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  • 2020-2023  (1)
  • 2000-2004  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 27 (2000), S. 371-376 
    ISSN: 1432-2021
    Keywords: Key words Enstatite ; Forsterite ; 1H NMR ; FTIR ; Water ; Nominally anhydrous minerals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Samples of enstatite and forsterite were crystallized in the presence of a hydrous fluid at 15 kbar and 1100 °C. Water contents in quenched samples were measured by 1H MAS NMR and by FTIR. If the samples were prepared in the same way, similar water concentrations were obtained by both methods. There is no evidence that one or the other method would severely over or underestimate water contents in nominally anhydrous minerals. However, measured water contents vary by orders of magnitude depending on sample preparation. The lowest water contents are measured by polarized FTIR spectroscopy on clear, inclusion-free single crystals. These water contents probably reflect the real point defect solubility in the crystals. Polycrystalline material shows much higher total water concentrations, presumably due to hydrous species on grain boundaries, growth defects, and in submicroscopic fluid inclusions. Grinding the sample in air further increases water concentration. This effect is even more pronounced if the sample is ground in water and subsequently dried at 150 °C. Polarized FTIR measurements on clear single crystals of enstatite saturated at 15 kbar and 1100 °C give 199 ± 25 ppm by weight of water. The spectra show sharp and strongly polarized bands. These bands are also present in spectra measured through turbid, polycrystalline aggregates of enstatite. However, in these spectra, they are superimposed on much broader, nearly isotropic bands resulting from hydrous species in grain boundaries, growth defects, and submicroscopic fluid or melt inclusions. Total water contents for these polycrystalline aggregates are between 2000 and 4000 ppm. Water contents measured by FTIR on enstatite powders are 5300 ppm after grinding in air and 12 600 ppm after grinding under water und subsequent drying at 150 °C.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2020-02-12
    Keywords: 550 - Earth sciences
    Type: info:eu-repo/semantics/article
    Format: application/pdf
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  • 3
    Publication Date: 2022-08-18
    Description: The solubility of N2 in basaltic (MORB) and haplogranitic melts was studied at oxidizing conditions (oxygen fugacity about two log units above the Ni–NiO buffer). Under these conditions, N2 is expected to be the only significant nitrogen species present in the melt. Experiments were carried out from 0.1 to 2 GPa and 1000–1450 ˚C using either an externally heated TZM pressure vessel, an internally heated gas pressure vessel or a piston cylinder apparatus. Nitrogen contents in run product glasses were quantified by SIMS (secondary ion mass spectrometry). To discriminate against atmospheric contamination, 15N-enriched AgN3 was used as the nitrogen source in the experiments. According to infrared and Raman spectra, run product glasses contain N2 as their only dissolved nitrogen species. Due to interactions with the matrix, the N2 molecule becomes slightly infrared active. Nitrogen solubility in the melts increases linearly with pressure over the entire range studied; the effect of temperature on solubility is small. The data may, therefore, be described by simple Henry constants Khaplogranite = (1461 ± 26) ppm N2/GPa and KMORB = (449 ± 21) ppm N2/GPa, recalculated to ppm by weight (μg/g) of isotopically normal samples. These equations describe the solubility of nitrogen during MORB generation and during melting in the crust, as we show by thermodynamic analysis that N2 is the only significant nitrogen species in these environments. Nitrogen solubility in the haplogranitic melt is about three times larger than for the MORB melt, as is expected from ionic porosity considerations. If expressed on a molar basis, nitrogen solubility is significantly lower than argon solubility, in accordance with the larger size of the N2 molecule. Notably, N2 solubility in felsic melts is also much lower than CO2 solubility, even on a molar basis. This implies that the exsolution of nitrogen may drive vapor oversaturation in felsic melts derived from nitrogen-rich sediments. We also measured the partitioning of nitrogen between olivine, pyroxenes, plagioclase, garnet, and basaltic melt by slowly cooling MORB melts to sub-liquidus temperatures to grow large crystals. The mineral/melt partition coefficients of nitrogen range from 0.001 to 0.002, and are similar to argon partition coefficients. These new data, therefore, support the assumption that there is little fractionation between nitrogen and argon during mantle melting and that the N2/Ar ratio in basalts and xenoliths is, therefore, representative of the N2/Ar ratio in the mantle source. This assumption is essential for assessing the size of the nitrogen reservoir in the mantle. Our data also show that for an upper mantle oxidation state that is similar to the one observed today, nitrogen outgassing by partial melting is extremely efficient and even low melt fractions in the range of a few percent may extract nearly all nitrogen from the mantle source.
    Language: English
    Type: info:eu-repo/semantics/article
    Format: application/pdf
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