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 1250 kg/h · 50% sugarStream 2ṁ₂ = ? · 5% sugarProduct25% sugar

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

ṁ1 = 250 kg/hx1 = 50 %x2 = 5 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2200 kg/h · 17% saltProduct P50% saltVapour W (pure water)W = ? kg/h

An evaporator concentrates a salt solution by boiling off pure water. Find the water evaporated W in kg/h.

F = 2200 kg/hxF = 17 %xP = 50 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 170 °C80 °Cwater · 20 °Ct = ? °C

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

ṁh = 2 kg/scp,h = 2.1 kJ/(kg·K)Th: 170 → 80 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 170 °C90 °Cwater · 10 °C25 °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: 170 → 90 °Ct: 10 → 25 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
250 g of ArP = 750 kPaT = 20 °CV = ?

What volume V does 250 g of Ar occupy at 750 kPa and 20 °C? Treat it as an ideal gas.

m = 250 gM = 39.95 g/molP = 750 kPaT = 20 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
Ar, M = 39.95 g/molP = 200 kPaT = 150 °Cρ = ?

Find the density ρ of Ar at 200 kPa and 150 °C, treating it as an ideal gas.

M = 39.95 g/molP = 200 kPaT = 150 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

4 g of H2 and 32 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(Al)n(Al)n(AlCl3​)m(AlCl3​)÷ M(Al)× 2/2× M(AlCl3​)

In the reaction 2Al + 3Cl2 → 2AlCl3, 10 g of Al reacts completely (the other reactants are in excess) and 38.55 g of AlCl3 is collected. Find the percent yield Y.

M(Al) = 26.98 g/molM(AlCl3) = 133.33 g/molactual: 38.55 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 = 9. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 9
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.400C−x+x+xE0.4 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 0.4 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.4 mol/LKc = 0.02
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 250 gT = 80 °Cc = 0.388 J/(g·°C)Waterm = 150 gT = 23 °Cc = 4.18 J/(g·°C)

A 250 g block of zinc (c = 0.388 J/(g·°C)) at 80 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 23 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.388 J/(g·°C)Tmetal = 80 °Cmwater = 150 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l).

ΔH°f(C2H6) = −84.7 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)X (%)t = ?90%

A zero-order reaction has k = 0.005 mol/(L·min) and starts at 1.2 mol/L. How long does it take to reach 90% conversion? Find t.

k = 0.005 mol/(L·min)CA0 = 1.2 mol/LX = 90 %
t = min
14.Reaction kineticsHard
Tk30 °C0.0540 °C0.178

The rate constant of a reaction is 0.05 min⁻¹ at 30 °C and 0.178 min⁻¹ at 40 °C. Find the activation energy Ea.

k1 = 0.05 min⁻¹T1 = 30 °Ck2 = 0.178 min⁻¹T2 = 40 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 40 L/minCA0​ = 1.5 mol/LCA​ = ?V = 200 L, k = 0.5 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.5 min⁻¹) runs in a 200 L plug-flow reactor (PFR). The feed enters at 40 L/min with CA0 = 1.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 200 LQ = 40 L/mink = 0.5 min⁻¹CA0 = 1.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
V = 200 LQ = 40 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 200 L CSTR fed at 40 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 40 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT150 °C40 °C110 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 250 kW. The hot fluid cools from 150 to 40 °C and the cold fluid heats from 25 to 110 °C. The overall heat transfer coefficient is 200 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 250 kWU = 200 W/(m²·K)Th: 150 → 40 °CTc: 25 → 110 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT120 °C75 °C?20 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.5 kg/s, cp = 2.5 kJ/(kg·K)) flows in the inner tube and cools from 120 to 75 °C. Water (0.2 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 20 °C. The inner tube has a diameter of 25 mm, and U = 150 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.5 kg/scp,h = 2.5 kJ/(kg·K)Th: 120 → 75 °Cṁc = 0.2 kg/sTc,in = 20 °CD = 25 mmU = 150 W/(m²·K)
L = m
19.Heat conductionMedium
Brick, k = 0.72200 mmMineral wool, k = 0.04150 mm17 °C1 °CTi​ = ?Q̇

A wall is made of 200 mm of brick and 150 mm of mineral wool, with an area of 12 m². The outer faces are at 17 °C and 1 °C. Find the temperature Ti at the interface between the two layers.

L1 = 200 mm, k1 = 0.72 W/(m·K)L2 = 150 mm, k2 = 0.04 W/(m·K)A = 12 m²T1 = 17 °CT3 = 1 °C
Ti = °C
20.Heat conductionHard
Concrete, k = 1.4200 mmGlass, k = 0.96100 mmroom 20 °Coutside 3 °CTs​ = ?Q̇

A wall of 200 mm concrete and 100 mm glass separates a room at 20 °C from outside air at 3 °C. The convection coefficients are 10 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 12 m². Find the temperature Ts of the inside surface of the wall.

L1 = 200 mm, k1 = 1.4 W/(m·K)L2 = 100 mm, k2 = 0.96 W/(m·K)A = 12 m²hi = 10 W/(m²·K)ho = 20 W/(m²·K)Troom = 20 °CTout = 3 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 2.1 m/sD = 150 mmL = 100 mf = 0.018

Water (ρ = 1000 kg/m³) flows at 2.1 m/s through a horizontal pipe, 100 m long, with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2.1 m/sL = 100 mD = 150 mmf = 0.018ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 10free outletH = ?L = 100 m, D = 300 mm, f = 0.0183× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 300 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), 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 200 L/s?

Q = 200 L/sL = 100 mD = 300 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 10
H = m
23.Pumps & pump powerMedium
PQ = 40 L/sH = 14 m

In a test, a pump delivers 40 L/s of water (ρ = 1000 kg/m³) against a head of 14 m while its shaft takes 7.3 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 40 L/sH = 14 mPshaft = 7.3 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 15 L/sΔz = 8 mL = 100 m, D = 100 mm, f = 0.015, ΣK = 5

A pump moves 15 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 8 m higher. The pipe is 100 m long with an inside diameter of 100 mm and a Darcy friction factor f = 0.015; the minor-loss coefficients add up to ΣK = 5 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 15 L/sΔz = 8 mL = 100 mD = 100 mmf = 0.015ΣK = 5
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 312.5 kg/h

Steady-state mass balance: in = out for the total and for each component. Blending problems combine both.

Balances

Total: ṁ3 = ṁ1 + ṁ2
sugar: ṁ1x1 + ṁ2x2 = (ṁ1 + ṁ2)x3

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 250·(50 − 25)/(25 − 5) = 312.5 kg/h

Answer

ṁ2 = 312.5 kg/h
2.Mass balance

Answer: W = 1452 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 = 2200·17/50 = 748 kg/h

Total balance

W = F − P = 2200 − 748 = 1452 kg/h

Answer

W = 1452 kg/h
3.Energy balance

Answer: tout = 50.14 °C

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

Heat released by the hot stream

Q = 2·2.1·(170 − 80) = 378 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 378/(3·4.18) = 50.14 °C

Answer

tout = 50.14 °C
4.Energy balance

Answer: ṁc = 7.809 kg/s

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

Heat released

Qh = 2·3.6·(170 − 90) = 576 kW

Heat that reaches the water

Qc = (1 − 0.15)·576 = 489.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 489.6/(4.18·15) = 7.809 kg/s

Answer

ṁc = 7.809 kg/s
5.Ideal gas law

Answer: V = 20.34 L

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

Moles

n = 250/39.95 = 6.258 mol
T = 20 + 273.15 = 293.1 K

Volume

V = nRT/P = 6.258·8.314·293.1/750 = 20.34 L

Answer

V = 20.34 L
6.Ideal gas law

Answer: ρ = 2.271 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 150 + 273.15 = 423.1 K

Density

ρ = 200·39.95/(8.314·423.1) = 2.271 kg/m³

Answer

ρ = 2.271 kg/m³
7.Stoichiometry

Answer: m = 35.75 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) = 4/2.016 = 1.984 mol
n(O2) = 32/32 = 1 mol

Limiting reactant

1.984/2 = 0.9921, 1/1 = 1 → H2

Mass of product

n(H2O) = 0.9921·2 = 1.984 mol
m = 1.984·18.02 = 35.75 g

Answer

m = 35.75 g
8.Stoichiometry

Answer: Y = 78.01 %

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(Al) = 10/26.98 = 0.3706 mol
m = 0.3706·2/2·133.33 = 49.42 g

Percent yield

Y = 38.55/49.42·100 = 78.01%

Answer

Y = 78.01%
9.Chemical equilibrium

Answer: [HI] = 0.48 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

9 = (2x)²/(0.4 − x)²

Take the square root

3 = 2x/(0.4 − x) → x = 0.4·3/(2 + 3) = 0.24 mol/L

Equilibrium concentration

[HI] = 2x = 0.48 mol/L

Answer

[HI] = 0.48 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.08 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

0.02 = x²/(0.4 − x) → x² + 0.02·x − 0.008 = 0

Solve the quadratic

x = (−0.02 + √(0.02² + 4·0.008))/2 = 0.08 mol/L

Equilibrium concentration

[Cl₂] = x = 0.08 mol/L

Answer

[Cl2] = 0.08 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 30.64 °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·(80 − Tf) = 150·4.18·(Tf − 23)

Solve for the final temperature

Tf = (97·80 + 627·23)/(97 + 627) = 30.64 °C

Answer

Tf = 30.64 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −3119 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

Answer

ΔH° = −3119 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 216 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 = 1.2·0.9 = 1.08 mol/L

Time

t = CA0·X/k = 1.08/0.005 = 216 min

Answer

t = 216 min
14.Reaction kinetics

Answer: Ea = 100.2 kJ/mol

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Absolute temperatures

T1 = 303.1 K, T2 = 313.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·1.27/(-1.053e-4) = 100217 J/mol
Ea = 100.2 kJ/mol

Answer

Ea = 100.2 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.1231 mol/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 = V/Q = 200/40 = 5 min

Outlet concentration

CA = 1.5·e−0.5·5 = 0.1231 mol/L

Answer

CA = 0.1231 mol/L

Conversion: X = 91.79%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 55.56 %

Ideal reactors, first-order reaction (−rA = k·CA) at steady state, with space time τ = V/Q. A CSTR is perfectly mixed, so the whole volume reacts at the low outlet concentration: τ = X/(k·(1 − X)) and CA = CA0/(1 + k·τ). In a PFR each slice of fluid reacts like a small batch reactor: τ = ln(1/(1 − X))/k and CA = CA0·e−k·τ. For the same conversion a CSTR always needs more volume than a PFR.

Space time

τ = V/Q = 200/40 = 5 min, kτ = 0.25·5 = 1.25

Conversion

X = kτ/(1 + kτ) = 1.25/(1 + 1.25) = 55.56%

Answer

X = 55.56%
17.Heat exchangers (LMTD)

Answer: A = 49.04 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 = 150 − 110 = 40 K
ΔT₂ = Th,out − Tc,in = 40 − 25 = 15 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (40 − 15)/ln(40/15) = 25.49 K

Area

A = Q̇/(U·ΔTlm) = 250000/(200·25.49) = 49.04 m²

Answer

A = 49.04 m²
18.Heat exchangers (LMTD)

Answer: L = 111.3 m

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

Heat duty and water outlet temperature

Q̇ = 0.5·2.5·(120 − 75) = 56.25 kW
Tc,out = 20 + 56.25/(0.2·4.18) = 87.28 °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 = 120 − 87.28 = 32.72 K
ΔT₂ = Th,out − Tc,in = 75 − 20 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (32.72 − 55)/ln(32.72/55) = 42.9 K

Area and length

A = 56250/(150·42.9) = 8.742 m²
L = A/(πD) = 8.742/(π·0.025) = 111.3 m

Answer

L = 111.3 m
19.Heat conduction

Answer: Ti = 15.9 °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)/(0.72·12) = 0.02315 K/W
R2 = L2/(k2A) = (150/1000)/(0.04·12) = 0.3125 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 16/0.3356 = 47.67 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 17 − 47.67·0.02315 = 15.9 °C

Answer

Ti = 15.9 °C
20.Heat conduction

Answer: Ts = 15.72 °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/(10·12) = 0.008333 K/W
R1 = L1/(k1A) = (200/1000)/(1.4·12) = 0.0119 K/W
R2 = L2/(k2A) = (100/1000)/(0.96·12) = 0.008681 K/W
Ro = 1/(hoA) = 1/(20·12) = 0.004167 K/W
ΣR = 0.03309 K/W

Heat loss

Q̇ = (20 − (3))/0.03309 = 513.8 W
Ts = Troom − Q̇·Ri = 20 − 513.8·0.008333 = 15.72 °C

Answer

Ts = 15.72 °C
21.Pipe friction & head loss

Answer: Δp = 26.46 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) = 0.018·(100/0.15)·2.1²/(2·9.81) = 2.697 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 = 1000·9.81·2.697 = 26460 Pa = 26.46 kPa

Answer

Δp = 26.46 kPa
22.Pipe friction & head loss

Answer: H = 7.508 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 = 0.2/0.07069 = 2.829 m/s
V²/(2g) = 0.408 m

Loss coefficients

f·L/D = 0.018·100/0.3 = 6
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 + 6 + 11.4)·0.408 = 7.508 m

Answer

H = 7.508 m
23.Pumps & pump power

Answer: η = 75.25 %

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 = 1000·9.81·0.04·14 = 5.494 kW

Efficiency

η = Ph/Pshaft = 5.494/7.3 = 75.25%

Answer

η = 75.25%
24.Pumps & pump power

Answer: H = 11.72 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 = 0.015/0.007854 = 1.91 m/s
V²/(2g) = 0.1859 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (15 + 5)·0.1859 = 3.718 m

Pump head

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

H = Δz + hL = 8 + 3.718 = 11.72 m

Answer

H = 11.72 m

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