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조철형,조성휴,조병욱,김정규,김숭평,권중근 조선대학교 생산기술연구소 1983 生産技術硏究 Vol.1983 No.-
Copolyesters containing oxybenzoate as a rigid rod molecule and methylene group and dimethyl tetramethyl disiloxane as flexible spacers were prepared by room temperature solution polymerization for the purpose of the developement of polymeric composite materials. The thermal properties and the characteristics of the polymers were investigated by DSC and a polarizing microscope. The polymers may be formed nematic liquid crystal phase, and the thermodynamic characteristics of their mesophase to isotropic phase transition could be explained on the basis of its structural features.
Kwon, Sooncheol,Park, Jin Kuen,Kim, Jehan,Kim, Geunjin,Yu, Kilho,Lee, Jinho,Jo, Yong-Ryun,Kim, Bong-Joong,Kang, Hongkyu,Kim, Junghwan,Kim, Heejoo,Lee, Kwanghee The Royal Society of Chemistry 2015 Journal of Materials Chemistry A Vol.3 No.15
<P>Processing additives have been widely utilized for high-performance organic bulk-heterojunction (BHJ) photovoltaic devices. However, the role of processing additives remained unclear due to the limited information relying on the final BHJ film state rather than the intermediate film state during solvent evaporation. Here, by using<I>in situ</I>GIWAXS measurements on the intermediate BHJ film, we propose a possible phase separation mechanism in efficient BHJ solar cells consisting of a narrow band gap polymer (P1) and PC71BM<I>via</I>the use of 1-chloronaphthalene (1-CN) as a processing additive. We found that adding small amounts of an additive, 1-CN, with a high boiling point and a high PC71BM solubility can prolong the solvent evaporation time and dissolve many PC71BM molecules, promoting the strong P1 polymer:solvent and PC71BM:solvent interaction to produce pure domains of each component. Thus, the bi-continuous networks for both P1 and PC71BM and their enlarged interfacial area are well fabricated in the BHJ films, inducing balanced photo-charge carrier densities for the electrons and holes and improving the overall photovoltaic performance. Therefore, our findings elucidate the kinetic motions of two organic phases affected by the physical properties of the solvents in the process of film formation and establish criteria for BHJ systems.</P>
이강춘,조종수,성용길,권중근,조병욱 한국약제학회 1992 Journal of Pharmaceutical Investigation Vol.22 No.4
Poly(ε-carbobenzoxy L-lysine)/poly(ethylene oxide)/poly(ε-carbobenzoxy L-lysine) (LEL) block copolymers containing poly(ε-carbobenzoxy L-lysine) (PCLL) as the A component and poly(ethylene oxide) (PEO) as the B component were investigated as drug delivery matrix. PCLL homopolymer and LEL block copolymer microspheres containing anticancer drug, cytarabine, were prepared by a solvent evaporation process and the release patterns of cytarabine from the microspheres were investigated in vitro. The size of PCLL homopolymer and LEL block copolymer microspheres was ranged from 0.2 ㎛ to 1 ㎛ in diameter and the shape of the microspheres was almost round. The release pattern of cytarabine from the block copolymers microspheres was dependent on the mole % of PEO of the block copolymers.
조종수,권중근,조병욱,이강춘,성용길,Cho, Chong-Su,Kwon, Joong-Kuen,Jo, Byung-Wook,Lee, Kang-Choon,Sung, Yong-Kiel 한국약제학회 1992 Journal of Pharmaceutical Investigation Vol.22 No.4
$Poly({\varepsilon}-carbobenzoxy\;L-lysine)/poly(ethylene oxide)/poly({\varepsilon}-carbobenzoxy\;L-lysine)$ (LEL) block copolymers containing $poly({\varepsilon}-carbobenzoxy\;L-lysine)$ (PCLL) as the A component and poly(ethylene oxide) (PEO) as the B component were investigated as drug delivery matrix. PCLL homopolymer and LEL block copolymer microspheres containing anticancer drug, cytarabine, were prepared by a solvent evaporation process and the release patterns of cytarabine from the microspheres were investigated in vitro. The size of PCLL homopolymer and LEL block copolymer microspheres was ranged from $0.2\;{\mu}m$ to $1\;{\mu}m$ in diameter and the shape of the microspheres was almost round. The release pattern of cytarabine from the block copolymer microspheres was dependent on the mole % of PEO of the block copolymers.