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Clotilde Gaillard

Researcher at University of Lyon

Publications -  43
Citations -  1952

Clotilde Gaillard is an academic researcher from University of Lyon. The author has contributed to research in topics: Ionic liquid & Uranyl. The author has an hindex of 23, co-authored 42 publications receiving 1788 citations. Previous affiliations of Clotilde Gaillard include Centre national de la recherche scientifique & Russian Academy of Sciences.

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Liquid–liquid extraction of actinides, lanthanides, and fission products by use of ionic liquids: from discovery to understanding

TL;DR: Liquid–liquid extraction of actinides and lanthanides by use of ionic liquids is reviewed, considering, first, phenomenological aspects, then looking more deeply at the various mechanisms.
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Task-specific ionic liquids bearing 2-hydroxybenzylamine units: synthesis and americium-extraction studies.

TL;DR: It is demonstrated that, whether pure or diluted, TSIL is able to extract americium ions, and recovery of americium from the IL phase into a receiving phase can be achieved under acidic conditions.
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Stability of divalent europium in an ionic liquid: Spectroscopic investigations in 1-methyl-3-butylimidazolium hexafluorophosphate

TL;DR: Results from small angle X-ray scattering indicate that the pure solvent exhibits a local organization in relation to 1-methyl-3-butylimidazolium hexafluorophosphate ionic liquid.
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Solvent extraction of U(VI) by task specific ionic liquids bearing phosphoryl groups

TL;DR: In this article, a novel class of hydrophobic ionic liquids based on quaternary ammonium cation and bearing phosphoryl groups was synthesized and the preliminary results of U(VI) extraction from aqueous solution into the ionic liquid were presented.
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Understanding the Extraction Mechanism in Ionic Liquids: UO2 2+/HNO3/TBP/C4-mimTf2N as a Case Study

TL;DR: In this paper, the authors proposed a chemical model to describe the data through a fit of uranyl distribution ratios, while some other suggestions are unable to do so, and proposed to proceed via cation exchange at low initial acidities and via anion exchange at high HNO3 concentrations.