Variable splitter for regulation of the solvent evaporation rate in the coupling of liquid chromatography with gas chromatography
✍ Scribed by Dolecka, Ewa ;Vreuls, Jolan J. ;de Jong, Gerhardus J. ;Th. Brinkman, Udo A. ;Maris, Frans A.
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 482 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0935-6304
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A system is described which accelerates the solvent evaporation rate in the retention gap. The evaporation is due to a saturation effect of the carrier gas stream, and a considerable increase in evaporation rate is obtained by inserting a split outlet between the retention gap and the capillary separation column in the gas chromatograph. By varying the backpressure of the spliter device, the flow rate through the retention gap can be adjusted and so too the evaporation rate. The evaporation process was monitored by inserting a dectecter in the split outlet line. The technique was applied to the on‐line LC trace enrichment/GC analysis of water containing a mixture of polycyclic aromatic hydrocarbons.
📜 SIMILAR VOLUMES
## Abstract An on‐line coupled supercritical fluid extraction–liquid chromatography–gas chromatography–mass spectrometry (SFE‐LC‐GC‐MS) system was constructed and applied for the quantitative analysis of selected organic acids. In SFE the analytes were derivatized __in situ__ with pentafluorobenzyl
## Abstract In trace analysis by capillary GC it is often desirable to use larger than normal injection volumes to obtain sufficient sensitivity. This, however, results in a wider solvent peak and tailing, and may reduce column efficiency. This paper describes the use of a short length of a capilla
## Abstract The triacylglycerol composition of olive oil samples has been determined by stereospecific analysis after partial hydrolysis with ethyl magnesium bromide, derivatization, preparative chiral HPLC, transesterification, and GC quantitation of fatty acid methyl esters. The data obtained for
## Abstract An optimized 2‐D liquid chromatography (LC×LC) set‐up, based on the different selectivities of a silver ion (Ag) and a non‐aqueous reversed phase (NARP), employed in the first (D1) and the second dimension (D2), respectively, in combination with evaporative light‐scattering detection (E