CHEMICAL ENGINEERING
Solutions to the Problems in Chemical Engineering
Volumes 2 and 3
Related Butterworth-Heinemann Titles in the Chemical Engineering Series by
J. M. COULSON & J. F. RICHARDSON
Chemical Engineering, Volume 1, Sixth edition
Fluid Flow, Heat Transfer and Mass Transfer
(with J. R. Backhurst and J. H. Harker)
Chemical Engineering, Volume 3, Third edition
Chemical and Biochemical Reaction Engineering, and Control
(edited by J. F. Richardson and D. G. Peacock)
Chemical Engineering, Volume 6, Third edition
Chemical Engineering Design
(R. K. Sinnott)
Chemical Engineering, Solutions to Problems in Volume 1
(J. R. Backhurst, J. H. Harker and J. F. Richardson)
Chemical Engineering, Solutions to Problems in Volume 2
(J. R. Backhurst, J. H. Harker and J. F. Richardson)
Coulson & Richardson’s
CHEMICAL ENGINEERING
J. M. COULSON and J. F. RICHARDSON
Solutions to the Problems in Chemical Engineering
Volume 2 (5th edition) and Volume 3 (3rd edition)
By
J. R. BACKHURST and J. H. HARKER
University of Newcastle upon Tyne
With
J. F. RICHARDSON
University of Wales Swansea
OXFORD AMSTERDAM BOSTON LONDON NEW YORK PARIS
SAN DIEGO SAN FRANCISCO SINGAPORE SYDNEY TOKYO
Butterworth-Heinemann
An imprint of Elsevier Science
Linacre House, Jordan Hill, Oxford OX2 8DP
225 Wildwood Avenue, Woburn, MA 01801-2041
First published 2002
Copyright 2002, J.F. Richardson and J.H. Harker. All rights reserved
The right of J.F. Richardson and J.H. Harker to be identified as the authors of this work
has been asserted in accordance with the Copyright, Designs
and Patents Act 1988
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ISBN 0 7506 5639 5
For information on all Butterworth-Heinemann publications visit our website at www.bh.com
Contents
Preface
Preface to the Second Edition of Volume 5
Preface to the First Edition of Volume 5
Factors for Conversion of SI units
vii
ix
xi
xiii
Solutions to Problems in Volume 2
2-1
Particulate solids
2-2
Particle size reduction and enlargement
2-3
Motion of particles in a fluid
2-4
Flow of fluids through granular beds and packed columns
2-5
Sedimentation
2-6
Fluidisation
2-7
Liquid filtration
2-8
Membrane separation processes
2-9
Centrifugal separations
2-10 Leaching
2-11 Distillation
2-12 Absorption of gases
2-13 Liquid–liquid extraction
2-14 Evaporation
2-15 Crystallisation
2-16 Drying
2-17 Adsorption
2-18 Ion exchange
2-19 Chromatographic separations
1
8
14
34
39
44
59
76
79
83
98
150
171
181
216
222
231
234
235
Solutions to Problems in Volume 3
3-1
Reactor design — general principles
3-2
Flow characteristics of reactors — flow modelling
3-3
Gas–solid reactions and reactors
3-4
Gas–liquid and gas–liquid–solid reactors
237
262
265
271
v
3-5
3-7
Biochemical reaction engineering
Process control
285
294
(Note: The equations quoted in Sections 2.1–2.19 appear in Volume 2 and those in
Sections 3.1–3.7 appear in Volume 3. As far as possible, the nomenclature used in this
volume is the same as that used in Volumes 2 and 3 to which reference may be made.)
vi
Preface
Each of the volumes of the Chemical Engineering Series includes numerical examples to
illustrate the application of the theory presented in the text. In addition, at the end of each
volume, there is a selection of problems which the reader is invited to solve in order to
consolidate his (or her) understanding of the principles and to gain a better appreciation
of the order of magnitude of the quantities involved.
Many readers who do not have ready access to assistance have expressed the desire for
solutions manuals to be available. This book, which is a successor to the old Volume 5, is
an attempt to satisfy this demand as far as the problems in Volumes 2 and 3 are concerned.
It should be appreciated that most engineering problems do not have unique solutions,
and they can also often be solved using a variety of different approaches. If therefore the
reader arrives at a different answer from that in the book, it does not necessarily mean
that it is wrong.
This edition of the Solutions Manual which relates to the fifth edition of Volume 2 and
to the third edition of Volume 3 incorporates many new problems. There may therefore
be some mismatch with earlier editions and, as the volumes are being continually revised,
they can easily get out-of-step with each other.
None of the authors claims to be infallible, and it is inevitable that errors will occur
from time to time. These will become apparent to readers who use the book. We have
been very grateful in the past to those who have pointed out mistakes which have then
been corrected in later editions. It is hoped that the present generation of readers will
prove to be equally helpful!
J. F. R.
vii
Preface to the Second Edition
of Volume 5
IT IS always a great joy to be invited to prepare a second edition of any book and on
two counts. Firstly, it indicates that the volume is proving useful and fulfilling a need,
which is always gratifying and secondly, it offers an opportunity of making whatever
corrections are necessary and also adding new material where appropriate. With regard
to corrections, we are, as ever, grateful in the extreme to those of our readers who have
written to us pointing out, mercifully minor errors and offering, albeit a few of what
may be termed ‘more elegant solutions’. It is important that a volume such as this is as
accurate as possible and we are very grateful indeed for all the contributions we have
received which, please be assured, have been incorporated in the preparation of this new
edition.
With regard to new material, this new edition is now in line with the latest edition,
that is the Fourth, of Volume 2 which includes new sections, formerly in Volume 3 with,
of course, the associated problems. The sections are: 17, Adsorption; 18, Ion Exchange;
19, Chromatographic Separations and 20, Membrane Separation Processes and we are
more than grateful to Professor Richardson’s colleagues at Swansea, J. H. Bowen, J.
R. Conder and W. R. Bowen, for an enormous amount of very hard work in preparing
the solutions to these problems. A further and very substantial addition to this edition
of Volume 5 is the inclusion of solutions to the problems which appear in Chemical
Engineering, Volume 3 — Chemical & Biochemical Reactors & Process Control and again,
we are greatly indebted to the authors as follows:
3.1
3.2
3.3
3.4
3.5
3.6
Reactor Design — J. C. Lee
Flow Characteristics of Reactors — J. C. Lee
Gas–Solid Reactions and Reactors — W. J. Thomas and J. C. Lee
Gas–Liquid and Gas–Liquid–Solid Reactors — J. C. Lee
Biological Reaction Engineering — M. G. Jones and R. L. Lovitt
Process Control — A. P. Wardle
and also of course, to Professor Richardson himself, who, with a drive and enthusiasm
which seems to be getting ever more vigorous as the years proceed, has not only arranged
for the preparation of this material and overseen our efforts with his usual meticulous
efficiency, but also continues very much in master-minding this whole series. We often
reflect on the time when, in preparing 150 solutions for the original edition of Volume 4,
the worthy Professor pointed out that we had only 147 correct, though rather reluctantly
agreed that we might still just merit first class honours! Whatever, we always have and
we are sure that we always will owe him an enormous debt of gratitude.
ix
We must also offer thanks to our seemingly ever-changing publishers for their drive,
efficiency and encouragement and especially to the present staff at Butterworth-Heinemann
for not inconsiderable efforts in locating the manuscript for the present edition which was
apparently lost somewhere in all the changes and chances of the past months.
We offer a final thought as to the future where there has been a suggestion that the titles
Volume 4 and Volume 5 may find themselves hijacked for new textural volumes, coupled
with a proposal that the solutions offered here hitherto may just find a new resting place
on the Internet. Whatever, we will continue with our efforts in ensuring that more and
more solutions find their way into the text in Volumes 1 and 2 and, holding to the view
expressed in the Preface to the First Edition of Volume 4 that ‘. . . worked examples are
essential to a proper understanding of the methods of treatment given in the various texts’,
that the rest of the solutions are accessible to the widest group of students and practising
engineers as possible.
Newcastle upon Tyne, 1997
J. R. BACKHURST
J. H. HARKER
(Note: Some of the chapter numbers quoted here have been amended in the later editions
of the various volumes.)
x
Preface to the First Edition
of Volume 5
IN THE preface to the first edition of Chemical Engineering, Volume 4, we quoted the
following paragraph written by Coulson and Richardson in their preface to the first edition
of Chemical Engineering, Volume 1:
‘We have introduced into each chapter a number of worked examples which we believe
are essential to a proper understanding of the methods of treatment given in the text.
It is very desirable for a student to understand a worked example before tackling
fresh practical problems himself. Chemical Engineering problems require a numerical
answer, and it is essential to become familiar with the different techniques so that the
answer is obtained by systematic methods rather than by intuition.’
It is with these aims in mind that we have prepared Volume 5, which gives our solutions
to the problems in the third edition of Chemical Engineering, Volume 2. The material is
grouped in sections corresponding to the chapters in that volume and the present book is
complementary in that extensive reference has been made to the equations and sources of
data in Volume 2 at all stages. The book has been written concurrently with the revision
of Volume 2 and SI units have been used.
In many ways these problems are more taxing and certainly longer than those in Volume 4, which gives the solutions to problems in Volume 1, and yet they have considerable
merit in that they are concerned with real fluids and, more importantly, with industrial
equipment and conditions. For this reason we hope that our efforts will be of interest to
the professional engineer in industry as well as to the student, who must surely take some
delight in the number of tutorial and examination questions which are attempted here.
We are again delighted to acknowledge the help we have received from Professors
Coulson and Richardson in so many ways. The former has the enviable gift of providing
the minimum of data on which to frame a simple key question, which illustrates the crux
of the problem perfectly, whilst the latter has in a very gentle and yet thorough way
corrected our mercifully few mistakes and checked the entire work. Our colleagues at the
University of Newcastle upon Tyne have again helped us, in many cases unwittingly, and
for this we are grateful.
Newcastle upon Tyne, 1978
J. R. BACKHURST
J. H. HARKER
xi
Factors for conversion of SI units
mass
1 lb
1 ton
length
1 in
1 ft
1 mile
time
1 min
1 h
1 day
1 year
area
1 in2
1 ft2
volume
1 in3
1 ft3
1 UK gal
1 US gal
force
1 pdl
1 lb
1 dyne
energy
1 ft lb
1 cal
1 erg
1 Btu
power
1 h.p.
1 Btu/h
0.454 kg
1016 kg
25.4 mm
0.305 m
1.609 km
60 s
3.6 ks
86.4 ks
31.5 Ms
645.2 mm2
0.093 m2
16,387.1 mm3
0.0283 m3
4546 cm3
3786 cm3
0.138 N
4.45 N
10−5 N
1.36 J
4.187 J
10−7 J
1.055 kJ
745 W
0.293 W
pressure
1 lbf/in2
1 atm
1 bar
1 ft water
1 in water
1 in Hg
1 mm Hg
viscosity
1 P
1 lb/ft h
1 stoke
1 ft2 /h
mass flow
1 lb/h
1 ton/h
1 lb/h ft2
thermal
1 Btu/h ft2
1 Btu/h ft2 ◦ F
1 Btu/lb
1 Btu/lb ◦ F
1 Btu/h ft ◦ F
energy
1 kWh
1 therm
6.895 kN/m2
101.3 kN/m2
100 kN/m
2.99 kN/m2
2.49 N/m2
3.39 kN/m2
133 N/m2
0.1 N s/m2
0.414 mN s/m2
10−4 m2 /s
0.258 cm2 /s
0.126 g/s
0.282 kg/s
1.356 g/s m2
3.155
5.678
2.326
4.187
1.731
W/m2
W/m2 K
kJ/kg
kJ/kg K
W/m K
3.6 MJ
106.5 MJ
calorific value
1 Btu/ft3
1 Btu/lb
37.26 kJ/m3
2.326 kJ/kg
density
1 lb/ft3
16.02 kg/m3
SECTION 2-1
Particulate Solids
PROBLEM 1.1
The size analysis of a powdered material on a mass basis is represented by a straight line
from 0 per cent at 1 µm particle size to 100 per cent by mass at 101 µm particle size.
Calculate the surface mean diameter of the particles constituting the system.
Solution
See Volume 2, Example 1.1.
PROBLEM 1.2
The equations giving the number distribution curve for a powdered material are dn/dd = d
for the size range 0–10 µm, and dn/dd = 100,000/d 4 for the size range 10–100 µm
where d is in µm. Sketch the number, surface and mass distribution curves and calculate
the surface mean diameter for the powder. Explain briefly how the data for the construction
of these curves may be obtained experimentally.
Solution
See Volume 2, Example 1.2.
PROBLEM 1.3
The fineness characteristic of a powder on a cumulative basis is represented by a straight
line from the origin to 100 per cent undersize at a particle size of 50 µm. If the powder
is initially dispersed uniformly in a column of liquid, calculate the proportion by mass
which remains in suspension in the time from commencement of settling to that at which
a 40 µm particle falls the total height of the column. It may be assumed that Stokes’ law
is applicable to the settling of the particles over the whole size range.
1
Solution
For settling in the Stokes’ law region, the velocity is proportional to the diameter squared
and hence the time taken for a 40 µm particle to fall a height h m is:
t = h/402 k
where k a constant.
During this time, a particle of diameter d µm has fallen a distance equal to:
kd 2 h/402 k = hd 2 /402
The proportion of particles of size d which are still in suspension is:
= 1 − (d 2 /402 )
and the fraction by mass of particles which are still in suspension is:
40
[1 − (d 2 /402 )]dw
=
0
Since dw/dd = 1/50, the mass fraction is:
40
[1 − (d 2 /402 )]dd
= (1/50)
0
= (1/50)[d − (d 3 /4800)]40
0
= 0.533 or 53.3 per cent of the particles remain in suspension.
PROBLEM 1.4
In a mixture of quartz of density 2650 kg/m3 and galena of density 7500 kg/m3 , the sizes
of the particles range from 0.0052 to 0.025 mm.
On separation in a hydraulic classifier under free settling conditions, three fractions
are obtained, one consisting of quartz only, one a mixture of quartz and galena, and one
of galena only. What are the ranges of sizes of particles of the two substances in the
original mixture?
Solution
Use is made of equation 3.24, Stokes’ law, which may be written as:
u0 = kd 2 (ρs − ρ),
where k (= g/18µ) is a constant.
For large galena: u0 = k(25 × 10−6 )2 (7500 − 1000) = 4.06 × 10−6 k m/s
For small galena: u0 = k(5.2 × 10−6 )2 (7500 − 1000) = 0.176 × 10−6 k m/s
For large quartz: u0 = k(25 × 10−6 )2 (2650 − 1000) = 1.03 × 10−6 k m/s
For small quartz: u0 = k(5.2 × 10−6 )2 (2650 − 1000) = 0.046 × 10−6 k m/s
2
If the time of settling was such that particles with a velocity equal to 1.03 × 10−6 k m/s
settled, then the bottom product would contain quartz. This is not so and hence the
maximum size of galena particles still in suspension is given by:
1.03 × 10−6 k = kd 2 (7500 − 1000)
or
d = 0.0000126 m
or 0.0126 mm.
Similarly if the time of settling was such that particles with a velocity equal to 0.176 ×
10−6 k m/s did not start to settle, then the top product would contain galena. This is not
the case and hence the minimum size of quartz in suspension is given by:
0.176 × 10−6 k = kd 2 (2650 − 1000)
or
d = 0.0000103 m
or
0.0103 mm.
It may therefore be concluded that, assuming streamline conditions, the fraction of
material in suspension, that is containing quartz and galena, is made up of particles of
sizes in the range 0.0103–0.0126 mm
PROBLEM 1.5
A mixture of quartz and galena of a size range from 0.015 mm to 0.065 mm is to be
separated into two pure fractions using a hindered settling process. What is the minimum
apparent density of the fluid that will give this separation? How will the viscosity of the
bed affect the minimum required density?
The density of galena is 7500 kg/m3 and the density of quartz is 2650 kg/m3 .
Solution
See Volume 2, Example 1.4.
PROBLEM 1.6
The size distribution of a dust as measured by a microscope is as follows. Convert these
data to obtain the distribution on a mass basis, and calculate the specific surface, assuming
spherical particles of density 2650 kg/m3 .
Size range (µm)
0–2
2–4
4–8
8–12
12–16
16–20
20–24
Number of particles in range (−)
2000
600
140
40
15
5
2
3
Solution
From equation 1.4, the mass fraction of particles of size d1 is given by:
x1 = n1 k1 d13 ρs ,
where k1 is a constant, n1 is the number of particles of size d1 , and ρs is the density of
the particles = 2650 kg/m3 .
x1 = 1 and hence the mass fraction is:
x1 = n1 k1 d13 ρs nkd 3 ρs .
In this case:
d
n
kd 3 nρs
x
1
3
6
10
14
18
22
200
600
140
40
15
5
2
5,300,000k
42,930,000k
80,136,000k
106,000,000k
109,074,000k
77,274,000k
56,434,400k
0.011
0.090
0.168
0.222
0.229
0.162
0.118
= 477,148,400k
= 1.0
The surface mean diameter is given by equation 1.14:
ds = (n1 d13 ) (n1 d12 )
and hence:
Thus:
d
n
nd 2
nd 3
1
3
6
10
14
18
22
2000
600
140
40
15
5
2
2000
5400
5040
4000
2940
1620
968
2000
16,200
30,240
40,000
41,160
29,160
21,296
= 21,968
= 180,056
ds = (180,056/21,968) = 8.20 µm
This is the size of a particle with the same specific surface as the mixture.
The volume of a particle 8.20 µm in diameter = (π/6)8.203 = 288.7 µm3 .
4
The surface area of a particle 8.20 µm in diameter = (π × 8.202 ) = 211.2 µm2
and hence: the specific surface = (211.2/288.7)
= 0.731 µm2 /µm3 or 0.731 × 106 m2 /m3
PROBLEM 1.7
The performance of a solids mixer was assessed by calculating the variance occurring in
the mass fraction of a component amongst a selection of samples withdrawn from the
mixture. The quality was tested at intervals of 30 s and the data obtained are:
mixing time (s)
sample variance (−)
30
0.025
60
0.006
90
0.015
120
0.018
150
0.019
If the component analysed represents 20 per cent of the mixture by mass and each of the
samples removed contains approximately 100 particles, comment on the quality of the
mixture produced and present the data in graphical form showing the variation of mixing
index with time.
Solution
See Volume 2, Example 1.3.
PROBLEM 1.8
The size distribution by mass of the dust carried in a gas, together with the efficiency of
collection over each size range is as follows:
Size range, (µm)
Mass (per cent)
Efficiency (per cent)
0–5
10
20
5–10
15
40
10–20
35
80
20–40
20
90
40–80
10
95
80–160
10
100
Calculate the overall efficiency of the collector and the percentage by mass of the emitted
dust that is smaller than 20 µm in diameter. If the dust burden is 18 g/m3 at entry and
the gas flow is 0.3 m3 /s, calculate the mass flow of dust emitted.
Solution
See Volume 2, Example 1.6.
PROBLEM 1.9
The collection efficiency of a cyclone is 45 per cent over the size range 0–5 µm, 80
per cent over the size range 5–10 µm, and 96 per cent for particles exceeding 10 µm.
5
Calculate the efficiency of collection for a dust with a mass distribution of 50 per cent
0–5 µm, 30 per cent 5–10 µm and 20 per cent above 10 µm.
Solution
See Volume 2, Example 1.5.
PROBLEM 1.10
A sample of dust from the air in a factory is collected on a glass slide. If dust on the slide
was deposited from one cubic centimetre of air, estimate the mass of dust in g/m3 of air
in the factory, given the number of particles in the various size ranges to be as follows:
Size range (µm)
Number of particles (−)
0–1
2000
1–2
1000
2–4
500
4–6
200
6–10
100
10–14
40
It may be assumed that the density of the dust is 2600 kg/m3 , and an appropriate allowance
should be made for particle shape.
Solution
If the particles are spherical, the particle diameter is d m and the density ρ = 2600 kg/m3 ,
then the volume of 1 particle = (π/6)d 3 m3 , the mass of 1 particle = 2600(π/6)d 3 kg
and the following table may be produced:
Size (µm)
0–1
1–2
2–4
4–6
Number of particles (−)
2000
1000
500
200
Mean diameter (µm)
0.5
1.5
3.0
5.0
−6
−6
−6
1.5 × 10
3.0 × 10
5.0 × 10−6
(m)
0.5 × 10
Volume (m3 )
6.54 × 10−20 3.38 × 10−18 1.41 × 10−17 6.54 × 10−17
Mass of one particle (kg) 1.70 × 10−16 8.78 × 10−15 3.68 × 10−14 1.70 × 10−13
Mass of one particles in
size range (kg)
3.40 × 10−13 8.78 × 10−12 1.83 × 10−11 3.40 × 10−11
Size (µm)
Number of particles (−)
Mean diameter (µm)
(m)
3
Volume (m )
Mass of one particle (kg)
Mass of one particles in
size range (kg)
6–10
100
8.0
8.0 × 10−6
2.68 × 10−16
6.97 × 10−13
10–14
40
12.0
12.0 × 10−6
9.05 × 10−16
2.35 × 10−12
6.97 × 10−11
9.41 × 10−11
6
Total mass of particles = 2.50 × 10−10 kg.
As this mass is obtained from 1 cm3 of air, the required dust concentration is given by:
(2.50 × 10−10 ) × 103 × 106 = 0.25 g/m3
PROBLEM 1.11
A cyclone separator 0.3 m in diameter and 1.2 m long, has a circular inlet 75 mm in
diameter and an outlet of the same size. If the gas enters at a velocity of 1.5 m/s, at what
particle size will the theoretical cut occur?
The viscosity of air is 0.018 mN s/m2 , the density of air is 1.3 kg/m3 and the density
of the particles is 2700 kg/m3 .
Solution
See Volume 2, Example 1.7.
7
SECTION 2-2
Particle Size Reduction
and Enlargement
PROBLEM 2.1
A material is crushed in a Blake jaw crusher such that the average size of particle is
reduced from 50 mm to 10 mm, with the consumption of energy of 13.0 kW/(kg/s). What
will be the consumption of energy needed to crush the same material of average size
75 mm to average size of 25 mm:
(a) assuming Rittinger’s Law applies,
(b) assuming Kick’s Law applies?
Which of these results would be regarded as being more reliable and why?
Solution
See Volume 2, Example 2.1.
PROBLEM 2.2
A crusher was used to crush a material with a compressive strength of 22.5 MN/m2 .
The size of the feed was minus 50 mm, plus 40 mm and the power required was
13.0 kW/(kg/s). The screen analysis of the product was:
Size of aperture (mm)
through
6.0
on
4.0
on
2.0
on
0.75
on
0.50
on
0.25
on
0.125
through
0.125
Amount of product (per cent)
all
26
18
23
8
17
3
5
What power would be required to crush 1 kg/s of a material of compressive strength
45 MN/m2 from a feed of minus 45 mm, plus 40 mm to a product of 0.50 mm average size?
8
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