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 · 30% sugarStream 2ṁ₂ = ? · 15% sugarProduct25% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 25% sugar? Find ṁ2.

ṁ1 = 200 kg/hx1 = 30 %x2 = 15 %x3 = 25 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2300 kg/h · 18% sugarProduct PP = ? · 30%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 = 2300 kg/hxF = 18 %xP = 30 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 170 °C140 °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 = 2.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 170 → 140 °Cṁc = 1 kg/scp,c = 4.18 kJ/(kg·K)tin = 30 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 140 °C80 °Cwater · 10 °C60 °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 = 1.5 kg/scp,h = 2.1 kJ/(kg·K)Th: 140 → 80 °Ct: 10 → 60 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
60 g of ArP = 300 kPaT = 10 °CV = ?

What volume V does 60 g of Ar occupy at 300 kPa and 10 °C? Treat it as an ideal gas.

m = 60 gM = 39.95 g/molP = 300 kPaT = 10 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
Ar, M = 39.95 g/molP = 950 kPaT = 60 °Cρ = ?

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

M = 39.95 g/molP = 950 kPaT = 60 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(CO2​)m(CO2​)÷ M(X)× 3/ν× M(CO2​)

30 g of Fe2O3 and 24 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(C6​H12​O6​)n(C6​H12​O6​)n(C2​H5​OH)m(C2​H5​OH)÷ M(C6​H12​O6​)× 2/1× M(C2​H5​OH)

In the reaction C6H12O6 → 2C2H5OH + 2CO2, 20 g of C6H12O6 reacts completely (the other reactants are in excess) and 6.34 g of C2H5OH is collected. Find the percent yield Y.

M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 6.34 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 = 36. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]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 = 0.04 at the reaction temperature. A container starts with 1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 1 mol/LKc = 0.04
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 100 gT = 130 °Cc = 0.388 J/(g·°C)Waterm = 150 gT = 15 °Cc = 4.18 J/(g·°C)

A 100 g block of zinc (c = 0.388 J/(g·°C)) at 130 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 15 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.388 J/(g·°C)Tmetal = 130 °Cmwater = 150 gTwater = 15 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H250 g C6​H12​O6​C6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 250 g of C6H12O6 (M = 180.16 g/mol) burns completely: C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C6H12O6) = −1274 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 = 0.8 L/(mol·min) and an initial concentration of 2 mol/L. Find its first half-life t½.

k = 0.8 L/(mol·min)CA0 = 2 mol/L
t½ = min
14.Reaction kineticsHard
t (min)X (%)60 minX = ?

A first-order reaction has k = 0.01 min⁻¹ at 30 °C and an activation energy of 60 kJ/mol. The batch reactor is now run at 60 °C for 60 min. Find the conversion X reached.

k1 = 0.01 min⁻¹T1 = 30 °CEa = 60 kJ/molT2 = 60 °Ct = 60 minR = 8.314 J/(mol·K)
X = %
15.Reactor sizing (CSTR & PFR)Medium
QX = 75%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 75% conversion. How many times larger must a CSTR be than a PFR for the same feed rate, rate constant and conversion? Find the ratio VCSTR/VPFR.

X = 75%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
Q = 50 L/minX = ?V = 150 L

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in a 150 L plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 150 LQ = 50 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT135 °C95 °C25 °C60 °CΔT₁ΔT₂parallel flow

A parallel-flow heat exchanger transfers 250 kW. Its heat transfer area is 20 m². The hot fluid cools from 135 to 95 °C and the cold fluid heats from 25 to 60 °C. Find the overall heat transfer coefficient U.

Q̇ = 250 kWA = 20 m²Th: 135 → 95 °CTc: 25 → 60 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT120 °C??10 °CΔT₁ΔT₂counter-flow

In a counter-flow heat exchanger both streams have the same heat capacity rate, ṁ·cp = 3 kW/K. The hot stream enters at 120 °C and the cold stream at 10 °C. The exchanger has A = 1.5 m² and U = 800 W/(m²·K). Find the hot outlet temperature Th,out.

Ch = Cc = 3 kW/KTh,in = 120 °CTc,in = 10 °CA = 1.5 m²U = 800 W/(m²·K)
Th,out = °C
19.Heat conductionMedium
Concrete, k = 1.4250 mmWood, k = 0.17150 mm21 °C-10 °CQ̇ = ?

A wall is made of 250 mm of concrete and 150 mm of wood, with an area of 15 m². The outer faces are at 21 °C and -10 °C. Find the heat flow Q̇ through the wall.

L1 = 250 mm, k1 = 1.4 W/(m·K)L2 = 150 mm, k2 = 0.17 W/(m·K)A = 15 m²T1 = 21 °CT3 = -10 °C
Q̇ = W
20.Heat conductionHard
Concrete, k = 1.450 mmBrick, k = 0.7225 mmroom 20 °Coutside -15 °CQ̇ = ?

A wall of 50 mm concrete and 25 mm brick separates a room at 20 °C from outside air at -15 °C. The convection coefficients are 6 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 6 m². Find the heat loss Q̇ through the wall.

L1 = 50 mm, k1 = 1.4 W/(m·K)L2 = 25 mm, k2 = 0.72 W/(m·K)A = 6 m²hi = 6 W/(m²·K)ho = 20 W/(m²·K)Troom = 20 °CTout = -15 °C
Q̇ = W
21.Pipe friction & head lossMedium
Q = 8 L/sD = 75 mmL = 1000 mf = 0.028

Water flows at 8 L/s through a pipe 1000 m long with an inside diameter of 75 mm. Use the Darcy friction factor f = 0.028 and g = 9.81 m/s². Find the friction head loss hf.

Q = 8 L/sL = 1000 mD = 75 mmf = 0.028g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 2free outletH = ?L = 150 m, D = 100 mm, f = 0.0184× bend (K = 0.3)

A pipe 150 m long with an inside diameter of 100 mm (Darcy friction factor f = 0.018) 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 = 2). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 15 L/s?

Q = 15 L/sL = 150 mD = 100 mmf = 0.018Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 2
H = m
23.Pumps & pump powerMedium
PQ = 10 L/sH = 42 m

A pump delivers 10 L/s of water (ρ = 1000 kg/m³) against a head of 42 m. The pump efficiency is 70% and the electric motor driving it has an efficiency of 94%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 10 L/sH = 42 mηpump = 70%ηmotor = 94%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 15 mL = 500 m, D = 150 mm, f = 0.015, 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 500 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.015; 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 = 500 mD = 150 mmf = 0.015ΣK = 6
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 100 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) = 200·(30 − 25)/(25 − 15) = 100 kg/h

Answer

ṁ2 = 100 kg/h
2.Mass balance

Answer: P = 1380 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 = 2300·18/30 = 1380 kg/h

Answer

P = 1380 kg/h
3.Energy balance

Answer: tout = 94.59 °C

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

Heat released by the hot stream

Q = 2.5·3.6·(170 − 140) = 270 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 30 + 270/(1·4.18) = 94.59 °C

Answer

tout = 94.59 °C
4.Energy balance

Answer: ṁc = 0.7687 kg/s

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

Heat released

Qh = 1.5·2.1·(140 − 80) = 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/(4.18·50) = 0.7687 kg/s

Answer

ṁc = 0.7687 kg/s
5.Ideal gas law

Answer: V = 11.79 L

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

Moles

n = 60/39.95 = 1.502 mol
T = 10 + 273.15 = 283.1 K

Volume

V = nRT/P = 1.502·8.314·283.1/300 = 11.79 L

Answer

V = 11.79 L
6.Ideal gas law

Answer: ρ = 13.7 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 = 950·39.95/(8.314·333.1) = 13.7 kg/m³

Answer

ρ = 13.7 kg/m³
7.Stoichiometry

Answer: m = 24.8 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) = 30/159.69 = 0.1879 mol
n(CO) = 24/28.01 = 0.8568 mol

Limiting reactant

0.1879/1 = 0.1879, 0.8568/3 = 0.2856 → Fe2O3

Mass of product

n(CO2) = 0.1879·3 = 0.5636 mol
m = 0.5636·44.01 = 24.8 g

Answer

m = 24.8 g
8.Stoichiometry

Answer: Y = 61.98 %

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

Theoretical yield

n(C6H12O6) = 20/180.16 = 0.111 mol
m = 0.111·2/1·46.07 = 10.23 g

Percent yield

Y = 6.34/10.23·100 = 61.98%

Answer

Y = 61.98%
9.Chemical equilibrium

Answer: [H2] = 0.25 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/(1 − x)²

Take the square root

6 = 2x/(1 − x) → x = 1·6/(2 + 6) = 0.75 mol/L

Equilibrium concentration

[H₂] = 1 − x = 0.25 mol/L

Answer

[H2] = 0.25 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.819 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/(1 − x) → x² + 0.04·x − 0.04 = 0

Solve the quadratic

x = (−0.04 + √(0.04² + 4·0.04))/2 = 0.181 mol/L

Equilibrium concentration

[PCl₅] = 1 − 0.181 = 0.819 mol/L

Answer

[PCl5] = 0.819 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 21.7 °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

100·0.388·(130 − Tf) = 150·4.18·(Tf − 15)

Solve for the final temperature

Tf = (38.8·130 + 627·15)/(38.8 + 627) = 21.7 °C

Answer

Tf = 21.7 °C
12.Calorimetry & enthalpy

Answer: q = 3888 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

Heat for the given mass

n = 250/180.16 = 1.388 mol
q = n·|ΔH°/1| = 1.388·2802 = 3888 kJ

Answer

q = 3888 kJ
13.Reaction kinetics

Answer: t½ = 0.625 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/(0.8·2) = 0.625 min

Answer

t½ = 0.625 min

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

14.Reaction kinetics

Answer: X = 99.4 %

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).

Rate constant at the new temperature

T1 = 303.1 K, T2 = 333.1 K
k2 = 0.01·e−(60000/8.314)·(1/333.1 − 1/303.1) = 0.08531 min⁻¹

Conversion

X = 1 − e−0.08531·60 = 1 − 0.005984 = 99.4 %

Answer

X = 99.4 %
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 2.164

Ideal reactors, first-order reaction (−rA = k·CA) at steady state, with space time τ = V/Q. A CSTR is perfectly mixed, so the whole volume reacts at the low outlet concentration: τ = X/(k·(1 − X)) and CA = CA0/(1 + k·τ). In a PFR each slice of fluid reacts like a small batch reactor: τ = ln(1/(1 − X))/k and CA = CA0·e−k·τ. For the same conversion a CSTR always needs more volume than a PFR.

k·τ for each reactor

CSTR: k·τ = X/(1 − X) = 0.75/0.25 = 3
PFR: k·τ = ln(1/(1 − X)) = ln(4) = 1.386

Ratio of volumes

VCSTR/VPFR = 3/1.386 = 2.164

Answer

VCSTR/VPFR = 2.164

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 52.76 %

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 = 150/50 = 3 min, kτ = 0.25·3 = 0.75

Conversion

X = 1 − e−kτ = 1 − e−0.75 = 52.76%

Answer

X = 52.76%
17.Heat exchangers (LMTD)

Answer: U = 190.9 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 = 135 − 25 = 110 K
ΔT₂ = Th,out − Tc,out = 95 − 60 = 35 K

Log-mean temperature difference

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

Overall coefficient

U = Q̇/(A·ΔTlm) = 250000/(20·65.49) = 190.9 W/(m²·K)

Answer

U = 190.9 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: Th,out = 88.57 °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.

Constant temperature difference

The cold outlet sits opposite the hot inlet: Tc,out = Tc,in + (Th,in − Th,out), so ΔT₁ = Th,in − Tc,out = Th,out − Tc,in = ΔT₂.

ΔTlm = Th,out − Tc,in

Energy balance equals rate equation

3·(120 − Th,out) = 1.2·(Th,out − 10)
Th,out = (3·120 + 1.2·10)/(3 + 1.2) = 88.57 °C

Answer

Th,out = 88.57 °C

Heat transferred: Q̇ = 94.29 kW; the cold stream leaves at 41.43 °C.

19.Heat conduction

Answer: Q̇ = 438.3 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)/(1.4·15) = 0.0119 K/W
R2 = L2/(k2A) = (150/1000)/(0.17·15) = 0.05882 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 31/0.07073 = 438.3 W

Answer

Q̇ = 438.3 W
20.Heat conduction

Answer: Q̇ = 731.4 W

Thermal resistance: steady heat flow through layers in series behaves like current through resistors in series: Q̇ = ΔT/ΣR, with R = L/(kA) for a conducting layer and R = 1/(hA) for a convecting surface. The temperature drop across each layer is proportional to its resistance.

Resistances in series

Ri = 1/(hiA) = 1/(6·6) = 0.02778 K/W
R1 = L1/(k1A) = (50/1000)/(1.4·6) = 0.005952 K/W
R2 = L2/(k2A) = (25/1000)/(0.72·6) = 0.005787 K/W
Ro = 1/(hoA) = 1/(20·6) = 0.008333 K/W
ΣR = 0.04785 K/W

Heat loss

Q̇ = (20 − (-15))/0.04785 = 731.4 W

Answer

Q̇ = 731.4 W
21.Pipe friction & head loss

Answer: hf = 62.4 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 = 0.008/0.004418 = 1.811 m/s

Velocity head

V²/(2g) = 1.811²/(2·9.81) = 0.1671 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.028·(1000/0.075)·1.811²/(2·9.81) = 62.4 m

Answer

hf = 62.4 m
22.Pipe friction & head loss

Answer: H = 5.893 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 = 0.015/0.007854 = 1.91 m/s
V²/(2g) = 0.1859 m

Loss coefficients

f·L/D = 0.018·150/0.1 = 27
ΣK = 0.5 + 4·0.3 + 2 = 3.7

Energy equation

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

H = (1 + 27 + 3.7)·0.1859 = 5.893 m

Answer

H = 5.893 m
23.Pumps & pump power

Answer: Pel = 6.262 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 = 1000·9.81·0.01·42 = 4.12 kW

Shaft power

Pshaft = 4.12/0.7 = 5.886 kW

Electrical power

Pel = 5.886/0.94 = 6.262 kW

Answer

Pel = 6.262 kW
24.Pumps & pump power

Answer: H = 37.85 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) = (50 + 6)·0.408 = 22.85 m

Pump head

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

H = Δz + hL = 15 + 22.85 = 37.85 m

Answer

H = 37.85 m

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