Electric field effect on chemical and phase equilibria in nano-TiB2–TiO2–TiBO3 system at <650 °C: an in situ time-resolved energy dispersive x-ray diffraction study with an ultrahigh energy synchrotron probe

Nano-TiB2 powder of 58 nm size with TiO2 and TiBO3 as secondary phases was heated with 20 °C to 1% TiB2 unit cell expansion, exceeding zero field thermally induced expansion. The current bursts also induced nonisothermal reaction between TiB2 and TiO2, yielding TiBO3 that is absent with no field. In...

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Veröffentlicht in:Journal of materials research 2017-01, Vol.32 (2), p.482-494
Hauptverfasser: Özdemir, Tevfik E., Akdoğan, Enver Koray, Şavklıyıldız, İlyas, Biçer, Hülya, Örnek, Metin, Zhong, Zhong, Tsakalakos, Thomas
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container_end_page 494
container_issue 2
container_start_page 482
container_title Journal of materials research
container_volume 32
creator Özdemir, Tevfik E.
Akdoğan, Enver Koray
Şavklıyıldız, İlyas
Biçer, Hülya
Örnek, Metin
Zhong, Zhong
Tsakalakos, Thomas
description Nano-TiB2 powder of 58 nm size with TiO2 and TiBO3 as secondary phases was heated with 20 °C to 1% TiB2 unit cell expansion, exceeding zero field thermally induced expansion. The current bursts also induced nonisothermal reaction between TiB2 and TiO2, yielding TiBO3 that is absent with no field. Increase from 16 to 40 V/cm shifts the TiB2 → TiBO3 reaction forward, decreases T onset but increases reaction rate. Analysis using Van’t Hoff relation, including electrochemical effects, precluded possibility of appreciable Joule heating, which was supported with adiabatic internal temperature calculations. The observed low temperature oxidation of TiB2 to TiBO3 that is electrochemically driven and is mediated by the TiO2 solid electrolyte.
doi_str_mv 10.1557/jmr.2016.466
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Mater. Res</addtitle><description>Nano-TiB2 powder of 58 nm size with TiO2 and TiBO3 as secondary phases was heated with 20 °C to &lt;650 °C in argon while applying an electric field. The powder became conductive at 520 and 305 °C (T onset) for 16 and 40 V/cm, respectively, at which point current bursts of 4.5 and 10.0 A (peak value) were observed. Current bursts were accompanied by &gt;1% TiB2 unit cell expansion, exceeding zero field thermally induced expansion. The current bursts also induced nonisothermal reaction between TiB2 and TiO2, yielding TiBO3 that is absent with no field. Increase from 16 to 40 V/cm shifts the TiB2 → TiBO3 reaction forward, decreases T onset but increases reaction rate. Analysis using Van’t Hoff relation, including electrochemical effects, precluded possibility of appreciable Joule heating, which was supported with adiabatic internal temperature calculations. 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Analysis using Van’t Hoff relation, including electrochemical effects, precluded possibility of appreciable Joule heating, which was supported with adiabatic internal temperature calculations. The observed low temperature oxidation of TiB2 to TiBO3 that is electrochemically driven and is mediated by the TiO2 solid electrolyte.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><doi>10.1557/jmr.2016.466</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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source Cambridge Journals; SpringerNature Journals
subjects Aluminum
Applied and Technical Physics
Biomaterials
Ceramics
Electric fields
Equilibrium
Grain boundaries
Grain growth
High temperature
Hot pressing
Inorganic Chemistry
Laboratories
Materials Engineering
Materials research
MATERIALS SCIENCE
Nanotechnology
Oxidation
phase transformation
Radiation
Sintering
title Electric field effect on chemical and phase equilibria in nano-TiB2–TiO2–TiBO3 system at <650 °C: an in situ time-resolved energy dispersive x-ray diffraction study with an ultrahigh energy synchrotron probe
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