Determination of several pesticides with a chemical ionization ion trap detector

1990 ◽  
Vol 38 (2) ◽  
pp. 402-407 ◽  
Author(s):  
Gregory C. Mattern ◽  
George M. Singer ◽  
Judy Louis ◽  
Mark Robson ◽  
Joseph D. Rosen
1997 ◽  
Vol 69 (24) ◽  
pp. 5121-5129 ◽  
Author(s):  
Mark A. Dearth ◽  
Keiji G. Asano ◽  
Kevin J. Hart ◽  
Michelle V. Buchanan ◽  
Douglas E. Goeringer ◽  
...  

1991 ◽  
Vol 74 (4) ◽  
pp. 611-618 ◽  
Author(s):  
Martin J Lynch ◽  
Franklyn R Mosher ◽  
Richard P Schneider ◽  
Hassan G Fouda ◽  
James E Risk

Abstract The Ion trap detector (ITD), in combination with a capillary gas chromatograph and under chemical ionization conditions, offers sufficient sensitivity to determine carbadoxrelated residues as the methyl ester derivative of quinoxaline- 2-carboxylic acid at 3 μg/kg or higher in porcine liver. A tetradeuterated internal standard of QME effectively compensates for losses incurred during sample preparation. The method produced mean levels of 3.3 (±0.5), 5.5 (±0.8), and 10.1 (±0.9) μg/kg for liver fortified at 3, 5, and 10 μg/kg. When applied to analysis of samples containing incurred residues of 14C-carbadox at the low μg/kg level, results were comparable to those obtained by reverse isotope dilution analysis.


1991 ◽  
Vol 247 (2) ◽  
pp. 243-248 ◽  
Author(s):  
B. Geypens ◽  
Y. Ghoos ◽  
M. Hiele ◽  
P. Rutgeerts ◽  
G. Vantrappen ◽  
...  

1997 ◽  
Vol 62 (9) ◽  
pp. 1403-1412 ◽  
Author(s):  
David Milde ◽  
Zbyněk Plzák ◽  
Miloslav Suchánek

A selective and rapid procedure was developed for the determination of trace amounts of butyltin compounds in sediments by capillary gas chromatography with mass spectrometric detection. Analytes were isolated from the sediment samples by extraction with a methanolic solution of HCl (0.5 mol l-1) followed by reextraction into a hexane solution of tropolone (0.1%). The organotin compounds were converted to the nonpolar methyl derivatives by methylation with a Grignard reagent. The recovery was determined for each step of the procedure. This efficient separation method combined with the ion trap based mass detection ensures a high selectivity even for concentrations approaching the detection limit (0.15 pg for Bu3SnMe) in real sediments. Chemical ionization using acetonitrile as the reaction gas, exhibiting a similar sensitivity of determination and reducing the background level, can serve as a convenient alternative of detection for sediments heavily contaminated by organics. The method was applied to a set of real samples and validated by analysis of a certified reference material.


1991 ◽  
Vol 74 (6) ◽  
pp. 982-986
Author(s):  
Gregory C Mattern ◽  
Judith B Louis ◽  
Joseph D Rosen

Abstract An improved method for the determination of trace levels of pesticides in surface water has been developed and was used to analyze 20 target pesticides in New Jersey. Pesticides were extracted from 2 L water samples, using a mixture of XAD-2 and XAD-7 resins, and were determined by gas chromatography/chemical ionization mass spectrometry with ion trap detection. Average recoveries (performed in triplicate at the 1 ppb level, except for captan and chlorothalonil at 5 ppb) were between 75 and 113%, with an average coefficient of variation of 9%. Most of the pesticides (alachlor, atrazine, butylate, carbofuran, chlorpyrifos, diazinon, fonofos, isofenphos, metolachlor, metribuzin, parathion, and simazine) had limits of detection (LODs) of 0.005 ppb or lower, while some (carbaryl, cyanazine, fenamiphos, linuron, pendlmethalin, and terbufos) had LODs between 0.005 and 0.05 ppb. Captan and chlorothalonil had LODs of 1 ppb. Of 31 samples analyzed, 29 contained one or more of the following pesticides: alachlor, atrazine, carbaryl, chlorpyrifos, cyanazine, diazinon, isofenphos, linuron, metolachlor, and simazine in concentrations between trace (<0.025 ppb) and 5.48 ppb.


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