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 1850 kg/h · 20% saltStream 2ṁ₂ = ? · 50% saltProduct30% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 30% salt? Find ṁ2.

ṁ1 = 850 kg/hx1 = 20 %x2 = 50 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2100 kg/h · 11% saltProduct P35% 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 = 2100 kg/hxF = 11 %xP = 35 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 150 °C60 °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 = 0.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 150 → 60 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 180 °C120 °Cwater · 15 °C85 °C · ṁ = ?10% lost

Hot glycol mix 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 = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 180 → 120 °Ct: 15 → 85 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
90 g of O₂V = 10 LT = 20 °CP = ?

A tank of 10 L contains 90 g of O₂ at 20 °C. Treat it as an ideal gas and find the pressure P.

m = 90 gM = 32 g/molV = 10 LT = 20 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 250 kPa, 2 L, 15 °C to 650 kPa and 190 °C. Find the new volume V2.

P1 = 250 kPaV1 = 2 LT1 = 15 °CP2 = 650 kPaT2 = 190 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(MgO)m(MgO)÷ M(X)× 2/ν× M(MgO)

24 g of Mg and 80 g of O2 react according to 2Mg + O2 → 2MgO. What mass m of MgO can form?

M(Mg) = 24.31M(O2) = 32M(MgO) = 40.3 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 15.58 g of MgO is collected. Find the percent yield Y.

M(Mg) = 24.31 g/molM(MgO) = 40.3 g/molactual: 15.58 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 = 36. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 36
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.200C−x+x+xE0.2 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.01 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.2 mol/LKc = 0.01
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 200 gT = 120 °Cc = 0.449 J/(g·°C)Waterm = 150 gT = 22 °Cc = 4.18 J/(g·°C)

A 200 g block of iron (c = 0.449 J/(g·°C)) at 120 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 22 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.449 J/(g·°C)Tmetal = 120 °Cmwater = 150 gTwater = 22 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H50 g CH4​CH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 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)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 1 L/(mol·min) and an initial concentration of 0.5 mol/L. Find its first half-life t½.

k = 1 L/(mol·min)CA0 = 0.5 mol/L
t½ = min
14.Reaction kineticsHard
t (min)X (%)20 minX = ?

A first-order reaction has k = 0.01 min⁻¹ at 20 °C and an activation energy of 75 kJ/mol. The batch reactor is now run at 30 °C for 20 min. Find the conversion X reached.

k1 = 0.01 min⁻¹T1 = 20 °CEa = 75 kJ/molT2 = 30 °Ct = 20 minR = 8.314 J/(mol·K)
X = %
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 L/minX = 90%V = ?, k = 0.15 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.15 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 90% conversion of A.

Q = 80 L/mink = 0.15 min⁻¹X = 90%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 10 L/minX = ?V = 200 L

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in a 200 L plug-flow reactor (PFR) fed at 10 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 10 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT105 °C80 °C80 °C25 °CΔT₁ΔT₂counter-flow

A shell-and-tube heat exchanger (one shell pass, two tube passes) must transfer 720 kW. The hot fluid cools from 105 to 80 °C and the cold fluid heats from 25 to 80 °C. The LMTD correction factor for this arrangement is F = 0.9, and U = 1000 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 720 kWF = 0.9U = 1000 W/(m²·K)Th: 105 → 80 °CTc: 25 → 80 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT85 °C60 °C34.17 °C25 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.3 kJ/(kg·K)) cools from 85 to 60 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 25 °C. With U = 200 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.3 kJ/(kg·K)Th: 85 → 60 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 25 °CU = 200 W/(m²·K)
A = m²
19.Heat conductionMedium
Gypsum board, k = 0.1750 mmExpanded polystyrene, k = 0.03575 mm20 °C8 °CQ̇ = ?

A wall is made of 50 mm of gypsum board and 75 mm of expanded polystyrene, with an area of 12 m². The outer faces are at 20 °C and 8 °C. Find the heat flow Q̇ through the wall.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 75 mm, k2 = 0.035 W/(m·K)A = 12 m²T1 = 20 °CT3 = 8 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.96200 mmExpanded polystyrene, k = 0.03575 mmroom 20 °Coutside 4 °CTs​ = ?Q̇

A wall of 200 mm glass and 75 mm expanded polystyrene separates a room at 20 °C from outside air at 4 °C. The convection coefficients are 10 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 4 m². Find the temperature Ts of the inside surface of the wall.

L1 = 200 mm, k1 = 0.96 W/(m·K)L2 = 75 mm, k2 = 0.035 W/(m·K)A = 4 m²hi = 10 W/(m²·K)ho = 25 W/(m²·K)Troom = 20 °CTout = 4 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 4 L/sD = 100 mmL = 150 mf = 0.018

Water flows at 4 L/s through a pipe 150 m long with an inside diameter of 100 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the friction head loss hf.

Q = 4 L/sL = 150 mD = 100 mmf = 0.018g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5free outletH = ?L = 150 m, D = 200 mm, f = 0.0183× bend (K = 0.3)

A pipe 150 m long with an inside diameter of 200 mm (Darcy friction factor f = 0.018) runs from an open reservoir and discharges as a free jet into the air. The minor losses are a square-edged entrance (K = 0.5), 3 bends (K = 0.3 each) and a valve (K = 5). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 40 L/s?

Q = 40 L/sL = 150 mD = 200 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×3)Kvalve = 5
H = m
23.Pumps & pump powerMedium
PQ = 60 L/sH = 60 m

A pump with an efficiency of 70% delivers 60 L/s of water (ρ = 1000 kg/m³) against a head of 60 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 60 L/sH = 60 mη = 70%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 21 mL = 600 m, D = 200 mm, f = 0.02, 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 21 m higher. The pipe is 600 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.02; 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 = 21 mL = 600 mD = 200 mmf = 0.02ΣK = 8
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 425 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) = 850·(20 − 30)/(30 − 50) = 425 kg/h

Answer

ṁ2 = 425 kg/h
2.Mass balance

Answer: W = 1440 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 = 2100·11/35 = 660 kg/h

Total balance

W = F − P = 2100 − 660 = 1440 kg/h

Answer

W = 1440 kg/h
3.Energy balance

Answer: tout = 17.54 °C

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

Heat released by the hot stream

Q = 0.5·2.1·(150 − 60) = 94.5 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 94.5/(3·4.18) = 17.54 °C

Answer

tout = 17.54 °C
4.Energy balance

Answer: ṁc = 0.9966 kg/s

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

Heat released

Qh = 1.5·3.6·(180 − 120) = 324 kW

Heat that reaches the water

Qc = (1 − 0.1)·324 = 291.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 291.6/(4.18·70) = 0.9966 kg/s

Answer

ṁc = 0.9966 kg/s
5.Ideal gas law

Answer: P = 685.5 kPa

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

Moles

n = m/M = 90/32 = 2.813 mol
T = 20 + 273.15 = 293.1 K

Pressure

P = nRT/V = 2.813·8.314·293.1/0.01 = 685.5 kPa

Answer

P = 685.5 kPa
6.Ideal gas law

Answer: V2 = 1.236 L

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

Absolute temperatures

T1 = 288.1 K, T2 = 463.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(250/650)·(463.1/288.1) = 1.236 L

Answer

V2 = 1.236 L
7.Stoichiometry

Answer: m = 39.79 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(Mg) = 24/24.31 = 0.9872 mol
n(O2) = 80/32 = 2.5 mol

Limiting reactant

0.9872/2 = 0.4936, 2.5/1 = 2.5 → Mg

Mass of product

n(MgO) = 0.4936·2 = 0.9872 mol
m = 0.9872·40.3 = 39.79 g

Answer

m = 39.79 g
8.Stoichiometry

Answer: Y = 93.98 %

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 = 15.58/16.58·100 = 93.98%

Answer

Y = 93.98%
9.Chemical equilibrium

Answer: [HI] = 0.6 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

36 = (2x)²/(0.4 − x)²

Take the square root

6 = 2x/(0.4 − x) → x = 0.4·6/(2 + 6) = 0.3 mol/L

Equilibrium concentration

[HI] = 2x = 0.6 mol/L

Answer

[HI] = 0.6 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.16 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

0.01 = x²/(0.2 − x) → x² + 0.01·x − 0.002 = 0

Solve the quadratic

x = (−0.01 + √(0.01² + 4·0.002))/2 = 0.04 mol/L

Equilibrium concentration

[PCl₅] = 0.2 − 0.04 = 0.16 mol/L

Answer

[PCl5] = 0.16 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 34.28 °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

200·0.449·(120 − Tf) = 150·4.18·(Tf − 22)

Solve for the final temperature

Tf = (89.8·120 + 627·22)/(89.8 + 627) = 34.28 °C

Answer

Tf = 34.28 °C
12.Calorimetry & enthalpy

Answer: q = 2775 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 = 50/16.04 = 3.117 mol
q = n·|ΔH°/1| = 3.117·890.3 = 2775 kJ

Answer

q = 2775 kJ
13.Reaction kinetics

Answer: t½ = 2 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/(1·0.5) = 2 min

Answer

t½ = 2 min

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

14.Reaction kinetics

Answer: X = 42.42 %

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).

Rate constant at the new temperature

T1 = 293.1 K, T2 = 303.1 K
k2 = 0.01·e−(75000/8.314)·(1/303.1 − 1/293.1) = 0.0276 min⁻¹

Conversion

X = 1 − e−0.0276·20 = 1 − 0.5758 = 42.42 %

Answer

X = 42.42 %
15.Reactor sizing (CSTR & PFR)

Answer: V = 1228 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))/0.15 = 2.303/0.15 = 15.35 min

Volume

V = Q·τ = 80·15.35 = 1228 L

Answer

V = 1228 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 86.47 %

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 = 200/10 = 20 min, kτ = 0.1·20 = 2

Conversion

X = 1 − e−kτ = 1 − e−2 = 86.47%

Answer

X = 86.47%
17.Heat exchangers (LMTD)

Answer: A = 21.03 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 (counter-flow)

In counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 105 − 80 = 25 K
ΔT₂ = Th,out − Tc,in = 80 − 25 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (25 − 55)/ln(25/55) = 38.05 K

Area

A = Q̇/(U·F·ΔTlm,cf) = 720000/(1000·0.9·38.05) = 21.03 m²

Answer

A = 21.03 m²
18.Heat exchangers (LMTD)

Answer: A = 6.777 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) = 1·2.3·25 = 57.5 kW
Tc,out = 25 + 57.5/(1.5·4.18) = 34.17 °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 = 85 − 34.17 = 50.83 K
ΔT₂ = Th,out − Tc,in = 60 − 25 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (50.83 − 35)/ln(50.83/35) = 42.42 K

Area

A = Q̇/(U·ΔTlm) = 57500/(200·42.42) = 6.777 m²

Answer

A = 6.777 m²
19.Heat conduction

Answer: Q̇ = 59.09 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)/(0.17·12) = 0.02451 K/W
R2 = L2/(k2A) = (75/1000)/(0.035·12) = 0.1786 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 12/0.2031 = 59.09 W

Answer

Q̇ = 59.09 W
20.Heat conduction

Answer: Ts = 19.36 °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/(10·4) = 0.025 K/W
R1 = L1/(k1A) = (200/1000)/(0.96·4) = 0.05208 K/W
R2 = L2/(k2A) = (75/1000)/(0.035·4) = 0.5357 K/W
Ro = 1/(hoA) = 1/(25·4) = 0.01 K/W
ΣR = 0.6228 K/W

Heat loss

Q̇ = (20 − (4))/0.6228 = 25.69 W
Ts = Troom − Q̇·Ri = 20 − 25.69·0.025 = 19.36 °C

Answer

Ts = 19.36 °C
21.Pipe friction & head loss

Answer: hf = 0.3569 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.

Mean velocity

A = π·0.1²/4 = 0.007854 m²
V = Q/A = 0.004/0.007854 = 0.5093 m/s

Velocity head

V²/(2g) = 0.5093²/(2·9.81) = 0.01322 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.018·(150/0.1)·0.5093²/(2·9.81) = 0.3569 m

Answer

hf = 0.3569 m
22.Pipe friction & head loss

Answer: H = 1.727 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 = 0.04/0.03142 = 1.273 m/s
V²/(2g) = 0.08263 m

Loss coefficients

f·L/D = 0.018·150/0.2 = 13.5
ΣK = 0.5 + 3·0.3 + 5 = 6.4

Energy equation

The outlet jet still carries its velocity head; it is not a loss but it has to be supplied.

H = (1 + 13.5 + 6.4)·0.08263 = 1.727 m

Answer

H = 1.727 m
23.Pumps & pump power

Answer: Pshaft = 50.45 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 = 1000·9.81·0.06·60 = 35.32 kW

Shaft power

Pshaft = Ph/η = 35.32/0.7 = 50.45 kW

Answer

Pshaft = 50.45 kW
24.Pumps & pump power

Answer: H = 40.75 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 = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (60 + 8)·0.2905 = 19.75 m

Pump head

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

H = Δz + hL = 21 + 19.75 = 40.75 m

Answer

H = 40.75 m

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