Published December 2019 | Version v1
Journal article

Determination of Sudan red contaminants at trace level from water samples by magnetic solid-phase extraction using Fe@NiAl-layered double hydroxide coupled with HPLC

  • 1. China University of Petroleum (Beijing), State Key Laboratory of Heavy Oil Processing, College of Chemical Engineering and Environment (China)

Description

Background

Sudan red dyes are widely used as color additions in various fields. Due to their potential carcinogenicity and large consumption, they have absorbed much more attention and become a research hot topic. There have been a few of existing methods for their analysis from samples; however, it is of great importance to develop simple, sensitive, and low-cost analytical method for public health and safety. This article described a new method based on magnetic Fe@NiAl-layered double hydroxides for enrichment of Sudan red dyes in combination with high-performance liquid chromatography.

Results

The as-prepared magnetic Fe@NiAl-layered double hydroxides (Fe@NiAl-LDHs) exhibited good adsorption capacity for Sudan red dyes, and could be used as an effective adsorbent for preconcentration of three Sudan Red dyes from environmental water samples. The proposed method provided low limits of detection in the range of 0.002–0.005 μg L−1 with magnetic solid-phase extraction in combination with high-performance liquid chromatography.

Conclusion

The developed method utilized the easy to prepare magnetic materials as adsorbents and conventional analytical instrument and provided high sensitivity, which provided a robust and low consumption of toxic organic solvent alternative method. The results of present study are of great value for interested laboratories to monitor the level of Sudan red dyes in water samples or develop sensitive determination methods to monitor other pollutants at trace level in environmental waters.

Additional details

Identifiers

Publishing Information

Journal Title
Environmental Sciences Europe
Journal Volume
31
Journal Issue
1
Journal Page Range
p. 1-10
ISSN
2190-4715

Optional Information

Copyright
Copyright (c) 2019 The Author(s)