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Ordered coalescence of nano crystallites contributing to the rapid anisotropic grain growth in silicon nitride ceramics
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
2013 (English)In: Scripta Materialia, ISSN 1359-6462, E-ISSN 1872-8456, Vol. 69, no 3, p. 270-273Article in journal (Refereed) Published
Abstract [en]

Microstructural characterization is performed on two dense Si3N4 ceramic samples consolidated by spark plasma sintering (SPS): one fabricated using alpha-Si3N4 and the other using beta-Si3N4 as the starting powder. A novel mechanism is revealed where ordered coalescence of nano beta-crystallites accelerate the rapid beta-Si3N4 anisotropic grain growth. The rapid alpha- to beta-Si3N4 phase transformation via a high supersaturation of dissolved Si3N4 in the melt favors this mechanism. The high heating rate by SPS is essential for achieving such supersaturation.

Place, publisher, year, edition, pages
2013. Vol. 69, no 3, p. 270-273
Keywords [en]
Abnormal grain growth, Phase transformations, Interface defects, Spark plasma sintering, HREM
National Category
Nano Technology Materials Chemistry Metallurgy and Metallic Materials
Research subject
Inorganic Chemistry
Identifiers
URN: urn:nbn:se:su:diva-89296DOI: 10.1016/j.scriptamat.2013.04.017ISI: 000320841900017OAI: oai:DiVA.org:su-89296DiVA, id: diva2:616935
Funder
Swedish Research Council
Note

AuthorCount: 2;

Available from: 2013-04-19 Created: 2013-04-19 Last updated: 2022-02-24Bibliographically approved
In thesis
1. Grain growth by Ordered Coalescence of crystallites in Ceramics: Grain Growth Mechanisms, Microstructure Evolution and Sintering
Open this publication in new window or tab >>Grain growth by Ordered Coalescence of crystallites in Ceramics: Grain Growth Mechanisms, Microstructure Evolution and Sintering
2013 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Grain growth and densification process play the two most crucial roles on the microstructure evolution and the achieved performances during sintering of ceramics. In this thesis, the grain growth of SrTiO3, BaTiO3-SrTiO3 solid solutions and Si3N4 ceramics during spark plasma sintering (SPS) were investigated by electron microscopy.

SrTiO3 ceramics starting from nanopowders were fabricated by SPS. A novel grain growth mechanism was discovered and named as ordered coalescence (OC) of nanocrystals. This mechanism involved nanocrystals as building blocks and is distinguished from atomic layer epitaxial growth (AEG) in classical sintering theory. The results also revealed that the dominant grain growth mechanism can be changed by varying heating rates. Low rate (10°C/min) gives AEG, whereas high rates (≥ 50°C/min) yields three-dimensional coalescence of nanocrystals, i.e. OC.

BaTiO3-SrTiO3 sintered bodies were made by SPS of BaTiO3 and SrTiO3 nanopowders mixtures. A novel Sr1-xBaxTiO3 “solid solution” with mosaic-like single crystal structure was manufactured by OC of the precursor crystallites. This reveals a new path for preparation of solid solution grains or composites.  

Si3N4 ceramics were prepared from α- or β-Si3N4 nanopowders at the same SPS conditions. The anisotropic OC of precipitated β-Si3N4 crystallites gives elongated β-Si3N4 grains at 1650°C using α-Si3N4 nanopowder. In contrast, AEG leads to the equi-axed β-Si3N4 grains using β-Si3N4 nanopowder. The metastable α- to β-Si3N4 phase transformation and OC accelerates anisotropic grain growth.

Grain motions contribute to the densification process during pressureless sintered 3Y-ZrO2 (>87%TD) or SPS of SrTiO3 (>92%TD) ceramics. This extends the sintering range for active grain re-arrangement over that predicted by classical theory.

In this thesis a new grain growth mechanism (OC) is proved by using SPS and nanopowders. By OC the microstructural evolution can be manipulated.

Place, publisher, year, edition, pages
Stockholm: Department of Materials and Environmental Chemistry (MMK), Stockholm University, 2013. p. 80
National Category
Materials Chemistry Inorganic Chemistry
Research subject
Inorganic Chemistry
Identifiers
urn:nbn:se:su:diva-88628 (URN)978-91-7447-677-4 (ISBN)
Public defence
2013-06-13, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, Stockholm, 13:00 (English)
Opponent
Supervisors
Note

At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 2: Accepted. Paper 3: Submitted. Paper 4: Manuscript. Paper 7: Accepted.

Available from: 2013-05-16 Created: 2013-03-22 Last updated: 2022-02-24Bibliographically approved

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Hu, JianfengShen, Zhijian

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