Magnetic Covalent Organic Framework for Efficient Solid-Phase Extraction of Uranium for on-Site Determination by Portable X-ray Fluorescence Spectrometry.

Anal Chem

Key Lab of Green Chemistry and Technology of MOE and College of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China.

Published: April 2024

AI Article Synopsis

  • - Uranium is crucial for the nuclear industry, but its accidental release can lead to significant health and environmental risks, necessitating effective contamination detection methods.
  • - A new technique was developed that integrates magnetic dispersive solid-phase extraction (MDSPE) with portable X-ray fluorescence (XRF) to quickly identify trace uranium in samples without complicated equipment.
  • - The method uses a stable magnetic covalent organic framework to extract uranium efficiently, achieving a very low detection limit and demonstrating reliable performance in assessing real water samples rapidly.

Article Abstract

Uranium plays a pivotal role in the nuclear industry; however, its inadvertent release has raised concerns regarding health and environmental implications. It is crucial for a prompt warning and accurate tracing of uranium contamination in emergency scenarios. In this study, a novel and simple method was proposed that combines magnetic dispersive solid-phase extraction (MDSPE) with portable X-ray fluorescence spectrometry (XRF) for the on-site sampling and determination of trace uranium in real samples. A magnetic covalent organic framework (FeO@COF) composite with excellent chemical stability and a large adsorption capacity of 311 mg/g was synthesized and employed as an efficient adsorbent for the solid-phase extraction of trace uranium. Without the need for a centrifuge or filter requirement, the established method by benchtop wavelength-dispersive X-ray fluorescence spectrometry (WDXRF) exhibits an exceptionally low limit of detection (LOD) of 0.008 μg/L with a sample volume of 50 mL and a fast adsorption time of 15 min, rendering it suitable for environmental monitoring of UO. Consequently, this approach, in combination with a hand-held portable XRF instrument with an LOD of 0.1 μg/L, was successfully implemented for the on-site extraction and quality assessment of real water samples, yielding accurate results and satisfactory spike recoveries.

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Source
http://dx.doi.org/10.1021/acs.analchem.4c00063DOI Listing

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