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.

New problemsBack to the course

In the print window, choose “Save as PDF” to keep a copy on your device.

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 · 45% NaOHStream 2ṁ₂ = ? · 10% NaOHProduct15% NaOH

How much of stream 2 must be added each hour to stream 1 so that the blended product contains 15% NaOH? Find ṁ2.

ṁ1 = 1000 kg/hx1 = 45 %x2 = 10 %x3 = 15 %
ṁ2 = kg/h
2.Mass balanceHard
EvaporatorFeed F1900 kg/h · 12% saltProduct PP = ? · 60%Vapour W (pure water)0% salt

An evaporator concentrates a salt solution by boiling off pure water. Find the product flow P in kg/h.

F = 1900 kg/hxF = 12 %xP = 60 %
P = kg/h
3.Energy balanceMedium
hot sidecold sideethanol · 170 °C130 °Cwater · 20 °Ct = ? °C

Hot ethanol cools water in a counter-flow heat exchanger with no heat loss. Find the water outlet temperature tout.

ṁh = 3 kg/scp,h = 2.44 kJ/(kg·K)Th: 170 → 130 °Cṁc = 1.5 kg/scp,c = 4.18 kJ/(kg·K)tin = 20 °C
tout = °C
4.Energy balanceHard
hot sidecold sidelight oil · 170 °C100 °Cwater · 20 °C60 °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 = 2 kg/scp,h = 2.1 kJ/(kg·K)Th: 170 → 100 °Ct: 20 → 60 °Ccp,c = 4.18 kJ/(kg·K)loss = 5 %
ṁc = kg/s
5.Ideal gas lawMedium
380 g of HeV = 5 LT = 60 °CP = ?

A tank of 5 L contains 380 g of He at 60 °C. Treat it as an ideal gas and find the pressure P.

m = 380 gM = 4.003 g/molV = 5 LT = 60 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
CO₂, M = 44.01 g/molP = 150 kPaT = 140 °Cρ = ?

Find the density ρ of CO₂ at 150 kPa and 140 °C, treating it as an ideal gas.

M = 44.01 g/molP = 150 kPaT = 140 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.StoichiometryMedium
m(X)n(X)n(Fe)m(Fe)÷ M(X)× 2/ν× M(Fe)

10 g of Fe2O3 and 64 g of CO react according to Fe2O3 + 3CO → 2Fe + 3CO2. What mass m of Fe can form?

M(Fe2O3) = 159.69M(CO) = 28.01M(Fe) = 55.85 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, 10 g of C6H12O6 reacts completely (the other reactants are in excess) and 4.35 g of C2H5OH is collected. Find the percent yield Y.

M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 4.35 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 = 36. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 36
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I1.500C−x+x+xE1.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 1.5 mol/LKc = 0.05
[Cl2] = mol/L
11.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 50 gT = 130 °Cc = 0.388 J/(g·°C)Waterm = 200 gT = 25 °Cc = 4.18 J/(g·°C)

A 50 g block of zinc (c = 0.388 J/(g·°C)) at 130 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.388 J/(g·°C)Tmetal = 130 °Cmwater = 200 gTwater = 25 °Ccwater = 4.18 J/(g·°C)
Tf = °C
12.Calorimetry & enthalpyHard
H2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l).

ΔH°f(C4H10) = −125.6 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)10 min0.24

In a first-order reaction the concentration of A falls from 0.8 mol/L to 0.24 mol/L in 10 min. Find the rate constant k.

CA0 = 0.8 mol/LCA = 0.24 mol/Lt = 10 min
k = min⁻¹
14.Reaction kineticsHard
CA0​ (mol/L)r (mol/(L·s))run 10.20.02run 20.60.18n = ?

Two experiments measure the initial rate of A → products. With CA0 = 0.2 mol/L the rate is 0.02 mol/(L·s); with CA0 = 0.6 mol/L it is 0.18 mol/(L·s). Find the reaction order n with respect to A.

CA0,1 = 0.2 mol/Lr1 = 0.02 mol/(L·s)CA0,2 = 0.6 mol/Lr2 = 0.18 mol/(L·s)
n =
15.Reactor sizing (CSTR & PFR)Medium
Q = 50 L/minX = 95%V = ?, k = 0.08 min⁻¹

A first-order liquid-phase reaction A → B with k = 0.08 min⁻¹ is carried out in a plug-flow reactor (PFR) fed at 50 L/min. The density is constant and the reactor is at steady state. Find the reactor volume V in litres for 95% conversion of A.

Q = 50 L/mink = 0.08 min⁻¹X = 95%
V = L
16.Reactor sizing (CSTR & PFR)Hard
V = 800 LQ = 50 L/minX = ?

A first-order liquid-phase reaction (k = 0.05 min⁻¹) runs in an 800 L CSTR fed at 50 L/min. The density is constant and the reactor is at steady state. Find the conversion X in percent.

V = 800 LQ = 50 L/mink = 0.05 min⁻¹
X = %
17.Heat exchangers (LMTD)Medium
lengthT120 °C15 °C50 °CΔT₁ΔT₂condensing steam

In a condenser, steam condenses at a constant 120 °C on the outside of the tubes. Cooling water (0.5 kg/s, cp = 4.18 kJ/(kg·K)) flows through the tubes and heats from 15 to 50 °C. The overall heat transfer coefficient is 3000 W/(m²·K). Find the heat transfer area A needed.

Ts = 120 °Cṁ = 0.5 kg/scp = 4.18 kJ/(kg·K)Tc: 15 → 50 °CU = 3000 W/(m²·K)
A = m²
18.Heat exchangers (LMTD)Hard
lengthT105 °C30 °C?ΔT₁ΔT₂condensing steam

Steam condenses at a constant 105 °C on the outside of the tubes of a condenser with a heat transfer area of 5 m² and U = 1500 W/(m²·K). Cooling water (1.5 kg/s, cp = 4.18 kJ/(kg·K)) enters the tubes at 30 °C. Find the water outlet temperature Tc,out.

Ts = 105 °CA = 5 m²U = 1500 W/(m²·K)ṁ = 1.5 kg/scp = 4.18 kJ/(kg·K)Tc,in = 30 °C
Tc,out = °C
19.Heat conductionMedium
Mineral wool, k = 0.04200 mmGypsum board, k = 0.1750 mm25 °C-1 °CQ̇ = ?

A wall is made of 200 mm of mineral wool and 50 mm of gypsum board, with an area of 4 m². The outer faces are at 25 °C and -1 °C. Find the heat flow Q̇ through the wall.

L1 = 200 mm, k1 = 0.04 W/(m·K)L2 = 50 mm, k2 = 0.17 W/(m·K)A = 4 m²T1 = 25 °CT3 = -1 °C
Q̇ = W
20.Heat conductionHard
Wood, k = 0.17200 mmGlass, k = 0.9625 mmroom 21 °Coutside -3 °CQ̇

A wall of 200 mm wood and 25 mm glass separates a room at 21 °C from outside air at -3 °C. The convection coefficients are 7.7 W/(m²·K) inside and 20 W/(m²·K) outside, and the wall area is 8 m². Find the overall heat transfer coefficient U of the wall.

L1 = 200 mm, k1 = 0.17 W/(m·K)L2 = 25 mm, k2 = 0.96 W/(m·K)A = 8 m²hi = 7.7 W/(m²·K)ho = 20 W/(m²·K)Troom = 21 °CTout = -3 °C
U = W/(m²·K)
21.Pipe friction & head lossMedium
Q = 25 L/sD = 250 mmL = 500 mf = 0.015

Water flows at 25 L/s through a pipe 500 m long with an inside diameter of 250 mm. Use the Darcy friction factor f = 0.015 and g = 9.81 m/s². Find the friction head loss hf.

Q = 25 L/sL = 500 mD = 250 mmf = 0.015g = 9.81 m/s²
hf = m
22.Pipe friction & head lossHard
K = 10free outletH = ?L = 200 m, D = 300 mm, f = 0.022× bend (K = 0.3)

A pipe 200 m long with an inside diameter of 300 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), 2 bends (K = 0.3 each) and a valve (K = 10). 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 = 300 mmf = 0.02Kentrance = 0.5Kbend = 0.3 (×2)Kvalve = 10
H = m
23.Pumps & pump powerMedium
PQ = 40 L/sH = 50 m

A pump with an efficiency of 72% delivers 40 L/s of water (ρ = 1000 kg/m³) against a head of 50 m. Use g = 9.81 m/s². Find the shaft power Pshaft needed, in kW.

Q = 40 L/sH = 50 mη = 72%g = 9.81 m/s²
Pshaft = kW
24.Pumps & pump powerHard
PQ = 50 L/sΔz = 22 mL = 400 m, D = 150 mm, f = 0.022, 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 22 m higher. The pipe is 400 m long with an inside diameter of 150 mm and a Darcy friction factor f = 0.022; the minor-loss coefficients add up to ΣK = 8 (entrance and exit included). Use g = 9.81 m/s². The pump efficiency is 65%. Find the shaft power Pshaft in kW.

Q = 50 L/sΔz = 22 mL = 400 mD = 150 mmf = 0.022ΣK = 8η = 65%
Pshaft = kW

3Solutions

1.Mass balance

Answer: ṁ2 = 6000 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) = 1000·(45 − 15)/(15 − 10) = 6000 kg/h

Answer

ṁ2 = 6000 kg/h
2.Mass balance

Answer: P = 380 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 = 1900·12/60 = 380 kg/h

Answer

P = 380 kg/h
3.Energy balance

Answer: tout = 66.7 °C

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

Heat released by the hot stream

Q = 3·2.44·(170 − 130) = 292.8 kW

Heat picked up by the water

tout = tin + Q/(ṁccp,c) = 20 + 292.8/(1.5·4.18) = 66.7 °C

Answer

tout = 66.7 °C
4.Energy balance

Answer: ṁc = 1.67 kg/s

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

Heat released

Qh = 2·2.1·(170 − 100) = 294 kW

Heat that reaches the water

Qc = (1 − 0.05)·294 = 279.3 kW

Water flow rate

ṁc = Qc/(cp,c·Δt) = 279.3/(4.18·40) = 1.67 kg/s

Answer

ṁc = 1.67 kg/s
5.Ideal gas law

Answer: P = 52587 kPa

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

Moles

n = m/M = 380/4.003 = 94.93 mol
T = 60 + 273.15 = 333.1 K

Pressure

P = nRT/V = 94.93·8.314·333.1/0.005 = 52587 kPa

Answer

P = 52587 kPa
6.Ideal gas law

Answer: ρ = 1.922 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 140 + 273.15 = 413.1 K

Density

ρ = 150·44.01/(8.314·413.1) = 1.922 kg/m³

Answer

ρ = 1.922 kg/m³
7.Stoichiometry

Answer: m = 6.995 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) = 10/159.69 = 0.06262 mol
n(CO) = 64/28.01 = 2.285 mol

Limiting reactant

0.06262/1 = 0.06262, 2.285/3 = 0.7616 → Fe2O3

Mass of product

n(Fe) = 0.06262·2 = 0.1252 mol
m = 0.1252·55.85 = 6.995 g

Answer

m = 6.995 g
8.Stoichiometry

Answer: Y = 85.05 %

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) = 10/180.16 = 0.05551 mol
m = 0.05551·2/1·46.07 = 5.114 g

Percent yield

Y = 4.35/5.114·100 = 85.05%

Answer

Y = 85.05%
9.Chemical equilibrium

Answer: [H2] = 0.2 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/(0.8 − x)²

Take the square root

6 = 2x/(0.8 − x) → x = 0.8·6/(2 + 6) = 0.6 mol/L

Equilibrium concentration

[H₂] = 0.8 − x = 0.2 mol/L

Answer

[H2] = 0.2 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 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

0.05 = x²/(1.5 − x) → x² + 0.05·x − 0.075 = 0

Solve the quadratic

x = (−0.05 + √(0.05² + 4·0.075))/2 = 0.25 mol/L

Equilibrium concentration

[Cl₂] = x = 0.25 mol/L

Answer

[Cl2] = 0.25 mol/L
11.Calorimetry & enthalpy

Answer: Tf = 27.38 °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

50·0.388·(130 − Tf) = 200·4.18·(Tf − 25)

Solve for the final temperature

Tf = (19.4·130 + 836·25)/(19.4 + 836) = 27.38 °C

Answer

Tf = 27.38 °C
12.Calorimetry & enthalpy

Answer: ΔH° = −5755 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° = [8·(−393.5) + 10·(−285.8)] − [2·(−125.6) + 13·0] = −5755 kJ

Answer

ΔH° = −5755 kJ

Negative: the reaction gives off heat (exothermic).

13.Reaction kinetics

Answer: k = 0.1204 min⁻¹

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Integrated first-order law

k = ln(CA0/CA)/t = ln(0.8/0.24)/10 = 1.204/10 = 0.1204 min⁻¹

Answer

k = 0.1204 min⁻¹
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 = 0.18/0.02 = 9
C2/C1 = 0.6/0.2 = 3

Order

n = ln(9)/ln(3) = 2

Answer

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

Answer: V = 1872 L

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

Space time

τ = ln(1/(1 − 0.95))/0.08 = 2.996/0.08 = 37.45 min

Volume

V = Q·τ = 50·37.45 = 1872 L

Answer

V = 1872 L
16.Reactor sizing (CSTR & PFR)

Answer: X = 44.44 %

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 = 800/50 = 16 min, kτ = 0.05·16 = 0.8

Conversion

X = kτ/(1 + kτ) = 0.8/(1 + 0.8) = 44.44%

Answer

X = 44.44%
17.Heat exchangers (LMTD)

Answer: A = 0.2825 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.

Heat duty from the water side

Q̇ = 0.5·4.18·(50 − 15) = 73.15 kW

End temperature differences

ΔT₁ = 120 − 15 = 105 K
ΔT₂ = 120 − 50 = 70 K

Log-mean temperature difference

ΔTlm = (ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂) = (105 − 70)/ln(105/70) = 86.32 K

Area

A = Q̇/(U·ΔTlm) = 73150/(3000·86.32) = 0.2825 m²

Answer

A = 0.2825 m²
18.Heat exchangers (LMTD)

Answer: Tc,out = 82.32 °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.

Combine the energy balance and the rate equation

With ΔT₁ = Ts − Tc,in and ΔT₂ = Ts − Tc,out, the difference ΔT₁ − ΔT₂ equals the water temperature rise, so the rise cancels.

ṁcp(ΔT₁ − ΔT₂) = U·A·(ΔT₁ − ΔT₂)/ln(ΔT₁/ΔT₂)
ln(ΔT₁/ΔT₂) = U·A/(ṁcp) = 1500·5/(1.5·4180) = 1.196

Outlet temperature

ΔT₂ = ΔT₁·e−1.196 = 75·0.3023 = 22.68 K
Tc,out = 105 − 22.68 = 82.32 °C

Answer

Tc,out = 82.32 °C

Heat transferred: Q̇ = 328.1 kW.

19.Heat conduction

Answer: Q̇ = 19.64 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)/(0.04·4) = 1.25 K/W
R2 = L2/(k2A) = (50/1000)/(0.17·4) = 0.07353 K/W

Heat flow

Q̇ = (T1 − T3)/(R1 + R2) = 26/1.324 = 19.64 W

Answer

Q̇ = 19.64 W
20.Heat conduction

Answer: U = 0.7234 W/(m²·K)

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

Resistances in series

Ri = 1/(hiA) = 1/(7.7·8) = 0.01623 K/W
R1 = L1/(k1A) = (200/1000)/(0.17·8) = 0.1471 K/W
R2 = L2/(k2A) = (25/1000)/(0.96·8) = 0.003255 K/W
Ro = 1/(hoA) = 1/(20·8) = 0.00625 K/W
ΣR = 0.1728 K/W

Overall coefficient

U = 1/(A·ΣR) = 1/(8·0.1728) = 0.7234 W/(m²·K)

Answer

U = 0.7234 W/(m²·K)
21.Pipe friction & head loss

Answer: hf = 0.3966 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) = 0.015·(500/0.25)·0.5093²/(2·9.81) = 0.3966 m

Answer

hf = 0.3966 m
22.Pipe friction & head loss

Answer: H = 1.459 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 = 0.075/0.07069 = 1.061 m/s
V²/(2g) = 0.05738 m

Loss coefficients

f·L/D = 0.02·200/0.3 = 13.33
ΣK = 0.5 + 2·0.3 + 10 = 11.1

Energy equation

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

H = (1 + 13.33 + 11.1)·0.05738 = 1.459 m

Answer

H = 1.459 m
23.Pumps & pump power

Answer: Pshaft = 27.25 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 = 1000·9.81·0.04·50 = 19.62 kW

Shaft power

Pshaft = Ph/η = 19.62/0.72 = 27.25 kW

Answer

Pshaft = 27.25 kW
24.Pumps & pump power

Answer: Pshaft = 37.13 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.

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) = (58.67 + 8)·0.408 = 27.2 m

Pump head

H = Δz + hL = 22 + 27.2 = 49.2 m

Shaft power

Pshaft = ρ·g·Q·H/η = 1000·9.81·0.05·49.2/0.65 = 37.13 kW

Answer

Pshaft = 37.13 kW

This is independent practice material. ExamProblems is not affiliated with or endorsed by the organisation that runs this exam, and the exam name is used only to describe the content. The FE exam is run by NCEES, which is not affiliated with ExamProblems and does not endorse it.

ExamProblems · examproblems.com/courses/fe-exam-chemical