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      KCI등재

      부틸글리시딜에테르와 이산화탄소의 부가반응에 대한 이온성 액체의 촉매 성능 고찰 = Catalytic Performance of Ionic Liquids for the Cycloaddition of Carbon Dioxide and Butyl Glycidyl Ether

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      https://www.riss.kr/link?id=A104429035

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      The synthesis of cyclic carbonate from butyl glycidyl ether (BGE) and carbon
      dioxide was performed in the presence of three different types of ionic liquid : quarternary
      ammonium salt, alkyl pyridinium salt, and alkylimidazolium salt. Ionic liquids of different alkyl
      groups (C3, C4, C6 and C8) and anions (Cl-, Br- and I-) were used for the reaction which was
      carried out in a batch autoclave reactor at 60~120 ℃. The catalytic activity was increased
      with increasing alkyl chain length in the order of C3 < C4 < C6. But the ionic liquid with
      longer alkyl chain length (C8) decreased the conversion of BGE because it is too bulky to
      form an intermediate with BGE. For the counter anion of the ionic liquid catalysts, the BGE
      conversion decreased in the order Cl- > Br-
      > I-
      .
      번역하기

      The synthesis of cyclic carbonate from butyl glycidyl ether (BGE) and carbon dioxide was performed in the presence of three different types of ionic liquid : quarternary ammonium salt, alkyl pyridinium salt, and alkylimidazolium salt. Ionic liquids of...

      The synthesis of cyclic carbonate from butyl glycidyl ether (BGE) and carbon
      dioxide was performed in the presence of three different types of ionic liquid : quarternary
      ammonium salt, alkyl pyridinium salt, and alkylimidazolium salt. Ionic liquids of different alkyl
      groups (C3, C4, C6 and C8) and anions (Cl-, Br- and I-) were used for the reaction which was
      carried out in a batch autoclave reactor at 60~120 ℃. The catalytic activity was increased
      with increasing alkyl chain length in the order of C3 < C4 < C6. But the ionic liquid with
      longer alkyl chain length (C8) decreased the conversion of BGE because it is too bulky to
      form an intermediate with BGE. For the counter anion of the ionic liquid catalysts, the BGE
      conversion decreased in the order Cl- > Br-
      > I-
      .

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      참고문헌 (Reference)

      1 L. A. Dominey, "Thermally stable lithium salts for polymer electrolytes" 37 : 1551-, 1992

      2 A. Rokicki, "The application of carbon dioxide as a direct material for polymer syntheses in polymerization and polycondensation reactions" 21 : 135-, 1981

      3 R. Nomura, "Synthesis of cyclic carbonates from carbon dioxide and epoxides in the presence of organoantimony compounds as novel catalysts" 45 : 3735-, 1980

      4 C. E. Song, "Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel -Crafts alkylation of aromatic compounds with alkenes" 1695-, 2000

      5 H. Matsumoto, "Room temperature molten salts based on tetraalkylammonium cations and bis(trifluoromethylsulfonyl)imide" 182 : 2001

      6 R. Hagiwara, "Room temperature ionic liquids of alkyl imidazolium cations and fluoroanions" 105 : 221-, 2000

      7 B. S. Yu, "React. Kinet" 84 : 175-, 2005

      8 A. Rokicki, "Poly(alkylene carbonates) with controlled molecular weight" 4 (4): 677-, 1990

      9 M. Freemantle, "Peter Debye award in physical chemistry" 78 : 120-, 2000

      10 S. Inoue, "Organic and Bioorganic Chemistry of Carbon dioxide" Kodansha Ltd. 1981

      1 L. A. Dominey, "Thermally stable lithium salts for polymer electrolytes" 37 : 1551-, 1992

      2 A. Rokicki, "The application of carbon dioxide as a direct material for polymer syntheses in polymerization and polycondensation reactions" 21 : 135-, 1981

      3 R. Nomura, "Synthesis of cyclic carbonates from carbon dioxide and epoxides in the presence of organoantimony compounds as novel catalysts" 45 : 3735-, 1980

      4 C. E. Song, "Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel -Crafts alkylation of aromatic compounds with alkenes" 1695-, 2000

      5 H. Matsumoto, "Room temperature molten salts based on tetraalkylammonium cations and bis(trifluoromethylsulfonyl)imide" 182 : 2001

      6 R. Hagiwara, "Room temperature ionic liquids of alkyl imidazolium cations and fluoroanions" 105 : 221-, 2000

      7 B. S. Yu, "React. Kinet" 84 : 175-, 2005

      8 A. Rokicki, "Poly(alkylene carbonates) with controlled molecular weight" 4 (4): 677-, 1990

      9 M. Freemantle, "Peter Debye award in physical chemistry" 78 : 120-, 2000

      10 S. Inoue, "Organic and Bioorganic Chemistry of Carbon dioxide" Kodansha Ltd. 1981

      11 G. Rokicki, "Monatsh" 115 : 205-, 1984

      12 N. Kihara, "Makromol" 193 : 1482-, 1992

      13 D. R. Bond, "Liquid clathrates" 1910-, 1989

      14 H. Olivier-Bourbigou, "Ionic liquids: perspectives for organic and catalytic reactions" 182 : 419-, 2002

      15 P. Wasserscheid, "Ionic liquids - new solutions for transition metal catalysis" 39 : 3772-, 2000

      16 D. R. MacFarlane, "High conductivity molten salts based on the imide ion" 45 : 1271-, 2000

      17 J. A. King, "Extractive method for the preparation of quaternary salts with perfluorinated anions" 5 (5): 696-, 1998

      18 F. H. Hurley, "Electrodeposition of metals from fused quaternary ammonium salts" 98 : 203-, 1951

      19 A. S. Larsen, "Designing ionic liquids: Imidazolium melts with inert carborane anions" 122 : 7264-, 2000

      20 S. Inoue, "Copolymerzation of carbon dioxide and epoxide" 7 : 287-, 1969

      21 M. S. Super, "Copolymerizations involving carbon dioxide: the use of CO2 as a monomer" 5 (5): 236-, 1997

      22 J. D. Holbrey, "Clean Prod" 1 : 223-, 1999

      23 D. J. Darensbourg, "Catalysts for the reactions of epoxides and carbon dioxide" 153 : 155-, 1996

      24 D. W. Park, "Catal" 98 : 499-, 2004

      25 T. Aida, "Alternating copolymerization of carbon dioxide and epoxide catalyzed by the aluminum porphyrin-quaternary organic salt ortriphenylphosphine system" 19 (19): 1986

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 계속평가 신청대상 (계속평가)
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      외국어명 : Journal of Oil & Applied Science -> Journal of the Korean Applied Science and Technology
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      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2017-06-01 학술지명변경 한글명 : 韓國油化學會誌 -> 오일 및 응용과학 학회지
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      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.3 0.3 0.3
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.27 0.24 0.354 0.08
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