• 제목/요약/키워드: Ethyl levulinate

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Chitosan으로부터 균일 산 촉매를 이용한 Ethyl Levulinate의 합성 (Synthesis of Ethyl levulinate from Chitosan Using Homogeneous Acid Catalyst)

  • 정귀택;김성구
    • Korean Chemical Engineering Research
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    • 제58권2호
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    • pp.266-272
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    • 2020
  • 본 연구에서는 갑각류의 껍질로부터 추출한 chitosan으로부터 황산을 촉매로 사용하여 가수분해 및 에스테르화 반응과 반응표면분석 실험계획법을 적용하여 화학 원료 및 연료로 사용 가능한 ethyl levulinate의 생산 가능성을 조사하였다. 반응물 중 수분함량의 영향을 조사한 결과, chitosan의 가수분해와 동시에 탈수반응과 ethyl levulinate로의 에스테르화와 반응은 5% 수분함량에서 가장 높았다. 반응표면분석 실험계획법을 이용하여 반응인자를 최적화한 결과, 200 ℃, 3.19% chitosan, 0.49M 황산 촉매, 5% 수분함량(95% 에탄올 용매), 그리고 58분의 반응조건에서 30.1%의 ethyl levulinate의 생성 수율을 얻었다. 또한, ethyl levulinate의 생성 수율은 반응의 가혹도가 증가할수록 증가하는 경향을 나타내었다. 이러한 결과는 chitosan이 화학 원료 및 연료의 생산에 사용될 수 있는 바이오매스로서의 잠재력이 있다고 판단된다.

Synthesis of Renewable Jet Fuel Precursors from C-C Bond Condensation of Furfural and Ethyl Levulinate in Water

  • Cai, Chiliu;Liu, Qiying;Tan, Jin;Wang, Tiejun;Zhang, Qi;Ma, Longlong
    • Korean Chemical Engineering Research
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    • 제54권4호
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    • pp.519-526
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    • 2016
  • Biomass derived jet fuel is proven as a potential alternative for the currently used fossil oriented energy. The efficient production of jet fuel precursor with special molecular structure is prerequisite in producing biomass derived jet fuel. We synthesized a new jet fuel precursor containing branched $C_{15}$ framework by aldol condensation of furfural (FA) and ethyl levulinate (EL), where the latter of two could be easily produced from lignocellulose by acid catalyzed processes. The highest yield of 56% for target jet fuel precursor could be obtained at the optimal reaction condition (molar ratio of FA/EL of 2, 323 K, 50 min) by using KOH as catalyst. The chemical structure of $C_{15}$ precursor was specified as (3E, 5E)-6-(furan-2-yl)-3-(furan-2-ylmethylene)-4-oxohex-5-enoic acid ($F_2E$). For stabilization, this yellowish solid precursor was hydrogenated at low temperature to obtain C=C bonds saturated product, and the chemical structure was proposed as 4-oxo-6-(tetrahydrofuran-2-yl)-3-(tetrahydrofuran-2-yl)-methyl hexanoic acid ($H-F_2E$). The successful synthesis of the new jet fuel precursors showed the significance that branched jet fuel could be potentially produced from biomass derived FA and EL via fewer steps.

A Convenient Allylation of 1,n-Dicarbonyl Compounds Using Organoindium Reagents

  • 이필호;동서문;이구연
    • Bulletin of the Korean Chemical Society
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    • 제22권12호
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    • pp.1380-1384
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    • 2001
  • The chemoselective reactions of 1,n-dicarbonyl compounds with allyl halides using indium metal were investigated. $\alpha-Ketoesters$ such as ethyl pyruvate, ethyl 3-methyl-2-oxobutyrate and ethyl benzoylformate reacted with a variety of allyl halides i n the presence of indium to afford hydroxy unsaturated carbonyl compounds in good to excellent yields in MeOH/HCl at $25^{\circ}C.$ For the allyl bromide, the presence of various substituents at the $\alpha$ or $\gamma$ position exhibited little effects on both the reaction rates and yields. Ethyl acetoacetate or ethyl levulinate was treated with allylindium reagent to give hydroxy unsaturated carbonyl compounds in good yield. These results mean that both reactivity and selectivity are independent of the distance between carbonyl groups. 2,3-Butanedione or 1-phenyl-1,2-propanedione reacted with allylindium to produce monoallylation product as major compound.

Conversion of Glucose and Xylose to 5-Hydroxymethyl furfural, Furfural, and Levulinic Acid Using Ethanol Organosolv Pretreatment under Various Conditions

  • Ki-Seob, GWAK;Chae-Hwi, YOON;Jong-Chan, KIM;Jong-Hwa, KIM;Young-Min, CHO;In-Gyu, CHOI
    • Journal of the Korean Wood Science and Technology
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    • 제50권6호
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    • pp.475-489
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    • 2022
  • The objective of this study was to understand the conversion characteristics of glucose and xylose using the major monosaccharide standards for lignocellulosic biomass. The acid-catalyzed organosolv pretreatment conducted using ethanol was significantly different from the acid-catalyzed process conducted in an aqueous medium. 5-hydroxymethylfurfural (5-HMF), levulinic acid and furfural were produced from glucose conversion. The maximum yield of 5-HMF was 5.5%, at 200℃, when 0.5% sulfuric acid was used. The maximum yield of levulinic acid was 21.5%, at 220℃, when 1.0% sulfuric acid was used. Furfural was produced from xylose conversion and under 0.5% sulfuric acid, furfural reached the maximum yield 48.5% at 210℃. Ethyl levulinate and methyl levulinate were also formed from the glucose standard following the esterification reaction conducted under conditions of the combined conversion method, which proceeded under both ethanol-rich and water-rich conditions.

Biorefinery 산업과 Furfural 생산 및 응용 분야 (Production of Furfural and its Application in Biorefinery)

  • 김승수
    • 공업화학
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    • 제27권1호
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    • pp.10-15
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    • 2016
  • 에너지 수요의 증가와 화석연료 고갈에 대비해 재생가능한 자원에 대한 관심이 높다. 목질계 바이오매스는 지속 및 재생 가능하며, 원유로부터 생산되는 화학물질을 대체할 수 있고, 바이오 기반의 화학물질과 바이오연료를 생산하는 원료물질로 인식되고 있다. 푸르푸랄은 푸란을 기반으로 하는 메틸퓨란, 터트라하이드로퓨판, 메틸테트라하이드로퓨란, 에틸테트라하이드로퓨릴 이써, 에틸 레부리네이트, 레불루닉산과 알칸 등 화학물질 및 용매 생산을 위한 천연 전구체이며, 바이오 화학물질과 바이오연료를 위한 재생 가능한 화학 플랫폼으로 잠재력을 가지고 있다. 본 논문에서는 바이오리파이너리 개념, 푸르푸랄의 생산과 응용분야에 대해 고찰을 하였다.