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Separation of the Minor Actinides Americium(III) and Curium(III) by Hydrophobic and Hydrophilic BTPhen Ligands: Exploiting Differences in their Rates of Extraction and Effective Separations at Equilibrium

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68407700%3A21340%2F18%3A00321447" target="_blank" >RIV/68407700:21340/18:00321447 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1080/07366299.2018.1429358" target="_blank" >http://dx.doi.org/10.1080/07366299.2018.1429358</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/07366299.2018.1429358" target="_blank" >10.1080/07366299.2018.1429358</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Separation of the Minor Actinides Americium(III) and Curium(III) by Hydrophobic and Hydrophilic BTPhen Ligands: Exploiting Differences in their Rates of Extraction and Effective Separations at Equilibrium

  • Original language description

    The complexation and extraction of the adjacent minor actinides Am(III) and Cm(III) by both hydrophobic and hydrophilic pre-organized 2,9-bis(1,2,4-triazin-3-yl)-1,10-phenanthroline (BTPhen) ligands has been studied in detail. It has been shown that Am(III) is extracted more rapidly than Cm(III) by the hydrophobic CyMe4-BTPhen ligand into different organic diluents under non-equilibrium extraction conditions, leading to separation factors for Am over Cm (SFAm/Cm) as high as 7.9. Furthermore, the selectivity for Am(III) over Cm(III) can be tuned through careful choice of the extraction conditions (organic diluent, contact time, mixing speed, ligand concentration). This `kinetic’ effect is attributed to the higher presumed kinetic lability of the Am(III) aqua complex towards ligand substitution. A dependence of the Am(III)/Cm(III) selectivity on the structure of the alkyl groups attached to the triazine rings is also observed, and BTPhens bearing linear alkyl groups are less able to discriminate between Am(III) and Cm(III) than CyMe4-BTPhen. Under equilibrium extraction conditions, hydrophilic tetrasulfonated BTPhen ligands complex selectively Am(III) over Cm(III) and prevent the extraction of Am(III) from nitric acid by the hydrophobic O-donor ligand N,N,N’,N’-tetraoctyldiglycolamide (TODGA), giving separation factors for Cm(III) over Am(III) (SFCm/Am) of up to 4.6. These results further underline the utility of the BTPhen ligands for the challenging separation of the chemically similar minor actinides Am(III) and Cm(III).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10400 - Chemical sciences

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Solvent Extraction and Ion Exchange

  • ISSN

    0736-6299

  • e-ISSN

    1532-2262

  • Volume of the periodical

    36

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    21

  • Pages from-to

    115-135

  • UT code for WoS article

    000430081400001

  • EID of the result in the Scopus database

    2-s2.0-85040996866