Have a personal or library account? Click to login
Application of Molecular Imprinted Polymers for Selective Solid Phase Extraction of Bisphenol A Cover

Application of Molecular Imprinted Polymers for Selective Solid Phase Extraction of Bisphenol A

Open Access
|Dec 2016

Abstract

Selective molecularly imprinted polymers (MIPs) with bisphenol A as template were synthesized using the non-covalent imprinting approach. MIPs were prepared using thermally initiated polymerization with 1,1’-azobis(cyclohexanecarbonitryle) (ACHN) as initiator and ethylene glycol dimethacrylate (EDMA) as a cross-linking agent. The tested functional monomers included methacrylic acid, acrylamide, and 4-vinylpyridine. The selectivity of the BPA-MIP for the solid phase extraction of bisphenol A was tested in samples containing other related alkylphenols. The polymers prepared in acetonitrile using methacrylic acid or acrylamide as monomer showed the highest selectivity towards target analyte (the selectivity ratio 8:1, respectively for MIP and NIP). The proposed procedure has been proven to be an effective for selective extraction of bisphenol A in aqueous samples (recoveries over 85%) enabling detection and quantification limits of 25 and 70 μg/dm3, respectively based on 10 cm3 of sample volume, with relative standard deviations (RSD) lower than 6%. The obtained molecularly imprinted material showed interesting properties for selective extraction and preconcentration of studied analyte from large volumes of aqueous samples without any problems of cartridge clogging.

DOI: https://doi.org/10.1515/eces-2016-0046 | Journal eISSN: 2084-4549 | Journal ISSN: 1898-6196
Language: English
Page range: 651 - 664
Published on: Dec 30, 2016
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2016 Anna Poliwoda, Małgorzata Mościpan, Piotr P. Wieczorek, published by Society of Ecological Chemistry and Engineering
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.