Facile preparation of surface-exchangeable core@shell iron oxide@gold nanoparticles for magnetic solid-phase extraction: Use of gold shell as the intermediate platform for versatile adsorbents with varying self-assembled monolayers
Creators
- 1. Graduate School, University of Chinese Academy of Sciences, Beijing 100049 (China)
- 2. Beijing National Laboratory of Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China)
Description
Graphical abstract: -- Highlights: •The core@shell Fe3O4@Au nanoparticles functionalized with SAMs were successfully constructed. •The SAMs could be transformed from one kind to another via thiol exchange process. •The developed nanomaterials could be applied in mode switching MSPE. -- Abstract: The core@shell Fe3O4@Au nanoparticles (NPs) functionalized with exchangeable self-assembled monolayers have been developed for mode switching magnetic solid-phase extraction (MSPE) using high performance liquid chromatography with ultraviolet detection. The adsorbents were synthesized by chemical coprecipitation to prepare magnetic cores followed by sonolysis to produce gold shells. Functionalization of Fe3O4@Au NPs surface was realized through self-assembly of commercially available low molecular weight thiol-containing ligands using gold shells as intermediate platform and the dynamic nature of Au–S chemistry allowed substituent of one thiol-containing ligand with another simply by thiol exchange process. The resultant adsorbents were characterized by transmission electronic microscopy, Fourier transform infrared spectroscopy, elemental analysis, contact angle measurement, and vibrating sample magnetometry. To evaluate the versatile performance of the developed MSPE adsorbents, they were applied for normal-phase SPE followed by reversed-phase SPE. A few kinds of diphenols and polycyclic aromatic hydrocarbons (PAHs) were employed as model analytes, respectively. The predominant parameters affecting extraction efficiency were investigated and optimized. Under the optimum experimental conditions, wide dynamic linear range (6.25–1600 μg L−1 for diphenols and 1.56–100 μg L−1 for PAHs) with good linearity (r2 ≥ 0.989) and low detection limits (0.34–16.67 μg L−1 for diphenols and 0.26–0.52 μg L−1 for PAHs) were achieved. The advantage of the developed method is that the Fe3O4@Au NPs could be reutilized for preconcentrating diverse target analytes in different SPE modes sequentially simply through treatment with desired thiol-containing ligands
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aca.2013.12.020Additional details
Identifiers
- DOI
- 10.1016/j.aca.2013.12.020;
- PII
- S0003-2670(13)01569-9;
Publishing Information
- Journal Title
- Analytica Chimica Acta
- Journal Volume
- 811
- Journal Page Range
- p. 36-42
- ISSN
- 0003-2670
- CODEN
- ACACAM
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45040860
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ADSORBENTS; EXTRACTION; FERRITES; FOURIER TRANSFORM SPECTROMETERS; GOLD; HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY; IRON OXIDES; MAGNETIC CORES; NANOSTRUCTURES; PARTICLES; PHENOLS; POLYCYCLIC AROMATIC HYDROCARBONS; SOLIDS; THIOLS; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- AROMATICS; CHALCOGENIDES; CHROMATOGRAPHY; ELECTRON MICROSCOPY; ELEMENTS; FERRIMAGNETIC MATERIALS; HYDROCARBONS; HYDROXY COMPOUNDS; IRON COMPOUNDS; LIQUID COLUMN CHROMATOGRAPHY; MAGNETIC MATERIALS; MAGNETIC STORAGE DEVICES; MATERIALS; MEASURING INSTRUMENTS; MEMORY DEVICES; METALS; MICROSCOPY; ORGANIC COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; SEPARATION PROCESSES; SPECTROMETERS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.