• Journal of Technologic Dentistry
• /
• v.26 no.1
• /
• pp.49-58
• /
• 2004

Two diketones, 1-phenyl-1,2-propanedione(PD) and 2,3-butanedione (BD) were investigated as new visible light photosensitizers for a dental resin composite of bis-GMA in order to improve photopolymerization effect. And the photopolymerization efficiency of mixed photosensitizers, PD-CQ and DA-CQ, was studied. Photopolymerization effect of photosensitizers were compared with that of camphorquinone(CQ), the most widely used photosensitizer. The photopolymerization efficiency of bis-GMA containing the photosensitizer increased with irradiation time. The increase was in the order: BD < CQ < PD. The photopolymerization efficiency of this mixture was not so efficient as CQ or PD.

• Journal of Technologic Dentistry
• /
• v.28 no.1
• /
• pp.43-52
• /
• 2006

Three t-amines, 4-(dimethylamino)benzoic acid (ABA), 4-(dimethylamino)benzaldehyde (MBA), 4-(dimethylamino)benzophenone (MBP), were investigated as new visible light photoinitiators for a dental resin composite of UDMA in order to improve photopolymerization effect. Three t-amines mixed with three photosensiizers, CQ, PD and DA, respectively. And the photopolymerization effect of photoinitiators were compared with that of 4-(dimethylamino)ethyl methacrylate (AEM), the most widely used photoinitiator. The photopolymerization efficiency of UDMA containing the photoinitiator increased with irradiation time. The increase was in the order: MBP

• Journal of dental hygiene science
• /
• v.8 no.3
• /
• pp.109-115
• /
• 2008

Two t-amines, N,N-dimethylaniline (MA), N,N-dimethyl-p-toluidine (MPT), were investigated as new visible light amine initiators for a dental resin composite of UDMA in order to improve photopolymerization effect. Three t-amines mixed with three photosensitizers, camphorquinone(CQ), 1-phenyl-1,2-propane dione(PD) and diacetyl (DA), respectively. And then this mixtures are added to resin monomer, UDMA. Photopolymerization efficiency of UDMA was studied through the use of FT-IR absorption spectroscopy. The photopolymerization effect of amine initiators were compared with that of 4-(dimethylamino)ethyl methacrylate (AEM), the most widely used photoinitiator. The photopolymerization efficiency of UDMA containing the amine initiator increased with irradiation time. The relative polymerization efficiency containing the CQ photosensitizer increase was in the order: AEM < MPT < MA. And the relative polymerization efficiency containing the PD photosensitizer increase was in the order: MPT < AEM < MA. This result shows that MA is most efficient amine initiator with CQ and PD.

• Journal of dental hygiene science
• /
• v.9 no.2
• /
• pp.189-195
• /
• 2009

Two diketones, 1,2-phenylpropanedione (PD) and diacetyl (DA) were investigated as new visible light photosensitizers for dental composite resin of bis-GMA in order to improve the photopolymerization effect. The photopolymerization efficiency of bis-GMA composite resin containing PD and DA was studied by IR absorption spectroscopy. And the results were compared with that of camphorquinone (CQ). Relative photopolymerization efficiency of the photosensitizers increased in the order of DA < CQ < PD. Thus. PO is a new visible light photosensitizer for dental composite resin with higher photopolymerization efficiency than that of CQ.

• Journal of Technologic Dentistry
• /
• v.23 no.2
• /
• pp.49-59
• /
• 2002

The photopolymerization efficiency and surface hardness of composite resin containing 1,2-phenylpropanedione (PD) and diacetyl (DA) as photoinitiators were studied by IR and Vickers hardness and the results were compared with that of camphorquinone (CQ). Relative photopolymerization efficiency of the photoinitiators increased in the order of DA < CQ < PD. Vickers hardness of composite resin containing the photoinitiators increased in the order of CQ < PD < DA. Thus, PD is a new visible light photoinitiator for dental composite resin with higher photopolymerization efficiency and surface hardness than that of CQ. Mechanical properties such as Vickers hardness, diametral tensile strength, and flexural strength of the experimental resin composite prepared by addition of the photosensitizer into a resin of bis-GMA improved with increasing the photosensitizer content and irradiation time. The resin composite of bis-GMA containing DA or PD shows better mechanical properties than that of CQ.

• 한국정보디스플레이학회:학술대회논문집
• /
• 2004.08a
• /
• pp.1208-1211
• /
• 2004

When irradiated with visible light in HPDLC, photoinitiator and coinitiator produce a radical for photopolymerization. According to the kinds of photoinitiator and coinitiator, quantity and rate of produced a radical is different. It is influence on photopolymerization rate relate on diffraction efficiency. Thus, this paper is about the effect of photoinitiator/coinitiator combinations in terms of diffraction efficiency and real-time first order diffraction efficiency.

• Journal of Technologic Dentistry
• /
• v.35 no.3
• /
• pp.209-218
• /
• 2013

Purpose: The purpose of this study was to know the availability of two photosensitizers, PD, DA, as a photosensitizer instead of CQ in UDMA dental composite resin. We want to know photopolymerization effect of UDMA unfilled resin and surface hardness of composite resin containing PD and DA were compared with those of CQ, most widely used photosensitizer for dental composite resins. Methods: The photopolymerization effect of UDMA studied by FT-IR spectroscopy increased with irradiation time and the amount of photosensitizer. Knoop hardness of experimental composite resins prepared by the addition of the photosensitizer content and irradiation time. Results: The relative photopolymerization effect of UDMA increased in the order of PD > CQ > DA. The composite resin of UDMA containing DA or PD, which shows better Knoop hardness than that containing CQ. Conclusion: PD and DA show as effective photosensizers, suitable for UDMA dental composite resin compare with a higher efficiency than CQ.

• Journal of the Optical Society of Korea
• /
• v.11 no.4
• /
• pp.183-191
• /
• 2007

The highest diffraction efficiency(DE) value after illumination and post-curing of photopolymer films were obtained at the $SeO_2$/Acrylamide(AA) Ratios of AA 3.0 g, $SeO_2$ 1.0g and the DE's were stable values of over 90%. By the addition of $SeO_2$, the maximum DE at the initial stage of illumination was reached at 300 seconds, which suggests $SeO_2$ slows down the photopolymerization of AA, which enhances the maximum DE value by giving more migration time. DE variation curve for the optimum composition during extended-time illumination of 9,000 seconds resembles a sine curve due to the combination of the monomer diffusion and the photopolymerization, and the photopolymer film expanded by about 8% after photopolymerization due to monomer migration.

• Korean Journal of Optics and Photonics
• /
• v.9 no.1
• /
• pp.31-37
• /
• 1998

We fabricated acrylamie photopolymer holographic recording materials by photopolymerization of acrylamide, and described hologram formation process. Light absorption and phtobleaching process by MB(methylene blue) dye and radical polymerization process due to TEA(triethanolamind) are explained in detail. We adopted the Beer-lambert law in order to explain the photobleaching kinetics. Dependencies of diffraction efficiency of the hologram on monomer amout and the exposure are investigated. The scattering effect caused by grain of polymer crystal, and fixing method are also illustrated.

• Macromolecular Research
• /
• v.14 no.2
• /
• pp.155-165
• /
• 2006

The present article describes the experimental and theoretical observations on the formation of holographic, polymer-dispersed, liquid crystals and electrically switchable, photonic crystals. A phase diagram of the starting mixture of nematic liquid crystal and photo-reactive triacrylate monomer was established by means of differential scanning calorimetry (DSC) and cloud point measurement. Photolithographic patterns were imprinted on the starting mixture of LC/triacrylate via multi-beam interference. A similar study was extended to a dendrimer/photocurative mixture as well as to a single component system (tetra-acrylate). Theoretical modeling and numerical simulation were carried out based on the combination of Flory-Huggins free energy of mixing and Maier-Saupe free energy of nematic ordering. The combined free energy densities were incorporated into the time-dependent Ginzburg-Landau (Model C) equations coupled with the photopolymerization rate equation to elucidate the spatio-temporal structure growth. The 2-D photonic structures thus simulated were consistent with the experimental observations. Furthermore, 3-D simulation was performed to guide the fabrication of assorted photonic crystals under various beam-geometries. Electro-optical performance such as diffraction efficiency was evaluated during the pattern photopolymerization process and also as a function of driving voltage.