• 한국염색가공학회지
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• 제11권4호
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• pp.50-56
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• 1999

The adhesive properties of polyester cord in rubber matrix were investigated according to the surface modification. The polyester cord was oxidized in sodium hypochlorite solution, and graft-polymerized with acrylic acid under the irradiation with ultraviolet light, and then coated with resorcinol-formaldehyde latex (RFL). The modified surface was checked with scanning electron microscope. The adhesive properties were measured by the full-Out method, and evaluated with regard to the energy of adhesion and the maximum load. The polyester was not oxidized in sodium hypochlorite solution, so the surface was not able to etch to produce the coarse topology. As the concentration of acrylic acid and the reaction time were increased, the graft yields were also increased. It was considered that the acrylic acid would swell the polyester and diffuse easily to the inner side of substrate. The adhesive properties of polyeser to rubber matrix were affected by the surface condition. Namely, the maximum load was almost same, but the energy of adhesion was rather higher In the polyester grafted with acrylic acid than in control one. We concluded that the flexible aliphatic chains of polyacrylic acid situated in the interface of cord and rubber matrix were distributed well the stress and strain all over the filler resulting the high energy of adhesion.

• 방사선산업학회지
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• 제8권1호
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• pp.53-57
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• 2014

The kenaf is quickly developing as a renewable resource. Kenaf can be grown under a wide range of weather conditions. Modification of kenaf fiber by graft polymerization provides a significant route to alter the chemical properties, including surface hydrophilicity or hydrophobicity. In this study, kenaf fiber surfaces were grafted with acrylic acid as a hydrophilic group using electron beam irradiation. The grafting rate increased with an increase in grafting time. The FT-IR results confirmed that acrylic acid was successfully grafted onto the kenaf fibers. The wettability of the kenaf fiber was increased, accompanied by acylic acid grafting on the fiber surface. According to the permeability test result, it was found that acrylic acid grafted kenaf fiber reinforced cement composite was more reduced than non-grafted kenaf fiber reinforced cement composite.

• 생명과학회지
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• 제13권6호
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• pp.836-842
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• 2003

1,2-phenylenediamino과 2,5-dimethoxytetrahydro- furan을 빙초산 용매하에서 1-(2-aminophenyl)- pyrrole 5를 합성하였다. 1,3-phenylenediamine과 2,5-dimethoxytetrahydrofuran을 빙초산을 사용하여 1-(3-aminophenyl)pyrrole 7과 1,3-dipyrrolyl-benzene 8을 합성하였다. 1,4-phenyl-enediamine과 2,5-dimethoxytetrahydrofuran을 빙초산을 사용하여 1,4-dipyrrolylbenzene 10을 합성하였다. 1,2-phenylenediamine, 1,3-phenylenediamine 그리고 1,4-phenyl-enediamine과 2,5-dimethoxytetra- hydrofuran을 (가) 빙초산 대신, (나) 용매없이, (다) acrylic acid, (라) silica gel, (마) acrylic acid와 silicagel, 그리고 (바) silica gel과 acetic acid를 사용하여 각각 반응시켜 그에 상응하는 amino-phenylpyrroles 5, 7과 dipyrrolylbenzenes 8, 10을 합성하였다. 여러 가지 방법 중 (마) silicagel과 acetic acid를 사용한 경우에 dipyrrolylbenzenes 8, 10의 합성에 관한 반응성이 가장 좋았다. 또한 dicarbazolylbenzene을 합성하기 위한 전단계로 9-phenylcarbazole 11을 합성하였다.

• 폴리머
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• 제24권4호
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• pp.469-476
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• 2000

아크릴 공중합체와 점착부여제와의 상용성을 점착제의 물성에 영향을 주었다. 특히 높은 분자량과 좁은 분자량 분포를 가진 아크릴 공중합체가 혼합된 점착제는 상용계에 한해서만 점착 부여제의 함량증가에 따른 체계적인 물성 향상을 보였으며 이들 두 성분간의 상용성을 확인하는 것은 점착제의 물성에 매우 중요하다는 것을 알게 되었다.

• 폴리머
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• 제29권5호
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• pp.463-467
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• 2005

Fluoroalkyl methacrylate, 아크릴산, 2-hydroxyethyl methacrylate(HEMA)를 공중합한 불소화 아크릴계 이온성 고분자로 제조한 이온성 고분자-백금 복합재료(IPMC)의 구동력을 증대시키기 위하여, HEMA의 OH기를 1,3-diethoxy-1,1,3,3-tetramethyldisiloxane으로 가교하였다. 가교반응에 의하여 IPMC의 수분흡수가 감소하면서, 기계적 강도, 구동력이 증가함을 관찰하였다. 그러나 IPMC의 구동성, 즉 외부 전위에 의한 변위와 전류량은 가교에 의해 감소하였다.

• 접착 및 계면
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• 제20권4호
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• pp.135-139
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• 2019

본 연구에서는 인계 난연성 단량체를 점착성 아크릴 단량체인 butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, acrylic acid, 2-hydroxyethyl methacrylate와 고형분 65%에서 공중합을 진행하여 난연성 수성 아크릴 에멀젼 점착제를 합성하였다. 이때 전환율은 100%를 보이며 인계 난연 단량체의 첨가량에 따라 점착제의 점도에 차이가 발생하였고 최대 5500cps의 점도를 나타내었다. FT-IR로 아크릴 점착제의 구조분석을 진행하였고, differential scanning calorimeter (DSC) 열적 특성을 측정하였다. 인계 난연 단량체의 첨가에 따라 유리전이온도(Tg)는 미첨가시 -44.1℃에서 최대첨가량 15part에서 -31.4℃로 증가하였다. 박리강도는 미첨가시 2100gf/inch였으며 첨가량 15part에서는 200gf/inch를 나타내었고 난연성 수성 아크릴 에멀젼 점착제의 방염성을 평가하여 난연성 점착제로서의 특성 확인하였다.

• 접착 및 계면
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• 제9권3호
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• pp.27-33
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• 2008

무기계 킬레이트의 일종인 aluminum acetylacetonate (AlACA)를 점착제의 -COOH 당량비에 따라 0, 0.25, 0.5, 0.75, 1의 비율로 변화 시키고, 점착제는 acrylic acid의 함량을 3 wt%, 7 wt%, 10 wt%으로 변화를 시켜 그에 따른 경화거동을 살펴 보았다. 킬레이트의 함량이 증가하면서 가교 구조가 형성되고, 이에 따라 probe tack의 fibrillation이 줄어들고, peel strength도 줄어드는 경향을 보였다. SAFT의 경우 점착제의 acrylic acid 함량이 증가함에 따라 확연히 증가하였다. 본 연구 결과, aluminum acetylacetonate는 점착물성을 크게 변화시키지 않는 범위에서 점착제를 가교 시킬 수 있음을 확인하였다.

• 한국의류학회지
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• 제23권7호
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• pp.1064-1072
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• 1999

Nylon fabric was grafted for the purpose of the development of detergency against the hemoglobin as a protein soil. By free-radical producing chemical initiator systems the graft using acrylic acid(AA) as a hydrophilic vinyl monomer was performed to change surface energies in the presence of ammonium persulfate(APS) as an initiator and then acrylic acid grafted Nylon was treated with NaOH solution. The surface morphology for Nylon-g-NaAA with changing graft rate were studied by scanning electron microscopy (SEM) The properties of the Nylon such as diameter tenacity elongation contact angle and the hemoglobin removal were also investigated. The diameter of grafted Nylon fiber increased as the graft ratio increased. The tenacity of grafted Nylon also increased with increasing graft ratio up to 15% The elongation however decreased gradually according to graft, The contact angle decreased after graft and alkaline treatment. The amount of hemoglobin on the grafted Nylon increased in proportion to the graft ratio. Hemoglobin was easily removed from grafted Nylon while it was difficult to be removed from ungrafted Nylon. The detergency of hemoglobin for grafted Nylon decreased when the graft ratio exceeded 15% The removal of hemoglobin increased markedly with increasing hemoglobin content and revolution speed. Therefore the removal of hemoglobin was improved due to graft and alkaline treatment.

• 폴리머
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• 제25권1호
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• pp.90-97
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• 2001

Poly(ethylene-co-acrylic acid) (PEAA)를 암모늄과 나트륨의 두 가지 서로 다른 반대 이온을 사용하여 수분산 하고 이의 필름을 제조하였다. 얻어진 필름에 대한 urea 수용액의 확산계수를 측정하고 필름의 물리, 화학적 구조와의 상관관계를 조사하였다. 측정된 구조적 특징은 DSC에 의한 유리전이온도와 결정화도, WAXD에 의한 결정 및 이온성 클러스터의 구조, 그리고 FT-IR에 의한 carboxyl기의 존재 형태 등이었다. 결정성 고분자인 폴리에틸렌 이오노머의 투과특성은 반대이온의 종류나 중화도는 물론 필름형성시의 조건, 그리고 초기 입자의 크기와 같은 다양한 변수에 영향을 받음을 관찰하였다.

• 약학회지
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• 제41권1호
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• pp.22-29
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• 1997

Poloxamer-poly (acrylic acid) (PAA) interpenetrating polymer networks (IPNs) were prepared via matrix polymerization of acrylic acid with poloxamer prepolymer. The equilibrium s welling of poloxamer/PAA IPNs was determined in various pH medium. The swelling of poloxamer/PAA IPNs was more affected by pH difference compared with the swelling of homo PAA gel due to protonation and deprotonation of the PAA network, followed by reversible formation and dissociation of the interpolymer complex due to hydrogen bonding between acidic hydrogens and ether oxygens. Nonionic/anionic/cationic drugs were incorporated into IPN matriceds as a model drug and their release behavior was studied. Nonionic, drug revealed release patterns depending solely on pH dependent swelling kinetics. In contrast, the release of ionic drugs was significantly affected by ionic drug-polymer interaction as well as the swelling kinetics.