| 释义 |
- Vivianite group
- Structure
- Appearance
- Optical properties
- Physical properties
- Geological setting
- Oxidation
- Pigment
- Localities
- See also
- References
{{Infobox mineral
| name = Vivianite
| category = Phosphate mineral
Vivianite group
| image = 7314M-vivianite2.jpg
| caption = Vivianite tabular crystal, transparent, with a deep green color. Crystal size: 82 mm x 38 mm x 11 mm. From Huanuni mine, Dalence Province, Oruro Department, Bolivia
| formula = {{Chem|Fe|2+|Fe|2+|2|(PO|4|)|2|·8H|2|O}}
| 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 = B2/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 {010}
| 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
| density =
| polish =
| opticalprop = Biaxial (+)
| 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
| extinction =
| length fast/slow =
| fluorescence= Not fluorescent
| absorption =
| melt = {{convert|1114|C}}
| fusibility =
| diagnostic =
| solubility = Easily soluble in acids
| other =
| alteration = Metavivianite
| references =
}}Vivianite ({{Chem|Fe|2+|Fe|2+|2|(PO|4|)|2|·8H|2|O}}) is a hydrated iron phosphate mineral found in a number of geological environments. Small amounts of manganese Mn2+, magnesium Mg and calcium Ca may substitute for iron Fe2+ in the structure.[1] 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. It was named by Abraham Gottlob Werner in 1817, the year of his death, after John Henry Vivian (1785–1855), a Welsh-Cornish politician, mine owner and mineralogist living in Truro, Cornwall, England. John Vivian discovered the mineral at Wheal Kind, in St Agnes, Cornwall.[3] Vivianite group Vivianite group minerals have the general formula A3(XO4)2·8H2O, where A is a divalent transition metal cation and X is either phosphorus or arsenic, and they are monoclinic.[2][3]
Group members are:
| Mineral | Chemical formula | Crystal system |
|---|
| Annabergite | Ni3(AsO4)2·8H2O | Monoclinic | | Arupite | Ni3(PO4)2·8H2O | Monoclinic | | Baricite | (Mg2+,Fe2+)3(PO4)2·8H2O | Monoclinic | | Erythrite | Co3(AsO4)2·8H2O | Monoclinic | | Hörnesite | Mg3(AsO4)2·8H2O | Monoclinic | | Köttigite | 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+{{math|3−x}},Fe3+{{mvar|x}})(PO4)2(OH){{mvar|x}}·{{math|size=100%|(8-x)}}H2O.[1]
- Note: Metavivianite, that vivianite readily alters to, is not a member of the vivianite group because it contains trivalent Fe3+ cations.
Structure 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 (PO4)−3, 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.[1]
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°[3][1] a = 10.06 Å, b = 13.41 Å, c = 4.696 Å, β = 104.3°[4] 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)°[15] Appearance The mineral may occur as crystals, or as masses or concretions.[1] The crystals are usually prismatic parallel to the c crystal axis, and flattened perpendicular to the b axis. Equant crystals are rarer.[[3][1] They may also occur as stellate (star-shaped) groups, or encrustations with a bladed or fibrous structure.[1]] 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.[[3][4][1]] Optical properties 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[1] nα = 1.579 - 1.616 nβ = 1.602 - 1.656 nγ = 1.629 - 1.675[[3]] nα=1.58-1.626, nβ=1.598-1.662, nγ=1.627-1.699[4] Birefringence: δ = 0.050 - 0.059[3] or 0.0470 - 0.0730[4] The refractive indices increase with increasing oxidation, the birefringence decreases, and the pleochroism on {010} becomes stronger.[3][1]
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°.[3][4] The dispersion of the optic axes is weak, with r[3][1] or non-existent.[4]
Vivianite is pleochroic with X= blue, deep blue or indigo-blue; Y= pale yellowish green, pale bluish green or yellow-green; Z= pale yellowish green or olive-yellow. X is parallel to the b crystal axis and Z is inclined to the c crystal axis at an angle of 28.5°. Physical properties Vivianite is a soft mineral, with Mohs hardness only {{frac|1|1|2}} 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.[3][1]
It has a melting point of {{convert|1114|C}},[3] it darkens in color in H2O2[3] and is not radioactive.[4] Geological setting 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.[49] Some authors say that it is particularly associated with gossan, but this is disputed by Petrov.[4] Associated minerals include metavivianite, ludlamite, pyrite, siderite and pyrrhotite.[[4]] Hydrothermal veins produce the best crystal specimens with the classic gemmy green color.[4] The type locality is Wheal Kind (Wheal Kine), West Wheal Kitty group, St Agnes, St Agnes District, Cornwall, England.[3] Oxidation 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+Fe3+2(PO4)2(OH)·(H2O)7, which usually occurs as paramorphs after vivianite.[5] Pigment Vivianite was known as a pigment since Roman times but its use in oil painting was rather limited.[6] It has been found in Vermeer's The Procuress in the blue-grey parts of the carpet in the foreground.[7] Localities - Brazil. Cigana Mine, Galileia, Minas Gerais, with muscovite and pyrite.[8] Typically wedge-shaped crystals of vivianite to 11 cm across, of medium lustre, smoke-blue color and good transparency on matrix of sharp silvery muscovite plates, some with druses of pyrite microcrystals.[9]
- Brazil: Llallagua, Potosi: Crystals to 10 cm at the Siglio XX mine.[1] Transparent bottle green crystals to 10 cm from the San Jose/San Firmin vein. In general the vivianite occurs as prismatic crystals on a matrix of botryoidal goethite derived from the alteration of pyrite and marcasite. Specimens found in 2000 were associated with childrenite, cronstedtite, pyrrhotite, frankeite and pink massive sphalerite.[10]
- Cameroon: The world’s largest vivianite crystals (more than a meter long) from mud.[4]
- Canada: In bog iron at Côte St Charles, Vaudreuil-Soulanges, Montérégie, Québec.[1]
- Germany: In the limonite ores in Amberg-Auerbach and in the pegmatites of Hagendorf, Bavaria.[1]
- Japan: At Nagasawa, Iwama-machi, Ibaraki Prefecture, vivianite was found along fractures in rocks rich in graphite, pyrite and pyrrhotite. The vivianite is intimately associated with pyrite and occurs as very thin tabular crystals, up to 10 cm in length.[15]
- Kosovo. Trepča Mines, Stari Trg. Thick prismatic crystals up to 10 cm long and 2 cm thick, relatively stable. Deep green in color and transparent, commonly resting on pyrrhotite or pyrite, and in some cases on quartz or carbonates.[11]
- Mexico: In blue-green gem quality crystals to 8 cm at the San Antonio Mine, Santa Eulalia, Chihuahua.[1]
- Russia: In sedimentary iron ores and in fossil shells in the Kerch and Taman peninsula on the Black Sea.[1][4]
- Spain: At the Brunita mine, Cartagena, Murcia, vivianite was found as deep green crystals, up to 8 cm[12]
- USA: In diatomite in a tertiary lake bed near Burey, Shasta County, California.[1]
- USA: In green sand at Middletown, New Castle County, Delaware.[1]
- USA: Blackbird Mine, Lemhi County, Idaho. Crystals in shades of pink, green, greyish blue, purple and purplish black, as well as colorless. The unique deep purple color of some Blackbird mine specimens is characteristic of the locality. Some single crystals have both purple and green zones. Vivianite crystals from the Blackbird Mine are usually elongated and blade-like. They occur as singles and groups on dark altered schist and on white quartz. Associated minerals include ludlamite, quartz and siderite.[13]
- USA: Abundant in the pegmatites of Newry, Maine.[1]
- New Zealand: Small amounts of vivianite are present within the sediments of Lake Kohangapiripiri.[14]
See also- List of minerals
- List of minerals named after people
- Vivianite as a pigment at ColourLex
References{{commons category| Vivianite}}1. ^1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 Gaines et al (1997) Dana’s New Mineralogy Eighth Edition. Wiley
2. ^Journal of the Russell Society (2006) 9:3
3. ^{{Cite book |first1=Malcolm E. |last1=Back |title=Fleischer’s Glossary of Mineral Species |year=2014 |edition=11 |publisher=Mineralogical Record Inc. |pages=434 |location=Tucson AZ}}
4. ^1 2 3 4 5 {{cite web|url=https://www.mindat.org/article.php/137/A+Scientific+Study+of+the+Absorption+of+Evil+by+Vivianite|title=Alfredo Petrov - A Scientific Study of the Absorption of Evil by Vivianite|last=Petrov|first=Alfredo|date=1 January 2008|publisher=Mindat.org|accessdate=23 September 2018}}
5. ^Alfredo Petrov, 2006 on Mindat
6. ^Vivianite at ColourLex
7. ^H. Stege, C. Tilenschi und A. Unger. Bekanntes und Unbekanntes – neue Untersuchungen zur Palette Vermeers auf dem Gemälde „Bei der Kupplerin“. In: Uta Neidhardt und Marlies Giebe (Ed.), Johannes Vermeer – Bei der Kupplerin, Ausstellungskatalog Dresden 2004, pp. 76-82.
8. ^The Mineralogical Record (2004) 35-2:156
9. ^The Mineralogical Record (2004) 35-3:252
10. ^The Mineralogical Record (2006) 37-2:156
11. ^The Mineralogical Record (2007) 38-4:290
12. ^{{Cite book|title=Minerales y Minas de España. Fosfatos, Arseniatos y Vanadatos|last=Calvo|first=Miguel|publisher=Escuela Técnica Superior de Ingenieros de Minas de Madrid. Fundación Gómez Pardo. Madrid, Spain|year=2015|isbn=978-84-95063-96-0|location=|pages=297}}
13. ^The Mineralogical Record (2010) 41-4:366
14. ^Cochran, U., Goff, J., Hannah, M., and Hull, A. (1999) Relative stability on a tectonically active coast: paleoenvironment during the last 7000 years at Lake Kohangapiripiri, Wellington, New Zealand, Quaternary International, 56, 53-63
15. ^1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Vivianite (Mindat.org)
16. ^1 2 3 4 5 6 7 8 9 Webmineral data
17. ^1 2 {{cite journal |title=Vivianite from Nagasawa, Iwama-machi, Ibaraki Prefecture, Japan. New finding from meta-pelitic rocks |url=http://sciencelinks.jp/j-east/article/199911/000019991199A0349754.php |author1=Banno Yasuyuki |author2=Bunno Michiaki |author3=Haruna Makoto |author4=Kono Masahide |last-author-amp=yes |journal=Bulletin of the Geological Survey of Japan |issn=0016-7665 |volume=50 |pages=117–121 |year=1999 |issue=2 |language=ja |access-date=2008-03-20 |archive-url=https://web.archive.org/web/20120229033717/http://sciencelinks.jp/j-east/article/199911/000019991199A0349754.php |archive-date=2012-02-29 |dead-url=yes |df= }}
18. ^{{cite book |title = A Dictionary of the Names of Minerals Including Their History and Etymology |url = http://books.google.pt/books?id=-UNwRAAACAAJ |author = Albert Huntington Chester |publisher = BiblioBazaar |year = 2010 |isbn = 1-142-13314-1}}
}}
}}
3 : Iron minerals|Phosphate minerals|Monoclinic minerals |