Optimization of large-volume on-column injection conditions in gas chromatography by monitoring the actual carrier gas flow

Citation
T. Hankemeier et al., Optimization of large-volume on-column injection conditions in gas chromatography by monitoring the actual carrier gas flow, J CHROMAT A, 841(1), 1999, pp. 75-94
Citations number
18
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
841
Issue
1
Year of publication
1999
Pages
75 - 94
Database
ISI
SICI code
Abstract
The change of the evaporation rate of the solvent during injection and evap oration is the most critical aspect during optimization of large-volume on- column injection conditions in gas chromatography. The change is caused by the pressure drop along the retention gap when using an early solvent vapou r exit (SVE) and can be described by a mathematical model. Four procedures for the optimization of the injection conditions were compared. It was foun d that different procedures often yield different evaporation rates, which may also depend on the injection speeds used during optimization. For optim ization of a new set-up, i.e. if little is known about the optimal injectio n conditions, the evaporation rate should be determined by increasing the i njection time at a fixed injection speed, injection temperature and head pr essure; subsequently, an appropriate injection speed can be calculated. If a mere re-optimization is required as e.g, after the exchange of the retent ion gap, adjusting the evaporation rate to the injection speed by varying t he injection temperature at a constant injection speed is the preferred pro cedure. With both methods, optimization can be achieved by means of 2-5 inj ections of pure solvent and monitoring the helium carrier gas flow. That is , optimization of the injection conditions takes less than 1 h. When using this strategy, analytes as volatile as monochlorobenzene can be determined in aqueous samples by in-vial liquid-liquid extraction-gas chromatography-m ass spectrometry. Closing the SVE at the very end of solvent evaporation re sults in a considerable increase of the capacity of the retention gap compa red to closing the SVE before all solvent is evaporated. (C) 1999 Elsevier Science B.V. All rights reserved.