RF plasma processing of ultra-fine hydroxyaptite powders

Citation
R. Kumar et al., RF plasma processing of ultra-fine hydroxyaptite powders, J MATER PR, 113(1-3), 2001, pp. 456-462
Citations number
16
Categorie Soggetti
Material Science & Engineering
Journal title
JOURNAL OF MATERIALS PROCESSING TECHNOLOGY
ISSN journal
09240136 → ACNP
Volume
113
Issue
1-3
Year of publication
2001
Pages
456 - 462
Database
ISI
SICI code
0924-0136(20010615)113:1-3<456:RPPOUH>2.0.ZU;2-N
Abstract
The study of biocompatible materials has intensified over the last decade d riven by the growing awareness of an aging population. The need for alterna tive medical solutions has not only extended the requirement for biomedical devices to offer more than just functionality but also bioactivity. A new generation of bioactive materials has emerged promising better properties o ver existing biomaterials because of their ability-to promote intimate bone growth and rapid fixation. In particular, hydroxyapatite (HA) has been rec ognised as one bioactive material having the potential and opportunity for development as bone substitutes. Although HA has a similar chemical composi tion to that of natural bone, it lacks sufficient strength and toughness fo r use in load bearing applications. Very often it requires blending with a low modulus polymer to achieve adequate toughness. However, the properties of HA composites is highly dependent on the particle size and morphology of the HA filler. Much has been suggested on the benefit of nano particulate materials in achieving higher mechanical properties. The need now arises in developing and processing HA of sufficient fineness for this purpose. As s uch the synthesis of ultra-fine HA was initiated using RF induction suspens ion plasma spraying with a wet suspension of HA as feedstock. This was axia lly injected into the RF plasma at various plate powers (plasma energies), chamber pressures, probe distances and plasma gas flow rates. The processed powders varied in size according to the cyclones designed to collect the p owders from medium to ultra-fine. The chamber collecting ultrafine powder c ontained particles ranging from 10 nm to 4 mum. The particle size, morpholo gy and phase concentration of the powders were characterised using SEM, TEM , XRD and FTIR. In general, the particle size decreased with increasing pla te power, while the reverse was observed for the volume of nano-sized parti cles produced. Decomposition into other phases such as tricalcium phosphate (TCP), tetracalcium phosphate (TTCP) and calcium oxide (CaO) increased wit h increasing plate power. This study suggests that the processing parameter s associated with the production of the ultra-fine powders interact in a co mplex manner but can be rationalised by considering the overall thermal tre atment experienced by the particulates during plasma treatment. (C) 2001 El sevier Science B.V. All rights reserved.