• 접착 및 계면
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• 제10권4호
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• pp.191-198
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• 2009

지방족 에폭시 수지인 glycerol diglycidyl ether (GDE)에 단관능성 아크릴 수지인 2-carboxyethyl acrylate (2-CEA) 또는 2-hydroxyethyl acrylate (2-HEA)를 반응시켜 지방족 에폭시 아크릴레이트를 제조하였다. FT-IR, $^1H$-NMR, 그리고 $^{13}C$-NMR를 사용하여 생성물을 확인하였고, 수율은 prep-LC를 사용하여 얻었다. 생성물의 자외선 경화거동은 photo-DSC를 사용하였고, 열경화 반응성은 DSC를 사용하여 얻었다. 2-CEA의 반응성이 2-HEA보다 월등히 높음을 알 수 있었고, 2-CEA로부터 제조한 지방족 에폭시 아크릴레이트(GEA-C)의 수율은 약 83%이었다. 촉매를 제거한 GEA-C 생성물의 자외선 경화반응($T_{max}$)은 약 10 s로 빠르게 진행되었다. GEA-C는 투명하고, 내열성이 우수하며 저점도를 갖고 있음을 확인할 수 있었다. ${\Delta}E^*$는 2.51, 점도는 192 cps, 5% 중량감소 때의 온도는 $299^{\circ}C$이었다. Kissinger와 Ozawa-Flynn-Wall 식으로 얻은 GEA-C의 열경화 반응의 활성화에너지($E_a$)는 91~92 kJ/mol이었다.

• 멤브레인
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• 제34권1호
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• pp.70-78
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• 2024

본 연구에서는 역전기투석용 4차 암모늄이온을 음이온교환기로 갖는 폴리아크릴레이트계 광가교형 음이온교환막을 개발하였다. 역전기투석은 청정 재생에너지 생산 시스템이지만 출력이 낮고 핵심 소재인 분리막의 가격이 비싸다는 단점으로 인해 상용화에 제한이 있다. 이에, 지지체가 없는 광가교형 음이온교환소재를 제조하였으며 개발한 고분자의 주쇄는 우수한 물성의 엔지니어링 플라스틱을 기반으로 제조하였다. 제조된 분리막은 우수한 물리적, 화학적, 전기화학적 특성을 보였으며 상용 음이온교환막인 AMV와 비교하여 약 50% 낮은 분리막 저항을 보였다. 더욱이 CQAPPOA-35는 40 ㎛의 얇은 분리막 두께에도 불구하고 상용막과 동등 수준의 선택도를 보이는 것을 확인할 수 있었다. CQAPPOA-35을 적용한 RED 스택은 최대 2.327 W m^-2 (flow rate : 100 mL min^-1)의 출력 밀도를 보여 AMV가 도입된 것보다 15% 향상된 성능 특성을 보였다. 개발된 CQAPPOA-35이 광경화를 통해 쉽고 저렴하게 제조할 수 있으며 RED 스택 특성도 매우 우수하다는 점을 고려할 때, 개발된 CQAPPOA-35은 RED용 음이온교환막으로 상용 활용을 위한 대안이 될 수 있을 것으로 기대된다.

• Bulletin of the Korean Chemical Society
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• 제31권7호
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• pp.1891-1896
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• 2010

Submicron-sized polymeric colloidal particles can self assemble into 3-dimensional (3D) opal structure which is a useful template for photonic crystal. Narrowly dispersed polymer microspheres can be synthesized by emulsion polymerization in water using water-soluble radical initiator. In this report, we demonstrate a facile and reproducible emulsion polymerization method to prepare various polymeric microspheres within 200 - 400 nm size ranges which can be utilized as colloidal photonic crystal template. By controlling the amount of monomer and surfactant, monodisperse polymer colloids of polystyrene (PS) and acrylates with various sizes were successfully prepared without complicated synthetic procedures. Such polymer colloids self-assembled into 3D opal structure exhibiting bright colors by reflection of visible light. The colloidal particles and the resulting opal structures were rigorously characterized, and the wavelength of the structural color from the colloidal crystal was confirmed to have quantitative relationship with the size of constituting colloidal particles as predicted by Bragg equation. The tunability of the structural color was achieved not only by varying the particle size but also by infiltration of the colloidal crystal with liquids having different refractive indices.

• Macromolecular Research
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• 제15권6호
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• pp.533-540
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• 2007

We designed and successfully synthesized UV curable, functional acrylate monomers having a polarizing group, i.e., an electron-withdrawing and/or electron-donating group for the optical materials of high refractive index. Optical polymer films made from the functional methacrylate monomers were achieved with photo crosslinking under UV illumination. A monomer having amino and cyano groups (Dimer-CN) exhibited the highest refractive index ($n_{TE}$=1.595 at 850nm) among the studied methacrylate derivatives, due to the large polarizability of the dipolar monomer structures with electron-donating and withdrawing groups. By controlling the compositions of the functional acrylate monomer of copolymers, the refractive indices of the polymers were readily adjusted within a wide range of 1.498-1.595. The copolymers showed a high glass transition temperature $(T_g)$ and good thermal stability, which are desirable for optical applications. $T_g$ and $T_{10%}$ (10%-weight loss occurred) of the copolymers ranged from $120-140^{\circ}C$ and from $329-387^{\circ}C$, respectively.

• Bulletin of the Korean Chemical Society
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• 제28권12호
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• pp.2139-2152
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• 2007

Ruthenium complex-catalyzed reactions often require highly qualified tuning of reaction conditions with substrates to attain high yield and selectivity of the products. In this review, our strategies for achieving characteristic ruthenium complex-catalyzed co-oligomerization of different alkenes are disclosed: 1) The codimerization of 2-norbornenes with acrylic compounds by new ruthenium catalyst systems of RuCl3(tpy)/Zn [tpy = 2,2':6',2''-terpyridine] or [RuCl2(η6-C6H6)]2/Zn in alcohols, 2) A novel synthesis of 2-alkylidenetetrahydrofurans from dihydrofurans and acrylates by zerovalent ruthenium catalysts, such as Ru(η4-cod)(η6-cot) [cod = 1,5-cyclooctadiene, cot = 1,3,5-cyclooctatriene] and Ru(η6-cot)(η2-dmfm)2 [dmfm = dimethyl fumarate], 3) Regio- and stereoselective synthesis of enamides by Ru(η6-cot)(η2-dmfm)2-catalyzed codimerization of N-vinylamides with alkenes, and 4) Unusual head-to-head dimerization of styrenes and linear codimerization of styrenes with ethylene by Ru(η6-cot)(η2-dmfm)2 catalyst in the presence of primary alcohols.

• 한국응용과학기술학회지
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• 제17권4호
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• pp.262-266
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• 2000

Acrylic pressure sensitive adhesives of n-butyl acrylate, 2-ethyl acrylate, methyl acrylate, vinyl acetate, acrylic acid, acrylonitrile and 2-hydroxyethyl acrylate were synthesized and basic physical properties of pressure sensitive adhesives with increasing the contents of 2-hydroxyethyl acrylate were investigated. 2-Hydroxyethyl acrylates effects on glass transition temperature, viscosity, hardening time and peel strength. Glass transition temperature(Tg) decreased with increasing the contents of 2-hydroxyethyl acrylate. Viscosity and hardening time were increased with increasing the contents of 2-hydroxyethyl acrylate. On the other hands, peel strength increased with increasing the contents of 2-hydroxyethyl acrylate up to 6 wt% and the decreased at further higher contents of 2-hydroxyethyl acrylate. In peel test, interfacial failure was occured in 8 wt% and 10wt%.

• 분석과학
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• 제15권4호
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• pp.341-345
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• 2002

UV 광 중합 반응의 진행정도를 near-IR 분광학적 방법을 사용하여 관찰하였다. 광중합반응의 반응체는 4차 암모늄염을 포함하고 있는 아크릴 모노머를 사용하였으며 광 개시제로는 Darocur 1174를 사용하였다. 반응의 진척도는 광중합 반응의 정도를 나타내 주는 척도가 되는 중합 반응체인 아크릴 모노머의 -C=$CH_2$ 기와 관련된 흡수 띠인 1615 nm(6190 $cm^{-1}$)와 2105 nm(4750 $cm^{-1}$)에서 관찰된 띠 세기의 전환율로부터 구하였다. Near-IR 분광법이 광 중합 반응의 진행정도를 관찰하는데 효과적인 방법이 될 수 있음을 알 수 있었다.

• Macromolecular Research
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• 제14권5호
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• pp.517-523
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• 2006

The effects of particle content, size and shape on the thermal conductivity (k) and adhesion properties of thermally conductive, pressure-sensitive adhesives (PSAs) were investigated. The matrix resins were thermally crosslinkable, 2-ethylhexyl acrylic polyol and ultraviolet (UV)-curable, random copolymer consisting of acrylic oligomer and various acrylates. We found that k increased with increasing diameter and particle aspect ratio, and was further enhanced due to the reduction of the interfacial thermal barrier when the coupling agent, which increases the adhesion between particles and the matrix resin, was used. On the other hand, adhesion properties such as peel strength and tack of the thermally crosslinkable resin decreased sharply with increasing particle content. However, for UV curable resin, increased particle addition inhibited the decrease in adhesion properties.

• 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.

• Macromolecular Research
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• 제16권7호
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• pp.614-619
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• 2008

Copolymers of phenyl alkyl acrylates/methacrylates are used clinically as soft materials for the foldable intraocular lens (IOL) to treat cataracts. In this study, copolymers of 2-phenylethyl acrylate (PEA) and 2-phenylethyl methacrylate (PEMA) of various compositions were prepared using free radical polymerization in solution. The composition of the copolymers was determined by $^1H$-NMR analysis. The reactivity ratios of the monomers were calculated using the conventional Fineman-Ross or Kelen-Tudos method. The reactivity ratio of PEA ($r_1$) and PEMA ($r_2$) were estimated to be 0.280 and 2.085 using the Kelen-Tudos method, respectively. These values suggest that PEMA is more reactive in copolymerization than PEA, and the copolymers will have a higher content of PEMA units. The glass transition temperature ($T_g$) of the copolymers increased with increasing PEMA content. The molecular weight and polydispersity indices ($M_w/M_n$) of the polymers were determined by GPC. Overall, these results are expected to be quite useful in applications to foldable soft IOL materials.