MULTI-SPECTROSCOPIC STUDY OF FE(II) IN SILICATE GLASSES: IMPLICATIONS FOR THE COORDINATION ENVIRONMENT OF FE(II) IN SILICATE MELTS

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dc.contributor.author Jackson W.E.
dc.contributor.author Farges F.
dc.contributor.author Yeager M.
dc.contributor.author Mabrouk P.A.
dc.contributor.author Rossano S.
dc.contributor.author Waychunas G.A.
dc.contributor.author Solomon E.I.
dc.contributor.author Brown Jr.G.E.
dc.date.accessioned 2023-11-18T10:28:12Z
dc.date.available 2023-11-18T10:28:12Z
dc.date.issued 2005
dc.identifier https://www.elibrary.ru/item.asp?id=12092112
dc.identifier.citation Geochimica et Cosmochimica Acta, 2005, 69, 17, 4315-4332
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/41827
dc.description.abstract The coordination environment of Fe(II) has been examined in seven anhydrous ferrosilicate glasses at 298 K and 1 bar using 57Fe Mössbauer, Fe K-edge X-ray near edge structure (XANES), and extended X-ray absorption fine structure (EXAFS), UV-Vis-NIR, and magnetic circular dichroism (MCD) spectroscopies. Glasses of the following compositions were synthesized from oxide melts (abbreviation and nonbridging oxygen:tetrahedral cation ratio (NBO/T) in parentheses): Li2FeSi3O8 (LI2: 1.33), Rb2FeSi3O8 (RB2: 1.33), Nal.08Fel.l7Si3.l3O8 (NAl: 1.09), Nal.46Ca0.24Fel.08Si2.97O8 (NC6: 1.38), Nal.09Ca0.51Fe0.72Si3.10O8 (NC2: 1.15), Na0.99Ca0.92Fe0.24 Si3.17O8 (NCl: 1.04), and Na0.29Mg0.53Ca0.52Fe0.56Al0.91Si2.44O8 (BAS: 1.05). Mössbauer, XANES, and EXAFS information suggests that iron is dominantly ferrous in all glasses (
dc.title MULTI-SPECTROSCOPIC STUDY OF FE(II) IN SILICATE GLASSES: IMPLICATIONS FOR THE COORDINATION ENVIRONMENT OF FE(II) IN SILICATE MELTS
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2005.01.008


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