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Aggregation of P,P{prime}-di(2-ethylhexyl) methanediphosphonic acid and its Fe(III) complexes

Journal Article · · Solvent Extraction and Ion Exchange
; ;  [1];  [2]
  1. Argonne National Lab., IL (United States)
  2. Loyola Univ., Chicago, IL (United States). Dept. of Chemistry

The aggregation of P,P{prime}-di(2-ethylhexyl) methanediphosphonic acid, H{sub 2}DEH[MDP], dissolved in deuterated toluene has been investigated by small angle neutron scattering (SANS). The title compound was shown to exist in solution as a dimer under all conditions. Dimer formation is independent of the acidity of the aqueous solution with which the organic solution is pre-equilibrated. Solutions of H{sub 2}DEH[MDP] containing increasing amounts of Fe(III) extracted from aqueous solutions in the acidity range from 0.1 to 5 M were also investigated. The SANS results confirm the tendency of H{sub 2}DEH[MDP]-Fe(III) species in aromatic diluents to form rod-like aggregates characterized by a constant cross section and a length which increases with increasing amounts of metal in the organic phase. Particle growth is independent of the acidity of the aqueous solutions from which the metal is extracted. These results are important for understanding the chemistry underlying the solvent extraction behavior of H{sub 2} DEH[MDP] and its practical application in separation procedures.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
346979
Journal Information:
Solvent Extraction and Ion Exchange, Journal Name: Solvent Extraction and Ion Exchange Journal Issue: 5 Vol. 16; ISSN 0736-6299; ISSN SEIEDB
Country of Publication:
United States
Language:
English

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