Solvent trapping reconcentrates volatile components after injection or on-line transfer of large volumes. When an early vapor exit is used, typically after a 5-10 m x 0.53 mm i.d. uncoated precolumn, the solvent trapping process differs from that described previously. The visual experiments and the conclusions drawn therefrom, as described in a previous paper, are supplemented with chromatographic results. They show that even hexane ran be quantitatively analyzed in 250 mu l of a pentane solution. Injection of a volume of 250 mu 1 by vaporizer/precolumn solvent splitting was used in the analysis of gasoline in drinking water. Conditions for the transfer of a 1000 mu l volume can easily be adjusted through detection of the front end of the f...
The iterative trapping method has been developed for concentrating gaseous volatile organic compound...
The use of a programmed temperature vaporiser (PTV) with a packed liner was evaluated for the inject...
The application range of the on-line solid-phase extraction-gas chromatographic (SPE-GC) analysis of...
In the present study the retaining precolumn, which is commonly used in a set-up for large-volume on...
When 0.53 mm i.d. uncoated precolumns connected to a solvent vapor exit are used for sample introduc...
0.53 mm i.d. uncoated precolumns of about 10 m in length followed by a solvent vapor exit have becom...
The change of the evaporation rate of the solvent during injection and evaporation is the most criti...
Monitoring of the helium flow into a gas chromatograph (GC) by means of an electronic flow meter has...
In the first part of this thesis, strategies for avoiding systematic errors when quantifying the mai...
In gas chromatography (GC) large volume injection of samples containing very high molecular weight a...
A new method for the introduction of large sample sizes using a temperature programmed injector and ...
To be productive the columns are usually overloaded in preparative chromatography. It is well known ...
The newly developed dynamic solvent effect (DSE) sampling technique for capillary gas chromatography...
In preparative chromatography often the solubility of samples to be separated is low in mobile phase...
The iterative trapping method has been developed for concentrating gaseous volatile organic compound...
The use of a programmed temperature vaporiser (PTV) with a packed liner was evaluated for the inject...
The application range of the on-line solid-phase extraction-gas chromatographic (SPE-GC) analysis of...
In the present study the retaining precolumn, which is commonly used in a set-up for large-volume on...
When 0.53 mm i.d. uncoated precolumns connected to a solvent vapor exit are used for sample introduc...
0.53 mm i.d. uncoated precolumns of about 10 m in length followed by a solvent vapor exit have becom...
The change of the evaporation rate of the solvent during injection and evaporation is the most criti...
Monitoring of the helium flow into a gas chromatograph (GC) by means of an electronic flow meter has...
In the first part of this thesis, strategies for avoiding systematic errors when quantifying the mai...
In gas chromatography (GC) large volume injection of samples containing very high molecular weight a...
A new method for the introduction of large sample sizes using a temperature programmed injector and ...
To be productive the columns are usually overloaded in preparative chromatography. It is well known ...
The newly developed dynamic solvent effect (DSE) sampling technique for capillary gas chromatography...
In preparative chromatography often the solubility of samples to be separated is low in mobile phase...
The iterative trapping method has been developed for concentrating gaseous volatile organic compound...
The use of a programmed temperature vaporiser (PTV) with a packed liner was evaluated for the inject...
The application range of the on-line solid-phase extraction-gas chromatographic (SPE-GC) analysis of...