4.7 Article

Preparation and Characterization of Superparamagnetic Molecularly Imprinted Polymers for Selective Adsorption and Separation of Vanillin in Food Samples

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 62, Issue 46, Pages 11138-11145

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jf504144g

Keywords

superparamagnetism; water-compatible; magnetic molecularly imprinted polymers; vanillin; selective adsorption

Funding

  1. National Natural Science Foundation of China [21201098, 51102131, 31160317, 21275158, 21105117]
  2. Jiangxi Department of Education Fund [GJJ13039]
  3. Specialized Research Fund for the Doctoral Program of Higher Education [20113601110004]

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Novel water-compatible superparamagnetic molecularly imprinted polymers (M-MIPs) were prepared by coating superparamagnetic Fe3O4 nanoparticles with MIPs in a methanol-water reaction system. The M-MIPs were used for the selective adsorption and separation of vanillin from aqueous solution. The M-MIPs were characterized by X-ray powder diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), and scanning electron microscopy (SEM). Results indicated that a core shell structure of M-MIPs was obtained by coating a layer of silica and MIPs on the surface of the Fe3O4 nanoparticles. The obtained M-MIPs possess a loose and porous structure and can be rapidly separated from the solution using a magnet. The adsorption experiments showed that the binding capacity of the M-MIPs was significantly higher than that of the superparamagnetic non-molecularly imprinted polymers (M-NIPs). Meanwhile, the adsorption of M-MIP's reached equilibrium within 100 min, and the apparent maximum adsorption quantity (Q(max)) and dissociation constant (K-d) were 64.12 mu mol g(-1) and 58.82 mu mol L-1, respectively. The Scatchard analysis showed that homogeneous binding sites were formed on the M-MIP surface. The recoveries of 83.39-95.58% were achieved when M-MIPs were used for the pre-concentration and selective separation of vanillin in spiked food samples. These results provided the possibility for the separation and enrichment of vanillin from complicated food matrices by M-MIPs.

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