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Magnetron Sputtering Deposition of Calcium Phosphate Films with Nanoscale Grain Morphology in their Surface

Published online by Cambridge University Press:  26 February 2011

Wilfredo Otaño
Affiliation:
wotano@cayey.upr.edu, University of Puerto Rico at Cayey, Mathematics-Physics, 205 A. Barcelo Avenue, Cayey, 00736, Puerto Rico, 787-738-2161, 787-263-6426
Víctor M. Pantojas
Affiliation:
vpantojas@hotmail.com, University of Puerto Rico at Cayey, Mathematics-Physics, 205 A. Barcelo Avenue, Cayey, 00736, Puerto Rico
Juan M. Figueroa
Affiliation:
juanm_figueroa@yahoo.com, University of Puerto Rico at Cayey, Mathematics-Physics, 205 A. Barcelo Avenue, Cayey, 00736, Puerto Rico
Darimar Hernández
Affiliation:
dary-17@hotmail.com, University of Puerto Rico at Cayey, Mathematics-Physics, 205 A. Barcelo Avenue, Cayey, 00736, Puerto Rico
Alejandro Rodríguez-Navarro
Affiliation:
anava@ugr.es, Universidad de Granada, Instituto Andaluz de Ciencias de la Tierra-CSIC, Campus de Fuentenueva, Granada, 18002, Spain
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Abstract

Hydroxyapatite (HA) is a calcium phosphate mineral analogous to the mineral part of bone. This similarity makes this material bioactive and suitable to coat medical implants. However, at present, there is not a coating technique which gives the coated implant the desired properties and long life required for medical implants.

In an effort to produce HA coatings with improved properties, calcium phosphate films were prepared using magnetron sputtering deposition on a silicon substrate at 600°C. Initial efforts resulted in the deposition of amorphous films with a distinctive grain-like surface morphology. The morphological grain size was studied using SEM and found that it was possible to control the average diameter value of the round shaped grains by adjusting the deposition time. Increasing the deposition time increases the mean grain diameter. EDS spectra showed the unintentional addition of carbon, iron and nickel to the samples during deposition. After eliminating the impurities, it was possible to prepare calcium phosphate films in the HA phase but without the grain-like surface morphology. These results suggested that the impurities prevented the formation of the calcium phosphate HA phase while acting as nuclei for the heterogeneous nucleation of the grains. This is an important result where the deposition process parameters can be controlled to functionalize the films in order to produce distinctive nanoscale features in the surface morphology.

Type
Research Article
Copyright
Copyright © Materials Research Society 2007

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References

REFERENCES

1. LeGeros, R.Z., LeGeros, J.P., Kim, Y., Kijkowska, R., Zheng, R., Bautista, C., and Wong, J. L., Calcium Phosphates in Plasma-Sprayed HA Coatings, in Bioceramics: Materials and Applications, G., Fischman, A., Clare and L., Hench, eds, Ceramics Transactions 48, American Ceramic Society (1995) 173189.Google Scholar
2. Erkmen, Z. E., Journal of Biomedical Materials Research 48 (1999) 861.Google Scholar
3. Gu, Y.W., Khor, K.A., and Cheang, P., Biomaterials 24 (2003) 16031611.Google Scholar
4. Koch, B., Wolke, J.G.C., and deGroot, K., Journal of Biomedical Materials Research 24 (1991) 655667.Google Scholar
5. Clèries, L., Fernández-Pradas, J.M., Sardin, G., and Morenza, J.L., Biomaterials 19 (1998) 14831487.Google Scholar
6. Fernández-Pradas, J.M., Sardin, G., Clèries, L., Serra, P., Ferrater, C., and Morenza, J.L., TiN Solid Films 317 (1998) 393396.Google Scholar
7. Cui, F.Z., Luo, Z.S., and Feng, Q.L., Journal of Materials Science: Materials in Medicine 8 (1997) 403405.Google Scholar
8. Handi, M., Hakamata, S., and Ektessabi, A.M., presented at the International Conference on Metallurgical Coatings and Thin Films, San Diego, California, (2000).Google Scholar
9. Ozeki, K., Yuhta, T., Aoki, H., Fukui, Y., and Aoki, H., Surface and Coatings Technology 160 (2002) 5461.Google Scholar
10. Van Dijk, K., Schaeken, H.G., Wolke, J.G.C., Marée, C.H.M., Habraken, F.H.P.M., Verhoeven, J. and Jansen, J.A., Journal of Biomedical Materials Research 29 (1995) 269276.Google Scholar
11. Yang, Y., Agrawal, C.M., Kim, K.H., Martin, H., Schulz, K., Bumgardner, I.D., and Ong, J.L., Journal of Oral Implantology 29 (2003) 270.Google Scholar
12. Jansen, J.A., Wolke, J.G.C., Swann, S., van der Waerden, J.P.C.M., and deGroot, K., Clinical Oral Implants Research 4 (1993) 2834.Google Scholar
13. Nieh, T.G., Jankowski, A.F., and Koike, J., Journal of Materials Research 16 (2001) 32383245.Google Scholar
14. Nelea, V., Morosanu, C., Iiiescu, M., and Milhailescu, I.N., Surface & Coatings Technology, 173 (2003) 315.Google Scholar
15. Ding, S.-J., Biomaterials, 24 (2003) 4233.Google Scholar
16. Clèries, L., Fernández-Pradas, J.M., Sardin, G., and Morenza, J.L, Biomaterials 20 (1999) 14011405.Google Scholar