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 · 40% NaOHStream 2ṁ₂ = ? · 10% NaOHProduct35% NaOH

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

ṁ1 = 450 kg/hx1 = 40 %x2 = 10 %x3 = 35 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3200 kg/h · 18% saltProduct P60% 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 = 3200 kg/hxF = 18 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 140 °C110 °Cwater · 15 °Ct = ? °C

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

ṁh = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 140 → 110 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 120 °C80 °Cwater · 30 °C55 °C · ṁ = ?10% lost

Hot light oil 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 = 1 kg/scp,h = 2.1 kJ/(kg·K)Th: 120 → 80 °Ct: 30 → 55 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
340 g of N₂V = 5 LT = 80 °CP = ?

A tank of 5 L contains 340 g of N₂ at 80 °C. Treat it as an ideal gas and find the pressure P.

m = 340 gM = 28.01 g/molV = 5 LT = 80 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 400 kPa, 2 L, 25 °C to 700 kPa and 60 °C. Find the new volume V2.

P1 = 400 kPaV1 = 2 LT1 = 25 °CP2 = 700 kPaT2 = 60 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(Fe)m(Fe)÷ M(X)× 2/ν× M(Fe)

16 g of Fe2O3 and 48 g of CO react according to Fe2O3 + 3CO → 2Fe + 3CO2. What mass m of Fe can form?

M(Fe2O3) = 159.69M(CO) = 28.01M(Fe) = 55.85 g/mol
m = g
8.StoichiometryHard
m(Mg)n(Mg)n(MgO)m(MgO)÷ M(Mg)× 2/2× M(MgO)

In the reaction 2Mg + O2 → 2MgO, 10 g of Mg reacts completely (the other reactants are in excess) and 9.12 g of MgO is collected. Find the percent yield Y.

M(Mg) = 24.31 g/molM(MgO) = 40.3 g/molactual: 9.12 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.40.40C−x−x+2xE0.4 − x0.4 − x2x

0.4 mol/L of H₂ and 0.4 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 54. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 54
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.800C−x+x+xE0.8 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.8 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.8 mol/LKc = 0.1
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 250 gT = 90 °Cc = 0.449 J/(g·°C)Waterm = 300 gT = 15 °Cc = 4.18 J/(g·°C)

A 250 g block of iron (c = 0.449 J/(g·°C)) at 90 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 15 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.449 J/(g·°C)Tmetal = 90 °Cmwater = 300 gTwater = 15 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H25 g C4​H10​2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 25 g of C4H10 (M = 58.12 g/mol) burns completely: 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l). Give q as a positive number.

ΔH°f(C4H10) = −125.6 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)C (mol/L)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.02 L/(mol·min) and an initial concentration of 0.2 mol/L. Find its first half-life t½.

k = 0.02 L/(mol·min)CA0 = 0.2 mol/L
t½ = min
14.Reaction kineticsHard
1/Tln kT = 40 °Cln 0.1ln A = ?Ea​ = 75 kJ/mol

A first-order reaction has a rate constant of 0.1 s⁻¹ at 40 °C and an activation energy of 75 kJ/mol. Find the pre-exponential factor A in the Arrhenius equation.

k = 0.1 s⁻¹T = 40 °CEa = 75 kJ/molR = 8.314 J/(mol·K)
A = s⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 100 L/minCA0​ = 0.5 mol/LCA​ = ?V = 100 L, k = 0.4 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.4 min⁻¹) runs in a 100 L plug-flow reactor (PFR). The feed enters at 100 L/min with CA0 = 0.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 100 LQ = 100 L/mink = 0.4 min⁻¹CA0 = 0.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
Q = 20 L/minX = ?V = 150 L

A first-order liquid-phase reaction (k = 0.05 min⁻¹) runs in a 150 L plug-flow reactor (PFR) fed at 20 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 150 LQ = 20 L/mink = 0.05 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT130 °C15 °C75 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 130 °C on the outside of the tubes. Cooling water (1 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 15 to 75 °C. The overall heat transfer coefficient is 2000 W/(m²·K). Find the heat transfer area A needed.

Ts = 130 °Cṁ = 1 kg/scp = 4.18 kJ/(kg·K)Tc: 15 → 75 °CU = 2000 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT130 °C50 °C?10 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.2 kg/s, cp = 2.5 kJ/(kg·K)) flows in the inner tube and cools from 130 to 50 °C. Water (1 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 10 °C. The inner tube has a diameter of 25 mm, and U = 500 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.2 kg/scp,h = 2.5 kJ/(kg·K)Th: 130 → 50 °Cṁc = 1 kg/sTc,in = 10 °CD = 25 mmU = 500 W/(m²·K)
L = m
19.Heat conductionMedium
Brick, k = 0.72250 mmMineral wool, k = 0.0450 mm15 °C-8 °CTi​ = ?Q̇

A wall is made of 250 mm of brick and 50 mm of mineral wool, with an area of 15 m². The outer faces are at 15 °C and -8 °C. Find the temperature Ti at the interface between the two layers.

L1 = 250 mm, k1 = 0.72 W/(m·K)L2 = 50 mm, k2 = 0.04 W/(m·K)A = 15 m²T1 = 15 °CT3 = -8 °C
Ti = °C
20.Heat conductionHard
Glass, k = 0.96150 mmExpanded polystyrene, k = 0.03525 mmroom 20 °Coutside -7 °CTs​ = ?Q̇

A wall of 150 mm glass and 25 mm expanded polystyrene separates a room at 20 °C from outside air at -7 °C. The convection coefficients are 6 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 = 150 mm, k1 = 0.96 W/(m·K)L2 = 25 mm, k2 = 0.035 W/(m·K)A = 8 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 20 °CTout = -7 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.4 m/sD = 50 mmL = 800 mf = 0.018

Water (ρ = 1000 kg/m³) flows at 1.4 m/s through a horizontal pipe, 800 m long, with an inside diameter of 50 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 1.4 m/sL = 800 mD = 50 mmf = 0.018ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2Δz = ?L = 300 m, D = 200 mm, f = 0.022× bend (K = 0.3)

Two open reservoirs are joined by a pipe 300 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.02. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 2) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². What difference in water level Δz between the reservoirs gives a flow rate of 60 L/s?

Q = 60 L/sL = 300 mD = 200 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 40 L/sH = 16 m

A pump with an efficiency of 78% delivers 40 L/s of water (ρ = 1000 kg/m³) against a head of 16 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 40 L/sH = 16 mη = 78%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 120 L/sΔz = 6 mL = 400 m, D = 250 mm, f = 0.02, ΣK = 3

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 6 m higher. The pipe is 400 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 = 3 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 120 L/sΔz = 6 mL = 400 mD = 250 mmf = 0.02ΣK = 3
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
NaOH: ṁ1x1 + ṁ2x2 = (ṁ1 + ṁ2)x3

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 450·(40 − 35)/(35 − 10) = 90 kg/h

Answer

ṁ2 = 90 kg/h
2.Mass balance

Answer: W = 2240 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 = 3200·18/60 = 960 kg/h

Total balance

W = F − P = 3200 − 960 = 2240 kg/h

Answer

W = 2240 kg/h
3.Energy balance

Answer: tout = 37.61 °C

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

Heat released by the hot stream

Q = 1.5·2.1·(140 − 110) = 94.5 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 94.5/(1·4.18) = 37.61 °C

Answer

tout = 37.61 °C
4.Energy balance

Answer: ṁc = 0.7234 kg/s

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

Heat released

Qh = 1·2.1·(120 − 80) = 84 kW

Heat that reaches the water

Qc = (1 − 0.1)·84 = 75.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 75.6/(4.18·25) = 0.7234 kg/s

Answer

ṁc = 0.7234 kg/s
5.Ideal gas law

Answer: P = 7128 kPa

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

Moles

n = m/M = 340/28.01 = 12.14 mol
T = 80 + 273.15 = 353.1 K

Pressure

P = nRT/V = 12.14·8.314·353.1/0.005 = 7128 kPa

Answer

P = 7128 kPa
6.Ideal gas law

Answer: V2 = 1.277 L

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

Absolute temperatures

T1 = 298.1 K, T2 = 333.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(400/700)·(333.1/298.1) = 1.277 L

Answer

V2 = 1.277 L
7.Stoichiometry

Answer: m = 11.19 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(Fe2O3) = 16/159.69 = 0.1002 mol
n(CO) = 48/28.01 = 1.714 mol

Limiting reactant

0.1002/1 = 0.1002, 1.714/3 = 0.5712 → Fe2O3

Mass of product

n(Fe) = 0.1002·2 = 0.2004 mol
m = 0.2004·55.85 = 11.19 g

Answer

m = 11.19 g
8.Stoichiometry

Answer: Y = 55.01 %

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(Mg) = 10/24.31 = 0.4114 mol
m = 0.4114·2/2·40.3 = 16.58 g

Percent yield

Y = 9.12/16.58·100 = 55.01%

Answer

Y = 55.01%
9.Chemical equilibrium

Answer: [HI] = 0.6288 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

54 = (2x)²/(0.4 − x)²

Take the square root

7.348 = 2x/(0.4 − x) → x = 0.4·7.348/(2 + 7.348) = 0.3144 mol/L

Equilibrium concentration

[HI] = 2x = 0.6288 mol/L

Answer

[HI] = 0.6288 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.5628 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

0.1 = x²/(0.8 − x) → x² + 0.1·x − 0.08 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.08))/2 = 0.2372 mol/L

Equilibrium concentration

[PCl₅] = 0.8 − 0.2372 = 0.5628 mol/L

Answer

[PCl5] = 0.5628 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 21.16 °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

250·0.449·(90 − Tf) = 300·4.18·(Tf − 15)

Solve for the final temperature

Tf = (112.3·90 + 1254·15)/(112.3 + 1254) = 21.16 °C

Answer

Tf = 21.16 °C
12.Calorimetry & enthalpy

Answer: q = 1238 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° = [8·(−393.5) + 10·(−285.8)] − [2·(−125.6) + 13·0] = −5755 kJ

Heat for the given mass

n = 25/58.12 = 0.4301 mol
q = n·|ΔH°/2| = 0.4301·2877 = 1238 kJ

Answer

q = 1238 kJ
13.Reaction kinetics

Answer: t½ = 250 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/(0.02·0.2) = 250 min

Answer

t½ = 250 min

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

14.Reaction kinetics

Answer: A = 3.241 × 10¹¹ s⁻¹

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

Absolute temperature

T = 40 + 273.15 = 313.1 K

Solve Arrhenius for A

Ea/(RT) = 75000/(8.314·313.1) = 28.81
A = k·e28.81 = 0.1·3.241 × 10¹² = 3.241 × 10¹¹ s⁻¹

Answer

A = 3.241 × 10¹¹ s⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.3352 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 = 100/100 = 1 min

Outlet concentration

CA = 0.5·e−0.4·1 = 0.3352 mol/L

Answer

CA = 0.3352 mol/L

Conversion: X = 32.97%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 31.27 %

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 = 150/20 = 7.5 min, kτ = 0.05·7.5 = 0.375

Conversion

X = 1 − e−kτ = 1 − e−0.375 = 31.27%

Answer

X = 31.27%
17.Heat exchangers (LMTD)

Answer: A = 1.542 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 = 1·4.18·(75 − 15) = 250.8 kW

End temperature differences

ΔT₁ = 130 − 15 = 115 K
ΔT₂ = 130 − 75 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (115 − 55)/ln(115/55) = 81.35 K

Area

A = Q̇/(U·ΔTlm) = 250800/(2000·81.35) = 1.542 m²

Answer

A = 1.542 m²
18.Heat exchangers (LMTD)

Answer: L = 14.69 m

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 = 0.2·2.5·(130 − 50) = 40 kW
Tc,out = 10 + 40/(1·4.18) = 19.57 °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 = 130 − 19.57 = 110.4 K
ΔT₂ = Th,out − Tc,in = 50 − 10 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (110.4 − 40)/ln(110.4/40) = 69.36 K

Area and length

A = 40000/(500·69.36) = 1.153 m²
L = A/(πD) = 1.153/(π·0.025) = 14.69 m

Answer

L = 14.69 m
19.Heat conduction

Answer: Ti = 10 °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) = (250/1000)/(0.72·15) = 0.02315 K/W
R2 = L2/(k2A) = (50/1000)/(0.04·15) = 0.08333 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 23/0.1065 = 216 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 15 − 216·0.02315 = 10 °C

Answer

Ti = 10 °C
20.Heat conduction

Answer: Ts = 15.86 °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/(6·8) = 0.02083 K/W
R1 = L1/(k1A) = (150/1000)/(0.96·8) = 0.01953 K/W
R2 = L2/(k2A) = (25/1000)/(0.035·8) = 0.08929 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.1359 K/W

Heat loss

Q̇ = (20 − (-7))/0.1359 = 198.7 W
Ts = Troom − Q̇·Ri = 20 − 198.7·0.02083 = 15.86 °C

Answer

Ts = 15.86 °C
21.Pipe friction & head loss

Answer: Δp = 282.2 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) = 0.018·(800/0.05)·1.4²/(2·9.81) = 28.77 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 = 1000·9.81·28.77 = 282240 Pa = 282.2 kPa

Answer

Δp = 282.2 kPa
22.Pipe friction & head loss

Answer: Δz = 6.34 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 = 0.06/0.03142 = 1.91 m/s
V²/(2g) = 0.1859 m

Loss coefficients

f·L/D = 0.02·300/0.2 = 30
ΣK = 0.5 + 2·0.3 + 2 + 1.0 = 4.1

Total head loss

hf = 30·0.1859 = 5.577 m
hm = 4.1·0.1859 = 0.7622 m
Δz = hf + hm = 6.34 m

Answer

Δz = 6.34 m
23.Pumps & pump power

Answer: Pshaft = 8.049 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 = 1000·9.81·0.04·16 = 6.278 kW

Shaft power

Pshaft = Ph/η = 6.278/0.78 = 8.049 kW

Answer

Pshaft = 8.049 kW
24.Pumps & pump power

Answer: H = 16.66 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) = (32 + 3)·0.3046 = 10.66 m

Pump head

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

H = Δz + hL = 6 + 10.66 = 16.66 m

Answer

H = 16.66 m

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