Sol–gel synthesis of Tb‐doped hydroxyapatite with high performance as photocatalyst for 2, 4 dichlorophenoxyacetic acid mineralization
BACKGROUND Tb3+doped hydroxyapatite was synthetized by the sol–gel technique, using amounts of the dopant source ranging from 2 to 12 wt%, with respect to the calcium former material. The solids were analyzed using several techniques in order to determine their structural, textural and optical prope...
Gespeichert in:
Veröffentlicht in: | Journal of chemical technology and biotechnology (1986) 2017-07, Vol.92 (7), p.1521-1530 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | BACKGROUND
Tb3+doped hydroxyapatite was synthetized by the sol–gel technique, using amounts of the dopant source ranging from 2 to 12 wt%, with respect to the calcium former material. The solids were analyzed using several techniques in order to determine their structural, textural and optical properties. The photoactivity of the materials was tested in the degradation of 2,4‐dichlorophenoxyacetic acid, under UV irradiation.
RESULTS
The analysis of the samples by X‐ray diffraction, energy‐dispersive X‐ray spectroscopy and Fourier transform infrared spectroscopy indicates the formation of hydroxyapatite with calcium deficiency, with a stoichiometry close to the ideal in the sample doped with 10 wt% of terbium. The highest photoluminescence emission, production of •OH radicals under UV in the terephtalic acid reaction, as well as photocatalytic activity in the photodegradation of 2,4‐dichlorophenoxyacetic acid (2,4‐D) was found in the sample doped with 10 wt% of terbium, reaching almost total degradation and 95% of mineralization of the organic molecule, after 240 min irradiation.
CONCLUSION
Terbium doping during the synthesis of hydroxyapatite significantly improves its efficiency as photocatalyst. © 2017 Society of Chemical Industry |
---|---|
ISSN: | 0268-2575 1097-4660 |
DOI: | 10.1002/jctb.5270 |