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Determination of glyphosate in water samples with the combination of cation-exchange chromatography and capillary electrophoresis

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
An analytical method for determination of pesticide Glyphosate in water as a combination of cation-exchange chromatography and capillary electrophoresis is presented. Pure water was spiked with Glyphosate at concentrations 0.1, 0.25, 0.5 and 1 mM and percolated through a strong cation-exchange column packed with Dowex 50WX4-400 resin in its H+ form. The extract was further analyzed by capillary electrophoresis in indirect detection mode. The calibration curve for the pesticide in the range 0.1–2.5 mM was linear and with high degree of reproducibility. The obtained recoveries for all the studied concentrations amount 85%. Afterwards, the possibility to determine Glyphosate at the concentration 0.001mM (0.17 µg/ml) was checked by percolation of 100 ml of water sample through a column. The calculated recovery was 97.7%
Rocznik
Tom
Strony
56--63
Opis fizyczny
Bibliogr. 12 poz., rys., tab.
Twórcy
autor
  • Institute of Chemistry, University of Opole, Oleska 48, 45-052 Opole, Poland
autor
  • Institute of Chemistry, University of Opole, Oleska 48, 45-052 Opole, Poland
autor
  • Institute of Chemistry, University of Opole, Oleska 48, 45-052 Opole, Poland
Bibliografia
  • [1] US Environmental Protection Agency, National Pesticide Survey. Phase I Report PB-91-125765, National Technical Information Service, Springfield, VA, 1990
  • [2] US Environmental Protection Agency, National Pesticide Survey of Drinking Water Wells. Phase II Report EPA 570/9-91-020, National Technical Information Service, Springfield, VA, 1992
  • [3] Directive 76/464/EEC. Pollution Caused by Certain Dangerous Substances Discharged into Aquatic Environment of the Community (Black List). Off. J. Eur. Commun. L129/7 (1976)
  • [4] C.D. Stalkas, C.N. Konidari, J. Chromatogr. A., 2001, 907, 1-19.
  • [5] A. Royer, S. Beguin, J.C. Tabet, S.S. Hulot, M.A. Reding, P.Y. Anal. Chem., 2000, 72, 3826-3832.
  • [6] M. Tsuji, Y. Akiyama, M. Yano, Anal. Sci., 1997, 13, 283.
  • [7] C.D. Stalikas, G.A. Pilidis, M.I. Karayannis, Chromatographia., 2000, 51, 741-746.
  • [8] E.A. Lee, L.R. Zimmerman, B.S. Bhullar, E.M. Thurman, Anal. Chem., 2002, 74, 4937-4943.
  • [9] E. Mallat, D. Barceló, J. Chromatogr. A., 1998, 823, 129-136.
  • [10] M.G. Cikalo, D.M. Goodall, W. Matthews, J. Chromatogr. A., 1996, 745, 189-200.
  • [11] J.L. Tadeo, C. Sánchez-Brunete, R.A. Pérez, M.D. Fernández, J. Chromatogr. A., 2000, 882, 175-191.
  • [12] P.L. Alferness, L.A. Wiebe, J. AOAC Int., 2001, 84, 823-846.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATA-0007-0018
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