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 1750 kg/h · 35% NaOHStream 2ṁ₂ = ? · 10% NaOHProduct15% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 15% NaOH? Find ṁ2.

ṁ1 = 750 kg/hx1 = 35 %x2 = 10 %x3 = 15 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2800 kg/h · 10% NaOHProduct PP = ? · 60%Vapour W (pure water)0% NaOH

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

F = 2800 kg/hxF = 10 %xP = 60 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 120 °C80 °Cwater · 20 °Ct = ? °C

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

ṁh = 2.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 120 → 80 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 130 °C60 °Cwater · 15 °C30 °C · ṁ = ?10% lost

Hot ethanol 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 = 2.44 kJ/(kg·K)Th: 130 → 60 °Ct: 15 → 30 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
130 g of CH₄V = 20 LT = 10 °CP = ?

A tank of 20 L contains 130 g of CH₄ at 10 °C. Treat it as an ideal gas and find the pressure P.

m = 130 gM = 16.04 g/molV = 20 LT = 10 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of O₂ goes from 200 kPa, 5 L, 10 °C to 200 kPa and 190 °C. Find the new volume V2.

P1 = 200 kPaV1 = 5 LT1 = 10 °CP2 = 200 kPaT2 = 190 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(NH3​)m(NH3​)÷ M(X)× 2/ν× M(NH3​)

4 g of N2 and 10 g of H2 react according to N2 + 3H2 → 2NH3. What mass m of NH3 can form?

M(N2) = 28.02M(H2) = 2.016M(NH3) = 17.03 g/mol
m = g
8.StoichiometryHard
m(C6​H12​O6​)n(C6​H12​O6​)n(CO2​)m(CO2​)÷ M(C6​H12​O6​)× 2/1× M(CO2​)

In the reaction C6H12O6 → 2C2H5OH + 2CO2, 10 g of C6H12O6 reacts completely (the other reactants are in excess) and 3.03 g of CO2 is collected. Find the percent yield Y.

M(C6H12O6) = 180.16 g/molM(CO2) = 44.01 g/molactual: 3.03 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.50.50C−x−x+2xE0.5 − x0.5 − x2x

0.5 mol/L of H₂ and 0.5 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 64. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 64
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

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

[PCl₅]₀ = 0.5 mol/LKc = 0.2
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 100 gT = 90 °Cc = 0.897 J/(g·°C)Waterm = 150 gT = 16 °Cc = 4.18 J/(g·°C)

A 100 g block of aluminium (c = 0.897 J/(g·°C)) at 90 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 16 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.897 J/(g·°C)Tmetal = 90 °Cmwater = 150 gTwater = 16 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H50 g CH3​OH2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 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)C (mol/L)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.02 L/(mol·min) and an initial concentration of 0.5 mol/L. Find its first half-life t½.

k = 0.02 L/(mol·min)CA0 = 0.5 mol/L
t½ = min
14.Reaction kineticsHard
Tk30 °C0.00545 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 30 °C and an activation energy of 60 kJ/mol. Find the rate constant k2 at 45 °C.

k1 = 0.005 min⁻¹T1 = 30 °CT2 = 45 °CEa = 60 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minCA0​ = 1.5 mol/LCA​ = ?V = 100 L, k = 0.3 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.3 min⁻¹) runs in a 100 L plug-flow reactor (PFR). The feed enters at 25 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 = 100 LQ = 25 L/mink = 0.3 min⁻¹CA0 = 1.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
V = 200 LQ = 10 L/minX = ?

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in a 200 L CSTR fed at 10 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 10 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT130 °C105 °C55 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 410 kW. The hot fluid cools from 130 to 105 °C and the cold fluid heats from 25 to 55 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 410 kWU = 800 W/(m²·K)Th: 130 → 105 °CTc: 25 → 55 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT155 °C50 °C104.2 °C10 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.5 kJ/(kg·K)) cools from 155 to 50 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 10 °C. With U = 300 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.5 kJ/(kg·K)Th: 155 → 50 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 10 °CU = 300 W/(m²·K)
A = m²
19.Heat conductionMedium
Wood, k = 0.17250 mmGlass, k = 0.9675 mm21 °C4 °CQ̇ = ?

A wall is made of 250 mm of wood and 75 mm of glass, with an area of 4 m². The outer faces are at 21 °C and 4 °C. Find the heat flow Q̇ through the wall.

L1 = 250 mm, k1 = 0.17 W/(m·K)L2 = 75 mm, k2 = 0.96 W/(m·K)A = 4 m²T1 = 21 °CT3 = 4 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.03550 mmConcrete, k = 1.4100 mmroom 21 °Coutside -15 °CQ̇

A wall of 50 mm expanded polystyrene and 100 mm concrete separates a room at 21 °C from outside air at -15 °C. The convection coefficients are 8 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 8 m². Find the overall heat transfer coefficient U of the wall.

L1 = 50 mm, k1 = 0.035 W/(m·K)L2 = 100 mm, k2 = 1.4 W/(m·K)A = 8 m²hi = 8 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = -15 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
Q = 3 L/sD = 50 mmL = 500 mf = 0.03

Water flows at 3 L/s through a pipe 500 m long with an inside diameter of 50 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the friction head loss hf.

Q = 3 L/sL = 500 mD = 50 mmf = 0.03g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10Δz = ?L = 100 m, D = 150 mm, f = 0.0252× bend (K = 0.3)

Two open reservoirs are joined by a pipe 100 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.025. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 10) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². What difference in water level Δz between the reservoirs gives a flow rate of 25 L/s?

Q = 25 L/sL = 100 mD = 150 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 10Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 14 m

A pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 14 m. The pump efficiency is 60% and the electric motor driving it has an efficiency of 92%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 10 L/sH = 14 mηpump = 60%ηmotor = 92%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 40 L/sΔz = 6 mL = 400 m, D = 150 mm, f = 0.018, 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 6 m higher. The pipe is 400 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.018; the minor-loss coefficients add up to ΣK = 8 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 78%. Find the shaft power Pshaft in kW.

Q = 40 L/sΔz = 6 mL = 400 mD = 150 mmf = 0.018ΣK = 8η = 78%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 3000 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) = 750·(35 − 15)/(15 − 10) = 3000 kg/h

Answer

ṁ2 = 3000 kg/h
2.Mass balance

Answer: P = 466.7 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 = 2800·10/60 = 466.7 kg/h

Answer

P = 466.7 kg/h
3.Energy balance

Answer: tout = 39.46 °C

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

Heat released by the hot stream

Q = 2.5·2.44·(120 − 80) = 244 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 244/(3·4.18) = 39.46 °C

Answer

tout = 39.46 °C
4.Energy balance

Answer: ṁc = 6.129 kg/s

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

Heat released

Qh = 2.5·2.44·(130 − 60) = 427 kW

Heat that reaches the water

Qc = (1 − 0.1)·427 = 384.3 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 384.3/(4.18·15) = 6.129 kg/s

Answer

ṁc = 6.129 kg/s
5.Ideal gas law

Answer: P = 954 kPa

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

Moles

n = m/M = 130/16.04 = 8.105 mol
T = 10 + 273.15 = 283.1 K

Pressure

P = nRT/V = 8.105·8.314·283.1/0.02 = 954 kPa

Answer

P = 954 kPa
6.Ideal gas law

Answer: V2 = 8.179 L

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

Absolute temperatures

T1 = 283.1 K, T2 = 463.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(200/200)·(463.1/283.1) = 8.179 L

Answer

V2 = 8.179 L
7.Stoichiometry

Answer: m = 4.862 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(N2) = 4/28.02 = 0.1428 mol
n(H2) = 10/2.016 = 4.96 mol

Limiting reactant

0.1428/1 = 0.1428, 4.96/3 = 1.653 → N2

Mass of product

n(NH3) = 0.1428·2 = 0.2855 mol
m = 0.2855·17.03 = 4.862 g

Answer

m = 4.862 g
8.Stoichiometry

Answer: Y = 62.02 %

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(C6H12O6) = 10/180.16 = 0.05551 mol
m = 0.05551·2/1·44.01 = 4.886 g

Percent yield

Y = 3.03/4.886·100 = 62.02%

Answer

Y = 62.02%
9.Chemical equilibrium

Answer: [H2] = 0.1 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

64 = (2x)²/(0.5 − x)²

Take the square root

8 = 2x/(0.5 − x) → x = 0.5·8/(2 + 8) = 0.4 mol/L

Equilibrium concentration

[H₂] = 0.5 − x = 0.1 mol/L

Answer

[H2] = 0.1 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.2317 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

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

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.1))/2 = 0.2317 mol/L

Equilibrium concentration

[Cl₂] = x = 0.2317 mol/L

Answer

[Cl2] = 0.2317 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 25.26 °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

100·0.897·(90 − Tf) = 150·4.18·(Tf − 16)

Solve for the final temperature

Tf = (89.7·90 + 627·16)/(89.7 + 627) = 25.26 °C

Answer

Tf = 25.26 °C
12.Calorimetry & enthalpy

Answer: q = 1134 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 = 50/32.04 = 1.561 mol
q = n·|ΔH°/2| = 1.561·726.4 = 1134 kJ

Answer

q = 1134 kJ
13.Reaction kinetics

Answer: t½ = 100 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).

Second-order half-life

t½ = 1/(k·CA0) = 1/(0.02·0.5) = 100 min

Answer

t½ = 100 min

Each later half-life is twice as long, because C₀ has halved.

14.Reaction kinetics

Answer: k2 = 0.01536 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 = 303.1 K, T2 = 318.1 K

Arrhenius ratio

ln(k2/k1) = −(60000/8.314)·(1/318.1 − 1/303.1) = 1.122
k2 = 0.005·e1.122 = 0.01536 min⁻¹

Answer

k2 = 0.01536 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.4518 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 = 100/25 = 4 min

Outlet concentration

CA = 1.5·e−0.3·4 = 0.4518 mol/L

Answer

CA = 0.4518 mol/L

Conversion: X = 69.88%.

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 = 200/10 = 20 min, kτ = 0.1·20 = 2

Conversion

X = kτ/(1 + kτ) = 2/(1 + 2) = 66.67%

Answer

X = 66.67%
17.Heat exchangers (LMTD)

Answer: A = 6.615 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 = 130 − 55 = 75 K
ΔT₂ = Th,out − Tc,in = 105 − 25 = 80 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (75 − 80)/ln(75/80) = 77.47 K

Area

A = Q̇/(U·ΔTlm) = 410000/(800·77.47) = 6.615 m²

Answer

A = 6.615 m²
18.Heat exchangers (LMTD)

Answer: A = 29.05 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) = 1.5·2.5·105 = 393.8 kW
Tc,out = 10 + 393.8/(1·4.18) = 104.2 °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 = 155 − 104.2 = 50.8 K
ΔT₂ = Th,out − Tc,in = 50 − 10 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (50.8 − 40)/ln(50.8/40) = 45.19 K

Area

A = Q̇/(U·ΔTlm) = 393750/(300·45.19) = 29.05 m²

Answer

A = 29.05 m²
19.Heat conduction

Answer: Q̇ = 43.91 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)/(0.17·4) = 0.3676 K/W
R2 = L2/(k2A) = (75/1000)/(0.96·4) = 0.01953 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 17/0.3872 = 43.91 W

Answer

Q̇ = 43.91 W
20.Heat conduction

Answer: U = 0.597 W/(m²·K)

Thermal resistance: steady heat flow through layers in series behaves like current through resistors in series: Q̇ = ΔT/ΣR, with R = L/(kA) for a conducting layer and R = 1/(hA) for a convecting surface. The temperature drop across each layer is proportional to its resistance.

Resistances in series

Ri = 1/(hiA) = 1/(8·8) = 0.01563 K/W
R1 = L1/(k1A) = (50/1000)/(0.035·8) = 0.1786 K/W
R2 = L2/(k2A) = (100/1000)/(1.4·8) = 0.008929 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.2094 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(8·0.2094) = 0.597 W/(m²·K)

Answer

U = 0.597 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 35.69 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·0.05²/4 = 0.001963 m²
V = Q/A = 0.003/0.001963 = 1.528 m/s

Velocity head

V²/(2g) = 1.528²/(2·9.81) = 0.119 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.03·(500/0.05)·1.528²/(2·9.81) = 35.69 m

Answer

hf = 35.69 m
22.Pipe friction & head loss

Answer: Δz = 2.934 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 = 0.025/0.01767 = 1.415 m/s
V²/(2g) = 0.102 m

Loss coefficients

f·L/D = 0.025·100/0.15 = 16.67
ΣK = 0.5 + 2·0.3 + 10 + 1.0 = 12.1

Total head loss

hf = 16.67·0.102 = 1.7 m
hm = 12.1·0.102 = 1.234 m
Δz = hf + hm = 2.934 m

Answer

Δz = 2.934 m
23.Pumps & pump power

Answer: Pel = 2.488 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 = 1000·9.81·0.01·14 = 1.373 kW

Shaft power

Pshaft = 1.373/0.6 = 2.289 kW

Electrical power

Pel = 2.289/0.92 = 2.488 kW

Answer

Pel = 2.488 kW
24.Pumps & pump power

Answer: Pshaft = 10.38 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.

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) = (48 + 8)·0.2611 = 14.62 m

Pump head

H = Δz + hL = 6 + 14.62 = 20.62 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.04·20.62/0.78 = 10.38 kW

Answer

Pshaft = 10.38 kW

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