A multi-technique study devoted to investigate the surface features of nanosized hydroxyapatite (HA) was carried out. UHR-TEM observation provided evidence that HA nanoparticles are constituted by a crystalline core, elongated in the direction of the crystallographic c-axis, coated by an amorphous layer 1-2 nm thick. By means of IR spectroscopy and microgravimetry, the amount of water and hydroxyls on the surface was evaluated. For the as prepared material, it was found that the first hydration layer is mainly constituted by H2O molecules interacting through a coordinative bond with Ca2+ in a 1:1 ratio, while hydroxyls account only for ca. 20% of surface hydration species. Outgassing at increasing temperatures up to 300°C resulted in a complete surface dehydration, accompanied by a decrease of the capability to readsorb water. Possible changes of the local structure of surface Ca2+ ions were probed by IR spectra of adsorbed CO. The combination of these data with rehydration tests suggested that a significant part of surface Ca2+ ions, once dehydrated, can undergo a relaxation inward the surface, progressively more irreversible as the outgassing temperature increases.

Surface structure, hydration and cationic sites of nanohydroxyapatite: UHR-TEM, IR and microgravimetric studies

COLUCCIA, Salvatore;MARTRA, Gianmario
2007-01-01

Abstract

A multi-technique study devoted to investigate the surface features of nanosized hydroxyapatite (HA) was carried out. UHR-TEM observation provided evidence that HA nanoparticles are constituted by a crystalline core, elongated in the direction of the crystallographic c-axis, coated by an amorphous layer 1-2 nm thick. By means of IR spectroscopy and microgravimetry, the amount of water and hydroxyls on the surface was evaluated. For the as prepared material, it was found that the first hydration layer is mainly constituted by H2O molecules interacting through a coordinative bond with Ca2+ in a 1:1 ratio, while hydroxyls account only for ca. 20% of surface hydration species. Outgassing at increasing temperatures up to 300°C resulted in a complete surface dehydration, accompanied by a decrease of the capability to readsorb water. Possible changes of the local structure of surface Ca2+ ions were probed by IR spectra of adsorbed CO. The combination of these data with rehydration tests suggested that a significant part of surface Ca2+ ions, once dehydrated, can undergo a relaxation inward the surface, progressively more irreversible as the outgassing temperature increases.
2007
111
4027
4035
bioceramics; adsorbed water; hydroxyls; surface Ca2+; effect of de-hydration
BERTINETTI L; TAMPIERI A; LANDI E; DUCATI C; COLUCCIA S; MARTRA G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/7343
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