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dc.contributor.authorOymak, Tülay
dc.contributor.authorTokalıoğlu, Şerife
dc.contributor.authorCam, Şafak
dc.contributor.authorDemir, Selçuk
dc.date.accessioned2020-12-19T19:35:00Z
dc.date.available2020-12-19T19:35:00Z
dc.date.issued2020
dc.identifier.citationOymak, T., Tokalıoğlu, Ş., Cam, Ş., & Demir, S. (2020). Determination of color additive tartrazine (E 102) in food samples after dispersive solid phase extraction with a zirconium-based metal-organic framework (UiO-66(Zr)-(COOH)2). Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 37(5), 731–741. https://doi.org/10.1080/19440049.2020.1726501en_US
dc.identifier.issn1944-0049
dc.identifier.issn1944-0057
dc.identifier.urihttps://doi.org/10.1080/19440049.2020.1726501
dc.identifier.urihttps://hdl.handle.net/11436/1211
dc.descriptionDemir, Selcuk/0000-0002-5719-7145en_US
dc.descriptionWOS: 000515051900001en_US
dc.descriptionPubMed: 32083510en_US
dc.description.abstractA new and rapid dispersive solid phase extraction method by using a green-synthesised UiO-66(Zr)-(COOH)(2) (Zr-BTeC) adsorbent with body-centred cubic (bcu) topology was developed for determination of tartrazine in food samples. Zr-BTeC was used for the first time as an adsorbent for tartrazine. It was synthesised and characterised by X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, Brunauer-Emmett-Teller surface area analysis, and zeta potential measurements. Tartrazine was determined at 405 nm spectrophotometrically. Experimental conditions were optimised in order to achieve quantitative recoveries. the sample acidity was found to be 0.02 mol L-1 HCl. the amount of Zr-BTeC was 10 mg. Both adsorption and elution contact times were only 5 s without the need for vortexing. Elution was with 2 mL of 0.5 mol L-1 NH3. A sample volume of 45 mL was selected as optimum. the adsorption capacity for tartrazine with Zr-BTeC was found to be 185 mg g(-1) and the adsorbent was reusable up to 40 cycles. the tartrazine concentrations found by the developed method in food supplements were compared with the results obtained by HPLC method for the same samples. Statistical analysis results showed that there are insignificant differences between the results of the two methods (p = .05). the method was successfully applied to the determination of tartrazine in spiked chewing gums, lemon flavoured icing glaze, and jelly samples.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTartrazineen_US
dc.subjectMetal-organic frameworken_US
dc.subjectGreen synthesisen_US
dc.subjectDispersive solid phase extractionen_US
dc.subjectSpectrophotometryen_US
dc.titleDetermination of color additive tartrazine (E 102) in food samples after dispersive solid phase extraction with a zirconium-based metal-organic framework (UiO-66(Zr)-(COOH)(2))en_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Fen - Edebiyat Fakültesi, Kimya Bölümüen_US
dc.contributor.institutionauthorCam, Şafak
dc.contributor.institutionauthorDemir, Selçuk
dc.identifier.doi10.1080/19440049.2020.1726501
dc.identifier.volume37en_US
dc.identifier.issue5en_US
dc.identifier.startpage731en_US
dc.identifier.endpage741en_US
dc.relation.journalFood Additives and Contaminants Part A-Chemistry Analysis Control Exposure & Risk Assessmenten_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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