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American Mineralogist
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Disponibilidad
Institución detectada | Período | Navegá | Descargá | Solicitá |
---|---|---|---|---|
No detectada | desde feb. 1998 / hasta dic. 2023 | GeoScienceWorld |
Información
Tipo de recurso:
revistas
ISSN impreso
0003-004X
ISSN electrónico
1945-3027
País de edición
Estados Unidos
Fecha de publicación
1916-
Cobertura temática
Tabla de contenidos
doi: 10.2138/am-2022-8272
Characterization of vandenbrandeite: A potential alteration product of spent nuclear fuel
Victoria L. Frankland; Antoni E. Milodowski; Robert A. Lawrence; Marco Sacchi; David Read
<jats:title>Abstract</jats:title> <jats:p>The use of copper canisters in the Swedish KBS-3 concept for spent nuclear fuel disposal could result in the formation of copper-bearing uranyl phases should a canister suffer from defects or if the containment were to fail before reducing conditions are established in the repository. Most uranyl species would be expected to display higher solubility than the original uranium(IV) dioxide fuel, leading to enhanced release, though this would depend on the phase and prevailing groundwater conditions. Secondary alteration products may also be poorly crystalline or even amorphous, making characterization difficult during the pre-closure period owing to the high radiation field close to the canister. Vandenbrandeite, [CuUO2(OH)4], is a rare mineral in nature but known to form by alteration of primary uraninite through interaction with oxidizing groundwater containing dissolved copper. Consequently, an attempt has been made to characterize two vandenbrandeite specimens of varying crystallinity by luminescence and multiple-laser Raman spectroscopy; techniques amenable to remote, robotic deployment and which have proved useful in discriminating other uranyl oxy-hydroxides, silicates, and phosphates. The first reported luminescence emission and excitation spectra for vandenbrandeite revealed near-negligible luminescence, with a slightly enhanced signal for the specimen displaying poorer crystallinity. This observation agrees well with density functional theory calculations. The simulated projected density of state and band structure show an unlikely transition from the U f-orbitals to Cu d-orbitals, or O states, would be required for luminescence to be detectable; this probably improves for poorly crystalline specimens as the spatial overlap between the orbitals increases. Furthermore, negligible differences in the number of peaks and peak positions were detected in the laser wavelength-dependent Raman spectra although again, variation in background noise and peak shape was observed based on the degree of crystallinity. Good agreement was obtained between experimental and simulated Raman spectra, particularly with the environmentally sensitive axial uranyl stretching modes, validating the crystal system derived in this study. The findings of this study suggest luminescence spectroscopy, when combined with Raman spectroscopy, may be able to both identify vandenbrandeite and distinguish between crystalline and amorphous forms based on their relative luminescence intensity.</jats:p>
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 695-708
doi: 10.2138/am-2022-8403
The NaCl-CaCO3 and NaCl-MgCO3 systems at 6 GPa: Link between saline and carbonatitic diamond forming melts
Anton Shatskiy; Ivan V. Podborodnikov; Anastasia S. Fedoraeva; Anton V. Arefiev; Altyna Bekhtenova; Konstantin D. Litasov
<jats:title>Abstract</jats:title> <jats:p>The frequent occurrence of chlorides and carbonates in the form of microinclusions of melts or high-density fluid (HDF) in diamonds and igneous minerals of kimberlites worldwide generates genuine interest in their phase diagrams under pressure. Here, we present the first experimental results on the phase relations in the NaCl-CaCO3 and NaCl-MgCO3 systems at 6 GPa in the range 1000–1600 °C performed using a multi-anvil press. We found that both systems have the eutectic type of phase diagrams. The subsolidus assemblages are represented by halite + aragonite and halite + magnesite. Halite-aragonite eutectic is situated just below 1200 °C and has a composition of 40 wt% NaCl and 60 wt% CaCO3. Halite-magnesite eutectic is located at 1300 °C and has a composition of 72 wt% NaCl and 28 wt% MgCO3. The halite melting point was established at 1500 °C. Complete miscibility between carbonate and chloride liquids was observed up to 1600 °C. The results support the hypotheses that saline HDF is either a low-temperature derivative or precursor of mantle carbonatite HDF. The data also do not exclude an alternative hypothesis, according to which saline HDF are formed as a result of the reduction of the carbonate component of chloride-containing carbonatite melts to diamond.</jats:p>
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 709-718
Presentation of the Dana Medal of the Mineralogical Society of America for 2022 to Cin-Ty Lee
Roberta L. Rudnick; Fang-Zhen Teng
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 775-775
Acceptance of the Dana Medal of the Mineralogical Society of America for 2022
Cin-Ty Lee
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 776-776
Presentation of the Mineralogical Society of America Award for 2022 to Benjamin M. Tutolo
W.E. Seyfried; Nicholas J. Tosca
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 777-778
Acceptance of the Mineralogical Society of America Award for 2022
Benjamin M. Tutolo
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 779-780
Presentation of the 2022 Roebling Medal of the Mineralogical Society of America to John W. Valley
Jade Star Lackey; William H. Peck
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 781-781
Acceptance of the 2022 Roebling Medal of the Mineralogical Society of America
John W. Valley
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 782-783
New Mineral Names
Aaron J. Celestian
<jats:title>Abstract</jats:title> <jats:p>This issue of New Mineral Names provides a summary of five new species: pohlite, muonionalustaite, medvedevite, gysinite-(La), and nioboheftetjernite.</jats:p>
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 784-785
Book Review
Max Wilke
Palabras clave: Geochemistry and Petrology; Geophysics.
Pp. 786-786