Determination of Chlorinated Pesticide Residues in Foods. III. Simultaneous Analysis of Chlorinated Pesticide and Phthalate Ester Residues by Using AgNO3-Coated Florisil Column Chromatography for Cleanup of Various Samples

1979 ◽  
Vol 62 (3) ◽  
pp. 689-694
Author(s):  
Takashi Suzuki ◽  
Kiyoshi Ishikawa ◽  
Nobutoshi Sato ◽  
Kei-Ichi Sakai

Abstract A simplified method suitable for simultaneous analysis of chlorinated pesticide and phthalate ester residues in various foods was developed. Chemical residues were quantitatively extracted from fatty and vegetable samples with acetonitrile as follows: Chemical standard in 0.5 mL ethanol solution was added to 10 g homogenized sample. After 3 hr, pork and beef were extracted 3 times with 20 mL portions of acetonitrile. The acetonitrile layers were diluted with water and extracted with n-hexane. Rice samples were combined with 10 mL water, 5 mL acetonitrile, and 1 mL ethanol and extracted 3 times with 20 mL portions of n-hexane. The re-hexane concentrate from each sample was submitted to AgNO3-coated Florisil column chromatography. The AgNO3 coating adequately adsorbed interfering coextractives. Extracts of fish and vegetable samples were separated into 2 fractions by the above column chromatography. Supplemental cleanup procedures were also developed to accurately determine phthalate esters eluted in the second fraction. Satisfactory gas chromatograms were obtained for most samples.

1987 ◽  
Vol 70 (4) ◽  
pp. 740-745
Author(s):  
Ronald G. Luchtefeld

Abstract A method is described for determining substituted urea herbicides in foods. The residues are extracted from the product with methanol, and the food coextractives are removed by using solvent partitioning and Florisil column chromatography. The extract is analyzed using liquid chromatography with postcolumn photodegradation, chemical derivatization with orthophthalaldehyde, and spectrofluorometry. Recoveries were determined by spiking 8 different food products with 6 phenylureas—chlorbromuron, chloroxuron, diuron, fluometuron, linuron, and metobromuron—at 0.05 and 0.5 ppm. Three determinations were made at each level for each product. Average recovery at 0.05 ppm was 95% (with a standard deviation of 7.9%), and at 0.5 ppm, 98% (with a standard deviation of 6.9%).


1974 ◽  
Vol 38 (9) ◽  
pp. 1661-1667
Author(s):  
Masayuki Katayama ◽  
Ching Tsang Hou ◽  
Norman C. Chen ◽  
Takako Hirota ◽  
Toshiko Kiribuchi ◽  
...  

1984 ◽  
Vol 67 (4) ◽  
pp. 783-789
Author(s):  
Fred M Gretch ◽  
Joseph D Rosen

Abstract An automated, continuous flow system is described for Florisil column chromatography of pesticide residues from food extracts. Evaluation of the system using 5 common organochlorine and organophosphorus pesticides in 2 crop matrices demonstrates essentially no difference in recovery or precision between automated and currently used manual analyses. The automated procedure uses only 20% of the solvents and adsorbents used in the manual procedure and is 3 times faster.


1987 ◽  
Vol 70 (4) ◽  
pp. 740-745
Author(s):  
Ronald G Luchtefeld

Abstract A method is described for determining substituted urea herbicides in foods. The residues are extracted from the product with methanol, and the food coextractives are removed by using solvent partitioning and Florisil column chromatography. The extract is analyzed using liquid chromatography with postcolumn photodegradation, chemical derivatization with orthophthalaldehyde, and spectrofluorometry. Recoveries were determined by spiking 8 different food products with 6 phenylureas—chlorbromuron, chloroxuron, diuron, fluometuron, linuron, and metobromuron—at 0.05 and 0.5 ppm. Three determinations were made at each level for each product. Average recovery at 0.05 ppm was 95% (with a standard deviation of 7.9%), and at 0.5 ppm, 98% (with a standard deviation of 6.9%).


1974 ◽  
Vol 38 (9) ◽  
pp. 1661-1667 ◽  
Author(s):  
Masayuki KATAYAMA ◽  
Ching Tsang HOU ◽  
Norman C. CHEN ◽  
Takako HIROTA ◽  
Toshiko KIRIBUCHI ◽  
...  

2000 ◽  
Vol 63 (11) ◽  
pp. 1563-1569 ◽  
Author(s):  
HAE-JUNG LEE ◽  
MYUNG-WOO BYUN ◽  
KYONG-SU KIM

The method consists of the extraction of fat from perilla seeds, separation of hydrocarbons and 2-alkylcyclobutanones with florisil column chromatography, and identification of hydrocarbons and 2-alkylcyclobutanones by gas chromatography–mass spectroscopy (GC-MS). Concentrations of hydrocarbons and 2-alkylcyclobutanones increased with the irradiation dose. The major hydrocarbons in the irradiated perilla seeds were 8-heptadecene and 1,7-hexadecadiene from oleic acid and 6,9-heptadecadiene and 1,7,10-hexadecatriene from linoleic acid. One of the 2-alkylcyclobutanones, 2-(5′-tetradecenyl)cyclobutanone, was found in the highest concentration in the irradiated perilla seeds. Radiation-induced hydrocarbons in the perilla seeds were detected at doses of 0.5 kGy and higher, and radiation-induced 2-alkylcyclobutanones were detected at doses of 1 kGy and higher. These compounds were not detected in nonirradiated perilla seeds.


1974 ◽  
Vol 57 (3) ◽  
pp. 645-647
Author(s):  
Oliver Dean Decker ◽  
Richard Frank

Abstract Two methods are described for the determination of isopropalin (2,6-dinitro-N,N-dipropylcumidine) in technical grade material (a concentrate in xylene) and emulsifiable concentrate formulations. Samples measured spectrophotometrically are purified by Florisil column chromatography. Samples measured gas chromatographically are dissolved in chloroform, mixed with the internal standard, and then injected into a gas chromatograph equipped with a flame ionization detector.


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