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CLASSICAL PHYSICS OF MATTER
Edited by John Bolton
0 CRC Press
Taylor & Francis Group
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Taylor & Francis Group, an informa business
Institute of Physics Publishing

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in association with
The Open
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The Physical World Course Team
Course Team Chair Robert Lambourne
Academic Editors John Bolton, Alan Durrant , Robert Lambourne, Joy Manners,
Andrew Norton
Authors David Broadhurst, Derek Capper, Andrew Conway, Dan Dubin,
Tony Evans, !an Halliday, Carole Haswell, Keith Higgins, Keith
Hodgkinson, Mark Jones , Sally Jordan , Ray Mackintosh, David
Martin, John Perring, Michael de Podesta, Sean Ryan, !an Saunders,
Richard Skelding, Tony Sudbery, Stan Zochow ski
Consultants Alan Cayless, Melvin Davies, Graham Farmelo , Stuart Freake,
Gloria Medina , Kerry Parker, Alice Peasgood, Graham Read,
Russell Stannard, Chris Wigglesworth
Course Managers Gillian Knight, Michael Watkins
Course Secretaries Tracey Moore, Tracey Woodcraft
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The CourseTeam wishes to thank Richard Skelding, !an Saunders, John Perring,
Robert Lambourne, Mark Jones, Alan Cayless, Gloria Medina and Chris Denham for their
contributions to this book.
First Published in 2000 by Institute of Physics Publishing

Published 2020 by CRC Press
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Copyright© 2000 by The Open University

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DOl: 10.1201/9780429187780
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Library of Congress Cataloging-in-Publication Data are available.
This text forms part of an Open University course, S207 The Physical World. The complete list of texts that
make up this course can be found on the back cover.
1.1
s207book4i 1.1
2
CLASSICAL PHYSICS OF MATTER
Introduction 6
Chapter I From atoms to the phases of matter 8
I A puzzle 8
2 Atoms: the building blocks of matter 8
2. 1 The concept of an atom 8
2.2 Atomic sizes 11
2.3 Isotopes and ions 14
2.4 Atomic masses IS
2.5 Interactions between atoms 16
3 Atomic descriptions of the phases of matter 19
3.1 The gas phase 20
3.2 The liquid phase 23
3.3 The solid phase 24
4 Macroscopic variables 26
4. 1 Density 26
4.2 Pressure 26
4.3 Temperature 28
4.4 Internal energy 31
4.5 Molar quantities 31
4.6 Response functions 33
5 Macroscopic equilibrium in ideal gases 34
5. 1 Experiments on gases 35
5.2 The absolute temperature scale 37
5.3 The equation of state of an ideal gas 38
5.4 Internal energy equations of ideal gases 42
5.5 A puzzle resolved 43
6 Macroscopic descriptions of the phases of matter 44
6. 1 The generic PVT surface and phases of matter 44
6.2 The generic UPT surface and latent heats 46
7 Closing items 48
Chapter 2 Microscopic models of gases 52
I Introduction 52
2 Chance and probability 53
2. I Probability 53
2.2 Average values 55
2.3 Fluctuations 57
2.4 Dicing with Boltzmann 58
3 The pressure of a gas 61
3.1 Molecular bombardment 61
3.2 The simple gas model 62
3.3 Calculating the pressure 63
4 Distributions of speed and translational energy in gases 68
4.1 Measuring the distribution of molecular speeds 68
4.2 Analysing the experiment in terms of translational energy 71
3
The Physical World
4.3 What do the distributions of speed and translational

energy depend on? 72
4.4 Distribution functions 73
5 Statistical mechanics 76
S.l From chance to practical certainty 76
S.2 Defining configurations in a gas 78
S.3 Assigning probabilities to configurations 79
S.4 The Boltzmann distribution law 80
S.S The distribution of molecular speed 84
S.6 The distribution of molecular translational energy 87
6 The equipartition of energy 92
6. 1 Application to gases 94
6.2 Application to solids 97
7 Closing items 98
Appendix to Chapter 2 Computer simulations 103
Chapter 3 Thermodynamics and entropy 105
I Engine efficiency - an effect of thermodynamics lOS
2 The first law of thermodynamics 107
2.1 Systems, states and processes 107
2.2 Heat and work 109
2.3 The first law of thermodynamics 112
2.4 The first law and heat capacities 117
2.S Isothermal and adiabatic processes 122
3 The second law of thermodynamics 127
3.1 Reversible and irreversible processes 127
3.2 Adiabatic accessibility and the second law 128
3.3 Defining entropy 132
3.4 Entropy and heat flow 138
3.S But what is entropy anyway? 139
4 Entropy, engines and refrigerators 141
4.1 Heat engines 141
4.2 Refrigerators 147
4.3 The third law of thermodynamics ISO
5 Closing items ISO
Chapter 4 The physics of fluids 154
I Introduction 154
2 Fluids at rest ISS
2.1 Pressure in a fluid ISS
2.2 The pressure experienced by a diver IS6
2.3 The pressure experienced by a mountaineer IS9
2.4 Buoyancy and Archimedes' principle 166
3 Ideal fluids in motion 169
3.1 Ideal flow 169
3.2 Conservation of mass and the equation of continuity 171
3.3 Conservation of energy and Bernoulli's equation 172
3.4 Bernoulli's principle in action 174
4
Classical physics of matter
4 Non-ideal fluids in motion 175

4.1 Viscosity 175
4.2 Dynamical similarity and Reynolds number 178
4.3 Turbulence and its onset 181
4.4 The boundary layer 183
5 Flight 186
6 Closing items 187
Chapter 5 Consolidation and skills development 190
I Introduction 190
2 Overview of Chapters I to 4 190
2. 1 The atomic hypothesis 191
2.2 The macroscopic view 192
2.3 A statistical approach to physics 193
2.4 The laws of thermodynamics 194
2.5 The meaning of temperature 195
2.6 The physics of fluids 196
3 Writing precise physical statements 197
4 Basic skills and knowledge test 201
5 Interactive questions 206
6 Physica problems 206
Answers and comments 207
Acknowledgements 229
Index 230
5
The Physical World
Introduction
Understanding and using the properties of matter have gone hand in hand with
technological progress and the rise and fall of civilizations. We speak of the Stone
Age, the Bronze Age and the Iron Age, because the properties of these materials
helped to shape the nature of human existence. More recently, we have emerged
from the Age of Steam, flirted with the Age of Uranium and, with the rise of
computers, are surely living in the Age of Silicon.
Materials do have a remarkable range of properties. Take a paper clip, a pane of
glass and a rubber ball. The paper clip is shiny, can be bent, is attracted to magnets
and conducts heat and electricity well. The pane of glass is transparent, brittle, non-
magnetic and conducts heat and electricity poorly. The rubber ball is soft and
bounces when dropped. It is easy to take these properties for granted as part of the
environment we are born into, and most people are content to leave things that way.
They simply accept that glass has glassy properties because that is the way glass is.
Science, however, does not thrive on easy acceptance; it is based on a much more
adventurous curiosity. Taking nothing for granted, and looking with fresh eyes at the
substances around us, we are led to ask a profound question: why do these
substances behave as they do?
This question becomes more sharply focused once we recognize that all normal
matter, whether solid, liquid or gas, is composed of atoms. You can think of an atom
as being a tiny sphere, about I0- 10 m in diameter. There are over 100 different types
of atom, corresponding to the different types of chemical element. Once we know
that different substances contain a limited number of different types of atom, we can
try to explain the transparency of glass, the magnetism of iron or the stretchiness of
rubber on an atomic scale.
The central importance of atoms has been emphasized by Richard Feynman, Nobel
laureate and one of the greatest physicists of recent times. Feynman once asked a
group of students:
'If in some cataclysm, all of scientific knowledge were to be destroyed and

only one sentence passed on to the next generation of creatures, what
statement would contain the most information in the fewest words?'
There is no record of the replies given by the students, but we do know Feynman's
own answer:
'I believe that it is the atomic hypothesis ... that all things are made of
atoms - little particles that move around in perpetual motion, attracting
each other when they are a little distance apart, but repelling one another
upon being squeezed together. In that one sentence, you will see, there is an
enormous amount of information about the world, if just a little imagination
and thinking are applied.'
The relationship between the properties of materials and the properties of atoms can
be quite straightforward: the mass of a raindrop, for instance, is just the sum of the
masses of its atoms. But many of the properties of materials emerge in a far more
subtle way - steel is not strong because it is made from strong atoms; and rubber is
not stretchy because it is made from stretchy atoms! Establishing the link between
the scale of everyday life and the scale of atoms has proved to be one of the major
challenges of physics.
6 DOl: 10.1201/9780429187780-1
At first, the problem was that very little was known about atoms, and their very
existence was seriously in doubt. This is not surprising. Even the tiniest scrap of
dust, just visible to the naked eye, contains 10 15 atoms or more, so individual atoms
lie well beyond the limits of our senses. Throughout the nineteenth century, many
scientists suspected that atoms existed, but had very little idea of their properties.
Amid this uncertainty, two different traditions emerged.
One group of physicists simply assumed that atoms exist, picturing them as tiny
particles bouncing around in accordance with Newton's laws. The enormous number
of particles involved meant that it was impossible to keep detailed track of them as
they collided with one another. Nevertheless, a variety of statistical methods allowed
predictions to be made about the behaviour of matter on a large scale. The other
group of physicists chose to ignore the possible existence of atoms and to deduce
what they could by treating matter as a continuous medium; this gave rise to two
subjects - thermodynamics and fluid mechanics - which remain important today.
This book will look at both traditions. Although I have stressed the ultimate aim of
looking for explanations at an atomic level, I do not wish to downplay the value of
thermodynamics and fluid mechanics. The truth is that many questions of practical
and technological importance are best answered within these two subjects. This is
partly because the goal of understanding matter in terms of the properties of atoms is
yet to be completely fulfilled. Where it has been attained, we can be very satisfied;
elsewhere, thermodynamics and fluid mechanics remain the best tools available.
Ironically, just as the existence of atoms was being demonstrated beyond any
reasonable doubt at the beginning of the twentieth century, the foundations of
Newtonian mechanics were being shaken by the first glimmerings of quantum
theory. The arrival of quantum mechanics gave new insights into the behaviour of
matter, and it is now apparent that many important and useful properties of materials
are due to quantum mechanical effects. In this course, our discussion of the physics
of matter is split into two parts. The present book is based on classical physics.
Many aspects of the properties of matter can be explained in this way, without any
need for quantum mechanics, and we shall explore these aspects now. Following an
introduction to quantum mechanics, the course will return to the properties of matter
in Quantum physics of matter and discuss those properties that can only be
understood in quantum mechanical terms.
Open Uni versity students shoul d note that the video assoc iated with thi s
book is Video 4 Maiden Flights; thi s is best viewed toward s the e nd of
Chapter 4.
7
The Physical World
Chapter I From atoms to the

phases of matter
I A puzzle
Suppose you go into a cold room and turn on an electric fire. After a while, you
begin to feel more comfortable - the chill has been taken out of the room, and you
settle down to take a well-deserved snooze. Would it surprise you to learn that the
total energy of the air in the warm room is the same as it was in the cold room?
Turning on the fire did not increase the energy of the air in the room at all!
This surprising fact illustrates some of the subtleties that arise in discussing the
properties of matter in general, and the properties of gases in particular. We leave it
as a puzzle, with the promise that we will come back to it before this chapter closes.
2 Atoms: the building blocks of matter

2.1 The concept of an atom
'All these things being consider'd, it seems probably to me, that God form'd
matter in solid, massy, hard, impenetrable particles ... '
Isaac Newton, Query 31, Opticks, 1706.
The concept of an atom is an extremely ancient one, dating back at least to the fifth
century BC when the Greek philosophers Leucippus and Democritus proposed that
all matter is made up of atoms in ceaseless motion. Different substances were
supposed to be produced by different combinations of the fundamental atom·s. This
opposed the view that matter was a continuum which could be divided into smaller
and smaller parts, ad infinitum. The atomic ideawas never part of the mainstream of
Greek philosophy, but it survived as a minority view, and Newton clearly favoured
it, though he lacked convincing experimental evidence.
The first persuasive arguments for atoms came at the beginning of the nineteenth
century, from chemists who had found that certain substances could not be broken
down into simpler components. These substances were called elements, and each
pure substance was regarded as being either an element or a combination of different
elements (a compound). It gradually became clear that each compound contained a
fixed proportion (by mass) of its constituent elements. And, when one element
combined with another to produce more than one compound, the ratios of the masses
of the elements could be expressed as simple integers.
John Dalton (c. 1766-1844) realized thatthese facts could be explained quite
naturally if matter were made up of atoms, and if different elements had different
atoms. (Newton did not have this understanding because the chemical notion of an
element was not fully developed in his day.) Dalton gave lectures on this idea and, in
1808, published a revolutionary book called A New System of Chemical Philosophy
John Dalton (c. 1766-1844) which asserted that:
8 DOl: 10.1201/9780429187780-2
Each ele ment has a di stincti ve kind of atom with its o wn characteri sti c
properti es. A macroscopic sampl e of an ele ment consists of a large number of
these atoms. Atoms o f onetype cann ot b e co nverted into a toms of another
type, but atoms ca n bind together in specific ways.
The images shown in Figure 1.1 are taken from Dalton's book. Although they should
not be taken too literally, they clearly show the essential idea that elements have
atoms of distinct types and these can combine together to form new substances.
l i!lll
Q o.' Y5"' Z inc

~ Ploosplw" " .9
. @ ,Copper
ffi SulpJ,,, )~ <!) Lei\fl
(}) M.',\'"""·' 2 ® Silver
e L llu r 24 0 Cold
(J]) Sod a 'f 8 ®
® Polaslt 1!
2 3 4 5 6
i i ~ w® ~
Figure 1.1 (al D.tlton\
"Ymhols •or suhsta·1ces t 1at he
7 8 9 10 11
!'loug'lt were elmnt~: several of
~ ~ ~
them subsequently were found to
& ~
he compounds (h) Part ot
Dalton's onginal pllture of atoms
(b) comhiring together to form
molecules.
9
The Physical World
Each arrangement of atoms is now called a molecule. There are several cases to
consider (Figure 1.2):
Atoms of different types can combine together to form a molecule of a
compound. Thus, a water molecule is formed when two hydrogen atoms bind
with one oxygen atom. Much larger and more complicated molecules can form,
such as DNA, the famous carrier of the genetic code.
2 Atoms of the same type can also join together to form a molecule. Thus, two
oxygen atoms join together to form an oxygen molecule. It is also possible for
three oxygen atoms to join together to form a different type of molecule, known
as an ozone molecule.
3 Finally, some elements, such as argon, have atoms that do not easily combine
with others - argon gas consists of individual argon atoms. It is convenient to
continue to use the terminology of molecules in this case, so an argon molecule
is just a single argon atom.
The words monatomic, diatomic and triatomic are often used to describe molecules
containing one, two and three atoms respectively.
We are perhaps fortunate that Dalton lived in Cumbria, a rainy part of Britain. It is
said that his concerns about the origin of rain led him to a detailed study of gases
which culminated in the atomic theory. By the time of his death, in 1844, the idea of
an atom had spread far beyond the small community of scientists; Dalton's lying-in-
state in Manchester Town Hall was attended by no fewer than 40 000 people!
The popular appeal of the atomic model was justified, as simplicity is generally an
excellent guide to truth. But it was not to everyone's taste. It neatly fitted the
chemical facts but there was no direct evidence or proof. That is why it was referred
(a) (b)
Figure 1.2
Modern representations of
molecules: (a) argon: (b) oxygen;
(c) ozone; (d) water; and
(c) (d) (e) segment of DNA.
10
to as the atomic hypothesis, and why some scientists regarded it as a fiction, useful
for accounting purposes but not reflecting deep reality. The debate about whether
atoms exist or not was destined to run for the whole of the nineteenth century, only
to be finally settled around 1908, the centenary of Dalton's original insight.
2.2 Atomic sizes

Once the ideas of atoms and molecules had been proposed, physicists worked hard
to see if this structure of matter would have any large-scale consequences. At the
same time, knowledge of atomic properties became of great intrinsic interest. Many
questions had been left unanswered by Dalton's ideas: what size and mass do atoms
have and what forces act between them?
We will begin with atomic sizes. Clearly, atoms and molecules must be small -
below the limits of sight- but how small, exactly? Is their diameter I o- 10 m, or is it
more like I0-20 m?
A simple observation, first performed by Lord Rayleigh, provides a clue. If a drop of
oil is lowered carefully onto the surface of a lake, it spreads out, forming a circular
patch on the surface. The patch soon becomes too thin to be seen directly, but makes
its presence felt because the water is particularly calm and unruffled over the area of
the patch. The patch is surprisingly large: a tiny drop of oil of radius 0.5 mm spreads
to a circular patch with a radius of around 0.4 m.
e Use the information given above to estimate the thickness of the oil film.
0 We can take the oil drop to be a sphere of radius r, and treat the oil patch as a
very thin circular cylinder of radius R and thickness t (Figure 1.3). Then, setting
the volume of the initial oil drop equal to the volume of the oil patch gives
so t= _± X ~ = _± X (0.5 X 1o-3 m)3 "" 1o-9 m. •

3 R2 3 (0.4 m) 2
Figure 1.3 A drop of oil spreads

out on the surface of a lake.
The oil film cannot be less than one molecule thick, so we have an upper limit for
the linear dimensions of an oil molecule - around 1o-9 m. Clearly, atoms must be
smaller than this.
Throughout the nineteenth century, physicists devised several other ways of
estimating the sizes of atoms and molecules. Many of these involved the properties
of gases - especially the rate at which molecules, energy and momentum spread
from one region in a gas to another. When a gas molecule moves from one side of a
room to another, it does so at a rate that depends on the number of collisions it
makes with other molecules. If it makes no collisions, it will make very rapid
11
The Physical World
progress, but if it collides frequently, it will follow a highly irregular zigzag path and
its progress will be much slower. The rate of collisions, of course, depends on the
size of the molecule. This fact, and a great deal of careful measurement, quantitative
analysis and plausible assumptions, gave physicists a way of estimating the size of
molecules. By the end of the nineteenth century the consensus had emerged that
atoms would have to be about 1-2 x 10- 10 m across and small molecules would
therefore be slightly larger (depending on the number of atoms they contain).
Although the victory of the atomists has long been complete, it is only recently that
we have been able to obtain images that give us the impression of seeing atoms. To
explain how this is possible, I need to say something about the nature of light. The
most important point is that light is a wave-like phenomenon. Rather like water-
Light is discussed more fully in the waves travelling towards a shore, light propagates as a series of peaks and troughs.
book Dynamic fields and waves. One of the key parameters that describes a light wave is its wavelength -the
distance between one crest in the wave and the next. In fact, the wavelength of a
light wave is directly related to its colour: red light has a wavelength of about
7 x 10-7 m while violet light has a wavelength of about 4 x 10-7 m.
Wavelength becomes very important when we consider how waves flow around an
obstacle. The example of water waves can illustrate this point (Figure 1.4). In Figure
1.4a, the object is larger than the wavelength of the waves. In this case the object has
a significant effect on the way the waves propagate, so it should be possible for
observers downstream to infer the presence of the object by measuring the waves
that reach them. In Figure 1.4b, the object is smaller than the wavelength of the
waves. In this case, the waves are scarcely affected by the object and observers
would be very hard-pressed to detect it, simply by observing the waves.
Figure 1.4 Water waves flowing

around an object. (a) If the object is
larger than the wavelength, the
wave propagation is significantly
affected. (b) If the object is smaller
than the wavelength, the wave (a) (b)
propagation is almost unchanged.
Very similar considerations apply to light: it is practically impossible to see any
object whose linear dimensions are smaller than the wavelength of the light that is
used to illuminate it. With ordinary light, the smallest object that can be seen, even
with a microscope, is roughly 1o-6 m across. This is about I 0000 times larger than
the size of an atom.
In order to 'see' atoms we must use waves with much smaller wavelengths than
visible light. It turns out that electrons can behave as waves. High energy electrons
propagate as waves of very short wavelength, and this fact is used to form very
detailed images in electron microscopes. The most powerful electron microscopes
are able to resolve individual atoms (Figure 1.5).
12
Figure 1.5 An image of gold atoms

formed by a very powerful electron
microscope. The atoms are arranged in a
very regular array so each tiny dot in the
central region represents a column of atoms.
In 1982, the scanning tunnelling microscope (STM) was invented, which gave an
alternative way of viewing atoms. The STM relies on the fact that atoms contain
negatively charged electrons which are attracted to positive charges. In order to
deduce the arrangement of atoms on the surface of a solid, a very sharply pointed,
positively charged metal tip is allowed to approach the surface, coming almost into
contact with it. When the metal tip gets close enough to the surface, it starts to suck
electrons out of the surface, like a miniature vacuum cleaner. The flow of electrons
into the metal tip depends very sensitively on the distance between the tip and the
surface.
The operator of the STM scans the tip over the surface, whilst making tiny
adjustments to its distance from the surface in order to ensure that the flow of
electrons remains steady. Since the surface under investigation contains bumps
(where the atoms are) and hollows (in between the atoms), the metal tip has to move
in and out to follow these tiny surface features. By keeping note of the precise
movements of the metal tip, the bumps and hollows can be mapped out, and a
picture of the atomic positions formed. Figure 1.6 A surface map
obtained with a STM . Each
If someone came to you with a plan for a new device, operating along the lines just
pinkish-red blob is an atom,
described, would you be inclined to invest money in it? Perhaps not. The plan
though these colours have been
requires the position of a metal tip to be controlled to within less than the size of an assigned by the computer purely
atom (l0- 10 m), which sounds rather fanciful. But, amazingly enough, this proves to to increase the visual impact. The
be no problem. Precise positioning of this kind can be achieved with quartz rods, atoms have been carefully
which have the property of changing their lengths in response to applied electrical positioned (also using the STM)
voltages. Figure 1.6 is the proof of the pudding: an STM image showing exactly so that they form the Japanese
where all the surface atoms are located. characters for the word 'atom'.
13
The Physical World
2.3 Isotopes and ions

Atoms, as originally conceived by Dalton, were tiny, impenetrable spheres. In order
to explore the properties of atoms in more detail, including their masses, we must
adopt a more modern viewpoint, and recognize that atoms have internal structure.
Any atom consists of three types of particle: electrons, protons and neutrons,
which have the physical properties shown in Table 1.1 . An atom is electrically
neutral, so it contains equal numbers of negatively charged electrons and positively
charged protons. The protons and neutrons are tightly bound together in the nucleus
- a tiny, dense core at the centre of the atom. Since protons and neutrons are much
more massive than electrons, nearly all the atom's mass is locked up in its nucleus.
The electrons occupy the region outside the nucleus, so they roam over nearly all of
the atom's volume.
Table 1.1 Properties of electrons, protons and neutrons. The coulomb (C) is the SI
unit of electric charge; it is discussed fully in Static fields and potential.\·.
Mass/1 o-30 kg Charge/1.602 x I0-19 C
electron 0.9109 -1
proton 1673 +1
neutron 1675 0
Each element has atoms with a definite number of electrons and an equal number of
protons. For example, iron has atoms with 26 electrons and 26 protons; silver has
atoms with 47 electrons and 47 protons. However, atoms of a given element need
not all have the same number of neutrons. Most iron atoms contain 30 neutrons, but
about 6% contain 28 neutrons and 2% contain 31 neutrons. Each species of at01;n,
with a fixed number of electrons, protons and neutrons, is called an isotope:
Isotopes
A g iven element may have a number of different isotopes, each with the same
nu mber of electrons, an equ al number of protons, but diffe rent numbers of
neutrons. Different isotopes of the same e lement have sli ghtl y different masses,
bu t essentially the same c hemi cal properties.
Isotopes are conventionally labelled by giving two numbers. The atomic number Z
is the number of protons (or electrons) in the atom. This is the same for all isotopes
of a given element. The mass number A is the sum of the numbers of protons and
neutrons. This number varies from isotope to isotope. For example, the most
common isotope of iron, with 26 electrons, 26 protons and 30 neutrons, has Z =26
and A =56. The less common isotopes mentioned above haveA =54 and A =57.
Very often, the mass number is just tagged on to the name of the element, so that we
talk of iron-56, iron-54 or iron-57, for example.
e How would you describe an isotope of silver with 47 protons and 60 neutrons?
0 The isotope is described as silver-107. •
One consequence of the internal structure of atoms is the fact that they can gain or
lose electrons. In the simplest case, a neutral atom loses a single electron and so
becomes positively charged, since there is now one more positively charged proton
14
than there are negatively charged electrons. The positively charged object that Molecules can also lose
remains after the electron has been removed is called an ion. Electrons are very light, electrons to form ions.
so the ion has almost the same mass as the atom from which it was prepared, but it
behaves quite differently: because it is electrically charged, an ion responds to electrical
forces. This means that ions can be controlled more easily than uncharged atoms.
2.4 Atomic masses

Dalton's atomic theory developed from the observation that the masses of elements
that combine to form compounds can be expressed as simple ratios. If the elements
are gases, it turns out that their volumes, at a given temperature and pressure, are
also in simple ratios. How can both these facts be true? Shortly after Dalton had
published his theory, Amedeo Avogadro (1776-1856) suggested a simple explanation:
Avogadro's hypothesis
Equ al vo lumes of different gases, at the same temperature a nd pressure,
contain the sa me number of molec ul es.
This suggestion lay dormant for 50 years before it was realized that it could be put to
use - by weighing equal volumes of different gases under specified conditions of
temperature and pressure, the mass of one type of molecule could be related to the
mass of another. Of course, no absolute measurements could be taken in this way,
but a scale of relative masses could be established. For example, an oxygen
molecule was found to be 16 times more massive than a hydrogen molecule.
In order to establish a definite scale, a particular isotope is chosen as a reference. A
natural choice would be hydrogen (Z = 1, A = 1). This is the lightest and simplest of
all atoms - a single electron and a single proton bound together. For technical
reasons, a slightly different (but almost equivalent) choice is made:
The atomic mass unit

Masses of atoms and molec ules are co mmonly meas ured in term s of the Note In some books, the symbol
atomic mass unit (amu) . This is defined to be 1/1 2 the mass of a carbon-1 2 'u' is used instead of amu.
atom - an atom with 6 protons, 6 n eutrons a nd 6 e lectron s. By definition, a
carbon-1 2 a tom ahs a mass of exactly 12amu . Hydrogen has two stable
isotopes with masses close to 1 amu and 2 amu.
Relative atomic and molecular masses

The mass of an atom,di vided b y 1 amu, is known as the relative atomic
mass of the a tom.So, if t he relati ve atomic mass is Mn the mass of one atom is
Mramu.
Similarly, the mass of a molecule, divided by 1amu , is called the relative
molecular mass of the molecule. If the relative molecul ar mass is M,., the mass
of one molecul e is Mr amu .
Relati ve atomi c masses and relative molecul ar masses were formerly know n as
atomic weights and molecular weights, and thi s termin ology is still sometimes
used today, though it is generally di sco uraged. Both are ratios of masses, so
they have no units.
IS
The Physical World
Nowadays, it is possible to obtain direct measurements of the masses of atoms (more

strictly, ions), using a time-of-flight mass spectrometer (Figure 1.7). The idea is to
accelerate an ion from rest, giving it aknown kinetic energy. The speed of the ion
can be found by measuring the time taken for it to travel a fixed distance and its
mass can then be deduced by rearranging the formula for kinetic energy:
E= -!-mv 2 •
When absolute measurements of this kind are made, a carbon-12 atom is found to
have a mass of 1.9926 x I0- 26kg, allowing us to establish that
Figure I. 7 A time-of-flight mass 1amu = 1 bx 1.9926 x 10-26 kg= 1.6605 x 10-27 kg.
spectrometer. Such an instrument Atoms have masses that vary by a factor of about 300, from the lightest, hydrogen, to the
can be used to measure the masses heaviest man-made atoms. You might therefore wonder why we quoted the size of an
of different ions. and their atom as being around IQ- 10 m. Shouldn't the heaviest atoms be much larger than the
abundance in a given sample. It is lightest? In fact, the diameter of atoms only varies by a factor of two or three .
very sensitive and quite compact, Although the heaviest atoms contain more than 100 electrons, these electrons are
and so can be loaded on board strongly attracted to the nucleus and are closely packed in around it, so the diameters
space probes to analyse the of all atoms are of the same order of magnitude.
atmospheres of our neighbouring
planets. Question 1.1 A molecular ion with kinetic energy 2 .0 X 10- 19 J takes 3.0X 10-3 s to
travel 0.6 m. What are the mass and the magnitude of the momentum of the ion? •
2.5 Interactions between atoms

A moment's thought shows that atoms and molecules must interact with one another.
The fact that atoms combine together to form molecules shows that attractive forces
exist, persuading the atoms to stick together. On the other hand, when a solid metal
bar is squeezed, it resists being crushed. This suggests that atoms exert repulsive
forces on each other when they get too close. This combination of attractive and
repulsive forces makes good sense. If there were only attractive forces, matter would
implode. If there were only repulsive forces, it would fly apart. Matter is
mechanically stable because atoms attract one another when they are pulled apart,
and repel one another when they are crushed together.
The force-separation curve

The simplest case to consider is that of a diatomic molecule which consists of two
atoms, A and B, separated by a variable distance r (Figure 1.8). The two atoms exert
forces on one another, equal in magnitude and opposite in direction. We concentrate
on the force experienced by atom B, and represent this force by its radial component
F,, which is positive when B is repelled by A (Figure 1.8a) and negative when B is
attracted to A (Figure 1.8b).
repulsion
1- r - ~
(a)
Figure 1.8 Forces exerted by
atoms on one another. (a) When the attractio n
atoms are very close, they repel one ~
another. (b) When the atoms are
further apart, they attract one
another.
16
Figure 1.9 shows a typical graphof Fr against r. This type of graph is called a force-
separation curve. There are a number of points to notice:
• There is one separation, r0 , at which the force is zero. According to Newtonian
mechanics, the atoms can remain stationary when separated by this distance,
so it is called the equilibrium separation. A typical value for r0 is around
3 X 10- 10 m.
• For separations smaller than the equilibrium separation, Fr is positive and rises
to very high values, indicating a strong repulsion. This shows that Newton's idea
that atoms are 'hard impenetrable particles' is not so far from the truth.
• For separations greaterthan the equilibrium separation, Fr is negative, indicating
an attraction. The attraction is significant at separations between r0 and 2r0 but
becomes negligible for very large separations. Thus each atom has a relatively
small region of influence within which its attraction is strongly felt.
5
4
3
2
z r0
"'0
I
0
2 4 5 s- 9
r.••:- - ] r / 10- 10 m
-2
-3
-4
Figure 1.9 A typical force-
-5
separation curve.
It is possible for the atoms to remain stationary at their equilibrium separation, r0 ,

where the force is zero. More commonly though, the atoms oscillate as if joined by a
spring. During one half of the oscillation the separation is greater than r0 , and the
atoms attract one another; during the other half of the oscillation the separation is
less than r0 , and the atoms repel one another. The frequency of oscillation is of
interest because a molecule vibrating at a given frequency will strongly absorb and
emit light that has exactly this frequency.
The frequency of the oscillation is related to the shape of the force-separation curve
and the masses of the atoms. As shown in Figure 1. 9, the force-separation graph is
practically a straight line in the immediate vicinity of the equilibrium separation so,
provided the amplitude of the oscillation is small, the force can be written as
Fr=-C(r-ro) (1.1)
where C (the magnitude of the slope of the force-separation curve) is a constant.
Because the force is proportional to (r-r0 ), and acts in a direction that restores the
atoms towards their equilibrium separation, the oscillation will be simple harmonic.
A little care is needed to predict the frequency of oscillation because the equations of
simple harmonic motion refer to the oscillation of a particle about a fixed point, and
neither of the atoms in the molecule is fixed. To take a definite case, consider an
oxygen molecule, composed of two identical oxygen atoms. The centre of mass of
the molecule (mid-way between the atoms) can be taken to be stationary, with the
17
The Physical World
atoms vibrating to and fro about it, as shown in Figure l.lOa. Relative to this fixed
centre of mass, atom B has position x = r/2 and equilibrium position x 0 = rof2, so
Equation 1.1 can be written as
F, = -2C(x-x0 ).
This shows that the effective force constant for the oscillation is 2C. Using the
standard equation for the frequency of a simple harmonic oscillator, it follows that
the frequency of oscillation of an oxygen molecule is
J=-1 f2C.
21t f--;;;
f-o - x=r/2 - ~ m8 ) ( mA )
( mA + m.B r mA + mB r
f-o- x 0 = r0 !2-J 1-o , - ~- ~
centre of centre of
mass mass
:1--- ----- - - - - - - -- ---i ms
,_ _ _ _ ,.0 - - - -----1 , _______ ,. _______ ~
f..., _ _ _ _ _ _ _ ,. _ _ _ _ _ __
(a) (b)
Figure 1.10 (<.) Pos tton" of Question I .2 Figure 1.1 Ob shows the position of the centre of mass for a
aton's rel,ltive to the centre of molecule composed of two different atoms, A and B, of masses mA and m 8 . Use an
mass in an oxy,ren molecule. argument similar to that given above to show that the frequency of vibration of this
(b) Positions of atoms relativ.:' to molecule is
the centre of ma'i'i i'1 a ?eneral
diatomic molecule . f = _1 C(mA +ms)
27t mAmB
where C is the magnitude of the gradient of the force-separation graph at the

equilibrium separation.
Question 1.3 Estimate the frequency of oscillation of a molecule composed of

two atoms whose force-separation curve is given in Figure 1.9 and whose masses
are 2.2 X I0-25 kg and 8.8 X 1Q-26 kg. •
The potential energy-separation curve

The interaction between atoms can also be described in terms of potential energy.
Figure 1.11 shows a graph of potential energy against separation, r, with the zero of
potential energy corresponding to atoms that are infinitely far apart. Although this
graph is superficially similar to Figure 1.9, it is actually very different, and the
relationship between the two graphs is quite subtle.
You may remember from Chapter 2 of Predicting motion that
dEpot
F.=---·
r dr
This means that the force-separation graph plotted in Figure 1.9 is minus the
gradient of the potential energy-separation graph plotted in Figure 1.11 . Notice, in
particular, that the equilibrium separation of the atoms, r0 , corresponds to the lowest
point on the potential energy graph, where the gradient of the graph, and hence the
18
1.5
1.0
_, 0.5 r0
00
I
0
0
0 2 3 4 7- s- 9
lt.lc. r/10- IO m
-0.5
Figure 1.1 I The potential
- 1.0 energy-separation curve
corresponding to the
- 1.5 force-separation curve shown
in Figure 1.9.
force, is zero. For separations smaller than r0 , the gradient of the potential energy
graph is negative, corresponding to a positive radial force component and a repulsive
force. For separations greater than r0 , the gradient of the potential energy graph is
positive, corresponding to a negative radial force component and an attractive force.
We are often interested in the minimum energy needed to take two atoms in a
diatomic molecule, initially at the equilibrium separation, and move them infinitely
far apart. This is known as the binding energy of the molecule. Taking the potential
energy at the bottom of the potential energy curve to be -Eb and the potential energy
at infinite separation to be 0, we have
binding energy = 0 - (-Eb) = Eb.
In other words, the binding energy is the 'depth' of the potential energy well.
The above discussion referred to atoms in a diatomic molecule. However, similar
considerations apply to other forms of matter. For example, similar forces exist between
molecules, and between atoms in a solid. The situation is slightly more complicated
for atoms in a solid because any given atom will experience forces due to all the atoms
around it. However, the forces between atoms are quite short in range so the most
important influences come from an atom's nearest neighbours. Thus, in a solid, we can
again expect the typical spacing between atoms to be close to r0 and the atoms will
again move to and fro, making small vibrations about fixed equilibrium positions.
We can also imagine separating all the atoms in a solid from their equilibrium
· positions until they are infinitely far apart. The energy required to do this is the
binding energy of the solid.
Question 1.4 Two atoms are initially at their equilibrium separation in a diatomic
molecule, with forces and potential energies as shown in Figures 1.9 and 1.11. Use
these graphs to estimate the minimum force and minimum energy needed to split the
molecule into completely separate atoms. • ·
3 Atomic descriptions of the phases of

matter
A water molecule is a tightly bound combination of one oxygen and two hydrogen
atoms. Steam, liquid water and ice are just collections of these water molecules. It is
intriguing that the same building blocks are capable of producing such distinct
phases, and that one phase can change into another quite abruptly: at 99 °C we have
19
The Physical World
liquid water, and at 101 oc gaseous steam. In this section we will examine the three
familiar phases of matter- gas, liquid and solid- and try to relate their behaviour
to that of the underlying atoms and molecules. We start by noting that the phases
have distinctive properties:
Gases occur at high temperatures. They are not very dense and are able to flow,
adopting the shape and volume of any empty container they are placed in. They can
be compressed quite easily.
Liquids form at lower temperatures. They are much denser than gases. Although they
are able to flow, they do not expand to fill the whole volume of any empty container.
If the volume of the container is greater than the volume of the liquid, the liquid will
generally occupy the bottom of the container, but if the volume of the liquid is
greater than that of the container, it will overflow. Liquids resist being compressed.
Solids form at even lower temperatures. They have roughly the same density as
liquids (slightly greater in most cases) and are not able to flow. In fact they are rigid
- kick one end of a brick, and the whole brick will move forward, maintaining a
practically constant shape. Rigidity is a special property of solids that distinguishes
them from both liquids and gases.
These distinctions are generalizations. A gas can be pressurized and made more
dense so that it behaves rather like a liquid. Putty could be thought of either as a soft
solid or a thick liquid. Nevertheless, the distinction between gases, liquids and solids
is usually clear enough, especially when there are clear transitions from one to
another, as when ice melts or liquid water boils.
The precise phase that is found, whether gas, liquid or solid, depends on two
competing influences - binding energy and kinetic energy. Binding energy
measures the attraction between molecules. If this were the only influence, the
molecules would huddle closely together, with nearest neighbours being close to
their equilibrium separation. While binding energy causes molecules to cohere
together, kinetic energy has the opposite influence. If the molecules move around
very energetically, they can easily shake themselves free from one another. Any
small clump of molecules that does manage to cohere will soon be split apart when it
is bombarded by other high-energy molecules.
The role of temperature is significant. As the temperature rises, so does the average
kinetic energy of the molecules and this, in very broad terms, explains why solids
melt and liquids vaporize. At low temperatures, the binding energy is much greater
than the kinetic energy, and the molecules cling together vibrating about fixed
equilibrium positions: this is the rigid, solid phase. As the temperature rises, the
molecules achieve the freedom to move past one another, although they still stay in
close contact: this is the liquid phase. At higher temperatures, the molecules break
loose and the much more tenuous gas phase is formed. This is not quite the end of
the story, for at even higher temperatures, molecules split apart into separate atoms,
and atoms disintegrate into electrons and nuclei. A fully ionized gas has very
distinctive properties and is regarded as a new phase of matter- the plasma phase.
Although plasmas are widespread in the Universe, in stars and in the interstellar
medium, we shall not discuss them further, but will concentrate on the three phases
most familiar in everyday life: gases, liquids and solids.
3.1 The gas phase

We have just seen that gases appear at high temperatures, where the effects of kinetic
energy dominate those of binding energy. Since the forces between molecules play a
relatively minor role in gases, we can expect all gases to behave in roughly similar
20
ways. This makes the gas phase a good place to start, as it is really the simplest
phase to discuss.
To have a gas phase, it is not necessary for the kinetic energy to exceed the binding
energy. The disruptive effect of collisions is such that a gas will generally form if the
average kinetic energy per atom is greater than 10% of the binding energy per atom.
This is shown in Figure 1.12. The strong correlation between the binding energy per
atom and the average kinetic energy of an atom when the boiling point is reached,
confirms the idea that there is a competition between binding energy and kinetic
energy. In the gas phase, kinetic energy has the upper hand.
-, 1.2
•
"'I
0
•
• •
\tungs ten
..._ •
~ 1.0
<;:;
::l •
... •
E
0)
Q.
..,.
B 0. 8
bl) ••• • •
c • •• • ••
·c.;
0.6
• • .
••• • · ~ ri o n
,
.D
<;:;
>. •• •
t:_ll
0)
c0) 0.4
.~
0:5
.'•
_• •
...
c • • .____ magnes ium

:.Q
0)
0/)
0.2 •••
e
0)
•
>
"'
0 5 10 15
binding energy/ I0- 19 J
Figure 1.12 The average kinetic energy per atom for a range of selected elements at
their boiling temperatures, plotted against the binding energy per atom. (To compare like
with like. elements have been selected that vaporize into separate atoms. Thus elements
such as nitrogen and oxygen. which have diatomic molecules in the gas phase, have been
excluded.)
The density of a fixed mass of gas depends on the size of its container, but we can
take the air in your living room as a typical example. The average spacing between
molecules in air is about 3.3 x I0-9 m. While this may seem very small, it is much
larger than the typical range of intermolecular forces so each molecule in a gas
spends most of its time beyond the range of influence of others. You can picture the
molecules in a gas as moving around freely, occasionally colliding with one another
when their paths cross. This is why a gas expands to fill an empty vessel: the
molecules experience no strong forces holding them together, so they just drift apart
until they occupy the vessel more or less uniformly.
Figure 1.13 Typical paths
Figure 1.13a shows a typical path followed by a gas molecule. The path is highly followed by a gas molecule
erratic because each collision with another molecule involves an exchange of (a) The path for a molecule of
momentum and energy, and usually a sharp change in direction. A larger molecule small radius . (b) The path for a
would collide more frequently and its path would be even more erratic (Figure molecule of larger radius. The
1.13b) so, if the molecules were those of scents emerging from perfume bottles into number of molecules per unit
still air, the smaller molecule would delight your nose first. volume is the same in both cases.
21
The Physical World
The random motion of a gas molecule is invisible, and can only be inferred
indirectly. But if smoke particles are allowed to drift in air, and are observed under
high magnification, their zigzag paths can be seen directly. This phenomenon (which
is also observed in suspensions of particles in liquids) is called Brownian motion
after its discoverer, the botanist Robert Brown. It is a direct consequence of
collisions between molecules in the surrounding medium and the suspended particle.
For a smoke particle, each zig and zag does not correspond to a single collision. The
collisions occur at random, so that the smoke particle is continually jostled this way
and that, but usually on a scale that is not visible. Occasionally, a number of
collisions push the particle in the same direction, and it gains enough momentum to
make a visible step forward. Historically, Brownian motion was important in
establishing the reality of molecules and thus of atoms. Indeed, Einstein's 1905
paper on Brownian motion, and subsequent measurements carried out by Perrin in
1908, marked the end of all serious resistance to the atomic hypothesis.
If you could take a sn_apshot of the individual molecules in a gas you would see an
almost random arrangement, as shown in Figure 1.14. Randomness can be a tricky
concept to understand. Looking at Figure 1.14, you can see that there are areas
where molecules are quite closely packed, and areas where they are further apart. It
is tempting to assume that this reveals a lack of randomness, but this is not true. If
all the molecules were more or less uniformly spaced, that would be a non-random
arrangement. Randomness implies a spread in particle spacings. It also implies a
spread in particle speeds. If Figure 1.14 could be turned into a movie, you would see
some molecules travelling very quickly and others moving very slowly. The word
'gas' is a corruption of the Greek chaos, which turned out to be an apt choice .
....
One way of describing the randomness in a gas is to say that there is no correlation
between the positions of molecules in a gas. In other words, if I know that there is a
molecule at a given place, that does not affect the chances of finding another
molecule somewhere else. This is because the intermolecular forces between gas
molecules have a negligible role. To visualize this idea more clearly, imagine
choosing one particular molecule as a reference and counting the number of
molecules, N, whose centres lie in a thin spherical shell centred on this molecule
(Figure 1.15). If the spherical shell has radius rand thickness !lr, its volume is
4nr2 fir, so the number of molecules per unit volume at a distance r from the chosen
Figure 1.14 A 'snapshot' of molecule is NI( 4nr2 fir). As the molecules move around, this quantity fluctuates, but
molecules in a gas. we are interested in its value averaged over time:
Figure 1.15 A spherical shell

used to define the radial density
function.
22
The radial density function n(r) is defined as the time-averaged value of n (r)
N/(4n r2 1'1.r) , where N is the nu mber of molecul es whose centres li e in a thin
spheri cal shell of radiu s ra nd thickness 1'1.r, centred on a chosen m olecul e.
The radial density function measures the average number of molecules per unit
volume as we step outwards from a given molecule. Figure 1.16 shows the radial
density function for a gas. For most separations this is practically a horizontal line,
which confirms that one molecule has no influence on the position of another - the 0 2 4 6 8
r/ I0- 10 m
molecules are in random, uncorrelated positions. The only significant detail occurs at
very low separations, where there is a dip in the radial density function. This is not igure 1.16 I "'-• I uJlill UeJ1SJty
surprising because the molecules repel one another if pressed too closely together - funct.(' 1 of .t g.. s.
they cannot sit exactly on top of one another. Apart from the occasional collisions
that occur when molecules get too close, the overall picture is one of independent
molecules travelling around freely, with a range of speeds and kinetic energies.
3.2 The liquid phase

When a gas is cooled, 'the kinetic energy of its molecules falls until it reaches a point
where collisions are no longer able to prevent the clumping together of molecules.
At this point, a gas turns into a liquid.
The transformation of steam into water can be taken as a typical example. Rare
clumps of molecules may form briefly in the steam, but are rapidly tom apart. As the
temperature drops these clumps grow, persist for longer, and can be thought of as
tiny droplets of water. Eventually, a few droplets become so large that, instead of
decaying, they grow, enveloping molecules or other droplets that strike their surface.
The steam then rapidly condenses into water.
You will have seen one of the key signatures of this process whenever you boil a
kettle. Steam is actually colourless and transparent. The white haze you see forming
a little way from the spout of the kettle is a suspension of water droplets formed as
the steam condenses (Figure 1.17). These water droplets have grown to sizes that are '-Vater conde~i. f•om -;k'..tm
comparable to, or larger than, the wavelength of visible light, so they are able to catte• h,rt>t stro'lrly wht n thev
scatter light strongly. Exactly the same thing happens in clouds as water vapour !'row to '1e larger than the
contained in the atmosphere condenses. wavelenrtr of v s bk I~r 11
Liquids are much denser than gases because their molecules are much closer
together. Neighbouring molecules are within one another's spheres
of influence, so you would expect the positions of the molecules to
be much more correlated than for a gas. Figure 1.18 shows the
radial density function for water at a variety of temperatures. In the
lower graphs (4 °C, 25 °C), there are clear peaks and troughs which
die away with distance. Each peak represents a surplus of molecules
over the average, and each trough a deficit. These features show
that the molecules of a liquid are arranged in a more orderly way
than in a gas, but this order only persists over a short distance;
beyond 4-6 molecular diameters from the chosen particle, the
average density of particles is practically constant. Liquids are said
to have short-range order. The upper graphs in Figure 1.18 show
the radial density function for water at higher temperatures. Notice
Figure 1.18 Radial density function for water at different

temperatures. Note that the graphs are displaced vertically from one 2 3 4 5 6 7 8 9 10
another so that they can be easily distinguished. r!I0- 10 m
23
The Physical World
that the peaks and troughs diminish in size as the temperature rises. This is because
the average kinetic energy of the molecules increases with temperature, and the
fragile short-range order created by intermolecular forces starts to break down.
The motion of molecules in a liquid is nothing like the free motion of molecules in a
gas. Figure 1.19 shows the sort of path a molecule in a liquid follows. The molecule
spends much of its time jogging to and fro in a small region, but occasionally makes
a longer jump into a neighbouring region. An analogy can be made with a country
dance, where people are initially arranged into sets who dance together but, as the
dance proceeds, some dancers move from one set to another. In a dance, these
motions would be choreographed, but in a liquid the same effect is achieved in a
more serendipitous way.
Figure 1.19 Path followed by a
molecule in a liquid. e Liquids are much harder to compress than gases. Use a microscopic model to
explain why this behaviour is expected.
0 The molecules in a liquid are very close together so further compression invokes
the strong repulsive force shown in Figure 1.9. The molecules in a gas can be
brought closer together without invoking this force. •
3.3 The solid phase

For all substances (except helium), liquids do not persist down to the lowest
temperatures. Sooner or later, a temperature is reached at which the liquid turns into
a solid. In a solid, each atom is tied to a specific equilibrium position. Although it
vibrates to and fro about this position, an atom is very unlikely to move from its 'home'
relative to its neighbours (Figure 1.20). That is why a solid is rigid. If you tap a solid
gently it moves as a whole, rather than allowing the atoms to change their relative
positions.
In many cases, the solid is crystalline, either consisting of a single crystal, as in a
gemstone, or a collection of microscopic crystals, as in most metals. In a crystal,
the atoms oscillate around equilibrium positions that are regularly ordered. The
Figure 1.20 Movement of an atoms can be pictured like soldiers on parade, shuffling from one foot to another,
atom in a solid. but not moving from their position in the array. Figure 1.21 shows the equilibrium
arrangement of water molecules in ice. Although it is rather difficult to see the
details, you can discern that the whole structure is formed by repeating a simple
pattern endlessly and periodically throughout space. This is rather like saying that
a wallpaper pattern is produced by regularly spaced repetitions of a given motif
(Figure 1.22).
y
I
I
Figure 1.21 Arrangement of Figure 1.22 A wallpaper pattern.

water molecules in ice.
24
Once we know the structure of a crystal, and the immediate environment of a given
atom, we can predict the positions of atoms many thousands of atomic spacings
away. For this reason, a crystal is said to have long-r~e order, in contrast with
liquids, which have only short-range order, and gases, which are disordered. The
long-range order in a crystalline solid leads to a radial density function with very
sharp peaks, extending far from the central atom (Figure 1.23).
n (r )
0 2 3 4 5
r/lQ- IO m
Figure 1.23 The radial density function in a solid.
Another distinctive feature of crystals is their symmetry. In ice, for example, the
molecules pack together in an hexagonal arrangement. Intriguingly, this hexagonal
symmetry has an influence on a much larger scale, in the beautiful form adopted by
snowflakes (Figure 1.24). Also reflecting their underlying atomic arrangement,
crystals cleave along lines of particular weakness, between one plane of atoms and
the next. Even diamonds, the hardest of all substances, are cleaved in this way before
being polished to produce gemstones (Figure 1.25). The study of crystals turns out to
be full of fascinating detail. Ice, for example, has at least seven crystalline phases,
with the water molecules arranged differently in each. In the case of steel, the
existence of different phases is of major technological importance. Steel generally
consists of a myriad of tiny crystals, so small that they can only be seen under the
microscope (Figure 1.26). By arranging to have a suitable blend of crystals in
different phases, it is possible to control the hardness and flexibility of different
types of steel.
Figure 1.24 A snowflake. Figure 1.25 A diamond crystal. Figure 1.26 Microscopic crystals in steel.
25
The Physical World
4 Macroscopic variables
So far, we have looked at matter from an atomic perspective. For the rest of this
chapter, we will take a more everyday view, on the scale of millimetres and above,
rather than nanometres and below. The larger scale is often described as being
macroscopic, while the smaller one is microscopic. Of course, the real interest lies
in linking these two different scales: understanding the whole in terms of its parts.
To obtain a more quantitative description, we will introduce variables, such as
density, pressure, temperature and internal energy, that are often used to describe
matter on a large scale. Although you may be familiar with these concepts, it is
worth reading on, to check that your understanding is in line with the technical
meaning of these terms.
4.1 Density
The density, p, of a sample of matter is defined to be its mass per unit volume,
M (1.2)
p=-
v
so the SI unit of density is kilogram per cubic metre (kg m-3). The volume V should
be chosen judiciously so that the sample of matter appears to be homogeneous. It
1
must be large enough to avoid the grainy nature of matter on an atomic scale, and
small enough to be unaffected by any large-scale variations. If the volume is chosen
1
10 core of neutron star reasonably, thedensity will be quite insensitive to the exact choice.
10 1
1
core of wh ite dwarf star
Some typical densities are shown in Figure 1.27. Of course, solids and liquids have
much higher densities than gases, but even amongst solids there are large differences
-the density of solid osmium is more than 40 times that of solid lithium. Under
10 6 extreme conditions, the atomic nature of matter breaks down and very high densities
centre of Sun are produced. Neutron stars, for example, are composed of matter with the density of
10 5
uranium atomic nuclei, roughly 10 15 times greater than found in ordinary matter.
10 4
iron You will also come across the term number density for the number of molecules per
10 3 water unit volume. If each molecule has mass m, the number density is given by
10 2 number density = plm. (1.3)
""I
E 10
~
bD
air at sea-level
4.2 Pressure
Q. An asteroid, in empty space, would experience no pressure from its surroundings.
But the matter we are familiar with on Earth is generally at some non-zero pressure,
high vac uum if only because the weight of the atmosphere presses down on it.
10-·I
10 - 5 The upper surface of a flat roof, with dimensions 10 m x 10 m say, experiences a
downward force due to the pressure of the Earth's atmosphere. The magnitude of this
,. ~I force is about 107 N, equivalent to the weight of a 1000 tonne object! This sounds
alarming, but the space beneath the roof also contains atmosphere which exerts a
Io- 9 ultra-hi gh vacuum force of 107 N on the lower surface of the roof, in an upward direction. So the roof
will be slightly compressed, but it should not collapse on your head.
best laboratory vac uum
The large forces applied by the Earth's atmosphere only become apparent when they
10-'t
Io- 2o interstellar space are unbalanced. This is what happens when a jam jar is sealed with a partial vacuum
inside it. A more spectacular demonstration was given in 1657 by Otto von Guericke,
one-time mayor of Magdeburg, Germany. Von Guericke placed two large copper
Figure 1.27 Some typical hemispheres together to form a sphere (Figure 1.28). The hemispheres had been
densit1es . carefully made so that they fitted snugly together. He then pumped some of the air
26
Figure 1.28 Otto von Guericke's

demonstration of the large forces
that are applied by atmospheric
pressure .
out of the sphere, and challenged people to pull it apart into separate hemispheres.
To the amazement of the assembled crowd, no one could, nor could two teams of
eight horses. The pressure inside was very small but the atmospheric pressure of
about 105 newtons per square metre provided alarge inward force, pressing the
hemispheres together.
Pressure is quantified in terms of the force exerted on a flat surface. If a uniform
force presses down on a surface, in a direction perpendicular to the surface, the
pressure is defined to be
P= F
A
where F is the magnitude of the force and A is the area of the surface.
If the force F is not perpendicular to the area (Figure 1.29), the pressure is defined in
terms ofFJ.• the component of the force that is perpendicular to the surface:
p = FJ. = Fcos(} . (1.4)

A A
The area is taken to be small enough for the force to be uniform across it. In the - areaA
limiting case where the area is taken to be very sm,all, the pressure is defined at a
given point.
Unlike force, pressure is a scalar quantity. In SI units, it is measured in newtons per
square metre (N m-2). This unit is called a pascal (Pa) in honour of the French Figure 1.29 Definition of
scientist Blaise Pascal (1623-1662) who gave an early definition of pressure and pressure.
investigated its variation with altitude. In the context of these investigations, Pascal
was fortunate in his sister's choice of husband. Just four years after the invention of
the barometer, he asked his brother-in-law to carry a barometer up a mountain and
observe any change in the pressure recorded. So Pascal's brother-in-law was the first
27
The Physical World
to observe that pressure decreases with altitude, a topic we return to in Chapter 4.

l centre o f Sun
Normal atmospheric pressure at sea-level is around 105 Pa, but Figure 1.30 shows a
range of values that are encountered in other contexts.
he lium - metalli c solid Sometimes, the pressure of a system is quoted as an overpressure. This is the amount
centre o f Earth by which the pressure of the system exceeds a standard value (such as normal
graphite diam o nd
atmospheric pressure). Tyre pressures, for example, are generally quoted in this way.
botto m o f ocea n When performing calculations in physics, though, it is usually advisable to convert
overpressures into actual pressures.
V
gf atmos p I 1en. c press ure
~ at sea level
Question 1.5 A woman wearing high-heel shoes pivots in such a way that, for a
~
~ pain thres ho ld fo r so und
brief instant, all her weight is on one heel. If the woman has a mass of 56 kg and the
~ heel has a cross-sectional area of 0.49 cm 2, what is the pressure exerted by the heel
c.. best vacuum with
~ mechani cal pump
on the floor? •
§
0
10- 5 = 4.3 Temperature
atm os pheri c press ure a t
an a ltitude of 300 mil es
We are used to ambient temperatures that vary over a relatively rather narrow range.
In Britain, for example, we would regard 30 oc as a very hot day, and -10 °C as a
bes t labo ratory vacuum bitterly cold one. Although some parts of the world are hotter than others, large
temperature differences are moderated by winds and ocean currents which transport
interpl anetary space energy from hotter regions to cooler ones.
10- 15
We know that our bodies work best within a narrow range of temperature and we do
our best, with houses, clothing, ice creams and air conditioning to stay within that
Figure 1.30 Some typical
range. When these artificial protection mechanisms let us down, our bodies take over
pressures.
by shivering or sweating. In a way, we all act as thermometers. Our skin contains
special nerve endings, or receptors, which are sensitive to temperature (Figure 1.31 ).
Between about 15 oc and 45 °C, the active receptors are those that respond to cold or
warmth; outside this range, pain receptors start to function. Thus, we literally have a
'feel' for the meaning of temperature.
warmth receptors
N 10
:c
>.,
u
=
V
::l
cold receptors
l
V
~ 5
0..
E
temper atu refCC
Figure 1.31 Four types of receptors in the skin respond to temperature. The frequency
with which each receptor transmits impulses to the central nervous system varies with
temperature. Note that the response curves for the cold receptors and warmth receptors
overlap around the core body temperature (- 37 °C).
28
The ability to sense temperatures is essential to our survival, but temperature is more
than a vague, subjective feeling. It is a scientific variable with a precise meaning.
Perhaps the most important point to emphasize is the distinction between
temperature and heat. In the early days there was much confusion between these two
terms, but they refer to very different things.
If two bodies, at different temperatures, are brought into contact, energy flows from
the warm body to the cool body (Figure 1.32a). In the process, the temperature of the
warm body falls and the temperature of the cool body rises. The energy transfer
continues until both bodies are at the same temperature, when further change ceases
(Figure 1.32b). The bodies are then said to be in thermal equilibrium. A
The e nergy transferred fro m a warm body to a coo l body, as a result of a

diffe rence in temperature, is know n as heat, a nd thi s type of energy transfer i s
known as heating. If no other energy transfers take pl ace, the e nergy lost by (b)
the warm body is equal to the e nergy gained by the coo l body, ensuring that
energy is conserved overall. Figure 1.32 Temperature
differences control the now of
energy (heat) from one body to
It is tempting, but WRONG, to think of temperature in the same way as energy. another. (a) So long as the
The first person to realize this was the Scottish physicist, Joseph Black. In 1760, temperature of body A is greater
Black placed a number of different objects, in turn, in contact with a hot object. than that of body B, energy will
For the same loss in temperature of the hot object, he found that different flow from A to B. (b) Thermal
objects, of the same mass, were warmed to different temperatures. Such results equilibrium is achieved when both
could never be interpreted in terms of a flow of temperature from one body to bodies have the same temperature.
another.
So what is temperature? We will arrive at many different answers to this question
during this course, but the following statement makes an excellent starting point:
Temperature is a label which d etermines the direction of heat fl ow between

two bodies placed in contact with one a no ther. Heat fl ows fro m the body with
the hj gher temperature to t he body w ith the lower t emperature, and keeps on
fl ow ing until , in thermal equilibrium , both bodies are a t th e same temperature.
Several points can be lifted out of this statement:

1 Heat always flows in a definite direction. We define temperature in such a way
that heat flows from a high-temperature body to a low-temperature body.
2 So long as there is a temperature difference between two bodies in contact, or
within a single body, heat will flow and the system will not be in a state of
equilibrium.
3 When the temperature is uniform, a state of thermal equilibrium is reached in
which no more heat is transferred.
So far, we just know that temperature is a label that determines the direction of heat
flow. For the moment, we will use the symbol () to denote temperature, so if body 1
has temperature ()1 and body 2 has temperature ()2 , with ()1 > ()2 , heat will flow from
body 1 to body 2. To proceed further, we must say something about how the
labelling is carried out. In other words, we must decide how to calibrate a
thermometer so that quantitative readings can be taken. This turns out to be a subtle
issue but, to get started, we can consider an ordinary mercury-in-glass thermometer.
29
The Physical World
Following the instructions in Box 1.1, you could produce a calibrated thermometer
which could be used to read off any temperature (in degrees Celsius) between 0 °C
and 100°C.
Box 1.1 Instructions for calibrating a thermometer

Suppose you had a merc ury-in-glass thermo me te r before it had been calibrated .
B ecause merc ury expand s whe n heated yo u will see the le ngth of merc ury in
the c olumn inc reas in g as the te mperature increases. To calibrate the
thermometer, you could the n ta ke the fo ll ow ing ste ps:
Plun ge th e thermometer into a beak e r of ice, meltin g unde r normal
atmosphe ri c pressure. All ow the thermo me ter t o settle down a nd reach the
same tempe rature as the melting ice, the n m ark the positio n of th e e nd of the
mercury co lumn as 0 °C.
2 Imme rse the therm ome ter in water, boiling under norm al atmospheri c
pressure. All ow the thermo meter to settle down a nd reach the sa me
temperature as the boiling water, t hen m rak the pos iti o n of the e nd of the
merc ury column as l OO oc.
3 Constru ct a linearl y g radu a ted sca le be tween these two calibrati o n p o ints.
Thi s can b e do ne as fo llows:
S uppose /0 a nd / 100 are the le ngth s of the mercury co lumn whe n the
thermo meter is in the rmal equilibrium with melting ice a nd boiling water
res pecti vely. By definition, these correspond to 0 °C a nd lOO °C on our
te mperature scale, and thi s is s how n b y the pos iti ons of the red d ots o n
Figure 1.33. A linearly g radu ated scale is fo rmed b y drawin g a s traight line
between these two points a nd taking readin gs fro m it. So, whe n the le ngth of
the merc ury co lumn is midway between !0 a nd / 100 , the te mpe rature is take n to
be 50 °C. M ore generally, whe n the le ngth of the me rcury co lumn is /, th e
te mperature is take n to be
e = 0 °C + I - lo X 100 °C. ( 1.5)

l10o - lo
I !cm
0 100
Figure 1.33 Forming a temperature scale.
Question 1.6 The length of mercury in the column of an uncalibrated mercury-

in-glass thermometer is found to be 3.3 cm when it is held in contact with melting
ice and 6.9 cm when it is immersed in boiling water. Estimate the temperature,
measured by this thermometer on the Celsius scale, when the length of mercury in
the column is 4.2 cm. •
30
4.4 Internal energy

Energy has an important role to play in explaining the properties of matter, but care
is needed, because some contributions to the energy have no influence on the
properties of matter. For example, a steel bar may rotate about an axis. This motion
certainly contributes to the total energy of the bar, but has a negligible effect on the
bar's material properties, such as its strength or flexibility. Similarly, taking the bar
to the top of a mountain will affect its gravitational potential energy, but will not
affect the bar's ability to conduct electricity or heat. For present purposes, we can
restrict attention to samples of matter that are macroscopically at rest, and far from
all external influences, such as gravity. Under these circumstances, the total energy
of the sample is referred to as its internal energy.
In microscopic terms, we can picture individual atoms or molecules moving around
within the sample. These particles have kinetic energy and mutual potential energy.
The internal energy can then be thought of as the sum of all these atomic or
molecular contributions. (This energy is sometimes referred to as thermal energy,
but should never be called heat, or heat energy, as this would clash with the careful
definition of heat given earlier.)
As always, we must settle on a choice for the zero of potential energy. One common
convention is to take the potential energy to be zero when the individual atoms or
molecules are infinitely far apart. This implies that internal energies can be negative,
as well as positive, depending on the precise combination of kinetic and potential
energies. Alternatively, we can take the potential energy to be zero when the atoms
are in their equilibrium positions in the solid phase. The choice is arbitrary and
unimportant because internal energy itself cannot be measured. However, we can
measure changes in internal energy. This is because energy is a conserved quantity
so, if we keep track of the energy entering or leaving a system, we know by how
much its energy has changed.
We can distinguish two ways of increasing the internal energy of a system. The first,
called heating, has been described above. Heat is any transfer of energy that occurs
because of a temperature difference, the energy flowing from a high-temperature
region to a low-temperature region. Thus, if you place a frying pan on top of a
glowing hot plate, the frying pan will be heated, according to our strict definition of
the term. The term work is used for all energy transfers that are not classified as
heat. Work often involves mechanical processes, such as compressing a gas, stirring
a liquid, or scouring a solid. It may also involve electrical processes, as when the
filament in a light bulb is made to glow by passing an electrical current through it.
Calculations of heat, work and changes in internal energy form part of the subject of
thermodynamics which will be discussed in Chapter 3 of this book.
4.5 Molar quantities

Many properties of matter depend on how large a sample is under consideration. It is
therefore a good idea to specify a standard quantity of matter, relative to which all
measured values are quoted. The simplest choice is to take one kilogram as this
standard quantity. However, another choice, based on the concept of a mole, is
equally important.
A mole contains adefinite number of 'basic particles' (atoms or molecules). To see
how it is defined, consider a pure substance composed of identical basic particles of
mass Mr amu. (These could be molecules of relative molecularmass Mr or atoms of
relative atomic mass Mr.)
31
The Physical World
The abbreviation for mole is mol.

Then one mole of the substance is defined to be a sampl e of mass M .. x w-3 kg.
Thi s is a macroscopic qu antity of matter, s uchas you mi ght hold in your hand .
Note that the definition of a mole only applies to pure substances. We cannot talk of
a mole of concrete, for example, because concrete is a mixture of several different
chemicals, of different relative molecularmasses. The factor I0-3 is an historical
curiosity. It occurs because the definition of the mole dates back to a time when grams
were regarded as fundamental units of mass, rather than kilograms, but it would be
too risky to make changes now, given the widespread use of moles in medicine.
Avogadro's number, N A• is defined as the number of basic particles in a mole. Since
each basic particle has mass Mr amu, we can write:
mass of 1 mole= Mr x 10-3 kg= N A x (Mr amu)
_10- 3 kg 3
so N A- lQ- kg = 6.022 X 10 23 .
1amu 1.6605 X 10-27 kg
The enormous size of Avogadro's number shows that ordinary samples of matter
contain a vast number of molecules or atoms, giving the illusion that matter is
continuous. Note that Avogadro's number is independent of the substance under
consideration.
One mole of any pure substance co ntains 6.022 x 1023 basic particles. That i s
why a mole is a useful way of specify in g a standard quantity of matter. Many
properti es of matter areexpected t o depend on the number of bas ic parti cles
in vo lved, so pattern s a re likely to emer
ge more c learl y if meas urements a re
ex pressed pe r mole of the s ubstance.
Although it may seem like splitting hairs, it is conventional to distinguish between

the number of particles in one mole, and the number of particles per mole in any
given sample. The former is Avogadro's number, NA = 6.022 x 1023 . Of course, this
is just a pure number, with no units. By contrast, the number of particles per mole
has the units of mol- 1. To keep track of units, including moles, it is sensible to
introduce a new symbol, Nm, for the number of particles per mole. This quantity is
called Avogadro's constant, and is defined by
Nm = NAmol- 1•
Having defined the mole, we can express other molar quantities, as values per mole.
The molar mass, M m• is the mass per mole so, by definition,
Mm= Mrx I0-3 kgmol- 1•
The molar volume, Vm• is the volume per mole. This is related to the molar mass via
the density,
Vm=Mmlp.
For a gas at room temperature and atmospheric pressure, the molar volume is of the
order of a cubic foot per mole. A typical value for most solid elements is more like a
cubic inch per mole.
The molar internal energy, Urn, is the internal energy per mole. This depends on the
substance involved and the zero chosen for potential energy, but a typical room
temperature value is of the order of 1()4 to 105 joules per mole.
32
e Lead has a relative atomic mass of 207. How many lead atoms are there in
(a) one mole of lead and (b) one kilogram of lead?
0 (a) By definition, one mole of lead contains Avogadro's number (6.022 x 1023 )
of atoms.
(b) One mole of lead has a mass of 207 x 1o-3 kg and contains 6.022 x 1023
atoms. Thus 1 kg of lead contains
1.0 X kg
6.022 x 10 23 x = 2.9 x 10 24 atoms. •
207 x to-3 kg
4.6 Response functions

A useful way of gauging the properties of a substance is to make a small change in
one quantity and observe how some other quantity responds. For example, we could
increase the temperature slightly, and see how much the volume increases; or we
could increase the pressure slightly and see how much the internal energy changes.
Thermal expansion provides a familiar example. Consider a sample of matter that
initially has volume V, pressure P and temperature 0. If this sample is heated at
constant pressure, itwill generally expand. The change in volume, ~V, is therefore
positive, and would be expected to be proportional to the change in temperature, ~(},
and to the initial volume, V. We can therefore write
~V= av~e (1.6)
where a is a coefficient of proportionality, which depends on the substance that is
being heated. This quantity is known as the (isobaric) expansivity of the material,
where isobaric means 'at constant pressure'. The factor of V on the right-hand side
of Equation 1.6 ensures that a is independent of V, and so characterizes the
substance under study (e.g. copper or steel), no matter what the size of the sample.
A second example is provided by compression. If you squeeze a sample of matter
slightly, increasing the pressure, whilst keeping the temperature constant, there will
be a small decrease in the sample's volume (it squashes). The change in volume is
therefore negative, and would be expected to be proportional to the change in
pressure, M and to the initial volume, V. This implies that
~V=-f3M (1 .7)
where f3 is a coefficient of proportionality, which depends on the substance that is
being squeezed and is known as the (isothermal) compressibility of the substance.
Isothermal means 'at constant temperature'. Rubber has a large value of f3 because
it is very squashy, while steel has a much smaller value. The isothermal
compressibility depends on a number of factors, but tables exist for a variety of
materials under a range of conditions, so that designers and technologists can choose
an appropriate material for a particular use.
Similar definitions can be made for otherpairs of stimuli and responses. The
coefficients of proportionality that occur in this way are called response functions .
In the limiting case of small changes, Equations 1.6 and 1.7 give
1 dV
a=-- (at constant pressure) (1.8)
V dO
f3 =_ _!_ dV (at constant temperature). (1.9)

V dP
33
The Physical World
All response functions can be defined in terms of derivatives describing how rapidly
one quantity varies with respect to another, supplemented by conditions specifying
which quantities are held constant during the change.
Question I. 7 When a metal block is heated by 5 °C at constant pressure, it

expands. The pressure acting on the block is then increased at constant temperature
until the bar contracts back to its initial volume. During the expansion, the
expansivity is 3.6 X 10-6 oc-l, and during the contraction the compressibility is
3.0 x I0- 11 Pa- 1• By how much was the pressure increased? •
5 Macroscopic equilibrium in ideal gases

Some macroscopic variables (such as pressure and temperature) help us to specify
the state of a given sample of matter. Others (such as expansivity and
compressibility) help us to quantify the inherent differences between one material
and another. Either way, as soon as we start to look closely at these variables, a vast
range of questions emerges. Usually, when we change the value of one macroscopic
variable, many other variables will change, and we would like to understand these
changes. With understanding comes power, so we can hope that an understanding of
the properties of matter will allow us to control the behaviour of materials and shape
them for our own ends.
When confronting a difficult question - such as trying to understand the properties
of matter- it is a good idea to consider a particularly simple situation, to see if that
can be understood first. For this reason, we shall concentrate first on gases which are
in equilibrium, that is, in a settled, unchanging state.
At first sight, equilibrium may seem dull. The still air in a sealed room may seem
less exciting than the air in a tornado or a furnace. Perhaps so, but equilibrium itself
contains a great mystery, which deserves careful thought. The mystery can be stated
in very general terms:
Any equilibrium state of a macroscopic sampl e of matter can b e c ahracteri zed

by an amazingly small number of macroscopic variables- often just two or
three are s uffici ent.
To take a definite case, consider a fixed quantity of oxygen gas, contained in a

cylinder with a closely fitting but adjustable piston (Figure 1.34). The volume of the
gas is easily controlled by adjusting the position of the piston: sliding the piston in
reduces the volume and sliding it out increases the volume. The temperature of the
gas can be controlled by immersing itin a large thermal reservoir (sometimes called
a 'heat bath') which has a known, fixed temperature. If the gas is colder than the
thermal reservoir, heat will flow into the gas and it will get warmer; if the gas is
warmer than the reservoir, heat will flow out of the gas and it will get cooler. When
the gas has settled down to a state of equilibrium, its temperature is the same as that
of the thermal reservoir. Now for the surprise:
Hav ing fixed the temperature a nd volume of ou r sa mpl e of oxygen, all other
Figure 1.34 A sample of oxygen macroscopic properties of this sample are determined. The pressure, internal
gas, studied under controlled energy, compress ibility, density and all other properties have definite va lues
conditions. which can be reproduced whenever the sampl e has the same volume and
temperature.
34
The surprising thing about this situation is that it is so simple. A typical macroscopic
sample of matter contains 10 18 molecules or more, each of which is described by
three position coordinates and three velocity components so, from a microscopic
point of view, a vast number of variables is needed to specify the gas completely.
Yet, from a macroscopic point of view, all the equilibrium properties are determined
by the volume and temperature. This extreme contrast between the microscopic and
macroscopic descriptions is the essence of the mystery described above. How can we
get away with such a simple macroscopic description of equilibrium states when the
underlying microscopic description is so complicated?
The answer to this question will emerge in the next chapter, where you will see that
the macroscopic properties of a gas are determined by the most likely, average
behaviour of its molecules. In other words, the gulf between the macroscopic and
microscopic viewpoints will eventually be bridged with help from statistics.
S.l Experiments on gases

It is possible to perform experiments on gases, to see how different variables such as Figure 1.35 Robert Boyle
pressure, volume, temperature and internal energy are related to one another. An ( 1627- 91) was an Irish chemist who
experiment of this type was carried out by Newton's contemporary, Robert Boy le did much to advance the concept of
(Figure 1.35). a chemical element and the atomic
hypothesis. Using a vacuum pump.
Boyle's law Boyle demonstrated that Galileo was
Boy le knew of Pascal's work and was stimulated to investigate the effects of correct in asserting that all falling
pressure on what he called 'the spring of the air'. In 1662, he observed 'not without objects accelerate downwards at the
delight and satisfaction', that the more a gas is compressed, the more its pressure same rate. and went on to perform
rises. By taking a fixed mass of gas, and maintaining it at a fixed temperature, he the experiments which led to
Boyle's law.
was able to establish the following law:
Boyle's law
If a f ixed m ass of gas is held at a co nstant temperature, its p ressure is in versely
proporti onal to its vo lume.
We can express this in terms of a proportionality:

1
Poc- p
V
or as an equation:
PV =constant (fixed quantity, constant temperature)
where the constant on the right-hand side depends on the amount (i.e. number of
moles) of gas and on the temperature. Figure 1.36 shows what this equation means,
in graphical terms.
Boyle needed skill and care to arrive at this conclusion. Normally, when you
compress a gas, it warms up (you may have noticed the temperature rise that occurs
when you pump up a cycle tyre). Boyle was able to obtain a simple result only
because he had the patience to let the compressed gas cool down to its initial V
temperature. This was good scientific practice: in order to investigate how one
variable depends on another, it is generally a good idea to ensure that other variables, Figure 1.36 Boyle's law. At
which could influence the result, are held constant. constant temperature. pressure is
inversely proportional to volume.
According to Boyle's law, each doubling of the pressure leads to a halving of the The precise shape of the curve
volume, so we can compress a gas to a very small volume indeed, provided we apply depends on the fixed temperature:
a high enough pressure. This suggests that Boyle's law has its limitations. At very in this figure. el < e2 < e,.
35
The Physical World
high pressures, the molecules will be squeezed together so closely that the strong
repulsive forces shown in Figure 1.9 will come into play. These forces will help the
gas to resist further compression, so that further doublings of the pressure will not
produce halvings of the volume, and deviations from Boyle's law will be observed.
Nevertheless, Boyle's law works well for most ordinary gases, provided the pressure
is not too high. In particular, it works well for air at room temperature and
atmospheric pressure.
Charles's law and the absolute temperature scale

Ballooning, which became popular in the second half of the eighteenth century,
provided strong motivation for more detailed studies of gases (Figure 1.37). In 1783,
Jacques and Robert Charles completed the first manned ascent in a hydrogen
balloon. As his fame spread, J acques Charles ( 1746-1823) studied the properties of
gases more thoroughly. One of the favoured means of ascent was in hot air balloons,
so he studied the expansion that occurs when a gas is heated, arriving at the
following conclusion:
Figure 1.37 A hot <11r balloon.
Heating the air ins1de the bJ.IIoon Charles's law
causes it to expand ...md ~he
reductiOn m derslty produces If a fi xed mass of gas is heated at constant press ure, the increase in volume is
buoyancy. proporti onal to the increase in temperature.
So, if we plot a graph of volume against temperature at constant pressure, we will

get a straight line (Figure 1.38). As with Boyle's law, there are deviations at very
high pressures, but Charles's law works well enough for gases under normal
conditions, and becomes exactly true in the limiting case of low pressures.
Figure 1.38 prompts an intriguing question. Since gases expand when they are
heated, they must contract when they are cooled. What would happen if we carried
on cooling a low-pressure gas indefinitely? If we simply extrapolate the straight
lines in Figure 1.38 to very low temperatures, we get the strange situation shown in
Figure 1.39. At a temperature of -273.15 cc the extrapolated volume for any gas is
zero, and at temperatures lower than this, it is actually negative! Such a state of
affairs is clearly impossible, so Charles's law cannot apply at temperatures below
-273.15 °C. The reason for this turns outto be simple, and profound: temperatures
lower than -273.15 °C do not exist.
V V
Figure 1.39 Charles's law

0 -273.15 0 extrapolated to very low
temperatures.
Figure 1.38 (... ) ChJ.rles s law
between 0 cc and :00 ~ c. At
constant pressure. the volume of
the gas is linearly reiJted to the The absolute zero of temperature
temperature. fhe slope or the line The lowest conceivable temperature is-273. 15 °C. This is known as the
depends on the fixed pressure: m absolute zero of temperature; it can b e approached, but never quite reached.
th1s f1gure. P 1 < P, < P 1. No system in a s tate of equilibrium can have a temperature below absolute zero.
36
5.2 The absolute temperature scale T/K

The idea that -273.15 °C is the lower limit for temperature suggests that it would centre of supernova
be useful to introduce a new temperature scale in which this lowest conceivable
temperature is taken to be zero. This new scale is called the absolute temperature 10 9
scale. 10 8
centre of Sun
So far, we have used the symbol ()to represent a temperature on the Celsius scale, 10 7
and the symbol °C for the Celsius degree. Thus, the temperature of boiling water has
been specified as () = 100 °C. To avoid confusion, it is a good idea to use different 10 6 all atoms ioni zed
symbols for our new scale. We shall use the symbol T to represent a temperature on 10 5
the absolute temperature scale and we shall also introduce a new unit, the kelvin,
abbreviated to K, for the new scale. The numerical value of a temperature on the 10 4 surface of Sun
absolute scale is found by adding 273.15 to the numerical value on the Celsius scale, 10 3
centre of Earth
so in terms of symbols room temperature
10 2
TIK =ere+ 273.15. (1.10) nitrogen liquefies
You have seen that the lowest conceivable temperature on the Celsius scale is 10
helium liquefies
0= -273.15 °C. Using Equation 1.10, the corresponding value on the absolute scale is
T/K =-273.15 °C/°C + 273.15 = 0,
so the absolute zero of temperature on the absolute scale is T = 0 K, as required.
e What is the temperature of boiling water on the absolute scale? I o-3 3 He superfluid
0 Using Equation 1.1 0,

TIK = 100°C/°C + 273.15 = 373.15. Figure 1.40 A range of
So the temperature of boiling water is T = 373.15 K. • tempr.u~ .
If a temperature on the Celsius scale increases by I °C, the corresponding

temperature on the absolute scale increases by I K. This means that quantities we
defined earlier in terms of ()can be easily re-expressed in terms ofT. For example,
the isobaric expansivity can be written as:
I dV
a=-- (at constant pressure). (Eqn 1.8)
V dT
In spite of this close relationship, it is important to preserve the distinction between
oc and K, so that it is clear that a temperature quoted as 300 oc refers to the Celsius
scale, while one quoted as 300 K refers to the absolute scale. Figure 1.40 shows a
range of temperatures found on Earth and in the Universe, all expressed on the
absolute scale. Normal room temperature is around 295 K.
Finally, returning to Charles's law, Figure 1.41 shows the linear
V
relationship between volume and temperature, expressed in terms of
the absolute temperature scale. The straight line now passes through
the origin, corresponding to the proportionality
Voc T
or the equation
V= constant x T (fixed quantity, constant pressure) 0 T/K
where the constant depends on the amount (i.e. number of moles) of
gas and on the pressure. Figure 1.41 Charles· law expressed in terms o~
the absolute temperature scale
37
The Physical World
5.3 The equation of state of an ideal gas

Boyle's law and Charles's law were important milestones in understanding the
properties of gases. Charles's law, especially, pointed the way to the absolute zero of
temperature and the absolute temperature scale. However, it is not necessary to
remember these laws individually, because they are both special cases of a more
powerful statement.
Suppose that n moles of a gas are in equilibrium, at pressure P, volume V and
absolute temperature T. Then, it is found that
PV=nRT ( 1.11 )
where R =8.314 J K- 1 mol- 1 is called the universal gas constant or the molar gas
constant.
Equation 1.11 works well for most ordinary gases, but deviations appear when the
pressure becomes too high. We can simplify the discussion by introducing the
concept of an ideal gas. An ideal gas is one with negligible forces between its
molecules, and which obeys Equation 1.11 exactly. Any equation that links the
equilibrium values of P, V and T is called an equation of state, so Equation 1.11 is
known as the ideal gas equation of state.
The behaviour of a real gas becomes completely indistinguishable from that of an
ideal gas in the limit of low pressure. This is understandable - as the pressure
decreases, the molecules move further apart (on average), which reduces the
importance of intermolecular forces. But, even under normal conditions, most real
gases are approximately ideal, and Equation 1.11 provides an excellent description
of their behaviour.
The fact that Equation 1.11 provides such a good description of gases, especially at
low pressures, is used to construct the ideal gas temperature scale. This is done by
defining temperature in such a way that Equation 1.11 is automatically satisfied at very
low pressures. More explicitly, imagine taking measurements of the pressure P and
volume V of a fixed mass of a gas at a fixed temperature.For each pressure, the quantity
PV/nR can be calculated. As the pressure becomes smaller and smaller, the value of
PV/nR is found to approach a limiting value. This limiting value is defined to be the
temperature on the ideal gas temperature scale. In terms of symbols, we can write
T = P~O lim (PV)

nR
This is much more satisfactory way of defining temperature than using the
expansion of a mercury column. There are more fundamental ways of defining
temperature, based on statistical mechanics or thermodynamics but, for practical
purposes, they are all equivalent to temperature defined on the ideal gas scale.
The ability of an equation to give a concise summary of many facts is well illustrated
by the ideal gas equation of state. By considering this equation under special
circumstances, we can recover all the facts about gases discussed earlier, and
more besides.
1 Boyle's law For a fixed number of moles at a constant temperature, the right-
hand side of Equation 1.11 is a constant, so we recover Boyle's law:
PV = constant.
38
2 Charles's law According to Equation 1.11,

V nR
-=-·
T p
So, for a fixed number of moles at a constant pressure, we recover Charles's law:
V
- = constant.
T
3 Avogadro's hypothesis According to Equation 1.11,
PV
n=-·
RT
So, if two samples of different ideal gases are maintained at the same temperature T
and pressure P, and occupy the same volume V, they must contain the same number
of moles, n. Since a mole contains a definite number of molecules (6.022 x 1023 ), the
two samples must also contain the same number of molecules, in agreement with
Avogadro's hypothesis.
4 Universal behaviour Because the ideal gas equation of state contains a
constant, R, which is the same for all ideal gases, many properties of ideal gases are
universal (i.e. independent of whether the gas is hydrogen, oxygen or whatever).
This can be illustrated by calculating the (isobaric) expansivity of an ideal gas. The
equation of state of an ideal gas gives
V= nRT
p
so, at constant pressure, the rate of increase of volume with temperature"is
dV nR
=
dT p
Using Equation 1.8, the (isobaric) expansivity is then
1 dV nR 1
a=--=-=-
V dT PV T'
where the last equality follows from Equation 1.11. We conclude that:
All ideal gases at the same temperature have the sa me ( isobaric) e xpansivity,
irrespecti ve of th eir molecul ar compos iti on.
This fact was known to Charles, and must have been of interest to him as he planned
future ballooning exploits.
Question 1.8 We stated earlier that 1 mol of any gas, under normal conditions of
pressure and temperature, occupies a volume of about a cubic foot. Use the ideal gas
equation of state to establish this fact.
Question I. 9 A sample of ideal gas occupies a volume of 5.00 m 3 and is at a

pressure of 1.00 x 105 Pa and a temperature of 300 K. (a) How many moles of
the gas are there in the sample? (b) How many molecules are there in the sample?
(c) If the gas is made of hydrogen molecules, with a relative molecular mass of 2.02,
what is the density ofthe gas? •
39
The Physical World
Alternative ways of writing the equation of state

The ideal gas equation of state can be written in many different, but fundamentally
equivalent, ways. The most common variant is to express it in terms of the number
of molecules, N, rather than the number of moles, n. Remembering that the number
of molecules per mole is given by Avogadro's constant, Nm, the total number of
molecules is
N = nNm.
The equation of state can therefore be written as
PV = .!!_RT
Nm
or PV=NkT ( 1.12)
where we have introduced a new constant,
k = _!__ = 1.381 X 10-23 J K-1,

Nm
known as Boltzmann's constant. You will see Boltzmann's constant appearing in
many equations of physics - especially where temperature is involved.
A third way of expressing the equation of state is also worth mentioning. If we have
a gas composed of N molecules, each of mass m, the total mass of the gas is
M=Nm
T and the density of the gas is
M Nm
p=-=-·
V V
Combining this with Equation 1.12 gives
mP
( 1.1 3)
(a)
p = kT .
V
This form of the equation of state would be of direct interest to balloonists as the
density of the gas within the balloon needs to be less than that of the surrounding air to
produce buoyancy. The equation suggests three different strategies for achieving this:
• choose a gas with a low molecular mass;
• use a sealed container containing gas at very low pressure;
• heat the gas in a balloon that is not sealed.
The PVT surface - visualizing the ideal gas equation of state

A useful way of visualizing the equation of state for a fixed quantity of ideal gas is
to display it as a 'three-dimensional graph', with T and V plotted along two
horizontal axes and P plotted along a vertical axis. Figure 1.42a shows how any
single point is plotted. The set of all points generated in this way produces a
continuous surface, known as the PVT surface for an ideal gas (Figure 1.42b).
Figure 1.42 (a) Plotting a single Each point on the PVT surface corresponds to a combination of pressure, volume and
point on the PVT surface. (b) The temperature values that can be achieved in a fixed quantity of an ideal gas in
PVT surface of an ideal gas. The equilibrium. Conversely, any set of pressure, volume and temperature values that
surface is normally drawn for one does not lie on this surface does not satisfy Equation 1.11, and so cannot be achieved
mole of a substance. in the fixed quantity of ideal gas in equilibrium.
40
Figure 1.43 (a) Slicmg through

the PVT surface of an ideal gas at
constant temperature T2 . The cut
V surface reveals (b) the dependence
(b) of pressure on volume at constant
temperature (Boyle's law) .
Figure 1.44 (a) Slicing through

the PVT surface of an ideal gas at
constant pressure P 2. The cut
0 T surface reveals (b) the dependence
(b) of volume on temperature at
constant pressure (Charles's law) .
Figure 1.43 shows a slice through the PVT surface at constant temperature. The
cross-section revealed is identical to Figure 1.36 for Boyle's law. Figure 1.44 shows
a slice through the PVT surface at constant pressure. This gives a cross-section
identical to Figure 1.41 for Charles's law.
The PVT surface can also be used to visualize processes, such as compression or
heating. Provided the process is gentle, the system will have time to adjust to the
changing conditions, and can be thought of as being in equilibrium at each instant.
Changes that are gentle enough for this to be a fair description are said to be
quasi-static. Because quasi-static processes are effectively successions of
equilibrium states, they can be represented by paths that lie on the PVT surface.
Figure 1.45 shows two paths that occur when a gas is compressed by a certain
amount. The red path a-b shows what happens ifthe temperature is held constant
during the compression, while the blue a--c path shows what happens when the gas
is allowed to warm up as it compresses. The two paths arequite different, and the
pressure at point c is greater than the pressure at point b. This illustrates the care
that is needed when describing processes: it is not sufficient to say that a gas is Figure 1.45 Two paths across a
compressed: we must also know how the temperature varies (or does not vary) PVT surface representing quasi-
during the compression. static processes.
41
The Physical World
5.4 Internal energy equations of ideal gases

You have seen that the equation of state relates the pressure of a gas to other
variables -the number of moles, the volume and the temperature. We can also ask
whether the internal energy of a gas is linked to these variables. For example, you
might expect the internal energy of a gas to be proportional to the number of moles
of the gas, and to increase with temperature. To say any more, we need to turn to
experiments for guidance.
James Prescott Joule (1818-1889) conducted a number of experiments on the nature
and effect of heat which did much to establish the general principle of the
conservation of energy. At the same time, he investigated the factors that affect the
internal energy of gases.
Joule found that the internal energy of a gas is proportional to the number of moles
and increases with temperature. However, at fixed temperature, he found that the
internal energy is practically independent of pressure and volume. The phrase 'at
fixed temperature' is significant because, when a gas is compressed, its temperature
will generally rise, leading to an increase in internal energy. But if the gas is allowed
to cool back to its initial temperature, the internal energy returns to its initial value,
with the gas at a smaller volume than before. So, at a fixed temperature, the internal
energy of the gas is unaffected by the volume change. This result can be interpreted
by recalling that intermolecular forces play a negligible role in gases.
In a solid, the individual molecules are close together and interact strongly.
Reducing the volume of a solid brings the molecules even closer together, and is
accompanied by large changes in potential energy. In a gas, though, the molecules
are so far apart that bringing them a little closer together makes practically no
difference to their mutual potential energy. Provided the temperature remains fixed,
the kinetic energy of the molecules also remains constant, so the total internal energy
does not depend on the volume of the gas.
It is again convenient to summarize our discussion by using the concept of an ideal
gas, in which molecular interactions have a negligible effect.
In equilibrium, the internal energy of an ideal gas is independent of pressure

and vo lume, and can be written as
U = nF(T) ( 1.1 4)
where n is the number of moles of the gas and F(D is some f uncti on of th e
absolute temperature. Thi s result is kn own as Joule ' s law of ideal gases.
In some ways, Joule's law is simpler than the ideal gas equation of state, but the
result is less universal because the function F(D depends on the type of gas under
investigation, especially on the number of atoms per molecule.
As always, when discussing energy, it is important to specify a zero of energy. We
will take the zero of energy to correspond to a situation where the molecules are at
rest, an infinite distance apart. With this convention, the internal energy of n moles
of any monatomic gas is accurately described by the equation
U = tnRT (1.15a)
where R is the universal gas constant introduced earlier and T is the absolute temperature.
Diatomic gases, such as nitrogen and oxygen, have higher internal energies than
monatomic gases at the same temperature. Their internal energies depend on
42
temperature in a complicated way, but around room temperature a typical diatomic

molecule has
U = tnRT. (1.16a)
The simple relationships expressed by Equations 1.15a and 1.16a intrigued

physicists in the nineteenth century, and they invested much effort to explain them.
You will see some of their arguments in the next chapter. For the moment, you can
accept Equations 1.15a and 1.16a as experimental results.
These equations can also be rewritten in terms of the number of molecules, N, rather
than the number of moles, n. When this is done, the internal energy equation for a
monatomic ideal gas becomes
U = lNkT
2
(1.15b)
and that of a typical diatomic gas at room temperature is

U = -fNkT (1.16b)
where k is Boltzmann's constant introduced earlier. As with the equation of state,
we can visualize these results graphically, by plotting athree-dimensional graph of u
internal energy against pressure and temperature to produce the UPT surface of an
ideal gas (Figure 1.46). This is simply a plane sloping upwards as temperature
increases, but not sloping asP varies, in accordance with Joule's law. The slope is
greater for diatomic gases than for monatomic gases.
Absolute zero and kinetic energy

Equations 1.15 and 1.16 suggest that the internal energy of an ideal gas vanishes as
the temperature falls to absolute zero. Because intermolecular forces have a
negligible effect in an ideal gas, the internal energy contains no contributions from
potential energy, and we can say that the kinetic energy of the molecules becomes
zero at absolute zero. Figure 1.46 The UPT surface
This turns out to be a general statement, valid for all phases of matter, throughout for an ideal gas.
classical physics. The lower the temperature falls, the slower the molecules move
until, at absolute zero, they stop moving and have zero kinetic energy. This helps to
explain why absolute zero is a fundamental limiting temperature. The process of
cooling slows the molecules down, but once the molecules have come to rest, no
further cooling is possible.
Question 1.1 0 Oxygen exists usually as a diatomic molecule and has a relative
molecular mass of 32. How much energy is needed to increase the temperature of
1.6 kg of oxygen gas from 0 cc to 100 cc?
Question 1.1 I Helium is a monatomic gas. Suppose 0.2 kg of helium gas initially
has a volume of 3.2 X I0-3 m 3, at a temperature of 0 cc. The gas is then heated at
constant pressure and its internal energy increases by 6.5 x 103 J. By how much do
the temperature and volume of the gas increase? •
5.5 A puzzle resolved

We started the chapter with a puzzle, claiming that turning on an electric fire does
not increase the internal energy of the air in a room. We can now investigate this
statement, to see why it is true, and why the glowing fire nevertheless provides a
comforting experience.
43
The Physical World
The key to the solution is to combine the equation of state with the internal energy
equation. Air is mostly nitrogen and oxygen, both diatomic gases, so it is appropriate
to use Equation 1.16 to describe the internal energy. Combining Equations 1.12 and
1.16b gives
U = tPV. ( 1.17)
The volume of air in the room is clearly unaffected by lighting the fire (i.e. the
volume of the room does not change). The pressure of air in the room is unaffected
too, remaining at atmospheric pressure. The pressure remains constant because the
room is not completely sealed - tiny gaps underneath doors or between floorboards,
for example, allow air to escape, and the pressure to equalize with that outside. We
can be sure that this happens because it is easy to open the door of the room from the
outside, showing that there is no extra pressure inside the room to press against.
With both the pressure and the volume remaining constant, Equation 1.17 shows that
the internal energy of the air in the room remains constant too, as we claimed.
However, something has changed. Rearranging Equation 1.12 gives
N= PV
kT
so, as the temperature increases, the number of gas molecules in the room decreases.
This agrees with our description of air escaping through tiny gaps. The average
energy per molecule is
U = lkT
N 2
which certainly increases with temperature, but the number of air molecules in the
room decreases so the total internal energy remains unchanged. The fire nevertheless
does its job, partly because heat is radiated directly in the form of infrared radiation,
but also because the molecules that remain in the room have increased average
energies, and so are more effective in transferring energy to us.
6 Macroscopic descriptions of the phases

of matter
6.1 The generic PVT surface and phases of matter
You have seen that a PVT surface is useful in visualizing the equation of state of
an ideal gas. It is even more useful when considering different phases of matter.
You should not, of course, assume that the ideal gas equation of state applies to
liquids or solids - there will be quite different equations of state between pressure,
temperature and volume for these phases, and the precise relationship will vary from
substance to substance. Nevertheless, each phase of each substance will have a
definite relationship linking pressure, temperature and volume for a fixed quantity of
substance, so we can plot a PVT surface encompassing a wide range of temperatures
and volumes, beyond any one phase. Each substance has its own characteristic PVT
surface. Rather than look at any particular case we shall consider a so-called generic
PVT surface, which illustrates the general features expected for a typical substance,
and allows us to point out the important features without getting immersed in
specific detail.
Figure 1.47 shows a generic PVT surface. This surface shows the conditions under
which a substance is in a particular phase, or combination of phases. For example,
44
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correspondence,” he added, “is enormous, employing six
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with amazement and delight at the sight which met my eyes. This
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engines in process of completion, most of them larger and some a
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bordering on ecstasy, heightened of course by the suddenness of
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me the old shop engine which I had not seen for twenty-three years.
Everything looked familiar except its speed. He said to me, “we have
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Under date of Oct. 31, 1907, Mr. Brooks writes me, “the business
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Three or four years ago I was spending a few days at the Mohonk
Lake Mountain House, Mr. Albert K. Smiley’s famous summer resort,
and one day strolled into the power house, where were three
dynamos, each driven by a Ball & Wood engine, the latter making, I
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I fell into conversation with the engineer, rather an old man and
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I mentioned this to the old man, who replied impatiently: “O, that
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Transcriber’s Notes
The text of this document follows that of the source;
inconsistent spelling and hyphenation have been
retained, except as mentioned below.
Depending on the hard- and software used to read
this text, and on their settings, not all elements
may display as intended. The scales as provided
in the indicator diagrams are, of course, not
necessarily correct.
Page 93: ... H laid on its side, thus ⌶: the symbol is
used to represent the shape of the rotated letter
H, not an I or an I-beam.
Page 137, bill for American belt: there are some
errors in the calculations, these have not been
corrected.
Page 147, paragraph starting The day after the
opening ...: the single and double quote marks do
not match.
Page 155, ... exposition of the action of the
reciprocating parts was given Mr. Edwin Reynolds
...: should possibly read ... exposition of the action
of the reciprocating parts was given by Mr. Edwin
Reynolds ....
Page 202, ... half the distance to the mid-stroke or to
E, Fig. 32, ...: presumably this refers to the figure
on page 201; there is no figure 32 in the book.
Page 217, If I went, that I would be the end of the
business: the second I should probably be
deleted.
Page 293: Presumably the references in the text to
Figure 1 and Figure 2 are to the top and bottom
illustration respectively; the source document
does not provide figure numbers.
Page 328-330: The use of quote marks in these
letters differs from that in other correspondence;
this has not been standardised.
Changes made
Illustrations and tables were moved out of text
paragraphs.
Texts in a
dashed box
is not present as text in the source document, but
has been transcribed from the accompanying
illustration. The transcribed texts provide an
approximate indication of the positions of the
elements relative to each other.
Some obvious minor typographical and punctuation
errors have been corrected silently.
Dimensions m×n and m × n have been standardised
to m×n, multiplications x×y and x × y to x × y;
cross-head and crosshead were standardised to
cross-head.
Page xii: illustration numbers have been added;
Diagrams from English Locomotive ... has been
changed to Diagrams from English Locomotives
... as in the illustration caption.
Page 40: a closing single quote mark was inserted
after ... do not require any governor,
Page 79: pièce de resistance changed to pièce de
résistance.
Page 91, illustration caption: English Locomtlvoes
changed to English Locomotives.
Page 175: ... told me had had supplied all the
money ... changed to ... told me he had supplied
all the money ....
Page 287: ... this they had been keen kept in
ignorance of ... changed to ... this they had been
kept in ignorance of ....
Page 294: b′ and c′ in the text changed to b¹ and c¹
as in the illustration.
Page 303: ... to very the speed ... changed to ... to
vary the speed ....
Page 331: ... before I left planning a smaller engine
... changed to ... before I left, planning a smaller
engine ....
Page 333: closing quote mark inserted after ...
employing six typewriters.
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Classical Physics of Matter John Bolton Full Chapter

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CRC Press is an imprint of the

Institute of Physics Publishing

First Published in 2000 by Institute of Physics Publishing

Copyright© 2000 by The Open University

No claim to original U.S. Government works

ISBN 13:978-0-7503-0717-8 (pbk)

4.3 What do the distributions of speed and translational

4 Non-ideal fluids in motion 175

'If in some cataclysm, all of scientific knowledge were to be destroyed and

Chapter I From atoms to the

2 Atoms: the building blocks of matter

Q o.' Y5"' Z inc

2.2 Atomic sizes

so t= _± X ~ = _± X (0.5 X 1o-3 m)3 "" 1o-9 m. •

Figure 1.3 A drop of oil spreads

Figure 1.4 Water waves flowing

Figure 1.5 An image of gold atoms

2.3 Isotopes and ions

Mass/1 o-30 kg Charge/1.602 x I0-19 C

2.4 Atomic masses

The atomic mass unit

Relative atomic and molecular masses

Nowadays, it is possible to obtain direct measurements of the masses of atoms (more

2.5 Interactions between atoms

The force-separation curve

It is possible for the atoms to remain stationary at their equilibrium separation, r0 ,

,_ _ _ _ ,.0 - - - -----1 , _______ ,. _______ ~

where C is the magnitude of the gradient of the force-separation graph at the

Question 1.3 Estimate the frequency of oscillation of a molecule composed of

The potential energy-separation curve

3 Atomic descriptions of the phases of

3.1 The gas phase

c • • .____ magnes ium

Figure 1.15 A spherical shell

3.2 The liquid phase

Figure 1.18 Radial density function for water at different

3.3 The solid phase

Figure 1.21 Arrangement of Figure 1.22 A wallpaper pattern.

Figure 1.23 The radial density function in a solid.

Figure 1.28 Otto von Guericke's

p = FJ. = Fcos(} . (1.4)

to observe that pressure decreases with altitude, a topic we return to in Chapter 4.

temper atu refCC

The e nergy transferred fro m a warm body to a coo l body, as a result of a

Temperature is a label which d etermines the direction of heat fl ow between

Several points can be lifted out of this statement:

Box 1.1 Instructions for calibrating a thermometer

e = 0 °C + I - lo X 100 °C. ( 1.5)

Question 1.6 The length of mercury in the column of an uncalibrated mercury-

4.4 Internal energy

4.5 Molar quantities

The abbreviation for mole is mol.

Although it may seem like splitting hairs, it is conventional to distinguish between

4.6 Response functions

f3 =_ _!_ dV (at constant temperature). (1.9)

Question I. 7 When a metal block is heated by 5 °C at constant pressure, it

5 Macroscopic equilibrium in ideal gases

,_ _ _ _ ,.0 - - - -----1 , _ ,. _ ~