International
Tables for
Crystallography
Volume H
Powder diffraction
Edited by C. J. Gilmore, J. A. Kaduk and H. Schenk

International Tables for Crystallography (2018). Vol. H, ch. 3.9, p. 362

Figure 3.9.14 

I. C. Madsen,a* N. V. Y. Scarlett,a R. Kleebergb and K. Knorrc

aCSIRO Mineral Resources, Private Bag 10, Clayton South 3169, Victoria, Australia,bTU Bergakademie Freiberg, Institut für Mineralogie, Brennhausgasse 14, Freiberg, D-09596, Germany, and cBruker AXS GmbH, Oestliche Rheinbrückenstr. 49, 76187 Karlsruhe, Germany
Correspondence e-mail:  ian.madsen@csiro.au

[Figure 3.9.14]
Figure 3.9.14

Raw in situ XRD data (Co Kα radiation) collected during the synthesis of the iron-ore sinter bonding phase SFCA-I (Webster et al., 2013[link]). The data, collected as a function of heating temperature, are viewed down the intensity axis with red representing the highest intensity and blue the lowest intensity. The identified phases include gibbsite Al(OH)3, calcite CaCO3, haematite Fe2O3, lime CaO, calcium ferrites CF and CFF, calcium alumina-ferrite C2F1−xAx, magnetite Fe3O4, and SFCA-I.