Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.chroma.2009.09.019
DC FieldValue
dc.titleCommercial polymeric fiber as sorbent for solid-phase microextraction combined with high-performance liquid chromatography for the determination of polycyclic aromatic hydrocarbons in water
dc.contributor.authorHii, T.M.
dc.contributor.authorBasheer, C.
dc.contributor.authorLee, H.K.
dc.date.accessioned2014-10-16T08:23:05Z
dc.date.available2014-10-16T08:23:05Z
dc.date.issued2009-10-30
dc.identifier.citationHii, T.M., Basheer, C., Lee, H.K. (2009-10-30). Commercial polymeric fiber as sorbent for solid-phase microextraction combined with high-performance liquid chromatography for the determination of polycyclic aromatic hydrocarbons in water. Journal of Chromatography A 1216 (44) : 7520-7526. ScholarBank@NUS Repository. https://doi.org/10.1016/j.chroma.2009.09.019
dc.identifier.issn00219673
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93329
dc.description.abstractA novel microextraction method making use of commercial polymer fiber as sorbent, coupled with high-performance liquid chromatography-fluorescence detection for the determination of polycyclic aromatic hydrocarbons (PAHs) in water has been developed. In this technique, the extraction device was simply a length (8 cm) of a strand of commercial polymer fiber, Kevlar (each strand consisted of 1000 filaments, each of diameter ca. 9.23 μm), that was allowed to tumble freely in the aqueous sample solution during extraction. The extracted analytes were desorbed ultrasonically before the extract was injected into HPLC system for analysis. Extraction parameters such as extraction time, desorption time, type of desorption solvent and sample volume were optimized. Each fiber could be used for up to 50 extractions and the method showed good precision, reproducibility and linear response within a concentration range 0.05-5.00 μg L-1 with correlation coefficients of up to 0.9998. Limits of detection between 0.4 and 4.4 ng L-1 for seven PAHs could be achieved. The relative standard deviations (n = 3) of this technique were between 2.9% and 12.1%. © 2009 Elsevier B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.chroma.2009.09.019
dc.sourceScopus
dc.subjectHigh-performance liquid chromatography
dc.subjectPolycyclic aromatic hydrocarbons
dc.subjectPolymeric fiber
dc.subjectSolid-phase microextraction
dc.subjectWater analysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.chroma.2009.09.019
dc.description.sourcetitleJournal of Chromatography A
dc.description.volume1216
dc.description.issue44
dc.description.page7520-7526
dc.description.codenJCRAE
dc.identifier.isiut000271250500028
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