Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

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Publications (1/1 displayed)

  • 2002A SAXS/WAXS XAFS study of crystallisation in cordierite glass16citations

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Bras, W.
1 / 13 shared
Greaves, G. N.
1 / 6 shared
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2002

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  • Bras, W.
  • Greaves, G. N.
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article

A SAXS/WAXS XAFS study of crystallisation in cordierite glass

  • Oversluizen, M.
  • Bras, W.
  • Greaves, G. N.
Abstract

<p>New Cr X-ray absorption fine structure (XAFS) data have been combined with the results of small angle X-ray scattering (SAXS) and wide angle X-ray scattering (WAXS) experiments to probe in detail the crystallisation mechanism in cordierite (Mg<sub>2</sub>Al<sub>4</sub>Si<sub>5</sub>O<sub>18</sub> glass doped with 0.34 mol% Cr<sub>2</sub>O<sub>3</sub>. By direct comparison with chromo-aluminate spinels (MgCr<sub>2x</sub>Al<sub>2(1-x)</sub>O<sub>4</sub> Cr XAFS is used to determine the composition of the devitrified Cr species. This is identified as MgCr<sub>0.18</sub>Al<sub>1.82</sub>O<sub>4</sub>, which can be directly related to the Cr content in the starting glass and as a result the total crystalline volume in the fully developed ceramic is predicted to be 4%. In situ WAXS not only reveals the presence of the spinel phase but also a silica-rich stuffed quartz phase. This grows independently of the spinel and is probably nucleated from the glass surface. From our knowledge of the compositions of both crystalline phases we are able to deduce that the SAXS contrast between the surrounding glass and the spinel crystallites is 30 times greater than that between the quartz crystallites and the glass matrix, and therefore dominates the measured scattered intensity and the SAXS invariant that is derived from it. As a consequence we are able to show that the spinel crystalline volume fraction inherent in the SAXS is in close agreement with the 4% value obtained from the Cr XAFS. Furthermore in situ SAXS reveals the gradual development of the spinel particle size and shape during heat treatment. This is conducted in the super-cooled region just above the glass transition temperature, T<sub>g</sub>. By employing a two-step annealing process nucleation can be separated from growth and from time-resolved SAXS measurements the alumino-chromate nanocrystals are found to be closely monodispersed. Over a total time course of 600 min they grow from rough crystallites to smooth spherical particles of radius 21 ± 2 nm, with a final density of (1.2 ± 0.4) × 10<sup>21</sup> m<sup>-3</sup>. As the process of ceramic formation takes place in the viscous melt, growth is indeed found to be limited by diffusion and is complete when all the Cr is exhausted. We use this comprehensive in situ study of crystallisation in cordierite glass to demonstrate the advantages of combining SAXS, WAXS and XAFS for probing the time-resolved chemistry, the microstructure and its development from nucleation sites, that underpins the processing of nanoparticle ceramics.</p>

Topics
  • nanoparticle
  • density
  • impedance spectroscopy
  • microstructure
  • surface
  • experiment
  • melt
  • crystalline phase
  • glass
  • glass
  • glass transition temperature
  • annealing
  • small angle x-ray scattering
  • cordierite
  • X-ray absorption fine structure spectroscopy