Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13492
Title: Graphene/polyvinylpyrrolidone/polyaniline nanocomposite-modified electrode for simultaneous determination of parabens by high performance liquid chromatography
Authors: Kajornkavinkul S.
Punrat E.
Siangproh W.
Rodthongkum N.
Praphairaksit N.
Chailapakul O.
Keywords: Beverages
Chromatographic analysis
Cosmetics
Electrochemical electrodes
Graphene
High performance liquid chromatography
Liquids
Nanocomposites
Polyaniline
Propylparaben
Amperometric detection
Electrochemical behaviors
Electrospraying
Modified electrodes
Polyanilines (PAni)
Polyvinyl pyrrolidone
Screen-printed carbon electrodes
Simultaneous determinations
Parabens
4 hydroxybenzoic acid ester
aniline derivative
graphite
nanocomposite
polyaniline
povidone
chemistry
devices
electrospray mass spectrometry
high performance liquid chromatography
ion selective electrode
procedures
Aniline Compounds
Chromatography, High Pressure Liquid
Graphite
Ion-Selective Electrodes
Nanocomposites
Parabens
Povidone
Spectrometry, Mass, Electrospray Ionization
Issue Date: 2016
Abstract: A nanocomposite of graphene (G), polyvinylpyrrolidone (PVP) and polyaniline (PANI) modified onto screen-printed carbon electrode (SPCE) using an electrospraying technique was developed for simultaneous determination of five parabens in beverages and cosmetic products by high performance liquid chromatography. PVP and PANI were used as the dispersing agents of graphene, and also for the enhancement of electrochemical conductivity of the electrode. The electrochemical behavior of each paraben was investigated using the G/PVP/PANI nanocomposite-modified SPCE, compared to the unmodified SPCE. Using HPLC along with amperometric detection at a controlled potential of +1.2 V vs Ag/AgCl, the chromatogram of five parabens obtained from the modified SPCE exhibits well defined peaks and higher current response than those of its unmodified counterpart. Under the optimal conditions, the calibration curves of five parabens similarly provide a linear range between 0.1 and 30 μg mL-1 with the detection limits of 0.01 μg mL-1for methyl paraben (MP), ethyl paraben (EP) and propyl paraben (PP), 0.02 and 0.03 μg mL-1 for isobutyl paraben (IBP) and butyl paraben (BP), respectively. Furthermore, this proposed method was applied for the simultaneous determination of five parabens in real samples including a soft drink and a cosmetic product with satisfactory results, yielding the recovery in the range of 90.4-105.0%. © 2015 Elsevier B.V.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13492
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84949097632&doi=10.1016%2fj.talanta.2015.05.044&partnerID=40&md5=7e13d3160ea4a8f0519d41f19e5075fe
ISSN: 399140
Appears in Collections:Scopus 1983-2021

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