• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.101-101
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• 2006

We have studied the micellisation of poly(n-butyl acrylate)-block-poly(acrylic acid) and poly(n-butyl acrylate)-graft-poly(acrylic acid) in aqueous solution. The size and structure of the formed micelles was elucidated by scattering and imaging techniques. The micelle structure depends on pH, composition, and topology: graft copolymers form much smaller micelles that block copolymers of similar composition. We have also synthesized block copolymers of acrylic acid and N-isopropylacrylamide (NIPAAm) or N,N-diethylacrylamide (DEAAm). Due to the LCST of polyNIPAAm and polyDEAAm, these block copolymers spontaneously form micelles upon heating and they form inverse micelles upon decreasing pH below 4. If the LCST block is much longer than the PAA one, this presents a very convenient way to prepare crew-cut micelles. The polymers have been successfully used as stabilizers in emulsion polymerization. They also have been conjugated to streptavidin. The conjugates reversibly form mesoscopic particles on heating.

• 한국염색가공학회지
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• 제14권6호
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• pp.313-318
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• 2002

Chitosan is known to be an excellent biocompatible natural polymer. Recently, with a growing interest of health and environment, chitosan which is good in no harmful effect on human body and environment, has been watched as the finish treatment of hygiene and pleasantness. The purpose of this study is to develop multi functional fabrics by chitosan added on acrylic acid grafted cotton fabrics. Therefore physical properties such as moisture regain, air permeability, whiteness, static voltage and tensile strength of chitosan added on acrylic acid grafted cotton fabrics were investigated. The results are as follows ; According to increased chitosan's concentration, grafting yield was decreased. Therefore thickness of film by treated chitosan added on acrylic acid grafted cotton fabric became thin. FT R spectra of chitosan add on acrylic acid grafted cotton fabric clearly showed peaks of COOH and $NH_2$, Moisture regain, static voltage of chitosan add on acrylic acid grafted cotton fabrics were increased than control. Air permeability, whiteness and tensile strength were decreased than control.

• 접착 및 계면
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• 제14권1호
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• pp.43-48
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• 2013

압력감응성 아크릴 점착제의 물성은 가교를 위한 관능성그룹을 가진 단량체를 이용하여 쉽게 물성을 조절할 수 있다. 본 연구에서는 두개의 다른 가교제, isocyanate 및 epoxy형 가교제에 따른 아크릴 점착제의 가교특성과 물성을 연구하였다. 2-Ethylhexyl acrylate, acrylic acid (AA)와 2-hydroxyethyl methacrylate를 주 단량체로 하여 이소시아네이트 또는 에폭시형 가교제로 가교한 점착제의 박리점착 특성, 볼텍, 유지력 및 수축성을 고찰하였다. 점착특성은 AA함량 증가와 더불어 증가하였고 가교점이 많고 ether와 같은 유연한 결합을 생성하는 에폭시형 가교제에서 우수한 물성을 나타내었다.

• 한국응용과학기술학회지
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• 제24권1호
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• pp.10-22
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• 2007

To prepare weather-resistant silicone/acrylic resin coatings for an architectural purpose, tetrapolymers were synthesized by a radical polymerization. 3-Methacryloxypropyltrimethoxysilane (MPTS) as a silicone monomer and n-butyl acrylate, methyl methacrylate, and n-butyl methacrylate as acrylic monomers were used. The compositions of monomers were adjusted to fix the glass transition temperature of acrylic polymer for $20^{\circ}C$. The composition of MPTS in the synthesized polymer were varied from 10 wt% to 30 wt%. On the basis of synthesized resin amber paints were prepared and their physical properties and effects for weatherability were examined. The presence of MPTS in silicone/acrylic resins generally resulted in low molecular weight and broad molecular weight distribution, and also lowered the viscosity of the copolymers. The coated films prepared from these resins showed good and balanced properties in general. Adhesion to the substrate was outstanding in particular. Weatherability tests were carried out in three different types such as outdoor exposure, QUV, and SWO. The test results showed that the silicone/acrylic resins containing 30 wt% of MPTS had weather-resistant properties.

• 폴리머
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• 제28권3호
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• pp.273-280
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• 2004

고형분 80%인 아크릴수지 (에틸 메타크릴레이트-2-히드록시프로필 메타크릴레이트-노르말부틸 아크릴레이트-아크릴산 : EHBC)를 합성한 후 이를 헥사메틸렌 디이소시아네이트-뷰렛 경화제로서 상온경화시켜 고 고형분 도료 (에틸 메타크릴레이트-2-히드록시프로필 메타크릴레이트-노르말부틸 아크릴레이트-아즈릴산/헥사메틸렌 디이소시아네이트-뷰렛 : EHBCN)를 제조하였다. 진동자법에 의한 점탄성 측정에서 제조된 도료인 EHBCN-4 (EHBC-4 정적 $T_{g}$ $0^{\circ}C$)와 EHBCN-7 (EHBC-7 : 정적 $T_{g}$ 3$0^{\circ}C$)의 경화시간은 6.2시간과 4.5시간으로, 또한 경화된 도막의 동적 $T_{g}$ 는 $14^{\circ}C$ 와 $39^{\circ}C$로 각각 나타났다. 도막 물성 중 접착력과 굴곡성은 카프로락톤 아크릴레이트 단량체 성분이 함유된 EHBCN쪽의 물성이 현저히 좋게 나타나, 카프로락톤 아크릴레이트 성분이 접착력과 굴곡성을 증진시켰음이 입증되었다.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2008년도 추계학술발표대회 및 제15회 신소재 심포지엄
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• pp.29.1-29.1
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• 2008

• 폴리머
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• 제38권6호
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• pp.801-808
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• 2014

광경화 아크릴고분자 필름에서 이온이동에 관한 연구를 하였다. 고분자에 결합된 아민기와 카르복실산 작용기의 함량을 조절하여 수소이온과 수산화이온의 이동에 적합한 필름을 제조하였다. 수소이온 이동 검출을 위해 p-methylred(PMR) 유도체를 사용하였고 수산화이온 검출을 위해 페놀프탈레인 유도체를 합성하여 각각 고분자에 도입하였다. 수소이온의 이동은 아민기의 함량이 많을수록 빠르게 진행되었고 수산화이온은 카르복실산의 함량이 높을수록 빠르게 이동하였다. 수소이온 이동은 필름표면과 내부로 빠르게 진행하였고 PMR 포함 필름의 흡수스펙트럼을 통해 관찰되었다. 산 용액에 감응하는 필름을 사용하여 색상변화의 가역성을 관찰하였고 연속 50회를 실시하는 동안 정확히 재현되었다. 구리(II) 이온은 카르복실산 작용기의 함량이 높은 필름에서 빠르게 이동하였다. 로다민이 도입된 필름에서 구리이온의 배위로 로다민의 고리열림 반응이 진행되었고 광흡수 및 발광특성 측정을 통해 구리이온의 이동을 추적하였다.

• Journal of Pharmaceutical Investigation
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• 제36권2호
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• pp.83-87
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• 2006

Poly(acrylic acid) (PAA) was identified to possess good mucoadhesive properties ensuring its application to extend the retention times of the formulations at the oral cavity, intended route of administration using the polymer. In the noncross-linked state, PAA will swell and become eroded owing to the presence of salivary flow from the site of application. The formation of cross-links between the polymer chains will allow swelling but prevents the erosion of the dosage form. In the current study, cross-linking was achieved by esterification of the PAA chains with sucrose. The density of crosslinking was modified by changing sucrose concentration and the duration of cure time. The cross-linking density of the polymer hydrogel was assessed by equilibrium swelling studies. The mucoadhesion testing method allowed a comparative study of the hydrogels prepared. An inverse relationship between equilibrium swelling and peak detachment force showed that increased PAA chain density per unit area enhanced the mucoadhesive interaction.

• 공업화학
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• 제7권3호
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• pp.536-542
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• 1996

본 연구에서는 유화중합을 통해 water jet loom용 경사 호제인 비용제형 수용성 아크릴 호제(GSW-7000)를 합성하였다. 이 호제는 아크릴계 호제의 암모늄염 형태로 제조되어 weaving force에 대한 저항력과 water jet loom 사용에 있어 물에 대한 저항력이 우수하였다. 제조한 GSW-7000은 sizing에 적당한 점도를 가지고 있고, 신도와 접착력, 용해성, 침투성 및 호부착성이 우수하였다. 또한 본 호제로 처리된 호부사는 접착강도가 높아 기존 용제형 아크릴 호제에 비하여 sizing시 호제 소모량을 70~80% 수준으로 저하시켜도 우수한 집속성 및 포합력을 나타내었으며, 호피막이 유연하며 평활성 및 내마모성이 우수하여 호부시 유제 및 대전 방지제를 사용하지 않아도 sizing 및 제직이 가능하였다.

• 폴리머
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• 제34권4호
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• pp.386-389
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• 2010

Thermal behaviors of water in the poly(acrylic acid) (PAA)/water mixtures with 0.1 M NaCl, HCl, and NaOH were investigated by DSC. It showed that adding ions in the mixtures affected the crystallization of water evidently. Compared with the PAA/water mixtures, the $T_m$ of freezable bound water in the mixtures with ions moved to lower values and varied with different cations and anions, due to the stabilization or destabilization of the hydrogen-bonding hydration between polymers and water molecules through ionic hydration. The content of non-freezable bound water in the non-crystalline phase of the PAA/water mixtures with ions was not constant, it increased with total water content gradually, owing to the more binding sites created by ions. The ions could change the distribution of different states of water in the polymer aqueous solutions evidently.