Iis Sopyan
Ceramics Technology Group, Materials Technology Center Agency for the Assesment and Application of Technology (BPPT) Gedung BPPT II Lantai 22, Jalan M.H. Thamrin 8, Jakarta 10340

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PREPARATION OF HYDROXYAPATITE POWDERS FOR MEDICALAPPLICATIONS VIA SOL-GEL TECHNIQUE Iis Sopyan
Jurnal Sains Materi Indonesia Vol 4, No 2: FEBRUARI 2003
Publisher : Center for Science & Technology of Advanced Materials - National Nuclear Energy Agency

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.17146/jsmi.2003.4.2.4883

Abstract

PREPARATION OF HYDROXYAPATITE POWDERS FOR MEDICALAPPLICATIONS VIA SOL-GEL TECHNIQUE. Hydroxyapatite (HA) powders have been prepared via sol-gel procedure using calcium nitrate tetrahydrate and di-ammonium hydrogen phosphate as the precursors for calcium and phosphorus, respectively. An ammoniacal solution of the monomers was heated at 100°C for about 3 –4 h until a white gel of hydroxyapatite mixture were obtained. The obtained gel was then dried at 340°C for 7 h and subsequently subjected to an 820°C calcination for 2 h. The yield of the powder mixture ranged between 50 to 53 g. XRD measurement shown that the powder contained hydroxyapatite crystal with b-TCP ( 15-20%) and calcium oxide (4-6%) as secondary phases. Further treatment was conducted to gain hydroxyapatite powder of higher purity, thus the correct Ca/P ratio, by adding an appropriate amount of di-ammonium hydrogen phosphate and heated while stirring at 90°C for 4 h. Good purity (almost 100%) of the obtained hydroxyapatite was confirmed by XRD analysis.This result proved that our HA powder meets the medical prerequisite: a HA purity of above 95%. Morphological evaluation by SEM measurement shows that the particles of the HA agglomerate are globular in shape with an average size of 1-2 mm in diameter. Meanwhile, the primary particles have a diameter of 70-150 nm in average. Surface area of the powder is 7 m2/g and the mean particle size as measured using X ray sedimentation method is ca. 1 mm. The measurements are not in good agreement with the morphological investigation. We consider, accordingly, that the particles presumably have high surface potentials, thus forming very tightly bonded agglomerates