• Polymer(Korea)
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• v.25 no.5
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• pp.617-624
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• 2001

The core-shell composite latexes were synthesized by stage emulsion polymerization of methyl methacrylate (MMA) and styrene (St) with ammonium persulfate after preparing monomer pre-emulsion in the presence of anionic surfactant. However, in preparation of core-shell composite latex, several unexpected results are observed, such as, particle coagulation, low degree of polymerization, and formation of new particles during shell polymerization. To solve the disadvantages, We study the effect of initiator concentrations, surfactant concentrations, and reaction temperature on the core-shell structure of polymethyl methacrylate/polystyrene and polystyrene/polymethyl methacrylate. Particle size and particle size distribution were measured using particle size analyzer, and the morphology of the core-shell composite latex was determined using transmission electron microscope. Glass temperature was also measured using differential scanning calorimeter. To identify the core-shell structure, pH of the two composite latex solutions were measured.

• Journal of the Korean Chemical Society
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• v.17 no.1
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• pp.40-46
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• 1973

The afterpolymerization of nylon 6 was carried out in three different reaction conditions, nitrogen flow, sealing and evacuation. The viscosity and reduced weight of polymer were increased by increasing the reaction time and temperature, and viscosity of polymers at constant reaction temperature was decreased as the following order: nitrogen flow >sealing >evacuation. The activation energy of afterpolymerization was 10.5 kcal/mole.

• Polymer(Korea)
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• v.36 no.3
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• pp.302-308
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• 2012

The objective of this study is to investigate optimum reaction conditions for the grafting of poly($N$-vinyl- 2-pyrrolidone) (PVP) onto the surface of plasma-treated polypropylene film. The plasma treatment conditions were fixed as 200 W rf power, 6 LPM Ar flow rate, 30 sec treatment time, and 5 min exposure time after treatment. For graft copolymerization, we investigated the change of grafting degree with respect to reaction time, reaction temperature and $N$-vinyl-2-pyrrolidone concentration. Maximum grafting degree was obtained at the conditions of 6 h reaction time, $90^{\circ}C$ reaction temperature, and 40% $N$-vinyl-2-pyrrolidone concentration. The introduction of PVP was confirmed by ATR-FTIR, XPS, and SEM analysis.

• Elastomers and Composites
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• v.48 no.4
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• pp.294-299
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• 2013

Solution polymerization was conducted with water-soluble methacrylic acid (MAA) as a monomer and potassium persulfate (KPS) as an initiator at a selected temperature between $70^{\circ}C$ and $90^{\circ}C$. When the ratio between MAA and water was reduced or initiator concentration increased, molecular weights decreased. Molecular weights of poly(methacrylic acid) (PMAA) showed nearly no dependence on reaction temperature. The Weissenberg effect was observed in most polymerization reactions, while its effect weakened at $90^{\circ}C$. The polydispersity index was less than 1.5 in most of the reactions. An increase in the stirring speed produced PMAAs with increasing molecular weights. When the stirring speed reached 800 rpm, we retrieved a monodisperse PMAA with both the number and weight average molecular weights of 791,000 g/mol. The glass transition temperature was found to be $162^{\circ}C$.

• Proceedings of the Korean Institute of Industrial Safety Conference
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• 2003.10a
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• pp.148-153
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• 2003

고분자 물질은 유기용제를 사용하여 제조되는 경우가 일반적이다. 이들 중에서 용제형 아크릴계 고분자는 점착강도, 내습성, 내수성 그리고 내열성 등이 우수하여 페인트, 접ㆍ점착제, 섬유 등의 산업전반에 이용되고 있으나 용제사용에 따른 화재의 위험성과 환경적인 문제점 때문에 규제의 대상이 되고 있다. 이러한 위험성과 환경문제점은 유화중합법에 의해 고분자물질을 제조함으로써 해결되며, 그 중에서 단계 유화중합법은 다른 중합법에 비해 온도조절이 용이하며, 반응속도와 분자량을 조절할 수 있다는 장점 때문에 latex 공업이나 고분자 blending 기술면에서 많이 이용되고 있는 실정이다.(중략)

• Proceedings of the Membrane Society of Korea Conference
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• 1998.04a
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• pp.17-20
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• 1998

1. 서론 : 계면중합은 제조에 따른 박막의 성능 조절이 가능한 이유로 해서 역삼투용 복합막의 주요 제조 방법으로 제시되어 왔다. 계면중합을 응용하여 제조된 복합막의 성능은 반응 단량체의 종류, 용재의 종류, 단량체의 농도, 반응시간, 열처리 유무 및 온도와 시간 등에 의해 변한다. 한편 위의 변수에 절대적인 영향을 받고 아울러 단량체간의 몰 비가 성립하지 않음으로 해서 최적의 막 성능으로 제시되는 조건을 만족하기 위하여 주로 시행착오에 의한 방법을 동원하여 여러 변수에 다른 제조 막의 성능 고찰을 실시하여 왔다. (생략)

• Electrical & Electronic Materials
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• v.6 no.4
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• pp.354-360
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• 1993

열수축성 튜브 제조에 적합한 조성을 얻기 위하여 PVC의 방사선가교에 대하여 검토하였다. 중합도가 각각 다른 PVC에 가소제, 가교제를 변화시켜 배합한 혼합물을 방사선 가교시켰을 때 가교도는 가교제, 가소제, 중합도 및 조사선량이 증가됨에 따라 증가되었다. 가교제로서는 삼관능성 단량체가 높은 가교효율을 나타내었다. 가교 PVC 필름의 열수축성은 연신배율과 수축 온도를 높여줌으로써 증가되었으나 가교제 및 가소제의 증가량에 의한 열수축성의 증가는 나타내지 않았고 저중합도 PVC의 열수축성은 극히 저조하였다.

• Journal of the Korean Chemical Society
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• v.21 no.6
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• pp.440-444
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• 1977

The anionic polymerization of ${\varepsilon}$-caprolactam via $CS_2$/KOH catalysis was carried out under various conditions. The inherent viscosity of the polymers and percent conversion of the polymers were determined. It was observed that the percent conversion was increased as an increasing concentration of catalyst and initiator. The percent conversion was relatively low at low temperature and the highest percent conversion was obtained at temperature between $130^{\circ}C,\;to\;155^{\circ}C$ with any $CS_2$/KOH mole ratio.

• Journal of Biosystems Engineering
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• v.29 no.4
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• pp.347-356
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• 2004

치아인회석, 키토산, 시아노아크릴레이트 등의 생분해성 생체재료를 이용해 새로운 생체흡수성 골시멘트를 개발하고자 하였다. 이들 골시멘트들에 대해서 중합온도, 응고시간 등의 조작특성과 압축강도, 전단강도 등의 물성을 분석하였다. 특히, 치아인회석과 키토산의 미립가루와 부틸 시아노아크릴레이트의 강력접착제를 이용한 시멘트(B)에 대해서는 직접 접촉방법과 XTT 방법을 통해 세포독성을 분석하였고, 또한 쥐를 이용한 동물실험에서 시멘트(B)의 처리그룹에 따라 생체적합성을 분석하였다. 시아노아크릴레이트를 이용한 골시멘트의 최대중합온도는 약 33$^{\circ}C$, 조작(응고)시간은 3-6분, 압축강도는 약 15-25㎫, 전단강도는 약 0.4-l.7 ㎫를 나타내었다. 첨가제로 사용된 Lipiodol은 골시멘트의 주사성과 강력접착제의 초기 중합지연도를 높였고, 특히 송진가루는 시아노아크릴레이트의 초기중합을 지연시켰다. 시아노아크릴레이트를 이용한 시멘트(B)의 세포독성을 분석한 결과, 대부분의 처리 그룹에서 낮게 나타났고, 특히 키토산과 치아인회석을 사용한 경우 각각 세포 독성이 더 낮게 나타났다. 그리고 골시멘트(B)의 동물 생체적합성 실험의 방사선상 및 조직학적 분석에서도 뼈 형성 및 결합이 우수하게 나타났다.

• Fire Science and Engineering
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• v.10 no.3
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• pp.3-9
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• 1996

The Polyimide thin films based on PMDA and 4,$4^{\circ}$'-DDE were fabricated by VDPM, and their heat resistance characteristics were invastigated by TGA(Thermogravimetry Analyzer). It was found that deposition rate decreased with increasing substrate temperature and the thin films were not fabricated over the substrate temperature of $70^{\circ}$. $T_{TG}$ of weight loss temperature is $565^{\circ}$, $397^{\circ}$ and $210^{\circ}$ at the substrate temperature of $20^{\circ}$, $40^{\circ}$ and $70^{\circ}$, respectively. It is realized that the endurace temperature for 20,000 hour of thin films fabricated at $20^{\circ}$ and $40^{\circ}$ is $230^{\circ}$ and $200^{\circ}$, respectively.