Transitions in polymers Flashcards

1
Q

Polymer definition

A

A polymer is a large, chain-like molecule made up of monomers, which are small molecules
We can find ‘natural’ and ‘synthetic’ polymers

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2
Q

Natural polymers

A
Collagen
Silk
Natural rubber
DNA
Protein
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3
Q

Synthetic polymers

A

Everywhere
Polystyrene
Polyamide
Low-density polymer

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4
Q

Applications in dentistry

A
Dentures (bases, liners, artificial teeth)
Cavity filling materials (composites)
Sealants
Impression materials
Cements (resin based)
Orthodontics (elastics)
Equipment (mixing bowl)
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5
Q

Denture base acrylic

A

Denture-base material –> pouring –> typical acrylic denture

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6
Q

Denture resins

A

1853 Vulcanised rubber introduced
1890 Gutta-percha temp crowns and cavity fillings, root canal filling materials
1936 PMMA introduced
1940 Room-T PMs e.g. bis-GMA (self-curing prosthetic and restorative resins)
1950 Self-curing dimethacrylates reinforced by dispersed phase ceramic particle ‘filler’ in late 50s

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7
Q

PMMA uses

A

Bone cements
Contact and intraocular lens
Screw fixation in bone
Filler for bone cavities and skull defects
Vertebrae stabilisation in osteoporotic patients

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8
Q

PMMA advantages

A

Good mechanical properties (rigidity, strength, wear resistance)
Suitable manipulation/ processing properties (easy to mix, shapeable simple to process and cure)
Acceptable cost of both material and processing method
Biocompatible (tasteless, odourless, non-toxic, non-irritating, resistance to microbial colonisation)
Aesthetic properties translucency and transparency

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9
Q

PMMA problems

A

Colour stability
Shrinking problems
Adhesion

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10
Q

How can shrinkage of PMMA be reduced

A

Adding MMA

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11
Q

Self-curing dimethacrylate with dispersed phase ceramic particle ‘filler’ advantages

A

Self-curable
UV-photocurable
Blue-light photopolymerisable resins

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12
Q

What do the physical properties of polymers depend on?

A

How their molecules are arranged (polymer structure) - covalent bonds
The strength of forces between these molecules (intermolecular forces)

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13
Q

Strength and flexibility of polymer depends on:

A

Chain length (longer chain, stronger polymer)
Side groups (intramolecular forces e.g. H-bonds give stronger attraction between polymer chains, making polymer stronger)
Branching (straight and unbranched more dense, therefore crystalline and stronger)
Cross-linking (if polymer chains linked together by covalent bonds, polymer is harder and more difficult to melt)

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14
Q

Crystallinity of polymers

A
Aligned parts 'crystal-like' ordered structure
Crystallisation affects
-optical
-mechanical
-thermal
-chemical properties
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15
Q

Some highly crystalline polymers

A
Crystalline PET (CPET)
Nylon
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16
Q

Some highly amorphous (random structure) polymers

A

Acrylonitrile buadeine styrene (ABS)

Polycarbonate

17
Q

Thermoplastic polymers

A

Linear/ branched structures
Flow when heated and can be reshaped
Easily moulded and extruded into films
e.g. polypropylene

18
Q

Thermosetting polymers

A

Crosslinked structures
Cannot be reshaped upon heating
Hard and durable
e.g. epxoy resin

19
Q

Elastomers

A

Rubbery polymers
Can be stretched easily
Return to original dimensions when applied stress released

20
Q

Polymer properties: Tg (see graph on slides)

A

Tg is glass transition T: the T at which polymer chains begin to flow past each other
Below Tg polymer is solid (hard and glassy)
Above Tg the polymer can flow (soft and rubbery)
Tg is always lower than melting T (Tm)
The weaker the secondary bonds the lower the Tg

21
Q

Polymerisation: mechanisms

A

Chemical reaction in which monomers of low molecular weight are converted into chains of polymers with high molecular weight
Monomer molecules bonded by covalent bonds

22
Q

Types of polymerisation

A

Addition polymerisation

Condensation polymerisation

23
Q

Addition polymerisation

A

Addition polymerisation occurs when reaction between 2 molecules produces larger molecule without elimination of smaller molecule

24
Q

Addition polymerisation steps

A
  1. Activation (by heat/ chemical compounds e.g. tertiary amines/ light)
  2. Initiation (free radical initiates polymerisation e.g. benzoyloxy radical from benzoyl peroxide)
  3. Propagation (reactive end-groups of a polymer chain react with a new monomer molecule transferring the reactive group to the last unit)
  4. Termination (ceases the formation of reactive intermediates in a chain propagation)
25
Q

Common polymers formed via addition polymerisation

A

Polyethylene (low and high density)
Polystyrene
PTFE, Teflon
PMMA

26
Q

Condensation polymerisation

A

Occurs when reaction between 2 molecules produces a larger molecule with the elimination of a smaller moecule
e.g. silicone impression material setting reaction, producing water

27
Q

Blend

A

Mixing polymer prior to moulding
Polymers generally miscible
Moderate changes in mechanical properties
e.g. PLA + PCL to combine properties

28
Q

Copolymer

A

2 different types of monomers joined in same polymer chain

More noticeable changes in mechanical properties

29
Q

Plasticizer

A

Small molecule added to polymer
Reduces attraction forces between polymer chains
Big effect in mechanical properties: lowers Tg and elastic modulus (e.g. good for brittle polymers)

30
Q

Composite

A

Combination of materials with different mechanical properties in which the combination material offers superior properties comparing them to the individual components

e. g. matrix and filler
e. g. glass reinforced polymer