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Simultaneous determination of phenmedipham, desmedipham, and ethofumesate in a pesticide formulation by normal-phase high-performance liquid chromatography

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A normal-phase high-performance liquid-chromatographic method has been developed for simultaneous quantitative analysis of phenmedipham, desmedipham, and ethofumesate in a pesticide formulation. Analysis was performed on a 25 cm × 0.4 cm, 5- µm particle, CN column with n-hexane-dichloromethane 40:60 (v/v) as mobile phase at a flow rate of 1 mL min-1. UV detection was performed at 270 nm; the constant column temperature was 25°C. The run time under these chromatographic conditions was less than 8 min. Calibration plots were linear in the concentration range 76-380 µg mL-1 for phenmedipham, 72-360 µg mL-1 for desmedipham, and 52-260 µg mL-1 for ethofumesate. Statistical evaluation by analysis of variance showed the intra-day repeatability (n = 8) and inter-day precision (n = 3) of the assay were satisfactory. The sensitivity of the method, as the limits of detection (LOD) and quantification (LOQ) for each active ingredient, was also determined.
Słowa kluczowe
Rocznik
Strony
109--118
Opis fizyczny
Bibliogr. 23 poz., rys., tab.
Twórcy
autor
  • Laboratory for Pesticide Formulation Control, Department of Chemistry, Faculty of Agricultural Sciences and Food, the "St. Cyril and Methodius" University, Bul.: "Aleksandar Makedonski" bb, P.O. Box 297, 1000 Skopje, Republic of Macedonia
Bibliografia
  • [1] I. Deveikyte and V. Seibutis, Agron. Res., 4, 159 (2006)
  • [2] B.R. Weeden, A Report for the Rural Industries Research and Development Corporation, Project No DAQ-211A, 2000
  • [3] C. Tomlin, The Pesticide Manual Incorporating the Agrochemicals Handbook, 11th edn (Crop Protection Publications), 1997, pp. 291–292, 410–411, 787–788
  • [4] T. Krongaard, K. K. Petersen, and C. Christoffersen, NERI Technical Report, No. 461, 2003
  • [5] European Commission, Health and Consumer Protection Directorate—General (Phenmedipham), Appendix I, 2004
  • [6] EPA, Reregistration Eligibility Decision for Phenmedipham, 2005
  • [7] European Commission, Health and Consumer Protection Directorate-General (Desmedipham), Appendix I, 2004
  • [8] EPA, Reregistration Eligibility Decision for Desmedipham, 1996
  • [9] European Commission, Health and Consumer Protection Directorate-General (Ethofumesate), Appendix I, 2002
  • [10] EPA, Reregistration Eligibility Decision for Ethofumesate, 2005
  • [11] CIPAC Method Handbook C (Phenmedipham), 77/TC/M/3.2, 1985, pp. 2181–2186
  • [12] CIPAC Method Handbook J (Ethofumesate), 233/TC/M/3, 2000, pp. 43–50
  • [13] C. Hidalgo, J.V. Sancho, F.J. Lopez, and F. Hernandez, J. Chromatogr. A., 823(1–2), 121 (1998)
  • [14] V. Tatarkovicova and Z. Stransky, Collect. Czech. Chem. Commun., 57(8), 1632 (1992)
  • [15] V. Tatarkovicova and R. Machac, Collect. Czech. Chem. Commun., 57(11), 2295 (1992)
  • [16] J. Tekel, P. Farkas, J. Kovacicova, and A. Szokolay, Nahrung, 32(4), 357 (1988)
  • [17] D. Perret, A. Gentili, S.Marchese, A. Marino, and F. Bruno, JAOAC Int., 84(5), 1407 (2001)
  • [18] M.P. Garcia de Llasera and M. Bernal-Gonzalez, Water Res., 35(8), 1933 (2001)
  • [19] Omega, Perkin–Elmer Corporation, Norwalk, USA, 1989
  • [20] D.R. Jenke, J. Liq. Chromatogr. Related Technol., 19(5), 737 (1996)
  • [21] W.J. Lough and I.W. Wainer, High Performance Liquid Chromatography (Fundamental Principles and Practise), Blackie Academic and Professional, Chapman and Hall, Glasgow, UK, 1996, pp. 47, 50, 156–163
  • [22] V.R. Meyer, Practical High-Performance Liquid Chromatography, 2nd edn, John Wiley and Sons, Chichester, 1994, pp. 259–260
  • [23] J.C. Miller and J.N. Miller, Statistics for Analytical Chemistry, 3rd edn, Ellis Horwood, Prentice Hall, 1993, pp. 101–104.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATE-0001-0009
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