Chlorite group: Difference between revisions
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{{Short description| | {{Short description|Group of phyllosilicate minerals}} | ||
{{for|the chemistry term|chlorite}} | {{for|the chemistry term|chlorite}} | ||
{{Infobox mineral | {{Infobox mineral | ||
| name = Chlorite group | | name = Chlorite group | ||
| category = [[ | | category = [[Phyllosilicate]] [[minerals]] | ||
| image = ChloriteUSGOV.jpg | | image = ChloriteUSGOV.jpg | ||
| imagesize = 260px | | imagesize = 260px | ||
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}} | }} | ||
The '''chlorites''' are the group of [[phyllosilicate]] [[mineral]]s common in low-grade [[metamorphic rock]]s and in [[Mineral alteration|altered]] [[igneous rocks]]. [[Greenschist]], formed by metamorphism of [[basalt]] or other low-silica volcanic rock, typically contains significant amounts of chlorite. | The '''chlorites''' are the group of [[phyllosilicate]] [[mineral]]s common in low-grade [[metamorphic rock]]s and in [[Mineral alteration|altered]] [[igneous rocks]]. | ||
Chlorite minerals do not contain the element [[chlorine]]. The name ''chlorite'' is from the [[Greek language|Greek]] ''chloros'' (χλωρός), meaning "green", in reference to its color. [[Greenschist]], formed by metamorphism of [[basalt]] or other low-silica volcanic rock, typically contains significant amounts of chlorite mineral (but not the chlorite ion, nor chlorine in any other form). | |||
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 diffraction|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 circulation|hydrothermal]] rocks and deeply buried sediments. | 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 diffraction|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 circulation|hydrothermal]] rocks and deeply buried sediments. | ||
==Properties== | ==Properties== | ||
Chlorite forms blue-green crystals resembling [[mica]]. However, while the plates are flexible, they are not elastic like mica, and are less easily pulled apart. [[Talc]] is much softer and feels soapy between the fingers.<ref>{{cite book |last1=Sinkankas |first1=John |title=Mineralogy for amateurs. |date=1964 |publisher=Van Nostrand |location=Princeton, N.J. |isbn= | Chlorite forms blue-green crystals resembling [[mica]]. However, while the plates are flexible, they are not elastic like mica, and are less easily pulled apart. [[Talc]] is much softer and feels soapy between the fingers.<ref>{{cite book |last1=Sinkankas |first1=John |title=Mineralogy for amateurs. |date=1964 |publisher=Van Nostrand |location=Princeton, N.J. |isbn=0-442-27624-9 |page=486}}</ref><ref>{{cite book |last1=Klein |first1=Cornelis |last2=Hurlbut |first2=Cornelius S. Jr. |title=Manual of mineralogy: (after James D. Dana) |date=1993 |publisher=Wiley |location=New York |isbn=0-471-57452-X |edition=21st |page=514}}</ref> | ||
The typical general formula for chlorite is {{Chem2|(Mg,Fe)3(Si,Al)4O10(OH)2*(Mg,Fe)3(OH)6}}. This formula emphasizes the structure of the group, which is described as ''TOT-O'' and consists of alternating ''TOT'' layers and ''O'' layers.<ref name=Nesse2000>{{cite book |last1=Nesse |first1=William D. |title=Introduction to mineralogy |date=2000 |publisher=Oxford University Press |location=New York |isbn= | The typical general formula for chlorite is {{Chem2|(Mg,Fe)3(Si,Al)4O10(OH)2*(Mg,Fe)3(OH)6}}. This formula emphasizes the structure of the group, which is described as ''TOT-O'' and consists of alternating ''TOT'' layers and ''O'' layers.<ref name=Nesse2000>{{cite book |last1=Nesse |first1=William D. |title=Introduction to mineralogy |date=2000 |publisher=Oxford University Press |location=New York |isbn=978-0-19-510691-6 |pages=251–260}}</ref> The ''TOT'' layer ('''T'''etrahedral-'''O'''ctahedral-'''T'''etrahedral = '''''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 force]]s. 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.{{sfn|Klein|Hurlbut|1993|pp=500-501}} | ||
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Chlorite is considered a [[clay mineral]]. It is a nonswelling clay mineral,<ref>{{cite journal |last1=Osacky |first1=Marek |last2=Geramian |first2=Mirjavad |last3=Ivey |first3=Douglas G. |last4=Liu |first4=Qi |last5=Etsell |first5=Thomas H. |title=Influence of Nonswelling Clay Minerals (Illite, Kaolinite, and Chlorite) on Nonaqueous Solvent Extraction of Bitumen |journal=Energy & Fuels |date=16 July 2015 |volume=29 |issue=7 |pages=4150–4159 |doi=10.1021/acs.energyfuels.5b00269}}</ref> since water is not adsorbed in the interlayer spaces, and it has a relatively low [[cation exchange capacity]].<ref>{{cite journal |last1=Nadziakiewicza |first1=Małgorzata |last2=Kehoe |first2=Sylvia |last3=Micek |first3=Piotr |title=Physico-Chemical Properties of Clay Minerals and Their Use as a Health Promoting Feed Additive |journal=Animals |date=23 September 2019 |volume=9 |issue=10 | | Chlorite is considered a [[clay mineral]]. It is a nonswelling clay mineral,<ref>{{cite journal |last1=Osacky |first1=Marek |last2=Geramian |first2=Mirjavad |last3=Ivey |first3=Douglas G. |last4=Liu |first4=Qi |last5=Etsell |first5=Thomas H. |title=Influence of Nonswelling Clay Minerals (Illite, Kaolinite, and Chlorite) on Nonaqueous Solvent Extraction of Bitumen |journal=Energy & Fuels |date=16 July 2015 |volume=29 |issue=7 |pages=4150–4159 |doi=10.1021/acs.energyfuels.5b00269}}</ref> since water is not adsorbed in the interlayer spaces, and it has a relatively low [[cation exchange capacity]].<ref>{{cite journal |last1=Nadziakiewicza |first1=Małgorzata |last2=Kehoe |first2=Sylvia |last3=Micek |first3=Piotr |title=Physico-Chemical Properties of Clay Minerals and Their Use as a Health Promoting Feed Additive |journal=Animals |date=23 September 2019 |volume=9 |issue=10 |page=714 |doi=10.3390/ani9100714|pmid=31548509 |pmc=6827059 |doi-access=free }}</ref> | ||
==Occurrence== | ==Occurrence== | ||
[[File:Quartz-Chlorite-Group-139575.jpg|thumb|150px|Quartz crystal with chlorite inclusions from [[Minas Gerais]], [[Brazil]] (size: 4.2 × 3.9 × 3.3 cm)]] | [[File:Quartz-Chlorite-Group-139575.jpg|thumb|150px|Quartz crystal with chlorite inclusions from [[Minas Gerais]], [[Brazil]] (size: 4.2 × 3.9 × 3.3 cm)]] | ||
Chlorite is a common mineral, found in metamorphic, igneous, and sedimentary rocks. It is an important rock-forming mineral in low- to medium-grade metamorphic rock formed by metamorphism of [[mafic]] or [[pelitic]] rock.{{sfn|Nesse|2000|p=252}} It is also common in igneous rocks, usually as a secondary mineral, formed by alteration of mafic minerals such as [[biotite]], [[hornblende]], [[pyroxene]], or [[garnet]].{{sfn|Klein|Hurlbut|1993|p=522}} The glassy rims of [[pillow basalt]] on the ocean floor is often altered to pure chlorite, in part by exchange of chemicals with seawater.<ref>{{cite book |last1=Yardley |first1=B. W. D. |title=An introduction to metamorphic petrology |date=1989 |publisher=Longman Scientific & Technical |location=Harlow, Essex, England |isbn= | Chlorite is a common mineral, found in metamorphic, igneous, and sedimentary rocks. It is an important rock-forming mineral in low- to medium-grade metamorphic rock formed by metamorphism of [[mafic]] or [[pelitic]] rock.{{sfn|Nesse|2000|p=252}} It is also common in igneous rocks, usually as a secondary mineral, formed by alteration of mafic minerals such as [[biotite]], [[hornblende]], [[pyroxene]], or [[garnet]].{{sfn|Klein|Hurlbut|1993|p=522}} The glassy rims of [[pillow basalt]] on the ocean floor is often altered to pure chlorite, in part by exchange of chemicals with seawater.<ref>{{cite book |last1=Yardley |first1=B. W. D. |title=An introduction to metamorphic petrology |date=1989 |publisher=Longman Scientific & Technical |location=Harlow, Essex, England |isbn=0-582-30096-7 |page=121}}</ref> The green color of many igneous rocks, [[slate]]s, and [[schist]]s is due to fine particles of chlorite disseminated throughout the rock.{{sfn|Klein|Hurlbut|1993|p=522}} Chlorite is a common [[weathering]] product and is widespread in [[clay]] and in sedimentary rock containing clay minerals.{{sfn|Nesse|2000|p=252}} Chlorite is found in [[pelites]] along with [[quartz]], [[albite]], [[sericite]], and [[garnet]], and is also found in associate with [[actinolite]] and [[epidote]].{{sfn|Klein|Hurlbut|1993|p=522}} | ||
In his pioneering work on [[metamorphic facies]] in the Scottish Highlands, [[George Barrow (geologist)|G.M. Barrow]] identified the chlorite zone as the zone of mildest metamorphism.{{sfn|Yardley|1989|p=8}} In modern petrology, chlorite is the diagnostic mineral of the [[greenschist]] facies.{{sfn|Klein|Hurlbut|1993|p=522}} This facies is characterized by temperatures near {{convert|450|C|sigfig=2|sp=us}} and pressures near 5 kbar.{{sfn|Yardley|1989|p=50}} 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.{{sfn|Yardley|1989|pp=64-68}} | In his pioneering work on [[metamorphic facies]] in the Scottish Highlands, [[George Barrow (geologist)|G.M. Barrow]] identified the chlorite zone as the zone of mildest metamorphism.{{sfn|Yardley|1989|p=8}} In modern petrology, chlorite is the diagnostic mineral of the [[greenschist]] facies.{{sfn|Klein|Hurlbut|1993|p=522}} This facies is characterized by temperatures near {{convert|450|C|sigfig=2|sp=us}} and pressures near 5 kbar.{{sfn|Yardley|1989|p=50}} 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.{{sfn|Yardley|1989|pp=64-68}} | ||
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[[File:Chlorite-Group-Garnet-Group-65646.jpg|thumb|150px|Chlorite [[pseudomorph]] after [[garnet]] from Michigan (size: 3.5 × 3.1 × 2.7 cm)]] | [[File:Chlorite-Group-Garnet-Group-65646.jpg|thumb|150px|Chlorite [[pseudomorph]] after [[garnet]] from Michigan (size: 3.5 × 3.1 × 2.7 cm)]] | ||
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]] [[magma]]s are generated.<ref>{{cite journal |last1=Manthilake |first1=Geeth |last2=Bolfan-Casanova |first2=Nathalie |last3=Novella |first3=Davide |last4=Mookherjee |first4=Mainak |last5=Andrault |first5=Denis |title=Dehydration of chlorite explains anomalously high electrical conductivity in the mantle wedges |journal=Science Advances |date=6 May 2016 |volume=2 |issue=5 | | 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]] [[magma]]s are generated.<ref>{{cite journal |last1=Manthilake |first1=Geeth |last2=Bolfan-Casanova |first2=Nathalie |last3=Novella |first3=Davide |last4=Mookherjee |first4=Mainak |last5=Andrault |first5=Denis |title=Dehydration of chlorite explains anomalously high electrical conductivity in the mantle wedges |journal=Science Advances |date=6 May 2016 |volume=2 |issue=5 |article-number=e1501631 |doi=10.1126/sciadv.1501631|pmid=27386526 |pmc=4928900 |bibcode=2016SciA....2E1631M }}</ref><ref>{{cite journal|title=The influence of H<sub>2</sub>O on mantle wedge melting|journal=[[Earth and Planetary Science Letters|Earth Planet. Sci. Lett.]]|volume=249|issue=1–2|pages=74–89|display-authors=3|vauthors=Grove TL, Chatterjee N, Parman SW, Médard E|date=2006|bibcode=2006E&PSL.249...74G|doi=10.1016/j.epsl.2006.06.043}}</ref> | ||
== Members of the chlorite group == | == Members of the chlorite group == | ||
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Chlorite does not have any specific industrial uses of any importance. Some rock types containing chlorite, such as chlorite schist, have minor decorative uses or as construction stone. However, chlorite is a common mineral in [[clay]], which has a vast number of uses.{{sfn|Nesse|2000|p=252}} | Chlorite does not have any specific industrial uses of any importance. Some rock types containing chlorite, such as chlorite schist, have minor decorative uses or as construction stone. However, chlorite is a common mineral in [[clay]], which has a vast number of uses.{{sfn|Nesse|2000|p=252}} | ||
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.{{ | 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.{{citation needed|date=November 2024}} | ||
==See also== | ==See also== | ||
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== Further reading == | == Further reading == | ||
*{{Cite web|url=http://www.gc.maricopa.edu/earthsci/imagearchive/chlorite.htm|title=Chlorite|website=Maricopa.edu|archive-url=https://web.archive.org/web/20041112090955/http://www.gc.maricopa.edu/earthsci/imagearchive/chlorite.htm|archive-date=12 November 2004 | *{{Cite web|url=http://www.gc.maricopa.edu/earthsci/imagearchive/chlorite.htm|title=Chlorite|website=Maricopa.edu|archive-url=https://web.archive.org/web/20041112090955/http://www.gc.maricopa.edu/earthsci/imagearchive/chlorite.htm|archive-date=12 November 2004|access-date=22 Mar 2019}}] | ||
{{commons category|Chlorite}} | {{commons category|Chlorite}} | ||
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[[Category:Clay minerals group]] | [[Category:Clay minerals group]] | ||
[[Category:Monoclinic minerals]] | [[Category:Monoclinic minerals]] | ||
[[Category: | [[Category:Chlorite group| ]] | ||
Latest revision as of 19:57, 22 December 2025
Template:Short description Script error: No such module "For". Script error: No such module "Infobox".Template:Template otherScript error: No such module "Check for unknown parameters".
The chlorites are the group of phyllosilicate minerals common in low-grade metamorphic rocks and in altered igneous rocks.
Chlorite minerals do not contain the element chlorine. The name chlorite is from the Greek chloros (χλωρός), meaning "green", in reference to its color. Greenschist, formed by metamorphism of basalt or other low-silica volcanic rock, typically contains significant amounts of chlorite mineral (but not the chlorite ion, nor chlorine in any other form).
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.
Properties
Chlorite forms blue-green crystals resembling mica. However, while the plates are flexible, they are not elastic like mica, and are less easily pulled apart. Talc is much softer and feels soapy between the fingers.[1][2]
The typical general formula for chlorite is Template:Chem2. This formula emphasizes the structure of the group, which is described as TOT-O and consists of alternating TOT layers and O layers.[3] 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.Template:Sfn
-
Crystal structure of chlorite viewed along [100] (looking along the layers)
-
Chlorite structure viewed along [001] showing pseudohexagonal structure
Chlorite is considered a clay mineral. It is a nonswelling clay mineral,[4] since water is not adsorbed in the interlayer spaces, and it has a relatively low cation exchange capacity.[5]
Occurrence
Chlorite is a common mineral, found in metamorphic, igneous, and sedimentary rocks. It is an important rock-forming mineral in low- to medium-grade metamorphic rock formed by metamorphism of mafic or pelitic rock.Template:Sfn It is also common in igneous rocks, usually as a secondary mineral, formed by alteration of mafic minerals such as biotite, hornblende, pyroxene, or garnet.Template:Sfn The glassy rims of pillow basalt on the ocean floor is often altered to pure chlorite, in part by exchange of chemicals with seawater.[6] The green color of many igneous rocks, slates, and schists is due to fine particles of chlorite disseminated throughout the rock.Template:Sfn Chlorite is a common weathering product and is widespread in clay and in sedimentary rock containing clay minerals.Template:Sfn Chlorite is found in pelites along with quartz, albite, sericite, and garnet, and is also found in associate with actinolite and epidote.Template:Sfn
In his pioneering work on metamorphic facies in the Scottish Highlands, G.M. Barrow identified the chlorite zone as the zone of mildest metamorphism.Template:Sfn In modern petrology, chlorite is the diagnostic mineral of the greenschist facies.Template:Sfn This facies is characterized by temperatures near Script error: No such module "convert". and pressures near 5 kbar.Template:Sfn 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.Template:Sfn
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.[7]
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 magmas are generated.[8][9]
Members of the chlorite group
Baileychlore IMA1986-056 Template:Chem2 Borocookeite IMA2000-013 Template:Chem2 Chamosite year: 1820 Template:Chem2 Clinochlore year: 1851 Template:Chem2 Cookeite year: 1866 Template:Chem2 Donbassite year: 1940 Template:Chem2 Gonyerite year: 1955 Template:Chem2 Nimite year: 1968 Template:Chem2 Pennantite year: 1946 Template:Chem2 Ripidolite chlinochlore var. Template:Chem2 Sudoite IMA1966-027 Template:Chem2
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.[10]
Uses
Chlorite does not have any specific industrial uses of any importance. Some rock types containing chlorite, such as chlorite schist, have minor decorative uses or as construction stone. However, chlorite is a common mineral in clay, which has a vast number of uses.Template:Sfn
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.Script error: No such module "Unsubst".
See also
References
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Further reading
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