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Cobaltite

Cobaltite is a sulfosalt with the CoAsS, consisting of , , and in a 1:1:1 ratio. It crystallizes in the orthorhombic system and typically forms metallic, pseudocubic crystals or granular masses. Cobaltite exhibits a silvery-white to reddish-silver color, with a grayish-black streak, metallic luster, and a Mohs of 5.5. It has perfect cleavage on the {001} plane, a specific gravity of 6.33, and is brittle with an uneven fracture. The mineral is opaque and shows weak in reflected light. It occurs primarily in high-temperature hydrothermal deposits and veins within contact-metamorphosed rocks, often associated with minerals such as , , , , and other cobalt-nickel sulfides or arsenides. Notable localities include the Cobalt-Gowganda region in , ; Broken Hill in ; and the Skutterud mine in . The name "cobaltite" derives from the German word "," meaning , due to the troublesome content encountered by early miners. As a primary of , cobaltite serves as an important source for extracting this critical metal, which is used in alloys, batteries, and pigments. When found in sufficient quantities, it is mined for its cobalt content, contributing to industrial applications like superalloys and rechargeable batteries.

Etymology and history

Etymology

The name cobaltite derives from the chemical element cobalt, which itself originates from the German word Kobold, meaning "goblin" or "mischievous underground spirit." This linguistic root reflects historical mining folklore in Europe, where cobalt-bearing ores were associated with supernatural interference due to their failure to smelt into valuable metals and their emission of toxic arsenic vapors that harmed workers. In the 16th century, silver miners in , , encountered these troublesome ores, which they believed were cursed by goblins who substituted worthless material for silver, reinforcing the name's superstitious origins. The connection to ancient mining superstitions persisted, as cobalt minerals like cobaltite were often blamed on these mythical entities for causing illness and disappointment in ore processing. The mineral was first scientifically described in 1797 by German chemist , who analyzed specimens and termed it Glanzkobalt (shining ) to highlight its metallic luster and composition. The specific name cobaltite (or cobaltine in French) was introduced in 1832 by mineralogist François Sulpice Beudant in his Traité Élémentaire de Minéralogie, formalizing its recognition in mineralogical nomenclature based on its primary content.

Historical discovery

Cobaltite was first described in 1797 by the German chemist Martin Heinrich Klaproth, who conducted a chemical analysis of specimens obtained from mines in Sweden. Klaproth identified its composition as containing cobalt, arsenic, and sulfur, distinguishing it from other cobalt-bearing minerals known at the time. His work, published in Beiträge zur chemischen Kenntniss der Mineralkörper, marked the initial scientific recognition of the mineral, based on samples from the Tunaberg ore field. The type locality for cobaltite is the Tunaberg ore field in , . Notable localities include the Håkansboda mine in , where exceptional crystals were documented and collected during early activities. This site, part of the mining district, yielded high-quality specimens that exemplified the mineral's characteristic silver-white, metallic luster and cubic to pyritohedral forms, contributing to its study in the late 18th and early 19th centuries. In the early , cobaltite gained recognition across as a primary source of for production and , with Swedish chemists performing detailed analyses of local ores to refine extraction methods and compositional understanding. These efforts highlighted its economic value in regions like and , where cobalt ores supported the growing demand for blue glass and coloring agents.

Chemical composition

Molecular formula

Cobaltite is a with the ideal CoAsS, representing sulfarsenide. This includes one atom, one atom, and one atom per . The molecular weight of the CoAsS is 165.92 g/mol. Cobaltite is classified as a and serves as the prototype for the cobaltite group, which encompasses related sulfarsenides with similar structures.

Impurities and varieties

Cobaltite's composition often includes iron substituting for cobalt, with Fe contents typically reaching up to 10 wt.%, leading to the generalized (Co,Fe)AsS. This substitution is common in natural samples, where iron occupies a portion of the cation site without significantly altering the mineral's overall structure. analyses reveal variability in iron content across specimens, frequently ranging from less than 1 wt.% to around 4-10 wt.%, depending on the deposit and formation conditions. For instance, analyses from , show Fe at approximately 4.11 wt.%, while other occurrences exhibit higher levels approaching the upper limit. These variations arise from local geochemical environments during hydrothermal deposition. Nickel and other metals, such as in trace amounts, can substitute for cobalt in rare cases, but such impurities are generally minor and do not exceed a few percent. Cobaltite has no formally recognized varieties, though it participates in a series with alloclasite, the monoclinic polymorph sharing the ideal composition CoAsS but accommodating higher iron contents, often up to 25% of the cation site. This series reflects polymorphic transitions influenced by iron substitution and temperature, with alloclasite forming under conditions favoring more Fe-rich compositions.

Crystal structure and physical properties

Crystal system and habit

Cobaltite crystallizes in the , often exhibiting pseudocubic due to nearly equal lattice parameters. The crystal class is pyramidal, corresponding to the point group mm2. Its structure is described by the space group Pca21 (No. 29). The unit cell dimensions are a = 5.5833(7) Å, b = 5.5892(6) Å, and c = 5.5812(8) Å, with Z = 4 formula units per cell. These parameters reflect the close-packed arrangement of , , and atoms, contributing to the mineral's metallic luster and density. In terms of , cobaltite most commonly occurs as granular or massive aggregates, though well-formed are rare and can reach up to 8 cm in size. When crystalline, it typically displays pseudocubic or pseudopyritohedral forms, including pseudo-octahedra, with striated faces being a distinctive feature. Twinning is infrequent but occurs about the direction as a pseudocubic threefold axis, with twin planes on {011} and {111}, often resulting in flamelike textures visible in polished sections.

Physical characteristics

Cobaltite is an opaque with a metallic luster, displaying colors ranging from reddish silver-white to steel-gray or . Its streak is grayish-. The mineral exhibits perfect on the {001} plane and distinct cleavage on {110}. Fracture is uneven, and tenacity is brittle. Cobaltite has a Mohs of 5.5. Its specific is 6.33 g/cm³ (measured). In reflected light, cobaltite appears isotropic with very weak observed at grain boundaries. values are approximately 51% at 546 nm, increasing to higher values in the red spectrum (e.g., 53.8% at 700 nm).

Geological occurrence

Formation environments

Cobaltite primarily forms through in high-temperature hydrothermal veins, typically at temperatures between 200 and 400°C, where magmatic or metamorphic fluids transport and deposit , , and . These veins develop in structurally controlled features such as shear zones and fractures, often linked to plutons or intrusions that provide the necessary heat and metal sources. The mineral is commonly associated with contact metamorphic rocks, where interaction between intrusive magmas and surrounding sediments or volcanics facilitates its crystallization. Precipitation of cobaltite occurs from arsenic- and sulfur-rich hydrothermal fluids in reduced environments, characterized by saline brines with chloride complexes that enable metal transport, followed by deposition upon fluid mixing, cooling, or pressure changes. These conditions often prevail in greenschist- to amphibolite-facies metamorphism, promoting the formation of sulfarsenides like cobaltite alongside associated minerals such as skutterudite and pyrite. Upon exposure to surface , primary cobaltite undergoes secondary alteration in oxidative zones, converting to (Co₃(AsO₄)₂·8H₂O), a hydrated cobalt , through hydration and oxidation processes that mobilize and into more soluble forms. This alteration is typically confined to thin zones near the surface, influenced by rainwater and atmospheric oxygen.

Notable localities

Cobaltite's type locality is the Tunaberg copper-cobalt ore field near in , , where it was first described in 1797 by as "Glanzkobalt." Among the most notable deposits worldwide, significant occurrences include the Håkansboda mine in Västmanland, Sweden, renowned for well-formed crystals since the 18th century; the Cobalt-Gowganda mining district in , , , a major historical source of high-grade cobaltite in silver veins; the Skutterud mine in Modum, , a historic site known for cobalt minerals including cobaltite; the Røros copper mines in , , where cobaltite appears in polymetallic assemblages; the Schneeberg district in , , a classic site for cobaltite in silver-cobalt-nickel veins mined since the ; in , , a significant locality for cobaltite in deposits; the Bou Azzer district in , , hosting cobaltite in quartz-calcite veins associated with serpentinites; the Katanga Copperbelt in , , a key modern producer where cobaltite occurs in sediment-hosted copper-cobalt deposits; and the Mount Cobalt mine in Cloncurry Shire, , , an abandoned site yielding cobaltite with arsenides since 1919. In these deposits, cobaltite is commonly associated with , , , , , and , often forming in hydrothermal systems. Historically, silver-cobalt-nickel mines in regions like , , and supplied much of the world's cobaltite for production from the 16th to 19th centuries, while contemporary output predominantly derives from African deposits in the and , contributing to global supply.

Uses and economic importance

As a cobalt ore

Cobaltite serves as a primary mineral for the extraction of , containing approximately 35.5% by weight in its of CoAsS. This high content makes it economically viable for dedicated operations in suitable deposits, where it is often associated with other sulfides like and . Unlike many sources that occur as byproducts of or , cobaltite enables targeted recovery of the metal for industrial applications. Mining of cobaltite typically employs methods for vein-hosted deposits in metamorphic or hydrothermal environments, allowing access to narrow, high-grade bodies. For larger, shallower deposits, open-pit techniques are used, involving excavation and blasting to remove and extract the efficiently. These approaches are selected based on deposit , depth, and economics, with examples including operations in the Cobalt Belt and the Bou Azzer district. Post-extraction, the undergoes crushing and flotation to concentrate the cobaltite prior to further processing. Processing of cobaltite involves either pyrometallurgical or hydrometallurgical routes to separate from and . In pyrometallurgical treatment, the concentrate is roasted to volatilize and then smelted to produce a , which is subsequently refined. Hydrometallurgical methods include acid —often with under pressure—followed by solvent extraction and to yield high-purity metal or salts. These processes are tailored to handle the arsenical nature of the ore, ensuring effective recovery while managing hazardous elements. Although cobaltite accounts for a minor share of global cobalt production—less than 5% of the annual output of approximately 290,000 metric tons as of 2024—the Democratic Republic of Congo dominates overall cobalt supply through its sedimentary copper-cobalt deposits, while cobaltite production occurs at specialized sites such as Morocco's Bou Azzer mine and the Idaho Cobalt Belt in the United States. This limited but strategic role underscores cobaltite's importance in diversifying supply away from dominant sedimentary sources. A significant environmental challenge in cobaltite and processing is the release of byproducts, which can contaminate soil and water if not properly managed. volatilization during roasting or dissolution in requires specialized treatment, such as stabilization or , to mitigate risks to ecosystems and communities. Ongoing research focuses on innovative techniques to immobilize , enabling safer extraction from domestic deposits like those .

Other applications

In historical contexts, cobaltite crystals from , , known locally as sehta, have been used by artisans to create blue enamels for decorating gold and silver jewelry and ornamental items through extraction of cobalt compounds. Synthetic cobaltite (CoAsS) is produced in laboratories primarily for mineralogical research, enabling detailed examination of its structural variations. Studies have shown that synthetic cobaltite exhibits a continuous series, ranging from CoAs0.86S1.19 to CoAs0.42S1.58 under controlled conditions at 550°C, which helps understand isomorphous substitutions and phase stability. This synthetic form is also explored in research due to its electronic properties, particularly for thermoelectric applications where alloying with elements like modifies thermal conductivity and enhances the . For instance, ordered CoAsS demonstrates effective n-type and p-type thermoelectric behavior depending on synthesis and doping parameters, with reduced lattice thermal conductivity improving overall performance. Beyond research, natural cobaltite holds significant value as a collector's , prized for its brilliant silvery-white, metallic luster and well-formed cubic or pyritohedral . Exceptional specimens are preserved in institutions like the Smithsonian , where they are showcased for their aesthetic and scientific appeal.

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