Liquid chromatographic determination of aliphatic amines in water using solid support assisted derivatization with 9-fluorenylmethyl chloroformate

2002 ◽  
Vol 55 (3-4) ◽  
pp. 129-134 ◽  
Author(s):  
J. Verdú-Andrés ◽  
P. Campíns-Falcó ◽  
R. Herráez-Hernández
1974 ◽  
Vol 57 (4) ◽  
pp. 954-956
Author(s):  
Robert G Parker

Abstract In the method described, anethole is extracted from the liqueur sample with chloroform, which eliminates interference from the large amount of sugar present, and is determined by gas-liquid chromatography, using 10% K-20M Carbowax as stationary phase on Chromosorb W (AWDMCS) as solid support. Anethole concentrations were measured in 8 different bottle samples, consisting of 4 different brands produced by 3 different manufacturers. There is a significant difference in the anethole concentration for the 4 brands tested.


2016 ◽  
Vol 12 (6) ◽  
pp. 560-567
Author(s):  
Marwa F. Mansour ◽  
Ehab F. El-Kady ◽  
Mona M. Abd El-Moety ◽  
Nabawia M. El-Guindi ◽  
Ann Van Schepdael ◽  
...  

1975 ◽  
Vol 58 (5) ◽  
pp. 1051-1061
Author(s):  
William P Cochrane ◽  
James F Lawrence ◽  
Young W Lee ◽  
Ronald B Maybury ◽  
Brian P Wilson

Abstract An interlaboratory investigation of technical chlordane residues in food crops was carried out to determine the most practical and consistent method of reporting results. Using a technical chlordane reference standard, 8 gas chromatographic stationary phases were studied for their resolution capabilities. The best separations were obtained with SE-30 and its OV-1 equivalent. Using these columns and electron capture detection, potatoes and carrots from supervised field experiments were analyzed in duplicate and quantitated by using 4 methods of calculation. The data were statistically treated to determine the precision and bias for each method. Also, 1 sample was analyzed in duplicate on 2 different occasions by 6 laboratories to substantiate the initial conclusions. Based on the criterion of high precision it is suggested that a comparison of total area under the chromatogram of the sample with total area of a standard technical chlordane be the method of quantitation. Only peaks which are common to both standard and sample have any significance in this type of calculation.


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