Dental Materials Science

LECTURE
NOTES
Dental Material Science I
DENTAL TECHNOLOGY DIPLOMA

General Introduction
Welcome to Dental Materials Science.
Please have the notes with you during lectures, when the material will be further
explained. Although you may find taking some notes is useful to give an extra
view on some points, these notes cover all the material you will need to pass the
module. You will not need to take any notes during the lecture, which will go
over the material in these notes again by a Powerpoint presentation, or on the
board.
You may also find it useful to purchase the recommended materials science
textbook, or to read the reference textbooks in the library. These books have been
listed in the resources section which follows shortly.
These notes have also been designed to allow you to study and learn the material
away from class. Being able to cover the material at your own speed and with
your own pattern of learning is beneficial for many students. To help with this,
there are questions typical of some of those asked in the examinations at the end
of each section. These allow you to check your knowledge of each section as you
proceed.
Module Overview
This module has been designed to build your knowledge of atoms, material
structure, chemical bonding, and properties of materials. This knowledge leads to
a better understanding of the chemical, physical and mechanical properties of
materials. In later sections of the course this knowledge will be valuable in
understanding the reasons for using a particular dental restorative material, and
the techniques necessary to fabricate it.
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Dental Material Science
Recommended Textbook
Title: Dental Materials properties and Manipulation.

Author: R.C. Craig, J.M.Powers, & J.C. Wataha.
Publisher: Mosby
ISBN: 0-323-02520-X
Reference Textbook
Title: Dental Materials: Properties and Selection.

Author: O’Brien, William, J.
Publisher: Quintessence Publishing Company
Pub Place: Chicago
Pub Date: 1989
ISBN: 0867151994
Your college may have a copy that you can borrow or you can purchase it
yourself.
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LEARNING OUTCOME 1
CLASSIFICATION OF MATTER.
Assessment criteria:
You will have achieved this learning outcome when you can:
• Distinguish the different states of matter.
• Classify matter as elements, mixtures or compounds.
COMM SERV HEALTH TOURISM HOSP ESD©

PARAMEDICAL STUDIES PROGRAM AREA
1
TOPIC 1 - Classification of Matter.
Recommended Time - 2 hrs
Introduction
In explaining to you the properties and use of various dental materials, we need
first to understand what material, or matter, is. Scientists describe matter as
belonging to different types in order to help understand its properties, For
example, we often divide solid materials into metals, plastics (polymers) or
ceramics, a classification we will learn more about later. Topic 1 introduces you
to some of the ways scientists describe and classify matter. You will learn about:
• States of matter (ways in which matter can exist)
• Classification of matter as elements, mixtures or compounds.
Matter
Matter is defined as anything which has mass and occupies a volume. Mass is
the amount of material present. For example, when you see bubbles in a liquid,
the bubbles have a volume, and the mass of the air can be determined. At the
same time, you can observe differences between a gaseous and a liquid state of
matter. This simple observation shows that the same matter can to exist in
different states. Changing from one to another state of matter is a reversible,
physical change. We can change water (a liquid form of hydrogen oxide) to ice
(a solid form of the same compound) by cooling it sufficiently. We can change
the ice back into water by heating it
States of Matter
Matter can exist in one of 4 forms:

(i) Solid.
(ii) Liquid.
(iii) Gas.
(iv) Plasma
Plasma is a rare state of existence for matter on this planet and needn’t bother us
much for dental work, but it is important to understand the other three.
The differences in the behaviour of matter as solid, liquid and gas is caused by
the behaviour of its atoms in that state. For example, water can exist as a solid
(ice) below 00C, as a liquid above 0oC, and as a gas if heated above 1000C.
What causes the properties of these different states of matter is the how mobile
the atoms are each state. In the solid state, the atoms or molecules are fixed in
position due to strong forces between molecules. Because the molecules or atoms
remain in these fixed positions, the only movement possible is vibration. Every
solid has a fixed volume and a fixed, definite shape. However, when the solid
is heated, the atoms or molecules react to the extra energy by vibrating with
increased frequency and amplitude. They are still held firmly in place, however,
and cannot break free of the forces holding them in place until their energy
becomes great enough. At this point, the matter becomes a liquid. We say that it
has reached its melting point.
The forces between molecules are much weaker in liquids so the particles have
greater mobility. Liquids are able to flow, a property due to the constant motion
of their particles relative to one another. This is why they have no definite
shape. The particles have only limited movement, however. They cannot move
apart much, so that liquids have a constant, or fixed volume at any one
temperature. Most particles of a liquid are held within the liquid due to forces of
attraction between molecules (surface tension), but particles can gain enough
energy to escape and form a vapour. This is called evaporation. As a liquid is
heated, more and more particles evaporate until the temperature reaches the
boiling point and a complete change of state from liquid to gas occurs.
In the gaseous state the particles are in constant motion and free to move in any
direction. As a result, gases are not only fluid (like liquids, they have no fixed
shape), they also have no fixed volume. As the particles in a gas regularly
collide and rebound from each other at high speed, they move around until they
fill the whole container. If they are not contained they will fly away due to their
highly mobile state. As gases are heated, the heat energy is transferred to
increased motion (velocity) of the particles, and can be observed as an increase in
pressure.
At room temperature, if a substance appears as a liquid then it has a melting point

below room temperature. If a substance is a gas at room temperature then it has a
boiling point below room temperature.
Kinetic Theory of Matter
This theory explains how matter can be changed from one state to another. We
know that all matter is be made up of tiny particles (atoms or molecules.) At any
temperature above absolute zero, these particles are in a state of constant motion.
The amount of motion of a substance in any state of matter is due to its particles
responding to the available energy. Heat is a form of energy. If a substance is

3
liquid at room temperature, its particles are mobile, or in the liquid state. Its
melting point is below room temperature. For water, with a melting point of 00C,
there is enough energy at 200C to keep water particles mobile and able to flow.
As the temperature of water is decreased the mobility of the molecules decrease

until they cannot move fast enough to overcome the forces of attraction between
them. The substance then changes state to become a solid. The molecules are no
longer free to move, but they are still able to vibrate in positions fixed relative to
each other.
If we decrease the temperature further, particle vibration decreases until -2730C is

reached. This is referred to absolute zero, since at this point all vibration stops.
The temperature at which we observe changes of state are exact for pure
substances. If we change the purity of the substance, the melting point and
boiling point will also change.
Homogenous and Heterogeneous Matter
We use these terms describe the composition and properties of matter. For
example, if we have pure water in a container, then a sample taken from
anywhere in the liquid will have the same composition, and properties. Because
of this, only one value of a property is needed to fully describe pure matter. It is
said to be homogenous, its properties are identical at any point in it.
If two elements or substances are mixed together, such as oil and water, they will
quickly separate. We are able to easily separate the two distinct parts by physical
means. This is called heterogeneous matter. The properties will not be the same
at any point in the body. They will depend on which of the mixture components
has been sampled.
Elements, Mixtures and Compounds
A pure substance is composed of only one type of atom or molecule, and it will
have homogeneous properties. An atom is the smallest part of an element that
still has the properties of that element
A pure substance composed only of one sort of atom is called an element. A pure
substance made from one sort of molecule is called a compound.
A compound is a pure substance made by combining two or more elements in

a fixed proportion by weight. A molecule is the smallest part of a compound
that still has the properties of that compound
When a second element is introduced to a first, the chemical and physical

properties will change. For example, pure water melts at 00C and boils at 1000C.
If we dissolve salt in the water, its composition changes. It is no longer pure. If
we re-measure its melting and boiling points, they will have changed also.
The difference in composition and properties between pure water and salt water
explains the difference between a pure substance and a mixture. The properties
of a mixture are a mixture of the properties of the individual substances. As the
amounts of each substance vary, so will the properties.
Mixtures do not have fixed melting points or boiling points; they change with
composition. There is no chemical reaction involved in their formation so they
are still easily separated. In the case of salt water, the water can be evaporated to
form pure water leaving pure salt water behind.
If two or more pure elements are made to react together chemically, then the
result will be the formation of a compound. The compound formed will be a
pure substance and will be different in composition and properties to the original
elements. An example of forming a compound is the combustion of pure
hydrogen in the presence of oxygen to form pure water. The compound formed is
in a different state of matter at room temperature, does not resemble its gaseous
reactants, and cannot easily be reversed to hydrogen and oxygen. A chemical
reaction is needed to do that.
Another example is mixing pure iron and sulphur together. Only when the
mixture is heated will a chemical reaction occur to form a new compound, iron
sulphide. This has different composition and properties to its reactants.

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ELEMENTS, MIXTURES & COMPOUNDS – Practical
Assignment I
AIM
To examine some of the properties of elements, mixtures and compounds.
METHOD (1)
(i) Weigh out 5g of iron (Fe) and 3g of sulphur (S).
(ii) Place these two elements in a mortar and grind them into a fine
powder with a pestle.
(iii) Spread this powder on a piece of filter paper and examine it with a
magnifying glass. Is it uniform throughout (homogeneous) or is it
non-uniform (heterogeneous)?
(iv) Pass a magnet under the filter paper and observe what happens. Is
there any separation? Does this indicate a homogeneous or
heterogeneous material?
(v) Fill a clean test tube to a depth of approximately 10 mm with the

ground material and shake it up. Is there any separation? Half fill
the test tube with water and shake. Is there any separation?
METHOD (2)
(i) Place 10mm of the ground material into a Pyrex test tube. Heat it
over a bunsen flame in a fume cupboard. Note any reactions.
(ii) Allow the mass in the test tube to cool. Remove it form the test
tube and grind it up in the mortar and pestle. Place some of the
ground powder on a filter paper and examine it with a magnifying
glass. Compare the results to those obtained in 1(iii).
(iii) Test the powder with a magnet as in 1(iv) and compare the results.
(iv) Place some of the material obtained in part 2 in a test tube to a

depth of 10 mm and repeat 1(v). Compare the results.
RESULTS
It would be helpful to record all your observations of the results in a tabulated
form.
CONCLUSIONS
Consider the results you have written down. Do they indicate that we have an
element, a mixture , or a compound at each stage of the experiment? What do the
results show you about In light of your discussion draw some conclusions about
elements, mixtures and compounds.
Check Your Progress
Self Evaluation Questions
Listed below are questions which will help you to review Topic 1,
Write your answer to each question on the lines below the question.
You can check your answers with the ones given at the end of this topic.
Q1. List three (3) different states of matter.

(i) _____________________
(ii) _____________________
(iii) _____________________
Q2. Describe the motion of particle of matter in each state you listed in Q1.
(i) _____________________________________________________
(ii) _____________________________________________________
(iii) _____________________________________________________
Q3. Briefly describe the Kinetic Theory of Matter.

_______________________________________________________________
_______________________________________________________________
_______________________________________________________________
Q4. Define the following terms:
•
(i) Homogeneous
•
(ii) Heterogeneous
•
(iii) Element
•
(iv) Mixture
•
(v) Compound

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Suggested Responses for Topic 1
Q1. (i) solid

(i) liquid
(ii) gas
Q2. (i) Vibration of particles only – rigidly restrained.

(ii) Particles have constant motion and can flow.
(iii) Particles are free to move in any direction.
Q3. All matter consist of particles which are in a constant state of motion.
Changes in temperature increase or decrease motion and cause changes of
state.
Q4. Define the following terms:
• chemical properties are uniform

(i) Homogeneous
• only one physical distinct property throughout the
material.
• show two or more different property which allows
(ii) Heterogeneous
separation easily by physical means
• A pure substance composed of only one type of
(iii) Element
atom.
• A substance containing with two or more elements
(iv) Mixture
or compounds combined in no fixed proportions.
It shows the properties of each of its components.
• The components are easily separated by physical
means (heterogeneous)
• This is a pure substance made by chemically
(v) Compound
combining atoms of two or more elements in fixed
proportions by weight. A compound has its own
chemical and physical properties, different from
those of its components. It is still homogeneous.
LEARNING OUTCOME 2
DISTINGUISH BETWEEN METALS AND

NON-METALS, USING KNOWLEDGE OF
ATOMIC STRUCTURE.
Assessment Criteria:
• Name and describe sub-atomic particles.
• Describe the arrangement of sub-atomic particles within the atom.
• Relate the atomic number of an atom to its structure.
• Classify atoms as metals or non-metals based on their structure.
• Name, write the symbol for and describe the atomic structure of the first
twelve elements.
• Name, and write the symbol(s) for the elements within the periodic table that
are of interest to dental restoration study.

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TOPIC 2 - Atomic Structure.
Introduction
We now understand that materials can be classified according to their different
behaviour, both physical and chemical. To understand why materials are
different from each other, we first must understand some basic chemistry about
how matter is made, and how this influences its properties. This topic starts the
process of understanding the basic structure of materials by introducing you to the
structure of atoms, under the following headings:
• The type and nature of sub atomic particles.

• The arrangement of sub atomic particles in an atom.
• The relationship between atomic number and structure.
• The classification of atoms, including the division into metals or non
metals.
• Important properties of the first twelve elements.
• Identifying elements that are present in dental materials.
History of Atomic Theory (just read this, not examinable)

Precisely what goes to make up matter or substances is a problem that has
fascinated scientific philosophers for centuries.
Early philosophies considered matter to be made from of four elements: earth,

fire, air and water. Around 400 BC Greek philosophers proposed that matter
consisted of tiny indivisible particles called atoms.
In the early 1800’s John Dalton proposed a revolutionary new approach:

• All elements are made up of atoms
• Atoms cannot be created or destroyed (they are indivisible)
• Atoms of different elements may combine with atoms of another
element in definite ratios.
• Atoms of one element are different from atoms of another element.
By 1820, laboratory experiment had found the presence of smaller particles in

atoms, which suggested the presence of sub-atomic particles. Atoms could be
taken apart, contrary to Dalton’s ideas.
In 1911, Ernest Rutherford confirmed the presence of sub-atomic particles, and
made the following conclusions:
• Each atoms has a nucleus which is positively charged.
• Most of the atomic mass is contained in the nucleus.
• The nucleus is surrounded by an almost empty space that makes up the rest
of the atom.
• Negatively charged electrons are present in this space around the nucleus.
The negative charge on the electrons balances the positive charge of the
nucleus.
In 1913, Niels Bohr suggested that the nucleus contains two different types of sub
atomic particles. This gave rise to the modern atomic theory.
Modern Atomic Theory
Bohr conclude his atomic theory as:

• Atoms consist of subatomic particles
• The nucleus contains protons (+ charge) and neutrons (no charge).
• A cloud of electrons (- charge) orbits the nucleus.
• The volume of the nucleus is extremely small compared to the volume of

an atom.
• The atom is electrically neutral since the number of electrons = number of

protons.
Properties of Subatomic Particles
Subatomic Symbol Charge Mass Mass Location

Particle (grams) a.m.u
Electron e- -1 9.07x10-28 0.00055 outside nucleus
Proton p+ +1 1.672x10-24 1.0073 inside nucleus
Neutron n 0 1.672x10-24 1.0087 inside nucleus
All elements are made up of different combinations of these subatomic particles.

The number of each type of sub-atomic particle in an atom can be determined
from the information about that particular element contained in the Periodic
Table. This is a table of all the known elements and their basic properties,
arranged in order of atomic number.

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e
e
n
n
p Electron
n
n orbits
n
pn
p
e
n Nucleus
The arrangement of particles in an atom. PROTONS (+ charge), NEUTRONS

(no charge) and ELECTRONS (- charge).
Atomic Number and Mass Number
What makes the difference between elements? To determine this we have to look
at the arrangement of subatomic particles that make up each atom. This
arrangement is different for each element. The information can be determined
from the Atomic Number and the Mass Number:
Atomic number = number of protons in the nucleus
Mass number = number of protons plus neutrons in the nucleus
As each atom must be electrically neutral, the number of electrons must be equal
to the number of protons, which is the atomic number. If you look at the table of
elements, you will see, for instance;
Atomic Number Mass Number

Carbon 6 12
From this. we can work out that that carbon has:

6 protons (atomic number)
6 neutrons (mass number minus atomic number)
6 electrons (number of electrons = number of protons)
Element Atomic Number Mass Number
(Z) (A)
Hydrogen 1 1
Helium 2 4
Lithium 3 7
Beryllium 4 9
Boron 5 11
Carbon 6 12
Nitrogen 7 14
Oxygen 8 16
We know now that the central nucleus contains the protons and neutrons, but we
don’t know how the electron orbits are arranged. For example, carbon has 6
protons (atomic number) and to be electrically neutral, must have 6 electrons.
Logically there must be some consistent arrangement of these electrons, because
they are moving around the nucleus without crashing into each other,
Electron Structure
Bohr described electrons as moving in fixed circular orbits around the nucleus,
rather like planets orbiting around a sun. This is why his description is often
referred to as the “Planetary Model” of an atom. These orbits, shells, or orbitals
are different distances away from the nucleus, so each electron in a different shell
must have a different energy. The electrons in the furthest orbit form the nucleus
have the most energy, while those closer to the nucleus have less energy.
Bohr identified each electron shell with a number, n. The shell closest to the
nucleus had n=1 which is the lowest energy level. The next shell, n=2, has a
higher energy level and so on for n=3,4,5,6.
It seems logical that the outer shells, being larger, could hold more electrons. In
fact, it turns out that the maximum number of electrons which can fit in each shell
is governed by the formulae:
Maximum Number of electrons in any shell “n” = 2n2

n can be 1,2,3,4,5,6.
For example in the first electron shell, n=1.and n2 = 1. The maximum number of
electrons which can be fitted into that shell is 2, because 2x(1)2=2.
For the second shell n=2. n2 = 4 The maximum number of electrons in this shell is
8, because 2x(2)2 = 8
For the third shell n = 3. n2 = 9. The maximum number of electrons in the third
shell is 18 because 2x(3)2 = 18

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Consider the case of carbon. As we discussed earlier, it has six electrons. Its
electron configuration can thus be calculated as
2 electrons in the 1st shell (n=1)

4 electrons in the 2nd shell (n=2)
The second shell could hold a maximum of eight electrons, but carbon only has
six. After putting two into the first shell there are only four left, so the second
shell can only have the remaining four electrons in it.
Under normal conditions electrons in their shells are referred to as in their

“ground state.” If atoms are heated, electrons gain energy and they may jump to
higher energy levels. When dropping back to the ground state, they may re-emit
the same amount of energy.
If we gave each shell a number to identify it, this could become confused with the
number of electrons in the shell, so chemists have identified each shell with a
letter instead The closest shell to the nucleus is called K. The next is L followed
by M, N etc.
The following table shows the electron configuration for the first twelve
elements. Remember, the maximum number of electrons is expressed by 2n2.
Element Number of Maximum Electron

(chemical symbol) electrons number in shell Configuration
K,L,M,N
Hydrogen (H) 1 2 1
Helium (He) 2 2 2
Lithium (Li) 3 2, 8 2, 1
Beryllium (Be) 4 2, 8 2, 2
Boron ( B) 5 2, 8 2, 3
Carbon (C) 6 2, 8 2, 4
Nitrogen (N) 7 2, 8 2, 5
Oxygen (O) 8 2, 8 2, 6
Fluorine (F) 9 2, 8 2, 7
Neon (Ne) 10 2, 8 2, 8
Sodium (Na) 11 2, 8, 18 2, 8, 1
Magnesium (Mg) 12 2, 8, 18 2, 8, 2
Names and symbols of elements
As you can see from the table above, each different element has been given a
name by its discoverer, and a symbol of one or two letters made up from the
element’s name or from its Latin name. The elements are named after greek or
roman gods, scientists, countries, or anything else which took their discoverer’s
fancy at the time. The symbols are used as a type of short-hand to represent the
elements in chemical formulae and equations. For the purposes of this course,
you should know the names and symbols of the first twelve elements, and their
symbols, and those of another fourteen common elements or those of interest in
dental work. These are set out in the next table
Element Symbol Element Symbol Element Symbol

Hydrogen H Gold Au Chlorine Cl
Helium He Silver Ag Sulfur S
Lithium Li Palladium Pd Phosphorus P
Beryllium Be Platinum Pt Mercury Hg
Boron B Iron Fe Zinc Zn
Carbon C Cobalt Co Calcium Ca
Nitrogen N Nickel Ni
Oxygen O Chromium Cr
Fluorine F Tin Sn
Neon Ne Copper Cu
Sodium Na Aluminium Al
Magnesium Mg Lead Pb
Periodic Table
You will notice that the first twelve elements in the table have been listed in order
of their Mass Number, which is the way that they were listed as the number of
elements being discovered grew. The normal way of considering all the elements
at once is the Periodic Table. Scientists in the 1800’s discovered that some
elements had very similar chemical properties to each other, even though their
atomic and mass numbers were different. To find out why this was so, they
arranged groups of elements with similar properties in columns and rows and
looked for patterns in their properties or the numbers. In this way they made early
versions of a periodic classification.
The modern Periodic Table lists the elements in a series of boxes arranged in
columns and rows.. In the horizontal row, elements increase in atomic number
from left to right. Each box contains important information about the element:
Atomic number, or “Z”

Mass number, or “A”
Chemical symbol
Electron configuration

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Originally, elements with similar chemical properties had their boxes arranged in
a vertical column. This arrangement is still used. For example, Helium, Neon,
Argon, Krypton and Xenon are all inert gases and are found in a column on the
right hand side of the periodic table.
Look at the periodic table shown below. Although it is more than seventy years
old, little has changed except for the addition of a few extra heavy elements with
atomic weights above 105. Note that elements which have very obvious metallic
properties are found on the left of the table. The less “typical” metals are found
in the middle, the transition metals. Just before the non-metals on the right,
separated by the stepped vertical line, there are elements which have some
properties of both metals and non-metals, the “metalloids” such as arsenic, or
silicon. Why should these obvious groupings occur? What determines the
difference between metals and non-metals, so that arranging the elements in order
of atomic number and similar chemical properties will reveal it?
It turns out that the chemical properties of any element are controlled mainly
by the number of electrons in its outer shells. This is a most important fact.
Properties of Metal and Non-Metals
We now know, from a study of the types of chemical reactions they undergo, that
what distinguishes metallic from non-metallic elements is the number of electrons
they have in the outermost shell of their atoms. We call these valence electrons.
An element will behave as a metal if it easily loses, or donates, one or more
electrons when forming chemical bonds. Metals thus are those elements with
only a few electrons in their outer shell. Look at the second column from the left
in the periodic table. Use the atomic numbers to work out how many electrons
each one has, and you’ll find they all have two electrons in their outermost shell.
Non-Metals are elements that have outer electron shells that are close to being
full. They readily accept electrons during chemical bonding.
A comparison of the common properties of metals and non metals is shown in the
following table:
Metal Non Metal

 Have 1, 2, or 3 valence  Have 4, or more valence
electrons. electrons.
 Lose electrons easily.  Tend to gain electrons.
 Form compounds with non  Form compounds with metals.
metals.  Low electrical conductivity.
 High electrical conductivity.  Low thermal conductivity.
 High thermal conductivity.  Non ductile (brittle).
 Malleable and Ductile.

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Check Your Progress
With a self-paced learning package like this one, we provide regular opportunities
for you to check your knowledge as you go. You’ll find a set of questions for you
to answer, and so review your knowledge, at the end of each topic.
Listed below are questions that will help you to review Topic 2. Write your
answer to each question on the lines below the question, and when you have
finished you can check your answers with the ones given at the end of this topic.
Q1 Give the name and charge of each of the particles that make up an atom
(i)……………………………………………………………………………
(i) ……………………………………………………………………………
(ii) ……………………………………………………………………………
(ii) ………………………………………………………………………….
Q2 Define what is meant by the following terms.
(i) Atomic Number ……………………….…………………………………….

…………………………………………………………………………………
(ii) Mass Number ………………………………………………………………..
…………………………………………………………………………………...
Q3 The maximum number of electrons in any shell with number “n” is calculated
from which formula?………………………………………………………….
Q4. List three (3) properties of metals and non metals.
Metals Non Metals

(i) (i)
(ii) (ii)
(iii) (iii)
Q1 Give the name and charge of each of the particles that go to make up an atom.
(i) proton (+)
(ii) electron (-)
(iii) neutron (0)
Q2. Complete the following sentences:.

(iii) The Atomic Number of an atom is The number of protons in the
nucleus.
(iv) The Mass Number of an atom is The number of protons plus the
number of neutrons in the nucleus.
Q3. The maximum number of electrons in any shell with number “n” is calculated
from the formula :- Maximum number =2n2 where n = shell number
Q4. List three (3) properties of metals and non-metals.
Metals Non-Metals
(i) 1,2 or 3 valence electrons (i) 4 or more valence electrons
(ii) lose electrons easily (ii) tend to gain electrons
(iii) malleable (iii) brittle

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So, how did you go with the topics under Learning outcome 2? Did you answer all the
questions correctly? Do you feel confident in being able to meet the assessment
criteria listed under the learning outcome? If you did, congratulations and please
proceed to Learning outcome 2. If you answered a question incorrectly or you had
difficulty with any of the activities, go back and have a look at the information again.
If any part of this module is not clear, it is very important to contact your teacher and
discuss this with him or her before you start Learning outcome 3.
LEARNING OUTCOME 3
RELATE CHEMICAL REACTIONS AND

BONDING TO THE STRUCTURE OF
MATTER.
• Describe primary and secondary bonding in matter.
• Classify the bonding in different materials.
• Write balanced chemical equations to describe chemical reactions.

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TOPIC 3 - Chemical Bonding and Reactions
Introduction
The way that elements are combined to make compounds often has much to do
with their properties as possible dental materials. This topic introduces you to
important information about:
 Nature and types of primary and secondary bonds in matter.

 Specific types of bonding in materials.
 Writing and balancing chemical equation to represent reactions.
If you think about what might happen as two atoms are brought closer together, it
is obvious that what they do will be controlled by their outer electron shells,
which are the first parts to come together.
We now know that atoms will be in a lower state of energy if their outer
electron shells are full of electrons. If they are close to another atom, they can
achieve this condition by obtaining extra electrons from it and filling their
outer shell, or by giving electrons to it, so as to empty their outer shell and
expose the full shell next to it, or by sharing electrons with the other atom so
that both have a full outer shell. When atoms do this, they very often bond
together to form a new substance, a compound
Valency
The combining power of an atom is known as its valency, or valence, and is an
important property of each different element. It is determined by the number of
electrons the atom will acquire, give away, or share during chemical bonding.
electrons, as these high energy electrons are the ones involved in chemical
bonding to from compounds.
Metallic atoms have 1, 2, or 3 valence electrons which they lose easily during
bonding to form a positive ion. An Ion is an atom that has been given a positive
or negative charge by losing or gaining electrons.
Non metallic atoms tend to gain electrons during bonding, so the number of
vacant site in the outermost shell is their valency. Examples are shown in the
following table. These elements form negative ions. Also in the table are a
number of negative ions and one positive ion which are made from a number of
atoms, not one. These negative or positive groups of atoms are called “functional
groups”, because they can function as, or take the place of, a single atom or ion.
Positive valency ions Negative valency ions

Lithium Li1+ Carbon C4-
Beryllium Be2+ Chloride CI1-
Boron B3+ Carbonate CO32-
Sodium Na1+ Fluoride FI3-
Magnesium Mg2+ Hydroxide OH1-
Aluminium AI3+ Oxide O2-
Potassium K1+ Nitrate NO31-
Calcium Ca2+ Sulfate SO42-
Hydrogen H1+ Phosphate PO43-
Iron Fe2+ or Fe3+
Copper Cu1+ or Cu2+
Silver Ag1+
Gold Au1+
Ammonium NH41+
Chemical Bonding in Compounds
The simplest form of bonding which occurs to form a compound is shown by non-
metals such as oxygen, hydrogen or nitrogen. Two gas atoms like these can bond
together to produce a stable diatomic molecule. The chemical formulae shows
this:
Oxygen - O2
Chlorine - CI2 Diatomic gases
Nitrogen - N2
Hydrogen - H2
For bonding to occur between metals and non-metals, an ion may have to be
formed. This is a charged atom, an atom with some electrons missing, or some
extra electrons added. For example, aluminium has 3 valence electrons, but
bonding is not possible until an ion has been formed by removing these.
Al (element) → Al3+ + 3 electrons

Na (element) → Na1+ + 1 electron

23
An ion of aluminium has been formed form the element by losing 3 electrons.
Similarly Sodium loses 1 electron to form an ion.
As an example of a non-metal, the element chlorine can gain one electron to form
a chloride ion for bonding.
Cl (element) + e → Cl1-
Ions of opposite charges attract each other, and may join together to form an ionic
compound.
An example of an ionic compound is sodium chloride
Na1+ + Cl1- → NaCl
The ions involved are Na1+ and Cl1- As they both have the same valency they are
going to react in a 1:1 ratio, that is one ion of sodium (Na1+) will react with one
chloride ion (Cl1-) to form the new compound NaCl.
Another example is the reaction between zinc ions (Zn2+) and chloride ions (Cl1-).
In this case the valency of zinc allows it to react with two chloride ions Zinc has
two electrons to lose, and each chlorine atom can only pick up one of them, so the
ratio of Zinc ions to Chlorine ions in the new compound is 1:2.
(Zn2+) + Cl1- → ZnCl2
Notice how we use the abbreviated symbols given to the elements to describe the
chemical reaction and also to construct a formula for the new compounds formed.
How do these ions, in their fixed ratios, come together to form what we see as
large amounts of matter, material, or substances? To answer this question, we
must discuss chemical bonding, what holds atoms together
Primary Chemical Bonds
1. Ionic Bonds
The stability and strength of these bonds can be explained by looking at

the formation of sodium chloride we discussed above. Sodium has 1
electron in its outer shell which it will freely give up so that its next
innermost shell is full, a more stable arrangement. Chlorine needs 1
electron to fill its most outermost shell, similarly becoming more stable.
When these two elements react, electrons are taken from the sodium to the
chloride atoms. The positive sodium ions and negative chloride ions
formed have a strong electrostatic attraction to each other, and are held in
place in a fixed structure to from a solid compound (at room temperature.)
This newly formed compound, sodium chloride, normal table salt, is a
solid, normally small clear crystals. Its properties are very different from
those of the reactive shiny metal which is sodium and the green poisonous
gas, chlorine. This difference proves the formation of a new substance.
Ionic compounds such as sodium chloride have high melting points, are
usually solid at room temperature and are soluble in water. They conduct
electricity when they melt or when dissolved in water because they
separate into ions (dissociate) which can carry an electric current.
Steps in ionic bond formation:
i) formation of sodium ion Na → Na1+ + 1 electron

ii) chlorine accept electron Cl + 1e → CI1-
iii) elecrostatic attraction forms new Na+ + Cl- → NaCI

compound
2. Covalent Bonds
Atoms may achieve stable electron configurations by sharing electrons

with adjacent atoms rather than donating or accepting them like elements
which form ionic bonds. The gases we discussed earlier – oxygen,
hydrogen and carbon, all share electrons to fill their outer shells, which
makes them more stable. Sharing outer shell electrons between atoms
makes a new outer shell which encloses both atoms. A molecule of a new
substance is created, with its atoms held together by a covalent bond.
For example, consider a hydrogen atom with its single electron.
Two hydrogen atoms pair together to become a diatomic. molecule. To do

this, they share their two electrons, which form a single orbital around
both atoms. The orbital has a figure-eight shape.

25
We can write this as an equation, showing the reagent atoms and their
product molecule.
H. + H. → H–H (hydrogen gas molecule, formula H2)
Other non metallic atoms can share atoms to form covalently bonded
molecules. For example a molecule of water (formula, H2O) is formed
from two atoms of hydrogen and one of oxygen.
H O H
H. + H + O → H–O–H (water)
The bond which holds the atoms together in a molecule forms because the
positive nucleus of each atom is strongly attracted to the cloud of shared
electrons surrounding the atoms.
A more extensive example of covalent bonding is found in methane, CH4.

Here carbon, shares each of its four outer shell electrons in a bond with
one of four separate hydrogen atoms. This results in eight electrons in a
complex orbital around the carbon, and two around each hydrogen atom.
All the atoms have an effectively full outer shell.
The “structural” diagram for this is simpler, but does not show each
electron.
H
|
H−C−H
|
H
H
H C H
Atoms undergoing covalent bonding may also share more than 2 electrons.
Sharing four electrons, for example, produces a double bond An example
can be seen in the gas ethylene. There is a double bond between the two
carbon atoms, which also share an electron in turn to each of two hydro
atoms. Each carbon atom has thus shared its outer four electrons with
another four from different atoms to give a total number of eight in its
outer shell. The ethylene molecule forms a very reactive gas.
H H
\ /
C=C
/ \
H H
The atomic or electronic diagram shows us the structure of each bond

27
H H
C C
H H
3. Metallic Bonds
This type of bonding is only formed between metallic atoms. There are
not enough valence electrons in metals to share between atoms to make a
true covalent bond. So, each atom contributes its valence electron to form
a loose ‘cloud’ of electrons. These electrons are not associated with any
of the positive metallic ions formed, but are free to move between them.
This produces a strong electrostatic attraction between the positively
charged ions and the ‘cloud’ of mobile electrons.
Atoms
Electron
cloud
The strength of the metallic bond produces very close packing of the ions
in a regular lattice arrangement. The freely moving electron cloud
produces good electrical conductivity, and the close packing gives metals
their typically high densities.
4. Secondary Chemical Bonds
Secondary bonds are formed by the attraction of weak intermolecular

forces between dipoles. A dipole is part of a covalently bonded molecule
where charge is not evenly distributed. An example is water. The
hydrogen atoms are not bonded to form a linear molecule, in fact the bond
angle between the hydrogen is only 104.50 degrees instead of 180 degrees.
O
H H
104. 50
+
This produces a weakly positive electrostatic charge on one side of the

molecule and a weak negative charge on the opposite side. Attraction is
now possible between oppositely charged poles of other polar molecules.
Chemical Reactions and Equations
During the previous paragraphs, we have been coming close to describing the
reaction between elements to from new compounds not just in words, but also by
using the symbols which are the shorthand identification for the elements. Now
we will expand this idea so that you can learn how scientists describe complicated
chemical reactions in a brief and precise way.
Chemical reactions involve substances which are present before the reaction.
These substances are called reactants, or reagents The reaction produces new
substances formed in a chemical change which are called products. There are
many different types of chemical reactions, but for our purposes we only need to
consider the general type described by the following form. Two or more
elements, or one or more compounds (the Reagents) react or break down to make
one or more different elements or compounds (the Products)
REAGENT + REAGENT → PRODUCT + PRODUCT
Balancing Chemical Equations

29
Chemical equations can tell us not only what elements and compounds are
involved, but also how much of each one is needed, and how much is produced.
For them to do this, they need to be Balanced.
We say that an equation is balanced if it tells us tell us the exact truth about the
reaction. It must show the correct reagents and products, and the correct amounts
of each one. We test for a balanced equation by using the principal that we
cannot make (or lose) atoms. Therefore exactly the same number of atoms of
each element involved should be present in the reagent compounds as is in the
product compounds. Where atoms combine in different ratios the correct number
of atoms is important to complete the reaction. Balancing is achieved as a
number of steps:
1. Write the equation for the reaction in words, making sure that the
correct reagents and products are specified. In many cases, such as
your examinations, the equation will be given to you already in
symbols, in which case you cam leave out this step.
2. Express the products and reactants as the correct chemical symbols
and formulae, and that the correct formulae are used for each one.
3. Count the number of atoms of each type of element in the reagents
and in the products.
4. Balance the elements one at a time, using as many steps as needed.
Example Hydrogen burns in oxygen to make water
Step 1 Oxygen + Hydrogen → Water
Step 2 O2 + H2 → H2 O
Note The formula for oxygen and hydrogen are correct; we know
that these gases are normally present as diatomic molecules. Also,
the formula for water is correct, we know it is made up from two
atoms of hydrogen and one atom of oxygen Remember the
molecular formulae for these in previous pages?
Step 3 Note. There are two atoms of hydrogen in the reagents and in the
product. The equation is balanced for hydrogen. There are two
atoms of oxygen in the reagents, but only one atom of oxygen in
the products. The equation is not balanced for oxygen
Step 4A O2 + H2 → 2 H2 O
Note. Now we have doubled the number of water molecules
produced, we have balanced the equation for oxygen (two atoms in
reagents and products) but it is unbalanced for hydrogen.
Step 4B O2 + 2 H2 → 2 H2 O
Note. Now both oxygen and hydrogen are balanced. There are two
atoms of oxygen and four atoms of hydrogen on both sides of the
equation.
The equation now shows the same number of each type of atom among the
reagents as among the products. We say that it is a balanced equation. Note that
we cannot change the small numbers below the line in each formula, such as the
2 in H2 O. These numbers are part of the formula; they show us the exact numbers
of each atom in a molecule of a compound. To change them would be to change
the compound into another one. For example, we could change H2O to H2O2, but
this would be changing the compound from water to hydrogen peroxide, an
entirely different compound!
What we have to do is increase or reduce the number of molecules of each

compound, or atoms of each free element until the equation balances. We show
this variation by altering the large numbers placed before the formula for the
compound or element. For example, H2O means one molecule of water,
containing two hydrogen atoms and one oxygen atom. 2H2O means two
molecules of water, therefore four atoms of hydrogen and two atoms of oxygen.
For clarity, these numbers are bold, italic, and bigger in the equations above.
Example: Sodium metal reacts with water
Step 1: Sodium+ water → Sodium Hydroxide + hydrogen gas
Step 2: Na + H2O → NaOH + H2
Step 2 Note. There is one atom of sodium on each side of the equation,
and one atom of oxygen. But there are two toms of hydrogen in the
reagents and three in the products.
Step 4A: Na +2H2O → NaOH + H2
Step 4B Na + 2H2O → 2NaOH + H2

Step 4C 2Na + 2H2O → NaOH + H2
Now we will try a harder equation to balance:
Balance the reaction for calcium hydroxide and nitric acid.
Step 1: Nitric acid + Calcium Hydroxide → Calcium nitrate + water
Step 2: HNO3 + Ca(OH)2 → Ca(NO3)2 + H2O
Step 3 Note The reagents have 3xH, 5xO, 1xN, 1xCa. The products have
2xH, 7xO, 1xN, 1xCa
Step 4A: 2HNO3 + Ca(OH)2 →Ca(NO3)2 + H2O

Note. this balances the N, but H and O are still unbalanced.
31
Step 4B 2HNO3 + Ca(OH)2 →Ca(NO3)2 + 2H2O
Note4xH, 2xN, 1xCa, 8x0 → 4xH, 2xN, 1xCa, 8x0
Same number of atoms on both side. – it balances!
Activity 1 – Student Exercise
Try balancing the following equations.
The answers are at the end of this unit.
1. C2H6 + O2 → CO2 + H2O
2. Ca + HCI → CaCI2 + H2
3. KOH + AI(NO3)3 → KNO3 + AI(OH)3
4. H2SO4 + AI(OH)3 → H2O + AI2 (SO4)3
5. FeCI2 + Na3PO4 → Fe3(PO4)2 + NaCI
6. CaCO3 + H3PO4 → Ca3(PO4)2 + H2O + CO2

7 Mg + O2 → MgO

33
Activity 1 - Answersheet
1. 2C2H6 + 7O2 → 4CO2 + 6H2O
2. Ca + 2HCI → H2 + CaCI2
3. 3KOH + AI(NO3)3 → 3KNO3 + AI(OH)3
4. 3H2SO4 + 2AI(OH)3 → 6H2O + AI2(SO4)3
5. 3FeCI2 + 2Na3PO4 → Fe3(PO4)2 + 6NaCI
6. 3CaCO3 + 2H3PO4 → Ca3(PO4)2 + 3H2O + 3CO2
7. Mg + O2 → MgO
PHYSICAL & CHEMICAL CHANGE = Assignment 2
AIM
To observe and describe changes of properties of various materials and to classify
them as:
a) physical
b) chemical
c) allotropic change
An allotropic change is a special form of physical change where the material

changes its solid state structure, that is, the arrangement of atoms used to put it
together.
METHOD
1. (i) Dissolve a small amount of ammonium dichromate in water in a test
tube. Record what is happening. Retain the solution.
(ii) Ignite a small quantity of dry ammonium dichromate in an

evaporating basin in a fume cupboard. Note any reactions, sparks
evolved, colour changes or volume changes. Dissolve some of the
reaction product in water and compare with 1 (i).
2. (i) Gently heat (in a fume cupboard) a small quantity of napthalene in a

crucible until melting occurs. Allow to cool, and note all changes.
(ii) Reheat strongly (in a fume cupboard) projecting the flame down
onto the material. Note all reactions.
3. (i) Place a lump of limestone (calcium carbonate) in a test tube and add
a few drops of water. Note any reactions.
(iii) Add a few drops of hydrochloric acid to the test tube in 3(i). Note any
reactions.
4. (i) Dissolve some salt (sodium chloride) in 5 ml water. Evaporate to

dryness. Note the changes that have occurred.
5. (i) Heat (in a fume cupboard), a test tube 1/3 full of sulphur. Note any
changes in state, viscosity and colour as the sulphur reacts to the
heating. Note each change carefully. (Do not heat to strongly as
sulphur will ignite).
(ii) Warm the sides of the test tube and pour the ,molten sulphur into a
beaker of water. Compare the properties of the solid produced with
the original sulphur. Note the changes that have occurred.

35
RESULTS
Record all the results in tabulated form. Include chemical equations where
applicable.
CONCLUSION
To come to some conclusions about what has happened, you need to look at the
results you observed, and decide whether there was a physical reaction, a
chemical reaction, or an allotropic reaction in each case.
Check Your Progress
Listed below are questions which will help you to review Topic 3,
You can check your answer with the one given at the end of this topic.
Q1. Fill in the missing words
(i) Metallic atoms have ……………………………valence electrons.

(ii) Non metallic atoms have ………………………valence electrons.
Q2. How do metallic ions form from a metal atom?

(i) Metallic ions are formed by
…………………………………………………………………………..
(ii) Give an example: ……………………………………………….
Q3. Write an equation to represent an ionic bond.

…………………………………………………………………………………
Q4. What type of force holds ionic compounds such as sodium chloride together?
…………………………………………………………………………………
Q5. Covalent bonds are characterized by ………………………………………….
Q6. Write an equation which gives an example of covalent bonding.

…………………………………………………………………………………..
Q7. Describe metallic bonding.

…………………………………………………………………………………..
…………………………………………………………………………………..
Q8 Describe Secondary bonds……………………………………………………...

…………………………………………………………………………………………..
Q9. Balance this equation: C3H2COOH + O2 → CO2 + H2O

37
Q1. (i) 1, 2 or 3.
(ii) 4 or more.
Q2. (i) Losing their valence electrons to gain a positive valence.

(ii) Al → Al3+ + 3e
Q3. Sodium plus chlorine → salt

+
Na + CI -
→ NaCI
Q4. A very strong electrostatic attraction between the positive sodium ion and the
negative chloride ion.
Q5. Sharing electrons to fill the outer shell.
Q6. . . . .
H + O + H → : :
H O H (water)
Q7. The positively charged metallic ions are strongly attracted to a freely moving
negative electron cloud.
Q8 Weak intermolecular forces of attraction between oppositely charged dipoles.
Q9. C3H2 COOH + 5O2 → 4CO2 + 4H2O


39
LEARNING OUTCOME 4
MATERIALS
CLASSIFICATION, ALLOYS,
POLYMERS OR CERAMICS.
• Describe the bonding in alloys, polymers or ceramics.
• Categorise common dental materials as alloys, polymers or ceramics.
TOPIC 4 - Structure of Materials
Recommended Time - 1 hr
Introduction
Dental applications involve some of the most fascinating and varied materials
used nowadays, but, since no one type of materials possess all the desired
properties for a particular dental application, we have to use a range of different
materials, or combinations of them. .
Later in the Diploma of Dental Technology the modules you study will include
discussions of the properties and uses of Dental Metals, Dental Polymers, and
Dental Ceramics. First, however, we need an introduction to these groups of
materials, which we will find in this topic.
This topic introduces you to important basic information about:

• The bonding which constructs alloys, polymers and ceramics.
• Classifying dental materials as alloys, polymers or ceramics.
Classification of Materials
Materials used in dental applications can be divided into 4 families:
(i) metals and their alloys

(ii) ceramics and glasses
(iii) low and high molecular weight polymers and elastomers
(iv) composites
Each of these material groups has specific properties which make them useful as
dental materials. There is also great variation for these properties. For example,
metals and ceramics show very limited flexibility (they are comparatively stiff, or
rigid,) whereas polymers can be compounded to give the rubbery behaviour
necessary in impression materials.
Metals (metallic bonding)
We can explain the chemical behaviour of materials by the number of their outer
shell electrons. The mechanical properties of materials are caused by the way that
41
atoms are arranged in order to make bulk material, We call this arrangement the
structure of the material. The mechanical and physical properties of metals can
be explained in terms of their metallic bonding. As discussed earlier in this unit,
positive metallic ions are held rigidly in a close packed crystalline lattice
structure, around which an electron cloud freely moves. This electron cloud can
transmit energy with little loss, and so produces the characteristic metallic
properties of electrical and thermal conductivity.
If light is shone on a metal surface, it is reflected, producing a characteristic

lustre. Most metals have high melting points, which is explained by the strength
of the metallic bond. The ions need much heat energy to overcome electrostatic
bonding forces and break free of each other, change state and become liquid.
In terms of mechanical properties, most metals are as tough and ductile. They can
be stressed below a certain limit and return to their original dimensions when the
stress is released (elastic behaviour) or they can be stressed above their elastic
limit and become permanently deformed (this plastic behaviour makes them
formable, a useful property). Deformation without fracture is possible because
layers of the crystalline arrangements can slip past one another under stress,
another property of the metallic bond structure.
Polymers (covalent bonding)
Organic materials involve covalent bonding which involves sharing electrons

They commonly form large molecules or macromolecules.by a process of
repeated joining of a basic group of atoms, called polymerisation. These
molecules may be many hundreds of thousands of atoms in size. In may polymers
the molecules take the form of long chains of atoms, where the atoms are joined
by covalent bonding, but the chains are only held to each other by weaker
secondary bonds. Other polymers may have very large three-dimensional
structures of atoms.
When polymers melt the molecules separate from one another and move
independently. Polymer melting points are much lower than those of metals or
ceramics because only secondary bonds need to be broken. For the same reason.
the strengths of polymers will also be much lower than that of metals or ceramics.
. The rigidity of polymers is also lower than that of metals or ceramics.
However, the low weight of most of the atoms in polymer molecules, and their
relatively large spaces between chains makes polymers much less denseThe
bonding of polymer atoms in chains or rings is strong, but the secondary bonds
between chains are weak unless there is covalently bonded crosslinking.
Increased temperature causes separation of the chains to allow each one to vibrate
more. This phenomenon gives polymers much higher thermal expansion than
metals or ceramics. Also, water can penetrate the weak bonding between chains,
producing a susceptibility to swelling and degradation.
Ceramics (ionic bonding)
A simple definition of a ceramic is, “A compound of metal ions and non-metal

ions with ionic bonding,” although there are some ceramics, such as glasses, with
covalent bonding. A simpler definition of a ceramic is a material whose structure
has been caused by firing it. Either way, their high strength bonds make ceramics
very stable, with high melting points and rigidity (stiffness.) They are poor
conductors, since the electrons donated by metal ions are strongly held by the
non-metallic ion. On melting the crystal structure of the compound separates
making the ions mobile, so ceramics can carry electric currents. when molten.
Ceramics are also characterised by their high hardness and brittleness, as well as
outstanding resistance to high temperatures. These properties are due to the
electron behaviour of the constituent ions. Also due to this electron behaviour,
ceramics are usually electrical and thermal insulators.
Ceramics may be transparent (window glass) or coloured by absorption of ions as

well as the suspension of pigments. This property is again due to the absence of
free electrons in the material. Colouring is important to dental ceramics as their
final shading must be matched to the patients natural tooth colour and stains.
Hardening and strengthening of ceramics is possible by incorporating other ionic

compounds like alumina (A1203). This increases their strength and rigidity.
A big disadvantage of ceramics is their brittleness. Unlike metals, and a number

of polymers, the strong ionic bond and crystalline structure does not allow any
localised movement under stress. At higher stresses, the only response possible
from the structure is to fracture. A brittle failure results, with a sudden release of
energy. Many ceramic articles are made by firing powder until the particles fuse,
because the ceramic melting points are inconveniently high for casting, unlike
many metals. The spaces between the particles results in small entrapped voids
which are hard to remove. Ceramics are poor heat conductors, so the outer
surface cools faster, placing it under a tensile stress which produces small cracks.
Although very strong in compression, the combination of surface cracks and

internal defects like porosity makes ceramics much weaker in tension than many
metals. As a result, ceramics are most suitable for use in applications where they
are stressed in compression. Ceramics for dental applications are selected for
their high strength and ease of processing. Their brittleness can be improved by
forming a type of composite material when they are fused to the surface of a
reinforcing metal structure which has a much greater toughness.
Composites (covalent bonding matrix – metallic or ionically

bonded fillers).
A composite is a material with two or more distinct phases. One phase is usually
much harder than the other, and more brittle. The softer phase is generally

43
tougher. The combination of materials has properties that each of the separate
ones cannot match. For example, human teeth can be repaired by a composite of a
setting acrylic polymer with hard glass (ceramic) particles mixed in with it. This
gives the composite the following properties:
(i) good strength and toughness

(ii) good bonding to natural teeth
(iii) wear resistance
(iv) rapid setting (polymerised by light)
(v) ease of use
Check Your Progress
Listed below are questions which will help you to review Topic 4.
You can check your answer with the script section at the end of this topic.
Q1. List four (4) families of material

(i) ______________________________
(ii) ______________________________
(iii) ______________________________
(iv) ______________________________
Q2. List three (3) properties of metals

(i) ______________________________
(ii) ______________________________
(iii) ______________________________
Q3. Define what is meant y a “polymer”

___________________________________________________
______________________________________________________________
Q4. List three (3) properties of polymers

(i) _____________________________
(ii) _____________________________
(iii) _____________________________
Q5. Crosslinking is _______________________________________________
Q6. Ceramics are _______________________ bonded.
Q7. List 3 properties of ceramics

(i) _____________________________
(ii) _____________________________
(iii) _____________________________
Q8. The biggest disadvantage of ceramics is their ______________________

which is due to ______________________________________________
Q9. Composites have ______ phases, one of which is ____________ and the
other __________

45
Q1. i) metals and alloys

ii) ceramics and glasses
iii) polymers and elastomers
iv) composites
Q2. i) high melting point

ii) metallic bonding
iii) high density
Q3. organic materials characterised by long chains which are covalently

bonded
Q4. i) low density

ii) low softening points
iii) covalent bonding
Q5. chemical bonding between polymer chains
Q6. ionically
Q7. i) poor electrical conductors

ii) brittle
iii) high hardness
Q8. brittleness, surface cracks and internal defects
Q9. two, hard, soft


47
LEARNING OUTCOME 5
RATIONALISE THE USE OF

SELECTED MATERIALS
ACCORDING TO THEIR
PROPERTIES.
• Classify the properties of materials as chemical, physical or mechanical.
• Relate selected properties of materials to their use in dental technology
applications.
• Define and calculate specific properties using data for selected dental
materials.
TOPIC 5 - Properties of Materials
Introduction
Now that we know about the basic differences between types of material, we need
to start looking at their properties. Selection of materials for dental uses involves
matching these properties against those needed for the particular application. In
order to specify what properties we need, we must start by considering what
properties there are, and which ones are relevant to the particular use.
This topic introduces you to important basic information about:

• Classification of chemical, physical and mechanical properties useful for
dental applications.
• Properties which are desired in various dental materials.
• Calculating specific properties from data obtained by testing dental

materials.
Property Classification
The properties of materials can be classified into three categories:
(i) chemical
(ii) physical
(iii) mechanical
(i) Chemical Properties
The chemical properties of a material describe the types of chemical reactions

that it will undergo in various circumstances. Some physical properties are also
linked to the chemical structure of the material.
The chemical properties of elements include valency and reactivity., stability,

corrosion resistance, acidity or alkalinity, and composition. Of particular
dental importance, are the reactions the material may have with human tissue.

49
(ii) Physical Properties
The physical properties of a substance are describe how it reacts to the physical
universe. Often, these properties are used to identify a substance. Examples are
boiling point, melting point, electrical conductivity, or density.
(iii) Mechanical Properties
These properties describe how substances react to applied forces. They are often
measured by destructive testing, such as by tensile, compressive or impact
tests. Typical properties include tensile or compressive strengths, stiffness,
(rigidity) hardness, brittleness, fatigue resistance and impact toughness.
These properties are usually related to how the atoms are arranged in a substance.
Before looking at the properties needed for specific dental applications, we need
to examine some of them more fully.
(i) Chemical Properties
Bonding - The adhesion of one substance to another is an important chemical

property. For example, if they cannot bond to the natural tooth,
then restorative materials would be useless.
Wetting - The wetting characteristics determine if molecules are compatible

in terms of their bonding energy. Good wetting produces high
strength bonding. The surface tension of the material is a measure
of this energy. If materials like solders, enamels or adhesives do not
wet a surface, they will not join to it.
Stability - Material in the oral environment must not react or change in any
way which alters its properties. If the material absorbs fluid and
swells, or is attacked by oral fluids then its usefulness is limited.
Toxicity Ideally dental materials are fully “bio-compatible” That is, they
can become integrated with human tissue without unfavourable
results. Any material used certainly should not cause trauma or
tissue damage to the patient. Care must be taken when some
degradation may occur, or where certain materials may be toxic or
reactive to patient or technician if used in certain ways.
(ii) Physical Properties
Dimensional -The material should not shrink or contract and so cause discomfort
Stability for the patient and so diminished usefulness of the appliance.
Rheology - This is the behaviour of materials moving under stress, such as
when mixing, or when being squeezed out of a tube. The flow and
viscosity of some materials used to make dental appliances are also
important.
Density - This is the mass per unit volume of a material. Polymers have low
densities and metals have high densities. This property needs
consideration when selecting materials, as it controls the weight of
an appliance. It may also control how much the material costs
Melting
Point - The temperature at which a substance changes from solid to liquid
state. It is important in determining how easy a metal is to cast,
because it partly determines the energy needed for melting it.
Boiling
Point - This is the temperature at which a substance changes from liquid to
gaseous states. It will affect how a material is to be processed, or
how it may react in dental use.
Optical
Properties - There are a number of these, such as colour (accurately defined and
quantified), opacity and reflectance. These determine how light is
transmitted, absorbed, or changed in wavelength on meeting the
material. This controls its appearance, which is dentally important.
These properties are vitally important to dental ceramics.
Coefficient
Of Thermal
Expansion - Almost all substances expand as their temperature rises, and
contract if cooled. As a result they change size with temperature,
and the amount can be significant to the accuracy of metal castings,
polymer restorations, and ceramics. In a mixture of two different
materials (such as dental metal/ceramic restorations) two different
rates of expansion can set up destructive stresses on cooling
Comparison of the varying amounts by which different materials

expand is given by their coefficient of expansion. This is the
amount a material will expand for every degree Celsius its
temperature rises and for every unit of its original length. So,
dental chromium alloys have a coefficient of linear expansion,
(called “α”). of 15 x 10-6 mm per mm of original length, per oC rise
in temperature. We use the formula: L1 = Lo + Lo x α x ∆T, where
L1 = Final length, after expansion or contraction
Lo = Original length, before expansion or contraction
α = coefficient of linear expansion of the materials
∆T = Change in temperature

51
Substances also have expansion coefficients of area (β) and volume
(γ)
To illustrate the importance of this property, consider a dental

chromium/cobalt alloy partial denture casting measuring 75mm
across. This would solidify at 1425oC, and after solidifying it will
contract by 1.6mm (15 x 10-6 x 1400 x 75 mm) as it cools to room
temperature. Unless some allowance is made for this (which is
done, as you will learn in the Module “Removable Alloy Partial
Dentures”) such a casting can become significantly undersized.
Specific heat This is a measure of the capacity of a material to absorb energy,

while changing temperature. It is measured as the energy required
to raise the temperature of one unit of mass of the substance by one
degree. So, for example, calories per gram per degree Celsius
(Cal/g/oC) Metal with high specific heat takes longer heating
(more energy) from a gas torch to reach the same temperature as a
metal with lower specific heat.
Viscosity This is a measure of the resistance to flow of a fluid. The unit in

the metric system is the Poise. For example, a fluid like honey has
a higher viscosity than water. Fluids with high viscosity flow less
under pressure. An example where the viscosity is important in
dental work is where the fluid must be poured to shape, such as an
impression material.
Surface
Tension This can be a difficult property to understand, but is of vital
importance in dental work whenever a fluid needs to wet and flow
over a surface. Surface tension is a measure of the force with
which one material is attracted to another at their surface, and is
related to the chemical phenomenon of wetting.
Look at the diagrams below. An atom within the body of a liquid;

it is evenly surrounded by other atoms of the same type. Their
attraction for it is evenly distributed, which holds the atom in one
place. On the surface of the liquid, however, the same atom is
partly surrounded by atoms in the surface of whatever substance the
liquid is touching. The force on the atom is now unbalanced; it
may be attracted towards the new material surface, or back into the
liquid, depending on how much it is attracted to atoms in the new
surface. This imbalance means that the liquid will be attracted to,
or repelled by a different material. Such a force mean that liquids
will wet a new surface such as a solid, and spread across it, or they
will not wet it, and withdraw from it.
An atom in the centre is pulled An atom at the surface is pulled
evenly in all directions by other inwards or outwards. This
atoms creates a “surface tension”
The results of surface tension are seen in the capacity of surfaces to

pull liquid upwards against gravity. Examples are liquid soaking
into finely porous material, or in sap rising in trees
Latent Heat This is the amount of energy, expressed in calories per gram,
which a substance takes up or gives off when it changes state. So,
there is a latent heat of fusion, needed to melt material already at
its melting point, and a latent heat of vaporisation, needed to boil
material already at its boiling point.
Material with a high specific heat, high latent heat of fusion, and
high melting point, needs much more energy to melt it, say for
casting, than material with lower values for these properties
(iii) Mechanical Properties
To give satisfactory service in the oral environment, any material

needs to have sufficient strength to withstand the stresses involved.
A number of properties like the strength of a material can be
measured from a Tensile Test. To carry out this test, we take a
material specimen of suitable size. We measure the length to be
tested, and the cross-sectional area at right angles to the applied
force. We apply a gradually increasing force to the material, and
measure the increase in length which occurs and the increasing
force needed to continue extending the material. The test machine
will gives us an applied force, measured in Newtons in the metric
system, and an extension of the specimen, in millimetres.
Before describing the results from such a test, we need to consider

the units we are measuring. We need to understand exactly what a
Force, and a Stress are.

53
A force is defined as applying energy to a substance, so that it
tends to move.
Applying a force, f, to a body of mass m, produces an acceleration,

a
F=mxa
A Force can be applied to a body in a number of ways.

If we apply a linear force, the body is in tension, or in compression
TENSION, A TENSILE FORCE
COMPRESSION, A COMPRESSIVE FORCE
Other forces include bending, twisting and shear forces
A BENDING
FORCE
TORSION,
A TWISTING FORCE
SHEAR, A PARTING
FORCE
A typical test graph for a tensile test is shown on the next page, but
what is plotted on the diagram is not the force and extension the
test machine measured, but the related properties of stress and
strain. Stress is defined as the force applied to a substance,
divided by the area of material across which the force is applied.
Strain is the resulting change in size of the body of material (say,
its extra length) divided by the original size
We need stress and strain because they are properties of the

material independent of the size of the specimen used. Consider
two steel bolts, one with a cross-section area of ten square
millimetres, and one with a cross-sectional area of twenty square
millimetres. It will take twice as much force to break the bigger
bolt in a tensile test, not because the steel in it is stronger, but
because there is twice as much of it. But if we divide the force used
to break each bolt by the area of the bolt, we will get the identical
stress..
The unit of stress in the metric system is the Pascal, which is

defined as a Newton of force per square metre of area.
Unfortunately, the Pascal is such a small amount of stress that we
commonly find ourselves measuring things in millions of Pascals,
or “ MegaPascals” Conveniently for our test, if we measure the
force in Newtons, and the area of cross-section of the specimen in
square millimetres, the resulting stress comes out in MegaPascals.
Similarly, we want to measure as a material property, not the

extension produced, but the strain, or percentage extension, which
won’t vary with the original length of the specimen.
A B
It takes twice as much force to break piece A than piece B, but if

we divide the force by the cross-section area of the piece, the
resulting stress experience by the material is the same

55
The next diagram is a graph of the stress against strain that happens
when a piece of material is subjected to a tensile force
Maximum, or Ultimate Stress
Elastic limit C Breaking Stress

or B D
Yield Point
S
t
r
e
s
s
Elastic region Plastic region
% Elongation
Now, let us see what the important areas on this diagram can tell us
about the mechanical properties of the material tested,
Elastic Limit This is sometimes called the Yield Point of the material, point B on
the diagram It is the stress at which the material stops behaving
elastically and starts behaving plastically. That means that, if we
were to remove the test force below the point B, the material would
return to its original length (behave elastically) After the stress at
point B, if we remove the applied force, the material will not return
to its original length. It will have become plastically, or
permanently deformed. So, the Yield Point or Elastic Limit, is the
value of the stress at point B, is a measure of how easy it is to
deform (say bend, or stretch) the material.
Elastic
Modulus - Alternatively called stiffness or rigidity or the modulus of
rigidity, or Young’s Modulus, after its inventor, it describes how
much material may elastically distort in use. In our diagram, the
rigidity of a material is shown by the slope of the elastic part of the
test line, A-B. The rigidity would be found from the stress at the
point B divided by the strain at the point B.
In the diagrams below, a) shows the stress/strain relationship for a

material of high rigidity, such as a chromium alloy, whereas b)
shows the curve for a material of low rigidity, such as a polymer.
The rigidity of a material is a measure of how stiff it is, how

much it resists deflection
stress stress
strain strain
a) High rigidity material b) Low rigidity material
Ultimate
Tensile
Strength - This is the maximum stress a material can withstand, the stress at
point C on the test diagram.
The Ultimate Tensile Stress or U.T.S. is a measure of how much

stress a material will carry before it breaks. This is what is called
strength
Plasticity - Often called ductility, this is a measure of the amount of

deformation a material can withstand up to its failure at point D.
Brittle materials, such as glass have low plasticity, whereas ductile
materials have high plasticity. A completely brittle material would
have a stress/strain diagram like b) below, whereas a ductile
material would show a curve like a), and give a large value of strain
at the breaking point
Ductility is thus a measure of how much we can change the shape

of a material before it breaks.

57
stress stress
strain at
breaking
strain strain
a) Stress/ strain curve for b) Stress/strain curve for

ductile material brittle material (no plastic
deformation
Resilience - This is the ability of a material to store elastic energy and release it
when the force is removed. This can be considered as the area
under the elastic part of the curve, shaded in the diagram below.
Resilience is the amount of energy a material can store before
deforming, obviously an important property for assessing material
for making springs
resilience
stress
strain
Toughness- This the amount of energy a material can absorb without fracture.
On a stress/strain diagram it is represented by the total area under
the curve. Toughness can be seen as the total amount of energy a
material will store before breaking
stress toughness
strain
Fatigue - This is the resistance of a material to failure by repeated stressing

and unloading at a level of force lower than is required to break the
material by one application e.g. mastication. Think of it as
cumulative damage
Hardness - Hardness is related to wear resistance, an important property which

can control the useful life of a material in dental application.
Hardness is defined as the resistance of a substance to
indentation. It is measured by making a test indentation in the
substance using an indenter of specific shape and size, and applying
a set load to it. After the indentation is made, measuring its depth
or width and referring to a set of charts will give a relative hardness
number on the scale measured by the particular test method. Notice
that, unlike strength, hardness is not a property which allows us to
do any further calculations about what forces a substance will
resist. Hardness is just a comparative figure.
There are three basic hardness tests whose results might be found in
materials textbooks; BRINELL, ROCKWELL, AND VICKERS
The Brinell test uses a round steel ball about 12mm in diameter as
an indenter. In use this indenter is gradually forced into the surface
of the test specimen by applying weight gradually, controlled by a
hydraulic piston. It makes a circular indentation whose diameter is
measured using a small microscope. Looking up a set of tables
using the indentation diameter and the test load give s a Brinell
Hardness Number, or BHN.
` Because this test makes a fairly large indentation, it is not much use
on thin or small specimens, although it is statistically more valid on
large ones. It also cannot test substances which are harder than the
hardened steel ball.
The Vickers test uses a similar, but smaller machine, and a much
smaller indenter made of industrial diamond, so it can test any
material. This indenter is in the shape of a four-sided pyramid, so it
leaves a square-shaped dent, whose size is easier to measure.
Again, the size of this dent and the test load are used to look up a
hardness result, the Vickers Hardness Number, or VHN.
The Vickers test is fussy, and harder to use, but it can test any
material. It is probably the one most commonly found in dental
textbooks to indicating the hardness of a material.
The Rockwell test uses a range of different sizes steel balls and
diamond cone indenters for material of differing hardness. It
measures the depth, not the width of the indentation, and so can
give a direct reading of hardness from its dial, without any need for
looking up tables. Although it is hard to compare its results with
other hardness tests, it is the quickest and easiest to use. Its results

59
are given, for example, as 55Rc, meaning a hardness of 55 on the
Rockwell C scale.
Examples of mechanical and physical properties of various

materials
In the previous section the properties of polymers, metals and ceramics were
discussed in general terms. Now that we know what the particular properties
mean, we should consider the values of important properties to show the
difference between metals, polymers and ceramics.
Melting point
The melting point of metal ranges up to that of tungsten at 3410OC, with many of
them melting in between 500 and 1500OC. Ceramics have a similar maximum to
metals, over 3000OC, but many of the common ones soften above the melting
point of most metals. Polymers are generally much lower, only silicone polymers
softening at above 4000C
Density
Metals are the densest materials. The common ones vary from as low as 2.5g/cm3
for aluminium to Lead at 11g/cm3. Gold has a very high density of 19.6g/cm3 and
Platinum is the highest at 21.45g/cm3. Chrome alloys have density about
8.5g/cm3. Ceramics have lower densities, from 2.5g/cm3 to 5, and polymers are
generally between 0.9g/cm3 and 2.2g/cm3 unless foamed or filled.
Hardness
Human teeth have a hardness in healthy enamel of about 300V.H.N.. Metals can
be as low in hardness as 60V.H.N., for lead, to about 600V.H.N. for tool steels.
Dental gold alloys are about 250 VHN and chrome alloys about 400V.H.N..
Dental polymers are much softer, generally about 30 or 40V.H.N. Ceramics are
harder, though some minerals are very soft because of their structure. Ceramics
vary from about 600 V.H.N for silicates up to 3500V.H.N. or more for abrasives.
Coefficient of expansion
Natural teeth have a coefficient of expansion typically about 11 x10-6mm/mm/OC,

varying from 7 to 14. Ceramics generally have a slightly lower value, but can be
made to match human teeth fairly easily. Metals generally have slightly higher
values, with chrome alloys at 15x10-6mm/mm/OC, but can be made to match tooth
expansion. Polymers have much higher expansion coefficients, up to 300 or more
x10-6 mm/mm/OC, although mineral filled dental composites are much lower, they
do not have values a slow as that for human teeth.
Strength
Metals have a tensile strength varying from below 100 Mpa (MegaPascals) to as
high as 2300Mpa for heat treated high alloy steels. By comparison, only the
strongest of polymers get over 100Mpa. Ceramics are weaker in tension than
metals, and difficult to test, but the strongest are comparable to metals. The
compressive strength of ceramics can get over several thousand Mpa, but they are
normally tested in a “flexural strength” test
Ductility
Ceramics have no ductility, being brittle, they fail under stress without any
permanent change of shape. Polymers can extend by many hundreds of percent if
they are above their transition temperature. Metals have ductility ranging from
fairly brittle at a few percent extension to the formable metals such as brass and
aluminium which can be extended by 40 or 50%.
Application of Dental Materials – Properties.
Considering the properties in the previous couple of pages, it is obvious that no

one material will completely match the properties of human dental materials. The
task then becomes one of selecting the best material for a particular application
by considering all of its properties, including cost and appearance.
In this section we will look briefly at some typical dental materials and relate the
properties of the materials used to their purpose.
The properties of all these materials will be examined in much greater detail in
later sections of the course in the appropriate theory section. Consequently the
following introduction to dental materials is intended to be read for information
only, and would not be examinable in the Materials Science Exam
1) Impression Materials
The first step in many dental applications is to make a working copy of the
patient’s oral structure. For a material to suitably record oral morphology, it must
be fluid during application, and set in a reasonable time. These properties are
related to its chemical and physical properties. The material should not be toxic
or allergenic to the patient or the dental technician, and should not be unpleasant
in any way during setting (taste, smell, surface feeling).
The material should be easily removed from the mouth without distortion. After
removal the material should be dimensionally stable until the model of the
patient’s dentition can be taken from it.
The impression it has taken must be accurate in dimension and in surface detail.
This means that the impression material must be fluid enough to flow over and

61
duplicate surface detail, but not so fluid that it is difficult to use or flows out of
the tray into the patient’s throat.
Although non-elastic, or rigid, materials have been used in the past, the
impression materials used nowadays are elastic. That means that they can be
elastically deformed sufficiently to be distorted over undercuts in the shape of the
patient’s dentition when being removed.
Elastic materials - polyether

- polysulphide
- addition silicone
- condensation silicone
- hydrocolloid
Water based
- alginate
2) Tooth replacement materials
The forces of mastication necessitate high strength and wear resistance in

restorative materials. They must be strong under compressive and shear stress,
and have a high hardness. The ability of a material to remain rigid (elastic
modulus) and not distort is also important as damage to other surfaces may result
if a restoration distorts in use, even if it returns to shape later..
Corrosion resistance, dimensional stability, good aesthetics, and ease of handling

and ease of polishing are important. Porosity and moisture uptake are not
desirable, for hygienic reasons.
Commonly used materials are:
• polymethyl methacrylate (acrylic) dentures

• ceramics of various types –commonly called “porcelain”
• Precious metal alloys, gold and palladium based (crowns, bridges and
copings, partial dentures)
• base metal alloys, cobalt, nickel and titanium alloys (crowns and copings,
partial dentures)
3) Restorative Materials
These materials are used to repair or restore natural tooth structures. The material
must have good wetting characteristics so that high bond strengths to the natural
structure can occur. The expansion and contraction of the material should be
similar to the bonded material, otherwise fatigue failure may be a problem. Ease
of use and moisture (saliva) tolerance is important for fitting.
Where special adhesives and surface treatments are necessary the process should
not be toxic and present minor discomfort to the patient. Working times should
be as suitable, and the aesthetics should be pleasing.
Typical materials are:

• amalgam
• composites
• acrylic
4) Casts, Model and Die Materials
These materials are required for creating replicas of the patient’s dentition over
which the final appliance can be constructed.. Both of these applications require
strength and abrasion resistance, and the commonly used material is a specially
hardened gypsum “stone.”
Casts have to be made from this, “type IV stone” for high strength to withstand
clamping forces. Die materials need abrasion resistance to withstand damaging
during wearing. Both requirements necessitate materials which are easy to use,
reproduce detail well, and have a low setting expansion. Additives are used to
control setting expansion and time.
Other materials include:

• acrylic resins
• polyester and epoxy resins
5) Investment Materials
To produce a cast metal appliance, a negative image must be created as a cavity

in a mould made from a refractory material to withstand the high temperatures
during casting. Such materials are called investment materials and consist of a
binder and refractory particles. .Refractory particles are necessary to withstand
the heat of casting and cause expansion. Modifying agents are used to control
properties and produce setting and thermal expansion – the total of which has to
be equal the solid state contraction of the alloy as it cools. Cristobalite and quartz
are commonly used to produce the desired thermal expansions.

• gypsum bonded investment – low melting point alloys
• phosphate bonded investment – high melting point alloys
6) Dental Castings
Reproducing a lost tooth structure can easily be done by replicating the shape in
wax and investing to form a mould. The mould is then filled with an alloy with
has the following properties

63
• corrosion resistance
• ready flow in the molten state
• ease of cleaning and polishing
• no toxicity
• compatibility with current materials
• hardenability (for example, gold/copper alloys)
• strength
• toughness
• hygienic
• aesthetic appeal
• compatibility with dental porcelain
• ease of melting and casting
Two types of alloys are used:

i) precious metal casting alloys (various alloys of Au, or Pd)
ii) base metal casting alloys (alloys of Ni,Cr,Co or Ti)
7) Implant Materials
These special materials are used where there is available bond to support the
implant. The alloy used must have
• biocompatibility
• corrosion resistance
• high strength and elastic modulus
• reasonable price
• compatibility to dental coatings (hydroxyapatite)
• ease of processing and installation
• excellent wear resistance

titanium based alloys.
MATERIALS SCIENCE -SURFACE TENSION
The property of SURFACE TENSION has been defined as the capacity of surface
of material to wet, or be attracted to the surface of another. In practice this can be seen
by the tendency of liquids to be pulled up the inside of thin tubing.
PRACTICAL METHOD
Place some water in a beaker. Select a thin bore glass tube, and measure its inside
diameter by using the thin wire gauge supplied. Place this tube in the liquid in the
beaker.
From the side of the beaker, observe how far the liquid in the tube is raised above the
surface of the liquid in the beaker. This is a measure of the surface tension of the
water for glass tubing.
Repeat the experiment using methylated spirits instead of water. Does methylated
spirits have a higher or lower surface tension than water?
Rinse the beaker and the tubing, and repeat the experiment with a couple of drops of
detergent in the water. What effect has the detergent had on the surface tension of
water on glass.
Repeat the experiment using water with a few drops of WAXIT in it. WAXIT is a
proprietary surface tension reducer used in dental technician’s work. What is its effect
on surface tension?
•
• cobalt based alloys
• ceramics

65
Check Your Progress
Listed below are questions which will help you to review Topic 5.
You can check your answer with the script section at the end of this topic.
Q1. List three (3) types of material properties:

(i) ______________________________
(ii) ______________________________
(iii) ______________________________
Q2. Define the following properties:

(i) bonding __________________________________________________
(ii) toxicity __________________________________________________
(iii) dimension stability _________________________________________
(iv) melting point _____________________________________________
(v) elastic modulus ____________________________________________
(vi) resilience _________________________________________________
(vii) plasticity _________________________________________________
Q3 Which type of material shows extensive plastic deformation in a tensile test,

ductile, or brittle _________________________________________________
Q4 What property is given by the slope of the elastic part of the tensile test
curve?_______________________________________________________
Q5 If the maximum force which can be resisted by a piece of material is 3000

Newtons (3kiloNewtons, or3kN) and it is 10mm square in cross section,
what is the stress applied to it? ___________________________________
Q6 A material has a strength of 2000 Mpa, melts at 1500OC, and has a density
of 9g/cm3. Is it a polymer, a ceramic, or a metal?…………………………...
Q7 A material has a softening temperature of 1500C, a density of 1.0g/cm3 ,

and a strength of 40Mpa. Is it a ceramic, a metal, or a polymer?…………...
Q1. (i) chemical

(ii) physical
(iii) mechanical
Q2. (i) bonding - adhesion of a material to a substrate

(ii) toxicity - the ability of a material to cause tissue trauma
(iii) dimensional stability - material should not absorb fluid and swell
(iv) melting point - temperature state changes from solid to liquid
(v) elastic modules - rigidity or stiffness of a metal or alloy
(vi) resilience - the storage and release of elastic energy
(vii) plasticity - amount of deformation before failure
Q3 Ductile
Q4 Rigidity, Modulus of elasticity
Q5 30Mpa (stress = force/area, =3000N/100mm2
Q6 A metal
Q7 A polymer

67
69
LEARNING OUTCOME 6
RATIONALISE THE USE OF

IMPRESSION AND MODEL-
MAKING MATERIALS
ACCORDING TO THEIR
PROPERTIES.
• List, describe and explain the important properties of alginate impression Relate selected
properties of materials to their use in dental technology applications.
• List, describe and explain the important properties of plaster, stone and die stone as used
for making dental models
•
TOPIC 6 - Properties of Materials used to make dental models
Introduction
Now that we know about the basic differences between types of material and their properties,
we need to start looking at the first ones used in dentistry.
The procedure their properties which begins the construction of a dental appliance is usually
the taking of an impression of the surface of the patients dentition. The next step is to make
from this impression a model in solid material of the patient’s dentition. This is used as a
basis for constructing the appliance.
This topic introduces you to the properties which control the techniques of using:
Gypsum products
• Alginate impression materials.
71
GYPSUM PRODUCTS
The major materials used to make models are types of gypsum; calcium sulfate dihydrate. This is a
mineral with 2 molecules of water in the structure of its crystals, combined with one molecule of
calcium sulfate, CaSO4٠2 H2O. When this material is heated, or calcined, it loses three molecules
of water of crystallisation for every two molecules of gypsum, to form plaster of Paris,
(CaSO4)2·H2O. The chemical formula for this is often wrongly described as CaSO4٠1/2H2O, which
gives the material its common name, Calcium sulfate hemi-hydrate. When it is mixed with water,
plaster of Paris forms gypsum again, and sets. The resulting solid makes very accurate models; it is
reasonably strong, it is cheap, and it sets fairly quickly. It is convenient to use and non-toxic. It is,
however, brittle. Like all brittle materials, its strength in tension is much lower than its strength in
compression. The actual ratio is about 1:5. As a result it has little resistance to tensile and bending
loads, and has a low shock resistance. In practice this means that set gypsum products such as
models will fracture if dropped, and the surface is easy to chip or flake during repeated use.
Chemistry of Plaster and stone
To understand how this material should be used, we need to know how it is made, how it
mixes with water and how it sets. The term “plaster” covers not only dental plaster, but also
stone, and improved stones. These products are categorised in order of increasing strength, for
example by the American Dental Association, as:
• Impression plaster, ADA type I

• Model Plaster, ADA type II
• Dental Stone, ADA type III
• High strength Dental Stone, ADA type IV
These products are actually chemically identical. The difference between plaster, medium
strength plaster (stone) and high strength plaster (improved stone, or die stone) is the size and
shape of the their particles of calcium sulfate hemi-hydrate. This difference, however, can
have a great effect on the strength of the material. The particles vary in size and shape because
of the way they are formed as the plaster sets.
Plaster is made by heating gypsum between 120OC and 180OC. The gypsum gives off water, and
the eventual product at room temperature is calcium sulfate hemi-hydrate.
2CaSO4٠2H2O → (CaSO4)2·H2O +3 H2O
This is the process is called calcination, or calcining
Stone
Particles of plaster made by calcining are roughly the same shape and size as the ground particles of
gypsum from which they have been made. However, if the process is carried out by heating
gypsum with superheated steam, at about 120OC for several hours, followed by drying, the
formation of the particles of plaster is controlled by crystallisation. They are less porous, more
geometrically shaped and more even in size and shape than particles of dry calcined plaster. Stone
is also reground after calcining, making a certain amount of fine powder particles as well. The
stone particles with some fines make a powder whose particles pack together more closely,
increasing the bulk density of the dry powder. When the stone powder is mixed with water and
reset, the resulting gypsum has smaller crystals because it starts to set from more points. It is also
more densely packed, and this resulting “stone” has a compressive strength double that of “dental”
plaster, or model plaster.
a) b) c)
THE “BULK DENSITY OF a) PLASTER, b) STONE, and c) DIE STONE.

Each cylinder contains 100g of calcium sulfate hemi-hydrate
High-strength Stone
By using chemical additions to further control the shape and size of the crystals of the hemi-hydrate
grown during calcining, the stone produced can be made stronger again. “Modified” or “die”stones
such as this will have a compressive strength four times that of dental plaster.
Although the particle size and strength of stone and modified stone is different from plaster, they all
set in the same way when mixed with. For this purpose, they can all be considered as one material.
The setting reaction
When one of the powder products plaster, stone or die stone, is mixed with water, it eventually sets
as gypsum.
(CaSO4)2·H2O + 3H2O → 2CaSO4·2H2O + Heat
his makes a solid mass of interlocking crystals of gypsum. Obviously, this reaction is the reverse of
the calcining reaction, but that only tells us what the product is, not how the reaction works.
Plaster has low solubility in water, and dissolves slowly, although it is still more soluble than
gypsum. As a result, when plaster powder is mixed with water, it takes time to dissolve. Eventually
the amount of calcium sulfate in the water becomes high enough that gypsum, because of its lower
solubility, begins to form solid crystals. As it does so, a little more plaster dissolves, and more
gypsum crystals form. Because of this slow dissolution and resetting process, plaster sets gradually.
This is a valuable property because it gives technicians some time for mixing and pouring the
plaster into a mould before it starts to set.
Understanding this process gives us information about how to control it better. There are a number
of variables which must be properly controlled by the technician before the best possible product
can be ensured.
73
Setting stages
Observing the setting of gypsum will show how it should be used. Mixing water with powder
initially produces a liquid “slurry,” a fluid paste. The proper mixture will be a little too stiff to flow
easily, but it will flow readily if assisted by vibration. As solid gypsum crystals form the mixture
becomes too viscous to be poured, although it remains sufficiently plastic to be moulded by
applying pressure, say with the hands. Eventually all the water present is used, and the surface of
the plaster loses its glossy wet look. This stage, called “gloss-off,” is often used by technicians to
indicate that the plaster has set. In fact there will continue to be some smaller crystals growing in
between the others for some time. The solid mass will not gain its full strength until it is completely
dry.
Because of the gradual way the crystals form, plaster also changes dimensions during setting. There
is actually a shrinkage in the liquid stage as setting starts, but this is not large enough to be obvious.
Once gloss-off is reached, the growing crystals of di-hydrate push against each other and cause a
slight expansion of the final solid bulk. Mixed with the correct amount of water, plaster will expand
about 0.3% on setting, and stones about 0.1%.
If the plaster is in contact with an excess of water during the later stages of setting (after gloss-off)
it will expand further. The final crystals are grow in an excess of water rather than coated with a
thin film of it. They are not restrained by pushing against each other as they grow. This is
commonly, but not altogether correctly, called hygroscopic expansion.
It can be achieved by immersing the setting plaster block in water after the gloss-off stage. This
technique is used to cause compensatory setting expansion of investments mixtures.
Additives
Commercial plaster and stone mixtures generally have a number of additives:
• Accelerators. These make the gypsum set faster. Fine dry plaster powder is one, as are a
number of ionic salts such as sulfates and chlorides, in low concentrations.
• Retarders: These slow gypsum setting. Included are acetate, borate, tartrate and citrate salts,
and any colloid, such as gelatine.
The amount of accelerators and retarders in plaster products is carefully controlled because many of
them also reduce the setting expansion and the strength of the set product Because they are added
as a mixture to the dry powder, it becomes important that the plaster in a container is evenly mixed
before using it.
Water to Powder ratios, W:P
The ratio of water to plaster powder in the original mixture has a number of effects on the setting
process, and on the properties of the set plaster
The amount of water needed for plaster to set usefully depends on two things:
• The amount of water needed for all the plaster particles to dissolve and precipitate as
gypsum
• The amount of water that is needed by the technician to make a pourable liquid mixture,
with each particle of powder exposed to water in the time available.
Theoretically plaster only needs a W:P ratio of 0.186 (0.186g water for each 1g of plaster) to
set fully. However, a mixture made to this ratio of water would be too dry to mix evenly.
Some particles would remain dry and unset. In order to make a mixture which is smooth and
even, and can be poured into a mould, W:P ratios about 0.5 or 0.6 are needed for plaster.
Dental stone needs a W:P ratio of about 0.33, and die stones need about 0.25. The smaller
particles in the stones allow full and even mixing with less water than is needed for plaster.
Although exposing plaster to an excess of water during the final stages of solidification may
increase the setting expansion, using a higher initial W:P ratio will result in reduced setting
expansion.
Strength of plaster products

As stated above, stone and die stone have much greater strength than plaster, due to their
smaller and better packed crystals.
STRENGTHS OF SET PLASTER
Product Compressive strength, MPa Tensile strength, MPa
Plaster 25 4
Stone 65 7
Die stone 80 10
Note that the results in the above table are typical of fully dry plaster. If the plaster is still wet, or
has been re-wet after drying, its strength in both tension and compression will be halved! Only a
small amount of added water is necessary to produce this effect on dry plaster.
Increasing the W:P ratio (making a runnier mix) will substantially reduce the strength of the set
plaster products because it makes the resulting set plaster more porous.
EFFECT of W/P RATIO ON THE STRENGTH OF SET DRY PLASTER
Water/ Plaster Ratio Compressive strength,

MPa
0.45 26.2
0.60 17.9
0.80 11.0
Hardeners
For some purposes the brittleness of plaster and its tendency to flake at the surface can be a
nuisance. In such cases, such as making dies, hardeners can be used. These are either
preparations painted on the plaster surface, or additives made to the plaster during mixing.
75
Strictly speaking these are not hardeners, as the hardness of the plaster is not affected. They
are better described as strengtheners, or tougheners
Surface hardeners.
These are usually polymers dissolved in solvent. Cyanoacrylate, acrylic, and polystyrene. have all
been used. It is not hard for the technician to make his or her own in a small nail-polish bottle,
though dissolving the polymer in a solvent, such as acetone, should be done in a well-ventilated
space. The mixture is applied with a small brush to the wearing surfaces of the model. The mixture
should be thin enough that it will soak into the pores of the plaster and set there, binding the
crystals together. It is not intended to add the polymer as a surface layer of added thickness (unless
this is necessary, to create a later spacing effect)
An alternative to polymer hardeners is to use colloidal silica in water or alcohol based solutions.
This is the same material which is used to set phosphate and silicate-bonded investments. Provided
it is used thin enough to avoid a “paint-on” layer, it penetrates and sets in the surface of the plaster
as a gel, making the plaster much tougher
Mix-in hardeners
Again polymer solutions or colloidal silica can be used, though the polymers will need to be
dissolved in a water compatible solvent such as an alcohol. The addition of colloidal silica
liquid to the plaster at the same time as the water is mixed will add 20 to 40% to the
compressive strength of the plaster. There is a risk in using high concentrations of this liquid
with the powder. Depending on what they are carried in, some of the silica colloids can invert
and set, apparently due to the pH of the plaster mix. It can cause greatly decreased setting rates
for the plaster. If you are using some left-over investment fluid rather than a specific gypsum
hardener, make a trial mix first.
USING PLASTER PRODUCTS

In the light of the above information, a number of points can be made about good practice in using
plaster products in dentistry:
• It is important to mix the plaster and water in a smooth fashion, not beating it. Any air
entrained in the plaster can result in bubbles that will remain after setting and weaken it.
• Mix plaster with water by sifting the powder onto the water surface. That way every
powder particle is more evenly wetted. Pouring the water over a heap of powder will result
in the outside of the heap starting to set first. It will be difficult to mix evenly. This problem
will be much more pronounced with large amounts of plaster.
• Using mechanical mixing machines will assist in producing easy and even mixing within
the available working time.
• If the plaster starts to set before you have poured it into the impression, adding extra water
will not correct matters. It will still set, just as quickly, but now you will have a lumpy set
material with uneven texture and low strength.
• Adding more water than recommended to a mix produces a lower strength solid. For
example, a die stone with a W:P ratio of about 0.2 will have maximum strength at that
value. Mixing it to a ratio of 0.25 will make the resulting solid roughly 40% weaker.
• If an extremely accurate set product is desired, i.e. a setting expansion or contraction of 0%,
use a slightly higher W:P ratio. However, the product will be slightly weaker.
• If the strongest possible set product is desired, use a slightly lower W:P ratio. However, the
setting expansion will be increased.
• Store plaster in an airtight bag and keep the lid on the container. Atmospheric moisture will
set plaster gradually if it is exposed. What most commonly happens is that the moisture
wets the surface of the powder and sets some of it, working from the outside inwards on
each particle. The result is a powder made from half-set particles. This will make a gritty,
lumpy mix, and sets to form a weaker solid.
• The accelerators and retarders in plaster may settle out over a long period of storage,
particularly where there is some vibration. This will produce plaster where material at the
top of the tin will have different setting properties from material at the bottom. It is good
practice to invert, or shake stored tins every few weeks to avoid this.
77
PRACTICAL ASSIGNMENT - DENTAL GYPSUM PRODUCTS
AIM
To examine some of the physical and mechanical properties of dental gypsum products
METHOD
Prepare test cylinders of plaster by setting 60g of plaster in the plastic moulds supplied. These
moulds are tapered slightly to make it easier to remove the set plaster, which may fit rather
tightly because it expands a little during setting. The moulds may be also be greased lightly to
make it easier to remove the set plaster.
Experiment (1) – The effect of Water/Plaster ratio
Make the specimens in the lists below, for plaster, stone and die stone. These are based on using
the same amount of plaster, but with a different water amount for each sample. Make sure that there
are no air bubbles in the plaster mould, as this would reduce the subsequent test strength. If the
mixture is too dry to make a mould, note this and comment. After removal of the plaster specimen
from the mould, write your group name on it with a pencil to avoid confusion during later testing
While the material is setting, observe:-

a) The setting time, using a surface needle such as a Vicat or Gilmore.
b) The consistency, or fluidity of the mix.
c) The suitability of the mix for dental use
After setting, measure d), The effect of W/P ratio on the strength of the set mixture by keeping the
set specimens for a week, then testing their compressive strength using a hydraulic pressure frame.
Before placing the specimens in the machine, make sure that the top and bottom surfaces are flat
and level by scraping them with a plaster knife.
Samples
i) Plaster W/P Ratio Plaster Water

0.25 60g 15ml
0.30 60g 18ml
0.50 60g 30ml
0.60 60g 36ml
ii) Stone 0.25 60g 15ml

0.30 60g 18ml
0.50 60g 30ml
0.60 60g 36ml
iii) Die stone
0.20 60g 12ml
0.25 60g 15ml
0.30 60g 18ml
0.50 60g 30ml
0.60 60g 36ml
Experiment (2) – The effect of water temperature
Prepare six plaster cylinders using a W/P ratio of 0.5 (60g water, 30g plaster,) but using water
at different temperatures for each one. Use water at:-
i) Room temperature (about 20oC) iv) Water at 70oC
o
ii) Water at 30 C v) Water at 90oC
iii) Water at 50oC vi) Water at boiling point
Record the setting time for each mixture, and plot a graph of setting time versus temperature.
Experiment (3) – Accelerators and Retarders
Make a specimen at W/P ratio 0.5 (60g plaster, 30ml water,) but dissolve 0.5g of
potassium sulfate in the water before mixing.
Repeat this experiment, but using sodium chloride, borax, and sodium citrate as the additives.
By comparing the setting time of this specimen with that of the 0.5 W/P ratio specimen
without additions from Experiment (1) determine which chemicals are accelerators, and
which are retarders.
Experiment (4) – Setting expansion
Using the expansion micrometer provided, measure the setting expansion of plaster, stone and die
stone. Set the micrometer to zero, which will leave a 100mm trough length. Grease the sides of the
trough, and pour the plaster mixture in. Immediately after the plaster has become rigid (Gloss-off)
back the micrometer end block off a couple of millimetres to allow the plaster to expand. After 1
hour, close the micrometer onto the end of the plaster block and measure any expansion.
RESULTS
Record the results from each experiment in a table
DISCUSSION /CONCLUSION
Compare the results from each experiment with what you would expect from previous theory
sections. What significance do these results have for dental use of plaster products?
79
IMPRESSION MATERIALS
The next material we consider is the “Impression” material, the substance that is used to take
an impression of the patient’s oral structure. This can be one of two types, rigid or flexible, ,
sometimes (wrongly) called non-elastic and elastic. The rigid ones were the original materials,
now no longer used, and the more recent materials are flexible, or elastic
Rigid impression materials:

Plaster
Zinc oxide/Eugenol
Impression compound
Flexible impression materials:

Alginate
Agar
Polyether
Polysulfide
Silicone (addition)
Silicone (condensation)
The difference between the two groups is that the rigid impression materials cannot not be
flexed to any extent after they have set without breaking them. Flexible, or elastomeric,
materials have can have a large amount of elastic, or rubbery behaviour. After a force is
applied to flex them, they will return to their original shape when the force is removed. In use
rigid materials cannot be used to take an impression of any dental surface which contains any
undercuts, or reverse angles, because the only way they can be removed from such a surface is
to break them into pieces and subsequently re-assemble the bits. While this used to be done
when rigid impression materials were the only ones available, the more recent flexible
materials have taken over because they can be used more easily for all types of impressions.
In this part of Materials Science we will look at the agar and alginate materials. The synthetic
polymer materials will be dealt with at a later stage in the course.
Hydrocolloid materials, Agar and Alginates

Agar is the first of the flexible, or elastic impression materials to be used in dentistry. It is
cheap, but complicated to use, and difficult to disinfect satisfactorily. It has been replaced by
the synthetic rubber polymers for oral impressions, but still finds occasional use as a material
for duplicating from stone models.
Agar and alginates are colloid materials. Colloids are one member of a group of materials
called suspensions. These are constructed of a very fine suspension of one substance in
another. The particles of the first substance are so fine that they do not settle. For example,
mist, or clouds, or steam are a colloidal suspension of water droplets in air, sometimes called
an aerosol. (liquid in gas suspension) Smoke is a suspension of solid particles in air (solid in
gas suspension), Margarine and hand cream are suspensions of oil droplets in water, called an
emulsions (liquid in liquid suspension).
Agar is made from a natural material derived from seaweed, which forms a colloidal
suspension of solidified particles in water. Above a certain temperature, the particles are
separated in the water, and the suspension behaves like a thick liquid. Below this temperature
the particles join together and form a brush or fibril structure, long molecules with a structure
like tiny combs. The water is contained in the spaces between these fibres, and the material
now behaves like a rubbery solid. In the solid form, this suspension is called a Gel, in the
liquid form it is called a Sol.
Interlocking fibril structure of colloidal material
The change from a gel to a sol and from as sol to a gel takes place at about 43OC, just above mouth
temperature so that the material can be heated to form a thick fluid, then placed in the mouth on a
water-cooled tray where it will become a sol and take an impression.
Because the change from gel to sol structures involves a lot of movement of atoms to make or
break up the fibril structure, the change is slow. Often the liquefaction temperature will be well
above the gelation temperature, because the material is warming up while it liquefies.
Agar is an accurate impression material. The elastic recovery is 98.8%. This means that the
material will regain 98.8% of its shape to after the elastic strain of being removed from undercuts.
The flexibility is rated at 11, a reasonable value which indicates that the material is not too stiff to
remove from undercuts.
Like most polymers agar will flow, that is, it will gradually change shape with time under a light
load. This is a property like the flow of a liquid, and leads to materials like colloids being referred
to as “semi-solids” It is thus recommended to remove agar (and any other flexible impression
material) rapidly rather than gradually, to minimise flow.
The mechanical properties of agar are dependent on the amount of water in its structure. More
water decreases the strength and stiffness, and increases flexibility and flow.
The usual mixture of agar is supplied as a gel containing 15% agar, and a little borax, potassium
sulfate, preservatives and colouring agents. The Borax strengthens the mix. The potassium sulfate
is there to act as an accelerator on the surface of the subsequent stone model poured in the agar. If
the sulfate were not there, the water in the gelled agar would act to slow down the setting of the
surface of the plaster, leaving wet, weak patches.
The major problem with agar is that it is dimensionally unstable. Because its structure contains a
large and variable amount of water, it will easily change shape and dimensions depending on the
water content of the air around it. The expansion of agar placed in contact with water is called
imbibition, and its shrinkage if placed in air of less than 100% humidity is called syneresis. The
uncertainty of its dimensional stability means that models must be poured into agar immediately
after it has set.
81
Agar is cheap, accurate (if poured up immediately), and reusable. However, it needs a water boiler
to heat it, and water-cooled trays. Its re-useability cannot be applied to oral impressions because of
the risk of infection transfer. Its equipment cost, and its dimensional instability have led to its being
used nowadays only for model duplications. For oral impressions, alginates and the rubber
impression materials have superseded it.
Alginate
Alginate is a synthetic colloid based on the compound, sodium alginate. This undergoes a
chemical reaction and sets with a similar molecular structure to agar, but it has increased
strength and reduced shrinkage due to the presence of a large amount of fillers included. These
large amounts of filler also make set alginate stiffer and stronger than agar.
The alginate is supplied as a powder containing about 15% sodium alginate, about 10%
gypsum (calcium sulfate di-hydrate), some phosphates or carbonates as retarders and 70%
inert filler, usually a silicate powder.
When the powder is mixed with water, the sodium alginate dissolves immediately. The
gypsum dissolves slowly, Setting occurs when the calcium sulfate reacts with the sodium
alginate to form calcium alginate, which is insoluble in water. It forms as a set solid and
includes a lot of water in its structure. The phosphate present slows the reaction by using up
some of the calcium sulfate.
Sodium alginate + calcium sulfate → calcium alginate↓ + sodium alginate
Because it sets by a chemical reaction, not the physical gelation of agar, alginate sets more
quickly and does not need complicate cooling trays. Because it sets by a chemical reaction
which is not easily reversed, alginate is not re-usable.
Mainly because of its ease of use, alginate has taken over from agar as a flexible impression
material. It has a lower elastic recovery of 97.2%. Like agar, however it has only a moderate
resistance to tearing, and this strength is reduced if too much water is used in the mixture.
Because alginate is a colloidal material, its structure still contains considerable amounts of
water. Like agar it will suffer from substantial shrinkage after use due to syneresis, The model
must have the modelling material poured into it immediately after setting. Not only do agar
and alginate tend to shrink after setting, but if they are placed in contact with variable amounts
of water, they may not only shrink, but also distort as different areas experience different
amounts of syneresis or imbibition
USING ALGINATE IMPRESSION MATERIAL
• Alginate needs to be mixed with care to avoid lumps which form grainy patches after
setting; it is, however, relatively fast setting, so more than one minute mixing is
unadvisable, even for large mixes.
• Cooling the mixing water will prolong the setting time, warming the water will shorten
it. This is because the alginate reaction is a chemical reaction, and speeds up as the
temperature is raised. In contrast, agar’s physical setting reaction is slowed by heating.
• Using extra water in the mix, above that recommended, will increase the flexibility, but
decrease the stiffness and tear resistance of the set product. Conversely, less water and
more powder makes a stronger, but stiffer product.
• It may not always be possible to pour the model immediately after the alginate has set.
In such cases the dimensional change of the alginate can be reduced, or even prevented,
by storing the impression in an atmosphere saturated with water. This is usually
achieved by putting it in a plastic bag together with a wet rag, but it is better done by
putting the wet rag or paper into a container with a perforated lid, made from a polish
tin or spice jar. In this case the impression is surrounded by uniformly moist air, but
cannot come into full contact with extra water in the wet rag, which might cause
localised expansion of some part of the impression, and so produce distortion. This
procedure usually minimises the alginate shrinkage for a few hours, but it is hard to
know if it has worked. It is still much better practice to pour the model immediately.
• To reduce the chances of subsequent distortion, the set impression should be kept in the
tray and not have any weight placed on it.
Agar will usually contain a small amount of accelerator for the plaster which will be set on
it. Like agar, its water content can otherwise cause unset patches on the surface of the
subsequent model. This small amount of accelerator can settle in the storage container
with time or vibration during storage, so it is a good idea to mix the powder before each
use. Do this by shaking the closed tin. Stirring the powder in an open tin can is a
potential long-term health hazard, as the filler is usually some form of fine silicate
powder and should not be breathed.
83

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LECTURE

DENTAL TECHNOLOGY DIPLOMA

Welcome to Dental Materials Science.

Title: Dental Materials properties and Manipulation.

Title: Dental Materials: Properties and Selection.

COMM SERV HEALTH TOURISM HOSP ESD©

Recommended Time - 2 hrs

• Classification of matter as elements, mixtures or compounds.

Matter can exist in one of 4 forms:

At room temperature, if a substance appears as a liquid then it has a melting point

Kinetic Theory of Matter

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As the temperature of water is decreased the mobility of the molecules decrease

If we decrease the temperature further, particle vibration decreases until -2730C is

Homogenous and Heterogeneous Matter

Elements, Mixtures and Compounds

A compound is a pure substance made by combining two or more elements in

When a second element is introduced to a first, the chemical and physical

COMM SERV HEALTH TOURISM HOSP ESD©

(v) Fill a clean test tube to a depth of approximately 10 mm with the

(iv) Place some of the material obtained in part 2 in a test tube to a

Q1. List three (3) different states of matter.

Q3. Briefly describe the Kinetic Theory of Matter.

Q4. Define the following terms:

COMM SERV HEALTH TOURISM HOSP ESD©

Q1. (i) solid

Q2. (i) Vibration of particles only – rigidly restrained.

Q4. Define the following terms:

• chemical properties are uniform

DISTINGUISH BETWEEN METALS AND

COMM SERV HEALTH TOURISM HOSP ESD©

Recommended Time - 3 hrs

• The type and nature of sub atomic particles.

History of Atomic Theory (just read this, not examinable)

Early philosophies considered matter to be made from of four elements: earth,

In the early 1800’s John Dalton proposed a revolutionary new approach:

By 1820, laboratory experiment had found the presence of smaller particles in

Modern Atomic Theory

Bohr conclude his atomic theory as:

• The nucleus contains protons (+ charge) and neutrons (no charge).

• A cloud of electrons (- charge) orbits the nucleus.

• The volume of the nucleus is extremely small compared to the volume of

• The atom is electrically neutral since the number of electrons = number of

Properties of Subatomic Particles

Subatomic Symbol Charge Mass Mass Location

All elements are made up of different combinations of these subatomic particles.

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The arrangement of particles in an atom. PROTONS (+ charge), NEUTRONS

Atomic Number and Mass Number

Atomic number = number of protons in the nucleus

Mass number = number of protons plus neutrons in the nucleus

Atomic Number Mass Number

From this. we can work out that that carbon has:

Maximum Number of electrons in any shell “n” = 2n2

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2 electrons in the 1st shell (n=1)

Under normal conditions electrons in their shells are referred to as in their

Element Number of Maximum Electron

Element Symbol Element Symbol Element Symbol

Atomic number, or “Z”

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Properties of Metal and Non-Metals

Metal Non Metal