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Cerium oxide for the destruction of chemical warfare agents: A comparison of synthetic routes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F16%3A00458193" target="_blank" >RIV/61388980:_____/16:00458193 - isvavai.cz</a>

  • Alternative codes found

    RIV/44555601:13520/16:43886868 RIV/44555601:13440/16:43886868

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jhazmat.2015.10.069" target="_blank" >http://dx.doi.org/10.1016/j.jhazmat.2015.10.069</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jhazmat.2015.10.069" target="_blank" >10.1016/j.jhazmat.2015.10.069</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Cerium oxide for the destruction of chemical warfare agents: A comparison of synthetic routes

  • Original language description

    Four different synthetic routes were used to prepare active forms of cerium oxide that are capable of destroying toxic organophosphates: a sol-gel process (via a citrate precursor), homogeneous hydrolysis and a precipitation/calcination procedure (via carbonate and oxalate precursors). The samples prepared via homogeneous hydrolysis with urea and the samples prepared via precipitation with ammonium bicarbonate (with subsequent calcination at 500 degrees C in both cases) exhibited the highest degradation efficiencies towards the extremely dangerous nerve agents soman (O-pinacolyl methylphosphonofluoridate) and VX (O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothioate) and the organophosphate pesticide parathion methyl. These samples were able to destroy more than 90% of the toxic compounds in less than 10 min. The high degradation efficiency of cerium oxide is related to its complex surface chemistry (presence of surface -OH groups and surface non-stoichiometry) and to its nanocrystalline nature, which promotes the formation of crystal defects on which the decomposition of organophosphates proceeds through a nucleophilic substitution mechanism that is not dissimilar to the mechanism of enzymatic hydrolysis of organic phosphates by phosphotriesterase.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CA - Inorganic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Hazardous Materials

  • ISSN

    0304-3894

  • e-ISSN

  • Volume of the periodical

    304

  • Issue of the periodical within the volume

    MAR

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    259-268

  • UT code for WoS article

    000367699200029

  • EID of the result in the Scopus database

    2-s2.0-84946606173