The mutual solubilities and related liquid-liquid equilibria of C 10 hydrocarbons with water are exhaustively and critically reviewed. Reports of experimental determination of solubility in 20 chemically distinct binary systems that appeared in the primary literature prior to end of 2002 are compiled. For ten systems sufficient data are available to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units. In addition to the standard evaluation criteria used throughout the Solubility Data Series, a new method based on the evaluation of the all experimental data for a given homologous series of aliphatic and aromatic hydrocarbons was used.

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The mutual solubilities and related liquid–liquid equilibria of C10 hydrocarbons with water are exhaustively and critically reviewed. Reports of experimental determination of solubility in 20 chemically distinct binary systems that appeared in the primary literature prior to end of 2002 are compiled. For ten systems sufficient data are available to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units. In addition to the standard evaluation criteria used throughout the Solubility Data Series, a new method based on the evaluation of the all experimental data for a given homologous series of aliphatic and aromatic hydrocarbons was used.

The mutual solubilities and related liquid–liquid equilibria of C13–C36 hydrocarbons with water are exhaustively and critically reviewed. Reports of experimental determination of solubility in 56 chemically distinct binary systems that appeared in the primary literature prior to end of 2002 are compiled. For 17 systems sufficient data are available to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units. In addition to the standard evaluation criteria used throughout the Solubility Data Series, a new method based on the evaluation of all the experimental data for a given homologous series of aliphatic and aromatic hydrocarbons was used.

long axis of the base, the measurements are relatively insensitive to base roll.9 Therefore, while the base tilt is close to 0°, the base inclination could be different if the base pairs are propellered or if there is significant base roll. It will now be interesting to see how DNA length and other experimental parameters affect the properties of the DNA liquid crystals.