Published December 2021 | Version v1
Journal article

Anomalous phase transformation of Li2TiO3 during sintering in oxygen atmosphere: A dilatometry study

  • 1. Powder Metallurgy Division, Bhabha Atomic Research Centre, Vashi Complex, Navi Mumbai, 400705 (India)
  • 2. Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400085 (India)

Description

Highlights: • Remarkably improved sinterability was observed in BeO doped Li2TiO3. • For the first time, monoclinic-to-cubic phase transformation in Li2TiO3 was observed at unusually low sintering temperature. • Monoclinic-to-cubic phase transformation was not observed after small quantity of BeO doping in Li2TiO3. Augmenting the sinter-ability of powder is helpful to address problems such as Li sublimation and rapid grain growth related to the sintering of lithium-bearing ceramics as tritium breeder materials. In the present work, the sintering behavior of pure phase Li2TiO3 powders with and without BeO doping synthesized by urea assisted solid-state method was probed employing dilatometry analysis in the O2 atmosphere. Results revealed surprisingly low sintering onset temperature (∼715 °C) of un-doped Li2TiO3. Increasing sintering temperature to about 970 °C resulted in an anomalous monoclinic-to-cubic phase transformation characterized by unusually low transformation temperature and irreversible nature. Such phase transformation of Li2TiO3 has been usually reported in temperature range 1150–1250 °C which is significantly higher than observed in the present work. Interestingly, after BeO doping, a further reduction in sintering temperature with improved densification and suppression of the phase transformation was observed.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.fusengdes.2021.112950

Additional details

Identifiers

DOI
10.1016/j.fusengdes.2021.112950;
PII
S0920379621007262;

Publishing Information

Journal Title
Fusion Engineering and Design
Journal Volume
173
Journal Page Range
vp.
ISSN
0920-3796
CODEN
FEDEEE

Optional Information

Copyright
Copyright (c) 2021 Elsevier B.V. All rights reserved.