• 한국응용과학기술학회지
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• 제24권2호
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• pp.149-159
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• 2007

In order to prepare high-solid coatings, acrylic resins, HSCs [poly (EA/EMA/2-HEMA/CLA)] that contain 90% solid, were synthesized by copolymerization of ethyl acrylate (EA), ethyl methacrylate (EMA), 2-hydroxyethyl methacrylate (2-HEMA) and caprolactone acrylate (CLA). The high-solid coatings named as CHSCs (HSCs/HDI-trimer) were prepared by the curing reaction between the acrylic resins containing 90% solid contents and the isocyanates (HDI-trimer) curing agent room temperature. The curing behavior and various properties were examined on the film coated with the both high-solid coatings. The glass transition temperatures $(T_g)$ of CHSCs increased proportionally with increasing the predicted $T_g$ value by Fox equation, and had nothing to do with the solid contents. The prepared film showed good properties for $60^{\circ}$ specular gloss, impact resistance, cross-hatch adhesion and heat resistance, and bad properties for pencil hardness, drying time, and pot-life. Among the film properties, the heat resistance was very excellent and could be explained by the introduction of functional monomers of CLA.

• 반도체디스플레이기술학회지
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• 제16권1호
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• pp.45-51
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• 2017

Poly(urethane acrylate) siloxane oligomers with Interpenetrating polymer netwoked nanoparticles were prepared to synthesize hard coating solution by reaction with diisocyanates. The diisocyanate combined siloxane hard coating solution showed more flexibility than the siloxane solution. In addition, diisocyanate resulted in improvement of curl property and surface hardness in the siloxane solution. Of the used diisocyanates, isophorone diisocyanate and acryloyloxy ethyl diisocyanate were good for UV hard coating solution. This effect will decrease brittleness in the siloxane solution using for plastic display plate.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 춘계학술대회 논문집
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• pp.270-273
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• 2009

A comb-like copolymer consisting of a poly(vinylidene fluoride-co-chlorotrifluoro-ethylene) backbone and poly(hydroxy ethyl acrylate) side chains, i.e. P(VDF-co-CTFE)-g-PHEA, was synthesized through atom transfer radical polymerization (ATRP) using CTFE units as a macroinitiator. Successful synthesis and a microphase-separated structure of the copolymer were confirmed by proton nuclear magnetic resonance (1H-NMR), FT-IR spectroscopy, and transmission electron microscopy (TEM). This comb-like polymer was crosslinked with 4,5-imidazole dicarboxylic acid (IDA) via the esterification of the -OH groups of PHEA and the -COOH groups of IDA. Upon doping with phosphoric acid ($H_3PO_4$) to form imidazole-$H_3PO_4$ complexes, the proton conductivity of the membranes continuously increased with increasing $H_3PO_4$ content. A maximum proton conductivity of 0.015 S/cm was achieved at $120^{\circ}C$ under anhydrous conditions. In addition, these P(VDF-co-CTFE)-g-PHEA/IDA/$H_3PO_4$ membranes exhibited good mechanical properties (765 MPa of Young's modulus), and high thermal stability up to $250^{\circ}C$, as determined by a universal testing machine (UTM) and thermal gravimetric analysis (TGA), respectively.

• 공업화학
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• 제8권4호
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• pp.673-678
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• 1997

본 연구에서는 associative macromonomer로서 비이온성 vinyl surfactant ester(alkyloxy $poly(ethyleneoxy)_n$ ethyl acrylate)[VSE]를 사용한 유화중합을 통하여 회합형 아크릴 증점제를 합성하고, 유성학적 물성을 고찰하였다. VSE의 소수성 말단기의 탄소수, ethoxylation 정도에 따라 회합형 증점제의 증점제의 증점효과가 크게 영향을 받았다. VSE의 종류를 고정하고, 공단량체 조성을 달리하여 제조한 아크릴 회합형 증점제의 수용액 점도 병화를 고찰한 결과, VSE의 양이 늘어날수록 증점효과가 증가하였다. 이것은 VSE의 소수성 말단기의 상호작용에 의한 회합 증점 메카니즘에 의해 증점효과가 향상되었기 때문이다. 또한 사슬전이제에 의한 분자량이 감소할수록 hydrodynamic volume이 작아져 증점효과가 감소하였다.