Effect of temperature on the protonation of N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid in aqueous solutions: Potentiometric and calorimetric studies

Xingliang Li, Zhicheng Zhang, Francesco Endrizzi, Leigh R. Martin, Shunzhong Luo, Linfeng Rao

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

The TALSPEAK process (Trivalent Actinide Lanthanide Separations by Phosphorus-reagent Extraction from Aqueous Komplexes) has been demonstrated in several pilot-scale operations to be effective at separating trivalent actinides (An3+) from trivalent lanthanides (Ln3+). However, fundamental studies have revealed undesired aspects of TALSPEAK, such as the significant partitioning of Na+, lactic acid, and water into the organic phase, thermodynamically unpredictable pH dependence, and the slow extraction kinetics. In the modified TALSPEAK process, the combination of the aqueous holdback complexant HEDTA (N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid) with the extractant HEH[EHP] (2-ethyl(hexyl) phosphonic acid mono-2-ethylhexyl ester) in the organic phase has been found to exhibit a nearly flat pH dependence between 2.5 and 4.5 and more rapid phase transfer kinetics for the heavier lanthanides. To help understand the speciation of Ln3+ and An3+ in the modified TALSPEAK, systematic studies are underway on the thermodynamics of major reactions in the HEDTA system under conditions relevant to the process (e.g., higher temperatures). Thermodynamics of the protonation and complexation of HEDTA with Ln3+ were studied at variable temperatures. Equilibrium constants and enthalpies were determined by a combination of techniques including potentiometry and calorimetry. This paper presents the protonation constants of HEDTA at T = (25 to 70) °C. The potentiometric titrations have demonstrated that, stepwise, the first two protonation constants decrease and the third one slightly increases with the increase of temperature. This trend is in good agreement with the enthalpy of protonation directly determined by calorimetry. The results of NMR analysis further confirm that the first two protonation reactions occur on the diamine nitrogen atoms, while the third protonation reaction occurs on the oxygen of a carboxylate group. These data, in conjunction with the thermodynamic parameters of Ln3+/An3+ complexes with HEDTA at different temperatures, will help to predict the speciation and temperature-dependent behavior of Ln3+/An3+ in the modified TALSPEAK process.

Original languageEnglish
Pages (from-to)35-41
Number of pages7
JournalJournal of Chemical Thermodynamics
Volume85
DOIs
StatePublished - Jun 2015
Externally publishedYes

Funding

This work was supported by the Fuel Cycle Research and Development (FCR&D) Thermodynamics and Kinetics Program, Office of Nuclear Energy, the U.S. Department of Energy under Contract Number DE-AC02-05CH11231 at Lawrence Berkeley National Laboratory. The authors are thankful to Dr. Wayne Lukens for help with the NMR studies. L.R. Martin acknowledges the support from DOE NE FCR&D Thermodynamics and Kinetics program , under DOE Idaho Operations Office Contract DE-AC07-05ID14517 while preparing this manuscript.

FundersFunder number
DOE NE FCR&D Thermodynamics and Kinetics program
Fuel Cycle Research and Development
Kinetics Program
U.S. Department of EnergyDE-AC02-05CH11231, DE-AC07-05ID14517
Office of Nuclear Energy
Lawrence Berkeley National Laboratory

    Keywords

    • Actinide/lanthanide separations
    • N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid
    • Protonation
    • Temperature effect

    Fingerprint

    Dive into the research topics of 'Effect of temperature on the protonation of N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid in aqueous solutions: Potentiometric and calorimetric studies'. Together they form a unique fingerprint.

    Cite this