4.6 Article

One-pot fabrication of functional magnetic adsorbent for efficient capture of mercury species in aqueous samples prior to HPLC analysis

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1685, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.chroma.2022.463622

关键词

Magnetic solid phase microextraction; Mercury species; Sorbent; Aqueous sample

资金

  1. National Natural Science Founda- tion of China
  2. Natural Science Foundation of Fu- jian Province
  3. XMU Training Program of Innovation and Enterpreneurship for Undergraduates
  4. [21976149]
  5. [2020J01045]

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Efficient extraction of mercury speciation was achieved by fabricating a new magnetic adsorbent using 4-vinylbenzeneboronic acid and 9-vinylanthracene. The adsorbent showed satisfactory entrapment performance towards different mercury species, and a sensitive and reliable approach for quantifying trace mercury was developed using HPLC/DAD. The established method exhibited low detection limits and good precision.
Efficient extraction is a vital step in mercury speciation. In this context, using 4-vinylbenzeneboronic acid and 9-vinylanthracene as functional monomers, a new magnetic adsorbent was fabricated accord-ing to one-pot hydrothermal approach. Various characterization results prove the as-prepared adsorbent presented abundant functional groups and saturation magnetism. Combining with magnetic solid phase extraction (MSPE), the adsorbent exhibited satisfactory entrapment performance towards different mer-cury species which had been pre-coordinated with dithizone to form metal-organic coordination. A series of parameters influencing the extraction performance were inspected in detail. Under the most beneficial conditions, sensitive and reliable approach to quantify trace methylmercury, ethylmercury, phenylmer-cury and inorganic mercury in aqueous samples was developed by the combination of HPLC/DAD. Limits of detection and precision located in the ranges of 0.012-0.074 mu g/L and 2.5-9.8%, respectively. Recoveries with low, medium and high fortified contents in actual waters varied from 79.8 to 119%. Confirmatory ex-periments were performed to evidence the accuracy and reliability of established approach. In addition, a possible mechanism was suggested based on the chemical nature of analytes, extraction conditions and characterization results.(c) 2022 Elsevier B.V. All rights reserved.

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