Specific gravity in the context of Settling basin

Brackish water, sometimes termed brack water, is water occurring in a natural environment that has more salinity than freshwater, but not as much as seawater. It may result from mixing seawater (salt water) and fresh water together, as in estuaries, or it may occur in brackish fossil aquifers. The word comes from the Middle Dutch root brak. Certain human activities can produce brackish water, in particular civil engineering projects such as dikes and the flooding of coastal marshland to produce brackish water pools for freshwater prawn farming. Brackish water is also the primary waste product of the salinity gradient power process. Because brackish water is hostile to the growth of most terrestrial plant species, without appropriate management it can be damaging to the environment (see article on shrimp farms).

Technically, brackish water contains between 0.5 and 30 grams of salt per litre—more often expressed as 0.5 to 30 parts per thousand (‰), which is a specific gravity of between 1.0004 and 1.0226. Thus, brackish covers a range of salinity regimes and is not considered a precisely defined condition. It is characteristic of many brackish surface waters that their salinity can vary considerably over space or time. Water with a salt concentration greater than 30‰ is considered saline.

A hydrometer or lactometer is an instrument used for measuring density or relative density of liquids based on the concept of buoyancy. They are typically calibrated and graduated with one or more scales such as specific gravity.

A hydrometer usually consists of a sealed hollow glass tube with a wider bottom portion for buoyancy, a ballast such as lead or mercury for stability, and a narrow stem with graduations for measuring. The liquid to test is poured into a tall container, often a graduated cylinder, and the hydrometer is gently lowered into the liquid until it floats freely. The point at which the surface of the liquid touches the stem of the hydrometer correlates to relative density. Hydrometers can contain any number of scales along the stem corresponding to properties correlating to the density.

Cinnabar (/ˈsɪnəˌbɑːr/; from Ancient Greek κιννάβαρι (kinnábari)), also called cinnabarite (/ˌsɪnəˈbɑːraɪt/) or mercurblende, is the bright scarlet to brick-red form of mercury(II) sulfide (HgS). It is the most common source ore for refining elemental mercury and is the historic source for the brilliant red or scarlet pigment termed vermilion and associated red mercury pigments.

Cinnabar generally occurs as a vein-filling mineral associated with volcanic activity and alkaline hot springs. The mineral resembles quartz in symmetry and it exhibits birefringence. Cinnabar has a mean refractive index near 3.2, a hardness between 2.0 and 2.5, and a specific gravity of approximately 8.1. The color and properties derive from a structure that is a hexagonal crystalline lattice belonging to the trigonal crystal system, crystals that sometimes exhibit twinning.

In geology, felsic is a modifier describing igneous rocks that are relatively rich in elements that form feldspar and quartz. It is contrasted with mafic rocks, which are richer in magnesium and iron. Felsic refers to silicate minerals, magma, and rocks which are enriched in the lighter elements such as silicon, oxygen, aluminium, sodium, and potassium. Molten felsic magma and lava is more viscous than molten mafic magma and lava. Felsic magmas and lavas have lower temperatures of melting and solidification than mafic magmas and lavas.

Felsic rocks are usually light in color and have specific gravities less than 3. The most common felsic rock is granite. Common felsic minerals include quartz, muscovite, orthoclase, and the sodium-rich plagioclase feldspars (albite-rich).

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.

Chlorargyrite is the mineral form of silver chloride (AgCl). Chlorargyrite occurs as a secondary mineral phase in the oxidation of silver mineral deposits. It crystallizes in the isometric–hexoctahedral crystal class. Typically massive to columnar in occurrence it also has been found as colorless to variably yellow cubic crystals. The color changes to brown or purple on exposure to light. It is quite soft with a Mohs hardness of 1 to 2 and dense with a specific gravity of 5.55. It is also known as cerargyrite and, when weathered by desert air, as horn silver. Bromian chlorargyrite (or embolite) is also common. Chlorargyrite is water-insoluble.

It occurs associated with native silver, cerussite, iodargyrite, atacamite, malachite, jarosite and various iron–manganese oxides.

Scoria or cinder is a pyroclastic, highly vesicular, dark-colored volcanic rock formed by ejection from a volcano as a molten blob and cooled in the air to form discrete grains called clasts. It is typically dark in color (brown, black or purplish-red), and basaltic or andesitic in composition. Scoria has relatively low density, as it is riddled with macroscopic ellipsoidal vesicles (gas bubbles), but in contrast to pumice, scoria usually has a specific gravity greater than 1 and sinks in water. Some scoria can have a specific gravity similar to pumice especially if the vesicles are large and abundant alongside the walls being thin causing it to float. Examples of floating scoria were observed at the Taal Caldera lake in 2023. Scoria from a 1993 undersea eruption near Socorro Island in the Pacific Ocean was observed to float on the ocean surface for up to 15 minutes before it sank.

Scoria may form as part of a lava flow, typically near its surface as a crust, or more commonly as fragmental ejecta (lapilli, volcanic blocks, and volcanic bombs), for instance in Strombolian eruptions that form steep-sided scoria cones, also called cinder cones. Basaltic to andesitic Plinian eruptions can also form scoria like when Taal erupted in 2020 which was of andesitic composition. Scoria's holes or vesicles form when gases dissolved in the original magma come out of solution as it erupts, creating bubbles in the molten rock, some of which are frozen in place as the rock cools and solidifies. Most scoria is composed of glassy fragments and may contain phenocrysts. A sample from Yemen was mainly composed of volcanic glass with a few zeolites (e.g., clinoptilolite).

Mellite, also called honeystone, is an unusual mineral being also an organic chemical. It is chemically identified as an aluminium salt of mellitic acid, and specifically as aluminium benzenehexacarboxylate hexadecahydrate, with the chemical formula Al₂C₆(COO)₆·16H₂O.

It is a translucent honey-coloured crystal which can be polished and faceted to form striking gemstones. It crystallizes in the tetragonal system and occurs both in good crystals and as formless masses. It is soft with a Mohs hardness of 2 to 2.5 and has a low specific gravity of 1.6.

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.

Litharge (from Greek lithargyros, lithos 'stone' + argyros 'silver' λιθάργυρος) is one of the natural mineral forms of lead(II) oxide, PbO. Litharge is a secondary mineral which forms from the oxidation of galena ores. It forms as coatings and encrustations with internal tetragonal crystal structure. It is dimorphous with the yellow orthorhombic form massicot. It forms soft (Mohs hardness of 2), red, greasy-appearing crusts with a very high specific gravity of 9.14–9.35. PbO may be prepared by heating lead metal in air at approximately 600 °C (lead melts at only 300 °C). At this temperature it is also the end product of heating of other lead oxides in air. This is often done with a set of bellows pumping air over molten lead and causing the oxidized product to slip or fall off the top into a receptacle, where it quickly solidifies in minute scales.

Massicot is lead (II) oxide mineral with an orthorhombic lattice structure.Lead(II) oxide (formula: PbO) can occur in one of two lattice formats, orthorhombic and tetragonal. The red tetragonal form is called litharge. PbO can be changed from massicot to litharge (or vice versa) by controlled heating and cooling. At room temperature massicot forms soft (Mohs hardness of 2) yellow to reddish-yellow, earthy, scaley masses which are very dense, with a specific gravity of 9.64. Massicot can be found as a natural mineral, though it is only found in minor quantities. In bygone centuries it was mined. Nowadays massicot arises during industrial processing of lead and lead oxides, especially in the glass industry, which is the biggest user of PbO.

The definition of massicot as orthorhombic PbO dates from the 1840s, but the substance massicot and the name massicot has been in use since the late medieval era. There is some evidence that the ancient Romans used the substance.

Diopside is a monoclinic pyroxene mineral with composition MgCaSi
₂O
₆. It forms complete solid solution series with hedenbergite (FeCaSi
₂O
₆) and augite, and partial solid solutions with orthopyroxene and pigeonite. 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 n_α=1.663–1.699, n_β=1.671–1.705, and n_γ=1.693–1.728. The optic angle is 58° to 63°.

Arsenopyrite (IMA symbol: Apy) is an iron arsenic sulfide (FeAsS). It is a hard (Mohs 5.5–6) metallic, opaque, steel grey to silver white mineral with a relatively high specific gravity of 6.1.

When dissolved in nitric acid, it releases elemental sulfur. When arsenopyrite is heated, it produces sulfur and arsenic vapor. With 46% arsenic content, arsenopyrite, along with orpiment, is a principal ore of arsenic. When deposits of arsenopyrite become exposed to the atmosphere, the mineral slowly converts into iron arsenates. Arsenopyrite is generally an acid-consuming sulfide mineral, unlike iron pyrite which can lead to acid mine drainage.

Muscovite (also known as common mica, isinglass, or potash mica) is a hydrated phyllosilicate mineral of aluminium and potassium with formula KAl₂(AlSi₃O₁₀)(F,OH)₂, or (KF)₂(Al₂O₃)₃(SiO₂)₆(H₂O). It has a highly perfect basal cleavage yielding remarkably thin laminae (sheets) which are often highly elastic. Sheets of muscovite 5 by 3 meters (16.4 ft × 9.8 ft) have been found in Nellore, India.

Muscovite has a Mohs hardness of 2–2.25 parallel to the [001] face, 4 perpendicular to the [001] and a specific gravity of 2.76–3. It can be colorless or tinted through grays, violet or red, and can be transparent or translucent. It is anisotropic and has high birefringence. Its crystal system is monoclinic. The green, chromium-rich variety is called fuchsite; mariposite is also a chromium-rich type of muscovite.

Siderite is a mineral composed of iron(II) carbonate (FeCO₃). Its name comes from the Ancient Greek word σίδηρος (sídēros), meaning "iron". A valuable iron ore, it consists of 48% iron and lacks sulfur and phosphorus. Zinc, magnesium, and manganese commonly substitute for the iron, resulting in the siderite-smithsonite, siderite-magnesite, and siderite-rhodochrosite solid solution series.

Siderite has Mohs hardness of 3.75 to 4.25, a specific gravity of 3.96, a white streak and a vitreous or pearly luster. Siderite is antiferromagnetic below its Néel temperature of 37 K (−236 °C) that can assist in its identification.

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.

Anatase is a metastable mineral form of titanium dioxide (TiO₂) with a tetragonal crystal structure. Although colorless or white when pure, anatase in nature is usually a black solid due to impurities. Three other polymorphs (or mineral forms) of titanium dioxide are known to occur naturally: brookite, akaogiite, and rutile, with rutile being the most common and most stable of the bunch. Anatase is formed at relatively low temperatures and found in minor concentrations in igneous and metamorphic rocks. Glass coated with a thin film of TiO₂ shows antifogging and self-cleaning properties under ultraviolet radiation.

Anatase is always found as small, isolated, and sharply developed crystals, and like rutile, it crystallizes in a tetragonal system. Anatase is metastable at all temperatures and pressures, with rutile being the equilibrium polymorph. Nevertheless, anatase is often the first titanium dioxide phase to form in many processes due to its lower surface energy, with a transformation to rutile taking place at elevated temperatures. Although the degree of symmetry is the same for both anatase and rutile phases, there is no relation between the interfacial angles of the two minerals, except in the prism-zone of 45° and 90°. The common octahedral crystal habit of anatase, with four perfect cleavage planes, has an angle over its polar edge of 82°9', whereas rutile octahedra only has a polar edge angle of 56°52½'. The steeper angle gives anatase crystals a longer vertical axis and skinnier appearance than rutile. Additional important differences exist between the physical characters of anatase and rutile. For example, anatase is less hard (5.5–6 vs. 6–6.5 on the Mohs scale) and less dense (specific gravity about 3.9 vs. 4.2) than rutile. Anatase is also optically negative, whereas rutile is optically positive. Anatase has a more strongly adamantine or metallic-adamantine luster than that of rutile as well.