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 · 50% NaOHStream 2ṁ₂ = ? · 5% NaOHProduct25% NaOH

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

ṁ1 = 550 kg/hx1 = 50 %x2 = 5 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4200 kg/h · 5% saltProduct PP = ? · 30%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 = 4200 kg/hxF = 5 %xP = 30 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 140 °C80 °Cwater · 25 °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: 140 → 80 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 130 °C60 °Cwater · 10 °C70 °C · ṁ = ?10% lost

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

ṁh = 2.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 130 → 60 °Ct: 10 → 70 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
20 g of N₂V = 20 LT = 30 °CP = ?

A tank of 20 L contains 20 g of N₂ at 30 °C. Treat it as an ideal gas and find the pressure P.

m = 20 gM = 28.01 g/molV = 20 LT = 30 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
He, M = 4.003 g/molP = 850 kPaT = 190 °Cρ = ?

Find the density ρ of He at 850 kPa and 190 °C, treating it as an ideal gas.

M = 4.003 g/molP = 850 kPaT = 190 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

4 g of Na and 32 g of Cl2 react according to 2Na + Cl2 → 2NaCl. What mass m of NaCl can form?

M(Na) = 22.99M(Cl2) = 70.9M(NaCl) = 58.44 g/mol
m = g
8.StoichiometryHard
m(CaCO3​)n(CaCO3​)n(CaO)m(CaO)÷ M(CaCO3​)× 1/1× M(CaO)

In the reaction CaCO3 → CaO + CO2, 10 g of CaCO3 reacts completely (the other reactants are in excess) and 4.93 g of CaO is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CaO) = 56.08 g/molactual: 4.93 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 = 54. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 54
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.200C−x+x+xE0.2 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.5 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.2 mol/LKc = 0.5
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 250 gT = 140 °Cc = 0.388 J/(g·°C)Waterm = 300 gT = 25 °Cc = 4.18 J/(g·°C)

A 250 g block of zinc (c = 0.388 J/(g·°C)) at 140 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.388 J/(g·°C)Tmetal = 140 °Cmwater = 300 gTwater = 25 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC3​H8​ + 5O₂reactants3CO₂ + 4H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C3H8 + 5O₂ → 3CO₂ + 4H₂O(l).

ΔH°f(C3H8) = −103.8 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 min0.75

In a first-order reaction the concentration of A falls from 1.5 mol/L to 0.75 mol/L in 5 min. Find the rate constant k.

CA0 = 1.5 mol/LCA = 0.75 mol/Lt = 5 min
k = min⁻¹
14.Reaction kineticsHard
Tk20 °C0.00535 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 20 °C and an activation energy of 100 kJ/mol. Find the rate constant k2 at 35 °C.

k1 = 0.005 min⁻¹T1 = 20 °CT2 = 35 °CEa = 100 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minX = 90%V = ?, k = 0.08 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.08 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 25 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 = 25 L/mink = 0.08 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 400 LQ = 50 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 400 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 = 400 LQ = 50 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT95 °C70 °C75 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 490 kW. The hot fluid cools from 95 to 70 °C and the cold fluid heats from 25 to 75 °C. The overall heat transfer coefficient is 200 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 490 kWU = 200 W/(m²·K)Th: 95 → 70 °CTc: 25 → 75 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT95 °C60 °C49.26 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (0.5 kg/s, cp = 2.3 kJ/(kg·K)) cools from 95 to 60 °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 = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 0.5 kg/scp,h = 2.3 kJ/(kg·K)Th: 95 → 60 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Glass, k = 0.96250 mmMineral wool, k = 0.0425 mm17 °C-13 °CQ̇ = ?

A wall is made of 250 mm of glass and 25 mm of mineral wool, with an area of 10 m². The outer faces are at 17 °C and -13 °C. Find the heat flow Q̇ through the wall.

L1 = 250 mm, k1 = 0.96 W/(m·K)L2 = 25 mm, k2 = 0.04 W/(m·K)A = 10 m²T1 = 17 °CT3 = -13 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.9650 mmGypsum board, k = 0.17150 mmroom 20 °Coutside -5 °CQ̇ = ?

A wall of 50 mm glass and 150 mm gypsum board separates a room at 20 °C from outside air at -5 °C. The convection coefficients are 6 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 20 m². Find the heat loss Q̇ through the wall.

L1 = 50 mm, k1 = 0.96 W/(m·K)L2 = 150 mm, k2 = 0.17 W/(m·K)A = 20 m²hi = 6 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = -5 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 1.8 m/sD = 300 mmL = 150 mf = 0.015

Water flows at a mean velocity of 1.8 m/s through a pipe 150 m long with an inside diameter of 300 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the friction head loss hf.

V = 1.8 m/sL = 150 mD = 300 mmf = 0.015g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10free outletH = ?L = 150 m, D = 250 mm, f = 0.023× bend (K = 0.3)

A pipe 150 m long with an inside diameter of 250 mm (Darcy friction factor f = 0.02) 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 = 10). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 100 L/s?

Q = 100 L/sL = 150 mD = 250 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 10
H = m
23.Pumps & pump powerMedium
PQ = 30 L/sH = 36 m

A pump with an efficiency of 82% delivers 30 L/s of water (ρ = 1000 kg/m³) against a head of 36 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 30 L/sH = 36 mη = 82%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 40 L/sΔz = 31 mL = 100 m, D = 150 mm, f = 0.025, ΣK = 8

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 31 m higher. The pipe is 100 m long with an inside diameter of 150 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 = 40 L/sΔz = 31 mL = 100 mD = 150 mmf = 0.025ΣK = 8
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 687.5 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·(50 − 25)/(25 − 5) = 687.5 kg/h

Answer

ṁ2 = 687.5 kg/h
2.Mass balance

Answer: P = 700 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 = 4200·5/30 = 700 kg/h

Answer

P = 700 kg/h
3.Energy balance

Answer: tout = 63.76 °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·(140 − 80) = 324 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 324/(2·4.18) = 63.76 °C

Answer

tout = 63.76 °C
4.Energy balance

Answer: ṁc = 1.319 kg/s

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

Heat released

Qh = 2.5·2.1·(130 − 60) = 367.5 kW

Heat that reaches the water

Qc = (1 − 0.1)·367.5 = 330.8 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 330.8/(4.18·60) = 1.319 kg/s

Answer

ṁc = 1.319 kg/s
5.Ideal gas law

Answer: P = 89.98 kPa

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

Moles

n = m/M = 20/28.01 = 0.714 mol
T = 30 + 273.15 = 303.1 K

Pressure

P = nRT/V = 0.714·8.314·303.1/0.02 = 89.98 kPa

Answer

P = 89.98 kPa
6.Ideal gas law

Answer: ρ = 0.8836 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 190 + 273.15 = 463.1 K

Density

ρ = 850·4.003/(8.314·463.1) = 0.8836 kg/m³

Answer

ρ = 0.8836 kg/m³
7.Stoichiometry

Answer: m = 10.17 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(Na) = 4/22.99 = 0.174 mol
n(Cl2) = 32/70.9 = 0.4513 mol

Limiting reactant

0.174/2 = 0.08699, 0.4513/1 = 0.4513 → Na

Mass of product

n(NaCl) = 0.08699·2 = 0.174 mol
m = 0.174·58.44 = 10.17 g

Answer

m = 10.17 g
8.Stoichiometry

Answer: Y = 87.99 %

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(CaCO3) = 10/100.09 = 0.09991 mol
m = 0.09991·1/1·56.08 = 5.603 g

Percent yield

Y = 4.93/5.603·100 = 87.99%

Answer

Y = 87.99%
9.Chemical equilibrium

Answer: [HI] = 0.6288 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

54 = (2x)²/(0.4 − x)²

Take the square root

7.348 = 2x/(0.4 − x) → x = 0.4·7.348/(2 + 7.348) = 0.3144 mol/L

Equilibrium concentration

[HI] = 2x = 0.6288 mol/L

Answer

[HI] = 0.6288 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.04689 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

0.5 = x²/(0.2 − x) → x² + 0.5·x − 0.1 = 0

Solve the quadratic

x = (−0.5 + √(0.5² + 4·0.1))/2 = 0.1531 mol/L

Equilibrium concentration

[PCl₅] = 0.2 − 0.1531 = 0.04689 mol/L

Answer

[PCl5] = 0.04689 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 33.26 °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

250·0.388·(140 − Tf) = 300·4.18·(Tf − 25)

Solve for the final temperature

Tf = (97·140 + 1254·25)/(97 + 1254) = 33.26 °C

Answer

Tf = 33.26 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −2220 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° = [3·(−393.5) + 4·(−285.8)] − [1·(−103.8) + 5·0] = −2220 kJ

Answer

ΔH° = −2220 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.1386 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(1.5/0.75)/5 = 0.6931/5 = 0.1386 min⁻¹

Answer

k = 0.1386 min⁻¹
14.Reaction kinetics

Answer: k2 = 0.03684 min⁻¹

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 = 293.1 K, T2 = 308.1 K

Arrhenius ratio

ln(k2/k1) = −(100000/8.314)·(1/308.1 − 1/293.1) = 1.997
k2 = 0.005·e1.997 = 0.03684 min⁻¹

Answer

k2 = 0.03684 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 719.6 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))/0.08 = 2.303/0.08 = 28.78 min

Volume

V = Q·τ = 25·28.78 = 719.6 L

Answer

V = 719.6 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 = 400/50 = 8 min, kτ = 0.25·8 = 2

Conversion

X = kτ/(1 + kτ) = 2/(1 + 2) = 66.67%

Answer

X = 66.67%
17.Heat exchangers (LMTD)

Answer: A = 79.47 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 = 95 − 75 = 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) = 490000/(200·30.83) = 79.47 m²

Answer

A = 79.47 m²
18.Heat exchangers (LMTD)

Answer: A = 0.719 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) = 0.5·2.3·35 = 40.25 kW
Tc,out = 30 + 40.25/(0.5·4.18) = 49.26 °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 = 95 − 49.26 = 45.74 K
ΔT₂ = Th,out − Tc,in = 60 − 30 = 30 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (45.74 − 30)/ln(45.74/30) = 37.32 K

Area

A = Q̇/(U·ΔTlm) = 40250/(1500·37.32) = 0.719 m²

Answer

A = 0.719 m²
19.Heat conduction

Answer: Q̇ = 338.8 W

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)/(0.96·10) = 0.02604 K/W
R2 = L2/(k2A) = (25/1000)/(0.04·10) = 0.0625 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 30/0.08854 = 338.8 W

Answer

Q̇ = 338.8 W
20.Heat conduction

Answer: Q̇ = 440.7 W

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) = (50/1000)/(0.96·20) = 0.002604 K/W
R2 = L2/(k2A) = (150/1000)/(0.17·20) = 0.04412 K/W
Ro = 1/(hoA) = 1/(30·20) = 0.001667 K/W
ΣR = 0.05672 K/W

Heat loss

Q̇ = (20 − (-5))/0.05672 = 440.7 W

Answer

Q̇ = 440.7 W
21.Pipe friction & head loss

Answer: hf = 1.239 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) = 1.8²/(2·9.81) = 0.1651 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.015·(150/0.3)·1.8²/(2·9.81) = 1.239 m

Answer

hf = 1.239 m
22.Pipe friction & head loss

Answer: H = 5.161 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 = 0.1/0.04909 = 2.037 m/s
V²/(2g) = 0.2115 m

Loss coefficients

f·L/D = 0.02·150/0.25 = 12
ΣK = 0.5 + 3·0.3 + 10 = 11.4

Energy equation

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

H = (1 + 12 + 11.4)·0.2115 = 5.161 m

Answer

H = 5.161 m
23.Pumps & pump power

Answer: Pshaft = 12.92 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 = 1000·9.81·0.03·36 = 10.59 kW

Shaft power

Pshaft = Ph/η = 10.59/0.82 = 12.92 kW

Answer

Pshaft = 12.92 kW
24.Pumps & pump power

Answer: H = 37.44 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) = (16.67 + 8)·0.2611 = 6.441 m

Pump head

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

H = Δz + hL = 31 + 6.441 = 37.44 m

Answer

H = 37.44 m

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