J Adv Prosthodont.  2011 Dec;3(4):216-220. 10.4047/jap.2011.3.4.216.

Polymerization behavior and thermal characteristics of two new composites at five temperatures: refrigeration to preheating

Affiliations
  • 1Department of Dental Materials, Faculty of Dentistry, Tehran University of Medical Sciences; Research Center for Medical and Technology in Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran.
  • 2Dentist, Pharmacy School, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • 3Department of Pharmaceutics, Pharmacy School, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • 4Department of Prosthodontics, Faculty of Dentistry, Tehran University of Medical Sciences; Secretary of the Dentistry and Specialties, Deputy of Education, Ministry of Health and Medical Education, Tehran, Iran.
  • 5Department of Dental Materials, Faculty of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.
  • 6Department of Dental Anatomy and Morphology, Dental Branch, Islamic Azad University, Tehran, Iran. vahid.rakhshan@gmail.com

Abstract

PURPOSE
Heat of composite polymerization (HP) indicates setting efficacy and temperature increase of composite in clinical procedures. The purpose of this in vitro experimental study was to evaluate the effects of 5 temperatures on HP of two new composites.
MATERIALS AND METHODS
From each material (Core Max II [CM] and King Dental [KD]), 5 groups of 5 specimens each were prepared and their total HPs (J/gr) were measured and recorded, at one of the constant temperatures 0degrees C, 15degrees C, 23degrees C, 37degrees C and 60degrees C (2 x 5 x 5 specimens) using a differential scanning calorimetry (DSC) analyzer. The data were analyzed using a two-way ANOVA, a Tukey's test, an independent-samples t-test, and a linear regression analysis (alpha=0.05).
RESULTS
No polymerization reactions occurred at 0degrees C; then this temperature was excluded from statistical analyses. The mean HP of the remaining 20 KD specimens was 20.5 +/- 14.9 J/gr, while it was 40.7 +/- 12.9 J/gr for CM. The independent-samples t-test showed that there were significant differences between the HP of the two materials at the temperatures 15degrees C (P=.0001), 23degrees C (P=.0163), 37degrees C (P=.0039), and 60degrees C (P=.0106). Linear regression analysis showed statistically significant correlations between environment temperatures and HP of CM (R2=0.777).
CONCLUSION
Using CM is advantageous over conventional composite because of its better polymerization capacity. However due to its high HP, further studies should assess its temperature increase in vivo. Preheating KD is recommended. Refrigerating composites can negatively affect their polymerization potential.

Keyword

Dental Materials; Composite Resins; Polymerization; Differential Thermal Analysis; Differential Scanning Calorimetry (DSC)

MeSH Terms

Calorimetry, Differential Scanning
Composite Resins
Dental Materials
Differential Thermal Analysis
Hot Temperature
Linear Models
Polymerization
Polymers
Refrigeration
Composite Resins
Dental Materials
Polymers

Figure

  • Fig. 1 Mean (SD) HPs of the tested materials (J/gr) at different temperatures (℃).


Reference

1. Shillingburg HT, Hobo S, Whitsett LD, Jacobi R, Brackett SE. Fundamentals of fixed prosthodontics. 1997. Chicag: Quintessence Publishing.
2. Kovarik RE, Breeding LC, Caughman WF. Fatigue life of three core materials under simulated chewing conditions. J Prosthet Dent. 1992. 68:584–590.
3. Antonucci JM, Toth EE. Extent of polymerization of dental resins by differential scanning calorimetry. J Dent Res. 1983. 62:121–125.
4. Prasanna N, Pallavi Reddy Y, Kavitha S, Lakshmi Narayanan L. Degree of conversion and residual stress of preheated and room-temperature composites. Indian J Dent Res. 2007. 18:173–176.
5. Cotti E, Scungio P, Dettori C, Ennas G. Comparison of the Degree of Conversion of Resin Based Endodontic Sealers Using the DSC Technique. Eur J Dent. 2011. 5:131–138.
6. Daronch M, Rueggeberg FA, De Goes MF. Monomer conversion of pre-heated composite. J Dent Res. 2005. 84:663–667.
7. Awliya WY. The influence of temperature on the efficacy of polymerization of composite resin. J Contemp Dent Pract. 2007. 8:9–16.
8. Faria-E-Silva AL, Piva E, Moraes RR. Time-dependent effect of refrigeration on viscosity and conversion kinetics of dental adhesive resins. Eur J Dent. 2010. 4:150–155.
9. Daronch M, Rueggeberg FA, Moss L, de Goes MF. Clinically relevant issues related to preheating composites. J Esthet Restor Dent. 2006. 18:340–350. discussion 351.
10. Lohbauer U, Zinelis S, Rahiotis C, Petschelt A, Eliades G. The effect of resin composite pre-heating on monomer conversion and polymerization shrinkage. Dent Mater. 2009. 25:514–519.
11. Choudhary N, Kamat S, Mangala T, Thomas M. Effect of pre-heating composite resin on gap formation at three different temperatures. J Conserv Dent. 2011. 14:191–195.
12. Driscoll CF, Woolsey G, Ferguson WM. Comparison of exothermic release during polymerization of four materials used to fabricate interim restorations. J Prosthet Dent. 1991. 65:504–506.
13. Hussey DL, Biagioni PA, McCullagh JJ, Lamey PJ. Thermographic assessment of heat generated on the root surface during post space preparation. Int Endod J. 1997. 30:187–190.
14. Lipski M. Root surface temperature rises during root canal obturation, in vitro, by the continuous wave of condensation technique using System B HeatSource. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005. 99:505–510.
15. Behnia A, McDonald NJ. In vitro infrared thermographic assessment of root surface temperatures generated by the thermafil plus system. J Endod. 2001. 27:203–205.
16. Atai M, Ahmadi M, Babanzadeh S, Watts DC. Synthesis, characterization, shrinkage and curing kinetics of a new low-shrinkage urethane dimethacrylate monomer for dental applications. Dent Mater. 2007. 23:1030–1041.
17. Lee H, Colby C. Heat of polymerization of nine mono-, di-, and trimethacrylate esters tested neat and with low levels of peroxide by dynamic differential scanning calorimetry. Dent Mater. 1986. 2:175–178.
18. Martín JL. Kinetic analysis of an asymmetrical DSC peak in the curing of an unsaturated polyester resin catalysed with MEKP and cobalt octoate. Polymer. 1999. 40:3451–3462.
19. Tanimoto Y, Hayakawa T, Nemoto K. Analysis of photopolymerization behavior of UDMA/TEGDMA resin mixture and its composite by differential scanning calorimetry. J Biomed Mater Res B Appl Biomater. 2005. 72:310–315.
20. Atai M, Motevasselian F. Temperature rise and degree of photopolymerization conversion of nanocomposites and conventional dental composites. Clin Oral Investig. 2009. 13:309–316.
21. Chung KH, Greener EH. Correlation between degree of conversion, filler concentration and mechanical properties of posterior composite resins. J Oral Rehabil. 1990. 17:487–494.
22. Guiraldo RD, Consani S, De Souza AS, Consani RL, Sinhoreti MA, Correr-Sobrinho L. Influence of light energy density on heat generation during photoactivation of dental composites with different dentin and composite thickness. J Appl Oral Sci. 2009. 17:289–293.
23. Bayne SC, Thompson JY. Roberson TM, Heymann HO, Ritter AV, editors. Biomaterials. Sturdevant's art and science of operative dentistry. 2006. St. Louis: The CV Mosby Co.;135–242.
24. Pojman JA, Ilyashenko VM, Khan AM. Free-radical frontal polymerization: self-propagating thermal reaction waves. J Chem Soc Faraday Trans. 1996. 92:2825–2837.
25. Daronch M, Rueggeberg FA, Hall G, De Goe MF. Effect of composite temperature on in vitro intrapulpal temperature rise. Dent Mater. 2007. 23:1283–1288.
26. Tantbirojn D, Chongvisal S, Augustson DG, Versluis A. Hardness and postgel shrinkage of preheated composites. Quintessence Int. 2011. 42:e51–e59.
Full Text Links
  • JAP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr