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 1450 kg/h · 10% saltStream 2ṁ₂ = ? · 40% saltProduct15% salt

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

ṁ1 = 450 kg/hx1 = 10 %x2 = 40 %x3 = 15 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F600 kg/h · 5% NaOHProduct P55% NaOHVapour W (pure water)W = ? kg/h

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

F = 600 kg/hxF = 5 %xP = 55 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 140 °C80 °Cwater · 10 °Ct = ? °C

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

ṁh = 3 kg/scp,h = 2.44 kJ/(kg·K)Th: 140 → 80 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 140 °C80 °Cwater · 20 °C65 °C · ṁ = ?15% lost

Hot light oil 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 = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 140 → 80 °Ct: 20 → 65 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
430 g of HeP = 250 kPaT = 30 °CV = ?

What volume V does 430 g of He occupy at 250 kPa and 30 °C? Treat it as an ideal gas.

m = 430 gM = 4.003 g/molP = 250 kPaT = 30 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
N₂, M = 28.01 g/molP = 250 kPaT = 160 °Cρ = ?

Find the density ρ of N₂ at 250 kPa and 160 °C, treating it as an ideal gas.

M = 28.01 g/molP = 250 kPaT = 160 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

4 g of Na and 8 g of Cl2 react according to 2Na + Cl2 → 2NaCl. What mass m of NaCl can form?

M(Na) = 22.99M(Cl2) = 70.9M(NaCl) = 58.44 g/mol
m = g
8.StoichiometryHard
m(C6​H12​O6​)n(C6​H12​O6​)n(C2​H5​OH)m(C2​H5​OH)÷ M(C6​H12​O6​)× 2/1× M(C2​H5​OH)

In the reaction C6H12O6 → 2C2H5OH + 2CO2, 20 g of C6H12O6 reacts completely (the other reactants are in excess) and 5.63 g of C2H5OH is collected. Find the percent yield Y.

M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 5.63 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.20.20C−x−x+2xE0.2 − x0.2 − x2x

0.2 mol/L of H₂ and 0.2 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 16
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 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 = 0.05
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 150 gT = 90 °Cc = 0.385 J/(g·°C)Waterm = 100 gT = 19 °Cc = 4.18 J/(g·°C)

A 150 g block of copper (c = 0.385 J/(g·°C)) at 90 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 19 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.385 J/(g·°C)Tmetal = 90 °Cmwater = 100 gTwater = 19 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H25 g C3​H8​C3​H8​ + 5O₂reactants3CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 25 g of C3H8 (M = 44.1 g/mol) burns completely: C3H8 + 5O₂ → 3CO₂ + 4H₂O(l). Give q as a positive number.

ΔH°f(C3H8) = −103.8 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = kJ
13.Reaction kineticsMedium
t (min)X (%)t = ?75%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.2 L/(mol·min) and starts at 1 mol/L. How long does it take to reach 75% conversion? Find t.

k = 0.2 L/(mol·min)CA0 = 1 mol/LX = 75 %
t = min
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.50.01run 210.0283n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.5 mol/L the rate is 0.01 mol/(L·s); with CA0 = 1 mol/L it is 0.0283 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.5 mol/Lr1 = 0.01 mol/(L·s)CA0,2 = 1 mol/Lr2 = 0.0283 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
QX = 85%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 85% 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 = 85%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
V = 500 LQ = 50 L/minX = ?

A first-order liquid-phase reaction (k = 0.3 min⁻¹) runs in a 500 L CSTR fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 500 LQ = 50 L/mink = 0.3 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT95 °C75 °C85 °C10 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 360 kW. Its heat transfer area is 6 m². The hot fluid cools from 95 to 75 °C and the cold fluid heats from 10 to 85 °C. Find the overall heat transfer coefficient U.

Q̇ = 360 kWA = 6 m²Th: 95 → 75 °CTc: 10 → 85 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT180 °C70 °C100.7 °C20 °CΔT₁ΔT₂counter-flow

Hot oil (2 kg/s, cp = 2.3 kJ/(kg·K)) cools from 180 to 70 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 20 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 2 kg/scp,h = 2.3 kJ/(kg·K)Th: 180 → 70 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 20 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Concrete, k = 1.450 mmGlass, k = 0.96100 mm22 °C10 °CTi​ = ?Q̇

A wall is made of 50 mm of concrete and 100 mm of glass, with an area of 8 m². The outer faces are at 22 °C and 10 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 1.4 W/(m·K)L2 = 100 mm, k2 = 0.96 W/(m·K)A = 8 m²T1 = 22 °CT3 = 10 °C
Ti = °C
20.Heat conductionHard
Wood, k = 0.17200 mmGypsum board, k = 0.17150 mmroom 21 °Coutside -7 °CQ̇ = ?

A wall of 200 mm wood and 150 mm gypsum board separates a room at 21 °C from outside air at -7 °C. The convection coefficients are 6 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 20 m². Find the heat loss Q̇ through the wall.

L1 = 200 mm, k1 = 0.17 W/(m·K)L2 = 150 mm, k2 = 0.17 W/(m·K)A = 20 m²hi = 6 W/(m²·K)ho = 25 W/(m²·K)Troom = 21 °CTout = -7 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 2 m/sD = 250 mmL = 1000 mf = 0.028

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 = 0.028 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2 m/sL = 1000 mD = 250 mmf = 0.028ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 0.2Δz = 28 mL = 100 m, D = 100 mm, f = 0.024× bend (K = 0.3)

Two open reservoirs are joined by a pipe 100 m long with an inside diameter of 100 mm and a Darcy friction factor f = 0.02. The water surface of the upper reservoir is 28 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 4 bends (K = 0.3 each), a valve (K = 0.2) 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 = 28 mL = 100 mD = 100 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 0.2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 25 L/sH = 60 m

In a test, a pump delivers 25 L/s of water (ρ = 1000 kg/m³) against a head of 60 m while its shaft takes 17.3 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 25 L/sH = 60 mPshaft = 17.3 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
200 kPa (gauge)PQ = 40 L/sΔz = 9 mL = 200 m, D = 150 mm, f = 0.022, ΣK = 4

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 9 m higher. The pipe is 200 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.022; 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 200 kPa. Find the head H the pump must add.

Q = 40 L/sΔz = 9 mL = 200 mD = 150 mmf = 0.022ΣK = 4ptank = 200 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 90 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) = 450·(10 − 15)/(15 − 40) = 90 kg/h

Answer

ṁ2 = 90 kg/h
2.Mass balance

Answer: W = 545.5 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 = 600·5/55 = 54.55 kg/h

Total balance

W = F − P = 600 − 54.55 = 545.5 kg/h

Answer

W = 545.5 kg/h
3.Energy balance

Answer: tout = 115.1 °C

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

Heat released by the hot stream

Q = 3·2.44·(140 − 80) = 439.2 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 439.2/(1·4.18) = 115.1 °C

Answer

tout = 115.1 °C
4.Energy balance

Answer: ṁc = 0.8541 kg/s

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

Heat released

Qh = 1.5·2.1·(140 − 80) = 189 kW

Heat that reaches the water

Qc = (1 − 0.15)·189 = 160.7 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 160.7/(4.18·45) = 0.8541 kg/s

Answer

ṁc = 0.8541 kg/s
5.Ideal gas law

Answer: V = 1083 L

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

Moles

n = 430/4.003 = 107.4 mol
T = 30 + 273.15 = 303.1 K

Volume

V = nRT/P = 107.4·8.314·303.1/250 = 1083 L

Answer

V = 1083 L
6.Ideal gas law

Answer: ρ = 1.944 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 160 + 273.15 = 433.1 K

Density

ρ = 250·28.01/(8.314·433.1) = 1.944 kg/m³

Answer

ρ = 1.944 kg/m³
7.Stoichiometry

Answer: m = 10.17 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(Na) = 4/22.99 = 0.174 mol
n(Cl2) = 8/70.9 = 0.1128 mol

Limiting reactant

0.174/2 = 0.08699, 0.1128/1 = 0.1128 → Na

Mass of product

n(NaCl) = 0.08699·2 = 0.174 mol
m = 0.174·58.44 = 10.17 g

Answer

m = 10.17 g
8.Stoichiometry

Answer: Y = 55.04 %

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) = 20/180.16 = 0.111 mol
m = 0.111·2/1·46.07 = 10.23 g

Percent yield

Y = 5.63/10.23·100 = 55.04%

Answer

Y = 55.04%
9.Chemical equilibrium

Answer: [H2] = 0.06667 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/(0.2 − x)²

Take the square root

4 = 2x/(0.2 − x) → x = 0.2·4/(2 + 4) = 0.1333 mol/L

Equilibrium concentration

[H₂] = 0.2 − x = 0.06667 mol/L

Answer

[H2] = 0.06667 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.1351 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

0.05 = x²/(0.5 − x) → x² + 0.05·x − 0.025 = 0

Solve the quadratic

x = (−0.05 + √(0.05² + 4·0.025))/2 = 0.1351 mol/L

Equilibrium concentration

[Cl₂] = x = 0.1351 mol/L

Answer

[Cl2] = 0.1351 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 27.62 °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

150·0.385·(90 − Tf) = 100·4.18·(Tf − 19)

Solve for the final temperature

Tf = (57.75·90 + 418·19)/(57.75 + 418) = 27.62 °C

Answer

Tf = 27.62 °C
12.Calorimetry & enthalpy

Answer: q = 1258 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

Heat for the given mass

n = 25/44.1 = 0.5669 mol
q = n·|ΔH°/1| = 0.5669·2220 = 1258 kJ

Answer

q = 1258 kJ
13.Reaction kinetics

Answer: t = 15 min

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Concentration at the end

CA = 1·(1 − 0.75) = 0.25 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (4 − 1)/0.2 = 15 min

Answer

t = 15 min
14.Reaction kinetics

Answer: n = 1.501

Method of initial rates: for r = k·Cⁿ, comparing two runs that differ only in the starting concentration removes k: r₂/r₁ = (C₂/C₁)ⁿ. Doubling C doubles the rate for first order and quadruples it for second order.

Ratios

r2/r1 = 0.0283/0.01 = 2.83
C2/C1 = 1/0.5 = 2

Order

n = ln(2.83)/ln(2) = 1.501

Answer

n = 1.501
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 2.987

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) = 0.85/0.15 = 5.667
PFR: k·τ = ln(1/(1 − X)) = ln(6.667) = 1.897

Ratio of volumes

VCSTR/VPFR = 5.667/1.897 = 2.987

Answer

VCSTR/VPFR = 2.987

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 75 %

Ideal reactors, first-order reaction (−rA = k·CA) at steady state, with space time τ = V/Q. A CSTR is perfectly mixed, so the whole volume reacts at the low outlet concentration: τ = X/(k·(1 − X)) and CA = CA0/(1 + k·τ). In a PFR each slice of fluid reacts like a small batch reactor: τ = ln(1/(1 − X))/k and CA = CA0·e−k·τ. For the same conversion a CSTR always needs more volume than a PFR.

Space time

τ = V/Q = 500/50 = 10 min, kτ = 0.3·10 = 3

Conversion

X = kτ/(1 + kτ) = 3/(1 + 3) = 75%

Answer

X = 75%
17.Heat exchangers (LMTD)

Answer: U = 2042 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 = 95 − 85 = 10 K
ΔT₂ = Th,out − Tc,in = 75 − 10 = 65 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (10 − 65)/ln(10/65) = 29.38 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 360000/(6·29.38) = 2042 W/(m²·K)

Answer

U = 2042 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: A = 5.31 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) = 2·2.3·110 = 506 kW
Tc,out = 20 + 506/(1.5·4.18) = 100.7 °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 = 180 − 100.7 = 79.3 K
ΔT₂ = Th,out − Tc,in = 70 − 20 = 50 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (79.3 − 50)/ln(79.3/50) = 63.53 K

Area

A = Q̇/(U·ΔTlm) = 506000/(1500·63.53) = 5.31 m²

Answer

A = 5.31 m²
19.Heat conduction

Answer: Ti = 18.94 °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) = (50/1000)/(1.4·8) = 0.004464 K/W
R2 = L2/(k2A) = (100/1000)/(0.96·8) = 0.01302 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 12/0.01749 = 686.3 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 22 − 686.3·0.004464 = 18.94 °C

Answer

Ti = 18.94 °C
20.Heat conduction

Answer: Q̇ = 247.2 W

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

Resistances in series

Ri = 1/(hiA) = 1/(6·20) = 0.008333 K/W
R1 = L1/(k1A) = (200/1000)/(0.17·20) = 0.05882 K/W
R2 = L2/(k2A) = (150/1000)/(0.17·20) = 0.04412 K/W
Ro = 1/(hoA) = 1/(25·20) = 0.002 K/W
ΣR = 0.1133 K/W

Heat loss

Q̇ = (21 − (-7))/0.1133 = 247.2 W

Answer

Q̇ = 247.2 W
21.Pipe friction & head loss

Answer: Δp = 224 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) = 0.028·(1000/0.25)·2²/(2·9.81) = 22.83 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 = 1000·9.81·22.83 = 224000 Pa = 224 kPa

Answer

Δp = 224 kPa
22.Pipe friction & head loss

Answer: Q = 38.47 L/s

Pipe flow: the Reynolds number Re = V·D/ν = ρ·V·D/μ tells laminar flow (Re below about 2000) from turbulent flow (above about 4000). Friction along a pipe costs the Darcy–Weisbach head loss hf = f·(L/D)·V²/(2g). Fittings, valves, the entrance and the exit add minor losses hm = ΣK·V²/(2g). Between two open reservoir surfaces the energy equation gives Δz = hf + hm, with the exit loss K = 1 included.

Loss coefficients

f·L/D = 0.02·100/0.1 = 20
ΣK = 0.5 + 4·0.3 + 0.2 + 1.0 = 2.9

Energy equation

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

28 = (20 + 2.9)·V²/(2·9.81)
V = √(2·9.81·28/22.9) = 4.898 m/s

Flow rate

Q = V·π·D²/4 = 4.898·0.007854 = 0.03847 m³/s = 38.47 L/s

Answer

Q = 38.47 L/s
23.Pumps & pump power

Answer: η = 85.06 %

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 = 1000·9.81·0.025·60 = 14.71 kW

Efficiency

η = Ph/Pshaft = 14.71/17.3 = 85.06%

Answer

η = 85.06%
24.Pumps & pump power

Answer: H = 38.09 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 = 0.04/0.01767 = 2.264 m/s
V²/(2g) = 0.2611 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (29.33 + 4)·0.2611 = 8.705 m

Pressure head

p/(ρ·g) = 200000/(1000·9.81) = 20.39 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 9 + 20.39 + 8.705 = 38.09 m

Answer

H = 38.09 m

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