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Voltammetric Determination of Nitronaphthalenes at a Silver Solid Amalgam Electrode

  1. 1.
    SYSNO ASEP0330470
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleVoltammetric Determination of Nitronaphthalenes at a Silver Solid Amalgam Electrode
    TitleVoltametrické stanovení nitronaftalenů na stříbrné pevné analgámové elektrodě
    Author(s) Pecková, K. (CZ)
    Barek, J. (CZ)
    Navrátil, Tomáš (UFCH-W) RID, ORCID
    Josypčuk, Bohdan (UFCH-W) RID, SAI, ORCID
    Zima, J. (CZ)
    Source TitleAnalytical Letters. - : Taylor & Francis - ISSN 0003-2719
    Roč. 42, č. 15 (2009), s. 2339-2363
    Number of pages25 s.
    Languageeng - English
    CountryUS - United States
    Keywordscyclic voltammetry ; differential pulse voltammetry ; elimination voltammetry with linear scan ; silver amalgam electrode
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGA203/07/1195 GA ČR - Czech Science Foundation (CSF)
    IAA400400806 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    LC06035 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000270544700001
    DOI10.1080/00032710903142442
    AnnotationElectrodes based on amalgam materials were re-introduced in electroanalytical chemistry in the year 2000, partially as reaction to unsubstantiated public fears of liquid mercury. In this publication, the voltammetric behavior of 1-nitronaphthalene and 2-nitronaphthalene was investigated at a mercury meniscus-modified silver solid amalgam electrode. The reduction mechanism in mixed neutral buffer-methanol medium includes the four-electron reduction to hydroxylaminoderivative followed by a two-electron reduction to the amine in acidic medium, similarly to mercury electrodes. In alkaline media, both compounds show the splitting of the main four-electron reduction peak typical for mercury electrodes in two new ones, the first one corresponding to a one electron reduction of the nitroderivative to the nitro radical anion, which was confirmed by microcoulometry.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2010
Number of the records: 1  

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