1997
DOI: 10.1016/s0304-386x(96)00040-0
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Interfacial activity of bis(2-ethylhexyl) phosphoric acid in model liquid-liquid extraction systems

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Cited by 24 publications
(14 citation statements)
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“…However, in a previous work it was shown that the molecules of long chain alcohols such as isodecanol compete with HDEHP for adsorption at the liquid±liquid interfaces. 23 In fact, Table 3 shows that there is indeed competition, but that the HDEHP molecules remain present at the interface, even in the presence of isodecanol at high concentration. Logically, the same phenomenon should occur when PENRECO 1 170 ES is used as a diluent and the presence of HDEHP at the interface should be not very strongly depressed.…”
Section: Es and At The Aqueous/penrecomentioning
confidence: 95%
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“…However, in a previous work it was shown that the molecules of long chain alcohols such as isodecanol compete with HDEHP for adsorption at the liquid±liquid interfaces. 23 In fact, Table 3 shows that there is indeed competition, but that the HDEHP molecules remain present at the interface, even in the presence of isodecanol at high concentration. Logically, the same phenomenon should occur when PENRECO 1 170 ES is used as a diluent and the presence of HDEHP at the interface should be not very strongly depressed.…”
Section: Es and At The Aqueous/penrecomentioning
confidence: 95%
“…23,29,30 Trimeric species have also occasionally been reported. 31 It is also well known that long chain alcohols often used as phase modi®ers may solvate extractant molecules and, as a result, have the tendency to depress the selfassociation of the latter in organic phases.…”
Section: Es and At The Aqueous/penrecomentioning
confidence: 95%
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“…It is not clear whether this effect is to be attributed primarily to a decrease in the interfacial tension or to a fluidification of the extractant film; maybe both effects act simultaneously. In addition one can find alternative explanations in relation to specific effects of modifiers, which have been well documented (55,(60)(61)(62), such as their ability to give coassociation with extractant molecules or to coadsorb at the interface. If the addition of long-chain alcohols more or less inhibits the interfacial adsorption of extractant molecules, this will be expected to decrease the rate of metal extraction if the extractant is rejected in the organic phase, but the reverse may be true if it is rejected in the aqueous phase.…”
Section: Factors Influencing Distribution Coefficients and Favoring Imentioning
confidence: 97%
“…El agua, si está presente de alguna manera en la fase orgánica, puede actuar de la misma forma, disminuyendo la asociación de las oximas. Existe otro factor que debe ser considerado al tener en cuenta la posibilidad de asociación en las oximas, tanto el grupo hidroxilo como el oximino presentan una baja acidez e hidrofilidad; por esto, las oximas con estructuras como la representada en la figura 1, no forman micelas inversas ni microemulsiones como los derivados organofosforados ácidos o los ácidos sulfónicos (17). Como ya se ha mencionado, los derivados piridínicos (Fig.5) al no presentar en su estructura áto-mos de hidrógeno lábiles, no pueden dar lugar a asociaciones intramoleculares.…”
Section: Intraasociacion De Los Agentes De Extracciónunclassified