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Natural Alteration of Mica and Reactions between Released Ions in Mineral Deposits

Published online by Cambridge University Press:  01 July 2024

J. Rimsaite
J. Rimsaite*
Affiliation:
Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A OE8, Canada
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Abstract

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Chemical changes during the natural alteration of micas were studied by electron microprobe and classical chemical analyses of fresh and altered portions of mica flakes from 10 Canadian mineral deposits. Results of 50 new analyses are discussed in five examples, starting from simple changes in the interlayer followed by exsolution of titania and ending with complex replacements of anions and cations in all layers of the mica structure. Alteration of micas starts along 001 cleavage planes and fractures and gradually extends into the entire flake leaving some or no remnants of the host mica. The removal of ions from the mica structure and from the flake takes place by gradual depletion, by exsolution of oxides, and/or by alternating removal and redeposition of a newly-formed oxide, illustrated in the following example of the removal of Ti;

  1. (1) removal of Ti from the mica structure and exsolution of rutile in the parent mica

  2. (2) destruction of rutile and recrystallization as anatase on the surface of the mica; and

  3. (3) destruction of anatase, removal of Ti from the surface of the host and crystallization of anatase away from the parent mica.

Residual minerals replacing the original micas are secondary and recrystallized micas, chlorite, vermiculite, serpentine, talc and depleted, optically amorphous flakes. Newly-formed minerals which may incorporate the released ions into their structures are rutile, anatase, sericite, hydronepheline, chlorite-serpentine aggregates, goethite and jarosite. The following partly-altered micas are indicative of sulphide mineralization;

  1. (a) bright-green, partly altered phlogopite from ultrabasic rocks and from Co-Cu-Fe-Ni sulphide assemblages. The green phlogopite formed by replacement of K, Al and Ti by Fe, Mg and OH

  2. (b) depleted mica coated with jarosite and Ni-goethite in the oxidation zone of a nickel deposit.

    The jarosite formed from released S and Fe from decomposed Fe-Ni sulphides and K released from the host mica; and

  3. (c) chlorite-sericite-biotite alteration zones adjacent to Pb-Zn-Cu-Fe deposits.

Type
Research Article
Information
Clays and Clay Minerals , Volume 23 , Issue 3 , June 1975 , pp. 247 - 255
Copyright
Copyright © 1975, The Clay Minerals Society

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