• 폴리머
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• 제36권1호
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• pp.65-70
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• 2012

글리시딜메타크릴레이트(GMA)의 플라즈마 유도 그래프트 공중합을 통해 기재로 사용한 평판형 폴리프로필렌 위에 에폭시 그룹을 도입하였다. 그래프트 공중합은 에멀젼 공중합법을 적용하였고, 기존의 용액 공중합과 비교하여 그 효과를 확인하고자 하였다. 대기압 플라즈마 처리 조건은 RF power 200 W, 처리시간 30초, Ar 기체 유속 6 LPM으로 고정하였고, 처리 후의 대기 중 노출시간 역시 5분으로 고정하였다. 중합반응에서는 GMA의 농도, 반응온도, 반응시간에 따라 표면 그래프트도의 변화를 최적화하였다. 그 결과, GMA 농도 12%, 반응온도 $90^{\circ}C$, 반응시간 5시간으로 중합하였을 때 가장 높은 그래프트도를 나타내었다. 분석 결과, 같은 반응조건 하에서 에멀젼 중합이 용액 중합에 비하여 더 많은 에폭시 그롭 도입에 효과적임을 확인하였다.

• 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.

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.2966-2970
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• 2012

Fullerene/polystyrene ($C_{60}$/PS) nano particle was prepared by using emulsion polymerization. Styrene and fullerene were emulsified in aqueous media in the presence of poly(N-vinyl pyridine) as an emulsion stabilizer, and polymerization was initiated by water soluble radical initiator, potassium persulfate. The obtained nano particles have an average diameter in the range of 400-500 nm. The fullerene contents in the nano particle can be controlled up to 15 wt % by varying the feed ratio, which was confirmed by themogravimetric analysis (TGA) and elemental analysis (EA). The structure and morphologies of the $C_{60}$/PS nano particles were examined by various analytical techniques such as dynamic light scattering (DLS), scanning electron microscope (SEM), transmission electron microscope (TEM), electron diffraction (ED) pattern, X-ray powder diffraction (XRD), and UV spectroscopy. Unlike conventional $C_{60}$/PS particles initiated by organic free radical initiators, in which the fullerene is copolymerized forming a covalent bond with styrene monomer, the prepared $C_{60}$/PS nano particles contain pristine fullerene as secondary particles homogeneously distributed in the polystyrene matrix.

• 한국응용과학기술학회지
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• 제23권2호
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• pp.169-176
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• 2006

Acrylic adhesives for automobiles protection were prepared by emulsion polymerization. Monomers used were n-butyl acrylate(BA), acrylonitrile (AN), butyl methacrylate(BMA), glycidyl methacrylate(GMA), and acrylic acid (AA). Emulsifiers used were sodium lauryl sulfate and polyoxyethylene lauryl ether, which are an anionic emulsifier and a nonionic emulsifier respectively. Potassium persulfate was used as an initiator and polyvinyl alcohol was used as a stabilizer. Emulsion polymerization was carried out in a semi-batch reactor at $70^{\circ}C$ and agitation speed was kept at 200 rpm. Water resistance, heat resistance, acid resistance, alkali resistance and smoke resistance were examined. As a result, when each 0.03 mole of GMA and AA was introduced, the adhesion properties and various above mentioned resistances of the prepared adhesives were satisfied the standard for automobiles.

• 한국응용과학기술학회지
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• 제22권4호
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• pp.332-338
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• 2005

This study was conducted to prepare acrylic removable protective coatings by emulsion polymerization. Monomers used were n-butyl acrylate, acrylonitrile, butyl methacrylate. Emulsifiers used were sodium lauryl sulfate and polyoxyethylene lauryl ether, which are an anionic emulsifier and a nonionic emulsifier respectively. Potassium persulfate was used as an initiator and polyvinyl alcohol was used as a stabilizer. Emulsion polymerization was carried out in a semi-batch reactor at $70^{\circ}C$ and agitation speed was 200 rpm. Tensile strength, extension, peel strength, viscosity, and solid contents of the synthesized coatings were examined. The coatings prepared with BA:AN = 60:20 (in weight ratio) satisfied the standard for automobile in terms of extension and peel strength. When the concentration of BMA was in a range of $18{\sim}23$ wt%, the prepared coatings satisfied the standard for automobile in terms of peel strength and water resistance.

• 한국응용과학기술학회지
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• 제6권1호
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• pp.1-7
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• 1989

To developed new process for obtaining maximum molecular weight of anionic acrylamide and acrylic acid copolymer by inverse emulsion polymerization. Concentration of initiator, reducing agent, surfactant and mole ratio of acrylamide-acrylic acid were studied for the process. Semi-batch processes with method of redox, control of reaction temperature, feeding method of monomer and reaction time, was suitable for maximum molecular weight of P(AMAC) from this process obtained $3.09\;{\time}\;10^6({\bar{M}}n.)$ and $4.41\;{\time}\;10^6({\bar{M}}w.)$ in molecular weight measured by the intrinsic viscosity method. inverse emulsion polymerization mechanism of P(AMAC) does not followed the Smith-Ewart and Medvedev theory, but selected for concentration of initiator, reducing agent, surfactant, water solubility of monomer.

• 한국응용과학기술학회지
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• 제19권2호
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• pp.131-136
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• 2002

As model waterborne acrylic coatings, mono-dispersed poly(butyl acrylate-methyl methacrylate) copolymer latexes of random copolymer and core/shell type graft copolymer were prepared by seeded multi-staged emulsion polymerization with particle size of $180{\sim}200$ nm using semi-batch type process. Sodium lauryl sulfate and potassium persulfate were used as an emulsifier and an initiator, respectively. The effect of particle texture including core/shell phase ratio, glass transition temperature and crosslinking density, and film forming temperature on the film formation and final properties of film was investigated using SEM, AFM, and UV in this study. The film formation behavior of model latex was traced simultaneously by the weight loss measurement and by the change of tensile properties and UV transmittance during the entire course of film formation. It was found that the increased glass transition temperature and higher crosslinking degree of latex resulted in the delay of the onset of coalescence of particles by interdiffusion during film forming process. This can be explained qualitatively in terms of diffusion rate of polymer chains. However, the change of weight loss during film formation was insensitive to discern each film forming stages-I, II and III.

• 한국응용과학기술학회지
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• 제28권1호
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• pp.10-14
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• 2011

Emulsion polymerization was carried out using RMA like MMA, EMA, BMA and Styrene(St.) as monomer for core-shell latex preparation. It was synthesized at $80^{\circ}C$ in the presence of anionic surfactant SLS. FT-IR, TGA and DSC analysis are used to confirm synthesized core-shell emulsion latexes and to investigate the thermal characteristics of them. From analysis of TGA and DSC, the differences of the decomposition rate and the activation energy are not so large. It considers that the pendent group is not affect of the thermal characteristics and stability on core-shell latexes, which is synthesized with RMA and Styrene.

• Korea-Australia Rheology Journal
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• 제16권3호
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• pp.153-160
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• 2004

Open microcellular foams having small-sized cell and good mechanical properties are desirable for many practical applications. As an effort to reduce the cell size, the microcellular foams combining viscosity improvers into the conventional formulation of styrene and water system were prepared via high internal phase emulsion polymerization. Since the material properties of foam are closely related to the solution properties of emulsion state before polymerization, the flow behavior of emulsions was investigated using a controlled stress rheometer. The yield stress and the storage modulus increased as viscosity improver concentration and agitation speed increased, due to the reduced cell size reflecting both a competition between the continuous phase viscosity and the viscosity ratio and an increase of shear force. Appreciable tendency was found between the rheological data of emulsions and the cell sizes of polymerized foams. Cell size reduction with the concentration of viscosity improver could be explained by the relation between capillary number and viscosity ratio. A correlative study for the cell size reduction with agitation speed was also attempted and the result was in a good accordance with the hydrodynamic theory.

• 공업화학
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• 제9권2호
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• pp.300-305
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• 1998

세 종류의 모노머로 구성된 삼모노머중합의 동력학을 입자성장이 끝난 interval II 동안 pseudo-homopolymerization (PHP) 방법에 의하여 연구하였다. 삼모노머중합의 Smith-Ewart 확장식과 순간중합조성식을 단일유화중합의 해당식과 유사하게 나타낼 수 있었다. 입자당 평균라디칼수와 순간중합조성을 라텍스입자내의 모노머조성을 변화시킴으로써 입자당 자유라디칼수가 한 개 이하인 계에서 예측하였다. 모델계산의 예로서 Styrene-Methyl methacrylate-Acrylonitrile(SMA)계의 속도상수들을 사용하였다.