• 文献标题:   Development of a new strategy for the synthesis of graphene oxide-alumina nanocomposite as an efficient adsorbent for dispersive solid-phase extraction of parabens
  • 文献类型:   Article
  • 作  者:   TAHMASEBI E, SATTARI R
  • 作者关键词:   alumina, aluminium polycation, graphene oxide, paraben, solidphase extraction
  • 出版物名称:   JOURNAL OF SEPARATION SCIENCE
  • ISSN:   1615-9306 EI 1615-9314
  • 通讯作者地址:  
  • 被引频次:   0
  • DOI:   10.1002/jssc.202200698 EA NOV 2022
  • 出版年:   2023

▎ 摘  要

The present study investigates the synthesis and application of the graphene oxide-alumina nanocomposite as a new adsorbent for the dispersive solid-phase extraction of three parabens and their determination using high-performance liquid chromatography-ultraviolet detection. The characterization of the synthesized material was accomplished and its size, morphology, chemical composition, porosity, and thermal stability were studied. Application of the proposed strategy for the synthesis of the nanocomposite resulted in the incorporation of Al2O3 nanoparticles into graphene oxide nanosheets, further resulting in the exfoliation of graphene oxide nanosheets increasing their surface area. An orthogonal rotatable central composite design was used to optimize the extraction. Under the optimum conditions, the analytical performance of the method showed a suitable linear dynamic range (0.2-100.0 mu g/L), reasonable limits of detection (0.03-0.05 mu g/L), and preconcentration factors ranging from 128 to 173. Finally, the new validated method was applied for the determination of parabens in some real samples including wastewater, cream, toothpaste, and juice samples with satisfactory recoveries (88%-109%), and relative standard deviations less than 8.7% (n = 3). Results demonstrated that inserting alumina nanoparticles into graphene oxide nanosheets improved the extraction efficiency of parabens, as polar acidic compounds, by providing additional efficient interactions including hydrogen bonding, dipole-dipole, and Bronsted and Lewis acid-base interactions.