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 · 5% saltStream 2ṁ₂ = ? · 35% saltProduct10% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 10% salt? Find ṁ2.

ṁ1 = 900 kg/hx1 = 5 %x2 = 35 %x3 = 10 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3200 kg/h · 13% sugarProduct PP = ? · 50%Vapour W (pure water)0% sugar

An evaporator concentrates a sugar solution by boiling off pure water. Find the product flow P in kg/h.

F = 3200 kg/hxF = 13 %xP = 50 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 130 °C70 °Cwater · 25 °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 = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 130 °C80 °Cwater · 10 °C35 °C · ṁ = ?15% lost

Hot glycol mix heats water in an exchanger that loses 15% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 3 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 80 °Ct: 10 → 35 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
370 g of CH₄V = 10 LT = 100 °CP = ?

A tank of 10 L contains 370 g of CH₄ at 100 °C. Treat it as an ideal gas and find the pressure P.

m = 370 gM = 16.04 g/molV = 10 LT = 100 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
Ar, M = 39.95 g/molP = 650 kPaT = 10 °Cρ = ?

Find the density ρ of Ar at 650 kPa and 10 °C, treating it as an ideal gas.

M = 39.95 g/molP = 650 kPaT = 10 °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 20 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, 12 g of C6H12O6 reacts completely (the other reactants are in excess) and 3.81 g of C2H5OH is collected. Find the percent yield Y.

M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 3.81 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 = 25. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 25
[H2] = 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​ = ?Leadm = 150 gT = 180 °Cc = 0.129 J/(g·°C)Waterm = 300 gT = 21 °Cc = 4.18 J/(g·°C)

A 150 g block of lead (c = 0.129 J/(g·°C)) at 180 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 21 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.129 J/(g·°C)Tmetal = 180 °Cmwater = 300 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)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.5 L/(mol·min) and an initial concentration of 0.8 mol/L. Find its first half-life t½.

k = 0.5 L/(mol·min)CA0 = 0.8 mol/L
t½ = min
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.250.01run 210.04n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.25 mol/L the rate is 0.01 mol/(L·s); with CA0 = 1 mol/L it is 0.04 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.25 mol/Lr1 = 0.01 mol/(L·s)CA0,2 = 1 mol/Lr2 = 0.04 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 5 L/minCA0​ = 2.5 mol/LCA​ = ?V = 50 L, k = 0.3 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.3 min⁻¹) runs in a 50 L plug-flow reactor (PFR). The feed enters at 5 L/min with CA0 = 2.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 50 LQ = 5 L/mink = 0.3 min⁻¹CA0 = 2.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
V = 500 LV = 500 LQ = 10 L/minX = ?

A first-order liquid-phase reaction (k = 0.15 min⁻¹) runs in two equal CSTRs in series, each of 500 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 = 500 L (×2)Q = 10 L/mink = 0.15 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT110 °C20 °C90 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 110 °C on the outside of the tubes. Cooling water (3 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 20 to 90 °C. The overall heat transfer coefficient is 2500 W/(m²·K). Find the heat transfer area A needed.

Ts = 110 °Cṁ = 3 kg/scp = 4.18 kJ/(kg·K)Tc: 20 → 90 °CU = 2500 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT80 °C55 °C37.48 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (0.5 kg/s, cp = 2.5 kJ/(kg·K)) cools from 80 to 55 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 500 W/(m²·K), find the heat transfer area A needed.

ṁh = 0.5 kg/scp,h = 2.5 kJ/(kg·K)Th: 80 → 55 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 500 W/(m²·K)
A = m²
19.Heat conductionMedium
Glass, k = 0.96200 mmGypsum board, k = 0.1725 mm19 °C-13 °CQ̇ = ?

A wall is made of 200 mm of glass and 25 mm of gypsum board, with an area of 10 m². The outer faces are at 19 °C and -13 °C. Find the heat flow Q̇ through the wall.

L1 = 200 mm, k1 = 0.96 W/(m·K)L2 = 25 mm, k2 = 0.17 W/(m·K)A = 10 m²T1 = 19 °CT3 = -13 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.035100 mmMineral wool, k = 0.0450 mmroom 22 °Coutside -5 °CTs​ = ?Q̇

A wall of 100 mm expanded polystyrene and 50 mm mineral wool separates a room at 22 °C from outside air at -5 °C. The convection coefficients are 6 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 20 m². Find the temperature Ts of the inside surface of the wall.

L1 = 100 mm, k1 = 0.035 W/(m·K)L2 = 50 mm, k2 = 0.04 W/(m·K)A = 20 m²hi = 6 W/(m²·K)ho = 30 W/(m²·K)Troom = 22 °CTout = -5 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.3 m/sD = 250 mmL = 400 mf = 0.03

Water (ρ = 1000 kg/m³) flows at 1.3 m/s through a horizontal pipe, 400 m long, with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.3 m/sL = 400 mD = 250 mmf = 0.03ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 5Δz = 38 mL = 200 m, D = 200 mm, f = 0.0153× bend (K = 0.3)

Two open reservoirs are joined by a pipe 200 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.015. The water surface of the upper reservoir is 38 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 = 5) 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 = 38 mL = 200 mD = 200 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 5Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 150 L/sH = 30 m

A pump delivers 150 L/s of water (ρ = 1000 kg/m³) against a head of 30 m. The pump efficiency is 78% and the electric motor driving it has an efficiency of 90%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 150 L/sH = 30 mηpump = 78%ηmotor = 90%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
300 kPa (gauge)PQ = 120 L/sΔz = 14 mL = 200 m, D = 250 mm, f = 0.02, ΣK = 5

A pump moves 120 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 14 m higher. The pipe is 200 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.02; the minor-loss coefficients add up to ΣK = 5 (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 300 kPa. Find the head H the pump must add.

Q = 120 L/sΔz = 14 mL = 200 mD = 250 mmf = 0.02ΣK = 5ptank = 300 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 180 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) = 900·(5 − 10)/(10 − 35) = 180 kg/h

Answer

ṁ2 = 180 kg/h
2.Mass balance

Answer: P = 832 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 = 3200·13/50 = 832 kg/h

Answer

P = 832 kg/h
3.Energy balance

Answer: tout = 36.67 °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) = 25 + 146.4/(3·4.18) = 36.67 °C

Answer

tout = 36.67 °C
4.Energy balance

Answer: ṁc = 4.392 kg/s

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

Heat released

Qh = 3·3.6·(130 − 80) = 540 kW

Heat that reaches the water

Qc = (1 − 0.15)·540 = 459 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 459/(4.18·25) = 4.392 kg/s

Answer

ṁc = 4.392 kg/s
5.Ideal gas law

Answer: P = 7156 kPa

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

Moles

n = m/M = 370/16.04 = 23.07 mol
T = 100 + 273.15 = 373.1 K

Pressure

P = nRT/V = 23.07·8.314·373.1/0.01 = 7156 kPa

Answer

P = 7156 kPa
6.Ideal gas law

Answer: ρ = 11.03 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 10 + 273.15 = 283.1 K

Density

ρ = 650·39.95/(8.314·283.1) = 11.03 kg/m³

Answer

ρ = 11.03 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) = 20/70.9 = 0.2821 mol

Limiting reactant

0.174/2 = 0.08699, 0.2821/1 = 0.2821 → 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 = 62.08 %

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) = 12/180.16 = 0.06661 mol
m = 0.06661·2/1·46.07 = 6.137 g

Percent yield

Y = 3.81/6.137·100 = 62.08%

Answer

Y = 62.08%
9.Chemical equilibrium

Answer: [H2] = 0.1429 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

25 = (2x)²/(0.5 − x)²

Take the square root

5 = 2x/(0.5 − x) → x = 0.5·5/(2 + 5) = 0.3571 mol/L

Equilibrium concentration

[H₂] = 0.5 − x = 0.1429 mol/L

Answer

[H2] = 0.1429 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 = 23.42 °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

150·0.129·(180 − Tf) = 300·4.18·(Tf − 21)

Solve for the final temperature

Tf = (19.35·180 + 1254·21)/(19.35 + 1254) = 23.42 °C

Answer

Tf = 23.42 °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: t½ = 2.5 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).

Second-order half-life

t½ = 1/(k·CA0) = 1/(0.5·0.8) = 2.5 min

Answer

t½ = 2.5 min

Each later half-life is twice as long, because C₀ has halved.

14.Reaction kinetics

Answer: n = 1

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 = 0.04/0.01 = 4
C2/C1 = 1/0.25 = 4

Order

n = ln(4)/ln(4) = 1

Answer

n = 1
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.1245 mol/L

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

Space time

τ = V/Q = 50/5 = 10 min

Outlet concentration

CA = 2.5·e−0.3·10 = 0.1245 mol/L

Answer

CA = 0.1245 mol/L

Conversion: X = 95.02%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 98.62 %

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 = 500/10 = 50 min, kτ = 0.15·50 = 7.5

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 7.5) = 0.1176
C2/CA0 = 1/(1 + kτ)² = 0.01384
X = 1 − 0.01384 = 98.62%

Answer

X = 98.62%
17.Heat exchangers (LMTD)

Answer: A = 7.544 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 from the water side

Q̇ = 3·4.18·(90 − 20) = 877.8 kW

End temperature differences

ΔT₁ = 110 − 20 = 90 K
ΔT₂ = 110 − 90 = 20 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (90 − 20)/ln(90/20) = 46.54 K

Area

A = Q̇/(U·ΔTlm) = 877800/(2500·46.54) = 7.544 m²

Answer

A = 7.544 m²
18.Heat exchangers (LMTD)

Answer: A = 1.895 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) = 0.5·2.5·25 = 31.25 kW
Tc,out = 30 + 31.25/(1·4.18) = 37.48 °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 = 80 − 37.48 = 42.52 K
ΔT₂ = Th,out − Tc,in = 55 − 30 = 25 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (42.52 − 25)/ln(42.52/25) = 32.99 K

Area

A = Q̇/(U·ΔTlm) = 31250/(500·32.99) = 1.895 m²

Answer

A = 1.895 m²
19.Heat conduction

Answer: Q̇ = 900.4 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) = (200/1000)/(0.96·10) = 0.02083 K/W
R2 = L2/(k2A) = (25/1000)/(0.17·10) = 0.01471 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 32/0.03554 = 900.4 W

Answer

Q̇ = 900.4 W
20.Heat conduction

Answer: Ts = 20.96 °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/(6·20) = 0.008333 K/W
R1 = L1/(k1A) = (100/1000)/(0.035·20) = 0.1429 K/W
R2 = L2/(k2A) = (50/1000)/(0.04·20) = 0.0625 K/W
Ro = 1/(hoA) = 1/(30·20) = 0.001667 K/W
ΣR = 0.2154 K/W

Heat loss

Q̇ = (22 − (-5))/0.2154 = 125.4 W
Ts = Troom − Q̇·Ri = 22 − 125.4·0.008333 = 20.96 °C

Answer

Ts = 20.96 °C
21.Pipe friction & head loss

Answer: Δp = 40.56 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) = 0.03·(400/0.25)·1.3²/(2·9.81) = 4.135 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 = 1000·9.81·4.135 = 40560 Pa = 40.56 kPa

Answer

Δp = 40.56 kPa
22.Pipe friction & head loss

Answer: Q = 181.2 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 = 0.015·200/0.2 = 15
ΣK = 0.5 + 3·0.3 + 5 + 1.0 = 7.4

Energy equation

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

38 = (15 + 7.4)·V²/(2·9.81)
V = √(2·9.81·38/22.4) = 5.769 m/s

Flow rate

Q = V·π·D²/4 = 5.769·0.03142 = 0.1812 m³/s = 181.2 L/s

Answer

Q = 181.2 L/s
23.Pumps & pump power

Answer: Pel = 62.88 kW

Pump power: the power given to the water is the hydraulic power Ph = ρ·g·Q·H = Q·Δp. The shaft must deliver more because the pump loses some: Pshaft = Ph/ηpump, and the motor draws Pel = Pshaft/ηmotor. The pump head H follows from the energy equation: static lift + pressure head + all friction and minor losses.

Hydraulic power

Ph = ρ·g·Q·H = 1000·9.81·0.15·30 = 44.15 kW

Shaft power

Pshaft = 44.15/0.78 = 56.6 kW

Electrical power

Pel = 56.6/0.9 = 62.88 kW

Answer

Pel = 62.88 kW
24.Pumps & pump power

Answer: H = 50.98 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 = 0.12/0.04909 = 2.445 m/s
V²/(2g) = 0.3046 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (16 + 5)·0.3046 = 6.397 m

Pressure head

p/(ρ·g) = 300000/(1000·9.81) = 30.58 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 14 + 30.58 + 6.397 = 50.98 m

Answer

H = 50.98 m

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