                             !  " ## $#  ! %&   ’# (##    ##   ! $#  !   %&  )* +, - .-/0 ’# (##     !   %&  1# # *  2## 2## 2## /32##   , 4    567   In this work, nanosized hydroxyapatite (HA) powder was synthesized via mechanochemical method by a dry mixture of calcium hydroxide Ca(OH) 2 and di-ammonium hydrogen phosphate (NH 4 ) 2 HPO 4 powders. The effect of mechanochemical process on powder properties was investigated. Three rotation speeds of 170 rpm, 270 rpm and 370 rpm were chose with 15 hours milling time respectively. Characterization of nanopowders was accomplished by Fourier transform infra red (FTIR), X-ray diffraction (XRD) and nanosizer analysis. The green compacted powders with 200 MPa isostatically pressed were prepared and sintered in atmosphere condition at various temperatures ranging from 1150 o C - 1350 o C. The results showed that the rotation speed affected the obtained powders where the crystallite size was found increased with rotation speed (9 – 21 nm). In contrast, the particle size distribution decreased with rotation speed (322-192 nm). The sintering process has influenced the stability of powder by yielding TCP phase at a lower sintering temperature, 1150 o C. However, powder synthesized at 370 rpm has showed a significant hardness, 5.3 GPa after compacted and sintered at 1250 o C with the relative density of 95%. This phenomenon is believed to be related with the nanosize powder synthesized at high speed which has contributes the high strength of the sintered bodies.  Hydroxyapatite (HA) is usually used for a number of biomedical applications in the forms of granules, blocks, coatings, dense bodies [1-4], for bone augmentation and middle-ear implants [4]. HA also has shown the benefits in therapeutic antitumor vaccine [5] and was useful for drug delivery and antibiotics [6-7]. It naturally contained in human bone as the crystals within collagen. The high strength is necessary for the reliable work of an implant in the body [8]. Many improvements have been made earlier to overcome the limitation of HA in loading application by controlling microstructures via novel sintering technique or utilization of nano powders [9]. Development of dense HA ceramics with superior mechanical properties is possible if the starting powder is stoichiometric with better powder properties such as crystallinity, agglomeration, and morphology. A decrease in grain size to nano scale in dense sintered materials is a desired parameter to enhance the mechanical and biological properties of HA-based bioceramic materials [10]. There have been several methods applied in synthesized HA nanocrystalline powder consist of co-precipitation [6], emulsion/microemulsion [11], sol-gel [12], hydrothermal [13] and mechanochemical [14]. Mechanochemical is a simple and low cost method compared to others. The chemical processes occurring during mechanical action on solids became to be more specific and versatile. Besides, mechanochemical treatment has been recently receiving attention as an alternative route in preparing materials characterized by better biocompatibility with natural bone Materials Science Forum Vol. 694 (2011) pp 118-122 Online available since 2011/Jul/27 at www.scientific.net © (2011) Trans Tech Publications, Switzerland doi:10.4028/www.scientific.net/MSF.694.118 All rights reserved. No part of contents of this paper may be reproduced or transmitted in any form or by any means without the written permission of TTP, www.ttp.net. (ID: 210.48.222.7-28/07/11,05:17:21)