scholarly journals Efficiencies of different methods for determination of organophosphate pesticide residues in fermented wheat substrate

2013 ◽  
Vol 28 (2) ◽  
pp. 133-140 ◽  
Author(s):  
Tijana Djordjevic ◽  
Slavica Siler-Marinkovic ◽  
Rada Djurovic-Pejcev ◽  
Suzana Dimitrijevic-Brankovic ◽  
Jelena Gajic-Umiljendic

In the present work, the efficiencies of three different sample preparation methods for GC/ MS determination of pirimiphos-methyl and chlorpyrifos-methyl residues in wheat (Triticum spelta) samples fermented by Lactobacillus plantarum were compared. All three methods were based on methanol:acetone=1:1 extraction, while further purification of the obtained samples was altered. First purification was through a column containing a mixture of aluminium oxide and activated charcoal slurry-packed and eluted with dichlormethane, the second was purification on a florisil column slurry-packed and eluted with ethyl acetate:acetone=4:1, while the third was based on a combination of the former two methods, i.e. clean-up through columns filled with a mixture of aluminum oxide and activated charcoal slurry-packed and eluted with ethyl acetate:acetone=4:1. The second method was found the most effective for obtaining satisfactory recoveries at four fortification levels. For pirimiphos-methyl, recoveries were in the range of 91.3-96.0% and had good reproducibility, i.e. RSD ranging from 2.2-4.1%, while the corresponding range for chlorpyrifos-methyl was 81.6-88.2%, and the RSD range 2.5-5.4%. The chosen method was further optimized in order to establish the optimum volume of elution solvent used during the clean-up procedures. The highest recoveries of 93.7?3.5% for pirimiphos-methyl and 85.3?2.5% for chlorpyrifos-methyl were obtained after elution with 25 ml volume of solvent. Considering all, simple, efficient and reliable GC/MS detection of pirimiphosmethyl and chlorpyrifos-methyl residues in wheat grain substrate altered by fermentation with L. plantarum was achieved by the two-steps extraction with 25 ml of methanol:acetone=1:1 solvent mix for 30 min, followed by a clean-up procedure through a glass column with florisil coupled with elution by 25 ml of ethyl acetate:acetone=4:1.

2012 ◽  
Vol 27 (2) ◽  
pp. 167-174 ◽  
Author(s):  
Tijana Djordjevic ◽  
Rada Djurovic ◽  
Jelena Gajic-Umiljendic

Efficiency of three different sample preparation methods for GC/MS determination of bifenthrin residues in wheat (Triticum spelta) samples fermented by Lactobacillus plantarum was tested. The first method was based on a methanol:acetone=1:1 extraction folowed by a purification on columns containing mixture of aluminium oxide and activated charcoal slurry-packed and eluted with dichlormethane, the second was based on methanol:acetone=1:1 extraction folowed by the purification on florisil column and elution by ethil acetate:acetone=4:1, while the third tested method was based on a combination of the first two mentioned methods, thus methanol:acetone=1:1 extraction and clean-up throught columns filled with a mixture of aluminum oxide and activated charcoal slurrypacked and eluted with ethil acetate:acetone=4:1. The second method was the most effective for obtaining satisfactory recoveries for bifenthrin in a range of 79-83% for four fortification levels, with good reproducibility i.e. RSD% in a range of 2.2-7.4%. The chosen method was further optimized by assessing the optimum volume of elution solvent used during the clean-up procedures. The highest recovery of 82.1% was obtained after elution with 25 ml of solvent. Overall, two-step extraction with 25 ml of methanol:acetone=1:1 solvent mix for 30 min, followed by clean-up procedure through a glass column with florisil coupled with elution with 25 ml of ethyl acetate: acetone=4:1, allows simple, efficient and reliable GC/MS detection of bifenthrin residues from wheat grain fermented by L. plantarum.


1988 ◽  
Vol 32 ◽  
pp. 221-226
Author(s):  
Wayne Watson ◽  
Jim Parker ◽  
Anthony R. Harding

AbstractVarious sample preparation methods for Energy Dispersive X-ray Fluorescence (EDXRF) analysis of Portland cement were compared in order to evaluate improvement in analytical accuracy and precision. Sample preparation requirements for EDXRF are slightly different than for Wavelength Dispersive X-ray Fluorescence (WDXRF), and the methods commonly used in WDXRF are not optimized for EDXRF. Primarily, the work focuses on techniques for producing a fused sample with the lowest practical concentration of lithium borate flux. Determination of minimum detection limits were made from samples with varying proportions of flux in order to evaluate analytical optimization. Ease and reproducibility of preparation of the sample was also considered.


1968 ◽  
Vol 51 (4) ◽  
pp. 771-773
Author(s):  
Aaron E Rash

Abstract The nitric-perchloric acid digestion, 22.070(b) and 22.073, for the determination of phosphorus in grains and stock feeds was compared with three other methods of sample preparation (destruction of organic material) : quinoline molybdate precipitation, perchloric-sulfuric-sodium molybdate digestion, and the plant method. The values obtained by the nitric-perchloric acid method were not in good agreement with those obtained by the other methods studied. Six samples of commercial feeds and one barley sample were analyzed. The barley sample gave very poor recoveries by method 22.073.


2004 ◽  
Vol 60 (1-2) ◽  
Author(s):  
Hohyun Kim ◽  
Kyu Young Chang ◽  
Chang Hun Park ◽  
Moon Sun Jang ◽  
Jung-Ae Lee ◽  
...  

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