Please use this identifier to cite or link to this item:
|Title:||Headspace liquid-phase microextraction of chlorobenzenes in soil with gas chromatography-electron capture detection|
|Citation:||Shen, G., Lee, H.K. (2003-01-01). Headspace liquid-phase microextraction of chlorobenzenes in soil with gas chromatography-electron capture detection. Analytical Chemistry 75 (1) : 98-103. ScholarBank@NUS Repository. https://doi.org/10.1021/ac020428b|
|Abstract:||The organic solvent film formed in a microsyringe barrel was used as an extraction interface in headspace liquidphase microextraction (HS-LPME) of chlorobenzenes. Some common organic solvents with different vapor pressures (9.33-12 918.9 Pa) were studied as extractants. The results indicated that even the solvent with the highest vapor pressure (cyclohexane) can be used to carry out the extraction successfully. In general, the reasons for successful extraction are the very small space (5 mm3) within the microsyringe barrel and the fast equilibrium between gaseous analytes and organic solvent film. Both of these factors significantly reduced the risk of solvent loss during extraction. Thus, the choice of extraction solvent for the present method was very flexible. From the viewpoint of extraction efficiency, toluene (which has relatively low vapor pressure) was found to provide the best extraction efficiency. The effects of sampling volume, organic solvent volume, syringe withdrawal rate, and number of extraction cycles were also investigated. The procedure with respect to repeatability and limits of detection was evaluated by soil spiked with chlorobenzenes. Repeatability was between 5.7 and 17.7%, and the limits of detection were 6-14 ng/g. HS-LPME was shown to be an inexpensive, fast, and simple sample preparation method for volatile compounds.|
|Source Title:||Analytical Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Dec 11, 2018
WEB OF SCIENCETM
checked on Dec 3, 2018
checked on Dec 14, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.