II. INTERNATIONAL PERGE SCIENTIFIC STUDIES CONGRESS , Antalya, Türkiye, 11 - 12 Ocak 2025, ss.140, (Özet Bildiri)
Particle-filled polymeric composite materials have
become indispensable in many technological fields, including dental treatments.
In dental composites developed for this purpose, the organic matrix, which acts
as a binder, is frequently prepared from monomers such as Diurethane
dimethacrylate (UDMA), Bisphenol A glycidyl methacrylate (Bis-GMA), and Ethoxylated
bisphenol A glycidyl methacrylate (Bis-EMA). Due to their high molecular
weight, especially Bis-GMA and Bis-EMA monomers have high viscosity, which
makes it difficult to prepare composite structures with the addition of ceramic
particles. Therefore, acrylate-based solvents with cross-linking properties,
such as Triethylene glycol dimethacrylate (TEGDMA), are used. In this study,
the monomer mixtures of DUDMA:TEGDMA:Bis-GMA and DUDMA:TEGDMA:Bis-EMA were kept
constant at a weight ratio of 60:40:20, respectively, as the organic matrix.
Barium borosilicate with particle sizes of 3 μm and 0.7 μm was added as a
ceramic particle at a weight ratio of 55% and 24%, respectively, to prepare the
composite composition. Camphorquinone (CQ), a light-activated radical
initiator, was used at 0.5% of the total composite weight for the
polymerization reaction.
Bis-GMA and Bis-EMA are high molecular weight monomers
frequently used interchangeably in the preparation of dental composites.
Therefore, in this study, all other components of the composite were kept
constant, while the organic matrix was varied between Bis-GMA and Bis-EMA to
prepare test specimens. Water sorption and
solubility values of the prepared specimens were determined according to ISO
4049, "Dentistry-Polymer based restorative materials". To evaluate
the impact of water sorption on mechanical behavior, specimens were immersed in
water for various durations (3, 6, 9, 12, and 15 days) and then subjected to
flexural, compressive, and fracture toughness testing using a universal testing
machine, following ISO 4049 protocols.
When the compressive test results of the specimens
were examined, it was found that the compressive strength of the composites
prepared with Bis-GMA increased by approximately 50 MPa after 15 days, while
the compressive strength values of the composites prepared with Bis-EMA
decreased by an average of 25 MPa. No significant change was observed in the
flexural strength values of both types of composites after 15 days. When the
fracture toughness values were examined, no significant change was observed in
the composites prepared with Bis-GMA due to water interaction, while the
fracture toughness value of the composite composition prepared with Bis-EMA
increased from 0.80 MPa m1/2 to 1.20 MPa m1/2.