| Nickeline | |
| Category: | Arsenide mineral |
| Formula: | nickel arsenide (NiAs) |
| Imasymbol: | Nc[1] |
| Strunz: | 2.CC.05 |
| System: | Hexagonal |
| Class: | Dihexagonal dipyramidal (6/mmm) H-M symbol: (6/m 2/m 2/m) |
| Symmetry: | P63/mmc |
| Unit Cell: | a = 3.602 Å, c = 5.009 Å; Z = 2 |
| Color: | Pale copper red with blackish tarnish. white with strong yellowish pink hue on polished section strongly anisotropic |
| Habit: | Massive columnar to reniform, rarely as distorted, horizontally striated, terminated crystals |
| Twinning: | On producing fourlings |
| Cleavage: | Imperfect, Imperfect |
| Fracture: | Conchoidal |
| Tenacity: | Brittle |
| Mohs: | 5 – 5.5 |
| Luster: | metallic |
| Diaphaneity: | Opaque |
| Pleochroism: | Strong (reflected light) |
| Streak: | brownish black |
| Gravity: | 7.8 |
| Fusibility: | 2 |
| Other: | garlic odor on heating |
| References: | [2] [3] |
Nickeline or niccolite is a mineral consisting primarily of nickel arsenide (NiAs). The naturally-occurring mineral contains roughly 43.9% nickel and 56.1% arsenic by mass, but composition of the mineral may vary slightly.[2]
Small quantities of sulfur, iron and cobalt are usually present, and sometimes the arsenic is largely replaced by antimony. This last forms an isomorphous series with breithauptite (nickel antimonide).
Medieval miners looking for copper in the German Ore Mountains would sometimes find a red mineral, superficially resembling copper ore. Upon attempting extraction, no copper was produced, and subsequently, the miners would be afflicted with mysterious illness. They blamed a mischievous sprite of German mythology, Nickel (similar to Old Nick) for besetting the copper (German: Kupfer).[4] This German equivalent of "copper-nickel" was used as early as 1694 (other old German synonyms are Rotnickelkies and Arsennickel).
In 1751, Baron Axel Fredrik Cronstedt was attempting to extract copper from kupfernickel mineral, and obtained instead a white metal which he named "nickel", after the sprite.[5] In modern German, Kupfernickel and Kupfer-Nickel designates the alloy Cupronickel.
The names subsequently given to the ore, nickeline from F. S. Beudant, 1832, and niccolite, from J. D. Dana, 1868, refer to the presence of nickel; in Latin, niccolum.
In 1971, the International Mineralogical Association recommended use of the name nickeline rather than niccolite.[6]
The main compound within nickeline, nickel arsenide (NiAs), can be prepared by direct combination of the elements:
Nickeline is formed by hydrothermal modification of ultramafic rocks and associated ore deposits, and may be formed by replacement of nickel-copper bearing sulfides (replacing pentlandite, and in association with copper arsenic sulfides), or via metasomatism of sulfide-free ultramafic rocks, where metasomatic fluids introduce sulfur, carbonate, and arsenic. This typically results in mineral assemblages including millerite, heazelwoodite and metamorphic pentlandite-pyrite via sulfidation and associated arsenopyrite-nickeline-breithauptite. Associated minerals include: arsenopyrite, barite, silver, cobaltite, pyrrhotite, pentlandite, chalcopyrite, breithauptite and maucherite. Nickeline alters to annabergite (a coating of green nickel arsenate) on exposure to moist air.
Most of these minerals can be found in the areas surrounding Sudbury and Cobalt, Ontario. Other localities include the eastern flank of the Widgiemooltha Dome, Western Australia, from altered pentlndite-pyrite-pyrrhotite assemblages within the Mariners, Redross and Miitel nickel mines where nickeline is produced by regional Au-As-Ag-bearing alteration and carbonate metasomatism. Other occurrences include within similarly modified nickel mines of the Kambalda area.
The unit cell of nickeline is used as the prototype of a group of crystalline solids with similar crystal structures.[8] The structure consists of two interpenetrating sublattices: a primitive hexagonal nickel sublattice and a hexagonal close-packed arsenic sublattice. Each nickel atom is octahedrally coordinated to six arsenic atoms, while each arsenic atom is trigonal prismatically coordinated to six nickel atoms.[9] Compounds adopting the NiAs structure are generally the chalcogenides, arsenides, antimonides and bismuthides of transition metals.
The following are the members of the nickeline group:
Nickeline is rarely used as a source of nickel due to the presence of arsenic, which is deleterious to most smelting and milling techniques. When nickel sulfide ore deposits have been altered to produce nickeline, often the presence of arsenic renders the ore uneconomic when concentrations of As reach several hundred parts per million. However, arsenic bearing nickel ore may be treated by blending with 'clean' ore sources, to produce a blended feedstock which the mill and smelter can handle with acceptable recovery.
The primary problem for treating nickeline in conventionally constructed nickel mills is the specific gravity of nickeline versus that of pentlandite. This renders the ore difficult to treat via the froth flotation technique. Within the smelter itself, the nickeline contributes to high arsenic contents which require additional reagents and fluxes to strip from the nickel metal.