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ELASTOMERIC IMPRESSION MATERIALS
PRESENTED BY
DR. SHAILJA SHARDA
MDS – I
DEPARTMENT OF PROSTHODONTICS, CROWN AND BRIDGE
BHARATI VIDYAPEETH DEEMED TO BE UNIVERSITY
DEFINITION
Elastomer : A polymer that has a
glass transition temperature that is
below its service temperature
(usually room temperature); these
materials are characterized by low
stiffness and extremely large
elastic strains.
Elastomeric impression material : A
group of flexible chemical
polymers that are either chemically
chemically or physically cross-
linked; generally, they can be easily
easily stretched and rapidly
recover their original dimensions
when applied stresses are released.
DEVELOPMENT
1950s
1955
1960s
Polyether impression
material developed in
Germany.
1970s
Addition silicone was
introduced as a dental
impression material.
1988
Latest addition and light cure
elastomers.
1990–2000
New auto devices and
delivery systems.
First elastomeric impression
material - Polysulfide
Condensation
silicone
IDEAL REQUISITES
Sufficiently fluid to
adapt to the oral
tissues
Viscous enough to be
contained in a tray
Able to transform (set)
into a rubbery or rigid
solid in the mouth in a
reasonable time (less
than 7 min).
Resistant to distortion
or tearing when
removed from the
mouth,
Dimensionally stable
long enough to allow
one or more casts to
be poured.
Biocompatible
Cost-effective in terms
of time as well as the
expense of the
associated processing
equipment.
CLINICAL
APPLICATION
 1) Impression material for all applications including
- Fixed partial dentures
- Dentulous and edentulous impressions
 2) Border moulding of special trays(polyether)
 3) Bite registration
 4) As duplicating material for refractory casts
INTRODUCTION TO ELASTOMERIC IMPRESSION MATERIALS
Also called as Rubber Base
Impression materials.
Elastomers are rubber like
materials with long chained
polymers, slightly crosslinked
& coiled having glass
transition temperature much
lower than room
temperatures.
Accepted in dentistry to
overcome 2 main problems
associated with Hydrocolloids
:
Poor tear resistance Poor dimensional stability
ELASTOMERIC
IMPRESSION
MATERIALS
Elastomers are of 3 types
1) POLYSULPHIDE
2) SILICONES :
a) Addition Silicones
b) Condensation Silicones.
3) POLYETHERS :
a) Light activated polyethers.
b) Chemically activated polyethers.
POLYSULPHIDES
First elastomeric
impression material to
be introduced.
Alternate names: a) Thiokol impression
material (By the name
of first manufacturer)
b) Mercaptan impression
material (by chemistry)
c) Vulcanizing
impression material (by
processing terminology).
Viscosities – light,
medium, heavy.
Commercial names -
permlastic, coe-
flex, omniflex.
COMPOSITION
THE BASE
Polysulphide polymer (-SH, mercaptan group) Principal ingredient
Titanium oxide and zinc Fillers
Sulphate, copper carbonate or silica Strengthener
Dibutyl pthalate Plasticizer
THE ACCELERATOR
Lead dioxide Reactor, gives it characteristic brown colour
Sulphur Promoter, accelerates the reaction
Oleic acid or Stearic acid Reactor, controls setting reaction
PROPERTIES
BIOLOGICAL:
1) Non toxic, non
poisonous.
2) Bad odor due to
lead dioxide &
Mercaptan group.
3) Easy to disinfect
(glutaraldehyde)
RHEOLOGICAL
PROPERTIES:
1) Available in variety
of viscosities (Low,
Medium, Heavy in
increasing order of
filler content)
2) Working time = 3-
6 min
3) Setting time = 10-
20 min.
PROPERTIES
MECHANICAL
PROPERTIES:
1) Highly flexible of all
the elastomers.
2) Elastic recovery
improves with time
(viscoelasticity).
3) High tear strength.
4) Not dimensionally
stable. Curing shrinkage
– high and continues
after setting ; highest
permanent deformation.
5) Hardness increases by
increasing filler content.
Hydrophobic.
1) LONGER WORKING
TIME.
2) HIGHEST
FLEXIBILITY.
3) HIGHEST TEAR
STRENGTH.
4) CAN BE
ELECTROPLATED
WITH SILVER.
5) LONG SHELF LIFE. 6) INEXPENSIVE AS
COMPARED TO
OTHER ELASTOMERS.
ADVANTAGES
DISADVANTAGES
1) Unpleasant
odour and taste.
2) Long setting
time.
3) Dimensional
change due to
loss of by-
product.
4) Cloth staining.
5) Multiple die
pouring not
accurate.
POLYETHER
 Polyether was introduced in Germany in 1960.
 Commercial names are, Impregum, Remitec, Polyjel etc.
 Polyether is available in 3 viscosities (Light, Regular and heavy
body)
 Dispensed as 3 paste system
 1) Base paste.
 2) Reactor/Accelerator paste.
 3) Modifier (thinner) paste.
COMPOSITION
BASE
Polyether polymer Cross-linked to form rubber
Colloidal silica Acts as filler
Glycol (ether) or pthalate Plasticizer
ACCELERATOR
Alkyl aromatic sulfonate Initiates cross-linking
Colloidal silica Filler
Pthalate Plasticizer
PROPERTIES
BIOLOGICAL:
1) Nontoxic, Non poisonous.
2) Pleasant Odor and Colour
3) Can cause irritation due to presence of aromatic sulphonic acid catalyst in
reactor paste.
4) Can cause hypersensitivity in some patients due to presence of ethylene
imine rings in base paste.
RHEOLOGICAL:
1) Available in 3 consistencies (L,R & Heavy body)
2) Flow after 1 hour is < 0.03%
MECHANICAL
PROPERTIES
1) Elastic recovery
=98.9%
2) Permanent
deformation is 0.8-
1.6%
3) Flexibility is low
(3%)
4) Mixing time is
45 sec to 1 minute.
5) Working time is
2 minutes; Setting
time is 6-
8 minutes.
6)hydrophilic
7) Good
dimensional
stability due to
a) Addition
polymerization
reaction.
b) Less
polymerization
shrinkage.
ADVANTAGES
Good pseudoplastic
properties i.e. same
mixture can be used
as tray as well as
syringe material.
Dimensionally stable.
Less polymerization
shrinkage.
No by product
formed.
Pour more accurate
casts.
Multiple cast pouring
is possible.
Cast pouring can be
delayed for few
hours, even a week.
Long shelf life.
Catalyst can
be sensitive to
some patients.
Electroplating
not easy.
Low tear
strength.
High stiffness.
Very expensive
when
compared with
other
elastomers.
DISADVANTAGES
LIGHT ACTIVATED
POLYETHER
 It was introduced in
1988.
 Available in 2
viscosities.
Light body supplied in
syringes.
Heavy body supplied
as tubes
INGREDIENT FUNCTION
Urethane
dimethacrylate
elastomer resin
Visible light curing
polyether
Champhoroquinone Photoiniator
Dimethyl amino ethyl
methacrylate
Photoaccelerator
Silicon dioxide Fillers
Excellent elasticity.
It has operator
control over the
polymerization.
Infinite working
time.
Short setting time.
Low volume
shrinkage on
setting.
Impression can be
stored upto 2
weeks.
PROPERTIES
CONDENSATION SILICONE
INTRODUCTION
First type of silicone
material ; also known
as conventional
silicone.
Also known as RTV
silicone (room
temperature
vulcanization
silicone)
Available as : - Two- paste system
- Base paste(larger)
and catalyst
paste (smaller tube)
- Two putty system.
Viscosities - light,
medium, putty.
Commerical names -
Sil 21, coltex
COMPOSITION
BASE CATALYST
• Polydimethyl siloxane - undergoes cross
linking to form rubber
• Colloidal silica – filler
• Colour pigments
• Tetra ethyl alkyl silicates
• Stannous octoate
SETTING REACTION
Dimethyl siloxane
+
Orthoethyl silicate
Silicone rubber
+
Ethyl alcohol
PROPERTIES
Biological : non-
toxic.
pleasant color
and odor.
Mechanical:
Stiffer than
plosulfide.
Dimensional
stability: poor
due to loss of by-
product.
Hydrophobic
Setting time: 6-9
mins, mixing
time: 45s
ADDITION SILICONE
INTRODUCTION
Also called polyvinyl
siloxane or vinyl poly-
siloxane impression
material, most widely
used elastomer.
They have better
properties than
condensation silicone.
Available in four
viscosities : Light
bodied, medium
bodied , heavy
bodied and putty.
Commercial names-
reprosil, provil,
president.
Supplied as- tubes
(base& catalyst),
cartridges form with
static mixing tips,
Putty jars
COMPOSITION
BASE ACCELERATOR
• Polymethylhydrosiloxane
• Divinylpolysiloxane
• Fillers
• Divinylpolysiloxane
• Platinum
• Fillers
• Palladium
SETTING REACTION
No reaction byproduct unlike condensation silicone
Residual polymethylsiloxane can undergo secondary reaction with each other or with
moisture and produce hydrogen gas
They do not affect the dimensional stability ; but can cause pinpoint voids in the
gypsum casts
Palladium is added in the catalyst paste which acts as hydrogen scavenger.
PROPERTIES
Biological: avoid
skin contact, can
cause allergic
reaction.
Plesant odor
& color.
Mechanical:
Best dimensional
stability.
Hydrophobic, added
surfactant makes it
hydrophilic.
Setting time: 5-9
mins, mixing time:
45s
MAKING
IMPRESSIONS
Preparing
a tray
01
Managing
tissue
02
Preparing
the
material
03
Making an
impression
04
Removing
the
impression
05
Preparing
stone casts
and dies
06
STEPS IN MAKING IMPRESSION :
IMPRESSION TRAYS
Stock tray or custom tray
can be used to record
impression
Custom tray allows
uniform distribution of
material between the
tray and the object that
improves accuracy
Addition silicone doesn’t
need custom tray,
disposable stock tray
can be used
Prior to making an
impression uniform
thickness of tray
adhesive is applied on
the tray and allowed to
dry
MIXING
SYSTEMS
3 types of systems are available to
mix catalyst and base thoroughly.
1. Hand mixing system.
2. Static mixing system.
3. Dynamic mechanical mixing
system.
1. Impression pastes
are dispensed from
collapsible tubes.
2. Equal lengths of
catalyst and base
paste are dispensed
on a paper pad.
3. Initial mixing is
accomplished with
a circular motion.
4. Final mixing is
done with broad
strokes of spatula.
5. Final mix should
be smooth.
6. Mixing is readily
accomplished in 45
seconds.
All 4 types of
elastomers are
available for mixing
in this fashion.
HAND MIXING SYSTEM
2. STATIC MIXING
This technique transforms two fluid material into a homogenous mix
Mixing is done with a help of a gun with two-cylinder cartridge, and a mixing tip
Porosities due to mixing with air can be avoided as no mechanical mixing is involved
It provides greater uniformity in proportioning and mixing, yields fewer voids in the mix and
reduces the mixing time
Lesser possibilities of contamination of the material
Mixed material is directly injected into adhesive coated tray or onto the prepared teeth
3. DYNAMIC
MECHANICAL
MIXING
The device uses a motor to drive parallel
plungers, forcing the materials into a mixing
top and out into an impression tray or syringe
Thorough mixing of the higher viscosity
materials can be achieved by minimal effort
Both polyether and addition silicone
impression materials of various viscosities are
available with this dispensing system
MAKING AN IMPRESSION
MULTIPLE MIX TECHNIQUE
• Light body and heavy body are used in this technique
; mixed by different person. But with the mechanical
devices it can be done by single person
• Lighter material is injected from the static mixing gun
within and around the tooth preparation. Filled tray is
then inserted in the mouth and seated over the
syringe material
• If partially set material is seated, it will be
compressed elastically and cause spring back of the
1. Often taken with medium viscosity material.
2. When forced through impression syringe, the viscosity
decreases but when used with tray the viscosity is
unaffected.
3. Addition silicones and Poly ethers are well suited for
this technique.
SINGLE VISCOSITY
TECHNIQUE (Monophase):
PUTTY WASH TECHNIQUE
Originally developed for condensation
silicone to minimize the dimensional
changes
Preliminary impression made with thick
putty material ; will serve as intra oral
custom made tray
Space for the light body is then provided
by this polyethylene sheet as a spacer or
by cutting away some of the putty
Then thin consistency wash material is
placed into the putty impression and on to
the preparation, then the tray is seated
REMOVAL OF THE IMPRESSION
Viscoelastic property
of the elastomers have
to be considered
01
It is necessary to use a
quick snap to
minimise plastic
deformation of the
impression
02
Should not be
removed until the
curing has progressed
sufficiently to provide
adequate elasticity to
prevent distortion
03
DISINFECTION
Rubber impression materials
: 10 mins in 2%
Glutaraldehyde, 3 mins
in Chlorine compounds;
other disinfectants-
iodophors and phenolics can
be used.
Disinfection time should be
short to prevent any loss of
surface quality or accuracy
Long immersion may cause
the surfactant in the
hydrophilic polyvinyl
siloxane to leach out.
RECENT ADVANCES
VINYL POLYETHER SILOXANE
• Combination of polyether and polyvinylsiloxane
• This new elastomer boasts of immediate hydrophilicity, at the same time
combining favourable characteristics of both polyether and vinyl poly-
siloxane.
• Optimized elastomeric properties: dimensionally accurate recovery and
easy removal from the mouth.
REFERENCE
 Impression materials, Phillips' science of Dental
Materials
 Elastomeric Impression materials, Basic Dental
Materials, John J. Manappallil
 Vinyl polysiloxane ether : a breakthrough in elastomeric
impression materials, Dr. Mohan Shetty, Dr. Ganesh R.
Bhandari, Dr. Deepak Mehta
 Comparative evaluation of dimensional accuracy of
addition silicone and condensation silicone impression
materials - An invitro study, Dr. Pramod Joshi, Dr, Bhat
GS, Dr. Shenoy V
THANK YOU!

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ELASTOMERS.pptx

  • 1. ELASTOMERIC IMPRESSION MATERIALS PRESENTED BY DR. SHAILJA SHARDA MDS – I DEPARTMENT OF PROSTHODONTICS, CROWN AND BRIDGE BHARATI VIDYAPEETH DEEMED TO BE UNIVERSITY
  • 2. DEFINITION Elastomer : A polymer that has a glass transition temperature that is below its service temperature (usually room temperature); these materials are characterized by low stiffness and extremely large elastic strains. Elastomeric impression material : A group of flexible chemical polymers that are either chemically chemically or physically cross- linked; generally, they can be easily easily stretched and rapidly recover their original dimensions when applied stresses are released.
  • 3. DEVELOPMENT 1950s 1955 1960s Polyether impression material developed in Germany. 1970s Addition silicone was introduced as a dental impression material. 1988 Latest addition and light cure elastomers. 1990–2000 New auto devices and delivery systems. First elastomeric impression material - Polysulfide Condensation silicone
  • 4. IDEAL REQUISITES Sufficiently fluid to adapt to the oral tissues Viscous enough to be contained in a tray Able to transform (set) into a rubbery or rigid solid in the mouth in a reasonable time (less than 7 min). Resistant to distortion or tearing when removed from the mouth, Dimensionally stable long enough to allow one or more casts to be poured. Biocompatible Cost-effective in terms of time as well as the expense of the associated processing equipment.
  • 5. CLINICAL APPLICATION  1) Impression material for all applications including - Fixed partial dentures - Dentulous and edentulous impressions  2) Border moulding of special trays(polyether)  3) Bite registration  4) As duplicating material for refractory casts
  • 6. INTRODUCTION TO ELASTOMERIC IMPRESSION MATERIALS Also called as Rubber Base Impression materials. Elastomers are rubber like materials with long chained polymers, slightly crosslinked & coiled having glass transition temperature much lower than room temperatures. Accepted in dentistry to overcome 2 main problems associated with Hydrocolloids : Poor tear resistance Poor dimensional stability
  • 7. ELASTOMERIC IMPRESSION MATERIALS Elastomers are of 3 types 1) POLYSULPHIDE 2) SILICONES : a) Addition Silicones b) Condensation Silicones. 3) POLYETHERS : a) Light activated polyethers. b) Chemically activated polyethers.
  • 8. POLYSULPHIDES First elastomeric impression material to be introduced. Alternate names: a) Thiokol impression material (By the name of first manufacturer) b) Mercaptan impression material (by chemistry) c) Vulcanizing impression material (by processing terminology). Viscosities – light, medium, heavy. Commercial names - permlastic, coe- flex, omniflex.
  • 9. COMPOSITION THE BASE Polysulphide polymer (-SH, mercaptan group) Principal ingredient Titanium oxide and zinc Fillers Sulphate, copper carbonate or silica Strengthener Dibutyl pthalate Plasticizer THE ACCELERATOR Lead dioxide Reactor, gives it characteristic brown colour Sulphur Promoter, accelerates the reaction Oleic acid or Stearic acid Reactor, controls setting reaction
  • 10. PROPERTIES BIOLOGICAL: 1) Non toxic, non poisonous. 2) Bad odor due to lead dioxide & Mercaptan group. 3) Easy to disinfect (glutaraldehyde) RHEOLOGICAL PROPERTIES: 1) Available in variety of viscosities (Low, Medium, Heavy in increasing order of filler content) 2) Working time = 3- 6 min 3) Setting time = 10- 20 min.
  • 11. PROPERTIES MECHANICAL PROPERTIES: 1) Highly flexible of all the elastomers. 2) Elastic recovery improves with time (viscoelasticity). 3) High tear strength. 4) Not dimensionally stable. Curing shrinkage – high and continues after setting ; highest permanent deformation. 5) Hardness increases by increasing filler content. Hydrophobic.
  • 12. 1) LONGER WORKING TIME. 2) HIGHEST FLEXIBILITY. 3) HIGHEST TEAR STRENGTH. 4) CAN BE ELECTROPLATED WITH SILVER. 5) LONG SHELF LIFE. 6) INEXPENSIVE AS COMPARED TO OTHER ELASTOMERS. ADVANTAGES
  • 13. DISADVANTAGES 1) Unpleasant odour and taste. 2) Long setting time. 3) Dimensional change due to loss of by- product. 4) Cloth staining. 5) Multiple die pouring not accurate.
  • 14. POLYETHER  Polyether was introduced in Germany in 1960.  Commercial names are, Impregum, Remitec, Polyjel etc.  Polyether is available in 3 viscosities (Light, Regular and heavy body)  Dispensed as 3 paste system  1) Base paste.  2) Reactor/Accelerator paste.  3) Modifier (thinner) paste.
  • 15. COMPOSITION BASE Polyether polymer Cross-linked to form rubber Colloidal silica Acts as filler Glycol (ether) or pthalate Plasticizer ACCELERATOR Alkyl aromatic sulfonate Initiates cross-linking Colloidal silica Filler Pthalate Plasticizer
  • 16. PROPERTIES BIOLOGICAL: 1) Nontoxic, Non poisonous. 2) Pleasant Odor and Colour 3) Can cause irritation due to presence of aromatic sulphonic acid catalyst in reactor paste. 4) Can cause hypersensitivity in some patients due to presence of ethylene imine rings in base paste. RHEOLOGICAL: 1) Available in 3 consistencies (L,R & Heavy body) 2) Flow after 1 hour is < 0.03%
  • 17. MECHANICAL PROPERTIES 1) Elastic recovery =98.9% 2) Permanent deformation is 0.8- 1.6% 3) Flexibility is low (3%) 4) Mixing time is 45 sec to 1 minute. 5) Working time is 2 minutes; Setting time is 6- 8 minutes. 6)hydrophilic 7) Good dimensional stability due to a) Addition polymerization reaction. b) Less polymerization shrinkage.
  • 18. ADVANTAGES Good pseudoplastic properties i.e. same mixture can be used as tray as well as syringe material. Dimensionally stable. Less polymerization shrinkage. No by product formed. Pour more accurate casts. Multiple cast pouring is possible. Cast pouring can be delayed for few hours, even a week. Long shelf life.
  • 19. Catalyst can be sensitive to some patients. Electroplating not easy. Low tear strength. High stiffness. Very expensive when compared with other elastomers. DISADVANTAGES
  • 20. LIGHT ACTIVATED POLYETHER  It was introduced in 1988.  Available in 2 viscosities. Light body supplied in syringes. Heavy body supplied as tubes INGREDIENT FUNCTION Urethane dimethacrylate elastomer resin Visible light curing polyether Champhoroquinone Photoiniator Dimethyl amino ethyl methacrylate Photoaccelerator Silicon dioxide Fillers
  • 21. Excellent elasticity. It has operator control over the polymerization. Infinite working time. Short setting time. Low volume shrinkage on setting. Impression can be stored upto 2 weeks. PROPERTIES
  • 23. INTRODUCTION First type of silicone material ; also known as conventional silicone. Also known as RTV silicone (room temperature vulcanization silicone) Available as : - Two- paste system - Base paste(larger) and catalyst paste (smaller tube) - Two putty system. Viscosities - light, medium, putty. Commerical names - Sil 21, coltex
  • 24. COMPOSITION BASE CATALYST • Polydimethyl siloxane - undergoes cross linking to form rubber • Colloidal silica – filler • Colour pigments • Tetra ethyl alkyl silicates • Stannous octoate
  • 25. SETTING REACTION Dimethyl siloxane + Orthoethyl silicate Silicone rubber + Ethyl alcohol
  • 26. PROPERTIES Biological : non- toxic. pleasant color and odor. Mechanical: Stiffer than plosulfide. Dimensional stability: poor due to loss of by- product. Hydrophobic Setting time: 6-9 mins, mixing time: 45s
  • 28. INTRODUCTION Also called polyvinyl siloxane or vinyl poly- siloxane impression material, most widely used elastomer. They have better properties than condensation silicone. Available in four viscosities : Light bodied, medium bodied , heavy bodied and putty. Commercial names- reprosil, provil, president. Supplied as- tubes (base& catalyst), cartridges form with static mixing tips, Putty jars
  • 29. COMPOSITION BASE ACCELERATOR • Polymethylhydrosiloxane • Divinylpolysiloxane • Fillers • Divinylpolysiloxane • Platinum • Fillers • Palladium
  • 30. SETTING REACTION No reaction byproduct unlike condensation silicone Residual polymethylsiloxane can undergo secondary reaction with each other or with moisture and produce hydrogen gas They do not affect the dimensional stability ; but can cause pinpoint voids in the gypsum casts Palladium is added in the catalyst paste which acts as hydrogen scavenger.
  • 31. PROPERTIES Biological: avoid skin contact, can cause allergic reaction. Plesant odor & color. Mechanical: Best dimensional stability. Hydrophobic, added surfactant makes it hydrophilic. Setting time: 5-9 mins, mixing time: 45s
  • 32.
  • 35. IMPRESSION TRAYS Stock tray or custom tray can be used to record impression Custom tray allows uniform distribution of material between the tray and the object that improves accuracy Addition silicone doesn’t need custom tray, disposable stock tray can be used Prior to making an impression uniform thickness of tray adhesive is applied on the tray and allowed to dry
  • 36. MIXING SYSTEMS 3 types of systems are available to mix catalyst and base thoroughly. 1. Hand mixing system. 2. Static mixing system. 3. Dynamic mechanical mixing system.
  • 37. 1. Impression pastes are dispensed from collapsible tubes. 2. Equal lengths of catalyst and base paste are dispensed on a paper pad. 3. Initial mixing is accomplished with a circular motion. 4. Final mixing is done with broad strokes of spatula. 5. Final mix should be smooth. 6. Mixing is readily accomplished in 45 seconds. All 4 types of elastomers are available for mixing in this fashion. HAND MIXING SYSTEM
  • 38. 2. STATIC MIXING This technique transforms two fluid material into a homogenous mix Mixing is done with a help of a gun with two-cylinder cartridge, and a mixing tip Porosities due to mixing with air can be avoided as no mechanical mixing is involved It provides greater uniformity in proportioning and mixing, yields fewer voids in the mix and reduces the mixing time Lesser possibilities of contamination of the material Mixed material is directly injected into adhesive coated tray or onto the prepared teeth
  • 39.
  • 40. 3. DYNAMIC MECHANICAL MIXING The device uses a motor to drive parallel plungers, forcing the materials into a mixing top and out into an impression tray or syringe Thorough mixing of the higher viscosity materials can be achieved by minimal effort Both polyether and addition silicone impression materials of various viscosities are available with this dispensing system
  • 41.
  • 42. MAKING AN IMPRESSION MULTIPLE MIX TECHNIQUE • Light body and heavy body are used in this technique ; mixed by different person. But with the mechanical devices it can be done by single person • Lighter material is injected from the static mixing gun within and around the tooth preparation. Filled tray is then inserted in the mouth and seated over the syringe material • If partially set material is seated, it will be compressed elastically and cause spring back of the
  • 43. 1. Often taken with medium viscosity material. 2. When forced through impression syringe, the viscosity decreases but when used with tray the viscosity is unaffected. 3. Addition silicones and Poly ethers are well suited for this technique. SINGLE VISCOSITY TECHNIQUE (Monophase):
  • 44. PUTTY WASH TECHNIQUE Originally developed for condensation silicone to minimize the dimensional changes Preliminary impression made with thick putty material ; will serve as intra oral custom made tray Space for the light body is then provided by this polyethylene sheet as a spacer or by cutting away some of the putty Then thin consistency wash material is placed into the putty impression and on to the preparation, then the tray is seated
  • 45.
  • 46. REMOVAL OF THE IMPRESSION Viscoelastic property of the elastomers have to be considered 01 It is necessary to use a quick snap to minimise plastic deformation of the impression 02 Should not be removed until the curing has progressed sufficiently to provide adequate elasticity to prevent distortion 03
  • 47. DISINFECTION Rubber impression materials : 10 mins in 2% Glutaraldehyde, 3 mins in Chlorine compounds; other disinfectants- iodophors and phenolics can be used. Disinfection time should be short to prevent any loss of surface quality or accuracy Long immersion may cause the surfactant in the hydrophilic polyvinyl siloxane to leach out.
  • 49. VINYL POLYETHER SILOXANE • Combination of polyether and polyvinylsiloxane • This new elastomer boasts of immediate hydrophilicity, at the same time combining favourable characteristics of both polyether and vinyl poly- siloxane. • Optimized elastomeric properties: dimensionally accurate recovery and easy removal from the mouth.
  • 50.
  • 51. REFERENCE  Impression materials, Phillips' science of Dental Materials  Elastomeric Impression materials, Basic Dental Materials, John J. Manappallil  Vinyl polysiloxane ether : a breakthrough in elastomeric impression materials, Dr. Mohan Shetty, Dr. Ganesh R. Bhandari, Dr. Deepak Mehta  Comparative evaluation of dimensional accuracy of addition silicone and condensation silicone impression materials - An invitro study, Dr. Pramod Joshi, Dr, Bhat GS, Dr. Shenoy V