This paper reports a systematic investigation on Mg-substituted hydroxyapatite (Ca10−xMgx(PO4)6(OH)2) nanopowders produced by precipitation of Ca(NO3)2·4H2O and Mg(NO3)2. The Mg content ranged between 0.6 and 2.4 wt%. Semicrystalline Mg-substituted hydroxyapatite powders made up of needle-like nanoparticles were obtained, the specific surface area ranged between 87 and 142m2/g. Pure hydroxyapatite nanopowder decomposed around 1000 ◦C. Mg-substituted hydroxyapatites were thermally stable up to 660 ◦C (x=1.0), 760 ◦C (x=0.5) and 840 ◦C (x=0.25) showing a distinct decreased thermal stability with respect to the pure sample. A relevant displacement of the sintering curve at lower temperature as a function of Mg content was observed, comparing to the behaviour of a pure HAp material, synthesized following the same procedure, and ascribed to the -TCP formation.

Mg-substituted hydroxyapatite nanopowders: Synthesis, thermal stability and sintering behaviour / Cacciotti, I; Bianco, A; Lombardi, Mariangela; Montanaro, Laura. - In: JOURNAL OF THE EUROPEAN CERAMIC SOCIETY. - ISSN 0955-2219. - STAMPA. - 29:(2009), pp. 2969-2978. [10.1016/j.jeurceramsoc.2009.04.038]

Mg-substituted hydroxyapatite nanopowders: Synthesis, thermal stability and sintering behaviour

LOMBARDI, MARIANGELA;MONTANARO, Laura
2009

Abstract

This paper reports a systematic investigation on Mg-substituted hydroxyapatite (Ca10−xMgx(PO4)6(OH)2) nanopowders produced by precipitation of Ca(NO3)2·4H2O and Mg(NO3)2. The Mg content ranged between 0.6 and 2.4 wt%. Semicrystalline Mg-substituted hydroxyapatite powders made up of needle-like nanoparticles were obtained, the specific surface area ranged between 87 and 142m2/g. Pure hydroxyapatite nanopowder decomposed around 1000 ◦C. Mg-substituted hydroxyapatites were thermally stable up to 660 ◦C (x=1.0), 760 ◦C (x=0.5) and 840 ◦C (x=0.25) showing a distinct decreased thermal stability with respect to the pure sample. A relevant displacement of the sintering curve at lower temperature as a function of Mg content was observed, comparing to the behaviour of a pure HAp material, synthesized following the same procedure, and ascribed to the -TCP formation.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11583/2144577
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