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 11000 kg/h · 35% NaOHStream 2ṁ₂ = ? · 10% NaOHProduct25% NaOH

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

ṁ1 = 1000 kg/hx1 = 35 %x2 = 10 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4500 kg/h · 7% sugarProduct P60% 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 = 4500 kg/hxF = 7 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 140 °C100 °Cwater · 30 °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: 140 → 100 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 140 °C70 °Cwater · 25 °C45 °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 = 3 kg/scp,h = 2.44 kJ/(kg·K)Th: 140 → 70 °Ct: 25 → 45 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
360 g of CH₄V = 10 LT = 20 °CP = ?

A tank of 10 L contains 360 g of CH₄ at 20 °C. Treat it as an ideal gas and find the pressure P.

m = 360 gM = 16.04 g/molV = 10 LT = 20 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
He, M = 4.003 g/molP = 650 kPaT = 20 °Cρ = ?

Find the density ρ of He at 650 kPa and 20 °C, treating it as an ideal gas.

M = 4.003 g/molP = 650 kPaT = 20 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(AlCl3​)m(AlCl3​)÷ M(X)× 2/ν× M(AlCl3​)

24 g of Al and 40 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(Fe2​O3​)n(Fe2​O3​)n(CO2​)m(CO2​)÷ M(Fe2​O3​)× 3/1× M(CO2​)

In the reaction Fe2O3 + 3CO → 2Fe + 3CO2, 24 g of Fe2O3 reacts completely (the other reactants are in excess) and 13.89 g of CO2 is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(CO2) = 44.01 g/molactual: 13.89 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII110C−x−x+2xE1 − x1 − x2x

1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 16
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.800C−x+x+xE0.8 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.5 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 = 0.5
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 150 gT = 140 °Cc = 0.449 J/(g·°C)Waterm = 150 gT = 21 °Cc = 4.18 J/(g·°C)

A 150 g block of iron (c = 0.449 J/(g·°C)) at 140 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 21 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.449 J/(g·°C)Tmetal = 140 °Cmwater = 150 gTwater = 21 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC3​H8​ + 5O₂reactants3CO₂ + 4H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C3H8 + 5O₂ → 3CO₂ + 4H₂O(l).

ΔH°f(C3H8) = −103.8 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)C (mol/L)40 min0.96

In a first-order reaction the concentration of A falls from 1.2 mol/L to 0.96 mol/L in 40 min. Find the rate constant k.

CA0 = 1.2 mol/LCA = 0.96 mol/Lt = 40 min
k = min⁻¹
14.Reaction kineticsHard
1/Tln kT = 100 °Cln 0.05ln A = ?Ea​ = 40 kJ/mol

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

k = 0.05 s⁻¹T = 100 °CEa = 40 kJ/molR = 8.314 J/(mol·K)
A = s⁻¹
15.Reactor sizing (CSTR & PFR)Medium
QX = 75%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 75% 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 = 75%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
V = 200 LV = 200 LQ = 10 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in two equal CSTRs in series, each of 200 L. The feed rate is 10 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 200 L (×2)Q = 10 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT160 °C100 °C55 °C20 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 170 kW. Its heat transfer area is 20 m². The hot fluid cools from 160 to 100 °C and the cold fluid heats from 20 to 55 °C. Find the overall heat transfer coefficient U.

Q̇ = 170 kWA = 20 m²Th: 160 → 100 °CTc: 20 → 55 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT170 °C100 °C120.5 °C15 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.1 kJ/(kg·K)) cools from 170 to 100 °C in a counter-flow exchanger. It heats 0.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 15 °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: 170 → 100 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 15 °CU = 200 W/(m²·K)
A = m²
19.Heat conductionMedium
Concrete, k = 1.4150 mmMineral wool, k = 0.0450 mm16 °C-9 °CTi​ = ?Q̇

A wall is made of 150 mm of concrete and 50 mm of mineral wool, with an area of 12 m². The outer faces are at 16 °C and -9 °C. Find the temperature Ti at the interface between the two layers.

L1 = 150 mm, k1 = 1.4 W/(m·K)L2 = 50 mm, k2 = 0.04 W/(m·K)A = 12 m²T1 = 16 °CT3 = -9 °C
Ti = °C
20.Heat conductionHard
Gypsum board, k = 0.1750 mmWood, k = 0.17100 mmroom 21 °Coutside -4 °CTs​ = ?Q̇

A wall of 50 mm gypsum board and 100 mm wood separates a room at 21 °C from outside air at -4 °C. The convection coefficients are 10 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 8 m². Find the temperature Ts of the inside surface of the wall.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 100 mm, k2 = 0.17 W/(m·K)A = 8 m²hi = 10 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = -4 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 2.8 m/sD = 250 mmL = 200 mf = 0.02

Water flows at a mean velocity of 2.8 m/s through a pipe 200 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 friction head loss hf.

V = 2.8 m/sL = 200 mD = 250 mmf = 0.02g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5Δz = ?L = 150 m, D = 250 mm, f = 0.0254× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.025. The minor losses are a square-edged entrance (K = 0.5), 4 bends (K = 0.3 each), a valve (K = 5) 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 60 L/s?

Q = 60 L/sL = 150 mD = 250 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 5Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 50 L/sH = 64 m

In a test, a pump delivers 50 L/s of water (ρ = 1000 kg/m³) against a head of 64 m while its shaft takes 48.3 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 50 L/sH = 64 mPshaft = 48.3 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
100 kPa (gauge)PQ = 75 L/sΔz = 7 mL = 100 m, D = 250 mm, f = 0.015, ΣK = 4

A pump moves 75 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 7 m higher. The pipe is 100 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.015; the minor-loss coefficients add up to ΣK = 4 (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 100 kPa. Find the head H the pump must add.

Q = 75 L/sΔz = 7 mL = 100 mD = 250 mmf = 0.015ΣK = 4ptank = 100 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 666.7 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) = 1000·(35 − 25)/(25 − 10) = 666.7 kg/h

Answer

ṁ2 = 666.7 kg/h
2.Mass balance

Answer: W = 3975 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 = 4500·7/60 = 525 kg/h

Total balance

W = F − P = 4500 − 525 = 3975 kg/h

Answer

W = 3975 kg/h
3.Energy balance

Answer: tout = 50.1 °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·(140 − 100) = 168 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 168/(2·4.18) = 50.1 °C

Answer

tout = 50.1 °C
4.Energy balance

Answer: ṁc = 5.516 kg/s

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

Heat released

Qh = 3·2.44·(140 − 70) = 512.4 kW

Heat that reaches the water

Qc = (1 − 0.1)·512.4 = 461.2 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 461.2/(4.18·20) = 5.516 kg/s

Answer

ṁc = 5.516 kg/s
5.Ideal gas law

Answer: P = 5470 kPa

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

Moles

n = m/M = 360/16.04 = 22.44 mol
T = 20 + 273.15 = 293.1 K

Pressure

P = nRT/V = 22.44·8.314·293.1/0.01 = 5470 kPa

Answer

P = 5470 kPa
6.Ideal gas law

Answer: ρ = 1.068 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 20 + 273.15 = 293.1 K

Density

ρ = 650·4.003/(8.314·293.1) = 1.068 kg/m³

Answer

ρ = 1.068 kg/m³
7.Stoichiometry

Answer: m = 50.15 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) = 24/26.98 = 0.8895 mol
n(Cl2) = 40/70.9 = 0.5642 mol

Limiting reactant

0.8895/2 = 0.4448, 0.5642/3 = 0.1881 → Cl2

Mass of product

n(AlCl3) = 0.1881·2 = 0.3761 mol
m = 0.3761·133.33 = 50.15 g

Answer

m = 50.15 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(Fe2O3) = 24/159.69 = 0.1503 mol
m = 0.1503·3/1·44.01 = 19.84 g

Percent yield

Y = 13.89/19.84·100 = 70%

Answer

Y = 70%
9.Chemical equilibrium

Answer: [HI] = 1.333 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

16 = (2x)²/(1 − x)²

Take the square root

4 = 2x/(1 − x) → x = 1·4/(2 + 4) = 0.6667 mol/L

Equilibrium concentration

[HI] = 2x = 1.333 mol/L

Answer

[HI] = 1.333 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.4301 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

0.5 = x²/(0.8 − x) → x² + 0.5·x − 0.4 = 0

Solve the quadratic

x = (−0.5 + √(0.5² + 4·0.4))/2 = 0.4301 mol/L

Equilibrium concentration

[Cl₂] = x = 0.4301 mol/L

Answer

[Cl2] = 0.4301 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 32.54 °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

150·0.449·(140 − Tf) = 150·4.18·(Tf − 21)

Solve for the final temperature

Tf = (67.35·140 + 627·21)/(67.35 + 627) = 32.54 °C

Answer

Tf = 32.54 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −2220 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° = [3·(−393.5) + 4·(−285.8)] − [1·(−103.8) + 5·0] = −2220 kJ

Answer

ΔH° = −2220 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.005579 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(1.2/0.96)/40 = 0.2231/40 = 0.005579 min⁻¹

Answer

k = 0.005579 min⁻¹
14.Reaction kinetics

Answer: A = 19883 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 = 100 + 273.15 = 373.1 K

Solve Arrhenius for A

Ea/(RT) = 40000/(8.314·373.1) = 12.89
A = k·e12.89 = 0.05·3.977 × 10⁵ = 19883 s⁻¹

Answer

A = 19883 s⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 2.164

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) = 0.75/0.25 = 3
PFR: k·τ = ln(1/(1 − X)) = ln(4) = 1.386

Ratio of volumes

VCSTR/VPFR = 3/1.386 = 2.164

Answer

VCSTR/VPFR = 2.164

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 97.22 %

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 = 0.25·20 = 5

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 5) = 0.1667
C2/CA0 = 1/(1 + kτ)² = 0.02778
X = 1 − 0.02778 = 97.22%

Answer

X = 97.22%
17.Heat exchangers (LMTD)

Answer: U = 92.46 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 = 160 − 55 = 105 K
ΔT₂ = Th,out − Tc,in = 100 − 20 = 80 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (105 − 80)/ln(105/80) = 91.93 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 170000/(20·91.93) = 92.46 W/(m²·K)

Answer

U = 92.46 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: A = 16.79 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) = 1.5·2.1·70 = 220.5 kW
Tc,out = 15 + 220.5/(0.5·4.18) = 120.5 °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 = 170 − 120.5 = 49.5 K
ΔT₂ = Th,out − Tc,in = 100 − 15 = 85 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (49.5 − 85)/ln(49.5/85) = 65.66 K

Area

A = Q̇/(U·ΔTlm) = 220500/(200·65.66) = 16.79 m²

Answer

A = 16.79 m²
19.Heat conduction

Answer: Ti = 14.03 °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)/(1.4·12) = 0.008929 K/W
R2 = L2/(k2A) = (50/1000)/(0.04·12) = 0.1042 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 25/0.1131 = 221.1 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 16 − 221.1·0.008929 = 14.03 °C

Answer

Ti = 14.03 °C
20.Heat conduction

Answer: Ts = 18.58 °C

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

Resistances in series

Ri = 1/(hiA) = 1/(10·8) = 0.0125 K/W
R1 = L1/(k1A) = (50/1000)/(0.17·8) = 0.03676 K/W
R2 = L2/(k2A) = (100/1000)/(0.17·8) = 0.07353 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.129 K/W

Heat loss

Q̇ = (21 − (-4))/0.129 = 193.7 W
Ts = Troom − Q̇·Ri = 21 − 193.7·0.0125 = 18.58 °C

Answer

Ts = 18.58 °C
21.Pipe friction & head loss

Answer: hf = 6.393 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 head

V²/(2g) = 2.8²/(2·9.81) = 0.3996 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.02·(200/0.25)·2.8²/(2·9.81) = 6.393 m

Answer

hf = 6.393 m
22.Pipe friction & head loss

Answer: Δz = 1.729 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 = 0.06/0.04909 = 1.222 m/s
V²/(2g) = 0.07615 m

Loss coefficients

f·L/D = 0.025·150/0.25 = 15
ΣK = 0.5 + 4·0.3 + 5 + 1.0 = 7.7

Total head loss

hf = 15·0.07615 = 1.142 m
hm = 7.7·0.07615 = 0.5863 m
Δz = hf + hm = 1.729 m

Answer

Δz = 1.729 m
23.Pumps & pump power

Answer: η = 64.99 %

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 = 1000·9.81·0.05·64 = 31.39 kW

Efficiency

η = Ph/Pshaft = 31.39/48.3 = 64.99%

Answer

η = 64.99%
24.Pumps & pump power

Answer: H = 18.38 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 = 0.075/0.04909 = 1.528 m/s
V²/(2g) = 0.119 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (6 + 4)·0.119 = 1.19 m

Pressure head

p/(ρ·g) = 100000/(1000·9.81) = 10.19 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 7 + 10.19 + 1.19 = 18.38 m

Answer

H = 18.38 m

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