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 1500 kg/h · 50% 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 = 500 kg/hx1 = 50 %x2 = 20 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3400 kg/h · 17% sugarProduct PP = ? · 65%Vapour W (pure water)0% sugar

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

F = 3400 kg/hxF = 17 %xP = 65 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 180 °C70 °Cwater · 30 °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: 180 → 70 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 120 °C60 °Cwater · 30 °C70 °C · ṁ = ?10% lost

Hot glycol mix heats water in an exchanger that loses 10% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 1.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 120 → 60 °Ct: 30 → 70 °Ccp,c = 4.18 kJ/(kg·K)loss = 10 %
ṁc = kg/s
5.Ideal gas lawMedium
420 g of N₂V = 50 LT = 15 °CP = ?

A tank of 50 L contains 420 g of N₂ at 15 °C. Treat it as an ideal gas and find the pressure P.

m = 420 gM = 28.01 g/molV = 50 LT = 15 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
He, M = 4.003 g/molP = 550 kPaT = 110 °Cρ = ?

Find the density ρ of He at 550 kPa and 110 °C, treating it as an ideal gas.

M = 4.003 g/molP = 550 kPaT = 110 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 1/ν× M(CO2​)

16 g of CH4 and 20 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(Mg)n(Mg)n(MgO)m(MgO)÷ M(Mg)× 2/2× M(MgO)

In the reaction 2Mg + O2 → 2MgO, 8 g of Mg reacts completely (the other reactants are in excess) and 7.29 g of MgO is collected. Find the percent yield Y.

M(Mg) = 24.31 g/molM(MgO) = 40.3 g/molactual: 7.29 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII110C−x−x+2xE1 − x1 − x2x

1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 1 mol/LKc = 16
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

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

[PCl₅]₀ = 0.5 mol/LKc = 0.5
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 50 gT = 120 °Cc = 0.129 J/(g·°C)Waterm = 400 gT = 19 °Cc = 4.18 J/(g·°C)

A 50 g block of lead (c = 0.129 J/(g·°C)) at 120 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 19 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.129 J/(g·°C)Tmetal = 120 °Cmwater = 400 gTwater = 19 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H20 g C2​H5​OHC2​H5​OH + 3O₂reactants2CO₂ + 3H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 20 g of C2H5OH (M = 46.07 g/mol) burns completely: C2H5OH + 3O₂ → 2CO₂ + 3H₂O(l). Give q as a positive number.

ΔH°f(C2H5OH) = −277.7 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)X (%)t = ?75%

A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.8 L/(mol·min) and starts at 0.5 mol/L. How long does it take to reach 75% conversion? Find t.

k = 0.8 L/(mol·min)CA0 = 0.5 mol/LX = 75 %
t = min
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.50.008run 210.0226n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.5 mol/L the rate is 0.008 mol/(L·s); with CA0 = 1 mol/L it is 0.0226 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.5 mol/Lr1 = 0.008 mol/(L·s)CA0,2 = 1 mol/Lr2 = 0.0226 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 100 L/minX = 85%V = ?, k = 0.3 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.3 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 85% conversion of A.

Q = 100 L/mink = 0.3 min⁻¹X = 85%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 40 L/minX = ?V = 400 L

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 400 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 = 400 LQ = 40 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT130 °C105 °C20 °C10 °CΔT₁ΔT₂counter-flow

A shell-and-tube heat exchanger (one shell pass, two tube passes) must transfer 150 kW. The hot fluid cools from 130 to 105 °C and the cold fluid heats from 10 to 20 °C. The LMTD correction factor for this arrangement is F = 0.85, and U = 300 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 150 kWF = 0.85U = 300 W/(m²·K)Th: 130 → 105 °CTc: 10 → 20 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT145 °C35 °C30.18 °C10 °CΔT₁ΔT₂counter-flow

Hot oil (0.5 kg/s, cp = 2.3 kJ/(kg·K)) cools from 145 to 35 °C in a counter-flow exchanger. It heats 1.5 kg/s of water (cp = 4.18 kJ/(kg·K)) that enters at 10 °C. With U = 1500 W/(m²·K), find the heat transfer area A needed.

ṁh = 0.5 kg/scp,h = 2.3 kJ/(kg·K)Th: 145 → 35 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)Tc,in = 10 °CU = 1500 W/(m²·K)
A = m²
19.Heat conductionMedium
Expanded polystyrene, k = 0.035100 mmConcrete, k = 1.4150 mm22 °C-5 °CQ̇ = ?

A wall is made of 100 mm of expanded polystyrene and 150 mm of concrete, with an area of 8 m². The outer faces are at 22 °C and -5 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.035 W/(m·K)L2 = 150 mm, k2 = 1.4 W/(m·K)A = 8 m²T1 = 22 °CT3 = -5 °C
Q̇ = W
20.Heat conductionHard
Expanded polystyrene, k = 0.035250 mmGlass, k = 0.96150 mmroom 21 °Coutside -8 °CQ̇

A wall of 250 mm expanded polystyrene and 150 mm glass separates a room at 21 °C from outside air at -8 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 15 m². Find the overall heat transfer coefficient U of the wall.

L1 = 250 mm, k1 = 0.035 W/(m·K)L2 = 150 mm, k2 = 0.96 W/(m·K)A = 15 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 21 °CTout = -8 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 2.4 m/sD = 150 mmL = 300 mf = 0.025

Water flows at a mean velocity of 2.4 m/s through a pipe 300 m long with an inside diameter of 150 mm. Use the Darcy friction factor f = 0.025 and g = 9.81 m/s². Find the friction head loss hf.

V = 2.4 m/sL = 300 mD = 150 mmf = 0.025g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5free outletH = ?L = 300 m, D = 300 mm, f = 0.022× bend (K = 0.3)

A pipe 300 m long with an inside diameter of 300 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), 2 bends (K = 0.3 each) and a valve (K = 5). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 75 L/s?

Q = 75 L/sL = 300 mD = 300 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 5
H = m
23.Pumps & pump powerMedium
PQ = 100 L/sH = 66 m

In a test, a pump delivers 100 L/s of water (ρ = 1000 kg/m³) against a head of 66 m while its shaft takes 107.9 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 100 L/sH = 66 mPshaft = 107.9 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 75 L/sΔz = 20 mL = 100 m, D = 200 mm, f = 0.025, ΣK = 5

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 20 m higher. The pipe is 100 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.025; 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 = 75 L/sΔz = 20 mL = 100 mD = 200 mmf = 0.025ΣK = 5
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 2500 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) = 500·(50 − 25)/(25 − 20) = 2500 kg/h

Answer

ṁ2 = 2500 kg/h
2.Mass balance

Answer: P = 889.2 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 = 3400·17/65 = 889.2 kg/h

Answer

P = 889.2 kg/h
3.Energy balance

Answer: tout = 124.7 °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·(180 − 70) = 792 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 792/(2·4.18) = 124.7 °C

Answer

tout = 124.7 °C
4.Energy balance

Answer: ṁc = 1.744 kg/s

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

Heat released

Qh = 1.5·3.6·(120 − 60) = 324 kW

Heat that reaches the water

Qc = (1 − 0.1)·324 = 291.6 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 291.6/(4.18·40) = 1.744 kg/s

Answer

ṁc = 1.744 kg/s
5.Ideal gas law

Answer: P = 718.4 kPa

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

Moles

n = m/M = 420/28.01 = 14.99 mol
T = 15 + 273.15 = 288.1 K

Pressure

P = nRT/V = 14.99·8.314·288.1/0.05 = 718.4 kPa

Answer

P = 718.4 kPa
6.Ideal gas law

Answer: ρ = 0.6911 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 110 + 273.15 = 383.1 K

Density

ρ = 550·4.003/(8.314·383.1) = 0.6911 kg/m³

Answer

ρ = 0.6911 kg/m³
7.Stoichiometry

Answer: m = 13.75 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) = 16/16.04 = 0.9975 mol
n(O2) = 20/32 = 0.625 mol

Limiting reactant

0.9975/1 = 0.9975, 0.625/2 = 0.3125 → O2

Mass of product

n(CO2) = 0.3125·1 = 0.3125 mol
m = 0.3125·44.01 = 13.75 g

Answer

m = 13.75 g
8.Stoichiometry

Answer: Y = 54.97 %

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Theoretical yield

n(Mg) = 8/24.31 = 0.3291 mol
m = 0.3291·2/2·40.3 = 13.26 g

Percent yield

Y = 7.29/13.26·100 = 54.97%

Answer

Y = 54.97%
9.Chemical equilibrium

Answer: [H2] = 0.3333 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

16 = (2x)²/(1 − x)²

Take the square root

4 = 2x/(1 − x) → x = 1·4/(2 + 4) = 0.6667 mol/L

Equilibrium concentration

[H₂] = 1 − x = 0.3333 mol/L

Answer

[H2] = 0.3333 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.191 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

0.5 = x²/(0.5 − x) → x² + 0.5·x − 0.25 = 0

Solve the quadratic

x = (−0.5 + √(0.5² + 4·0.25))/2 = 0.309 mol/L

Equilibrium concentration

[PCl₅] = 0.5 − 0.309 = 0.191 mol/L

Answer

[PCl5] = 0.191 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 19.39 °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

50·0.129·(120 − Tf) = 400·4.18·(Tf − 19)

Solve for the final temperature

Tf = (6.45·120 + 1672·19)/(6.45 + 1672) = 19.39 °C

Answer

Tf = 19.39 °C
12.Calorimetry & enthalpy

Answer: q = 593.3 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) + 3·(−285.8)] − [1·(−277.7) + 3·0] = −1367 kJ

Heat for the given mass

n = 20/46.07 = 0.4341 mol
q = n·|ΔH°/1| = 0.4341·1367 = 593.3 kJ

Answer

q = 593.3 kJ
13.Reaction kinetics

Answer: t = 7.5 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 = 0.5·(1 − 0.75) = 0.125 mol/L

Integrated second-order law

t = (1/CA − 1/CA0)/k = (8 − 2)/0.8 = 7.5 min

Answer

t = 7.5 min
14.Reaction kinetics

Answer: n = 1.498

Method of initial rates: for r = k·Cⁿ, comparing two runs that differ only in the starting concentration removes k: r₂/r₁ = (C₂/C₁)ⁿ. Doubling C doubles the rate for first order and quadruples it for second order.

Ratios

r2/r1 = 0.0226/0.008 = 2.825
C2/C1 = 1/0.5 = 2

Order

n = ln(2.825)/ln(2) = 1.498

Answer

n = 1.498
15.Reactor sizing (CSTR & PFR)

Answer: V = 632.4 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))/0.3 = 1.897/0.3 = 6.324 min

Volume

V = Q·τ = 100·6.324 = 632.4 L

Answer

V = 632.4 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 91.79 %

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 = 400/40 = 10 min, kτ = 0.25·10 = 2.5

Conversion

X = 1 − e−kτ = 1 − e−2.5 = 91.79%

Answer

X = 91.79%
17.Heat exchangers (LMTD)

Answer: A = 5.749 m²

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

End temperature differences (counter-flow)

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

ΔT₁ = Th,in − Tc,out = 130 − 20 = 110 K
ΔT₂ = Th,out − Tc,in = 105 − 10 = 95 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (110 − 95)/ln(110/95) = 102.3 K

Area

A = Q̇/(U·F·ΔTlm,cf) = 150000/(300·0.85·102.3) = 5.749 m²

Answer

A = 5.749 m²
18.Heat exchangers (LMTD)

Answer: A = 1.431 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) = 0.5·2.3·110 = 126.5 kW
Tc,out = 10 + 126.5/(1.5·4.18) = 30.18 °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 − 30.18 = 114.8 K
ΔT₂ = Th,out − Tc,in = 35 − 10 = 25 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (114.8 − 25)/ln(114.8/25) = 58.92 K

Area

A = Q̇/(U·ΔTlm) = 126500/(1500·58.92) = 1.431 m²

Answer

A = 1.431 m²
19.Heat conduction

Answer: Q̇ = 72.87 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)/(0.035·8) = 0.3571 K/W
R2 = L2/(k2A) = (150/1000)/(1.4·8) = 0.01339 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 27/0.3705 = 72.87 W

Answer

Q̇ = 72.87 W
20.Heat conduction

Answer: U = 0.134 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/(7.7·15) = 0.008658 K/W
R1 = L1/(k1A) = (250/1000)/(0.035·15) = 0.4762 K/W
R2 = L2/(k2A) = (150/1000)/(0.96·15) = 0.01042 K/W
Ro = 1/(hoA) = 1/(30·15) = 0.002222 K/W
ΣR = 0.4975 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(15·0.4975) = 0.134 W/(m²·K)

Answer

U = 0.134 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 14.68 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) = 2.4²/(2·9.81) = 0.2936 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.025·(300/0.15)·2.4²/(2·9.81) = 14.68 m

Answer

hf = 14.68 m
22.Pipe friction & head loss

Answer: H = 1.555 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 = 0.075/0.07069 = 1.061 m/s
V²/(2g) = 0.05738 m

Loss coefficients

f·L/D = 0.02·300/0.3 = 20
ΣK = 0.5 + 2·0.3 + 5 = 6.1

Energy equation

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

H = (1 + 20 + 6.1)·0.05738 = 1.555 m

Answer

H = 1.555 m
23.Pumps & pump power

Answer: η = 60.01 %

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 = 1000·9.81·0.1·66 = 64.75 kW

Efficiency

η = Ph/Pshaft = 64.75/107.9 = 60.01%

Answer

η = 60.01%
24.Pumps & pump power

Answer: H = 25.08 m

Pump power: the power given to the water is the hydraulic power Ph = ρ·g·Q·H = Q·Δp. The shaft must deliver more because the pump loses some: Pshaft = Ph/ηpump, and the motor draws Pel = Pshaft/ηmotor. The pump head H follows from the energy equation: static lift + pressure head + all friction and minor losses.

Velocity

V = Q/A = 0.075/0.03142 = 2.387 m/s
V²/(2g) = 0.2905 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (12.5 + 5)·0.2905 = 5.083 m

Pump head

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

H = Δz + hL = 20 + 5.083 = 25.08 m

Answer

H = 25.08 m

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