Send to

Choose Destination
J Chromatogr A. 2013 Mar 29;1283:20-6. doi: 10.1016/j.chroma.2013.01.110. Epub 2013 Feb 4.

Preparation of polydopamine coated Fe₃O₄ nanoparticles and their application for enrichment of polycyclic aromatic hydrocarbons from environmental water samples.

Author information

State Key Laboratory of Environmental Chemistry and Ecotoxicology of Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.


Core/shell structured magnetic Fe3O4/polydopamine (Fe3O4/PDA) nanoparticles have been successfully synthesized and developed as a magnetic solid-phase extraction (SPE) adsorbent in dispersion mode for the determination of trace polycyclic aromatic hydrocarbons (PAHs) in environmental samples. The Fe3O4/PDA synthetic procedure is simple and involves no organic solvents. Only 20mg of Fe3O4/PDA adsorbents are required to extract PAHs from 500mL water samples. The adsorption attains equilibrium rapidly and analysts are eluted with acetonitrile readily. The extraction efficiency is not influenced by salt concentrations up to 300mM and pH values over the range 4-11. Under optimized conditions, the detection limits of PAHs are in the range of 0.5-1.9ngL(-1). The accuracy of the method is evaluated by the recoveries of PAHs from environmental samples. Good recoveries (76.4-107%) with low relative standard deviations from 1.0% to 9.7% are achieved. Comparison study shows that the recoveries of target PAHs are low when they are extracted using traditional SPE method even with the addition of methanol or tetrabutylammonium bromide surfactants in water samples, suggesting great application potential of magnetic SPE method to preconcentrate highly hydrophobic contaminants (such as PAHs) from large volume of water samples. This new SPE method provides several advantages, such as simplicity, low environmental impact, high extraction efficiency, high breakthrough volumes, convenient extraction procedure, and short analysis time.

[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center