4.7 Article

Densification mechanism and microstructure characteristics of nano- and micro-crystalline alumina by high-pressure and low temperature sintering

Journal

JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
Volume 41, Issue 1, Pages 635-645

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jeurceramsoc.2020.08.018

Keywords

Spark plasma sintering; Densification; Plastic deformation; Grain growth

Funding

  1. National Natural Science Foundation of China [51521001, 51832003, 51902233, 51972243]
  2. National Key Research and Development Plan of China [2017YF130310400]
  3. Self-determined and Innovative Research Funds of Wuhan University of Technology [2019III059XZ]

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High-pressure sintering can effectively produce dense ceramics at relatively low temperatures. Research shows that sintering densification temperature and starting threshold temperature of grain growth increase with grain size and applied pressure. Ceramics sintered under high pressure and low temperature exhibit higher grain boundary energy, residual stress, and dislocation density compared to samples sintered without additional pressure.
Fully dense ceramics with retarded grain growth can be attained effectively at relatively low temperatures using a high-pressure sintering method. However, there is a paucity of in-depth research on the densification mechanism, grain growth process, grain boundary characterization, and residual stress. Using a strong, reliable die made from a carbon-fiber-reinforced carbon (C-f/C) composite for spark plasma sintering, two kinds of commercially pure alpha-Al2O3 powders, with average particle sizes of 220 nm and 3 m, were sintered at relatively low temperatures and under high pressures of up to 200 MPa. The sintering densification temperature and the starting threshold temperature of grain growth (T-sg) were determined by the applied pressure and the surface energy relative to grain size, as they were both observed to increase with grain size and to decrease with applied pressure. Densification with limited grain coarsening occurred under an applied pressure of 200 MPa at 1050 degrees C for the 220 nm Al2O3 powder and 1400 degrees C for the 3 m A1203 powder. The grain boundary energy, residual stress, and dislocation density of the ceramics sintered under high pressure and low temperature were higher than those of the samples sintered without additional pressure. Plastic deformation occurring at the contact area of the adjacent particles was proved to be the dominant mechanism for sintering under high pressure, and a mathematical model based on the plasticity mechanics and close packing of equal spheres was established. Based on the mathematical model, the predicted relative density of an Al2O3 compact can reach 80 % via the plastic deformation mechanism, which fits well with experimental observations. The densification kinetics were investigated from the sintering parameters, i.e., the holding temperature, dwell time, and applied pressure. Diffusion, grain boundary sliding, and dislocation motion were assistant mechanisms in the final stage of sintering, as indicated by the stress exponent and the microstructural evolution. During the sintering of the 220 nm alumina at 1125 degrees C and 100 MPa, the deformation tends to increase defects and vacancies generation, both of which accelerate lattice diffusion and thus enhance grain growth.

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