Product Code Database
The chlorites are the group of phyllosilicate common in low-grade and in altered igneous rocks. Greenschist, formed by metamorphism of basalt or other low-silica volcanic rock, typically contains significant amounts of chlorite.
Chlorite minerals show a wide variety of compositions, in which magnesium, iron, aluminium, and silicon substitute for each other in the crystal structure. A complete solid solution series exists between the two most common end members, magnesium-rich clinochlore and iron-rich chamosite. In addition, manganese, zinc, lithium, and calcium species are known. The great range in composition results in considerable variation in physical, optical, and X-ray properties. Similarly, the range of chemical composition allows chlorite group minerals to exist over a wide range of temperature and pressure conditions. For this reason chlorite minerals are ubiquitous minerals within low and medium temperature metamorphic rocks, some igneous rocks, hydrothermal rocks and deeply buried sediments.
The name chlorite is from the Greek language chloros (χλωρός), meaning "green", in reference to its color. Chlorite minerals do not contain the element chlorine, also named from the same Greek root.
The typical general formula for chlorite is . This formula emphasizes the structure of the group, which is described as TOT-O and consists of alternating TOT layers and O layers. (2025). 9780195106916, Oxford University Press. ISBN 9780195106916 The TOT layer ( Tetrahedral- Octahedral- Tetrahedral = T-O-T) is often referred to as a talc layer, since talc is composed entirely of stacked TOT layers. The TOT layers of talc are electrically neutral and are bound only by relatively weak van der Waals forces. By contrast, the TOT layers of chlorite contain some aluminium in place of silicon, which gives the layers an overall negative charge. These TOT layers are bound together by positively charged O layers, sometimes called brucite layers. Mica is also composed of aluminium-rich, negatively charged TOT layers, but these are bonded together by individual cations (such as potassium, sodium, or calcium ions) rather than a positively charged brucite layer.
Chlorite is considered a clay mineral. It is a nonswelling clay mineral, since water is not adsorbed in the interlayer spaces, and it has a relatively low cation exchange capacity.
In his pioneering work on metamorphic facies in the Scottish Highlands, G.M. Barrow identified the chlorite zone as the zone of mildest metamorphism. In modern petrology, chlorite is the diagnostic mineral of the greenschist facies. This facies is characterized by temperatures near and pressures near 5 kbar. At higher temperatures, much of the chlorite is destroyed by reactions with either potassium feldspar or phengite mica which produce biotite, muscovite, and quartz. At still higher temperatures, other reactions destroy the remaining chlorite, often with release of water vapor.
Chlorite is one of the most common minerals produced by propylitic alteration by hydrothermal systems, where it occurs in the "green rock" environment with epidote, actinolite, albite, hematite, and calcite.
Experiments indicate that chlorite can be stable in peridotite of the Earth's mantle above the ocean lithosphere carried down by subduction, and chlorite may even be present in the mantle volume from which island arc are generated.
Clinochlore, pennantite, and chamosite are the most common varieties. Several other sub-varieties have been described. A massive compact variety of clinochlore used as a decorative carving stone is referred to by the trade name seraphinite. It occurs in the Korshunovskoye iron skarn deposit in the Irkutsk Oblast of Eastern Siberia.
Chlorite schist has been used as roofing granules, the mineral granules adhered to asphalt composition shingles due to the green color. It was quarried near Ely, Minnesota, US, until superseded by synthetic materials.
|
|
