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 1200 kg/h · 15% NaOHStream 2ṁ₂ = ? · 50% NaOHProduct35% NaOH

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

ṁ1 = 200 kg/hx1 = 15 %x2 = 50 %x3 = 35 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1000 kg/h · 11% sugarProduct P60% sugarVapour W (pure water)W = ? kg/h

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

F = 1000 kg/hxF = 11 %xP = 60 %
W = kg/h
3.Energy balanceMedium
hot sidecold sidelight oil · 180 °C90 °Cwater · 30 °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: 180 → 90 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sideglycol mix · 120 °C60 °Cwater · 30 °C80 °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 = 0.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 120 → 60 °Ct: 30 → 80 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
240 g of N₂V = 10 LT = 60 °CP = ?

A tank of 10 L contains 240 g of N₂ at 60 °C. Treat it as an ideal gas and find the pressure P.

m = 240 gM = 28.01 g/molV = 10 LT = 60 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
O₂, M = 32 g/molP = 950 kPaT = 60 °Cρ = ?

Find the density ρ of O₂ at 950 kPa and 60 °C, treating it as an ideal gas.

M = 32 g/molP = 950 kPaT = 60 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NH3​)m(NH3​)÷ M(X)× 2/ν× M(NH3​)

30 g of N2 and 40 g of H2 react according to N2 + 3H2 → 2NH3. What mass m of NH3 can form?

M(N2) = 28.02M(H2) = 2.016M(NH3) = 17.03 g/mol
m = g
8.StoichiometryHard
m(N2​)n(N2​)n(NH3​)m(NH3​)÷ M(N2​)× 2/1× M(NH3​)

In the reaction N2 + 3H2 → 2NH3, 24 g of N2 reacts completely (the other reactants are in excess) and 26.55 g of NH3 is collected. Find the percent yield Y.

M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 26.55 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.250.250C−x−x+2xE0.25 − x0.25 − x2x

0.25 mol/L of H₂ and 0.25 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 50. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 50
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.1 mol/LKc = 0.02
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 250 gT = 80 °Cc = 0.388 J/(g·°C)Waterm = 200 gT = 20 °Cc = 4.18 J/(g·°C)

A 250 g block of zinc (c = 0.388 J/(g·°C)) at 80 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 20 °C in an insulated cup. Find the final temperature Tf.

mmetal = 250 gcmetal = 0.388 J/(g·°C)Tmetal = 80 °Cmwater = 200 gTwater = 20 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HCH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction CH4 + 2O₂ → CO₂ + 2H₂O(l).

ΔH°f(CH4) = −74.8 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)C (mol/L)20 min0.96

In a first-order reaction the concentration of A falls from 1.2 mol/L to 0.96 mol/L in 20 min. Find the rate constant k.

CA0 = 1.2 mol/LCA = 0.96 mol/Lt = 20 min
k = min⁻¹
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.250.008run 20.50.0226n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.25 mol/L the rate is 0.008 mol/(L·s); with CA0 = 0.5 mol/L it is 0.0226 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.25 mol/Lr1 = 0.008 mol/(L·s)CA0,2 = 0.5 mol/Lr2 = 0.0226 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 80 L/minX = 50%V = ?, k = 0.05 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.05 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 80 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 50% conversion of A.

Q = 80 L/mink = 0.05 min⁻¹X = 50%
V = L
16.Reactor sizing (CSTR & PFR)Hard
Q = 10 L/minX = ?V = 200 L

A first-order liquid-phase reaction (k = 0.2 min⁻¹) runs in a 200 L plug-flow reactor (PFR) fed at 10 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 200 LQ = 10 L/mink = 0.2 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT80 °C50 °C10 °C20 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 340 kW. Its heat transfer area is 6 m². The hot fluid cools from 80 to 50 °C and the cold fluid heats from 10 to 20 °C. Find the overall heat transfer coefficient U.

Q̇ = 340 kWA = 6 m²Th: 80 → 50 °CTc: 10 → 20 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT95 °C50 °C?25 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.3 kg/s, cp = 2.5 kJ/(kg·K)) flows in the inner tube and cools from 95 to 50 °C. Water (1 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 25 °C. The inner tube has a diameter of 50 mm, and U = 250 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.3 kg/scp,h = 2.5 kJ/(kg·K)Th: 95 → 50 °Cṁc = 1 kg/sTc,in = 25 °CD = 50 mmU = 250 W/(m²·K)
L = m
19.Heat conductionMedium
Expanded polystyrene, k = 0.035250 mmGypsum board, k = 0.1750 mm22 °C-12 °CQ̇ = ?

A wall is made of 250 mm of expanded polystyrene and 50 mm of gypsum board, with an area of 12 m². The outer faces are at 22 °C and -12 °C. Find the heat flow Q̇ through the wall.

L1 = 250 mm, k1 = 0.035 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 12 m²T1 = 22 °CT3 = -12 °C
Q̇ = W
20.Heat conductionHard
Glass, k = 0.96250 mmGypsum board, k = 0.17100 mmroom 22 °Coutside 4 °CQ̇

A wall of 250 mm glass and 100 mm gypsum board separates a room at 22 °C from outside air at 4 °C. The convection coefficients are 7.7 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 4 m². Find the overall heat transfer coefficient U of the wall.

L1 = 250 mm, k1 = 0.96 W/(m·K)L2 = 100 mm, k2 = 0.17 W/(m·K)A = 4 m²hi = 7.7 W/(m²·K)ho = 20 W/(m²·K)Troom = 22 °CTout = 4 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
V = 2.4 m/sD = 200 mmL = 150 mf = 0.03

Water (ρ = 1000 kg/m³) flows at 2.4 m/s through a horizontal pipe, 150 m long, with an inside diameter of 200 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the pressure drop Δp over the pipe in kPa.

V = 2.4 m/sL = 150 mD = 200 mmf = 0.03ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 400 m, D = 300 mm, f = 0.0152× bend (K = 0.3)

A pipe 400 m long with an inside diameter of 300 mm (Darcy friction factor f = 0.015) 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 = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 150 L/s?

Q = 150 L/sL = 400 mD = 300 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 80 L/sH = 78 m

A pump delivers 80 L/s of water (ρ = 1000 kg/m³) against a head of 78 m. The pump efficiency is 60% 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 = 80 L/sH = 78 mηpump = 60%ηmotor = 92%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
200 kPa (gauge)PQ = 50 L/sΔz = 9 mL = 300 m, D = 150 mm, f = 0.022, ΣK = 4

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 9 m higher. The pipe is 300 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.022; the minor-loss coefficients add up to ΣK = 4 (entrance and exit included). Use g = 9.81 m/s². The upper tank is closed and the air above its water is at a gauge pressure of 200 kPa. Find the head H the pump must add.

Q = 50 L/sΔz = 9 mL = 300 mD = 150 mmf = 0.022ΣK = 4ptank = 200 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 266.7 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) = 200·(15 − 35)/(35 − 50) = 266.7 kg/h

Answer

ṁ2 = 266.7 kg/h
2.Mass balance

Answer: W = 816.7 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 = 1000·11/60 = 183.3 kg/h

Total balance

W = F − P = 1000 − 183.3 = 816.7 kg/h

Answer

W = 816.7 kg/h
3.Energy balance

Answer: tout = 75.22 °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·(180 − 90) = 283.5 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 283.5/(1.5·4.18) = 75.22 °C

Answer

tout = 75.22 °C
4.Energy balance

Answer: ṁc = 0.4392 kg/s

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

Heat released

Qh = 0.5·3.6·(120 − 60) = 108 kW

Heat that reaches the water

Qc = (1 − 0.15)·108 = 91.8 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 91.8/(4.18·50) = 0.4392 kg/s

Answer

ṁc = 0.4392 kg/s
5.Ideal gas law

Answer: P = 2373 kPa

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

Moles

n = m/M = 240/28.01 = 8.568 mol
T = 60 + 273.15 = 333.1 K

Pressure

P = nRT/V = 8.568·8.314·333.1/0.01 = 2373 kPa

Answer

P = 2373 kPa
6.Ideal gas law

Answer: ρ = 10.98 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 60 + 273.15 = 333.1 K

Density

ρ = 950·32/(8.314·333.1) = 10.98 kg/m³

Answer

ρ = 10.98 kg/m³
7.Stoichiometry

Answer: m = 36.47 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(N2) = 30/28.02 = 1.071 mol
n(H2) = 40/2.016 = 19.84 mol

Limiting reactant

1.071/1 = 1.071, 19.84/3 = 6.614 → N2

Mass of product

n(NH3) = 1.071·2 = 2.141 mol
m = 2.141·17.03 = 36.47 g

Answer

m = 36.47 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(N2) = 24/28.02 = 0.8565 mol
m = 0.8565·2/1·17.03 = 29.17 g

Percent yield

Y = 26.55/29.17·100 = 91.01%

Answer

Y = 91.01%
9.Chemical equilibrium

Answer: [H2] = 0.05512 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

50 = (2x)²/(0.25 − x)²

Take the square root

7.071 = 2x/(0.25 − x) → x = 0.25·7.071/(2 + 7.071) = 0.1949 mol/L

Equilibrium concentration

[H₂] = 0.25 − x = 0.05512 mol/L

Answer

[H2] = 0.05512 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.06417 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/(0.1 − x) → x² + 0.02·x − 0.002 = 0

Solve the quadratic

x = (−0.02 + √(0.02² + 4·0.002))/2 = 0.03583 mol/L

Equilibrium concentration

[PCl₅] = 0.1 − 0.03583 = 0.06417 mol/L

Answer

[PCl5] = 0.06417 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 26.24 °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

250·0.388·(80 − Tf) = 200·4.18·(Tf − 20)

Solve for the final temperature

Tf = (97·80 + 836·20)/(97 + 836) = 26.24 °C

Answer

Tf = 26.24 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −890.3 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° = [1·(−393.5) + 2·(−285.8)] − [1·(−74.8) + 2·0] = −890.3 kJ

Answer

ΔH° = −890.3 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.01116 min⁻¹

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).

Integrated first-order law

k = ln(CA0/CA)/t = ln(1.2/0.96)/20 = 0.2231/20 = 0.01116 min⁻¹

Answer

k = 0.01116 min⁻¹
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 = 0.5/0.25 = 2

Order

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

Answer

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

Answer: V = 1109 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 − 0.5))/0.05 = 0.6931/0.05 = 13.86 min

Volume

V = Q·τ = 80·13.86 = 1109 L

Answer

V = 1109 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 98.17 %

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 = 200/10 = 20 min, kτ = 0.2·20 = 4

Conversion

X = 1 − e−kτ = 1 − e−4 = 98.17%

Answer

X = 98.17%
17.Heat exchangers (LMTD)

Answer: U = 1200 W/(m²·K)

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 = 80 − 10 = 70 K
ΔT₂ = Th,out − Tc,out = 50 − 20 = 30 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (70 − 30)/ln(70/30) = 47.21 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 340000/(6·47.21) = 1200 W/(m²·K)

Answer

U = 1200 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: L = 21.11 m

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 = 0.3·2.5·(95 − 50) = 33.75 kW
Tc,out = 25 + 33.75/(1·4.18) = 33.07 °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 = 95 − 33.07 = 61.93 K
ΔT₂ = Th,out − Tc,in = 50 − 25 = 25 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (61.93 − 25)/ln(61.93/25) = 40.71 K

Area and length

A = 33750/(250·40.71) = 3.316 m²
L = A/(πD) = 3.316/(π·0.05) = 21.11 m

Answer

L = 21.11 m
19.Heat conduction

Answer: Q̇ = 54.86 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)/(0.035·12) = 0.5952 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·12) = 0.02451 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 34/0.6197 = 54.86 W

Answer

Q̇ = 54.86 W
20.Heat conduction

Answer: U = 0.9723 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/(7.7·4) = 0.03247 K/W
R1 = L1/(k1A) = (250/1000)/(0.96·4) = 0.0651 K/W
R2 = L2/(k2A) = (100/1000)/(0.17·4) = 0.1471 K/W
Ro = 1/(hoA) = 1/(20·4) = 0.0125 K/W
ΣR = 0.2571 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(4·0.2571) = 0.9723 W/(m²·K)

Answer

U = 0.9723 W/(m²·K)
21.Pipe friction & head loss

Answer: Δp = 64.8 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·(150/0.2)·2.4²/(2·9.81) = 6.606 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 = 1000·9.81·6.606 = 64800 Pa = 64.8 kPa

Answer

Δp = 64.8 kPa
22.Pipe friction & head loss

Answer: H = 5.531 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 = 0.15/0.07069 = 2.122 m/s
V²/(2g) = 0.2295 m

Loss coefficients

f·L/D = 0.015·400/0.3 = 20
ΣK = 0.5 + 2·0.3 + 2 = 3.1

Energy equation

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

H = (1 + 20 + 3.1)·0.2295 = 5.531 m

Answer

H = 5.531 m
23.Pumps & pump power

Answer: Pel = 110.9 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 = 1000·9.81·0.08·78 = 61.21 kW

Shaft power

Pshaft = 61.21/0.6 = 102 kW

Electrical power

Pel = 102/0.92 = 110.9 kW

Answer

Pel = 110.9 kW
24.Pumps & pump power

Answer: H = 48.97 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) = (44 + 4)·0.408 = 19.59 m

Pressure head

p/(ρ·g) = 200000/(1000·9.81) = 20.39 m

Pump head

Both surfaces are practically at rest, so there is no velocity head term.

H = Δz + p/(ρ·g) + hL = 9 + 20.39 + 19.59 = 48.97 m

Answer

H = 48.97 m

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