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| image = Jarosite on quartz Potassium iron sulfate Arabia District, Pershing County, Nevada 2779.jpg
| image = Jarosite on quartz Potassium iron sulfate Arabia District, Pershing County, Nevada 2779.jpg
| caption = Jarosite on quartz from the Arabia District, Pershing County, Nevada
| caption = Jarosite on quartz from the Arabia District, Pershing County, Nevada
| formula = KFe<sup>3+</sup><sub>3</sub>(OH)<sub>6</sub>(SO<sub>4</sub>)<sub>2</sub>
| formula = KFe<sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>
| IMAsymbol = Jrs<ref>{{Cite journal|last=Warr|first=L.N.|date=2021|title=IMA–CNMNC approved mineral symbols|journal=Mineralogical Magazine|volume=85|issue=3|pages=291–320|doi=10.1180/mgm.2021.43|bibcode=2021MinM...85..291W|s2cid=235729616|doi-access=free}}</ref>
| molweight = 500.8 g/mol
| molweight = 500.8 g/mol
| strunz = 7.BC.10
| strunz = 7.BC.10
| dana = 30.2.5.1
| dana = 30.2.5.1
| system = [[Trigonal]]
| system = [[Trigonal]]
| class = Rhombohedral ({{overline|3}}m) <br/>[[H-M symbol]]: ({{overline|3}}m)
| class = Rhombohedral ({{overline|3}}m) <br />[[H-M symbol]]: ({{overline|3}}m)
| symmetry = ''R''{{overline|3}}m
| symmetry = ''R''{{overline|3}}m
| unit cell = a = 7.304&nbsp;[[Ångstrom|Å]], c = 17.268&nbsp;Å; Z&nbsp;=&nbsp;3
| unit cell = a = 7.304&nbsp;[[Ångstrom|Å]], c = 17.268&nbsp;Å; Z&nbsp;=&nbsp;3
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| fracture = Uneven to conchoidal
| fracture = Uneven to conchoidal
| tenacity = Brittle
| tenacity = Brittle
| mohs = 2.5 - 3.5
| mohs = 2.5–3.5
| luster = Subadamantine to vitreous, resinous on fractures
| luster = Subadamantine to vitreous, resinous on fractures
| refractive = n<sub>ω</sub> = 1.815 to 1.820; n<sub>ε</sub> = 1.713 to 1.715
| refractive = n<sub>ω</sub> = 1.815 to 1.820; n<sub>ε</sub> = 1.713 to 1.715
| opticalprop = Uniaxial (-), usually anomalously biaxial with very small 2V
| opticalprop = Uniaxial (), usually anomalously biaxial with very small 2V
| birefringence = 0.102 to 0.105
| birefringence = 0.102 to 0.105
| pleochroism = E colorless, very pale yellow, or pale greenish yellow, O deep golden yellow or reddish brown
| pleochroism = E colorless, very pale yellow, or pale greenish yellow, O deep golden yellow or reddish brown
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| fusibility =
| fusibility =
| diagnostic =
| diagnostic =
| solubility = Insoluble in water. Soluble in HCl.
| solubility = Insoluble in water. Soluble in HCl.
| diaphaneity = Transparent to translucent
| diaphaneity = Transparent to translucent
| other = Strongly [[pyroelectric]]. Non-fluorescent. Barely detectable radioactivity
| other = Strongly [[pyroelectric]]. Non-fluorescent. Barely detectable radioactivity
| references = <ref name=Dana>Gaines et al (1997) Dana's New Mineralogy Eighth Edition, Wiley</ref><ref name=Mindat>http://www.mindat.org/min-2078.html</ref><ref name=HOM>http://rruff.geo.arizona.edu/doclib/hom/jarosite.pdf</ref>}}
| references = <ref name=Dana>Gaines et al (1997) Dana's New Mineralogy Eighth Edition, Wiley</ref><ref name=Mindat>{{Cite web|url=http://www.mindat.org/min-2078.html|title = Jarosite}}</ref><ref name=HOM>{{cite web |last1=Anthony |first1=John W. |last2=Bideaux |first2=Richard A. |last3=Bladh |first3=Kenneth W. |last4=Nichols |first4=Monte C. |title=Jarosite |url=http://www.handbookofmineralogy.org/pdfs/jarosite.pdf |website=Handbook of Mineralogy |publisher=Mineral Data Publishing |access-date=14 March 2022 |date=2005}}</ref>}}


'''Jarosite''' is a basic [[hydrate|hydrous]] [[sulfate]] of [[potassium]] and [[iron]] with a chemical formula of KFe<sup>3+</sup><sub>3</sub>(OH)<sub>6</sub>(SO<sub>4</sub>)<sub>2</sub>. This [[sulfate mineral]] is formed in [[ore]] deposits by the [[oxidation]] of iron [[sulfide]]s. Jarosite is often produced as a byproduct during the purification and refining of [[zinc]] and is also commonly associated with [[acid mine drainage]] and [[acid sulfate soil]] environments.
'''Jarosite''' is a basic [[hydrate|hydrous]] [[sulfate]] of [[potassium]] and ferric [[iron]] (Fe-III) with a chemical formula of KFe<sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>. This [[sulfate mineral]] is formed in [[ore]] deposits by the [[oxidation]] of iron [[sulfide]]s. Jarosite is often produced as a byproduct during the purification and refining of [[zinc]] and is also commonly associated with [[acid mine drainage]] and [[acid sulfate soil]] environments.


==Physical properties==
==Physical properties==
[[File:Jarosite-34304.jpg|thumb|left|Jarosite crystals from Sierra Peña Blanca, Aldama, Chihuahua, Mexico (5.6 x 3.1 x 1.6 cm)]]
[[File:Jarosite-34304.jpg|thumb|left|Jarosite crystals from Sierra Peña Blanca, Aldama, Chihuahua, Mexico (5.6 × 3.1 × 1.6 cm)]]
Jarosite has a [[trigonal]] crystal structure and is brittle, with basal cleavage, a [[Mohs scale of mineral hardness|hardness]] of 2.5-3.5, and a [[specific gravity]] of 3.15-3.26. It is translucent to opaque with a vitreous to dull luster, and is colored dark yellow to yellowish-brown. It can sometimes be confused with [[limonite]] or [[goethite]] with which it commonly occurs in the [[gossan]] (oxidized cap over an ore body). Jarosite is an iron analogue of the potassium aluminium sulfate, [[alunite]].
Jarosite has a [[trigonal]] crystal structure and is brittle, with basal cleavage, a [[Mohs scale of mineral hardness|hardness]] of 2.5–3.5, and a [[specific gravity]] of 3.15–3.26. It is translucent to opaque with a vitreous to dull luster, and is colored dark yellow to yellowish-brown. It can sometimes be confused with [[limonite]] or [[goethite]] with which it commonly occurs in the [[gossan]] (oxidized cap over an ore body). Jarosite is an iron analogue of the potassium aluminium sulfate, [[alunite]].


== Solid solution series ==
== Solid solution series ==
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The alunite supergroup includes the [[alunite]], jarosite, [[beudantite]], [[crandallite]] and [[florencite]] subgroups. The alunite supergroup minerals are isostructural with each other and substitution between them occurs, resulting in several [[solid solution]] series. The alunite supergroup has the general formula AB<sub>3</sub>(TO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>. In the alunite subgroup B is Al, and in the jarosite subgroup B is Fe<sup>3+</sup>. The beudantite subgroup has the general formula AB<sub>3</sub>(XO<sub>4</sub>)(SO<sub>4</sub>)(OH)<sub>6</sub>, the crandallite subgroup AB<sub>3</sub>(TO<sub>4</sub>)<sub>2</sub>(OH)<sub>5</sub>•H<sub>2</sub>O and the florencite subgroup AB<sub>3</sub>(TO<sub>4</sub>)<sub>2</sub>(OH)<sub>5&thinsp;or&thinsp;6</sub>.
The alunite supergroup includes the [[alunite]], jarosite, [[beudantite]], [[crandallite]] and [[florencite]] subgroups. The alunite supergroup minerals are isostructural with each other and substitution between them occurs, resulting in several [[solid solution]] series. The alunite supergroup has the general formula AB<sub>3</sub>(TO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>. In the alunite subgroup B is Al, and in the jarosite subgroup B is Fe<sup>3+</sup>. The beudantite subgroup has the general formula AB<sub>3</sub>(XO<sub>4</sub>)(SO<sub>4</sub>)(OH)<sub>6</sub>, the crandallite subgroup AB<sub>3</sub>(TO<sub>4</sub>)<sub>2</sub>(OH)<sub>5</sub>•H<sub>2</sub>O and the florencite subgroup AB<sub>3</sub>(TO<sub>4</sub>)<sub>2</sub>(OH)<sub>5&thinsp;or&thinsp;6</sub>.


[[File:Jarosite crystal structure.png|thumb|left|upright=1.25|Crystal structure of jarosite Color code: Potassium, K: purple; Sulfur, S: olive; Iron, Fe: violet-blue; Cell: sky-blue]]
[[File:Jarosite crystal structure.png|thumb|left|upright=1.25|Crystal structure of jarosite Color code: Potassium, K: purple; Sulfur, S: olive; Iron, Fe: violet-blue; Cell: sky-blue.]]
In the jarosite-alunite series Al may substitute for Fe and a complete solid solution series between jarosite and alunite, KAl<sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, probably exists, but intermediate members are rare. The material from [[Kopec (Prostiboř)|Kopec]], [[Czech Republic]], has about equal Fe and Al, but the amount of Al in jarosite is usually small.
In the jarosite-alunite series Al may substitute for Fe and a complete solid solution series between jarosite and alunite, KAl<sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, probably exists, but intermediate members are rare. The material from [[Kopec (Prostiboř)|Kopec]], [[Czech Republic]], has about equal Fe and Al, but the amount of Al in jarosite is usually small.


When jarosite forms from [[pyrite]] [[oxidation]] in sedimentary clays, the main sources of K<sup>+</sup> are [[illite]], a non-swelling clay, or [[K-feldspar]]. In other geological settings [[mica]]'s alteration can also be a source of potassium.
In the jarosite-natrojarosite series Na substitutes for K to at least Na/K = 1:2.4 but the pure sodium end member NaFe<sup>3+</sup><sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub> is not known in nature. Minerals with Na > K are known as [[natrojarosite]]. End member formation (jarosite and natrojarosite) is favoured by a low temperature environment, less than 100&nbsp;°C, and is illustrated by the oscillatory zoning of jarosite and natrojarosite found in samples from the Apex Mine, Arizona, and [[Gold Hill, Utah]]. This indicates that there is a wide [[miscibility gap]] between the two end members,<ref name=AM92>American Mineralogist (2007) 92:444-447</ref> and it is doubtful whether a complete series exists between jarosite and natrojarosite.


In the jarosite-natrojarosite series Na substitutes for K to at least Na/K = 1:2.4 but the pure sodium end member NaFe<sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub> is not known in nature. Minerals with Na > K are known as [[natrojarosite]]. End member formation (jarosite and natrojarosite) is favoured by a low temperature environment, less than 100&nbsp;°C, and is illustrated by the oscillatory zoning of jarosite and natrojarosite found in samples from the Apex Mine, Arizona, and [[Gold Hill, Utah]]. This indicates that there is a wide [[miscibility gap]] between the two end members,<ref name=AM92>American Mineralogist (2007) 92:444–447</ref> and it is doubtful whether a complete series exists between jarosite and natrojarosite.
In [[hydroniumjarosite]]<ref name=AM921464>American Mineralogist (2007) 92:1464-1473</ref> the [[hydronium]] ion H<sub>3</sub>O<sup>+</sup> can also substitute for K<sup>+</sup>, with increased hydronium ion content causing a marked decrease in the lattice parameter ''c'', although there is little change in ''a''.<ref name=AM50>American Mineralogist (1965) 50:1595-1607</ref> Hydroniumjarosite will only form from alkali-deficient solutions, as alkali-rich jarosite forms preferentially.


In [[hydroniumjarosite]]<ref name=AM921464>American Mineralogist (2007) 92:1464–1473</ref> the [[hydronium]] ion H<sub>3</sub>O<sup>+</sup> can also substitute for K<sup>+</sup>, with increased hydronium ion content causing a marked decrease in the lattice parameter ''c'', although there is little change in ''a''.<ref name=AM50>American Mineralogist (1965) 50:1595–1607</ref> Hydroniumjarosite will only form from alkali-deficient solutions, as alkali-rich jarosite forms preferentially.
Divalent cations may also substitute for the monovalent cation K<sup>+</sup> in the A site.<ref name=AM72>American Mineralogist (1987) 72:178-187</ref> Charge balance may be achieved in three ways.

Divalent cations may also substitute for the monovalent cation K<sup>+</sup> in the A site.<ref name=AM72>American Mineralogist (1987) 72:178–187</ref> Charge balance may be achieved in three ways.
:Firstly by replacing two monovalent cations by one divalent cation, and leaving an A site vacancy, as in [[plumbogummite]], Pb<sup>2+</sup>Al<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub>(OH)<sub>5</sub>.H<sub>2</sub>O, which is a member of the crandallite subgroup.
:Firstly by replacing two monovalent cations by one divalent cation, and leaving an A site vacancy, as in [[plumbogummite]], Pb<sup>2+</sup>Al<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub>(OH)<sub>5</sub>.H<sub>2</sub>O, which is a member of the crandallite subgroup.
:Secondly by incorporating divalent ions in the B sites, as in [[osarizawaite]], Pb<sup>2+</sup>Cu<sup>2+</sup>Al<sub>2</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, alunite subgroup, and [[beaverite]], Pb<sup>2+</sup>Cu<sup>2+</sup>(Fe<sup>3+</sup>,Al)<sub>2</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, jarosite subgroup.
:Secondly by incorporating divalent ions in the B sites, as in [[osarizawaite]], Pb<sup>2+</sup>Cu<sup>2+</sup>Al<sub>2</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, alunite subgroup, and [[beaverite]], Pb<sup>2+</sup>Cu<sup>2+</sup>(Fe<sup>3+</sup>,Al)<sub>2</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, jarosite subgroup.
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== History ==
== History ==
Jarosite was first described in 1852 by [[August Breithaupt]] in the Barranco del Jaroso in the Sierra Almagrera (near Los Lobos, Cuevas del Almanzora, [[Almería (province)|Almería]], [[Spain]]). The name jarosite is also directly derived from Jara, the Spanish name of a yellow flower that belongs to the genus ''[[Cistus]]'' and grows in this sierra. The mineral and the flower have the same color.
Jarosite was first described in 1852 by [[August Breithaupt]] in the Barranco del Jaroso in the Sierra Almagrera (near Los Lobos, Cuevas del Almanzora, [[Almería (province)|Almería]], [[Spain]]). The name jarosite is directly derived from "jara", the Spanish name of a yellow flower that belongs to the genus ''[[Cistus]]'' and grows in the sierra. The mineral and the flower have the same color.


Mysterious spheres of clay 1.5 to 5 inches in diameter and covered with jarosite have been found beneath the [[Temple of the Feathered Serpent]] an ancient six level stepped pyramid 30 miles from Mexico City.<ref>[http://news.discovery.com/history/archaeology/mysterious-spheres-emerge-from-ancient-temple-1304291.htm Discovery News (2013) "Robot Finds Mysterious Spheres in Ancient Temple"]</ref>
Mysterious spheres of clay, {{convert|1.5|to|5|in|round=5}} in diameter and covered with jarosite, have been found beneath the [[Temple of the Feathered Serpent]], an ancient six-level stepped pyramid {{convert|30|mi|round=5}} from Mexico City.<ref>{{Cite web |url=http://news.discovery.com/history/archaeology/mysterious-spheres-emerge-from-ancient-temple-1304291.htm |title=Discovery News (2013) "Robot Finds Mysterious Spheres in Ancient Temple" |access-date=2013-04-30 |archive-date=2015-03-19 |archive-url=https://web.archive.org/web/20150319032519/http://news.discovery.com/history/archaeology/mysterious-spheres-emerge-from-ancient-temple-1304291.htm |url-status=dead }}</ref>


=== Mars exploration ===
=== Mars exploration ===
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| first = Kenneth
| first = Kenneth
| date = 2009-05-19
| date = 2009-05-19
| title = Mars rover’s 5 working wheels are stuck in hidden soft spot
| title = Mars rover's 5 working wheels are stuck in hidden soft spot
| work = The New York Times
| work = The New York Times
| access-date = 2009-05-19
| access-date = 2009-05-19
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=== Antarctica deep borehole ===
=== Antarctica deep borehole ===
On Earth, jarosite is mainly associated with the ultimate stage of [[acid mine drainage|pyrite oxidation]] in clay environment and can also be found in [[mine tailings]] waste where acidic conditions prevail. Against all expectations, jarosite has also been fortuitously discovered in minute quantities in the form of small dust particules in ice cores recovered from a deep borehole in [[Antarctica]]. This surprising discovery was made by geologists who were searching for specific minerals capable to indicate ice age cycles within the layers of a 1620 meters-long ice core.<ref name="Joosse2021">{{cite journal|last1=Joosse|first1=Tess|title=Substance found in Antarctic ice may solve a martian mystery|journal=Science|year=2021|issn=0036-8075|doi=10.1126/science.abg7690}}</ref> Geologists speculate that jarosite dust could also have accumulated within ice on glaciers on Mars. However, this hypothesis is a matter of controverses, because on Mars jarosite deposits can be very thick (up to 10 meters); but Mars is also a very dusty planet and in the absence of [[plate tectonic]] on Mars glacial dust deposits might have accumulated during long periods of time.
On Earth, jarosite is mainly associated with the ultimate stage of [[acid mine drainage|pyrite oxidation]] in clay environment, and can also be found in [[mine tailings]] waste where acidic conditions prevail. Against all expectations, jarosite has also been fortuitously discovered in minute quantities in the form of small dust particles in ice cores recovered from a deep borehole in [[Antarctica]]. That surprising discovery was made by geologists who were searching for specific minerals capable of indicating ice age cycles within the layers of a 1620-meter-long ice core.<ref name="Joosse2021">{{cite journal |last1=Joosse |first1=Tess |title=Substance found in Antarctic ice may solve a martian mystery |journal=Science |year=2021 |issn=0036-8075 |doi=10.1126/science.abg7690 |s2cid=234047108}}</ref> Geologists speculate that jarosite dust could also have accumulated within ice in glaciers on Mars.<ref name="Baccolo2021">{{cite journal |last1=Baccolo |first1=Giovanni |last2=Delmonte |first2=Barbara |last3=Niles |first3=P. B. |last4=Cibin |first4=Giannantonio |last5=Di Stefano |first5=Elena |last6=Hampai |first6=Dariush |last7=Keller |first7=Lindsay |last8=Maggi |first8=Valter |last9=Marcelli |first9=Augusto|last10=Michalski |first10=Joseph |last11=Snead |first11=Christopher |last12=Frezzotti |first12=Massimo |title=Jarosite formation in deep Antarctic ice provides a window into acidic, water-limited weathering on Mars|journal=Nature Communications |volume=12 |issue=1 |year=2021 |page=436 |issn=2041-1723 |doi=10.1038/s41467-020-20705-z |pmid=33469027 |pmc=7815727 |bibcode=2021NatCo..12..436B |doi-access=free}}</ref> However, that hypothesis is a matter of controversy because, on Mars, jarosite deposits can be very thick (up to 10 meters). However, Mars is also a very dusty planet and, in the absence of [[plate tectonics]] on Mars, glacial dust deposits might have accumulated over long periods of time.


== Use in materials science ==
== Use in materials science ==
Jarosite is also a more generic term denoting an extensive family of compounds of the form AM<sub>3</sub>(OH)<sub>6</sub>(SO<sub>4</sub>)<sub>2</sub>, where A<sup>+</sup> = [[Sodium|Na]], [[Potassium|K]], [[Rubidium|Rb]], [[Ammonium|NH<sub>4</sub>]], [[Hydronium|H<sub>3</sub>O]], [[Silver|Ag]], [[Thallium|Tl]] and M<sup>3+</sup> = [[Iron|Fe]], [[Chromium|Cr]], [[Vanadium|V]]. In [[condensed matter physics]] and [[materials science]] they are renowned for containing layers with [[kagome lattice]] structure, relating to [[geometrically frustrated magnet]]s.<ref>{{cite journal | last = Harrison | first = A. | year = 2004 | title = First catch your hare: the design and synthesis of frustrated magnets | journal = J. Phys.: Condens. Matter | volume = 16 | issue = 9-12 | pages = S553–S572 | doi = 10.1088/0953-8984/16/11/001 |bibcode = 2004JPCM...16S.553H }}</ref><ref>{{cite journal | last = Wills | first = A. S. | year = 2000 | title = Magnetic properties of pure and diamagnetically doped jarosites: Model kagomé antiferromagnets with variable coverage of the magnetic lattice | journal = Phys. Rev. B | volume = 61 | issue = 9 | pages = 6156–6169 | doi = 10.1103/PhysRevB.61.6156 | last2 = Harrison | first2 = A. | last3 = Ritter | first3 = C. | last4 = Smith | first4 = R.|bibcode = 2000PhRvB..61.6156W |display-authors=etal}}</ref>
Jarosite is also a more generic term denoting an extensive family of compounds of the form AM<sub>3</sub>(OH)<sub>6</sub>(SO<sub>4</sub>)<sub>2</sub>, where A<sup>+</sup> = [[Sodium|Na]], [[Potassium|K]], [[Rubidium|Rb]], [[Ammonium|NH<sub>4</sub>]], [[Hydronium|H<sub>3</sub>O]], [[Silver|Ag]], [[Thallium|Tl]] and M<sup>3+</sup> = [[Iron|Fe]], [[Chromium|Cr]], [[Vanadium|V]]. In [[condensed matter physics]] and [[materials science]] they are renowned for containing layers with [[kagome lattice]] structure, relating to [[geometrically frustrated magnet]]s.<ref>{{cite journal | last = Harrison | first = A. | year = 2004 | title = First catch your hare: the design and synthesis of frustrated magnets | journal = J. Phys.: Condens. Matter | volume = 16 | issue = 9–12 | pages = S553–S572 | doi = 10.1088/0953-8984/16/11/001 |bibcode = 2004JPCM...16S.553H | s2cid = 250736993 }}</ref><ref>{{cite journal | last1 = Wills | first1 = A. S. | year = 2000 | title = Magnetic properties of pure and diamagnetically doped jarosites: Model kagomé antiferromagnets with variable coverage of the magnetic lattice | journal = Phys. Rev. B | volume = 61 | issue = 9 | pages = 6156–6169 | doi = 10.1103/PhysRevB.61.6156 | last2 = Harrison | first2 = A. | last3 = Ritter | first3 = C. | last4 = Smith | first4 = R.|bibcode = 2000PhRvB..61.6156W |display-authors=etal}}</ref>


==See also==
==See also==
Line 94: Line 97:
* [http://webmineral.com/data/Jarosite.shtml Webmineral data]
* [http://webmineral.com/data/Jarosite.shtml Webmineral data]
* [http://www.news.cornell.edu/Chronicle/04/3.4.04/jarosite.html Cornell University (2004) ''How an obscure mineral provided a vital clue to Martian water.'']
* [http://www.news.cornell.edu/Chronicle/04/3.4.04/jarosite.html Cornell University (2004) ''How an obscure mineral provided a vital clue to Martian water.'']
* [http://news.discovery.com/history/archaeology/mysterious-spheres-emerge-from-ancient-temple-1304291.htm Discovery News (2013) "Robot Finds Mysterious Spheres in Ancient Temple"]
* [http://news.discovery.com/history/archaeology/mysterious-spheres-emerge-from-ancient-temple-1304291.htm Discovery News (2013) "Robot Finds Mysterious Spheres in Ancient Temple"] {{Webarchive|url=https://web.archive.org/web/20150319032519/http://news.discovery.com/history/archaeology/mysterious-spheres-emerge-from-ancient-temple-1304291.htm |date=2015-03-19 }}


==External links==
==External links==

Latest revision as of 20:46, 17 January 2024

Jarosite
Jarosite on quartz from the Arabia District, Pershing County, Nevada
General
CategorySulfate minerals
Formula
(repeating unit)
KFe3(SO4)2(OH)6
IMA symbolJrs[1]
Strunz classification7.BC.10
Dana classification30.2.5.1
Crystal systemTrigonal
Crystal classRhombohedral (3m)
H-M symbol: (3m)
Space groupR3m
Unit cella = 7.304 Å, c = 17.268 Å; Z = 3
Identification
Formula mass500.8 g/mol
ColorAmber yellow or dark brown
Crystal habitCrystals are usually pseudocubic or tabular, also as granular crusts, nodules, fibrous masses or concretionary.
CleavageDistinct on {0001}
FractureUneven to conchoidal
TenacityBrittle
Mohs scale hardness2.5–3.5
LusterSubadamantine to vitreous, resinous on fractures
Streaklight yellow
DiaphaneityTransparent to translucent
Specific gravity2.9 to 3.3
Optical propertiesUniaxial (−), usually anomalously biaxial with very small 2V
Refractive indexnω = 1.815 to 1.820; nε = 1.713 to 1.715
Birefringence0.102 to 0.105
PleochroismE colorless, very pale yellow, or pale greenish yellow, O deep golden yellow or reddish brown
SolubilityInsoluble in water. Soluble in HCl.
Other characteristicsStrongly pyroelectric. Non-fluorescent. Barely detectable radioactivity
References[2][3][4]

Jarosite is a basic hydrous sulfate of potassium and ferric iron (Fe-III) with a chemical formula of KFe3(SO4)2(OH)6. This sulfate mineral is formed in ore deposits by the oxidation of iron sulfides. Jarosite is often produced as a byproduct during the purification and refining of zinc and is also commonly associated with acid mine drainage and acid sulfate soil environments.

Physical properties[edit]

Jarosite crystals from Sierra Peña Blanca, Aldama, Chihuahua, Mexico (5.6 × 3.1 × 1.6 cm)

Jarosite has a trigonal crystal structure and is brittle, with basal cleavage, a hardness of 2.5–3.5, and a specific gravity of 3.15–3.26. It is translucent to opaque with a vitreous to dull luster, and is colored dark yellow to yellowish-brown. It can sometimes be confused with limonite or goethite with which it commonly occurs in the gossan (oxidized cap over an ore body). Jarosite is an iron analogue of the potassium aluminium sulfate, alunite.

Solid solution series[edit]

The alunite supergroup includes the alunite, jarosite, beudantite, crandallite and florencite subgroups. The alunite supergroup minerals are isostructural with each other and substitution between them occurs, resulting in several solid solution series. The alunite supergroup has the general formula AB3(TO4)2(OH)6. In the alunite subgroup B is Al, and in the jarosite subgroup B is Fe3+. The beudantite subgroup has the general formula AB3(XO4)(SO4)(OH)6, the crandallite subgroup AB3(TO4)2(OH)5•H2O and the florencite subgroup AB3(TO4)2(OH)5 or 6.

Crystal structure of jarosite Color code: Potassium, K: purple; Sulfur, S: olive; Iron, Fe: violet-blue; Cell: sky-blue.

In the jarosite-alunite series Al may substitute for Fe and a complete solid solution series between jarosite and alunite, KAl3(SO4)2(OH)6, probably exists, but intermediate members are rare. The material from Kopec, Czech Republic, has about equal Fe and Al, but the amount of Al in jarosite is usually small.

When jarosite forms from pyrite oxidation in sedimentary clays, the main sources of K+ are illite, a non-swelling clay, or K-feldspar. In other geological settings mica's alteration can also be a source of potassium.

In the jarosite-natrojarosite series Na substitutes for K to at least Na/K = 1:2.4 but the pure sodium end member NaFe3(SO4)2(OH)6 is not known in nature. Minerals with Na > K are known as natrojarosite. End member formation (jarosite and natrojarosite) is favoured by a low temperature environment, less than 100 °C, and is illustrated by the oscillatory zoning of jarosite and natrojarosite found in samples from the Apex Mine, Arizona, and Gold Hill, Utah. This indicates that there is a wide miscibility gap between the two end members,[5] and it is doubtful whether a complete series exists between jarosite and natrojarosite.

In hydroniumjarosite[6] the hydronium ion H3O+ can also substitute for K+, with increased hydronium ion content causing a marked decrease in the lattice parameter c, although there is little change in a.[7] Hydroniumjarosite will only form from alkali-deficient solutions, as alkali-rich jarosite forms preferentially.

Divalent cations may also substitute for the monovalent cation K+ in the A site.[8] Charge balance may be achieved in three ways.

Firstly by replacing two monovalent cations by one divalent cation, and leaving an A site vacancy, as in plumbogummite, Pb2+Al3(PO4)2(OH)5.H2O, which is a member of the crandallite subgroup.
Secondly by incorporating divalent ions in the B sites, as in osarizawaite, Pb2+Cu2+Al2(SO4)2(OH)6, alunite subgroup, and beaverite, Pb2+Cu2+(Fe3+,Al)2(SO4)2(OH)6, jarosite subgroup.
Thirdly by replacing divalent anions with trivalent anions, as in beudantite, PbFe3+3(AsO4)3−(SO4)(OH)6, beudantite subgroup.

History[edit]

Jarosite was first described in 1852 by August Breithaupt in the Barranco del Jaroso in the Sierra Almagrera (near Los Lobos, Cuevas del Almanzora, Almería, Spain). The name jarosite is directly derived from "jara", the Spanish name of a yellow flower that belongs to the genus Cistus and grows in the sierra. The mineral and the flower have the same color.

Mysterious spheres of clay, 1.5 to 5 inches (40 to 125 mm) in diameter and covered with jarosite, have been found beneath the Temple of the Feathered Serpent, an ancient six-level stepped pyramid 30 miles (50 km) from Mexico City.[9]

Mars exploration[edit]

Ferric sulfate and jarosite have been detected by three martian rovers: Spirit, Opportunity and Curiosity. These substances are indicative of strongly oxidizing conditions prevailing at the surface of Mars. In May 2009, the Spirit rover became stuck when it drove over a patch of soft ferric sulfate that had been hidden under a veneer of normal-looking soil.[10] Because iron sulfate has very little cohesion, the rover's wheels could not gain sufficient traction to pull the body of the rover out of the iron sulfate patch. Multiple techniques were attempted to extricate the rover, but the wheels eventually sank so deeply into the iron sulfate that the body of the rover came to rest on the Martian surface, preventing the wheels from exerting any force on the material below them. As the JPL team failed to recover the mobility of Spirit, it signified the end of the journey for the rover.

Antarctica deep borehole[edit]

On Earth, jarosite is mainly associated with the ultimate stage of pyrite oxidation in clay environment, and can also be found in mine tailings waste where acidic conditions prevail. Against all expectations, jarosite has also been fortuitously discovered in minute quantities in the form of small dust particles in ice cores recovered from a deep borehole in Antarctica. That surprising discovery was made by geologists who were searching for specific minerals capable of indicating ice age cycles within the layers of a 1620-meter-long ice core.[11] Geologists speculate that jarosite dust could also have accumulated within ice in glaciers on Mars.[12] However, that hypothesis is a matter of controversy because, on Mars, jarosite deposits can be very thick (up to 10 meters). However, Mars is also a very dusty planet and, in the absence of plate tectonics on Mars, glacial dust deposits might have accumulated over long periods of time.

Use in materials science[edit]

Jarosite is also a more generic term denoting an extensive family of compounds of the form AM3(OH)6(SO4)2, where A+ = Na, K, Rb, NH4, H3O, Ag, Tl and M3+ = Fe, Cr, V. In condensed matter physics and materials science they are renowned for containing layers with kagome lattice structure, relating to geometrically frustrated magnets.[13][14]

See also[edit]

References[edit]

  1. ^ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
  2. ^ Gaines et al (1997) Dana's New Mineralogy Eighth Edition, Wiley
  3. ^ "Jarosite".
  4. ^ Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (2005). "Jarosite" (PDF). Handbook of Mineralogy. Mineral Data Publishing. Retrieved 14 March 2022.
  5. ^ American Mineralogist (2007) 92:444–447
  6. ^ American Mineralogist (2007) 92:1464–1473
  7. ^ American Mineralogist (1965) 50:1595–1607
  8. ^ American Mineralogist (1987) 72:178–187
  9. ^ "Discovery News (2013) "Robot Finds Mysterious Spheres in Ancient Temple"". Archived from the original on 2015-03-19. Retrieved 2013-04-30.
  10. ^ Chang, Kenneth (2009-05-19). "Mars rover's 5 working wheels are stuck in hidden soft spot". The New York Times. ISSN 0362-4331. Retrieved 2009-05-19.
  11. ^ Joosse, Tess (2021). "Substance found in Antarctic ice may solve a martian mystery". Science. doi:10.1126/science.abg7690. ISSN 0036-8075. S2CID 234047108.
  12. ^ Baccolo, Giovanni; Delmonte, Barbara; Niles, P. B.; Cibin, Giannantonio; Di Stefano, Elena; Hampai, Dariush; Keller, Lindsay; Maggi, Valter; Marcelli, Augusto; Michalski, Joseph; Snead, Christopher; Frezzotti, Massimo (2021). "Jarosite formation in deep Antarctic ice provides a window into acidic, water-limited weathering on Mars". Nature Communications. 12 (1): 436. Bibcode:2021NatCo..12..436B. doi:10.1038/s41467-020-20705-z. ISSN 2041-1723. PMC 7815727. PMID 33469027.
  13. ^ Harrison, A. (2004). "First catch your hare: the design and synthesis of frustrated magnets". J. Phys.: Condens. Matter. 16 (9–12): S553–S572. Bibcode:2004JPCM...16S.553H. doi:10.1088/0953-8984/16/11/001. S2CID 250736993.
  14. ^ Wills, A. S.; Harrison, A.; Ritter, C.; Smith, R.; et al. (2000). "Magnetic properties of pure and diamagnetically doped jarosites: Model kagomé antiferromagnets with variable coverage of the magnetic lattice". Phys. Rev. B. 61 (9): 6156–6169. Bibcode:2000PhRvB..61.6156W. doi:10.1103/PhysRevB.61.6156.

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