Lower mantle hydrogen partitioning between periclase and perovskite: A quantum chemical modelling. (15th January 2016)

• Record Type: Journal Article
• Authors: Merli, Marcello; Bonadiman, Costanza; Diella, Valeria; Pavese, Alessandro
• Is Part Of: Geochimica et cosmochimica acta. Volume 173(2016:Jan. 15)
• Page Start: 304
• Page End: 318
• Publication Date: 2016-01-15
• Subjects: Geochemistry -- Periodicals; Meteorites -- Periodicals; Géochimie -- Périodiques; Météorites -- Périodiques; Geochemie; Astrochemie; Electronic journals; 551.905
• DOI: 10.1016/j.gca.2015.10.025
• Languages: English
• ISSNs: 0016-7037

Abstract

Abstract: Partitioning of hydrogen (often referred to as H2 O) between periclase ( pe ) and perovskite ( pvk ) at lower mantle conditions (24–80 GPa) was investigated using quantum mechanics, equilibrium reaction thermodynamics and by monitoring two H-incorporation models. One of these (MSWV) was based on replacements provided by Mg 2+ ↔ 2H + and Si 4+ ↔ 4H + ; while the other (MSWA) relied upon substitutions in 2Mg 2+ ↔ Al 3+ + H + and Si 4+ ↔ Al 3+ + H + . H2 O partitioning in these phases was considered in the light of homogeneous (Bulk Silicate Earth; pvk : 75%– pe :16% model contents) and heterogeneous (Layered Mantle; pvk :78%– pe :14% modal contents) mantle geochemical models, which were configured for lower and upper bulk water contents ( BWC ) at 800 and 1500 ppm, respectively. The equilibrium constant, BWC K ( P, T ), for the reactions controlling the H-exchange between pe and pvk exhibited an almost negligible dependence on P, whereas it was remarkably sensitive to T, BWC and the hydrogen incorporation scheme. Both MSWV and MSWA lead to BWC K ( P, T ) ⩽ 1, which suggests a ubiquitous shift in the exchange reaction towards an H2 O-hosting perovskite. This took place more markedly in the latter incorporation mechanism, indicating that H2 O-partitioning is affected by the uptake mechanism. In general, the larger the BWC, the smaller the BWC K ( P, T ). Over the BWC reference range, MSWV led to BWC K ( P, T )-grand average (〈 BWC K 〉) calculated along lower mantle P – T -paths of ≈0.875. With regard to the MSWA mechanism, 〈 BWC K 〉 was more sensitive to BWC (and LM over BSE), but its values remained within the rather narrow 0.61–0.78 range. The periclase–perovskite H2 O concentration-based partition coefficient, Kd H 2 O pe / pvk, was inferred using 〈 BWC K 〉, assuming both hydrous and anhydrous-dominated systems. MSWV revealed a Kd H 2 O pe / pvk – BWC linear interpolation slope which was close to 0 and Kd H 2 O pe / pvk values of 0.36 and 0.56 (for anhydrous and hydrous system, respectively). MSWA, in turn, yielded a Kd H 2 O pe / pvk trend with a slightly steeper negative BWC -slope, while it may also be considered nearly invariant with Kd H 2 O pe / pvk values of 0.31–0.47 in the 800–1500 ppm interval. Combining the MSWV and MSWA results led to the supposition that Kd H 2 O pe / pvk lies in the narrow 0.31–0.56 interval, as far as the P – T – BWC values of interest are concerned. This implies that water always prefers pvk to pe . Furthermore, it also suggests that even in lower mantle with low or very low bulk water content, periclase rarely becomes a pure anhydrous phase.