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 · 40% sugarStream 2ṁ₂ = ? · 5% sugarProduct20% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 20% sugar? Find ṁ2.

ṁ1 = 550 kg/hx1 = 40 %x2 = 5 %x3 = 20 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1600 kg/h · 8% saltProduct P60% 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 = 1600 kg/hxF = 8 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 170 °C130 °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: 170 → 130 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 180 °C110 °Cwater · 10 °C35 °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 = 3 kg/scp,h = 3.6 kJ/(kg·K)Th: 180 → 110 °Ct: 10 → 35 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
330 g of CH₄P = 550 kPaT = 55 °CV = ?

What volume V does 330 g of CH₄ occupy at 550 kPa and 55 °C? Treat it as an ideal gas.

m = 330 gM = 16.04 g/molP = 550 kPaT = 55 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of He goes from 100 kPa, 2 L, 40 °C to 300 kPa and 180 °C. Find the new volume V2.

P1 = 100 kPaV1 = 2 LT1 = 40 °CP2 = 300 kPaT2 = 180 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 1/ν× M(CO2​)

30 g of CH4 and 32 g of O2 react according to CH4 + 2O2 → CO2 + 2H2O. What mass m of CO2 can form?

M(CH4) = 16.04M(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, 10 g of H2 reacts completely (the other reactants are in excess) and 81.34 g of H2O is collected. Find the percent yield Y.

M(H2) = 2.016 g/molM(H2O) = 18.02 g/molactual: 81.34 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​I0.200C−x+x+xE0.2 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.2 mol/LKc = 0.08
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 75 gT = 190 °Cc = 0.385 J/(g·°C)Waterm = 400 gT = 23 °Cc = 4.18 J/(g·°C)

A 75 g block of copper (c = 0.385 J/(g·°C)) at 190 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 23 °C in an insulated cup. Find the final temperature Tf.

mmetal = 75 gcmetal = 0.385 J/(g·°C)Tmetal = 190 °Cmwater = 400 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H20 g CH3​OH2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 20 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 = ?75%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.1 L/(mol·min) and starts at 2 mol/L. How long does it take to reach 75% conversion? Find t.

k = 0.1 L/(mol·min)CA0 = 2 mol/LX = 75 %
t = min
14.Reaction kineticsHard
Tk30 °Ck1​?5·k1​

A reaction has an activation energy of 100 kJ/mol. At 30 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 5 times faster?

Ea = 100 kJ/molT1 = 30 °Ck2/k1 = 5R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 20 L/minX = 80%V = ?, k = 0.05 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.05 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 20 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 80% conversion of A.

Q = 20 L/mink = 0.05 min⁻¹X = 80%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 500 LV = 500 LQ = 20 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in two equal CSTRs in series, each of 500 L. The feed rate is 20 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 500 L (×2)Q = 20 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT155 °C115 °C20 °C85 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 50 kW. The hot fluid cools from 155 to 115 °C and the cold fluid heats from 20 to 85 °C. The overall heat transfer coefficient is 200 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 50 kWU = 200 W/(m²·K)Th: 155 → 115 °CTc: 20 → 85 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT105 °C50 °C?20 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.8 kg/s, cp = 2.1 kJ/(kg·K)) flows in the inner tube and cools from 105 to 50 °C. Water (0.3 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 20 °C. The inner tube has a diameter of 50 mm, and U = 250 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.8 kg/scp,h = 2.1 kJ/(kg·K)Th: 105 → 50 °Cṁc = 0.3 kg/sTc,in = 20 °CD = 50 mmU = 250 W/(m²·K)
L = m
19.Heat conductionMedium
Expanded polystyrene, k = 0.035150 mmWood, k = 0.1725 mm21 °C-8 °CTi​ = ?Q̇

A wall is made of 150 mm of expanded polystyrene and 25 mm of wood, with an area of 12 m². The outer faces are at 21 °C and -8 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 0.035 W/(m·K)L2 = 25 mm, k2 = 0.17 W/(m·K)A = 12 m²T1 = 21 °CT3 = -8 °C
Ti = °C
20.Heat conductionHard
Expanded polystyrene, k = 0.03550 mmGypsum board, k = 0.17100 mmroom 20 °Coutside -9 °CQ̇ = ?

A wall of 50 mm expanded polystyrene and 100 mm gypsum board separates a room at 20 °C from outside air at -9 °C. The convection coefficients are 8 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 10 m². Find the heat loss Q̇ through the wall.

L1 = 50 mm, k1 = 0.035 W/(m·K)L2 = 100 mm, k2 = 0.17 W/(m·K)A = 10 m²hi = 8 W/(m²·K)ho = 25 W/(m²·K)Troom = 20 °CTout = -9 °C
Q̇ = W
21.Pipe friction & head lossMedium
Q = 8 L/sD = 100 mmL = 50 mf = 0.015

Water flows at 8 L/s through a pipe 50 m long with an inside diameter of 100 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the friction head loss hf.

Q = 8 L/sL = 50 mD = 100 mmf = 0.015g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2Δz = 6 mL = 150 m, D = 200 mm, f = 0.022× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.02. The water surface of the upper reservoir is 6 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 2) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². Find the flow rate Q in L/s.

Δz = 6 mL = 150 mD = 200 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 60 L/sH = 72 m

A pump with an efficiency of 80% delivers 60 L/s of water (ρ = 1000 kg/m³) against a head of 72 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 60 L/sH = 72 mη = 80%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 100 L/sΔz = 10 mL = 100 m, D = 250 mm, f = 0.02, ΣK = 4

A pump moves 100 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 10 m higher. The pipe is 100 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.02; 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 = 100 L/sΔz = 10 mL = 100 mD = 250 mmf = 0.02ΣK = 4
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 733.3 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) = 550·(40 − 20)/(20 − 5) = 733.3 kg/h

Answer

ṁ2 = 733.3 kg/h
2.Mass balance

Answer: W = 1387 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 = 1600·8/60 = 213.3 kg/h

Total balance

W = F − P = 1600 − 213.3 = 1387 kg/h

Answer

W = 1387 kg/h
3.Energy balance

Answer: tout = 22.78 °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·(170 − 130) = 97.6 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 97.6/(3·4.18) = 22.78 °C

Answer

tout = 22.78 °C
4.Energy balance

Answer: ṁc = 6.149 kg/s

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

Heat released

Qh = 3·3.6·(180 − 110) = 756 kW

Heat that reaches the water

Qc = (1 − 0.15)·756 = 642.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 642.6/(4.18·25) = 6.149 kg/s

Answer

ṁc = 6.149 kg/s
5.Ideal gas law

Answer: V = 102.1 L

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

Moles

n = 330/16.04 = 20.57 mol
T = 55 + 273.15 = 328.1 K

Volume

V = nRT/P = 20.57·8.314·328.1/550 = 102.1 L

Answer

V = 102.1 L
6.Ideal gas law

Answer: V2 = 0.9647 L

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

Absolute temperatures

T1 = 313.1 K, T2 = 453.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(100/300)·(453.1/313.1) = 0.9647 L

Answer

V2 = 0.9647 L
7.Stoichiometry

Answer: m = 22 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(CH4) = 30/16.04 = 1.87 mol
n(O2) = 32/32 = 1 mol

Limiting reactant

1.87/1 = 1.87, 1/2 = 0.5 → O2

Mass of product

n(CO2) = 0.5·1 = 0.5 mol
m = 0.5·44.01 = 22 g

Answer

m = 22 g
8.Stoichiometry

Answer: Y = 91 %

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) = 10/2.016 = 4.96 mol
m = 4.96·2/2·18.02 = 89.38 g

Percent yield

Y = 81.34/89.38·100 = 91%

Answer

Y = 91%
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] = 0.09266 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/(0.2 − x) → x² + 0.08·x − 0.016 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.016))/2 = 0.09266 mol/L

Equilibrium concentration

[Cl₂] = x = 0.09266 mol/L

Answer

[Cl2] = 0.09266 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 25.84 °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

75·0.385·(190 − Tf) = 400·4.18·(Tf − 23)

Solve for the final temperature

Tf = (28.88·190 + 1672·23)/(28.88 + 1672) = 25.84 °C

Answer

Tf = 25.84 °C
12.Calorimetry & enthalpy

Answer: q = 453.4 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 = 20/32.04 = 0.6242 mol
q = n·|ΔH°/2| = 0.6242·726.4 = 453.4 kJ

Answer

q = 453.4 kJ
13.Reaction kinetics

Answer: t = 15 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).

Concentration at the end

CA = 2·(1 − 0.75) = 0.5 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (2 − 0.5)/0.1 = 15 min

Answer

t = 15 min
14.Reaction kinetics

Answer: T2 = 42.82 °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 = 303.1 K

Solve Arrhenius for T₂

1/T2 = 1/303.1 − 8.314·ln(5)/100000 = 3.299 × 10⁻³ − 1.338 × 10⁻⁴ = 3.165 × 10⁻³ K⁻¹
T2 = 316 K = 42.82 °C

Answer

T2 = 42.82 °C
15.Reactor sizing (CSTR & PFR)

Answer: V = 643.8 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 − 0.8))/0.05 = 1.609/0.05 = 32.19 min

Volume

V = Q·τ = 20·32.19 = 643.8 L

Answer

V = 643.8 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 98.1 %

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 = 500/20 = 25 min, kτ = 0.25·25 = 6.25

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 6.25) = 0.1379
C2/CA0 = 1/(1 + kτ)² = 0.01902
X = 1 − 0.01902 = 98.1%

Answer

X = 98.1%
17.Heat exchangers (LMTD)

Answer: A = 3.581 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 = 155 − 20 = 135 K
ΔT₂ = Th,out − Tc,out = 115 − 85 = 30 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (135 − 30)/ln(135/30) = 69.81 K

Area

A = Q̇/(U·ΔTlm) = 50000/(200·69.81) = 3.581 m²

Answer

A = 3.581 m²
18.Heat exchangers (LMTD)

Answer: L = 122.8 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 = 0.8·2.1·(105 − 50) = 92.4 kW
Tc,out = 20 + 92.4/(0.3·4.18) = 93.68 °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 = 105 − 93.68 = 11.32 K
ΔT₂ = Th,out − Tc,in = 50 − 20 = 30 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (11.32 − 30)/ln(11.32/30) = 19.16 K

Area and length

A = 92400/(250·19.16) = 19.29 m²
L = A/(πD) = 19.29/(π·0.05) = 122.8 m

Answer

L = 122.8 m
19.Heat conduction

Answer: Ti = −7.038 °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) = (150/1000)/(0.035·12) = 0.3571 K/W
R2 = L2/(k2A) = (25/1000)/(0.17·12) = 0.01225 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 29/0.3694 = 78.51 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 21 − 78.51·0.3571 = −7.038 °C

Answer

Ti = −7.038 °C
20.Heat conduction

Answer: Q̇ = 132.9 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/(8·10) = 0.0125 K/W
R1 = L1/(k1A) = (50/1000)/(0.035·10) = 0.1429 K/W
R2 = L2/(k2A) = (100/1000)/(0.17·10) = 0.05882 K/W
Ro = 1/(hoA) = 1/(25·10) = 0.004 K/W
ΣR = 0.2182 K/W

Heat loss

Q̇ = (20 − (-9))/0.2182 = 132.9 W

Answer

Q̇ = 132.9 W
21.Pipe friction & head loss

Answer: hf = 0.3966 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 = 0.008/0.007854 = 1.019 m/s

Velocity head

V²/(2g) = 1.019²/(2·9.81) = 0.05288 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.015·(50/0.1)·1.019²/(2·9.81) = 0.3966 m

Answer

hf = 0.3966 m
22.Pipe friction & head loss

Answer: Q = 77.99 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 = 0.02·150/0.2 = 15
ΣK = 0.5 + 2·0.3 + 2 + 1.0 = 4.1

Energy equation

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

6 = (15 + 4.1)·V²/(2·9.81)
V = √(2·9.81·6/19.1) = 2.483 m/s

Flow rate

Q = V·π·D²/4 = 2.483·0.03142 = 0.07799 m³/s = 77.99 L/s

Answer

Q = 77.99 L/s
23.Pumps & pump power

Answer: Pshaft = 52.97 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 = 1000·9.81·0.06·72 = 42.38 kW

Shaft power

Pshaft = Ph/η = 42.38/0.8 = 52.97 kW

Answer

Pshaft = 52.97 kW
24.Pumps & pump power

Answer: H = 12.54 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 = 0.1/0.04909 = 2.037 m/s
V²/(2g) = 0.2115 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (8 + 4)·0.2115 = 2.538 m

Pump head

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

H = Δz + hL = 10 + 2.538 = 12.54 m

Answer

H = 12.54 m

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