Absorption Spectra and Bioactivity Behavior of Gamma Irradiated CeO2-Doped Bioglasses
The synthesis and characterization of some bioglasses based on Hench’s Bioglass® 45S5 with additions of CeO 2 (1.0, 2.0, or 3.0%) have been carried out. Two objectives have been focused upon; first, the effect of successive ionizing gamma irradiation on the undoped and CeO 2 -doped bioglass samples...
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Published in | SILICON Vol. 5; no. 2; pp. 171 - 181 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.04.2013
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | The synthesis and characterization of some bioglasses based on Hench’s Bioglass® 45S5 with additions of CeO
2
(1.0, 2.0, or 3.0%) have been carried out. Two objectives have been focused upon; first, the effect of successive ionizing gamma irradiation on the undoped and CeO
2
-doped bioglass samples has been evaluated with the aim of justifying the role of the rare earth oxide CeO
2
on gamma irradiation. The second objective was directed to test the bioactivity of such prepared CeO
2
-doped samples after soaking for 1 month in a simulated body fluid at 37 °C. The results indicate that the additions of CeO
2
suppress, to a marked extent, the generation of radiation induced defects especially in the visible region. The bioactivity results show that the studied CeO
2
-doped bioglass samples gave rise to a calcium phosphate surface layer upon immersion in a simulated body fluid for 1 month at 37 °C and the bioactivity extent was almost identical in the CeO
2
doping interval limit (1 → 3% CeO
2
) to that of the undoped base Hench’s Bioglass. The presence of both Ce
3+
and Ce
4+
ions were confirmed by optical absorption spectra. Electron spin resonance (ESR) studies of gamma irradiated CeO
2
-doped glasses indicate and confirm the dominance of Ce
4+
in the bioglass compositions and its transformation to Ce
3+
by high gamma irradiation. |
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ISSN: | 1876-990X 1876-9918 |
DOI: | 10.1007/s12633-012-9112-4 |