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 11000 kg/h · 35% sugarStream 2ṁ₂ = ? · 10% 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 = 1000 kg/hx1 = 35 %x2 = 10 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1400 kg/h · 9% sugarProduct PP = ? · 30%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 = 1400 kg/hxF = 9 %xP = 30 %
P = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 150 °C90 °Cwater · 20 °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: 150 → 90 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 180 °C100 °Cwater · 15 °C85 °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: 180 → 100 °Ct: 15 → 85 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
260 g of O₂P = 300 kPaT = 60 °CV = ?

What volume V does 260 g of O₂ occupy at 300 kPa and 60 °C? Treat it as an ideal gas.

m = 260 gM = 32 g/molP = 300 kPaT = 60 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
N₂, M = 28.01 g/molP = 200 kPaT = 30 °Cρ = ?

Find the density ρ of N₂ at 200 kPa and 30 °C, treating it as an ideal gas.

M = 28.01 g/molP = 200 kPaT = 30 °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)

10 g of H2 and 32 g of O2 react according to 2H2 + O2 → 2H2O. What mass m of H2O can form?

M(H2) = 2.016M(O2) = 32M(H2O) = 18.02 g/mol
m = g
8.StoichiometryHard
m(Na)n(Na)n(NaCl)m(NaCl)÷ M(Na)× 2/2× M(NaCl)

In the reaction 2Na + Cl2 → 2NaCl, 16 g of Na reacts completely (the other reactants are in excess) and 30.5 g of NaCl is collected. Find the percent yield Y.

M(Na) = 22.99 g/molM(NaCl) = 58.44 g/molactual: 30.5 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.80.80C−x−x+2xE0.8 − x0.8 − x2x

0.8 mol/L of H₂ and 0.8 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 9. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I1.500C−x+x+xE1.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 1.5 mol/LKc = 0.2
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 250 gT = 170 °Cc = 0.388 J/(g·°C)Waterm = 300 gT = 20 °Cc = 4.18 J/(g·°C)

A 250 g block of zinc (c = 0.388 J/(g·°C)) at 170 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 20 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.388 J/(g·°C)Tmetal = 170 °Cmwater = 300 gTwater = 20 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H25 g CH4​CH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 25 g of CH4 (M = 16.04 g/mol) burns completely: CH4 + 2O₂ → CO₂ + 2H₂O(l). Give q as a positive number.

ΔH°f(CH4) = −74.8 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = kJ
13.Reaction kineticsMedium
t (min)C (mol/L)20 minC = ?

A reaction with rate law −rA = k·CA² has k = 0.5 L/(mol·min) and starts at 1 mol/L. Find the concentration CA after 20 min.

k = 0.5 L/(mol·min)CA0 = 1 mol/Lt = 20 min
CA = mol/L
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.40.002run 21.20.054n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.4 mol/L the rate is 0.002 mol/(L·s); with CA0 = 1.2 mol/L it is 0.054 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.4 mol/Lr1 = 0.002 mol/(L·s)CA0,2 = 1.2 mol/Lr2 = 0.054 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 25 L/minX = 90%V = ?, k = 0.2 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.2 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 25 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 90% conversion of A.

Q = 25 L/mink = 0.2 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 150 LV = 150 LQ = 10 L/minX = ?

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in two equal CSTRs in series, each of 150 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 = 150 L (×2)Q = 10 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT135 °C70 °C30 °C40 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 280 kW. The hot fluid cools from 135 to 70 °C and the cold fluid heats from 30 to 40 °C. The overall heat transfer coefficient is 300 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 280 kWU = 300 W/(m²·K)Th: 135 → 70 °CTc: 30 → 40 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT90 °C50 °C15 °C?ΔT₁ΔT₂parallel flow

In a parallel-flow double-pipe heat exchanger, hot oil (0.5 kg/s, cp = 2.3 kJ/(kg·K)) flows in the inner tube and cools from 90 to 50 °C. Water (1.5 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 15 °C. The inner tube has a diameter of 32 mm, and U = 300 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.5 kg/scp,h = 2.3 kJ/(kg·K)Th: 90 → 50 °Cṁc = 1.5 kg/sTc,in = 15 °CD = 32 mmU = 300 W/(m²·K)
L = m
19.Heat conductionMedium
Expanded polystyrene, k = 0.03550 mmGypsum board, k = 0.1775 mm25 °C-3 °CQ̇ = ?

A wall is made of 50 mm of expanded polystyrene and 75 mm of gypsum board, with an area of 8 m². The outer faces are at 25 °C and -3 °C. Find the heat flow Q̇ through the wall.

L1 = 50 mm, k1 = 0.035 W/(m·K)L2 = 75 mm, k2 = 0.17 W/(m·K)A = 8 m²T1 = 25 °CT3 = -3 °C
Q̇ = W
20.Heat conductionHard
Mineral wool, k = 0.0450 mmBrick, k = 0.7275 mmroom 20 °Coutside -2 °CTs​ = ?Q̇

A wall of 50 mm mineral wool and 75 mm brick separates a room at 20 °C from outside air at -2 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 8 m². Find the temperature Ts of the inside surface of the wall.

L1 = 50 mm, k1 = 0.04 W/(m·K)L2 = 75 mm, k2 = 0.72 W/(m·K)A = 8 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = -2 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.3 m/sD = 250 mmL = 800 mf = 0.015

Water (ρ = 1000 kg/m³) flows at 1.3 m/s through a horizontal pipe, 800 m long, with an inside diameter of 250 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 = 1.3 m/sL = 800 mD = 250 mmf = 0.015ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2Δz = 14 mL = 200 m, D = 150 mm, f = 0.024× bend (K = 0.3)

Two open reservoirs are joined by a pipe 200 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.02. The water surface of the upper reservoir is 14 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 4 bends (K = 0.3 each), a valve (K = 2) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². Find the flow rate Q in L/s.

Δz = 14 mL = 200 mD = 150 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 50 L/sH = 32 m

A pump with an efficiency of 80% delivers 50 L/s of water (ρ = 1000 kg/m³) against a head of 32 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 50 L/sH = 32 mη = 80%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
250 kPa (gauge)PQ = 30 L/sΔz = 17 mL = 150 m, D = 150 mm, f = 0.018, ΣK = 8

A pump moves 30 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 17 m higher. The pipe is 150 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.018; 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 250 kPa. Find the head H the pump must add.

Q = 30 L/sΔz = 17 mL = 150 mD = 150 mmf = 0.018ΣK = 8ptank = 250 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 666.7 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) = 1000·(35 − 25)/(25 − 10) = 666.7 kg/h

Answer

ṁ2 = 666.7 kg/h
2.Mass balance

Answer: P = 420 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 = 1400·9/30 = 420 kg/h

Answer

P = 420 kg/h
3.Energy balance

Answer: tout = 42.61 °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·(150 − 90) = 189 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 189/(2·4.18) = 42.61 °C

Answer

tout = 42.61 °C
4.Energy balance

Answer: ṁc = 0.5167 kg/s

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

Heat released

Qh = 1·2.1·(180 − 100) = 168 kW

Heat that reaches the water

Qc = (1 − 0.1)·168 = 151.2 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 151.2/(4.18·70) = 0.5167 kg/s

Answer

ṁc = 0.5167 kg/s
5.Ideal gas law

Answer: V = 75.02 L

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

Moles

n = 260/32 = 8.125 mol
T = 60 + 273.15 = 333.1 K

Volume

V = nRT/P = 8.125·8.314·333.1/300 = 75.02 L

Answer

V = 75.02 L
6.Ideal gas law

Answer: ρ = 2.223 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 30 + 273.15 = 303.1 K

Density

ρ = 200·28.01/(8.314·303.1) = 2.223 kg/m³

Answer

ρ = 2.223 kg/m³
7.Stoichiometry

Answer: m = 36.04 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(H2) = 10/2.016 = 4.96 mol
n(O2) = 32/32 = 1 mol

Limiting reactant

4.96/2 = 2.48, 1/1 = 1 → O2

Mass of product

n(H2O) = 1·2 = 2 mol
m = 2·18.02 = 36.04 g

Answer

m = 36.04 g
8.Stoichiometry

Answer: Y = 74.99 %

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(Na) = 16/22.99 = 0.696 mol
m = 0.696·2/2·58.44 = 40.67 g

Percent yield

Y = 30.5/40.67·100 = 74.99%

Answer

Y = 74.99%
9.Chemical equilibrium

Answer: [H2] = 0.32 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

9 = (2x)²/(0.8 − x)²

Take the square root

3 = 2x/(0.8 − x) → x = 0.8·3/(2 + 3) = 0.48 mol/L

Equilibrium concentration

[H₂] = 0.8 − x = 0.32 mol/L

Answer

[H2] = 0.32 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.4568 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/(1.5 − x) → x² + 0.2·x − 0.3 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.3))/2 = 0.4568 mol/L

Equilibrium concentration

[Cl₂] = x = 0.4568 mol/L

Answer

[Cl2] = 0.4568 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 30.77 °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·(170 − Tf) = 300·4.18·(Tf − 20)

Solve for the final temperature

Tf = (97·170 + 1254·20)/(97 + 1254) = 30.77 °C

Answer

Tf = 30.77 °C
12.Calorimetry & enthalpy

Answer: q = 1388 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° = [1·(−393.5) + 2·(−285.8)] − [1·(−74.8) + 2·0] = −890.3 kJ

Heat for the given mass

n = 25/16.04 = 1.559 mol
q = n·|ΔH°/1| = 1.559·890.3 = 1388 kJ

Answer

q = 1388 kJ
13.Reaction kinetics

Answer: CA = 0.09091 mol/L

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).

Integrated second-order law

1/CA = 1/CA0 + kt = 1 + 0.5·20 = 11 L/mol
CA = 1/11 = 0.09091 mol/L

Answer

CA = 0.09091 mol/L
14.Reaction kinetics

Answer: n = 3

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 = 0.054/0.002 = 27
C2/C1 = 1.2/0.4 = 3

Order

n = ln(27)/ln(3) = 3

Answer

n = 3
15.Reactor sizing (CSTR & PFR)

Answer: V = 287.8 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 − 0.9))/0.2 = 2.303/0.2 = 11.51 min

Volume

V = Q·τ = 25·11.51 = 287.8 L

Answer

V = 287.8 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 87.24 %

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 = 150/10 = 15 min, kτ = 0.12·15 = 1.8

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 1.8) = 0.3571
C2/CA0 = 1/(1 + kτ)² = 0.1276
X = 1 − 0.1276 = 87.24%

Answer

X = 87.24%
17.Heat exchangers (LMTD)

Answer: A = 15.59 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 = 135 − 30 = 105 K
ΔT₂ = Th,out − Tc,out = 70 − 40 = 30 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (105 − 30)/ln(105/30) = 59.87 K

Area

A = Q̇/(U·ΔTlm) = 280000/(300·59.87) = 15.59 m²

Answer

A = 15.59 m²
18.Heat exchangers (LMTD)

Answer: L = 32.14 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 = 0.5·2.3·(90 − 50) = 46 kW
Tc,out = 15 + 46/(1.5·4.18) = 22.34 °C

End temperature differences

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

ΔT₁ = Th,in − Tc,in = 90 − 15 = 75 K
ΔT₂ = Th,out − Tc,out = 50 − 22.34 = 27.66 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (75 − 27.66)/ln(75/27.66) = 47.46 K

Area and length

A = 46000/(300·47.46) = 3.231 m²
L = A/(πD) = 3.231/(π·0.032) = 32.14 m

Answer

L = 32.14 m
19.Heat conduction

Answer: Q̇ = 119.8 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) = (50/1000)/(0.035·8) = 0.1786 K/W
R2 = L2/(k2A) = (75/1000)/(0.17·8) = 0.05515 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 28/0.2337 = 119.8 W

Answer

Q̇ = 119.8 W
20.Heat conduction

Answer: Ts = 18.12 °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/(7.7·8) = 0.01623 K/W
R1 = L1/(k1A) = (50/1000)/(0.04·8) = 0.1563 K/W
R2 = L2/(k2A) = (75/1000)/(0.72·8) = 0.01302 K/W
Ro = 1/(hoA) = 1/(30·8) = 0.004167 K/W
ΣR = 0.1897 K/W

Heat loss

Q̇ = (20 − (-2))/0.1897 = 116 W
Ts = Troom − Q̇·Ri = 20 − 116·0.01623 = 18.12 °C

Answer

Ts = 18.12 °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) = 0.015·(800/0.25)·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 = 52.29 L/s

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

Loss coefficients

f·L/D = 0.02·200/0.15 = 26.67
ΣK = 0.5 + 4·0.3 + 2 + 1.0 = 4.7

Energy equation

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

14 = (26.67 + 4.7)·V²/(2·9.81)
V = √(2·9.81·14/31.37) = 2.959 m/s

Flow rate

Q = V·π·D²/4 = 2.959·0.01767 = 0.05229 m³/s = 52.29 L/s

Answer

Q = 52.29 L/s
23.Pumps & pump power

Answer: Pshaft = 19.62 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 = 1000·9.81·0.05·32 = 15.7 kW

Shaft power

Pshaft = Ph/η = 15.7/0.8 = 19.62 kW

Answer

Pshaft = 19.62 kW
24.Pumps & pump power

Answer: H = 46.3 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 = 0.03/0.01767 = 1.698 m/s
V²/(2g) = 0.1469 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (18 + 8)·0.1469 = 3.819 m

Pressure head

p/(ρ·g) = 250000/(1000·9.81) = 25.48 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 17 + 25.48 + 3.819 = 46.3 m

Answer

H = 46.3 m

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