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 1300 kg/h · 20% sugarStream 2ṁ₂ = ? · 40% 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 = 300 kg/hx1 = 20 %x2 = 40 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1000 kg/h · 15% saltProduct P45% 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 = 1000 kg/hxF = 15 %xP = 45 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 180 °C140 °Cwater · 15 °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: 180 → 140 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 120 °C80 °Cwater · 25 °C40 °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 = 2.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 120 → 80 °Ct: 25 → 40 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
280 g of HeP = 750 kPaT = 80 °CV = ?

What volume V does 280 g of He occupy at 750 kPa and 80 °C? Treat it as an ideal gas.

m = 280 gM = 4.003 g/molP = 750 kPaT = 80 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
He, M = 4.003 g/molP = 100 kPaT = 90 °Cρ = ?

Find the density ρ of He at 100 kPa and 90 °C, treating it as an ideal gas.

M = 4.003 g/molP = 100 kPaT = 90 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NH3​)m(NH3​)÷ M(X)× 2/ν× M(NH3​)

12 g of N2 and 16 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(H2​)n(H2​)n(H2​O)m(H2​O)÷ M(H2​)× 2/2× M(H2​O)

In the reaction 2H2 + O2 → 2H2O, 30 g of H2 reacts completely (the other reactants are in excess) and 147.5 g of H2O is collected. Find the percent yield Y.

M(H2) = 2.016 g/molM(H2O) = 18.02 g/molactual: 147.5 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.80.80C−x−x+2xE0.8 − x0.8 − x2x

0.8 mol/L of H₂ and 0.8 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 = 0.8 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 = 0.1 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.5 mol/LKc = 0.1
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 75 gT = 170 °Cc = 0.449 J/(g·°C)Waterm = 400 gT = 23 °Cc = 4.18 J/(g·°C)

A 75 g block of iron (c = 0.449 J/(g·°C)) at 170 °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 = 0.449 J/(g·°C)Tmetal = 170 °Cmwater = 400 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H50 g C2​H6​2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 g of C2H6 (M = 30.07 g/mol) burns completely: 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C2H6) = −84.7 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)60 min0.24

In a first-order reaction the concentration of A falls from 1.2 mol/L to 0.24 mol/L in 60 min. Find the rate constant k.

CA0 = 1.2 mol/LCA = 0.24 mol/Lt = 60 min
k = min⁻¹
14.Reaction kineticsHard
Tk20 °C0.0540 °C0.407

The rate constant of a reaction is 0.05 min⁻¹ at 20 °C and 0.407 min⁻¹ at 40 °C. Find the activation energy Ea.

k1 = 0.05 min⁻¹T1 = 20 °Ck2 = 0.407 min⁻¹T2 = 40 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 10 L/minCA0​ = 0.5 mol/LCA​ = ?V = 100 L, k = 0.15 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.15 min⁻¹) runs in a 100 L plug-flow reactor (PFR). The feed enters at 10 L/min with CA0 = 0.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 100 LQ = 10 L/mink = 0.15 min⁻¹CA0 = 0.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
Q = 50 L/minX = ?V = 800 L

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in an 800 L plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 800 LQ = 50 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT145 °C125 °C25 °C85 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 310 kW. The hot fluid cools from 145 to 125 °C and the cold fluid heats from 25 to 85 °C. The overall heat transfer coefficient is 500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 310 kWU = 500 W/(m²·K)Th: 145 → 125 °CTc: 25 → 85 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT125 °C45 °C65.19 °C25 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.1 kJ/(kg·K)) cools from 125 to 45 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 25 °C. With U = 200 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 125 → 45 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 25 °CU = 200 W/(m²·K)
A = m²
19.Heat conductionMedium
Wood, k = 0.17100 mmGlass, k = 0.9625 mm24 °C-14 °CQ̇ = ?

A wall is made of 100 mm of wood and 25 mm of glass, with an area of 12 m². The outer faces are at 24 °C and -14 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.17 W/(m·K)L2 = 25 mm, k2 = 0.96 W/(m·K)A = 12 m²T1 = 24 °CT3 = -14 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.9650 mmGypsum board, k = 0.1750 mmroom 22 °Coutside -9 °CQ̇

A wall of 50 mm glass and 50 mm gypsum board separates a room at 22 °C from outside air at -9 °C. The convection coefficients are 8 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 6 m². Find the overall heat transfer coefficient U of the wall.

L1 = 50 mm, k1 = 0.96 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 6 m²hi = 8 W/(m²·K)ho = 30 W/(m²·K)Troom = 22 °CTout = -9 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
Q = 80 L/sD = 250 mmL = 100 mf = 0.015

Water flows at 80 L/s through a pipe 100 m long with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the friction head loss hf.

Q = 80 L/sL = 100 mD = 250 mmf = 0.015g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2Δz = ?L = 100 m, D = 300 mm, f = 0.0184× bend (K = 0.3)

Two open reservoirs are joined by a pipe 100 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.018. The minor losses are a square-edged entrance (K = 0.5), 4 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. What difference in water level Δz between the reservoirs gives a flow rate of 200 L/s?

Q = 200 L/sL = 100 mD = 300 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 150 L/sH = 30 m

A pump delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 30 m. The pump efficiency is 60% and the electric motor driving it has an efficiency of 88%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 150 L/sH = 30 mηpump = 60%ηmotor = 88%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 25 mL = 100 m, D = 150 mm, f = 0.025, ΣK = 6

A pump moves 50 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 25 m higher. The pipe is 100 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.025; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 50 L/sΔz = 25 mL = 100 mD = 150 mmf = 0.025ΣK = 6
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) = 300·(20 − 25)/(25 − 40) = 100 kg/h

Answer

ṁ2 = 100 kg/h
2.Mass balance

Answer: W = 666.7 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 = 1000·15/45 = 333.3 kg/h

Total balance

W = F − P = 1000 − 333.3 = 666.7 kg/h

Answer

W = 666.7 kg/h
3.Energy balance

Answer: tout = 55.19 °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·(180 − 140) = 168 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 168/(1·4.18) = 55.19 °C

Answer

tout = 55.19 °C
4.Energy balance

Answer: ṁc = 4.88 kg/s

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

Heat released

Qh = 2.5·3.6·(120 − 80) = 360 kW

Heat that reaches the water

Qc = (1 − 0.15)·360 = 306 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 306/(4.18·15) = 4.88 kg/s

Answer

ṁc = 4.88 kg/s
5.Ideal gas law

Answer: V = 273.8 L

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

Moles

n = 280/4.003 = 69.95 mol
T = 80 + 273.15 = 353.1 K

Volume

V = nRT/P = 69.95·8.314·353.1/750 = 273.8 L

Answer

V = 273.8 L
6.Ideal gas law

Answer: ρ = 0.1326 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 = 100·4.003/(8.314·363.1) = 0.1326 kg/m³

Answer

ρ = 0.1326 kg/m³
7.Stoichiometry

Answer: m = 14.59 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) = 12/28.02 = 0.4283 mol
n(H2) = 16/2.016 = 7.937 mol

Limiting reactant

0.4283/1 = 0.4283, 7.937/3 = 2.646 → N2

Mass of product

n(NH3) = 0.4283·2 = 0.8565 mol
m = 0.8565·17.03 = 14.59 g

Answer

m = 14.59 g
8.Stoichiometry

Answer: Y = 55 %

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) = 30/2.016 = 14.88 mol
m = 14.88·2/2·18.02 = 268.2 g

Percent yield

Y = 147.5/268.2·100 = 55%

Answer

Y = 55%
9.Chemical equilibrium

Answer: [H2] = 0.16 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/(0.8 − x)²

Take the square root

8 = 2x/(0.8 − x) → x = 0.8·8/(2 + 8) = 0.64 mol/L

Equilibrium concentration

[H₂] = 0.8 − x = 0.16 mol/L

Answer

[H2] = 0.16 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.3209 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/(0.5 − x) → x² + 0.1·x − 0.05 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.05))/2 = 0.1791 mol/L

Equilibrium concentration

[PCl₅] = 0.5 − 0.1791 = 0.3209 mol/L

Answer

[PCl5] = 0.3209 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 25.9 °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

75·0.449·(170 − Tf) = 400·4.18·(Tf − 23)

Solve for the final temperature

Tf = (33.68·170 + 1672·23)/(33.68 + 1672) = 25.9 °C

Answer

Tf = 25.9 °C
12.Calorimetry & enthalpy

Answer: q = 2593 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

Heat for the given mass

n = 50/30.07 = 1.663 mol
q = n·|ΔH°/2| = 1.663·1560 = 2593 kJ

Answer

q = 2593 kJ
13.Reaction kinetics

Answer: k = 0.02682 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(1.2/0.24)/60 = 1.609/60 = 0.02682 min⁻¹

Answer

k = 0.02682 min⁻¹
14.Reaction kinetics

Answer: Ea = 80.02 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 = 293.1 K, T2 = 313.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·2.097/(-2.179e-4) = 80016 J/mol
Ea = 80.02 kJ/mol

Answer

Ea = 80.02 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.1116 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 = 100/10 = 10 min

Outlet concentration

CA = 0.5·e−0.15·10 = 0.1116 mol/L

Answer

CA = 0.1116 mol/L

Conversion: X = 77.69%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 79.81 %

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 = 800/50 = 16 min, kτ = 0.1·16 = 1.6

Conversion

X = 1 − e−kτ = 1 − e−1.6 = 79.81%

Answer

X = 79.81%
17.Heat exchangers (LMTD)

Answer: A = 8.514 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 = 145 − 25 = 120 K
ΔT₂ = Th,out − Tc,out = 125 − 85 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (120 − 40)/ln(120/40) = 72.82 K

Area

A = Q̇/(U·ΔTlm) = 310000/(500·72.82) = 8.514 m²

Answer

A = 8.514 m²
18.Heat exchangers (LMTD)

Answer: A = 34.67 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) = 1.5·2.1·80 = 252 kW
Tc,out = 25 + 252/(1.5·4.18) = 65.19 °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 = 125 − 65.19 = 59.81 K
ΔT₂ = Th,out − Tc,in = 45 − 25 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (59.81 − 20)/ln(59.81/20) = 36.34 K

Area

A = Q̇/(U·ΔTlm) = 252000/(200·36.34) = 34.67 m²

Answer

A = 34.67 m²
19.Heat conduction

Answer: Q̇ = 742.3 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) = (100/1000)/(0.17·12) = 0.04902 K/W
R2 = L2/(k2A) = (25/1000)/(0.96·12) = 0.00217 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 38/0.05119 = 742.3 W

Answer

Q̇ = 742.3 W
20.Heat conduction

Answer: U = 1.982 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/(8·6) = 0.02083 K/W
R1 = L1/(k1A) = (50/1000)/(0.96·6) = 0.008681 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·6) = 0.04902 K/W
Ro = 1/(hoA) = 1/(30·6) = 0.005556 K/W
ΣR = 0.08409 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(6·0.08409) = 1.982 W/(m²·K)

Answer

U = 1.982 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 0.8123 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·0.25²/4 = 0.04909 m²
V = Q/A = 0.08/0.04909 = 1.63 m/s

Velocity head

V²/(2g) = 1.63²/(2·9.81) = 0.1354 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.015·(100/0.25)·1.63²/(2·9.81) = 0.8123 m

Answer

hf = 0.8123 m
22.Pipe friction & head loss

Answer: Δz = 4.366 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 + 4·0.3 + 2 + 1.0 = 4.7

Total head loss

hf = 6·0.408 = 2.448 m
hm = 4.7·0.408 = 1.918 m
Δz = hf + hm = 4.366 m

Answer

Δz = 4.366 m
23.Pumps & pump power

Answer: Pel = 83.61 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 = 1000·9.81·0.15·30 = 44.15 kW

Shaft power

Pshaft = 44.15/0.6 = 73.58 kW

Electrical power

Pel = 73.58/0.88 = 83.61 kW

Answer

Pel = 83.61 kW
24.Pumps & pump power

Answer: H = 34.25 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 = 0.05/0.01767 = 2.829 m/s
V²/(2g) = 0.408 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (16.67 + 6)·0.408 = 9.249 m

Pump head

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

H = Δz + hL = 25 + 9.249 = 34.25 m

Answer

H = 34.25 m

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