Development of bifunctional anion-exchange resins with improved selectivity and sorptive kinetics for pertechnetate: Batch-equilibrium experiments

Peter V. Bonnesen, Gilbert M. Brown, Spiro D. Alexandratos, Laurie Bates Bavoux, Derek J. Presley, Vijay Patel, Robert Ober, Bruce A. Moyer

Research output: Contribution to journalArticlepeer-review

128 Scopus citations

Abstract

A novel class of strong-base anion-exchange resins, bearing two different types of exchange sites, is described. These bifunctional resins have anion-exchange sites composed of two separate and differently sized trialkylammonium groups. In pertechnetate (TcO4-) uptake experiments from a solution matrix containing anions commonly encountered in groundwater, bifunctional resins containing exchange sites derived from tri-n-hexylamine in combination with either triethylamine, tri-n-propylamine, or tri-n-butylamine were shown to possess superior 24-h distribution ratios (K(d)) for pertechnetate over all monofunctional anion-exchange resins (derived from a single trialkylamine) examined. For example, although monofunctional resins containing a tri-n-hexylammonium exchange site possessed excellent selectivity for pertechnetate over other anions, the exchange kinetics were poor. The superior performance of these resins can be attributed to the combination of a large trialkylammonium site for enhanced selectivity for large anions and a smaller trialkylammonium site for the retention of good exchange kinetics.

Original languageEnglish
Pages (from-to)3761-3766
Number of pages6
JournalEnvironmental Science and Technology
Volume34
Issue number17
DOIs
StatePublished - Sep 1 2000

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