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 1800 kg/h · 5% sugarStream 2ṁ₂ = ? · 40% sugarProduct15% sugar

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

ṁ1 = 800 kg/hx1 = 5 %x2 = 40 %x3 = 15 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4700 kg/h · 19% NaOHProduct PP = ? · 35%Vapour W (pure water)0% NaOH

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

F = 4700 kg/hxF = 19 %xP = 35 %
P = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 120 °C80 °Cwater · 10 °Ct = ? °C

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

ṁh = 2 kg/scp,h = 2.1 kJ/(kg·K)Th: 120 → 80 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 130 °C60 °Cwater · 10 °C45 °C · ṁ = ?5% lost

Hot glycol mix heats water in an exchanger that loses 5% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 0.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 60 °Ct: 10 → 45 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
500 g of CO₂V = 50 LT = 100 °CP = ?

A tank of 50 L contains 500 g of CO₂ at 100 °C. Treat it as an ideal gas and find the pressure P.

m = 500 gM = 44.01 g/molV = 50 LT = 100 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
CO₂, M = 44.01 g/molP = 350 kPaT = 120 °Cρ = ?

Find the density ρ of CO₂ at 350 kPa and 120 °C, treating it as an ideal gas.

M = 44.01 g/molP = 350 kPaT = 120 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

30 g of CH4 and 8 g of O2 react according to CH4 + 2O2 → CO2 + 2H2O. What mass m of H2O can form?

M(CH4) = 16.04M(O2) = 32M(H2O) = 18.02 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 8.69 g of C2H5OH is collected. Find the percent yield Y.

M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 8.69 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 = 25. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.2 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 = 0.2 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.2 mol/LKc = 0.2
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 250 gT = 130 °Cc = 0.388 J/(g·°C)Waterm = 200 gT = 22 °Cc = 4.18 J/(g·°C)

A 250 g block of zinc (c = 0.388 J/(g·°C)) at 130 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 22 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.388 J/(g·°C)Tmetal = 130 °Cmwater = 200 gTwater = 22 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC2​H5​OH + 3O₂reactants2CO₂ + 3H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C2H5OH + 3O₂ → 2CO₂ + 3H₂O(l).

ΔH°f(C2H5OH) = −277.7 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)X (%)t = ?90%

A zero-order reaction has k = 0.04 mol/(L·min) and starts at 0.8 mol/L. How long does it take to reach 90% conversion? Find t.

k = 0.04 mol/(L·min)CA0 = 0.8 mol/LX = 90 %
t = min
14.Reaction kineticsHard
Tk35 °C0.00545 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 35 °C and an activation energy of 75 kJ/mol. Find the rate constant k2 at 45 °C.

k1 = 0.005 min⁻¹T1 = 35 °CT2 = 45 °CEa = 75 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 L/minX = 75%V = ?, k = 0.1 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.1 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 80 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 75% conversion of A.

Q = 80 L/mink = 0.1 min⁻¹X = 75%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 800 LQ = 40 L/minX = ?

A first-order liquid-phase reaction (k = 0.08 min⁻¹) runs in an 800 L CSTR fed at 40 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 800 LQ = 40 L/mink = 0.08 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT115 °C60 °C20 °C35 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 340 kW. The hot fluid cools from 115 to 60 °C and the cold fluid heats from 20 to 35 °C. The overall heat transfer coefficient is 200 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 340 kWU = 200 W/(m²·K)Th: 115 → 60 °CTc: 20 → 35 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT100 °C65 °C87.78 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.3 kJ/(kg·K)) cools from 100 to 65 °C in a counter-flow exchanger. It heats 0.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 1000 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.3 kJ/(kg·K)Th: 100 → 65 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 1000 W/(m²·K)
A = m²
19.Heat conductionMedium
Gypsum board, k = 0.1750 mmGlass, k = 0.9625 mm18 °C-4 °CTi​ = ?Q̇

A wall is made of 50 mm of gypsum board and 25 mm of glass, with an area of 20 m². The outer faces are at 18 °C and -4 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 25 mm, k2 = 0.96 W/(m·K)A = 20 m²T1 = 18 °CT3 = -4 °C
Ti = °C
20.Heat conductionHard
Brick, k = 0.72250 mmConcrete, k = 1.425 mmroom 22 °Coutside -7 °CQ̇

A wall of 250 mm brick and 25 mm concrete separates a room at 22 °C from outside air at -7 °C. The convection coefficients are 7.7 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 10 m². Find the overall heat transfer coefficient U of the wall.

L1 = 250 mm, k1 = 0.72 W/(m·K)L2 = 25 mm, k2 = 1.4 W/(m·K)A = 10 m²hi = 7.7 W/(m²·K)ho = 25 W/(m²·K)Troom = 22 °CTout = -7 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 2.9 m/sD = 100 mmL = 300 mf = 0.015

Water (ρ = 1000 kg/m³) flows at 2.9 m/s through a horizontal pipe, 300 m long, with an inside diameter of 100 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2.9 m/sL = 300 mD = 100 mmf = 0.015ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2Δz = ?L = 150 m, D = 100 mm, f = 0.0152× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 100 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 = 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 15 L/s?

Q = 15 L/sL = 150 mD = 100 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 15 L/sH = 22 m

A pump delivers 15 L/s of water (ρ = 1000 kg/m³) against a head of 22 m. The pump efficiency is 60% and the electric motor driving it has an efficiency of 94%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 15 L/sH = 22 mηpump = 60%ηmotor = 94%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
350 kPa (gauge)PQ = 75 L/sΔz = 5 mL = 200 m, D = 250 mm, f = 0.025, ΣK = 8

A pump moves 75 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 5 m higher. The pipe is 200 m long with an inside diameter of 250 mm and a Darcy friction factor f = 0.025; the minor-loss coefficients add up to ΣK = 8 (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 350 kPa. Find the head H the pump must add.

Q = 75 L/sΔz = 5 mL = 200 mD = 250 mmf = 0.025ΣK = 8ptank = 350 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 320 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) = 800·(5 − 15)/(15 − 40) = 320 kg/h

Answer

ṁ2 = 320 kg/h
2.Mass balance

Answer: P = 2551 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 = 4700·19/35 = 2551 kg/h

Answer

P = 2551 kg/h
3.Energy balance

Answer: tout = 36.79 °C

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

Heat released by the hot stream

Q = 2·2.1·(120 − 80) = 168 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 168/(1.5·4.18) = 36.79 °C

Answer

tout = 36.79 °C
4.Energy balance

Answer: ṁc = 0.8182 kg/s

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

Heat released

Qh = 0.5·3.6·(130 − 60) = 126 kW

Heat that reaches the water

Qc = (1 − 0.05)·126 = 119.7 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 119.7/(4.18·35) = 0.8182 kg/s

Answer

ṁc = 0.8182 kg/s
5.Ideal gas law

Answer: P = 704.9 kPa

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

Moles

n = m/M = 500/44.01 = 11.36 mol
T = 100 + 273.15 = 373.1 K

Pressure

P = nRT/V = 11.36·8.314·373.1/0.05 = 704.9 kPa

Answer

P = 704.9 kPa
6.Ideal gas law

Answer: ρ = 4.712 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 120 + 273.15 = 393.1 K

Density

ρ = 350·44.01/(8.314·393.1) = 4.712 kg/m³

Answer

ρ = 4.712 kg/m³
7.Stoichiometry

Answer: m = 4.505 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(CH4) = 30/16.04 = 1.87 mol
n(O2) = 8/32 = 0.25 mol

Limiting reactant

1.87/1 = 1.87, 0.25/2 = 0.125 → O2

Mass of product

n(H2O) = 0.125·2 = 0.25 mol
m = 0.25·18.02 = 4.505 g

Answer

m = 4.505 g
8.Stoichiometry

Answer: Y = 84.96 %

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 = 8.69/10.23·100 = 84.96%

Answer

Y = 84.96%
9.Chemical equilibrium

Answer: [H2] = 0.05714 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/(0.2 − x)²

Take the square root

5 = 2x/(0.2 − x) → x = 0.2·5/(2 + 5) = 0.1429 mol/L

Equilibrium concentration

[H₂] = 0.2 − x = 0.05714 mol/L

Answer

[H2] = 0.05714 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.1236 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

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

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.04))/2 = 0.1236 mol/L

Equilibrium concentration

[Cl₂] = x = 0.1236 mol/L

Answer

[Cl2] = 0.1236 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 33.23 °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

250·0.388·(130 − Tf) = 200·4.18·(Tf − 22)

Solve for the final temperature

Tf = (97·130 + 836·22)/(97 + 836) = 33.23 °C

Answer

Tf = 33.23 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −1367 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° = [2·(−393.5) + 3·(−285.8)] − [1·(−277.7) + 3·0] = −1367 kJ

Answer

ΔH° = −1367 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 18 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).

Amount converted

CA0·X = 0.8·0.9 = 0.72 mol/L

Time

t = CA0·X/k = 0.72/0.04 = 18 min

Answer

t = 18 min
14.Reaction kinetics

Answer: k2 = 0.01255 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 = 308.1 K, T2 = 318.1 K

Arrhenius ratio

ln(k2/k1) = −(75000/8.314)·(1/318.1 − 1/308.1) = 0.9201
k2 = 0.005·e0.9201 = 0.01255 min⁻¹

Answer

k2 = 0.01255 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 1109 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 − 0.75))/0.1 = 1.386/0.1 = 13.86 min

Volume

V = Q·τ = 80·13.86 = 1109 L

Answer

V = 1109 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 61.54 %

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 = 800/40 = 20 min, kτ = 0.08·20 = 1.6

Conversion

X = kτ/(1 + kτ) = 1.6/(1 + 1.6) = 61.54%

Answer

X = 61.54%
17.Heat exchangers (LMTD)

Answer: A = 32.42 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

In parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 115 − 20 = 95 K
ΔT₂ = Th,out − Tc,out = 60 − 35 = 25 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (95 − 25)/ln(95/25) = 52.43 K

Area

A = Q̇/(U·ΔTlm) = 340000/(200·52.43) = 32.42 m²

Answer

A = 32.42 m²
18.Heat exchangers (LMTD)

Answer: A = 5.577 m²

LMTD method: the temperature difference between the streams changes along the exchanger, so the rate equation uses its logarithmic mean: Q̇ = U·A·ΔTlm, with ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂), where ΔT₁ and ΔT₂ are the differences at the two ends. Counter-flow gives a larger ΔTlm than parallel flow for the same inlet and outlet temperatures.

Heat duty and water outlet temperature

Q̇ = ṁhcp,h(Th,in − Th,out) = 1.5·2.3·35 = 120.7 kW
Tc,out = 30 + 120.7/(0.5·4.18) = 87.78 °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 = 100 − 87.78 = 12.22 K
ΔT₂ = Th,out − Tc,in = 65 − 30 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (12.22 − 35)/ln(12.22/35) = 21.65 K

Area

A = Q̇/(U·ΔTlm) = 120750/(1000·21.65) = 5.577 m²

Answer

A = 5.577 m²
19.Heat conduction

Answer: Ti = −2.211 °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)/(0.17·20) = 0.01471 K/W
R2 = L2/(k2A) = (25/1000)/(0.96·20) = 0.001302 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 22/0.01601 = 1374 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 18 − 1374·0.01471 = −2.211 °C

Answer

Ti = −2.211 °C
20.Heat conduction

Answer: U = 1.869 W/(m²·K)

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/(7.7·10) = 0.01299 K/W
R1 = L1/(k1A) = (250/1000)/(0.72·10) = 0.03472 K/W
R2 = L2/(k2A) = (25/1000)/(1.4·10) = 0.001786 K/W
Ro = 1/(hoA) = 1/(25·10) = 0.004 K/W
ΣR = 0.05349 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(10·0.05349) = 1.869 W/(m²·K)

Answer

U = 1.869 W/(m²·K)
21.Pipe friction & head loss

Answer: Δp = 189.2 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) = 0.015·(300/0.1)·2.9²/(2·9.81) = 19.29 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 = 1000·9.81·19.29 = 189225 Pa = 189.2 kPa

Answer

Δp = 189.2 kPa
22.Pipe friction & head loss

Answer: Δz = 4.945 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 = 0.015/0.007854 = 1.91 m/s
V²/(2g) = 0.1859 m

Loss coefficients

f·L/D = 0.015·150/0.1 = 22.5
ΣK = 0.5 + 2·0.3 + 2 + 1.0 = 4.1

Total head loss

hf = 22.5·0.1859 = 4.183 m
hm = 4.1·0.1859 = 0.7622 m
Δz = hf + hm = 4.945 m

Answer

Δz = 4.945 m
23.Pumps & pump power

Answer: Pel = 5.74 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 = 1000·9.81·0.015·22 = 3.237 kW

Shaft power

Pshaft = 3.237/0.6 = 5.396 kW

Electrical power

Pel = 5.396/0.94 = 5.74 kW

Answer

Pel = 5.74 kW
24.Pumps & pump power

Answer: H = 44.01 m

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

Velocity

V = Q/A = 0.075/0.04909 = 1.528 m/s
V²/(2g) = 0.119 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (20 + 8)·0.119 = 3.332 m

Pressure head

p/(ρ·g) = 350000/(1000·9.81) = 35.68 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 5 + 35.68 + 3.332 = 44.01 m

Answer

H = 44.01 m

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