Analysis of cosolvent effect on supercritical carbon dioxide extraction for α-pinene and 1,8-cineole

被引:11
|
作者
Shimoyama, Yusuke [1 ]
Tokumoto, Hiroki [2 ]
Matsuno, Takumi [2 ]
Iwai, Yoshio [2 ]
机构
[1] Tokyo Inst Technol, Dept Chem Engn, Meguro Ku, Tokyo 1528550, Japan
[2] Kyushu Univ, Dept Chem Engn, Fac Engn, Nishi Ku, Fukuoka 8190395, Japan
来源
CHEMICAL ENGINEERING RESEARCH & DESIGN | 2010年 / 88卷 / 12A期
关键词
Extraction; Supercritical fluid; Cosolvent effect; Eucalyptus oil; VAPOR-LIQUID-EQUILIBRIA; ESSENTIAL OIL; PHASE-EQUILIBRIA; SOLUBILITY; ETHANOL; WATER; TEMPERATURES; MONOTERPENES;
D O I
10.1016/j.cherd.2010.04.009
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The solubilities of alpha-pinene and 1,8-cineole in supercritical carbon dioxide with and without cosolvent were measured by using a circulation type apparatus coupled with an on-line Fourier transform infrared (FT-IR) spectroscope at 323 K and 8.0 MPa. The cosolvents interested in this work were ethanol, water, acetone and hexane. The solubilities were measured under vapor-liquid two phases. The effects of cosolvents on the solubilities and selectivities of alpha-pinene and 1,8-cineole in supercritical CO2 were investigated. The selectivities at feed concentration of cosolvent of 0.056 mol L-1 were increased 1.23 times by ethanol and decreased 0.82 times by hexane. Peng-Robinson equation of state with a quadratic mixing rule was used for correlations of the solubilities for alpha-pinene and 1,8-cineole in supercritical CO2 with and without cosolvent. The correlated results reproduce the experimental data of cosolvent effects on the solubilities and selectivities of alpha-pinene and 1,8-cineole in supercritical CO2. (C) 2010 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1563 / 1568
页数:6
相关论文
共 50 条
  • [1] Catalytic isomerization of α-terpineol to 1,8-cineole in supercritical carbon dioxide
    Hong Y.
    Wang D.
    Li Z.
    Xu Y.
    Wang H.
    Su Y.
    Peng L.
    Li J.
    Huagong Xuebao/CIESC Journal, 2021, 72 (07): : 3680 - 3685
  • [2] Excess molar enthalpies for mixtures of supercritical carbon dioxide and 1,8-cineole
    Sanchez-Vicente, Yolanda
    Perez, Eduardo
    Cabanas, Albertina
    Renuncio, Juan A. R.
    Urieta, Jose S.
    Pando, Concepcion
    JOURNAL OF SUPERCRITICAL FLUIDS, 2007, 40 (03): : 331 - 335
  • [3] Mass transfer and hydrodynamic study of supercritical carbon dioxide extraction of 1,8-cineole from small cardamom seeds
    Paul, Kaninika
    Bhattacharjee, Paramita
    CHEMICAL ENGINEERING COMMUNICATIONS, 2018, 205 (08) : 1023 - 1033
  • [4] HYDROGENOLYSIS OF 1,8-CINEOLE
    HUGEL, HM
    JACKSON, WR
    KACHEL, CD
    RAE, ID
    AUSTRALIAN JOURNAL OF CHEMISTRY, 1977, 30 (06) : 1287 - 1292
  • [5] Phase behavior of the system lecithin-water -: The effects of addition of the hydrocarbon 1,8-cineole and supercritical carbon dioxide
    Francisco, JD
    Topgaard, D
    Sivik, B
    Bergenståhl, B
    JOURNAL OF SUPERCRITICAL FLUIDS, 2004, 31 (03): : 255 - 262
  • [6] Phase behavior of the monoolein-water system -: The effects of addition of the hydrocarbon 1,8-cineole and supercritical carbon dioxide
    Francisco, JD
    Topgaard, D
    Sivik, B
    Bergenståhl, B
    JOURNAL OF SUPERCRITICAL FLUIDS, 2004, 31 (03): : 263 - 271
  • [7] Mouse brain concentrations of -pinene, limonene, linalool, and 1,8-cineole following inhalation
    Satou, Tadaaki
    Hayakawa, Mako
    Kasuya, Hikaru
    Masuo, Yoshinori
    Koike, Kazuo
    FLAVOUR AND FRAGRANCE JOURNAL, 2017, 32 (01) : 36 - 39
  • [8] REARRANGEMENTS OF 1,8-CINEOLE DERIVATIVES
    BONDAVALLI, F
    CHIMICA & L INDUSTRIA, 1978, 60 (01): : 66 - 67
  • [9] Application of additives in 1,8-cineole purification
    Liu, Keguo
    Gu, Lili
    Hu, Huiguang
    Yang, Rong
    Tao, Jun
    ADVANCES IN CHEMICAL, MATERIAL AND METALLURGICAL ENGINEERING, PTS 1-5, 2013, 634-638 : 382 - 385
  • [10] PRODUCTS OF 1,8-CINEOLE OXIDATION BY A PSEUDOMONAD
    MACRAE, IC
    ALBERTS, V
    CARMAN, RM
    SHAW, IM
    AUSTRALIAN JOURNAL OF CHEMISTRY, 1979, 32 (04) : 917 - 922