journal article·2002-03

Nanosized hydroxyapatite powders derived from coprecipitation process

L. B. Kong, J. Ma, F. Boey

Journal of Materials Science· Volume 37· Issue 6
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Abstract

Nanosized hydoxyapatite (Ca10(PO4)6(OH)2 or HA) powders were prepared by a coprecipitation process using calcium nitrate and phosphoric acid as starting materials. The synthesized powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) specific area measurment techniques. Single phase HA, with an average grain size of about 60 nm and a BET surface area of 62 m2/g, was obtained. No grain coarsening was observed when the HA powders were heated at 600°C for 4 hours. HA ceramics were obtained by sintering the powders at temperatures from 1000°C to 1200°C. Dense HA ceramics with a theoretical density of 98% and grain size of 6.5 μm were achieved after sintering the HA powders at 1200°C for 2 hours. HA phase was observed to decompose into tricalcium phosphate when sintered at 1300°C. The microstructure development of the sintered HA ceramics with sintering temperature was also characterized and discussed.
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OpenAlex topics: Bone Tissue Engineering Materials · Luminescence Properties of Advanced Materials · Advanced ceramic materials synthesis

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References (17)

Show source-provided references
1. L. L. HENCH, J. Amer. Ceram. Soc. 74 (1991) 1487.10.1111/j.1151-2916.1991.tb07132.x ↗
2. M. ANDRÉS-VERGÉS, C. FERNÁNDEZ-GONZÁLEZ, M. MARTÍNEZ-GALLEGO, J. D. SOOLIER, I. CACHADIÑA and E. MATIJEVIĆ, J. Mater. Res. 15 (2000) 2526.10.1557/JMR.2000.0362 ↗
3. B. MAVIS and A. C. TAS, J. Amer. Ceram. Soc. 83 (2000) 989.10.1111/j.1151-2916.2000.tb01314.x ↗
4. W. WENG and J. L. BAPTISTA, ibid. 82 (1999) 27.10.1111/j.1151-2916.1999.tb01719.x ↗
5. S.W. RUSSELL, K. A. LUPTAK, C. T. A. SUCHICITAL, T. L. ALFORD and V. B. PIZZICONI, ibid 79(1996) 837.10.1111/j.1151-2916.1996.tb08514.x ↗
6. W. SUCHANEK and M. YOSHIMURA, J. Mater. Res. 13 (1998) 94.10.1557/JMR.1998.0015 ↗
7. W. L. SUCHANEK and M. YOSHIMURA, J. Amer. Ceram. Soc. 81 (1998) 765.10.1111/j.1151-2916.1998.tb02408.x ↗
8. G. K. LIM, J. WANG, S. C. NG and L. M. GAN, J. Mater. Chem. 9 (1999) 1635.10.1039/a809644i ↗
9. W. KIM, Q. ZHANG and F. SAITO, J. Mater. Sci. 35 (2000) 5401.10.1023/A:1004859231795 ↗
10. E. HAYEK and H. NEWESELY, Inorg. Synth. 7 (1963)63.10.1002/9780470132388.ch17 ↗
11. N. KIVRAK and A. C. TAS, J. Amer. Ceram. Soc. 81 (1998) 2245.10.1111/j.1151-2916.1998.tb02618.x ↗
12. M. G. S. MURRAY, J. WANG, C. B. PONTON and P. M. MARQUIS, J. Mater. Sci. 30 (1995) 3061.10.1007/BF01209218 ↗
13. D. C. HARRIS, “Quantitative Chemical Analysis” 3rd ed. (W.H. Freeman, New York, 1991) p. 136.
14. H. C. W. SKINNER, J. S. CKITTELBERGER and R. A. BEEBE, J. Phys. Chem. 74 (1975) 2017.10.1021/j100586a007 ↗
15. H. J. KLEEBE, E. F. BRÉS, D. BERNACHE-ASSOLANT and G. ZIEGLER, J. Amer. Ceram. Soc. 80 (1997) 37.10.1111/j.1151-2916.1997.tb02788.x ↗
16. H. K. VARMA and R. SIVAKUMAR, Mater. Lett. 29 (1996) 57.10.1016/S0167-577X(96)00121-8 ↗
17. P. L. CHEN and I. W. CHEN, J. Amer. Ceram. Soc. 79 (1996) 3129.10.1111/j.1151-2916.1996.tb08087.x ↗