• Proceedings of the Korean Fiber Society Conference
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• 2003.04a
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• pp.5-8
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• 2003

요오드화 아연과 수소화 요오드에 의해 개시되는 비닐에테르류 단량체의 양이온 리빙 중합이 보고$^{(1)}$ 된 이래 리빙 중합 개시계에 대한 연구가 많이 진행되어 왔다. 본 연구자들은 광양이온중합 개시제인 요오드화 디페닐요드늄과 할로젠화 아연 존재 하에서 비닐에테르 단량체의 광양이온중합을 실시하여 비극성 용매 하에서 연쇄이동이나 정지반응이 존재하지 않는 리빙중합을 보고한$^{(2-4)}$ 바 있는데 이 중합에서 비닐에테르 단량체와 프로톤산에 의하여 생성된 단량체 adduct의 C-I 결합이 안정한 공유결합을 형성하나 요오드화아연에 의해 C-I 결합의 분극화되어 활성화됨으로서 개시와 성장반응이 가능한 것으로 설명되었다. (중략)

• Microbiology and Biotechnology Letters
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• v.26 no.4
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• pp.338-344
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• 1998

New type of chitosan derivatives, chitosan-g-MAP, were synthesized by graft copolymerization of mono (2-methacryloyl oxyethyl) acid phosphate (MAP) into chitosan, in order to solubilize chitosan in water. Ceric ammonium nitrate was used as an initiator for graft copolymerization. The optimal conditions for graft copolymerization were determined on the basis of reaction temperature, time, and the concentration of initiator and monomer. The reaction conditions for the highest percentage of grafting were as follows: an initiator concentration, 3.5${\times}$10$\^$-3/ M; monomer concentration, 0.19 M; and reaction temperature, 40$^{\circ}C$ The reaction rate reached the maximum value after 4 hrs of reaction. Antifungal activity was tested against Candida albicans, Trichophyton rubrum and Trichophyton violaceum by using chitosan-g-MAP and two other chitosan samples which have degree of deacetylation of 70% (DA-7) and 90% (DA-90). Their antifungal activities were investigated in weak acidic range. Maximum antifungal activity of them was observed at pH 5.75. Chitosan-g-MAP inhibited thoroughly the growth of Candida albicans and Trichophyton violaceum. Howerver, DA-70 and DA-90 showed higher antifungal activities on Trichophyton rubrum than that of chitosan-g-MAP.

• Journal of the Korean Chemical Society
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• v.22 no.4
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• pp.268-274
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• 1978

The kinetics of the bulk polymerization of propylene sulfide initiated by o-sulfobenzoic anhydride were investigated, which proceeded by a zwitterionic mechanism.The instantaneous concentrations of monomer and initiator were determined by means of ir-and nmr-spectroscopy. The rate constant of propagation was found to be about three order of magnitude higher than that of initiation and this should be caused by a zwitterion mechanism.

• Journal of Korean Ophthalmic Optics Society
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• v.8 no.2
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• pp.129-134
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• 2003

A wide variety of unsaturated vinyl derivatives can be induced to undergo free-radical chain polymerization. The capability to carry out a thermodynamically feasible polymerization relies on its kinetic feasibility on whether the proceeds at a reasonable rate under a given set of reaction conditions. Initiator or promoter is often required to achieve the kinetic feasibility. Only a few unsaturated monomers including methyl methacrylate(MMA) are known to absorb light between 250 and 500 nm which is the most convenient wavelength range. Also, the polysilanes with unusual optical and electronic properties have been used as ceramic precursors, deep UV photoresists, photoconductors. The hydrosilation has been used to make many interesting types of silicon containing polymers such as copolymer, dendrimers. Bulk polymerization of monomers with different molar radio of hydrosilanes(9:1 through 1:9) were performed. A quartz test tube charged with monomer and hydrosilane was degassed and irradiated with 250 nm UV for 6 hours. The polymer was taken in toluene, precipitated in hexane, filtered off, and dried. It was found that the initiators appeared to competitively and concurrently function as both chain initiation and transfer agents in the polymerization of vinyl monomers.

• Elastomers and Composites
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• v.43 no.3
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• pp.157-165
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• 2008

Suspension polymerization was carried out to synthesize poly(butyl methacrylate) (PBMA) composite particles containing carbon black. Water was selected as a reaction medium, hydrophobic silica as a stabilizer and azobisisobutyronitrile as an initiator. Concentration of stabilizer was varied from 0.67 to 2.55 weight% with respect to the water, and that of initiator was varied from 0.25 to 3.00 weight% with respect to the butyl methacrylate (BMA) monomer. All polymerization reactions were conducted at 75$^{\circ}C$. It is found that stabilizer concentration has no impact on reaction kinetics, while an increase in initiator concentration enhances polymerization reaction rate. Increase of carbon black concentration from 1 to 3 to 5 wt% into PBMA displayed progressive decrease in reaction conversion. The particle diameter of PBMA composite particles containing carbon black was found to be between 5 and 30 ${\mu}m$. Glass transition was determined to range from 23.8 to 24.7$^{\circ}C$, irrespective of variation in the concentration of stabilizer, initiator or carbon black.

• Journal of the Korean Society of Industry Convergence
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• v.6 no.1
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• pp.17-21
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• 2003

5원환 고리아세탈 화합물인 4-methylenes(4,5)을 합성하고 저온조건 하에서 중합반응을 조사한 결과, 선택적인 개환중합이 일어났다. 보통의 양이온 개시제를 사용한 결과 $-78^{\circ}C$에서 가교체가 얻어졌으며, $CH_3SO_3H$를 개시제로 사용하면 같은 조건에서도 주사슬과 곁사슬에 이중결합을 가지는 개환중합체가 얻어진다. 이 중합체는 반응성을 가지는 불포화기를 포함하고 있으므로 prepolymer로써 널리 사용될 수 있다.

• Polymer(Korea)
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• v.25 no.1
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• pp.1-5
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• 2001

Monomer casting nylons were synthesized by casting anionic polymerization of ${\varepsilon}$-caprolactam. Polymerization rates, molecular weights of the products and the conversions were determined while varying the content of catalysts in the range of 0.2~0.6 mol% and 0.1~1.0 mol% for initiator. The polymerization rates were enhanced as the ratio of catalysts to initiator increased. The maximum molecular weight was observed when the ratio of catalysts to initiator was 0.8, and as the ratio increased the molecular weight decreased. On the other hand, when the ratio of catalysts to initiator was below 0.8, the conversions and the molecular weights were abruptly diminished due to the termination of growing chains.

• Proceedings of the International Microelectronics And Packaging Society Conference
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• 2002.11a
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• pp.59-63
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• 2002

Zinc-Magnesium borosilicate 유리에 CaF$_2$입자를 충진재로 첨가하여 혼합체의 소결거동, 결정화 거동 및 최종 소결체의 마이크로파 유전특성을 측정하였다. CaF$_2$첨가는 유리의 점도를 감소 시켜 결정화 및 수축개시온도를 감소시켰다. 이러한 CaF$_2$의 최대 첨가량은 주어진 유리조성에 있어서 15 vol. % 이었다. 이러한 소결성 및 결정화 개시온도의 변화는 모 유리와 CaF$_2$의 반응에 의한 결과로 보여지며 이 반응은 결정상의 변화나 이차상의 형성에는 영향을 미치지 않았다. 따라서 유전율 6.1에 품질계수가 40000GHz 인 CaF$_2$입자를 15 vol.% 첨가시 유전상수는 7.1에서 5.6로 품질계수는 2200에서 5000GHz로 유전특성이 향상되었고 소결온도는 75$0^{\circ}C$이었다.

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.457-460
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• 1998

일반적인 리빙중합의 정의는 개시반응과 사슬의 성장반응만이 있으며 사슬이동반응이나 종결반응 등의 부반응은 일어나지 않아서 중합반응 후에도 사슬의 성장활성이 오랫동안 유지되는 중합반응계를 말한다. 이러한 리빙중합은 여러 가지의 중합방법에 의해서 시도되어졌는데 가장 대표적이고 성공적인 방법으로서 이온중합에 의한 방법을 그 예로 들 수 있다. 그러나 이온중합에 의한 방법은 그 리빙성이 매우 우수한 반면에 중합가능한 단량체의 종류가 국한되어 있고 중합조건이 아주 까다로워서 실용성이 없다는 단점이 있다. (중략)

• Applied Chemistry for Engineering
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• v.5 no.3
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• pp.524-536
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• 1994

Chitosan is known to be a good biocompatible natural polymer. Polyethyleneglycol monomethacrylates(PEGM) were grafted onto chitosan and their reaction conditions and properties of the graft polymers obtained were estimated. Using ceric ammonium nitrate(CAN) as the initiator, the optimum condition for graft polymerization was determined amount of the initiator and monomer concentrations and reaction time. Grafting yields such as total conversion, the percentage of grafting and the efficiency of grafting were calculated and examined the optimum reaction condition for high grafting yields. The percentage of grafting and total conversion were maximum at condition that the concentration of initiator was $4{\sim}5{\times}10^{-3}M$, the concentration of monomer was 0.5~0.6M, the reaction time was 2~3 hours and the reaction temperature was about $40^{\circ}C$. Thermal characteristics, solubility for chitosan solvents and inherent viscosity of synthesized graft copolymers were investigated. In high initiator concentration, characteristics of chitosan were greatly diminshed. In case of inherent viscosities, chitosan-g-PE-90 was 2.81 dl/g, chitosan-g-PE-200, 3.01dl/g and chitosan-g-PE-350, 4.93dl/g. And a tendency of viscosity increase depending on the length of ethylene oxide residue was confirmed. Degree of swelling, tensile strength, elongation of membrane prepared from graft copolymers were determined. Properties of graft copolymers were affected by percentage of grafting and length of ethylene oxides residue in polyethylene glycol monomethacrylates. Tensile strength, elongation and degree of swelling of graft copolymers were remarkably improved than chitosan. As percentage of grafting increased, the amount of drug permeation was also increased.