Please use this identifier to cite or link to this item: https://doi.org/10.1021/ac020428b
DC FieldValue
dc.titleHeadspace liquid-phase microextraction of chlorobenzenes in soil with gas chromatography-electron capture detection
dc.contributor.authorShen, G.
dc.contributor.authorLee, H.K.
dc.date.accessioned2014-10-16T08:29:57Z
dc.date.available2014-10-16T08:29:57Z
dc.date.issued2003-01-01
dc.identifier.citationShen, 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
dc.identifier.issn00032700
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93916
dc.description.abstractThe 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ac020428b
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ac020428b
dc.description.sourcetitleAnalytical Chemistry
dc.description.volume75
dc.description.issue1
dc.description.page98-103
dc.description.codenANCHA
dc.identifier.isiut000180233300021
Appears in Collections:Staff Publications

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