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<dc:title>Liquid-liquid equilibria for the systems 2-ethoxy-benzenamine + CH3(CH2) CH3 (n = 6,8,10,12) and 4-ethoxy-benzenamine + CH3(CH2) CH3 (n = 5,6)</dc:title>
<dc:creator>Alonso Tristán, Cristina</dc:creator>
<dc:creator>González López, Juan Antonio</dc:creator>
<dc:creator>García de la Fuente, Isaías</dc:creator>
<dc:creator>Sanz, Luis Felipe</dc:creator>
<dc:creator>Cobos, José Carlos .</dc:creator>
<dc:subject>LLE</dc:subject>
<dc:subject>Phenetidine</dc:subject>
<dc:subject>Alkane</dc:subject>
<dc:subject>Substituted anilines or phenols</dc:subject>
<dc:subject>Intramolecular effects</dc:subject>
<dc:description>Liquid-liquid equilibria (LLE) phase diagrams have been determined for the systems: 2-ethoxy-benzenamine + octane, or +decane, or +dodecane, or +tetradecane and for 4-ethoxy-benzenamine + heptane, or +octane. The experimental method used is based on the observation, by mean of a laser scattering technique, of the turbidity produced on cooling when a second phase takes place. All the mixtures show an upper critical solution temperature, which increases with the alkane size. Dipolar interactions between like molecules become stronger in the sequence: 2-ethoxy-benzenamine &lt; aniline &lt; 4-ethoxy-benzenamine. Data available in the literature suggest that this relative variation is also valid for alkane mixtures containing other substituted anilines or phenols, characterized by having a second polar group. The dependence of the UCST values with the molecular structure of the polar aromatic compound involved is shortly discussed in terms of intramolecular and steric effects.</dc:description>
<dc:date>2021-05-17T10:28:58Z</dc:date>
<dc:date>2021-05-17T10:28:58Z</dc:date>
<dc:date>2019-01</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>0167-7322</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/5767</dc:identifier>
<dc:identifier>10.1016/j.molliq.2018.10.135</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Journal of Molecular Liquids. 2019, V. 274, p. 534-539</dc:relation>
<dc:relation>https://doi.org/10.1016/j.molliq.2018.10.135</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>Elsevier</dc:publisher>
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