4.6 Article

Surfactant-modified flowerlike layered double hydroxide-coated magnetic nanoparticles for preconcentration of phthalate esters from environmental water samples

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1414, Issue -, Pages 22-30

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2015.07.105

Keywords

Magnetic layered double hydroxide; Solid-phase extraction; Magnetic; Mixed hemimicelles; Surfactants; Concentration

Funding

  1. National Natural Science Foundation of China [41222026, 41130743, 21277152]

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A novel type of layered, flowerlike magnetic double hydroxide (MLDH) nanoparticles modified by surfactants has been successfully synthesized and was applied as an effective sorbent for pre-concentration of several phthalate ester pollutants (PAEs) from water prior to quantification. The MLDH was obtained via a simple ultrasound-assisted method by using silica coated Fe3O4 as the core and anisotropic Mg-Al layered double hydroxide (Mg-Al LDH) nanocrystals as the shell to which analytes were absorbed. Orientation and dimensionality hierarchical structure as well as the large expandable interlayer free space and positive charge of the Mg-Al LDH shell make it easier to form anionic surfactant micelles on its surface via self-assembly. Due to its high adsorption area, compared with non-mesoporous nano solid-phase extraction agents, mesoporous channel shell and reduction diffusion path, MLDH exhibited high extraction efficiency of organic target residues. Under optimized conditions, with a total of 30 mg of adsorbant added to from samples containing 400 mL water from the environment recoveries of DPP, DBP, DCP and DOP were consistent with ranges of 69-101%, 79-101%, 86-102% and 63-100%, respectively. Standard deviations of recoveries ranged from 1 to 7%, respectively and the method was sensitive with limits of detection of 12.3, 18.7, 36.5 and 15.6 ng L-1. To the best of our knowledge, this is the first report of use of surfactant-modified MLDH nanoparticles and its application as adsorbent to pre-concentration of PAEs from environmental water samples prior to instrumental analyses. (C) 2015 Elsevier B.V. All rights reserved.

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