Hostname: page-component-7479d7b7d-8zxtt Total loading time: 0 Render date: 2024-07-08T20:54:51.087Z Has data issue: false hasContentIssue false

Amorphization of Complex Ceramics by Heavy-Particle Irradiations

Published online by Cambridge University Press:  16 February 2011

R.C. Ewing
Affiliation:
Depart. of Earth and Planetary Sciences, U. of New Mexico, Albuquerque, NM 87131
L.M. Wang
Affiliation:
Depart. of Earth and Planetary Sciences, U. of New Mexico, Albuquerque, NM 87131
W.J. Weber
Affiliation:
Pacific Northwest Laboratory, Richland, WA 99352
Get access

Abstract

“Complex” ceramics, for the purpose of this paper, include materials that are generally strongly bonded (mixed ionic and covalent), refractory and frequently good insulators. They are distinguished from simple, compact ceramics (e.g., MgO and UO2) by structural features which include: 1.) open network structures, best characterized by a consideration of the shape, size and connectivity of coordination polyhedra; 2.) generally, complex compositions which characteristically lead to multiple cation sites and lower symmetry; 3.) directional bonding; 4.) bond-type variations, from bond-to-bond, within the structure. The heavy particle irradiations not only include ion-beam irradiations, but also recoil-nucleus damage resulting from a-decay events from constituent actinides. The latter effects are responsible for the radiation-induced transformation to the metamict state in minerals. The responses of these materials to irradiation are complex, as energy may be dissipated ballistically by transfer of kinetic energy from an incident projectile or radiolytically by conversion of radiation-induced electronic excitations into atomic motion. This results in isolated Frenkel defect pairs, defect aggregates, isolated collision cascades or bulk amorphization; all may occur concurrently. Thus, the amorphization process is heterogeneous. Only recently have there been systematic studies of heavy particle irradiations of “complex” ceramics on a wide variety of structure-types and compositions as a function of dose and temperature. In this paper, we review the conditions for amorphization for the tetragonal orthosilicate, zircon [ZrSiO4]; the hexagonal orthosilicate/phosphate apatite structure-type [X10(ZO4)6(F,Cl,O)2]; the isometric pyrochlores [A1-2B2O6(O,OH,F)o-1pH2O] and its monoclinic derivative zirconolite [CaZrTi2O7]; the olivine (derivative - hcp) structure types, α-VIA2IVBO4, and spinet (ccp,) γ-VIA2IVBO4.

Type
Research Article
Copyright
Copyright © Materials Research Society 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Naguib, H.M. and Kelly, R., Radiation Effects 24, 1, (1975).Google Scholar
2. Pabst, A., American Mineralogist 37, 137, (1952)Google Scholar
3. Ewing, R.C., Chakoumakos, B.C., Lumpkin, G.R. and Murakami, T., Mater. Res. Soc. Bull. 12(4), 58 (1987).Google Scholar
4. Ewing, R.C., Nucl. Instru. Meth. in Physics Res. B91, 22, (1994).Google Scholar
5. Lumpkin, G.R. and Ewing, R.C., Physics and Chemistry of Minerals 16, 2, (1988).Google Scholar
6. Weber, W.J., J. Mater. Res. 5,2687 (1990).Google Scholar
7. Murakami, T., Chakoumakos, B.C., Ewing, R.C., Lumpkin, G.R. and Weber, W.J., American Mineralogist 76, 1510, (1991).Google Scholar
8. Wang, L.M., Eby, R.K., Janeczek, J. and Ewing, R.C., Nucl. Instru. Meth. Physics Res. B59/60, 395, (1991).Google Scholar
9. Wang, L.M. and Ewing, R.C., Mat. Res. Soc. Bull. XVII, 38 (1992).Google Scholar
10. Eby, R.K., Ewing, R.C. and Birtcher, R.C., J. Mater. Res. 7, 3080, (1992).Google Scholar
11. Sreeram, A.N. and Hobbs, L.W., this volume.Google Scholar
12. Matzke, HJ., Radiation Effects 64, 3, (1982).Google Scholar
13. Devanathan, R., Lam, N.Q., Okamoto, P.R., Sabochick, M.J., and Meshii, M., Journal of Alloys and Compounds 194, 447, (1993).Google Scholar
14. Lam, N.Q. and Okamoto, P.R., Surface and Coatings Technology 65, 7, (1994).Google Scholar
15. Lam, N.Q. and Okamoto, P.R., MRS Bulletin XIX(7), 41 (1994).Google Scholar
16. Holland, H.D. and Gottfried, D., Acta Crystallogr. 8, 291, (1955).Google Scholar
17. Weber, W.J., J. Amer. Ceram. Soc. 76, 1729, (1993).Google Scholar
18. Weber, W.J., Ewing, R.C., and Wang, L.M., J. Mater. Res. 9, 688, (1994).Google Scholar
19. Wang, L.M., Ewing, R.C., Weber, W.J., and Eby, R.K., in Beam-Solid Interactions: Fundamentals and Applications, edited by Nastasi, M.A., Herbots, N., Harriott, L.R., and Averback, R.S. (Mater. Res. Soc. Symp. Proc. 279, Pittsburgh, PA, 1993) p. 451.Google Scholar
20. Harker, A.B. and Flintoff, J. F., in Scientific Basis for Nuclear Waste Management VII, McVay, G.L., Ed. (North Holland, New York, 1984) p. 513.Google Scholar
21. McConnell, D, Apatite (Springer-Verlag, New York, 1973).Google Scholar
22. Nelson, D.G.A., McLean, J.D., and Sanders, J.V., Radiat. Effects Lett. 68, 51, (1982).Google Scholar
23. Cameron, M., Wang, L.M., Crowley, K.D., and Ewing, R.C., in Proc. 50th Annual Meeting the Electron Microscope Society of America, Bailey, G.W., Bentley, J., and Small, J.A., Eds. (San Francisco Press, San Francisco, 1992) p. 378.Google Scholar
24. Wang, L.M., Cameron, M., Weber, W.J., Crowley, K.D., and Ewing, R.C., in Hydroxyapatite and Related Compounds, Brown, P.W. and Constantz, B., Eds. (CRC Press, Boca Raton, FL, 1994) p. 243.Google Scholar
25. Weber, W.J., Turcotte, R.P., Bunnell, L.R., Roberts, F.P., and Westsik, J.H. Jr, in Ceramics in Nuclear Waste Management, edited by Chikalla, T.D. and Mendel, J.E. (NTIS, Springfield, VA, 1979) p. 294.Google Scholar
26. Turcotte, R.P., Wald, J.W., Roberts, F.P., Rusin, J.M., and Lutze, W., J. Amer. Ceram. Soc. 65, 589, (1982).Google Scholar
27. Weber, W.J., Radiation Effects 77, 295, (1983).Google Scholar
28. Weber, W.J. and Wang, L.M., Nucl. Instr. and Meth. B 91, 63, (1994).Google Scholar
29. Chakoumakos, B.C., J. Solid State Chem. 53, 120, (1984).Google Scholar
30. Ewing, R.C., Weber, W.J. and Clinard, F.W. Jr, Progress in Nuclear Energy, in press.Google Scholar
31. Weber, W.J., Turcotte, R.P., Roberts, F.P., Radioactive Waste Management 2(3), 295 (1982).Google Scholar
32. White, T.J., Ewing, R.C., Wang, L.M., Forrester, J.S., Montross, C., in Scientific Basis for Nuclear Waste Management XVIII, Murakami, T. and Ewing, R.C., Eds. (Materials Research Society, Pittsburgh, in press).Google Scholar
33. Ewing, R.C. and Wang, L.M., Nucl. Instr. Meth. in Physics Res. B65, 319, (1992).Google Scholar
34. Headley, T.J., Arnold, G.W., Northrup, C.J.M., in Scientific Baiss for Radioactive Waste Management V, Lutze, W., Ed. (Materials Research Society, Pittsburgh, 1982) pp. 379388.Google Scholar
35. Clinard, F.W. Jr, Peterson, D.E., and Rohr, D.L., J. Nucl. Mater. 126, 245, (1984).Google Scholar
36. Yu, N., Sickafus, K.E. and Nastasi, M., Phil. Mag. Lett. 70, 235, (1994).Google Scholar
37. Wang, L.M., Gong, W.L., Bordes, N., Ewing, R.C. and Fei, Y., this volume.Google Scholar
38. Wang, L.M., Gong, W.L. and Ewing, R.C., Mat. Res. Soc. Symp. Proc. 316, 247, (1994).Google Scholar
39. Wang, L.M. and Ewing, R.C., Mat. Res. Soc. Symp. Proc. 235, 333, (1992).Google Scholar
40. Zemann, J., Z. Kristallogr. 175, 299, (1986).Google Scholar
41. Hazen, R.M. and Prewitt, A.T., American Mineralogist 62, 309, (1977).Google Scholar
42. Guyot, F. and Reynard, B., Chemical Geology 96, 411, (1992).Google Scholar
43. Koike, J., Okamoto, P.R. and Rehn, L.E., J. Mater. Res. 4, 1143, (1989).Google Scholar