Hagendorfite

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Hagendorfite
Hagendorfite-sea78b.jpg
General
CategoryIron phosphate minerals
Formula
(repeating unit)
(Na,Ca)MnFe2(PO4)3
IMA symbol Hag [1]
Strunz classification 8.AC.10
Crystal system Monoclinic
Crystal class Prismatic (2/m)
(same H-M symbol)
Space group C2/c
Unit cell a = 11.9721(9) Å
b = 12.5988(8) Å
c = 6.5029(5) Å
β = 114.841(8)°, Z = 4
Identification
ColorGreenish-black
Crystal habit Massive – uniformly indistinguishable crystals forming large masses.
Cleavage {001} good, {110} poor
Mohs scale hardness3.5
Streak Gray green
Diaphaneity Translucent
Specific gravity 3.71
Optical propertiesBiaxial (-)
Refractive index nα = 1.735 nβ = 1.742 nγ = 1.745
Birefringence 0.0100
Pleochroism (x): Yellowish brown (y): green (z): bluish green
2V angle Measured: 68° to 70°
References [2] [3] [4] [5] [6]

Hagendorfite is an iron phosphate mineral with the chemical formula of (Na,Ca)MnFe2(PO4)3 and is named after where the mineral was discovered, Hagendorf-Süd, Bavaria, Germany. [7]

Hagendorfite is in the monoclinic crystal class; the mineral's internal symmetry consists of three axes with unequal length. Furthermore, the angles between two of the axes is 90° while the other angle is less than 90°. [8] Monoclinic minerals contain a twofold rotation axis where they can be rotated 360° and have the crystal face repeat every 180°. They also have the characteristic mirror plane, which can produce a perfect mirror image when divided in two.

Hagendorfite belongs to the monoclinic crystal class, so it is assigned to the biaxial optical class. Hagendorfite's optic sign, which is negative, is proven by examining its interference figure. [4] Biaxial minerals, including Hagendorfite, have three indices of refraction which may or may not correspond with the mineral's unequally lengthened axes. A refractive index will provide the ratio of the speed of light in vacuum with the speed of light in the mineral. A single refractive index is given when two rays of light vibrate in the mineral's circular section and move along the optic axes.

Occurrence

The mineral is found in various locations around the world. Hagendorfite occurs in complex granite course-grained rocks called pegmatites or in the phosphate nodules in shale. Although hagendorfite was first discovered in Bavaria, Germany, it has since been found in the Southern Province in Rwanda, [9] the Sowie Mountains in Poland, [10] and New Hampshire in the US. [11] Hagendorfite is of interest to mineralogists researching phosphate-bearing pegmatites or the dickinsonite series. Hagendorfite is associated with the dickinsonite series and with other mineral members including varulite, alluarrdite, and manganalluaudite.

Related Research Articles

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Vivianite (Fe2+
Fe2+
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. 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.

<span class="mw-page-title-main">Alstonite</span>

Alstonite, also known as bromlite, is a low temperature hydrothermal mineral that is a rare double carbonate of calcium and barium with the formula BaCa(CO
3
)
2
, sometimes with some strontium. Barytocalcite and paralstonite have the same formula but different structures, so these three minerals are said to be trimorphous. Alstonite is triclinic but barytocalcite is monoclinic and paralstonite is trigonal. The species was named Bromlite by Thomas Thomson in 1837 after the Bromley-Hill mine, and alstonite by August Breithaupt of the Freiberg Mining Academy in 1841, after Alston, Cumbria, the base of operations of the mineral dealer from whom the first samples were obtained by Thomson in 1834. Both of these names have been in common use.

<span class="mw-page-title-main">Barytocalcite</span>

Barytocalcite is an anhydrous barium calcium carbonate mineral with the chemical formula BaCa(CO3)2. It is trimorphous with alstonite and paralstonite, that is to say the three minerals have the same formula but different structures. Baryte and quartz pseudomorphs after barytocalcite have been observed.

<span class="mw-page-title-main">Leadhillite</span> Lead sulfate carbonate hydroxide mineral

Leadhillite is a lead sulfate carbonate hydroxide mineral, often associated with anglesite. It has the formula Pb4SO4(CO3)2(OH)2. Leadhillite crystallises in the monoclinic system, but develops pseudo-hexagonal forms due to crystal twinning. It forms transparent to translucent variably coloured crystals with an adamantine lustre. It is quite soft with a Mohs hardness of 2.5 and a relatively high specific gravity of 6.26 to 6.55.

<span class="mw-page-title-main">Vauxite</span>

Vauxite is a phosphate mineral with the chemical formula Fe2+Al2(PO4)2(OH)2·6(H2O). It belongs to the laueite – paravauxite group, paravauxite subgroup, although Mindat puts it as a member of the vantasselite Al4(PO4)3(OH)3·9H2O group. There is no similarity in structure between vauxite and paravauxite Fe2+Al2(PO4)2(OH)2·8H2O or metavauxite Fe3+Al2(PO4)2(OH)2·8H2O, even though they are closely similar chemically, and all minerals occur together as secondary minerals. Vauxite was named in 1922 for George Vaux Junior (1863–1927), an American attorney and mineral collector.

<span class="mw-page-title-main">Marrite</span>

Marrite (mar'-ite) is a mineral with the chemical formula PbAgAsS3. It is the arsenic equivalent of freieslebenite (PbAgSbS3), but also displays close polyhedral characteristics with sicherite and diaphorite. Marrite was named in honor of geologist John Edward Marr (1857–1933) of Cambridge, England.

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<span class="mw-page-title-main">Sarabauite</span>

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Devilline is a sulfate mineral with the chemical formula CaCu4(SO4)2(OH)6•3H2O. The name originates from the French chemist's name, Henri Etienne Sainte-Claire Deville (1818–1881).

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Keyite is a mineral with the chemical formula Cu2+3Zn4Cd2(AsO4)6 · 2H2O. The name comes from Charles Locke Key, an American mineral dealer who furnished its first specimens. Keyite is monoclinic-prismatic, meaning its crystal form has three unequal axes, two of which have 90° angles between them and one with an angle less than 90°. Keyite belongs to the biaxial optical class, meaning it has more than one axis of anisotropy, in which light travels with zero birefringence, and three indices of refraction, nα = 1.800, nβ, and nγ = 1.870. Being a very rare cadmium copper arsenate, keyite is only found in Tsumeb, Namibia in the Tsumeb mine, a world-famous copper mine known for its abundance of rare and unusual minerals.

<span class="mw-page-title-main">Kröhnkite</span>

Kröhnkite ( Na2Cu(SO4)2•2H2O ) is a rare copper sulfate mineral named after B. Kröhnke who first researched it. Kröhnkite may be replaced by Saranchinaite, the anhydrous form of the mineral, if heated to temperatures above 200 °C (392 °F).

<span class="mw-page-title-main">Stellerite</span> Zeolite mineral

Stellerite is a rare mineral discovered by and named after Georg Wilhelm Steller, a German explorer and zoologist. The mineral has a general formula of Ca[Al2Si7O18]·7H2O. Like most rare minerals, there are few commercial uses for stellerite. Mineral collectors are lucky to find it in good enough crystal form. Zeolites, including stellerite, have been studied using a dehydration process to gauge the potential use of their phases as molecular sieves, sorbents, and catalysts.

<span class="mw-page-title-main">Laplandite-(Ce)</span>

Laplandite has a general formula of Na4CeTiPO4Si7O18•5H2O, and is found primarily in igneous rocks. This silicate mineral has been found as inclusions in pegmatites, primarily in the Kola Peninsula in Lappland, where the mineral's name gets its origin. Laplandite is orthorhombic, which states that crystallographically, it contains three axes of unequal lengths that all intersect at 90 degrees, perpendicular to one another. The shape of the crystal is bipyramidal, and is similar in structure to olivine or aragonite. Because of these different axes lengths, it shows anisotropism, which will allow for the visibility of birefringence. This property can give the mineral very distinct colors when viewed under cross-polarization. Laplandite has three different indices of refraction, which are measures of the speed of light in vacuum divided by the speed of light within the mineral, determined individually on each axis. Due to these different indices, Laplandite is a biaxial mineral, which states that the mineral will have two optic axes. Under the microscope, this mineral has moderate relief, which describes the contrast between Laplandite's refractive index and the refractive index of the mounting medium on which it is placed. The relief can be seen physically as how easily you can see the boundary lines of the mineral under plane polarized light in a petrographic microscope.

Samuelsonite is a complex mineral that is found near North Groton, Grafton County, New Hampshire, US. Additionally, it is most commonly found as a secondary mineral in granite pegmatite. Samuelsonite is named after Peter B. Samuelson, a prospector from Rumney, New Hampshire.

<span class="mw-page-title-main">Magnesiohastingsite</span>

Magnesiohastingsite is a calcium-containing amphibole and a member of the hornblende group. It is an inosilicate (chain silicate) with the formula NaCa2(Mg4Fe3+)(Si6Al2)O22(OH)2 and molar mass 864.69 g. In synthetic magnesiohastingsite it appears that iron occurs both as ferrous iron Fe2+ and as ferric iron Fe3+, but the ideal formula features only ferric iron. It was named in 1928 by Marland P. Billings. The name is for its relationship to hastingsite and its magnesium content. Hastingsite was named for the locality in Dungannon Township, Hastings County, Ontario, Canada.

<span class="mw-page-title-main">Pearceite</span>

Pearceite is one of the four so-called "ruby silvers", pearceite Cu(Ag,Cu)6Ag9As2S11, pyrargyrite Ag3SbS3, proustite Ag3AsS3 and miargyrite AgSbS2. It was discovered in 1896 and named after Dr Richard Pearce (1837–1927), a Cornish–American chemist and metallurgist from Denver, Colorado.

<span class="mw-page-title-main">Köttigite</span>

Köttigite is a rare hydrated zinc arsenate which was discovered in 1849 and named by James Dwight Dana in 1850 in honour of Otto Friedrich Köttig (1824–1892), a German chemist from Schneeberg, Saxony, who made the first chemical analysis of the mineral. It has the formula Zn3(AsO4)2·8H2O and it is a dimorph of metaköttigite, which means that the two minerals have the same formula, but a different structure: köttigite is monoclinic and metaköttigite is triclinic. There are several minerals with similar formulae but with other cations in place of the zinc. Iron forms parasymplesite Fe2+3(AsO4)2·8H2O; cobalt forms the distinctively coloured pinkish purple mineral erythrite Co3(AsO4)2·8H2O and nickel forms annabergite Ni3(AsO4)2·8H2O. Köttigite forms series with all three of these minerals and they are all members of the vivianite group.

<span class="mw-page-title-main">Carminite</span> Anhydrous arsenate mineral containing hydroxyl

Carminite (PbFe3+2(AsO4)2(OH)2) is an anhydrous arsenate mineral containing hydroxyl. It is a rare secondary mineral that is structurally related to palermoite (Li2SrAl4(PO4)4(OH)4). Sewardite (CaFe3+2(AsO4)2(OH)2) is an analogue of carminite, with calcium in sewardite in place of the lead in carminite. Mawbyite is a dimorph (same formula, different structure) of carminite; mawbyite is monoclinic and carminite is orthorhombic. It has a molar mass of 639.87 g. It was discovered in 1850 and named for the characteristic carmine colour.

<span class="mw-page-title-main">Serpierite</span>

Serpierite (Ca(Cu,Zn)4(SO4)2(OH)6·3H2O) is a rare, sky-blue coloured hydrated sulfate mineral, often found as a post-mining product. It is a member of the devilline group, which has members aldridgeite (Cd,Ca)(Cu,Zn)4(SO4)2(OH)6·3H2O, campigliaite Cu4Mn2+(SO4)2(OH)6·4H2O, devilline CaCu4(SO4)2(OH)6·3H2O, kobyashevite Cu5(SO4)2(OH)6·4H2O, lautenthalite PbCu4(SO4)2(OH)6·3H2O and an unnamed dimorph of devilline. It is the calcium analogue of aldridgeite and it is dimorphous with orthoserpierite CaCu4(SO4)2(OH)6·3H2O.

<span class="mw-page-title-main">Talmessite</span>

Talmessite is a hydrated calcium magnesium arsenate, often with significant amounts of cobalt or nickel. It was named in 1960 for the type locality, the Talmessi mine, Anarak district, Iran. It forms a series with β-Roselite, where cobalt replaces some of the magnesium, and with gaitite, where zinc replaces the magnesium. All these minerals are members of the fairfieldite group. Talmessite is dimorphic with wendwilsonite.

References

  1. Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi: 10.1180/mgm.2021.43 . S2CID   235729616.
  2. Strunz, H. (1955) Hagendorfite. American Mineralogist, 40, 553.
  3. Palache, C., Berman, H., and Frondel, C. (1951) The System of Mineralogy of James Dwight Dana and Edward Salisbury Dana, 669-670 p. New York, J. Wiley and Sons, inc.
  4. 1 2 Ralph, Jolyon, Hagendorfite
  5. Barthelmy, David, Hagendorfite Mineral Data
  6. Handbook of Mineralogy
  7. Redhammer, G.J., Tippelt, G., Bernoider, M., Lottermoser, W., Amthauer, G., and Roth, G. (2005) European Journal of Mineralogy,17, 915-932.
  8. Fisher, J. D. (1956) Hagendorfite Unit Cell. Geological Society of America Bulletin, 67, 1694-1695.
  9. Fransolet, A., Hatert F., and Fontan F (2004) Petrographic Evidence for Primary Hagendorfite in an Unusual Assemblage of Phosphate Minerals, Kibingo Granitic Pegmatite, Rwanda. Canadian Mineralogist, 42, 697–704.
  10. Pieczka A., Obos K., and Sachanbinski M. (2004) The First Occurrence of Elbaite in Poland. Mineralogia Polonica, 35, 5.
  11. Moore P. (1965) Huhnerkobelite Crystals from the Palermo No. 1 Pegmatite, North Groton, New Hampshire. American Mineralogist, 50, 713-717.