Scotlandite | |
---|---|
General | |
Category | Sulfite |
Formula (repeating unit) | Pb S O 3 |
IMA symbol | Sct [1] |
Strunz classification | 4/K.01-10 |
Crystal system | Monoclinic |
Crystal class | 2/m - Prismatic |
Space group | P21/m (no. 11) |
Unit cell | a = 4.505 Å, b = 5.333 Å c = 6.405 Å; β= 106.24°; Z = 2 |
Identification | |
Formula mass | 287.26 |
Color | Pale yellow, greyish-white, colorless, transparent |
Crystal habit | Spear-shaped crystals |
Cleavage | Perfect along {100} and good along {010} |
Tenacity | Radiating clusters |
Mohs scale hardness | 2 |
Luster | Adamantine, Pearly |
Diaphaneity | Transparent |
Density | 6.37 g/cm3 |
Optical properties | Biaxial positive |
Refractive index | nα= 2.035 nβ= 2.040 nγ= 2.085 |
Birefringence | δ = 0.050 |
Dispersion | v >> r strong |
Absorption spectra | Strong 900 cm−1 |
References | [2] [3] [4] [5] |
Scotlandite is a sulfite mineral first discovered in a mine at Leadhills in South Lanarkshire, Scotland, an area known to mineralogists and geologists for its wide range of different mineral species found in the veins that lie deep in the mine shafts. This specific mineral is found in the Susanna vein of Leadhills, where the crystals are formed as chisel-shaped or bladed. [4] Scotlandite was actually the first naturally occurring sulfite, which has the ideal chemical formula of Pb S O 3. The mineral has been approved by the Commission on New Minerals and Mineral Names, IMA, to be named scotlandite for Scotland. [2]
Scotlandite is found in association with pyromorphite, anglesite, lanarkite, leadhillite, susannite, and barite. It occurs in cavities in massive barite and anglesite, and is closely associated with lanarkite and susannite. Scotlandite represents the latest phase in the crystallization sequence of the associated lead secondary minerals. It can often be found in the vuggy anglesite as yellowish single crystals up to 1 millimeter in length that sometimes arrange in a fan-shaped aggregates. Anglesite can usually be recognized in a very thin coating on scotlandite which is used to protect the sulfite from further oxidation. A second variety of scotlandite can also occur in discontinuously distributed cavities between the anglesite mass containing the first variety and the barite matrix. This variety is characterized by tiny, whitish to water-clear crystals, and crystal clusters less than one millimeter in size, which encrust large portions of the interior of the cavities. Scotlandite is a uniquely rare mineral, as it occurs in small amounts in few locations around the world. [2]
Scotlandite is a pale yellow, greyish-white, colorless, transparent mineral with an adamantine or pearly luster. It exhibits a hardness of 2 on the Mohs hardness scale. [3] Scotlandite occurs as chisel-shaped or bladed crystals elongated along the c-axis, with a tendency to form radiating clusters. Its crystals are characterized by the {100}, {010}, {011}, {021}, {031}, and {032}. faces. Scotlandite shows perfect cleavage along the {100} plane and a less good one along the {010} plane. The measured density is 6.37 g/cm3. [2]
Scotlandite is biaxial positive, which means it will refract light along two axes. The mineral is optically biaxial positive, 2Vmeas. 35° 24'(Na). The refractive indices are: α ~ 2.035, β ~ 2.040, and γ ~ 2.085 (Na). Dispersion is strong, v >> r. The extinction is β//b, and α [001] = 20° (γ [100] = 4° in the obtuse angle β. H(Mohs) < 2. D = 6.37 and calculated Dx = 6.40 g cm−3. [2] The infrared spectrum of scotlandite shows conclusively that it is an anhydrous sulfite, with no OH groups or other polyatomic anions being present. It is also proven by electron microprobe analysis and infrared spectroscopy that scotlandite must be a polymorph of lead sulfite. [2]
Scotlandite is a sulfite compared with chemically related compounds, it is very close to the value of anglesite (6.38 g cm−3), but distinctly different from that of lanarkite (6.92 g cm−3). Orthorhombic lead sulfite is of higher density (Dmeas = 6.54, calculated Dx = 6.56 g cm−3), and has the same chemical properties as well. [2] The empirical chemical formula for scotlandite calculated on the basis of Pb+S = 2, is Pbl.06S0.94O2.94 or more ideally PbSO3. [3]
Oxide | wt% | Range |
---|---|---|
SO2 | 19.88 | 17.89-22.30 |
PbO | 77.85 | 79.03-77.70 |
Total | 97.73 | 96.92-100.00 |
A small crystal of scotlandite, showing some cleavage faces, was examined using Weissenberg and precession techniques. Scotlandite is in the monoclinic crystal system. The only systematic extinctions observed from the single crystal patterns were 0k0 where k was odd. Thus the possible space group is either P2 or P2/m. The unit cell parameters obtained from the single crystal study were used to index the X-ray powder pattern and were then refined with the indexed powder data. [2] A subsequent study determined the space group is P21/m (no. 11) with unit cell dimensions: a = 4.505 Å, b = 5.333 Å, c = 6.405 Å; β= 106.24°; Z = 2. If the present a and c axes are interchanged, the unit cell of scotlandite is very similar, isotypic, to that of molybdomenite, PbSeO3. Lead is coordinated to nine oxygen atoms with Pb-Oav=2.75 Å, and possibly further to one sulfur atom with Pb−S=3.46 Å. The average S−O distance in the pyramidal SO3 group is 1.52 Å. [5]
Anglesite is a lead sulfate mineral with the chemical formula PbSO4. It occurs as an oxidation product of primary lead sulfide ore, galena. Anglesite occurs as prismatic orthorhombic crystals and earthy masses, and is isomorphous with barite and celestine. It contains 74% of lead by mass and therefore has a high specific gravity of 6.3. Anglesite's color is white or gray with pale yellow streaks. It may be dark gray if impure.
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.
Todorokite is a rare complex hydrous manganese oxide mineral with the chemical formula (Na,Ca,K,Ba,Sr)
1-x(Mn,Mg,Al)
6O
12·3-4H
2O. It was named in 1934 for the type locality, the Todoroki mine, Hokkaido, Japan. It belongs to the prismatic class 2/m of the monoclinic crystal system, but the angle β between the a and c axes is close to 90°, making it seem orthorhombic. It is a brown to black mineral which occurs in massive or tuberose forms. It is quite soft with a Mohs hardness of 1.5, and a specific gravity of 3.49 - 3.82. It is a component of deep ocean basin manganese nodules.
Tsumcorite is a rare hydrated lead arsenate mineral that was discovered in 1971, and reported by Geier, Kautz and Muller. It was named after the TSUMeb CORporation mine at Tsumeb, in Namibia, in recognition of the Corporation's support for mineralogical investigations of the orebody at its Mineral Research Laboratory.
Susannite is a lead sulfate carbonate hydroxide mineral. It has the formula Pb4SO4(CO3)2(OH)2. Susannite is the higher temperature phase of the two and forms above 80 °C when fluids oxidize the lead ore deposits. It is trimorphous with leadhillite and macphersonite.
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.
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.
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.
Macphersonite, Pb4(SO4)(CO3)2 (OH)2, is a carbonate mineral that is trimorphous with leadhillite and susannite. Macphersonite is generally white, colorless, or a pale amber in color and has a white streak. It crystallizes in the orthorhombic system with a space group of Pcab. It is fairly soft mineral that has a high specific gravity.
Scandiobabingtonite was first discovered in the Montecatini granite quarry near Baveno, Italy in a pegmatite cavity. Though found in pegmatites, the crystals of scandiobabingtonite are sub-millimeter sized, and are tabular shaped. Scandiobabingtonite was the sixth naturally occurring mineral discovered with the rare earth element scandium, and grows around babingtonite, with which it is isostructural, hence the namesake. It is also referred to as scandian babingtonite. The ideal chemical formula for scandiobabingtonite is Ca2(Fe2+,Mn)ScSi5O14(OH).
Metarauchite is a member of the autunite group, found at the Jáchymov ore district, Czech Republic and in Schneeberg, Germany. Metarauchite is a member of the Autunite Group, which is a group of structured uranyl phosphates and arsenates, the other members of the group are Autunite, Bassetite, Heinrichite, Kahlerite, Nováčekite-I, Nováčekite-II, Rauchite, Sabugalite, Saléeite, Torbernite, Uranocircite, Uranospinite, Zeunerite. The mineral is named after Czech mineral collector Luděk Rauch, who died in the Jáchymov mines during mineral prospecting.
Mammothite is a mineral found in the Mammoth mine in Tiger, Arizona and also in Laurium, Attika, Greece. This mineral was named in 1985 by Donald R. Peacor, Pete J. Dunn, G. Schnorrer-Köhler, and Richard A. Bideaux, for the Mammoth vein (one of the two main veins in the mine) and the town of Mammoth, Arizona, which was named for the mine. The mammothite that is found in Arizona exist as euhedral crystals imbedded in micro granular, white colored anglesite with a saccharoidal texture. The associated minerals include phosgenite, wulfenite, leadhillite and caledonite. In Greece, the mammothite exists as small euhedral crystals and also as microscopic rock cavities lined with projecting crystals within the slags. The associated minerals here are cerussite, phosgenite and matlockite. The ideal chemical formula for mammothite is Pb6Cu4AlSb5+O2(OH)16Cl4(SO4)2.
Danielsite is a sulfide and sulfosalt that was first discovered in a pocket of supergene minerals in the north region of Western Australia. The location found was about 1 kilometre (0.62 mi) west of the locality known as Coppin Pool. The mineral danielsite was named after John L. Daniels who collected the sample in which the new mineral was found. The chemical formula of danielsite is (Cu,Ag)
14HgS
8. Danielsite is very fine grained and hard to observe in hand samples. It generally has a gray color with very brittle and soft physical characteristics.
Lahnsteinite is a basic sulfate mineral first discovered in the Friedrichssegen Mine, Germany in a goethite cavity. Though found in goethite, the crystals of Lahnsteinite are few millimeters in size, and are tabular shaped. Lahnsteinite was the first mineral discovered in the Lahn Valley deposits. The empirical formula for lahnsteinite is (Zn3.3,Fe0.27,Cu0.11)3.91(S0.98O4)(OH)5*3H2.10O.
Lemanskiite is a mineral that was first discovered in a mine at Abundancia mine, El Guanaco mining district, Chile, with the ideal formula of NaCaCu5(AsO4)4Cl•3H2O. Originally, this mineral was discovered as being dimorphus with lavendulan, but in 2018 it was revised to only have 3 water molecules. Lemanskiite typically occurs as rosette-shaped aggregates of thin lamellar or needle-shaped aggregates, such as lammerite. Lemanskiite is dark sky blue with a light blue streak, it is brittle with an excellent cleavage plane. It was found on a dumping site in the abandoned Abundancia mine, El Guanaco mining district, Region II, Antofagasta Province, Chile The new mineral has been named after Chester S. Lemanski, Jr. This mineral and name were then approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association.
Malhmoodite is a phosphate mineral first discovered at a mine called Union Carbide in Wilson Springs, Arkansas, United States. This mine is 10 km west of Magnet Cove, an alkaline igneous complex, and Union Carbide is in a contact region of alkalic igneous rocks and surrounding sedimentary rocks. The mineral has been approved by the Commission on New Minerals and Mineral Names, IMA, to be named for the late Bertha K. Malhmood, the Administrative Assistant of the Branch of Analytical Laboratories, U.S. Geological Survey.
Falcondoite, a member of the sepiolite group, was first discovered in the Dominican Republic, near the town of Bonao. The mineral was found in a deposit mined by Falconbridge Dominica, and so was named "falcondoite" after the company. Falcondoite is frequently associated with sepiolite, garnierite, talc, and serpentine, and is commonly nickel-bearing. While the chemical formula for falcondoite can vary, the mineral must contain more nickel than magnesium to be considered its own species. The ideal chemical formula for falcondoite is (Ni,Mg)4Si6O15(OH)2·6H2O.
Chukanovite is an iron(II) hydroxide-carbonate mineral with the ideal chemical formula Fe+22(CO3)(OH)2. It is a member of the rosasite mineral group and crystalizes in the monoclinic crystal system. Upon initial crystallization, it is typically pale green to colorless, but it takes on a brownish green hue after being altered at the surface. As a weathering product of meteoritic iron, chukanovite is a relatively uncommon mineral on Earth, having only been discovered in the year 2000. However, it is commonly formed artificially as a corrosion byproduct through the manufacturing of sand-deposited carbon steel.
Northstarite is an immensely rare lead-tellurite-thiosulfate mineral with an ideal formula of Pb6(Te4+ O3)5(S6+O3S2-). Northstarite was first discovered in 2019 by Charles Adan in the North Star Mine of the Tintic Mining District, Juab County, Utah, USA. Northstarite received its name after this type locality where it was originally discovered, the North Star Mine. Northstarite is the fourth thiosulfate mineral that exists on Earth, and although all thiosulfates have essential lead components, northstarite is the first thiosulfate species containing groups of both thiosulfate and tellurite (Te4+O3).
Vigezzite is a variant of the mineral aeschynite containing calcium, cerium, niobium, tantalum, and titanium. It was first discovered near Orcesco, Valle Vigezzo, Provo Novara, Northern Italy, in cavities of an albitic rock. The crystals of Vigezzite are flat prismatic crystals up to 2-3 mm length of an orange-yellow color.The name Vigezzite was chosen to draw attention to the locality that has produced the first occurrence of a Ca-Nb-Ta-mineral with Nb dominance over Ta, crystallizing with the aeschynite structure. The ideal chemical formula for vigezzite is (Ca,Ce),(Nb,Ta,Ti)2O6