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 11000 kg/h · 45% sugarStream 2ṁ₂ = ? · 15% sugarProduct35% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 35% sugar? Find ṁ2.

ṁ1 = 1000 kg/hx1 = 45 %x2 = 15 %x3 = 35 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3900 kg/h · 11% NaOHProduct PP = ? · 40%Vapour W (pure water)0% NaOH

An evaporator concentrates a NaOH solution by boiling off pure water. Find the product flow P in kg/h.

F = 3900 kg/hxF = 11 %xP = 40 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 160 °C60 °Cwater · 25 °Ct = ? °C

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

ṁh = 2 kg/scp,h = 3.6 kJ/(kg·K)Th: 160 → 60 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 25 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 130 °C90 °Cwater · 10 °C45 °C · ṁ = ?15% lost

Hot glycol mix heats water in an exchanger that loses 15% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 3 kg/scp,h = 3.6 kJ/(kg·K)Th: 130 → 90 °Ct: 10 → 45 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
270 g of HeV = 30 LT = 0 °CP = ?

A tank of 30 L contains 270 g of He at 0 °C. Treat it as an ideal gas and find the pressure P.

m = 270 gM = 4.003 g/molV = 30 LT = 0 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of Ar goes from 200 kPa, 10 L, 15 °C to 450 kPa and 210 °C. Find the new volume V2.

P1 = 200 kPaV1 = 10 LT1 = 15 °CP2 = 450 kPaT2 = 210 °C
V2 = L
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 3/ν× M(CO2​)

20 g of Fe2O3 and 80 g of CO react according to Fe2O3 + 3CO → 2Fe + 3CO2. What mass m of CO2 can form?

M(Fe2O3) = 159.69M(CO) = 28.01M(CO2) = 44.01 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, 4 g of CaCO3 reacts completely (the other reactants are in excess) and 1.91 g of CaO is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CaO) = 56.08 g/molactual: 1.91 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 = 36. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.1 mol/LKc = 36
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I100C−x+x+xE1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 1 mol/LKc = 0.02
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 75 gT = 80 °Cc = 0.129 J/(g·°C)Waterm = 100 gT = 18 °Cc = 4.18 J/(g·°C)

A 75 g block of lead (c = 0.129 J/(g·°C)) at 80 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 18 °C in an insulated cup. Find the final temperature Tf.

mmetal = 75 gcmetal = 0.129 J/(g·°C)Tmetal = 80 °Cmwater = 100 gTwater = 18 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H20 g CH3​OH2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 20 g of CH3OH (M = 32.04 g/mol) burns completely: 2CH3OH + 3O₂ → 2CO₂ + 4H₂O(l). Give q as a positive number.

ΔH°f(CH3OH) = −238.7 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 = 0.05 L/(mol·min) and an initial concentration of 1 mol/L. Find its first half-life t½.

k = 0.05 L/(mol·min)CA0 = 1 mol/L
t½ = min
14.Reaction kineticsHard
Tk20 °C0.150 °C0.672

The rate constant of a reaction is 0.1 min⁻¹ at 20 °C and 0.672 min⁻¹ at 50 °C. Find the activation energy Ea.

k1 = 0.1 min⁻¹T1 = 20 °Ck2 = 0.672 min⁻¹T2 = 50 °CR = 8.314 J/(mol·K)
Ea = kJ/mol
15.Reactor sizing (CSTR & PFR)Medium
Q = 100 L/minX = 75%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 100 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 75% conversion of A.

Q = 100 L/mink = 0.05 min⁻¹X = 75%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 40 L/minX = ?V = 1000 L

A first-order liquid-phase reaction (k = 0.12 min⁻¹) runs in a 1000 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 = 1000 LQ = 40 L/mink = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT130 °C80 °C20 °C45 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 460 kW. The hot fluid cools from 130 to 80 °C and the cold fluid heats from 20 to 45 °C. The overall heat transfer coefficient is 800 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 460 kWU = 800 W/(m²·K)Th: 130 → 80 °CTc: 20 → 45 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT145 °C115 °C30.05 °C20 °CΔT₁ΔT₂counter-flow

Hot oil (1 kg/s, cp = 2.1 kJ/(kg·K)) cools from 145 to 115 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 20 °C. With U = 200 W/(m²·K), find the heat transfer area A needed.

ṁh = 1 kg/scp,h = 2.1 kJ/(kg·K)Th: 145 → 115 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 20 °CU = 200 W/(m²·K)
A = m²
19.Heat conductionMedium
Wood, k = 0.17250 mmConcrete, k = 1.4100 mm25 °C-14 °CQ̇ = ?

A wall is made of 250 mm of wood and 100 mm of concrete, with an area of 12 m². The outer faces are at 25 °C and -14 °C. Find the heat flow Q̇ through the wall.

L1 = 250 mm, k1 = 0.17 W/(m·K)L2 = 100 mm, k2 = 1.4 W/(m·K)A = 12 m²T1 = 25 °CT3 = -14 °C
Q̇ = W
20.Heat conductionHard
Gypsum board, k = 0.17250 mmConcrete, k = 1.475 mmroom 20 °Coutside -5 °CTs​ = ?Q̇

A wall of 250 mm gypsum board and 75 mm concrete separates a room at 20 °C from outside air at -5 °C. The convection coefficients are 10 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 6 m². Find the temperature Ts of the inside surface of the wall.

L1 = 250 mm, k1 = 0.17 W/(m·K)L2 = 75 mm, k2 = 1.4 W/(m·K)A = 6 m²hi = 10 W/(m²·K)ho = 25 W/(m²·K)Troom = 20 °CTout = -5 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1 m/sD = 50 mmL = 200 mf = 0.03

Water (ρ = 1000 kg/m³) flows at 1 m/s through a horizontal pipe, 200 m long, with an inside diameter of 50 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 = 1 m/sL = 200 mD = 50 mmf = 0.03ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 0.2Δz = 11 mL = 150 m, D = 300 mm, f = 0.0252× bend (K = 0.3)

Two open reservoirs are joined by a pipe 150 m long with an inside diameter of 300 mm and a Darcy friction factor f = 0.025. The water surface of the upper reservoir is 11 m above that of the lower one. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 0.2) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². Find the flow rate Q in L/s.

Δz = 11 mL = 150 mD = 300 mmf = 0.025Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 0.2Kexit = 1.0
Q = L/s
23.Pumps & pump powerMedium
PQ = 25 L/sH = 72 m

In a test, a pump delivers 25 L/s of water (ρ = 1000 kg/m³) against a head of 72 m while its shaft takes 23.5 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 25 L/sH = 72 mPshaft = 23.5 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 15 mL = 200 m, D = 150 mm, f = 0.025, ΣK = 6

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 15 m higher. The pipe is 200 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.025; the minor-loss coefficients add up to ΣK = 6 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 50 L/sΔz = 15 mL = 200 mD = 150 mmf = 0.025ΣK = 6
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 500 kg/h

Steady-state mass balance: in = out for the total and for each component. Blending problems combine both.

Balances

Total: ṁ3 = ṁ1 + ṁ2
sugar: ṁ1x1 + ṁ2x2 = (ṁ1 + ṁ2)x3

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 1000·(45 − 35)/(35 − 15) = 500 kg/h

Answer

ṁ2 = 500 kg/h
2.Mass balance

Answer: P = 1073 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 = 3900·11/40 = 1073 kg/h

Answer

P = 1073 kg/h
3.Energy balance

Answer: tout = 139.8 °C

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

Heat released by the hot stream

Q = 2·3.6·(160 − 60) = 720 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 25 + 720/(1.5·4.18) = 139.8 °C

Answer

tout = 139.8 °C
4.Energy balance

Answer: ṁc = 2.51 kg/s

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

Heat released

Qh = 3·3.6·(130 − 90) = 432 kW

Heat that reaches the water

Qc = (1 − 0.15)·432 = 367.2 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 367.2/(4.18·35) = 2.51 kg/s

Answer

ṁc = 2.51 kg/s
5.Ideal gas law

Answer: P = 5106 kPa

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

Moles

n = m/M = 270/4.003 = 67.45 mol
T = 0 + 273.15 = 273.1 K

Pressure

P = nRT/V = 67.45·8.314·273.1/0.03 = 5106 kPa

Answer

P = 5106 kPa
6.Ideal gas law

Answer: V2 = 7.452 L

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

Absolute temperatures

T1 = 288.1 K, T2 = 483.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(200/450)·(483.1/288.1) = 7.452 L

Answer

V2 = 7.452 L
7.Stoichiometry

Answer: m = 16.54 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(Fe2O3) = 20/159.69 = 0.1252 mol
n(CO) = 80/28.01 = 2.856 mol

Limiting reactant

0.1252/1 = 0.1252, 2.856/3 = 0.952 → Fe2O3

Mass of product

n(CO2) = 0.1252·3 = 0.3757 mol
m = 0.3757·44.01 = 16.54 g

Answer

m = 16.54 g
8.Stoichiometry

Answer: Y = 85.22 %

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) = 4/100.09 = 0.03996 mol
m = 0.03996·1/1·56.08 = 2.241 g

Percent yield

Y = 1.91/2.241·100 = 85.22%

Answer

Y = 85.22%
9.Chemical equilibrium

Answer: [H2] = 0.025 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/(0.1 − x)²

Take the square root

6 = 2x/(0.1 − x) → x = 0.1·6/(2 + 6) = 0.075 mol/L

Equilibrium concentration

[H₂] = 0.1 − x = 0.025 mol/L

Answer

[H2] = 0.025 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.8682 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

0.02 = x²/(1 − x) → x² + 0.02·x − 0.02 = 0

Solve the quadratic

x = (−0.02 + √(0.02² + 4·0.02))/2 = 0.1318 mol/L

Equilibrium concentration

[PCl₅] = 1 − 0.1318 = 0.8682 mol/L

Answer

[PCl5] = 0.8682 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 19.4 °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

75·0.129·(80 − Tf) = 100·4.18·(Tf − 18)

Solve for the final temperature

Tf = (9.675·80 + 418·18)/(9.675 + 418) = 19.4 °C

Answer

Tf = 19.4 °C
12.Calorimetry & enthalpy

Answer: q = 453.4 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° = [2·(−393.5) + 4·(−285.8)] − [2·(−238.7) + 3·0] = −1453 kJ

Heat for the given mass

n = 20/32.04 = 0.6242 mol
q = n·|ΔH°/2| = 0.6242·726.4 = 453.4 kJ

Answer

q = 453.4 kJ
13.Reaction kinetics

Answer: t½ = 20 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/(0.05·1) = 20 min

Answer

t½ = 20 min

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

14.Reaction kinetics

Answer: Ea = 50.01 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 = 293.1 K, T2 = 323.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·1.905/(-3.167e-4) = 50015 J/mol
Ea = 50.01 kJ/mol

Answer

Ea = 50.01 kJ/mol
15.Reactor sizing (CSTR & PFR)

Answer: V = 2773 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 − 0.75))/0.05 = 1.386/0.05 = 27.73 min

Volume

V = Q·τ = 100·27.73 = 2773 L

Answer

V = 2773 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 95.02 %

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 = 1000/40 = 25 min, kτ = 0.12·25 = 3

Conversion

X = 1 − e−kτ = 1 − e−3 = 95.02%

Answer

X = 95.02%
17.Heat exchangers (LMTD)

Answer: A = 8.779 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 parallel flow both inlets are at the same end, and both outlets at the other.

ΔT₁ = Th,in − Tc,in = 130 − 20 = 110 K
ΔT₂ = Th,out − Tc,out = 80 − 45 = 35 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (110 − 35)/ln(110/35) = 65.49 K

Area

A = Q̇/(U·ΔTlm) = 460000/(800·65.49) = 8.779 m²

Answer

A = 8.779 m²
18.Heat exchangers (LMTD)

Answer: A = 3.01 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) = 1·2.1·30 = 63 kW
Tc,out = 20 + 63/(1.5·4.18) = 30.05 °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 = 145 − 30.05 = 115 K
ΔT₂ = Th,out − Tc,in = 115 − 20 = 95 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (115 − 95)/ln(115/95) = 104.7 K

Area

A = Q̇/(U·ΔTlm) = 63000/(200·104.7) = 3.01 m²

Answer

A = 3.01 m²
19.Heat conduction

Answer: Q̇ = 303.5 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) = (250/1000)/(0.17·12) = 0.1225 K/W
R2 = L2/(k2A) = (100/1000)/(1.4·12) = 0.005952 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 39/0.1285 = 303.5 W

Answer

Q̇ = 303.5 W
20.Heat conduction

Answer: Ts = 18.5 °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/(10·6) = 0.01667 K/W
R1 = L1/(k1A) = (250/1000)/(0.17·6) = 0.2451 K/W
R2 = L2/(k2A) = (75/1000)/(1.4·6) = 0.008929 K/W
Ro = 1/(hoA) = 1/(25·6) = 0.006667 K/W
ΣR = 0.2774 K/W

Heat loss

Q̇ = (20 − (-5))/0.2774 = 90.14 W
Ts = Troom − Q̇·Ri = 20 − 90.14·0.01667 = 18.5 °C

Answer

Ts = 18.5 °C
21.Pipe friction & head loss

Answer: Δp = 60 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·(200/0.05)·1²/(2·9.81) = 6.116 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 = 1000·9.81·6.116 = 60000 Pa = 60 kPa

Answer

Δp = 60 kPa
22.Pipe friction & head loss

Answer: Q = 269.9 L/s

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.

Loss coefficients

f·L/D = 0.025·150/0.3 = 12.5
ΣK = 0.5 + 2·0.3 + 0.2 + 1.0 = 2.3

Energy equation

Both surfaces are open to the air and practically at rest, so all of Δz is lost in the pipe.

11 = (12.5 + 2.3)·V²/(2·9.81)
V = √(2·9.81·11/14.8) = 3.819 m/s

Flow rate

Q = V·π·D²/4 = 3.819·0.07069 = 0.2699 m³/s = 269.9 L/s

Answer

Q = 269.9 L/s
23.Pumps & pump power

Answer: η = 75.14 %

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 = 1000·9.81·0.025·72 = 17.66 kW

Efficiency

η = Ph/Pshaft = 17.66/23.5 = 75.14%

Answer

η = 75.14%
24.Pumps & pump power

Answer: H = 31.05 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) = (33.33 + 6)·0.408 = 16.05 m

Pump head

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

H = Δz + hL = 15 + 16.05 = 31.05 m

Answer

H = 31.05 m

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