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EBB 220/3 Polymer Physics

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Title: EBB 220/3 Polymer Physics


1
EBB 220/3Polymer Physics
2
INTRODUCTION
  • Characteristics of
  • Thermoplastic (amorphous semicrystalline)
  • thermoset
  • rubber
  • Linear crosslink system?
  • Differences between
  • vulcanizing and curing?

3
INTRODUCTION
4
(No Transcript)
5
Structure
  • The structural properties of a polymer relate to
    the physical arrangement of monomers along the
    backbone of the chain.
  • Structure has a strong influence on the other
    properties of a polymer.

6
Structure
  • The simplest form of polymer molecule is a
    straight chain or linear polymer, composed of a
    single main chain. The flexibility of an
    unbranched chain polymer is characterized by its
    persistence length.
  • A branched polymer molecule is composed of a main
    chain with one or more substituent side chains or
    branches.
  • A cross-link suggests a branch point from which
    four or more distinct chains emanate. A polymer
    molecule with a high degree of crosslinking is
    referred to as a polymer network

7
Monomer arrangement in copolymers
  • Monomers within a copolymer may be organized
    along the backbone in variety of ways.
  • Alternating copolymers possess regularly
    alternating monomer residues
  • Random copolymers have a random sequence of
    monomer residue types
  • Block copolymers have two or more homopolymer
    subunits linked by covalent bonds. Block
    copolymers with two or three distinct blocks are
    called diblock copolymers and triblock
    copolymers, respectively.

8
Tacticity in polymers
  • This property describes the relative
    stereochemistry of chiral centers in neighboring
    structural units within a macromolecule. There
    are three types isotactic, atactic, and
    syndiotactic.
  • Precise knowledge of tacticity of a polymer also
    helps understanding at what temperature a polymer
    melts, how soluble it is in a solvent and its
    mechanical properties.

9
Melting point
  • The term "melting point" when applied to polymers
    suggests not a solid-liquid phase transition but
    a transition from a crystalline or
    semi-crystalline phase to a solid amorphous
    phase.
  • Though abbreviated as simply "Tm", the property
    in question is more properly called the
    "crystalline melting temperature".
  • Among synthetic polymers, crystalline melting is
    only discussed with regards to thermoplastics, as
    thermosetting polymers will decompose at high
    temperatures rather than melt.

10
Glass transition temperature (Tg)
  • A parameter of particular interest in synthetic
    polymer manufacturing is the glass transition
    temperature (Tg), which describes the temperature
    at which amorphous polymers undergo a second
    order phase transition from a rubbery, viscous
    amorphous solid to a brittle, glassy amorphous
    solid.
  • The glass transition temperature may be
    engineered by altering the degree of branching or
    cross-linking in the polymer or by the addition
    of plasticizer.

The Space Shuttle Challenger disaster was caused
by rubber O-rings that were below their glass
transition temperature on an unusually cold
Florida morning, and thus could not flex
adequately to form proper seals between sections
of the two solid-fuel rocket boosters.
11
Polymer Structure/Property relationships
  • Chain length
  • Increasing chain length tends to decrease chain
    mobility, increase strength and toughness, and
    increase the glass transition temperature (Tg).
  • This is a result of the increase in chain
    interactions such as Van der Waals attractions
    and entanglements that come with increased chain
    length.
  • These interactions tend to fix the individual
    chains more strongly in position and resist
    deformations and matrix breakup, both at higher
    stresses and higher temperatures.

12
Polymer Structure/Property relationships
  • Branching
  • Branching of polymer chains also affect the bulk
    properties of polymers.
  • Long chain branches may increase polymer
    strength, toughness, and Tg due to an increase in
    the number of entanglements per chain.
  • Random length and atactic short chains, on the
    other hand, may reduce polymer strength due to
    disruption of organization.
  • Short side chains may likewise reduce
    crystallinity due to disruption of the crystal
    structure. Reduced crystallinity may also be
    associated with increased transparency due to
    light scattering by small crystalline regions. A
    good example of this effect is related to the
    range of physical attributes of polyethylene.
  • High density polyethylene (HDPE) has a very low
    degree of branching, is quite stiff, and is used
    in applications such as milk jugs. Low density
    polyethylene (LDPE), on the other hand, has
    significant numbers of short branches, is quite
    flexible, and is used in applications such as
    plastic films.

13
Polymer Structure/Property relationships
  • Chemical cross-linking
  • Cross linking tends to increase Tg and increase
    strength and toughness.
  • Cross linking consists of the formation of
    chemical bonds between chains.
  • Among other applications, this process is used to
    strengthen rubbers in a process known as
    vulcanization, which is based on cross linking by
    sulfur. Car tires, for example, are highly cross
    linked in order to reduce the leaking of air out
    of the tire and to toughen their durability.
    Eraser rubber, on the other hand, is not cross
    linked to allow flaking of the rubber and prevent
    damage to the paper.

14
Polymer Structure/Property relationships
  • Inclusion of plasticizers
  • Inclusion of plasticizers tends to lower Tg and
    increase polymer flexibility.
  • Plasticizers are generally small molecules that
    are chemically similar to the polymer and create
    gaps between polymer chains for greater mobility
    and reduced interchain interactions.
  • A good example of the action of plasticizers is
    related to polyvinylchlorides or PVCs.
  • A uPVC or unplasticized polyvinylchloride is used
    for things such as pipes. A pipe has no
    plasticizers in it because it needs to remain
    strong and heat resistant. Plasticized PVC is
    used for clothing for a flexible quality.
    Plasticizers are also put in some types of cling
    film to make the polymer more flexible.

15
Polymer Structure/Property relationships
  • Degree of crystallinity
  • Increasing degree of crystallinity tends to make
    a polymer more rigid. It can also lead to greater
    brittleness.
  • Polymers with degree of crystallinity approaching
    zero or one will tend to be transparent, while
    polymers with intermediate degrees of
    crystallinity will tend to be opaque due to light
    scattering by crystalline / glassy regions.

16
Example of Thermoplastic Polymers
17
Example of Thermoplastic Polymers
18
EBB 220/3PRINCIPLE OFVISCO-ELASTICITY
19
INTRODUCTION
  • The differences between the polymeric materials
    behaviour and materials with totally elastic
    behaviours are
  • Time dependent characteristics
  • Temperature dependent characteristics
  • Polymeric materials will show the properties that
    dependent on stress strain ? that will
    influence when the loading being applied.

20
  • The response of polymeric materials with stress
    or strain that been applied dependent on
  • Loading rate
  • Loading time
  • The differences between materials behaviour are
  • Elastic materials
  • Viscous materials
  • Visco-elasticity

21
Behaviour of elastic material
  • Elastic behaviour is instantaneous/immediate.
  • The total deformation (or strain) occurs the
    instant the stress is applied or release.
  • Upon release of the external stress the
    deformation is totally recovered (deformation is
    reversible)
  • The specimens assumes its original deformation

22
Elastic materials
  • The spring (in the following figure) represents
    the elastic portion (usually short term) of a
    plastic material's response to load.
  • When a load is applied to the spring, it
    instantly deforms by an amount proportional to
    the load. When the load is removed, the spring
    instantly recovers to its original dimensions.
  • As with all elastic responses, this response is
    independent of time and the deformation is
    dependent on the spring constant.

23
Behaviour of viscous material
  • Deformation or strain is not instantaneously.
  • In response to an applied stress- deformation is
    delayed or dependent with time.
  • This deformation is not reversible or completely
    recovered after stress is released.

24
Viscous Behavior
  • The dash-pot in the following figure represents
    the viscous portion of a plastic's response.
  • The dash-pot consists of a cylinder holding a
    piston immersed in a viscous fluid. The fit
    between the piston and cylinder is not tight.
  • When a load is applied, the piston moves slowly
    in response. The higher the loading, the faster
    the piston moves. If the load is continued at the
    same level, the piston eventually bottoms out
    (representing failure of the part). The viscous
    response is generally time- and rate-dependent.

h viscosity de/dt strain rate
25
Summary Hookes law (elastic) Newtons Law
(plastic)
  • The behaviour of linear elastic were given by
    Hookes law

or
  • The behaviour of linear viscous were given by
    Newtons Law
  • E Elastic modulus
  • s Stress
  • e strain
  • de/dt strain rate
  • ds/dt stress rate
  • h viscosity

This equation only applicable at low strain
26
Visco elastic behaviour
  • Behaviour of most polymer is in between behaviour
    of elastic and viscous materials.
  • At low temperature high strain rate,
  • Polymer demonstrate elastic behaviour,
  • At high temperature low strain rate,
  • Polymer demonstrate viscous behaviour
  • At intermediate temperatures rate of strain
  • Polymer demonstrate visco-elastic behaviour

27
  • Polymer is called visco- elastic because
  • Showing both behaviour elastic viscous
    behaviour
  • Instantaneously elastic strain followed by
    viscous time dependent strain

28
Mechanical Model
  • Methods that used to predict the behaviour of
    visco-elasticity.
  • They consist of a combination of between elastic
    behaviour and viscous behaviour.
  • Two basic elements that been used in this model
  • Elastic spring with modulus which follows Hookes
    law
  • Viscous dashpots with viscosity h which follows
    Newtons law.
  • The models are used to explain the phenomena
    creep and stress relaxation of polymers involved
    with different combination of this two basic
    elements.

29
STRESS RELAXATION
CREEP
Constant strain is applied ? the stress relaxes
as function of time
Constant stress is applied ? the strain relaxes
as function of time
30
  • The common mechanical model that use to explain
    the viscoelastic phenomena are
  • Maxwell
  • Spring and dashpot ? align in series
  • Voigt
  • Spring and dashpot ? align in parallel
  • Standard linear solid
  • One Maxwell model and one spring ? align in
    parallel.

31
Maxwell Model
  • Maxwell model consist of spring and dashpot in
    series and was developed to explain the
    mechanical behaviour on tar.
  • On the application of stress, the strain in each
    elements are additive.
  • The total strain is the sum of strain in spring
    dashpot. The stress each elements endures is the
    same.

Elastic spring
Viscous dashpot
32
  • Overall stress s, overall strain e in the system
    is given by
  • es strain in spring and ed strain in dashpot
    dashpot
  • Because the elements were in series ? the stress
    is the same for all elements,
  • Equations for spring and dashpot can be written
    as

and
33
  • For Maxwell model, the strain rate is given as
  • In creep case, the stress at s s0 therefore
    ds/dt 0. The equations can be written as
  • Maxwell model can predict the Newtonian behaviour
    ? the strain is predict to increase with time

34
  • .
  • The behavior of Maxwell model during creep
    loading (constant stress, s0 ?strain is predicted
    to increased linearly with time

This is not the viscoelastic behaviour of
polymeric materials ? de/dt decreased with time
35
  • May be this model is useful to predict the
    behaviour of polymeric materials during stress
    relaxation.
  • In this case, the strain is constant ee0 applied
    to the system given de/dt 0
  • then
  • Integration at t0 s s0 given

?
so earlier stress
36
  • The term h/E is constant for Maxwell model and
    sometimes can be refered as time relaxation, t0
    written as
  • The exponential decreased in stress can be
    predicted ? give a better representation of
    polymeric materials behaviour.
  • Stress were predicted completely relaxed with
    time period ? it is not the normal case for
    polymer

37
Voigt Model
  • Can also known as the Kelvin model.
  • It consists of a spring and dashpot in parallel.
  • In application of strain, the stress of each
    element is additive, and the strain in each
    element is the same.

Elastic spring
Viscous dashpot
38
  • The parallel arrangement of spring and dashpot
    gives the strain e are the same for the system
    given by
  • es strain in spring and ed strain in
    dashpot
  • Because the elements in parallel ? stress s d in
    every elements are additive and the overall
    stress are
  • Equation for spring and dahpot can be written as

and
39
  • For Voigt model, the strain rate are
  • The accuracy of prediction the mechanical
    behaviour of Voigt model can be confirm.
  • In creep case, stress is s so so ds/dt 0.
    The equation can be written as
  • The simple differential equation given by

40
  • Constant ratio h/E can be replace with time
    relaxation, t0.
  • Changes in strain with time for Voigt model that
    having creep are given by

Figure shows polymer behavior under creep
deformation? strain rate decreased with time
e ?so /.E and t
41
  • Voigt model fails to predict the stress
    relaxation behaviour of polymer
  • When the strain is constant at e0 and de/dt 0
    the equation shows
  • ? The linear response is shown in the figure

or
Behavior of Voigt model at different loading ?
Stress relaxation
42
Standard linear solid
  • As shown
  • Maxwell model can accurately predict the
    phenomenon stress relaxation to a first
    approximation.
  • Voigt Model can accurately predict the phenomenon
    creep to a first approximation.
  • Standard linear solid model was developed to
    combined the Maxwell and Voigt model ? to
    describe both creep stress relaxation to a
    first approximation.

43
Elastic spring
Viscous dashpot
  • In consist ? one Maxwell elements in parallel
    with a spring.
  • The presence on this second spring will stop the
    tendency of Maxwell element undergoing viscous
    flow during creep loading ? but will still allow
    the stress relaxation to occur

44
General time dependent behaviour
  • The true mechanical properties that appropriate
    with time for polymeric materials dependent on ?
    types of stress or cycle of strain that been
    used.
  • Changes in stress an strain with time (t), can
    be shown in simple schema of polymer tensile.
  • It can be categorized based on 4 different
    deformation behaviour as
  • creep
  • Stress relaxation
  • Constant stress rate
  • Constant strain rate

45
INTRODUCTION
  • It is difficult to predict the creep and stress
    relaxation for polymeric materials.
  • It is easier to predict the behaviour of
    polymeric materials with the assumption ? it
    behaves as linear viscoelastic behaviour.
  • Deformation of polymeric materials can be divided
    to two components
  • Elastic component Hookes law
  • Viscous component Newtons law
  • Deformation of polymeric materials ? combination
    of Hookes law and Newtons law.

46
STRESS RELAXATION
CREEP
Constant strain is applied ? the stress relaxes
as function of time
Constant stress is applied ? the strain relaxes
as function of time
47
(a) Creep
  • During Creep loading
  • A constant load were applied to the specimen at
  • t 0,
  • The strain increased quickly at the beginning but
    become slowly with time after a long period of
    deformation.
  • For elastic solid ? the strain rate is constant

Constant stress
48
(b) Stress Relaxation
  • During stress relaxation
  • Strain is constant
  • Stress decreased slowly with time.
  • For elastic solid ? the stress is constant

49
(c) Constant stress rate
  • The increasing strain with time is not linear.
  • It becoming more steep with
  • Increasing time
  • Increasing stress rate

50
(d) Constant strain rate
  • The increasing stress with time is not linear.
  • The slope of the curve decreased with time
  • The slope become more steep with the increasing
    strain rate

51
Creep phenomenon
  • It were the general behaviour of polymeric
    materials and very important in engineering.
  • It can estimates the strength or the ability to
    sustained the stress that been applied
    permanently or constant.
  • Creep ? polymer is stressed at a constant level
    for a given a time and the strain increases
    during that time periods.
  • Creep can be used to estimate the life times of
    materials
  • Frequently run at temperatures where thermal
    degradation is significant ? data can be used to
    estimate of the elevate-temperature life of
    materials.

52
3 creep stages
  • There were 3 stages of creep
  • Primary Creep The slope of strain vs time
    decreased with time.
  • Secondary creep Constant strain rate.
  • Tertiary creep the strain rate increased
    rapidly until rupture (formation of crack,
    yielding and etc).

53
Creep strain, e
Rupture
Time, t
Graph for strain curve at constant loading.
54
  • After beginning of strain, specimen will having a
    slowly shape changes with time until the
    yielding occur that caused a rupture.
  • At primer area ?
  • Area of early stage of deformation when creep
    rate is decreased with time (slope of the curve
    decreased with time).
  • Polymeric materials having the increased in creep
    resistance or strain hardening.

55
  • Secondary area ?
  • Area where the creep rate where almost constant
  • Creep rate were explained by the equilibrium in
    between strain hardening and the ability to
    maintain/ retain its shape.
  • Tertier area ?
  • Where creep accelerate and rupture occurred.
  • Creep happens due to changes in microstructure.
  • Happen at higher stress for ductile materials.
  • Decreased in cross-section that make the rupture
    or creep rate increased rapidly.

56
  • Creep test normally run in extension/ tension
    test. (but can be done in shear, compression or
    flexural test)
  • Creep rate of polymeric materials were dependent
    on loading, time and temperatures.
  • Polymeric components will deformed rapidly at
    higher temperatures.
  • Creep results can been shown as
  • Isometric curve stress versus time
  • Modulus creep curve modulus versus time
  • Isochronous curve stress versus strain

57
Isometric curve
  • Stress that being applied will dependent on time.
  • At beginning ? stress is higher due to bonding
    forces between atoms is higher.
  • After a few moments ? slippage between atoms
    occur and the polymer crystallization rate
    decreased then the strain were increased with
    time.

58
Modulus curve
  • The elasticity of certain materials exists due to
    the materials decomposition of chain to become
    more order.
  • If the measurements is taken in the short
    periods? the decomposition of chain folding had
    not happened ? polymer are more like persistent
    materials.
  • This graph is very useful in determination of
    materials rigidity and persistent ? based on the
    life span of the materials.

59
Isochronous curve
  • The slope of the graph is equivalent to the
    modulus Young, E which is the determination the
    resistance towards the neighbouring separation of
    the atoms.
  • Modulus is the rigidity or the resistance of
    materials towards shapes changes.
  • The high modulus values ? resulting from small
    strain changes due to the applied stress.

60
The use of creep graph
  • The knowledge of knowing to interpret of creep
    graphs are useful for materials engineer.
  • Data from creep graph gives us the information
    about
  • The rupture/deformation of the materials
  • Yield and shape change of the materials.
  • Can estimating the life time of the materials
  • Can choose the materials based on materials
    applications.

61
Isochronous curve
  • Can comparing various types of polymeric
    materials during design because
  • ? The stress for materials were plotted at time
    for the specific loading being applied.

62
Example of the problem
  • One of the engineer has to design rigid structure
    can sustained the continuous load for 1000 hours
    with the strain not more than 2 .
  • Question
  • What is the maximum stress can be allowed?
  • Solution
  • Need to make a comparison from graph strain
    versus time for different stress for 1000 hours.
    ? strain at different stress can be resolved.
  • Graph stress versus strain at 1000 hours can be
    plotted ? the maximum stress allowed can be
    obtained.

63
Modulus curve
  • From graph ? creep modulus decreased with
    increasing time showing the visco-elastic
    behaviour.
  • This graph were useful because modulus were
    needed in engineering deflection.

64
Example of the application
  • To chosen the life span of component that being
    designing at modulus curve ? the modulus value is
    called design modulus.
  • The stress of the modulus is determine according
    to the alternative
  • If stress being determine ? The values should be
    taken from the modulus curve with the stress
    value is nearly to the value that needed.
  • If the stress needed not yet been determine ?
    Need to choose the modulus curve with the
    conservative stress value and need to be checked
    before starting the calculation.

65
Isometric curve
  • With observing materials behaviour during stress
    relaxation ? can estimate the long term materials
    behaviour.
  • Materials long term service can be estimate when
    the certain stress being applied not more than
    the rupture of the materials.

66
Example of application
  • For one bottle lid under constant strain for very
    long period ? low stress relaxation is needed.
  • That bottle lid will fail if the stress decreased
    instantly.
  • Time is a the main factor that will influenced
    the mechanical properties of the bottle lid
    because
  • At very short loading time ? higher stresses is
    needed for particular strain.
  • At long term loading ? lower stresses is needed
    to get the particular strain.

67
Example of the exams question
  • What is definition of visco-elasticity?
  • Please gives the differences between
    visco-elastic behavior and totally elastic
    behavior.
  • Gives the advantages of creep properties in
    materials engineering?

68
Effect of glass transition and temperature on
creep
  • Below Tg?
  • In the Tg region?
  • Above Tg?

69
Summary
  • There were a lots of attempts to discover more
    complex model that can give a good approximation
    to predict viscoelastic behaviour of polymeric
    materials.
  • When the elements used is increased ?
    mathematical can be more complex.
  • It can be emphasis that mechanical models can
    only gives mathematical representations for
    mechanical behaviour only ? it not much help to
    predict the behaviour of viscoelasticity at
    molecular level.

70
Example of the exams question
  • What is the purpose of mechanical model in
    visco-elasticity theories?
  • Gives a brief description how the chosen
    mechanical model can be used to estimate the
    creep or stress relaxation behavior for polymeric
    materials?

71
Thank you
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