Abstract
Several N-alkylcarbonyl-substituted N-phenylhydroxylamines (R-PHAs) were synthesized for use in lanthanoids(III) extraction. They were N-octanoyl-, N-(3,5,5-trimethylhexanoyl)-, N-(4-butylcyclohexanoyl)-, N-(4-butylbenzoyl)-, N-(2-propylpentanoyl)-, and N-(2-hexyldecanoyl)-N-phenylhydroxylamines. The distribution ratio of a lanthanoid(III) ion between the carbon tetrachloride and aqueous phases was examined as functions of the pH and R-PHA concentration at 298 K and the ionic strength, 0.1 (NaNO3). Sodium tartrate (1×l0−2mol dm−3) was present in the aqueous phase. Lanthanoids(III) were extracted as a self-adducted chelate, ML3(HL)2, with all the R-PHAs used. The conditional extraction constants and the separation factors of lanthanoids(III) with R-PHAs were evaluated. Among the R-PHAs, N-(2-hexyldecanoyl)-N-phenylhydroxylamine was most promising for the separation of heavy lanthanoids(III). Appropriate branching at the α-position of the carbonyl group seemed to transmit the R-PHAs different chemical properties with respect to the straight chain R-PHAs.
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Haraguchi, K., Yamazaki, Y., Saitoh, T. et al. Solvent Extraction of Lanthanoids(III) with N-Alkylcarbonyl-Substituted N-Phenylhydroxylamines. ANAL. SCI. 6, 877–882 (1990). https://doi.org/10.2116/analsci.6.877
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DOI: https://doi.org/10.2116/analsci.6.877