• 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)

• Journal of the Korean Society of Industry Convergence
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• v.9 no.4
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• pp.331-336
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• 2006

An efficient synthesis of 3,4-dihydro-2H-pyrans is achieved by $Ag_2CO_3$/celite mediated reaction of 1,3-dicarbonyl compounds with vinyl ether in moderate yields. This method has been applied to the synthesis of 3,4-dihydro-2H-pyranochromens and 3,4-dihydro-2H-benzochromen. 3,4-Dihydro-2H-pyranochromens were easily converted to 4H-pyranochromens by elimination of ethoxy group. The structures of these compound were identified by IR and $^1H$ NMR-Spectra.

• Journal of Information Display
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• v.12 no.4
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• pp.223-227
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• 2011

Electrophosphorescent devices with ionomer-type hole transport layers were investigated. On top of the 3,4-ethylenedioxy thiophene:poly(4-styrene sulfonate) [PEDOT:PSS] structures, fluoropolymer interfacial layers (FPIs) with different side chain lengths were introduced. Both for the PEDOT:PSS/FPI (layered) and PEDOT:PSS (mixed) structures with soluble phosphorescent emitters, the short-side-chain FPIs showed higher efficiency. The difference in the electrical properties of the two FPIs for bipolar (light-emitting) devices was not clear, but the hole-only device clearly showed the favored hole injection at the PEDOT:PSS/FPI structure with a shorter side chain, a copolymer of tetrafluoroethylene and sulfonyl fluoride vinyl ether.

• Journal of the Korean Society of Clothing and Textiles
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• v.20 no.3
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• pp.512-518
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• 1996

Microcapsules containing 2, 4, 4'-trichloro-2-hydroxydiphenyl ether and perfumes were prepared by the coacervation using poly (vinyl alcohol) and crosslinking agents. Effects of dispersing agents, core materials, agitating speed and crosslinking agents on microcapsule size were investigated. The mean and deviation of microcapsule diameters decreased with increasing agitation speed. The diameters of m;crocapsules decreased with increasing dispering agent concentration at 6, 000 rpm of agitation speed, but it was not changed at 10, 000 rpm. The dispering effect of PVA is better than that of gum arabic. The slight increase in the diameter of microcapsule was observed when the amount of core material was increased. As the amount of crosslinking agent was increased, the diameter of microcapsule was decreased.

• Proceedings of the Korean Society of Propulsion Engineers Conference
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• 2017.05a
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• pp.495-497
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• 2017

Thermoplastic propellants using thermoplastic elastomer binders show moderate performance and mechanical properties compared to thermoset propellants, but these propellants are widely used in a variety of fields due to low cost of raw materials, simple manufacturing process and stable handling process. In order to utilize thermoplastic solid propellants in various fields, we will study properties depending on the content of oxidants, metal fuels and additives.

• YAKHAK HOEJI
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• v.47 no.6
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• pp.356-360
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• 2003

Nitroso-2-naphthol-3,6-disulfonic acid, disodium salt (NRS) was used as an organic ligand to prepare basic drug-selective polymeric membrane electrode. The sensing membrane of the electrode consited of basic drug-meta1(II)-NRS as an ion-exchanger site in a poly(vinyl chloride) matrix plasticized with 2-nitrophenyl octyl ether (NPOE). The metal ions used were Fe$^{2+}$, Co$^{2+}$, Ni$^{2+}$ and Cu$^{2+}$. The electrodes exhibited fast and wide linear response in the basic drug concentration of 10$^{-5}$ ∼10$^{-3}$ mol/l with a response slope of 50∼60 mV/decade in a buffer solution of pH 4∼8. The electrodes exhibited good selectivity for many basic compounds.mpounds.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2000.07a
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• pp.265-269
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• 2000

Nowadays the hydrophilic polymeric networks (polymer hydrogels) due to the complex of benefit physico-chemical properties attract a wide attention of specialists working in various fields of science, medicine and technology. The special attention of chemists is aimed on so-called stimuli-sensitive or intelligent hydrogels, which can undergo a volume phase transition in response to change in environmental parameters such as temperature, pH, solvent composition, etc [1]. Scientific group of Kazak State National University, Department of Macromolecular Chemistry works in this field [2-5]. Here we report about our achievements on pH-sensitive hydrogens.

• Bulletin of the Korean Chemical Society
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• v.7 no.5
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• pp.372-376
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• 1986

Substituted 3,4-dihydro-2H-pyrans ($1_{a-e}$) were prepared by (4 + 2) cycloaddition reaction of dimethyl dicyanofumarate with the corresponding electron-rich olefins. The compounds $1_{a-e}$ were ring-open polymerized by cationic initiators to obtain polymers of 1:1 alternating sequence. Polymerizations were carried out with boron trifluoride etherate in methylene chloride at $-78^{\circ}C$. All the polymers obtained were soluble in common solvents and were reprecipitated by pouring its chloroform solution into diethyl ether. All the compounds $1_{a-e}$ were not as reactive as the corresponding pyrans derived from ${\alpha}$ -cyanoacrylate.

• Bulletin of the Korean Chemical Society
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• v.16 no.12
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• pp.1167-1172
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• 1995

A coverage of about 1 μm-sized pores of a membrane filter by four monolayers of maleic acids copolymers and poly(allylamine) (PAA) was attained by Langmuir-Blodgett (LB) technique through a covalent cross-linking followed a polyion complexation at the air-water interface. The copolymers were prepared to have side chains of hydrocarbon tail, carboxyl, and/or oligoether in the repeat unit. The surface pressure-area isotherms showed that the monolayers on an aqueous PAA have more expanded area than on pure water. The monolayers were transferable on a calcium fluoride substrate and a fluorocarbon membrane filter as Y deposition type, and the resulting LB films were characterized by FT-IR spectroscopy and scanning electron microscopy. A polymer network produced through interchain amide formation was confirmed in as-deposited films. The films were heat-treated in order to complete the cross-linking. SEM observation of the heat-treated film on a porous membrane filter showed that the four layer film was sufficiently stable to cover the filter pore of about 1 μm. Immersion of the film in water or in chloroform did not cause any change in its appearance on SEM and in FT-IR spectra.

• Bulletin of the Korean Chemical Society
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• v.16 no.4
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• pp.316-320
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• 1995

The incorporation of metal ion into the Langmuir-Blodgett (LB) film of an itaconate copolymer was investigated. The polymer was prepared via radical copolymerization of monooctadecyl itaconate with triethyleneglycol methyl vinyl ether. The metal ions employed were Na+, Cs+, Mg2+, Fe2+, Al3+, and Fe3+. The surface pressure-area isotherms indicated that all the monolayers studied on subphases with metal ions showed more expanded areas than that observed on pure water. The monolayers showed an irreversible collapse behavior. The collapse pressure of the monolayers was low on subphases containing trivalent metal ions. From the FT-IR spectra by reflection and transmission modes, the formation of carboxylate salts and the uprisen orientation of the pendant against substrate surface in the polymer LB film were determined. It was estimated by XPS measurement that ca. 13.1 repeat units of the polymer contain one Na+ ion, while one Mg2+ ion corresponds to 5.9 carboxyls.