## Abstract Large‐volume injection is an attractive means to improve detection limits when analyzing dilute sample extracts. There is now no need to achieve enrichment by means of solvent evaporation, which makes the total analytical procedure less reliable and less robust due to loss of volatile c
Large Volume Injection in Fast Gas Chromatography with On-Column Injector
✍ Scribed by Korytár, Peter ;Matisová, Eva ;Lefflerová, Henrieta ;Slobodník, Jaroslav
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 87 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0935-6304
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✦ Synopsis
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 -30-fold larger sample volumes without any distortion of peak shapes. In the set-up a normal-bore retention gap (1 m60.32 mm i. d.) was coupled to a narrow-bore (4.8 m60.1 mm i. d.60.4 lm film thickness) analytical column using a low dead volume column connector. The effects of the experimental conditions such as inlet pressure, sample volume, initial injection temperature, and oven temperature on a peak focusing are discussed. H-u curves for helium and hydrogen are used to compare their suitability for high speed gas chromatography and to show the dependence of separation efficiency on the carrier gas velocity at high inlet pressures. In the fast gas chromatography system a baseline separation of C 10 -C 28 n-alkanes was achieved in less than 3 minutes.
📜 SIMILAR VOLUMES
## Abstract A direct injection method for large volume samples which avoids severe tailing of the solvent peak has been developed using a packed column injector (up to 100 μl) leading into an ordinary capillary column (0.3 mm i.d.). Modifications are made to the cooler zones of the inlet port and o
Automated large volume (25-200 1-11) on-column injections into a gas chromatograph with a capillary column were successfully performed by coupling a retention gap technique with an air actuated rotary valve. The linearity, injection precision, and carryover were evaluated. Slight boiling point discr
## 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 with