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 1350 kg/h · 5% saltStream 2ṁ₂ = ? · 50% saltProduct35% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 35% salt? Find ṁ2.

ṁ1 = 350 kg/hx1 = 5 %x2 = 50 %x3 = 35 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3300 kg/h · 14% sugarProduct P65% sugarVapour W (pure water)W = ? kg/h

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

F = 3300 kg/hxF = 14 %xP = 65 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 130 °C80 °Cwater · 30 °Ct = ? °C

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

ṁh = 2 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 80 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 140 °C90 °Cwater · 20 °C65 °C · ṁ = ?5% lost

Hot ethanol heats water in an exchanger that loses 5% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 2 kg/scp,h = 2.44 kJ/(kg·K)Th: 140 → 90 °Ct: 20 → 65 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
480 g of ArV = 50 LT = 95 °CP = ?

A tank of 50 L contains 480 g of Ar at 95 °C. Treat it as an ideal gas and find the pressure P.

m = 480 gM = 39.95 g/molV = 50 LT = 95 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of CH₄ goes from 200 kPa, 5 L, 25 °C to 750 kPa and 70 °C. Find the new volume V2.

P1 = 200 kPaV1 = 5 LT1 = 25 °CP2 = 750 kPaT2 = 70 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(AlCl3​)m(AlCl3​)÷ M(X)× 2/ν× M(AlCl3​)

16 g of Al and 80 g of Cl2 react according to 2Al + 3Cl2 → 2AlCl3. What mass m of AlCl3 can form?

M(Al) = 26.98M(Cl2) = 70.9M(AlCl3) = 133.33 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, 12 g of H2 reacts completely (the other reactants are in excess) and 75.08 g of H2O is collected. Find the percent yield Y.

M(H2) = 2.016 g/molM(H2O) = 18.02 g/molactual: 75.08 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 = 36. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 36
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.800C−x+x+xE0.8 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.01 at the reaction temperature. A container starts with 0.8 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.8 mol/LKc = 0.01
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 200 gT = 160 °Cc = 0.449 J/(g·°C)Waterm = 100 gT = 21 °Cc = 4.18 J/(g·°C)

A 200 g block of iron (c = 0.449 J/(g·°C)) at 160 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 21 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.449 J/(g·°C)Tmetal = 160 °Cmwater = 100 gTwater = 21 °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 second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.05 L/(mol·min) and starts at 2 mol/L. How long does it take to reach 90% conversion? Find t.

k = 0.05 L/(mol·min)CA0 = 2 mol/LX = 90 %
t = min
14.Reaction kineticsHard
1/Tln kT = 40 °Cln 0.05ln A = ?Ea​ = 100 kJ/mol

A first-order reaction has a rate constant of 0.05 s⁻¹ at 40 °C and an activation energy of 100 kJ/mol. Find the pre-exponential factor A in the Arrhenius equation.

k = 0.05 s⁻¹T = 40 °CEa = 100 kJ/molR = 8.314 J/(mol·K)
A = s⁻¹
15.Reactor sizing (CSTR & PFR)Medium
QX = 90%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 90% conversion. How many times larger must a CSTR be than a PFR for the same feed rate, rate constant and conversion? Find the ratio VCSTR/VPFR.

X = 90%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
V = 50 LV = 50 LQ = 5 L/minX = ?

A first-order liquid-phase reaction (k = 0.05 min⁻¹) runs in two equal CSTRs in series, each of 50 L. The feed rate is 5 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 50 L (×2)Q = 5 L/mink = 0.05 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT175 °C120 °C30 °C20 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 430 kW. Its heat transfer area is 2 m². The hot fluid cools from 175 to 120 °C and the cold fluid heats from 20 to 30 °C. Find the overall heat transfer coefficient U.

Q̇ = 430 kWA = 2 m²Th: 175 → 120 °CTc: 20 → 30 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT160 °C??30 °CΔT₁ΔT₂counter-flow

In a counter-flow heat exchanger both streams have the same heat capacity rate, ṁ·cp = 2 kW/K. The hot stream enters at 160 °C and the cold stream at 30 °C. The exchanger has A = 3 m² and U = 200 W/(m²·K). Find the hot outlet temperature Th,out.

Ch = Cc = 2 kW/KTh,in = 160 °CTc,in = 30 °CA = 3 m²U = 200 W/(m²·K)
Th,out = °C
19.Heat conductionMedium
Glass, k = 0.96100 mmBrick, k = 0.72150 mm17 °C-4 °CQ̇ = ?

A wall is made of 100 mm of glass and 150 mm of brick, with an area of 8 m². The outer faces are at 17 °C and -4 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.96 W/(m·K)L2 = 150 mm, k2 = 0.72 W/(m·K)A = 8 m²T1 = 17 °CT3 = -4 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.035200 mmConcrete, k = 1.475 mmroom 20 °Coutside -14 °CQ̇

A wall of 200 mm expanded polystyrene and 75 mm concrete separates a room at 20 °C from outside air at -14 °C. The convection coefficients are 6 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 15 m². Find the overall heat transfer coefficient U of the wall.

L1 = 200 mm, k1 = 0.035 W/(m·K)L2 = 75 mm, k2 = 1.4 W/(m·K)A = 15 m²hi = 6 W/(m²·K)ho = 25 W/(m²·K)Troom = 20 °CTout = -14 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 2 m/sD = 250 mmL = 1000 mf = 0.02

Water (ρ = 1000 kg/m³) flows at 2 m/s through a horizontal pipe, 1000 m long, with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.02 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2 m/sL = 1000 mD = 250 mmf = 0.02ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2Δz = 10 mL = 100 m, D = 300 mm, f = 0.0223× 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 = 0.022. The water surface of the upper reservoir is 10 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 3 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 = 10 mL = 100 mD = 300 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 2Kexit = 1.0
Q = L/s
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 78% 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 = 10 L/sH = 14 mηpump = 78%ηmotor = 88%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
150 kPa (gauge)PQ = 25 L/sΔz = 6 mL = 400 m, D = 150 mm, f = 0.015, ΣK = 6

A pump moves 25 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 = 0.015; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². The upper tank is closed and the air above its water is at a gauge pressure of 150 kPa. Find the head H the pump must add.

Q = 25 L/sΔz = 6 mL = 400 mD = 150 mmf = 0.015ΣK = 6ptank = 150 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 700 kg/h

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

Balances

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

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 350·(5 − 35)/(35 − 50) = 700 kg/h

Answer

ṁ2 = 700 kg/h
2.Mass balance

Answer: W = 2589 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 = 3300·14/65 = 710.8 kg/h

Total balance

W = F − P = 3300 − 710.8 = 2589 kg/h

Answer

W = 2589 kg/h
3.Energy balance

Answer: tout = 87.42 °C

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

Heat released by the hot stream

Q = 2·3.6·(130 − 80) = 360 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 360/(1.5·4.18) = 87.42 °C

Answer

tout = 87.42 °C
4.Energy balance

Answer: ṁc = 1.232 kg/s

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

Heat released

Qh = 2·2.44·(140 − 90) = 244 kW

Heat that reaches the water

Qc = (1 − 0.05)·244 = 231.8 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 231.8/(4.18·45) = 1.232 kg/s

Answer

ṁc = 1.232 kg/s
5.Ideal gas law

Answer: P = 735.5 kPa

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

Moles

n = m/M = 480/39.95 = 12.02 mol
T = 95 + 273.15 = 368.1 K

Pressure

P = nRT/V = 12.02·8.314·368.1/0.05 = 735.5 kPa

Answer

P = 735.5 kPa
6.Ideal gas law

Answer: V2 = 1.535 L

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

Absolute temperatures

T1 = 298.1 K, T2 = 343.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(200/750)·(343.1/298.1) = 1.535 L

Answer

V2 = 1.535 L
7.Stoichiometry

Answer: m = 79.07 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(Al) = 16/26.98 = 0.593 mol
n(Cl2) = 80/70.9 = 1.128 mol

Limiting reactant

0.593/2 = 0.2965, 1.128/3 = 0.3761 → Al

Mass of product

n(AlCl3) = 0.2965·2 = 0.593 mol
m = 0.593·133.33 = 79.07 g

Answer

m = 79.07 g
8.Stoichiometry

Answer: Y = 70 %

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) = 12/2.016 = 5.952 mol
m = 5.952·2/2·18.02 = 107.3 g

Percent yield

Y = 75.08/107.3·100 = 70%

Answer

Y = 70%
9.Chemical equilibrium

Answer: [HI] = 1.2 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

36 = (2x)²/(0.8 − x)²

Take the square root

6 = 2x/(0.8 − x) → x = 0.8·6/(2 + 6) = 0.6 mol/L

Equilibrium concentration

[HI] = 2x = 1.2 mol/L

Answer

[HI] = 1.2 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.08458 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

0.01 = x²/(0.8 − x) → x² + 0.01·x − 0.008 = 0

Solve the quadratic

x = (−0.01 + √(0.01² + 4·0.008))/2 = 0.08458 mol/L

Equilibrium concentration

[Cl₂] = x = 0.08458 mol/L

Answer

[Cl2] = 0.08458 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 45.58 °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

200·0.449·(160 − Tf) = 100·4.18·(Tf − 21)

Solve for the final temperature

Tf = (89.8·160 + 418·21)/(89.8 + 418) = 45.58 °C

Answer

Tf = 45.58 °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 = 90 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 − 0.9) = 0.2 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (5 − 0.5)/0.05 = 90 min

Answer

t = 90 min
14.Reaction kinetics

Answer: A = 2.399 × 10¹⁵ s⁻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 temperature

T = 40 + 273.15 = 313.1 K

Solve Arrhenius for A

Ea/(RT) = 100000/(8.314·313.1) = 38.41
A = k·e38.41 = 0.05·4.797 × 10¹⁶ = 2.399 × 10¹⁵ s⁻¹

Answer

A = 2.399 × 10¹⁵ s⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 3.909

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.

k·τ for each reactor

CSTR: k·τ = X/(1 − X) = 0.9/0.1 = 9
PFR: k·τ = ln(1/(1 − X)) = ln(10) = 2.303

Ratio of volumes

VCSTR/VPFR = 9/2.303 = 3.909

Answer

VCSTR/VPFR = 3.909

The gap grows quickly at high conversion.

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 = 50/5 = 10 min, kτ = 0.05·10 = 0.5

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 0.5) = 0.6667
C2/CA0 = 1/(1 + kτ)² = 0.4444
X = 1 − 0.4444 = 55.56%

Answer

X = 55.56%
17.Heat exchangers (LMTD)

Answer: U = 1775 W/(m²·K)

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 = 175 − 30 = 145 K
ΔT₂ = Th,out − Tc,in = 120 − 20 = 100 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (145 − 100)/ln(145/100) = 121.1 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 430000/(2·121.1) = 1775 W/(m²·K)

Answer

U = 1775 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: Th,out = 130 °C

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.

Constant temperature difference

The cold outlet sits opposite the hot inlet: Tc,out = Tc,in + (Th,in − Th,out), so ΔT₁ = Th,in − Tc,out = Th,out − Tc,in = ΔT₂.

ΔTlm = Th,out − Tc,in

Energy balance equals rate equation

2·(160 − Th,out) = 0.6·(Th,out − 30)
Th,out = (2·160 + 0.6·30)/(2 + 0.6) = 130 °C

Answer

Th,out = 130 °C

Heat transferred: Q̇ = 60 kW; the cold stream leaves at 60 °C.

19.Heat conduction

Answer: Q̇ = 537.6 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)/(0.96·8) = 0.01302 K/W
R2 = L2/(k2A) = (150/1000)/(0.72·8) = 0.02604 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 21/0.03906 = 537.6 W

Answer

Q̇ = 537.6 W
20.Heat conduction

Answer: U = 0.1674 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/(6·15) = 0.01111 K/W
R1 = L1/(k1A) = (200/1000)/(0.035·15) = 0.381 K/W
R2 = L2/(k2A) = (75/1000)/(1.4·15) = 0.003571 K/W
Ro = 1/(hoA) = 1/(25·15) = 0.002667 K/W
ΣR = 0.3983 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(15·0.3983) = 0.1674 W/(m²·K)

Answer

U = 0.1674 W/(m²·K)
21.Pipe friction & head loss

Answer: Δp = 160 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) = 0.02·(1000/0.25)·2²/(2·9.81) = 16.31 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 = 1000·9.81·16.31 = 160000 Pa = 160 kPa

Answer

Δp = 160 kPa
22.Pipe friction & head loss

Answer: Q = 289 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 = 0.022·100/0.3 = 7.333
ΣK = 0.5 + 3·0.3 + 2 + 1.0 = 4.4

Energy equation

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

10 = (7.333 + 4.4)·V²/(2·9.81)
V = √(2·9.81·10/11.73) = 4.089 m/s

Flow rate

Q = V·π·D²/4 = 4.089·0.07069 = 0.289 m³/s = 289 L/s

Answer

Q = 289 L/s
23.Pumps & pump power

Answer: Pel = 2.001 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 = 1.373/0.78 = 1.761 kW

Electrical power

Pel = 1.761/0.88 = 2.001 kW

Answer

Pel = 2.001 kW
24.Pumps & pump power

Answer: H = 25.98 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 = 0.025/0.01767 = 1.415 m/s
V²/(2g) = 0.102 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (40 + 6)·0.102 = 4.692 m

Pressure head

p/(ρ·g) = 150000/(1000·9.81) = 15.29 m

Pump head

Both surfaces are practically at rest, so there is no velocity head term.

H = Δz + p/(ρ·g) + hL = 6 + 15.29 + 4.692 = 25.98 m

Answer

H = 25.98 m

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