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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/1614
Title: Adsorption of zearalenone by organomodified natural zeolitic tuff
Authors: Daković, Aleksandra
Matijasević, Srdan
Rottinghaus, George E
Dondur, Vera 
Pietrass, Tanja
Clewett, Catherine F M
Keywords: 1 H NMR;Adsorption;Clinoptilolite;Mycotoxins;Organozeolite;Zearalenone;Zeolite
Issue Date: 1-Jul-2007
Journal: Journal of colloid and interface science
Abstract: 
Adsorption of zearalenone (ZEN) by natural zeolitic tuff, modified with different numbers of octadecyldimethylbenzylammonium (ODMBA) ions, was investigated. The results of solid-state 1H NMR analysis of the starting material suggested that zeolitic tuff is rich in mineral clinoptilolite, confirming the results of previous thermal stability study. Three organozeolites (OZ-2, OZ-5, and OZ-10) were prepared with ODMBA surface coverages of 20, 50, and 100 mmol/100 g. The mechanism of ZEN sorption by the three organozeolites was investigated through the determination of the adsorption isotherms at pH 3, 7, and 9. Adsorption of ZEN by organozeolites was best represented by a linear type of isotherm at pH 3, while at pH 7 and 9, adsorption of ZEN by organozeolites followed a nonlinear (Langmuir) type of isotherm. The different shape of the ZEN adsorption isotherms for the three organozeolites with different levels of ODMBA at the zeolitic surface at different pH values suggests that the adsorption mechanism may be dependent on the form of ZEN in solution. Since, at pH 3, ZEN exists in solution as the neutral form, the linear isotherms at pH 3 suggested that hydrophobic interactions are probably responsible for adsorption of neutral, hydrophobic ZEN onto the hydrophobic surface of the organozeolites. At pH 7, the phenolate anion is present in water solution, while at pH 9, ZEN is almost entirely in the anionic form. The nonlinear isotherms obtained for ZEN adsorption by the three organozeolites suggest that sorption appears to be the result of the adsorption process as well as partitioning.
URI: https://dspace.ffh.bg.ac.rs/handle/123456789/1614
ISSN: 0021-9797
DOI: 10.1016/j.jcis.2007.02.033
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University of Belgrade
Faculty of Physical Chemistry
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PAC 105305
SERBIA
University of Belgrade Faculty of Physical Chemistry