DAROCUR (80 wt%) liquid. IRGACURE Phosphine oxide. – light yellow liquid at room temp. , viscous liquid. IRGACURE Fluorinated diaryl titanocene (Irgacure ) proved to be effective for initiating the polymerization of acrylate monomers under visible light. In this paper, a study of the photoinitiation mechanisms of Irgacure photosensitizer, in an epoxy resin matrix, is presented. We report our.

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The density of the cured resins was found to increase compared to that of the monomers and was found to be nearly constant —1. Add this article to your Mendeley library. These free radicals can also participate in polymer chain termination primary termination, and it is therefore necessary irgacuure understand their generation in order irgacuree predict the temporally varying kinetic effects present during holographic grating formation.

According to Figure 6the conversion 74 photocuring shows a significant light intensity dependence. That is, while most of the polymerization reaction occurs during the first minutes after irradiation, a irgacude portion of reaction may take place after curing [ 29 ]. The most common photopolymerization monomers are cyclic or linear epoxides cationic and acrylate-based monomers radical [ 1 ]. Since we used a green LED light source to initiate the photopolymerization process, knowing the characteristics of the lamp and sensitivity of the initiator in the green region of visible light is important.

This photoinitiator does not require an electron donor to produce free radicals so it is suitable for the substitution of CQ in dental photopolymer systems.

Advances in Condensed Matter Physics

This result shows that Irgacure can be irgavure effective when combined with the narrow-emission green LED. For the swelling studies, three of the samples at different light intensities, 0. To exclude oxygen, the photocuring process was performed under laminate conditions. China Manufacturer photoinitiator irgacure CAS The most common photoinitiator in dental practice is camphorquinone CQ in combination with tertiary amines as coinitiators [ 14 ].


Another important factor to consider for practical applications is the surface hardness of the material. The reaction rate of a theoretical radical chain polymerization is usually given by where is the degree of conversion, is the intensity of irgacre light in moles of light quanta per liter-second, is the quantum yield of initiation, and and are the rate constants for propagation irgacire termination, respectively.

The photopolymerization was performed at different light intensities ranging from 0. Herein, we report on our investigation into the effect of a LED light-curing unit on the mechanical properties and conversion rates of acrylate-based experimental resin containing Irgacure photoinitiator. In this paper, a study of the photoinitiation mechanisms of Irgacure photosensitizer, in rigacure epoxy resin matrix, is presented.

Irgacure , Irgacure Suppliers and Manufacturers at

Applied Biomaterialsvol. The kinetics of the photopolymerization was followed by Raman spectroscopy and conversion values were determined. Mechanical properties of the photocured resins at 1.

The subsequent mechanical measurements were performed at the chosen light intensity. So, as the photoinitiators present in oral biomaterials have light absorption spectra with distinct maxima, effective and rapid photopolymerization could result if the wavelength of the LED was chosen in this range [ 21 ].

An irgacure doped photopolymers for display holograms recording at nm – Semantic Scholar

Hardness is not the only property affecting the practical applicability of dental restorative materials. Another advantage of Irgacure is that it is not reliant on diffusion controlled electron transfer reactions because it undergoes unimolecular decomposition [ 19 ]. UDMA in a weight ratio of The results are presented in Figure 8. Unfortunately, 2 does not consider that the glass transition temperature of the restorative material must be higher than the maximum temperature that can be reached in the oral cavity, in order to prevent failures of the restorations due to thermal fatigue.

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As the photocuring progresses, of the network formed also increases, and the initially viscous liquid monomer mixture becomes a glassy solid. The samples were photopolymerized with the LED light source at 1.

An irgacure 784 doped photopolymers for display holograms recording at 532 nm

The applicability of a narrow-emission green LED light source, in combination with Irgacure during the photocuring of an acrylate-based dental resin, was studied. During sample preparation, we used the optimal composition [ 24 ] of BisGMA: The applicability of the model, describing the overall kinetic behavior, was tested by comparing the theoretical conversion data with the experimental data.

Abstract Low intensity green light emitting diodes LED were shown to be an effective light source to induce the photopolymerization of an acrylate-based photocurable dental restorative resin mixture of bisphenol A glycerolate dimethacrylate BisGMAtriethylene glycol dimethacrylate TEGDMAand diurethane dimethacrylate UDMAin combination with rigacure diaryl titanocene Irgacure The compressive strength and diametric tensile strength of the resins, cured at 1. With these measurements, the chosen light intensities varied between 0.

The surfaces of the wet disks were cautiously wiped dry and their weights were measured immediately. For dental applications, higher light intensities are favorable; however these values fall well below those previously reported for CQ [ 16 ].

The degree of conversion of the dental irggacure, which is the marker of polymerization efficiency, depends on the correlation between the spectral distribution of the light source and the absorption spectra of the photoinitiator [ 21 ].

Therefore, for further experiments, a 1. Vickers microhardness values for the samples cured by a LED light source at different intensities, with an irradiation time of 30 seconds, after storage for 24 hours and one week.