Xenotime

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Xenotime
Xenotime with Rutile-08-2-78ab.jpg
Xenotime with rutile
General
Category Phosphate minerals
Formula
(repeating unit)
YPO4
IMA symbol Xtm [1]
Strunz classification 8.AD.35
Crystal system Tetragonal
Crystal class Dipyramidal (4/mmm)
H-M symbol: (4/m)
Space group I41/a
Identification
ColorBrown, brownish yellow, gray
Crystal habit Prismatic, radial aggregates, granular
Cleavage Perfect [100]
Fracture Uneven to splintery
Mohs scale hardness4.5
Luster Vitreous to resinous
Streak Pale brown, yellowish or reddish, to white
Diaphaneity Translucent to opaque
Specific gravity 4.4–5.1
Refractive index 1.720–1.815
Birefringence δ = 0.096
Pleochroism Dichroic
Other characteristicsNot radioactive or luminescent
References [2] [3] [4] [5]

Xenotime is a rare-earth phosphate mineral, the major component of which is yttrium orthophosphate (Y P O 4). It forms a solid solution series with chernovite-(Y) (Y As O 4) and therefore may contain trace impurities of arsenic, as well as silicon dioxide and calcium. The rare-earth elements dysprosium, erbium, terbium and ytterbium, as well as metal elements such as thorium and uranium (all replacing yttrium) are the expressive secondary components of xenotime. Due to uranium and thorium impurities, some xenotime specimens may be weakly to strongly radioactive. Lithiophyllite, monazite and purpurite are sometimes grouped with xenotime in the informal "anhydrous phosphates" group. Xenotime is used chiefly as a source of yttrium and heavy lanthanide metals (dysprosium, ytterbium, erbium and gadolinium). Occasionally, gemstones are also cut from the finest xenotime crystals.

Contents

Etymology

The name xenotime is from the Greek words κενός vain and τιμή honor, akin to "vainglory". It was coined by French mineralogist François Sulpice Beudant as a rebuke of another scientist, Swedish chemist Jöns Jacob Berzelius, for the latter's premature claim to have found in the mineral a new chemical element (later understood to be previously discovered yttrium). The criticism was blunted, as over time "kenotime" was misread and misprinted "xenotime" [2] [3] [5] with the error suggesting the etymology ξένος + τιμή as "different honor". Xenotime was first described for an occurrence in Vest-Agder, Norway in 1824. [3]

Properties

Crystallising in the tetragonal (I41/amd) crystal system, xenotime is typically translucent to opaque (rarely transparent) in shades of brown to brownish yellow (most common) but also reddish to greenish brown and gray. Xenotime has a variable habit: It may be prismatic (stubby or slender and elongate) with dipyramidal terminations, in radial or granular aggregates, or rosettes. A soft mineral (Mohs hardness 4.5), xenotime is—in comparison to most other translucent minerals—fairly dense, with a specific gravity between 4.4–5.1. Its lustre, which may be vitreous to resinous, together with its crystal system, may lead to a confusion with zircon (ZrSiO4), the latter having a similar crystal structure and with which xenotime may sometimes occur.

Xenotime has two directions of perfect prismatic cleavage and its fracture is uneven to irregular (sometimes splintery). It is considered brittle and its streak is white. The refractive index of xenotime is 1.720–1.815 with a birefringence of 0.095 (uniaxial positive). Xenotime is dichroic with pink, yellow or yellowish brown seen in the extraordinary ray and brownish yellow, grayish brown or greenish brown seen in the ordinary ray. There is no reaction under ultraviolet light. While xenotime may contain significant amounts of thorium or uranium, the mineral does not undergo metamictization like sphene or zircon would.

Occurrence

Occurring as a minor accessory mineral, xenotime is found in pegmatites and other igneous rocks, as well as gneisses rich in mica and quartz. Associated minerals include biotite and other micas, chlorite group minerals, quartz, zircon, certain feldspars, analcime, anatase, brookite, rutile, siderite and apatite. Xenotime is also known to be diagenetic: It may form as minute grains or as extremely thin (less than 10 µ) coatings on detrital zircon grains in siliciclastic sedimentary rocks. The importance of these diagenetic xenotime deposits in the radiometric dating of sedimentary rocks is only beginning to be realised. [6]

Discovered in 1824, xenotime's type locality is Hidra (Hitterø), Flekkefjord, Vest-Agder, Norway. Other notable localities include: Arendal and Tvedestrand, Norway; Novo Horizonte, São Paulo, Novo Horizonte, Bahia and Minas Gerais, Brazil; Madagascar and California, Colorado, Georgia, North Carolina and New Hampshire, United States. A new discovery of gemmy, colour change (brownish to yellow) xenotime has been reported from Afghanistan and been found in Pakistan. North of Mount Funabuse in Gifu Prefecture, Japan, a notable basaltic rock is quarried at a hill called Maru-Yama: crystals of xenotime and zircon arranged in a radiating, flower-like pattern are visible in polished slices of the rock, which is known as chrysanthemum stone (translated from the Japanese 菊石 kiku-ishi). This stone is widely appreciated in Japan for its ornamental value.

Small tonnages of xenotime sand are recovered in association with Malaysian tin mining, etc. and are processed commercially. The lanthanide content is typical of "yttrium earth" minerals and runs about two-thirds yttrium, with the remainder being mostly the heavy lanthanides, where the even-numbered lanthanides (such as Gd, Dy, Er, or Yb) each being present at about the 5% level, and the odd-numbered lanthanides (such as Tb, Ho, Tm, Lu) each being present at about the 1% level. Dysprosium is usually the most abundant of the even-numbered heavies, and holmium is the most abundant of the odd-numbered heavies. The lightest lanthanides are generally better represented in monazite while the heaviest lanthanides are in xenotime.

See also

Related Research Articles

<span class="mw-page-title-main">Dysprosium</span> Chemical element, symbol Dy and atomic number 66

Dysprosium is a chemical element; it has symbol Dy and atomic number 66. It is a rare-earth element in the lanthanide series with a metallic silver luster. Dysprosium is never found in nature as a free element, though, like other lanthanides, it is found in various minerals, such as xenotime. Naturally occurring dysprosium is composed of seven isotopes, the most abundant of which is 164Dy.

<span class="mw-page-title-main">Erbium</span> Chemical element, symbol Er and atomic number 68

Erbium is a chemical element; it has symbol Er and atomic number 68. A silvery-white solid metal when artificially isolated, natural erbium is always found in chemical combination with other elements. It is a lanthanide, a rare-earth element, originally found in the gadolinite mine in Ytterby, Sweden, which is the source of the element's name.

<span class="mw-page-title-main">Holmium</span> Chemical element, symbol Ho and atomic number 67

Holmium is a chemical element; it has symbol Ho and atomic number 67. It is a rare-earth element and the eleventh member of the lanthanide series. It is a relatively soft, silvery, fairly corrosion-resistant and malleable metal. Like many other lanthanides, holmium is too reactive to be found in native form, as pure holmium slowly forms a yellowish oxide coating when exposed to air. When isolated, holmium is relatively stable in dry air at room temperature. However, it reacts with water and corrodes readily, and also burns in air when heated.

<span class="mw-page-title-main">Lutetium</span> Chemical element, symbol Lu and atomic number 71

Lutetium is a chemical element; it has symbol Lu and atomic number 71. It is a silvery white metal, which resists corrosion in dry air, but not in moist air. Lutetium is the last element in the lanthanide series, and it is traditionally counted among the rare earth elements; it can also be classified as the first element of the 6th-period transition metals.

The lanthanide or lanthanoid series of chemical elements comprises at least the 14 metallic chemical elements with atomic numbers 57–70, from lanthanum through ytterbium. In the periodic table, they fill the 4f orbitals. Lutetium is also sometimes considered a lanthanide, despite being a d-block element and a transition metal.

<span class="mw-page-title-main">Thorium</span> Chemical element, symbol Th and atomic number 90

Thorium is a chemical element; it has symbol Th and atomic number 90. Thorium is a weakly radioactive light silver metal which tarnishes olive gray when it is exposed to air, forming thorium dioxide; it is moderately soft and malleable and has a high melting point. Thorium is an electropositive actinide whose chemistry is dominated by the +4 oxidation state; it is quite reactive and can ignite in air when finely divided.

<span class="mw-page-title-main">Terbium</span> Chemical element, symbol Tb and atomic number 65

Terbium is a chemical element; it has symbol Tb and atomic number 65. It is a silvery-white, rare earth metal that is malleable, and ductile. The ninth member of the lanthanide series, terbium is a fairly electropositive metal that reacts with water, evolving hydrogen gas. Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite, xenotime and euxenite.

<span class="mw-page-title-main">Thulium</span> Chemical element, symbol Tm and atomic number 69

Thulium is a chemical element; it has symbol Tm and atomic number 69. It is the thirteenth and third-last element in the lanthanide series. Like the other lanthanides, the most common oxidation state is +3, seen in its oxide, halides and other compounds; however, the +2 oxidation state can also be stable. In aqueous solution, like compounds of other late lanthanides, soluble thulium compounds form coordination complexes with nine water molecules.

<span class="mw-page-title-main">Ytterbium</span> Chemical element, symbol Yb and atomic number 70

Ytterbium is a chemical element; it has symbol Yb and atomic number 70. It is a metal, the fourteenth and penultimate element in the lanthanide series, which is the basis of the relative stability of its +2 oxidation state. Like the other lanthanides, its most common oxidation state is +3, as in its oxide, halides, and other compounds. In aqueous solution, like compounds of other late lanthanides, soluble ytterbium compounds form complexes with nine water molecules. Because of its closed-shell electron configuration, its density, melting point and boiling point are much lower than those of most other lanthanides.

<span class="mw-page-title-main">Zircon</span> Zirconium silicate, a mineral belonging to the group of nesosilicates

Zircon is a mineral belonging to the group of nesosilicates and is a source of the metal zirconium. Its chemical name is zirconium(IV) silicate, and its corresponding chemical formula is ZrSiO4. An empirical formula showing some of the range of substitution in zircon is (Zr1–y, REEy)(SiO4)1–x(OH)4x–y. Zircon precipitates from silicate melts and has relatively high concentrations of high field strength incompatible elements. For example, hafnium is almost always present in quantities ranging from 1 to 4%. The crystal structure of zircon is tetragonal crystal system. The natural color of zircon varies between colorless, yellow-golden, red, brown, blue, and green.

<span class="mw-page-title-main">Rare-earth element</span> Any of the fifteen lanthanides plus scandium and yttrium

The rare-earth elements (REE), also called the rare-earth metals or rare earths or, in context, rare-earth oxides, and sometimes the lanthanides, are a set of 17 nearly indistinguishable lustrous silvery-white soft heavy metals. Compounds containing rare earths have diverse applications in electrical and electronic components, lasers, glass, magnetic materials, and industrial processes.

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

Baddeleyite is a rare zirconium oxide mineral (ZrO2 or zirconia), occurring in a variety of monoclinic prismatic crystal forms. It is transparent to translucent, has high indices of refraction, and ranges from colorless to yellow, green, and dark brown. See etymology below.

<span class="mw-page-title-main">Gadolinite</span> Nesosilicate mineral

Gadolinite, sometimes known as ytterbite, is a silicate mineral consisting principally of the silicates of cerium, lanthanum, neodymium, yttrium, beryllium, and iron with the formula (Ce,La,Nd,Y)2FeBe2Si2O10. It is called gadolinite-(Ce) or gadolinite-(Y), depending on the prominent composing element. It may contain 35.5% yttria sub-group rare earths, 2.2% ceria earths, as much as to 11.6% BeO, and traces of thorium. It is found in Sweden, Norway, and the US.

<span class="mw-page-title-main">Monazite</span> Mineral containing rare-earth elements

Monazite is a primarily reddish-brown phosphate mineral that contains rare-earth elements. Due to variability in composition, monazite is considered a group of minerals. The most common species of the group is monazite-(Ce), that is, the cerium-dominant member of the group. It occurs usually in small isolated crystals. It has a hardness of 5.0 to 5.5 on the Mohs scale of mineral hardness and is relatively dense, about 4.6 to 5.7 g/cm3. There are five different most common species of monazite, depending on the relative amounts of the rare earth elements in the mineral:

Metamictisation is a natural process resulting in the gradual and ultimately complete destruction of a mineral's crystal structure, leaving the mineral amorphous. The affected material is therefore described as metamict.

<span class="mw-page-title-main">Thorite</span> Nesosilicate mineral

Thorite, (Th,U)SiO4, is a rare nesosilicate of thorium that crystallizes in the tetragonal system and is isomorphous with zircon and hafnon. It is the most common mineral of thorium and is nearly always strongly radioactive. Thorite was discovered in 1828 on the island of Løvøya, Norway, by the vicar and mineralogist, Hans Morten Thrane Esmark. First specimens of Thorite were sent to his father, Jens Esmark, who was a professor of mineralogy and geology. It was named in 1829 to reflect its thorium content.

Thorium-232 is the main naturally occurring isotope of thorium, with a relative abundance of 99.98%. It has a half life of 14 billion years, which makes it the longest-lived isotope of thorium. It decays by alpha decay to radium-228; its decay chain terminates at stable lead-208.

Uranium–lead dating, abbreviated U–Pb dating, is one of the oldest and most refined of the radiometric dating schemes. It can be used to date rocks that formed and crystallised from about 1 million years to over 4.5 billion years ago with routine precisions in the 0.1–1 percent range.

<span class="mw-page-title-main">Yttrium</span> Chemical element, symbol Y and atomic number 39

Yttrium is a chemical element; it has symbol Y and atomic number 39. It is a silvery-metallic transition metal chemically similar to the lanthanides and has often been classified as a "rare-earth element". Yttrium is almost always found in combination with lanthanide elements in rare-earth minerals and is never found in nature as a free element. 89Y is the only stable isotope and the only isotope found in the Earth's crust.

<span class="mw-page-title-main">Huttonite</span> Thorium nesosilicate mineral

Huttonite is a thorium nesosilicate mineral with the chemical formula ThSiO4 and which crystallizes in the monoclinic system. It is dimorphous with tetragonal thorite, and isostructual with monazite. An uncommon mineral, huttonite forms transparent or translucent cream–colored crystals. It was first identified in samples of beach sands from the West Coast region of New Zealand by the mineralogist Colin Osborne Hutton (1910–1971). Owing to its rarity, huttonite is not an industrially useful mineral.

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. 1 2 Fontani, Marco; Costa, Mariagrazia; Orna, Virginia (2014). The Lost Elements: The Periodic Table's Shadow Side. Oxford University Press. p. 73. ISBN   978-0199383-344.
  3. 1 2 3 Mindat database.
  4. Webmineral.
  5. 1 2 Handbook of Mineralogy.
  6. "Geoconferences (WA) Inc". Archived from the original on December 14, 2006. Retrieved January 8, 2006. Daniela Vallini

Further reading

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