Article ID Journal Published Year Pages File Type
77201 Microporous and Mesoporous Materials 2006 7 Pages PDF
Abstract

The surface hydroxyl groups of zeolite Y were reacted with 1,1,3,3-tetramethyldisilazane, HN(SiHMe2)2 under ambient conditions and the grafting of siloxy functionality on the zeolite was confirmed by infrared, NMR spectroscopy and elemental analysis. Paraquat (methyl viologen) was ion-exchanged into the zeolite, followed by treatment with the disilazane reagent. Surface modification of paraquat-loaded zeolites encapsulates the guest molecules in the zeolite cages and release of paraquat by ion-exchange with sodium ions was studied. The total amount of paraquat released was dependent on the concentration of Na+ in solution, and was similar for the derivatized and underivatized samples. In the absence of surface modification, equilibration occurred within 20 min, whereas with surface modification, the equilibration time was extended to 7 days. These kinetics are reflected in the effective diffusion coefficients (D) of paraquat, with D = 1.2 × 10−15 cm2 s−1 for derivatized zeolite Y and D = 0.2–1.1 × 10−7 cm2 s−1 for the underivatized sample. Paraquat was chosen as the guest molecule, since it is widely used as an herbicide and its controlled release is of interest in agricultural applications.

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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