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Development of a rapid and sensitive method for the simultaneous determination of 1,2-dibromoethane, 1,4-dichlorobenzene and naphthalene residues in honey using HS-SPME coupled with GC-MS

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dc.contributor.author Tsimeli, K en
dc.contributor.author Triantis, TM en
dc.contributor.author Dimotikali, D en
dc.contributor.author Hiskia, A en
dc.date.accessioned 2014-03-01T01:28:09Z
dc.date.available 2014-03-01T01:28:09Z
dc.date.issued 2008 en
dc.identifier.issn 00032670 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/18732
dc.subject 1,4-Dichlorobenzene en
dc.subject Headspace solid-phase microextraction en
dc.subject Honey en
dc.subject Naphthalene and 1,2-dibromoethane en
dc.subject Residues en
dc.subject.other Benzene en
dc.subject.other Calibration en
dc.subject.other Correlation methods en
dc.subject.other Gas chromatography en
dc.subject.other Mass spectrometry en
dc.subject.other Naphthalene en
dc.subject.other 1,2-dibromoethane en
dc.subject.other Headspace solid-phase microextraction en
dc.subject.other Honey en
dc.subject.other Ion monitoring en
dc.subject.other Residues en
dc.subject.other Ethane en
dc.subject.other 1,2 dibromoethane en
dc.subject.other 1,4 dichlorobenzene en
dc.subject.other dimeticone en
dc.subject.other naphthalene en
dc.subject.other sodium chloride en
dc.subject.other accuracy en
dc.subject.other adsorption en
dc.subject.other article en
dc.subject.other calibration en
dc.subject.other concentration (parameters) en
dc.subject.other correlation coefficient en
dc.subject.other gas chromatography en
dc.subject.other headspace solid phase microextraction en
dc.subject.other honey en
dc.subject.other ion monitoring en
dc.subject.other mass spectrometry en
dc.subject.other measurement en
dc.subject.other priority journal en
dc.subject.other sensitivity analysis en
dc.subject.other solid phase microextraction en
dc.subject.other standard en
dc.subject.other temperature en
dc.subject.other thickness en
dc.subject.other time en
dc.title Development of a rapid and sensitive method for the simultaneous determination of 1,2-dibromoethane, 1,4-dichlorobenzene and naphthalene residues in honey using HS-SPME coupled with GC-MS en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.aca.2008.03.049 en
heal.identifier.secondary http://dx.doi.org/10.1016/j.aca.2008.03.049 en
heal.publicationDate 2008 en
heal.abstract A new method for the simultaneous determination of 1,4-dichlorobenzene (p-DCB), naphthalene and 1,2-dibromoethane (1,2-DBE) residues in honey has been developed. Analysis is carried out using gas chromatography-mass spectrometry (GC/MS) in selected ion monitoring mode (SIM), after extraction and preconcentration of target analytes by headspace solid-phase microextraction (HS-SPME), with a 100 μm film thickness polydimethylsiloxane (PDMS) fiber. Several parameters affecting the extension of the adsorption process (i.e., addition of salt, extraction time, extraction temperature) were studied. The optimal conditions for the determination of these analytes were established. The proposed HS-SPME method showed good sensitivity, without carryover between the samples. Linearity was studied from 5 to 2500 μg kg-1 for p-DCB, 0.5 to 500 μg kg-1 for naphthalene and 5 to 500 μg kg-1 honey for 1,2-DBE with correlation coefficients (r2) ranging from 0.9901 to 0.9999. Precision was assessed and both intra and inter-day R.S.D.s (%) were below 6.3%. The detection limits were found to be 1, 0.1 and 2 μg kg-1 honey for p-DCB, naphthalene and 1,2-DBE, respectively. The percentage recoveries that were evaluated with the proposed HS-SPME method and the standard addition calibration technique gave values among 72.8 and 104.3% for measurements in samples spiked with one target analyte or mixtures of the three. This method has been applied for the analysis of unknown honey samples. The results showed an excellent applicability of the proposed method for the determination of the target compounds in honey samples. © 2008 Elsevier B.V. All rights reserved. en
heal.journalName Analytica Chimica Acta en
dc.identifier.doi 10.1016/j.aca.2008.03.049 en
dc.identifier.volume 617 en
dc.identifier.issue 1-2 en
dc.identifier.spage 64 en
dc.identifier.epage 71 en


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