Characterization of dimethacrylate polymeric networks

A study of the crosslinked structure formed by monomers used in dental composites

Carmem Pfeifer, Zachary R. Shelton, Roberto R. Braga, Dario Windmoller, José C. MacHado, Jeffrey W. Stansbury

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

The resin phase of dental composites is mainly composed of combinations of dimethacrylate comonomers, with final polymeric network structure defined by monomer type/reactivity and degree of conversion. This fundamental study evaluates how increasing concentrations of the flexible triethylene glycol dimethacrylate (TEGDMA) influences void formation in bisphenol A diglycidyl dimethacrylate (BisGMA) co-polymerizations and correlates this aspect of network structure with reaction kinetic parameters and macroscopic volumetric shrinkage. Photopolymerization kinetics was followed in real-time by a near-infrared (NIR) spectroscopic technique, viscosity was assessed with a viscometer, volumetric shrinkage was followed with a linometer, free volume formation was determined by positron annihilation lifetime spectroscopy (PALS) and the sol-gel composition was determined by extraction with dichloromethane followed by 1H NMR analysis. Results show that, as expected, volumetric shrinkage increases with TEGDMA concentration and monomer conversion. Extraction/1H NMR studies show increasing participation of the more flexible TEGDMA towards the limiting stages of conversion/crosslinking development. As the conversion progresses, either based on longer irradiation times or greater TEGDMA concentrations, the network becomes more dense, which is evidenced by the decrease in free volume and weight loss after extraction in these situations. For the same composition (BisGMA/TEGDMA 60-40 mol%) light-cured for increasing periods of time (from 10 to 600 s), free volume decreased and volumetric shrinkage increased, in a linear relationship with conversion. However, the correlation between free volume and macroscopic volumetric shrinkage was shown to be rather complex for variable compositions exposed for the same time (600 s). The addition of TEGDMA decreases free-volume up to 40 mol% (due to increased conversion), but above that concentration, in spite of the increase in conversion/crosslinking, free volume pore size increases due to the high concentration of the more flexible monomer. In those cases, the increase in volumetric shrinkage was due to higher functional group concentration, in spite of the greater free volume. Therefore, through the application of the PALS model, this study elucidates the network formation in dimethacrylates commonly used in dental materials.

Original languageEnglish (US)
Pages (from-to)162-170
Number of pages9
JournalEuropean Polymer Journal
Volume47
Issue number2
DOIs
StatePublished - Feb 2011
Externally publishedYes

Fingerprint

Dental composites
Free volume
Glycols
shrinkage
monomers
Monomers
glycols
composite materials
Positron annihilation
crosslinking
positron annihilation
Crosslinking
Chemical analysis
Nuclear magnetic resonance
Spectroscopy
Dental materials
Dental Materials
life (durability)
nuclear magnetic resonance
bisphenols

Keywords

  • Dental resins
  • Free volume
  • Polymer network
  • Reaction kinetics
  • Volumetric shrinkage

ASJC Scopus subject areas

  • Polymers and Plastics
  • Physics and Astronomy(all)
  • Organic Chemistry

Cite this

Characterization of dimethacrylate polymeric networks : A study of the crosslinked structure formed by monomers used in dental composites. / Pfeifer, Carmem; Shelton, Zachary R.; Braga, Roberto R.; Windmoller, Dario; MacHado, José C.; Stansbury, Jeffrey W.

In: European Polymer Journal, Vol. 47, No. 2, 02.2011, p. 162-170.

Research output: Contribution to journalArticle

Pfeifer, Carmem ; Shelton, Zachary R. ; Braga, Roberto R. ; Windmoller, Dario ; MacHado, José C. ; Stansbury, Jeffrey W. / Characterization of dimethacrylate polymeric networks : A study of the crosslinked structure formed by monomers used in dental composites. In: European Polymer Journal. 2011 ; Vol. 47, No. 2. pp. 162-170.
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