Lamprophyllite

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Lamprophyllite
Lamprophyllite Basic sodium strontium barium titanium fluo-silicate Kola Peninsula, Russia 2882.jpg
General
Category Silicate mineral
IMA symbol Lmp [1]

Lamprophyllite (named for its lustrous cleavage) is a rare, but widespread mineral Ti-silicate mineral usually found in intrusive agpasitic igneous rocks. Yellow, reddish brown, Vitreous, Pearly. [2]

Lamprophyllite formula is (Sr,Ba,K,Na)2Na(Na,Fe,Mn)2Ti[Ti2O2(Si2O7)2[(O, OH,F)2 . Full isomorphic range between lampropyllite and baritollalpropyllite exist. [3]

The general crystal-chemical formula for lampropyllite-related minerals can be written as A2[(M1)(M2)2(M3)X2] [[5] L2(Si2O7)2O2], where the contents of the O and H sheets are given in square brackets in this order and A = Sr, Ba,K, Na; M1 = Na, Mn2+; M2 = Na, Mn2+, Fe2+, Ca; M3 = Ti, Mn2+, Mg, Fe3+, Fe2+; L = Ti, Fe3+; X = OH, O, F. [4]

Lamprophyllite is monoclinic, The mineral also has an orthorhombic polytype [5] Unit-cell parameters mainly depend from the cationic composition in the interlayer position A [6] The crystal structures of the lamprophyllite-related minerals are based upon HOH modules consisting of a central octahedral O sheet sandwiched between two heteropolyhedral H sheets. [7]

Lamprophyllite melts incongruently (880 °C) with formation of titanium oxides: rutile, tausonite, freudenbergite. Syntetic lamprophyllite synthesis was crystallized from melt. Tewly formed lamprophyllite show higher Sr/Ba ratioi than in equilibrium melt. [8]

Pseudobinare phase diagram lamprophyllite-nepheline Lam-Ne.jpg
Pseudobinare phase diagram lamprophyllite-nepheline

Related Research Articles

<span class="mw-page-title-main">Apophyllite</span> Phyllosilicate mineral

The name apophyllite refers to a specific group of phyllosilicates, a class of minerals. Originally, the group name referred to a specific mineral, but was redefined in 1978 to stand for a class of minerals of similar chemical makeup that comprise a solid solution series, and includes the members fluorapophyllite-(K), fluorapophyllite-(Na), hydroxyapophyllite-(K). The name apophyllite is derived from the Greek ἀποφυλλίζω apophylliso, meaning "it flakes off", a reference to this class's tendency to flake apart when heated, due to water loss. Exfoliation of apophyllite is also possible by treating it with acids or simply by rubbing it. These minerals are typically found as secondary minerals in vesicles in basalt or other volcanic rocks. A recent change (2008) in the nomenclature system used for this group was approved by the International Mineralogical Association, removing the prefixes from the species names and using suffixes to designate the species. A subsequent nomenclature change approved by the International Mineralogical Association in 2013 renamed the minerals to include both suffixes and prefixes, as shown above.

<span class="mw-page-title-main">Zanazziite</span>

Zanazziite is a complex hydrated phosphate mineral from the roscherite group. It is a magnesium beryllium phosphate mineral. Zanazziite arises as barrel-shaped crystals and can reach up to 4 mm. It grows alongside quartz minerals. It is found in the crevices of Lavra da Ilha pegmatite, near Taquaral, in northeastern Minas Gerais, Brazil. Zanazziite is named after Pier F. Zanazzi. Zanazziite has an ideal chemical formula of Ca2Mg5Be4(PO4)6(OH)4·6H2O.

Eudialyte group is a group of complex trigonal zircono- and, more rarely, titanosilicate minerals with general formula [N(1)N(2)N(3)N(4)N(5)]3[M(1a)M(1b)]3M(2)3M(4)Z3[Si24O72]O'4X2, where N(1) and N(2) and N(3) and N(5) = Na+ and more rarely H3O+ or H2O, N(4) = Na+, Sr2+, Mn2+ and more rarely H3O+ or H2O or K+ or Ca2+ or REE3+ (rare earth elements), M(1) and M(1b) = Ca2+, M(1a) = Ca2+ or Mn2+ or Fe2+, M(2) = Fe (both II and III), Mn and rarely Na+, K+ or Zr4+, M(3) = Si, Nb and rarely W, Ti and [] (vacancy), M(4) = Si and or rarely [], Z Zr4+ and or rarely Ti4+, and X = OH, Cl and more rarely CO32− or F. Some of the eudialyte-like structures can even be more complex, however, in general, its typical feature is the presence of [Si3O9]6− and [Si9O27]18− ring silicate groups. Space group is usually R3m or R-3m but may be reduced to R3 due to cation ordering. Like other zirconosilicates, the eudialyte group minerals possess alkaline ion-exchange properties, as microporous materials.

Nabalamprophyllite has a general formula of Ba(Na,Ba){Na3Ti[Ti2O2Si4O14](OH,F)2}. The name is given for its composition and relation to other lamprophyllite-group minerals. Lamprophyllite is a rare Ti-bearing silicate mineral usually found in intrusive igneous rocks.

The Hatrurim Formation or Mottled Zone is a geologic formation with outcrops all around the Dead Sea Basin: in the Negev Desert in Israel, in the Judaean Desert on the West Bank, and in western Jordan. It includes late Cretaceous to Eocene aged impure limestone along with coal bearing chalk and marl. The rocks have been subjected to pyrometamorphism resulting from combustion of contained or underlying coal or hydrocarbon deposits. The formation is named for exposures in the Hatrurim Basin which lies west of the Dead Sea.

<span class="mw-page-title-main">Ikranite</span> Mineral member of the eudialyte group

Ikranite is a member of the eudialyte group, named after the Shubinov Institute of Crystallography of the Russian Academy of Sciences. It is a cyclosilicate mineral that shows trigonal symmetry with the space group R3m, and is often seen with a pseudo-hexagonal habit. Ikranite appears as translucent and ranges in color from yellow to a brownish yellow. This mineral ranks a 5 on Mohs Scale of Hardness, though it is considered brittle, exhibiting conchoidal fracture when broken.

<span class="mw-page-title-main">Perettiite-(Y)</span>

Perettiite-(Y) is a complex silicate–borate mineral with the formula Y2Mn4FeSi2B8O24. It was first discovered in 2015 by Adolf Peretti of the Gemresearch Swisslab (GRS). It was found as inclusions in a phenakite crystal from Mogok, Myanmar.

Ilyukhinite is a very rare mineral of the eudialyte group, with formula (H3O,Na)14Ca6Mn2Zr3Si26O72(OH)2·3H2O. The formula given is simplified and does not show the presence of cyclic silicate groups. Ilyukhinite is the second group representative with species-defining hydronium ion after aqualite.

Dualite is a very rare and complex mineral of the eudialyte group, its complexity being expressed in its formula Na
30
(Ca,Na,Ce,Sr)
12
(Na,Mn,Fe,Ti)
6
Zr
3
Ti
3
MnSi
51
O
144
(OH,H
2
O,Cl)
9
. The formula is simplified as it does not show the presence of cyclic silicate groups. The name of the mineral comes from its dual nature: zircono- and titanosilicate at once. Dualite has two modules in its structure: alluaivite one and eudialyte one. After alluaivite and labyrinthite it stands for third representative of the eudialyte group with essential titanium.

Labyrinthite is a very rare mineral of the eudialyte group. When compared to other species in the group, its structure is extremely complex - with over 100 sites and about 800 cations and anions - hence its name, with its complexity expressed in its chemical formula (Na,K,Sr)35Ca12Fe3Zr6TiSi51O144(O,OH,H2O)9Cl3. The formula is simplified as it does not show the presence of cyclic silicate groups. Complexity of the structure results in symmetry lowering from the typical centrosymmetrical group to R3 space group. Other eudialyte-group representatives with such symmetry lowering include aqualite, oneillite, raslakite, voronkovite. Labyrinthite is the second dual-nature representative of the group after dualite and third with essential titanium after dualite and alluaivite.

Taseqite is a rare mineral of the eudialyte group, with chemical formula Na12Sr3Ca6Fe3Zr3NbSiO(Si9O27)2(Si3O9)2(O,OH,H2O)3Cl2. The formula given is derived from the original one and shows a separate silicon at the M4 site, basing on the nomenclature of the eudialyte group. Taseqite, khomyakovite and manganokhomyakovite are three group representatives with species-defining strontium, although many other members display strontium diadochy. Both strontium (N4Sr) and niobium (M3Nb) are essential in the crystal structure of taseqite. When compared to khomyakovite, taseqite differs in niobium- and chlorine-dominance.

<span class="mw-page-title-main">Manganoeudialyte</span>

Manganoeudialyte is an moderately rare mineral of the eudialyte group, with formula Na14Ca6Mn3Zr3Si2[Si24O72(OH)2]Cl2·4H2O. The formula given is one of the forms that can be given, based on the originally reported one, and shows dominance of silicon at both the M3 and M4 sites. As suggested by its name, it is the manganese-analogue of eudialyte.

<span class="mw-page-title-main">Raslakite</span>

Raslakite is a rare mineral of the eudialyte group with the chemical formula Na15Ca3Fe3(Na,Zr)3Zr3(Si,Nb)SiO(Si9O27)2(Si3O9)2(OH,H2O)3(Cl,OH). This formula is based on the original one, and is extended to show the presence of cyclic silicate groups. The additional silicon and oxygen shown in separation from the cyclic groups are in fact connected with two 9-fold rings. The mineral has lowered symmetry, similarly to some other eudialyte-group members: aqualite, labyrinthite, oneillite and voronkovite. The specific feature of raslakite is, among others, the presence of sodium and zirconium at the M2 site. Raslakite was named after Raslak Cirques located nearby the type locality.

<span class="mw-page-title-main">Jinshajiangite</span>

Jinshajiangite is a rare silicate mineral named after the Jinshajiang river in China. Its currently accepted formula is BaNaFe4Ti2(Si2O7)2O2(OH)2F. It gives a name of the jinshajiangite group. The mineral is associated with alkaline rocks. In jinshajiangite, there is a potassium-to-barium, calcium-to-sodium, manganese-to-iron and iron-to-titanium diadochy substitution. Jinshajiangite is the iron-analogue of surkhobite and perraultite. It is chemically related to bafertisite, cámaraite and emmerichite. Its structure is related to that of bafertisite. Jinshajiangite is a titanosilicate with heteropolyhedral HOH layers, where the H-layer is a mixed tetrahedral-octahedral layer, and the O-layer is simply octahedral.

<span class="mw-page-title-main">Shulamit Gross</span> Israeli geologist

Shulamit Gross was an Israeli mineralogist and geologist who studied the Hatrurim Formation.

<span class="mw-page-title-main">Freudenbergite</span> Oxide mineral

Freudenbergite is a mineral that is named in honor of Wilhelm Freudenberg, palaeontologist at the University of Tübingen and the University of Göttingen, and curator for mineralogy and geology at the National Collections of Natural History in Karlsruhe. He studied Katzenbuckel rocks.

The sulfate fluorides are double salts that contain both sulfate and fluoride anions. They are in the class of mixed anion compounds. Some of these minerals are deposited in fumaroles.

Lomonosovite is a phosphate–silicate mineral with the idealized formula Na10Ti4(Si2O7)2(PO4)2O4 early Na5Ti2(Si2O7)(PO4)O2 or Na2Ti2Si2O9*Na3PO4.

<span class="mw-page-title-main">Fumarole mineral</span> Minerals which are deposited by fumarole exhalations

Fumarole minerals are minerals which are deposited by fumarole exhalations. They form when gases and compounds desublimate or precipitate out of condensates, forming mineral deposits. They are mostly associated with volcanoes following deposition from volcanic gas during an eruption or discharge from a volcanic vent or fumarole, but have been encountered on burning coal deposits as well. They can be black or multicoloured and are often unstable upon exposure to the atmosphere.

<span class="mw-page-title-main">Ferricoronadite</span>

Ferricoronadite is a lead mineral discovered in 2016 by Chukanov et al. near Nezhilovo, North Macedonia. Its simplified elemental formula is Pb(Mn64+Fe23+)O16, and it is found in a matrix of zinc-dominant spinels. Ferricoronadite is named as an analogue of coronadite.

References

  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. "Lamprophyllite".
  3. Zaitsev V.A. Kogarko L.N. (2002). "Compositions of Minerals of the Lamprophyllite Group from Alkaline Massifs Worldwide". Geochemistry International. 40: 313–322.
  4. Rastsvetaeva, Ramiza K.; Chukanov, Nikita V.; Aksenov, Sergey M. (2016-12-31). "The crystal chemistry of lamprophyllite-related minerals: a review". European Journal of Mineralogy. 28 (5): 915–930. Bibcode:2016EJMin..28..915R. doi:10.1127/ejm/2016/0028-2560.
  5. Krivovichev, Sergey V.; Armbruster, Thomas; Yakovenchuk, Viktor N.; Pakhomovsky, Yakov A.; Men'shikov, Yuriy P. (2003-08-01). "Crystal structures of lamprophyllite-2M and lamprophyllite-2O from the Lovozero alkaline massif, Kola peninsula, Russia". European Journal of Mineralogy. 15 (4): 711–718. Bibcode:2003EJMin..15..711K. doi:10.1127/0935-1221/2003/0015-0711. ISSN   0935-1221.
  6. Zaitsev, V. A. (May 2005). "Numerical dependence of the unit-cell parameters of minerals of the lamprophyllite group on the cationic composition in the interlayer position". Crystallography Reports. 50 (3): 379–381. Bibcode:2005CryRp..50..379Z. doi:10.1134/1.1927593. ISSN   1063-7745. S2CID   98166023.
  7. Rastsvetaeva, Ramiza K.; Chukanov, Nikita V.; Aksenov, Sergey M. (2016-12-31). "The crystal chemistry of lamprophyllite-related minerals: a review". European Journal of Mineralogy. 28 (5): 915–930. Bibcode:2016EJMin..28..915R. doi:10.1127/ejm/2016/0028-2560.
  8. VA Zaitsev, LD Krigman, LN Kogarko (2004). "Pseudobinare phase diagram lamprophyllite-nepheline". Lithos. EMPG-X special volume.{{cite journal}}: CS1 maint: multiple names: authors list (link)