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SO 2 ‐rock interaction on Io: Reaction under highly oxidizing conditions
Author(s) -
Johnson M. L.,
Burnett D. S.
Publication year - 1993
Publication title -
journal of geophysical research: planets
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/92je02509
Subject(s) - albite , orthoclase , silicate , oxidizing agent , alkali metal , sulfate , geology , plagioclase , mineralogy , basalt , chemical composition , eutectic system , geochemistry , analytical chemistry (journal) , chemistry , crystallography , quartz , paleontology , organic chemistry , chromatography , microstructure
Laboratory simulations have been carried out to test the possibility that interactions of SO 2 and silicates can produce Na‐S compounds which can account for the observed surface enrichment of Na relative to Si on Io. A wide variety of silicate compositions were heated under oxidizing conditions with a SO 2 /O 2 = 1 gas phase at a mid‐level crustal temperature for Io (1123K). All experiments produced sulfate deposits on the silicate surfaces. The nature of the sulfate changed systematically with the silicate Ca/Na ratio, with mixtures of CaSO 4 and Na‐rich sulfate formed by basaltic compositions having higher Ca/Na but only alkali‐rich sulfates formed for more granitic (low Ca/Na) compositions. For crystalline albite and an albite‐orthoclase eutectic glass composition, K and Al‐rich sulfates were formed. Assuming that burial of SO 2 to the temperatures of our experiments is plausible on Io and that somewhat less oxidizing conditions do not qualitatively change the results, SO 2 ‐rock interactions producing Na‐rich sulfates could account for the Io surface enrichment in Na. Observations on minor elements, such as K or Ca, in the atomic cloud or in magnetospheric ion spectra could be used to identify sulfates as Io surface phases and, conceivably, even define Ionian crustal magma types. Many analyses show significant S excesses which are best interpreted as due to the presence of bisulfate (HSO 4 .) components, and NaHSO 4 deserves consideration as an Io surface mineral. The possibility of elemental S on Io can be regarded as a totally separate issue from the problem of the surface Na enrichment.

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