Influence of thermal expansion on shrinkage during photopolymerization of dental resins based on bis-GMA/TEGDMA

• Published in: Dental materials Vol. 25; no. 1; pp. 103 - 114
• Main Authors: Mucci, Veronica, Arenas, Gustavo, Duchowicz, Ricardo, Cook, Wayne D, Vallo, Claudia
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.01.2009
• Subjects: Advanced Basic Science; Bisphenol A-Glycidyl Methacrylate - chemistry; Bisphenol A-Glycidyl Methacrylate - radiation effects; Calorimetry; Composite Resins - chemistry; Dental Materials - chemistry; Dental Materials - radiation effects; Dental resins; Dentistry; Dimethacrylates; Exotherm; Fiber Optic Technology; Humans; Interferometric method; Interferometry; Light; Materials Testing; Methacrylates; Models, Chemical; para-Aminobenzoates; Phase Transition; Photopolymerization; Polyethylene Glycols - chemistry; Polymerization shrinkage; Polymers - chemistry; Polymers - radiation effects; Polymethacrylic Acids - chemistry; Reducing Agents; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared; Spectroscopy, Near-Infrared; Surface Properties; Temperature; Terpenes - chemistry; Dimethacrylates; Interferometric method; Exotherm; Photopolymerization; Polymerization shrinkage; Dental resins
• ISSN: 0109-5641; 1879-0097
• DOI: 10.1016/j.dental.2008.04.014

Abstract Objective The aim of this study was to assess volume changes that occur during photopolymerization of unfilled dental resins based on bis-GMA-TEGDMA. Methods The resins were activated for visible light polymerization by the addition of camphorquinone (CQ) in combination with dimethylamino ethylmethacrylate (DMAEMA) or ethyl-4-dimethyl aminobenzoate (EDMAB). A fibre-optic sensing method based on a Fizeau-type interferometric scheme was employed for monitoring contraction during photopolymerization. Measurements were carried out on 10 mm diameter specimens of different thicknesses (1 and 2 mm). Results The high exothermic nature of the polymerization resulted in volume expansion during the heating, and this effect was more pronounced when the sample thickness increased. Two approaches to assess volume changes due to thermal effects are presented. Due to the difference in thermal expansion coefficients between the rubbery and glassy resins, the increase of volume due to thermal expansion was greater than the decrease in volume due to thermal contraction. As a result, the volume of the vitrified resins was greater than that calculated from polymerization contraction. The observed trends of shrinkage versus sample thickness are explained in terms of light attenuation across the path length during photopolymerization. Significance Results obtained in this research highlight the inherent interlinking of non-isothermal photopolymerization and volumetric changes in bulk polymerizing systems.