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<field name="value">Alonso Tristán, Cristina</field>
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<field name="value">González López, Juan Antonio</field>
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<field name="value">García de la Fuente, Isaías</field>
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<field name="value">Sanz, Luis Felipe</field>
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<field name="value">Cobos, José Carlos .</field>
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<field name="value">The liquid–liquid equilibrium (LLE) curves for 2-phenylethan-1-ol (2-phenylethanol, 2PhEtOH) + octane, + decane, + dodecane, + tetradecane or + 2,2,4-trimethylpentane have been determined by a method of turbidimetry using a laser scattering technique. Experimental results reveal that the systems are characterized by an upper critical solution temperature (UCST), which increases linearly with the number of C atoms of the n-alkane. In addition, the LLE curves have a rather horizontal top and become skewed to higher mole fractions of the n-alkane, when its size increases. For a given n-alkane, UCST decreases as follows: phenol > phenylmethanol > 2-PhEtOH, indicating that dipolar interactions decrease in the same sequence. This has been ascribed to a weakening in the same order of the proximity effects between the phenyl and OH groups of the aromatic alkanols. DISQUAC interaction parameters for OH/aliphatic and OH/aromatic contacts in the investigated systems are reported. Phenol, or phenylmethanol or 2-PhEtOH, + n-alkane mixtures only differ by the first dispersive Gibbs energy interaction parameter for the (OH/aliphatic) contact</field>
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<field name="value">Journal of Chemical and Engineering Data. 2013, V. 73, n. 2, p. 429–435</field>
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<field name="value">Liquid−Liquid Equilibria for 2‑Phenylethan-1-ol + Alkane Systems</field>
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