4.6 Article

Effect of Environmental Factors on Estrogenic Compounds Adsorption by MIP

Journal

WATER AIR AND SOIL POLLUTION
Volume 210, Issue 1-4, Pages 255-264

Publisher

SPRINGER INTERNATIONAL PUBLISHING AG
DOI: 10.1007/s11270-009-0247-x

Keywords

Selective adsorption; Molecular imprinted polymer; Estrogenic compounds; Environmental factors

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In this study, the effects of environmental factors, including humic acid (HA), pH, ionic strength, and the coexistence of competing estrogenic compounds, on the adsorption of four typical estrogenic compounds, estrone (E1), 17 beta-estradiol (E2), 17 alpha-ethinylestradiol (EE2), and bisphenol A (BPA), were studied by molecularly imprinted polymer (MIP). The adsorption capacities of MIP for E2 were 116.3, 118.5, 127.0, and 109.0 A mu mol/g at HA concentrations of 0, 5, 15, and 20 mg/L in total organic carbon, respectively, while the corresponding adsorption capacities of nontemplate imprinted polymer (NIP) for E2 were 98.1, 109.4, 113.8, and 98.0 A mu mol/g. This implied that no significant trend could be found with the increasing HA concentrations. Furthermore, the selective adsorption capacity, represented by the difference in adsorption capacities between MIP and NIP, was not affected significantly. Similar observations were noted for E1, EE2, and BPA in the presence of HA. Ionic strength did not exert a considerable influence on the adsorption capacities of MIP and NIP for E1, E2, and BPA. However, at 0 mM of NaCl, EE2 adsorption capacities of MIP and NIP were 124.7 and 111.7 A mu mol/g, respectively, while the corresponding adsorption capacities were 144.7 and 138.2 A mu mol/g at 10 mM of NaCl due to the increased hydrophobic interactions. Nevertheless, the selective adsorption capacity was not significantly affected by the range of ionic strength tested in this study. The study demonstrated that there was no significant effect of pH on the adsorption capacity of both MIP and NIP from pH 3.1 to 9 and that no considerable effect of pH on selective adsorption capacity of MIP could be established. However, the adsorption capacities of MIP and NIP for E2 at pH 9 were 95.1 and 82.9 A mu mol/g, while at pH 11, the adsorption capacities were 12.1 and 5.9 A mu mol/g correspondingly. This means that adsorption capacity and selective adsorption capacity were influenced significantly due to the ionization of target compounds. A similar trend was observed for E1, EE2, and BPA. The study on the effect of the coexistence of competing estrogenic compounds demonstrated that selective adsorption capacities of MIP can be influenced. Differences between MIP and NIP for E1, E1, EE2, and BPA under competing conditions were 8.8, 6.8, 10.2, and 4.2 A mu mol/g, respectively, while the corresponding differences were 12.6, 18.2, 13.0, and 9.8 A mu mol/g, respectively, when adsorbed individually.

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