journal article·2010-02

Function of magnesium aluminate hydrate and magnesium nitrate as MgO addition in crystal structure and grain size control of α-Al2O3 during sintering

Soumen Pal, A. K. Bandyopadhyay, S. Mukherjee, B. N. Samaddar, P. G. Pal

Bulletin of Materials Science· Volume 33· Issue 1
Publisher page

Abstract

Chemically pure reactive alumina (α-Al2O3) which is commercially available was used for densification study in presence of widely accepted dopant MgO as additive. MgO was added both as spinel (MgAl2O4) forming precursor i.e. magnesium aluminate hydrate, and magnesium nitrate. Sintering investigations were conducted in the temperature range 1500–1600°C with 2 h soaking. Structural study of sintered pellets was carried out by extensive XRD analysis. Scanning electron mode SEM images of the specimens were considered to understand the effect of both types of additions. Addition of MgO within and beyond optimum amount had some effect on development of microstructure of sintered bodies. Densification, around 99% ρ th, with fine grain microstructure was achieved. These different types of additions caused two distinct changes in crystal structure of alumina—one small contraction and the other expansion of unit cell parameters.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Advanced ceramic materials synthesis · Aluminum Alloys Composites Properties · Microwave Dielectric Ceramics Synthesis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (17)

Show source-provided references
1. Cahoon H P and Christerson J 1956 J. Am. Ceram. Soc. 39 33710.1111/j.1151-2916.1956.tb15599.x ↗
2. Coble R L 1961 J. Appl. Phys. 32 79310.1063/1.1736108 ↗
3. Coble R L 1962 U.S. Patent 302610
4. Cohen Abraham, Van der Merwe C P and Kingon A I 1984 in Advances in ceramics (ed.) W D Kingery (Ohio, Columbus: Am. Ceram. Soc. Inc.) Vol. 10 pp 780–790
5. Cullity B D 1959 Elements of X-ray diffraction (USA: Addison-Wesley Publishing Company, Inc.) p. 309
6. Haroun N A and Budworth D W 1970 Br. Ceram. Trans. 69 73
7. Johnson W C and Coble R L 1978 J. Am. Ceram. Soc. 61 11010.1111/j.1151-2916.1978.tb09250.x ↗
8. Jorgensen P J 1965 J. Am. Ceram. Soc. 48 20710.1111/j.1151-2916.1965.tb14714.x ↗
9. Jorgensen P J and Westbrook J H 1964 J. Am. Ceram. Soc. 47 33210.1111/j.1151-2916.1964.tb12996.x ↗
10. Li C W and Kingery W D 1984 in Advances in ceramics (ed.) W D Kingery (Columbus, Ohio: Am. Ceram. Soc. Inc.) Vol. 10 pp 368–378
11. Mukherjee S G and Samaddar B N 1969 Indian J. Chem. 7 183
12. Paul P G and Samaddar B N 1985 Trans. Ind. Ceram. Soc. 44 13210.1080/0371750X.1985.10822763 ↗
13. Samaddar B N, Paul P G and Bhattacharyya Hemanta 1979 Trans. Ind. Ceram. Soc. 38 15110.1080/0371750X.1979.10840907 ↗
14. Smothers W J and Reynolds H J 1954 J. Am. Ceram. Soc. 37 58810.1111/j.1151-2916.1954.tb13993.x ↗
15. Taylor R I, Coad J P and Brook R J 1974 J. Am. Ceram. Soc. 57 53910.1111/j.1151-2916.1974.tb10809.x ↗
16. Taylor R I, Coad J P and Hughes A E 1976 J. Am. Ceram. Soc. 59 37410.1111/j.1151-2916.1976.tb10993.x ↗
17. Warman M O and Budworth D W 1967 Br. Ceram. Trans. 66 253