Portal:Minerals
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The Minerals Portal
In geology and mineralogy, a mineral or mineral species is, broadly speaking, a solid substance with a fairly well-defined chemical composition and a specific crystal structure that occurs naturally in pure form.
The geological definition of mineral normally excludes compounds that occur only in living organisms. However, some minerals are often biogenic (such as calcite) or organic compounds in the sense of chemistry (such as mellite). Moreover, living organisms often synthesize inorganic minerals (such as hydroxylapatite) that also occur in rocks.
The concept of mineral is distinct from rock, which is any bulk solid geologic material that is relatively homogeneous at a large enough scale. A rock may consist of one type of mineral or may be an aggregate of two or more different types of minerals, spacially segregated into distinct phases.
Some natural solid substances without a definite crystalline structure, such as opal or obsidian, are more properly called mineraloids. If a chemical compound occurs naturally with different crystal structures, each structure is considered a different mineral species. Thus, for example, quartz and stishovite are two different minerals consisting of the same compound, silicon dioxide. (Full article...)
Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical (including optical) properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization. (Full article...)
Selected articles
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Image 1
In crystallography, the cubic (or isometric) crystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals.
There are three main varieties of these crystals:- Primitive cubic (abbreviated cP and alternatively called simple cubic)
- Body-centered cubic (abbreviated cI or bcc)
- Face-centered cubic (abbreviated cF or fcc)
Note: the term fcc is often used in synonym for the cubic close-packed or ccp structure occurring in metals. However, fcc stands for a face-centered-cubic Bravais lattice, which is not necessarily close-packed when a motif is set onto the lattice points. E.g. the diamond and the zincblende lattices are fcc but not close-packed.
Each is subdivided into other variants listed below. Although the unit cells in these crystals are conventionally taken to be cubes, the primitive unit cells often are not. (Full article...) -
Image 2
Zircon (/ˈzɜːrkɒn, -kən/) is a mineral belonging to the group of nesosilicates and is a source of the metal zirconium. Its chemical name is zirconium(IV) silicate, and its corresponding chemical formula is ZrSiO4. An empirical formula showing some of the range of substitution in zircon is (Zr1–y, REEy)(SiO4)1–x(OH)4x–y. Zircon precipitates from silicate melts and has relatively high concentrations of high field strength incompatible elements. For example, hafnium is almost always present in quantities ranging from 1 to 4%. The crystal structure of zircon is tetragonal crystal system. The natural color of zircon varies between colorless, yellow-golden, red, brown, blue, and green.
The name derives from the Persian zargun, meaning "gold-hued". This word is changed into "jargoon", a term applied to light-colored zircons. The English word "zircon" is derived from Zirkon, which is the German adaptation of this word. Yellow, orange, and red zircon is also known as "hyacinth", from the flower hyacinthus, whose name is of Ancient Greek origin. (Full article...) -
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In crystallography, crystal structure is a description of the ordered arrangement of atoms, ions, or molecules in a crystalline material. Ordered structures occur from the intrinsic nature of the constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.
The smallest group of particles in the material that constitutes this repeating pattern is the unit cell of the structure. The unit cell completely reflects the symmetry and structure of the entire crystal, which is built up by repetitive translation of the unit cell along its principal axes. The translation vectors define the nodes of the Bravais lattice.
The lengths of the principal axes, or edges, of the unit cell and the angles between them are the lattice constants, also called lattice parameters or cell parameters. The symmetry properties of the crystal are described by the concept of space groups. All possible symmetric arrangements of particles in three-dimensional space may be described by the 230 space groups.
The crystal structure and symmetry play a critical role in determining many physical properties, such as cleavage, electronic band structure, and optical transparency. (Full article...) -
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Kaolinite (/ˈkeɪ.ələˌnaɪt, -lɪ-/ KAY-ə-lə-nyte, -lih-; also called kaolin) is a clay mineral, with the chemical composition Al2Si2O5(OH)4. It is a layered silicate mineral, with one tetrahedral sheet of silica (SiO4) linked through oxygen atoms to one octahedral sheet of alumina (AlO6).
Kaolinite is a soft, earthy, usually white, mineral (dioctahedral phyllosilicate clay), produced by the chemical weathering of aluminium silicate minerals like feldspar. It has a low shrink–swell capacity and a low cation-exchange capacity (1–15 meq/100 g).
Rocks that are rich in kaolinite, and halloysite, are known as kaolin (/ˈkeɪ.əlɪn/) or china clay. In many parts of the world kaolin is colored pink-orange-red by iron oxide, giving it a distinct rust hue. Lower concentrations of iron oxide yield the white, yellow, or light orange colors of kaolin. Alternating lighter and darker layers are sometimes found, as at Providence Canyon State Park in Georgia, United States.
Kaolin is an important raw material in many industries and applications. Commercial grades of kaolin are supplied and transported as powder, lumps, semi-dried noodle or slurry. Global production of kaolin in 2021 was estimated to be 45 million tonnes, with a total market value of $US4.24 billion. (Full article...) -
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Quartz is a hard, crystalline mineral composed of silica (silicon dioxide). The atoms are linked in a continuous framework of SiO4 silicon–oxygen tetrahedra, with each oxygen being shared between two tetrahedra, giving an overall chemical formula of SiO2. Quartz is, therefore, classified structurally as a framework silicate mineral and compositionally as an oxide mineral. Quartz is the second most abundant mineral in Earth's continental crust, behind feldspar.
Quartz exists in two forms, the normal α-quartz and the high-temperature β-quartz, both of which are chiral. The transformation from α-quartz to β-quartz takes place abruptly at 573 °C (846 K; 1,063 °F). Since the transformation is accompanied by a significant change in volume, it can easily induce microfracturing of ceramics or rocks passing through this temperature threshold.
There are many different varieties of quartz, several of which are classified as gemstones. Since antiquity, varieties of quartz have been the most commonly used minerals in the making of jewelry and hardstone carvings, especially in Europe and Asia.
Quartz is the mineral defining the value of 7 on the Mohs scale of hardness, a qualitative scratch method for determining the hardness of a material to abrasion. (Full article...) -
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Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe2+Fe3+2O4. It is one of the oxides of iron, and is ferrimagnetic; it is attracted to a magnet and can be magnetized to become a permanent magnet itself. With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth. Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism.
Magnetite is black or brownish-black with a metallic luster, has a Mohs hardness of 5–6 and leaves a black streak. Small grains of magnetite are very common in igneous and metamorphic rocks.
The chemical IUPAC name is iron(II,III) oxide and the common chemical name is ferrous-ferric oxide. (Full article...) -
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Gypsum is a soft sulfate mineral composed of calcium sulfate dihydrate, with the chemical formula CaSO4·2H2O. It is widely mined and is used as a fertilizer and as the main constituent in many forms of plaster, drywall and blackboard or sidewalk chalk. Gypsum also crystallizes as translucent crystals of selenite. It forms as an evaporite mineral and as a hydration product of anhydrite. The Mohs scale of mineral hardness defines gypsum as hardness value 2 based on scratch hardness comparison.
Fine-grained white or lightly tinted forms of gypsum known as alabaster have been used for sculpture by many cultures including Ancient Egypt, Mesopotamia, Ancient Rome, the Byzantine Empire, and the Nottingham alabasters of Medieval England. (Full article...) -
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Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical (including optical) properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization. (Full article...) -
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Crystallography is the experimental science of determining the arrangement of atoms in crystalline solids. Crystallography is a fundamental subject in the fields of materials science and solid-state physics (condensed matter physics). The word crystallography is derived from the Ancient Greek word κρύσταλλος (krústallos; "clear ice, rock-crystal"), and γράφειν (gráphein; "to write"). In July 2012, the United Nations recognised the importance of the science of crystallography by proclaiming that 2014 would be the International Year of Crystallography.
Before the development of X-ray diffraction crystallography (see below), the study of crystals was based on physical measurements of their geometry using a goniometer. This involved measuring the angles of crystal faces relative to each other and to theoretical reference axes (crystallographic axes), and establishing the symmetry of the crystal in question. The position in 3D space of each crystal face is plotted on a stereographic net such as a Wulff net or Lambert net. The pole to each face is plotted on the net. Each point is labelled with its Miller index. The final plot allows the symmetry of the crystal to be established.
Crystallographic methods depend mainly on analysis of the diffraction patterns of a sample targeted by a beam of some type. X-rays are most commonly used; other beams used include electrons or neutrons. Crystallographers often explicitly state the type of beam used, as in the terms X-ray crystallography, neutron diffraction and electron diffraction. These three types of radiation interact with the specimen in different ways.- X-rays interact with the spatial distribution of electrons in the sample.
- Neutrons are scattered by the atomic nuclei through the strong nuclear forces, but in addition, the magnetic moment of neutrons is non-zero. They are therefore also scattered by magnetic fields. When neutrons are scattered from hydrogen-containing materials, they produce diffraction patterns with high noise levels. However, the material can sometimes be treated to substitute deuterium for hydrogen. Because of these different forms of interaction, the three types of radiation are suitable for different crystallographic studies.
- Electrons are charged particles and therefore interact with the total charge distribution of both the atomic nuclei and the electrons of the sample.
It is hard to focus x-rays or neutrons, but since electrons are charged they can be focused and are used in electron microscope to produce magnified images. There are many ways that transmission electron microscopy and related techniques such as scanning transmission electron microscopy, high-resolution electron microscopy can be used to obtain images with in many cases atomic resolution from which crystallographic information can be obtained. There are also other methods such as low-energy electron diffraction, low-energy electron microscopy and reflection high-energy electron diffraction which can be used to obtain crystallographic information about surfaces. (Full article...) -
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Diamond is a solid form of the element carbon with its atoms arranged in a crystal structure called diamond cubic. Another solid form of carbon known as graphite is the chemically stable form of carbon at room temperature and pressure, but diamond is metastable and converts to it at a negligible rate under those conditions. Diamond has the highest hardness and thermal conductivity of any natural material, properties that are used in major industrial applications such as cutting and polishing tools. They are also the reason that diamond anvil cells can subject materials to pressures found deep in the Earth.
Because the arrangement of atoms in diamond is extremely rigid, few types of impurity can contaminate it (two exceptions are boron and nitrogen). Small numbers of defects or impurities (about one per million of lattice atoms) can color a diamond blue (boron), yellow (nitrogen), brown (defects), green (radiation exposure), purple, pink, orange, or red. Diamond also has a very high refractive index and a relatively high optical dispersion.
Most natural diamonds have ages between 1 billion and 3.5 billion years. Most were formed at depths between 150 and 250 kilometres (93 and 155 mi) in the Earth's mantle, although a few have come from as deep as 800 kilometres (500 mi). Under high pressure and temperature, carbon-containing fluids dissolved various minerals and replaced them with diamonds. Much more recently (hundreds to tens of million years ago), they were carried to the surface in volcanic eruptions and deposited in igneous rocks known as kimberlites and lamproites.
Synthetic diamonds can be grown from high-purity carbon under high pressures and temperatures or from hydrocarbon gases by chemical vapor deposition (CVD). Imitation diamonds can also be made out of materials such as cubic zirconia and silicon carbide. Natural, synthetic, and imitation diamonds are most commonly distinguished using optical techniques or thermal conductivity measurements. (Full article...) -
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Corundum is a crystalline form of aluminium oxide (Al2O3) 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.
The name "corundum" is derived from the Tamil-Dravidian word kurundam (ruby-sapphire) (appearing in Sanskrit as kuruvinda).
Because of corundum's hardness (pure corundum is defined to have 9.0 on the Mohs scale), it can scratch almost all other minerals. It is commonly used as an abrasive on sandpaper and on large tools used in machining metals, plastics, and wood. Emery, a variety of corundum with no value as a gemstone, is commonly used as an abrasive. It is a black granular form of corundum, in which the mineral is intimately mixed with magnetite, hematite, or hercynite.
In addition to its hardness, corundum has a density of 4.02 g/cm3 (251 lb/cu ft), which is unusually high for a transparent mineral composed of the low-atomic mass elements aluminium and oxygen. (Full article...) -
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Malachite is a copper carbonate hydroxide mineral, with the formula Cu2CO3(OH)2. This opaque, green-banded mineral crystallizes in the monoclinic crystal system, and most often forms botryoidal, fibrous, or stalagmitic masses, in fractures and deep, underground spaces, where the water table and hydrothermal fluids provide the means for chemical precipitation. Individual crystals are rare, but occur as slender to acicular prisms. Pseudomorphs after more tabular or blocky azurite crystals also occur. (Full article...) -
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Borax (also referred to as sodium borate, tincal (/ˈtɪŋkəl/) and tincar (/ˈtɪŋkər/)) is a salt (ionic compound), a hydrated or anhydrous borate of sodium, with the chemical formula Na2H20B4O17 (also written as Na2B4O7·10H2O).
It is a colorless crystalline solid that dissolves in water to make a basic solution.
It is commonly available in powder or granular form and has many industrial and household uses, including as a pesticide, as a metal soldering flux, as a component of glass, enamel, and pottery glazes, for tanning of skins and hides, for artificial aging of wood, as a preservative against wood fungus, and as a pharmaceutic alkalizer. In chemical laboratories, it is used as a buffering agent.
The terms tincal and tincar refer to native borax, historically mined from dry lake beds in various parts of Asia. (Full article...) -
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Tourmaline (/ˈtʊərməlɪn, -ˌliːn/ TOOR-mə-lin, -leen) is a crystalline silicate mineral group in which boron is compounded with elements such as aluminium, iron, magnesium, sodium, lithium, or potassium. This gemstone comes in a wide variety of colors.
The name is derived from the Sinhalese tōramalli (ටෝරමල්ලි), which refers to the carnelian gemstones. (Full article...) -
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Chalk is a soft, white, porous, sedimentary carbonate rock. It is a form of limestone composed of the mineral calcite and originally formed deep under the sea by the compression of microscopic plankton that had settled to the sea floor. Chalk is common throughout Western Europe, where deposits underlie parts of France, and steep cliffs are often seen where they meet the sea in places such as the Dover cliffs on the Kent coast of the English Channel.
Chalk is mined for use in industry, such as for quicklime, bricks and builder's putty, and in agriculture, for raising pH in soils with high acidity. It is also used for "blackboard chalk" for writing and drawing on various types of surfaces, although these can also be manufactured from other carbonate-based minerals, or gypsum. (Full article...) -
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Zeolite is a family of several microporous, crystalline aluminosilicate materials commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula Mn+
1/n(AlO
2)−
(SiO
2)
x・yH
2O where Mn+
1/n is either a metal ion or H+. These positive ions can be exchanged for others in a contacting electrolyte solution. H+
exchanged zeolites are particularly useful as solid acid catalysts.
The term was originally coined in 1756 by Swedish mineralogist Axel Fredrik Cronstedt, who observed that rapidly heating a material, believed to have been stilbite, produced large amounts of steam from water that had been adsorbed by the material. Based on this, he called the material zeolite, from the Greek ζέω (zéō), meaning "to boil" and λίθος (líthos), meaning "stone".
Zeolites occur naturally, but are also produced industrially on a large scale. , 253 unique zeolite frameworks have been identified, and over 40 naturally occurring zeolite frameworks are known. Every new zeolite structure that is obtained is examined by the International Zeolite Association Structure Commission (IZA-SC) and receives a three-letter designation. (Full article...) -
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Hematite (/ˈhiːməˌtaɪt, ˈhɛmə-/), also spelled as haematite, is a common iron oxide compound with the formula, Fe2O3 and is widely found in rocks and soils. Hematite crystals belong to the rhombohedral lattice system which is designated the alpha polymorph of Fe
2O
3. It has the same crystal structure as corundum (Al
2O
3) and ilmenite (FeTiO
3). With this it forms a complete solid solution at temperatures above 950 °C (1,740 °F).
Hematite naturally occurs in black to steel or silver-gray, brown to reddish-brown, or red colors. It is mined as an important ore mineral of iron. It is electrically conductive. Hematite varieties include kidney ore, martite (pseudomorphs after magnetite), iron rose and specularite (specular hematite). While these forms vary, they all have a rust-red streak. Hematite is not only harder than pure iron, but also much more brittle. Maghemite is a polymorph of hematite (γ-Fe
2O
3) with the same chemical formula, but with a spinel structure like magnetite.
Large deposits of hematite are found in banded iron formations. Gray hematite is typically found in places that have still, standing water or mineral hot springs, such as those in Yellowstone National Park in North America. The mineral can precipitate in the water and collect in layers at the bottom of the lake, spring, or other standing water. Hematite can also occur in the absence of water, usually as the result of volcanic activity.
Clay-sized hematite crystals can also occur as a secondary mineral formed by weathering processes in soil, and along with other iron oxides or oxyhydroxides such as goethite, which is responsible for the red color of many tropical, ancient, or otherwise highly weathered soils. (Full article...) -
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Andesite (/ˈændəzaɪt/) is a volcanic rock of intermediate composition. In a general sense, it is the intermediate type between silica-poor basalt and silica-rich rhyolite. It is fine-grained (aphanitic) to porphyritic in texture, and is composed predominantly of sodium-rich plagioclase plus pyroxene or hornblende.
Andesite is the extrusive equivalent of plutonic diorite. Characteristic of subduction zones, andesite represents the dominant rock type in island arcs. The average composition of the continental crust is andesitic. Along with basalts, andesites are a component of the Martian crust.
The name andesite is derived from the Andes mountain range, where this rock type is found in abundance. It was first applied by Christian Leopold von Buch in 1826. (Full article...) -
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Turquoise is an opaque, blue-to-green mineral that is a hydrous phosphate of copper and aluminium, with the chemical formula CuAl6(PO4)4(OH)8·4H2O. It is rare and valuable in finer grades and has been prized as a gemstone for millennia due to its hue.
Like most other opaque gems, turquoise has been devalued by the introduction of treatments, imitations, and synthetics into the market. The robin egg blue or sky blue color of the Persian turquoise mined near the modern city of Nishapur, Iran, has been used as a guiding reference for evaluating turquoise quality. (Full article...) -
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Cleavage, in mineralogy and materials science, is the tendency of crystalline materials to split along definite crystallographic structural planes. These planes of relative weakness are a result of the regular locations of atoms and ions in the crystal, which create smooth repeating surfaces that are visible both in the microscope and to the naked eye. If bonds in certain directions are weaker than others, the crystal will tend to split along the weakly bonded planes. These flat breaks are termed "cleavage". The classic example of cleavage is mica, which cleaves in a single direction along the basal pinacoid, making the layers seem like pages in a book. In fact, mineralogists often refer to "books of mica".
Diamond and graphite provide examples of cleavage. Each is composed solely of a single element, carbon. In diamond, each carbon atom is bonded to four others in a tetrahedral pattern with short covalent bonds. The planes of weakness (cleavage planes) in a diamond are in four directions, following the faces of the octahedron. In graphite, carbon atoms are contained in layers in a hexagonal pattern where the covalent bonds are shorter (and thus even stronger) than those of diamond. However, each layer is connected to the other with a longer and much weaker van der Waals bond. This gives graphite a single direction of cleavage, parallel to the basal pinacoid. So weak is this bond that it is broken with little force, giving graphite a slippery feel as layers shear apart. As a result, graphite makes an excellent dry lubricant.
While all single crystals will show some tendency to split along atomic planes in their crystal structure, if the differences between one direction or another are not large enough, the mineral will not display cleavage. Corundum, for example, displays no cleavage. (Full article...) -
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Opal is a hydrated amorphous form of silica (SiO2·nH2O); its water content may range from 3% to 21% by weight, but is usually between 6% and 10%. Due to its amorphous property, it is classified as a mineraloid, unlike crystalline forms of silica, which are considered minerals. It is deposited at a relatively low temperature and may occur in the fissures of almost any kind of rock, being most commonly found with limonite, sandstone, rhyolite, marl, and basalt.
The name opal is believed to be derived from the Sanskrit word upala (उपल), which means 'jewel', and later the Greek derivative opállios (ὀπάλλιος).
There are two broad classes of opal: precious and common. Precious opal displays play-of-color (iridescence); common opal does not. Play-of-color is defined as "a pseudo chromatic optical effect resulting in flashes of colored light from certain minerals, as they are turned in white light." The internal structure of precious opal causes it to diffract light, resulting in play-of-color. Depending on the conditions in which it formed, opal may be transparent, translucent, or opaque, and the background color may be white, black, or nearly any color of the visual spectrum. Black opal is considered the rarest, while white, gray, and green opals are the most common. (Full article...) -
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A ruby is a pinkish red to blood-red colored gemstone, a variety of the mineral corundum (aluminium oxide). Ruby is one of the most popular traditional jewelry gems and is very durable. Other varieties of gem-quality corundum are called sapphires. Ruby is one of the traditional cardinal gems, alongside amethyst, sapphire, emerald, and diamond. The word ruby comes from ruber, Latin for red. The color of a ruby is due to the element chromium.
Some gemstones that are popularly or historically called rubies, such as the Black Prince's Ruby in the British Imperial State Crown, are actually spinels. These were once known as "Balas rubies".
The quality of a ruby is determined by its color, cut, and clarity, which, along with carat weight, affect its value. The brightest and most valuable shade of red, called blood-red or pigeon blood, commands a large premium over other rubies of similar quality. After color follows clarity: similar to diamonds, a clear stone will command a premium, but a ruby without any needle-like rutile inclusions may indicate that the stone has been treated. Ruby is the traditional birthstone for July and is usually pinker than garnet, although some rhodolite garnets have a similar pinkish hue to most rubies. The world's most valuable ruby to be sold at auction is the Sunrise Ruby. (Full article...) -
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Cinnabar (/ˈsɪnəˌbɑːr/; from Ancient Greek κιννάβαρι (kinnábari)), or cinnabarite (/ˌsɪnəˈbɑːraɪt/), 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.
Cinnabar generally occurs as a vein-filling mineral associated with volcanic activity and alkaline hot springs. The mineral resembles quartz in symmetry and it exhibits birefringence. Cinnabar has a mean refractive index near 3.2, a hardness between 2.0 and 2.5, and a specific gravity of approximately 8.1. The color and properties derive from a structure that is a hexagonal crystalline lattice belonging to the trigonal crystal system, crystals that sometimes exhibit twinning.
Cinnabar has been used for its color since antiquity in the Near East, including as a rouge-type cosmetic, in the New World since the Olmec culture, and in China since as early as the Yangshao culture, where it was used in coloring stoneware.
Associated modern precautions for the use and handling of cinnabar arise from the toxicity of the mercury component, which was recognized as early as ancient Rome. (Full article...) -
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Galena, also called lead glance, is the natural mineral form of lead(II) sulfide (PbS). It is the most important ore of lead and an important source of silver.
Galena is one of the most abundant and widely distributed sulfide minerals. It crystallizes in the cubic crystal system often showing octahedral forms. It is often associated with the minerals sphalerite, calcite and fluorite. (Full article...) -
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Sapphire is a precious gemstone, a variety of the mineral corundum, consisting of aluminium oxide (α-Al2O3) with trace amounts of elements such as iron, titanium, cobalt, lead, chromium, vanadium, magnesium, boron, and silicon. The name sapphire is derived from the Latin word sapphirus, itself from the Greek word sappheiros (σάπφειρος), which referred to lapis lazuli. It is typically blue, but natural "fancy" sapphires also occur in yellow, purple, orange, and green colors; "parti sapphires" show two or more colors. Red corundum stones also occur, but are called rubies rather than sapphires. Pink-colored corundum may be classified either as ruby or sapphire depending on locale. Commonly, natural sapphires are cut and polished into gemstones and worn in jewelry. They also may be created synthetically in laboratories for industrial or decorative purposes in large crystal boules. Because of the remarkable hardness of sapphires – 9 on the Mohs scale (the third hardest mineral, after diamond at 10 and moissanite at 9.5) – sapphires are also used in some non-ornamental applications, such as infrared optical components, high-durability windows, wristwatch crystals and movement bearings, and very thin electronic wafers, which are used as the insulating substrates of special-purpose solid-state electronics such as integrated circuits and GaN-based blue LEDs. Sapphire is the birthstone for September and the gem of the 45th anniversary. A sapphire jubilee occurs after 65 years. (Full article...)
Selected mineralogist
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Samuel Fowler (October 30, 1779 – February 20, 1844) was a doctor, state legislator, and member of the United States House of Representatives from northwestern New Jersey. As the owner of zinc and iron mines and an iron works at Franklin, New Jersey, he became a noted mineralogist who discovered several varieties of rare minerals (chiefly various ores of zinc). (Full article...) -
Image 2João da Silva Barbosa or João da Silva Feijó, (1760 in Rio de Janeiro – 1824), was a naturalist, mineralogist and Portuguese soldier, born in Brazil.
João da Silva Feijó studied philosophy and mathematics at the University of Coimbra and adopted the name Feijó in homage to Benito Jerónimo Feijoo, Spanish philosopher, who at the time was respected among natural history students. (Full article...) -
Image 3
Johan Gadolin (5 June 1760 – 15 August 1852) was a Finnish chemist, physicist and mineralogist. Gadolin discovered a "new earth" containing the first rare-earth compound yttrium, which was later determined to be a chemical element. He is also considered the founder of Finnish chemistry research, as the second holder of the Chair of Chemistry at the Royal Academy of Turku (or Åbo Kungliga Akademi). Gadolin was ennobled for his achievements and awarded the Order of Saint Vladimir and the Order of Saint Anna. (Full article...) -
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Joseph Henry Collins FGS, (16 March 1841 – 12 April 1916) was a British mining engineer, mineralogist and geologist. He died at his home, Crinnis House, near St Austell, on 12 April 1916 and is buried in Campdowns cemetery, Charlestown. (Full article...) -
Image 5Andrew Ketcham Barnett (1852–1914) was a mineral collector and dealer in Penzance, Cornwall, in the United Kingdom. He was Principal of the Penzance School of Mines (now part of the Camborne School of Mines), lectured on mining, and helped to build their mineral collection. He also served as Mayor of Penzance on seven occasions from 1906 to 1913.
Cooper writes of him:
:"Barnett was born in Chacewater, Cornwall in 1852. He was an original member of the Mineralogical Society, a Fellow of the Geological Society from 1875, and President of the Royal Geological Society of Cornwall 1907–08, having been awarded their Bolitho Medal in 1906. His classes on mineralogy in 1873 led to the establishment of the Mining and Science School at Penzance of which he became Principal. He was mayor of Penzance seven times from 1906 to 1913. Active as a mineral dealer from at least 1876 to 1887 at Chyandour, Penzance, he specialized in local specimens and occasionally sold minerals brought back from Australia by "Cousin Jack." In the 1881 Census he described himself as an assayer. He is the author of the now-rare Elementary Inorganic Chemistry; lecture notes, ca. 1900." (Full article...) -
Image 6
George R. Rossman is an American mineralogist and the Professor of Mineralogy at the California Institute of Technology. (Full article...) -
Image 7Vittorio Simonelli (May 1860, in Arezzo – 9 February 1929, in San Quirico d'Orcia) was an Italian geologist and paleontologist. (Full article...)
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Alexandra Navrotsky (born 20 June 1943 in New York City) is a physical chemist in the field of nanogeoscience. She is an elected member of the United States National Academy of Sciences (NAS) and the American Philosophical Society (APS). She was a board member of the Earth Sciences and Resources division of the NAS from 1995 until 2000.
In 2005, she was awarded the Urey Medal, by the European Association of Geochemistry.
In 2006, she was awarded the Harry H. Hess Medal, by the American Geophysical Union.
She is currently the director of NEAT ORU (Nanomaterials in Environment, Agriculture, and Technology Organized Research Unit), a primary program in nanogeoscience. She is distinguished professor at University of California, Davis. (Full article...) -
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Johannes Martin Bijvoet ForMemRS (23 January 1892, Amsterdam – 4 March 1980, Winterswijk) was a Dutch chemist and crystallographer at the van 't Hoff Laboratory at Utrecht University. He is famous for devising a method of establishing the absolute configuration of molecules. In 1946, he became member of the Royal Netherlands Academy of Arts and Sciences.
The concept of tetrahedrally bound carbon in organic compounds stems back to the work by van 't Hoff and Le Bel in 1874. At this time, it was impossible to assign the absolute configuration of a molecule by means other than referring to the projection formula established by Fischer, who had used glyceraldehyde as the prototype and assigned randomly its absolute configuration. (Full article...) -
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Karl Johann Bernhard Karsten (26 November 1782 – 22 August 1853) was a German mineralogist known for contributions made to the German metallurgy industry. (Full article...) -
Image 11Wilhelm Hermann Julius Eitel (6 May 1891, Frankfurt am Main – 20 July 1979, United States) was a German-American scientist. (Full article...)
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Image 12
Georgius Agricola (/əˈɡrɪkələ/; born Georg Bauer; 24 March 1494 – 21 November 1555) was a German Humanist scholar, mineralogist and metallurgist. Born in the small town of Glauchau, in the Electorate of Saxony of the Holy Roman Empire, he was broadly educated, but took a particular interest in the mining and refining of metals. He was the first to drop the Arabic definite article al-, exclusively writing chymia and chymista in describing activity that we today would characterize as chemical or alchemical, giving chemistry its modern name. For his groundbreaking work De Natura Fossilium published in 1546, he is generally referred to as the Father of Mineralogy and the founder of geology as a scientific discipline.
He is well known for his pioneering work De re metallica libri XII, that was published in 1556, one year after his death. This 12-volume work is a comprehensive and systematic study, classification and methodical guide on all available factual and practical aspects, that are of concern for mining, the mining sciences and metallurgy, investigated and researched in its natural environment by means of direct observation. Unrivalled in its complexity and accuracy, it served as the standard reference work for two centuries. Agricola stated in the preface, that he will exclude "all those things which I have not myself seen, or have not read or heard of". He continued, "That which I have neither seen, nor carefully considered after reading or hearing of, I have not written about." (Full article...) -
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Adolf Karl Remelé (17 July 1839, Uerdingen – 16 November 1915, Eberswalde) was a German geologist and mineralogist.
He received his education at the University of Bonn, at the École des Mines in Paris and from the University of Berlin, receiving his doctorate in 1864 with the dissertation "De rubro uranico". In 1867 he qualified as a lecturer at Berlin, and during the following year, succeeded Lothar Meyer at the Forestry Academy in Eberswalde, where he taught classes in chemistry, geognosy and mineralogy. (Full article...) -
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James Tennant (8 February 1808 – 23 February 1881) was an English mineralogist, the master of the Worshipful Company of Turners and mineralogist to Queen Victoria. (Full article...) -
Image 15Harald Bjørlykke (14 September 1901 – 28 February 1968) was a Norwegian geologist. (Full article...)
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Image 16Enrico Clerici (15 October 1862 – 26 August 1938) was an Italian mineralogist and geologist. From 1903 on he worked at the University of Rome. He published in 1907 the composition of a solution with a density of 4.25 g/cm3 at 20 °C, to determine the density of minerals. The Clerici solution is a mixture of thallium formate (Tl(CHO2)) and thallium malonate (Tl(C3H3O4)) in water. (Full article...)
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Ullmannite or Nickel glance (trivial name) is a nickel antimony sulfide mineral with formula: NiSbS. Considerable substitution occurs with cobalt and iron in the nickel site along with bismuth and arsenic in the antimony site. A solid solution series exists with the high cobalt willyamite. (Full article...) -
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Henri Longchambon (27 July 1896 in Clermont-Ferrand, Puy-de-Dôme – 20 March 1969 in Le Kremlin-Bicêtre) was a French politician and scientist. (Full article...) -
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Christian Samuel Weiss (26 February 1780 – 1 October 1856) was a German mineralogist born in Leipzig.
Following graduation, he worked as a physics instructor in Leipzig from 1803 until 1808. and in the meantime, conducted geological studies of mountain formations in Tyrol, Switzerland and France (1806–08). In 1810 he became a professor of mineralogy at the University of Berlin, where in 1818/19 and 1832/33, he served as university rector. He died near Eger in Bohemia. (Full article...) -
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Emil Wilhelm Cohen (12 October 1842 – 13 April 1905) was a German mineralogist and petrographer, born in Jutland. (Full article...) -
Image 21Carl Schulz (12 November 1851 – 15 August 1944) was a Norwegian educator and politician for the Liberal Party. He became known as a teacher of physics, electrotechnics and mineralogy before advancing to being school director. (Full article...)
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Image 22
Karl Rössler (6 May 1788, in Wiesbaden – 23 August 1863, in Hanau) was a German manufacturer and mineralogist.
After a business apprenticeship in Frankfurt am Main, he acquired in 1818 a hat factory, which he transformed into a highly successful company. He had a keen interest in the geology, mineralogy and paleontology of the Wetterau, and accordingly, collected numerous minerals and fossils of the region. During his career, he worked closely with geologist Leopold von Buch. (Full article...) -
Image 23
Johann Wolfgang von Goethe (28 August 1749 – 22 March 1832) was a German polymath and writer, who is widely regarded as the greatest and most influential writer in the German language. His work has had a profound and wide-ranging influence on Western literary, political, and philosophical thought from the late 18th century to the present day. Goethe was a German poet, playwright, novelist, scientist, statesman, theatre director, and critic. His works include plays, poetry and aesthetic criticism, as well as treatises on botany, anatomy, and color.
Goethe took up residence in Weimar in November 1775 following the success of his first novel, The Sorrows of Young Werther (1774). He was ennobled by the Duke of Saxe-Weimar, Karl August, in 1782. Goethe was an early participant in the Sturm und Drang literary movement. During his first ten years in Weimar, Goethe became a member of the Duke's privy council (1776–1785), sat on the war and highway commissions, oversaw the reopening of silver mines in nearby Ilmenau, and implemented a series of administrative reforms at the University of Jena. He also contributed to the planning of Weimar's botanical park and the rebuilding of its Ducal Palace. (Full article...) -
Image 24Bertram Eugene Warren (June 28, 1902 – June 27, 1991) was an American crystallographer. His studies of X-rays provided much knowledge and understanding of both crystalline and non-crystalline materials. He also worked on changing amorphous solids to a crystalline state. (Full article...)
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Prof Ferdinand Zirkel FRS(For) HFRSE (20 May 1838 – 11 June 1912) was a German geologist and petrographer. (Full article...)
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For editor resources and to collaborate with other editors on improving Wikipedia's Minerals-related articles, see WikiProject Rocks and minerals.
General images
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Image 2Native gold. Rare specimen of stout crystals growing off of a central stalk, size 3.7 x 1.1 x 0.4 cm, from Venezuela. (from Mineral)
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Image 3Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
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Image 6Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
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Image 7Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
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Image 9Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
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Image 10Epidote often has a distinctive pistachio-green colour. (from Mineral)
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Image 12Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
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Image 13Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
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Image 14An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
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Image 15When minerals react, the products will sometimes assume the shape of the reagent; the product mineral is termed a pseudomorph of (or after) the reagent. Illustrated here is a pseudomorph of kaolinite after orthoclase. Here, the pseudomorph preserved the Carlsbad twinning common in orthoclase. (from Mineral)
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Image 18Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
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Image 19Schist is a metamorphic rock characterized by an abundance of platy minerals. In this example, the rock has prominent sillimanite porphyroblasts as large as 3 cm (1.2 in). (from Mineral)
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Image 20Mohs Scale versus Absolute Hardness (from Mineral)
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Image 21Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
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Image 22Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
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Image 23Gypsum desert rose (from Mineral)
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Image 25Pink cubic halite (NaCl; halide class) crystals on a nahcolite matrix (NaHCO3; a carbonate, and mineral form of sodium bicarbonate, used as baking soda). (from Mineral)
Did you know ...?
- ... that Treak Cliff Cavern (pictured) is one of only two remaining active sources of the ornamental mineral Blue John?
- ...that chalcocite, a profitable and desirable kind of copper ore, was particularly plentiful in the now-depleted copper mines of Cornwall, England and Bristol, Connecticut?
- ... that Gloria J. Romero is leading a campaign in the California Legislature to remove serpentine as the official state rock because it is a source of cancer-causing asbestos?
- ... that the mineral abelsonite probably formed from chlorophyll and is the only known crystalline geoporphyrin?
Subcategories
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Topics
Overview | ||
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Common minerals |
Ore minerals, mineral mixtures and ore deposits | |||||||||
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Ores |
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Deposit types |
Borates | |||||
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Carbonates | |||||
Oxides |
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Phosphates | |||||
Silicates | |||||
Sulfides | |||||
Other |
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Crystalline | |||||||
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Cryptocrystalline | |||||||
Amorphous | |||||||
Miscellaneous | |||||||
Notable varieties |
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Oxide minerals |
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Silicate minerals | |||||
Other |
Gemmological classifications by E. Ya. Kievlenko (1980), updated | |||||||||
Jewelry stones |
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Jewelry-Industrial stones |
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Industrial stones |
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Mineral identification | |
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"Special cases" ("native elements and organic minerals") |
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"Sulfides and oxides" |
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"Evaporites and similars" |
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"Mineral structures with tetrahedral units" (sulfate anion, phosphate anion, silicon, etc.) |
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