1.
Crystal habit
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In mineralogy, crystal habit is the characteristic external shape of an individual crystal or crystal group. A single crystals habit is a description of its shape and its crystallographic forms. Recognizing the habit may help in identifying a mineral, when the faces are well-developed due to uncrowded growth a crystal is called euhedral, one with partially developed faces is subhedral, and one with undeveloped crystal faces is called anhedral. The long axis of a quartz crystal typically has a six-sided prismatic habit with parallel opposite faces. Aggregates can be formed of individual crystals with euhedral to anhedral grains, the arrangement of crystals within the aggregate can be characteristic of certain minerals. For example, minerals used for asbestos insulation often grow in a fibrous habit, the terms used by mineralogists to report crystal habits describe the typical appearance of an ideal mineral. Recognizing the habit can aid in identification as some habits are characteristic, most minerals, however, do not display ideal habits due to conditions during crystallization. Minerals belonging to the crystal system do not necessarily exhibit the same habit. Some habits of a mineral are unique to its variety and locality, For example, while most sapphires form elongate barrel-shaped crystals, ordinarily, the latter habit is seen only in ruby. Sapphire and ruby are both varieties of the mineral, corundum. Some minerals may replace other existing minerals while preserving the originals habit, a classic example is tigers eye quartz, crocidolite asbestos replaced by silica. While quartz typically forms prismatic crystals, in tigers eye the original fibrous habit of crocidolite is preserved, the names of crystal habits are derived from, Predominant crystal faces. Abnormal grain growth Grain growth Crystallization
2.
Fracture (mineralogy)
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In the field of mineralogy, fracture is the texture and shape of a rocks surface formed when a mineral is fractured. Minerals often have a highly distinctive fracture, making it a feature used in their identification. Fracture differs from cleavage in that the latter involves clean splitting along the planes of the minerals crystal structure. All minerals exhibit fracture, but when very strong cleavage is present, conchoidal fracture breakage that resembles the concentric ripples of a mussel shell. It often occurs in amorphous or fine-grained minerals such as flint, opal or obsidian, subconchoidal fracture is similar to conchoidal fracture, but with less significant curvature. Earthy fracture is reminiscent of freshly broken soil and it is frequently seen in relatively soft, loosely bound minerals, such as limonite, kaolinite and aluminite. Hackly fracture is jagged, sharp and not even and it occurs when metals are torn, and so is often encountered in native metals such as copper and silver. Splintery fracture comprises sharp elongated points and it is particularly seen in fibrous minerals such as chrysotile, but may also occur in non-fibrous minerals such as kyanite. Uneven fracture is a surface or one with random irregularities. It occurs in a range of minerals including arsenopyrite, pyrite and magnetite. Rudolf Duda and Lubos Rejl, Minerals of the World http, //www. galleries. com/minerals/property/fracture. htm
3.
Mohs scale of mineral hardness
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The Mohs scale of mineral hardness is a qualitative ordinal scale characterizing scratch resistance of various minerals through the ability of harder material to scratch softer material. Created in 1812 by German geologist and mineralogist Friedrich Mohs, it is one of several definitions of hardness in materials science, while greatly facilitating the identification of minerals in the field, the Mohs scale does not show how well hard materials perform in an industrial setting. Despite its lack of precision, the Mohs scale is highly relevant for field geologists, the Mohs scale hardness of minerals can be commonly found in reference sheets. Reference materials may be expected to have a uniform Mohs hardness, the Mohs scale of mineral hardness is based on the ability of one natural sample of mineral to scratch another mineral visibly. The samples of matter used by Mohs are all different minerals, Minerals are pure substances found in nature. Rocks are made up of one or more minerals, as the hardest known naturally occurring substance when the scale was designed, diamonds are at the top of the scale. The hardness of a material is measured against the scale by finding the hardest material that the material can scratch. For example, if material is scratched by apatite but not by fluorite. Scratching a material for the purposes of the Mohs scale means creating non-elastic dislocations visible to the naked eye, frequently, materials that are lower on the Mohs scale can create microscopic, non-elastic dislocations on materials that have a higher Mohs number. The Mohs scale is an ordinal scale. For example, corundum is twice as hard as topaz, the table below shows the comparison with the absolute hardness measured by a sclerometer, with pictorial examples. On the Mohs scale, a streak plate has a hardness of 7.0, using these ordinary materials of known hardness can be a simple way to approximate the position of a mineral on the scale. The table below incorporates additional substances that may fall between levels, Comparison between Hardness and Hardness, Mohs hardness of elements is taken from G. V, samsonov in Handbook of the physicochemical properties of the elements, IFI-Plenum, New York, USA,1968. The Hardness of Minerals and Rocks
4.
Lustre (mineralogy)
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Lustre or luster is the way light interacts with the surface of a crystal, rock, or mineral. The word traces its origins back to the latin lux, meaning light, a range of terms are used to describe lustre, such as earthy, metallic, greasy, and silky. Similarly, the term refers to a glassy lustre. A list of terms is given below. Lustre varies over a continuum, and so there are no rigid boundaries between the different types of lustre. The terms are frequently combined to describe types of lustre. Some minerals exhibit unusual optical phenomena, such as asterism or chatoyancy, a list of such phenomena is given below. Adamantine minerals possess a superlative lustre, which is most notably seen in diamond, such minerals are transparent or translucent, and have a high refractive index. Minerals with an adamantine lustre are uncommon, with examples being cerussite. Minerals with a degree of lustre are referred to as subadamantine, with some examples being garnet. Dull minerals exhibit little to no lustre, due to coarse granulations which scatter light in all directions, a distinction is sometimes drawn between dull minerals and earthy minerals, with the latter being coarser, and having even less lustre. Greasy minerals resemble fat or grease, a greasy lustre often occurs in minerals containing a great abundance of microscopic inclusions, with examples including opal and cordierite. Many minerals with a greasy lustre also feel greasy to the touch, metallic minerals have the lustre of polished metal, and with ideal surfaces will work as a reflective surface. Examples include galena, pyrite and magnetite, pearly minerals consist of thin transparent co-planar sheets. Light reflecting from these layers give them a lustre reminiscent of pearls, such minerals possess perfect cleavage, with examples including muscovite and stilbite. Resinous minerals have the appearance of resin, chewing gum or plastic, a principal example is amber, which is a form of fossilized resin. Silky minerals have an arrangement of extremely fine fibres, giving them a lustre reminiscent of silk. Examples include asbestos, ulexite and the satin spar variety of gypsum, a fibrous lustre is similar, but has a coarser texture
5.
Transparency and translucency
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In the field of optics, transparency is the physical property of allowing light to pass through the material without being scattered. On a macroscopic scale, the photons can be said to follow Snells Law, in other words, a translucent medium allows the transport of light while a transparent medium not only allows the transport of light but allows for image formation. The opposite property of translucency is opacity, transparent materials appear clear, with the overall appearance of one color, or any combination leading up to a brilliant spectrum of every color. When light encounters a material, it can interact with it in different ways. These interactions depend on the wavelength of the light and the nature of the material, photons interact with an object by some combination of reflection, absorption and transmission. Some materials, such as glass and clean water, transmit much of the light that falls on them and reflect little of it. Many liquids and aqueous solutions are highly transparent, absence of structural defects and molecular structure of most liquids are mostly responsible for excellent optical transmission. Materials which do not transmit light are called opaque, many such substances have a chemical composition which includes what are referred to as absorption centers. Many substances are selective in their absorption of light frequencies. They absorb certain portions of the spectrum while reflecting others. The frequencies of the spectrum which are not absorbed are either reflected or transmitted for our physical observation and this is what gives rise to color. The attenuation of light of all frequencies and wavelengths is due to the mechanisms of absorption. Transparency can provide almost perfect camouflage for animals able to achieve it and this is easier in dimly-lit or turbid seawater than in good illumination. Many marine animals such as jellyfish are highly transparent, at the atomic or molecular level, physical absorption in the infrared portion of the spectrum depends on the frequencies of atomic or molecular vibrations or chemical bonds, and on selection rules. Nitrogen and oxygen are not greenhouse gases because there is no absorption because there is no molecular dipole moment. With regard to the scattering of light, the most critical factor is the scale of any or all of these structural features relative to the wavelength of the light being scattered. Primary material considerations include, Crystalline structure, whether or not the atoms or molecules exhibit the long-range order evidenced in crystalline solids, glassy structure, scattering centers include fluctuations in density or composition. Microstructure, scattering centers include internal surfaces such as boundaries, crystallographic defects
6.
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
7.
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
8.
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
9.
Stainless steel
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In metallurgy, stainless steel, also known as inox steel or inox from French inoxydable, is a steel alloy with a minimum of 10. 5% chromium content by mass. Stainless steel is notable for its resistance, and it is widely used for food handling. Stainless steel does not readily corrode, rust or stain with water as ordinary steel does, however, it is not fully stain-proof in low-oxygen, high-salinity, or poor air-circulation environments. There are various grades and surface finishes of stainless steel to suit the environment the alloy must endure, Stainless steel is used where both the properties of steel and corrosion resistance are required. Stainless steel differs from carbon steel by the amount of chromium present, unprotected carbon steel rusts readily when exposed to air and moisture. This iron oxide film is active and accelerates corrosion by making it easier for more iron oxide to form, since iron oxide has lower density than steel, the film expands and tends to flake and fall away. In comparison, stainless steels contain sufficient chromium to undergo passivation and this layer prevents further corrosion by blocking oxygen diffusion to the steel surface and stops corrosion from spreading into the bulk of the metal. Passivation occurs only if the proportion of chromium is high enough, Stainless steel’s resistance to corrosion and staining, low maintenance, and familiar lustre make it an ideal material for many applications. Storage tanks and tankers used to transport orange juice and other food are made of stainless steel. This also influences its use in kitchens and food processing plants, as it can be steam-cleaned and sterilized. High oxidation resistance in air at ambient temperature is achieved with addition of a minimum of 13% chromium. The chromium forms a layer of chromium oxide when exposed to oxygen. The layer is too thin to be visible, and the metal remains lustrous, the layer is impervious to water and air, protecting the metal beneath, and this layer quickly reforms when the surface is scratched. This phenomenon is called passivation and is seen in other metals, corrosion resistance can be adversely affected if the component is used in a non-oxygenated environment, a typical example being underwater keel bolts buried in timber. When stainless steel parts such as nuts and bolts are forced together, when forcibly disassembled, the welded material may be torn and pitted, a destructive effect known as galling. Galling can be avoided by the use of materials for the parts forced together, for example bronze and stainless steel. However, two different alloys electrically connected in a humid, even mildly acidic environment may act as a voltaic pile, nitronic alloys, made by selective alloying with manganese and nitrogen, may have a reduced tendency to gall. Additionally, threaded joints may be lubricated to provide a film between the two parts and prevent galling, low-temperature carburizing is another option that virtually eliminates galling and allows the use of similar materials without the risk of corrosion and the need for lubrication
10.
Yukon
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Yukon is the smallest and westernmost of Canadas three federal territories. The territory has the smallest population of any province or territory in Canada, Whitehorse is the territorial capital and Yukons only city. The territory was split from the Northwest Territories in 1898 and was named the Yukon Territory, though officially bilingual, the Yukon Government also recognizes First Nations languages. At 5,959 m, Yukons Mount Logan, in Kluane National Park and Reserve, is the highest mountain in Canada, most of Yukon has a subarctic climate, characterized by long cold winters and brief warm summers. The Arctic Ocean coast has a tundra climate, notable rivers include the Yukon River, after which the territory was named, as well as the Pelly, Stewart, Peel, White and Tatshenshini rivers. Long before the arrival of Europeans, central and southern Yukon was populated by First Nations people, sites of archeological significance in Yukon hold some of the earliest evidence of the presence of human occupation in North America. The sites safeguard the history of the first people and the earliest First Nations of the Yukon, the volcanic eruption of Mount Churchill in approximately 800 AD in what is now the U. S. Coastal and inland First Nations had extensive trading networks, European incursions into the area only began early in the 19th century with the fur trade, followed by missionaries. By the 1870s and 1880s gold miners began to arrive and this drove a population increase that justified the establishment of a police force, just in time for the start of the Klondike Gold Rush in 1897. The increased population coming with the gold led to the separation of the Yukon district from the Northwest Territories. Its northern coast is on the Beaufort Sea and its ragged eastern boundary mostly follows the divide between the Yukon Basin and the Mackenzie River drainage basin to the east in the Mackenzie mountains. Most of the territory is in the watershed of its namesake, the southern Yukon is dotted with a large number of large, long and narrow glacier-fed alpine lakes, most of which flow into the Yukon River system. The larger lakes include Teslin Lake, Atlin Lake, Tagish Lake, Marsh Lake, Lake Laberge, Kusawa Lake, bennett Lake on the Klondike Gold Rush trail is a lake flowing into Nares Lake, with the greater part of its area within Yukon. Canadas highest point, Mount Logan, is in the territorys southwest, Mount Logan and a large part of the Yukons southwest are in Kluane National Park and Reserve, a UNESCO World Heritage Site. Other national parks include Ivvavik National Park and Vuntut National Park in the north, other watersheds include the Mackenzie River, the Peel Watershed and the Alsek–Tatshenshini, and a number of rivers flowing directly into the Beaufort Sea. The two main Yukon rivers flowing into the Mackenzie in the Northwest Territories are the Liard River in the southeast, notable widespread tree species within Yukon are the black spruce and white spruce. Many trees are stunted because of the growing season and severe climate. The capital, Whitehorse, is also the largest city, with about three-quarters of the population, the second largest is Dawson City, which was the capital until 1952
11.
Serpentinite
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Serpentinite is a rock composed of one or more serpentine group minerals. Minerals in this group are formed by serpentinization, a hydration, the mineral alteration is particularly important at the sea floor at tectonic plate boundaries. Serpentinization is a geological low-temperature metamorphic process involving heat and water in which low-silica mafic and ultramafic rocks are oxidized and hydrolyzed with water into serpentinite. Peridotite, including dunite, at and near the seafloor and in mountain belts is converted to serpentine, brucite, magnetite, and other minerals — some rare, such as awaruite, and even native iron. In the process large amounts of water are absorbed into the increasing the volume. The density changes from 3.3 to 2.7 g/cm3 with a concurrent volume increase on the order of 30-40%, the reaction is highly exothermic and rock temperatures can be raised by about 260 °C, providing an energy source for formation of non-volcanic hydrothermal vents. The magnetite-forming chemical reactions produce hydrogen gas under anaerobic conditions prevailing deep in the mantle, carbonates and sulfates are subsequently reduced by hydrogen and form methane and hydrogen sulfide. The hydrogen, methane, and hydrogen sulfide provide energy sources for deep sea chemotroph microorganisms, serpentinite is formed from olivine via several reactions, some of which are complementary. Olivine is a solution between the magnesium-endmember forsterite and the iron-endmember fayalite. Serpentinite reaction 1a and 1b, below, exchange silica between forsterite and fayalite to form serpentine group minerals and magnetite, Reaction 1c describes the hydration of olivine with water only to yield serpentine and Mg2. Talc and magnesian chlorite are possible products, together with the serpentine minerals antigorite, lizardite, the final mineralogy depends both on rock and fluid compositions, temperature, and pressure. Antigorite forms in reactions at temperatures that can exceed 600 °C during metamorphism, lizardite and chrysotile can form at low temperatures very near the Earths surface. In the presence of carbon dioxide, however, serpentinitization may form either magnesite or generate methane and it is thought that some hydrocarbon gases may be produced by serpentinite reactions within the oceanic crust. Or, in balanced form, Reaction 2a is favored if the serpentinite is Mg-poor or if there isnt enough carbon dioxide to promote talc formation, Reaction 2b is favored in highly magnesian compositions and low partial pressure of carbon dioxide. If an olivine composition contains sufficient fayalite, then olivine plus water can completely metamorphose to serpentine, serpentinitization of a mass of peridotite usually destroys all previous textural evidence because the serpentine minerals are weak and behave in a very ductile fashion. Serpentine is the product of the reaction between water and fayalites ferrous ions, the process is effected by bacteria under anaerobic conditions. The two unoxidised ferrous ions still available in the three units of fayalite finally combine with the four ferric cations and oxide anions to form two formula units of magnetite. Serpentinization has been proposed as an alternative source for the observed methane traces
12.
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
