Abstract
Si3N4 powder has been milled using a planetary ball mill. The specific surface area, crystallite size and lattice distortions were studied as a function of milling time using the Brunauer-Emmett-Teller (BET) technique and X-ray powder diffractometry. The crystallite size decreased rapidly during the first 50 h of milling. Above 170 h no further decrease of the crystallite size occurred. The smallest crystallite size obtained was 0.074 μm. Lattice distortions were small and decreased slightly during the first 50 h of milling. Specific surface area increased linearly with time. Rapid wear of the milling parts occurred during the first 50 h. Increasing the milling time produced only minor wear. The oxygen content increased linearly with milling time. Reaction with the milling fluid produced an increase in carbon content.
Similar content being viewed by others
References
D. W. Richerson, “Modern Ceramic Engineering”, (Marcel Dekker, New York, 1982) p. 126.
G. Wötting and G. Ziegler, Interceram. 35 (1986) 32.
I. J. Mccolm, “Ceramic Science for Materials Technologists”, (Chapman and Hall, New York, 1983) p. 107.
Y. Kanno, Powder Met. 44 (1985) 93.
T. P. Herbell, T. K. Glasgow and N. W. Orth, Ceramic Bulletin 63 (1984) 1176.
T. P. Herbell, M. R. Freedman and J. D. Kiser, Ceram. Eng. Sci. Proc. 7 (1986) 817.
M. R. Freedman, J. D. Kiser and T. P. Herbell, ibid. 6 (1985) 1124.
L. T. Gankevich, S. G. Titov, S. L. Bochkov, K. K. Uzbekova, E. M. Cherednik and A. F. Kuteinikov, Poroshk. Metall. 9 (1987) 1.
K. Suzuki and Y. Kuwahara, Kona 2 (1984) 2.
B. C. Lippens and M. E. A. Hermans, Powder Met. 7 (1961) 66.
G. K. Williamson and W. H. Hall, Acta Met. 1 (1953) 22.
G. K. Williamson and R. E. Smallman, Phil. Mag. 1 (1956) 34.
M. J. Klein and P. S. Rudman, ibid. 14 (1966) 1199.
K. R. Evans and W. F. Flanagan, ibid. 14 (1966) 1131.
R. W. Heckel and J. L. Youngblood, J. Amer. Ceram. Soc. 51 (1967) 398.
N. F. M. Henry, H. Lipson and W. A. Wooster, “The Interpretation of X-ray Diffraction Photographs”, (Macmillan, London, 1960) p. 212.
G. Ziegler, Powder Met. Int. 10 (1978) 70.
Idem. Keram Z. 33 (1981) 287.
Idem., ibid..
T. Ekström, C. Chatfield, W. Wruss and M. Maly-Schreiber, J. Mater. Sci. 20 (1985) 1266.
R. D. Deslattes and A. Henins, Phys. Rev. Lett. 31 (1972) 972.
B. Noläng, unpublished, Institute of Chemistry, University of Uppsala, (1990).
C. P. Gazzara and D. R. Messier, Ceramic Bulletin 56 (1977) 777.
G. Petzow and R. Sersale, Pure & Appl. Chem. 59 (1987) 1673.
K. Yvon, W. Jeitschko and E. Parthe, J. Appl. Crystallogr. 10 (1977) 73.
R. Marchand, Y. Laurent and J. Lang, Acta Cryst. 25B (1969) 2157.
O. Borgen and H. M. Seip, Acta Chem. Scand. 15 (1961) 1789.
H. P. Klug and L. E. Alexander, “X-ray Diffraction Procedures for Polycrystalline and Amorphous Materials”, (Wiley, New York, 1974) p. 659.
E. A. Faulkner, Phil. Mag. 5 (1960) 519.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Lönnberg, B. Characterization of milled Si3N4 powder using X-ray peak broadening and surface area analysis. JOURNAL OF MATERIALS SCIENCE 29, 3224–3230 (1994). https://doi.org/10.1007/BF00356667
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF00356667