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 · 15% sugarStream 2ṁ₂ = ? · 30% sugarProduct20% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 20% sugar? Find ṁ2.

ṁ1 = 600 kg/hx1 = 15 %x2 = 30 %x3 = 20 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1900 kg/h · 12% saltProduct PP = ? · 35%Vapour W (pure water)0% salt

An evaporator concentrates a salt solution by boiling off pure water. Find the product flow P in kg/h.

F = 1900 kg/hxF = 12 %xP = 35 %
P = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 180 °C140 °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: 180 → 140 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 180 °C80 °Cwater · 15 °C40 °C · ṁ = ?15% lost

Hot light oil 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 = 3 kg/scp,h = 2.1 kJ/(kg·K)Th: 180 → 80 °Ct: 15 → 40 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
410 g of N₂P = 350 kPaT = 60 °CV = ?

What volume V does 410 g of N₂ occupy at 350 kPa and 60 °C? Treat it as an ideal gas.

m = 410 gM = 28.01 g/molP = 350 kPaT = 60 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of O₂ goes from 300 kPa, 20 L, 20 °C to 250 kPa and 180 °C. Find the new volume V2.

P1 = 300 kPaV1 = 20 LT1 = 20 °CP2 = 250 kPaT2 = 180 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(NH3​)m(NH3​)÷ M(X)× 2/ν× M(NH3​)

10 g of N2 and 10 g of H2 react according to N2 + 3H2 → 2NH3. What mass m of NH3 can form?

M(N2) = 28.02M(H2) = 2.016M(NH3) = 17.03 g/mol
m = g
8.StoichiometryHard
m(C3​H8​)n(C3​H8​)n(H2​O)m(H2​O)÷ M(C3​H8​)× 4/1× M(H2​O)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 12 g of C3H8 reacts completely (the other reactants are in excess) and 13.73 g of H2O is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 13.73 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.40.40C−x−x+2xE0.4 − x0.4 − x2x

0.4 mol/L of H₂ and 0.4 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 36. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 36
[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​ = ?Copperm = 75 gT = 180 °Cc = 0.385 J/(g·°C)Waterm = 250 gT = 19 °Cc = 4.18 J/(g·°C)

A 75 g block of copper (c = 0.385 J/(g·°C)) at 180 °C is dropped into 250 g of water (c = 4.18 J/(g·°C)) at 19 °C in an insulated cup. Find the final temperature Tf.

mmetal = 75 gcmetal = 0.385 J/(g·°C)Tmetal = 180 °Cmwater = 250 gTwater = 19 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l).

ΔH°f(C4H10) = −125.6 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 = 0.05 L/(mol·min) and starts at 1 mol/L. How long does it take to reach 50% conversion? Find t.

k = 0.05 L/(mol·min)CA0 = 1 mol/LX = 50 %
t = min
14.Reaction kineticsHard
Tk30 °C0.0155 °C0.0613

The rate constant of a reaction is 0.01 min⁻¹ at 30 °C and 0.0613 min⁻¹ at 55 °C. Find the activation energy Ea.

k1 = 0.01 min⁻¹T1 = 30 °Ck2 = 0.0613 min⁻¹T2 = 55 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minX = 70%V = ?, k = 0.2 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.2 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 70% conversion of A.

Q = 50 L/mink = 0.2 min⁻¹X = 70%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 20 L/minX = ?V = 200 L

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in a 200 L plug-flow reactor (PFR) fed at 20 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 20 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT130 °C70 °C110 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 410 kW. The hot fluid cools from 130 to 70 °C and the cold fluid heats from 25 to 110 °C. The overall heat transfer coefficient is 1000 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 410 kWU = 1000 W/(m²·K)Th: 130 → 70 °CTc: 25 → 110 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT115 °C60 °C?15 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.2 kg/s, cp = 2.1 kJ/(kg·K)) flows in the inner tube and cools from 115 to 60 °C. Water (0.8 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 15 °C. The inner tube has a diameter of 40 mm, and U = 300 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.2 kg/scp,h = 2.1 kJ/(kg·K)Th: 115 → 60 °Cṁc = 0.8 kg/sTc,in = 15 °CD = 40 mmU = 300 W/(m²·K)
L = m
19.Heat conductionMedium
Mineral wool, k = 0.0450 mmWood, k = 0.17150 mm25 °C-15 °CTi​ = ?Q̇

A wall is made of 50 mm of mineral wool and 150 mm of wood, with an area of 4 m². The outer faces are at 25 °C and -15 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 0.04 W/(m·K)L2 = 150 mm, k2 = 0.17 W/(m·K)A = 4 m²T1 = 25 °CT3 = -15 °C
Ti = °C
20.Heat conductionHard
Wood, k = 0.17100 mmConcrete, k = 1.475 mmroom 20 °Coutside -2 °CTs​ = ?Q̇

A wall of 100 mm wood and 75 mm concrete separates a room at 20 °C from outside air at -2 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 4 m². Find the temperature Ts of the inside surface of the wall.

L1 = 100 mm, k1 = 0.17 W/(m·K)L2 = 75 mm, k2 = 1.4 W/(m·K)A = 4 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = -2 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 40 L/sD = 250 mmL = 150 mf = 0.025

Water flows at 40 L/s through a pipe 150 m long with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.025 and g = 9.81 m/s². Find the friction head loss hf.

Q = 40 L/sL = 150 mD = 250 mmf = 0.025g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 200 m, D = 200 mm, f = 0.0252× bend (K = 0.3)

A pipe 200 m long with an inside diameter of 200 mm (Darcy friction factor f = 0.025) 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 = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 75 L/s?

Q = 75 L/sL = 200 mD = 200 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 20 L/sH = 10 m

In a test, a pump delivers 20 L/s of water (ρ = 1000 kg/m³) against a head of 10 m while its shaft takes 3 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 20 L/sH = 10 mPshaft = 3 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 80 L/sΔz = 33 mL = 400 m, D = 200 mm, f = 0.02, ΣK = 8

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 33 m higher. The pipe is 400 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.02; the minor-loss coefficients add up to ΣK = 8 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 82%. Find the shaft power Pshaft in kW.

Q = 80 L/sΔz = 33 mL = 400 mD = 200 mmf = 0.02ΣK = 8η = 82%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 300 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) = 600·(15 − 20)/(20 − 30) = 300 kg/h

Answer

ṁ2 = 300 kg/h
2.Mass balance

Answer: P = 651.4 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 = 1900·12/35 = 651.4 kg/h

Answer

P = 651.4 kg/h
3.Energy balance

Answer: tout = 41.75 °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·(180 − 140) = 210 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 210/(3·4.18) = 41.75 °C

Answer

tout = 41.75 °C
4.Energy balance

Answer: ṁc = 5.124 kg/s

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

Heat released

Qh = 3·2.1·(180 − 80) = 630 kW

Heat that reaches the water

Qc = (1 − 0.15)·630 = 535.5 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 535.5/(4.18·25) = 5.124 kg/s

Answer

ṁc = 5.124 kg/s
5.Ideal gas law

Answer: V = 115.8 L

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

Moles

n = 410/28.01 = 14.64 mol
T = 60 + 273.15 = 333.1 K

Volume

V = nRT/P = 14.64·8.314·333.1/350 = 115.8 L

Answer

V = 115.8 L
6.Ideal gas law

Answer: V2 = 37.1 L

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

Absolute temperatures

T1 = 293.1 K, T2 = 453.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 20·(300/250)·(453.1/293.1) = 37.1 L

Answer

V2 = 37.1 L
7.Stoichiometry

Answer: m = 12.16 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(N2) = 10/28.02 = 0.3569 mol
n(H2) = 10/2.016 = 4.96 mol

Limiting reactant

0.3569/1 = 0.3569, 4.96/3 = 1.653 → N2

Mass of product

n(NH3) = 0.3569·2 = 0.7138 mol
m = 0.7138·17.03 = 12.16 g

Answer

m = 12.16 g
8.Stoichiometry

Answer: Y = 70 %

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(C3H8) = 12/44.1 = 0.2721 mol
m = 0.2721·4/1·18.02 = 19.61 g

Percent yield

Y = 13.73/19.61·100 = 70%

Answer

Y = 70%
9.Chemical equilibrium

Answer: [H2] = 0.1 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

36 = (2x)²/(0.4 − x)²

Take the square root

6 = 2x/(0.4 − x) → x = 0.4·6/(2 + 6) = 0.3 mol/L

Equilibrium concentration

[H₂] = 0.4 − x = 0.1 mol/L

Answer

[H2] = 0.1 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 = 23.33 °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

75·0.385·(180 − Tf) = 250·4.18·(Tf − 19)

Solve for the final temperature

Tf = (28.88·180 + 1045·19)/(28.88 + 1045) = 23.33 °C

Answer

Tf = 23.33 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −5755 kJ

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

Enthalpy of reaction

ΔH° = [8·(−393.5) + 10·(−285.8)] − [2·(−125.6) + 13·0] = −5755 kJ

Answer

ΔH° = −5755 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 20 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·(1 − 0.5) = 0.5 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (2 − 1)/0.05 = 20 min

Answer

t = 20 min
14.Reaction kinetics

Answer: Ea = 59.99 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 = 328.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·1.813/(-2.513e-4) = 59985 J/mol
Ea = 59.99 kJ/mol

Answer

Ea = 59.99 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: V = 301 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 − 0.7))/0.2 = 1.204/0.2 = 6.02 min

Volume

V = Q·τ = 50·6.02 = 301 L

Answer

V = 301 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 69.88 %

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 = 200/20 = 10 min, kτ = 0.12·10 = 1.2

Conversion

X = 1 − e−kτ = 1 − e−1.2 = 69.88%

Answer

X = 69.88%
17.Heat exchangers (LMTD)

Answer: A = 13.3 m²

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

End temperature differences

In counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 130 − 110 = 20 K
ΔT₂ = Th,out − Tc,in = 70 − 25 = 45 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (20 − 45)/ln(20/45) = 30.83 K

Area

A = Q̇/(U·ΔTlm) = 410000/(1000·30.83) = 13.3 m²

Answer

A = 13.3 m²
18.Heat exchangers (LMTD)

Answer: L = 9.262 m

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 = 0.2·2.1·(115 − 60) = 23.1 kW
Tc,out = 15 + 23.1/(0.8·4.18) = 21.91 °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 − 21.91 = 93.09 K
ΔT₂ = Th,out − Tc,in = 60 − 15 = 45 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (93.09 − 45)/ln(93.09/45) = 66.16 K

Area and length

A = 23100/(300·66.16) = 1.164 m²
L = A/(πD) = 1.164/(π·0.04) = 9.262 m

Answer

L = 9.262 m
19.Heat conduction

Answer: Ti = 1.552 °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)/(0.04·4) = 0.3125 K/W
R2 = L2/(k2A) = (150/1000)/(0.17·4) = 0.2206 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 40/0.5331 = 75.03 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 25 − 75.03·0.3125 = 1.552 °C

Answer

Ti = 1.552 °C
20.Heat conduction

Answer: Ts = 16.45 °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/(7.7·4) = 0.03247 K/W
R1 = L1/(k1A) = (100/1000)/(0.17·4) = 0.1471 K/W
R2 = L2/(k2A) = (75/1000)/(1.4·4) = 0.01339 K/W
Ro = 1/(hoA) = 1/(30·4) = 0.008333 K/W
ΣR = 0.2013 K/W

Heat loss

Q̇ = (20 − (-2))/0.2013 = 109.3 W
Ts = Troom − Q̇·Ri = 20 − 109.3·0.03247 = 16.45 °C

Answer

Ts = 16.45 °C
21.Pipe friction & head loss

Answer: hf = 0.5077 m

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

Mean velocity

A = π·0.25²/4 = 0.04909 m²
V = Q/A = 0.04/0.04909 = 0.8149 m/s

Velocity head

V²/(2g) = 0.8149²/(2·9.81) = 0.03384 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.025·(150/0.25)·0.8149²/(2·9.81) = 0.5077 m

Answer

hf = 0.5077 m
22.Pipe friction & head loss

Answer: H = 8.453 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 = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Loss coefficients

f·L/D = 0.025·200/0.2 = 25
ΣK = 0.5 + 2·0.3 + 2 = 3.1

Energy equation

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

H = (1 + 25 + 3.1)·0.2905 = 8.453 m

Answer

H = 8.453 m
23.Pumps & pump power

Answer: η = 65.4 %

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 = 1000·9.81·0.02·10 = 1.962 kW

Efficiency

η = Ph/Pshaft = 1.962/3 = 65.4%

Answer

η = 65.4%
24.Pumps & pump power

Answer: Pshaft = 46.77 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) = (40 + 8)·0.3305 = 15.86 m

Pump head

H = Δz + hL = 33 + 15.86 = 48.86 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.08·48.86/0.82 = 46.77 kW

Answer

Pshaft = 46.77 kW

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