1981
DOI: 10.1007/bf02262893
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Gas chromatographic separation of ethanolamines and ethylene glycols without preliminary derivatization

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1986
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Cited by 8 publications
(4 citation statements)
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“…A somewhat better reproducibility was achieved when 15% Carbowax 20M on 80-100 mesh Porapak Q was used, as suggested by Boneva and Dimov (1979). We had, however, some problems with the detection of small amounts of TEA since its peak was quite broad.…”
Section: Methodsmentioning
confidence: 82%
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“…A somewhat better reproducibility was achieved when 15% Carbowax 20M on 80-100 mesh Porapak Q was used, as suggested by Boneva and Dimov (1979). We had, however, some problems with the detection of small amounts of TEA since its peak was quite broad.…”
Section: Methodsmentioning
confidence: 82%
“…The paper of Boneva and Dimov (1981) drew our attention to the possibility of using capillary columns. We therefore tested three fused-silica columns with bonded phases having different polarities.…”
Section: Methodsmentioning
confidence: 99%
“…If reaction conditions are not strictly maintained, it may cause inaccurate estimations of the analyte due to incomplete derivatization. The proposed analytical instruments are numerous for both separation including GC, LC, ion chromatography, and capillary electrophoresis and for detection including flame ionization detector (FID) or nitrogen phosphorous selective detector (NPD), MS, fluorescence or UV detection [18,20,22,[28][29][30][31][32][33][34][35]. A recently proposed approach uses impregnated glass fiber filters followed by the derivatization and LC-MS or LC-UV detection [20].…”
mentioning
confidence: 99%
“…HPLC with refractive index detection can be used to measure DEG reliably only down to 20-50 mg/L (Bonn, 1985; Day et al, 1985), much higher than the Canadian limit. Recent methods (Kaplan et al, 1982;Holzer, 1985;Bandion et al, 1985; Boneva and Dimov, 1981) utilizing capillary gas chromatography provide enough sensitivity, but the direct injection of wine results in a variety of chromatographic problems such as rapid degradation of column performance, contamination of the injector liner, adsorption, and poor reproducibility. In addition, the resulting chromatograms from direct analysis on polar columns are usually very complex and thus make the identification and quantitation difficult.…”
mentioning
confidence: 99%