Determination of volatile halogenated hydrocarbons in tap water, seawater and industrial effluents by glass capillary gas chromatography and electron capture detection

1978 ◽  
Vol 1 (1) ◽  
pp. 34-40 ◽  
Author(s):  
Göran Eklund ◽  
Björn Josefsson ◽  
Claes Roos
Keyword(s):  
Gas Chromatography ◽  
Electron Capture ◽  
Capillary Gas Chromatography ◽  
Tap Water ◽  
Industrial Effluents ◽  
Halogenated Hydrocarbons ◽  
Electron Capture Detection ◽  
Glass Capillary ◽  
Volatile Halogenated Hydrocarbons

Determination of Type A and B Trichothecenes in Cereals by Gas Chromatography with Electron Capture Detection

1992 ◽  
Vol 75 (6) ◽  
pp. 1049-1053 ◽  
Author(s):  
Tord E Möller ◽  
Håkan F Gustavsson
Keyword(s):  
Gas Chromatography ◽  
Ethyl Acetate ◽  
Electron Capture ◽  
Capillary Gas Chromatography ◽  
Quantitative Method ◽  
Type A ◽  
Electron Capture Detection

Abstract A quantitative method has been developed for determination of nonmacrocyclic trichothecenes in cereals. The mycotoxins are extracted with acetonitrile- ethyl acetate-water, and the extracts are quickly defatted with hexane and purified on a Sep- Pak Florisil cartridge. The trichothecenes are then silylated with Tri-Sil/TBT and quantitated by capillary gas chromatography with electron capture detection. High recoveries of 13 tested trichothecenes were achieved in experiments on wheat at the 250 μg/kg level. The method was also tested on barley, maize, oats, and rye with good results

Surrogate-Assisted Determination of 2,3,7,8-Tetrachlorodibenzo-p-Dioxin in Fish by Electron Capture Capillary Gas Chromatography

1986 ◽  
Vol 69 (6) ◽  
pp. 976-980
Author(s):  
Richard A Niemann
Keyword(s):  
Gas Chromatography ◽  
Electron Capture ◽  
Capillary Gas Chromatography ◽  
Capillary Column ◽  
Electron Capture Detection ◽  
Matrix Interference ◽  
Relative Standard ◽  
Tetrachlorodibenzo P Dioxin ◽  
Liquid Chromatographic

Abstract Surrogate spiking the sample with 1000 parts per trillion (pptr) 1,3,7,8-tetrachlorodibenzo-p-dioxin (1378-TCDD) has doubled analytical throughput in determining toxic 2378-TCDD (analyte) at the low partper- trillion level in fish, using multicolumn high resolution liquid chromatographic cleanup before quantitation by capillary gas chromatography with electron capture detection. The 1378- and 2378-TCDD were recovered equally and were well separated by the capillary column so that the earlier-eluting surrogate did not interfere with the quantitation of levels of analyte many-fold lower. Matrix interference contributed <1 % bias in surrogate quantitation. Using surrogate recovery to correct for analyte losses during analysis, accuracy averaged (n = 7) 105% in determining 18 or 45 pptr 2378-TCDD added to fish without detectable bioincurred analyte. Analyses of selected fish with bioincurred 2378-TCDD gave results comparable to earlier work where recovery correction required a second analysis of sample fortified with analyte. With surrogate fortification, repeatability of determination (n = 3 or 4) improved markedly to <5% relative standard deviation at 37-46 pptr.

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