• 유변학
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• 제10권4호
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• pp.247-255
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• 1998

이축 압출기에서 삼성분계 블렌드가 용융 혼련될 때 상구조의 형성과정에 대하여 연구하였다. 삼성분계 블렌드의 연속상은 polycarbonate(PC)로 고정하였고 나머지 분산상을 이루는 성분으로는 acrylonitrile-butadiene-styrene(ABS), methyl methacrylate-butadiene-ethyl acrylate(MBE), styrene-acrylonitrile(SAM) 공중합체, 그리고 poly(methyl methacrylate)(PMMA)를 사용하였다. 블렌드의 여러 가지 조성에 따라 최종 상구조는 현저한 차이를 보였고 특히 MBE와 PMMA의 경우는 각각 PC-SAN의 계면에 선택적으로 위치하였다. 삼성분계 고분자 블렌드의 상구조 형성과정은 성분간의 계면장력과 합체 현상의 상호 작용에 의하여 지배되었으며 합체의 정도는 계면에서의 점도에 의하여 민감하게 변화되었다.

• 폴리머
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• 제34권4호
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• pp.313-320
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• 2010

신나메이트기를 갖는 새로운 자기 경화형 감습성 고분자 및 고분자형 앵커제로 사용하기 위하여 [2-[(methacryloyloxy) ethyl]dimethyl]propyl ammonium bromide(MEPAB), methyl methacrylate(MMA), 3-(trimethoxysilyl) propyl methacrylate(TMSPM) 및 2-(cinnamoyloxy)ethyl methacrylate(CEMA)의 공중합체들 을 합성하였다. 광가교성 공중합체들로서 MEPAB/MMA/TMSPM/CEMA＝70/20/0/10의 조성을 갖는 공중합체는 감습성 전해질 고분자로서, 그리고 50/0/20/30과 0/0/50/50 조성은 고분자형 부착제로 사용하였다. 이들 광가교형 고분자 실란커플링 처리제의 전극 표면과 부착 특성을 비교하기 위하여 3-(triethoxysilyl)propyl cinnamate(TESPC)도 표면 부착을 위한 표면처리제로서 사용하였다. 표면처리제는 전극의 기재 표면 위에 공유결합을 통하여 광가교성 신나 메이트 박막을 형성시킬 수 있었으며 센서에 UV가 조사되었을 때 전해질 고분자가 [2$\pi$+2$\pi$] 환화반응을 이용한 가교반응으로 기재에 부착되었다. 이렇게 고분자 표면처리제 및 TESPC로 처리된 센서들은 24시간 물에 침적시켰을 때 60~85%의 저항 증가가 생겼으며 이것은 상대습도 변화로서 2.25~3.15%RH에 해당하였다. 또한, -0.2%RH 이하의 양호한 히스테리시스, 90초의 응답 및 회복속도, 그리고 80 $^{\circ}C$ 및 90%RH의 고온 고습에서 매우 좋은 신뢰성을 보여주었다.

• Macromolecular Research
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• 제15권5호
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• pp.418-423
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• 2007

A methacrylate copolymer based on isobornyl methacrylate (IBMA) and methyl methacrylate (MMA) was synthesized in an aqueous suspension via free-radical polymerization. The potential of this copolymer as a heat-resistant optical polymer is also discussed. 1,1,3,3-tetramethylbutyl peroxy-2-ethyl hexanoate and n-octyl mercaptan were used as the initiator and chain transfer agents, respectively. The effect of IBMA on the properties of the copolymer was investigated. The composition of the copolymer was analyzed using $^1H-NMR$, and the heat resistance by measuring the glass transition temperature, which exhibited a linear dependency on the IBMA content in the copolymer. Variation of the chain transfer content used in the synthesis step was effective for the optimization of the copolymer for practical use.

• 한국막학회:학술대회논문집
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• 한국막학회 1992년도 추계 총회 및 학술발표회
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• pp.47-48
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• 1992

Polymer containing monomers with pendant phospholipid polar group, 2-(metha-cryloyoxy) ethyl-2-(trimethylammonium) ethyl phosphate(MTP) were synthesized and blood compatibility of the copolymers was evaluated. Good permeability of biocomponents of molecular weight below 10$^4$ through cellulosic membrane coated with the copolymer of 2-(methacryloyoxy) ethyl-2-(tri-methylammonium)ethyl phosphate, butylmethacrylate(BMA), and glycidyl methacrylate(GMA) was observed, (Fig.1).

• 한국산업보건학회지
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• 제29권4호
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• pp.452-463
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• 2019

Objectives: The purpose of this study is to evaluate airborne concentrations of volatile organic compounds(VOCs) during nail art practice by college students. Methods: Personal samples for students were measured using passive samplers(OVM 3500) during three kinds of practice, including polish nail, gel nail and acrylic French sculpture at two universities located in Gyeongsangbuk-do Province. We also monitored area concentrations using active samplers and real-time total VOC monitors(ppbRAE 3000). All samples were analyzed with a gas chromatography flame ionized detector. Statistical analysis for monitored data were conducted using a web-based Bayesian toolkit, EXPOSTATS(www.expostats.ca). Results: Twenty-four personal samples and ten area samples were collected and five chemicals(acetone, butyl acetate, ethyl acetate, ethyl methacrylate(EMA) and methyl methacrylate(MMA)) were detected. Acetone was detected in all personal samples and ranged from 2.58 ppm to 50.3 ppm. EMA was detected in all personal and area samples with a maximum concentration of 9.78 ppm during acrylic French sculpture. Personal exposure levels to acetone, butyl acetate and mixtures were significantly higher with high occupant density (p<0.05). Geometric mean (GM) concentrations of 3.61 ppm for EMA personal samples were significantly higher than that of area samples, 1.5 ppm (p<0.05). Since there was no local ventilation, total VOC concentration continued to increase as the practice progressed. Conclusions: In order to minimize VOCs exposure for trainees, it is necessary to introduce a local ventilation system and maintain adequate occupant density.

• 한국응용과학기술학회지
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• 제20권3호
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• pp.221-229
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• 2003

A copolymer ${\sim}$550cps ; $M_n$, 2590${\sim}$2850 ; and conversion, 82${\sim}$89%, respectively. It was found from the plotting of $T_g$ versus viscosity and $T_g$ versus molecular weight that viscosity increased with $T_g$ while number averaged molecular weight decreased with increasing $T_g$.

• 한국염색가공학회지
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• 제6권4호
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• pp.40-45
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• 1994

To improve the blood compatibility of cellulose membrane, 2-(methacryloyloxy)ethyl-2-(trimethylammonium)ethyl phosphate(MTP), which is a methacrylate with phospholipid polar group, and glycidyl methacrylate(GMA) were grafted simultaneously on the surface of membrane and the biocompatibility of grafted membrane was investigated. There was no difference of permeability between the MTP and GMA-grafted and the original cellulose membrane. The permeation pathway for a solute whose molecular weight was above 10$^{4}$ is maintained after grafting on the surface of membrane. The cellulose membrane grafted with MTP and GMA effectively suppressed thrombogenicity for the rabbit blood. This effect became more clear with increasing the surface distribution of phospholipid polar groups.

• 대한치과기공학회지
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• 제28권1호
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• pp.43-52
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• 2006

Three t-amines, 4-(dimethylamino)benzoic acid (ABA), 4-(dimethylamino)benzaldehyde (MBA), 4-(dimethylamino)benzophenone (MBP), were investigated as new visible light photoinitiators for a dental resin composite of UDMA in order to improve photopolymerization effect. Three t-amines mixed with three photosensiizers, CQ, PD and DA, respectively. And the photopolymerization effect of photoinitiators were compared with that of 4-(dimethylamino)ethyl methacrylate (AEM), the most widely used photoinitiator. The photopolymerization efficiency of UDMA containing the photoinitiator increased with irradiation time. The increase was in the order: MBP

• Macromolecular Research
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• 제10권4호
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• pp.215-220
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• 2002

The electrorheological (ER) and dielectric behaviors of the polypyrrole(PPy)-coated poly(ethyl methacrylate)(PEMA) suspensions in mineral oil were investigated. PPy was coated on PEMA particles to enhance the particle polarization, which would lead to the enhanced ER response. Various PPy-coated PEMA particles were synthesized by controlling the oxidant amount during the pyrrole polymerization, and the ER responses of their suspensions were investigated. The ER response initially increases with the oxidant amount, passes through a maximum, and then decreases with the oxidant amount. The initial increase in the ER response with oxidant amounts is due to the enhanced particle polarization with the increased particle surface conductivity. The dielectric properties of the corresponding suspensions support that the ER enhancement arises from the enhanced particle polarization. The decrease in the ER response at large oxidant amounts seems to arise from the increased conduction between the PPy-coated PEMA particles.

• 한국응용과학기술학회지
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• 제18권4호
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• pp.316-324
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• 2001

To prepare an acrylic type pressure-sensitive adhesive, quarternary polymers were synthesized from butyl acrylate (BA), 2-ethyl hexyl acrylate (2-EHA), methyl methacrylate (MMA), and 2-hydroxy ethyl methacrylate (2-HEMA). The quarternary polymers were identified by FT-IR and Molecular weight was measured by Gel Pearmeation Chromatography. Also, viscosity, solid content and peel strength were examined. The peel strength was 160 $g_{f}/25$ mm when the volume ratio of feed monomer to solvent was 1.3:1, and the ratio was relevant to commercial usage. The pot life of adhesive was 30 sec at the 50 m/min of heat treatment rate at, and it indicated that the minimum drying time was 30 sec. In weathering resistance test, peel strength of $160{\sim}180$ $g_{f}/25$ mm after 1000 h, with no residual remains on the adhesive surface.