Abstract
Determination of omethoate by cathodically sweeping oscillopolarography is described. The product of the alkaline hydrolysis exhibited a sensitive second derivative wave at −0.50 V (vs. SCE) in a 1.0 ×10−5mol/L sodium dodecylbenzene sulfonate (SDBS)+0.1 mol/L HAc-NaAc (pH 4.0) buffer. The peak current was linearly proportional to the concentration of omethoate in the range from 6.4×10−7 to 5.1×10−5 mol/L. The detection limit is 2.0×10−7 mol/L with the relative standard derivation (RSD) of 3.5%. The hydrolysis procedure and the electrode reaction were studied by voltammetry.
Similar content being viewed by others
References
Wu Shichang.New Pesticide Collection. Beijing: Chinese Agriculture Technology Press, 1992. 86–87
Roach J A G, Carson L J. Collisionally actived decomposition mass spectrometry-mass spectrometry determination of organophosphorous pesticide in food.J Asso Off Anal Chem, 1987,70(3): 439–442
Ferreira J R, Falcao M M, Tainha A. Residues of dimethoate and omethoate in peaches and apples following repeated applications of dimethoate.J Agric Food Chem, 1987,35(4):506–508
Drescher W, Fiedler L. Mothode zum Nachweis von Ruckstanden der Insektixide Acephat, Dimethoate, Methamidophos und Omethoate in Kleinen Nektarmengen.Chemosphere, 1983,12: 1605–1610
Fu Z Ge.The Purification and Quantitation of Standard Pesticides. Beijing: Chinese Foreign Economy and Trading Press, 1995. 73–74
Author information
Authors and Affiliations
Additional information
Supported by the Foundation of Chinese-Franch Cooperation Programme on the Advanced Research
Wang Yu: born in 1964. Lecturer. Cangzhou Teacher’s College, Cangzhou, Hebei, 061001
Rights and permissions
About this article
Cite this article
Yu, W., Yuansi, S., Junhua, H. et al. Determination of omethoate by cathodically sweeping oscillopolarography. Wuhan Univ. J. Nat. Sci. 3, 469–472 (1998). https://doi.org/10.1007/BF02830053
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02830053