• 한국염색가공학회지
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• 제19권5호
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• pp.1-7
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• 2007

A new UV-curable coating was carried out to impart the flame-retardant property to cotton fabric using Bis[2-(methacryloyloxy)ehtyl]phosphate(DMEP) and 2-hydroxy-2-methyl-1-phenyl-propan-l-one(HMPP) as a UV-curable monomer and a photoinitiator, respectively. The cotton fabrics were applied with various amounts of DMEP and HMPP via padding and UV irradiation, and the optimal concentrations of DMEP and HMPP in the formulation were 40%(w/w) and 7%omp respectively. A limiteed oxygen index(LOI) up to 28.9 was obtained for the UV-cured fabric, which may occur through a condensed phase mechanism as verified by the increased residue number with increased application level. The characterization of the UV-cured coating was made by IR analysis, thermo-gravimetric analysis, LOI test, and scanning electron microscopy.

• 한국염색가공학회지
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• 제35권4호
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• pp.231-238
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• 2023

Microporous gel films of 29 m were prepared by the gel drawing of UHMWPE/soybean oil blend (4:6, w/w) up to 800%. The stretched films containing the optimal photoinitiator concentration, depending on the film thickness, was cross-linked under 365 nm LED-UV irradiation and the oil was extracted with n-hexane, resulting in a gel fraction of 95 % or more. With the formation of the cross-linked structure, the melt-down temperature and melt-down elongation increased by 16 ℃ and by 63% respectively. Also the thermal stability of the crosslinked UHMWPE was proved by the area shrinkage under the heat treatment decreased to 3.8 % compared to 17.4 % for the pristine film, and by the reductions in the combustion heat. The enhanced thermal stability of the crosslinked UHMWPE microporous membranes can be used for various industrial applications such as filters, electric vehicles and energy storage systems.

• Fibers and Polymers
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• 제2권3호
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• pp.122-128
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• 2001

UV-curable polyurethane acrylate prepolymers were prepared from diisocyanates [isophorone diisocyanate (IPDI), 2,4-toluene diisocyanate (TDI), or 4,4'-dicyclohexylmethane diisocyanate (H$_{12}$MDI)], diols [ethylene glycol (EG), 1,4-butane diol (BD), or 1,6-hexane diol (HD)], polypropylene glycol as a polyol. UY-curable mixtures were formulated from the prepolymer (90 wt%), reactive diluent monomer trimethylol propane triacrylate (10 wt%). and photoinitiator 1-hydroxycy-clohexyl ketone (3 wt% based on prepolymer/diluent). The effects of different diisocyanates/low molecular weigh dial on the dynamic mechanical thermal properties and elastic recovery of UV-cured polyurethane acrylate films were examined. The tensile storage modulus increased a little in the order of EG > BD > HD at the same diisocyanate. Two loss modulus peaks for all samples are observed owing to the glads transition of softs segments ($T_gh$) and the glass transition temperature of hard segments ($T_gh$). For the same diisocyanate, $T_gh$, decreased, however, $T_gh$ increased, in the order of HD > BD > EG. The elastic recovery also increased in the order of HD > BD > EG at the same diisocyanate. In case of same diols, $T_gh$ increased in the order of $H_12$MDl > TDI > IPDI significantly. The ultimate elongation and elastic recovery increased in the order of TDI > IPDI > $H_12$MDl at the same diol.l.

• Korean Chemical Engineering Research
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• 제50권4호
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• pp.621-626
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• 2012

본 연구에서는 마이크로 기공의 중공구를 유기 고분자 수지와 복합화한 유/무기 하이브리드 물질을 제조하여 우수한 단열 성능을 갖는 코팅유리를 개발하고자 하였다. 유기 고분자 물질로는 투명성과 접착성이 우수한 6관능기의 우레탄 아크릴레이트(UP118), 3관능기의 trimethylolpropane triacrylate (TMPTA), 2관능기의 1,6-hexanediol diacrylate (HDDA), 광 개시제(Irgacure184) 등으로 구성된 자외선 경화형 수지를 사용하였다. 유리 및 실리카 중공구를 고분자 수지에 각각 10~40 vol%까지 첨가하여 얻어진 코팅 졸을 투명유리에 바(bar)코팅 방식으로 박막을 형성시킨 후 자외선 경화를 통해 최종 코팅유리를 제조하였다. 마이크로 중공구의 종류 및 함량이 제조된 코팅유리의 광 투과율, 열전도도, 접착성 및 표면 경도에 미치는 영향을 조사하였다. 복합물 코팅유리는 중공구가 과량 첨가되어도 우수한 접착성(5B)을 유지하였으며, 단열 성능은 각 중공구가 20 vol%만 함유되어도 뚜렷하게 향상된 결과를 나타냈다. 또한 실리카 중공구(SP)를 단열 재료로 사용하였을 경우 광 투과율 80 %의 투명 코팅유리를 얻을 수 있었다.

• 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.

• Journal of the Korean Wood Science and Technology
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• 제36권6호
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• pp.121-129
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• 2008

고경도, 고광택, 고내마모성 및 고내산성 등의 물성이 요구되는 마루바닥재의 상도용 도료로는 물성이 우수하면서도 환경친화적인 자외선경화형 도료가 많이 사용되고 있다. 그 중에서도 특히 에폭시 아크릴레이트계의 올리고머는 높은 열안정성과 속경화 특성으로 인하여 목재내장재의 도료로써 많이 사용되고 있다. 본 연구에서는 아크릴레이트 관능기 수가 자외선 경화형 에폭시 아크릴레이트 도료의 열안정성 및 표면경도에 미치는 영향을 분석하고자 하였다. 조성분을 이루는 모노머, 올리고머, 광개시제 각각의 열분해 거동 및 아크릴레이트 관능기수가 달리 배합된 에폭시 아크릴레이트 도료의 열안정성을 열중량분석기(TGA)를 사용하여 평가하였으며, 열안정성과 물리적 물성과의 관계를 확인하기 위하여 진자경도계를 이용하여 표면경도를 측정하였다. 경화 전 후의 열분해 거동 및 표면경도를 비교한 결과, 자외선 경화 중에 발생하는 가교에 의해 도막의 열안정성이 부여되며, 관능기의 수가 많아짐에 따라 열안정성뿐만 아니라 표면경도도 향상됨을 확인하였다.

• 한국도로학회논문집
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• 제13권2호
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• pp.1-8
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• 2011

본 연구의 목적은 중온화 첨가제(LEADCAP$^{(R)}$)를 사용한 중온 아스팔트 바인더의 노화 방법에 따른 물성 변화 특성을 평가하고자 하였다. 아스팔트 바인더의 노화 거동을 모사하기 위해 단기노화인 RFTO를 실시하였으며, 햇빛에 의한 자연 노화 거동을 알아보기 위해 자외선 경화기를 이용하여 자외선에 의한 열화거동을 모사하였다. 이러한 열화 중온 아스팔트 바인더의 역학적인 물성과 유변동학적인 특성을 시험하기 위해서 만능시험기(UTM)과 동적전단유동기를 이용하여 직접인장력과 유변동학적인 거동을 평가하였다. 또한, 열분석 장비를 이용하여 온도에 따른 중온 아스팔트 바인더의 특성을 평가하여, 자외선 노출에 따른 열화가 발생하여도 온도에 따른 물성 변화가 많이 발생하지 않음을 발견하였다. $70^{\circ}C$에서 중온화 첨가제가 첨가한 단기노화 중온 아스팔트 바인더의 경우, PG 등급에서의 고온 등급의 기준값을 만족함을 알 수 있었다. 또한 저온에서 중온 아스팔트 바인더의 인장 특성을 평가한 결과, 인장강도 향상과 함께 인장력이 증가됨을 알 수 있었다.

• 한국응용과학기술학회지
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• 제26권4호
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• pp.467-472
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• 2009

Ultraviolet curable coating solution was prepared with poly(ethylene glycol) acrylate oligomer and various mono and multi-functional acrylate monomers. The optical properties of UV cured coating layer on PET film with acrylate coating solution containing metal oxides, such as fumed silica and alumina, were also investigated to reduce light reflection on films. Poly(ethylene glycol) diacrylate which has 575 of average molecular weight was used as oligomer acrylate, and pentaerythritol triacrylate and dipentaerythritolpenta-/hexa acrylate were used as multi-functional acrylate monomers. Also, butyl acrylate was used to improve the adhesion as well as to reduce glass transition temperature to give a better flexability. 1-hydroxy cyclohexyl phenyl ketone was used as photoinitiator. We found out the metal oxides in acrylate coating solution showed a homogeneous dispersion from energy dispersive spectroscopy data. Transmittance and light reflection of coated PET film was measured with UV/vis spectrometer and gloss meter, respectively. When 1.00 g of both metal oxides was added into coating solution, the transmittance and the glossiness were reduced from 90% to 30% and from 190 GU to 35 GU, respectively. However, adding up to 1.00 g of the metal oxide into coating solution did not affect on the hardness of coating layer and adhesion between coated layer and PET film. Conclusively, we can control transmittance and light reflection of coated film by adjusting the amounts of metal oxide in coating solution.

• The Journal of Advanced Prosthodontics
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• 제7권5호
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• pp.386-391
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• 2015

PURPOSE. The purpose of this preliminary study was to investigate the effects of adding 4,4'-bis(N,N-diethylamino) benzophenone (DEABP) as a co-initiator to a binary photoinitiating system (camphorquinone-amine) to analyze on the degree of conversion (DC) of a light-cured resin for dental 3D printing. MATERIALS AND METHODS. Cylindrical specimens (N=60, n=30 per group, ${\phi}5mm{\times}1mm$) were fabricated using bisphenol A glycerolate dimethacrylate (BisGMA) both with and without DEABP. The freshly mixed resins were exposed to light in a custom-made closed chamber with nine light-emitting diode lamps (wavelength: 405 nm; power: $840mW/cm^2$) for polymerization at each incidence of light-irradiation at 10, 30, 60, 180, and 300 seconds, while five specimens at a time were evaluated at each given irradiation point. Fourier-transform infrared (FTIR) spectroscopy was used to measure the DC values of the resins. Two-way analysis of variance and the Duncan post hoc test were used to analyze statistically significant differences between the groups and given times (${\alpha}$=.05). RESULTS. In the DEABP-containing resin, the DC values were significantly higher at all points in time (P<.001), and also the initial polymerization velocity was faster than in the DEABP-free resin. CONCLUSION. The addition of DEABP significantly enhanced the DC values and, thus, could potentially become an efficient photoinitiator when combined with a camphorquinone-amine system and may be utilized as a more advanced photopolymerization system for dental 3D printing.

• 대한치과기공학회지
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• 제33권4호
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• pp.291-297
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• 2011

Purpose: The purpose of this study was to know the availability of three photosensitizers, CQ, PD, DA, as a photosensitizer of dental resin composite. We want to know abortion band around visible light region for the using potential possibility as a photosensitizer for visible light cured dental composite resin. And I studied to know the relative photodecomposition ratio of three photosensitizers with or without photoinitiator, DAEM. Methods: The photodecomposition of three photosensitizers were studied by UV absorption spectroscopy in ethanol and determined by same instrument with irradiation time for relative photodecomposition. In order to study the effect of amine on photodecomposition was added the DAEM in the photosensitizer solution and the relative rate was measured by the same procedure with aove mentioned. Results: The all of three photosensitizers are absorbed around visible light region. The relative rate of decrease in absorbance incereased in the order: CQ < BD < PD. The effect of DAEM on the photodecomposition of the photosensitizers was appeared different results without DAEM. The photodecomposition rate of PD and DA decreased somewhat with the addition of amine, while that of CQ increased. The rtealtive photodecomposition rate increased in the oprder: BD ${\leq}$ CQ < PD with the addition of amine, but the differnce was not significant. Conclusion: PD and DA like CQ gives to the possibility of use as a photosensitizer for visible light cured dental composite resin by absorption around visible light region and photodecomposition in the maximum absorption wavelength. And it is showed that PD and DA are not effective decomposed with amine initiator, DAEM but CQ decomposed with DAEM effectively. This result may be due to a different mechanism operating for the decomposition of photosensitizers in the presence of amine.