• 제목/요약/키워드: Graft Copolymerization

검색결과 83건 처리시간 0.031초

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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단백질에 대한 그라프트 공중합 (제3보). Cerium (IV) 이온에 의한 비닐 단위체의 그라프트 공중합에 대한 메카니즘 (Graft Copolymerization to Proteins (III). Mechanism of Cerium (IV) Ion-Initiated Graft Copolymerization)

  • 조의환;안광덕
    • 대한화학회지
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    • 제20권4호
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    • pp.316-320
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    • 1976
  • 단백질에 대한 비닐 단위체의 그라프트 공중합 실험결과를 기초로하여 유기물과 Ce(IV)이온의 산화환원계에 의하여 개시되는 중합반응에 대하여 중합반응 메카니즘을 추구하였다. Ce(IV) 이온에 의한 산화성 종결반응을 고려하여 반응속도식을 유도 하였으며 Ce(IV) 이온 농도가 클때와 작을 때를 별개로 취급하여 Ce(IV) 이온 농도의 변화에 따라 그라프트 수득률의 최대점이 나타나는 현상을 설명하였다.

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Effect of Graft Copolymerization Conditions on Grafting Yield of AA and MA onto Polyester Fiber

  • Park, Myung-Ja
    • The International Journal of Costume Culture
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    • 제6권2호
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    • pp.134-146
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    • 2003
  • Polyester of linear homopolymer poly(ethylene terephthalate)(PET) was chemically modified through the formation of branched copolymer to improve the undesirable properties of fiber. Photo-induced graft copolymerization of the acrylic monomers acrylic acid (AA) and methyl acrylate (MA) in the liquid and vapor phase, respectively, onto N,N-dimetylformamide (DMF)-pretreated PET fibers was carried out. The effect of various synthesis conditions and DMF pretreatment of the PET on the graft yield was investigated. Grafting mechanism was analysed. The grafting was promoted by increasing DMF pretreatment temperature and amount of DMF retention in the fiber. The increasing biacetyl and monomer flow time, and irradiation time enhanced the grafting up to a certain amount and thereafter it decreased.

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Chloroprene 고무에 대한 Methyl Methacrylate의 Graft공중합 (Graft Copolymerization of Methyl Methacrylate on to Chloroprene Rubber)

  • 박찬영;김병규;박천욱
    • Elastomers and Composites
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    • 제26권2호
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    • pp.109-114
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    • 1991
  • The graft copolymerization of chloroprene rubber with methyl methacrylate in toluene solution has been carried out varying the concentration of monomer, initiator, CR, reaction time, and reaction temperature, etc.. It is observed that the grafting reaction follows conventional kinetic behavior under the present experimental conditions. Identification of grafting on to chloroprene rubber was obtained through characterization of the graft copolymer by infrared spectrometer.

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면섬유(綿纖維)에의 MMA/4-Vinylpyridine의 공(共)그라프트 중합(重合) (Graft Copolymerization of MMN4-Vinylpyridine onto Cotton Fiber)

  • 배현숙;김성련
    • 한국의류학회지
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    • 제17권3호
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    • pp.347-358
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    • 1993
  • Graft copolymerization of MMN4-VP onto cotton fiber using Ce(IV) salt as an initiator and triton X-100 as an emulsifier was performed under various polymerization conditions. In cograft polymerization, the polymeization behavior according to variation of 4-VP feed composition and the characteristics of MMA/4-VP graft polymer such as affinity for acid dye owing to cationization of cotton, antibacterial activity and thermal behavior were investigated. The results of this study were as follows : 1. While in copolymerization of MMA and 4-VP, 4-VP content in copolymer was more than that of monomer feed composition. 2. Increasing 4-VP content, graft yield was decreased, but graft efficiency was increased. In case of MMA/4-VP graft polymerization, the highest graft yield was obtained at higher CAN concentration than in MMA graft polymerization, the reason is that the behavior of 4-VP was disturbed by Ce(IV) sail 3. Elevation of temperature resulted in increase of graft yield and the apparent activation energy of MMA/4-VP graft polymerization was higher than that of MMA graft polymerization. 4. MMA/4-VP grafted cotton fiber showed affinity for acid dye, antibacterial activity and higher moisture regain than MMA grafted cotton fiber. MMA/4-VP grafted cotton fabric showed improvement of wrinkle recovery up to 40~50% graft yield and decreased thereafter. MMA/4-VP and MMA grafted cotton fabric did not showed significant difference in wrinkle recovery and stiffness.

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천연고무 Latex에 Poly(Methyl Methacrylate)의 그라프트 공중합 (Graft Copolymerization of Poly(Methyl Methacrylate) onto Natural Rubber Latex)

  • 김공수;신무호;최석규;금기문
    • Elastomers and Composites
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    • 제28권3호
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    • pp.191-197
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    • 1993
  • The graft copolymerization of methyl methacrylate(MMA) onto natural rubber latex(NRL) initiated by t-butyl hydroperoxide(t-BHPO) was investigated in aquous medium. The grafting percentage, grafting efficiency and total conversion were observed in various reaction conditions such as monomer, initiator and emulsifier concentration, reaction temperature, reaction time and agitation speed. The optimum conditions for the graft copolymerization onto natural rubber latex were as follows ; At given monomer concentration of $3{\times}10^{-2}mole/l$, the maximum grafting percentage was appeared in the case of grading in initiator concentration of $4{\times}10^{-2}mo1e/l$ and emulsifier concentration of 0.2wt.% at $40^{\circ}C$ for 5hrs.

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클로로프렌고무와 글리시딜메타아크릴과의 그라프트 공중합 반응과 그 공중합물의 접착능에 관한 연구 (Studies on the Graft Copolymerization of Glycidylmethacrylate to Chloroprene Rubber and the Adhesive Nature of the Copolymer)

  • 손진언;최병권
    • Elastomers and Composites
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    • 제11권1호
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    • pp.54-62
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    • 1976
  • It has been studied the graft copolymerization of glycidyl-methacrylate monomer containing two functional groups (vinyl- & epoxyl-) to chloroprene rubber. The reaction occured in the manner of chain transfer mechanism was carried out by means of solution polymerization in toluene in the presence of benzoyl peroxide as the radical initiator. The graft copolymer obtained from this work was analyzed by using IR spectrum, and the physical properties of the polymer such as the thermal behavior were also studied according to TG-DTA methods, and the potency of adhesiveness for the purpose of commercial application was investigated. Experimental results for the graft copolymerization are summarized as follows. 1) A small amount of initiator (0.5%) and 50% of monomer showed the best result for the grafting of monomer to the polymer chain of rubber while the 15% of rubber solution was found to be most suitable to raise either for the grafting ratio or the polymerization ratio. 2) Optimum temperature for better yield of graft copolymer was proved to he at $75^{\circ}C\sim80^{\circ}C$ while those of reaction time was to be $1\sim2$ hours.

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면섬유에 대한 Methyl Methacrylate의 유화 그라프트 중합 (Emulsion Graft Copolymerization of Methyl Methacrylate onto Cotton Fiber)

  • 배현석;류효선;김성련
    • 한국의류학회지
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    • 제15권3호
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    • pp.271-280
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    • 1991
  • Emulsion graft copolymerization of MMA onto cotton fiber using Ce(IV) salt as an initiator was carried out. Graft yield and graft efficiency were observed according to the kinds and concentrations of emulsifier and polymerization conditions. The physical properties of MMA grafted cotton fabric were investigated. The results of this study were as follows: 1. The heighest graft yield of emulsion graft polymerization occurred at the concentration below cmc of emulsifier, which was different from emulsion polymerization. Nonionic sur- factant as an emulsifier was more effective than anionic one. 2. The highest graft yield was obtained at the initiator concentration $1{\times}10^{-2}mol/l$. The viscometric molecular weight of PMMA was in the order of 106. 3. As reaction time increased, the graft yield increased but the graft efficiency decreased. 4. Elevation of reaction temperature resulted in increase of graft yield. The apparent activation energy of MMA graft polymerization was 4.72 Kcal/mol. 5. Physical properties of MMA grafted cotton fabric varied with increase of grafting. Thickness and stiffness showed a noticeable increase, whereas tensile strength and elongation was slightly increased. Crease recovery increased as the graft yield increase up to $50\%$ and decreased thereafter.

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Preparation and Evaluation of Chitin Derivatives and Their Utilization for Waste-water Treatement

  • Aly, Aly Sayed;Jeon, Byeong-Dae;Kim, Young-Jun;Park, Yun-Heum
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 1996년도 추계 학술발표회
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    • pp.53-58
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    • 1996
  • The Chitin Thiocarbonate-Fe(II)-H2O2 redox initiator system was investigated for the graft copolymerization of acrylonitrile(AN) and acrylic acid(AA) monomers onto chitin powder. The reactions with vinyl monomers onto chitin were carried out under various the graft copolymerization conditions to elucidate the polymerization behavior in terms of graft yield. Reactions of chitin-acrylonitrile graft copolymer with hydroxyl amine hydrochloride and those with sodium hydroxide were conducted in order to obtain chitin-(amidoxime-co-acrylonitrile) and chitin-(acrylate-co-acrylamide) graft copolymers, respectively. The reaction efficiency was observed to depend on the alkali concentration, time, temperature, and the reactant concentrations. The prepared chitin derivatives were evaluated to find potential applications for use in wastewater treatments for adsorption and desorption of heavy metal ions as well as acidic and basic dyes.

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메타과요오드산소다에 의한 알긴산소다의 MMA graft 중합 (Graft Polymerization of MMA onto Sodium Alginate by Sodium Metaperiodate)

  • 박천욱
    • Elastomers and Composites
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    • 제14권1호
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    • pp.7-12
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    • 1979
  • Graft copolymerization of methlymethacrylate(MMA) onto sodium alginate(SA) aqueous solution by sodium metaperiodate$(NaIO_4)$ as an initiator was carried out with the variation of the reaction time, the reaction temperature and the concentrations of initiator and monomer. The results obtained were as follows: 1. SA was easily separated from the reaction mixture of homopolymer, graft polymer and sodium alginate ungrafted by the treatment of concentrated boiling $Na_3PO_4$, solution with the small amount of $Na_2SO_3$ to the mixture and then isolated as the acid form by acidifying the salts solution containing SA. 2. The amount of graft polymer was larger than that of homopolymer below $70^{\circ}C$ whereas above $70^{\circ}C$ the amount of homopolymer was larger. 3. The sum of each amount of graft polymer ana homopolymer was always increased with increase of the reaction time, the reaction temperature and the concentrations of initiator and monomer. 4. With increase of the concentration of initiator, the graft efficiency was increased below $70^{\circ}C$ while decreased above $70^{\circ}C$. 5. Graft copolymerization of MMA onto SA in aqueous solution was carried out without initiator.

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