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 1900 kg/h · 30% sugarStream 2ṁ₂ = ? · 20% 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 = 900 kg/hx1 = 30 %x2 = 20 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4400 kg/h · 7% saltProduct P65% 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 = 4400 kg/hxF = 7 %xP = 65 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 130 °C70 °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 = 1 kg/scp,h = 2.44 kJ/(kg·K)Th: 130 → 70 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 140 °C90 °Cwater · 25 °C50 °C · ṁ = ?15% lost

Hot ethanol 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 = 3 kg/scp,h = 2.44 kJ/(kg·K)Th: 140 → 90 °Ct: 25 → 50 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
400 g of CO₂P = 700 kPaT = 85 °CV = ?

What volume V does 400 g of CO₂ occupy at 700 kPa and 85 °C? Treat it as an ideal gas.

m = 400 gM = 44.01 g/molP = 700 kPaT = 85 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 400 kPa, 20 L, 40 °C to 350 kPa and 230 °C. Find the new volume V2.

P1 = 400 kPaV1 = 20 LT1 = 40 °CP2 = 350 kPaT2 = 230 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

20 g of Na and 40 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(C3​H8​)n(C3​H8​)n(CO2​)m(CO2​)÷ M(C3​H8​)× 3/1× M(CO2​)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 20 g of C3H8 reacts completely (the other reactants are in excess) and 44.91 g of CO2 is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(CO2) = 44.01 g/molactual: 44.91 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.50.50C−x−x+2xE0.5 − x0.5 − x2x

0.5 mol/L of H₂ and 0.5 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 4. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 4
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.200C−x+x+xE0.2 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.04 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.2 mol/LKc = 0.04
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 100 gT = 150 °Cc = 0.385 J/(g·°C)Waterm = 100 gT = 22 °Cc = 4.18 J/(g·°C)

A 100 g block of copper (c = 0.385 J/(g·°C)) at 150 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 22 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.385 J/(g·°C)Tmetal = 150 °Cmwater = 100 gTwater = 22 °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)X (%)t = ?80%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.25 L/(mol·min) and starts at 0.5 mol/L. How long does it take to reach 80% conversion? Find t.

k = 0.25 L/(mol·min)CA0 = 0.5 mol/LX = 80 %
t = min
14.Reaction kineticsHard
Tk40 °C0.00580 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 40 °C and an activation energy of 55 kJ/mol. Find the rate constant k2 at 80 °C.

k1 = 0.005 min⁻¹T1 = 40 °CT2 = 80 °CEa = 55 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 20 L/minX = 95%V = ?, k = 0.25 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.25 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 20 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 95% conversion of A.

Q = 20 L/mink = 0.25 min⁻¹X = 95%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 1500 LV = 1500 LQ = 80 L/minX = ?

A first-order liquid-phase reaction (k = 0.08 min⁻¹) runs in two equal CSTRs in series, each of 1500 L. The feed rate is 80 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 1500 L (×2)Q = 80 L/mink = 0.08 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT110 °C95 °C100 °C20 °CΔT₁ΔT₂counter-flow

A shell-and-tube heat exchanger (one shell pass, two tube passes) must transfer 650 kW. The hot fluid cools from 110 to 95 °C and the cold fluid heats from 20 to 100 °C. The LMTD correction factor for this arrangement is F = 0.8, and U = 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 650 kWF = 0.8U = 800 W/(m²·K)Th: 110 → 95 °CTc: 20 → 100 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT175 °C125 °C19.17 °C10 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.3 kJ/(kg·K)) cools from 175 to 125 °C in a counter-flow exchanger. It heats 3 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 10 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.3 kJ/(kg·K)Th: 175 → 125 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 10 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Brick, k = 0.72100 mmExpanded polystyrene, k = 0.03550 mm17 °C3 °CQ̇ = ?

A wall is made of 100 mm of brick and 50 mm of expanded polystyrene, with an area of 8 m². The outer faces are at 17 °C and 3 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.72 W/(m·K)L2 = 50 mm, k2 = 0.035 W/(m·K)A = 8 m²T1 = 17 °CT3 = 3 °C
Q̇ = W
20.Heat conductionHard
Mineral wool, k = 0.0450 mmGlass, k = 0.9625 mmroom 20 °Coutside 3 °CTs​ = ?Q̇

A wall of 50 mm mineral wool and 25 mm glass separates a room at 20 °C from outside air at 3 °C. The convection coefficients are 6 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 6 m². Find the temperature Ts of the inside surface of the wall.

L1 = 50 mm, k1 = 0.04 W/(m·K)L2 = 25 mm, k2 = 0.96 W/(m·K)A = 6 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 20 °CTout = 3 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 200 L/sD = 300 mmL = 150 mf = 0.018

Water flows at 200 L/s through a pipe 150 m long with an inside diameter of 300 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the friction head loss hf.

Q = 200 L/sL = 150 mD = 300 mmf = 0.018g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10Δz = ?L = 300 m, D = 300 mm, f = 0.0152× bend (K = 0.3)

Two open reservoirs are joined by a pipe 300 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.015. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 10) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². What difference in water level Δz between the reservoirs gives a flow rate of 80 L/s?

Q = 80 L/sL = 300 mD = 300 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 10Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 150 L/sH = 14 m

In a test, a pump delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 14 m while its shaft takes 26.4 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 150 L/sH = 14 mPshaft = 26.4 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 80 L/sΔz = 9 mL = 200 m, D = 200 mm, f = 0.022, ΣK = 4

A pump moves 80 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 200 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. Find the head H the pump must add.

Q = 80 L/sΔz = 9 mL = 200 mD = 200 mmf = 0.022ΣK = 4
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 900 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) = 900·(30 − 25)/(25 − 20) = 900 kg/h

Answer

ṁ2 = 900 kg/h
2.Mass balance

Answer: W = 3926 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 = 4400·7/65 = 473.8 kg/h

Total balance

W = F − P = 4400 − 473.8 = 3926 kg/h

Answer

W = 3926 kg/h
3.Energy balance

Answer: tout = 33.35 °C

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

Heat released by the hot stream

Q = 1·2.44·(130 − 70) = 146.4 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 146.4/(1.5·4.18) = 33.35 °C

Answer

tout = 33.35 °C
4.Energy balance

Answer: ṁc = 2.977 kg/s

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

Heat released

Qh = 3·2.44·(140 − 90) = 366 kW

Heat that reaches the water

Qc = (1 − 0.15)·366 = 311.1 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 311.1/(4.18·25) = 2.977 kg/s

Answer

ṁc = 2.977 kg/s
5.Ideal gas law

Answer: V = 38.66 L

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

Moles

n = 400/44.01 = 9.089 mol
T = 85 + 273.15 = 358.1 K

Volume

V = nRT/P = 9.089·8.314·358.1/700 = 38.66 L

Answer

V = 38.66 L
6.Ideal gas law

Answer: V2 = 36.73 L

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

Absolute temperatures

T1 = 313.1 K, T2 = 503.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 20·(400/350)·(503.1/313.1) = 36.73 L

Answer

V2 = 36.73 L
7.Stoichiometry

Answer: m = 50.84 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) = 20/22.99 = 0.8699 mol
n(Cl2) = 40/70.9 = 0.5642 mol

Limiting reactant

0.8699/2 = 0.435, 0.5642/1 = 0.5642 → Na

Mass of product

n(NaCl) = 0.435·2 = 0.8699 mol
m = 0.8699·58.44 = 50.84 g

Answer

m = 50.84 g
8.Stoichiometry

Answer: Y = 75 %

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(C3H8) = 20/44.1 = 0.4535 mol
m = 0.4535·3/1·44.01 = 59.88 g

Percent yield

Y = 44.91/59.88·100 = 75%

Answer

Y = 75%
9.Chemical equilibrium

Answer: [HI] = 0.5 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

4 = (2x)²/(0.5 − x)²

Take the square root

2 = 2x/(0.5 − x) → x = 0.5·2/(2 + 2) = 0.25 mol/L

Equilibrium concentration

[HI] = 2x = 0.5 mol/L

Answer

[HI] = 0.5 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.1283 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

0.04 = x²/(0.2 − x) → x² + 0.04·x − 0.008 = 0

Solve the quadratic

x = (−0.04 + √(0.04² + 4·0.008))/2 = 0.07165 mol/L

Equilibrium concentration

[PCl₅] = 0.2 − 0.07165 = 0.1283 mol/L

Answer

[PCl5] = 0.1283 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 32.8 °C

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Heat balance

100·0.385·(150 − Tf) = 100·4.18·(Tf − 22)

Solve for the final temperature

Tf = (38.5·150 + 418·22)/(38.5 + 418) = 32.8 °C

Answer

Tf = 32.8 °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: t = 32 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 = 0.5·(1 − 0.8) = 0.1 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (10 − 2)/0.25 = 32 min

Answer

t = 32 min
14.Reaction kinetics

Answer: k2 = 0.05472 min⁻¹

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Absolute temperatures

T1 = 313.1 K, T2 = 353.1 K

Arrhenius ratio

ln(k2/k1) = −(55000/8.314)·(1/353.1 − 1/313.1) = 2.393
k2 = 0.005·e2.393 = 0.05472 min⁻¹

Answer

k2 = 0.05472 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 239.7 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 = ln(1/(1 − 0.95))/0.25 = 2.996/0.25 = 11.98 min

Volume

V = Q·τ = 20·11.98 = 239.7 L

Answer

V = 239.7 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 84 %

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 = 1500/80 = 18.75 min, kτ = 0.08·18.75 = 1.5

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 1.5) = 0.4
C2/CA0 = 1/(1 + kτ)² = 0.16
X = 1 − 0.16 = 84%

Answer

X = 84%
17.Heat exchangers (LMTD)

Answer: A = 31.48 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 (counter-flow)

In counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 110 − 100 = 10 K
ΔT₂ = Th,out − Tc,in = 95 − 20 = 75 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (10 − 75)/ln(10/75) = 32.26 K

Area

A = Q̇/(U·F·ΔTlm,cf) = 650000/(800·0.8·32.26) = 31.48 m²

Answer

A = 31.48 m²
18.Heat exchangers (LMTD)

Answer: A = 0.5705 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) = 1·2.3·50 = 115 kW
Tc,out = 10 + 115/(3·4.18) = 19.17 °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 = 175 − 19.17 = 155.8 K
ΔT₂ = Th,out − Tc,in = 125 − 10 = 115 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (155.8 − 115)/ln(155.8/115) = 134.4 K

Area

A = Q̇/(U·ΔTlm) = 115000/(1500·134.4) = 0.5705 m²

Answer

A = 0.5705 m²
19.Heat conduction

Answer: Q̇ = 71.45 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)/(0.72·8) = 0.01736 K/W
R2 = L2/(k2A) = (50/1000)/(0.035·8) = 0.1786 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 14/0.1959 = 71.45 W

Answer

Q̇ = 71.45 W
20.Heat conduction

Answer: Ts = 18.1 °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/(6·6) = 0.02778 K/W
R1 = L1/(k1A) = (50/1000)/(0.04·6) = 0.2083 K/W
R2 = L2/(k2A) = (25/1000)/(0.96·6) = 0.00434 K/W
Ro = 1/(hoA) = 1/(20·6) = 0.008333 K/W
ΣR = 0.2488 K/W

Heat loss

Q̇ = (20 − (3))/0.2488 = 68.33 W
Ts = Troom − Q̇·Ri = 20 − 68.33·0.02778 = 18.1 °C

Answer

Ts = 18.1 °C
21.Pipe friction & head loss

Answer: hf = 3.672 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·0.3²/4 = 0.07069 m²
V = Q/A = 0.2/0.07069 = 2.829 m/s

Velocity head

V²/(2g) = 2.829²/(2·9.81) = 0.408 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.018·(150/0.3)·2.829²/(2·9.81) = 3.672 m

Answer

hf = 3.672 m
22.Pipe friction & head loss

Answer: Δz = 1.769 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 = 0.08/0.07069 = 1.132 m/s
V²/(2g) = 0.06529 m

Loss coefficients

f·L/D = 0.015·300/0.3 = 15
ΣK = 0.5 + 2·0.3 + 10 + 1.0 = 12.1

Total head loss

hf = 15·0.06529 = 0.9793 m
hm = 12.1·0.06529 = 0.79 m
Δz = hf + hm = 1.769 m

Answer

Δz = 1.769 m
23.Pumps & pump power

Answer: η = 78.03 %

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 = 1000·9.81·0.15·14 = 20.6 kW

Efficiency

η = Ph/Pshaft = 20.6/26.4 = 78.03%

Answer

η = 78.03%
24.Pumps & pump power

Answer: H = 17.59 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 = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (22 + 4)·0.3305 = 8.593 m

Pump head

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

H = Δz + hL = 9 + 8.593 = 17.59 m

Answer

H = 17.59 m

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