Qualitative and quantitative determination of extractives in heartwood of Scots pine (Pinus sylvestris L.) by gas chromatography

2006 ◽  
Vol 1109 (2) ◽  
pp. 267-272 ◽  
Author(s):  
Dag Ekeberg ◽  
Per-Otto Flæte ◽  
Morten Eikenes ◽  
Monica Fongen ◽  
Carl Fredrik Naess-Andresen
1974 ◽  
Vol 20 (2) ◽  
pp. 249-254 ◽  
Author(s):  
M A Evenson ◽  
G L Lensmeyer

Abstract A rapid, simple, accurate, and precise isothermal gas-chromatographic method is introduced for determination of methaqualone (2-methyl-3-o-tolyl-4(3H)-quinazolinone) in serum. A single extraction of 2 ml of serum, without derivative formation, will give adequate sensitivity for quantitation of therapeutic serum concentrations of the drug within 15 min. The method is free of interferences from biological substances, as well as from commonly used drugs. A non-drug internal standard compensates for variables in extraction, injection, and instrumental changes during analysis. The coefficient of variation, day-to-day, is 5.6%. Mean recovery of added methaqualone was 80%. To compensate for the nonquantitative yield and ensure accurate results, we prepared all analytical methaqualone standards in serum.


1965 ◽  
Vol 48 (5) ◽  
pp. 952-954
Author(s):  
Alfred D Thruston

Abstract The qualitative and quantitative determination of chlordane residues on raw agricultural products has been best achieved by gas chromatography techniques. While good recoveries (90–100% at the 0.1 ppm level) have been obtained from plant extracts with added standard chlordane, weathered chlordane residues show changes in number and size of gas chromatographic peaks. Chlordane at the 50 µg level, when exposed to the air at room temperature over a period of time, showed progressive decomposition and loss of the many components that make up chlordane.


1974 ◽  
Vol 20 (2) ◽  
pp. 141-147 ◽  
Author(s):  
Mavis S Greaves

Abstract Accurate methods are described for the qualitative and quantitative determination of medazepam, diazepam, and nitrazepam in 5 ml of whole blood. Medazepam and diazepam are analyzed intact and nitrazepam is chromatographed as its trimethylsilyl derivative by flame-ionization gas-chromatography on "1% OV-17." A supplementary column of "2% OV-1" is used to separate nitrazepam TMS from diazepam when both are present in the same extract. Essential data given include the percentage recovery of medazepam, and the flame-ionization detector responses of diazepam and silylated nitrazepam relative to medazepam, calculated after extraction from blood and gas-chromatographic analysis. Chromatograms are illustrated of extracts of blood taken from patients on medazepam and diazepam therapy and from a patient who had taken an overdose of nitrazepam.


Author(s):  
E. Nesemann ◽  
F. Seehofer

AbstractA screening method has been developed for the qualitative and quantitative determination of vanillin, ethylvanillin, coumarin and dihydrocoumarin. The compounds are qualitatively determined by thin-layer chromatography after extraction of tobacco and purification of the extract. The quantitative determination is made by gas chromatography: Coumarin and dihydrocoumarin are determined directly and vanillin and ethylvanillin after silylation in the form of trimethylsilyl derivatives. Detection limit: thin-layer chromatography = 1 µg, gas chromatography = 0.02 µg. The coefficient of variation of the results obtained amounts to 2.4 % for vanillin and to 6.7 % for coumarin


2021 ◽  
Author(s):  
Yiwen Cao ◽  
Shenjie Zhu ◽  
Lin Zhang ◽  
Qun Cui ◽  
Haiyan Wang

Aiming at the difficulty in qualitative and quantitative analysis of trace compositions in food preservative propionic acid, the trace compositions and the key components influencing the total aldehyde content in...


1971 ◽  
Vol 54 (3) ◽  
pp. 711-712
Author(s):  
Martha Fuzesi

Abstract A gas chromatographic method is described for the quantitative determination of N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-tolindine and α,α,α-trifluoro-2,6-dinitro-N,N-dipropyI-p-toluidine herbicides in formulations. The sample is extracted with benzene, and equal amounts of sample and reference solution in the same concentration range are analyzed by gas chromatography, using an electron capture detector and an SE-30/Diatoport S column. The method has been applied successfully to laboratory-prepared and commercial samples.


1987 ◽  
Vol 20 (4) ◽  
pp. 290-291
Author(s):  
M. Moss ◽  
C.S.Y. Wong ◽  
T. McMahon ◽  
C. Cousins ◽  
C. Jacklyn

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