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 1550 kg/h · 45% NaOHStream 2ṁ₂ = ? · 15% NaOHProduct40% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 40% NaOH? Find ṁ2.

ṁ1 = 550 kg/hx1 = 45 %x2 = 15 %x3 = 40 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3500 kg/h · 14% NaOHProduct P55% 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 = 3500 kg/hxF = 14 %xP = 55 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 160 °C100 °Cwater · 20 °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 → 100 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 180 °C150 °Cwater · 25 °C55 °C · ṁ = ?15% lost

Hot glycol mix heats water in an exchanger that loses 15% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 2 kg/scp,h = 3.6 kJ/(kg·K)Th: 180 → 150 °Ct: 25 → 55 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
450 g of HeV = 10 LT = 35 °CP = ?

A tank of 10 L contains 450 g of He at 35 °C. Treat it as an ideal gas and find the pressure P.

m = 450 gM = 4.003 g/molV = 10 LT = 35 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of He goes from 250 kPa, 2 L, 30 °C to 500 kPa and 140 °C. Find the new volume V2.

P1 = 250 kPaV1 = 2 LT1 = 30 °CP2 = 500 kPaT2 = 140 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 3/ν× M(CO2​)

16 g of C3H8 and 16 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(Na)n(Na)n(NaCl)m(NaCl)÷ M(Na)× 2/2× M(NaCl)

In the reaction 2Na + Cl2 → 2NaCl, 12 g of Na reacts completely (the other reactants are in excess) and 25.93 g of NaCl is collected. Find the percent yield Y.

M(Na) = 22.99 g/molM(NaCl) = 58.44 g/molactual: 25.93 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 = 36. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 36
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I1.500C−x+x+xE1.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 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 = 0.1
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 100 gT = 200 °Cc = 0.385 J/(g·°C)Waterm = 200 gT = 24 °Cc = 4.18 J/(g·°C)

A 100 g block of copper (c = 0.385 J/(g·°C)) at 200 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 24 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.385 J/(g·°C)Tmetal = 200 °Cmwater = 200 gTwater = 24 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H250 g C2​H6​2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 250 g of C2H6 (M = 30.07 g/mol) burns completely: 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C2H6) = −84.7 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = kJ
13.Reaction kineticsMedium
t (min)X (%)t = ?20%

A zero-order reaction has k = 0.02 mol/(L·min) and starts at 2 mol/L. How long does it take to reach 20% conversion? Find t.

k = 0.02 mol/(L·min)CA0 = 2 mol/LX = 20 %
t = min
14.Reaction kineticsHard
Tk25 °Ck1​?2·k1​

A reaction has an activation energy of 60 kJ/mol. At 25 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 2 times faster?

Ea = 60 kJ/molT1 = 25 °Ck2/k1 = 2R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minX = 70%V = ?, k = 0.05 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.05 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 = 0.05 min⁻¹X = 70%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 250 LQ = 50 L/minX = ?

A first-order liquid-phase reaction (k = 0.2 min⁻¹) runs in a 250 L CSTR fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 250 LQ = 50 L/mink = 0.2 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT85 °C65 °C15 °C30 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 450 kW. Its heat transfer area is 3 m². The hot fluid cools from 85 to 65 °C and the cold fluid heats from 15 to 30 °C. Find the overall heat transfer coefficient U.

Q̇ = 450 kWA = 3 m²Th: 85 → 65 °CTc: 15 → 30 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT110 °C80 °C53.92 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (2 kg/s, cp = 2.5 kJ/(kg·K)) cools from 110 to 80 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 200 W/(m²·K), find the heat transfer area A needed.

ṁh = 2 kg/scp,h = 2.5 kJ/(kg·K)Th: 110 → 80 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 200 W/(m²·K)
A = m²
19.Heat conductionMedium
Expanded polystyrene, k = 0.035100 mmBrick, k = 0.7225 mm25 °C-12 °CTi​ = ?Q̇

A wall is made of 100 mm of expanded polystyrene and 25 mm of brick, with an area of 20 m². The outer faces are at 25 °C and -12 °C. Find the temperature Ti at the interface between the two layers.

L1 = 100 mm, k1 = 0.035 W/(m·K)L2 = 25 mm, k2 = 0.72 W/(m·K)A = 20 m²T1 = 25 °CT3 = -12 °C
Ti = °C
20.Heat conductionHard
Wood, k = 0.1750 mmGypsum board, k = 0.1750 mmroom 22 °Coutside 0 °CTs​ = ?Q̇

A wall of 50 mm wood and 50 mm gypsum board separates a room at 22 °C from outside air at 0 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 6 m². Find the temperature Ts of the inside surface of the wall.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 6 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 22 °CTout = 0 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.1 m/sD = 300 mmL = 200 mf = 0.02

Water (ρ = 1000 kg/m³) flows at 1.1 m/s through a horizontal pipe, 200 m long, with an inside diameter of 300 mm. Use the Darcy friction factor f = 0.02 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.1 m/sL = 200 mD = 300 mmf = 0.02ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2Δz = ?L = 300 m, D = 250 mm, f = 0.0182× bend (K = 0.3)

Two open reservoirs are joined by a pipe 300 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.018. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 2) 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 60 L/s?

Q = 60 L/sL = 300 mD = 250 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 15 L/sH = 18 m

In a test, a pump delivers 15 L/s of water (ρ = 1000 kg/m³) against a head of 18 m while its shaft takes 4.4 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 15 L/sH = 18 mPshaft = 4.4 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
400 kPa (gauge)PQ = 40 L/sΔz = 9 mL = 100 m, D = 150 mm, f = 0.022, ΣK = 5

A pump moves 40 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 9 m higher. The pipe is 100 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.022; the minor-loss coefficients add up to ΣK = 5 (entrance and exit included). Use g = 9.81 m/s². The upper tank is closed and the air above its water is at a gauge pressure of 400 kPa. Find the head H the pump must add.

Q = 40 L/sΔz = 9 mL = 100 mD = 150 mmf = 0.022ΣK = 5ptank = 400 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 110 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) = 550·(45 − 40)/(40 − 15) = 110 kg/h

Answer

ṁ2 = 110 kg/h
2.Mass balance

Answer: W = 2609 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 = 3500·14/55 = 890.9 kg/h

Total balance

W = F − P = 3500 − 890.9 = 2609 kg/h

Answer

W = 2609 kg/h
3.Energy balance

Answer: tout = 97.51 °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 − 100) = 324 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 324/(1·4.18) = 97.51 °C

Answer

tout = 97.51 °C
4.Energy balance

Answer: ṁc = 1.464 kg/s

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

Heat released

Qh = 2·3.6·(180 − 150) = 216 kW

Heat that reaches the water

Qc = (1 − 0.15)·216 = 183.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 183.6/(4.18·30) = 1.464 kg/s

Answer

ṁc = 1.464 kg/s
5.Ideal gas law

Answer: P = 28800 kPa

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

Moles

n = m/M = 450/4.003 = 112.4 mol
T = 35 + 273.15 = 308.1 K

Pressure

P = nRT/V = 112.4·8.314·308.1/0.01 = 28800 kPa

Answer

P = 28800 kPa
6.Ideal gas law

Answer: V2 = 1.363 L

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

Absolute temperatures

T1 = 303.1 K, T2 = 413.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(250/500)·(413.1/303.1) = 1.363 L

Answer

V2 = 1.363 L
7.Stoichiometry

Answer: m = 13.2 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) = 16/44.1 = 0.3628 mol
n(O2) = 16/32 = 0.5 mol

Limiting reactant

0.3628/1 = 0.3628, 0.5/5 = 0.1 → O2

Mass of product

n(CO2) = 0.1·3 = 0.3 mol
m = 0.3·44.01 = 13.2 g

Answer

m = 13.2 g
8.Stoichiometry

Answer: Y = 85.01 %

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(Na) = 12/22.99 = 0.522 mol
m = 0.522·2/2·58.44 = 30.5 g

Percent yield

Y = 25.93/30.5·100 = 85.01%

Answer

Y = 85.01%
9.Chemical equilibrium

Answer: [HI] = 0.75 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/(0.5 − x)²

Take the square root

6 = 2x/(0.5 − x) → x = 0.5·6/(2 + 6) = 0.375 mol/L

Equilibrium concentration

[HI] = 2x = 0.75 mol/L

Answer

[HI] = 0.75 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 1.159 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/(1.5 − x) → x² + 0.1·x − 0.15 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.15))/2 = 0.3405 mol/L

Equilibrium concentration

[PCl₅] = 1.5 − 0.3405 = 1.159 mol/L

Answer

[PCl5] = 1.159 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 31.75 °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

100·0.385·(200 − Tf) = 200·4.18·(Tf − 24)

Solve for the final temperature

Tf = (38.5·200 + 836·24)/(38.5 + 836) = 31.75 °C

Answer

Tf = 31.75 °C
12.Calorimetry & enthalpy

Answer: q = 12967 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

Heat for the given mass

n = 250/30.07 = 8.314 mol
q = n·|ΔH°/2| = 8.314·1560 = 12967 kJ

Answer

q = 12967 kJ
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).

Amount converted

CA0·X = 2·0.2 = 0.4 mol/L

Time

t = CA0·X/k = 0.4/0.02 = 20 min

Answer

t = 20 min
14.Reaction kinetics

Answer: T2 = 33.79 °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 = 298.1 K

Solve Arrhenius for T₂

1/T2 = 1/298.1 − 8.314·ln(2)/60000 = 3.354 × 10⁻³ − 9.605 × 10⁻⁵ = 3.258 × 10⁻³ K⁻¹
T2 = 306.9 K = 33.79 °C

Answer

T2 = 33.79 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 1204 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))/0.05 = 1.204/0.05 = 24.08 min

Volume

V = Q·τ = 50·24.08 = 1204 L

Answer

V = 1204 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 = 250/50 = 5 min, kτ = 0.2·5 = 1

Conversion

X = kτ/(1 + kτ) = 1/(1 + 1) = 50%

Answer

X = 50%
17.Heat exchangers (LMTD)

Answer: U = 2971 W/(m²·K)

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 = 85 − 15 = 70 K
ΔT₂ = Th,out − Tc,out = 65 − 30 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (70 − 35)/ln(70/35) = 50.49 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 450000/(3·50.49) = 2971 W/(m²·K)

Answer

U = 2971 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: A = 14.16 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) = 2·2.5·30 = 150 kW
Tc,out = 30 + 150/(1.5·4.18) = 53.92 °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 = 110 − 53.92 = 56.08 K
ΔT₂ = Th,out − Tc,in = 80 − 30 = 50 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (56.08 − 50)/ln(56.08/50) = 52.98 K

Area

A = Q̇/(U·ΔTlm) = 150000/(200·52.98) = 14.16 m²

Answer

A = 14.16 m²
19.Heat conduction

Answer: Ti = −11.56 °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) = (100/1000)/(0.035·20) = 0.1429 K/W
R2 = L2/(k2A) = (25/1000)/(0.72·20) = 0.001736 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 37/0.1446 = 255.9 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 25 − 255.9·0.1429 = −11.56 °C

Answer

Ti = −11.56 °C
20.Heat conduction

Answer: Ts = 18.2 °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/(7.7·6) = 0.02165 K/W
R1 = L1/(k1A) = (50/1000)/(0.17·6) = 0.04902 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·6) = 0.04902 K/W
Ro = 1/(hoA) = 1/(30·6) = 0.005556 K/W
ΣR = 0.1252 K/W

Heat loss

Q̇ = (22 − (0))/0.1252 = 175.7 W
Ts = Troom − Q̇·Ri = 22 − 175.7·0.02165 = 18.2 °C

Answer

Ts = 18.2 °C
21.Pipe friction & head loss

Answer: Δp = 8.067 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) = 0.02·(200/0.3)·1.1²/(2·9.81) = 0.8223 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 = 1000·9.81·0.8223 = 8067 Pa = 8.067 kPa

Answer

Δp = 8.067 kPa
22.Pipe friction & head loss

Answer: Δz = 1.957 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 = 0.018·300/0.25 = 21.6
ΣK = 0.5 + 2·0.3 + 2 + 1.0 = 4.1

Total head loss

hf = 21.6·0.07615 = 1.645 m
hm = 4.1·0.07615 = 0.3122 m
Δz = hf + hm = 1.957 m

Answer

Δz = 1.957 m
23.Pumps & pump power

Answer: η = 60.2 %

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 = 1000·9.81·0.015·18 = 2.649 kW

Efficiency

η = Ph/Pshaft = 2.649/4.4 = 60.2%

Answer

η = 60.2%
24.Pumps & pump power

Answer: H = 54.91 m

Pump power: the power given to the water is the hydraulic power Ph = ρ·g·Q·H = Q·Δp. The shaft must deliver more because the pump loses some: Pshaft = Ph/ηpump, and the motor draws Pel = Pshaft/ηmotor. The pump head H follows from the energy equation: static lift + pressure head + all friction and minor losses.

Velocity

V = Q/A = 0.04/0.01767 = 2.264 m/s
V²/(2g) = 0.2611 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (14.67 + 5)·0.2611 = 5.136 m

Pressure head

p/(ρ·g) = 400000/(1000·9.81) = 40.77 m

Pump head

Both surfaces are practically at rest, so there is no velocity head term.

H = Δz + p/(ρ·g) + hL = 9 + 40.77 + 5.136 = 54.91 m

Answer

H = 54.91 m

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