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dc.contributor.authorAydoʇan, C. and Karakoç, V. and Denizli, A.
dc.date.accessioned2021-04-08T12:08:56Z
dc.date.available2021-04-08T12:08:56Z
dc.date.issued2015
dc.identifier10.1016/j.foodchem.2015.04.062
dc.identifier.issn03088146
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84928478097&doi=10.1016%2fj.foodchem.2015.04.062&partnerID=40&md5=327ea2e99381fcdbda69b18fc971da36
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4724
dc.description.abstractThis study describes the application of an open tubular capillary column for chiral ligand-exchange separation and determination of malic acid enantiomers in apple juice by open-tubular capillary electrochromatography (OT-CEC). The open tubular column was prepared by in-situ grafting polymerization of 3-chloro-2-hydroxypropyl methacrylate (HPMA-Cl) and followed by l-Histidine (l-His) modification. l-His was used as a chiral ligand-exchange selector and copper (II) as a central ion. The electrochromatographic characterization of the open tubular column was performed with the use of thiourea as an electroosmotic flow (EOF) marker. Factors affecting electrochromatographic enantioseparation of malic acid were also studied. The running buffer conditions for optimum enantioseparation of malic acid were found to be ACN/5.0 mM CuSO4, 20.0 mM (NH4)2SO4 (60/40%, v/v) adjusted to pH 3.0. The separation and determination of the enantiomers of malic acid in the apple juice solution diluted 10- to 40-folds were successfully achieved. © 2015 Elsevier Ltd. All rights reserved.
dc.language.isoEnglish
dc.sourceFood Chemistry
dc.titleChiral ligand-exchange separation and determination of malic acid enantiomers in apple juice by open-tubular capillary electrochromatography


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