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 · 40% sugarStream 2ṁ₂ = ? · 20% sugarProduct30% sugar

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 30% sugar? Find ṁ2.

ṁ1 = 1000 kg/hx1 = 40 %x2 = 20 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3500 kg/h · 12% sugarProduct PP = ? · 40%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 = 3500 kg/hxF = 12 %xP = 40 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 180 °C140 °Cwater · 15 °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 → 140 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 15 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 140 °C90 °Cwater · 30 °C90 °C · ṁ = ?15% lost

Hot ethanol 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 kg/scp,h = 2.44 kJ/(kg·K)Th: 140 → 90 °Ct: 30 → 90 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
300 g of N₂V = 5 LT = 50 °CP = ?

A tank of 5 L contains 300 g of N₂ at 50 °C. Treat it as an ideal gas and find the pressure P.

m = 300 gM = 28.01 g/molV = 5 LT = 50 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
N₂, M = 28.01 g/molP = 1000 kPaT = 130 °Cρ = ?

Find the density ρ of N₂ at 1000 kPa and 130 °C, treating it as an ideal gas.

M = 28.01 g/molP = 1000 kPaT = 130 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 4/ν× M(H2​O)

6 g of C3H8 and 20 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of H2O can form?

M(C3H8) = 44.1M(O2) = 32M(H2O) = 18.02 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, 30 g of N2 reacts completely (the other reactants are in excess) and 22.61 g of NH3 is collected. Find the percent yield Y.

M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 22.61 g
Y = %
9.Chemical equilibriumMedium
H2​I2​HII0.80.80C−x−x+2xE0.8 − x0.8 − x2x

0.8 mol/L of H₂ and 0.8 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 49. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 49
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.800C−x+x+xE0.8 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.8 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.8 mol/LKc = 0.2
[PCl5] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 100 gT = 120 °Cc = 0.385 J/(g·°C)Waterm = 150 gT = 25 °Cc = 4.18 J/(g·°C)

A 100 g block of copper (c = 0.385 J/(g·°C)) at 120 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.385 J/(g·°C)Tmetal = 120 °Cmwater = 150 gTwater = 25 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
HC2​H5​OH + 3O₂reactants2CO₂ + 3H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction C2H5OH + 3O₂ → 2CO₂ + 3H₂O(l).

ΔH°f(C2H5OH) = −277.7 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)2 minC = ?

A reaction with rate law −rA = k·CA² has k = 0.4 L/(mol·min) and starts at 2 mol/L. Find the concentration CA after 2 min.

k = 0.4 L/(mol·min)CA0 = 2 mol/Lt = 2 min
CA = mol/L
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.50.02run 220.32n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.5 mol/L the rate is 0.02 mol/(L·s); with CA0 = 2 mol/L it is 0.32 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.5 mol/Lr1 = 0.02 mol/(L·s)CA0,2 = 2 mol/Lr2 = 0.32 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
QX = 60%same Q, k and X as the CSTR

A first-order liquid-phase reaction must reach 60% 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 = 60%first order, same k and Q
VCSTR/VPFR =
16.Reactor sizing (CSTR & PFR)Hard
V = 1000 LQ = 10 L/minX = ?

A first-order liquid-phase reaction (k = 0.2 min⁻¹) runs in a 1000 L CSTR fed at 10 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 1000 LQ = 10 L/mink = 0.2 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT170 °C155 °C110 °C25 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 210 kW. Its heat transfer area is 5 m². The hot fluid cools from 170 to 155 °C and the cold fluid heats from 25 to 110 °C. Find the overall heat transfer coefficient U.

Q̇ = 210 kWA = 5 m²Th: 170 → 155 °CTc: 25 → 110 °C
U = W/(m²·K)
18.Heat exchangers (LMTD)Hard
lengthT145 °C100 °C?25 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.8 kg/s, cp = 2.5 kJ/(kg·K)) flows in the inner tube and cools from 145 to 100 °C. Water (0.8 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 = 500 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.8 kg/scp,h = 2.5 kJ/(kg·K)Th: 145 → 100 °Cṁc = 0.8 kg/sTc,in = 25 °CD = 50 mmU = 500 W/(m²·K)
L = m
19.Heat conductionMedium
Brick, k = 0.7250 mmWood, k = 0.1775 mm22 °C-8 °CQ̇ = ?

A wall is made of 50 mm of brick and 75 mm of wood, with an area of 15 m². The outer faces are at 22 °C and -8 °C. Find the heat flow Q̇ through the wall.

L1 = 50 mm, k1 = 0.72 W/(m·K)L2 = 75 mm, k2 = 0.17 W/(m·K)A = 15 m²T1 = 22 °CT3 = -8 °C
Q̇ = W
20.Heat conductionHard
Mineral wool, k = 0.04200 mmBrick, k = 0.7275 mmroom 20 °Coutside -9 °CTs​ = ?Q̇

A wall of 200 mm mineral wool and 75 mm brick separates a room at 20 °C from outside air at -9 °C. The convection coefficients are 8 W/(m²·K) inside and 25 W/(m²·K) outside, and the wall area is 15 m². Find the temperature Ts of the inside surface of the wall.

L1 = 200 mm, k1 = 0.04 W/(m·K)L2 = 75 mm, k2 = 0.72 W/(m·K)A = 15 m²hi = 8 W/(m²·K)ho = 25 W/(m²·K)Troom = 20 °CTout = -9 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 3 m/sD = 100 mmL = 1000 mf = 0.03

Water flows at a mean velocity of 3 m/s through a pipe 1000 m long with an inside diameter of 100 mm. Use the Darcy friction factor f = 0.03 and g = 9.81 m/s². Find the friction head loss hf.

V = 3 m/sL = 1000 mD = 100 mmf = 0.03g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5free outletH = ?L = 150 m, D = 250 mm, f = 0.0224× bend (K = 0.3)

A pipe 150 m long with an inside diameter of 250 mm (Darcy friction factor f = 0.022) runs from an open reservoir and discharges as a free jet into the air. The minor losses are a square-edged entrance (K = 0.5), 4 bends (K = 0.3 each) and a valve (K = 5). Use g = 9.81 m/s². How far H must the reservoir surface be above the pipe outlet for a flow rate of 60 L/s?

Q = 60 L/sL = 150 mD = 250 mmf = 0.022Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 5
H = m
23.Pumps & pump powerMedium
PQ = 30 L/sH = 14 m

A pump delivers 30 L/s of water (ρ = 1000 kg/m³) against a head of 14 m. The pump efficiency is 82% and the electric motor driving it has an efficiency of 95%. Use g = 9.81 m/s². Find the electrical power Pel the motor draws, in kW.

Q = 30 L/sH = 14 mηpump = 82%ηmotor = 95%g = 9.81 m/s²
Pel = kW
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 25 mL = 300 m, D = 150 mm, f = 0.015, ΣK = 8

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 25 m higher. The pipe is 300 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 = 8 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 50 L/sΔz = 25 mL = 300 mD = 150 mmf = 0.015ΣK = 8
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 1000 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·(40 − 30)/(30 − 20) = 1000 kg/h

Answer

ṁ2 = 1000 kg/h
2.Mass balance

Answer: P = 1050 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 = 3500·12/40 = 1050 kg/h

Answer

P = 1050 kg/h
3.Energy balance

Answer: tout = 49.45 °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 − 140) = 288 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 15 + 288/(2·4.18) = 49.45 °C

Answer

tout = 49.45 °C
4.Energy balance

Answer: ṁc = 0.4135 kg/s

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

Heat released

Qh = 1·2.44·(140 − 90) = 122 kW

Heat that reaches the water

Qc = (1 − 0.15)·122 = 103.7 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 103.7/(4.18·60) = 0.4135 kg/s

Answer

ṁc = 0.4135 kg/s
5.Ideal gas law

Answer: P = 5755 kPa

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

Moles

n = m/M = 300/28.01 = 10.71 mol
T = 50 + 273.15 = 323.1 K

Pressure

P = nRT/V = 10.71·8.314·323.1/0.005 = 5755 kPa

Answer

P = 5755 kPa
6.Ideal gas law

Answer: ρ = 8.357 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 130 + 273.15 = 403.1 K

Density

ρ = 1000·28.01/(8.314·403.1) = 8.357 kg/m³

Answer

ρ = 8.357 kg/m³
7.Stoichiometry

Answer: m = 9.01 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(C3H8) = 6/44.1 = 0.1361 mol
n(O2) = 20/32 = 0.625 mol

Limiting reactant

0.1361/1 = 0.1361, 0.625/5 = 0.125 → O2

Mass of product

n(H2O) = 0.125·4 = 0.5 mol
m = 0.5·18.02 = 9.01 g

Answer

m = 9.01 g
8.Stoichiometry

Answer: Y = 62 %

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) = 30/28.02 = 1.071 mol
m = 1.071·2/1·17.03 = 36.47 g

Percent yield

Y = 22.61/36.47·100 = 62%

Answer

Y = 62%
9.Chemical equilibrium

Answer: [HI] = 1.244 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

49 = (2x)²/(0.8 − x)²

Take the square root

7 = 2x/(0.8 − x) → x = 0.8·7/(2 + 7) = 0.6222 mol/L

Equilibrium concentration

[HI] = 2x = 1.244 mol/L

Answer

[HI] = 1.244 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.4877 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

0.2 = x²/(0.8 − x) → x² + 0.2·x − 0.16 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.16))/2 = 0.3123 mol/L

Equilibrium concentration

[PCl₅] = 0.8 − 0.3123 = 0.4877 mol/L

Answer

[PCl5] = 0.4877 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 30.5 °C

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

Heat balance

100·0.385·(120 − Tf) = 150·4.18·(Tf − 25)

Solve for the final temperature

Tf = (38.5·120 + 627·25)/(38.5 + 627) = 30.5 °C

Answer

Tf = 30.5 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −1367 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

Answer

ΔH° = −1367 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: CA = 0.7692 mol/L

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).

Integrated second-order law

1/CA = 1/CA0 + kt = 0.5 + 0.4·2 = 1.3 L/mol
CA = 1/1.3 = 0.7692 mol/L

Answer

CA = 0.7692 mol/L
14.Reaction kinetics

Answer: n = 2

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 = 0.32/0.02 = 16
C2/C1 = 2/0.5 = 4

Order

n = ln(16)/ln(4) = 2

Answer

n = 2
15.Reactor sizing (CSTR & PFR)

Answer: VCSTR/VPFR = 1.637

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) = 0.6/0.4 = 1.5
PFR: k·τ = ln(1/(1 − X)) = ln(2.5) = 0.9163

Ratio of volumes

VCSTR/VPFR = 1.5/0.9163 = 1.637

Answer

VCSTR/VPFR = 1.637

The gap grows quickly at high conversion.

16.Reactor sizing (CSTR & PFR)

Answer: X = 95.24 %

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 = 1000/10 = 100 min, kτ = 0.2·100 = 20

Conversion

X = kτ/(1 + kτ) = 20/(1 + 20) = 95.24%

Answer

X = 95.24%
17.Heat exchangers (LMTD)

Answer: U = 463.9 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 counter-flow the hot inlet faces the cold outlet, and the hot outlet faces the cold inlet.

ΔT₁ = Th,in − Tc,out = 170 − 110 = 60 K
ΔT₂ = Th,out − Tc,in = 155 − 25 = 130 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (60 − 130)/ln(60/130) = 90.53 K

Overall coefficient

U = Q̇/(A·ΔTlm) = 210000/(5·90.53) = 463.9 W/(m²·K)

Answer

U = 463.9 W/(m²·K)
18.Heat exchangers (LMTD)

Answer: L = 13.69 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 = 0.8·2.5·(145 − 100) = 90 kW
Tc,out = 25 + 90/(0.8·4.18) = 51.91 °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 − 51.91 = 93.09 K
ΔT₂ = Th,out − Tc,in = 100 − 25 = 75 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (93.09 − 75)/ln(93.09/75) = 83.72 K

Area and length

A = 90000/(500·83.72) = 2.15 m²
L = A/(πD) = 2.15/(π·0.05) = 13.69 m

Answer

L = 13.69 m
19.Heat conduction

Answer: Q̇ = 881.3 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) = (50/1000)/(0.72·15) = 0.00463 K/W
R2 = L2/(k2A) = (75/1000)/(0.17·15) = 0.02941 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 30/0.03404 = 881.3 W

Answer

Q̇ = 881.3 W
20.Heat conduction

Answer: Ts = 19.31 °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/(8·15) = 0.008333 K/W
R1 = L1/(k1A) = (200/1000)/(0.04·15) = 0.3333 K/W
R2 = L2/(k2A) = (75/1000)/(0.72·15) = 0.006944 K/W
Ro = 1/(hoA) = 1/(25·15) = 0.002667 K/W
ΣR = 0.3513 K/W

Heat loss

Q̇ = (20 − (-9))/0.3513 = 82.56 W
Ts = Troom − Q̇·Ri = 20 − 82.56·0.008333 = 19.31 °C

Answer

Ts = 19.31 °C
21.Pipe friction & head loss

Answer: hf = 137.6 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) = 3²/(2·9.81) = 0.4587 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.03·(1000/0.1)·3²/(2·9.81) = 137.6 m

Answer

hf = 137.6 m
22.Pipe friction & head loss

Answer: H = 1.592 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 = 0.06/0.04909 = 1.222 m/s
V²/(2g) = 0.07615 m

Loss coefficients

f·L/D = 0.022·150/0.25 = 13.2
ΣK = 0.5 + 4·0.3 + 5 = 6.7

Energy equation

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

H = (1 + 13.2 + 6.7)·0.07615 = 1.592 m

Answer

H = 1.592 m
23.Pumps & pump power

Answer: Pel = 5.289 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 = 1000·9.81·0.03·14 = 4.12 kW

Shaft power

Pshaft = 4.12/0.82 = 5.025 kW

Electrical power

Pel = 5.025/0.95 = 5.289 kW

Answer

Pel = 5.289 kW
24.Pumps & pump power

Answer: H = 40.51 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) = (30 + 8)·0.408 = 15.51 m

Pump head

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

H = Δz + hL = 25 + 15.51 = 40.51 m

Answer

H = 40.51 m

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