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dc.contributor.authorTemel N.K.
dc.contributor.authorGürkan R.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:33:31Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:33:31Z
dc.date.issued2017
dc.identifier.issn1936-9751
dc.identifier.urihttps://dx.doi.org/10.1007/s12161-017-0973-4
dc.identifier.urihttps://hdl.handle.net/20.500.12418/5764
dc.description.abstractIn the present study, due to use of formaldehyde (FA) as a food additive as well as its endogenous and natural occurrence in aquatic products, a new preconcentration method for the quantification of free formaldehyde (FA) in beverages was developed before analysis by spectrophotometry at 538 nm. The method is based on spontaneously Cannizzaro disproportionation of FA with Variamine blue (VBH2) in the presence of ionic surfactant, sodium dodecylsulfate (SDS) as both sensitivity enhancer and counter ion at pH 7.0, and then extraction of the formed ion-pairing complex into the nonionic surfactant, polyethylene glycol tert-octylphenyl ether (Triton X-114). The effect of analytical variables was evaluated in detail, and the optimal working conditions were established. There was a rectilinear relationship in the range of 2–400 ?g L?1 with changing sensitivity. The limits of detection and quantification of the method with a sensitivity enhancement of 65 after preconcentration were 0.53 and 1.76 ?g L?1, respectively. The accuracy was validated by using two spiked quality control samples in linear working range and by comparing the results obtained from the samples with those of independent method, which is known as a slight modified acetylacetone method. It has been observed that the results obtained by both methods are statistically compatible with a t value ranging from 0.09 to 0.65 (tcritical 2.31). The intra-day and inter-day precisions as a result of stabilization of mixed micellar system were lower than 4.9% (as RSD%, n 5), and the recoveries were quantitatively higher than 95% for the two quality control samples spiked with 10, 25, and 50 ?g L?1 with satisfactory results. The method was successfully applied to the quantification of low levels of free FA in selected beverage matrices. © 2017, Springer Science+Business Media, LLC.en_US
dc.language.isoengen_US
dc.publisherSpringer New York LLCen_US
dc.relation.isversionof10.1007/s12161-017-0973-4en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBeveragesen_US
dc.subjectFormaldehydeen_US
dc.subjectSDSen_US
dc.subjectSpectrophotometryen_US
dc.subjectTriton X-114en_US
dc.subjectUA-CPEen_US
dc.subjectVariamine blueen_US
dc.titleExtraction, Preconcentration, and Quantification of Low Levels of Free Formaldehyde from Some Beverage Matrices by Combination of Ultrasound-Assisted-Cloud Point Extraction with Spectrophotometryen_US
dc.typearticleen_US
dc.relation.journalFood Analytical Methodsen_US
dc.contributor.departmentTemel, N.K., Department of Chemistry, University of Cumhuriyet, Faculty of Sciences, Sivas, 58140, Turkey -- Gürkan, R., Department of Chemistry, University of Cumhuriyet, Faculty of Sciences, Sivas, 58140, Turkeyen_US
dc.identifier.volume10en_US
dc.identifier.issue12en_US
dc.identifier.endpage4037en_US
dc.identifier.startpage4024en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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