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Published in Soil Sci Soc Am J 43:908-912 (1979)
© 1979 Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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The Microbiological Formation of Basic Ferric Sulfates: II. Crystallization in Presence of Potassium-, Ammonium-, and Sodium-Salts1

K. C. Ivarson, G. J. Ross and N. M. Miles2

ABSTRACT

Solutions of ferrous sulfate (pH 2.95) containing equivalent amounts of K+, NH4+, or Na+, either singly or in pairs, were inoculated with the iron-oxidizing bacterium (Thiobacillus ferrooxidans) and allowed to incubate for 42 weeks. Successive quantitative analyses of the alkali cations in the single cation systems showed that after 3 to 4 weeks, virtually all of the K+ in solutions had reacted to form jarosite [KFe8(SO4)2(OH)6]. On the other hand, after 42 weeks, about 80% of the NH4+ and 60% of the Na+ had entered into their respective basic ferric sulfates—ammoniojarosite [NH4Fe3(SO4)2(OH)6] and natrojarosite [Na Fe3 (SO4)2(OH)6]. Progressive increases in peak intensities of the resultant X-ray diffractograms and rates of acid production in solution agreed very well with rates of jarosite formation. In systems containing two alkali cations, solid solutions formed and the rate at which each cation disappeared from solution was similar to that in the single cation systems.

The results are in accord with reported field analyses of acid sulfate soils, i.e., jarosite is the most abundant basic ferric sulfate in these soils and the soils invariably contain Fe2+ and T. ferrooxidans.


NOTES

1 Contribution no. 1068 of the Chemistry and Biology Research Inst., Agric. Canada, Ottawa, K1A 0C6.

2 Soil Microbiologist and Soil Mineralogists, respectively.

Received for publication February 5, 1979. Accepted for publication April 3, 1979.




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MORPHOLOGY OF JAROSITE-GROUP COMPOUNDS PRECIPITATED FROM BIOLOGICALLY AND CHEMICALLY OXIDIZED Fe IONS
Can Mineral, February 1, 2000; 38(1): 45 - 56.
[Abstract] [Full Text] [PDF]




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