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Voltammetric determination of ethylvanillin and methylvanillin sum at carbon paste electrode modified by sodium dodecyl sulfate in selected foodstuffs

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F18%3A39912545" target="_blank" >RIV/00216275:25310/18:39912545 - isvavai.cz</a>

  • Result on the web

    <a href="https://link.springer.com/content/pdf/10.1007%2Fs00706-018-2266-z.pdf" target="_blank" >https://link.springer.com/content/pdf/10.1007%2Fs00706-018-2266-z.pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00706-018-2266-z" target="_blank" >10.1007/s00706-018-2266-z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Voltammetric determination of ethylvanillin and methylvanillin sum at carbon paste electrode modified by sodium dodecyl sulfate in selected foodstuffs

  • Original language description

    A new voltammetric method without using high cost and health risk nanomaterials has been developed for quantitative determination of ethylvanillin and methylvanillin sum, compounds that are used as food additives. The method is based on direct electrochemical oxidation of these biologically active compounds using square wave voltammetry at carbon paste electrode with surface modified by sodium dodecyl sulfate (SDS/CPE) performed in 0.1 M phosphate pH 6.0 buffer. Working conditions such as pH value of supporting electrolyte, type of surfactant, accumulation time of surfactant, and parameters of square wave voltammetry were optimized. In comparison with bare carbon paste electrode, excellent reproducibility characterized by a relative standard deviation of approximately 0.3% was obtained at the SDS/CPE. Linear range from 1.0 x 10(-6) to 2.0 x 10(-5) M, limits of quantification 9.8 x 10(-8) M and detection 2.9 x 10(-8) M were found at pulse amplitude 70 mV and frequency 50 Hz selected as optimum for ethylvanillin quantification. For methylvanillin, a linear range from 7.0 x 10(-8) to 2.0 x 10(-5) M and limits of quantification 7.0 x 10(-8) M and detection 2.0 x 10(-8) M were also determined. The procedure was validated using standard high-performance liquid chromatography method in the analysis of selected complex foodstuffs such as commercial baking sugar, biscuits, and an alcoholic drink. The results showed that a direct voltammetric approach is economically advantageous and reliable for the determination of ethyl- and methylvanillin, which is fully comparable to the reverse phase HPLC used as the ISO standard.

  • 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

    10406 - Analytical chemistry

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Monatshefte fur Chemie

  • ISSN

    0026-9247

  • e-ISSN

  • Volume of the periodical

    149

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    9

  • Pages from-to

    1945-1953

  • UT code for WoS article

    000446500100002

  • EID of the result in the Scopus database

    2-s2.0-85052953554