Kasolite | |
---|---|
General | |
Category | Mineral |
Formula (repeating unit) | Pb(UO2)(SiO4) · H2O |
IMA symbol | Kso |
Strunz classification | 09.AK.15 |
Dana classification | 53.03.01.01 |
Crystal system | Monoclinic |
Crystal class | Prismatic H-M symbol: 2/m |
Space group | P 21/a |
Unit cell | 596.48 |
Identification | |
Formula mass | 587.33 |
Color | Reddish orange, yellow, yellow brown, green, gray green |
Cleavage | Perfect on {001} Good on {010}, {100} |
Fracture | Uneven |
Tenacity | Brittle |
Mohs scale hardness | 4 - 5 |
Luster | Resinous, Greasy |
Streak | Light brownish yellow |
Diaphaneity | Transparent, translucent, opaque |
Specific gravity | 5.83 - 6.5 |
Density | Measured: 5.83 - 6.5 Calculated: 6.256 |
Optical properties | Biaxial (+) |
Refractive index | nα = 1.890 nβ = 1.910 nγ = 1.950 |
Birefringence | 0.060 |
Pleochroism | Weak X =Y = Pale yellow Z = Colorless to slightly grayish |
2V angle | Measured: 43° Calculated: 72° |
Dispersion | Strong |
Ultraviolet fluorescence | Radioactive |
Common impurities | As, P, Ba, Fe, Mg, Ca |
Other characteristics | Radioactive |
Kasolite is an uncommon lead uranyl silicate monohydrate mineral. It is an IMA approved mineral, that had been a valid species before the foundation of the association, that had been first described and published in 1921 by Schoep. It is a grandfathered mineral, meaning the name kasolite is still believed to refer to a valid species to this day. The mineral's name originates from its type locality, namely the Shinkolobwe Mine, also known as Kasolo Mine. Kasolite is possibly the lead analogue of the unnamed phase UM1956-02-SiO:CaHU, and it is the only accepted lead-uranium silicate. [1]
Kasolite occurs in prismatic, lath-like crystals. It typically forms either clusters of radial acicular crystals, [2] microcrystals, or a coating on top of the altered specimens. [3] Individual crystals can grow up to a few millimeters. [4] Massive specimens tend to have a dull to earthy luster. Kasolite is a weakly pleochroic mineral, which is an optical phenomenon. The mineral's color seems to be changing depending on the axis it is inspected on. On the X and Y axes, it appears in a pale yellow color, while on the Z, it can have a colorless to slightly grayish coloration. [1]
Kasolite mainly consists of uranium (40.53%), lead (35.28%) and oxygen (19.07%), but otherwise contains silicon (4.78%) and a small amount of hydrogen (0.34%). It has a very strong, 2,893,809.61 radioactivity measured in Gamma Ray American Petroleum Institute Units caused by its uranium concentration. [2] Typically it can have arsenic, potassium, barium, iron, magnesium and calcium impurities. The crystal structure has a strong hydrogen bonding, where the water molecules are distributed in pairs, [1] held together by two symmetrically related hydrogen bonds. It is further described to have formed from uranyl silicate layers having the uranophane sheet anion-topology. Water molecules are in the lead interlayer ions' coordination structure and reinforce it with hydrogen bonding between the uranyl silicate sheets. Its crystal structure is described as mechanically stable and very isotropic, which is unexpected as layered structures tend to be very anisotropic. Its large mechanical isotropy can be explained due to the strong dual hydrogen bonding between the uranyl silicate sheets. Because of the hydrogen bonding, the bonding strength along the direction perpendicular to sheets and that along the other directions are similar. [5]
Carbonate and fluoride complexes play a major role in the formation of the mineral. Hydrothermal solutions reacting with uranium-bearing metamictized minerals form uranous fluoride complexes. These complexes are predominant at pH 4 and in reducing atmosphere. As the fluids pass through fractures, approaching the surface, the pH and the oxygen fugacity increases due to the loss of volatile components. Under these conditions, the uranous fluorides go through metamorphosis, becoming uranyl fluoride complexes. The fluorine ion activity decays due to the precipitation of fluorite and the dilution of the hydrothermal solutions, which both contribute to temperature decrease. When these conditions meet, uranyl-carbonate complexes are favored, which, when they combine with lead and silica, form kasolite. As lead is neither radiogenic nor a uranium substitute, the source of lead in the mineral structure might originate from galena's mineralization. [6]
Kasolite is an oxidation product of uraninite. [4] This is the reason why it can usually be found in oxidized uranium deposits. [3] In Kasolo, Congo, the mineral occurs in association with torbernite, curite, dewindtite and uraninite, and in Nabarlek, Australia, it can be found in association with rutherfordine, sklodowskite and curite as well. The top distributors of the mineral are Congo, Gabon, Germany, England, France, Australia, Canada, Mexico and the United States, however, there are numerous minor distributors as well. [4]
Kaolinite ( KAY-ə-lə-nyte, -lih-) is a clay mineral, with the chemical composition Al2Si2O5(OH)4. It is a layered silicate mineral, with one tetrahedral sheet of silica (SiO4) linked through oxygen atoms to one octahedral sheet of alumina (AlO6) octahedra.
In geology and mineralogy, a mineral or mineral species is, broadly speaking, a solid substance with a fairly well-defined chemical composition and a specific crystal structure that occurs naturally in pure form.
Coffinite is a uranium-bearing silicate mineral with formula: U(SiO4)1−x(OH)4x.
Torbernite, also known as chalcolite, is a relatively common mineral with the chemical formula Cu[(UO2)(PO4)]2(H2O)12. It is a radioactive, hydrated green copper uranyl phosphate, found in granites and other uranium-bearing deposits as a secondary mineral. The chemical formula of torbernite is similar to that of autunite in which a Cu2+ cation replaces a Ca2+ cation. Torbernite tends to dehydrate to metatorbernite with the sum formula Cu[(UO2)(PO4)]2(H2O)8.
Afwillite is a calcium hydroxide nesosilicate mineral with formula Ca3(SiO3OH)2·2H2O. It occurs as glassy, colorless to white prismatic monoclinic crystals. Its Mohs scale hardness is between 3 and 4. It occurs as an alteration mineral in contact metamorphism of limestone. It occurs in association with apophyllite, natrolite, thaumasite, merwinite, spurrite, gehlenite, ettringite, portlandite, hillebrandite, foshagite, brucite and calcite.
Hydrogen fluoride (fluorane) is an inorganic compound with chemical formula HF. It is a very poisonous, colorless gas or liquid that dissolves in water to yield an aqueous solution termed hydrofluoric acid. It is the principal industrial source of fluorine, often in the form of hydrofluoric acid, and is an important feedstock in the preparation of many important compounds including pharmaceuticals and polymers, e.g. polytetrafluoroethylene (PTFE). HF is also widely used in the petrochemical industry as a component of superacids. Due to strong and extensive hydrogen bonding, it boils at near room temperature, much higher than other hydrogen halides.
The uranyl ion is an oxycation of uranium in the oxidation state +6, with the chemical formula UO2+
2. It has a linear structure with short U–O bonds, indicative of the presence of multiple bonds between uranium and oxygen. Four or more ligands may be bound to the uranyl ion in an equatorial plane around the uranium atom. The uranyl ion forms many complexes, particularly with ligands that have oxygen donor atoms. Complexes of the uranyl ion are important in the extraction of uranium from its ores and in nuclear fuel reprocessing.
Uranyl peroxide or uranium peroxide hydrate (UO4·nH2O) is a pale-yellow, soluble peroxide of uranium. It is found to be present at one stage of the enriched uranium fuel cycle and in yellowcake prepared via the in situ leaching and resin ion exchange system. This compound, also expressed as UO3·(H2O2)·(H2O), is very similar to uranium trioxide hydrate UO3·nH2O. The dissolution behaviour of both compounds are very sensitive to the hydration state (n can vary between 0 and 4). One main characteristic of uranium peroxide is that it consists of small needles with an average AMAD of about 1.1 μm.
Uranium compounds are compounds formed by the element uranium (U). Although uranium is a radioactive actinide, its compounds are well studied due to its long half-life and its applications. It usually forms in the +4 and +6 oxidation states, although it can also form in other oxidation states.
A chemical compound is a chemical substance composed of many identical molecules containing atoms from more than one chemical element held together by chemical bonds. A molecule consisting of atoms of only one element is therefore not a compound. A compound can be transformed into a different substance by a chemical reaction, which may involve interactions with other substances. In this process, bonds between atoms may be broken and/or new bonds formed.
Uranyl carbonate refers to the inorganic compound with the formula UO2CO3. Also known by its mineral name rutherfordine, this material consists of uranyl (UO22+) and carbonate (CO32-). Like most uranyl salts, the compound is a polymeric, each uranium(VI) center being bonded to eight O atoms. Hydrolysis products of rutherfordine are also found in both the mineral and organic fractions of coal and its fly ash and is the main component of uranium in mine tailing seepage water.
Curite is a rare mineral with the chemical composition Pb3[(UO2)4|O4|(OH)3]2·2 H2O. It is therefore a hydrated lead uranyl oxide, which forms red needles or orange, massive aggregates.
The purpose of a mineralizer is to facilitate the transport of insoluble “nutrient” to a seed crystal by means of a reversible chemical reaction. Over time, the seed crystal accumulates the material that was once in the nutrient and grows. Mineralizers are additives that aid the solubilization of the nutrient solid. When used in small quantities, mineralizers function as catalysts. Typically, a more stable solid is crystallized from a solution that consists of a less stable solid and a solvent. The process is done by dissolution-precipitation or crystallization process.
Paulscherrerite, UO2(OH)2, is a newly named mineral of the schoepite subgroup of hexavalent uranium hydrate/hydroxides. It is monoclinic, but no space group has been determined because no single-crystal study has been done. Paulscherrerite occurs as a canary yellow microcrystalline powdery product with a length of ~500 nm. It forms by the weathering and ultimate pseudomorphism of uranium-lead bearing minerals such as metaschoepite. The type locality for paulscherrerite is the Number 2 Workings, Radium Ridge near Mount Painter, North Flinders Ranges, South Australia, an area where radiogenic heat has driven hydrothermal activity for millions of years. It is named for Swiss physicist Paul Scherrer, co-inventor of the Debye-Scherrer X-ray powder diffraction camera. Study of paulscherrerite and related minerals is important for understanding the mobility of uranium around mining sites, as well as designing successful strategies for the storage of nuclear weapons and the containment of nuclear waste.
In chemistry, molecular oxohalides (oxyhalides) are a group of chemical compounds in which both oxygen and halogen atoms are attached to another chemical element A in a single molecule. They have the general formula AOmXn, where X is a halogen. Known oxohalides have fluorine (F), chlorine (Cl), bromine (Br), and/or iodine (I) in their molecules. The element A may be a main group element, a transition element, a rare earth element or an actinide. The term oxohalide, or oxyhalide, may also refer to minerals and other crystalline substances with the same overall chemical formula, but having an ionic structure.
Bijvoetite-(Y) is a very rare rare-earth and uranium mineral with the formula (Y,REE)8(UO2)16(CO3)16O8(OH)8·39H2O. When compared to the original description, the formula of bijvoetite-(Y) was changed in the course of crystal structure redefinition. Bijvoetite-(Y) is an example of natural salts containing both uranium and yttrium, the other examples being kamotoite-(Y) and sejkoraite-(Y). Bijvoetite-(Y) comes from Shinkolobwe deposit in Republic of Congo, which is famous for rare uranium minerals. The other interesting rare-earth-bearing uranium mineral, associated with bijvoetite-(Y), is lepersonnite-(Gd).
Sodium hydrogenoxalate is salt of formula NaHC
2O
4, consisting of sodium cations Na+
and hydrogenoxalate anions HC
2O−
4 or HO(O=)C-C(=O)O−
. The anion can be described as the result of removing one hydrogen ion H+
from oxalic acid H
2C
2O
4, or adding one to the oxalate anion C
2O2−
4.
Sayrite (Pb2(UO2)5O6(OH)24(H2O)) is an alteration product of uraninite named after the X-ray crystallographer David Sayre. Sayrite contains hydrogen, oxygen, uranium, and lead. It is mined at Shinkolobwe Mine, (Kasolo Mine), Kambove District, Haut-Katanga, Democratic Republic of the Congo. It is usually orange in color, but also can be reddish and yellowish. It is in the monoclinic crystal system.
A carbonate fluoride, fluoride carbonate, fluorocarbonate or fluocarbonate is a double salt containing both carbonate and fluoride. The salts are usually insoluble in water, and can have more than one kind of metal cation to make more complex compounds. Rare-earth fluorocarbonates are particularly important as ore minerals for the light rare-earth elements lanthanum, cerium and neodymium. Bastnäsite is the most important source of these elements. Other artificial compounds are under investigation as non-linear optical materials and for transparency in the ultraviolet, with effects over a dozen times greater than Potassium dideuterium phosphate.
Zellerite is a uranium mineral, named after its discoverer, geologist Howard Davis Zeller. It has a type locality of the Lucky MC uranium mine in Wyoming, USA. It was approved by the IMA in 1965, but was first published a year after its approval.
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