1.
Diopside
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Diopside is a monoclinic pyroxene mineral with composition MgCaSi2O6. It forms complete solid solution series with hedenbergite and augite, and partial solid solutions with orthopyroxene and it forms variably colored, but typically dull green crystals in the monoclinic prismatic class. It has two distinct prismatic cleavages at 87 and 93° typical of the pyroxene series. It has a Mohs hardness of six, a Vickers hardness of 7.7 GPa at a load of 0.98 N, and a specific gravity of 3.25 to 3.55. It is transparent to translucent with indices of refraction of nα=1. 663–1.699, nβ=1. 671–1.705, the optic angle is 58° to 63°. Diopside is found in igneous rocks, and diopside-rich augite is common in mafic rocks, such as olivine basalt. Diopside is also found in a variety of rocks, such as in contact metamorphosed skarns developed from high silica dolomites. It is an important mineral in the Earths mantle and is common in peridotite xenoliths erupted in kimberlite, some vermiculite deposits, most notably those in Libby, Montana, are contaminated with chrysotile that formed from diopside. At relatively high temperatures, there is a miscibility gap between diopside and pigeonite, and at lower temperatures, between diopside and orthopyroxene. Chrome diopside is a constituent of peridotite xenoliths, and dispersed grains are found near kimberlite pipes. Occurrences are reported in Canada, South Africa, Russia, Brazil, much chromian diopside from the Green River Basin localities and several of the State Line Kimberlites have been gem in character. Gemstone quality diopside is found in two forms, the black star diopside and the chrome diopside, at 5. 5–6.5 on the Mohs scale, chrome diopside is relatively soft to scratch. Violane is a variety of diopside, violet to light blue in color. Diopside derives its name from the Greek dis, twice, and òpsè, Diopside was discovered and first described about 1800, by Brazilian naturalist Jose Bonifacio de Andrada e Silva. Diopside based ceramics and glass-ceramics have potential applications in various technological areas, a diopside based glass-ceramic named silceram was produced by scientists from Imperial College, UK during the 1980s from blast furnace slag and other waste products. The as produced glass-ceramic is a structural material. Similarly, diopside based ceramics and glass-ceramics have potential applications in the field of biomaterials, nuclear waste immobilization, S. Carter, C. B. Ponton, R. D. Rawlings, P. S. Rogers, Microstructure, chemistry, elastic properties and internal-friction of silceram glass-ceramics, T. Nonami, S. Tsutsumi, Study of diopside ceramics for biomaterials, Journal of Materials Science, Materials in Medicine 10 475-479
2.
Afghanistan
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Afghanistan, officially the Islamic Republic of Afghanistan, is a landlocked country located within South Asia and Central Asia. It has a population of approximately 32 million, making it the 42nd most populous country in the world. It is bordered by Pakistan in the south and east, Iran in the west, Turkmenistan, Uzbekistan, and Tajikistan in the north and its territory covers 652,000 km2, making it the 41st largest country in the world. The land also served as the source from which the Kushans, Hephthalites, Samanids, Saffarids, Ghaznavids, Ghorids, Khiljis, Mughals, Hotaks, Durranis, the political history of the modern state of Afghanistan began with the Hotak and Durrani dynasties in the 18th century. In the late 19th century, Afghanistan became a state in the Great Game between British India and the Russian Empire. Following the Third Anglo-Afghan War in 1919, King Amanullah unsuccessfully attempted to modernize the country and it remained peaceful during Zahir Shahs forty years of monarchy. A series of coups in the 1970s was followed by a series of wars that devastated much of Afghanistan. The name Afghānistān is believed to be as old as the ethnonym Afghan, the root name Afghan was used historically in reference to a member of the ethnic Pashtuns, and the suffix -stan means place of in Persian. Therefore, Afghanistan translates to land of the Afghans or, more specifically in a historical sense, however, the modern Constitution of Afghanistan states that he word Afghan shall apply to every citizen of Afghanistan. An important site of historical activities, many believe that Afghanistan compares to Egypt in terms of the historical value of its archaeological sites. The country sits at a unique nexus point where numerous civilizations have interacted and it has been home to various peoples through the ages, among them the ancient Iranian peoples who established the dominant role of Indo-Iranian languages in the region. At multiple points, the land has been incorporated within large regional empires, among them the Achaemenid Empire, the Macedonian Empire, the Indian Maurya Empire, and the Islamic Empire. Archaeological exploration done in the 20th century suggests that the area of Afghanistan has been closely connected by culture and trade with its neighbors to the east, west. Artifacts typical of the Paleolithic, Mesolithic, Neolithic, Bronze, urban civilization is believed to have begun as early as 3000 BCE, and the early city of Mundigak may have been a colony of the nearby Indus Valley Civilization. More recent findings established that the Indus Valley Civilisation stretched up towards modern-day Afghanistan, making the ancient civilisation today part of Pakistan, Afghanistan, in more detail, it extended from what today is northwest Pakistan to northwest India and northeast Afghanistan. An Indus Valley site has found on the Oxus River at Shortugai in northern Afghanistan. There are several smaller IVC colonies to be found in Afghanistan as well, after 2000 BCE, successive waves of semi-nomadic people from Central Asia began moving south into Afghanistan, among them were many Indo-European-speaking Indo-Iranians. These tribes later migrated further into South Asia, Western Asia, the region at the time was referred to as Ariana
3.
Pyroxenite
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Pyroxenite is an ultramafic igneous rock consisting essentially of minerals of the pyroxene group, such as augite, diopside, hypersthene, bronzite or enstatite. Pyroxenites are classified into clinopyroxenites, orthopyroxenites, and the websterites which contain both types of pyroxenes, closely allied to this group are the hornblendites, consisting essentially of hornblende and other amphiboles. They are essentially of igneous origin, though some pyroxenites are included in the metamorphic Lewisian complex of Scotland and this connection is indicated also by their mode of occurrence, for they usually accompany masses of gabbro and peridotite and seldom are found by themselves. They are often very coarse-grained, containing individual crystals which may be several inches in length, the principal accessory minerals, in addition to olivine and feldspar, are chromite and other spinels, garnet, magnetite, rutile, and scapolite. Pyroxenites can be formed as cumulates in ultramafic intrusions by accumulation of crystals at the base of the magma chamber. Here they are associated with gabbro and anorthite cumulate layers and are typically high up in the intrusion. They may be accompanied by layers, ilmenite layers. Pyroxenites are also found as layers within masses of peridotite and these layers most commonly have been interpreted as products of reaction between ascending magmas and peridotite of the upper mantle. The layers typically are a few centimeters to a meter or so in thickness, pyroxenites that occur as xenoliths in basalt and in kimberlite have been interpreted as fragments of such layers. Although some mantle pyroxenites contain garnet, they are not eclogites, as clinopyroxene in them is less sodic than omphacite, purely pyroxene-bearing volcanic rocks are rare, restricted to spinifex-textured sills, lava tubes and thick flows in the Archaean greenstone belts. This is in similar to the formation of olivine spinifex textures in komatiite lava flows. They frequently occur in the form of dikes or segregations in gabbro and peridotite, in Shetland, Cortland on the Hudson River, North Carolina, Baltimore, New Zealand and they are also found in the Bushveld Igneous Complex in South Africa and Zimbabwe. The pyroxenites are often subject serpentinization under low temperature retrograde metamorphism, under pressure-metamorphism hornblende is developed and various types of amphibolite and hornblende-schist are produced. Sobolev, A. V. and others,2007, The amount of recycled crust in sources of mantle-derived melts, Science 316, media related to Pyroxenite at Wikimedia Commons Flett, John Smith
4.
Allan Hills 84001
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Allan Hills 84001 is a meteorite that was found in Allan Hills, Antarctica on December 27,1984 by a team of U. S. meteorite hunters from the ANSMET project. Like other members of the group of SNCs, ALH84001 is thought to be from Mars, however, it does not fit into any of the previously discovered SNC groups. On discovery, its mass was 1.93 kilograms. S, president Bill Clinton giving a speech about the potential discovery. This rock is considered to be one of the oldest Martian meteorites, based on chemical analyses, it is thought to have originated on Mars from a period when liquid water existed on the now arid planets surface. According to the analysis, Eos Chasma in the Valles Marineris canyon appears to be the source of the meteorite, the analysis was not conclusive, in part because it was limited to areas of Mars not obscured by dust. The theory holds that ALH84001 was blasted off from the surface of Mars by an impact about 17 million years ago. These dates were established by a variety of dating techniques, including samarium-neodymium, rubidium-strontium, potassium-argon. Other meteorites that have potential biological markings have generated less interest because they do not contain rock from a wet Mars, ALH84001 is the only meteorite collected from such a time period. In October 2011 it was reported that isotopic analysis indicated that the carbonates in ALH84001 were precipitated at a temperature of 18 °C with water and carbon dioxide from the Martian atmosphere. On August 6,1996, ALH84001 became newsworthy when it was claimed that the meteorite may contain evidence of traces of life from Mars, under the scanning electron microscope structures were revealed that some scientists interpreted as fossils of bacteria-like lifeforms. The structures found on ALH84001 are 20–100 nanometres in diameter, similar in size to theoretical nanobacteria, the announcement of possible extraterrestrial life caused considerable controversy. David S. McKay at NASA argued that likely microbial terrestrial contamination found in other Martian meteorites does not resemble the shapes in the ALH84001. In particular, the shapes within the ALH84001 look intergrown or embedded in the indigenous material, while likely contamination does not. While it has not yet conclusively been shown how the features in the meteorite were formed, David McKay says these results were obtained using unrealistically pure raw materials as a starting point, and will not explain many of the features described by us in ALH84001. According to McKay, a plausible inorganic model must explain all of the properties that we. The rest of the community disagreed with McKay. However, the consensus is that morphology alone cannot be used unambiguously as a tool for primitive life detection. Interpretation of morphology is notoriously subjective, and its use alone has led to errors of interpretation
5.
Silicate minerals
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Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of rock-forming minerals and they are classified based on the structure of their silicate groups, which contain different ratios of silicon and oxygen. Nesosilicates, or orthosilicates, have the orthosilicate ion, which constitute isolated 4− tetrahedra that are connected only by interstitial cations and these exist as 3-member 6− and 6-member 12− rings, where T stands for a tetrahedrally coordinated cation. Inosilicates, or chain silicates, have interlocking chains of silicate tetrahedra with either SiO3,1,3 ratio, for single chains or Si4O11,4,11 ratio, for double chains. Nickel–Strunz classification,09. D Pyroxene group Enstatite – orthoferrosilite series Enstatite – MgSiO3 Ferrosilite – FeSiO3 Pigeonite – Ca0.251, all phyllosilicate minerals are hydrated, with either water or hydroxyl groups attached. Serpentine subgroup Antigorite – Mg3Si2O54 Chrysotile – Mg3Si2O54 Lizardite – Mg3Si2O54 Clay minerals group Halloysite – Al2Si2O54 Kaolinite – Al2Si2O54 Illite – 24O10 Montmorillonite –0 and this group comprises nearly 75% of the crust of the Earth. Tectosilicates, with the exception of the group, are aluminosilicates. Nickel–Strunz classification,09. F and 09. G,04. A, an introduction to the rock-forming minerals. Wise, W. S. Zussman, J. Rock-forming minerals, P.982 pp. Hurlbut, Cornelius S. Danas Manual of Mineralogy. Mindat. org, Dana classification Webmineral, Danas New Silicate Classification Media related to Silicates at Wikimedia Commons
6.
Mineral
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A mineral is a naturally occurring chemical compound, usually of crystalline form and abiogenic in origin. A mineral has one specific chemical composition, whereas a rock can be an aggregate of different minerals or mineraloids, the study of minerals is called mineralogy. There are over 5,300 known mineral species, over 5,070 of these have been approved by the International Mineralogical Association, the silicate minerals compose over 90% of the Earths crust. The diversity and abundance of species is controlled by the Earths chemistry. Silicon and oxygen constitute approximately 75% of the Earths crust, which translates directly into the predominance of silicate minerals, minerals are distinguished by various chemical and physical properties. Differences in chemical composition and crystal structure distinguish the various species, changes in the temperature, pressure, or bulk composition of a rock mass cause changes in its minerals. Minerals can be described by their various properties, which are related to their chemical structure. Common distinguishing characteristics include crystal structure and habit, hardness, lustre, diaphaneity, colour, streak, tenacity, cleavage, fracture, parting, more specific tests for describing minerals include magnetism, taste or smell, radioactivity and reaction to acid. Minerals are classified by key chemical constituents, the two dominant systems are the Dana classification and the Strunz classification, the silicate class of minerals is subdivided into six subclasses by the degree of polymerization in the chemical structure. All silicate minerals have a unit of a 4− silica tetrahedron—that is, a silicon cation coordinated by four oxygen anions. These tetrahedra can be polymerized to give the subclasses, orthosilicates, disilicates, cyclosilicates, inosilicates, phyllosilicates, other important mineral groups include the native elements, sulfides, oxides, halides, carbonates, sulfates, and phosphates. The first criterion means that a mineral has to form by a natural process, stability at room temperature, in the simplest sense, is synonymous to the mineral being solid. More specifically, a compound has to be stable or metastable at 25 °C, modern advances have included extensive study of liquid crystals, which also extensively involve mineralogy. Minerals are chemical compounds, and as such they can be described by fixed or a variable formula, many mineral groups and species are composed of a solid solution, pure substances are not usually found because of contamination or chemical substitution. Finally, the requirement of an ordered atomic arrangement is usually synonymous with crystallinity, however, crystals are also periodic, an ordered atomic arrangement gives rise to a variety of macroscopic physical properties, such as crystal form, hardness, and cleavage. There have been recent proposals to amend the definition to consider biogenic or amorphous substances as minerals. The formal definition of an approved by the IMA in 1995, A mineral is an element or chemical compound that is normally crystalline. However, if geological processes were involved in the genesis of the compound, Mineral classification schemes and their definitions are evolving to match recent advances in mineral science
7.
Igneous rock
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Igneous rock, or magmatic rock, is one of the three main rock types, the others being sedimentary and metamorphic. Igneous rock is formed through the cooling and solidification of magma or lava, the magma can be derived from partial melts of existing rocks in either a planets mantle or crust. Typically, the melting is caused by one or more of three processes, an increase in temperature, a decrease in pressure, or a change in composition, solidification into rock occurs either below the surface as intrusive rocks or on the surface as extrusive rocks. Igneous rock may form with crystallization to form granular, crystalline rocks, Igneous and metamorphic rocks make up 90–95% of the top 16 km of the Earths crust by volume. Igneous rocks form about 15% of the Earths current land surface, most of the Earths oceanic crust is made of igneous rock. In terms of modes of occurrence, igneous rocks can be either intrusive or extrusive, the mineral grains in such rocks can generally be identified with the naked eye. Intrusive rocks can also be classified according to the shape and size of the intrusive body, typical intrusive formations are batholiths, stocks, laccoliths, sills and dikes. When the magma solidifies within the earths crust, it cools slowly forming coarse textured rocks, such as granite, gabbro, the central cores of major mountain ranges consist of intrusive igneous rocks, usually granite. When exposed by erosion, these cores may occupy huge areas of the Earths surface, intrusive igneous rocks that form at depth within the crust are termed plutonic rocks and are usually coarse-grained. Intrusive igneous rocks that form near the surface are termed subvolcanic or hypabyssal rocks, hypabyssal rocks are less common than plutonic or volcanic rocks and often form dikes, sills, laccoliths, lopoliths, or phacoliths. Extrusive igneous rocks, also known as rocks, are formed at the crusts surface as a result of the partial melting of rocks within the mantle. Extrusive igneous rocks cool and solidify quicker than intrusive igneous rocks and they are formed by the cooling of molten magma on the earths surface. The magma, which is brought to the surface through fissures or volcanic eruptions, hence such rocks are smooth, crystalline and fine-grained. Basalt is an extrusive igneous rock and forms lava flows, lava sheets. Some kinds of basalt solidify to form long polygonal columns, the Giants Causeway in Antrim, Northern Ireland is an example. The molten rock, with or without suspended crystals and gas bubbles, is called magma and it rises because it is less dense than the rock from which it was created. When magma reaches the surface from beneath water or air, it is called lava, eruptions of volcanoes into air are termed subaerial, whereas those occurring underneath the ocean are termed submarine. Black smokers and mid-ocean ridge basalt are examples of volcanic activity
8.
Metamorphic rock
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Metamorphic rocks arise from the transformation of existing rock types, in a process called metamorphism, which means change in form. The original rock is subjected to heat and pressure, causing profound physical and/or chemical change, the protolith may be a sedimentary, an igneous, or even an existing type of metamorphic rock. Metamorphic rocks make up a part of the Earths crust. They are classified by texture and by chemical and mineral assemblage and they may be formed simply by being deep beneath the Earths surface, subjected to high temperatures and the great pressure of the rock layers above it. They can form from tectonic processes such as continental collisions, which cause horizontal pressure and they are also formed when rock is heated up by the intrusion of hot molten rock called magma from the Earths interior. The study of rocks provides information about the temperatures and pressures that occur at great depths within the Earths crust. Some examples of rocks are gneiss, slate, marble, schist. Metamorphic minerals are those that only at the high temperatures and pressures associated with the process of metamorphism. These minerals, known as index minerals, include sillimanite, kyanite, staurolite, andalusite, and some garnet. Other minerals, such as olivines, pyroxenes, amphiboles, micas, feldspars, and quartz, may be found in metamorphic rocks and these minerals formed during the crystallization of igneous rocks. They are stable at temperatures and pressures and may remain chemically unchanged during the metamorphic process. However, all minerals are only within certain limits. The change in the size of the rock during the process of metamorphism is called recrystallization. Both high temperatures and pressures contribute to recrystallization, high temperatures allow the atoms and ions in solid crystals to migrate, thus reorganizing the crystals, while high pressures cause solution of the crystals within the rock at their point of contact. The layering within metamorphic rocks is called foliation, and it occurs when a rock is being shortened along one axis during recrystallization. This causes the platy or elongated crystals of minerals, such as mica and chlorite and this results in a banded, or foliated rock, with the bands showing the colors of the minerals that formed them. Textures are separated into foliated and non-foliated categories, foliated rock is a product of differential stress that deforms the rock in one plane, sometimes creating a plane of cleavage. For example, slate is a metamorphic rock, originating from shale
9.
Rock (geology)
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Rock or stone is a natural substance, a solid aggregate of one or more minerals or mineraloids. For example, granite, a rock, is a combination of the minerals quartz, feldspar. The Earths outer solid layer, the lithosphere, is made of rock, rock has been used by mankind throughout history. The minerals and metals found in rocks have been essential to human civilization, three major groups of rocks are defined, igneous, sedimentary, and metamorphic. The scientific study of rocks is called petrology, which is a component of geology. At a granular level, rocks are composed of grains of minerals, the aggregate minerals forming the rock are held together by chemical bonds. The types and abundance of minerals in a rock are determined by the manner in which the rock was formed, many rocks contain silica, a compound of silicon and oxygen that forms 74. 3% of the Earths crust. This material forms crystals with other compounds in the rock, the proportion of silica in rocks and minerals is a major factor in determining their name and properties. Rocks are geologically classified according to such as mineral and chemical composition, permeability, the texture of the constituent particles. These physical properties are the end result of the processes that formed the rocks, over the course of time, rocks can transform from one type into another, as described by the geological model called the rock cycle. These events produce three general classes of rock, igneous, sedimentary, and metamorphic, the three classes of rocks are subdivided into many groups. However, there are no hard and fast boundaries between allied rocks, hence the definitions adopted in establishing rock nomenclature merely correspond to more or less arbitrary selected points in a continuously graduated series. Igneous rock forms through the cooling and solidification of magma or lava and this magma can be derived from partial melts of pre-existing rocks in either a planets mantle or crust. Typically, the melting of rocks is caused by one or more of three processes, an increase in temperature, a decrease in pressure, or a change in composition, igneous rocks are divided into two main categories, plutonic rock and volcanic. Plutonic or intrusive rocks result when magma cools and crystallizes slowly within the Earths crust, a common example of this type is granite. Volcanic or extrusive rocks result from magma reaching the surface either as lava or fragmental ejecta, the chemical abundance and the rate of cooling of magma typically forms a sequence known as Bowens reaction series. Most major igneous rocks are found along this scale, about 64. 7% of the Earths crust by volume consists of igneous rocks, making it the most plentiful category. Of these, 66% are basalts and gabbros, 16% are granite, only 0. 6% are syenites and 0. 3% peridotites and dunites
10.
Calcium
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Calcium is a chemical element with symbol Ca and atomic number 20. Calcium is a soft grayish-yellow alkaline earth metal, fifth-most-abundant element by mass in the Earths crust, the ion Ca2+ is also the fifth-most-abundant dissolved ion in seawater by both molarity and mass, after sodium, chloride, magnesium, and sulfate. Free calcium metal is too reactive to occur in nature, Calcium is produced in supernova nucleosynthesis. Calcium is a trace element in living organisms. It is the most abundant metal by mass in animals, and it is an important constituent of bone, teeth. In cell biology, the movement of the calcium ion into, Calcium carbonate and calcium citrate are often taken as dietary supplements. Calcium is on the World Health Organizations List of Essential Medicines, Calcium has a wide variety of applications, almost all of which are associated with calcium compounds and salts. Calcium metal is used as a deoxidizer, desulfurizer, and decarbonizer for production of ferrous and nonferrous alloys. In steelmaking and production of iron, Ca reacts with oxygen, Calcium carbonate is used in manufacturing cement and mortar, lime, limestone and aids in production in the glass industry. It also has chemical and optical uses as mineral specimens in toothpastes, Calcium hydroxide solution is used to detect the presence of carbon dioxide in a gas sample bubbled through a solution. The solution turns cloudy where CO2 is present, Calcium arsenate is used in insecticides. Calcium carbide is used to make acetylene gas and various plastics, Calcium chloride is used in ice removal and dust control on dirt roads, as a conditioner for concrete, as an additive in canned tomatoes, and to provide body for automobile tires. Calcium citrate is used as a food preservative, Calcium cyclamate is used as a sweetening agent in several countries. In the United States, it has been outlawed as a suspected carcinogen, Calcium gluconate is used as a food additive and in vitamin pills. Calcium hypochlorite is used as a swimming pool disinfectant, as an agent, as an ingredient in deodorant. Calcium permanganate is used in rocket propellant, textile production, as a water sterilizing agent. Calcium phosphate is used as a supplement for animal feed, fertilizer, in production for dough and yeast products, in the manufacture of glass. Calcium phosphide is used in fireworks, rodenticide, torpedoes, Calcium sulfate is used as common blackboard chalk, as well as, in its hemihydrate form, Plaster of Paris
11.
Sodium
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Sodium is a chemical element with symbol Na and atomic number 11. It is a soft, silvery-white, highly reactive metal, Sodium is an alkali metal, being in group 1 of the periodic table, because it has a single electron in its outer shell that it readily donates, creating a positively charged atom—the Na+ cation. Its only stable isotope is 23Na, the free metal does not occur in nature, but must be prepared from compounds. Sodium is the sixth most abundant element in the Earths crust, Sodium was first isolated by Humphry Davy in 1807 by the electrolysis of sodium hydroxide. Among many other useful compounds, sodium hydroxide is used in soap manufacture, and sodium chloride is a de-icing agent. Sodium is an element for all animals and some plants. Sodium ions are the major cation in the fluid and as such are the major contributor to the ECF osmotic pressure. Loss of water from the ECF compartment increases the sodium concentration, isotonic loss of water and sodium from the ECF compartment decreases the size of that compartment in a condition called ECF hypovolemia. In nerve cells, the charge across the cell membrane enables transmission of the nerve impulse—an action potential—when the charge is dissipated. The melting and boiling points of sodium are lower than those of lithium but higher than those of the alkali metals potassium, rubidium. All of these high-pressure allotropes are insulators and electrides.3 nm, spin-orbit interactions involving the electron in the 3p orbital split the D line into two, at 589.0 and 589.6 nm, hyperfine structures involving both orbitals cause many more lines. Twenty isotopes of sodium are known, but only 23Na is stable, 23Na is created in the carbon-burning process in stars by fusing two carbon atoms together, this requires temperatures above 600 megakelvins and a star of at least three solar masses. Two nuclear isomers have been discovered, the one being 24mNa with a half-life of around 20.2 milliseconds. Sodium atoms have 11 electrons, one more than the stable configuration of the noble gas neon. This process requires so little energy that sodium is oxidized by giving up its 11th electron. In contrast, the ionization energy is very high, because the 10th electron is closer to the nucleus than the 11th electron. As a result, sodium usually forms ionic compounds involving the Na+ cation, the most common oxidation state for sodium is +1. It is generally less reactive than potassium and more reactive than lithium, Sodium metal is highly reducing, with the reduction of sodium ions requiring −2.71 volts, though potassium and lithium have even more negative potentials
12.
Iron
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Iron is a chemical element with symbol Fe and atomic number 26. It is a metal in the first transition series and it is by mass the most common element on Earth, forming much of Earths outer and inner core. It is the fourth most common element in the Earths crust, like the other group 8 elements, ruthenium and osmium, iron exists in a wide range of oxidation states, −2 to +6, although +2 and +3 are the most common. Elemental iron occurs in meteoroids and other low oxygen environments, but is reactive to oxygen, fresh iron surfaces appear lustrous silvery-gray, but oxidize in normal air to give hydrated iron oxides, commonly known as rust. Unlike the metals that form passivating oxide layers, iron oxides occupy more volume than the metal and thus flake off, Iron metal has been used since ancient times, although copper alloys, which have lower melting temperatures, were used even earlier in human history. Pure iron is soft, but is unobtainable by smelting because it is significantly hardened and strengthened by impurities, in particular carbon. A certain proportion of carbon steel, which may be up to 1000 times harder than pure iron. Crude iron metal is produced in blast furnaces, where ore is reduced by coke to pig iron, further refinement with oxygen reduces the carbon content to the correct proportion to make steel. Steels and iron alloys formed with metals are by far the most common industrial metals because they have a great range of desirable properties. Iron chemical compounds have many uses, Iron oxide mixed with aluminium powder can be ignited to create a thermite reaction, used in welding and purifying ores. Iron forms binary compounds with the halogens and the chalcogens, among its organometallic compounds is ferrocene, the first sandwich compound discovered. Iron plays an important role in biology, forming complexes with oxygen in hemoglobin and myoglobin. Iron is also the metal at the site of many important redox enzymes dealing with cellular respiration and oxidation and reduction in plants. A human male of average height has about 4 grams of iron in his body and this iron is distributed throughout the body in hemoglobin, tissues, muscles, bone marrow, blood proteins, enzymes, ferritin, hemosiderin, and transport in plasma. The mechanical properties of iron and its alloys can be evaluated using a variety of tests, including the Brinell test, Rockwell test, the data on iron is so consistent that it is often used to calibrate measurements or to compare tests. An increase in the content will cause a significant increase in the hardness. Maximum hardness of 65 Rc is achieved with a 0. 6% carbon content, because of the softness of iron, it is much easier to work with than its heavier congeners ruthenium and osmium. Because of its significance for planetary cores, the properties of iron at high pressures and temperatures have also been studied extensively
13.
Magnesium
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Magnesium is a chemical element with symbol Mg and atomic number 12. Magnesium is the ninth most abundant element in the universe and it is produced in large, aging stars from the sequential addition of three helium nuclei to a carbon nucleus. When such stars explode as supernovas, much of the magnesium is expelled into the medium where it may recycle into new star systems. Magnesium is the eighth most abundant element in the Earths crust and the fourth most common element in the Earth, making up 13% of the planets mass and it is the third most abundant element dissolved in seawater, after sodium and chlorine. Magnesium occurs naturally only in combination with elements, where it invariably has a +2 oxidation state. The free element can be produced artificially, and is highly reactive, the free metal burns with a characteristic brilliant-white light. The metal is now obtained mainly by electrolysis of magnesium salts obtained from brine, Magnesium is less dense than aluminium, and the alloy is prized for its combination of lightness and strength. Magnesium is the eleventh most abundant element by mass in the body and is essential to all cells. Magnesium ions interact with polyphosphate compounds such as ATP, DNA, hundreds of enzymes require magnesium ions to function. Magnesium compounds are used medicinally as common laxatives, antacids, elemental magnesium is a gray-white lightweight metal, two-thirds the density of aluminium. Magnesium has the lowest melting and the lowest boiling point 1,363 K of all the alkaline earth metals, Magnesium reacts with water at room temperature, though it reacts much more slowly than calcium, a similar group 2 metal. When submerged in water, hydrogen bubbles form slowly on the surface of the metal—though, if powdered, the reaction occurs faster with higher temperatures. Magnesiums reversible reaction with water can be harnessed to store energy, Magnesium also reacts exothermically with most acids such as hydrochloric acid, producing the metal chloride and hydrogen gas, similar to the HCl reaction with aluminium, zinc, and many other metals. Magnesium is highly flammable, especially when powdered or shaved into thin strips, flame temperatures of magnesium and magnesium alloys can reach 3,100 °C, although flame height above the burning metal is usually less than 300 mm. Once ignited, such fires are difficult to extinguish, with combustion continuing in nitrogen, carbon dioxide, Magnesium may also be used as an igniter for thermite, a mixture of aluminium and iron oxide powder that ignites only at a very high temperature. When burning in air, magnesium produces a light that includes strong ultraviolet wavelengths. Magnesium powder was used for illumination in the early days of photography. Later, magnesium filament was used in electrically ignited single-use photography flashbulbs, Magnesium powder is used in fireworks and marine flares where a brilliant white light is required
14.
Zinc
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Zinc is a chemical element with the symbol Zn and atomic number 30. It is the first element in group 12 of the periodic table, in some respects zinc is chemically similar to magnesium, both elements exhibit only one normal oxidation state, and the Zn2+ and Mg2+ ions are of similar size. Zinc is the 24th most abundant element in Earths crust and has five stable isotopes, the most common zinc ore is sphalerite, a zinc sulfide mineral. The largest workable lodes are in Australia, Asia, and the United States, Zinc is refined by froth flotation of the ore, roasting, and final extraction using electricity. Zinc metal was not produced on a large scale until the 12th century in India and was unknown to Europe until the end of the 16th century, the mines of Rajasthan have given definite evidence of zinc production going back to the 6th century BC. To date, the oldest evidence of pure zinc comes from Zawar, in Rajasthan, alchemists burned zinc in air to form what they called philosophers wool or white snow. The element was named by the alchemist Paracelsus after the German word Zinke. German chemist Andreas Sigismund Marggraf is credited with discovering pure metallic zinc in 1746, work by Luigi Galvani and Alessandro Volta uncovered the electrochemical properties of zinc by 1800. Corrosion-resistant zinc plating of iron is the application for zinc. Other applications are in batteries, small non-structural castings. A variety of compounds are commonly used, such as zinc carbonate and zinc gluconate, zinc chloride, zinc pyrithione, zinc sulfide. Zinc is an essential mineral perceived by the public today as being of exceptional biologic and public health importance, Zinc deficiency affects about two billion people in the developing world and is associated with many diseases. In children, deficiency causes growth retardation, delayed sexual maturation, infection susceptibility, enzymes with a zinc atom in the reactive center are widespread in biochemistry, such as alcohol dehydrogenase in humans. Consumption of excess zinc can cause ataxia, lethargy and copper deficiency, Zinc is a bluish-white, lustrous, diamagnetic metal, though most common commercial grades of the metal have a dull finish.6 pm. The metal is hard and brittle at most temperatures but becomes malleable between 100 and 150 °C, above 210 °C, the metal becomes brittle again and can be pulverized by beating. Zinc is a conductor of electricity. For a metal, zinc has relatively low melting and boiling points, the melting point is the lowest of all the transition metals aside from mercury and cadmium. Many alloys contain zinc, including brass, Other metals long known to form binary alloys with zinc are aluminium, antimony, bismuth, gold, iron, lead, mercury, silver, tin, magnesium, cobalt, nickel, tellurium, and sodium
15.
Manganese
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Manganese is a chemical element with symbol Mn and atomic number 25. It is not found as an element in nature, it is often found in minerals in combination with iron. Manganese is a metal with important industrial metal alloy uses, particularly in stainless steels, by the mid-18th century, Swedish chemist Carl Wilhelm Scheele had used pyrolusite to produce chlorine. Scheele and others were aware that pyrolusite contained a new element, johan Gottlieb Gahn was the first to isolate an impure sample of manganese metal in 1774, which he did by reducing the dioxide with carbon. Manganese phosphating is used for rust and corrosion prevention on steel, ionized manganese is used industrially as pigments of various colors, which depend on the oxidation state of the ions. The permanganates of alkali and alkaline earth metals are powerful oxidizers, Manganese dioxide is used as the cathode material in zinc-carbon and alkaline batteries. In biology, manganese ions function as cofactors for a variety of enzymes with many functions. Manganese enzymes are essential in detoxification of superoxide free radicals in organisms that must deal with elemental oxygen. Manganese also functions in the complex of photosynthetic plants. The element is a trace mineral for all known living organisms but is a neurotoxin. In larger amounts, and apparently with far greater effectiveness through inhalation, Manganese is a silvery-gray metal that resembles iron. It is hard and very brittle, difficult to fuse, Manganese metal and its common ions are paramagnetic. Manganese tarnishes slowly in air and oxidizes like iron in water containing dissolved oxygen, naturally occurring manganese is composed of one stable isotope, 55Mn. Eighteen radioisotopes have been isolated and described, the most stable being 53Mn with a half-life of 3.7 million years, 54Mn with a half-life of 312.3 days, and 52Mn with a half-life of 5.591 days. All of the radioactive isotopes have half-lives of less than three hours, and the majority of less than one minute. Manganese also has three meta states, Manganese is part of the iron group of elements, which are thought to be synthesized in large stars shortly before the supernova explosion. 53Mn decays to 53Cr with a half-life of 3.7 million years, because of its relatively short half-life, 53Mn is relatively rare, produced by cosmic rays impact on iron. Manganese isotopic contents are combined with chromium isotopic contents and have found application in isotope geology
16.
Lithium
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Lithium is a chemical element with the symbol Li and atomic number 3. It is a soft, silver-white metal belonging to the metal group of chemical elements. Under standard conditions, it is the lightest metal and the least dense solid element, like all alkali metals, lithium is highly reactive and flammable. For this reason, it is stored in mineral oil. When cut open, it exhibits a metallic luster, but contact with moist air corrodes the surface quickly to a silvery gray. Because of its reactivity, lithium never occurs freely in nature, and instead, appears only in compounds. Lithium occurs in a number of minerals, but due to its solubility as an ion, is present in ocean water and is commonly obtained from brines. On a commercial scale, lithium is isolated electrolytically from a mixture of lithium chloride, the nucleus of the lithium atom verges on instability, since the two stable lithium isotopes found in nature have among the lowest binding energies per nucleon of all stable nuclides. Because of its relative instability, lithium is less common in the solar system than 25 of the first 32 chemical elements even though the nuclei are very light in atomic weight. For related reasons, lithium has important links to nuclear physics, the transmutation of lithium atoms to helium in 1932 was the first fully man-made nuclear reaction, and lithium-6 deuteride serves as a fusion fuel in staged thermonuclear weapons. These uses consume more than three quarters of lithium production, Lithium is found in variable amounts in foods, primary food sources are grains and vegetables, in some areas, the drinking water also provides significant amounts of the element. Human dietary lithium intakes depend on location and the type of foods consumed, traces of lithium were detected in human organs and fetal tissues already in the late 19th century, leading to early suggestions as to possible specific functions in the organism. However, it took another century until evidence for the essentiality of lithium became available, in studies conducted from the 1970s to the 1990s, rats and goats maintained on low-lithium rations were shown to exhibit higher mortalities as well as reproductive and behavioral abnormalities. Lithium appears to play an important role during the early fetal development as evidenced by the high lithium contents of the embryo during the early gestational period. The available experimental evidence now appears to be sufficient to accept lithium as essential, the lithium ion Li+ administered as any of several lithium salts has proven to be useful as a mood-stabilizing drug in the treatment of bipolar disorder in humans. Like the other metals, lithium has a single valence electron that is easily given up to form a cation. Because of this, lithium is a conductor of heat and electricity as well as a highly reactive element. Lithiums low reactivity is due to the proximity of its electron to its nucleus
17.
Chromium
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Chromium is a chemical element with symbol Cr and atomic number 24. It is the first element in Group 6 and it is a steely-grey, lustrous, hard and brittle metal which takes a high polish, resists tarnishing, and has a high melting point. The name of the element is derived from the Greek word χρῶμα, chrōma, meaning color, Chromium metal is of high value for its high corrosion resistance and hardness. A major development was the discovery that steel could be highly resistant to corrosion and discoloration by adding metallic chromium to form stainless steel. Stainless steel and chrome plating together comprise 85% of the commercial use, trivalent chromium ion is an essential nutrient in trace amounts in humans for insulin, sugar and lipid metabolism, although the issue is debated. While chromium metal and Cr ions are not considered toxic, hexavalent chromium is toxic and carcinogenic, abandoned chromium production sites often require environmental cleanup. Chromium is remarkable for its properties, it is the only elemental solid which shows antiferromagnetic ordering at room temperature. Above 38 °C, it changes to paramagnetic, Chromium metal left standing in air is passivated by oxidation, forming a thin, protective, surface layer. This layer is a structure only a few molecules thick. It is very dense, and prevents the diffusion of oxygen into the underlying metal and this is different from the oxide that forms on iron and carbon steel, through which elemental oxygen continues to migrate, reaching the underlying material to cause incessant rusting. Passivation can be enhanced by short contact with oxidizing acids like nitric acid, passivated chromium is stable against acids. Passivation can be removed with a reducing agent that destroys the protective oxide layer on the metal. Chromium metal treated in this way readily dissolves in weak acids, Chromium, unlike such metals as iron and nickel, does not suffer from hydrogen embrittlement. However, it suffer from nitrogen embrittlement, reacting with nitrogen from air. Chromium is the 22nd most abundant element in Earths crust with a concentration of 100 ppm. Chromium compounds are found in the environment from the erosion of chromium-containing rocks, Chromium is mined as chromite ore. About two-fifths of the ores and concentrates in the world are produced in South Africa, while Kazakhstan, India, Russia. Untapped chromite deposits are plentiful, but geographically concentrated in Kazakhstan, although rare, deposits of native chromium exist
18.
Aluminium
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Aluminium or aluminum is a chemical element in the boron group with symbol Al and atomic number 13. It is a silvery-white, soft, nonmagnetic, ductile metal, Aluminium metal is so chemically reactive that native specimens are rare and limited to extreme reducing environments. Instead, it is combined in over 270 different minerals. The chief ore of aluminium is bauxite, Aluminium is remarkable for the metals low density and its ability to resist corrosion through the phenomenon of passivation. Aluminium and its alloys are vital to the industry and important in transportation and structures, such as building facades. The oxides and sulfates are the most useful compounds of aluminium, despite its prevalence in the environment, no known form of life uses aluminium salts metabolically, but aluminium is well tolerated by plants and animals. Because of these salts abundance, the potential for a role for them is of continuing interest. Aluminium is a soft, durable, lightweight, ductile. It is nonmagnetic and does not easily ignite, a fresh film of aluminium serves as a good reflector of visible light and an excellent reflector of medium and far infrared radiation. The yield strength of aluminium is 7–11 MPa, while aluminium alloys have yield strengths ranging from 200 MPa to 600 MPa. Aluminium has about one-third the density and stiffness of steel and it is easily machined, cast, drawn and extruded. Aluminium atoms are arranged in a cubic structure. Aluminium has an energy of approximately 200 mJ/m2. Aluminium is a thermal and electrical conductor, having 59% the conductivity of copper. Aluminium is capable of superconductivity, with a critical temperature of 1.2 kelvin. Aluminium is the most common material for the fabrication of superconducting qubits, the strongest aluminium alloys are less corrosion resistant due to galvanic reactions with alloyed copper. This corrosion resistance is reduced by aqueous salts, particularly in the presence of dissimilar metals. In highly acidic solutions, aluminium reacts with water to form hydrogen, primarily because it is corroded by dissolved chlorides, such as common sodium chloride, household plumbing is never made from aluminium
19.
Cobalt
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Cobalt is a chemical element with symbol Co and atomic number 27. Like nickel, cobalt is found in the Earths crust only in chemically combined form, the free element, produced by reductive smelting, is a hard, lustrous, silver-gray metal. In 1735, such ores were found to be reducible to a new metal, today, some cobalt is produced specifically from various metallic-lustered ores, for example cobaltite, but the main source of the element is as a by-product of copper and nickel mining. The copper belt in the Democratic Republic of the Congo, Central African Republic, cobalt is primarily used in the preparation of magnetic, wear-resistant and high-strength alloys. The compounds, cobalt silicate and cobalt aluminate give a deep blue color to glass, ceramics, inks, paints. Cobalt occurs naturally as only one isotope, cobalt-59. Cobalt-60 is an important radioisotope, used as a radioactive tracer. Cobalt is the center of coenzymes called cobalamins, the most common example of which is vitamin B12. As such, it is a trace dietary mineral for all animals. Cobalt in inorganic form is also a micronutrient for bacteria, algae, cobalt is a ferromagnetic metal with a specific gravity of 8.9. The Curie temperature is 1,115 °C and the moment is 1. 6–1.7 Bohr magnetons per atom. Cobalt has a relative permeability two-thirds that of iron, metallic cobalt occurs as two crystallographic structures, hcp and fcc. The ideal transition temperature between the hcp and fcc structures is 450 °C, but in practice, the difference is so small that random intergrowth of the two is common. Cobalt is a weakly reducing metal that is protected from oxidation by an oxide film. It is attacked by halogens and sulfur, heating in oxygen produces Co3O4 which loses oxygen at 900 °C to give the monoxide CoO. The metal reacts with fluorine at 520 K to give CoF3, with chlorine, bromine and iodine and it does not react with hydrogen gas or nitrogen gas even when heated, but it does react with boron, carbon, phosphorus, arsenic and sulfur. At ordinary temperatures, it reacts slowly with mineral acids, and very slowly with moist, common oxidation states of cobalt include +2 and +3, although compounds with oxidation states ranging from −3 to +5 are also known. A common oxidation state for simple compounds is +2 and these salts form the pink-colored metal aquo complex 2+ in water
20.
Scandium
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Scandium is a chemical element with symbol Sc and atomic number 21. A silvery-white metallic d-block element, it has historically been classified as a rare earth element, together with yttrium. It was discovered in 1879 by spectral analysis of the minerals euxenite and gadolinite from Scandinavia, Scandium is present in most of the deposits of rare earth and uranium compounds, but it is extracted from these ores in only a few mines worldwide. Because of the low availability and the difficulties in the preparation of metallic scandium, the positive effects of scandium on aluminium alloys were discovered in the 1970s, and its use in such alloys remains its only major application. The global trade of scandium oxide is about 10 tonnes per year, the properties of scandium compounds are intermediate between those of aluminium and yttrium. A diagonal relationship exists between the behavior of magnesium and scandium, just as there is between beryllium and aluminium, in the chemical compounds of the elements in group 3, the predominant oxidation state is +3. Scandium is a metal with a silvery appearance. It develops a slightly yellowish or pinkish cast when oxidized by air and it is susceptible to weathering and dissolves slowly in most dilute acids. It does not react with a 1,1 mixture of acid and 48% hydrofluoric acid. Scandium turnings ignite in air with a brilliant yellow flame to form scandium oxide, in nature, scandium is found exclusively as the isotope 45Sc, which has a nuclear spin of 7/2. Thirteen radioisotopes have been characterized with the most stable being 46Sc, which has a half-life of 83.8 days, 47Sc,3.35 days, the positron emitter 44Sc,4 h, and 48Sc,43.7 hours. All of the radioactive isotopes have half-lives less than 4 hours. This element also has five meta states, with the most stable being 44mSc, the isotopes of scandium range from 36Sc to 60Sc. The primary decay mode at masses lower than the stable isotope, 45Sc, is electron capture. The primary decay products at atomic weights below 45Sc are calcium isotopes, in Earths crust, scandium is not rare. Estimates vary from 18 to 25 ppm, which is comparable to the abundance of cobalt, Scandium is only the 50th most common element on Earth, but it is the 23rd most common element in the Sun. However, scandium is distributed sparsely and occurs in trace amounts in many minerals, rare minerals from Scandinavia and Madagascar such as thortveitite, euxenite, and gadolinite are the only known concentrated sources of this element. Thortveitite can contain up to 45% of scandium in the form of scandium oxide, the stable form of scandium is created in supernovas via the r-process
21.
Titanium
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Titanium is a chemical element with symbol Ti and atomic number 22. It is a transition metal with a silver color, low density. Titanium is resistant to corrosion in sea water, aqua regia, titanium was discovered in Cornwall, Great Britain, by William Gregor in 1791, and it is named by Martin Heinrich Klaproth for the Titans of Greek mythology. The metal is extracted from its principal mineral ores by the Kroll, the most common compound, titanium dioxide, is a popular photocatalyst and is used in the manufacture of white pigments. Other compounds include titanium tetrachloride, a component of smoke screens and catalysts, and titanium trichloride, the two most useful properties of the metal are corrosion resistance and strength-to-density ratio, the highest of any metallic element. In its unalloyed condition, titanium is as strong as some steels, there are two allotropic forms and five naturally occurring isotopes of this element, 46Ti through 50Ti, with 48Ti being the most abundant. Although they have the number of valence electrons and are in the same group in the periodic table. As a metal, titanium is recognized for its high strength-to-weight ratio and it is a strong metal with low density that is quite ductile, lustrous, and metallic-white in color. The relatively high melting point makes it useful as a refractory metal and it is paramagnetic and has fairly low electrical and thermal conductivity. Commercial grades of titanium have ultimate tensile strength of about 434 MPa, equal to that of common, low-grade steel alloys, titanium is 60% denser than aluminium, but more than twice as strong as the most commonly used 6061-T6 aluminium alloy. Certain titanium alloys achieve tensile strengths of over 1400 MPa, however, titanium loses strength when heated above 430 °C. Titanium is not as hard as some grades of heat-treated steel, it is non-magnetic, machining requires precautions, because the material might gall unless sharp tools and proper cooling methods are used. Like steel structures, those made from titanium have a limit that guarantees longevity in some applications. The metal is an allotrope of an hexagonal α form that changes into a body-centered cubic β form at 882 °C. The specific heat of the α form increases dramatically as it is heated to this transition temperature but then falls, similar to zirconium and hafnium, an additional omega phase exists, which is thermodynamically stable at high pressures, but metastable at ambient pressures. This phase is usually hexagonal or trigonal and can be considered to be due to a soft longitudinal acoustic phonon of the β phase causing collapse of planes of atoms, like aluminium and magnesium, titanium metal and its alloys oxidize immediately upon exposure to air. Titanium readily reacts with oxygen at 1,200 °C in air and it is, however, slow to react with water and air at ambient temperatures because it forms a passive oxide coating that protects the bulk metal from further oxidation. When it first forms, this layer is only 1–2 nm thick but continues to grow slowly
22.
Vanadium
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Vanadium is a chemical element with symbol V and atomic number 23. It is a hard, silvery grey, ductile, and malleable transition metal, the elemental metal is rarely found in nature, but once isolated artificially, the formation of an oxide layer stabilizes the free metal somewhat against further oxidation. Four years later, however, he was convinced by other scientists that erythronium was identical to chromium, both names were attributed to the wide range of colors found in vanadium compounds. Del Rios lead mineral was later renamed vanadinite for its vanadium content, in 1867 Henry Enfield Roscoe obtained the pure element. Vanadium occurs naturally in about 65 different minerals and in fossil fuel deposits and it is produced in China and Russia from steel smelter slag, other countries produce it either from the flue dust of heavy oil, or as a byproduct of uranium mining. It is mainly used to produce specialty steel alloys such as high-speed tool steels, the most important industrial vanadium compound, vanadium pentoxide, is used as a catalyst for the production of sulfuric acid. Large amounts of ions are found in a few organisms. The oxide and some salts of vanadium have moderate toxicity. Particularly in the ocean, vanadium is used by life forms as an active center of enzymes. Vanadium was discovered by Andrés Manuel del Río, a Spanish-Mexican mineralogist, Del Río extracted the element from a sample of Mexican brown lead ore, later named vanadinite. He found that its salts exhibit a variety of colors. Later, Del Río renamed the element erythronium because most of the salts turned red upon heating, Del Río accepted Collet-Descotils statement and retracted his claim. In 1831, the Swedish chemist Nils Gabriel Sefström rediscovered the element in a new oxide he found working with iron ores. Later that same year, Friedrich Wöhler confirmed del Ríos earlier work, Sefström chose a name beginning with V, which had not been assigned to any element yet. He called the element vanadium after Old Norse Vanadís, because of the many beautifully colored chemical compounds it produces, in 1831, the geologist George William Featherstonhaugh suggested that vanadium should be renamed rionium after del Río, but this suggestion was not followed. The isolation of vanadium metal proved difficult, in 1831, Berzelius reported the production of the metal, but Henry Enfield Roscoe showed that Berzelius had in fact produced the nitride, vanadium nitride. Roscoe eventually produced the metal in 1867 by reduction of chloride, VCl2. In 1927, pure vanadium was produced by reducing vanadium pentoxide with calcium, the first large-scale industrial use of vanadium was in the steel alloy chassis of the Ford Model T, inspired by French race cars
23.
Feldspar
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Feldspars are a group of rock-forming tectosilicate minerals that make up about 40% of the Earths continental crust. Feldspars crystallize from magma as veins in both intrusive and extrusive rocks and are also present in many types of metamorphic rock. Rock formed almost entirely of plagioclase feldspar is known as anorthosite. Feldspars are also found in types of sedimentary rocks. The name feldspar derives from the German Feldspat, a compound of the words Feld, field, and Spat, the change from Spat to -spar was influenced by the English word spar, a synonym for mineral. Feldspathic refers to materials that contain feldspar, the alternate spelling, felspar, has largely fallen out of use. This group of minerals consists of tectosilicates, solid solutions between albite and anorthite are called plagioclase, or more properly plagioclase feldspar. Only limited solid solution occurs between K-feldspar and anorthite, and in the two solid solutions, immiscibility occurs at temperatures common in the crust of the earth. Albite is considered both a plagioclase and alkali feldspar, the alkali feldspars are as follows, orthoclase —KAlSi3O8 sanidine —AlSi3O8 microcline —KAlSi3O8 anorthoclase —AlSi3O8 Sanidine is stable at the highest temperatures, and microcline at the lowest. Perthite is a texture in alkali feldspar, due to exsolution of contrasting alkali feldspar compositions during cooling of an intermediate composition. The perthitic textures in the alkali feldspars of many granites can be seen with the naked eye, microperthitic textures in crystals are visible using a light microscope, whereas cryptoperthitic textures can be seen only with an electron microscope. Barium feldspars are also considered alkali feldspars, barium feldspars form as the result of the substitution of barium for potassium in the mineral structure. The barium feldspars are monoclinic and include the following, celsian—BaAl2Si2O8 hyalophane—4O8 The plagioclase feldspars are triclinic, the immiscibility gaps in the plagioclase solid solutions are complex compared to the gap in the alkali feldspars. The play of colours visible in some feldspar of labradorite composition is due to very fine-grained exsolution lamellae, chemical weathering of feldspars results in the formation of clay minerals. About 20 million tonnes of feldspar were produced in 2010, mostly by three countries, Italy, Turkey, and China, Feldspar is a common raw material used in glassmaking, ceramics, and to some extent as a filler and extender in paint, plastics, and rubber. In glassmaking, alumina from feldspar improves product hardness, durability, in ceramics, the alkalis in feldspar act as a flux, lowering the melting temperature of a mixture. Fluxes melt at a stage in the firing process, forming a glassy matrix that bonds the other components of the system together. In the US, about 66% of feldspar is consumed in glassmaking, including glass containers, ceramics and other uses, such as fillers, accounted for the remainder
24.
Amphibole
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Amphiboles can be green, black, colorless, white, yellow, blue, or brown. The International Mineralogical Association currently classifies amphiboles as a mineral supergroup, amphiboles crystallize into two crystal systems, monoclinic and orthorhombic. In chemical composition and general characteristics they are similar to the pyroxenes, the chief differences from pyroxenes are that amphiboles contain essential hydroxyl or halogen and the basic structure is a double chain of tetrahedra. Most apparent, in specimens, is that amphiboles form oblique cleavage planes. Amphiboles are also less dense than the corresponding pyroxenes. In optical characteristics, many amphiboles are distinguished by their stronger pleochroism, amphiboles are the primary constituent of amphibolites. Amphiboles are minerals of either igneous or metamorphic origin, in the former case occurring as constituents of rocks, such as granite, diorite, andesite. Calcium is sometimes a constituent of naturally occurring amphiboles and those of metamorphic origin include examples such as those developed in limestones by contact metamorphism and those formed by the alteration of other ferromagnesian minerals. Pseudomorphs of amphibole after pyroxene are known as uralite, the name amphibole was used by René Just Haüy to include tremolite, actinolite, tourmaline and hornblende. The group was so named by Haüy in allusion to the variety, in composition and appearance. This term has since applied to the whole group. Numerous sub-species and varieties are distinguished, the important of which are tabulated below in two series. The formulae of each will be seen to be built on the general double-chain silicate formula RSi4O11, four of the amphibole minerals are among the minerals commonly called asbestos. These are, anthophyllite, riebeckite, cummingtonite/grunerite series, and actinolite/tremolite series, the cummingtonite/grunerite series is often termed amosite or brown asbestos, riebeckite is known as crocidolite or blue asbestos. These are generally called amphibole asbestos, anthophyllite occurs as brownish, fibrous or lamellar masses with hornblende in mica-schist at Kongsberg in Norway and some other localities. An aluminous related species is known as gedrite and a deep green Russian variety containing little iron as kupfferite, hornblende is an important constituent of many igneous rocks. It is also an important constituent of amphibolites formed by metamorphism of basalt, actinolite is an important and common member of the monoclinic series, forming radiating groups of acicular crystals of a bright green or greyish-green color. It occurs frequently as a constituent of greenschists, the name is a translation of the old German word Strahlstein
25.
Tetrahedron
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In geometry, a tetrahedron, also known as a triangular pyramid, is a polyhedron composed of four triangular faces, six straight edges, and four vertex corners. The tetrahedron is the simplest of all the ordinary convex polyhedra, the tetrahedron is the three-dimensional case of the more general concept of a Euclidean simplex. The tetrahedron is one kind of pyramid, which is a polyhedron with a polygon base. In the case of a tetrahedron the base is a triangle, like all convex polyhedra, a tetrahedron can be folded from a single sheet of paper. For any tetrahedron there exists a sphere on which all four vertices lie, a regular tetrahedron is one in which all four faces are equilateral triangles. It is one of the five regular Platonic solids, which have known since antiquity. In a regular tetrahedron, not only are all its faces the same size and shape, regular tetrahedra alone do not tessellate, but if alternated with regular octahedra they form the alternated cubic honeycomb, which is a tessellation. The regular tetrahedron is self-dual, which means that its dual is another regular tetrahedron, the compound figure comprising two such dual tetrahedra form a stellated octahedron or stella octangula. This form has Coxeter diagram and Schläfli symbol h, the tetrahedron in this case has edge length 2√2. Inverting these coordinates generates the dual tetrahedron, and the together form the stellated octahedron. In other words, if C is the centroid of the base and this follows from the fact that the medians of a triangle intersect at its centroid, and this point divides each of them in two segments, one of which is twice as long as the other. The vertices of a cube can be grouped into two groups of four, each forming a regular tetrahedron, the symmetries of a regular tetrahedron correspond to half of those of a cube, those that map the tetrahedra to themselves, and not to each other. The tetrahedron is the only Platonic solid that is not mapped to itself by point inversion, the regular tetrahedron has 24 isometries, forming the symmetry group Td, isomorphic to the symmetric group, S4. The first corresponds to the A2 Coxeter plane, the two skew perpendicular opposite edges of a regular tetrahedron define a set of parallel planes. When one of these intersects the tetrahedron the resulting cross section is a rectangle. When the intersecting plane is one of the edges the rectangle is long. When halfway between the two edges the intersection is a square, the aspect ratio of the rectangle reverses as you pass this halfway point. For the midpoint square intersection the resulting boundary line traverses every face of the tetrahedron similarly, if the tetrahedron is bisected on this plane, both halves become wedges
26.
Monoclinic crystal system
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In crystallography, the monoclinic crystal system is one of the 7 crystal systems. A crystal system is described by three vectors, in the monoclinic system, the crystal is described by vectors of unequal lengths, as in the orthorhombic system. They form a rectangular prism with a parallelogram as its base, hence two vectors are perpendicular, while the third vector meets the other two at an angle other than 90°. There is only one monoclinic Bravais lattice in two dimensions, the oblique lattice, two monoclinic Bravais lattices exist, the primitive monoclinic and the centered monoclinic lattices. In this axis setting, the primitive and base-centered lattices interchange in centering type, sphenoidal is also monoclinic hemimorphic, Domatic is also monoclinic hemihedral, Prismatic is also monoclinic normal. Crystal structure Hurlbut, Cornelius S. Klein, Cornelis, hahn, Theo, ed. International Tables for Crystallography, Volume A, Space Group Symmetry
27.
Orthorhombic crystal system
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In crystallography, the orthorhombic crystal system is one of the 7 crystal systems. All three bases intersect at 90° angles, so the three lattice vectors remain mutually orthogonal, there are two orthorhombic Bravais lattices in two dimensions, Primitive rectangular and centered rectangular. The primitive rectangular lattice can also be described by a centered rhombic unit cell, there are four orthorhombic Bravais lattices, primitive orthorhombic, base-centered orthorhombic, body-centered orthorhombic, and face-centered orthorhombic. In this axis setting, the primitive and base-centered lattices interchange in centering type, crystal structure Overview of all space groups Hurlbut, Cornelius S. Klein, Cornelis. Hahn, Theo, ed. International Tables for Crystallography, Volume A, Space Group Symmetry
28.
Glass
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Glass is a non-crystalline amorphous solid that is often transparent and has widespread practical, technological, and decorative usage in, for example, window panes, tableware, and optoelectronics. The most familiar, and historically the oldest, types of glass are silicate glasses based on the chemical compound silica, the primary constituent of sand. The term glass, in usage, is often used to refer only to this type of material. Many applications of silicate glasses derive from their optical transparency, giving rise to their use as window panes. Glass can be coloured by adding metallic salts, and can also be painted and printed with vitreous enamels and these qualities have led to the extensive use of glass in the manufacture of art objects and in particular, stained glass windows. Although brittle, silicate glass is extremely durable, and many examples of glass fragments exist from early glass-making cultures, because glass can be formed or moulded into any shape, it has been traditionally used for vessels, bowls, vases, bottles, jars and drinking glasses. In its most solid forms it has also used for paperweights, marbles. Some objects historically were so commonly made of glass that they are simply called by the name of the material, such as drinking glasses. Porcelains and many polymer thermoplastics familiar from everyday use are glasses and these sorts of glasses can be made of quite different kinds of materials than silica, metallic alloys, ionic melts, aqueous solutions, molecular liquids, and polymers. For many applications, like glass bottles or eyewear, polymer glasses are a lighter alternative than traditional glass, silica is a common fundamental constituent of glass. In nature, vitrification of quartz occurs when lightning strikes sand, forming hollow, fused quartz is a glass made from chemically-pure SiO2. It has excellent resistance to shock, being able to survive immersion in water while red hot. However, its high melting-temperature and viscosity make it difficult to work with, normally, other substances are added to simplify processing. One is sodium carbonate, which lowers the transition temperature. The soda makes the glass water-soluble, which is undesirable, so lime, some magnesium oxide. The resulting glass contains about 70 to 74% silica by weight and is called a soda-lime glass, soda-lime glasses account for about 90% of manufactured glass. Most common glass contains other ingredients to change its properties, lead glass or flint glass is more brilliant because the increased refractive index causes noticeably more specular reflection and increased optical dispersion. Adding barium also increases the refractive index, iron can be incorporated into glass to absorb infrared energy, for example in heat absorbing filters for movie projectors, while cerium oxide can be used for glass that absorbs UV wavelengths
29.
Mantle (geology)
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The mantle is a layer inside a terrestrial planet and some other rocky planetary bodies. For a mantle to form, the body must be large enough to have undergone the process of planetary differentiation by density. The mantle surrounds the planetary core, the mantle is surrounded by the crust. The terrestrial planets, the Moon, two of Jupiters moons and the asteroid Vesta each have a made of silicate rock. Interpretation of spacecraft data suggests that at least two moons of Jupiter, as well as Titan and Triton each have a mantle made of ice or other solid volatile substances. The interior of Earth, similar to the terrestrial planets, is divided into layers of different composition. The mantle is a layer between the crust and the outer core, Earths mantle is a silicate rocky shell with an average thickness of 2,886 kilometres. The mantle makes up about 84% of Earths volume and it is predominantly solid but in geological time it behaves as a very viscous fluid. The mantle encloses the hot core rich in iron and nickel, past episodes of melting and volcanism at the shallower levels of the mantle have produced a thin crust of crystallized melt products near the surface. A thin crust, the part of the lithosphere, surrounds the mantle and is about 5 to 75 km thick. In some places under the ocean the mantle is exposed on the surface of Earth. The mantle is divided into sections which are based upon results from seismology and these layers are the following, the upper mantle, the transition zone, the lower mantle, and anomalous core–mantle boundary with a variable thickness. The uppermost mantle plus overlying crust are relatively rigid and form the lithosphere, below the lithosphere the upper mantle becomes notably more plastic. In some regions below the lithosphere, the shear velocity is reduced. Inge Lehmann discovered a seismic discontinuity at about 220 km depth, although this discontinuity has been found in other studies, the transition zone is an area of great complexity, it physically separates the upper and lower mantle. Very little is known about the lower mantle apart from that it appears to be relatively seismically homogeneous, the D layer at the core–mantle boundary separates the mantle from the core. A principal source of the heat that drives plate tectonics is the decay of uranium, thorium. The mantle differs substantially from the crust in its properties as the direct consequence of the difference in composition
30.
Peridotite
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Peridotite is a dense, coarse-grained igneous rock consisting mostly of the minerals olivine and pyroxene. Peridotite is ultramafic, as the rock contains less than 45% silica and it is high in magnesium, reflecting the high proportions of magnesium-rich olivine, with appreciable iron. Peridotite is derived from the Earths mantle, either as solid blocks and fragments, the compositions of peridotites from these layered igneous complexes vary widely, reflecting the relative proportions of pyroxenes, chromite, plagioclase, and amphibole. Peridotite is the dominant rock of the part of the Earths mantle. The word peridotite comes from the gemstone peridot, which consists of pale green olivine, classic peridotite is bright green with some specks of black, although most hand samples tend to be darker green. Peridotitic outcrops typically range from bright yellow to dark green in color. While green and yellow are the most common colors, peridotitic rocks may exhibit a range of colors such as blue, brown. Dunite, more than 90% olivine, typically with Mg/Fe ratio of about 9,1, wehrlite, mostly composed of olivine plus clinopyroxene. Harzburgite, mostly composed of olivine plus orthopyroxene, and relatively low proportions of basaltic ingredients, lherzolite, most common form of peridotite, mostly composed of olivine, orthopyroxene, and clinopyroxene, and have relatively high proportions of basaltic ingredients. Partial fusion of lherzolite and extraction of the melt fraction can leave a residue of harzburgite. Magnesium-rich olivine forms a proportion of peridotite, and so magnesium content is high. Layered igneous complexes have more varied compositions, depending on the fractions of pyroxenes, chromite, plagioclase. Minor minerals and mineral groups in peridotite include plagioclase, spinel, garnet, amphibole, in peridotite, plagioclase is stable at relatively low pressures, aluminous spinel at higher pressures, and garnet at yet higher pressures. Peridotite is the dominant rock of the Earths mantle above a depth of about 400 km, below that depth, olivine is converted to the higher-pressure mineral wadsleyite. Oceanic plates consist of up to about 100 km of peridotite covered by a thin crust, the crust, commonly about 6 km thick, consists of basalt, gabbro, and minor sediments. The peridotite below the ocean crust, abyssal peridotite, is found on the walls of rifts in the sea floor. Oceanic plates are usually subducted back into the mantle in subduction zones, peridotites also occur as fragments carried up by magmas from the mantle. Among the rocks that commonly include peridotite xenoliths are basalt and kimberlite, certain volcanic rocks, sometimes called komatiites, are so rich in olivine and pyroxene that they also can be termed peridotite
31.
Xenolith
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A xenolith is a rock fragment which becomes enveloped in a larger rock during the latters development and solidification. In geology, the term xenolith is almost exclusively used to describe inclusions in igneous rock during magma emplacement, a xenocryst is an individual foreign crystal included within an igneous body. Examples of xenocrysts are quartz crystals in a silica-deficient lava and diamonds within kimberlite diatremes, although the term xenolith is most commonly associated with igneous inclusions, a broad definition could include rock fragments which have become encased in sedimentary rock. Xenoliths are sometimes found in recovered meteorites, xenoliths and xenocrysts provide important information about the composition of the otherwise inaccessible mantle. Basalts, kimberlites, lamproites and lamprophyres, which have their source in the mantle, often contain fragments. Xenoliths of dunite, peridotite and spinel lherzolite in basaltic lava flows are one example, kimberlites contain, in addition to diamond xenocrysts, fragments of lherzolites of varying composition. The aluminium-bearing minerals of these fragments provide clues to the depth of origin, calcic plagioclase is stable to a depth of 25 km. Between 25 km and about 60 km, spinel is the stable aluminium phase, at depths greater than about 60 km, dense garnet becomes the aluminium-bearing mineral. Some kimberlites contain xenoliths of eclogite, which is considered to be the high-pressure metamorphic product of basaltic oceanic crust, the large-scale inclusion of foreign rock strata at the margins of an igneous intrusion is called a roof pendant. Blatt, Harvey, and Robert J. Tracy
32.
Olivine
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The mineral olivine is a magnesium iron silicate with the formula 2SiO4. Thus it is a type of nesosilicate or orthosilicate and it is a common mineral in the Earths subsurface but weathers quickly on the surface. The ratio of magnesium and iron varies between the two endmembers of the solid solution series, forsterite and fayalite, compositions of olivine are commonly expressed as molar percentages of forsterite and fayalite. Forsterite has a high melting temperature at atmospheric pressure, almost 1,900 °C. The melting temperature varies smoothly between the two endmembers, as do other properties, olivine incorporates only minor amounts of elements other than oxygen, silicon, magnesium and iron. Manganese and nickel commonly are the elements present in highest concentrations. Olivine gives its name to the group of minerals with a structure which includes tephroite, monticellite and kirschsteinite. It has a structure similar to magnetite but uses one quadravalent. Olivine gemstones are called peridot and chrysolite, olivine is named for its typically olive-green color, though it may alter to a reddish color from the oxidation of iron. Translucent olivine is sometimes used as a gemstone called peridot, some of the finest gem-quality olivine has been obtained from a body of mantle rocks on Zabargad island in the Red Sea. Olivine occurs in mafic and ultramafic igneous rocks and as a primary mineral in certain metamorphic rocks. Mg-rich olivine crystallizes from magma that is rich in magnesium and low in silica and that magma crystallizes to mafic rocks such as gabbro and basalt. Ultramafic rocks such as peridotite and dunite can be left after extraction of magmas. Olivine and high pressure structural variants constitute over 50% of the Earths upper mantle, the metamorphism of impure dolomite or other sedimentary rocks with high magnesium and low silica content also produces Mg-rich olivine, or forsterite. In contrast, Mg-rich olivine does not occur stably with silica minerals, Mg-rich olivine is stable to pressures equivalent to a depth of about 410 km within Earth. Mg-rich olivine has also discovered in meteorites, on the Moon and Mars, falling into infant stars. Such meteorites include chondrites, collections of debris from the early Solar System, the spectral signature of olivine has been seen in the dust disks around young stars. The tails of comets often have the signature of olivine
33.
Spinel
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Spinel is the magnesium aluminium member of the larger spinel group of minerals. It has the formula MgAl2O4 in the crystal system. Its name comes from Latin spina, balas ruby is an old name for a rose-tinted variety of spinel. Spinel crystallizes in the system, common crystal forms are octahedra. It has an imperfect cleavage and a conchoidal fracture. Its hardness is 8, its gravity is 3. 5–4.1. It may be colorless, but is usually shades of red, blue, green, yellow, brown, black. There is a natural white spinel, now lost, that surfaced briefly in what is now Sri Lanka. The Samarian Spinel is the largest known spinel in the world, the transparent red spinels were called spinel-rubies or balas rubies. In the past, before the arrival of modern science, spinels, after the 18th century the word ruby was only used for the red gem variety of the mineral corundum and the word spinel came to be used. Balas is derived from Balascia, the ancient name for Badakhshan, mines in the Gorno Badakhshan region of Tajikistan was for centuries the main source for red and pink spinels. Spinel has long been found in the gravel of Sri Lanka and in limestones of the Badakshan Province in modern-day Afghanistan and Tajikistan. Recently gem quality spinels also found in the marbles of Luc Yen, Mahenge and Matombo, Tsavo and in the gravels of Tunduru and this is why spinel and ruby are often found together. Spinel, 2O4, is common in peridotite in the uppermost Earths mantle, Spinel, Al2O4, is a common mineral in the Ca-Al-rich inclusions in some chondritic meteorites. Synthetic spinel, accidentally produced in the middle of the 18th century, has described more recently in scientific publications in 2000 and 2004. By 2015, transparent spinel was being made in sheets and other shapes through sintering, synthetic spinel which looks like glass but has notably higher strength against pressure, can also have applications in military and commercial use. Spinel group Ceylonite The Samarian Spinel, the largest known spinel in the world, part of the Iranian Crown Jewels Black Princes Ruby Deer, Howie, an Introduction to the Rock-Forming Minerals, Longman, pp. 424–433, ISBN 0-582-44210-9. Gemstones of the World 3rd edition, Sterling, pp. 116–117, Spinel structure at the University of Wisconsin - Green Bay Spinel structure at the Institut for materials science of the University of Kiel Value of Spinel
34.
Basalt
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Basalt is a common extrusive igneous rock formed from the rapid cooling of basaltic lava exposed at or very near the surface of a planet or moon. Flood basalt describes the formation in a series of basalt flows. By definition, basalt is an igneous rock with generally 45-55% silica and less than 10% feldspathoid by volume. Basalt commonly features a very fine-grained or glassy matrix interspersed with visible mineral grains, the average density is 3.0 gm/cm3. Basalt is defined by its content and texture, and physical descriptions without mineralogical context may be unreliable in some circumstances. Basalt is usually grey to black in colour, but rapidly weathers to brown or rust-red due to oxidation of its mafic minerals into hematite, although usually characterized as dark, basaltic rocks exhibit a wide range of shading due to regional geochemical processes. Due to weathering or high concentrations of plagioclase, some basalts can be quite light-coloured and these phenocrysts usually are of olivine or a calcium-rich plagioclase, which have the highest melting temperatures of the typical minerals that can crystallize from the melt. Basalt with a texture is called vesicular basalt, when the bulk of the rock is mostly solid. Gabbro is often marketed commercially as black granite and these ultramafic volcanic rocks, with silica contents below 45% are usually classified as komatiites. Agricola applied basalt to the black rock of the Schloßberg at Stolpen. Tholeiitic basalt is relatively rich in silica and poor in sodium, included in this category are most basalts of the ocean floor, most large oceanic islands, and continental flood basalts such as the Columbia River Plateau. Basalt rocks are in some cases classified after their content in High-Ti and Low-Ti varieties. High-Ti and Low-Ti basalts have been distinguished in the Paraná and Etendeka traps and it has greater than 17% alumina and is intermediate in composition between tholeiite and alkali basalt, the relatively alumina-rich composition is based on rocks without phenocrysts of plagioclase. Alkali basalt is relatively poor in silica and rich in sodium and it is silica-undersaturated and may contain feldspathoids, alkali feldspar and phlogopite. Boninite is a form of basalt that is erupted generally in back-arc basins. Ocean island basalt Lunar basalt On Earth, most basalt magmas have formed by melting of the mantle. Basalt commonly erupts on Io, the third largest moon of Jupiter, and has formed on the Moon, Mars, Venus. The crustal portions of oceanic tectonic plates are composed predominantly of basalt, produced from upwelling mantle below, the mineralogy of basalt is characterized by a preponderance of calcic plagioclase feldspar and pyroxene
35.
Gabbro
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Gabbro refers to a large group of dark, often phaneritic, mafic intrusive igneous rocks chemically equivalent to basalt. It forms when magma is trapped beneath the Earths surface. Much of the Earths oceanic crust is made of gabbro, formed at mid-ocean ridges, Gabbro is also found as plutons associated with continental volcanism. Due to its variant nature, the term gabbro may be applied loosely to a range of intrusive rocks. The term gabbro was used in the 1760s to name a set of types that were found in the ophiolites of the Apennine Mountains in Italy. Then, in 1809, the German geologist Christian Leopold von Buch used the term more restrictively in his description of these Italian ophiolitic rocks and he assigned the name gabbro to rocks that geologists nowadays would more strictly call metagabbro. Von Buch named gabbro after Gabbro, a village in Rosignano Marittimo municipality of Tuscany, Gabbro is dense, greenish or dark-colored and contains pyroxene, plagioclase, and minor amounts of amphibole and olivine. The pyroxene content is mostly clinopyroxene, generally augite, but small amounts of orthopyroxene may also be present, if the amount of orthopyroxene is more than 95% of the total pyroxene content, then the rock is termed norite. On the other hand, gabbro has more than 95% of its pyroxenes in the form of the monoclinic clinopyroxene/s, the calcium rich plagioclase feldspar and pyroxene content vary between 10% - 90% in gabbro. If more than 90% plagioclase is present, then the rock is an anorthosite, if on the other hand, the rock contains more than 90% pyroxenes, it is termed pyroxenite. Gabbro may also contain amounts of olivine, amphibole and biotite. The quartz content in gabbro is less than 5% of total volume, quartz gabbros or monzogabbros are also known to occur, for example the cizlakite at Pohorje in northeastern Slovenia, and are probably derived from magma that was over-saturated with silica. Gabbros contain minor amounts, typically a few percent, of iron-titanium oxides such as magnetite, ilmenite, Gabbro is generally coarse grained, with crystals in the size range of 1 mm or greater. Finer grained equivalents of gabbro are called diabase, although the term microgabbro is often used when extra descriptiveness is desired, Gabbro may be extremely coarse grained to pegmatitic, and some pyroxene-plagioclase cumulates are essentially coarse grained gabbro, some may exhibit acicular crystal habits. Gabbro is usually equigranular in texture, although it may be porphyritic at times, cumulate gabbros are more properly termed pyroxene-plagioclase adcumulate. Gabbro is an part of the oceanic crust, and can be found in many ophiolite complexes as parts of zones III. Long belts of gabbroic intrusions are typically formed at proto-rift zones and around ancient rift zone margins, mantle plume hypotheses may rely on identifying mafic and ultramafic intrusions and coeval basalt volcanism. It is better to base a rock definition on descriptive characteristics of the rather than how or where it was formed
36.
Ion
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An ion is an atom or a molecule in which the total number of electrons is not equal to the total number of protons, giving the atom or molecule a net positive or negative electrical charge. Ions can be created, by chemical or physical means. In chemical terms, if an atom loses one or more electrons. If an atom gains electrons, it has a net charge and is known as an anion. Ions consisting of only a single atom are atomic or monatomic ions, because of their electric charges, cations and anions attract each other and readily form ionic compounds, such as salts. In the case of ionization of a medium, such as a gas, which are known as ion pairs are created by ion impact, and each pair consists of a free electron. The word ion comes from the Greek word ἰόν, ion, going and this term was introduced by English physicist and chemist Michael Faraday in 1834 for the then-unknown species that goes from one electrode to the other through an aqueous medium. Faraday also introduced the words anion for a charged ion. In Faradays nomenclature, cations were named because they were attracted to the cathode in a galvanic device, arrhenius explanation was that in forming a solution, the salt dissociates into Faradays ions. Arrhenius proposed that ions formed even in the absence of an electric current, ions in their gas-like state are highly reactive, and do not occur in large amounts on Earth, except in flames, lightning, electrical sparks, and other plasmas. These gas-like ions rapidly interact with ions of charge to give neutral molecules or ionic salts. These stabilized species are commonly found in the environment at low temperatures. A common example is the present in seawater, which are derived from the dissolved salts. Electrons, due to their mass and thus larger space-filling properties as matter waves, determine the size of atoms. Thus, anions are larger than the parent molecule or atom, as the excess electron repel each other, as such, in general, cations are smaller than the corresponding parent atom or molecule due to the smaller size of its electron cloud. One particular cation contains no electrons, and thus consists of a single proton - very much smaller than the parent hydrogen atom. Since the electric charge on a proton is equal in magnitude to the charge on an electron, an anion, from the Greek word ἄνω, meaning up, is an ion with more electrons than protons, giving it a net negative charge. A cation, from the Greek word κατά, meaning down, is an ion with fewer electrons than protons, there are additional names used for ions with multiple charges
37.
Enstatite
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Enstatite is a mineral, the magnesium endmember of the pyroxene silicate mineral series enstatite - ferrosilite. The magnesium rich members of the solid solution series are common rock-forming minerals found in igneous, the intermediate composition, SiO3, has historically been known as hypersthene, although this name has been formally abandoned and replaced by orthopyroxene. When determined petrographically or chemically the composition is given as relative proportions of enstatite and ferrosilite, most natural crystals are orthorhombic although three polymorphs are known. The high temperature, low pressure polymorphs are protoenstatite and protoferrosilite while the low temperature forms, weathered enstatite with a small amount of iron takes on a submetallic luster and a bronze-like color. This material is termed bronzite, although it is correctly called altered enstatite. Bronzite and hypersthene were known long before enstatite, which was first described by G. A. Kenngott in 1855, an emerald-green variety of enstatite is called chrome-enstatite and is cut as a gemstone. The green color is caused by traces of chromium, hence the varietal name, in addition, bronzite is also sometimes used as a gemstone. They also have a prismatic cleavage that is perfect in two directions at 90 degrees, Enstatite is white, gray, greenish, or brown in color, its hardness is 5–6 on the Mohs scale, and its specific gravity is 3. 2–3.3. Isolated crystals are rare, but orthopyroxene is a constituent of various types of igneous rocks. Magnesian orthopyroxene occurs in rocks such as gabbro and diorite. It may form small idiomorphic phenocrysts and also groundmass grains in volcanic rocks such as basalt, andesite, Enstatite, close to En90Fs10 in composition, is an essential mineral in typical peridotite and pyroxenite of the Earths mantle. Xenoliths of peridotite are common in kimberlite and in some basalt, orthopyroxene is an important constituent of some metamorphic rocks such as granulite. Orthopyroxene near pure enstatite in composition occurs in some metamorphosed serpentines, Enstatite is a common mineral in meteorites. Crystals have been found in stony and iron meteorites, including one that fell at Breitenbach in the Ore Mountains, Bohemia. In some meteorites, together with olivine it forms the bulk of the material, it can occur in small masses, or chondrules. Enstatite is one of the few minerals that have been observed in crystalline form outside the Solar System, particularly around evolved stars. Enstatite is thought to be a component of the E-type asteroids, in the Solar System. Deer, W. A. Howie, R. A. and Zussman, an introduction to the rock-forming minerals
38.
Pigeonite
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Pigeonite is a mineral in the clinopyroxene group. It has a formula of Si2O6. The calcium cation fraction can vary from 5% to 25%, with iron, pigeonite crystallizes in the monoclinic system, as does augite, and a miscibility gap exists between the two minerals. At lower temperatures, pigeonite is unstable relative to augite plus orthopyroxene, the presence of pigeonite in an igneous rock thus provides evidence for the crystallization temperature of the magma, and hence indirectly for the water content of that magma. Pigeonite is found as phenocrysts in volcanic rocks on Earth and as crystals in meteorites from Mars, in slowly cooled intrusive igneous rocks, pigeonite is rarely preserved. Slow cooling gives the calcium the necessary time to separate itself from the structure to form exsolution lamellae of calcic clinopyroxene, textural evidence of its breakdown to orthopyroxene plus augite may be present, as shown in the accompanying microscopic image. Pigeonite is named for its type locality on Lake Superiors shores at Pigeon Point, Minnesota and it was first described in 1900
39.
Augite
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Augite is a common rock-forming pyroxene mineral with formula 2O6. The crystals are monoclinic and prismatic, augite has two prominent cleavages, meeting at angles near 90 degrees. Augite is a solution in the pyroxene group. Diopside and hedenbergite are important endmembers in augite, but augite can also contain significant aluminium, titanium, with declining temperature, augite may exsolve lamellae of pigeonite and/or orthopyroxene. There is also a miscibility gap between augite and omphacite, but this gap occurs at higher temperatures, there are no industrial or economic uses for this mineral. Augite is a mineral in mafic igneous rocks, for example, gabbro and basalt. It also occurs in relatively high-temperature metamorphic rocks such as mafic granulite and it commonly occurs in association with orthoclase, sanidine, labradorite, olivine, leucite, amphiboles and other pyroxenes. Occasional specimens have an appearance that give rise to the minerals name. It was named by Abraham Gottlob Werner in 1792, transparent augites containing dendritic patterns are used as gems and ornamental stones known as shajar in parts of India. It is found near the Ken River, local jewelers export raw shajar stone and items to different parts of India. Banda is one city noted for trade of shazar stone, fassaite Deer, W. A. Howie, R. A. and Zussman, J. An introduction to the rock-forming minerals
40.
Wollastonite
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Wollastonite is a calcium inosilicate mineral that may contain small amounts of iron, magnesium, and manganese substituting for calcium. It forms when impure limestone or dolostone is subjected to temperature and pressure sometimes in the presence of silica-bearing fluids as in skarns or contact metamorphic rocks. Associated minerals include garnets, vesuvianite, diopside, tremolite, epidote, plagioclase feldspar, pyroxene and it is named after the English chemist and mineralogist William Hyde Wollaston. Some of the properties that make wollastonite so useful are its high brightness and whiteness, low moisture and oil absorption, Wollastonite is used primarily in ceramics, friction products, metalmaking, paint filler, and plastics. World production data for wollastonite is not available for many countries, estimated world production of crude wollastonite ore was in the range of 530,000 to 550,000 tonnes in 2010. World reserves of wollastonite were estimated to exceed 90 million tonnes, however, many large deposits have not been surveyed yet. In 2010, the producers were China, India, United States, Mexico. Finland has long been a major European supplier of wollastonite, in the United States, wollastonite is mined in Willsboro, New York and Gouverneur, New York. Deposits have also been mined commercially in North Western Mexico, in plastics, wollastonite improves tensile and flexural strength, reduces resin consumption, and improves thermal and dimensional stability at elevated temperatures. Surface treatments are used to improve the adhesion between the wollastonite and the polymers to which it is added, in some industries, it is used in different percentages of impurities, such as its use as a fabricator of mineral wool insulation, or as an ornamental building material. Ceramic applications probably account for 30% to 40% of wollastonite sales worldwide, followed by polymers with 30% to 35% of sales, the remaining sales were for construction, friction products, and metallurgical applications. The price of raw wollastonite varied in 2008 between US$80 and US$500 per tonne depending on the country and size and shape of the powder particles, in ceramics, wollastonite competes with carbonates, feldspar, lime, and silica as a source of calcium and silicon. Its use in ceramics depends on the formulation of the ceramic body, in a pure CaSiO3, each component forms nearly half of the mineral by weight,48. 3% of CaO and 51. 7% of SiO2. In some cases, small amounts of iron, and manganese, Wollastonite can form a series of solid solutions in the system CaSiO3-FeSiO3, or hydrothermal synthesis of phases in the system MnSiO3-CaSiO3. Wollastonite crystallizes triclinically in space group P1 with the constants a =7.94 Å, b =7.32 Å, c =7.07 Å, α =90, 03°, β =95, 37°, γ =103, 43°. Wollastonite was once classed structurally among the group, because both of these groups have a ratio of Si, O =1,3. In 1931, Warren and Biscoe showed that the structure of wollastonite differs from minerals of the pyroxene group. It has been shown that the chains are more kinked than those of pyroxene group
41.
Jadeite
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Jadeite is a pyroxene mineral with composition NaAlSi2O6. It has a Mohs hardness of about 6.5 to 7.0 depending on the composition, the mineral is dense, with a specific gravity of about 3.4. The name jadeite is derived from the Spanish phrase piedra de ijada which means stone of the side and it was believed to cure kidney stones if it was rubbed against the side of the afflicted persons body. The Latin version of the name, lapis nephriticus, is the origin of the term nephrite, Jadeite forms solid solutions with other pyroxene endmembers such as augite and diopside, aegirine, and kosmochlor. Pyroxenes rich in both the jadeite and augite endmembers are known as omphacite, Jadeite is formed in metamorphic rocks under high pressure and relatively low temperature conditions. Albite is a mineral of the Earths crust, and it has a specific gravity of about 2.6. With increasing pressure, albite breaks down to form the high-pressure assemblage of jadeite plus quartz, minerals associated with jadeite include, glaucophane, lawsonite, muscovite, aragonite, serpentine and quartz. Rocks that consist almost entirely of jadeite are called jadeitite, in all well-documented occurrences, jadeitite appears to have formed from subduction zone fluids in association with serpentinite. Jadeitite is resistant to weathering, and boulders of jadeitite released from the environments in which they formed are found in a variety of environments. Jadeites color commonly ranges from white through pale apple green to deep green but can also be blue-green, pink, lavender. Chloromelanite is a dark green to black variety. Color is largely affected by the presence of elements such as chromium. Its translucence can be anywhere from entirely solid through opaque to almost clear, variations in color and translucence are often found even within a single specimen. Jadeite is reported from California, US, Myanmar, New Zealand, Guatemala, Itoigawa, Japan, other localities of jadeite include Kazakhstan, Russia, British Columbia, Canada, Italy and Turkestan. Over 180 axe heads made from jadeitite quarried in northern Italy in the Neolithic era have been found across the British Isles, a great many jadeite beads and axe heads as well as the remains of jadeite workshops from the Neolithic era have been uncovered in Itoigawa, Japan. These beads and axes were traded throughout Japan and the Korean Peninsula and were produced by the worlds oldest known jadeite-using culture, Jadeite is one of the minerals recognized as the gemstone jade. Jadeite from the Motagua Valley, Guatemala, was used by the Olmec and Maya peoples, typically, the most highly valued colors of jadeite are the most intensely green, translucent varieties, though traditionally white has been considered the most valuable of the jades by the Chinese. It is thus difficult to obtain and as yet too rare, when purchasing jade, quality is determined by the degree of translucence, cleanness of color and purity of color
42.
Aegirine
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Aegirine is a member of the clinopyroxene group of inosilicates. Aegirine is the sodium endmember of the aegirine-augite series, aegirine has the chemical formula NaFeSi2O6 in which the iron is present as Fe3+. In the aegirine-augite series the sodium is replaced by calcium with iron. Aluminium also substitutes for the iron and it is also known as acmite, which is a fibrous, green-colored variety. Aegirine occurs as dark green prismatic crystals. It has a glassy luster and perfect cleavage, the Mohs hardness varies from 5 to 6 and the specific gravity is 3.2 to 3.4. Commonly occurs in igneous rocks, nepheline syenites, carbonatites and pegmatites. Also in regionally metamorphosed schists, gneisses, and iron formations, in blueschist facies rocks and it may occur as an authigenic mineral in shales and marls. It occurs in association with potassic feldspar, nepheline, riebeckite, arfvedsonite, aenigmatite, astrophyllite, catapleiite, eudialyte, serandite and apophyllite. Localities include Mont Saint-Hilaire, Quebec, Canada, Kongsberg, Norway, Narsarssuk, Greenland, Kola Peninsula, Russia, Magnet Cove, Arkansas, US, Kenya, Scotland and it was first described in 1835 for an occurrence in Rundemyr, Øvre Eiker, Buskerud, Norway. Aegirine was named after Ægir, the Teutonic god of the sea, a synonym for the mineral is acmite in reference to the typical pointed crystals. It is sometimes used as a gemstone
43.
X-ray crystallography
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By measuring the angles and intensities of these diffracted beams, a crystallographer can produce a three-dimensional picture of the density of electrons within the crystal. From this electron density, the positions of the atoms in the crystal can be determined, as well as their chemical bonds, their disorder. The method also revealed the structure and function of biological molecules, including vitamins, drugs, proteins. X-ray crystallography is still the method for characterizing the atomic structure of new materials. In a single-crystal X-ray diffraction measurement, a crystal is mounted on a goniometer, the goniometer is used to position the crystal at selected orientations. The crystal is illuminated with a finely focused monochromatic beam of X-rays, poor resolution or even errors may result if the crystals are too small, or not uniform enough in their internal makeup. X-ray crystallography is related to other methods for determining atomic structures. Similar diffraction patterns can be produced by scattering electrons or neutrons, for all above mentioned X-ray diffraction methods, the scattering is elastic, the scattered X-rays have the same wavelength as the incoming X-ray. By contrast, inelastic X-ray scattering methods are useful in studying excitations of the sample, Crystals, though long admired for their regularity and symmetry, were not investigated scientifically until the 17th century. Johannes Kepler hypothesized in his work Strena seu de Nive Sexangula that the symmetry of snowflake crystals was due to a regular packing of spherical water particles. The Danish scientist Nicolas Steno pioneered experimental investigations of crystal symmetry, hence, William Hallowes Miller in 1839 was able to give each face a unique label of three small integers, the Miller indices which remain in use today for identifying crystal faces. In the 19th century, a catalog of the possible symmetries of a crystal was worked out by Johan Hessel, Auguste Bravais, Evgraf Fedorov, Arthur Schönflies. Wilhelm Röntgen discovered X-rays in 1895, just as the studies of crystal symmetry were being concluded, physicists were initially uncertain of the nature of X-rays, but soon suspected that they were waves of electromagnetic radiation, in other words, another form of light. Single-slit experiments in the laboratory of Arnold Sommerfeld suggested that X-rays had a wavelength of about 1 angstrom, however, X-rays are composed of photons, and thus are not only waves of electromagnetic radiation but also exhibit particle-like properties. Albert Einstein introduced the concept in 1905, but it was not broadly accepted until 1922. Therefore, these properties of X-rays, such as their ionization of gases. Nevertheless, Braggs view was not broadly accepted and the observation of X-ray diffraction by Max von Laue in 1912 confirmed for most scientists that X-rays were a form of electromagnetic radiation, Crystals are regular arrays of atoms, and X-rays can be considered waves of electromagnetic radiation. Atoms scatter X-ray waves, primarily through the atoms electrons and this phenomenon is known as elastic scattering, and the electron is known as the scatterer
44.
Martian soil
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Martian soil is the fine regolith found on the surface of Mars. Its properties can differ significantly from those of terrestrial soil, the term Martian soil typically refers to the finer fraction of regolith. On Earth, the soil usually includes organic content. In contrast, planetary scientists adopt a definition of soil to distinguish it from rocks. Consequently, rocks classify as grains exceeding the size of cobbles on the Wentworth scale and this approach enables agreement across Martian remote sensing methods that span the electromagnetic spectrum from gamma to radio waves. ‘‘Soil’’ refers to all other, typically unconsolidated, material including those sufficiently fine-grained to be mobilized by wind, soil consequently encompasses a variety of regolith components identified at landing sites. Typical examples include, bedform armor, clasts, concretions, drift, dust, rocky fragments, Martian dust generally connotes even finer materials than Martian soil, the fraction which is less than 30 micrometres in diameter. Disagreement over the significance of soils definition arises due to the lack of a concept of soil in the literature. This definition emphasizes that soil is a body that retains information about its environmental history, Mars is covered with vast expanses of sand and dust and its surface is littered with rocks and boulders. The dust is occasionally picked up in vast planet-wide dust storms, Mars dust is very fine, and enough remains suspended in the atmosphere to give the sky a reddish hue. The sand is believed to move slowly in the Martian winds due to the very low density of the atmosphere in the present epoch. In the past, liquid water flowing in gullies and river valleys may have shaped the Martian regolith, Mars researchers are studying whether groundwater sapping is shaping the Martian regolith in the present epoch, and whether carbon dioxide hydrates exist on Mars and play a role. It is believed that large quantities of water and carbon dioxide ices remain frozen within the regolith in the parts of Mars. Water contents of Martian regolith range from <2% by weight to more than 60%, the presence of olivine, which is an easily weatherable primary mineral, has been interpreted to mean that physical rather than chemical weathering processes currently dominate on Mars. High concentrations of ice in soils are thought to be the cause of accelerated soil creep, scientists compared the soil near Mars north pole to that of backyard gardens on Earth, and concluded that it could be suitable for growth of plants.3. The presence of the perchlorate, if confirmed, would make Martian soil more exotic than previously believed, while our understanding of Martian soils is extremely rudimentary, their diversity may raise the question of how we might compare them with our Earth-based soils. On October 17,2012, the first X-ray diffraction analysis of Martian soil was performed, hawaiian volcanic ash has been used as Martian regolith simulant by researchers since 1998. However, terrestrial contamination, as the source of the organic compounds, on September 26,2013, NASA scientists reported the Mars Curiosity rover detected abundant, easily accessible water in soil samples at the Rocknest region of Aeolis Palus in Gale Crater
45.
CheMin
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CheMin, short for Chemistry and Mineralogy, is an instrument located in the interior of the Curiosity rover that is exploring the surface of Gale crater on Mars. David Blake, from NASA Ames Research Center, is the Principal Investigator, CheMin identifies and quantifies the minerals present in rocks and soil delivered to it by the rovers robotic arm. By determining the mineralogy in rocks and soils, CheMin assesses the involvement of water in their formation, deposition, in addition, CheMin data is useful in the search for potential mineral biosignatures, energy sources for life or indicators for past habitable environments. CheMin aboard the Curiosity rover on Mars won the 2013 NASA Government Invention of the year award, CheMin is an X-ray powder diffraction instrument that also has X-ray fluorescence capabilities. Raw CCD frames are processed into data products on board the rover to reduce the data volume and these data products are transmitted to Earth for further processing analyses. In operation, a collimated X-ray source produces and directs a beam through a sample cell containing powdered material. An X-ray sensitive CCD imager is positioned on the side of the sample from the source. The CCD can measure the charge generated by each photon, diffracted X-rays strike the detector and are identified by their energy, producing a two-dimensional image that constitutes the diffraction pattern of the sample. Both crystalline and amorphous materials can be analyzed in this fashion, the funnel contains a 1 mm mesh screen to limit the particle size. Five permanent cells are loaded with calibration standards, these are single minerals or synthetic ceramic, each analysis may take up to 10 hours, spread out over two or more Martian nights. Capacity, CheMin is planned to analyze as many as 74 dry samples, cross-contamination by cell reuse is expected to be less than 5%. CheMin does not have the capability to store previously analyzed samples for later reanalysis, detection limits, able to detect individual minerals that are present at the 3% level and above. The paragonetic tephra from a Hawaiian cinder cone has been mined to create Martian regolith simulant for researchers to use since 1998
46.
Curiosity (rover)
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Curiosity is a car-sized robotic rover exploring Gale Crater on Mars as part of NASAs Mars Science Laboratory mission. Curiosity was launched from Cape Canaveral on November 26,2011, at 15,02 UTC aboard the MSL spacecraft, the Bradbury Landing site was less than 2.4 km from the center of the rovers touchdown target after a 560 million km journey. Curiositys design will serve as the basis for the planned Mars 2020 rover, in December 2012, Curiositys two-year mission was extended indefinitely. As of April 7,2017, Curiosity has been on Mars for 1659 sols since landing on August 6,2012, the mission will also help prepare for human exploration. This data would be important for a manned mission. The remaining mass of the MSL craft was discarded in the process of carrying out this task, dimensions, Curiosity has a mass of 899 kg including 80 kg of scientific instruments. The rover is 2.9 m long by 2.7 m wide by 2.2 m in height, power source, Curiosity is powered by a radioisotope thermoelectric generator, like the successful Viking 1 and Viking 2 Mars landers in 1976. Radioisotope power systems are generators that produce electricity from the decay of isotopes, such as plutonium-238. Heat given off by the decay of this isotope is converted into electric voltage by thermocouples, providing constant power during all seasons and through the day, waste heat can be used via pipes to warm systems, freeing electrical power for the operation of the vehicle and instruments. Curiositys RTG is fueled by 4.8 kg of plutonium-238 dioxide supplied by the U. S. Department of Energy. The MMRTG produces less power over time as its plutonium fuel decays, at its minimum lifetime of 14 years, electrical power output is down to 100 watts. The power source will generate 9 MJ each day, much more than the solar panels of the Mars Exploration Rovers, the electrical output from the MMRTG charges two rechargeable lithium-ion batteries. This enables the power subsystem to meet power demands of rover activities when the demand temporarily exceeds the generator’s steady output level. Each battery has a capacity of about 42 ampere-hours, heat rejection system, The temperatures at the landing site can vary from −127 to 40 °C, therefore, the thermal system will warm the rover for most of the Martian year. It uses fluid pumped through 60 m of tubing in the body so that sensitive components are kept at optimal temperatures. The HRS also has the ability to cool components if necessary, the computers run the VxWorks real-time operating system. Each computers memory includes 256 kB of EEPROM,256 MB of DRAM, for comparison, the Mars Exploration Rovers used 3 MB of EEPROM,128 MB of DRAM, and 256 MB of flash memory. The RCE computers use the RAD750 CPU, which is a successor to the RAD6000 CPU of the Mars Exploration Rovers
47.
Rocknest (Mars)
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Rocknest is a sand patch on the surface of Aeolis Palus, between Peace Vallis and Aeolis Mons, in Gale crater on the planet Mars. The patch was encountered by the Curiosity rover on the way from Bradbury Landing to Glenelg Intrigue on September 28,2012, the approximate site coordinates are,4. 59°S137. 44°E / -4.59,137.44. The sand patch is downhill from a cluster of dark rocks, NASA determined the patch to be the location for the first use of the scoop on the arm of the Mars Curiosity rover. The Rocknest patch is about 1.5 m by 5 m, on October 7,2012, a mysterious bright object, discovered in the sand at Rocknest, drew scientific interest. Several close-up pictures were taken of the object and preliminary interpretations by scientists suggest the object to be debris from the spacecraft, nonetheless, further images in the nearby sand have detected other bright particles. These newly discovered objects are thought to be native Martian material. On October 17,2012 at Rocknest, the first X-ray diffraction analysis of Martian soil was performed, on September 26,2013, NASA scientists reported the Mars Curiosity rover detected abundant, easily accessible water in soil samples at the Rocknest region of Aeolis Palus in Gale Crater. In addition, NASA reported the rover found two principal types, a fine-grained mafic type and a locally derived, coarse-grained felsic type. The mafic type, similar to other soils and martian dust, was associated with hydration of the amorphous phases of the soil. NASA also reported that Jake M rock, a rock encountered by Curiosity on the way to Glenelg, was a mugearite, Curiosity Rover - Official Site NASA - Mars Exploration Program Volcanic rock classification
48.
Talc
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Talc is a clay mineral composed of hydrated magnesium silicate with the chemical formula H2Mg34 or Mg3Si4O102. In loose form, it, along with starch, was one of the most widely used substances known as baby powder It occurs as foliated to fibrous masses. It has a perfect cleavage, and the folia are not elastic. Mohs scale of hardness, based on scratch hardness comparison. As such, talc can easily be scratched by a fingernail, talc has a specific gravity of 2. 5–2.8, a clear or dusty luster, and is translucent to opaque. Talc is not soluble in water, but is soluble in dilute mineral acids. Its color ranges from white to grey or green and it has a greasy feel. Soapstone is a rock composed predominantly of talc. The word talc derives from Medieval Latin talcus, which in turn originates from Arabic, طلق ṭalq which in turn was derived from Persian, in the ancient times, the word was used for various related minerals, including talc, mica, and selenite. Talc is a mineral that results from the metamorphism of magnesian minerals such as serpentine, pyroxene, amphibole. This is known as talc carbonation or steatization and produces a suite of known as talc carbonates. This is typically associated with high-pressure, low-temperature minerals such as phengite, garnet, such rocks are typically white, friable, and fibrous, and are known as whiteschist. Talc is a trioctahedral layered mineral, its structure is similar to pyrophyllite, talc is a common metamorphic mineral in metamorphic belts that contain ultramafic rocks, such as soapstone, and within whiteschist and blueschist metamorphic terranes. Talc carbonate ultramafics are typical of areas of the Archaean cratons. Talc-carbonate ultramafics are also known from the Lachlan Fold Belt, eastern Australia, from Brazil, the Guiana Shield, and from the belts of Turkey, Oman. Notable economic talc occurrences include the Mount Seabrook talc mine, Western Australia, the France-based Luzenac Group is the worlds largest supplier of mined talc. Its largest talc mine at Trimouns near Luzenac in southern France produces 400,000 tonnes of talc per year, talc is used in many industries, including paper making, plastic, paint and coatings, rubber, food, electric cable, pharmaceuticals, cosmetics, and ceramics. A coarse grayish-green high-talc rock is soapstone or steatite, used for stoves, sinks, electrical switchboards, crayons, soap and it is often used for surfaces of laboratory table tops and electrical switchboards because of its resistance to heat, electricity and acids
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