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 · 15% NaOHStream 2ṁ₂ = ? · 45% 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 = 600 kg/hx1 = 15 %x2 = 45 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F4300 kg/h · 12% saltProduct P40% 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 = 4300 kg/hxF = 12 %xP = 40 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 150 °C100 °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 = 2 kg/scp,h = 2.1 kJ/(kg·K)Th: 150 → 100 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 130 °C100 °Cwater · 25 °C50 °C · ṁ = ?15% lost

Hot light oil 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 = 3 kg/scp,h = 2.1 kJ/(kg·K)Th: 130 → 100 °Ct: 25 → 50 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
160 g of HeV = 20 LT = 10 °CP = ?

A tank of 20 L contains 160 g of He at 10 °C. Treat it as an ideal gas and find the pressure P.

m = 160 gM = 4.003 g/molV = 20 LT = 10 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of CH₄ goes from 400 kPa, 10 L, 10 °C to 550 kPa and 100 °C. Find the new volume V2.

P1 = 400 kPaV1 = 10 LT1 = 10 °CP2 = 550 kPaT2 = 100 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 1/ν× M(CO2​)

4 g of CH4 and 64 g of O2 react according to CH4 + 2O2 → CO2 + 2H2O. What mass m of CO2 can form?

M(CH4) = 16.04M(O2) = 32M(CO2) = 44.01 g/mol
m = g
8.StoichiometryHard
m(C3​H8​)n(C3​H8​)n(H2​O)m(H2​O)÷ M(C3​H8​)× 4/1× M(H2​O)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 16 g of C3H8 reacts completely (the other reactants are in excess) and 23.8 g of H2O is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 23.8 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.50.50C−x−x+2xE0.5 − x0.5 − x2x

0.5 mol/L of H₂ and 0.5 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 = 0.5 mol/LKc = 9
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.04 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.1 mol/LKc = 0.04
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 250 gT = 130 °Cc = 0.449 J/(g·°C)Waterm = 100 gT = 19 °Cc = 4.18 J/(g·°C)

A 250 g block of iron (c = 0.449 J/(g·°C)) at 130 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 19 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.449 J/(g·°C)Tmetal = 130 °Cmwater = 100 gTwater = 19 °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 = ?75%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 1 L/(mol·min) and starts at 1 mol/L. How long does it take to reach 75% conversion? Find t.

k = 1 L/(mol·min)CA0 = 1 mol/LX = 75 %
t = min
14.Reaction kineticsHard
Tk50 °Ck1​?3·k1​

A reaction has an activation energy of 60 kJ/mol. At 50 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 3 times faster?

Ea = 60 kJ/molT1 = 50 °Ck2/k1 = 3R = 8.314 J/(mol·K)
T2 = °C
15.Reactor sizing (CSTR & PFR)Medium
Q = 10 L/minCA0​ = 2 mol/LCA​ = ?V = 50 L, k = 0.5 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.5 min⁻¹) runs in a 50 L plug-flow reactor (PFR). The feed enters at 10 L/min with CA0 = 2 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 50 LQ = 10 L/mink = 0.5 min⁻¹CA0 = 2 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
Q = 80 L/minX = ?V = 1000 L

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 1000 L plug-flow reactor (PFR) fed at 80 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 1000 LQ = 80 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT160 °C110 °C140 °C30 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 500 kW. The hot fluid cools from 160 to 110 °C and the cold fluid heats from 30 to 140 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 500 kWU = 800 W/(m²·K)Th: 160 → 110 °CTc: 30 → 140 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT110 °C30 °C?ΔT₁ΔT₂condensing steam

Steam condenses at a constant 110 °C on the outside of the tubes of a condenser with a heat transfer area of 3 m² and U = 1500 W/(m²·K). Cooling water (0.5 kg/s, cp = 4.18 kJ/(kg·K)) enters the tubes at 30 °C. Find the water outlet temperature Tc,out.

Ts = 110 °CA = 3 m²U = 1500 W/(m²·K)ṁ = 0.5 kg/scp = 4.18 kJ/(kg·K)Tc,in = 30 °C
Tc,out = °C
19.Heat conductionMedium
Expanded polystyrene, k = 0.035100 mmGlass, k = 0.9650 mm17 °C6 °CQ̇ = ?

A wall is made of 100 mm of expanded polystyrene and 50 mm of glass, with an area of 20 m². The outer faces are at 17 °C and 6 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.035 W/(m·K)L2 = 50 mm, k2 = 0.96 W/(m·K)A = 20 m²T1 = 17 °CT3 = 6 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.96150 mmWood, k = 0.1750 mmroom 20 °Coutside -9 °CQ̇

A wall of 150 mm glass and 50 mm wood separates a room at 20 °C from outside air at -9 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 10 m². Find the overall heat transfer coefficient U of the wall.

L1 = 150 mm, k1 = 0.96 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 10 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = -9 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
Q = 5 L/sD = 75 mmL = 400 mf = 0.018

Water flows at 5 L/s through a pipe 400 m long with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.018 and g = 9.81 m/s². Find the friction head loss hf.

Q = 5 L/sL = 400 mD = 75 mmf = 0.018g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10free outletH = ?L = 100 m, D = 300 mm, f = 0.0224× bend (K = 0.3)

A pipe 100 m long with an inside diameter of 300 mm (Darcy friction factor f = 0.022) 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 = 10). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 100 L/s?

Q = 100 L/sL = 100 mD = 300 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 10
H = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 24 m

A pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 24 m. The pump efficiency is 60% and the electric motor driving it has an efficiency of 90%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 10 L/sH = 24 mηpump = 60%ηmotor = 90%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 23 mL = 100 m, D = 200 mm, f = 0.018, ΣK = 6

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 23 m higher. The pipe is 100 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.018; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 65%. Find the shaft power Pshaft in kW.

Q = 75 L/sΔz = 23 mL = 100 mD = 200 mmf = 0.018ΣK = 6η = 65%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 300 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) = 600·(15 − 25)/(25 − 45) = 300 kg/h

Answer

ṁ2 = 300 kg/h
2.Mass balance

Answer: W = 3010 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 = 4300·12/40 = 1290 kg/h

Total balance

W = F − P = 4300 − 1290 = 3010 kg/h

Answer

W = 3010 kg/h
3.Energy balance

Answer: tout = 35.12 °C

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

Heat released by the hot stream

Q = 2·2.1·(150 − 100) = 210 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 210/(2·4.18) = 35.12 °C

Answer

tout = 35.12 °C
4.Energy balance

Answer: ṁc = 1.537 kg/s

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

Heat released

Qh = 3·2.1·(130 − 100) = 189 kW

Heat that reaches the water

Qc = (1 − 0.15)·189 = 160.7 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 160.7/(4.18·25) = 1.537 kg/s

Answer

ṁc = 1.537 kg/s
5.Ideal gas law

Answer: P = 4705 kPa

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

Moles

n = m/M = 160/4.003 = 39.97 mol
T = 10 + 273.15 = 283.1 K

Pressure

P = nRT/V = 39.97·8.314·283.1/0.02 = 4705 kPa

Answer

P = 4705 kPa
6.Ideal gas law

Answer: V2 = 9.584 L

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

Absolute temperatures

T1 = 283.1 K, T2 = 373.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(400/550)·(373.1/283.1) = 9.584 L

Answer

V2 = 9.584 L
7.Stoichiometry

Answer: m = 10.98 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(CH4) = 4/16.04 = 0.2494 mol
n(O2) = 64/32 = 2 mol

Limiting reactant

0.2494/1 = 0.2494, 2/2 = 1 → CH4

Mass of product

n(CO2) = 0.2494·1 = 0.2494 mol
m = 0.2494·44.01 = 10.98 g

Answer

m = 10.98 g
8.Stoichiometry

Answer: Y = 91.01 %

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(C3H8) = 16/44.1 = 0.3628 mol
m = 0.3628·4/1·18.02 = 26.15 g

Percent yield

Y = 23.8/26.15·100 = 91.01%

Answer

Y = 91.01%
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

9 = (2x)²/(0.5 − x)²

Take the square root

3 = 2x/(0.5 − x) → x = 0.5·3/(2 + 3) = 0.3 mol/L

Equilibrium concentration

[HI] = 2x = 0.6 mol/L

Answer

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

Answer: [Cl2] = 0.04633 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

0.04 = x²/(0.1 − x) → x² + 0.04·x − 0.004 = 0

Solve the quadratic

x = (−0.04 + √(0.04² + 4·0.004))/2 = 0.04633 mol/L

Equilibrium concentration

[Cl₂] = x = 0.04633 mol/L

Answer

[Cl2] = 0.04633 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 42.5 °C

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

Heat balance

250·0.449·(130 − Tf) = 100·4.18·(Tf − 19)

Solve for the final temperature

Tf = (112.3·130 + 418·19)/(112.3 + 418) = 42.5 °C

Answer

Tf = 42.5 °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 = 3 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).

Concentration at the end

CA = 1·(1 − 0.75) = 0.25 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (4 − 1)/1 = 3 min

Answer

t = 3 min
14.Reaction kinetics

Answer: T2 = 66.72 °C

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 temperature

T1 = 323.1 K

Solve Arrhenius for T₂

1/T2 = 1/323.1 − 8.314·ln(3)/60000 = 3.095 × 10⁻³ − 1.522 × 10⁻⁴ = 2.942 × 10⁻³ K⁻¹
T2 = 339.9 K = 66.72 °C

Answer

T2 = 66.72 °C
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.1642 mol/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 = V/Q = 50/10 = 5 min

Outlet concentration

CA = 2·e−0.5·5 = 0.1642 mol/L

Answer

CA = 0.1642 mol/L

Conversion: X = 91.79%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 95.61 %

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 = 1000/80 = 12.5 min, kτ = 0.25·12.5 = 3.125

Conversion

X = 1 − e−kτ = 1 − e−3.125 = 95.61%

Answer

X = 95.61%
17.Heat exchangers (LMTD)

Answer: A = 14.44 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 = 160 − 140 = 20 K
ΔT₂ = Th,out − Tc,in = 110 − 30 = 80 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (20 − 80)/ln(20/80) = 43.28 K

Area

A = Q̇/(U·ΔTlm) = 500000/(800·43.28) = 14.44 m²

Answer

A = 14.44 m²
18.Heat exchangers (LMTD)

Answer: Tc,out = 100.7 °C

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.

Combine the energy balance and the rate equation

With ΔT₁ = Ts − Tc,in and ΔT₂ = Ts − Tc,out, the difference ΔT₁ − ΔT₂ equals the water temperature rise, so the rise cancels.

ṁcp(ΔT₁ − ΔT₂) = U·A·(ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂)
ln(ΔT₁/ΔT₂) = U·A/(ṁcp) = 1500·3/(0.5·4180) = 2.153

Outlet temperature

ΔT₂ = ΔT₁·e−2.153 = 80·0.1161 = 9.29 K
Tc,out = 110 − 9.29 = 100.7 °C

Answer

Tc,out = 100.7 °C

Heat transferred: Q̇ = 147.8 kW.

19.Heat conduction

Answer: Q̇ = 75.62 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)/(0.035·20) = 0.1429 K/W
R2 = L2/(k2A) = (50/1000)/(0.96·20) = 0.002604 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 11/0.1455 = 75.62 W

Answer

Q̇ = 75.62 W
20.Heat conduction

Answer: U = 1.63 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/(7.7·10) = 0.01299 K/W
R1 = L1/(k1A) = (150/1000)/(0.96·10) = 0.01563 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·10) = 0.02941 K/W
Ro = 1/(hoA) = 1/(30·10) = 0.003333 K/W
ΣR = 0.06136 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(10·0.06136) = 1.63 W/(m²·K)

Answer

U = 1.63 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 6.267 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·0.075²/4 = 0.004418 m²
V = Q/A = 0.005/0.004418 = 1.132 m/s

Velocity head

V²/(2g) = 1.132²/(2·9.81) = 0.06529 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.018·(400/0.075)·1.132²/(2·9.81) = 6.267 m

Answer

hf = 6.267 m
22.Pipe friction & head loss

Answer: H = 2.044 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 = 0.1/0.07069 = 1.415 m/s
V²/(2g) = 0.102 m

Loss coefficients

f·L/D = 0.022·100/0.3 = 7.333
ΣK = 0.5 + 4·0.3 + 10 = 11.7

Energy equation

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

H = (1 + 7.333 + 11.7)·0.102 = 2.044 m

Answer

H = 2.044 m
23.Pumps & pump power

Answer: Pel = 4.36 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 = 1000·9.81·0.01·24 = 2.354 kW

Shaft power

Pshaft = 2.354/0.6 = 3.924 kW

Electrical power

Pel = 3.924/0.9 = 4.36 kW

Answer

Pel = 4.36 kW
24.Pumps & pump power

Answer: Pshaft = 30.97 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 = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (9 + 6)·0.2905 = 4.357 m

Pump head

H = Δz + hL = 23 + 4.357 = 27.36 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.075·27.36/0.65 = 30.97 kW

Answer

Pshaft = 30.97 kW

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