Surface Modification and Spectroscopic Characterization of TiO 2 Nanoparticles with 2-Aminoethyl Dihydrogen Phosphate
A common strategy for the surface modification of nano TiO 2 and other metal oxide nanoparticles is based on anchor groups using chelating ligands that can carry additional functionalities. This would allow the exploration of further applications of these materials. In the present work, we report th...
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Published in: | Journal of the Brazilian Chemical Society Vol. 26; no. 8; pp. 1608 - 1616 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English Portuguese |
Published: |
Sociedade Brasileira de Química
01-08-2015
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Subjects: | |
Online Access: | Get full text |
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Summary: | A common strategy for the surface modification of nano TiO 2 and other metal oxide nanoparticles is based on anchor groups using chelating ligands that can carry additional functionalities. This would allow the exploration of further applications of these materials. In the present work, we report the modification of TiO 2 nanoparticles from nano TiO 2 (Degussa P-25) dispersion in distilled water in the presence of 2-aminoethyl dihydrogen phosphate, followed by removing the excess of the capping agent through washing with water. The surface functionalization and the kind of surface interaction were analyzed applying different characterization methods like CHN elemental analysis, thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), attenuated total reflectance (ATR-FTIR), X-ray powder diffraction (XRD) and 1 H, 13 C, 31 P magic angle spinning nuclear magnetic resonance spectroscopy (MAS NMR), confirming the presence of modifying agent on the surface. In the study of modified nano TiO 2 by MAS NMR spectroscopy, a distinct downfield shift for 31 P signal has been seen comparing to the pure cappping agent due to P-O-Ti bond formation. The phosphate groups interact with the surface via quite strong covalent interaction, while according the analyses results, the surface amine groups remained uncoordinated. |
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ISSN: | 0103-5053 1678-4790 |
DOI: | 10.5935/0103-5053.20150131 |