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
- Image 1
Chalcopyrite (/ˌkælkəˈpaɪˌraɪt, -koʊ-/ KAL-kə-PY-ryte, -koh-) is a copper iron sulfide mineral and the most abundant copper ore mineral. It has the chemical formula CuFeS2 and crystallizes in the tetragonal system. It has a brassy to golden yellow color and a hardness of 3.5 to 4 on the Mohs scale. Its streak is diagnostic as green-tinged black.
On exposure to air, chalcopyrite tarnishes to a variety of oxides, hydroxides, and sulfates. Associated copper minerals include the sulfides bornite (Cu5FeS4), chalcocite (Cu2S), covellite (CuS), digenite (Cu9S5); carbonates such as malachite and azurite, and rarely oxides such as cuprite (Cu2O). It is rarely found in association with native copper. Chalcopyrite is a conductor of electricity.
Copper can be extracted from chalcopyrite ore using various methods. The two predominant methods are pyrometallurgy and hydrometallurgy, the former being the most commercially viable. (Full article...) - Image 2Galena with minor pyrite
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...) - Image 3
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...) - Image 4
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...) - Image 5
Crystal structure of table salt (sodium in purple, chlorine in green)
In crystallography, crystal structure is a description of ordered arrangement of atoms, ions, or molecules in a crystalline material. Ordered structures occur from intrinsic nature of constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.
The smallest group of particles in material that constitutes this repeating pattern is unit cell of the structure. The unit cell completely reflects symmetry and structure of the entire crystal, which is built up by repetitive translation of unit cell along its principal axes. The translation vectors define the nodes of Bravais lattice.
The lengths of principal axes/edges, of unit cell and angles between them are lattice constants, also called lattice parameters or cell parameters. The symmetry properties of crystal are described byconcept of space groups. All possible symmetric arrangements of particles in three-dimensional space may be described by 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...) - Image 6A ruby crystal from Dodoma Region, Tanzania
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, which sold for US$34.8 million. (Full article...) - Image 7Brazilian trigonal hematite crystal
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...) - Image 8
A rock containing three crystals of pyrite (FeS2). The crystal structure of pyrite is primitive cubic, and this is reflected in the cubic symmetry of its natural crystal facets.
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 9Beachy Head is a part of the extensive Southern England Chalk Formation.
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...) - Image 10Quartz crystal cluster from Brazil
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...) - Image 11
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...) - Image 12
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...) - Image 13
Rutile is an oxide mineral composed of titanium dioxide (TiO2), the most common natural form of TiO2. Rarer polymorphs of TiO2 are known, including anatase, akaogiite, and brookite.
Rutile has one of the highest refractive indices at visible wavelengths of any known crystal and also exhibits a particularly large birefringence and high dispersion. Owing to these properties, it is useful for the manufacture of certain optical elements, especially polarization optics, for longer visible and infrared wavelengths up to about 4.5 micrometres. Natural rutile may contain up to 10% iron and significant amounts of niobium and tantalum.
Rutile derives its name from the Latin rutilus ('red'), in reference to the deep red color observed in some specimens when viewed by transmitted light. Rutile was first described in 1803 by Abraham Gottlob Werner using specimens obtained in Horcajuelo de la Sierra, Madrid (Spain), which is consequently the type locality. (Full article...) - Image 14
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...) - Image 15A sample of andesite (dark groundmass) with amygdaloidal vesicles filled with zeolite. Diameter of view is 8 cm.
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...) - Image 16
Talc, or talcum, is a clay mineral composed of hydrated magnesium silicate, with the chemical formula Mg3Si4O10(OH)2. Talc in powdered form, often combined with corn starch, is used as baby powder. This mineral is used as a thickening agent and lubricant. It is an ingredient in ceramics, paints, and roofing material. It is a main ingredient in many cosmetics. It occurs as foliated to fibrous masses, and in an exceptionally rare crystal form. It has a perfect basal cleavage and an uneven flat fracture, and it is foliated with a two-dimensional platy form.
The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 1 as the hardness of talc, the softest mineral. When scraped on a streak plate, talc produces a white streak, though this indicator is of little importance, because most silicate minerals produce a white streak. Talc is translucent to opaque, with colors ranging from whitish grey to green with a vitreous and pearly luster. Talc is not soluble in water, and is slightly soluble in dilute mineral acids.
Soapstone is a metamorphic rock composed predominantly of talc. (Full article...) - Image 17
Green fluorite with prominent cleavage
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...) - Image 18The 423-carat (85 g) blue Logan Sapphire
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 the 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...) - Image 19Malachite from the Democratic Republic of the Congo
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...) - Image 20
The mineral pyrite (/ˈpaɪraɪt/ PY-ryte), or iron pyrite, also known as fool's gold, is an iron sulfide with the chemical formula FeS2 (iron (II) disulfide). Pyrite is the most abundant sulfide mineral.
Pyrite's metallic luster and pale brass-yellow hue give it a superficial resemblance to gold, hence the well-known nickname of fool's gold. The color has also led to the nicknames brass, brazzle, and brazil, primarily used to refer to pyrite found in coal.
The name pyrite is derived from the Greek πυρίτης λίθος (pyritēs lithos), 'stone or mineral which strikes fire', in turn from πῦρ (pŷr), 'fire'. In ancient Roman times, this name was applied to several types of stone that would create sparks when struck against steel; Pliny the Elder described one of them as being brassy, almost certainly a reference to what is now called pyrite.
By Georgius Agricola's time, c. 1550, the term had become a generic term for all of the sulfide minerals. (Full article...) - Image 21
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...) - Image 22A lustrous crystal of zircon perched on a tan matrix of calcite from the Gilgit District of Pakistan
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...) - Image 23Amethyst cluster from Artigas, Uruguay
Amethyst is a violet variety of quartz. The name comes from the Koine Greek αμέθυστος amethystos from α- a-, "not" and μεθύσκω (Ancient Greek) methysko / μεθώ metho (Modern Greek), "intoxicate", a reference to the belief that the stone protected its owner from drunkenness. Ancient Greeks wore amethyst and carved drinking vessels from it in the belief that it would prevent intoxification.
Amethyst, a semiprecious stone, is often used in jewelry. (Full article...) - Image 24Deep green isolated fluorite crystal resembling a truncated octahedron, set upon a micaceous matrix, from Erongo Mountain, Erongo Region, Namibia (overall size: 50 mm × 27 mm, crystal size: 19 mm wide, 30 g)
Fluorite (also called fluorspar) is the mineral form of calcium fluoride, CaF2. It belongs to the halide minerals. It crystallizes in isometric cubic habit, although octahedral and more complex isometric forms are not uncommon.
The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 4 as fluorite.
Pure fluorite is colourless and transparent, both in visible and ultraviolet light, but impurities usually make it a colorful mineral and the stone has ornamental and lapidary uses. Industrially, fluorite is used as a flux for smelting, and in the production of certain glasses and enamels. The purest grades of fluorite are a source of fluoride for hydrofluoric acid manufacture, which is the intermediate source of most fluorine-containing fine chemicals. Optically clear transparent fluorite has anomalous partial dispersion, that is, its refractive index varies with the wavelength of light in a manner that differs from that of commonly used glasses, so fluorite is useful in making apochromatic lenses, and particularly valuable in photographic optics. Fluorite optics are also usable in the far-ultraviolet and mid-infrared ranges, where conventional glasses are too opaque for use. Fluorite also has low dispersion, and a high refractive index for its density. (Full article...) - Image 25
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...)
Selected mineralogist
- Image 1
Teachers of the Forestry Academy in Eberswalde (ca. 1868); Adolf Remelé, 3rd figure from the right (standing).
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...) - Image 2Vladimir Vital'evich Shcherbina (1907–1978) was a prominent Soviet geochemist and mineralogist. He was a student of Alexander Fersman.
In 1931, he led a team from the USSR Academy of Sciences in the mineralogical examination of the Lovozero Massif. (Full article...) - Image 3
Charles Palache (July 18, 1869 – December 5, 1954) was an American mineralogist and crystallographer. In his time, he was one of the most important mineralogists in the United States. (Full article...) - Image 4Goethe in 1828, by Joseph Karl Stieler
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. A 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), and joined a thriving intellectual and cultural environment under the patronage of Duchess Anna Amalia that had already included Abel Seyler's theatre company and Christoph Martin Wieland, and that formed the basis of Weimar Classicism. 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 5
Otto Wilhelm Hermann Abich (11 December 1806 – 1 July 1886) was a German mineralogist and geologist who was among the first to conduct scientific studies in the Caucasus region and has been called the Father of Caucasian Geology. He worked briefly at the University of Dorpat and then travelled as part of the Corps of Mining Engineers of the Russian Empire. He collected minerals and fossils across the regions in which he travelled including Armenia, Persia, Italy and Daghestan. (Full article...) - Image 6
Ours-Pierre-Armand Petit-Dufrénoy (5 September 1792 – 20 March 1857) was a French geologist and mineralogist. (Full article...) - Image 7József Sándor Krenner or Joseph Krenner (3 March 1839 – 6 January 1920) was a Hungarian mineralogist. He discovered several new minerals.
Krenner was born in Buda and studied at the University of Pest, Vienna and Tübingen mineralogy and geology. He received his Ph.D. in 1865 for work with Friedrich August Quenstedt in Tübingen. Krenner worked in the mineralogy section of the Hungarian National Museum. From 1870 on he also lectured at the Technical University of Budapest. In 1888 he became a member of the Hungarian Academy of Science.
Krenner discovered several new minerals, for example, Krennerite which he discovered in 1877 in Sacaramb, Romania. The mineral is obviously named after himself. Another mineral he discovered was Semseyite, the lead antimony sulfide discovered in 1881 was named after Andor Semsey (1833–1923), a Hungarian nobleman and mineralogist. (Full article...) - Image 8
Carl Friedrich Christian Mohs (German: [moːs]; 29 January 1773 – 29 September 1839) was a German chemist and mineralogist. He was the creator of the Mohs scale of mineral hardness. Mohs also introduced a classification of the crystal forms in crystal systems independently of Christian Samuel Weiss. (Full article...) - Image 9
Gustav Adolph Kenngott, c. 1860
Gustav Adolph Kenngott (January 6, 1818 – March 7, 1897) was a German mineralogist. (Full article...) - Image 10John Henry Heuland (March 21, 1778 Bayreuth – November 16, 1856 Hastings) was a German born (Johann Heinrich) English mineralogist and dealer. He was a Fellow of the Geological Society of London. His collection is held by the Natural History Museum, London. In 1804 he purchased mineral specimens in Lisbon. He subsequently travelled through France, Germany, Sweden, and Russia, collecting and buying minerals. About the year 1806 he acquired minerals collected in Europe between the years 1766 and 1806 by his uncle Adolarius Jacob Forster whose London dealership later became Heuland's. Armand Lévy categorised his mineral collection.
The mineral Heulandite is named for him. He played a dubious role in the discovery of Palladium. (Full article...) - Image 11Robert Minard Garrels (August 24, 1916 – March 8, 1988) was an American geochemist. Garrels applied experimental physical chemistry data and techniques to geology and geochemistry problems. The book Solutions, Minerals, and Equilibria co-authored in 1965 by Garrels and Charles L. Christ revolutionized aqueous geochemistry.
Garrels earned a bachelor's degree in geology from the University of Michigan in 1937. He went on to earn an M.S. degree from Northwestern University in 1939, his thesis work was on iron ores of Newfoundland in 1938. His Ph.D. was awarded in 1941 based on lab studies of complex formation between lead and chloride ions in aqueous solution. (Full article...) - Image 12Stanley Robert Mitchell (12 February 1881 – 22 March 1963) was an Australian commercial metallurgist as well as an amateur mineralogist and ethnologist. (Full article...)
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Johann Gottlob Lehmann (4 August 1719 – 22 January 1767) was a German mineralogist and geologist noted for his work and research contributions to the geologic record leading to the development of stratigraphy. (Full article...) - Image 14François Alluaud (21 September 1778, Limoges – 18 February 1866, Limoges) was a French manufacturer of Limoges porcelain, geologist and mineralogist. He was the grandfather of entomologist Charles Alluaud (1861–1949).
Following the death of his father in 1799, who was also named François Alluaud, he took over ownership of the family porcelain factory in Limoges. The company operated its own quarries; a feldspar mine at Chanteloube and a kaolin quarry at Marcognac. (Full article...) - Image 15Peter John Wyllie (born 8 February 1930, in London, England) is a British petrologist and academic.
He was Professor of Geology at the California Institute of Technology from 1983 until his retirement in 1999. Prior to this, he held positions at the University of St Andrews (1955–56), Pennsylvania State University (1958–59 and 1961–66), the University of Leeds (1959–61), and the University of Chicago (1965–83). He is well known for his many contributions to the understanding of magmatism, particularly through his work on the experimental petrology of magmas and volatiles. In the early 1970s, Wyllie wrote two widely used textbooks; The Dynamic Earth (1971) and The Way the Earth Works (1976) which integrated the new understanding of magmatism and plate tectonics. He is also famous for his contributions to the coverage of earth sciences in the Encyclopædia Britannica, particularly his outline of the field in Part Two of the Propædia. Wyllie was President of the International Union of Geodesy and Geophysics (IUGG) from 1995 to 1999. (Full article...) - Image 16Adolf Pabst (30 November 1899, Chicago – 3 April 1990, Berkeley, California) was an American mineralogist and geologist. (Full article...)
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Hartvig Caspar Christie in 1873
Hartvig Caspar Christie (1 December 1826 – 3 March 1873) was a Norwegian mineralogist and physicist. (Full article...) - Image 18François Pierre Nicolas Gillet de Laumont (28 May 1747 – 1 June 1834) was a French mineralogist.
He was born in Paris, educated at a military school and served in the army from 1772 to 1784, when he was appointed inspector of mines. His attention in his leisure time was wholly given to mineralogy, and he assisted in organizing the new École des Mines in Paris. (Full article...) - Image 19
Karl Georg von Raumer (9 April 1783 – 2 June 1865) was a German geologist and educator. (Full article...) - Image 20Hilary Bauerman (16 March 1835 – 5 December 1909) was an English metallurgist, mineralogist and geologist. (Full article...)
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Frank Christopher Hawthorne CC FRSC (born 8 January 1946) is an English-born Canadian mineralogist, crystallographer and spectroscopist. He works at the University of Manitoba and is currently distinguished professor emeritus. By combining graph theory, bond-valence theory and the moments approach to the electronic energy density of solids he has developed bond topology
as a rigorous approach to understanding the atomic arrangements, chemical compositions and paragenesis of complex oxide and oxysalt minerals. (Full article...) - Image 22
Alice Mary Dowse Weeks (August 26, 1909 – August 29, 1988) was an American geologist. Weeksite is named after her. She identified uranophane in 1953 along with Mary E. Thompson. Weeks was the first to propose the concept of oxidation of ore deposits that contain uranium, vanadium, and other accessory metals. She founded the Geology Department at Temple University in Philadelphia, and was a strong proponent of women in geology. (Full article...) - Image 23Adolarius Jacob Forster (1739–1806) was a Prussian mineralogist and dealer in display specimen minerals. The Forster family left Yorkshire in 1649 and settled in Prussia. Adolarius Jacob Forster began dealing in mineral specimens around 1766, at the age of 27. He continued in that profession for 40 years and travelled widely. He had premises in London, Paris and St. Petersburg. The Covent Garden, London shop and one in Soho was run by his wife. His brother, Ingham Henry Forster (1725–1782) ran the business in Paris. Auction catalogues for sales in Paris were written by Romé de l'Isle.
He was related to Johann Georg Adam Forster and Johann Reinhold Forster and his sister married the London dealer naturalist George Humphrey at St-Martin-in-the-Fields, London on August 16, 1768. In 1802 Forster sold a collection to the museum of the St Petersburg Mining Institute, under the auspices of the Emperor of All Russia Alexander I. He spent the last ten years of his life in Russia, and died in St. Petersburg in 1806. The dealership was taken over by his nephew John Henry Heuland. (Full article...) - Image 24
Gregori Aminoff (8 February 1883 – 11 February 1947) was a Swedish mineralogist, artist, and a member of the Aminoff family. During his career, Aminoff introduced X-ray diffraction and electron diffraction to the Swedish scientific community and was a pioneer in crystallography in Sweden. (Full article...) - Image 25
Carl Johann Bernhard Karsten
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...)
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General images
- Image 3Pink 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)
- Image 5Schist 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)
- Image 6Mohs Scale versus Absolute Hardness (from Mineral)
- Image 7Perfect basal cleavage as seen in biotite (black), and good cleavage seen in the matrix (pink orthoclase). (from Mineral)
- Image 8Muscovite, a mineral species in the mica group, within the phyllosilicate subclass (from Mineral)
- Image 9When 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)
- Image 11Black andradite, an end-member of the orthosilicate garnet group. (from Mineral)
- Image 12Diamond is the hardest natural material, and has a Mohs hardness of 10. (from Mineral)
- Image 14Red cinnabar (HgS), a mercury ore, on dolomite. (from Mineral)
- Image 15Epidote often has a distinctive pistachio-green colour. (from Mineral)
- Image 17An example of elbaite, a species of tourmaline, with distinctive colour banding. (from Mineral)
- Image 18Gypsum desert rose (from Mineral)
- Image 19Hübnerite, the manganese-rich end-member of the wolframite series, with minor quartz in the background (from Mineral)
- Image 20Sphalerite crystal partially encased in calcite from the Devonian Milwaukee Formation of Wisconsin (from Mineral)
- Image 21Asbestiform tremolite, part of the amphibole group in the inosilicate subclass (from Mineral)
- Image 22Native 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)
- Image 25Mohs hardness kit, containing one specimen of each mineral on the ten-point hardness scale (from Mohs scale)
Did you know ...?
- ... that while manganese-bearing vesuvianite has been studied since 1883, manganvesuvianite (pictured) was not described until 2002?
- ... that the mineral rapidcreekite was discovered in Yukon, Canada, in 1983?
- ... that collinsite was discovered in British Columbia and named for the director of the Geological Survey of Canada?
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