Processing Flashcards
High impact resin
Styrene-butadiene
-Incorporating a rubber phase in the beads during polymerization
-Increasing impact strength and fatigue resistance
Composition and fxn of PMMA
Monomer
-MMA-
-Hydroquinone-Inhibitor
-Dimethyl-p-toluidine(tertiary amine)-Accelerator
-Dibutyl pthalate-Plasticizer
Polymer
-Pre-polymerized spheres of PMMA - reduces shrinkage
-Benzoyl peroxide- Initiator
-Butadiene-styrene-strength
-Titanium dioxide-opacifier
-Dibutyl pthalate-Plasticizer
Heat cure vs Cold cure PMMA
Heat
-Heat is activator-decomposes benzoyl peroxide after 60C to initiate polymerization
-LESS residual monomer (0.2-0.5%)
-MORE shrinkage
-MORE strength
-MORE color stability
-MORE biocompatibility
Cold
-Tertiary amine is activator
-MORE residual monomer(3%)
-LESS shrinkage
-LESS strength
-LESS color stability
-LESS biocompatible
Linear and Volumetric Shrinkage of PMMA during polymerization
Linear shrinkage
-More clinically significant
-Results in loss of fit/seal/occlusal contacts
-Greatest in heat cured compression molding
Volumetric
-Produces changes in density
Initial PMMA formation experiences 21% volumetric and 7% linear shrinkage
- PMMA beads are pre-polymerized
- 3:1 powder:liquid ratio
Decreases shrinkage to 6% volumetric and 0.5% for heat cured (0.25% for cold cure)