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 · 45% saltStream 2ṁ₂ = ? · 5% 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 = 45 %x2 = 5 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1400 kg/h · 10% NaOHProduct P30% 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 = 1400 kg/hxF = 10 %xP = 30 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 150 °C110 °Cwater · 15 °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 → 110 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 140 °C100 °Cwater · 10 °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 = 2.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 140 → 100 °Ct: 10 → 85 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
450 g of ArV = 5 LT = 25 °CP = ?

A tank of 5 L contains 450 g of Ar at 25 °C. Treat it as an ideal gas and find the pressure P.

m = 450 gM = 39.95 g/molV = 5 LT = 25 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 100 kPa, 10 L, 25 °C to 550 kPa and 240 °C. Find the new volume V2.

P1 = 100 kPaV1 = 10 LT1 = 25 °CP2 = 550 kPaT2 = 240 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 2/ν× M(H2​O)

8 g of H2 and 10 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(CaCO3​)n(CaCO3​)n(CO2​)m(CO2​)÷ M(CaCO3​)× 1/1× M(CO2​)

In the reaction CaCO3 → CaO + CO2, 30 g of CaCO3 reacts completely (the other reactants are in excess) and 11.21 g of CO2 is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CO2) = 44.01 g/molactual: 11.21 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.20.20C−x−x+2xE0.2 − x0.2 − x2x

0.2 mol/L of H₂ and 0.2 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 9. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 9
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.5 mol/LKc = 0.1
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 200 gT = 130 °Cc = 0.129 J/(g·°C)Waterm = 300 gT = 25 °Cc = 4.18 J/(g·°C)

A 200 g block of lead (c = 0.129 J/(g·°C)) at 130 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.129 J/(g·°C)Tmetal = 130 °Cmwater = 300 gTwater = 25 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l).

ΔH°f(C2H6) = −84.7 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
ΔH° = kJ
13.Reaction kineticsMedium
t (min)X (%)t = ?20%

A zero-order reaction has k = 0.05 mol/(L·min) and starts at 0.8 mol/L. How long does it take to reach 20% conversion? Find t.

k = 0.05 mol/(L·min)CA0 = 0.8 mol/LX = 20 %
t = min
14.Reaction kineticsHard
Tk25 °C0.0145 °C0.059

The rate constant of a reaction is 0.01 min⁻¹ at 25 °C and 0.059 min⁻¹ at 45 °C. Find the activation energy Ea.

k1 = 0.01 min⁻¹T1 = 25 °Ck2 = 0.059 min⁻¹T2 = 45 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
QX = 95%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 95% 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 = 95%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
Q = 40 L/minX = ?V = 200 L

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in a 200 L plug-flow reactor (PFR) fed at 40 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 40 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT165 °C105 °C135 °C10 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 450 kW. The hot fluid cools from 165 to 105 °C and the cold fluid heats from 10 to 135 °C. The overall heat transfer coefficient is 1500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 450 kWU = 1500 W/(m²·K)Th: 165 → 105 °CTc: 10 → 135 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT160 °C100 °C129 °C30 °CΔT₁ΔT₂counter-flow

Hot oil (1.5 kg/s, cp = 2.3 kJ/(kg·K)) cools from 160 to 100 °C in a counter-flow exchanger. It heats 0.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 30 °C. With U = 800 W/(m²·K), find the heat transfer area A needed.

ṁh = 1.5 kg/scp,h = 2.3 kJ/(kg·K)Th: 160 → 100 °Cṁc = 0.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 30 °CU = 800 W/(m²·K)
A = m²
19.Heat conductionMedium
Wood, k = 0.17100 mmBrick, k = 0.7250 mm22 °C-3 °CQ̇ = ?

A wall is made of 100 mm of wood and 50 mm of brick, with an area of 12 m². The outer faces are at 22 °C and -3 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.17 W/(m·K)L2 = 50 mm, k2 = 0.72 W/(m·K)A = 12 m²T1 = 22 °CT3 = -3 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.035200 mmConcrete, k = 1.450 mmroom 22 °Coutside 1 °CQ̇ = ?

A wall of 200 mm expanded polystyrene and 50 mm concrete separates a room at 22 °C from outside air at 1 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 4 m². Find the heat loss Q̇ through the wall.

L1 = 200 mm, k1 = 0.035 W/(m·K)L2 = 50 mm, k2 = 1.4 W/(m·K)A = 4 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 22 °CTout = 1 °C
Q̇ = W
21.Pipe friction & head lossMedium
V = 2.6 m/sD = 75 mmL = 300 mf = 0.025

Water flows at a mean velocity of 2.6 m/s through a pipe 300 m long with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.025 and g = 9.81 m/s². Find the friction head loss hf.

V = 2.6 m/sL = 300 mD = 75 mmf = 0.025g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10Δz = ?L = 100 m, D = 300 mm, f = 0.024× bend (K = 0.3)

Two open reservoirs are joined by a pipe 100 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.02. The minor losses are a square-edged entrance (K = 0.5), 4 bends (K = 0.3 each), a valve (K = 10) 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 80 L/s?

Q = 80 L/sL = 100 mD = 300 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 10Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 40 L/sH = 44 m

A pump delivers 40 L/s of water (ρ = 1000 kg/m³) against a head of 44 m. The pump efficiency is 75% and the electric motor driving it has an efficiency of 92%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 40 L/sH = 44 mηpump = 75%ηmotor = 92%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 80 L/sΔz = 9 mL = 600 m, D = 200 mm, f = 0.02, ΣK = 6

A pump moves 80 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 9 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 = 6 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 70%. Find the shaft power Pshaft in kW.

Q = 80 L/sΔz = 9 mL = 600 mD = 200 mmf = 0.02ΣK = 6η = 70%
Pshaft = kW

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·(45 − 25)/(25 − 5) = 600 kg/h

Answer

ṁ2 = 600 kg/h
2.Mass balance

Answer: W = 933.3 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 = 1400·10/30 = 466.7 kg/h

Total balance

W = F − P = 1400 − 466.7 = 933.3 kg/h

Answer

W = 933.3 kg/h
3.Energy balance

Answer: tout = 45.14 °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 − 110) = 126 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 126/(1·4.18) = 45.14 °C

Answer

tout = 45.14 °C
4.Energy balance

Answer: ṁc = 0.6029 kg/s

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

Heat released

Qh = 2.5·2.1·(140 − 100) = 210 kW

Heat that reaches the water

Qc = (1 − 0.1)·210 = 189 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 189/(4.18·75) = 0.6029 kg/s

Answer

ṁc = 0.6029 kg/s
5.Ideal gas law

Answer: P = 5584 kPa

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

Moles

n = m/M = 450/39.95 = 11.26 mol
T = 25 + 273.15 = 298.1 K

Pressure

P = nRT/V = 11.26·8.314·298.1/0.005 = 5584 kPa

Answer

P = 5584 kPa
6.Ideal gas law

Answer: V2 = 3.129 L

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

Absolute temperatures

T1 = 298.1 K, T2 = 513.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(100/550)·(513.1/298.1) = 3.129 L

Answer

V2 = 3.129 L
7.Stoichiometry

Answer: m = 11.26 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) = 8/2.016 = 3.968 mol
n(O2) = 10/32 = 0.3125 mol

Limiting reactant

3.968/2 = 1.984, 0.3125/1 = 0.3125 → O2

Mass of product

n(H2O) = 0.3125·2 = 0.625 mol
m = 0.625·18.02 = 11.26 g

Answer

m = 11.26 g
8.Stoichiometry

Answer: Y = 84.98 %

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(CaCO3) = 30/100.09 = 0.2997 mol
m = 0.2997·1/1·44.01 = 13.19 g

Percent yield

Y = 11.21/13.19·100 = 84.98%

Answer

Y = 84.98%
9.Chemical equilibrium

Answer: [HI] = 0.24 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/(0.2 − x)²

Take the square root

3 = 2x/(0.2 − x) → x = 0.2·3/(2 + 3) = 0.12 mol/L

Equilibrium concentration

[HI] = 2x = 0.24 mol/L

Answer

[HI] = 0.24 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.1791 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

0.1 = x²/(0.5 − x) → x² + 0.1·x − 0.05 = 0

Solve the quadratic

x = (−0.1 + √(0.1² + 4·0.05))/2 = 0.1791 mol/L

Equilibrium concentration

[Cl₂] = x = 0.1791 mol/L

Answer

[Cl2] = 0.1791 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 27.12 °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

200·0.129·(130 − Tf) = 300·4.18·(Tf − 25)

Solve for the final temperature

Tf = (25.8·130 + 1254·25)/(25.8 + 1254) = 27.12 °C

Answer

Tf = 27.12 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −3119 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° = [4·(−393.5) + 6·(−285.8)] − [2·(−84.7) + 7·0] = −3119 kJ

Answer

ΔH° = −3119 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: t = 3.2 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).

Amount converted

CA0·X = 0.8·0.2 = 0.16 mol/L

Time

t = CA0·X/k = 0.16/0.05 = 3.2 min

Answer

t = 3.2 min
14.Reaction kinetics

Answer: Ea = 69.99 kJ/mol

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 = 298.1 K, T2 = 318.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·1.775/(-2.108e-4) = 69990 J/mol
Ea = 69.99 kJ/mol

Answer

Ea = 69.99 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 6.342

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) = 0.95/0.05 = 19
PFR: k·τ = ln(1/(1 − X)) = ln(20) = 2.996

Ratio of volumes

VCSTR/VPFR = 19/2.996 = 6.342

Answer

VCSTR/VPFR = 6.342

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 45.12 %

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 = 200/40 = 5 min, kτ = 0.12·5 = 0.6

Conversion

X = 1 − e−kτ = 1 − e−0.6 = 45.12%

Answer

X = 45.12%
17.Heat exchangers (LMTD)

Answer: A = 5.32 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 = 165 − 135 = 30 K
ΔT₂ = Th,out − Tc,in = 105 − 10 = 95 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (30 − 95)/ln(30/95) = 56.39 K

Area

A = Q̇/(U·ΔTlm) = 450000/(1500·56.39) = 5.32 m²

Answer

A = 5.32 m²
18.Heat exchangers (LMTD)

Answer: A = 5.407 m²

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

Heat duty and water outlet temperature

Q̇ = ṁhcp,h(Th,in − Th,out) = 1.5·2.3·60 = 207 kW
Tc,out = 30 + 207/(0.5·4.18) = 129 °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 = 160 − 129 = 30.96 K
ΔT₂ = Th,out − Tc,in = 100 − 30 = 70 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (30.96 − 70)/ln(30.96/70) = 47.85 K

Area

A = Q̇/(U·ΔTlm) = 207000/(800·47.85) = 5.407 m²

Answer

A = 5.407 m²
19.Heat conduction

Answer: Q̇ = 456.1 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)/(0.17·12) = 0.04902 K/W
R2 = L2/(k2A) = (50/1000)/(0.72·12) = 0.005787 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 25/0.05481 = 456.1 W

Answer

Q̇ = 456.1 W
20.Heat conduction

Answer: Q̇ = 14.21 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/(7.7·4) = 0.03247 K/W
R1 = L1/(k1A) = (200/1000)/(0.035·4) = 1.429 K/W
R2 = L2/(k2A) = (50/1000)/(1.4·4) = 0.008929 K/W
Ro = 1/(hoA) = 1/(30·4) = 0.008333 K/W
ΣR = 1.478 K/W

Heat loss

Q̇ = (22 − (1))/1.478 = 14.21 W

Answer

Q̇ = 14.21 W
21.Pipe friction & head loss

Answer: hf = 34.45 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) = 2.6²/(2·9.81) = 0.3445 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.025·(300/0.075)·2.6²/(2·9.81) = 34.45 m

Answer

hf = 34.45 m
22.Pipe friction & head loss

Answer: Δz = 1.264 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 = 0.08/0.07069 = 1.132 m/s
V²/(2g) = 0.06529 m

Loss coefficients

f·L/D = 0.02·100/0.3 = 6.667
ΣK = 0.5 + 4·0.3 + 10 + 1.0 = 12.7

Total head loss

hf = 6.667·0.06529 = 0.4352 m
hm = 12.7·0.06529 = 0.8291 m
Δz = hf + hm = 1.264 m

Answer

Δz = 1.264 m
23.Pumps & pump power

Answer: Pel = 25.02 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 = 1000·9.81·0.04·44 = 17.27 kW

Shaft power

Pshaft = 17.27/0.75 = 23.02 kW

Electrical power

Pel = 23.02/0.92 = 25.02 kW

Answer

Pel = 25.02 kW
24.Pumps & pump power

Answer: Pshaft = 34.55 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.

Velocity

V = Q/A = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (60 + 6)·0.3305 = 21.81 m

Pump head

H = Δz + hL = 9 + 21.81 = 30.81 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.08·30.81/0.7 = 34.55 kW

Answer

Pshaft = 34.55 kW

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