Natroalunite

natroalunite

sillimanite

alunite

halloysite

Images

Formula: NaAl3(SO4)2(OH)6
Sulphate, alunite group
Crystal System: Trigonal
Specific gravity: 2.6 to 2.9 measured, 2.819 calculated
Hardness: 3½ to 4
Streak: White
Colour: White, greyish, yellowish, reddish, red-brown; colourless in transmitted light
Solubility: Insoluble in water
Electrical: Strongly pyroelectric
Common impurities: K
Environments

Sedimentary environments
Hydrothermal environments

Natroalunite is formed by solfataric or hydrothermal sulphate-bearing solutions reacting with clays, rarely with sillimanite; may be in laterites and as an authigenic sedimentary mineral. Associated minerals include alunite, kaolinite, halloysite, sillimanite and quartz (HOM).

Localities

At Ichetuyskoye, Dzhida Basin, Buryatia, Russia, the mineral assemblage consists of lazulite with variable amounts of scorzalite, trolleite, augelite, monazite, and members of the alunite supergroup (crandallite, florencite-(Ce), woodhouseite and svanbergite).
Numerous electron microprobe analyses are listed for strontian natroalunite (AM 86.200).

At Pofadder, Khâi-Ma, Namakwa District Municipality, Northern Cape, South Africa, large lenses of sillimanite occur in biotite-sillimanite schist. In one of the abandoned sillimanite quarries on the farms Hotson and Koenabib, the paragenesis sillimanite - natroalunite - zaherite - hotsonite was found. It is associated with silicates (kaolinite, pyrophyllite, topaz, muscovite and biotite), oxides (diaspore, rutile, ilmenite and corundum), sulphides (chalcopyrite, covellite and pyrite) and sulphide alteration products (covellite and goethite, atacamite and chalcanthite). The prevalent sequence of alteration is from sillimanite to natroalunite to zaherite to hotsonite, which is also the sequence of decreasing relative abundance, but sillimanite was directly transformed to zaherite wherever alkali elements were locally scanty. The necessary sulphate was apparently supplied during the oxidation of sulphides such as chalcopyrite and pyrite (CM 23.29-34).

The type locality is the Red Mountain Mining District, Colorado, USA. The Red Mountain district lies in the Tertiary volcanic rocks along the western border of the Silverton cauldron subsidence. It is characterised by strong hydrothermal alteration of the volcanic rocks and by the principal occurrences of ore deposits in chimney-like forms (Mindat).

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