Complexation and back extraction of various metals by water-soluble diglycolamide.

Water-soluble ligands, N,N,N',N'-tetramethyldiglycolamide (TMDGA), N,N,N',N'-tetraethyldiglycolamide (TEDGA), N,N,N',N'-tetrapropyldiglycolamide (TPDGA) and N,N-dipropyldiglycolamic acid (DPDGAc) were prepared and their abilities to complex with and to back-extract the metal cations were investigated. These results indicate that the DGA series and DPDGAc have a stronger complexing ability with Am(III) and Pu(IV) than comparable carboxylic and aminopolycarboxylic acids. Among these ligands, the trend of the strength of their complexing ability is TPDGA approximately TEDGA > TMDGA approximately DPDGAc. TPDGA has significant loss to the extraction solvent due to its high hydrophobicity. It is evident from the present work that TEDGA is the best reagent for the reverse-extraction of not only An(III), (IV) but also Ca(II), Sc(III), Y(III), Zr(IV), La(III), Hf(IV), and Bi(III).

Thermodynamics and the structural aspects of the ternary complexes of Am(III), Cm(III) and Eu(III) with Ox and EDTA + Ox.

The stability constants and the associated thermodynamic parameters of formation of the binary and the ternary complexes of Am(3+), Cm(3+) and Eu(3+) were determined by a solvent extraction to measure the variation in the distribution coefficient with temperature (0-60 degrees C) for aqueous solutions of I = 6.60 m (NaClO(4)). The formation of ternary complexes is favored by both the enthalpy (exothermic) and the entropy (endothermic) values. (13) C NMR, TRLFS and EXAFS spectral data was used to study the coordination modes of the ternary complexes. In the formation of the complex M(EDTA)(Ox)(3-), the EDTA retained all its coordination sites with Ox binding via two carboxylates and with one water of hydration remaining attached to the M(3+). In the complex M(EDTA)(Ox)(2)(5-), one carboxylate, either from EDTA or Ox, is not bounded to M(3+) and there were no water of hydration attached to these cations.

Uranyl coordination environment in hydrophobic ionic liquids: an in situ investigation.

Different inner-sphere coordination environments are observed for the uranyl nitrate complexes formed with octyl-phenyl-N,N-diisobutylcarbamoylmethylphosphine oxide and tributyl phosphate in dodecane and in the hydrophobic ionic liquids (ILs) [C(4)mim][PF(6)] and [C(8)mim][N(SO(2)CF(3))(2)]. Qualitative differences in the coordination environment of the extracted uranyl species are implied by changes in peak intensity patterns and locations for uranyl UV-visible spectral bands when the solvent is changed. EXAFS data for uranyl complexes in dodecane solutions is consistent with hexagonal bipyramidal coordination and the existence of UO(2)(NO(3))(2)(CMPO)(2). In contrast, the complexes formed when uranyl is transferred from aqueous nitric acid solutions into the ILs exhibit an average equatorial coordination number of approximately 4.5. Liquid/liquid extraction results for uranyl in both ILs indicate a net stoichiometry of UO(2)(NO(3))(CMPO)(+). The concentration of the IL cation in the aqueous phase increases in proportion to the amount of UO(2)(NO(3))(CMPO)(+) in the IL phase, supporting a predominantly cation exchange mechanism for partitioning in the IL systems.