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Mesoporous manganese oxide for the degradation of organophosphates pesticides

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    0469309 - ÚACH 2017 RIV US eng J - Článek v odborném periodiku
    Šťastný, Martin - Štengl, Václav - Henych, Jiří - Tolasz, Jakub - Vomáčka, Petr - Ederer, J.
    Mesoporous manganese oxide for the degradation of organophosphates pesticides.
    Journal of Materials Science. Roč. 51, č. 5 (2016), s. 2634-2642. ISSN 0022-2461. E-ISSN 1573-4803
    Grant ostatní: NATO(US) SPS984599
    Program: Science for Peace and Security
    Institucionální podpora: RVO:61388980
    Klíčová slova: transmission electron microscopy (TEM) * X-ray diffraction * electron microscopy * chemical synthesis * layered compounds * interfaces * Inorganic compounds
    Kód oboru RIV: CA - Anorganická chemie
    Impakt faktor: 2.599, rok: 2016

    Manganese(IV) oxide used for degradation of toxic organophosphorus compounds was prepared by homogeneous hydrolysis of potassium permanganate (KMnO4) with 2-chloroacetamide. The prepared sample was characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, and nitrogen physisorption. The degradation efficiency was determined with parathion methyl (PM) as representative of organophosphate pesticides using high-performance liquid chromatography. For a comparison, the commercially obtained product and the two synthesized manganese(IV) oxides prepared by direct reaction of manganese(II) sulfate (MnSO4 center dot H2O) and potassium permanganate (KMnO4) and potassium permanganate (KMnO4) with urea in aqueous solution were tested. The sample prepared by homogeneous hydrolysis of KMnO4 with 2-chloroacetamide showed the highest degradation efficacy. The reaction half-time in non-polar organic solvent (n-heptane) was around 0.9 min with the degradation efficiency of about 90 % within 2 h. It was shown that comparative samples of manganese(IV) oxides were variously effective in decomposition of PM by cleavage of the P-O-aryl bond in the pesticide molecule. The degradation mechanism for PM on the MnO2 surfaces was proposed.
    Trvalý link: http://hdl.handle.net/11104/0267112

     
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