Orthorhombic in the context of "Base (geometry)"

Anhydrite, or anhydrous calcium sulfate, is a mineral with the chemical formula CaSO₄. It is in the orthorhombic crystal system, with three directions of perfect cleavage parallel to the three planes of symmetry. It is not isomorphous with the orthorhombic barium (baryte) and strontium (celestine) sulfates, as might be expected from the chemical formulas. Distinctly developed crystals are somewhat rare, the mineral usually presenting the form of cleavage masses. The Mohs hardness is 3.5, and the specific gravity is 2.9. The color is white, sometimes greyish, bluish, or purple. On the best developed of the three cleavages, the lustre is pearly; on other surfaces it is glassy. When exposed to water, anhydrite readily transforms to the more commonly occurring gypsum, (CaSO₄·2H₂O) by the absorption of water. This transformation is reversible, with gypsum or calcium sulfate hemihydrate forming anhydrite by heating to around 200 °C (400 °F) under normal atmospheric conditions. Anhydrite is commonly associated with calcite, halite, and sulfides such as galena, chalcopyrite, molybdenite, and pyrite in vein deposits.

Cementite (or iron carbide) is a compound of iron and carbon, more precisely an intermediate transition metal carbide with the formula Fe₃C. By weight, it is 6.67% carbon and 93.3% iron. It has an orthorhombic crystal structure. It is a hard, brittle material, normally classified as a ceramic in its pure form, and is a frequently found and important constituent in ferrous metallurgy. While cementite is present in most steels and cast irons, it is produced as a raw material in the iron carbide process, which belongs to the family of alternative ironmaking technologies. The name cementite originated from the theory of Floris Osmond and J. Werth, in which the structure of solidified steel consists of a kind of cellular tissue, with ferrite as the nucleus and Fe₃C the envelope of the cells. The carbide therefore cemented the iron.

The pyroxenes (commonly abbreviated Px) are a group of important rock-forming inosilicate minerals found in many igneous and metamorphic rocks. Pyroxenes have the general formula XY(Si,Al)₂O₆, where X represents ions of calcium (Ca), sodium (Na), iron (Fe(II)) or magnesium (Mg) and more rarely zinc, manganese or lithium, and Y represents ions of smaller size, such as chromium (Cr), aluminium (Al), magnesium (Mg), cobalt (Co), manganese (Mn), scandium (Sc), titanium (Ti), vanadium (V) or even iron (Fe(II) or Fe(III)). Although aluminium substitutes extensively for silicon in silicates such as feldspars and amphiboles, the substitution occurs only to a limited extent in most pyroxenes. They share a common structure consisting of single chains of silica tetrahedra. Pyroxenes that crystallize in the monoclinic system are known as clinopyroxenes and those that crystallize in the orthorhombic system are known as orthopyroxenes.

The name pyroxene is derived from the Ancient Greek words for 'fire' (πυρ, pur) and 'stranger' (ξένος, xénos). Pyroxenes were so named due to their presence in volcanic lavas, where they are sometimes found as crystals embedded in volcanic glass; it was assumed they were impurities in the glass, hence the name meaning "fire stranger". However, they are simply early-forming minerals that crystallized before the lava erupted.

Anglesite is a lead sulfate mineral with the chemical formula PbSO₄. It occurs as an oxidation product of primary lead sulfide ore, galena. Anglesite occurs as prismatic orthorhombic crystals and earthy masses, and is isomorphous with barite and celestine. It contains 74% of lead by mass and therefore has a high specific gravity of 6.3. Anglesite's color is white or gray with pale yellow streaks. It may be dark gray if impure.

It was first recognized as a mineral species by William Withering in 1783, who discovered it in the Parys copper-mine in Anglesey; the name anglesite, from this locality, was given by F. S. Beudant in 1832. The crystals from Anglesey, which were formerly found abundantly on a matrix of dull limonite, are small in size and simple in form, being usually bounded by four faces of a prism and four faces of a dome; they are brownish-yellow in colour owing to a stain of limonite. Crystals from some other localities, notably from Monteponi [it] in Sardinia, are transparent and colourless, possessed of a brilliant adamantine lustre, and usually modified by numerous bright faces. The variety of combinations and habits presented by the crystals is very extensive, nearly two hundred distinct forms being figured by V. von Lang in his monograph of the species; without measurement of the angles the crystals are frequently difficult to decipher. There are distinct cleavages parallel to the faces of the prism (110) and the basal plane (001), but these are not so well developed as in the isomorphous minerals barite and celestite.

In crystallography, the monoclinic crystal system is one of the seven 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 parallelogram prism. Hence two pairs of vectors are perpendicular (meet at right angles), while the third pair makes an angle other than 90°.

Vaterite is a mineral, a polymorph of calcium carbonate (CaCO₃). It was named after the German mineralogist Heinrich Vater. It is also known as mu-calcium carbonate (μ-CaCO₃). Vaterite belongs to the hexagonal crystal system, whereas calcite is trigonal and aragonite is orthorhombic.

Vaterite, like aragonite, is a metastable phase of calcium carbonate at ambient conditions at the surface of the Earth. As it is less stable than either calcite, the most stable polymorph, or aragonite, vaterite has a higher solubility than either of these phases. Therefore, once vaterite is exposed to water, it converts to calcite (at low temperature) or aragonite (at high temperature: ~60 °C). At 37 °C for example a solution-mediated transition from vaterite to calcite occurs, where the vaterite dissolves and subsequently precipitates as calcite assisted by an Ostwald ripening process.

Boehmite or böhmite is an aluminium oxide hydroxide (γ-AlO(OH)) mineral, a component of the aluminium ore bauxite. It is dimorphous with diaspore. It crystallizes in the orthorhombic dipyramidal system and is typically massive in habit. It is white with tints of yellow, green, brown or red due to impurities. It has a vitreous to pearly luster, a Mohs hardness of 3 to 3.5 and a specific gravity of 3.00 to 3.07. It is colorless in thin section, optically biaxial positive with refractive indices of nα = 1.644 – 1.648, nβ = 1.654 – 1.657 and nγ = 1.661 – 1.668.

Boehmite occurs in tropical laterites and bauxites developed on alumino-silicate bedrock. It also occurs as a hydrothermal alteration product of corundum and nepheline. It occurs with kaolinite, gibbsite and diaspore in bauxite deposits; and with nepheline, gibbsite, diaspore, natrolite and analcime in nepheline pegmatites. Industrially, it is used as an inexpensive flame retardant additive for fire-safe polymers.

Diaspore (/ˈdaɪ.əˌspɔːr/) – also called diasporite, empholite, kayserite, or tanatarite – is an aluminium hydroxide oxide mineral, α-AlO(OH), crystallizing in the orthorhombic system and isomorphous with goethite. It occurs sometimes as flattened crystals, but usually as lamellar or scaly masses, the flattened surface being a direction of perfect cleavage on which the lustre is markedly pearly in character. It is colorless or greyish-white, yellowish, sometimes violet in color, and varies from translucent to transparent. It may be readily distinguished from other colorless transparent minerals with a perfect cleavage and pearly luster (e.g. mica, talc, brucite, and gypsum) by its greater hardness of 6.5–7. Its specific gravity is 3.4. When heated before the blowpipe, it decrepitates violently, breaking up into white pearly scales.

The mineral occurs as an alteration product of corundum or emery and is found in granular limestone and other crystalline rocks. Well-developed crystals are found in the emery deposits of the Ural Mountains and at Chester, Massachusetts, and in kaolin at Schemnitz in Hungary. If obtainable in large quantity, it would be of economic importance as a source of aluminium.

Stibnite, sometimes called antimonite, is a sulfide mineral, a mineral form of antimony trisulfide (Sb₂S₃). It is a soft, metallic grey crystalline solid with an orthorhombic space group. It is the most important source for the metalloid antimony. The name is derived from the Greek στίβι stibi through the Latin stibium as the former name for the mineral and the element antimony.