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| Vivianite | |
| Category: | Phosphate mineral Vivianite group |
| Imasymbol: | Viv[1] |
| Molweight: | 501.61 g/mol |
| Strunz: | 8.CE.40 (10 ed) 7/C.13-40 (8 ed) |
| Dana: | 40.3.6.1 |
| System: | Monoclinic |
| Class: | Prismatic (2/m) (same H-M symbol) |
| Symmetry: | C2/m |
| Unit Cell: | a = 10.086 Å, b = 13.441 Å c = 4.703 Å; β = 104.27°; Z = 2 |
| Color: | Colorless, very pale green, becoming dark blue, dark greenish blue, indigo-blue, then black with oxidation |
| Habit: | Flattened, elongated prismatic crystals, may be rounded or corroded; as stellate groups, incrustations, concretionary, earthy or powdery |
| Twinning: | Translation gliding |
| Cleavage: | Perfect on |
| Fracture: | Fibrous |
| Tenacity: | Flexible, sectile |
| Mohs: | 1.5–2 |
| Luster: | Vitreous, pearly on the cleavage, dull when earthy |
| Streak: | White, altering to dark blue, brown |
| Diaphaneity: | Transparent to translucent |
| Gravity: | 2.68 |
| Opticalprop: | Biaxial (+); moderate relief |
| Refractive: | nα = 1.579–1.616, nβ = 1.602–1.656, nγ = 1.629–1.675 |
| Birefringence: | δ = 0.050–0.059 |
| Pleochroism: | Visible; X = blue, deep blue, Indigo-blue; Y = pale yellowish green, pale bluish green, yellow-green; Z = pale yellowish green, olive-yellow |
| 2V: | Measured: 63° to 83.5°, Calculated: 78° to 88° |
| Dispersion: | r < v, weak |
| Fluorescence: | Not fluorescent |
| Solubility: | Easily soluble in acids |
| Alteration: | Metavivianite |
Vivianite is a hydrated iron(II) phosphate mineral found in a number of geological environments. Small amounts of manganese Mn2+, magnesium Mg2+, and calcium Ca2+ may substitute for iron Fe2+ in its structure.[2] Pure vivianite is colorless, but the mineral oxidizes very easily, changing the color, and it is usually found as deep blue to deep bluish green prismatic to flattened crystals. Vivianite crystals are often found inside fossil shells, such as those of bivalves and gastropods, or attached to fossil bone. Vivianite can also appear on the iron coffins or on the corpses of humans as a result of a chemical reaction of the decomposing body with the iron enclosure.
It was named by Abraham Gottlob Werner, the "father of German geology", in 1817, the year of his death, after either John Henry Vivian (1785–1855), a Welsh-Cornish politician, mine owner and mineralogist living in Truro, Cornwall, England, or after Jeffrey G. Vivian, an English mineralogist.[3] Vivianite was discovered at Wheal Kind, in St Agnes, Cornwall.
Vivianite group minerals have the general formula A3(XO4)2·8H2O, where A is a divalent metal cation and X is either phosphorus or arsenic, and they are monoclinic.[4] [5]
Group members are:
| Mineral | Chemical formula | Crystal system | |
|---|---|---|---|
| Ni3(AsO4)2·8H2O | Monoclinic | ||
| Arupite | Ni3(PO4)2·8H2O | Monoclinic | |
| Baricite | (Mg2+,Fe2+)3(PO4)2·8H2O | Monoclinic | |
| Co3(AsO4)2·8H2O | Monoclinic | ||
| Hörnesite | Mg3(AsO4)2·8H2O | Monoclinic | |
| Zn3(AsO4)2·8H2O | Monoclinic | ||
| Manganohörnesite | (Mn2+,Mg)3(AsO4)2·8H2O | Monoclinic | |
| Pakhomovskyite | Co3(PO4)2·8H2O | Monoclinic | |
| Parasymplesite | Fe2+3(AsO4)2·8H2O | Monoclinic | |
| Vivianite | Fe2+3(PO4)2·8H2O | Monoclinic |
Related:
– Bobierrite: Mg3(PO4)2·8H2O
– Symplesite: Fe2+3(AsO4)2·8H2O
– Metaköttigite: Zn3(AsO4)2·8H2O
– Metavivianite: (Fe2+,Fe3+)(PO4)2(OH)·H2O.[2]
Note: Metavivianite, that vivianite readily alters to, is not a member of the vivianite group because it contains trivalent Fe3+ cations.
In pure end member vivianite all the iron is divalent, Fe2+, but there are two distinct sites in the structure that these ions can occupy. In the first site, the Fe2+ is surrounded by four water molecules and two oxygens, making an octahedral group. In the second site, the Fe2+ is surrounded by two water molecules and four oxygens, again making an octahedral group. The oxygens are part of the phosphate groups (PO43−), that are tetrahedral. The vivianite structure has chains of these octahedra and tetrahedra that form sheets perpendicular to the a-crystal axis. The sheets are held together by weak bonds, and that accounts for the perfect cleavage between them.[2]
The crystals are monoclinic, class 2/m, space group C 2/m, with two formula units per unit cell (Z = 2). The approximate values of the unit cell parameters are:
a = 10.1 Å, b = 13.4 Å, c = 4.7 Å and β = 104.3°,with slightly different values given by different sources:
a = 10.086 Å, b = 13.441 Å, c = 4.703 Å, β = 104.27°[2]
a = 10.06 Å, b = 13.41 Å, c = 4.696 Å, β = 104.3°
a = 10.034–10.086 Å, b= 13.434–13.441 Å, c= 4.687–4.714 Å, β = 102.65–104.27°
a = 10.024(6) Å, b = 13.436(3) Å, c = 4.693(4) Å, β = 102.30(5)°
The mineral may occur as crystals, or as masses or concretions.[2] The crystals are usually prismatic parallel to the c-crystal axis, and flattened perpendicular to the b-axis. Equant crystals are rarer.[2] They may also occur as stellate (star-shaped) groups, or encrustations with a bladed or fibrous structure.[2] Unaltered specimens are colorless to very pale green, but they oxidize on exposure to light (and possibly also in situ) to blue, then darker green, brown, purple and purplish black. The streak is white, altering to dark blue or brown. Crystals are transparent to translucent with a vitreous luster, pearly on the cleavage surface, or dull and earthy.[2]
Vivianite is biaxial (+) with refractive indices approximately:
nα = 1.58, nβ = 1.6, nγ = 1.6, but different sources give somewhat different values
nα = 1.579, nβ = 1.602, nγ = 1.637[2]
nα = 1.579–1.616, nβ = 1.602–1.656, nγ = 1.629–1.675
nα = 1.58–1.626, nβ = 1.598–1.662, nγ = 1.627–1.699
Birefringence: δ = 0.050–0.059 or 0.0470–0.0730
The refractive indices increase with increasing oxidation, the birefringence decreases, and the pleochroism on becomes stronger.[2]
The angle between the optic axes, 2V, has been measured as between 63° and 83.5°; it can also be calculated from the refractive indices, giving a value between 78° and 88°. The dispersion of the optic axes is weak, with r
Vivianite is a soft mineral, with Mohs hardness only to 2, and specific gravity 2.7. It splits easily, with perfect cleavage perpendicular to the b-crystal axis, due to the sheet-like structure of the mineral. It is sectile, with a fibrous fracture, and thin laminae parallel to the cleavage plane are flexible. It is easily soluble in acids.[2] It has a melting point of, it darkens in color in H2O2, and is not radioactive.
Vivianite is a secondary mineral found in a number of geologic environments: the oxidation zone of metal ore deposits, in granite pegmatites containing phosphate minerals, in clays and glauconitic sediments, and in recent alluvial deposits replacing organic material such as peat, lignite, bog iron ores and forest soils (all). Bones and teeth buried in peat bogs are sometimes replaced by vivianite. Some authors say that it is particularly associated with gossan, but this is disputed by Petrov.[6]
Associated minerals include metavivianite, ludlamite, pyrite, siderite and pyrrhotite.[6] Hydrothermal veins produce the best crystal specimens with the classic gemmy green color.[6]
The type locality is Wheal Kind (Wheal Kine), West Wheal Kitty group, St Agnes, St Agnes District, Cornwall, England.
Oxidation of vivianite is an internal process; no oxygen or water enters or leaves the mineral from the outside. A visible light photon knocks a proton out of a water molecule, leaving a hydroxide ion (OH−). In turn, a divalent iron Fe2+ loses an electron to become Fe3+, i.e., it is oxidized and balances the charge. This process starts when visible light falls on the vivianite, and it can occur within a few minutes, drastically changing the color of the mineral. Eventually, the vivianite changes to a new species, metavivianite Fe2+2Fe3+(PO4)2(OH)·7H2O, which usually occurs as paramorphs after vivianite.[7]
Vivianite was known as a pigment since Roman times, but its use in oil painting was rather limited.[8] It has been found in Vermeer's The Procuress in the blue-grey parts of the carpet in the foreground.[9]