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 1850 kg/h · 5% NaOHStream 2ṁ₂ = ? · 50% NaOHProduct45% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 45% NaOH? Find ṁ2.

ṁ1 = 850 kg/hx1 = 5 %x2 = 50 %x3 = 45 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3200 kg/h · 18% NaOHProduct PP = ? · 65%Vapour W (pure water)0% NaOH

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

F = 3200 kg/hxF = 18 %xP = 65 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 120 °C60 °Cwater · 30 °Ct = ? °C

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

ṁh = 1.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 120 → 60 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 130 °C90 °Cwater · 10 °C70 °C · ṁ = ?5% lost

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

ṁh = 3 kg/scp,h = 2.1 kJ/(kg·K)Th: 130 → 90 °Ct: 10 → 70 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
420 g of N₂P = 400 kPaT = 15 °CV = ?

What volume V does 420 g of N₂ occupy at 400 kPa and 15 °C? Treat it as an ideal gas.

m = 420 gM = 28.01 g/molP = 400 kPaT = 15 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of Ar goes from 400 kPa, 10 L, 35 °C to 500 kPa and 210 °C. Find the new volume V2.

P1 = 400 kPaV1 = 10 LT1 = 35 °CP2 = 500 kPaT2 = 210 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

10 g of H2 and 16 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(N2​)n(N2​)n(NH3​)m(NH3​)÷ M(N2​)× 2/1× M(NH3​)

In the reaction N2 + 3H2 → 2NH3, 12 g of N2 reacts completely (the other reactants are in excess) and 8.02 g of NH3 is collected. Find the percent yield Y.

M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 8.02 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII110C−x−x+2xE1 − x1 − x2x

1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 49. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 49
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I100C−x+x+xE1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 at the reaction temperature. A container starts with 1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 1 mol/LKc = 0.08
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 150 gT = 100 °Cc = 0.388 J/(g·°C)Waterm = 100 gT = 16 °Cc = 4.18 J/(g·°C)

A 150 g block of zinc (c = 0.388 J/(g·°C)) at 100 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 16 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.388 J/(g·°C)Tmetal = 100 °Cmwater = 100 gTwater = 16 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H25 g CH3​OH2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 25 g of CH3OH (M = 32.04 g/mol) burns completely: 2CH3OH + 3O₂ → 2CO₂ + 4H₂O(l). Give q as a positive number.

ΔH°f(CH3OH) = −238.7 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 = ?60%

A zero-order reaction has k = 0.02 mol/(L·min) and starts at 1.5 mol/L. How long does it take to reach 60% conversion? Find t.

k = 0.02 mol/(L·min)CA0 = 1.5 mol/LX = 60 %
t = min
14.Reaction kineticsHard
Tk40 °Ck1​?5·k1​

A reaction has an activation energy of 75 kJ/mol. At 40 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 5 times faster?

Ea = 75 kJ/molT1 = 40 °Ck2/k1 = 5R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minX = 60%V = ?, k = 0.3 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.3 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 60% conversion of A.

Q = 50 L/mink = 0.3 min⁻¹X = 60%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 800 LQ = 25 L/minX = ?

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in an 800 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 = 800 LQ = 25 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT155 °C135 °C55 °C15 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 280 kW. Its heat transfer area is 8 m². The hot fluid cools from 155 to 135 °C and the cold fluid heats from 15 to 55 °C. Find the overall heat transfer coefficient U.

Q̇ = 280 kWA = 8 m²Th: 155 → 135 °CTc: 15 → 55 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT140 °C70 °C71.87 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (0.5 kg/s, cp = 2.5 kJ/(kg·K)) cools from 140 to 70 °C in a counter-flow exchanger. It heats 0.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 1000 W/(m²·K), find the heat transfer area A needed.

ṁh = 0.5 kg/scp,h = 2.5 kJ/(kg·K)Th: 140 → 70 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 1000 W/(m²·K)
A = m²
19.Heat conductionMedium
Concrete, k = 1.4200 mmExpanded polystyrene, k = 0.03525 mm17 °C-5 °CTi​ = ?Q̇

A wall is made of 200 mm of concrete and 25 mm of expanded polystyrene, with an area of 15 m². The outer faces are at 17 °C and -5 °C. Find the temperature Ti at the interface between the two layers.

L1 = 200 mm, k1 = 1.4 W/(m·K)L2 = 25 mm, k2 = 0.035 W/(m·K)A = 15 m²T1 = 17 °CT3 = -5 °C
Ti = °C
20.Heat conductionHard
Gypsum board, k = 0.17250 mmConcrete, k = 1.4100 mmroom 22 °Coutside 5 °CQ̇

A wall of 250 mm gypsum board and 100 mm concrete separates a room at 22 °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 8 m². Find the overall heat transfer coefficient U of the wall.

L1 = 250 mm, k1 = 0.17 W/(m·K)L2 = 100 mm, k2 = 1.4 W/(m·K)A = 8 m²hi = 6 W/(m²·K)ho = 30 W/(m²·K)Troom = 22 °CTout = 5 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 2.2 m/sD = 50 mmL = 150 mf = 0.02

Water flows at a mean velocity of 2.2 m/s through a pipe 150 m long with an inside diameter of 50 mm. Use the Darcy friction factor f = 0.02 and g = 9.81 m/s². Find the friction head loss hf.

V = 2.2 m/sL = 150 mD = 50 mmf = 0.02g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2Δz = 21 mL = 100 m, D = 200 mm, f = 0.0154× bend (K = 0.3)

Two open reservoirs are joined by a pipe 100 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.015. The water surface of the upper reservoir is 21 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 4 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. Find the flow rate Q in L/s.

Δz = 21 mL = 100 mD = 200 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 80 L/sH = 48 m

A pump with an efficiency of 80% delivers 80 L/s of water (ρ = 1000 kg/m³) against a head of 48 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 80 L/sH = 48 mη = 80%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 25 mL = 100 m, D = 200 mm, f = 0.025, ΣK = 8

A pump moves 75 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 100 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.025; the minor-loss coefficients add up to ΣK = 8 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 75 L/sΔz = 25 mL = 100 mD = 200 mmf = 0.025ΣK = 8
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 6800 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) = 850·(5 − 45)/(45 − 50) = 6800 kg/h

Answer

ṁ2 = 6800 kg/h
2.Mass balance

Answer: P = 886.2 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 = 3200·18/65 = 886.2 kg/h

Answer

P = 886.2 kg/h
3.Energy balance

Answer: tout = 56.27 °C

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

Heat released by the hot stream

Q = 1.5·2.44·(120 − 60) = 219.6 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 219.6/(2·4.18) = 56.27 °C

Answer

tout = 56.27 °C
4.Energy balance

Answer: ṁc = 0.9545 kg/s

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

Heat released

Qh = 3·2.1·(130 − 90) = 252 kW

Heat that reaches the water

Qc = (1 − 0.05)·252 = 239.4 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 239.4/(4.18·60) = 0.9545 kg/s

Answer

ṁc = 0.9545 kg/s
5.Ideal gas law

Answer: V = 89.81 L

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

Moles

n = 420/28.01 = 14.99 mol
T = 15 + 273.15 = 288.1 K

Volume

V = nRT/P = 14.99·8.314·288.1/400 = 89.81 L

Answer

V = 89.81 L
6.Ideal gas law

Answer: V2 = 12.54 L

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

Absolute temperatures

T1 = 308.1 K, T2 = 483.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(400/500)·(483.1/308.1) = 12.54 L

Answer

V2 = 12.54 L
7.Stoichiometry

Answer: m = 18.02 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) = 10/2.016 = 4.96 mol
n(O2) = 16/32 = 0.5 mol

Limiting reactant

4.96/2 = 2.48, 0.5/1 = 0.5 → O2

Mass of product

n(H2O) = 0.5·2 = 1 mol
m = 1·18.02 = 18.02 g

Answer

m = 18.02 g
8.Stoichiometry

Answer: Y = 54.98 %

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) = 12/28.02 = 0.4283 mol
m = 0.4283·2/1·17.03 = 14.59 g

Percent yield

Y = 8.02/14.59·100 = 54.98%

Answer

Y = 54.98%
9.Chemical equilibrium

Answer: [HI] = 1.556 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

49 = (2x)²/(1 − x)²

Take the square root

7 = 2x/(1 − x) → x = 1·7/(2 + 7) = 0.7778 mol/L

Equilibrium concentration

[HI] = 2x = 1.556 mol/L

Answer

[HI] = 1.556 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.7543 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

0.08 = x²/(1 − x) → x² + 0.08·x − 0.08 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.08))/2 = 0.2457 mol/L

Equilibrium concentration

[PCl₅] = 1 − 0.2457 = 0.7543 mol/L

Answer

[PCl5] = 0.7543 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 26.27 °C

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

Heat balance

150·0.388·(100 − Tf) = 100·4.18·(Tf − 16)

Solve for the final temperature

Tf = (58.2·100 + 418·16)/(58.2 + 418) = 26.27 °C

Answer

Tf = 26.27 °C
12.Calorimetry & enthalpy

Answer: q = 566.8 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° = [2·(−393.5) + 4·(−285.8)] − [2·(−238.7) + 3·0] = −1453 kJ

Heat for the given mass

n = 25/32.04 = 0.7803 mol
q = n·|ΔH°/2| = 0.7803·726.4 = 566.8 kJ

Answer

q = 566.8 kJ
13.Reaction kinetics

Answer: t = 45 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 = 1.5·0.6 = 0.9 mol/L

Time

t = CA0·X/k = 0.9/0.02 = 45 min

Answer

t = 45 min
14.Reaction kinetics

Answer: T2 = 58.53 °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(5)/75000 = 3.193 × 10⁻³ − 1.784 × 10⁻⁴ = 3.015 × 10⁻³ K⁻¹
T2 = 331.7 K = 58.53 °C

Answer

T2 = 58.53 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 152.7 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 − 0.6))/0.3 = 0.9163/0.3 = 3.054 min

Volume

V = Q·τ = 50·3.054 = 152.7 L

Answer

V = 152.7 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 76.19 %

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 = 800/25 = 32 min, kτ = 0.1·32 = 3.2

Conversion

X = kτ/(1 + kτ) = 3.2/(1 + 3.2) = 76.19%

Answer

X = 76.19%
17.Heat exchangers (LMTD)

Answer: U = 319.1 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 counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 155 − 55 = 100 K
ΔT₂ = Th,out − Tc,in = 135 − 15 = 120 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (100 − 120)/ln(100/120) = 109.7 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 280000/(8·109.7) = 319.1 W/(m²·K)

Answer

U = 319.1 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: A = 1.656 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) = 0.5·2.5·70 = 87.5 kW
Tc,out = 30 + 87.5/(0.5·4.18) = 71.87 °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 = 140 − 71.87 = 68.13 K
ΔT₂ = Th,out − Tc,in = 70 − 30 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (68.13 − 40)/ln(68.13/40) = 52.82 K

Area

A = Q̇/(U·ΔTlm) = 87500/(1000·52.82) = 1.656 m²

Answer

A = 1.656 m²
19.Heat conduction

Answer: Ti = 13.33 °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) = (200/1000)/(1.4·15) = 0.009524 K/W
R2 = L2/(k2A) = (25/1000)/(0.035·15) = 0.04762 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 22/0.05714 = 385 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 17 − 385·0.009524 = 13.33 °C

Answer

Ti = 13.33 °C
20.Heat conduction

Answer: U = 0.574 W/(m²·K)

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/(6·8) = 0.02083 K/W
R1 = L1/(k1A) = (250/1000)/(0.17·8) = 0.1838 K/W
R2 = L2/(k2A) = (100/1000)/(1.4·8) = 0.008929 K/W
Ro = 1/(hoA) = 1/(30·8) = 0.004167 K/W
ΣR = 0.2178 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(8·0.2178) = 0.574 W/(m²·K)

Answer

U = 0.574 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 14.8 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 head

V²/(2g) = 2.2²/(2·9.81) = 0.2467 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.02·(150/0.05)·2.2²/(2·9.81) = 14.8 m

Answer

hf = 14.8 m
22.Pipe friction & head loss

Answer: Q = 182.6 L/s

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.

Loss coefficients

f·L/D = 0.015·100/0.2 = 7.5
ΣK = 0.5 + 4·0.3 + 2 + 1.0 = 4.7

Energy equation

Both surfaces are open to the air and practically at rest, so all of Δz is lost in the pipe.

21 = (7.5 + 4.7)·V²/(2·9.81)
V = √(2·9.81·21/12.2) = 5.811 m/s

Flow rate

Q = V·π·D²/4 = 5.811·0.03142 = 0.1826 m³/s = 182.6 L/s

Answer

Q = 182.6 L/s
23.Pumps & pump power

Answer: Pshaft = 47.09 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 = 1000·9.81·0.08·48 = 37.67 kW

Shaft power

Pshaft = Ph/η = 37.67/0.8 = 47.09 kW

Answer

Pshaft = 47.09 kW
24.Pumps & pump power

Answer: H = 30.95 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 = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (12.5 + 8)·0.2905 = 5.955 m

Pump head

Both surfaces are open and practically at rest, so pressure and velocity terms drop out.

H = Δz + hL = 25 + 5.955 = 30.95 m

Answer

H = 30.95 m

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