TY - JOUR
T1 - Influence of the base and diluent monomer on network characteristics and mechanical properties of neat resin and composite materials
AU - de Godoy Fróes-Salgado, Nívea Regina
AU - Gajewski, Vinícius
AU - Ornaghi, Bárbara Pick
AU - Pfeifer, Carmem Silvia Costa
AU - Meier, Marcia Margarete
AU - Xavier, Tathy Aparecida
AU - Braga, Roberto Ruggiero
N1 - Funding Information:
The authors would like to express their gratitude to CAPES (Coordination for Enhancement of Higher Education Personnel) for the financial support (PNPD-CAPES 02436/09-4), to Antonio Carlos Lascala for the technical support and to FGM Produtos Odontológicos (Joinville, SC, Brazil) for preparing the experimental composites tested in this study.
Publisher Copyright:
© 2014, The Society of The Nippon Dental University.
PY - 2015/5/27
Y1 - 2015/5/27
N2 - This study evaluated the effect of the combination of two dimethacrylate-based monomers [bisphenol A diglycidyl dimethacrylate (BisGMA) or bisphenol A ethoxylated dimethacrylate (BisEMA)] with diluents either derived from ethylene glycol dimethacrylate (ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate) or 1,10-decanediol dimethacrylate (D3MA) on network characteristics and mechanical properties of neat resin and composite materials. The degree of conversion, maximum rate of polymerization and water sorption/solubility of unfilled resins and the flexural strength and microhardness of composites (after 24 h storage in water and 3 months storage in a 75 vol% ethanol aqueous solution) were evaluated. Data were analyzed with two-way ANOVA and Tukey’s test (α = 0.05). The higher conversion and lower water sorption presented by BisEMA co-polymers resulted in greater resistance to degradation in ethanol compared with BisGMA-based materials. In general, conversion and mechanical properties were optimized with the use of long-chain dimethacrylate derivatives of ethylene glycol. D3MA rendered more hydrophobic materials, but with relatively low conversion and mechanical properties.
AB - This study evaluated the effect of the combination of two dimethacrylate-based monomers [bisphenol A diglycidyl dimethacrylate (BisGMA) or bisphenol A ethoxylated dimethacrylate (BisEMA)] with diluents either derived from ethylene glycol dimethacrylate (ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate) or 1,10-decanediol dimethacrylate (D3MA) on network characteristics and mechanical properties of neat resin and composite materials. The degree of conversion, maximum rate of polymerization and water sorption/solubility of unfilled resins and the flexural strength and microhardness of composites (after 24 h storage in water and 3 months storage in a 75 vol% ethanol aqueous solution) were evaluated. Data were analyzed with two-way ANOVA and Tukey’s test (α = 0.05). The higher conversion and lower water sorption presented by BisEMA co-polymers resulted in greater resistance to degradation in ethanol compared with BisGMA-based materials. In general, conversion and mechanical properties were optimized with the use of long-chain dimethacrylate derivatives of ethylene glycol. D3MA rendered more hydrophobic materials, but with relatively low conversion and mechanical properties.
KW - Composite
KW - Degree of conversion
KW - Mechanical property
KW - Resin
KW - Water sorption
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U2 - 10.1007/s10266-014-0153-6
DO - 10.1007/s10266-014-0153-6
M3 - Article
C2 - 24728606
AN - SCOPUS:84933179506
SN - 1618-1247
VL - 103
SP - 160
EP - 168
JO - Odontology
JF - Odontology
IS - 2
ER -