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Journal ArticleDOI

Network structures of Bis-GMA/TEGDMA resins differ in DC, shrinkage-strain, hardness and optical properties as a function of reducing agent.

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TLDR
The resin containing DMAEMA showed higher DC, shrinkage-strain,shrinkage-Strain rate, and microhardness, in addition to better optical properties, in Besides, color stability and transmittance were evaluated after different periods of artificial aging, according to ISO 7491:2000.
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This article is published in Dental Materials.The article was published on 2011-05-01. It has received 54 citations till now.

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Citations
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Journal ArticleDOI

Progress in dimethacrylate-based dental composite technology and curing efficiency

TL;DR: A review of the key factors affecting the polymerization efficiency of light-activated resin-based composites highlights the apparent need for a more informative approach by manufacturers to relay appropriate information in order to optimize material properties of resin composites used in daily practice.
Journal ArticleDOI

New polymer-chemical developments in clinical dental polymer materials: Enamel–dentin adhesives and restorative composites

TL;DR: New bisacrylamide cross-linkers with improved hydrolytic stability and new strongly acidic polymerizable phosphonic acids and dihydrogen phosphates, in combination with the implementation of novel application devices, have significantly improved the performance of the current enamel–dentin adhesives.
Journal ArticleDOI

Effect of different photoinitiators and reducing agents on cure efficiency and color stability of resin-based composites using different LED wavelengths

TL;DR: After aging, CQ-based composites became more yellow and BAPO and TPO lighter and less yellow; despite the less yellowing of these alternative photoinitiators, camphorquinone presented higher color stability.
Journal ArticleDOI

Degree of Conversion of a Resin Cement Light-Cured Through Ceramic Veneers of Different Thicknesses and Types

TL;DR: The effect of different types and thicknesses of ceramic veneers on the degree of conversion of a light-cured resin-based cement (RelyX Veneer) depends on the thickness and type of ceramics employed when veneer thicker than 1.5 mm are cemented.
References
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Journal ArticleDOI

Correlation between hardness and degree of conversion during the setting reaction of unfilled dental restorative resins

TL;DR: Knoop hardness was correlated to degree of conversion (DC) of carbon double bonds, determined by IR, during the setting reaction of three unfilled dental resins, indicating increase in hardness correlates well with increases in DC during setting.
Journal ArticleDOI

Color stability of dental composite resin materials for crown and bridge veneers

TL;DR: The color stability of 3 light-polymerized veneer materials were investigated and compared to that of 3 conventional heat- and auto-polymers materials and the accelerated test had the ability to discriminate between the various products.
Journal ArticleDOI

Light intensity effects on resin-composite degree of conversion and shrinkage strain.

TL;DR: The correlation between DC and shrinkage strain values means that some reductions in the problems of shrinkage may be achieved by an acceptable reduction in DC, however, this must also be consistent with generating adequate curing performance in the resin-network.
Journal ArticleDOI

The Effects of Light Intensity, Temperature, and Comonomer Composition on the Polymerization Behavior of Dimethacrylate Dental Resins

TL;DR: It is concluded that the BisGMA portion of the mixture largely controls the polymerization mechanisms and kinetics, which suggests that TEGDMA is an excellent diluent, since it increases the mobility of the reacting medium; however, the high reactivity is due to the presence of BisGma.
Journal ArticleDOI

Filler features and their effects on wear and degree of conversion of particulate dental resin composites.

TL;DR: Filler size and geometry was found to have a significant effect on wear resistance and DC of composites, without compromising the percentage of reacted carbon double bonds at specific sizes and combinations.
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