Journal of

GEOsciences

  (Formerly Journal of the Czech Geological Society)

Original paper

Paolo Ballirano, Beatrice Celata, HenriK Skogby, Giovanni B. Andreozzi, Ferdinando Bosi

HT breakdown of Mn-bearing elbaite from the Anjanabonoina pegmatite, Madagascar

Journal of Geosciences, volume 67 (2022), issue 2, 151 - 161

DOI: http://doi.org/10.3190/jgeosci.347



The thermal behavior of a gem-quality purplish-red Mn-bearing elbaite from the Anjanabonoina pegmatite, Madagascar, with composition X(Na0.410.35Ca0.24)Σ1.00 Y(Al1.81Li1.00Fe3+0.04Mn3+0.02Mn2+0.12Ti0.004)Σ3.00ZAl6[T(Si5.60B0.40)Σ6.00O18](BO3)3(OH)3 W[(OH)0.50F0.13O0.37]Σ1.00 was investigated using both in situ High-Temperature X-Ray powder diffraction (HT-pXRD) and ex situ X-Ray single-crystal diffraction (SC-XRD) on two single crystals previously heated in the air up to 750 and 850 °C. The first occurrence of mullite diffraction peaks allowed us to constrain the breakdown temperature of Mn-bearing elbaite at ambient pressure, at 825 °C. The breakdown products from the HT-pXRD experiments were cooled down to ambient temperature and identified via pXRD, represented by B-mullite and &gama;-LiAlSi2O6. A thermally induced oxidation of Mn2+ to Mn3+ was observed with both in-situ and ex-situ techniques; it started at 470 °C and is assumed to be counterbalanced by deprotonation, according to the equation: Mn2+ + (OH)- → Mn3+ + O2- + 1/2H2. At temperatures higher than 752 °C, a partial disorder between the Y and Z sites is observed from unit-cell parameters and mean bond distances, possibly caused by the inter-site exchange mechanism YLi + ZAl → ZLi + YAl. 

Journal of Geosciences, Published by © Czech Geological Society, with support from the Czech Geological Survey.
Webdesign inspired by aTeo. Hosted at the server of the Institute of Petrology and Structural Geology, Charles University, Prague.
ISSN: 1803-1943 (online), 1802-6222 (print)
email: jgeosci(at)jgeosci.org
cover_rotated.gif, 15kB

SNIP (Scopus, 2022): 0.826

IF (WoS, 2022): 1.4

5 YEAR IF (WoS, 2022): 1.8

Policy: Open Access

ISSN: 1802-6222

E-ISSN: 1803-1943