• 제목/요약/키워드: polymerization

검색결과 3,130건 처리시간 0.029초

Living cationic polymerization of poly (isobutyl vinyl ether) and PVA derived therefrom

  • Mah, Soukil
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 2003년도 The Korea-Japan Joint Symposium
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    • pp.1-2
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    • 2003
  • Some new synthetic routes for the preparation of poly (isobutyl vinyl ether) (P(IBVE)) having a controllable molar mass with narrow distribution via catalytic or photoinduced living cationic polymerization and their conversion to corresponding PVA have been developed. It was found that the combination of iodomethyl methyl ether (IMME)-zinc iodide is effective in the initiation of the catalytic and the various combinations of diphenyliodonium halides, well known photocationic initiators (DPIX) with zinc halides (ZnX$_2$) are also useful in photoinduced living cationic polymerization of isobutyl vinyl ether (IBVE). Polymerization both in the catalytic and photoinduced systems precede until the full consumption of the monomer and the rate of polymerization increases as the concentration of the catalyst or photoinitiator. The number average molar mass of the resulting polymer is proportional with % conversion, which is determined by the ratio of monomer consumed and the initial values of the catalyst or initiator. The living nature was also confirmed by subsequent monomer addition technique.

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Reaction Condition Dependency of Propagating Behavior in the Polymerization Reaction by Thermal Front

  • Huh, Do-Sung;Choe, Sang-Joon;Lee, Burm-Jong
    • Bulletin of the Korean Chemical Society
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    • 제23권2호
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    • pp.325-329
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    • 2002
  • In this study, the dependency of the behavior of propagating front on the reaction condition in frontal polymerization reaction has been studied. We have used some multifunctional acrylates as a monomer and ammonium persulfate as an initiator for the polymerization reactions. In frontal polymerization, a method of producing polymeric materials via a thermal front that propagates through the unreacted monomer/initiator solution, the behavior of self propagating front shows various dynamic patterns depending on the reaction condition. We have obtained some spin modes of propagating front in the number of 'hot spots' or 'spin heads' by changing the reaction condition. The effect of the reactor tube diameter on the mode of propagating front has also been studied by using some reactor tubes with different size of tube diameter and it has been examined in some detail by adopting an experimental method of two-tubes system.

Living 양이온 중합의 구성원리와 현재동향 (Recent Trend in Living Carbocationic Polymerization)

  • 조창기
    • 공업화학
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    • 제2권3호
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    • pp.199-208
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    • 1991
  • 양이온 중합은 electron이 풍부한 단량체들을 중합하는데 널리 이용되나 많은 부 반응과 빠른 중합속도 때문에 반응을 제어하기가 어렵다. 최근에 이러한 반응 제어에 많은 연구가 되고 있는데 특히 living 중합에 의하여 중합반응을 제어하는 방법에 대한 연구가 활발하다. 본고에서는 종합활성점의 해리상태를 조절하여 중합반응을 제어하고 living 중합을 도모하는 방법에 대하여 기술하였다. 그리고 현재까지 알려진 여러 방법들을 이러한 기본원리하에서 설명하였다.

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Polymerization of 3-Ethynylphenol Try Transition Metal Catalysts

  • Gal, Yeong-Soon;Lee, Won-Chul;Jin, Sung-Ho;Lee, Hyung-Jong
    • Macromolecular Research
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    • 제8권5호
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    • pp.231-237
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    • 2000
  • The polymerization of 3-ethynylphenol, phenylacetylene having hydroxy functionality, was carried out by tungsten and molybdenum-based transition metal catalysts. The polymerization proceeded to give a moderate yield of polymer. The effects on the mole ratio of monomer to catalyst (M/C), initial monomer concentration ((Mb), and the polymerization temperature for the polymerization of 3-ethynylphenol were investigated. The catalytic activity of W-based catalysts was found to be greater than that of Mo-based catalysts. The resulting polymers were brown or black powders and mostly insoluble in organic solvents. Structural analysis of the polymer by instrumental methods revealed the conjugated polymer backbone structure carrying hydroxyphenyl moieties. Thermal and morphological properties of the resulting poly(3-ethynylphenol) were also discussed.

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비선형 예측제어 알고리즘을 이용한 회분식 중합 반응기의 온도제어 (Temperature control of a batch polymerization reactor using nonlinear predictive control algorithm)

  • 나상섭;노형준;이현구
    • 제어로봇시스템학회:학술대회논문집
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    • 제어로봇시스템학회 1996년도 한국자동제어학술회의논문집(국내학술편); 포항공과대학교, 포항; 24-26 Oct. 1996
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    • pp.1000-1003
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    • 1996
  • Nonlinear unified predictive control(UPC) algorithm was applied to the temperature control of a batch polymerization reactor for polymethylmethacrylate(PMMA). Before the polymerization reaction is initiated, the parameters of the process model are determined by the recursive least squares(RLS) method. During the reaction, nonlinearities due to generation of heat of reaction and variation of heat transfer coefficients are predicted through the nonlinear model developed. These nonlinearities are added to the process output from the linear process model. And then, the predicted process output is used to calculate the control output sequence. The performance of nonlinear control algorithm was verified by simulation and compared with that of the linear unified predictive control algorithm. In the experiment of a batch PMMA polymerization, nonlinear unified predictive control was implemented to regulate the temperature of the reactor, and the validity of the nonlinear model was verified through the experimental results. The performance of the nonlinear controller turned out to be superior to that of the linear controller for tracking abrupt changes in setpoint.

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Living cationic polymerization of Viny Ethers in Presence of Iodomethyl Methyl Ether and Zinc Iodide

  • Kwon, Soonhong;Lee, Yunsung;Mah, Soukil
    • Fibers and Polymers
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    • 제2권1호
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    • pp.131-134
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    • 2001
  • Living cationic polymerization behaviors of isobutyl vinyl ehters (IBVE), initiated by iodomethyl methyl ether (IMME)/zinc iodide ($Znl_2$) have been investigated. The polymerization was carried out at 0, -15, and $-30^{\circ}C$ in toluene. It was found that the rate of polymerization increased as the IMME concentration increased and decreased as temperature decreased. 100% conversion was always achieved without exception. Furthermore, the number-average molecular weight ($M_{n}$) of polymers increased in direct proportion to monomer conversion. The molecular weights of polymers were in good agreement with the theoretical values, calculated on the basis that one polymer chain was formed by one IMME molecule and the values of polydispersity index are always less than 1.2, revealing the living nature. The living nature was also confirmed by synthesis of poly(IBVE-b-TBVE) by subsequent monomer addition of t-butyl vinyl ether (TBVE).

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Kevlar 49 섬유 표면에 대한 MAN의 Graft 공중합에 관한 연구 (Graft Copolymerization of Methacrylonitrile(MAN) onto Kevlar 49 Fiber Surface)

  • 김은영;강주영;최재혁;김한도
    • 한국염색가공학회지
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    • 제7권1호
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    • pp.43-50
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    • 1995
  • The grafting of methacrylonitrile(MAN) onto Kevlar 49 filament surface was carried out by anionic polymerization using sodium methylsulfinylcarbanion formed from sodium hydride and dimethyl sulfoxide(DMSO). The effects of reaction conditions on the grafting percentage(GP) and on the tensile strength of the fiber were investgated. GP marktedly increased with increasing metalation time, and NaH concentration, polymerization temperature and time. The tensile strength of fiber decrased with increasing metalation time, and NaH concentration, polymerization temperature and time. The optimum conditions to increase over 40% of GP with below 10% reduction rate of tensile strength of fiber : NaH concentration ; 30.6 mmol/l/0.5g Kevlar, metalation time : 10min, polymerization tempera- ture : 5$0^{\circ}C$, polymerization time: 20 sec, monomer concentration : 1.12mol/l/0.5g Kevlar.

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Low Temperature Suspension Polymerization of Methyl Methacrylate for the Preparation of High Molecular Weight Poly(methyl methacrylate)/Silver Nanocomposite Microspheres

  • Yeum, Jeong-Hyun;Ghim, Han-Do;Deng, Yulin
    • Fibers and Polymers
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    • 제6권4호
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    • pp.277-283
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    • 2005
  • In order to prepare high molecular weight poly(methyl methacrylate) (PMMA)/silver nanocomposite microspheres, methyl methacrylate was suspension-polymerized in the presence of silver nanoparticles at low temperature with 2,2'-azobis(2,4-dimethylvaleronitrile) as an initiator. The rate of conversion was increased by increasing the initiator concentration. When silver nanoparticles were added, the rate of polymerization decreased slightly. High monomer conversion (about $85\%$) was obtained in spite of low polymerization temperature of $30^{\circ}C$. Under controlled conditions, PMMA/silver microspheres with various number-average degrees of polymerization (6,000-37,000) were prepared. Morphology studies revealed that except for normal suspension microspheres with a smooth surface, a golf ball-like appearance of the microspheres was observed, due to the migration and aggregation of the hydrophilic silver nanoparticles at the sublayer beneath the microsphere's surface.

Polymerization of Vinyl Monomers Initiated by Thianthrene Cation Radical with Potential Biological Activity

  • Lee, Beomgi;Kim, Seongsim;Park, Jaeyoung;Cheong, Hyeonsook;Noh, Ji Eun;Woo, Hee-Gweon
    • 통합자연과학논문집
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    • 제5권2호
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    • pp.127-130
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    • 2012
  • Polymerization of vinyl monomers is promoted by thianthrene cation radical as a part of our research concerning the reactions of various agents with readily isolable, yet highly reactive species and elucidate the biological activity. Thianthrene cation radical initiated the homopolymerization and copolymerization of styrene and ethyl vinyl ether. The polymerization yields decreased as the concentration of phenylacetylene or diphenylethylene increased. Such polymereization by cationic thianthrene radical could provide some clues for the reaction in living animals. Comments on possible polymerization mechanisms were suggested.