Portal:Minerals

Magnetite is a mineral and one of the main iron ores, with the chemical formula Fe²⁺Fe3+2O₄. It is one of the oxides of iron, and is ferrimagnetic; it is attracted to a magnet and can be magnetized to become a permanent magnet itself. With the exception of extremely rare native iron deposits, it is the most magnetic of all the naturally occurring minerals on Earth. Naturally magnetized pieces of magnetite, called lodestone, will attract small pieces of iron, which is how ancient peoples first discovered the property of magnetism.

Magnetite is black or brownish-black with a metallic luster, has a Mohs hardness of 5–6 and leaves a black streak. Small grains of magnetite are very common in igneous and metamorphic rocks.

The chemical IUPAC name is iron(II,III) oxide and the common chemical name is ferrous-ferric oxide. (Full article...)

Diamond is a solid form of the element carbon with its atoms arranged in a crystal structure called diamond cubic. Diamond is tasteless, odourless, strong, brittle solid, colourless in pure form, a poor conductor of electricity, and insoluble in water. Another solid form of carbon known as graphite is the chemically stable form of carbon at room temperature and pressure, but diamond is metastable and converts to it at a negligible rate under those conditions. Diamond has the highest hardness and thermal conductivity of any natural material, properties that are used in major industrial applications such as cutting and polishing tools.

Because the arrangement of atoms in diamond is extremely rigid, few types of impurity can contaminate it (two exceptions are boron and nitrogen). Small numbers of defects or impurities (about one per million of lattice atoms) can color a diamond blue (boron), yellow (nitrogen), brown (defects), green (radiation exposure), purple, pink, orange, or red. Diamond also has a very high refractive index and a relatively high optical dispersion.

Most natural diamonds have ages between 1 billion and 3.5 billion years. Most were formed at depths between 150 and 250 kilometres (93 and 155 mi) in the Earth's mantle, although a few have come from as deep as 800 kilometres (500 mi). Under high pressure and temperature, carbon-containing fluids dissolved various minerals and replaced them with diamonds. Much more recently (hundreds to tens of million years ago), they were carried to the surface in volcanic eruptions and deposited in igneous rocks known as kimberlites and lamproites.

Synthetic diamonds can be grown from high-purity carbon under high pressures and temperatures or from hydrocarbon gases by chemical vapor deposition (CVD). Natural and synthetic diamonds are most commonly distinguished using optical techniques or thermal conductivity measurements. (Full article...)

Turquoise is an opaque, blue-to-green mineral that is a hydrous phosphate of copper and aluminium, with the chemical formula CuAl₆(PO₄)₄(OH)₈·4H₂O. It is rare and valuable in finer grades and has been prized as a gemstone for millennia due to its hue.

The robin egg blue or sky blue color of the Persian turquoise mined near the modern city of Nishapur, Iran, has been used as a guiding reference for evaluating turquoise quality.

Like most other opaque gems, turquoise has been devalued by the introduction of treatments, imitations, and synthetics into the market. (Full article...)

Malachite (/ˈmæl.əˌkaɪt/) is a copper carbonate hydroxide mineral, with the formula Cu₂CO₃(OH)₂. This opaque, green-banded mineral crystallizes in the monoclinic crystal system, and most often forms botryoidal, fibrous, or stalagmitic masses, in fractures and deep, underground spaces, where the water table and hydrothermal fluids provide the means for chemical precipitation. Individual crystals are rare, but occur as slender to acicular prisms. Pseudomorphs after more tabular or blocky azurite crystals also occur. (Full article...)

Kaolinite (/ˈkeɪ.ələˌnaɪt, -lɪ-/ KAY-ə-lə-nyte, -⁠lih-; also called kaolin) is a clay mineral, with the chemical composition Al₂Si₂O₅(OH)₄. It is a layered silicate mineral, with one "tetrahedral" sheet of silicate tetrahedrons (SiO₄) linked to one "octahedral" sheet of aluminate octahedrons (AlO₂(OH)₄) through oxygen atoms on one side, and another such sheet through hydrogen bonds on the other side.

Kaolinite is a soft, earthy, usually white, mineral (dioctahedral phyllosilicate clay), produced by the chemical weathering of aluminium silicate minerals like feldspar. It has a low shrink–swell capacity and a low cation-exchange capacity (1–15 meq/100 g).

Rocks that are rich in kaolinite, and halloysite, are known as kaolin (/ˈkeɪ.əlɪn/) or china clay. In many parts of the world kaolin is colored pink-orange-red by iron oxide, giving it a distinct rust hue. Lower concentrations of iron oxide yield the white, yellow, or light orange colors of kaolin. Alternating lighter and darker layers are sometimes found, as at Providence Canyon State Park in Georgia, United States.

Kaolin is an important raw material in many industries and applications. Commercial grades of kaolin are supplied and transported as powder, lumps, semi-dried noodle or slurry. Global production of kaolin in 2021 was estimated to be 45 million tonnes, with a total market value of US $4.24 billion. (Full article...)

Beryl (/ˈbɛrəl/ BERR-əl) is a mineral composed of beryllium aluminium silicate with the chemical formula Be₃Al₂(SiO₃)₆. Well-known varieties of beryl include emerald and aquamarine. Naturally occurring hexagonal crystals of beryl can be up to several meters in size, but terminated crystals are relatively rare. Pure beryl is colorless, but it is frequently tinted by impurities; possible colors are green, blue, yellow, pink, and red (the rarest). It is an ore source of beryllium. (Full article...)

Zeolites are a group of several microporous, crystalline aluminosilicate minerals commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula Mⁿ⁺
_1/n(AlO
₂)⁻
(SiO
₂)
_x･yH
₂O where Mⁿ⁺
_1/n is either a metal ion or H⁺.

The term was originally coined in 1756 by Swedish mineralogist Axel Fredrik Cronstedt, who observed that rapidly heating a material, believed to have been stilbite, produced large amounts of steam from water that had been adsorbed by the material. Based on this, he called the material zeolite, from the Greek ζέω (zéō), meaning "to boil" and λίθος (líthos), meaning "stone".

Zeolites occur naturally, but are also produced industrially on a large scale. As of December 2018^[update], 253 unique zeolite frameworks have been identified, and over 40 naturally occurring zeolite frameworks are known. Every new zeolite structure that is obtained is examined by the International Zeolite Association Structure Commission (IZA-SC) and receives a three-letter designation. (Full article...)

In crystallography, crystal structure is a description of the ordered arrangement of atoms, ions, or molecules in a crystalline material. Ordered structures occur from the intrinsic nature of constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.

The smallest group of particles in a material that constitutes this repeating pattern is the unit cell of the structure. The unit cell completely reflects the symmetry and structure of the entire crystal, which is built up by repetitive translation of the unit cell along its principal axes. The translation vectors define the nodes of the Bravais lattice.

The lengths of principal axes/edges, of the unit cell and angles between them are lattice constants, also called lattice parameters or cell parameters. The symmetry properties of a crystal are described by the concept of space groups. All possible symmetric arrangements of particles in three-dimensional space may be described by 230 space groups.

The crystal structure and symmetry play a critical role in determining many physical properties, such as cleavage, electronic band structure, and optical transparency. (Full article...)

Dolomite (/ˈdɒl.əˌmaɪt, ˈdoʊ.lə-/) is an anhydrous carbonate mineral composed of calcium magnesium carbonate, ideally CaMg(CO₃)₂. The term is also used for a sedimentary carbonate rock composed mostly of the mineral dolomite (see Dolomite (rock)). An alternative name sometimes used for the dolomitic rock type is dolostone. (Full article...)

Fluorite (also called fluorspar) is the mineral form of calcium fluoride, CaF₂. It belongs to the halide minerals. It crystallizes in isometric cubic habit, although octahedral and more complex isometric forms are not uncommon.

The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 4 as fluorite.

Pure fluorite is colourless and transparent, both in visible and ultraviolet light, but impurities usually make it a colorful mineral and the stone has ornamental and lapidary uses. Industrially, fluorite is used as a flux for smelting, and in the production of certain glasses and enamels. The purest grades of fluorite are a source of fluoride for hydrofluoric acid manufacture, which is the intermediate source of most fluorine-containing fine chemicals. Optically clear transparent fluorite has anomalous partial dispersion, that is, its refractive index varies with the wavelength of light in a manner that differs from that of commonly used glasses, so fluorite is useful in making apochromatic lenses, and particularly valuable in photographic optics. Fluorite optics are also usable in the far-ultraviolet and mid-infrared ranges, where conventional glasses are too opaque for use. Fluorite also has low dispersion, and a high refractive index for its density. (Full article...)

Sapphire is a precious gemstone, a variety of the mineral corundum, consisting of aluminium oxide (α-Al₂O₃) with trace amounts of elements such as iron, titanium, cobalt, lead, chromium, vanadium, magnesium, boron, and silicon. The name sapphire is derived from the Latin word sapphirus, itself from the Greek word sappheiros (σάπφειρος), which referred to lapis lazuli. It is typically blue, but natural "fancy" sapphires also occur in yellow, purple, orange, and green colors; "parti sapphires" show two or more colors. Red corundum stones also occur, but are called rubies rather than sapphires. Pink-colored corundum may be classified either as ruby or sapphire depending on the locale. Commonly, natural sapphires are cut and polished into gemstones and worn in jewelry. They also may be created synthetically in laboratories for industrial or decorative purposes in large crystal boules. Because of the remarkable hardness of sapphires – 9 on the Mohs scale (the third-hardest mineral, after diamond at 10 and moissanite at 9.5) – sapphires are also used in some non-ornamental applications, such as infrared optical components, high-durability windows, wristwatch crystals and movement bearings, and very thin electronic wafers, which are used as the insulating substrates of special-purpose solid-state electronics such as integrated circuits and GaN-based blue LEDs. It occurs in assocation with ruby, zircon, biotite, muscovite, calcite, dravite and quartz. (Full article...)

Zircon (/ˈzɜːrkɒn, -kən/) is a mineral belonging to the group of nesosilicates and is a source of the metal zirconium. Its chemical name is zirconium(IV) silicate, and its corresponding chemical formula is ZrSiO₄. An empirical formula showing some of the range of substitution in zircon is (Zr_1–y, REE_y)(SiO₄)_1–x(OH)_4x–y. Zircon precipitates from silicate melts and has relatively high concentrations of high field strength incompatible elements. For example, hafnium is almost always present in quantities ranging from 1 to 4%. The crystal structure of zircon is tetragonal crystal system. The natural color of zircon varies between colorless, yellow-golden, red, brown, blue, and green.

The name derives from the Persian zargun, meaning "gold-hued". This word is changed into "jargoon", a term applied to light-colored zircons. The English word "zircon" is derived from Zirkon, which is the German adaptation of this word. Yellow, orange, and red zircon is also known as "hyacinth", from the flower hyacinthus, whose name is of Ancient Greek origin. (Full article...)

Quartz is a hard, crystalline mineral composed of silica (silicon dioxide). The atoms are linked in a continuous framework of SiO₄ silicon–oxygen tetrahedra, with each oxygen being shared between two tetrahedra, giving an overall chemical formula of SiO₂. Quartz is, therefore, classified structurally as a framework silicate mineral and compositionally as an oxide mineral. Quartz is the second most abundant mineral in Earth's continental crust, behind feldspar.

Quartz exists in two forms, the normal α-quartz and the high-temperature β-quartz, both of which are chiral. The transformation from α-quartz to β-quartz takes place abruptly at 573 °C (846 K; 1,063 °F). Since the transformation is accompanied by a significant change in volume, it can easily induce microfracturing of ceramics or rocks passing through this temperature threshold.

There are many different varieties of quartz, several of which are classified as gemstones. Since antiquity, varieties of quartz have been the most commonly used minerals in the making of jewelry and hardstone carvings, especially in Europe and Asia.

Quartz is the mineral defining the value of 7 on the Mohs scale of hardness, a qualitative scratch method for determining the hardness of a material to abrasion. (Full article...)

Borax (also referred to as sodium borate, tincal (/ˈtɪŋkəl/) and tincar (/ˈtɪŋkər/)) is a salt (ionic compound) normally encountered as a hydrated borate of sodium, with the chemical formula Na₂H₂₀B₄O₁₇. Borax mineral is a crystalline borate mineral that occurs in only a few places worldwide in quantities that enable it to be mined economically.

Borax can be dehydrated by heating into other forms with less water of hydration. The anhydrous form of borax can also be obtained from the decahydrate or other hydrates by heating and then grinding the resulting glasslike solid into a powder. It is a white crystalline solid that dissolves in water to make a basic solution due to the tetraborate anion.

Borax is commonly available in powder or granular form and has many industrial and household uses, including as a pesticide, as a metal soldering flux, as a component of glass, enamel, and pottery glazes, for tanning of skins and hides, for artificial aging of wood, as a preservative against wood fungus, as a food additive, and as a pharmaceutic alkalizer. In chemical laboratories it is used as a buffering agent.

The terms tincal and tincar refer to the naturally-occurring borax historically mined from dry lake beds in various parts of Asia. (Full article...)

Andesite (/ˈændəzaɪt/) is a volcanic rock of intermediate composition. In a general sense, it is the intermediate type between silica-poor basalt and silica-rich rhyolite. It is fine-grained (aphanitic) to porphyritic in texture, and is composed predominantly of sodium-rich plagioclase plus pyroxene or hornblende.

Andesite is the extrusive equivalent of plutonic diorite. Characteristic of subduction zones, andesite represents the dominant rock type in island arcs. The average composition of the continental crust is andesitic. Along with basalts, andesites are a component of the Martian crust.

The name andesite is derived from the Andes mountain range, where this rock type is found in abundance. It was first applied by Christian Leopold von Buch in 1826. (Full article...)

Crystallography is the branch of science devoted to the study of molecular and crystalline structure and properties. The word crystallography is derived from the Ancient Greek word κρύσταλλος (krústallos; "clear ice, rock-crystal"), and γράφειν (gráphein; "to write"). In July 2012, the United Nations recognised the importance of the science of crystallography by proclaiming 2014 the International Year of Crystallography.

Crystallography is a broad topic, and many of its subareas, such as X-ray crystallography, are themselves important scientific topics. Crystallography ranges from the fundamentals of crystal structure to the mathematics of crystal geometry, including those that are not periodic or quasicrystals. At the atomic scale it can involve the use of X-ray diffraction to produce experimental data that the tools of X-ray crystallography can convert into detailed positions of atoms, and sometimes electron density. At larger scales it includes experimental tools such as orientational imaging to examine the relative orientations at the grain boundary in materials. Crystallography plays a key role in many areas of biology, chemistry, and physics, as well new developments in these fields. (Full article...)

In crystallography, the cubic (or isometric) crystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals.

There are three main varieties of these crystals:

• Primitive cubic (abbreviated cP and alternatively called simple cubic)
• Body-centered cubic (abbreviated cI or bcc)
• Face-centered cubic (abbreviated cF or fcc)

Note: the term fcc is often used in synonym for the cubic close-packed or ccp structure occurring in metals. However, fcc stands for a face-centered cubic Bravais lattice, which is not necessarily close-packed when a motif is set onto the lattice points. E.g. the diamond and the zincblende lattices are fcc but not close-packed.
Each is subdivided into other variants listed below. Although the unit cells in these crystals are conventionally taken to be cubes, the primitive unit cells often are not. (Full article...)

Cleavage, in mineralogy and materials science, is the tendency of crystalline materials to split along definite crystallographic structural planes. These planes of relative weakness are a result of the regular locations of atoms and ions in the crystal, which create smooth repeating surfaces that are visible both in the microscope and to the naked eye. If bonds in certain directions are weaker than others, the crystal will tend to split along the weakly bonded planes. These flat breaks are termed "cleavage". The classic example of cleavage is mica, which cleaves in a single direction along the basal pinacoid, making the layers seem like pages in a book. In fact, mineralogists often refer to "books of mica".

Diamond and graphite provide examples of cleavage. Each is composed solely of a single element, carbon. In diamond, each carbon atom is bonded to four others in a tetrahedral pattern with short covalent bonds. The planes of weakness (cleavage planes) in a diamond are in four directions, following the faces of the octahedron. In graphite, carbon atoms are contained in layers in a hexagonal pattern where the covalent bonds are shorter (and thus even stronger) than those of diamond. However, each layer is connected to the other with a longer and much weaker van der Waals bond. This gives graphite a single direction of cleavage, parallel to the basal pinacoid. So weak is this bond that it is broken with little force, giving graphite a slippery feel as layers shear apart. As a result, graphite makes an excellent dry lubricant.

While all single crystals will show some tendency to split along atomic planes in their crystal structure, if the differences between one direction or another are not large enough, the mineral will not display cleavage. Corundum, for example, displays no cleavage. (Full article...)

Galena, also called lead glance, is the natural mineral form of lead(II) sulfide (PbS). It is the most important ore of lead and an important source of silver.

Galena is one of the most abundant and widely distributed sulfide minerals. It crystallizes in the cubic crystal system often showing octahedral forms. It is often associated with the minerals sphalerite, calcite and fluorite.

As a pure specimen held in the hand, under standard temperature and pressure, galena is insoluble in water and so is almost non-toxic. Handling galena under these specific conditions (such as in a museum or as part of geology instruction) poses practically no risk; however, as lead(II) sulfide is reasonably reactive in a variety of environments, it can be highly toxic if swallowed or inhaled, particularly under prolonged or repeated exposure. (Full article...)

Mineralogy is a subject of geology specializing in the scientific study of the chemistry, crystal structure, and physical (including optical) properties of minerals and mineralized artifacts. Specific studies within mineralogy include the processes of mineral origin and formation, classification of minerals, their geographical distribution, as well as their utilization. (Full article...)

Apatite is a group of phosphate minerals, usually hydroxyapatite, fluorapatite and chlorapatite, with high concentrations of OH⁻, F⁻ and Cl⁻ ion, respectively, in the crystal. The formula of the admixture of the three most common endmembers is written as Ca₁₀(PO₄)₆(OH,F,Cl)₂, and the crystal unit cell formulae of the individual minerals are written as Ca₁₀(PO₄)₆(OH)₂, Ca₁₀(PO₄)₆F₂ and Ca₁₀(PO₄)₆Cl₂.

The mineral was named apatite by the German geologist Abraham Gottlob Werner in 1786, although the specific mineral he had described was reclassified as fluorapatite in 1860 by the German mineralogist Karl Friedrich August Rammelsberg. Apatite is often mistaken for other minerals. This tendency is reflected in the mineral's name, which is derived from the Greek word ἀπατάω (apatáō), which means to deceive. (Full article...)

Halite (/ˈhælaɪt, ˈheɪlaɪt/ HAL-yte, HAY-lyte), commonly known as rock salt, is a type of salt, the mineral (natural) form of sodium chloride (NaCl). Halite forms isometric crystals. The mineral is typically colorless or white, but may also be light blue, dark blue, purple, pink, red, orange, yellow or gray depending on inclusion of other materials, impurities, and structural or isotopic abnormalities in the crystals. It commonly occurs with other evaporite deposit minerals such as several of the sulfates, halides, and borates. The name halite is derived from the Ancient Greek word for "salt", ἅλς (háls). (Full article...)

Ruby is a pinkish-red-to-blood-red-colored gemstone, a variety of the mineral corundum (aluminium oxide). Ruby is one of the most popular traditional jewelry gems and is very durable. Other varieties of gem-quality corundum are called sapphires; given that the rest of the corundum species are called as such, rubies are sometimes referred to as "red sapphires".

Ruby is one of the traditional cardinal gems, alongside amethyst, sapphire, emerald, and diamond. The word ruby comes from ruber, Latin for red. The color of a ruby is due to the presence of chromium.

Some gemstones that are popularly or historically called rubies, such as the Black Prince's Ruby in the British Imperial State Crown, are actually spinels. These were once known as "Balas rubies".

The quality of a ruby is determined by its color, cut, and clarity, which, along with carat weight, affect its value. The brightest and most valuable shade of red, called blood-red or pigeon blood, commands a large premium over other rubies of similar quality. After color comes clarity: similar to diamonds, a clear stone will command a premium, but a ruby without any needle-like rutile inclusions may indicate that the stone has been treated. Ruby is the traditional birthstone for July and is usually pinker than garnet, although some rhodolite garnets have a similar pinkish hue to most rubies. The world's most valuable ruby to be sold at auction is the Estrela de Fura, which sold for US$34.8 million. (Full article...)

Talc, or talcum, is a clay mineral composed of hydrated magnesium silicate, with the chemical formula Mg₃Si₄O₁₀(OH)₂. Talc in powdered form, often combined with corn starch, is used as baby powder. This mineral is used as a thickening agent and lubricant. It is an ingredient in ceramics, paints, and roofing material. It is a main ingredient in many cosmetics. It occurs as foliated to fibrous masses, and in an exceptionally rare crystal form. It has a perfect basal cleavage and an uneven flat fracture, and it is foliated with a two-dimensional platy form.

The Mohs scale of mineral hardness, based on scratch hardness comparison, defines value 1 as the hardness of talc, the softest mineral. When scraped on a streak plate, talc produces a white streak, though this indicator is of little importance, because most silicate minerals produce a white streak. Talc is translucent to opaque, with colors ranging from whitish grey to green with a vitreous and pearly luster. Talc is not soluble in water, and is slightly soluble in dilute mineral acids.

Soapstone is a metamorphic rock composed predominantly of talc. (Full article...)

Tourmaline (/ˈtʊərməlɪn, -ˌliːn/ ^ⓘ TOOR-mə-lin, -⁠leen) is a crystalline silicate mineral group in which boron is compounded with elements such as aluminium, iron, magnesium, sodium, lithium, or potassium. This gemstone comes in a wide variety of colors.

The name is derived from the Sinhalese tōramalli (ටෝරමල්ලි), which refers to the carnelian gemstones. (Full article...)

Karl August Lossen (born Kreuznach (Rhineland), 5 January 1841; died Berlin, 24 February 1893) was a German petrologist and geologist.

After finishing his studies at the gymnasium of Kreuznach in 1859 Lossen became a mining engineer; he began by two and a half years of practical work, then studied at the Universities of Berlin and Halle, where he graduated in 1866; in the same year he became assistant geologist of the Prussian national geological survey. He began immediately his well-known petrolographic studies of the Harz Mountains, which lasted till his death. In 1870 he became instructor in petrology at the Berlin mining academy, and at the same time lecturer at the university. In 1873, he was made a member of the newly founded Prussian National Geological Institute, and in 1882 received the title of professor; he was a fellow of the Görres Society from its foundation. In 1886, he became an associate professor in the university. (Full article...)

Alexander Filippovich Postels (Russian: Александр Филиппович Постельс; 24 August 1801 in Dorpat – 28 June 1871 in Vyborg) was a Russian naturalist, mineralogist and artist of Baltic German descent. (Full article...)

Félix Pisani (28 April 1831 in Constantinople – 7 November 1920 in Paris) was a French chemist and mineralogist.

He was born in Istanbul, where his Venetian father worked in the Russian diplomatic service. Beginning in 1854, he studied chemistry in Paris at a private school run by Charles Frédéric Gerhardt (1816–1856). (Full article...)

Franz-Joseph Müller, Freiherr von Reichenstein or Franz-Joseph Müller von Reichenstein (1 July 1740 or 4 October 1742 – 12 October 1825 or 1826) was an Austrian mineralogist and mining engineer. Müller held several positions in the Habsburg monarchy administration of mines and coinage in the Banat, Transylvania, and Tyrol. During his time in Transylvania he discovered tellurium in 1782. In his later career he became a member of the imperial council in Vienna and was knighted and elevated to the rank Freiherr in 1820. (Full article...)

Karl Friedrich August Rammelsberg (1 April 1813 – 28 December 1899) was a German mineralogist from Berlin, Prussia. (Full article...)

Clifford Howard Stockwell (September 26, 1897 – April 26, 1987) was a Canadian geologist, who published many scientific papers, reports and memoirs in the fields of Mineralogy, Structural Geology, Petrology, and Stratigraphy. He earned his PhD in geology at McGill University in Montreal in 1926. (Full article...)

Baron Jöns Jacob Berzelius (Swedish: [jœns ˈjɑ̌ːkɔb bæˈʂěːlɪɵs]; 20 August 1779 – 7 August 1848) was a Swedish chemist. Berzelius is considered, along with Robert Boyle, John Dalton, and Antoine Lavoisier, to be one of the founders of modern chemistry. Berzelius became a member of the Royal Swedish Academy of Sciences in 1808 and served from 1818 as its principal functionary. He is known in Sweden as the "Father of Swedish Chemistry". During his lifetime he did not customarily use his first given name, and was universally known simply as Jacob Berzelius.

Although Berzelius began his career as a physician, his enduring contributions were in the fields of electrochemistry, chemical bonding and stoichiometry. In particular, he is noted for his determination of atomic weights and his experiments that led to a more complete understanding of the principles of stoichiometry, which is the branch of chemistry pertaining to the quantitative relationships between elements in chemical compounds and chemical reactions and that these occur in definite proportions. This understanding came to be known as the "Law of Constant Proportions". (Full article...)

Ernst Heinrich Oskar Kasimir Weinschenk (6 April 1865, Esslingen am Neckar – 26 March 1921, Munich) was a German mineralogist and petrologist.

He served as a professor at the "Technische Hochschule" in Munich (1897–1921) and at the University of Munich (from 1900). His scientific research included mineralogical analysis of meteorites, and studies of contact-metamorphic mineralization in the Alpine region of central Europe. He also conducted investigations on the origin of the sulfidic ore deposit at Silberberg in the Bavarian Forest, as well as the genesis of graphite deposits near Passau. Through the use of polarizing microscopy and thin sectioning, he determined numerous new minerals. (Full article...)

Paul Niggli (26 June 1888 – 13 January 1953) was a Swiss crystallographer, mineralogist, and petrologist who was a leader in the field of X-ray crystallography. (Full article...)

Enrico Clerici (15 October 1862 – 26 August 1938) was an Italian mineralogist and geologist. From 1903 on he worked at the University of Rome. He published in 1907 the composition of a solution with a density of 4.25 g/cm³ at 20 °C, to determine the density of minerals. The Clerici solution is a mixture of thallium formate (Tl(CHO₂)) and thallium malonate (Tl(C₃H₃O₄)) in water. (Full article...)

Quintino Sella (Italian pronunciation: [kwinˈtino ˈsɛlla]; 7 July 1827 – 14 March 1884) was an Italian politician, economist and mountaineer. (Full article...)

John Scouler (31 December 1804 – 13 November 1871) was a Scottish naturalist. (Full article...)

Auguste Michel-Lévy (7 August 1844 – 27 September 1911) was a French geologist. He was born in Paris. (Full article...)

Carl Friedrich Christian Mohs (/moʊz/ MOHZ, German: [ˈfʁiːdʁɪç ˈmoːs]; 29 January 1773 – 29 September 1839) was a German chemist and mineralogist. He was the creator of the Mohs scale of mineral hardness. Mohs also introduced a classification of the crystal forms in crystal systems independently of Christian Samuel Weiss. (Full article...)

Johan Gadolin (5 June 1760 – 15 August 1852) was a Finnish chemist, physicist and mineralogist. Gadolin discovered a "new earth" containing the first rare-earth compound yttrium, which was later determined to be a chemical element. He is also considered the founder of Finnish chemistry research, as the second holder of the Chair of Chemistry at the Royal Academy of Turku (or Åbo Kungliga Akademi). Gadolin was ennobled for his achievements and awarded the Order of Saint Vladimir and the Order of Saint Anna. (Full article...)

William Babington FRS FGS (21 May 1756 – 29 April 1833) was an Anglo-Irish physician and mineralogist. (Full article...)

Antonio D'Achiardi (28 November 1839, in Pisa – 10 December 1902, in Pisa) was an Italian geologist, paleontologist and mineralogist known for his mineralogical and paleontological studies of Tuscany. He was the father of the mineralogist Giovanni D'Achiardi [it], and the artist, Pietro D'Achiardi.

In 1859 he received his doctorate in sciences from the University of Pisa, afterwards working as an assistant for chemistry (from 1861). Three months after this appointment, he lost the use of his left eye due to a laboratory accident involving nitric acid. He subsequently abandoned his career in chemistry, and instead devoted his attention to geology and mineralogy, becoming a student of Giuseppe Meneghini. He later became a professor of geology at Pavia and in 1874 was appointed a professor of mineralogy at the University of Pisa. In 1881 he established a laboratory of mineralogy at Pisa. (Full article...)

Sir William Lawrence Bragg (31 March 1890 – 1 July 1971) was an Australian-born British physicist who shared the 1915 Nobel Prize in Physics with his father William Henry Bragg "for their services in the analysis of crystal structure by means of X-rays", an important step in the development of X-ray crystallography.

As of 2024, he is the youngest ever Nobel laureate in physics, or in any science category, having received the award at the age of 25. Bragg was the director of the Cavendish Laboratory, Cambridge, when James D. Watson and Francis Crick reported the discovery of the structure of DNA in February 1953. (Full article...)

William James Lewis F.R.S. (10 January 1847 – 16 April 1926) was a Welsh mineralogist. (Full article...)

W. Gary Ernst (born December 14, 1931) is an American geologist specializing in petrology and geochemistry. He currently is the Benjamin M. Page Professor Emeritus in Stanford University's department of geological sciences. (Full article...)

Sarah Mawe (1767-1846) was an English mineralogist of the 19th century, appointed to serve Queen Victoria in that capacity from 1837 to 1840. (Full article...)

Leopold Heinrich Fischer (19 December 1817, Fribourg-en-Brisgau – 2 February 1886, Fribourg-en-Brisgau) was a German zoologist and mineralogist. (Full article...)

Andrew Ketcham Barnett (1852–1914) was a mineral collector and dealer in Penzance, Cornwall, in the United Kingdom. He was Principal of the Penzance School of Mines (now part of the Camborne School of Mines), lectured on mining, and helped to build their mineral collection. He also served as Mayor of Penzance on seven occasions from 1906 to 1913.

Cooper writes of him:
:"Barnett was born in Chacewater, Cornwall in 1852. He was an original member of the Mineralogical Society, a Fellow of the Geological Society from 1875, and President of the Royal Geological Society of Cornwall 1907–08, having been awarded their Bolitho Medal in 1906. His classes on mineralogy in 1873 led to the establishment of the Mining and Science School at Penzance of which he became Principal. He was mayor of Penzance seven times from 1906 to 1913. Active as a mineral dealer from at least 1876 to 1887 at Chyandour, Penzance, he specialized in local specimens and occasionally sold minerals brought back from Australia by "Cousin Jack." In the 1881 Census he described himself as an assayer. He is the author of the now-rare Elementary Inorganic Chemistry; lecture notes, ca. 1900." (Full article...)

Rodney Charles Ewing (September 20, 1946 – July 13, 2024) was an American mineralogist, a materials scientist and a nuclear safety expert whose research was focused on the properties of nuclear materials exposed to radiation and long-term geochemical alterations expected for radioactive waste disposal.

He was the Frank Stanton Professor in Nuclear Security at the Center for International Security and Cooperation, a Senior Fellow of the Freeman Spogli Institute for International Studies, a Senior Fellow of the Precourt Institute for Energy, an Affiliate of the Stanford Woods Institute for the Environment, and a professor in the School of Earth, Energy and Environmental Sciences at Stanford University. (Full article...)

Frank Charles Schrader (October 6, 1860 – April 1944) was an American geologist, mineralogist, and entomologist.

Born in Sterling, Illinois he received degrees from the University of Kansas (BS and MS) and Harvard University (BA and MA), before teaching at Harvard. (Full article...)