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 · 35% NaOHStream 2ṁ₂ = ? · 15% NaOHProduct30% NaOH

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

ṁ1 = 200 kg/hx1 = 35 %x2 = 15 %x3 = 30 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F3200 kg/h · 6% 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 = 3200 kg/hxF = 6 %xP = 30 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideglycol mix · 160 °C120 °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 = 2.5 kg/scp,h = 3.6 kJ/(kg·K)Th: 160 → 120 °Cṁc = 3 kg/scp,c = 4.18 kJ/(kg·K)tin = 10 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 150 °C100 °Cwater · 30 °C90 °C · ṁ = ?5% lost

Hot light oil heats water in an exchanger that loses 5% of the heat released by the hot stream to the surroundings. Find the water flow rate ṁc needed.

ṁh = 3 kg/scp,h = 2.1 kJ/(kg·K)Th: 150 → 100 °Ct: 30 → 90 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
100 g of HeV = 5 LT = 45 °CP = ?

A tank of 5 L contains 100 g of He at 45 °C. Treat it as an ideal gas and find the pressure P.

m = 100 gM = 4.003 g/molV = 5 LT = 45 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
O₂, M = 32 g/molP = 250 kPaT = 80 °Cρ = ?

Find the density ρ of O₂ at 250 kPa and 80 °C, treating it as an ideal gas.

M = 32 g/molP = 250 kPaT = 80 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(NaCl)m(NaCl)÷ M(X)× 2/ν× M(NaCl)

8 g of Na and 80 g of Cl2 react according to 2Na + Cl2 → 2NaCl. What mass m of NaCl can form?

M(Na) = 22.99M(Cl2) = 70.9M(NaCl) = 58.44 g/mol
m = g
8.StoichiometryHard
m(CH4​)n(CH4​)n(H2​O)m(H2​O)÷ M(CH4​)× 2/1× M(H2​O)

In the reaction CH4 + 2O2 → CO2 + 2H2O, 30 g of CH4 reacts completely (the other reactants are in excess) and 50.55 g of H2O is collected. Find the percent yield Y.

M(CH4) = 16.04 g/molM(H2O) = 18.02 g/molactual: 50.55 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 = 9. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.2500C−x+x+xE0.25 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 0.25 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.25 mol/LKc = 0.02
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 200 gT = 80 °Cc = 0.385 J/(g·°C)Waterm = 100 gT = 21 °Cc = 4.18 J/(g·°C)

A 200 g block of copper (c = 0.385 J/(g·°C)) at 80 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 21 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.385 J/(g·°C)Tmetal = 80 °Cmwater = 100 gTwater = 21 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l).

ΔH°f(C2H6) = −84.7 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)5 minC = ?

A reaction with rate law −rA = k·CA² has k = 0.1 L/(mol·min) and starts at 0.5 mol/L. Find the concentration CA after 5 min.

k = 0.1 L/(mol·min)CA0 = 0.5 mol/Lt = 5 min
CA = mol/L
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.40.012run 20.80.017n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.4 mol/L the rate is 0.012 mol/(L·s); with CA0 = 0.8 mol/L it is 0.017 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.4 mol/Lr1 = 0.012 mol/(L·s)CA0,2 = 0.8 mol/Lr2 = 0.017 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 10 L/minCA0​ = 2.5 mol/LCA​ = ?V = 100 L, k = 0.08 min⁻¹

A liquid-phase first-order reaction A → B (k = 0.08 min⁻¹) runs in a 100 L plug-flow reactor (PFR). The feed enters at 10 L/min with CA0 = 2.5 mol/L. The density is constant and the reactor is at steady state. Find the outlet concentration CA.

V = 100 LQ = 10 L/mink = 0.08 min⁻¹CA0 = 2.5 mol/L
CA = mol/L
16.Reactor sizing (CSTR & PFR)Hard
V = 250 LV = 250 LQ = 10 L/minX = ?

A first-order liquid-phase reaction (k = 0.25 min⁻¹) runs in two equal CSTRs in series, each of 250 L. The feed rate is 10 L/min, the density is constant and the reactors are at steady state. Find the overall conversion X in percent.

V = 250 L (×2)Q = 10 L/mink = 0.25 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT110 °C85 °C20 °C10 °CΔT₁ΔT₂counter-flow

A counter-flow heat exchanger transfers 310 kW. The hot fluid cools from 110 to 85 °C and the cold fluid heats from 10 to 20 °C. The overall heat transfer coefficient is 200 W/(m²·K). Find the heat transfer area A needed.

Q̇ = 310 kWU = 200 W/(m²·K)Th: 110 → 85 °CTc: 10 → 20 °C
A = m²
18.Heat exchangers (LMTD)Hard
lengthT105 °C65 °C?10 °CΔT₁ΔT₂counter-flow

In a counter-flow double-pipe heat exchanger, hot oil (0.2 kg/s, cp = 2.1 kJ/(kg·K)) flows in the inner tube and cools from 105 to 65 °C. Water (0.3 kg/s, cp = 4.18 kJ/(kg·K)) in the annulus enters at 10 °C. The inner tube has a diameter of 50 mm, and U = 200 W/(m²·K) is based on this diameter. Find the tube length L needed.

ṁh = 0.2 kg/scp,h = 2.1 kJ/(kg·K)Th: 105 → 65 °Cṁc = 0.3 kg/sTc,in = 10 °CD = 50 mmU = 200 W/(m²·K)
L = m
19.Heat conductionMedium
Wood, k = 0.17200 mmBrick, k = 0.7250 mm21 °C-1 °CQ̇ = ?

A wall is made of 200 mm of wood and 50 mm of brick, with an area of 6 m². The outer faces are at 21 °C and -1 °C. Find the heat flow Q̇ through the wall.

L1 = 200 mm, k1 = 0.17 W/(m·K)L2 = 50 mm, k2 = 0.72 W/(m·K)A = 6 m²T1 = 21 °CT3 = -1 °C
Q̇ = W
20.Heat conductionHard
Concrete, k = 1.4100 mmMineral wool, k = 0.04150 mmroom 20 °Coutside -1 °CTs​ = ?Q̇

A wall of 100 mm concrete and 150 mm mineral wool separates a room at 20 °C from outside air at -1 °C. The convection coefficients are 6 W/(m²·K) inside and 30 W/(m²·K) outside, and the wall area is 10 m². Find the temperature Ts of the inside surface of the wall.

L1 = 100 mm, k1 = 1.4 W/(m·K)L2 = 150 mm, k2 = 0.04 W/(m·K)A = 10 m²hi = 6 W/(m²·K)ho = 30 W/(m²·K)Troom = 20 °CTout = -1 °C
Ts = °C
21.Pipe friction & head lossMedium
Q = 25 L/sD = 250 mmL = 800 mf = 0.028

Water flows at 25 L/s through a pipe 800 m long with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.028 and g = 9.81 m/s². Find the friction head loss hf.

Q = 25 L/sL = 800 mD = 250 mmf = 0.028g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 5free outletH = ?L = 200 m, D = 200 mm, f = 0.024× bend (K = 0.3)

A pipe 200 m long with an inside diameter of 200 mm (Darcy friction factor f = 0.02) runs from an open reservoir and discharges as a free jet into the air. The minor losses are a square-edged entrance (K = 0.5), 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 75 L/s?

Q = 75 L/sL = 200 mD = 200 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×4)Kvalve = 5
H = m
23.Pumps & pump powerMedium
PQ = 100 L/sH = 52 m

In a test, a pump delivers 100 L/s of water (ρ = 1000 kg/m³) against a head of 52 m while its shaft takes 62.2 kW. Use g = 9.81 m/s². Find the pump efficiency η in percent.

Q = 100 L/sH = 52 mPshaft = 62.2 kWg = 9.81 m/s²
η = %
24.Pumps & pump powerHard
PQ = 80 L/sΔz = 8 mL = 400 m, D = 200 mm, f = 0.018, ΣK = 5

A pump moves 80 L/s of water (ρ = 1000 kg/m³) from an open lower reservoir to an upper tank whose water surface is 8 m higher. The pipe is 400 m long with an inside diameter of 200 mm and a Darcy friction factor f = 0.018; the minor-loss coefficients add up to ΣK = 5 (entrance and exit included). Use g = 9.81 m/s². Find the head H the pump must add.

Q = 80 L/sΔz = 8 mL = 400 mD = 200 mmf = 0.018ΣK = 5
H = m

3Solutions

1.Mass balance

Answer: ṁ2 = 66.67 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·(35 − 30)/(30 − 15) = 66.67 kg/h

Answer

ṁ2 = 66.67 kg/h
2.Mass balance

Answer: P = 640 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 = 3200·6/30 = 640 kg/h

Answer

P = 640 kg/h
3.Energy balance

Answer: tout = 38.71 °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·(160 − 120) = 360 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 10 + 360/(3·4.18) = 38.71 °C

Answer

tout = 38.71 °C
4.Energy balance

Answer: ṁc = 1.193 kg/s

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

Heat released

Qh = 3·2.1·(150 − 100) = 315 kW

Heat that reaches the water

Qc = (1 − 0.05)·315 = 299.3 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 299.3/(4.18·60) = 1.193 kg/s

Answer

ṁc = 1.193 kg/s
5.Ideal gas law

Answer: P = 13216 kPa

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

Moles

n = m/M = 100/4.003 = 24.98 mol
T = 45 + 273.15 = 318.1 K

Pressure

P = nRT/V = 24.98·8.314·318.1/0.005 = 13216 kPa

Answer

P = 13216 kPa
6.Ideal gas law

Answer: ρ = 2.725 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 80 + 273.15 = 353.1 K

Density

ρ = 250·32/(8.314·353.1) = 2.725 kg/m³

Answer

ρ = 2.725 kg/m³
7.Stoichiometry

Answer: m = 20.34 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(Na) = 8/22.99 = 0.348 mol
n(Cl2) = 80/70.9 = 1.128 mol

Limiting reactant

0.348/2 = 0.174, 1.128/1 = 1.128 → Na

Mass of product

n(NaCl) = 0.174·2 = 0.348 mol
m = 0.348·58.44 = 20.34 g

Answer

m = 20.34 g
8.Stoichiometry

Answer: Y = 74.99 %

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(CH4) = 30/16.04 = 1.87 mol
m = 1.87·2/1·18.02 = 67.41 g

Percent yield

Y = 50.55/67.41·100 = 74.99%

Answer

Y = 74.99%
9.Chemical equilibrium

Answer: [H2] = 0.32 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

9 = (2x)²/(0.8 − x)²

Take the square root

3 = 2x/(0.8 − x) → x = 0.8·3/(2 + 3) = 0.48 mol/L

Equilibrium concentration

[H₂] = 0.8 − x = 0.32 mol/L

Answer

[H2] = 0.32 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.06141 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/(0.25 − x) → x² + 0.02·x − 0.005 = 0

Solve the quadratic

x = (−0.02 + √(0.02² + 4·0.005))/2 = 0.06141 mol/L

Equilibrium concentration

[Cl₂] = x = 0.06141 mol/L

Answer

[Cl2] = 0.06141 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 30.18 °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

200·0.385·(80 − Tf) = 100·4.18·(Tf − 21)

Solve for the final temperature

Tf = (77·80 + 418·21)/(77 + 418) = 30.18 °C

Answer

Tf = 30.18 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −3119 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° = [4·(−393.5) + 6·(−285.8)] − [2·(−84.7) + 7·0] = −3119 kJ

Answer

ΔH° = −3119 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: CA = 0.4 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 = 2 + 0.1·5 = 2.5 L/mol
CA = 1/2.5 = 0.4 mol/L

Answer

CA = 0.4 mol/L
14.Reaction kinetics

Answer: n = 0.5025

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 = 0.017/0.012 = 1.417
C2/C1 = 0.8/0.4 = 2

Order

n = ln(1.417)/ln(2) = 0.5025

Answer

n = 0.5025
15.Reactor sizing (CSTR & PFR)

Answer: CA = 1.123 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 = 100/10 = 10 min

Outlet concentration

CA = 2.5·e−0.08·10 = 1.123 mol/L

Answer

CA = 1.123 mol/L

Conversion: X = 55.07%.

16.Reactor sizing (CSTR & PFR)

Answer: X = 98.1 %

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 = 250/10 = 25 min, kτ = 0.25·25 = 6.25

Conversion

C1/CA0 = 1/(1 + kτ) = 1/(1 + 6.25) = 0.1379
C2/CA0 = 1/(1 + kτ)² = 0.01902
X = 1 − 0.01902 = 98.1%

Answer

X = 98.1%
17.Heat exchangers (LMTD)

Answer: A = 18.84 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 = 110 − 20 = 90 K
ΔT₂ = Th,out − Tc,in = 85 − 10 = 75 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (90 − 75)/ln(90/75) = 82.27 K

Area

A = Q̇/(U·ΔTlm) = 310000/(200·82.27) = 18.84 m²

Answer

A = 18.84 m²
18.Heat exchangers (LMTD)

Answer: L = 7.931 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 = 0.2·2.1·(105 − 65) = 16.8 kW
Tc,out = 10 + 16.8/(0.3·4.18) = 23.4 °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 = 105 − 23.4 = 81.6 K
ΔT₂ = Th,out − Tc,in = 65 − 10 = 55 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (81.6 − 55)/ln(81.6/55) = 67.43 K

Area and length

A = 16800/(200·67.43) = 1.246 m²
L = A/(πD) = 1.246/(π·0.05) = 7.931 m

Answer

L = 7.931 m
19.Heat conduction

Answer: Q̇ = 105.9 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) = (200/1000)/(0.17·6) = 0.1961 K/W
R2 = L2/(k2A) = (50/1000)/(0.72·6) = 0.01157 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 22/0.2077 = 105.9 W

Answer

Q̇ = 105.9 W
20.Heat conduction

Answer: Ts = 19.13 °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/(6·10) = 0.01667 K/W
R1 = L1/(k1A) = (100/1000)/(1.4·10) = 0.007143 K/W
R2 = L2/(k2A) = (150/1000)/(0.04·10) = 0.375 K/W
Ro = 1/(hoA) = 1/(30·10) = 0.003333 K/W
ΣR = 0.4021 K/W

Heat loss

Q̇ = (20 − (-1))/0.4021 = 52.22 W
Ts = Troom − Q̇·Ri = 20 − 52.22·0.01667 = 19.13 °C

Answer

Ts = 19.13 °C
21.Pipe friction & head loss

Answer: hf = 1.185 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·0.25²/4 = 0.04909 m²
V = Q/A = 0.025/0.04909 = 0.5093 m/s

Velocity head

V²/(2g) = 0.5093²/(2·9.81) = 0.01322 m

Darcy–Weisbach

hf = f·(L/D)·V²/(2g) = 0.028·(800/0.25)·0.5093²/(2·9.81) = 1.185 m

Answer

hf = 1.185 m
22.Pipe friction & head loss

Answer: H = 8.046 m

Pipe flow: the Reynolds number Re = V·D/ν = ρ·V·D/μ tells laminar flow (Re below about 2000) from turbulent flow (above about 4000). Friction along a pipe costs the Darcy–Weisbach head loss hf = f·(L/D)·V²/(2g). Fittings, valves, the entrance and the exit add minor losses hm = ΣK·V²/(2g). Between two open reservoir surfaces the energy equation gives Δz = hf + hm, with the exit loss K = 1 included.

Velocity

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

Loss coefficients

f·L/D = 0.02·200/0.2 = 20
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 + 20 + 6.7)·0.2905 = 8.046 m

Answer

H = 8.046 m
23.Pumps & pump power

Answer: η = 82.01 %

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

Hydraulic power

Ph = ρ·g·Q·H = 1000·9.81·0.1·52 = 51.01 kW

Efficiency

η = Ph/Pshaft = 51.01/62.2 = 82.01%

Answer

η = 82.01%
24.Pumps & pump power

Answer: H = 21.55 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 = 0.08/0.03142 = 2.546 m/s
V²/(2g) = 0.3305 m

Head losses

hL = (f·L/D + ΣK)·V²/(2g) = (36 + 5)·0.3305 = 13.55 m

Pump head

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

H = Δz + hL = 8 + 13.55 = 21.55 m

Answer

H = 21.55 m

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