Pyromorphite
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Pyromorphite
Pyromorphite is a mineral species composed of lead chlorophosphate: Pb5( P O4)3 Cl, sometimes occurring in sufficient abundance to be mined as an ore of lead. Crystals are common, and have the form of a hexagonal prism terminated by the basal planes, sometimes combined with narrow faces of a hexagonal pyramid. Crystals with a barrel-like curvature are not uncommon. Globular and reniform masses are also found. It is part of a series with two other minerals: mimetite (Pb5( AsO4)3Cl) and vanadinite (Pb5( VO4)3Cl), the resemblance in external characters is so close that, as a rule, it is only possible to distinguish between them by chemical tests. They were formerly confused under the names green lead ore and brown lead ore (''German: Grünbleierz and Braunbleierz''). The phosphate was first distinguished chemically by M. H. Klaproth in 1784, and it was named pyromorphite by J. F. L. Hausmann in 1813. The name is derived from the Greek for ''pyr'' (fire) and ''morfe'' (form) due to ...
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Mimetite
Mimetite is a lead arsenate chloride mineral (Pb5(AsO4)3Cl) which forms as a secondary mineral in lead deposits, usually by the oxidation of galena and arsenopyrite. The name derives from the Greek Μιμητής ''mimetes'', meaning "imitator" and refers to mimetite's resemblance to the mineral pyromorphite. This resemblance is not coincidental, as mimetite forms a mineral series with pyromorphite () and with vanadinite (). Notable occurrences are Mapimi, Durango, Mexico and Tsumeb, Namibia. Properties Mimetite is a lead chloride arsenate mineral with the composition . It is a secondary mineral, formed by oxidation of primary lead minerals in arsenic-bearing lead deposits. It typically forms short hexagonal crystals that are yellow to brown to orange in color, very brittle, moderately hard (Mohs hardness 3.5-4), and dense (specific gravity 7.24). It is distinctive for its lack of transparency, its resinous to adamantine luster, and its solubility in nitric acid. Mimetite fo ...
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Vanadinite
Vanadinite is a mineral belonging to the apatite group of phosphates, with the chemical formula Pb5( V O4)3 Cl. It is one of the main industrial ores of the metal vanadium and a minor source of lead. A dense, brittle mineral, it is usually found in the form of red hexagonal crystals. It is an uncommon mineral, formed by the oxidation of lead ore deposits such as galena. First discovered in 1801 in Mexico, vanadinite deposits have since been unearthed in South America, Europe, Africa, and North America. Origins Vanadinite is an uncommon mineral, only occurring as the result of chemical alterations to a pre-existing material. It is therefore known as a secondary mineral. It is found in arid climates and forms by oxidation of primary lead minerals. Vanadinite is especially found in association with the lead sulfide, galena. Other associated minerals include wulfenite, limonite, and barite. It was originally discovered in Mexico by the Spanish mineralogist Andrés Manuel del Río ...
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Phosphate Mineral
Phosphate minerals contain the tetrahedrally coordinated phosphate (PO43−) anion along sometimes with arsenate (AsO43−) and vanadate (VO43−) substitutions, and chloride (Cl−), fluoride (F−), and hydroxide (OH−) anions that also fit into the crystal structure. The phosphate class of minerals is a large and diverse group, however, only a few species are relatively common. Applications Phosphate rock has high concentration of phosphate minerals, most commonly of the apatite group. It is the major resource mined to produce phosphate fertilizers for the agriculture sector. Phosphate is also used in animal feed supplements, food preservatives, anti-corrosion agents, cosmetics, fungicides, ceramics, water treatment and metallurgy. The largest use of minerals mined for their phosphate content is the production of fertilizer. Phosphate minerals are often used for control of rust and prevention of corrosion on ferrous materials applied with electrochemical conversion co ...
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Johann Friedrich Ludwig Hausmann
Johann Friedrich Ludwig Hausmann (22 February 1782, Hannover – 26 December 1859, Göttingen) was a German mineralogist. Biography He was born in Hannover and educated in Göttingen, where he obtained a PhD. Two years after making a geological tour of Denmark, Norway and Sweden in 1807, he was placed at the head of a government mining establishment in Westphalia, and established a school of mines at Clausthal in the Harz mountains. In 1811 he was appointed professor of technology and mining, and later of geology and mineralogy at the university of Göttingen, which he occupied until shortly before his death. Additionally, he was secretary of the Royal Academy of Sciences in Göttingen for many years. In 1813, he was elected a foreign member of the Royal Swedish Academy of Sciences. He published observations on the geology and mineralogy of Spain and Italy as well as that of central and northern Europe: he wrote on gypsum, pyrites, felspar, tachylite, cordierite and on some eru ...
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Mold (fungus)
A mold () or mould () is one of the structures certain fungi can form. The dust-like, colored appearance of molds is due to the formation of spores containing fungal secondary metabolites. The spores are the dispersal units of the fungi. Not all fungi form molds. Some fungi form mushrooms; others grow as single cells and are called microfungi (for example yeasts). A large and taxonomically diverse number of fungal species form molds. The growth of hyphae results in discoloration and a fuzzy appearance, especially on food. The network of these tubular branching hyphae, called a mycelium, is considered a single organism. The hyphae are generally transparent, so the mycelium appears like very fine, fluffy white threads over the surface. Cross-walls (septa) may delimit connected compartments along the hyphae, each containing one or multiple, genetically identical nuclei. The dusty texture of many molds is caused by profuse production of asexual spores ( conidia) formed by di ...
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Biomineralization
Biomineralization, also written biomineralisation, is the process by which living organisms produce minerals, often to harden or stiffen existing tissues. Such tissues are called mineralized tissues. It is an extremely widespread phenomenon; all six taxonomic kingdoms contain members that are able to form minerals, and over 60 different minerals have been identified in organisms. Examples include silicates in algae and diatoms, carbonates in invertebrates, and calcium phosphates and carbonates in vertebrates. These minerals often form structural features such as sea shells and the bone in mammals and birds. Organisms have been producing mineralized skeletons for the past 550 million years. Calcium carbonates and calcium phosphates are usually crystalline, but silica organisms (sponges, diatoms...) are always non crystalline minerals. Other examples include copper, iron and gold deposits involving bacteria. Biologically formed minerals often have special uses such as magnetic ...
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Lustre (mineralogy)
Lustre (British English) or luster (American English; see spelling differences) is the way light interacts with the surface of a crystal, rock, or mineral. The word traces its origins back to the Latin ''lux'', meaning "light", and generally implies radiance, gloss, or brilliance. A range of terms are used to describe lustre, such as ''earthy'', ''metallic'', ''greasy'', and ''silky''. Similarly, the term ''vitreous'' (derived from the Latin for glass, ''vitrum'') refers to a glassy lustre. A list of these terms is given below. Lustre varies over a wide continuum, and so there are no rigid boundaries between the different types of lustre. (For this reason, different sources can often describe the same mineral differently. This ambiguity is further complicated by lustre's ability to vary widely within a particular mineral species). The terms are frequently combined to describe intermediate types of lustre (for example, a "vitreous greasy" lustre). Some minerals exhibit unus ...
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Specific Gravity
Relative density, or specific gravity, is the ratio of the density (mass of a unit volume) of a substance to the density of a given reference material. Specific gravity for liquids is nearly always measured with respect to water (molecule), water at its densest (at ); for gases, the reference is air at room temperature (). The term "relative density" (often abbreviated r.d. or RD) is often preferred in scientific usage, whereas the term "specific gravity" is deprecation, deprecated. If a substance's relative density is less than 1 then it is less dense than the reference; if greater than 1 then it is denser than the reference. If the relative density is exactly 1 then the densities are equal; that is, equal volumes of the two substances have the same mass. If the reference material is water, then a substance with a relative density (or specific gravity) less than 1 will float in water. For example, an ice cube, with a relative density of about 0.91, will float. A substance wi ...
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Calcium
Calcium is a chemical element with the symbol Ca and atomic number 20. As an alkaline earth metal, calcium is a reactive metal that forms a dark oxide-nitride layer when exposed to air. Its physical and chemical properties are most similar to its heavier homologues strontium and barium. It is the fifth most abundant element in Earth's crust, and the third most abundant metal, after iron and aluminium. The most common calcium compound on Earth is calcium carbonate, found in limestone and the fossilised remnants of early sea life; gypsum, anhydrite, fluorite, and apatite are also sources of calcium. The name derives from Latin ''calx'' "lime", which was obtained from heating limestone. Some calcium compounds were known to the ancients, though their chemistry was unknown until the seventeenth century. Pure calcium was isolated in 1808 via electrolysis of its oxide by Humphry Davy, who named the element. Calcium compounds are widely used in many industries: in foods and pharma ...
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Isomorphism (crystallography)
In chemistry isomorphism has meanings both at the level of crystallography and at a molecular level. In crystallography, compounds are isomorphous if their symmetry is the same and their unit cell parameters are similar Molecules are isomorphous if they have similar shapes. The coordination complexes tris(acetylacetonato)iron (Fe(acac)3) and tris(acetylacetonato)aluminium (Al(acac)3) are isomorphous. These compounds, both of ''D''3 symmetry have very similar shapes, as determined by bond lengths and bond angles. Isomorphous compounds give rise to isomorphous crystals and form solid solutions. Historically, crystal shape was defined by measuring the angles between crystal faces with a goniometer. Whereas crystals of Fe(acac)3 are deep red and crystals of Al(acac)3 are colorless, a solid solution of the two, i.e. Fe1−xAlx(acac)3 will be deep or pale pink depending on the Fe/Al ratio, x. Double sulfates, such as Tutton's salt, with the generic formula MI2MII(SO4)2.6H2O, wh ...
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Stříbro
Stříbro (; german: Mies) is a town in Tachov District in the Plzeň Region of the Czech Republic. It has about 7,400 inhabitants. The town centre with the Renaissance Stříbro bridge is well preserved and is protected by law as an urban monument zone. Administrative parts Villages of Butov, Jezerce, Lhota u Stříbra, Milíkov, Otročín and Těchlovice are administrative parts of Stříbro. Etymology The Czech name derives from "silver" ( cs, stříbro), which used to be mined there. The German name ''Mies'' comes from the name of the river Mies/Mže ( la, Misa). Geography Stříbro is located about west of Plzeň. It lies in the Plasy Uplands. The highest point is the hill Jirná at above sea level. The Mže River flows through the town. The confluence of the river Mže and Úhlavka is located on the southern outskirts of the town. A part of the Hracholusky Reservoir, built on the Mže, lies in the eastern part of the territory. History According to the 16th century chr ...
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Bohemia
Bohemia ( ; cs, Čechy ; ; hsb, Čěska; szl, Czechy) is the westernmost and largest historical region of the Czech Republic. Bohemia can also refer to a wider area consisting of the historical Lands of the Bohemian Crown ruled by the Bohemian kings, including Moravia and Czech Silesia, in which case the smaller region is referred to as Bohemia proper as a means of distinction. Bohemia was a duchy of Great Moravia, later an independent principality, a kingdom in the Holy Roman Empire, and subsequently a part of the Habsburg monarchy and the Austrian Empire. After World War I and the establishment of an independent Czechoslovak state, the whole of Bohemia became a part of Czechoslovakia, defying claims of the German-speaking inhabitants that regions with German-speaking majority should be included in the Republic of German-Austria. Between 1938 and 1945, these border regions were joined to Nazi Germany as the Sudetenland. The remainder of Czech territory became the Second ...
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