Please use this identifier to cite or link to this item:
https://doi.org/10.1109/DSR.2011.6026836
Title: | Physiochemical stability of chemically-modified nanoapatites sintered at different temperatures |
Authors: | Lim, P.N. Tong, J.Y.E. Thian, E.S. Tay, B.Y. Chan, C.M. |
Keywords: | Co-substitution Hydroxyapatite Silicon Silver Sintering |
Issue Date: | 2011 |
Source: | Lim, P.N.,Tong, J.Y.E.,Thian, E.S.,Tay, B.Y.,Chan, C.M. (2011). Physiochemical stability of chemically-modified nanoapatites sintered at different temperatures. 2011 Defense Science Research Conference and Expo, DSR 2011 : -. ScholarBank@NUS Repository. https://doi.org/10.1109/DSR.2011.6026836 |
Abstract: | Nanostructured apatite has been widely used as a bone substitute material due to its biological similarity to the natural bone mineral. To enhance further the biomineralisation and introduce bactericidal property into HA, co-substitution of Ag and Si has been investigated. A co-substituted nanosized apatite (Ag/Si-HA) containing Ag (0.3 wt %) and Si (0.8 wt %) was synthesized by an aqueous precipitation technique. Bone-apatite mimicking morphology of dimensions ∼50 nm in length and ∼10 nm in width was observed for the Ag/Si-HA nano powder. XRF detected the presence of Ag and Si in phase-pure Ag/Si-HA. The Ag/Si-HA nano powders were then compacted and sintered at various temperatures (900-1300 °C) and found to achieve a maximum densification of 93 % at 1300 °C, with a grain size of approximately 1 m. Phase-purity was maintained up to a temperature of 1300 °C, as observed from the XRD pattern. This study thus demonstrated that a phase-pure Ag/Si-HA was synthesized via an aqueous precipitation technique. © 2011 IEEE. |
Source Title: | 2011 Defense Science Research Conference and Expo, DSR 2011 |
URI: | http://scholarbank.nus.edu.sg/handle/10635/86054 |
ISBN: | 9781424492763 |
DOI: | 10.1109/DSR.2011.6026836 |
Appears in Collections: | Staff Publications |
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.