Determination of the lifetime of intermediate products in the reduction of oxygen by means of oscillographic polarography

1973 ◽  
Vol 6 (5) ◽  
pp. 582-584
Author(s):  
N. A. Gordienko ◽  
L. I. Antropov
2020 ◽  
Vol 56 (14) ◽  
pp. 1379-1383
Author(s):  
Cao Nhat Linh ◽  
O. V. Duvanova ◽  
S. Yu. Nikitina ◽  
A. N. Zyablov

1969 ◽  
Vol 52 (4) ◽  
pp. 811-817
Author(s):  
Raymond J Gajan

Abstract Ten laboratories collaboratively studied several single sweep oscillopolarographic methods designed to be used as confirmative procedures for several organophosphorus pesticide residues determined by GLC. Polarographic methods for the detection and determination of parathion, methyl parathion, diazinon, and/or malathion at 0.5 and 2.0 ppm in extracts of apples and lettuce were included in this study. All 10 laboratories successfully detected the organophosphorus pesticide residues and quantitative results were reported by seven laboratories. These results show that the polarographic methods can be used for rapidly confirming results obtained by the multiple detection procedures now in use.


2006 ◽  
Vol 5 (5) ◽  
pp. 477 ◽  
Author(s):  
M. Tamimi ◽  
S. Qourzal ◽  
A. Assabbane ◽  
J.-M. Chovelon ◽  
C. Ferronato ◽  
...  

2010 ◽  
Vol 439-440 ◽  
pp. 109-112
Author(s):  
Ji Hong Zhou ◽  
Yan Jun Lian

Manganese in water has low toxicity. The product will form the yellow stain when the industrial water content is high. There are many ways to monitor it. The determination of trace Manganese in the YangjiaoPu source water by oscillographic polarography is introduced in this paper. The result indicate that the standard deviation of this method is 0.001~0.002 mg/L, the relative standard deviation is 2.3~2.5% and the mark-on recovery ranged from 96.8%~105.8%. At the same time several problems needing attention about experiment process are posed in this paper.


1965 ◽  
Vol 48 (5) ◽  
pp. 958-962 ◽  
Author(s):  
Raymond J Gajan ◽  
Walter R Benson ◽  
Josephine M Finocchiaro

Abstract The insecticide carbaryl can be determined quantitatively in the presence of a-naphthol by means of oscillographic polarography. A characteristic peak for the hydrolysis product of nitrosated carbaryl is obtained which has a peak potential of –0.45 ± .05 v vs. a mercury pool reference electrode. Using a modified cleanup method, as little as 0.2 ppm of carbaryl residues on certain fruils and vegetables has been determined. Recoveries from fortified crops averaged 95.3% ± 9 . 0% at the 0.2, 5.0, and 10.0 ppm levels. Among those pesticides tested, only o-phenylphenol interfered.


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