Transcript Document

What happens to Tg with increasing pressure?
Bar = 1 atm = 100 kPa
Why?
A Demonstration of Polymer
Viscoelasticity
Poly(ethylene oxide) in water
“Memory” of Previous State
Poly(styrene)
Tg ~ 100 °C
Chapter 5. Viscoelasticity
Is “silly putty” a solid or a liquid?
Why do some injection molded parts warp?
What is the source of the die swell phenomena that is often
observed in extrusion processing?
Expansion of a jet
of an 8 wt% solution of
polyisobutylene in decalin
Under what circumstances am I justified in ignoring viscoelastic
effects?
What is Rheology?
Rheology is the science of flow and
deformation of matter
Rheology Concepts, Methods, & Applications, A.Y. Malkin and A.I. Isayev; ChemTec Publishing, 2006
Temperature & Strain Rate
Time dependent processes:
Viscoelasticity
The response of
polymeric liquids,
such as melts and
solutions, to an
imposed stress may
resemble the behavior
of a solid or a liquid,
depending on the
situation.
De 
characteristic materialtime C

timescale of thedeformation tS
Stress
increasing loading rate
Strain
Network of Entanglements
There is a direct analogy between chemical crosslinks in
rubbers and “physical” crosslinks that are created by the
entanglements.
The physical entanglements can support stress (for short
periods up to a time tT), creating a “transient” network.
Entanglement Molecular Weights, Me, for
Various Polymers
Me (g/mole)
Poly(ethylene)
1,250
Poly(butadiene)
1,700
Poly(vinyl acetate)
6,900
Poly(dimethyl siloxane)
8,100
Poly(styrene)
19,000
Pitch drop experiment
•Started in 1927 by University of
Queensland Professor Thomas Parnell.
•A drop of pitch falls every 9 years
Pitch drop experiment apparatus
Pitch can be shattered by a hammer
Viscoelasticity and Stress Relaxation
Whereas steady-shear measurements probe material
responses under a steady-state condition, creep and stress
relaxation monitor material responses as a function of time.
t stress)
o
?
strain)
to=0
time
to=0
time
– Stress relaxation studies the effect of a step-change in strain on
stress.
Physical Meaning of the Relaxation Time

Constant strain applied
time
s
Stress relaxation:
Stress relaxes over time
as molecules re-arrange
s (t ) = Ge
t
time
t
Introduction to Viscoelasticity
All viscous liquids deform
continuously under the influence of an
applied stress – They exhibit viscous
behavior.
Solids deform under an applied stress,
but soon reach a position of
equilibrium, in which further
deformation ceases. If the stress is
removed they recover their original
shape – They exhibit elastic behavior.
Viscous fluid
Viscoelastic fluid
Elastic solid
Viscoelastic fluids can exhibit both
viscosity and elasticity, depending on
the conditions.
Polymers display VISCOELASTIC properties
Static Testing of Rubber Vulcanizates
• Static tensile tests measure
retractive stress at a constant
elongation (strain) rate.
– Both strain rate and
temperature influence the
result
Note that at common static
test conditions, vulcanized
elastomers store energy
efficiently, with little loss of
inputted energy.
Dynamic Testing of Rubber Vulcanizates: Resilience
Resilience tests reflect the ability of an
elastomeric compound to store and
return energy at a given frequency
and temperature.
Change of rebound
resilience (h/ho) with
temperature T for:
•1. cis-poly(isoprene);
•2. poly(isobutylene);
•3. poly(chloroprene);
•4. poly(methyl methacrylate).
Hooke and Newton
•
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 – Hooke’s law

Viscous component – Newton’s law
Deformation of polymeric materials  combination of Hooke’s
law and Newton’s law.
Hooke’s law & Newton’s Law
•
The behaviour of linear elastic were given by Hooke’s
law:
s  Ee
•
or
The behaviour of linear
viscous were given by
Newton’s Law:
de
s 
dt
ds
de
E
dt
dt
E= Elastic modulus
s = Stress
e = strain
de/dt = strain rate
ds/dt = stress rate
= viscosity
** This equation only applicable at low strain
Viscoelasticity and Stress Relaxation
Stress relaxation can be measured by shearing the polymer melt in a
viscometer (for example cone-and-plate or parallel plate). If the
.
rotation is suddenly stopped, ie. =0, the measured stress will not fall
to zero instantaneously, but will decay in an exponential manner.
Relaxation is slower
for Polymer B than for
Polymer A, as a result
of greater elasticity.
These differences may
arise from polymer
microstructure
(molecular weight,
branching).
CREEP
Constant stress is applied
 the strain relaxes as
function of time
STRESS RELAXATION
Constant strain is applied
 the stress relaxes as
function of time
Time-dependent behavior of Polymers
The response of polymeric liquids, such as melts and solutions, to an
imposed stress may under certain conditions resemble the behavior of a
solid or a liquid, depending on the situation.
Reiner used the biblical expression that “mountains flowed in front of
God” to define the DEBORAH number
De 
characteristic materialtime C

timescale of thedeformation t S
metal
elastomer
Viscous liquid
Static Modulus of Amorphous PS
Glassy
Leathery
Rubbery
Viscous
Polystyrene
Stress applied at x
and removed at y
Stress Relaxation Test
Strain
Elastic
Viscoelastic
Stress
Viscous fluid
0
Time, t
Stress relaxation
Stress relaxation after a step strain o is the fundamental way in which we define the
relaxation modulus:
G( t ) 
t( t )
o
Go (or GNo) is the
“plateau modulus”:
RT
G 
Me
o
N
where Me is the
average mol. weight
between
entanglements
G(t) is defined for shear flow. We can
also define a relaxation modulus for
extension:
E( t ) 
s( t )
o
Stress relaxation of an uncrosslinked melt
Glassy behavior
Transition Zone
Plateau Zone
Terminal Zone
(flow region)
slope = -1
perse
Mc: critical molecular weight above which entanglements exist
3.24
Network of Entanglements
There is a direct analogy between chemical crosslinks in
rubbers and “physical” crosslinks that are created by the
entanglements.
The physical entanglements can support stress (for short
periods up to a time tT), creating a “transient” network.
Relaxation Modulus for Polymer Melts
Elastic
tT = terminal
relaxation time
Viscous
flow
tT
Viscosity of Polymer Melts
Extrapolation to
low shear rates
gives us a value of
the “zero-shearrate viscosity”, o.
o
Shear thinning
behaviour

Poly(butylene terephthalate) at 285 ºC
For comparison:  for water is
10-3 Pa s at room temperature.
Rheology and Entanglements.
The elastic properties of linear thermo-plastic polymers are due to
chain entanglements. Entanglements will only occur above a critical
molecular weight.
When plotting melt viscosity o against molecular weight we see a
change of slope from 1 to 3.45 at the critical entanglement molecular
weight.
Slope = 3.4
Entanglement
molecular weight
o
Slope = 1
Mn
Scaling of Viscosity: o ~ N3.4
 ~ tTGP
o ~
N3.4
N0
Viscosity is shear-strain rate
dependent. Usually measure in
the limit of a low shear rate: o
~
N3.4
3.4
Universal behaviour for
linear polymer melts
Applies for higher N:
N>NC
Why?
G.Strobl, The Physics of Polymers,
p. 221
Data shifted
for clarity!
Application of Theory:
Electrophoresis
From Giant Molecules
Mechanical Model
•
Methods that used to predict the behaviour of viscoelasticity.
•
They consist of a combination of between elastic
behaviour and viscous behaviour.
•
Two basic elements that been used in this model:
1. Elastic spring with modulus which follows Hooke’s
law
2. Viscous dashpots with viscosity 
Newton’s law.
•
which follows
The models are used to explain the phenomena creep
and stress relaxation of polymers involved with different
combination of this two basic elements.
Dynamic Viscosity (dashpot)
• Lack of slipperiness
• Resistance to flow
• Interlayer friction
Shear stress
t


SI Unit: Pascal-second
1 centi-Poise = milli Pascal-second
  Slope of line
Shear rate
stress
stress input
dashpot
27/06/46
Strain in dashpot
42

Maxwell model


In series
Viscous strain remains after load removal.
stress input
Model
Strain Response
Maxwell model
27/06/46
43

Kelvin or Voigt model



In parallel
Nonlinear increase in strain with time
Strain decreases with time after load removal because of the
action of the spring (and dashpot).
stress input
Model
Strain Response
Voigt model
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44
Typical Viscosities (Pa.s)
Asphalt Binder --------------Polymer Melt ----------------Molasses ---------------------Liquid Honey ----------------Glycerol ----------------------Olive Oil ----------------------Water -------------------------Acetic Acid --------------------
100,000
1,000
100
10
1
0.01
0.001
0.00001
Courtesy: TA Instruments
Shear stress
Non Newtonian
Fluids
Shear rate
The Theory of Viscoelasticity
The liquid behavior can be simply represented by the Newtonian model.
We can represent the Newtonian behavior by using a “dashpot”
mechanical analog:
t   
The simplest elastic solid model is the Hookean model, which we can
represent by the “spring” mechanical analog.
tG
t
stress

strain

viscosity
G
modulus
Maxwell Model
Let’s create a VISCOELASTIC material:
At least two components are needed, one to characterize elastic and the
other viscous behavior. One such model is the Maxwell model:
t
stress

strain

viscosity
G
modulus
Maxwell Model
Let’s try to deform the Maxwell element
t
stress

strain

viscosity
G
modulus
Maxwell: solid line
Experiment: circles
Maxwell model too primitive
Maxwell Model
The deformation rate of the Maxwell model is equal to the sum of the
individual deformation rates:
   fluid   solid
t t
  
 G

t  t   
G
t  t   
 is the relaxation time
If the mechanical model is suddenly extended to a position and held there
.
(=const., =0):
t  t oe
t
stress
t / 

Exponential decay in stresses
strain

viscosity
G
modulus
Examples of Viscoelastic
Materials

Mattress, Pillow

Tissue, skin
27/06/46
52
Elastic
•
Viscous
The common mechanical model that use to explain
the viscoelastic phenomena are:
1.
•
Maxwell
Spring and dashpot  align in series
2.
•
Voigt
Spring and dashpot  align in parallel
3.
•
Standard linear solid
One Maxwell model and one spring  align in
parallel.
Measurements of Shear Viscosity
•
•
•
•
•
Melt Flow Index
Capillary Rheometer
Coaxial Cylinder Viscometer (Couette)
Cone and Plate Viscometer (Weissenberg rheogoniometer)
Disk-Plate (or parallel plate) viscometer
Weissenberg Effect
Dough Climbing: Weissenberg Effect
Other effects:
Barus
Kaye
Courtesy: Dr. Osvaldo Campanella
Dynamic Mechanical Testing
Response for Classical Extremes
Purely Elastic Response
(Hookean Solid)
Purely Viscous
Response
(Newtonian Liquid)
 = 90°
 = 0°
Stress
Stress
Strain
Strain
Courtesy: TA Instruments
Dynamic Mechanical Testing Viscoelastic
Material Response
Phase angle
0° <  <
90°
Strain
Stress
Courtesy: TA Instruments
DMA Viscoelastic Parameters:
The Complex, Elastic, & Viscous Stress
The stress in a dynamic experiment is referred to as the
complex stress s*
The complex stress can be separated into two components:
1) An elastic stress in phase with the strain. s' = s*cos
s' is the degree to which material behaves like an elastic solid.
2) A viscous stress in phase with the strain rate. s" = s*sin
s" is the degree to which material behaves like an ideal liquid.
Phase angle 
Complex Stress, s*
Strain, 
s* = s' + is"
Courtesy: TA Instruments
DMA Viscoelastic Parameters
The Complex Modulus: Measure of
materials overall resistance to
deformation.
G* = Stress*/Strain
G* = G’ + iG”
The Elastic (Storage) Modulus:
Measure of elasticity of material. The
ability of the material to store energy.
G' = (stress*/strain)cos
The Viscous (loss) Modulus:
The ability of the material to dissipate
energy. Energy lost as heat.
G" = (stress*/strain)sin
Tan Delta:
Measure of material damping - such
as vibration or sound damping.
Tan = G"/G'
Courtesy: TA Instruments
DMA Viscoelastic Parameters: Damping, tan 
Dynamic measurement
represented as a vector
It can be seen here that
G* = (G’2 +G”2)1/2
G*
G"
Phase angle 
G'
The tangent of the phase angle is the ratio of the
loss modulus to the storage modulus.
tan  = G"/G'
"TAN DELTA" (tan ) is a measure of the
damping ability of the material.
Courtesy: TA Instruments
Frequency Sweep: Material Response
Terminal
Region
Rubbery
Plateau
Region
Transition
Region
Glassy Region
1
2
Storage Modulus (E' or G')
Loss Modulus (E" or G")
log Frequency (rad/s or Hz)
Courtesy: TA Instruments
Viscoelasticity in Uncrosslinked,
Amorphous Polymers
Logarithmic plots of G’ and G” against angular frequency for
uncrosslinked poly(n-octyl methacrylate) at 100°C (above Tg),
molecular weight 3.6x106.
Dynamic Characteristics of Rubber Compounds
•Why do E’ and E” vary with frequency and temperature?
– The extent to which a polymer chains can store/dissipate energy depends
on the rate at which the chain can alter its conformation and its
entanglements relative to the frequency of the load.
•Terminal Zone:
– Period of oscillation is so long that chains can snake through their
entanglement constraints and completely rearrange their conformations
•Plateau Zone:
– Strain is accommodated by entropic changes to polymer segments between
entanglements, providing good elastic response
•Transition Zone:
– The period of oscillation is becoming too short to allow for complete
rearrangement of chain conformation. Enough mobility is present for
substantial friction between chain segments.
•Glassy Zone:
– No configurational rearrangements occur within the period of oscillation.
Stress response to a given strain is high (glass-like solid) and tanis on the
order of 0.1
Dynamic Temperature Ramp or Step and
Hold: Material Response
Glassy Region
Transition
Region
Rubbery Plateau
Region
Terminal Region
1
Storage Modulus (E' or G')
2
Loss Modulus (E" or G")
Temperature
Courtesy: TA Instruments
One more time: Dynamic (Oscillatory) Testing
In the general case when the sample is deformed sinusoidally, as a
response the stress will also oscillate sinusoidally at the same frequency,
but in general will be shifted by a phase angle  with respect to the strain
wave. The phase angle will depend on the nature of the material
(viscous, elastic or viscoelastic)
Input
   o sin(t )
Response
t  t o sin(t  )
where 0°<<90°
t
stress

strain

viscosity
G
modulus
3.29
One more time: Dynamic (Oscillatory) Testing
By using trigonometry:
t  to sin(t  )  to sin(t )  to cos(t )
In-phase component of
the stress, representing
solid-like behavior
Let’s define:
where:
(3-1)
Out-of-phase component
of the stress,
representing liquid-like
behavior
to  G o and to  G o
in  phasestress to

, Elasticor Storage Modulus
maximumstrain  o
out  of  phasestress to
G() 
 , Viscous or LossModulus
maximumstrain
o
G() 
3.30
Physical Meaning of G’, G”
Equation (3-1) becomes:
t   o G() sin(t )  G" () cos(t )
We can also define the loss tangent:
G 
tan  
G
For solid-like response:
tspring  G  G o sin(t )
 G  G, G  0, tan  0,   0
For liquid-like response:
tdashpot     ocos(t )
G  0, G  , tan  ,   90
G’
storage modulus
G’’
loss modulus
Typical Oscillatory Data
Rubber
G’
G’
storage modulus
log G
G’’
G’’
log 
Rubbers – Viscoelastic solid response:
G’ > G” over the whole range of frequencies
loss modulus
Typical Oscillatory Data
Melt or solution
G0
G’
storage modulus
log G
G’’
loss modulus
G’’
G’
log 
Polymeric liquids (solutions or melts) Viscoelastic liquid response:
G” > G’ at low frequencies
Response becomes solid-like at high frequencies
G’ shows a plateau modulus and decreases with -2 in the limit of low
frequency (terminal region)
G” decreases with -1 in the limit of low frequency
Typical Oscillatory Data





For Rubbers – Viscoelastic solid
response:
G’ > G” over the whole range of
frequencies
For polymeric liquids (solutions
or melts) – Viscoelastic liquid
response:
G”>G’ at low frequencies
Response becomes solid-like at
high frequencies
G’ shows a plateau modulus and
decreases with -2 in the limit of
low frequency (terminal region)
G” decreases with -1 in the limit
of low frequency
•Sample is strained (pulled, ) rapidly
to pre-determined strain (s)
•Stress required to maintain this
strain over time is measured at
constant T
•Stress decreases with time due to
molecular relaxation processes
•Relaxation modulus defined as:
Er(t) = s(t)/e0
•Er(t) also a function
of temperature