DM L1 Composites pt 1 Flashcards

1
Q

what is a composite

A

2 or more materials put together with each contributing to overall properties

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2
Q

name 5 uses of composites

A
restorative filling materials
fissure sealants
indirect restorations
endo post + cores
luting agents
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3
Q

what are the 3 main phases/components of dental composites

A

organic matrix
inorganic filler
coupling agents

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4
Q

what is the organic matrix phase of the dental composites

A

plastic monomer/resin material that polymerises (sets/cures) to form continuous phase
where binding the filler particles (via coupling agent)
hydrophobic

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5
Q

what is the inorganic filler phase of the dental composites

A

enhances material’s mechanic properties

reinforcing particles and/or fibres dispersed in the matrix

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6
Q

what is the coupling agent phase of the dental composites

A

bonding agent promotes adhesion between filler + resin matrix
hydrophilic end - chemically bonds to inorganic filler

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7
Q

what is the organic matrix made of

A

monomers - chemically active components of composite - polymerises
-> glassy polymer in set state

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8
Q

how do monomers form polymers in the organic matrix

A

monomer - viscous fluid, polymerises -> rigid polymeric material
free radical, addition polymerisation reaction

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9
Q

what monomer does organic matrix contain

A

Bis-GMA = Bowens’ monomer
made from bisphenol A + glycidal methacrylate
2 metha
crylate groups , ends

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10
Q

what is and why is another monomer used instead of Bis GMA in the organic matrix stage

A

Bis GMA = viscous monomer
so UDMA = urethane dimethacrylate used
UDMA less viscous than Bis GMA but still viscous

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11
Q

except UDMA, what is alternate monomer can be used in the organic matrix

A

Ethoxylated Bisphenol A derivative

2 methacrylate undergo polymerisation - break C=C

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12
Q

what does characteristics of monomers in organic matrix mean + how is it solved

A

Bis GMA - super viscous
UDMA - little less viscous
high viscous - monomers unworkable + add filler viscous increases more

diluent monomers (viscosity controllers added)
= gylcol dimethacrylates
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13
Q

why dimethacrylates used in composites

A

low molecular weight of MMA (methyl methacrylate ) + low molar vol –> high vol shrinkage after polymerisation

high mole weight + low vol of Bis GMA –> lower vol shrinkage after polymerisation

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14
Q

what happens to Bis GMA, UDMA + diluents when they polymerise

A

all have 2 sets of C=C double bonds

all polymerise + contribute to overall shrinkage of material when set

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15
Q

what other 7 additives does organic matrix contain

A
  1. hydroquinone = stabilises free radicals, prevents initiation inhibitor -> increases shelf life
  2. Activator/initiator system for Room temp cure = DHPT/Benzoyl peroxide
  3. Light cure = DHPT/Camphorquinone
    o Fillers
    o Pigments e.g. iron oxide
    o UV stabilisers
    o Optical brighteners
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16
Q

what are 6 advantages of using fillers in composites

A

Advantages:
o Reduce setting shrinkage ∴ more filler-↓monomer/resin required
o Reduce coefficient of thermal expansion - closer to tooth tissue
o Enhance modulus and strength (compressive), hardness
o May provide radio-opacity e.g. quartz, fused silica, radio-opaque glass
o Control of aesthetics e.g. translucency, fluorescence, colour
o higher filler amounts, mech properties of composite increases

17
Q

what is important wheen choosing filler for composite

A

refractive index of filler + resin must closely match - avoid scattering light
–>otherwise full depth of cure not achieved on light curing the resin

end result = translucent material

18
Q

what must the filler be treated with and why is particle size of filler important

A

silane treated
o Single filler insufficient- many types used
o Avg particle size and particle size distribution = determines amt of incorporated filler
o Fillers have an effect on surface finish; i.e. smaller particles = smoother finish)

19
Q

what are 3 types of fillers

A

conventional/Macro
hybrid/blended or small particle hybrid
microfine/ microfillers

20
Q

what was 1st type of macro used in fillers and why is it not used much nowadays

A
>1µm
- 1 st used = ground quartz
- Good strength  BUT
Poor finish of composite - dull appearance ∵
protruding particles from resin surface
21
Q

what eg of microfillers used in fillers and why were they good + why bad

A

colloidal silica
increased viscosity to an already
viscous resin (more diluent had to be added)
- Can b e polished; v smooth surface finish
- V Large s.a. in contact with resin ∴ difficult to
obtain high filler loading ∴ mechanical props inferior
- CANNOT be used in post cavities

22
Q

what was the 2 stage process of microfillers

A

micro-filled composite polymerised - then ground into tiny particles
tiny particles put in another organic matrix to fill resin matrix
increases filler loading

23
Q

what are hybrid composites

A

contain large filler particles + small amount of colloidal silica

small particle hybrid comps -achieves high polished surfaces
packing density increases - as 2 diff sizes used as fillers

24
Q

what are 4 advantages of hybrid fillers + 1 disadvantage

A
  • Favourable physical, mech and opt properties
  • great wear resistance (compared to macrofilled)
  • Surface morphology: superior to ; Conventional
  • Radiopacity possible
    Disadvantages:
  • ↑ surface roughness with time; resin wears
25
Q

what are characteristics of nano filled composites

A

Nano-filled composites:
Strength of a hybrid and polishing finish of a
microfilled material  to be researched

26
Q

when are micro-filled + hybrid composites used in teeth

A

micro-filled - anterior restorations –> low filler loading - so mech properties compromised
hybrid - posterior restoration - high filler loading

27
Q

what is coupling agent + how it works

A

silane

imp for filler + resin bonded -> so composite has acceptable mech properties
results in improved wear resistance of final result

28
Q

how is silane used with the filler particles

A

silane coated AROUND the filler particles (critical factor)

= silane treatment = γ-MPTS

29
Q

how does silane coupling agent bond to filler + organic matrix

A

silane coupling agent (hydrophilic) reacts with surface hydroxyl groups of filler - via condensation reaction

methacrylate group of silane (hydrophobic) bonds to (hydrophobic) organic resin - free radical polymerisation

30
Q

what is the other way for silane coupling agent to bind to filler + matrix

A

acid treating coupling agent

hydroxyl groups replaced with methoxy groups that carry out the reaction)

31
Q

why is stable adhesion bond needed between coupling agent + resin

A

o No bond; stress transfer between filler + resin insufficient -> creep/fracture/wear
o No bond; crack initiation sites -> fatigue failure
o Unstable bond = fracture -> disintegration

32
Q

what are advs of direct composites

A

excellent aesthetics
command set = light cure
conservative tooth tissue preparation

33
Q

what are disadvs of direct composites

A
polymerisation shrinkage
required bonding procedure
required incremental placement
residual monomer present
water uptake -> staining 
breakdown of bonding
wear of resin matrix