(Tf − 23)

Solve for the final temperature

Tf = (89.7·200 + 627·23)/(89.7 + 627) = 45.15 °C

Answer

Tf = 45.15 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −890.3 kJ

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Enthalpy of reaction

ΔH° = [1·(−393.5) + 2·(−285.8)] − [1·(−74.8) + 2·0] = −890.3 kJ

Answer

ΔH° = −890.3 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.2408 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(1.5/0.45)/5 = 1.204/5 = 0.2408 min⁻¹

Answer

k = 0.2408 min⁻¹
14.Reaction kinetics

Answer: T2 = 48.29 °C

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

Absolute temperature

T1 = 313.1 K

Solve Arrhenius for T₂

1/T2 = 1/313.1 − 8.314·ln(2)/70000 = 3.193 × 10⁻³ − 8.233 × 10⁻⁵ = 3.111 × 10⁻³ K⁻¹
T2 = 321.4 K = 48.29 °C

Answer

T2 = 48.29 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 959.4 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))/0.12 = 2.303/0.12 = 19.19 min

Volume

V = Q·τ = 50·19.19 = 959.4 L

Answer

V = 959.4 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 66.67 %

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 = 100/25 = 4 min, kτ = 0.5·4 = 2

Conversion

X = kτ/(1 + kτ) = 2/(1 + 2) = 66.67%

Answer

X = 66.67%
17.Heat exchangers (LMTD)

Answer: A = 2.609 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 = 2·4.18·(75 − 10) = 543.4 kW

End temperature differences

ΔT₁ = 130 − 10 = 120 K
ΔT₂ = 130 − 75 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (120 − 55)/ln(120/55) = 83.32 K

Area

A = Q̇/(U·ΔTlm) = 543400/(2500·83.32) = 2.609 m²

Answer

A = 2.609 m²
18.Heat exchangers (LMTD)

Answer: A = 2.649 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) = 0.5·2.5·55 = 68.75 kW
Tc,out = 25 + 68.75/(1·4.18) = 41.45 °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 = 115 − 41.45 = 73.55 K
ΔT₂ = Th,out − Tc,in = 60 − 25 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (73.55 − 35)/ln(73.55/35) = 51.91 K

Area

A = Q̇/(U·ΔTlm) = 68750/(500·51.91) = 2.649 m²

Answer

A = 2.649 m²
19.Heat conduction

Answer: Ti = 6.48 °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)/(1.4·12) = 0.01488 K/W
R2 = L2/(k2A) = (50/1000)/(0.72·12) = 0.005787 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 16/0.02067 = 774.1 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 18 − 774.1·0.01488 = 6.48 °C

Answer

Ti = 6.48 °C
20.Heat conduction

Answer: Ts = 15.2 °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) = (250/1000)/(0.72·20) = 0.01736 K/W
R2 = L2/(k2A) = (25/1000)/(0.17·20) = 0.007353 K/W
Ro = 1/(hoA) = 1/(20·20) = 0.0025 K/W
ΣR = 0.03555 K/W

Heat loss

Q̇ = (22 − (-7))/0.03555 = 815.8 W
Ts = Troom − Q̇·Ri = 22 − 815.8·0.008333 = 15.2 °C

Answer

Ts = 15.2 °C
21.Pipe friction & head loss

Answer: hf = 158.6 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.

Mean velocity

A = π·0.05²/4 = 0.001963 m²
V = Q/A = 0.005/0.001963 = 2.546 m/s

Velocity head

V²/(2g) = 2.546²/(2·9.81) = 0.3305 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.03·(800/0.05)·2.546²/(2·9.81) = 158.6 m

Answer

hf = 158.6 m
22.Pipe friction & head loss

Answer: H = 0.8681 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 = 0.06/0.04909 = 1.222 m/s
V²/(2g) = 0.07615 m

Loss coefficients

f·L/D = 0.022·100/0.25 = 8.8
ΣK = 0.5 + 3·0.3 + 0.2 = 1.6

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 + 1.6)·0.07615 = 0.8681 m

Answer

H = 0.8681 m
23.Pumps & pump power

Answer: η = 82.13 %

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 = 1000·9.81·0.15·12 = 17.66 kW

Efficiency

η = Ph/Pshaft = 17.66/21.5 = 82.13%

Answer

η = 82.13%
24.Pumps & pump power

Answer: Pshaft = 40.38 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 = 0.12/0.04909 = 2.445 m/s
V²/(2g) = 0.3046 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (40 + 6)·0.3046 = 14.01 m

Pump head

H = Δz + hL = 10 + 14.01 = 24.01 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.12·24.01/0.7 = 40.38 kW

Answer

Pshaft = 40.38 kW

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