Published April 2008 | Version v1
Journal article

Solubility of perfumery and fragrance raw materials based on cyclohexane in 1-octanol under ambient and high pressures up to 900 MPa

  • 1. Physical Chemistry Division, Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw (Poland)

Description

The (solid + liquid) phase equilibria (SLE) of binary mixtures containing 1-octanol and fragrance raw materials based on cyclohexane were investigated. The systems {1-octanol (1) + cyclohexyl carboxylic acid (CCA), or cyclohexyl acetic acid (CAA), or cyclohexyl acetate (CA), or 2-cyclohexyl ethyl acetate (2CEA), or 2-cyclohexyl ethanol (2CE)(2)} have been measured by a dynamic method in wide range of temperatures from (220 to 320) K and ambient pressure. For all systems SLE diagrams were detected as eutectic mixtures with complete miscibility in the liquid phase. The experimental data were correlated by means of the Wilson and NRTL equations, utilizing parameters derived from the (solid + liquid) equilibrium. The root-mean-square deviations of the solubility temperatures for all calculated data are dependent upon the particular system and the particular equation used. Additionally, the SLE in binary mixture that contain {1-octanol (1) + CCA (2)} has been measured under very high pressures up to about 900 MPa at the temperature range from T = (303.15 to 353.15) K. The thermostatted apparatus for the measurements of transition pressures from the (liquid + solid) state was used. The freezing and melting temperatures at a constant composition increase monotonously with pressure. The high pressure experimental results obtained at isothermal conditions (p-x) were interpolated to more convenient T-x diagram. Data of the (pressure + temperature) composition relation at the high pressure (solid + liquid) phase equilibria was correlated by the polynomial based on the Yang model. The basic thermodynamic properties of pure substances viz. the melting point, enthalpy of fusion, enthalpy of solid-solid phase transition, and glass transition, have been determined by the differential scanning calorimetry (DSC)

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jct.2007.10.004

Additional details

Identifiers

DOI
10.1016/j.jct.2007.10.004;
PII
S0021-9614(07)00195-4;

Publishing Information

Journal Title
Journal of Chemical Thermodynamics
Journal Volume
40
Journal Issue
4
Journal Page Range
p. 710-717
ISSN
0021-9614
CODEN
JCTDAF

Optional Information

Copyright
Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.