Phase equilibria of phenolic compounds in water or ethanol

被引:31
作者
Cesari, Laetitia [1 ]
Namysl, Sylvain [1 ]
Canabady-Rochelle, Laetitia [1 ]
Mutelet, Fabrice [1 ]
机构
[1] Univ Lorraine, Ecole Natl Super Ind Chim, UMR CNRS 7274, Lab React & Genie Proc, 1 Rue Grandville, F-54000 Nancy, France
关键词
Phase equilibria; Phenolic compounds; NRTL; Water; Ethanol; LIQUID-LIQUID EQUILIBRIUM; BINARY-MIXTURES; AQUEOUS SOLUBILITIES; TERNARY-SYSTEMS; FAST PYROLYSIS; IONIC LIQUID; LIQUEFACTION; BIOMASS; LIGNIN; ACID;
D O I
10.1016/j.fluid.2017.09.008
中图分类号
O414.1 [热力学];
学科分类号
摘要
The mutual solubilities of water and eight phenolic compounds (i.e. phenol, guaiacol, syringol, pyrocatechol, o-, m-, p-cresol and vanillin) were investigated between 293.15 and 323.15K. The solubility of the phenolic compounds in water increases as follows: vanillin < syringol < guaiacol < p-cresol < m cresol < o-cresol < phenol < pyrocatechol. For the molecules presenting liquid-liquid equilibria, the solubility of water into the phenolic phase increases as follows: guaiacol < o-cresol < m-cresol < p cresol < syringol. The vapor-liquid equilibria of binary mixtures composed of ethanol and phenol or guaiacol or o-cresol were measured in a range of pressure from 0.09 bar to atmospheric pressure. Finally, the mixing enthalpies of the phenolic compounds with ethanol indicate that the reactions are exothermic. It was found that NRTL model is suitable for the representation of phase diagrams of systems containing phenolic compounds and water or ethanol. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 66
页数:9
相关论文
共 59 条
  • [1] Performance of an absorption heat transformer using new working binary systems composed of {ionic liquid and water}
    Abumandour, EI-Shaimaa
    Mutelet, Fabrice
    Alonso, Dominique
    [J]. APPLIED THERMAL ENGINEERING, 2016, 94 : 579 - 589
  • [2] Aqueous solubilities of phenol derivatives by conductivity measurements
    Achard, C
    Jaoui, M
    Schwing, M
    Rogalski, M
    [J]. JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1996, 41 (03) : 504 - 507
  • [3] Ab initio studies on the molecular conformation of lignin model compounds I.: Conformational preferences of the phenolic hydroxyl and methoxy groups in guaiacol
    Agache, C
    Popa, VI
    [J]. MONATSHEFTE FUR CHEMIE, 2006, 137 (01): : 55 - 68
  • [4] Separation of phenols from Eucalyptus wood tar
    Amen-Chen, C
    Pakdel, H
    Roy, C
    [J]. BIOMASS & BIOENERGY, 1997, 13 (1-2) : 25 - 37
  • [5] [Anonymous], ULLMANNS ENCY IND CH
  • [6] [Anonymous], 2009, C80 BROCH
  • [7] [Anonymous], 2010, C80 COMM
  • [8] The increased solubility of phenolic substances in water on addition of a third substance
    Bailey, CR
    [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1923, 123 : 2579 - 2590
  • [9] An overview of fast pyrolysis of biomass
    Bridgwater, AV
    Meier, D
    Radlein, D
    [J]. ORGANIC GEOCHEMISTRY, 1999, 30 (12) : 1479 - 1493
  • [10] Brusset H., 1972, CHEM INF, V3