• 제목/요약/키워드: co-initiator

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무유화중합에 의한 단분산 Submicron 크기의 고분자 미립자의 제조 (Preparation of Monodisperse Submicron-Sized Polymeric Particles by Emulsifier-Free Emulsion Polymerization)

  • 이기창
    • 접착 및 계면
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    • 제13권3호
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    • pp.101-108
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    • 2012
  • 음이온개시제인 $K_2S_2O_8$ (KPS)와 양이온개시제인 2,2' azobis(2-methyl-propionamidine) dihydrochloride (AIBA)를 이용하여 MMA와 BMA 단량체간의 무유화공중합을 성공적으로 수행하여 PSD가 1.002~1.008인 단분산성이 우수한 poly(BMA-co-MMA)와 PBMA 라텍스들을 제조하였다. 실험결과, 160~494 nm 범위의 수평균입자경과 (1.25~7.55) ${\times}10^4$ 범위의 수평균분자량을 나타내었다. MMA/BMA 유화중합에 따르는 중합속도와 단량체 및 개시제 농도, DVB/EGDMA 가교제 농도, 중합온도 변화에 따르는 수평균입자경과 수평균분자량의 영향을 조사하였다. MMA/BMA 단량체 중 MMA 농도가 증가함에 따라 중합속도가 증가하였으며 일반적으로 이들 라텍스의 평균입자경과 평균분자량은 MMA/BMA 단량체중량비, 단량체량, 개시제량, 중합온도에 따라 쉽게 조절됨을 발견하였다.

합금도금강판 내식성 향상을 위한 UV 경화형 유무기 하이브리드 코팅 (Improvement of anti-corrosive property for alloy plated steel sheet by UV curable organic-inorganic hybrid coatings)

  • 박종원;이경황;나현주;박병규;남영섭;홍신협
    • Corrosion Science and Technology
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    • 제12권1호
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    • pp.27-33
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    • 2013
  • According to its merits about high curing speed and low emission of volatile organic compounds, UV curable inorganic-organic coating technology has been developed as an alternative for toxic and carcinogenic chromate-based treatments for years. It is consistently observed that ultra-thin films offer excellent corrosion protection as well as paint adhesion to metals. Based on the tetra-ethylorthosilicate(TEOS) and methacryloxypropyl trimethoxysilane(MPTMS), inorganic sol was synthesized and formed hybrid networks with UV curable acrylic monomer, 6-hexanediol diacrylate(HDDA), trimethylolpropane triacrylate(TMPTA), pentaerylthritol triacrylate(PETA). Several methods were used to test their properties such as salt spray test, potentiodynamic measurement, tape peel test, etc. It was shown that anti-corrosive property and stability of storage were affected by the molecular ratios of inorganic and organic compounds. It was not only the stability of storage, but had a excellent anti-corrosive, paint adhesive, and anti-solvent properties in a final molar ratios of 0.6/0.04/0.86/0.005 (TEOS/MPTMS/Acetone/HNO3) and 0.08/0.106/0.081/0.02 (TMPTA/HDDA/PETA/photo initiator).

비닐아세테이트/알킬아크릴레이트계 에멀젼 공중합과 등온 열분해 특성 (Characteristics of Isothermal Analysis and Emulsion Copolymerization of Vinyl Acetate/Alkyl Acrylate)

  • 조대훈;최성일;설수덕
    • 접착 및 계면
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    • 제13권2호
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    • pp.64-72
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    • 2012
  • 비닐아세테이트와 알킬아크릴레이트계 에멀젼공중합에서 개시제인 ammonium persulfate (APS)의 농도, 보호 콜로이드인 poly(vinyl alcohol) (PVA)의 종류와 농도, 공단량체인 methyl acrylate (MA), ethyl acrylate (EA), n-butyl acrylate (BA)의 혼합비를 변화시켜 중합하였다. 제조된 poly(vinyl acetate-co-methyl acrylate) (PVAc/PMA), poly(vinyl acetate-co-ethyl acrylate) (PVAc/PEA), poly(vinyl acetate-co-n-butyl acrylate) (PVAc/PBA)에 대하여 다음과 같은 결론을 얻었다. 등온 열분해법으로 $100{\sim}200^{\circ}C$ 영역에서 구한 비닐아세테이트와 알킬아크릴레이트 공중합체에 대한 등온 열분해 활성화에너지는 PVAc/PMA > PVAc/PEA > PVAc/PBA이었으며, 플라스마 처리 전과 후의 접착박리강도는 PVAc/PMA > PVAc/PEA > PVAc/PBA의 순이었다.

초임계 이산화탄소를 이용한 pH 감응성 하이드로젤 입자의 합성 (Synthesis of pH-Sensitive Hydrogel Nanoparticles in Supercritical Carbon Dioxide)

  • 양주승;류원선;이상민;김규식;최문재;이영무;김범상
    • Korean Chemical Engineering Research
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    • 제47권4호
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    • pp.453-458
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    • 2009
  • 최근 환경문제가 크게 대두됨에 따라 고분자 합성과 가공 공정에서도 유기용매를 사용하지 않는 새로운 친환경적 공정의 개발이 요구되고 있다. 초임계 이산화탄소는 고분자 합성에서 용매로 사용될 경우, 기존의 유기용매와 비교하여 불연성이고 독성이 없으며 생성물과의 분리가 용이하다는 장점을 가지고 있다. 본 연구에서는 초임계 이산화탄소를 이용하여 의약학 및 화장품 분야에서 지능형 약물전달체로 사용할 수 있는 pH 감응형 하이드로젤인 P(MAA-co-EGMA) 하이드로젤을 수 백 nm 수준의 입자 형태로 합성하는 방법을 개발하였다. 그리고 중합과정에서 사용하는 분산안정제인 PtBuMA-PEO와 중합개시제인 AIBN이 하이드로젤 입자의 합성에 미치는 영향을 살펴보았다. 입자의 합성에서 PtBuMA-PEO의 함량이 증가할수록 입자 크기는 감소하였으나 AIBN의 함량에 따른 입자 크기의 변화는 관찰할 수 없었다. 합성된 P(MAA-co-EGMA) 하이드로젤 입자의 pH에 따른 팽윤 실험결과, PMAA의 $pK_a$인 pH 5를 전후하여 급격한 하이드로젤의 평형 질량팽윤비의 변화를 관찰할 수 있었다. 즉, pH 5보다 낮은 pH에서는 낮은 팽윤비를, 반면에 pH 5보다 높은 pH에서는 매우 높은 팽윤비를 나타내었다. 그리고 Rh-B를 이용한 방출실험에서는 높은 pH에서는 다량의 Rh-B가 하이드로젤 입자로부터 방출되었으나 낮은 pH에서는 Rh-B가 거의 방출되지 않는 pH에 따른 선택적 방출 특성을 나타내었다.

SBR Latex의 개질 및 접착특성 (Modification of SBR Latex and its Adhesion Characteristic)

  • 김구니;전용철;오상택;박승현;이창호;유종선;민병권
    • Elastomers and Composites
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    • 제29권5호
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    • pp.444-452
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    • 1994
  • Emulsion graft copolymerizations of vinyl monomers, butyl acrylate(BA), methyl methacrylate(MMA), 2-ethylhexyl acrylate (EHA), glycidyl methacrylate (GMA), 2-hydroxyethyl methacrylate(HEMA), methacrylonitrile(MAN), dimethylaminoethyl methacrylate(DAMA) or 2-vinyl pyridine(VP), onto carboxyl-terminated SBR latex were carried out under different experimental conditions. In case of synthesizing SBR-g-poly(butyl acrylate), the degree of grafting was increased with increasing the amount of emulsifier, polymerization temperature and the amount of initiator. Pull-out strength of resorcinol-formaldehyde-latex(RFL) adhesives formulated with modified latexes was very higher than that of RFL adhesive formulated with ungrafted latex. When the modified latexes with GMA, HEMA, MAN, DAMA or VP were used, the break occurred at cords. Peel strength of RFL adhesives formulated with SBR-g-poly(GMA), SBR-g-poly(HEMA) or SBR-g-poly(VP) was higher by about 1.3 times than that of RFL adhesives formulated with unmodified SBR against nylon cord and was higher by about 2.0 times against polyester cord.

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Synthesis of Montmorillonite/Poly(acrylic acid-co-2-acrylamido-2-methyl-1-propane sulfonic acid) Superabsorbent Composite and the Study of its Adsorption

  • Zhu, Linhui;Zhang, Lili;Tang, Yaoji
    • Bulletin of the Korean Chemical Society
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    • 제33권5호
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    • pp.1669-1674
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    • 2012
  • A novel superabsorbent composite was prepared by intercalation polymerization of acrylic acid (AA) and 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS) in the presence of montmorillonite (MMT), using ammonium persulfate (APS) as an initiator and $N,N'$-methylenebisacrylamide (MBA) as a cross linker. The superabsorbent composite was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Maximum absorbency of the composite in distilled water and 0.9% sodium chloride solution was 722 and 108 g/g, respectively. The composite was used for removal of heavy metal ions from aqueous solutions. Maximum amount of adsorption for $Ni^{2+}$, $Cu^{2+}$ and $Pb^{2+}$ was 211.0, 159.6 and 1646.0 mg/g, respectively, and the adsorption was in accordance with both Langmuir and Freundlich model. The composite could be regenerated and reused in wastewater treatment.

알루미늄/GFRP 혼성 사각튜브의 정적 압축 붕괴 및 에너지 흡수 특성 (Axial Crush and Energy Absorption Characteristics of Aluminum/GFRP Hybird Square Tubes)

  • 김구현;이정주;신금철
    • 한국자동차공학회논문집
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    • 제8권6호
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    • pp.208-219
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    • 2000
  • In this study, static axial crush tests were performed with the new aluminum/GFRP hybrid tube. Glass/Epoxy prepregs were wrapped around an aluminum tube and co-cured. The failure of the hybrid tube was stable and progressive without trigger mechanism, and specific energy absorption was increased to the maximum of 33% in comparison with the aluminum tube. Effective energy absorption is possible for an inner aluminum tube because a wrapped composite tube constrains the deflection of an aluminum tube. The failure of a hybrid composite tube was stable without trigger mechanism because the inner aluminum tube could play the role of the crack initiator and controller. Mean crushing load could be calculated by modifying the plastic hinge collapse model for hybrid materials. The predicted results by this analytical model showed good agreement with the experimental results. It can be said that Aluminum/Glass-Epoxy hybrid tube is suitable for the vehicle front structure because this hybrid tube shows effective energy absorption, easy production, and simple application capability for RTM process.

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연속반응기에서 ${\alpha}$-Methylstyrene과 Acrylonitrile 라디칼 공중합 속도론 (The Kinetics of Radical Copolyerization of ${\alpha}$-Methylstyrene with Acrylonitrile in a CSTR)

  • 김남석;박근호
    • 한국응용과학기술학회지
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    • 제19권1호
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    • pp.33-42
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    • 2002
  • Copolymerization of ${\alpha}$-Methylstyrene(AMS) with Acrylonitrile(AN) was carried out with benzoylperoxide(BPO) as an initiator in toluene at $80^{\circ}C$ in a continuous stirred tank reactor. Reaction volume and residence time were 0.6 liters and 3 hours, respectively. The monomer reactivity ratios, $r_{AMS}$ and $r_{AN}$ determined by both the Kele$T{\"{u}}d\"{o}s$ method and the Fineman-Ross method were $r_{AMS}$=0.16(0.14), $r_{AN}$=0.04(0.06). The cross-termination factor ${\Phi}$ of the copolymer over the entire AMS composition ranged from 0.75 to 0.92. The ${\Phi}$ factors of poly(AMS-co-AN) were increased with increasing AMS content. The simulated conversions and copolymerization rates were compared with the experimental results. It was observed that the average time to reach dynamic steady-state was three times the residence time.

Higher Order Polymer Architectures Containing Ethylene and Functionalized Comonomers

  • Bazan, Guillermo;Diamanti, Steve;Coffin, Robert;Hotta, Atsushi;Khanna, Vikram;Fredrickson, Glenn;Kramer, Ed
    • 한국고분자학회:학술대회논문집
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    • 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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    • pp.156-157
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    • 2006
  • Quasi-living polymerization conditions for the copolymerization of ethylene and functionalized norbornenes can be achieved by using an initiator system comprising $[N-(2,6-diisopropylphenyl)-2-(2,6-diisopropylphenylimino)-propanamidato-{\kappa}^2N,O]Ni({\Box}^1-CH_2Ph)(PMe_3)\;and\;Ni(COD)_2$. It is possible with this polymerization system to obtain block-copolymer and tapered structures. The latter form microdomains similar to those of standard block co-polymers. The mechanism of the reaction will also be discussed.

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Acryloyllactam형 단량체의 공중합 및 그 공중합체를 이용한 음이온 그라프트 중합 (Anionic Graft Copolymerization Using Copolymer of Acryloyllactam Type Monomer)

  • 우희권;최삼권
    • 대한화학회지
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    • 제26권3호
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    • pp.179-187
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    • 1982
  • N-acryloylpyrrolidone과 acrylonitrile을 혼성중합시켜 각 단위체의 반응성비를 구한 결과 생성되는 혼성중합체는 pyrrolidone이 음이온 중합에 매우 좋은 개시제임을 알 수 가 있었다. ($r_1$ = 0.43과 $r_2$ = 1.56) 그리고 그 혼성중합체를 개시제로 하여 그라프트된 nylon-4를 합성하여 중합속도 상수를 구했으며, 그에 따르는 여러 인자들의 효과를 관찰하였다. 그 결과 중합속도 상수로 40$^{\circ}$C에서 2.82${\times}10^3$(l/mole, min)와 50$^{\circ}$C에서 2.93${\times}10^3$(l/mole, min)을 얻었다.

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