Hostname: page-component-cd9895bd7-mkpzs Total loading time: 0 Render date: 2024-12-26T22:01:20.169Z Has data issue: false hasContentIssue false

Comparison of powder synthesis routes for fabricating (Ba0.65Sr0.35)TiO3 ceramics

Published online by Cambridge University Press:  01 June 2006

N.J. Ali
Affiliation:
Institute of Materials Research, University of Leeds, Leeds, LS2 9JT, United Kingdom
S.J. Milne*
Affiliation:
Institute of Materials Research, University of Leeds, Leeds, LS2 9JT, United Kingdom
*
a) Address all correspondence to this author. e-mail: s.j.milne@leeds.ac.uk
Get access

Abstract

Powders of Ba0.65Sr0.35TiO3 have been prepared by solution-based and conventional mixed-oxide routes. Powders made by freeze-drying a precursor solution of mixed catecholate complexes of BaTiO3 and SrTiO3 had the smallest particle size, but secondary grain growth during sintering negated the anticipated benefits of the nano-sized powder in relation to ceramic densification and microstructural control. Addition of manganese oxide suppressed secondary grain growth for catecholate powders, allowing 97% dense ceramics to be produced at a sintering temperature of 1300 °C, with grain sizes of ≤5 μm. Doped mixed-oxide samples continued to show secondary grain growth, leading to coarse microstructures with grain sizes ≤100 μm after sintering at 1400 °C. Curie peaks for catecholate samples were sharper than those for mixed-oxide samples, suggesting a more uniform distribution of Ba and Sr ions in the powders. Difficulties were encountered in controlling the (Ba + Sr)/Ti ratio of powders made by an oxalate solution-precipitation route.

Type
Articles
Copyright
Copyright © Materials Research Society 2006

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.Clabaugh, W.S., Swiggard, E.M., Gilchrist, R.: Preparation of barium titanyl oxalate for conversion to barium titanate of high purity. J. Res. Natl. Bur. Stand. 56, 289 (1956).CrossRefGoogle Scholar
2.Osseo-Asare, K., Arriagada, F.J., Adair, J.H. Solubility relationships in the co-precipitation synthesis of barium titanate: Heterogeneous equilibria in the Ba–Ti–C2O4–H2O system, in Ceramic Transactions. Vol. I, edited by Messing, G.L., Fuller, E.R., and Hausner, H. (The American Ceramic Society, Columbus, Ohio, 1987), p. 47.Google Scholar
3.Murata, M.: U.S. Patent No. 4 061 583 (Dec. 6, 1977).Google Scholar
4.Pechini, M. P.: U.S. Patent No. 3 330 697 (July 11, 1967).Google Scholar
5.Mazdiyasni, K.S., Dollof, R.T., Smith, J.S.: Preparation of high purity submicron barium titanate powders. J. Am. Ceram. Soc. 52, 523 (1969).CrossRefGoogle Scholar
6.Phule, P.P., Risbud, S.H.: Low-temperature synthesis and processing of electronic materials in the BaO–TiO2 system. J. Mater. Sci. 25, 1169 (1990).CrossRefGoogle Scholar
7.Yang, W., Chang, A., Yang, B.: Preparation of barium strontium titanate ceramic by sol-gel method and microwave sintering. J. Mater. Synth. Process. 10, 303 (2002).CrossRefGoogle Scholar
8.Ali, N.J., Milne, S.J.: Synthesis and processing characteristics of Ba0.65Sr0.35TiO3 powders. J. Am. Ceram. Soc. 76, 2321 (1993).CrossRefGoogle Scholar
9.Roeder, R.K., Slamovich, E.B.: Stoichiometry control and phase selection in hydrothermally derived BaxSr1−xTiO3 powders. J. Am. Ceram. Soc. 82, 1665 (1999).CrossRefGoogle Scholar
10.Deshpande, S.B., Khollam, Y., Bhoraskar, Y.B., Date, S.K., Sainkara, S.R., Potdar, H.S.: Synthesis and characterisation of microwave-hydrothermally derived Ba1−xSrx TiO3 powders. Mater. Lett. 59, 293 (2005).CrossRefGoogle Scholar
11.Gallagher, P.K., Schrey, F., DiMarcello, F.V.: Preparation of semi-conducting titanate by chemical methods. J. Am. Ceram. Soc. 46, 359 (1963).CrossRefGoogle Scholar
12.Schrey, F.: Effect of pH on the chemical preparation of barium strontium titanate. J. Am. Ceram. Soc. 48, 401 (1965).CrossRefGoogle Scholar
13.Gallagher, P.K., Thomson, J.: Thermal analysis of some barium and strontium titanyl oxalates. J. Am. Ceram. Soc. 48, 644 (1965).CrossRefGoogle Scholar
14.Kudaha, K., Lizuni, K., Sasaki, : Preparation of stoichiometric barium titanyl oxalate tetrahydrate. Am. Ceram. Soc. Bull. 61, 1236 (1982).Google Scholar
15.Khollam, Y.B., Bhoraskar, S.V., Deshpande, S.B., Potdar, H.S., Pavaskar, N.R., Sainkar, S.R., Date, S.K.: Simple chemical route for the quantitative precipitation of barium strontium titanyl oxalate precursor leading to Ba1−xSrxTiO3 powders. Mater. Lett. 57, 1871 (2003).CrossRefGoogle Scholar
16.Herring, C.: Effect of change of scale on sintering phenomena. J. Appl. Phys. 21, 301 (1950).CrossRefGoogle Scholar
17.Wei, X.Z., Padture, N.P.: Hydrothermal synthesis of tetragonal BST powders. J. Ceram. Proc. Res. 5, 175 (2004).Google Scholar
18.Song, H., Coble, R.L., Brook, R.J. The applicability of Herring's scaling law to the sintering of powders, in Materials Science Research, Vol. 16, edited by Kuczynski, G.C., Miller, A.E., and Sargent, G.A. (Plenum Press, New York, 1984), pp. 6379.CrossRefGoogle Scholar
19.Rhodes, W.H.: Agglomerate and particle size effects on sintering yttria stabilised zirconia. J. Am. Ceram. Soc. 64, 19 (1981).CrossRefGoogle Scholar
20.Yan, M.F. Effect of physical, chemical and kinetic factors on ceramic sintering, in Advances in Ceramic Vol. 21, edited by Messing, G.L., Mazdiyasni, K.S., McCauley, J.W., and Haber, R.A. (American Ceramic Society, Columbus, OH, 1987), p. 635.Google Scholar
21.Harmer, M.P. Science of sintering as related to ceramic powder processing, in Ceramic Transactions, Vol. 1, edited by Messing, G.L.Fuller, E.R., and Hausner, H. (American Ceramic Society, Columbus OH, 1988), p. 824.Google Scholar
22.Brook, R.J., Tuan, W.H., Xue, L.A. Critical issues and future directions in sintering science, in Ceramic Transactions Vol. 1, edited by Messing, G.L., Fuller, E.R., and Hausner, H. (American Ceramic Society, Columbus, OH, 1988), p 811.Google Scholar
23.Evans, A.G.: Consideration of inhomogeneity effects in sintering. J. Am. Ceram. Soc. 65, 497 (1982).CrossRefGoogle Scholar
24.Lange, F.F.: Sinterability of agglomerated powders. J. Am. Ceram. Soc. 67, 83 (1984).CrossRefGoogle Scholar
25.Raj, R., Bordia, R.K.: Sintering behaviour of bimodal powder compacts. Acta Metall. 32, 1003 (1984).CrossRefGoogle Scholar
26.Tuan, W.H.: Sintering stresses and the fabrication of ceramic composites. Ph.D. Thesis, University of Leeds, Leeds, UK (1988).Google Scholar
27.Xue, L.A.: Additives and the control of grain growth in BaTiO3 ceramics. Ph.D. Thesis, University of Leeds, Leeds, UK, (1987).Google Scholar
28.Kulscar, F.: A microstructure study of BaTiO3 ceramics. J. Am. Ceram. Soc. 39, 13 (1956).Google Scholar
29.Jaffe, B., Cooke, W.R., Jaffe, H.: Piezoelectric Ceramics (Academic Press, London, UK, 1971).Google Scholar
30.Mostaghaci, H. Fast firing and hot pressing of BaTiO3 composition. Ph.D. Thesis, University of Leeds, Leeds, UK (1982).Google Scholar
31.Hennings, D. Recrystallisation of BaTiO3 ceramics, in Science of Ceramics Vol. 12, edited by. Vincenzini, P. (Ceramurgia, Italy, 1984), p. 341.Google Scholar
32.Jonker, G.H., Noorlander, W. Grain size of sintered BaTiO3, in Science of Ceramics Vol. 1, edited by Stewart, G.H. (Academic Press, London, UK, 1962) p. 255.Google Scholar
33.Desu, S.B., Payne, D.A.: Interfacial segregation in perovskites, I. Theory and II. Experimental evidence. J. Am. Ceram. Soc. 73, 3391 (1990).CrossRefGoogle Scholar