Synthesis and Screening of t-Bu-CyMe4-BTBP, and Comparison with CyMe4-BTBP
Journal article, 2014
The effect of adding a t-butyl group to the core molecule of CyMe4-BTBP, with the aim of improving solubility in organic diluents, has been studied with regard to the extraction of Am(III) and Eu(III) from HNO3. Synthesis of t-Bu-CyMe4-BTBP is described in detail. Metal nitrates are extracted from nitric acid in the form of 1:2 complexes, M(NO3)(3)(BTBP)(2). Whether in 1-octanol, kerosene, or cyclohexanone diluents, t-Bu-CyMe4-BTBP extracts with larger distribution ratios but with slower kinetics than CyMe4-BTBP. The general trends previously observed for CyMe4-BTBP regarding the diluent and modifier influence were also found for t-Bu-CyMe4-BTBP.
solubility
DONOR
ACTINIDES
AMERICIUM(III)
solvent extraction
BTBP
LIGANDS
SOLVENT
EXTRACTION
QUADRIDENTATE
C5-BTBP
kinetics
LANTHANIDES
actinides
lanthanides
ACTINIDE(III)/LANTHANIDE(III) SEPARATION
RADIOLYTIC STABILITY
side group
Author
Teodora Retegan Vollmer
Chalmers, Chemical and Biological Engineering, Nuclear Chemistry
M. Drew
University of Reading
Christian Ekberg
Chalmers, Chemical and Biological Engineering, Nuclear Chemistry
Elin Löfström Engdahl
Chalmers, Chemical and Biological Engineering, Nuclear Chemistry
M. J. Hudson
University of Reading
Anna Fermvik
Chalmers, Chemical and Biological Engineering, Nuclear Chemistry
Mark Foreman
Chalmers, Chemical and Biological Engineering, Nuclear Chemistry
G. Modolo
Forschungszentrum Jülich
A. Geist
Karlsruhe Institute of Technology (KIT)
Solvent Extraction and Ion Exchange
0736-6299 (ISSN) 1532-2262 (eISSN)
Vol. 32 7 720-736Subject Categories
Analytical Chemistry
DOI
10.1080/07366299.2014.940767