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At least 145 records · Page 8

Superionic iron oxide–hydroxide in Earth’s deep mantle

Water ice becomes a superionic phase under the high pressure and temperature conditions of deep planetary interiors of ice planets such as Neptune and Uranus, which affects interior structures and generates magnetic fields. The solid Earth, however, contains only hydrous minerals with a negligible amount of ice. Here we combine high pressure and temperature electrical conductivity experiments, Raman spectroscopy and first-principles simulations to investigate the state of hydrogen in the pyrite-type FeO 2 H x (x ≤ 1), which is a potential H-bearing phase near the core–mantle boundary. We find that when the pressure increases beyond 73 GPa at room temperature, symmetric hydroxyl bonds are softened and the H + (or proton) becomes diffusive within the vicinity of its crystallographic site. Increasing temperature under pressure, the diffusivity of hydrogen is extended beyond the individual unit cell to cover the entire solid, and the electrical conductivity soars, indicating a transition to the superionic state, which is characterized by freely moving protons and a solid FeO 2 lattice. Furthermore, the highly diffusive hydrogen provides fresh transport mechanisms for charge and mass, which dictate the geophysical behaviours of electrical conductivity and magnetism, as well as geochemical processes of redox, hydrogen circulation and hydrogen isotopic mixing in Earth’s deep mantle.

58 GEOSCIENCES↗

Effect of Dipole Interactions on Blocking Temperature and Relaxation Dynamics of Superparamagnetic Iron-Oxide (Fe 3 O 4 ) Nanoparticle Systems

The effects of dipole interactions on magnetic nanoparticle magnetization and relaxation dynamics were investigated using five nanoparticle (NP) systems with different surfactants, carrier liquids, size distributions, inter-particle spacing, and NP confinement. Dipole interactions were found to play a crucial role in modifying the blocking temperature behavior of the superparamagnetic nanoparticles, where stronger interactions were found to increase the blocking temperatures. Consequently, the blocking temperature of a densely packed nanoparticle system with stronger dipolar interactions was found to be substantially higher than those of the discrete nanoparticle systems. The frequencies of the dominant relaxation mechanisms were determined by magnetic susceptibility measurements in the frequency range of 100 Hz–7 GHz. The loss mechanisms were identified in terms of Brownian relaxation (1 kHz–10 kHz) and gyromagnetic resonance of Fe 3 O 4 (~1.12 GHz). It was observed that the microwave absorption of the Fe 3 O 4 nanoparticles depend on the local environment surrounding the NPs, as well as the long-range dipole–dipole interactions. These significant findings will be profoundly important in magnetic hyperthermia medical therapeutics and energy applications.

36 MATERIALS SCIENCE↗

Iron Oxides of Mars: Evidence for Contemporary Weathering

Reflectance spectra of Mars were analyzed using a multiple high order derivative spectroscopy technique. Among the results of the analysis was the presence of suites of bands in each of the spectra that can be attributed to Fe(3e) phases. Several of the spectra contained bands that are very close to the band positions in the laboratory spectra of goethite, an hexagonal hydrated ferric oxide. Spectra of other areas showed absorption bands that were within 3% of the positions for hematite, and hexagonal close packed unhydrated Fe203. Remaining areas showed bands that are intermediate in position to the goethite and hematite bands, suggesting that there may be mixtures of goethite and hematite, and/or intermediate (partially dehydrated goethite) phases present in those areas. Both bright areas and dark areas showed suites of goethite bands and hematite bands, and there does not therefore appear to be a correlation with albedo. The areas that showed the goethite bands are, however, within zones of ongoing or historically frequent dust cloud activity, and the areas with the hematite bands were outside of the zones of frequent dust cloud activity. This suggests the possiblility that the more hydrated phase may occur within a mobile dust component.

Huguenin, R. L.↗

Observational evidence of crystalline iron oxides on Mars

A series of new spectral observations of Mars was obtained at Mauna Kea Observatory in the 0.4-1.0-micron wavelength range during the extremely favorable 1988 opposition, which yielded new spectral reflectance and relative reflectance data for a number of distinct spots on the Martian surface at 500-600 km spatial resolution. The new spectra revealed absorptions at 0.62-0.72 micron and at 0.81-0.94 micron, both seen clearly for the first time. These absorption features are interpreted as Fe(3+) electronic transition bands that indicate the presence of crystalline ferric oxide or hydroxide minerals on the Martian surface.

Bell, James F., III↗

The Isotopic Composition of Molecular Water Formed by Hydrogen Reduction of Iron Oxides: A Proxy for Endogenous Water Formed From Solar Wind Implantation

Many workers have successfully utilized a variety of lunar materials to infer the sources and processing history of volatiles on the Moon. In situ techniques via NanoSIMS have enabled a plethora of hydrogen isotope measurements of isolated grains in regolith and apatite within igneous rocks, revealing an extraordinarily large range of δD values from ~ -900 to +1000‰. The lowest of these δD values are related to the incorporation of solar wind hydrogen, which is pure 1 H. Exposure to solar wind results in structural damage to crystalline phases, forming ubiquitous tens-to-hundreds of nanometer thick amorphous rims on mature regolith grains. Solar wind implantation of H + is also is also thought to result in the formation of nanophase Fe 0 (npFe), a quantitative metric of surface exposure time (e.g., Is/FeO). The formation of npFe can be generally described via the reaction: Fe 2+ O + H 2 = Fe 0 + H 2 O, resulting in the formation of endogenous molecular water reservoirs.

lunar water↗