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Kalyan Maity.
91 / OLT / 091013
 The most important thermoset material used for the
preparation of molding compounds , adhesives ,
coatings.
 The most common type of resin for composites and
marine services.
 The least expensive composite resin.
 The easiest-to-cure composite resin.
 Polyesters are made from two types of monomers:
 Di-acids
 Glycols
+ acid + glycol + acid + glycol +... => ...acidglycolacidglyc
ol... + n water
 one stage process.
 The conventional technique results both high and low
molecular weight fractions.
 The high-molecular-weight resin fractions raise the
viscosity .
 The low-molecular-weight fraction are detrimental to
both coating performance and enamel solids or
volatile organic content(VOC) due to volatisation
during cure
 Condensation time : 8-30 hours
 Water removal is enhanced by vacuum or nitrogen
stripping .
Monomers
Glycols G
(di-alcohols)
Acids A
(di-acids)
G
G
G
G
A
A
A
A
A
Polyester polymer
 Di-acids have active -OH groups on both ends.
 Glycols have active -H groups on both ends.
 One end of the di-acid (the OH group) reacts with
one end of the glycol (the H group) to form water
(H−OH) .
 The water separates from the polymer and condenses
out as a liquid.
 This type of polymerization reactions are called
condensation reactions.
OH C A C OH
O O
1st Step
O C A C OH
O O
OH C A C OH
O O
Many Steps
( )
Ester
Di-acid
Ester Ester Ester
Di-acid
Di-acid
Di-acid
Ester (new bond)
O ...O C A C O
O O
... O C A C
O O
O
HO G OH
Glycol
HO-G
HO G OH
Glycol
G G
GlycolGlycol
Di-Acids/Anhydrides Attributes
Maleic/Fumaric Unsaturation (crosslink sites)
Orthophthalic Low cost, styrene compatibility
Isophthalic Toughness,
water/chemical resistance
Terephthalic High HDT
Adipic Flexibility, toughness
Brominated Flammability resistance
Glycols Attributes
Ethylene Low cost, rigidity
Propylene Excellent styrene compatibility
Dipropylene Flexibility, toughness
Diethylene Flexibility
Neopentyl UV stability, water/chemical resistance
Bis-phenol A Water/chemical resistance, strength
Solvents Attributes
Styrene Cost
Vinyl toluene Strength, stiffness
Acrylic (PMMA) Low flammability, flexibility
 The relatively easy accessible raw materials - PTA or
DMT and MEG.
 The very well understood and described simple
chemical process of polyester synthesis.
 The low toxicity level of all raw materials and side
products during polyester production and processing.
 The possibility to produce PET in a closed loop at low
emissions to the environment.
 The outstanding mechanical and chemical properties
of polyester.
 The recyclability.
 The wide variety of intermediate and final products
made of polyester.
Modifications of unsaturated polyester resins have been
done in order to-
 achieve lower styrene emission.
 better styrene solubility.
 lower processing viscosity.
Two concepts are used:-
 Introduction of liquid crystalline segments into the
unsaturated polyester.
 End-capping the unsaturated polyester with
poly(ethylene glycol)ols of various molar mass.
C C C
C
Unsaturated portion
Polyesters must have unsaturated portions to
crosslink
 Initiators are sometimes called catalysts.
 The crosslinking reaction is began when an initiator
reacts with the double bond.
 The most common initiators are peroxides.
 The peroxides are effective initiators because they split
into free radicals (i.e. they have unshared electrons)
which react easily with the double bonds.
C C C
C
IInitiator ●
C C C
CI
●●
●
C C C
CI
●
Bond (2 electrons)
Unshared electron
C C C
CI
*
Free radical (unshared (unbonded) electron)
Free radicals react readily with any
Carbon-carbon double bond they encounter
 To react and form a crosslink, the free radical on the
polymer needs to encounter (collide with) a double bond
on another polymer.
 The polymers are long and entangled (highly viscous),
thus they don’t move very quickly.
 The polymers are bulky and it is hard to get the free
radical into the area of the double bond.
 Dissolve (dilute) the polymer with a solvent so that
the polymers can move around freely.
◦ Ideally, the solvent will react during the cross-linking
reaction so that it does not need to be removed from the
solid.
◦ These types of solvents are called “reactive solvents” or
“reactive diluents” or “co-reactants”.
 Added benefit:
◦ The solvent will also reduce the viscosity so that the
polymer will wet the fibres more easily.
 Styrene is the most common solvent for polyesters.
 The styrene reacts (is consumed) during the crosslinking
reaction because the styrene contains a double bond and
reacts with the free radical.
 The styrene serves as a bridge molecule between the polymer
chains (as part of the crosslink)
 There may be as many as 8 styrene molecules in a bridge.
C
C
C
C
C
C
C C
C C C
CI
The styrene is a bridge molecule between the polyester polymers
Styrene
C C C
C
New free radical*
New bonds
(crosslink)
The new free radical is available to react with another styrene
 Called addition or free radical cross-linking reaction.
 Proceeds as a chain reaction.
◦ Once started, it will keep going unless specifically terminated.
◦ Doesn’t need more initiator .
◦ Makes its own reactive sites.
 Inhibitors are added, usually by the resin
manufacturer, to slow down the cross-linking
reaction.
◦ Inhibitors typically absorb free radicals.
◦ Inhibitors protect the polymer during storage because
sunlight, heat, contaminants, etc. can start the curing
reaction.
◦ Molders must add sufficient initiator to overcome the
inhibitors and to cause the cross-linking to occur.
 Styrene produces the following complaints:
A.Considerable de-fatting of the skin.
B.Irritation of the mucous membrane of the eyes, nose,
throat, and trachea .
C.Narcosis ("styrene sickness").
precaution must be taken during polyester
resin handling.
 Flame Retardant UP-Formulations.
 VOC Emissions (volatile organic compounds).
 Odourless UP-resins and UP-Networks.
 Further Activities related to Human Health and Well Being.
A number of factors are creating opportunities to develop
new high performance polyesters at lower cost.
 Health concerns over bisphenol-A are also opening
the door for the use of polyesters in traditional epoxy
applications, such as interior can coatings.
 Strong growth in powder coatings, composites and coil
are increasing the market need for polyesters.
KALYAN MAITY.

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03 Polyesters - final

  • 1. Kalyan Maity. 91 / OLT / 091013
  • 2.  The most important thermoset material used for the preparation of molding compounds , adhesives , coatings.  The most common type of resin for composites and marine services.  The least expensive composite resin.  The easiest-to-cure composite resin.
  • 3.  Polyesters are made from two types of monomers:  Di-acids  Glycols + acid + glycol + acid + glycol +... => ...acidglycolacidglyc ol... + n water  one stage process.  The conventional technique results both high and low molecular weight fractions.
  • 4.  The high-molecular-weight resin fractions raise the viscosity .  The low-molecular-weight fraction are detrimental to both coating performance and enamel solids or volatile organic content(VOC) due to volatisation during cure  Condensation time : 8-30 hours  Water removal is enhanced by vacuum or nitrogen stripping .
  • 6.  Di-acids have active -OH groups on both ends.  Glycols have active -H groups on both ends.  One end of the di-acid (the OH group) reacts with one end of the glycol (the H group) to form water (H−OH) .  The water separates from the polymer and condenses out as a liquid.  This type of polymerization reactions are called condensation reactions.
  • 7. OH C A C OH O O 1st Step O C A C OH O O OH C A C OH O O Many Steps ( ) Ester Di-acid Ester Ester Ester Di-acid Di-acid Di-acid Ester (new bond) O ...O C A C O O O ... O C A C O O O HO G OH Glycol HO-G HO G OH Glycol G G GlycolGlycol
  • 8. Di-Acids/Anhydrides Attributes Maleic/Fumaric Unsaturation (crosslink sites) Orthophthalic Low cost, styrene compatibility Isophthalic Toughness, water/chemical resistance Terephthalic High HDT Adipic Flexibility, toughness Brominated Flammability resistance
  • 9. Glycols Attributes Ethylene Low cost, rigidity Propylene Excellent styrene compatibility Dipropylene Flexibility, toughness Diethylene Flexibility Neopentyl UV stability, water/chemical resistance Bis-phenol A Water/chemical resistance, strength
  • 10. Solvents Attributes Styrene Cost Vinyl toluene Strength, stiffness Acrylic (PMMA) Low flammability, flexibility
  • 11.  The relatively easy accessible raw materials - PTA or DMT and MEG.  The very well understood and described simple chemical process of polyester synthesis.  The low toxicity level of all raw materials and side products during polyester production and processing.
  • 12.  The possibility to produce PET in a closed loop at low emissions to the environment.  The outstanding mechanical and chemical properties of polyester.  The recyclability.  The wide variety of intermediate and final products made of polyester.
  • 13. Modifications of unsaturated polyester resins have been done in order to-  achieve lower styrene emission.  better styrene solubility.  lower processing viscosity. Two concepts are used:-  Introduction of liquid crystalline segments into the unsaturated polyester.  End-capping the unsaturated polyester with poly(ethylene glycol)ols of various molar mass.
  • 14. C C C C Unsaturated portion Polyesters must have unsaturated portions to crosslink
  • 15.  Initiators are sometimes called catalysts.  The crosslinking reaction is began when an initiator reacts with the double bond.  The most common initiators are peroxides.  The peroxides are effective initiators because they split into free radicals (i.e. they have unshared electrons) which react easily with the double bonds.
  • 18. C C C CI ● Bond (2 electrons) Unshared electron
  • 19. C C C CI * Free radical (unshared (unbonded) electron) Free radicals react readily with any Carbon-carbon double bond they encounter
  • 20.  To react and form a crosslink, the free radical on the polymer needs to encounter (collide with) a double bond on another polymer.  The polymers are long and entangled (highly viscous), thus they don’t move very quickly.  The polymers are bulky and it is hard to get the free radical into the area of the double bond.
  • 21.  Dissolve (dilute) the polymer with a solvent so that the polymers can move around freely. ◦ Ideally, the solvent will react during the cross-linking reaction so that it does not need to be removed from the solid. ◦ These types of solvents are called “reactive solvents” or “reactive diluents” or “co-reactants”.  Added benefit: ◦ The solvent will also reduce the viscosity so that the polymer will wet the fibres more easily.
  • 22.  Styrene is the most common solvent for polyesters.  The styrene reacts (is consumed) during the crosslinking reaction because the styrene contains a double bond and reacts with the free radical.  The styrene serves as a bridge molecule between the polymer chains (as part of the crosslink)  There may be as many as 8 styrene molecules in a bridge. C C C C C C C C
  • 23. C C C CI The styrene is a bridge molecule between the polyester polymers Styrene C C C C New free radical* New bonds (crosslink) The new free radical is available to react with another styrene
  • 24.  Called addition or free radical cross-linking reaction.  Proceeds as a chain reaction. ◦ Once started, it will keep going unless specifically terminated. ◦ Doesn’t need more initiator . ◦ Makes its own reactive sites.
  • 25.  Inhibitors are added, usually by the resin manufacturer, to slow down the cross-linking reaction. ◦ Inhibitors typically absorb free radicals. ◦ Inhibitors protect the polymer during storage because sunlight, heat, contaminants, etc. can start the curing reaction. ◦ Molders must add sufficient initiator to overcome the inhibitors and to cause the cross-linking to occur.
  • 26.  Styrene produces the following complaints: A.Considerable de-fatting of the skin. B.Irritation of the mucous membrane of the eyes, nose, throat, and trachea . C.Narcosis ("styrene sickness").
  • 27. precaution must be taken during polyester resin handling.
  • 28.  Flame Retardant UP-Formulations.  VOC Emissions (volatile organic compounds).  Odourless UP-resins and UP-Networks.  Further Activities related to Human Health and Well Being.
  • 29. A number of factors are creating opportunities to develop new high performance polyesters at lower cost.  Health concerns over bisphenol-A are also opening the door for the use of polyesters in traditional epoxy applications, such as interior can coatings.  Strong growth in powder coatings, composites and coil are increasing the market need for polyesters.