Kaitianite, Ti3+2Ti4+O5, a new titanium oxide mineral from Allende

1Chi Ma,1John R. Beckett
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13576]
1Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California, 91125 USA
Published by arrangement with John Wiley & Sons

Kaitianite, Ti3+2Ti4+O5, is a new titanium oxide mineral discovered in the Allende CV3 carbonaceous chondrite. The type grain coexists with tistarite (Ti2O3) and rutile. Corundum, xifengite, mullite, osbornite, and a new Ti,Al,Zr‐oxide mineral are also present, although not in contact. The chemical composition of type kaitianite is (wt%) Ti2O3 56.55, TiO2 39.29, Al2O3 1.18, MgO 1.39, FeO 0.59, V2O3 0.08 (sum 99.07), yielding an empirical formula of (Ti3+1.75Al0.05Ti4+0.10Mg0.08Fe0.02)(Ti4+1.00)O5, with Ti3+ and Ti4+ partitioned, assuming a stoichiometry of three cations and five oxygen anions pfu. The end‐member formula is Ti3+2Ti4+O5. Kaitianite is the natural form of γ‐Ti3O5 with space group C2/c and cell parameters a = 10.115 Å, b = 5.074 Å, c = 7.182 Å, β = 112º, V = 341.77 Å3, and Z = 4. Both the type kaitianite and associated rutile likely formed as oxidation products of tistarite at temperatures below 1200 K, but this oxidation event could have been in a very reducing environment, even more reducing than a gas of solar composition. Based on experimental data on the solubility of Ti3+ in equilibrium with corundum from the literature, the absence of tistarite in or on Ti3+‐rich corundum (0.27–1.45 mol% Ti2O3) suggests that these grains formed at higher temperatures than the kaitianite (>1579–1696 K, depending on the Ti concentration). The absence of rutile or kaitianite in or on corundum suggests that any exposure to the oxidizing environment producing kaitianite in tistarite was too short to cause the precipitation of Ti‐oxides in or on associated corundum.


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