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 1300 kg/h · 35% NaOHStream 2ṁ₂ = ? · 20% NaOHProduct25% NaOH

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

ṁ1 = 300 kg/hx1 = 35 %x2 = 20 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1700 kg/h · 12% sugarProduct P60% sugarVapour W (pure water)W = ? kg/h

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

F = 1700 kg/hxF = 12 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 120 °C80 °Cwater · 15 °Ct = ? °C

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

ṁh = 0.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 120 → 80 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 120 °C80 °Cwater · 20 °C40 °C · ṁ = ?15% lost

Hot ethanol 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 = 2.5 kg/scp,h = 2.44 kJ/(kg·K)Th: 120 → 80 °Ct: 20 → 40 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
10 g of CO₂V = 50 LT = 50 °CP = ?

A tank of 50 L contains 10 g of CO₂ at 50 °C. Treat it as an ideal gas and find the pressure P.

m = 10 gM = 44.01 g/molV = 50 LT = 50 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of O₂ goes from 200 kPa, 2 L, 35 °C to 400 kPa and 70 °C. Find the new volume V2.

P1 = 200 kPaV1 = 2 LT1 = 35 °CP2 = 400 kPaT2 = 70 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 4/ν× M(H2​O)

12 g of C3H8 and 24 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of H2O can form?

M(C3H8) = 44.1M(O2) = 32M(H2O) = 18.02 g/mol
m = g
8.StoichiometryHard
m(CaCO3​)n(CaCO3​)n(CaO)m(CaO)÷ M(CaCO3​)× 1/1× M(CaO)

In the reaction CaCO3 → CaO + CO2, 16 g of CaCO3 reacts completely (the other reactants are in excess) and 7.35 g of CaO is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CaO) = 56.08 g/molactual: 7.35 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.10.10C−x−x+2xE0.1 − x0.1 − x2x

0.1 mol/L of H₂ and 0.1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 64. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.1 mol/LKc = 64
[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 [PCl5].

[PCl₅]₀ = 0.2 mol/LKc = 0.2
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 150 gT = 180 °Cc = 0.388 J/(g·°C)Waterm = 400 gT = 25 °Cc = 4.18 J/(g·°C)

A 150 g block of zinc (c = 0.388 J/(g·°C)) at 180 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.388 J/(g·°C)Tmetal = 180 °Cmwater = 400 gTwater = 25 °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)X (%)t = ?90%

A zero-order reaction has k = 0.01 mol/(L·min) and starts at 0.5 mol/L. How long does it take to reach 90% conversion? Find t.

k = 0.01 mol/(L·min)CA0 = 0.5 mol/LX = 90 %
t = min
14.Reaction kineticsHard
Tk40 °C0.0150 °C?

A reaction has a rate constant of 0.01 min⁻¹ at 40 °C and an activation energy of 70 kJ/mol. Find the rate constant k2 at 50 °C.

k1 = 0.01 min⁻¹T1 = 40 °CT2 = 50 °CEa = 70 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 L/minX = 85%V = ?, k = 0.05 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.05 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 85% conversion of A.

Q = 80 L/mink = 0.05 min⁻¹X = 85%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 2000 LQ = 100 L/minX = ?

A first-order liquid-phase reaction (k = 0.1 min⁻¹) runs in a 2000 L CSTR fed at 100 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 2000 LQ = 100 L/mink = 0.1 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT110 °C10 °C65 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 110 °C on the outside of the tubes. Cooling water (1 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 10 to 65 °C. The overall heat transfer coefficient is 2500 W/(m²·K). Find the heat transfer area A needed.

Ts = 110 °Cṁ = 1 kg/scp = 4.18 kJ/(kg·K)Tc: 10 → 65 °CU = 2500 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT175 °C150 °C27.56 °C15 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.1 kJ/(kg·K)) cools from 175 to 150 °C in a counter-flow exchanger. It heats 1 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 15 °C. With U = 300 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.1 kJ/(kg·K)Th: 175 → 150 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 15 °CU = 300 W/(m²·K)
A = m²
19.Heat conductionMedium
Gypsum board, k = 0.1750 mmWood, k = 0.1750 mm17 °C-5 °CTi​ = ?Q̇

A wall is made of 50 mm of gypsum board and 50 mm of wood, with an area of 4 m². The outer faces are at 17 °C and -5 °C. Find the temperature Ti at the interface between the two layers.

L1 = 50 mm, k1 = 0.17 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 4 m²T1 = 17 °CT3 = -5 °C
Ti = °C
20.Heat conductionHard
Expanded polystyrene, k = 0.035100 mmMineral wool, k = 0.0425 mmroom 22 °Coutside 5 °CQ̇ = ?

A wall of 100 mm expanded polystyrene and 25 mm mineral wool separates a room at 22 °C from outside air at 5 °C. The convection coefficients are 10 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 8 m². Find the heat loss Q̇ through the wall.

L1 = 100 mm, k1 = 0.035 W/(m·K)L2 = 25 mm, k2 = 0.04 W/(m·K)A = 8 m²hi = 10 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = 5 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 2.2 m/sD = 75 mmL = 50 mf = 0.03

Water (ρ = 1000 kg/m³) flows at 2.2 m/s through a horizontal pipe, 50 m long, with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2.2 m/sL = 50 mD = 75 mmf = 0.03ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 100 m, D = 100 mm, f = 0.024× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 100 mm (Darcy friction factor f = 0.02) 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), 4 bends (K = 0.3 each) and a valve (K = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 10 L/s?

Q = 10 L/sL = 100 mD = 100 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 56 m

In a test, a pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 56 m while its shaft takes 7.6 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 10 L/sH = 56 mPshaft = 7.6 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 28 mL = 200 m, D = 150 mm, f = 0.018, ΣK = 5

A pump moves 50 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 28 m higher. The pipe is 200 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 = 5 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 50 L/sΔz = 28 mL = 200 mD = 150 mmf = 0.018ΣK = 5
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
NaOH: ṁ1x1 + ṁ2x2 = (ṁ1 + ṁ2)x3

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 300·(35 − 25)/(25 − 20) = 600 kg/h

Answer

ṁ2 = 600 kg/h
2.Mass balance

Answer: W = 1360 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 = 1700·12/60 = 340 kg/h

Total balance

W = F − P = 1700 − 340 = 1360 kg/h

Answer

W = 1360 kg/h
3.Energy balance

Answer: tout = 23.61 °C

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

Heat released by the hot stream

Q = 0.5·3.6·(120 − 80) = 72 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 72/(2·4.18) = 23.61 °C

Answer

tout = 23.61 °C
4.Energy balance

Answer: ṁc = 2.481 kg/s

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

Heat released

Qh = 2.5·2.44·(120 − 80) = 244 kW

Heat that reaches the water

Qc = (1 − 0.15)·244 = 207.4 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 207.4/(4.18·20) = 2.481 kg/s

Answer

ṁc = 2.481 kg/s
5.Ideal gas law

Answer: P = 12.21 kPa

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

Moles

n = m/M = 10/44.01 = 0.2272 mol
T = 50 + 273.15 = 323.1 K

Pressure

P = nRT/V = 0.2272·8.314·323.1/0.05 = 12.21 kPa

Answer

P = 12.21 kPa
6.Ideal gas law

Answer: V2 = 1.114 L

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

Absolute temperatures

T1 = 308.1 K, T2 = 343.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(200/400)·(343.1/308.1) = 1.114 L

Answer

V2 = 1.114 L
7.Stoichiometry

Answer: m = 10.81 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(C3H8) = 12/44.1 = 0.2721 mol
n(O2) = 24/32 = 0.75 mol

Limiting reactant

0.2721/1 = 0.2721, 0.75/5 = 0.15 → O2

Mass of product

n(H2O) = 0.15·4 = 0.6 mol
m = 0.6·18.02 = 10.81 g

Answer

m = 10.81 g
8.Stoichiometry

Answer: Y = 81.99 %

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(CaCO3) = 16/100.09 = 0.1599 mol
m = 0.1599·1/1·56.08 = 8.965 g

Percent yield

Y = 7.35/8.965·100 = 81.99%

Answer

Y = 81.99%
9.Chemical equilibrium

Answer: [H2] = 0.02 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

64 = (2x)²/(0.1 − x)²

Take the square root

8 = 2x/(0.1 − x) → x = 0.1·8/(2 + 8) = 0.08 mol/L

Equilibrium concentration

[H₂] = 0.1 − x = 0.02 mol/L

Answer

[H2] = 0.02 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.07639 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

[PCl₅] = 0.2 − 0.1236 = 0.07639 mol/L

Answer

[PCl5] = 0.07639 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 30.21 °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

150·0.388·(180 − Tf) = 400·4.18·(Tf − 25)

Solve for the final temperature

Tf = (58.2·180 + 1672·25)/(58.2 + 1672) = 30.21 °C

Answer

Tf = 30.21 °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: t = 45 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 = 0.5·0.9 = 0.45 mol/L

Time

t = CA0·X/k = 0.45/0.01 = 45 min

Answer

t = 45 min
14.Reaction kinetics

Answer: k2 = 0.02298 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 = 313.1 K, T2 = 323.1 K

Arrhenius ratio

ln(k2/k1) = −(70000/8.314)·(1/323.1 − 1/313.1) = 0.832
k2 = 0.01·e0.832 = 0.02298 min⁻¹

Answer

k2 = 0.02298 min⁻¹
15.Reactor sizing (CSTR & PFR)

Answer: V = 3035 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 − 0.85))/0.05 = 1.897/0.05 = 37.94 min

Volume

V = Q·τ = 80·37.94 = 3035 L

Answer

V = 3035 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 66.67 %

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 = 2000/100 = 20 min, kτ = 0.1·20 = 2

Conversion

X = kτ/(1 + kτ) = 2/(1 + 2) = 66.67%

Answer

X = 66.67%
17.Heat exchangers (LMTD)

Answer: A = 1.335 m²

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

Heat duty from the water side

Q̇ = 1·4.18·(65 − 10) = 229.9 kW

End temperature differences

ΔT₁ = 110 − 10 = 100 K
ΔT₂ = 110 − 65 = 45 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (100 − 45)/ln(100/45) = 68.88 K

Area

A = Q̇/(U·ΔTlm) = 229900/(2500·68.88) = 1.335 m²

Answer

A = 1.335 m²
18.Heat exchangers (LMTD)

Answer: A = 1.24 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) = 1·2.1·25 = 52.5 kW
Tc,out = 15 + 52.5/(1·4.18) = 27.56 °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 = 175 − 27.56 = 147.4 K
ΔT₂ = Th,out − Tc,in = 150 − 15 = 135 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (147.4 − 135)/ln(147.4/135) = 141.1 K

Area

A = Q̇/(U·ΔTlm) = 52500/(300·141.1) = 1.24 m²

Answer

A = 1.24 m²
19.Heat conduction

Answer: Ti = 6 °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)/(0.17·4) = 0.07353 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·4) = 0.07353 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 22/0.1471 = 149.6 W

Interface temperature

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

Ti = T1 − Q̇·R1 = 17 − 149.6·0.07353 = 6 °C

Answer

Ti = 6 °C
20.Heat conduction

Answer: Q̇ = 37.44 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.

Resistances in series

Ri = 1/(hiA) = 1/(10·8) = 0.0125 K/W
R1 = L1/(k1A) = (100/1000)/(0.035·8) = 0.3571 K/W
R2 = L2/(k2A) = (25/1000)/(0.04·8) = 0.07813 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.454 K/W

Heat loss

Q̇ = (22 − (5))/0.454 = 37.44 W

Answer

Q̇ = 37.44 W
21.Pipe friction & head loss

Answer: Δp = 48.4 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) = 0.03·(50/0.075)·2.2²/(2·9.81) = 4.934 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 = 1000·9.81·4.934 = 48400 Pa = 48.4 kPa

Answer

Δp = 48.4 kPa
22.Pipe friction & head loss

Answer: H = 2.041 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 = 0.01/0.007854 = 1.273 m/s
V²/(2g) = 0.08263 m

Loss coefficients

f·L/D = 0.02·100/0.1 = 20
ΣK = 0.5 + 4·0.3 + 2 = 3.7

Energy equation

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

H = (1 + 20 + 3.7)·0.08263 = 2.041 m

Answer

H = 2.041 m
23.Pumps & pump power

Answer: η = 72.28 %

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 = 1000·9.81·0.01·56 = 5.494 kW

Efficiency

η = Ph/Pshaft = 5.494/7.6 = 72.28%

Answer

η = 72.28%
24.Pumps & pump power

Answer: H = 39.83 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 = 0.05/0.01767 = 2.829 m/s
V²/(2g) = 0.408 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (24 + 5)·0.408 = 11.83 m

Pump head

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

H = Δz + hL = 28 + 11.83 = 39.83 m

Answer

H = 39.83 m

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