Abstract
We present a new technique for the quantification of water in glasses down to the parts per million level, using confocal microRaman spectroscopy with the recently developed “Comparator Technique.” To test this method, we used a suite of glasses and gemstone-quality garnets with varying chemical compositions. Water contents were independently determined with proton-proton (pp) scattering and infrared (IR) spectroscopy. Moreover, water concentrations obtained for the garnets were compared to data from a study by Maldener et al. (2003) using nuclear reaction analysis (NRA). For each sample, we recorded Raman spectra in the frequency range from 3100 to 3750 cm-1 and standardized them using an independently well-characterized glass. In this paper, we demonstrate the usefulness of this technique for quantifying water concentrations in natural and synthetic glass samples and garnets, and verify its adaptability for concentrations from 40 wt ppm up to 40 wt% H2O. However, in the case of absorbing material (e.g., Fe-bearing samples), the suggested method needs to be modified to overcome problems due to heating and melting of those phases. Furthermore, we propose an integrated molar absorption coefficient for water in quartz glass, εitot = 72 000 ± 12 000 Lmol-1H₂Ocm-2, for quantitative IR spectroscopy that is higher than a previously reported value of Paterson (1982) or that predicted by the general calibration trend determined by Libowitzky and Rossman (1997).
© 2015 by Walter de Gruyter Berlin/Boston
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Articles in the same Issue
- Amorphous materials: Properties, structure, and durability: Atomic structure and transport properties of MgO-Al2O3 melts: A molecular dynamics simulation study
- Amorphous Materials: Properties, structure, and durability: Oxidation state of iron in hydrous phono-tephritic melts
- Amorphous materials: Properties, structure, and durability: Quantitative Raman spectroscopy: Speciation of Na-silicate glasses and melts
- Dissolution-reprecipitation of zircon at low-temperature, high-pressure conditions (Lanzo Massif, Italy)
- High-pressure behavior of gypsum: A single-crystal X-ray study
- Presence and zoning of hydrous components in leucite from the Alban Hills volcano, Rome, Italy
- Herderite from Mogok, Myanmar, and comparison with hydroxyl-herderite from Ehrenfriedersdorf, Germany
- Application of Raman spectroscopy to quantify trace water concentrations in glasses and garnets
- Neutron diffraction study of δ-AlOOD at high pressure and its implication for symmetrization of the hydrogen bond
- A simple predictive model for the thermal expansion of AlSi3 feldspars
- New data on PGE alloy minerals from a very old collection (probably 1890s), California
- High-pressure study on lead fluorapatite
- High-pressure Al-rich hexagonal phases—What are their kin?
- Leucite at high pressure: Elastic behavior, phase stability, and petrological implications
- Thermodynamic mixing properties of Rb-K feldspars
- Demicheleite, BiSBr, a new mineral from La Fossa crater, Vulcano, Aeolian Islands, Italy
- A lattice dynamical study of the aragonite and post-aragonite phases of calcium carbonate rock
- Water in natural olivine—determined by proton-proton scattering analysis
- Factors affecting heat transfer in natural SiO2 solids
- A solution model for high-temperature PbS-AgSbS2-AgBiS2 galena
- Incorporation of molybdate anion into β-FeOOH
- Disordering of Fe2+ over octahedrally coordinated sites of tourmaline
- Raman spectroscopy of CaIrO3 postperovskite up to 30 GPa
- The thermal behavior of richterite
- The crystal structure of kelyanite, (Hg2)6(SbO6)BrCl2
- Comparison of crystallographic orientations between living (Emiliania huxleyi and Gephyrocapsa oceanica) and fossil (Watznaueria barnesiae) coccoliths using electron microscopes
- Letter. Iron partitioning between perovskite and post-perovskite: A transmission electron microscope study
- Letter. An isosymmetric phase transition of orthopyroxene found by high-temperature X-ray diffraction