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 1750 kg/h · 45% saltStream 2ṁ₂ = ? · 5% saltProduct40% salt

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 40% salt? Find ṁ2.

ṁ1 = 750 kg/hx1 = 45 %x2 = 5 %x3 = 40 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F2900 kg/h · 10% sugarProduct PP = ? · 45%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 = 2900 kg/hxF = 10 %xP = 45 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 130 °C70 °Cwater · 10 °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: 130 → 70 °Cṁc = 2 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sideethanol · 160 °C90 °Cwater · 25 °C75 °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: 160 → 90 °Ct: 25 → 75 °Ccp,c = 4.18 kJ/(kg·K)loss = 15 %
ṁc = kg/s
5.Ideal gas lawMedium
90 g of CH₄P = 550 kPaT = 80 °CV = ?

What volume V does 90 g of CH₄ occupy at 550 kPa and 80 °C? Treat it as an ideal gas.

m = 90 gM = 16.04 g/molP = 550 kPaT = 80 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
Ar, M = 39.95 g/molP = 300 kPaT = 10 °Cρ = ?

Find the density ρ of Ar at 300 kPa and 10 °C, treating it as an ideal gas.

M = 39.95 g/molP = 300 kPaT = 10 °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​)

24 g of N2 and 48 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(H2​)n(H2​)n(H2​O)m(H2​O)÷ M(H2​)× 2/2× M(H2​O)

In the reaction 2H2 + O2 → 2H2O, 16 g of H2 reacts completely (the other reactants are in excess) and 130.1 g of H2O is collected. Find the percent yield Y.

M(H2) = 2.016 g/molM(H2O) = 18.02 g/molactual: 130.1 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 = 49. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 49
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.400C−x+x+xE0.4 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 0.4 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.4 mol/LKc = 0.02
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 200 gT = 110 °Cc = 0.449 J/(g·°C)Waterm = 150 gT = 18 °Cc = 4.18 J/(g·°C)

A 200 g block of iron (c = 0.449 J/(g·°C)) at 110 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 18 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.449 J/(g·°C)Tmetal = 110 °Cmwater = 150 gTwater = 18 °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)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.25 L/(mol·min) and an initial concentration of 0.5 mol/L. Find its first half-life t½.

k = 0.25 L/(mol·min)CA0 = 0.5 mol/L
t½ = min
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.250.005run 20.750.026n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.25 mol/L the rate is 0.005 mol/(L·s); with CA0 = 0.75 mol/L it is 0.026 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.25 mol/Lr1 = 0.005 mol/(L·s)CA0,2 = 0.75 mol/Lr2 = 0.026 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minCA0​ = 2 mol/LCA​ = ?V = 400 L, k = 0.3 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.3 min⁻¹) runs in a 400 L plug-flow reactor (PFR). The feed enters at 50 L/min with CA0 = 2 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 400 LQ = 50 L/mink = 0.3 min⁻¹CA0 = 2 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
Q = 50 L/minX = ?V = 150 L

A first-order liquid-phase reaction (k = 0.12 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 = 0.12 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT175 °C80 °C145 °C15 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 280 kW. The hot fluid cools from 175 to 80 °C and the cold fluid heats from 15 to 145 °C. The overall heat transfer coefficient is 500 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 280 kWU = 500 W/(m²·K)Th: 175 → 80 °CTc: 15 → 145 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT160 °C??10 °CΔT₁ΔT₂counter-flow

In a counter-flow heat exchanger both streams have the same heat capacity rate, ṁ·cp = 4 kW/K. The hot stream enters at 160 °C and the cold stream at 10 °C. The exchanger has A = 2 m² and U = 800 W/(m²·K). Find the hot outlet temperature Th,out.

Ch = Cc = 4 kW/KTh,in = 160 °CTc,in = 10 °CA = 2 m²U = 800 W/(m²·K)
Th,out = °C
19.Heat conductionMedium
Brick, k = 0.72100 mmExpanded polystyrene, k = 0.03550 mm18 °C9 °CQ̇ = ?

A wall is made of 100 mm of brick and 50 mm of expanded polystyrene, with an area of 12 m². The outer faces are at 18 °C and 9 °C. Find the heat flow Q̇ through the wall.

L1 = 100 mm, k1 = 0.72 W/(m·K)L2 = 50 mm, k2 = 0.035 W/(m·K)A = 12 m²T1 = 18 °CT3 = 9 °C
Q̇ = W
20.Heat conductionHard
Concrete, k = 1.4100 mmWood, k = 0.1775 mmroom 22 °Coutside -12 °CTs​ = ?Q̇

A wall of 100 mm concrete and 75 mm wood separates a room at 22 °C from outside air at -12 °C. The convection coefficients are 7.7 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 6 m². Find the temperature Ts of the inside surface of the wall.

L1 = 100 mm, k1 = 1.4 W/(m·K)L2 = 75 mm, k2 = 0.17 W/(m·K)A = 6 m²hi = 7.7 W/(m²·K)ho = 30 W/(m²·K)Troom = 22 °CTout = -12 °C
Ts = °C
21.Pipe friction & head lossMedium
V = 1.2 m/sD = 100 mmL = 150 mf = 0.03

Water (ρ = 1000 kg/m³) flows at 1.2 m/s through a horizontal pipe, 150 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 pressure drop Δp over the pipe in kPa.

V = 1.2 m/sL = 150 mD = 100 mmf = 0.03ρ = 1000 kg/m³
Δp = kPa
22.Pipe friction & head lossHard
K = 2Δz = ?L = 200 m, D = 100 mm, f = 0.0152× bend (K = 0.3)

Two open reservoirs are joined by a pipe 200 m long with an inside diameter of 100 mm and a Darcy friction factor f = 0.015. The minor losses are a square-edged entrance (K = 0.5), 2 bends (K = 0.3 each), a valve (K = 2) and the exit into the lower reservoir (K = 1.0). Use g = 9.81 m/s². What difference in water level Δz between the reservoirs gives a flow rate of 15 L/s?

Q = 15 L/sL = 200 mD = 100 mmf = 0.015Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 2Kexit = 1.0
Δz = m
23.Pumps & pump powerMedium
PQ = 25 L/sH = 78 m

In a test, a pump delivers 25 L/s of water (ρ = 1000 kg/m³) against a head of 78 m while its shaft takes 24.5 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 25 L/sH = 78 mPshaft = 24.5 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
150 kPa (gauge)PQ = 50 L/sΔz = 12 mL = 100 m, D = 150 mm, f = 0.018, 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 12 m higher. The pipe is 100 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.018; 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 150 kPa. Find the head H the pump must add.

Q = 50 L/sΔz = 12 mL = 100 mD = 150 mmf = 0.018ΣK = 4ptank = 150 kPa
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 107.1 kg/h

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

Balances

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

Solve for ṁ2

ṁ2 = ṁ1(x1 − x3)/(x3 − x2) = 750·(45 − 40)/(40 − 5) = 107.1 kg/h

Answer

ṁ2 = 107.1 kg/h
2.Mass balance

Answer: P = 644.4 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 = 2900·10/45 = 644.4 kg/h

Answer

P = 644.4 kg/h
3.Energy balance

Answer: tout = 61.67 °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·(130 − 70) = 432 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 432/(2·4.18) = 61.67 °C

Answer

tout = 61.67 °C
4.Energy balance

Answer: ṁc = 0.6946 kg/s

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

Heat released

Qh = 1·2.44·(160 − 90) = 170.8 kW

Heat that reaches the water

Qc = (1 − 0.15)·170.8 = 145.2 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 145.2/(4.18·50) = 0.6946 kg/s

Answer

ṁc = 0.6946 kg/s
5.Ideal gas law

Answer: V = 29.95 L

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

Moles

n = 90/16.04 = 5.611 mol
T = 80 + 273.15 = 353.1 K

Volume

V = nRT/P = 5.611·8.314·353.1/550 = 29.95 L

Answer

V = 29.95 L
6.Ideal gas law

Answer: ρ = 5.091 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 10 + 273.15 = 283.1 K

Density

ρ = 300·39.95/(8.314·283.1) = 5.091 kg/m³

Answer

ρ = 5.091 kg/m³
7.Stoichiometry

Answer: m = 29.17 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) = 24/28.02 = 0.8565 mol
n(H2) = 48/2.016 = 23.81 mol

Limiting reactant

0.8565/1 = 0.8565, 23.81/3 = 7.937 → N2

Mass of product

n(NH3) = 0.8565·2 = 1.713 mol
m = 1.713·17.03 = 29.17 g

Answer

m = 29.17 g
8.Stoichiometry

Answer: Y = 91 %

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(H2) = 16/2.016 = 7.937 mol
m = 7.937·2/2·18.02 = 143 g

Percent yield

Y = 130.1/143·100 = 91%

Answer

Y = 91%
9.Chemical equilibrium

Answer: [HI] = 0.3889 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/(0.25 − x)²

Take the square root

7 = 2x/(0.25 − x) → x = 0.25·7/(2 + 7) = 0.1944 mol/L

Equilibrium concentration

[HI] = 2x = 0.3889 mol/L

Answer

[HI] = 0.3889 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.08 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/(0.4 − x) → x² + 0.02·x − 0.008 = 0

Solve the quadratic

x = (−0.02 + √(0.02² + 4·0.008))/2 = 0.08 mol/L

Equilibrium concentration

[Cl₂] = x = 0.08 mol/L

Answer

[Cl2] = 0.08 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 29.53 °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

200·0.449·(110 − Tf) = 150·4.18·(Tf − 18)

Solve for the final temperature

Tf = (89.8·110 + 627·18)/(89.8 + 627) = 29.53 °C

Answer

Tf = 29.53 °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: t½ = 8 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/(0.25·0.5) = 8 min

Answer

t½ = 8 min

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

14.Reaction kinetics

Answer: n = 1.501

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 = 0.026/0.005 = 5.2
C2/C1 = 0.75/0.25 = 3

Order

n = ln(5.2)/ln(3) = 1.501

Answer

n = 1.501
15.Reactor sizing (CSTR & PFR)

Answer: CA = 0.1814 mol/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 = V/Q = 400/50 = 8 min

Outlet concentration

CA = 2·e−0.3·8 = 0.1814 mol/L

Answer

CA = 0.1814 mol/L

Conversion: X = 90.93%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 30.23 %

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 = 0.12·3 = 0.36

Conversion

X = 1 − e−kτ = 1 − e−0.36 = 30.23%

Answer

X = 30.23%
17.Heat exchangers (LMTD)

Answer: A = 12.37 m²

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

End temperature differences

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

ΔT₁ = Th,in − Tc,out = 175 − 145 = 30 K
ΔT₂ = Th,out − Tc,in = 80 − 15 = 65 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (30 − 65)/ln(30/65) = 45.27 K

Area

A = Q̇/(U·ΔTlm) = 280000/(500·45.27) = 12.37 m²

Answer

A = 12.37 m²
18.Heat exchangers (LMTD)

Answer: Th,out = 117.1 °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

4·(160 − Th,out) = 1.6·(Th,out − 10)
Th,out = (4·160 + 1.6·10)/(4 + 1.6) = 117.1 °C

Answer

Th,out = 117.1 °C

Heat transferred: Q̇ = 171.4 kW; the cold stream leaves at 52.86 °C.

19.Heat conduction

Answer: Q̇ = 68.9 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)/(0.72·12) = 0.01157 K/W
R2 = L2/(k2A) = (50/1000)/(0.035·12) = 0.119 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 9/0.1306 = 68.9 W

Answer

Q̇ = 68.9 W
20.Heat conduction

Answer: Ts = 15.47 °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/(7.7·6) = 0.02165 K/W
R1 = L1/(k1A) = (100/1000)/(1.4·6) = 0.0119 K/W
R2 = L2/(k2A) = (75/1000)/(0.17·6) = 0.07353 K/W
Ro = 1/(hoA) = 1/(30·6) = 0.005556 K/W
ΣR = 0.1126 K/W

Heat loss

Q̇ = (22 − (-12))/0.1126 = 301.9 W
Ts = Troom − Q̇·Ri = 22 − 301.9·0.02165 = 15.47 °C

Answer

Ts = 15.47 °C
21.Pipe friction & head loss

Answer: Δp = 32.4 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·(150/0.1)·1.2²/(2·9.81) = 3.303 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 = 1000·9.81·3.303 = 32400 Pa = 32.4 kPa

Answer

Δp = 32.4 kPa
22.Pipe friction & head loss

Answer: Δz = 6.34 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 = 0.015·200/0.1 = 30
ΣK = 0.5 + 2·0.3 + 2 + 1.0 = 4.1

Total head loss

hf = 30·0.1859 = 5.577 m
hm = 4.1·0.1859 = 0.7622 m
Δz = hf + hm = 6.34 m

Answer

Δz = 6.34 m
23.Pumps & pump power

Answer: η = 78.08 %

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

Hydraulic power

Ph = ρ·g·Q·H = 1000·9.81·0.025·78 = 19.13 kW

Efficiency

η = Ph/Pshaft = 19.13/24.5 = 78.08%

Answer

η = 78.08%
24.Pumps & pump power

Answer: H = 33.82 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) = (12 + 4)·0.408 = 6.529 m

Pressure head

p/(ρ·g) = 150000/(1000·9.81) = 15.29 m

Pump head

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

H = Δz + p/(ρ·g) + hL = 12 + 15.29 + 6.529 = 33.82 m

Answer

H = 33.82 m

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