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 1600 kg/h · 30% saltStream 2ṁ₂ = ? · 20% saltProduct25% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 25% salt? Find ṁ2.

ṁ1 = 600 kg/hx1 = 30 %x2 = 20 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4900 kg/h · 12% NaOHProduct P60% NaOHVapour W (pure water)W = ? kg/h

An evaporator concentrates a NaOH solution by boiling off pure water. Find the water evaporated W in kg/h.

F = 4900 kg/hxF = 12 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 150 °C60 °Cwater · 10 °Ct = ? °C

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

ṁh = 1 kg/scp,h = 2.44 kJ/(kg·K)Th: 150 → 60 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 150 °C70 °Cwater · 30 °C55 °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 = 0.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 150 → 70 °Ct: 30 → 55 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
360 g of CO₂V = 30 LT = 35 °CP = ?

A tank of 30 L contains 360 g of CO₂ at 35 °C. Treat it as an ideal gas and find the pressure P.

m = 360 gM = 44.01 g/molV = 30 LT = 35 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of He goes from 400 kPa, 10 L, 20 °C to 500 kPa and 250 °C. Find the new volume V2.

P1 = 400 kPaV1 = 10 LT1 = 20 °CP2 = 500 kPaT2 = 250 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

4 g of Na and 32 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(N2​)n(N2​)n(NH3​)m(NH3​)÷ M(N2​)× 2/1× M(NH3​)

In the reaction N2 + 3H2 → 2NH3, 24 g of N2 reacts completely (the other reactants are in excess) and 20.42 g of NH3 is collected. Find the percent yield Y.

M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 20.42 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.250.250C−x−x+2xE0.25 − x0.25 − x2x

0.25 mol/L of H₂ and 0.25 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 50. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 50
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I1.500C−x+x+xE1.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 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 = 0.08
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 100 gT = 120 °Cc = 0.388 J/(g·°C)Waterm = 300 gT = 17 °Cc = 4.18 J/(g·°C)

A 100 g block of zinc (c = 0.388 J/(g·°C)) at 120 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 17 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.388 J/(g·°C)Tmetal = 120 °Cmwater = 300 gTwater = 17 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l).

ΔH°f(C6H12O6) = −1274 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)5 min0.5

In a first-order reaction the concentration of A falls from 1 mol/L to 0.5 mol/L in 5 min. Find the rate constant k.

CA0 = 1 mol/LCA = 0.5 mol/Lt = 5 min
k = min⁻¹
14.Reaction kineticsHard
Tk35 °C0.00565 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 35 °C and an activation energy of 100 kJ/mol. Find the rate constant k2 at 65 °C.

k1 = 0.005 min⁻¹T1 = 35 °CT2 = 65 °CEa = 100 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
QX = 60%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 60% conversion. How many times larger must a CSTR be than a PFR for the same feed rate, rate constant and conversion? Find the ratio VCSTR/VPFR.

X = 60%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
Q = 100 L/minX = ?V = 500 L

A first-order liquid-phase reaction (k = 0.3 min⁻¹) runs in a 500 L plug-flow reactor (PFR) fed at 100 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 500 LQ = 100 L/mink = 0.3 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT150 °C60 °C50 °C10 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 410 kW. The hot fluid cools from 150 to 60 °C and the cold fluid heats from 10 to 50 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 410 kWU = 800 W/(m²·K)Th: 150 → 60 °CTc: 10 → 50 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT80 °C50 °C33.92 °C10 °CΔT₁ΔT₂counter-flow

Hot oil (2 kg/s, cp = 2.5 kJ/(kg·K)) cools from 80 to 50 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 10 °C. With U = 500 W/(m²·K), find the heat transfer area A needed.

ṁh = 2 kg/scp,h = 2.5 kJ/(kg·K)Th: 80 → 50 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 10 °CU = 500 W/(m²·K)
A = m²
19.Heat conductionMedium
Concrete, k = 1.4100 mmMineral wool, k = 0.0450 mm25 °C-13 °CQ̇ = ?

A wall is made of 100 mm of concrete and 50 mm of mineral wool, with an area of 8 m². The outer faces are at 25 °C and -13 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 1.4 W/(m·K)L2 = 50 mm, k2 = 0.04 W/(m·K)A = 8 m²T1 = 25 °CT3 = -13 °C
Q̇ = W
20.Heat conductionHard
Gypsum board, k = 0.17250 mmConcrete, k = 1.475 mmroom 21 °Coutside 1 °CQ̇

A wall of 250 mm gypsum board and 75 mm concrete separates a room at 21 °C from outside air at 1 °C. The convection coefficients are 8 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 20 m². Find the overall heat transfer coefficient U of the wall.

L1 = 250 mm, k1 = 0.17 W/(m·K)L2 = 75 mm, k2 = 1.4 W/(m·K)A = 20 m²hi = 8 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = 1 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 2.2 m/sD = 150 mmL = 800 mf = 0.018

Water flows at a mean velocity of 2.2 m/s through a pipe 800 m long with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the friction head loss hf.

V = 2.2 m/sL = 800 mD = 150 mmf = 0.018g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5Δz = ?L = 150 m, D = 200 mm, f = 0.0184× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.018. The minor losses are a square-edged entrance (K = 0.5), 4 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. What difference in water level Δz between the reservoirs gives a flow rate of 75 L/s?

Q = 75 L/sL = 150 mD = 200 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 5Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 30 L/sH = 54 m

In a test, a pump delivers 30 L/s of water (ρ = 1000 kg/m³) against a head of 54 m while its shaft takes 19.9 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 30 L/sH = 54 mPshaft = 19.9 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 12 mL = 100 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 12 m higher. The pipe is 100 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. Find the head H the pump must add.

Q = 75 L/sΔz = 12 mL = 100 mD = 250 mmf = 0.025ΣK = 8
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 600 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) = 600·(30 − 25)/(25 − 20) = 600 kg/h

Answer

ṁ2 = 600 kg/h
2.Mass balance

Answer: W = 3920 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 = 4900·12/60 = 980 kg/h

Total balance

W = F − P = 4900 − 980 = 3920 kg/h

Answer

W = 3920 kg/h
3.Energy balance

Answer: tout = 36.27 °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·(150 − 60) = 219.6 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 219.6/(2·4.18) = 36.27 °C

Answer

tout = 36.27 °C
4.Energy balance

Answer: ṁc = 1.171 kg/s

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

Heat released

Qh = 0.5·3.6·(150 − 70) = 144 kW

Heat that reaches the water

Qc = (1 − 0.15)·144 = 122.4 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 122.4/(4.18·25) = 1.171 kg/s

Answer

ṁc = 1.171 kg/s
5.Ideal gas law

Answer: P = 698.6 kPa

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

Moles

n = m/M = 360/44.01 = 8.18 mol
T = 35 + 273.15 = 308.1 K

Pressure

P = nRT/V = 8.18·8.314·308.1/0.03 = 698.6 kPa

Answer

P = 698.6 kPa
6.Ideal gas law

Answer: V2 = 14.28 L

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

Absolute temperatures

T1 = 293.1 K, T2 = 523.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(400/500)·(523.1/293.1) = 14.28 L

Answer

V2 = 14.28 L
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) = 32/70.9 = 0.4513 mol

Limiting reactant

0.174/2 = 0.08699, 0.4513/1 = 0.4513 → 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 = 70 %

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(N2) = 24/28.02 = 0.8565 mol
m = 0.8565·2/1·17.03 = 29.17 g

Percent yield

Y = 20.42/29.17·100 = 70%

Answer

Y = 70%
9.Chemical equilibrium

Answer: [H2] = 0.05512 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

50 = (2x)²/(0.25 − x)²

Take the square root

7.071 = 2x/(0.25 − x) → x = 0.25·7.071/(2 + 7.071) = 0.1949 mol/L

Equilibrium concentration

[H₂] = 0.25 − x = 0.05512 mol/L

Answer

[H2] = 0.05512 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.3087 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

0.08 = x²/(1.5 − x) → x² + 0.08·x − 0.12 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.12))/2 = 0.3087 mol/L

Equilibrium concentration

[Cl₂] = x = 0.3087 mol/L

Answer

[Cl2] = 0.3087 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 20.09 °C

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

Heat balance

100·0.388·(120 − Tf) = 300·4.18·(Tf − 17)

Solve for the final temperature

Tf = (38.8·120 + 1254·17)/(38.8 + 1254) = 20.09 °C

Answer

Tf = 20.09 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −2802 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° = [6·(−393.5) + 6·(−285.8)] − [1·(−1274) + 6·0] = −2802 kJ

Answer

ΔH° = −2802 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.1386 min⁻¹

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).

Integrated first-order law

k = ln(CA0/CA)/t = ln(1/0.5)/5 = 0.6931/5 = 0.1386 min⁻¹

Answer

k = 0.1386 min⁻¹
14.Reaction kinetics

Answer: k2 = 0.1595 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 = 338.1 K

Arrhenius ratio

ln(k2/k1) = −(100000/8.314)·(1/338.1 − 1/308.1) = 3.463
k2 = 0.005·e3.463 = 0.1595 min⁻¹

Answer

k2 = 0.1595 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 1.637

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.

k·τ for each reactor

CSTR: k·τ = X/(1 − X) = 0.6/0.4 = 1.5
PFR: k·τ = ln(1/(1 − X)) = ln(2.5) = 0.9163

Ratio of volumes

VCSTR/VPFR = 1.5/0.9163 = 1.637

Answer

VCSTR/VPFR = 1.637

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 77.69 %

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 = 500/100 = 5 min, kτ = 0.3·5 = 1.5

Conversion

X = 1 − e−kτ = 1 − e−1.5 = 77.69%

Answer

X = 77.69%
17.Heat exchangers (LMTD)

Answer: A = 7.105 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 counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 150 − 50 = 100 K
ΔT₂ = Th,out − Tc,in = 60 − 10 = 50 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (100 − 50)/ln(100/50) = 72.13 K

Area

A = Q̇/(U·ΔTlm) = 410000/(800·72.13) = 7.105 m²

Answer

A = 7.105 m²
18.Heat exchangers (LMTD)

Answer: A = 6.982 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) = 2·2.5·30 = 150 kW
Tc,out = 10 + 150/(1.5·4.18) = 33.92 °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 − 33.92 = 46.08 K
ΔT₂ = Th,out − Tc,in = 50 − 10 = 40 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (46.08 − 40)/ln(46.08/40) = 42.97 K

Area

A = Q̇/(U·ΔTlm) = 150000/(500·42.97) = 6.982 m²

Answer

A = 6.982 m²
19.Heat conduction

Answer: Q̇ = 230.1 W

Thermal resistance: steady heat flow through layers in series behaves like current through resistors in series: Q̇ = ΔT/ΣR, with R = L/(kA) for a conducting layer and R = 1/(hA) for a convecting surface. The temperature drop across each layer is proportional to its resistance.

Layer resistances

R1 = L1/(k1A) = (100/1000)/(1.4·8) = 0.008929 K/W
R2 = L2/(k2A) = (50/1000)/(0.04·8) = 0.1563 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 38/0.1652 = 230.1 W

Answer

Q̇ = 230.1 W
20.Heat conduction

Answer: U = 0.5885 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/(8·20) = 0.00625 K/W
R1 = L1/(k1A) = (250/1000)/(0.17·20) = 0.07353 K/W
R2 = L2/(k2A) = (75/1000)/(1.4·20) = 0.002679 K/W
Ro = 1/(hoA) = 1/(20·20) = 0.0025 K/W
ΣR = 0.08496 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(20·0.08496) = 0.5885 W/(m²·K)

Answer

U = 0.5885 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 23.68 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 head

V²/(2g) = 2.2²/(2·9.81) = 0.2467 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.018·(800/0.15)·2.2²/(2·9.81) = 23.68 m

Answer

hf = 23.68 m
22.Pipe friction & head loss

Answer: Δz = 6.158 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 = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Loss coefficients

f·L/D = 0.018·150/0.2 = 13.5
ΣK = 0.5 + 4·0.3 + 5 + 1.0 = 7.7

Total head loss

hf = 13.5·0.2905 = 3.922 m
hm = 7.7·0.2905 = 2.237 m
Δz = hf + hm = 6.158 m

Answer

Δz = 6.158 m
23.Pumps & pump power

Answer: η = 79.86 %

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 = 1000·9.81·0.03·54 = 15.89 kW

Efficiency

η = Ph/Pshaft = 15.89/19.9 = 79.86%

Answer

η = 79.86%
24.Pumps & pump power

Answer: H = 14.14 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) = (10 + 8)·0.119 = 2.142 m

Pump head

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

H = Δz + hL = 12 + 2.142 = 14.14 m

Answer

H = 14.14 m

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