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 1500 kg/h · 35% sugarStream 2ṁ₂ = ? · 5% sugarProduct30% sugar

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

ṁ1 = 500 kg/hx1 = 35 %x2 = 5 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2100 kg/h · 6% sugarProduct PP = ? · 35%Vapour W (pure water)0% sugar

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

F = 2100 kg/hxF = 6 %xP = 35 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 160 °C60 °Cwater · 15 °Ct = ? °C

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

ṁh = 1 kg/scp,h = 2.44 kJ/(kg·K)Th: 160 → 60 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 170 °C90 °Cwater · 30 °C90 °C · ṁ = ?5% lost

Hot glycol mix 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 = 2.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 170 → 90 °Ct: 30 → 90 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
270 g of HeP = 350 kPaT = 40 °CV = ?

What volume V does 270 g of He occupy at 350 kPa and 40 °C? Treat it as an ideal gas.

m = 270 gM = 4.003 g/molP = 350 kPaT = 40 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
CO₂, M = 44.01 g/molP = 150 kPaT = 90 °Cρ = ?

Find the density ρ of CO₂ at 150 kPa and 90 °C, treating it as an ideal gas.

M = 44.01 g/molP = 150 kPaT = 90 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 3/ν× M(CO2​)

10 g of C3H8 and 8 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(H2​)n(H2​)n(H2​O)m(H2​O)÷ M(H2​)× 2/2× M(H2​O)

In the reaction 2H2 + O2 → 2H2O, 4 g of H2 reacts completely (the other reactants are in excess) and 22.17 g of H2O is collected. Find the percent yield Y.

M(H2) = 2.016 g/molM(H2O) = 18.02 g/molactual: 22.17 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 = 25. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 25
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 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 = 0.1
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 250 gT = 130 °Cc = 0.129 J/(g·°C)Waterm = 250 gT = 24 °Cc = 4.18 J/(g·°C)

A 250 g block of lead (c = 0.129 J/(g·°C)) at 130 °C is dropped into 250 g of water (c = 4.18 J/(g·°C)) at 24 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.129 J/(g·°C)Tmetal = 130 °Cmwater = 250 gTwater = 24 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2CH3OH + 3O₂ → 2CO₂ + 4H₂O(l).

ΔH°f(CH3OH) = −238.7 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)15 min0.6

In a first-order reaction the concentration of A falls from 1.2 mol/L to 0.6 mol/L in 15 min. Find the rate constant k.

CA0 = 1.2 mol/LCA = 0.6 mol/Lt = 15 min
k = min⁻¹
14.Reaction kineticsHard
Tk20 °C0.135 °C?

A reaction has a rate constant of 0.1 min⁻¹ at 20 °C and an activation energy of 80 kJ/mol. Find the rate constant k2 at 35 °C.

k1 = 0.1 min⁻¹T1 = 20 °CT2 = 35 °CEa = 80 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 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 80 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 = 80 L/mink = 0.08 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 250 LQ = 100 L/minX = ?

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in a 250 L CSTR fed at 100 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 250 LQ = 100 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT90 °C60 °C25 °C50 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 110 kW. The hot fluid cools from 90 to 60 °C and the cold fluid heats from 25 to 50 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 110 kWU = 800 W/(m²·K)Th: 90 → 60 °CTc: 25 → 50 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT145 °C115 °C?10 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (1 kg/s, cp = 2.3 kJ/(kg·K)) flows in the inner tube and cools from 145 to 115 °C. Water (0.2 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 10 °C. The inner tube has a diameter of 25 mm, and U = 500 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 1 kg/scp,h = 2.3 kJ/(kg·K)Th: 145 → 115 °Cṁc = 0.2 kg/sTc,in = 10 °CD = 25 mmU = 500 W/(m²·K)
L = m
19.Heat conductionMedium
Mineral wool, k = 0.0450 mmExpanded polystyrene, k = 0.03550 mm18 °C-6 °CQ̇ = ?

A wall is made of 50 mm of mineral wool and 50 mm of expanded polystyrene, with an area of 4 m². The outer faces are at 18 °C and -6 °C. Find the heat flow Q̇ through the wall.

L1 = 50 mm, k1 = 0.04 W/(m·K)L2 = 50 mm, k2 = 0.035 W/(m·K)A = 4 m²T1 = 18 °CT3 = -6 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.035250 mmConcrete, k = 1.475 mmroom 20 °Coutside 2 °CTs​ = ?Q̇

A wall of 250 mm expanded polystyrene and 75 mm concrete separates a room at 20 °C from outside air at 2 °C. The convection coefficients are 10 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 10 m². Find the temperature Ts of the inside surface of the wall.

L1 = 250 mm, k1 = 0.035 W/(m·K)L2 = 75 mm, k2 = 1.4 W/(m·K)A = 10 m²hi = 10 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = 2 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 12 L/sD = 100 mmL = 800 mf = 0.02

Water flows at 12 L/s through a pipe 800 m long with an inside diameter of 100 mm. Use the Darcy friction factor f = 0.02 and g = 9.81 m/s². Find the friction head loss hf.

Q = 12 L/sL = 800 mD = 100 mmf = 0.02g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10free outletH = ?L = 150 m, D = 250 mm, f = 0.0184× bend (K = 0.3)

A pipe 150 m long with an inside diameter of 250 mm (Darcy friction factor f = 0.018) 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), 4 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 60 L/s?

Q = 60 L/sL = 150 mD = 250 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 10
H = m
23.Pumps & pump powerMedium
PQ = 30 L/sH = 34 m

A pump with an efficiency of 70% delivers 30 L/s of water (ρ = 1000 kg/m³) against a head of 34 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 30 L/sH = 34 mη = 70%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 20 L/sΔz = 13 mL = 100 m, D = 100 mm, f = 0.025, ΣK = 4

A pump moves 20 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 13 m higher. The pipe is 100 m long with an inside diameter of 100 mm and a Darcy friction factor f = 0.025; the minor-loss coefficients add up to ΣK = 4 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 20 L/sΔz = 13 mL = 100 mD = 100 mmf = 0.025ΣK = 4
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 100 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) = 500·(35 − 30)/(30 − 5) = 100 kg/h

Answer

ṁ2 = 100 kg/h
2.Mass balance

Answer: P = 360 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 = 2100·6/35 = 360 kg/h

Answer

P = 360 kg/h
3.Energy balance

Answer: tout = 131.7 °C

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

Heat released by the hot stream

Q = 1·2.44·(160 − 60) = 244 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 244/(0.5·4.18) = 131.7 °C

Answer

tout = 131.7 °C
4.Energy balance

Answer: ṁc = 2.727 kg/s

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

Heat released

Qh = 2.5·3.6·(170 − 90) = 720 kW

Heat that reaches the water

Qc = (1 − 0.05)·720 = 684 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 684/(4.18·60) = 2.727 kg/s

Answer

ṁc = 2.727 kg/s
5.Ideal gas law

Answer: V = 501.7 L

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

Moles

n = 270/4.003 = 67.45 mol
T = 40 + 273.15 = 313.1 K

Volume

V = nRT/P = 67.45·8.314·313.1/350 = 501.7 L

Answer

V = 501.7 L
6.Ideal gas law

Answer: ρ = 2.186 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 90 + 273.15 = 363.1 K

Density

ρ = 150·44.01/(8.314·363.1) = 2.186 kg/m³

Answer

ρ = 2.186 kg/m³
7.Stoichiometry

Answer: m = 6.602 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) = 10/44.1 = 0.2268 mol
n(O2) = 8/32 = 0.25 mol

Limiting reactant

0.2268/1 = 0.2268, 0.25/5 = 0.05 → O2

Mass of product

n(CO2) = 0.05·3 = 0.15 mol
m = 0.15·44.01 = 6.602 g

Answer

m = 6.602 g
8.Stoichiometry

Answer: Y = 62.01 %

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(H2) = 4/2.016 = 1.984 mol
m = 1.984·2/2·18.02 = 35.75 g

Percent yield

Y = 22.17/35.75·100 = 62.01%

Answer

Y = 62.01%
9.Chemical equilibrium

Answer: [H2] = 0.2857 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

25 = (2x)²/(1 − x)²

Take the square root

5 = 2x/(1 − x) → x = 1·5/(2 + 5) = 0.7143 mol/L

Equilibrium concentration

[H₂] = 1 − x = 0.2857 mol/L

Answer

[H2] = 0.2857 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.0382 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

0.1 = x²/(0.1 − x) → x² + 0.1·x − 0.01 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.01))/2 = 0.0618 mol/L

Equilibrium concentration

[PCl₅] = 0.1 − 0.0618 = 0.0382 mol/L

Answer

[PCl5] = 0.0382 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 27.17 °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

250·0.129·(130 − Tf) = 250·4.18·(Tf − 24)

Solve for the final temperature

Tf = (32.25·130 + 1045·24)/(32.25 + 1045) = 27.17 °C

Answer

Tf = 27.17 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −1453 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

Answer

ΔH° = −1453 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.04621 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(1.2/0.6)/15 = 0.6931/15 = 0.04621 min⁻¹

Answer

k = 0.04621 min⁻¹
14.Reaction kinetics

Answer: k2 = 0.4942 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) = −(80000/8.314)·(1/308.1 − 1/293.1) = 1.598
k2 = 0.1·e1.598 = 0.4942 min⁻¹

Answer

k2 = 0.4942 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 2303 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 = 80·28.78 = 2303 L

Answer

V = 2303 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 23.08 %

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 = 250/100 = 2.5 min, kτ = 0.12·2.5 = 0.3

Conversion

X = kτ/(1 + kτ) = 0.3/(1 + 0.3) = 23.08%

Answer

X = 23.08%
17.Heat exchangers (LMTD)

Answer: A = 4.68 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 parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 90 − 25 = 65 K
ΔT₂ = Th,out − Tc,out = 60 − 50 = 10 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (65 − 10)/ln(65/10) = 29.38 K

Area

A = Q̇/(U·ΔTlm) = 110000/(800·29.38) = 4.68 m²

Answer

A = 4.68 m²
18.Heat exchangers (LMTD)

Answer: L = 23.21 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 = 1·2.3·(145 − 115) = 69 kW
Tc,out = 10 + 69/(0.2·4.18) = 92.54 °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 = 145 − 92.54 = 52.46 K
ΔT₂ = Th,out − Tc,in = 115 − 10 = 105 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (52.46 − 105)/ln(52.46/105) = 75.72 K

Area and length

A = 69000/(500·75.72) = 1.823 m²
L = A/(πD) = 1.823/(π·0.025) = 23.21 m

Answer

L = 23.21 m
19.Heat conduction

Answer: Q̇ = 35.84 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) = (50/1000)/(0.04·4) = 0.3125 K/W
R2 = L2/(k2A) = (50/1000)/(0.035·4) = 0.3571 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 24/0.6696 = 35.84 W

Answer

Q̇ = 35.84 W
20.Heat conduction

Answer: Ts = 19.75 °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/(10·10) = 0.01 K/W
R1 = L1/(k1A) = (250/1000)/(0.035·10) = 0.7143 K/W
R2 = L2/(k2A) = (75/1000)/(1.4·10) = 0.005357 K/W
Ro = 1/(hoA) = 1/(30·10) = 0.003333 K/W
ΣR = 0.733 K/W

Heat loss

Q̇ = (20 − (2))/0.733 = 24.56 W
Ts = Troom − Q̇·Ri = 20 − 24.56·0.01 = 19.75 °C

Answer

Ts = 19.75 °C
21.Pipe friction & head loss

Answer: hf = 19.04 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·0.1²/4 = 0.007854 m²
V = Q/A = 0.012/0.007854 = 1.528 m/s

Velocity head

V²/(2g) = 1.528²/(2·9.81) = 0.119 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.02·(800/0.1)·1.528²/(2·9.81) = 19.04 m

Answer

hf = 19.04 m
22.Pipe friction & head loss

Answer: H = 1.789 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 = 0.018·150/0.25 = 10.8
ΣK = 0.5 + 4·0.3 + 10 = 11.7

Energy equation

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

H = (1 + 10.8 + 11.7)·0.07615 = 1.789 m

Answer

H = 1.789 m
23.Pumps & pump power

Answer: Pshaft = 14.29 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 = 1000·9.81·0.03·34 = 10.01 kW

Shaft power

Pshaft = Ph/η = 10.01/0.7 = 14.29 kW

Answer

Pshaft = 14.29 kW
24.Pumps & pump power

Answer: H = 22.58 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 = 0.02/0.007854 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (25 + 4)·0.3305 = 9.585 m

Pump head

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

H = Δz + hL = 13 + 9.585 = 22.58 m

Answer

H = 22.58 m

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