Organophosphorus acids lanthanide complexes

Both carboxylic (e.g., Versatic acid) and organophosphorus acids have been used commercially to extract the lanthanides. The extraction follows the formation of the metal-extractant complex [Eq. (11.21)] and so depends on the pH of the feed. 

The lanthanides form many compounds with organic ligands. Some of these compounds are water-soluble, others oil-soluble. Water-soluble compounds have been used extensively for rare-earth separation by ion exchange (qv), for example, complexes form with citric acid, ethylenediaminetetraacetic acid (EDTA), and hydroxyethylethylenediaminetriacetic acid (HEEDTA) (see Chelating AGENTS). The complex formation is pH-dependent. Oil-soluble compounds are used extensively in the industrial separation of rare earths by liquid—liquid extraction. The preferred extractants are carboxylic acids, organophosphorus acids and esters, and tetraalkylammonium salts. 

A method is being developed to transform actinide ions in the near surface environment to less soluble, less reactive, thermodynamically stable phosphate minerals phases through application of organophosphorus complexants. These complexants decompose slowly, releasing phosphate to promote the formation of stable phosphate mineral phases, particularly with the more soluble trivalent, pentavalent, and hexavalent actinide ions. The complexant of choice, myo-inositol(hexakisphosphoric acid) or phytic acid, is a natural product widely used as a nutritional supplement. We have determined that phytic acid decomposes slowly in the absence of microbiological effects, that crystalline phosphate minerals are formed as a consequence of its decomposition, and that the formation of actinide (lanthanide) phosphates reduces the solubility of trivalent and hexavalent metal ions under environmental conditions. 

Metal-complexation/SFE using carbon dioxide has been successfully demonstrated for removal of lanthanides, actinides and various other fission products from solids and liquids (8-18), Direct dissolution of recalcitrant uranium oxides using nitric acid and metal-complexing agents in supercritical fluid carbon dioxide has also been reported (79-25). In this paper we explored supercritical fluid extraction of sorbed plutonium and americium from soil using common organophosphorus and beta-diketone complexants. We also qualitatively characterize actinide sorption to various soil fractions via use of sequential chemical extraction techniques. 

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