• 한국염색가공학회지
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• 제11권4호
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• pp.1-7
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• 1999

Urethane-acrylate propelymers for secondary coating of optical fiber and high - performance material were prepared from the 4,4'-diphenylmethane diisocyanate(MDI), poly(tetramethylene oxide)glycol(PTMG, Mw 650 or 1000), 1,6-hexanediol(HD), 2-hydroxyethyl acrylate(HEA), and dibutyltin dilaurate as a catalyst. UV-Curable polyurethane acrylates were formulated from the urethane-acrylate prepolymers, three types of reactive diluents(DTs) having mono-, di-, and trifunctional-phenoxyethyl acrylate(PEA), hexanediol diacrylate(HDDA), and trimethylolpropane triacrylate(TMPTA), and 1-hydtoxycyclohexyl phenyl ketone(Irgacure 184) as a photoinitiator. The UV-cured films of polyurethane acrylates were obtained by curing using a medium-pressure mercury lamp(U W/cm, $\lambda_{max}=365\;nm)$. In this work, the effects of molecular weights of polyol and diol with low molecular weight into polymer chain on mechanical and dynamic mechanical properties of UV-cured polyurethane acrylates were studied. The structure and properties of the films obtained from the UV photopolymerization of urethane-acrylate prepolymer were investigated by FT-IR spectroscopy, dynamic mechanical measurement, tensile testing, and X-ray diffractometry.

• 청정기술
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• 제23권2호
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• pp.148-157
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• 2017

To prepare UV-curable polyurethane-acrylate oligomer, NCO-terminated urethane prepolymers with trimethylolpropane, [TMP; 0 (0), 0.1 (0.021) and 0.2 (0.043) mole (mole fraction)] as crosslinkable tri-functional chain extender were end-capped with pentaerythritol triacrylate [PETA; 2.0 (0.400), 1.7 (0.354) and 1.4 (0.304) mole (mole fraction)] with one hydroxyl group/three vinyl functionalities. The stable as-formulated UV-curable polyurethane-acrylates [stable mixtures of PETA-capped oligomer/reactive acrylic monomer diluents without/with heptadecafluorodecyl methacrylate (PFA; 0, 6 and 9 wt%)] were formed up to 0.2 (0.043) mole (mole fraction) of TMP content in the prepolymer, while homogeneous-mixing failed at 0.3 (0.068) mole (mole fraction), in which the crosslink density in NCO-terminated urethane prepolymer was too high to enable the formation of stable mixture. This study examined the effect of TMP/PETA molar ratio and heptadecafluorodecyl methacrylate (PFA) content (wt%) on the properties of UV-cured polyurethane-acrylates as marine antifouling coating materials. The properties of UV-cured polyurethane-acrylate were found to be significantly dependent on the crosslinkable TMP/PETA ratio and PFA content. With the increasing of the TMP and PFA contents, the contact angles increased, and consequently the surface tension decreased. The adhesion of algae/barnacles to PFA contained film samples were found to be sufficiently weak to allow their easy removal. These results suggest that the UV-cured samples containing PFA have strong potential as coating materials for antifouling applications.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1996년도 추계 학술발표회
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• pp.468-472
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• 1996

A series of UV-curable polyurethane acrylate ionomer were synthesized from isophorone diisocyanate(IPDI), poly(tetramethylene ether glycol)(PTMG), 2,2-bis(hydroxymethyl)propionic acid (CMPA), triethylamine(TEA), 2-hydroxy ethyl acrylate (HEA), and dibutyl tin dilaurate (DBT) as a catalyst. 2,2-dimethoxy-2-phenyl acetophenone(DMPAP) was used as a photoinitiator. The films of UV-cured polyurethane acylate ionomer were prepared by casting the formulated materials onto a glass plate at room temperature and cured using a medium pressure mercury lamp (80 W/cm, max = 365nm). Effects of DMPA content, molecular weight of PTMG and degree of neutralization on the properties were invesigated. It is found that the storage modulus increased with increasing DMPA content. The glass transition temperature of sample A shifted to higher temperature as the content of DMPA was increased. Tensile modulus also increased with increasing DMPA content. Modulus and Tg decreased with increasing molecular weight of PTMG form 650 to 2000. With increasing the degree of nutralizaion, ionomers exhibited improved modulu.

• 접착 및 계면
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• 제18권4호
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• pp.159-165
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• 2017

본 연구에서는 반응성 희석제로 사용되는 BA의 함량에 따른 자외선 경화형 폴리우레탄 아크릴레이트 수지를 제조하여 수지의 열적 기계적 성질, 접착강도, 굴곡성을 확인하였다. BA의 함량이 40% 이상으로 증가할수록 Polyol의 Tg와 아크릴 수지의 Tg가 분리되어 나타난 것을 DSC로 통해 확인하였다. 또한 BA의 함량이 증가할수록 아크릴 수지의 낮은 기계적인 물성이 주도적으로 발현되어 인장강도와 신장률, 접착강도가 감소하는 것으로 나타났다. 굴곡성을 평가한 결과 BA의 함량이 40%인 경우 경도가 낮으면서 다른 수지에 비해 Tm이 낮아 굴곡성이 우수한 것으로 나타났다.

• 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.

• Fibers and Polymers
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• 제2권3호
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• pp.141-147
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• 2001

The effect of compositions of isophorone diisocyanate (IPDl)/4.4'-diphenylmethane diisocyalate (MDI) and polypropylene oxide diol (PPG, $M_w$: 3000)/1,4-butane diol (BD) on the properties of UV-cured polyurethane acrylate films based on 2-hydroxyethyl acrylate (HEA) was examined. UV-curable polyurethane acrylates were formulated from the prepolymer. trimethylol propane triacrylate (TMPTA) as a reactive diluent, and 1-hydroxycyclohexyl ketone (Irgacure 184) as a photoinitiator. Dynamic mechanical thermal properties and elastic properties of UV-cured polyurethane acrylates was fecund to depend on the chemical composition of IPDl/MDl and PPG/BD. As the BD content increased, the tensile storage modulus of all series samples increased significantly. The storage modulus increased in the order of samples A (IPDI based samples)> samples B (IPDI/MDl (7/3 molar ratio) based samples) > samples C (IPDI/MDl (5/5 molar ratio) based samples at the same composition. Two distinct louts modulus peaks for all samples are observed owing to the softs segment glass transition temperature ($T_gh$) and hard segment glass transition temperature ($T_gh$). The difference between $T_gh$, and $T_gh$, (Δ$T_g$) increases in the order of A > B > C at the same composition. In cycle test, the initial onset strain (%) was found to decrease with increasing BD content in PPG/BD and with increasing MDI content in IPDI/MDl.

• 한국환경과학회:학술대회논문집
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• 한국환경과학회 2020년도 정기학술대회 발표논문집
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• pp.226-226
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• 2020

• 한국환경과학회지
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• 제27권11호
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• pp.1023-1028
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• 2018

Shape memory materials are widely used in high-tech industries. Although shape memory polymers have been developed, they have a disadvantage, only unidirectional resilience. Shape memory polymers with bi-directional recovery resilience have been actively studied. In this study, a bidirectional shape memory polyurethane was synthesized using poly(${\varepsilon}$-caprolactone) diol, methylene dicyclohexyl diisocyanate, and hydroxyethyl acrylate. The first physical curing occurred between hard segments and hydrogen bondings when the solution was dried. The second curing in acrylate groups was performed by UV exposure. A degree of curing was analyzed by infrared spectroscopy. The shape memory properties of 2 step-cured polyurethanes were investigated as a function of UV curing time.

• 접착 및 계면
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• 제13권4호
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• pp.156-162
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• 2012

UV 경화형 우레탄아크릴레이트 수지와 유기화클레이를 혼합한 후 UV를 조사하여 경화시킴으로써 폴리우레탄-클레이 나노복합체를 제조하였다. 유기화클레이로서는 Closite20A (C20A) 및 이를 실란처리하여 표면에 아크릴기를 도입한 아크릴변성 C20A를 사용하였다. XRD와 TEM 분석으로부터 제조된 나노복합체는 삽입형 나노복합체이며, 아크릴 변성시킨 C20A가 변성시키지 않은 C20A에 비해 더 잘 분산되는 것을 알 수 있었다. DMTA, 연필경도분석, PET 필름에의 부착성 시험으로부터 클레이 첨가에 의해 유리전이온도와 저장탄성률 및 연필경도가 증가하고 PET 필름에의 부착성이 향상되며, 이러한 물리적 특성의 증가는 아크릴 변성시킨 C20A를 함유한 나노복합체에서 더 크게 발현됨을 알 수 있었다. 또한, 클레이 첨가에 의해 UV경화 시 수반되는 수축을 저하시킬 수 있음을 알았다. 한편, 제조된 나노복합체는 우수한 광투과도를 나타내었으나, 광택도는 나노입자를 함유하지 않은 경우에 비해 다소 저하되었다.

• 한국산학기술학회논문지
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• 제11권5호
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• pp.1773-1777
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• 2010

광경화(UV-curing)에 의한 PVC 바닥상재 코팅기술은 PVC 바닥상재 질의 개선을 위하여 사용되는 것이다. 본 연구에서 사용한 폴리우레탄 아크릴레이트 수지는 반응성 모노머, 광개시제, 그 외 첨가제를 배합하여 제조하였고, 올리고머는 상용화된 지방족 우레탄 아크릴레이트를 사용하였다. 제조한 코팅액을 바코팅(bar-coating) 방법으로 PVC 바닥상재에 코팅한 후 광경화법을 이용하여 상재표면에 코팅층을 형성하였다. 코팅에 사용된 코팅액은 FTIR로 측정하여 특성을 확인하였으며, PVC 상재 표면에 형성된 코팅층의 물성은 광택과 부착력으로 평가하였다. 코팅층의 물성은 코팅조성과 공정조건에 영향을 받았다.