A new analytical technique combining on-line supercritical fluid chromatography with capillary gas chromatography has been developed. The supercritical fluid sample effluent is decompressed througha restrictordirectlyintoaconventionalcapillary gas chromatographic injection port. This technique allow
On-line multidimensional chromatography using packed capillary liquid chromatography and capillary gas chromatography
β Scribed by Cortes, H. J. ;Pfeiffer, C. D. ;Richter, B. E.
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 427 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0935-6304
No coin nor oath required. For personal study only.
β¦ Synopsis
The introduction of selected fractions from a liquid chromatograph into a gas chromatograph has been described; however, analyses were performed by off-line experiments requiring collection and reinjection of the separate fractions or by on-line procedures where disadvantageously, only a fraction of the separated peak or a well resolved component in a mixturecould be introduced into a gas chromatograph. This disadvantage is overcome by the apparatus and method described in this paper, which utilizes a multidimensional chromatography system employing a high efficiency, packed capillary LCcolumn coupled on-line to a capillary gas chromatograph.
The liquid chromatograph (so designed) can act as a highly efficient clean-up or chemical class fractionation step prior to introduction into the gas chromatograph, significantly reducing sample preparation times in many applications. Thus minor components in a complex matrix can be determined without prior sample clean-up, an example of which is the determination of polychlorinated biphenyls in a complex hydrocarbon matrix. * The method and apparatus described in this publication are the subjects of pending patent applications.
π SIMILAR VOLUMES
## Abstract Capillary columns of 0.3β0.5 mm i.d. packed with 3β to 30βΞΌm silicaβbased stationary phases for liquid chromatography were used for gas chromatographic separation of hydrocarbons. Column efficiencies were evaluated for various commercially available packing material. The best column eff
In this article, fused silica capillaries with an inner diameter of 250 m were packed with 5-and 10-m spherical and irregular silica particles with pore sizes ranging from 60 to 300 A. The columns were investigated for high-speed Ε½ . separation seconds of light hydrocarbons under gas chromatographic
Reversed-phase packed capillary column liquid chromatography LC was investigated at column temperatures of 24ΠC, 40ΠC, 60ΠC, and 80ΠC. For a Ε½ . mixed mobile phase containing acetonitrile and water 72:28, vrv , the viscosity of the mobile phase decreased 2.2 times and the diffusion rate of the solut