Mineral group

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In geology and mineralogy, a mineral group is a set of mineral species with essentially the same crystal structure and composed of chemically similar elements. [1]

Contents

Silicon-oxygen double chain in the anions of amphibole minerals. Tremolite-chain.png
Silicon-oxygen double chain in the anions of amphibole minerals.

For example, the amphibole group consists of 15 or more mineral species, most of them with the general unit formula A
x
B
y
C
14-3x-2y
Si
8
O
22
(OH)
2
, where A is a trivalent cation such as Fe3+
or Al3+
, B is a divalent cation such as Fe2+
, Ca2+
, or Mg2+
, and C is an alkali metal cation such as Li+
, Na+
, or K+
. In all these minerals, the anions consist mainly of groups of four SiO
4
tetrahedra connected by shared oxygen corners so as to form a double chain of fused six-member rings. In some of the species, aluminum Al3+
may replace some silicon atoms Si4+
in the backbone, with extra B or C cations to balance the charges.

List of groups

[ citation needed ]

See also

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4
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The endmember hornblende tschermakite (☐Ca2(Mg3Al2)(Si6Al2)O22(OH)2) is a calcium rich monoclinic amphibole mineral. It is frequently synthesized along with its ternary solid solution series members tremolite and cummingtonite so that the thermodynamic properties of its assemblage can be applied to solving other solid solution series from a variety of amphibole minerals.

<span class="mw-page-title-main">Cookeite</span> Mineral species of the silicate group and the phyllosilicate subgroup, part of the chlorite family.

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Jimthompsonite is a magnesium iron silicate mineral with chemical formula (Mg,Fe2+)5Si6O16(OH)2. It is a triple chain silicate (or inosilicate) along with clinojimthompsonite and chesterite. They were described in 1977 by Burham and Veblen. They attracted great mineralogical attention because they were the first examples of new chain silicate structures among a large group known as biopyriboles whose name is derived from the words biotite, pyroxene, and amphiboles.

<span class="mw-page-title-main">Bicchulite</span> Tectosilicate mineral

Bicchulite has an ideal chemical formula of 2CaO•Al2O2•SiO2•H2O, which was formularized from the hydrothermal synthesis of synthetic gehlenite. Also, bicchulite was sighted in the mines of Japan with related minerals. This sodalite-type structured bicchulite has an uncommon ratio of aluminium to silicon, causing difficulties deciphering the structure. Because of bicchulite's structure it has a powdery texture, which leads to complications in obtaining information on the mineral's physical properties. Despite this problem, the color, specific gravity, and crystal size of bicchulite are known. Although bicchulite was only discovered about 40 years ago, technology has been rapidly advancing, allowing more accurate results to be made from experiments done today.

<span class="mw-page-title-main">Ferrogedrite</span> Amphibole, double chain inosilicate mineral

Ferrogedrite is an amphibole mineral with the complex chemical formula of ☐Fe2+2(Fe2+3Al2)(Si6Al2)O22(OH)2. It is sodium and calcium poor, making it part of the magnesium-iron-manganese-lithium amphibole subgroup. Defined as less than 1.00 apfu (atoms per formula unit) of Na + Ca and consisting of greater than 1.00 apfu of (Mg, Fe2+, Mn2+, Li) separating it from the calcic-sodic amphiboles. It is related to anthophyllite amphibole and gedrite through coupled substitution of (Al, Fe3+) for (Mg, Fe2+, Mn) and Al for Si. and determined by the content of silicon in the standard cell.

<span class="mw-page-title-main">Coupled substitution</span> Geological process by which two elements simultaneously substitute into a crystal

Coupled substitution is the geological process by which two elements simultaneous substitute into a crystal in order to maintain overall electrical neutrality and keep the charge constant. In forming a solid solution series, ionic size is more important than ionic charge, as this can be compensated for elsewhere in the structure.

References

  1. Stuart J. Mills, Frédéric Hatert, Ernest H. Nickel, and Giovanni Ferraris (2009): "The standardisation of mineral group hierarchies: application to recent nomenclature proposals". European Journal of Mineralogy, volume 21, number 5, pages 1073-1080. doi : 10.1127/0935-1221/2009/0021-1994