Christite | |
---|---|
General | |
Category | Sulfosalt mineral |
Formula (repeating unit) | TlHgAsS3 |
IMA symbol | Cri [1] |
Strunz classification | 2.HD.15 |
Crystal system | Monoclinic |
Crystal class | Prismatic (2/m) (same H-M symbol) |
Space group | P21/n |
Unit cell | a = 6.113 Å, b = 16.188 Å, c = 6.111 Å; β = 96.71°; V = 600.59 Å3; Z = 4 |
Identification | |
Formula mass | 576.09 g/mol |
Color | Crimson red, bright orange. |
Crystal habit | Subhedral grains, may be somewhat bladed or flattened |
Cleavage | {010} and {110} perfect, {101} good |
Fracture | Uneven |
Mohs scale hardness | 1-2 |
Luster | Adamantine |
Streak | light orange |
Diaphaneity | opaque to semitransparent |
Specific gravity | 6.2 |
Optical properties | Biaxial |
Pleochroism | Weak to strong, grayish green, dark violet, bluish violet |
References | [2] [3] [4] |
Christite is a mineral with the chemical formula Tl Hg As S 3. It is named after Dr. Charles L. Christ, a member of the U.S. Geological Survey. It usually comes in a crimson red or bright orange color. It has a density of 6.2 and has a rating between 1 and 2 on Mohs Hardness Scale. Christite has an adamantine luster and leaves behind an orange streak. [3] Its crystal system is monoclinic with possible crystal classes of twofold symmetry, mirror plane symmetry, and twofold with a mirror plane. This means it can have radial symmetry, mirror plane symmetry, or mirror plane symmetry perpendicular to the two-fold axis. [5] It is an anisotropic mineral, which means that it exhibits different properties when measured in different directions. In plane polarized light, its color is golden yellow. It is birefringent, which means that it has two distinct indices of refraction. This can be seen when one looks through the microscope with both polars crossed and sees the mineral change colors when it is rotated.
Christite occurs with baryte in hydrothermal veins in dolomite at the Carlin mine in Nevada and in pods within a mercury deposit, the Lanmuchang deposit, China. [4] It occurs associate with realgar, orpiment, lorandite, baryte and getchellite at the Carlin mine and with lorandite, baryte, pyrite and marcasite in the Lanmuchang. [4]
Corundum is a crystalline form of aluminium oxide typically containing traces of iron, titanium, vanadium, and chromium. It is a rock-forming mineral. It is a naturally transparent material, but can have different colors depending on the presence of transition metal impurities in its crystalline structure. Corundum has two primary gem varieties: ruby and sapphire. Rubies are red due to the presence of chromium, and sapphires exhibit a range of colors depending on what transition metal is present. A rare type of sapphire, padparadscha sapphire, is pink-orange.
Cinnabar, or cinnabarite, also known as mercurblende is the bright scarlet to brick-red form of mercury(II) sulfide (HgS). It is the most common source ore for refining elemental mercury and is the historic source for the brilliant red or scarlet pigment termed vermilion and associated red mercury pigments.
Baryte, barite or barytes ( BARR-eyet, BAIR- or bə-RYTE-eez) is a mineral consisting of barium sulfate (BaSO4). Baryte is generally white or colorless, and is the main source of the element barium. The baryte group consists of baryte, celestine (strontium sulfate), anglesite (lead sulfate), and anhydrite (calcium sulfate). Baryte and celestine form a solid solution (Ba,Sr)SO4.
Sodalite is a tectosilicate mineral with the formula Na
8(Al
6Si
6O
24)Cl
2, with royal blue varieties widely used as an ornamental gemstone. Although massive sodalite samples are opaque, crystals are usually transparent to translucent. Sodalite is a member of the sodalite group with hauyne, nosean, lazurite and tugtupite.
Stilbite is the name of a series of tectosilicate minerals of the zeolite group. Prior to 1997, stilbite was recognized as a mineral species, but a reclassification in 1997 by the International Mineralogical Association changed it to a series name, with the mineral species being named:
Anhydrite, or anhydrous calcium sulfate, is a mineral with the chemical formula CaSO4. It is in the orthorhombic crystal system, with three directions of perfect cleavage parallel to the three planes of symmetry. It is not isomorphous with the orthorhombic barium (baryte) and strontium (celestine) sulfates, as might be expected from the chemical formulas. Distinctly developed crystals are somewhat rare, the mineral usually presenting the form of cleavage masses. The Mohs hardness is 3.5, and the specific gravity is 2.9. The color is white, sometimes greyish, bluish, or purple. On the best developed of the three cleavages, the lustre is pearly; on other surfaces it is glassy. When exposed to water, anhydrite readily transforms to the more commonly occurring gypsum, (CaSO4·2H2O) by the absorption of water. This transformation is reversible, with gypsum or calcium sulfate hemihydrate forming anhydrite by heating to around 200 °C (400 °F) under normal atmospheric conditions. Anhydrite is commonly associated with calcite, halite, and sulfides such as galena, chalcopyrite, molybdenite, and pyrite in vein deposits.
Pyrrhotite is an iron sulfide mineral with the formula Fe(1-x)S. It is a nonstoichiometric variant of FeS, the mineral known as troilite. Pyrrhotite is also called magnetic pyrite, because the color is similar to pyrite and it is weakly magnetic. The magnetism decreases as the iron content increases, and troilite is non-magnetic. Pyrrhotite is generally tabular and brassy/bronze in color with a metallic luster. The mineral occurs with mafic igneous rocks like norites, and may form from pyrite during metamorphic processes. Pyrrhotite is associated and mined with other sulfide minerals like pentlandite, pyrite, chalcopyrite, and magnetite, and has been found globally.
Alunite is a hydroxylated aluminium potassium sulfate mineral, formula KAl3(SO4)2(OH)6. It was first observed in the 15th century at Tolfa, near Rome, where it was mined for the manufacture of alum. First called aluminilite by J.C. Delamétherie in 1797, this name was contracted by François Beudant three decades later to alunite.
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.
Austinite is a member of the adelite-descloizite group, adelite subgroup, the zinc (Zn) end member of the copper-Zn series with conichalcite. It is the zinc analogue of cobaltaustinite and nickelaustinite. At one time “brickerite” was thought to be a different species, but it is now considered to be identical to austinite. Austinite is named in honour of Austin Flint Rogers (1877–1957), American mineralogist from Stanford University, California, US.
Lorándite is a thallium arsenic sulfosalt with the chemical formula: TlAsS2. Though rare, it is the most common thallium-bearing mineral. Lorandite occurs in low-temperature hydrothermal associations and in gold and mercury ore deposits. Associated minerals include stibnite, realgar, orpiment, cinnabar, vrbaite, greigite, marcasite, pyrite, tetrahedrite, antimonian sphalerite, arsenic and barite.
Ajoite is a hydrated sodium potassium copper aluminium silicate hydroxide mineral. Ajoite has the chemical formula (Na,K)Cu7AlSi9O24(OH)6·3H2O, and minor Mn, Fe and Ca are usually also present in the structure. Ajoite is used as a minor ore of copper.
Getchellite is a rare sulfide of arsenic and antimony, AsSbS3, that was discovered by B. G. Weissberg of the New Zealand Department of Scientific and Industrial Research in 1963, and approved as a new species by the International Mineralogical Association in 1965. Many metal sulfides are grey to black, but a few are brightly colored. Orpiment is yellow to brownish gold, cinnabar is deep red and getchellite is a bright orange red.
Tsumebite is a rare phosphate mineral named in 1912 after the locality where it was first found, the Tsumeb mine in Namibia, well known to mineral collectors for the wide range of minerals found there. Tsumebite is a compound phosphate and sulfate of lead and copper, with hydroxyl, formula Pb2Cu(PO4)(SO4)(OH). There is a similar mineral called arsentsumebite, where the phosphate group PO4 is replaced by the arsenate group AsO4, giving the formula Pb2Cu(AsO4)(SO4)(OH). Both minerals are members of the brackebuschite group.
Mendipite is a rare mineral that was named for the locality where it is found, the Mendip Hills in Somerset, England. It is an oxyhalide of lead with formula Pb3Cl2O2.
Sarabauite (sar-a-bau'-ite) is a red monoclinic sulfide mineral with the chemical formula: CaSb10O10S6.
Babefphite is a rare phosphate mineral with the general formula BaBe(PO4)(F,OH). The name is given for its composition (Ba meaning barium, Be meaning beryllium, F meaning fluorine, and P for phosphorus).
Malayaite is a calcium tin silicate mineral with formula CaSnOSiO4. It is a member of the titanite group.
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.
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.