Compressional behavior and spin state of δ-(Al,Fe)OOH at high pressures

Author:

Ohira Itaru1,Jackson Jennifer M.2,Solomatova Natalia V.23,Sturhahn Wolfgang2,Finkelstein Gregory J.24,Kamada Seiji15,Kawazoe Takaaki67,Maeda Fumiya1,Hirao Naohisa8,Nakano Satoshi9,Toellner Thomas S.10,Suzuki Akio1,Ohtani Eiji1

Affiliation:

1. Department of Earth Science, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

2. Seismological Laboratory, California Institute of Technology, Pasadena, California 91125, U.S.A.

3. † Present address: Laboratoire de Géologie de Lyon, Ecole Normale Supérieure de Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5276, Lyon, France.

4. ‡ Present address: Hawaii Institute of Geophysics and Planetology, School of Ocean and Earth Sciences, University of Hawaii at Manoa, Honolulu, Hawaii 96822, U.S.A.

5. Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai 980-8578, Japan

6. Bayerisches Geoinstitut, University of Bayreuth, Bayreuth, 95440 Germany

7. Department of Earth and Planetary Systems Science, Graduate School of Science, Hiroshima University, Higashi-Hiroshima 739-8526, Japan

8. Japan Synchrotron Radiation Research Institute (JASRI), Hyogo, 679-5198, Japan

9. National Institute for Materials Science (NIMS), Tsukuba 305-0044, Japan

10. Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439, U.S.A.

Abstract

Abstract Hydrogen transport from the surface to the deep interior and distribution in the mantle are important in the evolution and dynamics of the Earth. An aluminum oxy-hydroxide, δ-AlOOH, might influence hydrogen transport in the deep mantle because of its high stability extending to lower mantle conditions. The compressional behavior and spin states of δ-(Al,Fe3+)OOH phases were investigated with synchrotron X-ray diffraction and Mössbauer spectroscopy under high pressure and room temperature. Pressure-volume (P-V) profiles of the δ-(Al0.908(9)57Fe0.045(1))OOH1.14(3) [Fe/(Al+Fe) = 0.047(10), δ-Fe5] and the δ-(Al0.832(5)57Fe0.117(1))OOH1.15(3) [Fe/(Al+Fe) = 0.123(2), δ-Fe12] show that these hydrous phases undergo two distinct structural transitions involving changes in hydrogen bonding environments and a high- to low-spin crossover in Fe3+. A change of axial compressibility accompanied by a transition from an ordered (P21nm) to disordered hydrogen bond (Pnnm) occurs near 10 GPa for both δ-Fe5 and δ-Fe12 samples. Through this transition, the crystallographic a and b axes become stiffer, whereas the c axis does not show such a change, as observed in pure δ-AlOOH. A volume collapse due to a transition from high- to low-spin states in the Fe3+ ions is complete below 32–40 GPa in δ-Fe5 and δ-Fe12, which i ~10 GPa lower than that reported for pure ε-FeOOH. Evaluation of the Mössbauer spectra of δ-(Al0.824(10)57Fe0.126(4))OOH1.15(4) [Fe/(Al+Fe) = 0.133(3), δ-Fe13] also indicate a spin transition between 32–45 GPa. Phases in the δ-(Al,Fe)OOH solid solution with similar iron concentrations as those studied here could cause an anomalously high ρ/νΦ ratio (bulk sound velocity, defined as K/ρ at depths corresponding to the spin crossover region (~900 to ~1000 km depth), whereas outside the spin crossover region a low ρ/νΦ anomaly would be expected. These results suggest that the δ-(Al,Fe)OOH solid solution may play an important role in understanding the heterogeneous structure of the deep Earth.

Publisher

Mineralogical Society of America

Subject

Geochemistry and Petrology,Geophysics

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