Synthesis of Nanocrystalline Hydroxyapatite by Natural Biopolymers Based Sol-Gel Technique

Article Preview

Abstract:

Nanocrystalline hydroxyapatite (HAp) powders were successfully synthesized by natural biopolymers based sol-gel technique. The biopolymers were extracted from the leaves of Yanang (Tiliacora triandra), Krueo Ma Noy (Cissampelos pareira) and Konjac (Amorphophallus konjac). To obtain HAp powders, the prepared precursors were calcined in air at 600, 700, and 800 °C for 2 h. The phase composition of the calcined samples was studied by X-ray diffraction (XRD) technique. The XRD results confirmed the formation of HAp phase with a small trace of β-tricalcium phosphate (β-TCP). The crystalline sizes of the samples were found to be 20-50 nm as evaluated by the XRD line broadening method. TEM investigation revealed that the synthesized HAp samples consisted of nanoparticles with a particle size in the range of 50-100 nm in diameter. The corresponding selected area electron diffraction (SAED) analysis further confirmed the formation of hexagonal structure of HAp.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

83-86

Citation:

Online since:

August 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] M.C. Chang, W.H. Douglas, J. Tanaka, J. Mater. Sci. -Mater. Med. 17 (2006) 387.

Google Scholar

[2] A. Afshar, N. Ghorbani, M.R. Ehsani, C.C. Sorrell, Mater. Des. 24 (2003) 197.

Google Scholar

[3] M.N. Salimi, R.H. Bridson, L.M. Grover, G.A. Leeke, Powder Technol. 218 (2012) 109.

Google Scholar

[4] Y. Wu, S. Bose, Langmuir 21 (2005) 3232.

Google Scholar

[5] G.C. Koumoulidis, T.C. Vaimakis, A.T. Sdoukos, N.K. Boukos, C.C. Trapalis, J. Am. Ceram. Soc. 84 (2001) 1203.

Google Scholar

[6] D. Tadic, F. Peters, M. Epple, Biomaterials, 23 (2002) 2553.

Google Scholar

[7] X. Guo, P. Xiao, J. Eur. Ceram. Soc. 26 (2006) 3383.

Google Scholar

[8] P. Shuk, W.L. Suchanek, T. Hao, E. Gulliver, R.E. Riman, M. Senna, K.S. TenHuisen, V.F. Janas, J. Mater. Res. 16 (2001) 1231.

DOI: 10.1557/jmr.2001.0170

Google Scholar

[9] W. Feng, L. Mu-sen, L. Yu-peng, Q. Yong-xin, Mater. Lett. 59 (2005) 916.

Google Scholar

[10] R.E. Riman, W.L. Suchanek, K. Byrappa, C.W. Chen, P. Shuk, C.S. Oakes, Solid State Ionics, 151 (2002) 393.

Google Scholar

[11] I.R. Gibson, W. Bonfield, J. Biomed. Mater. Res. 59 (2002) 697.

Google Scholar

[12] J. Singthong, S.W. Cui, S. Ningsanond, H.D. Goff, Carbohyd. Polym. 58 (2004) 391.

Google Scholar

[13] L.S. Liu, P.H. Cooke, D.R. Coffin, M.L. Fishman, K.B. Hicks, J. Appl. Polm. Sci. 92 (2004) 1893.

Google Scholar

[14] T.F. Vandamme, A. Lenourry, C. Charrueau, J.C. Chaumeil, Carbohydr. Polym. 48 (2001) 219.

Google Scholar

[15] L.S. Liu M.L. Fishman, J. Kost, K.B. Hicks, Biomaterials, 24 (2003) 3333.

Google Scholar

[16] B.D. Cullity, S.R. Stock, Elements of X–ray Diffraction, third ed., Prentice Hall, New Jersey, (2001).

Google Scholar