The main focus of the present research was the on-line coupling of two separation techniques, namely liquid chromatography (LC) and gas chromatography (GC). For such an analytical combination, a dedicated interface is required to remove solvent from the sample, leaving the latter in a sharp band at the head of the GC column. Considering such an objective, a lab-developed LC-GC interface is herein presented, based on the use of a six-port two-position valve and a programmed-temperature-vaporizing (PTV) injector. The PTV injector was derived from a commercial split/splitless injector body, heated using a resistance heating wire, and enabled a satisfactory recovery of low boiling compounds (≤ C13), working in the normal-phase mode. The lab-developed PTV injector allowed the use of a larger-volume liner (compared to the commercial one initially used), it being characterized by dimensions 95 mm length × 5.0 mm O.D. × 3.4 mm I.D. and a volume of 862 µL, thus facilitating the transfer of larger LC fractions. The developed system is fully automatized and controlled without the use of additional software. The interface was evaluated and used for the analysis of mineral oil saturated hydrocarbons in vegetable oils. Detection was carried out by using a flame ionization detector (FID), with quantification performed through external calibration, across the 5–1000 mg kg−1 range. The LC-GC-FID method linearity, limits of detection and quantification, accuracy and precision were measured. The resulting limits of detection and quantification values were 0.4 and 1.3 mg kg−1, respectively. The average accuracy at the 100 mg kg−1 level was 95.5% (ranging between 93.3 and 99.7%). Intra-day repeatability at levels of 5 and 100 mg kg−1 were 2.4% and 3.5%, respectively.
A lab-developed interface for liquid-gas chromatography coupling based on the use of a modified programmed-temperature-vaporizing injector
Zoccali M.Primo
;Tranchida P. Q.Secondo
;Mondello L.
Ultimo
2020-01-01
Abstract
The main focus of the present research was the on-line coupling of two separation techniques, namely liquid chromatography (LC) and gas chromatography (GC). For such an analytical combination, a dedicated interface is required to remove solvent from the sample, leaving the latter in a sharp band at the head of the GC column. Considering such an objective, a lab-developed LC-GC interface is herein presented, based on the use of a six-port two-position valve and a programmed-temperature-vaporizing (PTV) injector. The PTV injector was derived from a commercial split/splitless injector body, heated using a resistance heating wire, and enabled a satisfactory recovery of low boiling compounds (≤ C13), working in the normal-phase mode. The lab-developed PTV injector allowed the use of a larger-volume liner (compared to the commercial one initially used), it being characterized by dimensions 95 mm length × 5.0 mm O.D. × 3.4 mm I.D. and a volume of 862 µL, thus facilitating the transfer of larger LC fractions. The developed system is fully automatized and controlled without the use of additional software. The interface was evaluated and used for the analysis of mineral oil saturated hydrocarbons in vegetable oils. Detection was carried out by using a flame ionization detector (FID), with quantification performed through external calibration, across the 5–1000 mg kg−1 range. The LC-GC-FID method linearity, limits of detection and quantification, accuracy and precision were measured. The resulting limits of detection and quantification values were 0.4 and 1.3 mg kg−1, respectively. The average accuracy at the 100 mg kg−1 level was 95.5% (ranging between 93.3 and 99.7%). Intra-day repeatability at levels of 5 and 100 mg kg−1 were 2.4% and 3.5%, respectively.File | Dimensione | Formato | |
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