In this work a fast gas chromatography set-up with on-column injection was optimized and evaluated with a model mixture of C 8 -C 28 nalkanes. Usual injection volumes when using narrow-bore (e. g., 0.1 mm i.d.) analytical columns are ca. 0.1 lL. The presented configuration allows introduction of 10
Factors influencing chromatographic data in fast gas chromatography with on-column injection
✍ Scribed by Eva Matisová; Mária Šimeková; Svetlana Hrouzková; Peter Korytár; Milena Dömötörová
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 492 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The use of larger volume injection with on‐column injection and fast GC commercial instrumentation was evaluated with the model mixture of n‐alkanes of a broad range of volatility (C~10~–C~28~). The presented configuration allows introduction of 40–80‐fold larger sample volumes without any distortion of peak shapes compared to “usual” fast GC set‐ups using narrow‐bore columns. A normal‐bore retention gap (1–5 m×0.32 mm ID) was coupled to a narrow‐bore (5 m×0.1 mm ID×0.4 μm film thickness) analytical column using a standard press‐fit connector. The connection was tight and reliable, and hence suitable for hydrogen as carrier gas. The effect of pre‐column and analytical column connector, injection volume, pre‐column length, column inlet pressure, and analyte volatility on peak shape, peak broadening, and focusing are discussed. The precision of chromatographic data measurements and peak capacity under optimised temperature programmed conditions for fast separations with large volume injection were found to be very good. The presented fast GC set‐up with on‐column injection extends the applicability of the technique to trace analysis.
📜 SIMILAR VOLUMES
The dependence of the retention factor of compounds on the average pressure was theoretically considered for binary gas mixture on the basis of a new form of Langmuir adsorption equation taking into consideration the substitution reaction of the adsorbed molecule of the carrier gas for the adsorbed
A specific, sensitive, and accurate assay for quantitation of verapamil has been developed. The method involves a single extraction step with n-heptane, followed by evaporation at room temperature under nitrogen. 0.1 pi of the extract was injected into a capillary column coated with crosslinked 5% p