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      KCI등재 SCIE SCOPUS

      Catalytic production of hydroxymethylfurfural from sucrose using 1-methyl-3-octylimidazolium chloride ionic liquid

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      https://www.riss.kr/link?id=A104466366

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      다국어 초록 (Multilingual Abstract)

      Hydroxymethylfurfural (HMF) is an important chemical intermediate, but it has not been widely used because of low yields and high production costs. Sucrose is available at lower costs than other sugars and thus could be a biomass-derived abundant source for HMF production. In this study, a catalytic process for efficiently producing HMF from sucrose was scrutinized using 1-methyl-3-octylimidazolium chloride ([MOIM]Cl) as a reaction solvent, and HCl and metal chlorides (CrCl2 and Zncl2) as a catalyst. The rate of sucrose hydrolysis was relatively much faster in the reactions with HCl than without it. The hydrolysis of sucrose to fructose and glucose was affected by its reaction time.
      The mixed solvent of 50% [MOIM]Cl and 50% sucrose solution with HCl was more effective in HMF synthesis than single solvent alone. The addition of ZnCl2 and CrCl2 increased HMF yields by approximately 1.2-1.8-fold and its higher yield was found in the latter. The highest yield (82.0±3.9 wt%) in HMF production was achieved in the reaction mixture containing 5 g [MOIM]Cl and 5 mL of 20% sucrose solution with 0.5M HCl plus CrCl2 at 30 min reaction time. However,0.3 M HCl was more effective for the HMF productivity than 0.5 M HCl.
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      Hydroxymethylfurfural (HMF) is an important chemical intermediate, but it has not been widely used because of low yields and high production costs. Sucrose is available at lower costs than other sugars and thus could be a biomass-derived abundant sour...

      Hydroxymethylfurfural (HMF) is an important chemical intermediate, but it has not been widely used because of low yields and high production costs. Sucrose is available at lower costs than other sugars and thus could be a biomass-derived abundant source for HMF production. In this study, a catalytic process for efficiently producing HMF from sucrose was scrutinized using 1-methyl-3-octylimidazolium chloride ([MOIM]Cl) as a reaction solvent, and HCl and metal chlorides (CrCl2 and Zncl2) as a catalyst. The rate of sucrose hydrolysis was relatively much faster in the reactions with HCl than without it. The hydrolysis of sucrose to fructose and glucose was affected by its reaction time.
      The mixed solvent of 50% [MOIM]Cl and 50% sucrose solution with HCl was more effective in HMF synthesis than single solvent alone. The addition of ZnCl2 and CrCl2 increased HMF yields by approximately 1.2-1.8-fold and its higher yield was found in the latter. The highest yield (82.0±3.9 wt%) in HMF production was achieved in the reaction mixture containing 5 g [MOIM]Cl and 5 mL of 20% sucrose solution with 0.5M HCl plus CrCl2 at 30 min reaction time. However,0.3 M HCl was more effective for the HMF productivity than 0.5 M HCl.

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      참고문헌 (Reference)

      1 Y. Román-Leshkov, 447 : 982-, 2007

      2 A. S. Amarasekara, 100 : 5301-, 2009

      3 H.H. Szmant, 31 : 135-, 1981

      4 J. B. Binder, 131 : 1979-, 2009

      5 C. Lansalot-Matras, 4 : 517-, 2003

      6 C. Moreau, 11 : 237-, 2000

      7 C. Moreau, 253 : 165-, 2006

      8 Y. Su, 361 : 117-, 2009

      9 H. Zhao, 316 : 1597-, 2007

      10 Y. Román-Leshkov, 312 : 1933-, 2006

      1 Y. Román-Leshkov, 447 : 982-, 2007

      2 A. S. Amarasekara, 100 : 5301-, 2009

      3 H.H. Szmant, 31 : 135-, 1981

      4 J. B. Binder, 131 : 1979-, 2009

      5 C. Lansalot-Matras, 4 : 517-, 2003

      6 C. Moreau, 11 : 237-, 2000

      7 C. Moreau, 253 : 165-, 2006

      8 Y. Su, 361 : 117-, 2009

      9 H. Zhao, 316 : 1597-, 2007

      10 Y. Román-Leshkov, 312 : 1933-, 2006

      11 A. Corma, 107 : 2411-, 2007

      12 M. J. Antal, 199 (199): 1990

      13 G.W. Huber, 308 : 1446-, 2005

      14 E. L. Kunkes, 322 : 417-, 2008

      15 D.A. Fort, 9 : 63-, 2007

      16 J.G. Huddleston, 3 : 156-, 2001

      17 V. Kamavaram, 47 : 773-, 2008

      18 N.V. Plechkova, 37 : 123-, 2008

      19 R.C. Remsing, 112 : 11071-, 2008

      20 J. Lewkowski, 1 : 17-, 2001

      21 D. S. Pito, 100 : 4546-, 2009

      22 C. F. Kautz, 50 : 1022-, 1928

      23 G.W. Farr, 53 : 516-, 1974

      24 Y. Li, 33 : 1182-, 2009

      25 Shuai Xu, "Catalytic oxidation of 1,3-diisopropylbenzene using imidazolium ionic liquid as catalyst" 한국화학공학회 26 (26): 985-989, 2009

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      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2016-06-21 학술지명변경 한글명 : The Korean Journal of Chemical Engineering -> Korean Journal of Chemical Engineering
      외국어명 : The Korean Journal of Chemical Engineering -> Korean Journal of Chemical Engineering
      KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-09-27 학회명변경 영문명 : The Korean Institute Of Chemical Engineers -> The Korean Institute of Chemical Engineers KCI등재
      2007-09-03 학술지명변경 한글명 : The Korean Journal of Chemical Engineeri -> The Korean Journal of Chemical Engineering
      외국어명 : The Korean Journal of Chemical Engineeri -> The Korean Journal of Chemical Engineering
      KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.92 0.72 1.4
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.15 0.94 0.403 0.14
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