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
  • [41] Rogogic M, 2012, CHEM BIOCHEM ENG Q, V26, P155
  • [42] Schuster F., 1924, MONATSH CHEM, V45, P425
  • [43] CATALYTIC UPGRADING OF BIOMASS-DERIVED OILS TO TRANSPORTATION FUELS AND CHEMICALS
    SHARMA, RK
    BAKHSHI, NN
    [J]. CANADIAN JOURNAL OF CHEMICAL ENGINEERING, 1991, 69 (05) : 1071 - 1081
  • [44] On guaiacol solutions I. The electrical conductivity of sodium and potassium guaiacolates in guaiacol
    Shedlovsky, T
    Uhlig, HH
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1934, 17 (04) : 549 - 561
  • [45] The solubility of the nitrophenols and other isomeric disubstitution products of benzene.
    Sidgwick, NV
    Spurrell, WJ
    Davies, TE
    [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1915, 107 : 1202 - 1213
  • [46] Asymmetric Framework for Predicting Liquid-Liquid Equilibrium of Ionic Liquid-Mixed-Solvent Systems. 2. Prediction of Ternary Systems
    Simoni, Luke D.
    Chapeaux, Alexandre
    Brennecke, Joan F.
    Stadtherr, Mark A.
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2009, 48 (15) : 7257 - 7265
  • [47] Hydrothermal conversion of lignin to substituted phenols and aromatic ethers
    Singh, Rawel
    Prakash, Aditya
    Dhiman, Shashi Kumar
    Balagurumurthy, Bhavya
    Arora, Ajay K.
    Puri, S. K.
    Bhaskar, Thallada
    [J]. BIORESOURCE TECHNOLOGY, 2014, 165 : 319 - 322
  • [48] AQUEOUS SOLUBILITY OF CHLOROGUAIACOLS
    TAM, D
    VARHANICKOVA, D
    SHIU, WY
    MACKAY, D
    [J]. JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1994, 39 (01) : 83 - 86
  • [49] Terres E., 1955, Brennst. Chem, V36, P272
  • [50] Hydrocracking of solvolysis lignin in a batch reactor
    Thring, RW
    Breau, J
    [J]. FUEL, 1996, 75 (07) : 795 - 800