Back to Search Start Over

Ion-imprinted beads for molecular recognition based mercury removal from human serum

Authors :
Adil Denizli
Serap Şenel
Arzu Ersöz
Rıdvan Say
Sinem Mirel
Müge Andaç
Anadolu Üniversitesi, Fen Fakültesi, Fizik Bölümü
Say, Rıdvan
Ersöz, Arzu
Source :
International Journal of Biological Macromolecules. 40:159-166
Publication Year :
2007
Publisher :
Elsevier BV, 2007.

Abstract

WOS: 000243674800014<br />PubMed ID: 16950507<br />The aim of this study is to prepare ion-imprinted polymers which can be used for the selective removal of mercury ions [Hg2+] from human serum. N-Methacryloyl-(L)-cysteine (MAC) was chosen as the complexing monomer. In the first step, Hg2+ was complexed with MAC and the Hg2+-imprinted poly(hydroxyethyl methacrylate-N-methacryloyl-(L)-cysteine) (MIP) beads were synthesized by suspension polymerization. After that. the template ions (i.e., Hg2+) were removed using thiourea (0.5%, v/v) in 0.05 M HCl. The specific surface area of the MIP beads was found to be 59.04 m(2)/g with a size range of 63-140 mu m in diameter and the swelling ratio was 91.5%. According to the elemental analysis results, the MIP beads contained 87.0 mu mol MAC/g polymer. The maximum adsorption capacity was 0.45 mg Hg2+/g beads. The applicability of two kinetic models including pseudo-first order and pseudo-second order model was estimated on the basis of comparative analysis of the corresponding rate parameters, equilibrium capacity and correlation coefficients. Results suggest that chemisorption processes could be the rate-limiting step in the adsorption process. The relative selectivity coefficients of MIP beads for Hg2+/Cd2+, Hg2+/Zn2+ were 14.7 and 21.5 times greater than the non-imprinted (NIP) matrix. respectively. The MIP beads could be used many times without decreasing in their adsorption capacities significantly

Details

ISSN :
01418130
Volume :
40
Database :
OpenAIRE
Journal :
International Journal of Biological Macromolecules
Accession number :
edsair.doi.dedup.....a85b113fd0e1f8706cf886a3e88e8e1c
Full Text :
https://doi.org/10.1016/j.ijbiomac.2006.07.002