4.3 Article

Preparation and characterization of selenite substituted hydroxyapatite

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.msec.2012.09.011

Keywords

Hydroxyapatite; Apatite structure; Selenium; FTIR; XRD (X-ray diffraction)

Funding

  1. National Basic Research Program of China [2012CB933601]
  2. National Natural Science Foundation of China [81071263, 30870624]
  3. International S&T Cooperation Program of China [0102011DFA31430]
  4. National Key Technology Research and Development Program of China [2012BAI17B02]
  5. National High Technology Research and Development Program of China [2011 AA03105]

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Selenite-substituted hydroxyapatite (Se-HA) with different Se/P ratios was synthesized by a co-precipitation method, using sodium selenite (Na2SeO3) as a Se source. Selenium has been incorporated into the hydroxyapatite lattice by partially replacing phosphate (PO43-) groups with selenite (SeO32-) groups. X-ray diffraction (XRD). Fourier-transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) techniques reveal that substitutions of phosphate groups by selenite groups cause lower carbonate groups occupying at phosphate sites and change the lattice parameters of hydroxyapatite. The powders obtained are nano-crystalline hydroxyapatite when the Se/P ratios are not more than 0.1. The particle shape of Se-HA has not been altered compared with selenite-free hydroxyapatite but Se-incorporation reduces the crystallite size. The crystallinity was reduced as the Se/P ratios increased until amorphous phase (Se/P=0.3) appeared in the Se-HA powder obtained, and then another crystal phase presented as calcium selenite hydrate (Se/P=10). In addition, the sintering tests show that the Se-HA powders with the Se/P ratio of 0.1 have thermal stability at 900 degrees C for 2 h; hence they have great potential in the fabrication of bone repair scaffolds. (C) 2012 Elsevier B.V. All rights reserved.

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