<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-30T08:59:42Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/5767" metadataPrefix="etdms">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/5767</identifier><datestamp>2024-11-05T10:56:27Z</datestamp><setSpec>com_10259_4393</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_4394</setSpec></header><metadata><thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.0/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.0/ http://www.ndltd.org/standards/metadata/etdms/1.0/etdms.xsd">
<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)</title>
<creator>Alonso Tristán, Cristina</creator>
<creator>González López, Juan Antonio</creator>
<creator>García de la Fuente, Isaías</creator>
<creator>Sanz, Luis Felipe</creator>
<creator>Cobos, José Carlos .</creator>
<subject>LLE</subject>
<subject>Phenetidine</subject>
<subject>Alkane</subject>
<subject>Substituted anilines or phenols</subject>
<subject>Intramolecular effects</subject>
<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.</description>
<date>2021-05-17</date>
<date>2021-05-17</date>
<date>2019-01</date>
<type>info:eu-repo/semantics/article</type>
<identifier>0167-7322</identifier>
<identifier>http://hdl.handle.net/10259/5767</identifier>
<identifier>10.1016/j.molliq.2018.10.135</identifier>
<language>eng</language>
<relation>Journal of Molecular Liquids. 2019, V. 274, p. 534-539</relation>
<relation>https://doi.org/10.1016/j.molliq.2018.10.135</relation>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</rights>
<publisher>Elsevier</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>