Non-linear calibration of a nitrogen-phosphorus detector for the GC determination of amino acids

1991 ◽  
Vol 31 (9-10) ◽  
pp. 500-504 ◽  
Author(s):  
M. F. Philpott ◽  
M. J. Van der Merwe
1980 ◽  
Vol 63 (1) ◽  
pp. 43-46
Author(s):  
Keh-Chuh Ting ◽  
George A Root ◽  
George R Tichelaar

Abstract A simple, fast, and accurate method has been developed to determine residues of bromacil (5-bromo-3-sec-butyl-6-methyluracil) herbicide. Following sample extraction, filtration, and concentration, the herbicide is determined using a gas chromatograph equipped with a thermionic nitrogen/phosphorus detector. The method has been used to recover 0.04 ppm bromacil added to citrus, pineapple, soil, and water, and 0.1 ppm bromacil added to alfalfa hay.


Talanta ◽  
2007 ◽  
Vol 72 (3) ◽  
pp. 1004-1012 ◽  
Author(s):  
L.A. Tortajada-Genaro ◽  
P. Campíns-Falcó

1983 ◽  
Vol 262 ◽  
pp. 257-263 ◽  
Author(s):  
Richard E. Echols ◽  
Robert H. Miller ◽  
Willie Winzer ◽  
Darrell J. Carmen ◽  
Yonetta R. Ireland

1991 ◽  
Vol 74 (2) ◽  
pp. 295-309
Author(s):  
Kenneth W Edgell ◽  
Elizabeth L Jenkins ◽  
Viorica Lopez-Avila ◽  
James E Longbottom

Abstract A joint U.S. Environmental Protection Agency/AOAC interlaboratory method validation study was conducted on EPA Method 507, Determination of Nitrogen- and Phosphorus- Containing Pesticides In Finished Drinking Water by Gas Chromatography with a Nitrogen-Phosphorus Detector, to determine the mean recovery and precision for analyses of 45 nitrogen- or phosphorus-containing pesticides in reagent water and finished drinking waters. The study design was based on Youden's nonreplicate plan for collaborative tests of analytical methods. The waters were spiked with 45 nitrogen- or phosphorus-containing pesticides at 6 concentration levels, prepared as 3 Youden pairs. Ten volunteer laboratories extracted the spiked test waters with methylene chloride, performed a solvent exchange with methyl ferf-butyl ether, and analyzed an aliquot of each extract by gas chromatography using a nitrogen-phosphorus detector. Results were analyzed using an EPA computer program, which measured recovery and precision for each of the 45 pesticides and compared the performance of the method between water types. Method 507 was judged acceptable for all analytes tested except merphos, which thermally decomposed in the Injection port of the gas chromatograph. Five compounds (carboxin, disulfoton, metolachlor, pronamlde, and slmazlne) exhibited statistically significant matrix effects for the finished drinking water. The method has been adopted official first action by AOAC.


1989 ◽  
Vol 72 (5) ◽  
pp. 813-815
Author(s):  
Austin R Long ◽  
Lily C Hsieh ◽  
Marsha S Malbrough ◽  
Charles R Short ◽  
Steven A Barker

Abstract A method for the isolation and gas chromatographic determination of chlorsulfuron in milk is presented. Blank or chlorsulfuron-spiked milk samples were blended into C-18 (octadecylsilyl derivatized silica, ODS) packing material. A column made from the C-18/milk matrix was washed with hexane after which chlorsulfuron was eluted with dichloromethane (DCM). The DCM eluate contained chlorsulfuron which was free from interfering co-extractants when analyzed by gas chromatography utilizing a nitrogen/phosphorus detector. Chlorsulfuron was found to undergo a thermally induced decomposition to give 2-amino-4-methoxy-6-methyl-l,3,5-triazine, which was detected and quantitated by this method. Standard curves for these analyses were linear (r = 0.992 ± 0.004, n = 5), with an average percentage recovery of 91.6 ± 10.8%, over the concentration range examined (62.5-2000 ng/mL). The inter- and intra-assay variabilities were 11.6 ± 7.5% and 6.2%, respectively.


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