Aguilarite | |
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General | |
Category | Sulfosalt minerals |
Formula (repeating unit) | Ag4SeS |
IMA symbol | Agu [1] |
Strunz classification | 2.BA.55 |
Dana classification | 2.4.1.3 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) [2] |
Space group | P21/n [2] |
Unit cell | a = 4.2478(2), b =6.9432(3) c = 8.0042(5) [Å] β = 100.103(2)° Z = 4 [2] |
Identification | |
Color | Bright lead-gray on fresh surfaces; dull iron-black on exposure to air. |
Cleavage | None observed |
Fracture | Hackly |
Tenacity | Sectile |
Mohs scale hardness | 2.5 [3] 1–1.5 [2] |
Luster | Metallic |
Streak | Gray-black |
Diaphaneity | Opaque |
Ultraviolet fluorescence | Non-fluorescent [4] |
References | [3] |
Aguilarite is an uncommon sulfosalt mineral with formula Ag 4 Se S. It was described in 1891 and named for discoverer Ponciano Aguilar.
Aguilarite is bright lead-gray on fresh surfaces but becomes dull iron black when exposed to air. [3] The mineral occurs with massive habit, as elongated pseudododecahedral crystals up to 3 cm (1.2 in), or as intergrowths with acanthite or naumannite. [5]
In the late 19th century, Ponciano Aguilar, superintendent of the San Carlos mine in Guanajuato, Mexico, found several specimens of a mineral thought to be naumannite. [5] [6] The samples were given to F. A. Genth for identification, who, along with S. L. Penfield, discovered that it was a new mineral. The mineral was described in the American Journal of Science in 1891 and named aguilarite in honor of Ponciano Aguilar. [6] When the International Mineralogical Association was founded, aguilarite was grandfathered as a valid mineral species. [7]
Aguilarite is uncommon, and forms at relatively low temperatures in hydrothermal deposits rich in silver and selenium but deficient in sulfur. [5] The mineral is known from a number of countries in North and South America, Europe, Asia, and Australasia. [3] [5] Aguilarite occurs in association with acanthite, calcite, naumannite, pearceite, proustite, silver, stephanite, and quartz. [5]
In 2013, aguilarite's chemistry and crystal structure were reexamined by Bindi and Pingitore. [2] The significant reevaluation of aguilarite did not discredit its status as a valid mineral, but it was established as the selenium analogue of acanthite instead of sulfur-rich naumannite. [8] The sample primarily studied came from the Gem and Mineral Collection of the Department of Geosciences at Princeton University. [9]
The work of Petruk et al. in 1974 formed the basis of knowledge regarding the silver–sulfur–selenium system for about forty years. They indexed their x-ray diffraction patterns of aguilarite on an orthorhombic cell similar to naumannite. [10] Bindi and Pingitore determined that aguilarite is, in fact, monoclinic and is isostructural to acanthite and not naumannite. [2] Bindi and Pingitore believe that Petruk et al. were unable to resolve closely spaced peaks due to low resolution equipment, making aguilarite appear similar to naumannite. Additionally, a number of inconsistencies in unit cell dimensions in the 1974 work show that aguilarite does not have the same structure as naumannite. [11]
The crystal structure of aguilarite consists of planes nearly parallel to (010) composed of tetrahedrally coordinated nonmetal atoms and AgX3 triangles (where X is a nonmetal). The planes are joined by twofold-coordinated silver atoms. [12]
Aguilarite is part of the acanthite-like solid solution series Ag2S–Ag2S0.4Se0.6. The mineral comprises the range from 50 atomic percent selenium up to the transition from monoclinic to orthorhombic. [8]
Amphibole is a group of inosilicate minerals, forming prism or needlelike crystals, composed of double chain SiO
4 tetrahedra, linked at the vertices and generally containing ions of iron and/or magnesium in their structures. Its IMA symbol is Amp. Amphiboles can be green, black, colorless, white, yellow, blue, or brown. The International Mineralogical Association currently classifies amphiboles as a mineral supergroup, within which are two groups and several subgroups.
Arsenopyrite is an iron arsenic sulfide (FeAsS). It is a hard metallic, opaque, steel grey to silver white mineral with a relatively high specific gravity of 6.1. When dissolved in nitric acid, it releases elemental sulfur. When arsenopyrite is heated, it produces sulfur and arsenic vapor. With 46% arsenic content, arsenopyrite, along with orpiment, is a principal ore of arsenic. When deposits of arsenopyrite become exposed to the atmosphere, the mineral slowly converts into iron arsenates. Arsenopyrite is generally an acid-consuming sulfide mineral, unlike iron pyrite which can lead to acid mine drainage.
Bornite, also known as peacock ore, is a sulfide mineral with chemical composition Cu5FeS4 that crystallizes in the orthorhombic system (pseudo-cubic).
Calaverite, or gold telluride, is an uncommon telluride of gold, a metallic mineral with the chemical formula AuTe2, with approximately 3% of the gold replaced by silver. It was first discovered in Calaveras County, California in 1861, and was named for the county in 1868.
Acanthite is a form of silver sulfide with the chemical formula Ag2S. It crystallizes in the monoclinic system and is the stable form of silver sulfide below 173 °C (343 °F). Argentite is the stable form above that temperature. As argentite cools below that temperature its cubic form is distorted to the monoclinic form of acanthite. Below 173 °C acanthite forms directly. Acanthite is the only stable form in normal air temperature.
Chalcocite, copper(I) sulfide (Cu2S), is an important copper ore mineral. It is opaque and dark gray to black, with a metallic luster. It has a hardness of 2.5–3 on the Mohs scale. It is a sulfide with a monoclinic crystal system.
Krennerite is an orthorhombic gold telluride mineral which can contain variable amounts of silver in the structure. The formula is AuTe2, but specimen with gold substituted by up to 24% with silver have been found ([Au0.77Ag0.24]Te2). Both of the chemically similar gold-silver tellurides, calaverite and sylvanite, are in the monoclinic crystal system, whereas krennerite is orthorhombic.
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.
Triphylite is a lithium iron(II) phosphate mineral with the chemical formula LiFePO4. It is a member of the triphylite group and forms a complete solid solution series with the lithium manganese(II) phosphate, lithiophilite. Triphylite crystallizes in the orthorhombic crystal system. It rarely forms prismatic crystals and is more frequently found in hypidiomorphic rock. It is bluish- to greenish-gray in color, but upon alteration becomes brown to black.
Freieslebenite is a sulfosalt mineral composed of antimony, lead, and silver. Sulfosalt minerals are complex sulfide minerals with the formula: AmBnSp. The formula of freieslebenite is AgPbSbS3.
Empressite is a mineral form of silver telluride, AgTe. It is a rare, grey, orthorhombic mineral with which can form compact masses, rarely as bipyramidal crystals.
Silver selenide (Ag2Se) is the reaction product formed when selenium toning analog silver gelatine photo papers in photographic print toning. The selenium toner contains sodium selenite (Na2SeO3) as one of its active ingredients, which is the source of the selenide (Se2−) anion combining with the silver in the toning process.
Djurleite is a copper sulfide mineral of secondary origin with formula Cu31S16 that crystallizes with monoclinic-prismatic symmetry. It is typically massive in form, but does at times develop thin tabular to prismatic crystals. It occurs with other supergene minerals such as chalcocite, covellite and digenite in the enriched zone of copper orebodies. It is a member of the chalcocite group, and very similar to chalcocite, Cu2S, in its composition and properties, but the two minerals can be distinguished from each other by x-ray powder diffraction. Intergrowths and transformations between djurleite, digenite and chalcocite are common. Many of the reported associations of digenite and djurleite, however, identified by powder diffraction, could be anilite and djurleite, as anilite transforms to digenite during grinding.
Alacránite (As8S9) is an arsenic sulfide mineral first discovered in the Uzon caldera, Kamchatka, Russia. It was named for its occurrence in the Alacrán silver/arsenic/antimony mine. Pampa Larga, Chile. It is generally more rare than realgar and orpiment. Its origin is hydrothermal. It occurs as subhedral to euhedral tabular orange to pale gray crystals that are transparent to translucent. It has a yellow-orange streak with a hardness of 1.5. It crystallizes in the monoclinic crystal system. It occurs with realgar and uzonite as flattened and prismatic grains up to 0.5 mm across.
The silver antimonide mineral dyscrasite has the chemical formula Ag3Sb. It is an opaque, silver white, metallic mineral which crystallizes in the orthorhombic crystal system. It forms pyramidal crystals up to 5 cm (2.0 in) and can also form cylindrical and prismatic crystals.
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.
Brianyoungite is a secondary zinc carbonate mineral. The Commission on New Minerals, Nomenclature and Classification (CNMNC) of the International Mineralogical Association (IMA) classifies it as a carbonate with the formula Zn3(CO3)(OH)4, but sulfate groups SO4 also occupy the carbonate CO3 positions, in the ratio of about one sulfate to three carbonates, so other sources give the formula as Zn3(CO3,SO4)(OH)4, and Gaines et al. classify the mineral as a compound carbonate. It is similar in appearance to hydrozincite, another zinc carbonate. It was discovered in 1991 and designated IMA1991-053. In 1993 it was named "brianyoungite" after Brian Young (born 1947), a field geologist with the British Geological Survey, who provided the first specimens.
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.
Earlandite, [Ca3(C6H5O7)2(H2O)2]·2H2O, is the mineral form of calcium citrate tetrahydrate. It was first reported in 1936 and named after the English microscopist and oceanographer Arthur Earland FRSE. Earlandite occurs as warty fine-grained nodules ca. 1 mm in size in bottom sediments of the Weddell Sea, off Antarctica. Its crystal symmetry was first assigned as orthorhombic, then as monoclinic, and finally as triclinic.
Argentopyrite is a moderately rare sulfide mineral with the chemical formula AgFe2S3. It is one of the natural compounds of the MFe2S3 type, with M being caesium in very rare pautovite, copper in relatively common cubanite, potassium in rare rasvumite and thallium in rare picotpaulite. The type locality is Jáchymov in Czech Republic. Chemically similar mineral include sternbergite, lenaite, AgFeS2, and argentopentlandite, Ag(Fe,Ni)8S8.
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