• 대한치과기공학회지
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• 제26권1호
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• pp.49-58
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• 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.

• 대한치과기공학회지
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• 제28권1호
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• pp.43-52
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• 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

• 치위생과학회지
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• 제8권3호
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• pp.109-115
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• 2008

치과용 가시광선 중합형 복합수지의 광중합효율을 높이기 위해 2종의 새로운 액체형 amine 개시제인 MA, MPT와 현재 가장 많이 사용되고 있는 개시제인 AEM을 CQ, PD, DA에 각각 첨가하고 UDMA의 광중합효율을 알아본 결과 다음과 같은 결론을 얻었다. 1. 조사시간이 증가됨에 따라 amine 개시제의 종류에 관계없이 광중합효율이 점차 증가되었으며, 약 60초까지 조사였을 때에는 광중합효율이 급격히 증가되었으나 그 이상 조사하여도 광중합효율이 크게 증가되지 않았다. 2. AEM, MA와 MPT를 사용하였을 경우 모두 CQ > PD > DA의 순으로 광중합효율이 우수하게 나타났으나 AEM을 사용하였을 때 PD와 CQ는 큰 차이를 보이지 않았다. 3. CQ의 광중합효율은 새로운 광개시제인 MA와 MPT를 사용하였을 때가 범용으로 사용되고 있는 amine 개시제인 AEM을 사용하였을 경우보다 중합효율이 증가하는 결과를 보였다. 4. PD의 광중합효율은 MA와 함께 사용하였을 경우가 가장 높게 나타났으나 AEM의 경우와 큰 차이를 보이지는 않았다. 5. 이상의 결과로부터 MA와 CQ 및 PD를 함께 사용한 새로운 광중합시스템이 광중합효율을 높이는데 효율적인 것을 알 수 있었다.

• 치위생과학회지
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• 제9권2호
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• pp.189-195
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• 2009

치과용 가시광선 종합형 복합수지의 광중합효율을 높이기 위해 합성한 bis-GMA 레진에 2종의 새로운 광중감제인 PD, DA를 넣고 현재 가장 많이 사용되고 있는 광중감제인 CQ와 조사시간 및 광중감제의 양을 증가시키며 광중합효율을 비교한 결과 다음과 간은 결론을 얻었다. 1. Bis-GMA의 합성여부를 적외선 흡수 분광법, 핵자기공명 흡수법 등 분광학적인 방법으로 확인하였으며 핵자기 공명 흡수법으로 확인한 결과 이성질체가 존재함을 알 수 있었다. 2. 조사시간이 증가됨에 따라 광중감제의 종류에 관계없이 광중합효율이 점차 증가되었으며, 약 60초까지 조사였을 때에는 광중합효율이 급격히 증가되었으나 그 이상 조사하여도 광중합효율이 크게 증가되지 않았다. 3. 같은 시간 조사하였을 경우 대체적으로 광중합효율이 증가되었으나 CQ와 DA의 경우는 3.0 mol% 첨가하였을 때에 비해 6.0 mol% 첨가되었을 때의 광중합효율이 오히려 더 낮게 나타나는 양상을 보였다. 4. 같은 시간동안 조사하고, 같은 양의 광중감제를 첨가하였을 경우 DA < CQ < PD 순으로 광중합효율이 높게 나타나서 CQ에 비해 PD를 첨가하였을 때의 광중합효율이 높게 나타났다. 5. 이상의 결과로부터 PD가 CQ를 대체할 수 있는 효율이 좋은 새로운 광중감제로서 사용될 가능성을 보여주었다.

• 대한치과기공학회지
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• 제23권2호
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• pp.49-59
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• 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
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• 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
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• pp.1208-1211
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• 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.

• 대한치과기공학회지
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• 제35권3호
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• pp.209-218
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• 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
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• 제11권4호
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• pp.183-191
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• 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.

• 한국광학회지
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• 제9권1호
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• pp.31-37
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• 1998

Acrylamide의 광중합(photopolymerization)반응에 의해 형성되는 acrylamide photopolymer를 제작하고 홀로그램 형성과정을 설명하였다. MB(methylene blue) 색소에 의한 빛의 흡수 및 표백과정과 TEA(triethanolamine)에 의해 라디칼중합을 하는 acrylamide 중합과정에 대해 자세히 논하였다. Beer-Lambert의 광화학 표백 모델(photochemical bleaching model)을 이용하여, photopolymer의 흡수곁수와 표백률상수(bleaching rate constant)를 구하였다. 그리고 acrylamide photopolymer의 홀로그램 특성에 기여하는 홑몸체(monomer)의 양과 회절효율과의 관계 및 노출량에 따른 회절효율을 측정하였다. 고분자 결정(polymer crystal)의 grain에 의한 산란효과와 정착(fixing)방법에 대해서도 논하였다.

• Macromolecular Research
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• 제14권2호
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• pp.155-165
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• 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.