| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1420575 | Dental Materials | 2015 | 7 Pages |
•The results have shown that HP UDMA polymers have DC superior to that of the control group.•E′ and E″ were not significantly different between control and HP polymers.•The damping factor, tan δ , decreased with increasing pressure, while E′rubE′rub and Tg increased.•Polymerization at 150 MPa or higher resulted in significantly higher E′rubE′rub and Tg.•The results have also suggested that 200 MPa is an optimum polymerization pressure, resulting in polymers with significantly higher DC, E′rubE′rub, and Tg, while maintaining adequate damping capacity (tan δ).
ObjectivesThe aim of this study, part of our research to improve properties of resin composite blocks suitable for CAD/CAM and to better understand underlying mechanisms associated with high-temperature/high-pressure (HT/HP) polymerization, was to determine an optimum polymerization pressure of urethane dimethacrylate (UDMA) in the presence of an initiator (0.5% benzoyl peroxide) by determining the degree of conversion (DC) and viscoelastic properties of polymers obtained at 90 °C under varying HP.MethodsDC and viscoelastic properties of 16 UDMA polymers, two controls (thermo-cured and thermo-cured followed by post-cure relaxation) and 14 experimental groups (HP polymers, in the range of 50–350 MPa, in 50 MPa increments, without and with post-cure relaxation) were determined via near infrared spectroscopic analysis and dynamic mechanical analysis, respectively.ResultsThe results have shown that HP UDMA polymers have DC superior to that of the control group. With regards to E′ and E″, the results have shown no significant difference between control and HP polymers. The damping factor, tan δ , decreased with increasing pressure, while E′rubE′rub and Tg increased. Polymerization at 150 MPa or higher resulted in significantly higher E′rubE′rub and Tg.SignificanceThe results of this study suggested that HP polymerization at 90 °C of UDMA reduced the number of defects and the free volume, leading to a more homogeneous polymer network. The results have also suggested that 200 MPa is an optimum polymerization pressure, resulting in polymers with significantly higher DC, E′rubE′rub, and Tg, while maintaining adequate damping capacity (tan δ).
