Lutetium

Lutetium is a chemical element with the 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.[5]

Lutetium, 71Lu
Lutetium
Pronunciation/ljuːˈtiːʃiəm/ ​(lew-TEE-shee-əm)
Appearancesilvery white
Standard atomic weight Ar°(Lu)
  • 174.9668±0.0001
  • 174.97±0.01 (abridged)[1]
Lutetium in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
 Y
↑
Lu
↓
Lr
ytterbium ← lutetium → hafnium
Atomic number (Z)71
Groupgroup 3
Periodperiod 6
Block  d-block
Electron configuration[Xe] 4f14 5d1 6s2
Electrons per shell2, 8, 18, 32, 9, 2
Physical properties
Phase at STPsolid
Melting point1925 K ​(1652 °C, ​3006 °F)
Boiling point3675 K ​(3402 °C, ​6156 °F)
Density (near r.t.)9.841 g/cm3
when liquid (at m.p.)9.3 g/cm3
Heat of fusionca. 22 kJ/mol
Heat of vaporization414 kJ/mol
Molar heat capacity26.86 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1906 2103 2346 (2653) (3072) (3663)
Atomic properties
Oxidation states0,[2] +1, +2, +3 (a weakly basic oxide)
ElectronegativityPauling scale: 1.27
Ionization energies
  • 1st: 523.5 kJ/mol
  • 2nd: 1340 kJ/mol
  • 3rd: 2022.3 kJ/mol
Atomic radiusempirical: 174 pm
Covalent radius187±8 pm
Color lines in a spectral range
Spectral lines of lutetium
Other properties
Natural occurrenceprimordial
Crystal structure ​hexagonal close-packed (hcp)
Hexagonal close packed crystal structure for lutetium
Thermal expansionpoly: 9.9 µm/(m⋅K) (at r.t.)
Thermal conductivity16.4 W/(m⋅K)
Electrical resistivitypoly: 582 nΩ⋅m (at r.t.)
Magnetic orderingparamagnetic[3]
Young's modulus68.6 GPa
Shear modulus27.2 GPa
Bulk modulus47.6 GPa
Poisson ratio0.261
Vickers hardness755–1160 MPa
Brinell hardness890–1300 MPa
CAS Number7439-94-3
History
Namingafter Lutetia, Latin for: Paris, in the Roman era
DiscoveryCarl Auer von Welsbach and Georges Urbain (1906)
First isolationCarl Auer von Welsbach (1906)
Named byGeorges Urbain (1906)
Isotopes of lutetium
Main isotopes[4] Decay
abun­dance half-life (t1/2) mode pro­duct
173Lu synth 1.37 y ε 173Yb
174Lu synth 3.31 y ε 174Yb
175Lu 97.4% stable
176Lu 2.60% 3.78×1010 y β− 176Hf
177Lu synth 6.65 d β− 177Hf

Lutetium was independently discovered in 1907 by French scientist Georges Urbain, Austrian mineralogist Baron Carl Auer von Welsbach, and American chemist Charles James.[6] All of these researchers found lutetium as an impurity in the mineral ytterbia, which was previously thought to consist entirely of ytterbium. The dispute on the priority of the discovery occurred shortly after, with Urbain and Welsbach accusing each other of publishing results influenced by the published research of the other; the naming honor went to Urbain, as he had published his results earlier. He chose the name lutecium for the new element, but in 1949 the spelling was changed to lutetium. In 1909, the priority was finally granted to Urbain and his names were adopted as official ones; however, the name cassiopeium (or later cassiopium) for element 71 proposed by Welsbach was used by many German scientists until the 1950s.[7]

Lutetium is not a particularly abundant element, although it is significantly more common than silver in the Earth's crust. It has few specific uses. Lutetium-176 is a relatively abundant (2.5%) radioactive isotope with a half-life of about 38 billion years, used to determine the age of minerals and meteorites. Lutetium usually occurs in association with the element yttrium[8] and is sometimes used in metal alloys and as a catalyst in various chemical reactions. 177Lu-DOTA-TATE is used for radionuclide therapy (see Nuclear medicine) on neuroendocrine tumours. Lutetium has the highest Brinell hardness of any lanthanide, at 890–1300 MPa.[9]

Characteristics

Physical properties

A lutetium atom has 71 electrons, arranged in the configuration [Xe] 4f145d16s2.[10] Lutetium is generally encountered in the 3+ oxidation state, having lost its two outermost 6s and the single 5d-electron. The lutetium atom is the smallest among the lanthanide atoms, due to the lanthanide contraction,[11] and as a result lutetium has the highest density, melting point, and hardness of the lanthanides.[12] As lutetium's 4f orbitals are highly stabilized only the 5d and 6s orbitals are involved in chemical reactions and bonding;[13] thus it is characterized as a d-block rather than an f-block element,[14] and on this basis some consider it not to be a lanthanide at all, but a transition metal like its lighter congeners scandium and yttrium.[15][16]

Chemical properties and compounds

Lutetium's compounds always contain the element in the 3+ oxidation state .[17] Aqueous solutions of most lutetium salts are colorless and form white crystalline solids upon drying, with the common exception of the iodide, which is brown. The soluble salts, such as nitrate, sulfate and acetate form hydrates upon crystallization. The oxide, hydroxide, fluoride, carbonate, phosphate and oxalate are insoluble in water.[18]

Lutetium metal is slightly unstable in air at standard conditions, but it burns readily at 150 °C to form lutetium oxide. The resulting compound is known to absorb water and carbon dioxide, and it may be used to remove vapors of these compounds from closed atmospheres.[19] Similar observations are made during reaction between lutetium and water (slow when cold and fast when hot); lutetium hydroxide is formed in the reaction.[20] Lutetium metal is known to react with the four lightest halogens to form trihalides; except the fluoride they are soluble in water.

Lutetium dissolves readily in weak acids[19] and dilute sulfuric acid to form solutions containing the colorless lutetium ions, which are coordinated by between seven and nine water molecules, the average being [Lu(H2O)8.2]3+.[21]

2 Lu + 3 H2SO4 → 2 Lu3+ + 3 SO2−4 + 3 H2↑

Oxidation states

Lutetium is usually found in the +3 oxidation state, like most other lanthanides. However, it can also be in the 0, +1 and +2 states as well.

Isotopes
Main article: Isotopes of lutetium

Lutetium occurs on the Earth in form of two isotopes: lutetium-175 and lutetium-176. Out of these two, only the former is stable, making the element monoisotopic. The latter one, lutetium-176, decays via beta decay with a half-life of 3.78×1010 years; it makes up about 2.5% of natural lutetium.[4] To date, 39 synthetic radioisotopes of the element have been characterized, ranging in mass number from 149 to 189;[4][22] the most stable such isotopes are lutetium-174 with a half-life of 3.31 years, and lutetium-173 with a half-life of 1.37 years.[4] All of the remaining radioactive isotopes have half-lives that are less than 9 days, and the majority of these have half-lives that are less than half an hour.[4] Isotopes lighter than the stable lutetium-175 decay via electron capture (to produce isotopes of ytterbium), with some alpha and positron emission; the heavier isotopes decay primarily via beta decay, producing hafnium isotopes.[4]

The element also has 43 known nuclear isomers, with masses of 150, 151, 153–162, and 166–180 (not every mass number corresponds to only one isomer). The most stable of them are lutetium-177m, with a half-life of 160.4 days, and lutetium-174m, with a half-life of 142 days; these are longer than the half-lives of the ground states of all radioactive lutetium isotopes except lutetium-173, 174, and 176.[4]

History

Lutetium, derived from the Latin Lutetia (Paris), was independently discovered in 1907 by French scientist Georges Urbain, Austrian mineralogist Baron Carl Auer von Welsbach, and American chemist Charles James.[23][24] They found it as an impurity in ytterbia, which was thought by Swiss chemist Jean Charles Galissard de Marignac to consist entirely of ytterbium.[25] The scientists proposed different names for the elements: Urbain chose neoytterbium and lutecium,[26] whereas Welsbach chose aldebaranium and cassiopeium (after Aldebaran and Cassiopeia).[27] Both of these articles accused the other man of publishing results based on those of the author.[28][29][30][31][32]

The International Commission on Atomic Weights, which was then responsible for the attribution of new element names, settled the dispute in 1909 by granting priority to Urbain and adopting his names as official ones, based on the fact that the separation of lutetium from Marignac's ytterbium was first described by Urbain;[25] after Urbain's names were recognized, neoytterbium was reverted to ytterbium. Until the 1950s, some German-speaking chemists called lutetium by Welsbach's name, cassiopeium; in 1949, the spelling of element 71 was changed to lutetium. The reason for this was that Welsbach's 1907 samples of lutetium had been pure, while Urbain's 1907 samples only contained traces of lutetium.[33] This later misled Urbain into thinking that he had discovered element 72, which he named celtium, which was actually very pure lutetium. The later discrediting of Urbain's work on element 72 led to a reappraisal of Welsbach's work on element 71, so that the element was renamed to cassiopeium in German-speaking countries for some time.[33] Charles James, who stayed out of the priority argument, worked on a much larger scale and possessed the largest supply of lutetium at the time.[34] Pure lutetium metal was first produced in 1953.[34]

Occurrence and production
Monazite

Found with almost all other rare-earth metals but never by itself, lutetium is very difficult to separate from other elements. Its principal commercial source is as a by-product from the processing of the rare earth phosphate mineral monazite (Ce,La,...)PO
4, which has concentrations of only 0.0001% of the element,[19] not much higher than the abundance of lutetium in the Earth crust of about 0.5 mg/kg. No lutetium-dominant minerals are currently known.[35] The main mining areas are China, United States, Brazil, India, Sri Lanka and Australia. The world production of lutetium (in the form of oxide) is about 10 tonnes per year.[34] Pure lutetium metal is very difficult to prepare. It is one of the rarest and most expensive of the rare earth metals with the price about US$10,000 per kilogram, or about one-fourth that of gold.[36][37]

Crushed minerals are treated with hot concentrated sulfuric acid to produce water-soluble sulfates of rare earths. Thorium precipitates out of solution as hydroxide and is removed. After that the solution is treated with ammonium oxalate to convert rare earths into their insoluble oxalates. The oxalates are converted to oxides by annealing. The oxides are dissolved in nitric acid that excludes one of the main components, cerium, whose oxide is insoluble in HNO3. Several rare earth metals, including lutetium, are separated as a double salt with ammonium nitrate by crystallization. Lutetium is separated by ion exchange. In this process, rare-earth ions are sorbed onto suitable ion-exchange resin by exchange with hydrogen, ammonium or cupric ions present in the resin. Lutetium salts are then selectively washed out by suitable complexing agent. Lutetium metal is then obtained by reduction of anhydrous LuCl3 or LuF3 by either an alkali metal or alkaline earth metal.[18]

2 LuCl3 + 3 Ca → 2 Lu + 3 CaCl2

Applications

Because of production difficulty and high price, lutetium has very few commercial uses, especially since it is rarer than most of the other lanthanides but is chemically not very different. However, stable lutetium can be used as catalysts in petroleum cracking in refineries and can also be used in alkylation, hydrogenation, and polymerization applications.[38] A nitrogen-doped lutetium hydride may have a role in creating room temperature superconductors at 10 kbar.[39][40]

Lutetium aluminium garnet (Al5Lu3O12) has been proposed for use as a lens material in high refractive index immersion lithography.[41] Additionally, a tiny amount of lutetium is added as a dopant to gadolinium gallium garnet, which is used in magnetic bubble memory devices.[42] Cerium-doped lutetium oxyorthosilicate is currently the preferred compound for detectors in positron emission tomography (PET).[43][44] Lutetium aluminium garnet (LuAG) is used as a phosphor in light-emitting diode light bulbs.[45][46]

Aside from stable lutetium, its radioactive isotopes have several specific uses. The suitable half-life and decay mode made lutetium-176 used as a pure beta emitter, using lutetium which has been exposed to neutron activation, and in lutetium–hafnium dating to date meteorites.[47] The synthetic isotope lutetium-177 bound to octreotate (a somatostatin analogue), is used experimentally in targeted radionuclide therapy for neuroendocrine tumors.[48] Indeed, lutetium-177 is seeing increased usage as a radionuclide in neuroendocrine tumor therapy and bone pain palliation.[49][50] Research indicates that lutetium-ion atomic clocks could provide greater accuracy than any existing atomic clock.[51]

Lutetium tantalate (LuTaO4) is the densest known stable white material (density 9.81 g/cm3)[52] and therefore is an ideal host for X-ray phosphors.[53][54] The only denser white material is thorium dioxide, with density of 10 g/cm3, but the thorium it contains is radioactive.

Lutetium is also a compound of several scintillating materials, those which converts X-rays to visible light. It is part of LYSO, LuAg and Lutetium iodide scintilators.

Precautions

Like other rare-earth metals, lutetium is regarded as having a low degree of toxicity, but its compounds should be handled with care nonetheless: for example, lutetium fluoride inhalation is dangerous and the compound irritates skin.[19] Lutetium nitrate may be dangerous as it may explode and burn once heated. Lutetium oxide powder is toxic as well if inhaled or ingested.[19]

Similarly to the other rare-earth metals, lutetium has no known biological role, but it is found even in humans, concentrating in bones, and to a lesser extent in the liver and kidneys.[34] Lutetium salts are known to occur together with other lanthanide salts in nature; the element is the least abundant in the human body of all lanthanides.[34] Human diets have not been monitored for lutetium content, so it is not known how much the average human takes in, but estimations show the amount is only about several micrograms per year, all coming from tiny amounts absorbed by plants. Soluble lutetium salts are mildly toxic, but insoluble ones are not.[34]

See also

References
  1. "Standard Atomic Weights: Lutetium". CIAAW. 2007.
  2. Yttrium and all lanthanides except Ce and Pm have been observed in the oxidation state 0 in bis(1,3,5-tri-t-butylbenzene) complexes, see Cloke, F. Geoffrey N. (1993). "Zero Oxidation State Compounds of Scandium, Yttrium, and the Lanthanides". Chem. Soc. Rev. 22: 17–24. doi:10.1039/CS9932200017. and Arnold, Polly L.; Petrukhina, Marina A.; Bochenkov, Vladimir E.; Shabatina, Tatyana I.; Zagorskii, Vyacheslav V.; Cloke (2003-12-15). "Arene complexation of Sm, Eu, Tm and Yb atoms: a variable temperature spectroscopic investigation". Journal of Organometallic Chemistry. 688 (1–2): 49–55. doi:10.1016/j.jorganchem.2003.08.028.
  3. Lide, D. R., ed. (2005). "Magnetic susceptibility of the elements and inorganic compounds". CRC Handbook of Chemistry and Physics (PDF) (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  4. Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3): 030001. doi:10.1088/1674-1137/abddae.
  5. Scerri, E. (2012). "Mendeleev's Periodic Table Is Finally Completed and What To Do about Group 3?". Chemistry International. 34 (4). doi:10.1515/ci.2012.34.4.28. Archived from the original on 5 July 2017.
  6. "Lutetium Element Facts / Chemistry".
  7. "History of Lutetium".
  8. "lutetium - Dictionary Definition". Vocabulary.com. Retrieved 2020-03-06.
  9. Samsonov, G. V., ed. (1968). "Mechanical Properties of the Elements". Handbook of the physicochemical properties of the elements. New York, USA: IFI-Plenum. pp. 387–446. doi:10.1007/978-1-4684-6066-7_7. ISBN 978-1-4684-6066-7. Archived from the original on 2015-04-02.
  10. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 1223. ISBN 978-0-08-037941-8.
  11. Cotton, F. Albert; Wilkinson, Geoffrey (1988), Advanced Inorganic Chemistry (5th ed.), New York: Wiley-Interscience, pp. 776, 955, ISBN 0-471-84997-9
  12. Parker, Sybil P. (1984). Dictionary of Scientific and Technical Terms (3rd ed.). New York: McGraw-Hill.
  13. Jensen, William B. (2000). "The Periodic Law and Table" (PDF). Archived from the original (PDF) on 2020-11-10. Retrieved 10 December 2022.
  14. Jensen, William B. (2015). "The positions of lanthanum (actinium) and lutetium (lawrencium) in the periodic table: an update". Foundations of Chemistry. 17: 23–31. doi:10.1007/s10698-015-9216-1. S2CID 98624395. Archived from the original on 30 January 2021. Retrieved 28 January 2021.
  15. Winter, Mark (1993–2022). "WebElements". The University of Sheffield and WebElements Ltd, UK. Retrieved 5 December 2022.
  16. Cowan, Robert D. (1981). The Theory of Atomic Structure and Spectra. University of California Press. p. 598. ISBN 978-0-520-90615-0.
  17. "Lutetium".
  18. Patnaik, Pradyot (2003). Handbook of Inorganic Chemical Compounds. McGraw-Hill. p. 510. ISBN 978-0-07-049439-8. Retrieved 2009-06-06.
  19. Krebs, Robert E. (2006). The history and use of our earth's chemical elements: a reference guide. Greenwood Publishing Group. pp. 303–304. ISBN 978-0-313-33438-2.
  20. "Chemical reactions of Lutetium". Webelements. Retrieved 2009-06-06.
  21. Persson, Ingmar (2010). "Hydrated metal ions in aqueous solution: How regular are their structures?". Pure and Applied Chemistry. 82 (10): 1901–1917. doi:10.1351/PAC-CON-09-10-22. ISSN 0033-4545.
  22. Haak, K.; Tarasov, O. B.; Chowdhury, P.; et al. (2023). "Production and discovery of neutron-rich isotopes by fragmentation of 198Pt". Physical Review C. 108 (34608): 034608. doi:10.1103/PhysRevC.108.034608.
  23. James, C. (1907). "A new method for the separation of the yttrium earths". Journal of the American Chemical Society. 29 (4): 495–499. doi:10.1021/ja01958a010. In a footnote on page 498, James mentions that Carl Auer von Welsbach had announced " ... the presence of a new element Er, γ, which is undoubtedly the same as here noted, ... ." The article to which James refers is: C. Auer von Welsbach (1907) "Über die Elemente der Yttergruppe, (I. Teil)" (On the elements of the ytterbium group (1st part)), Monatshefte für Chemie und verwandte Teile anderer Wissenschaften (Monthly Journal for Chemistry and Related Fields of Other Sciences), 27 : 935-946.
  24. "Separation of Rare Earth Elements by Charles James". National Historic Chemical Landmarks. American Chemical Society. Retrieved 2014-02-21.
  25. Urbain, G. (1907). "Un nouvel élément: le lutécium, résultant du dédoublement de l'ytterbium de Marignac". Comptes Rendus. 145: 759–762.
  26. Urbain, G. (1909). "Lutetium und Neoytterbium oder Cassiopeium und Aldebaranium -- Erwiderung auf den Artikel des Herrn Auer v. Welsbach". Monatshefte für Chemie. 31 (10): 1. doi:10.1007/BF01530262. S2CID 101825980.
  27. Welsbach, Carl A. von (1908). "Die Zerlegung des Ytterbiums in seine Elemente" [Resolution of ytterbium into its elements]. Monatshefte für Chemie. 29 (2): 181–225, 191. doi:10.1007/BF01558944. S2CID 197766399. On page 191, Welsbach suggested names for the two new elements: "Ich beantrage für das an das Thulium, beziehungsweise Erbium sich anschließende, in dem vorstehenden Teile dieser Abhandlung mit Yb II bezeichnete Element die Benennung: Aldebaranium mit dem Zeichen Ad — und für das zweite, in dieser Arbeit mit Yb I bezeichnete Element, das letzte in der Reihe der seltenen Erden, die Benennung: Cassiopeïum mit dem Zeichen Cp." (I request for the element that is attached to thulium or erbium and that was denoted by Yb II in the above part of this paper, the designation "Aldebaranium" with the symbol Ad — and for the element that was denoted in this work by Yb I, the last in the series of the rare earths, the designation "Cassiopeïum" with the symbol Cp.)
  28. Weeks, Mary Elvira (1956). The discovery of the elements (6th ed.). Easton, PA: Journal of Chemical Education.
  29. Weeks, Mary Elvira (1932). "The discovery of the elements: XVI. The rare earth elements". Journal of Chemical Education. 9 (10): 1751–1773. Bibcode:1932JChEd...9.1751W. doi:10.1021/ed009p1751.
  30. Marshall, James L. Marshall; Marshall, Virginia R. Marshall (2015). "Rediscovery of the elements: The Rare Earths–The Beginnings" (PDF). The Hexagon: 41–45. Retrieved 30 December 2019.
  31. Marshall, James L. Marshall; Marshall, Virginia R. Marshall (2015). "Rediscovery of the elements: The Rare Earths–The Confusing Years" (PDF). The Hexagon: 72–77. Retrieved 30 December 2019.
  32. Marshall, James L. Marshall; Marshall, Virginia R. Marshall (2016). "Rediscovery of the elements: The Rare Earths–The Last Member" (PDF). The Hexagon: 4–9. Retrieved 30 December 2019.
  33. Thyssen, Pieter; Binnemans, Koen (2011). "Accommodation of the Rare Earths in the Periodic Table: A Historical Analysis". In Gschneider, Karl A. Jr.; Bünzli, Jean-Claude; Pecharsky, Vitalij K. (eds.). Handbook on the Physics and Chemistry of Rare Earths. Amsterdam: Elsevier. p. 63. ISBN 978-0-444-53590-0. OCLC 690920513. Retrieved 2013-04-25.
  34. Emsley, John (2001). Nature's building blocks: an A-Z guide to the elements. Oxford University Press. pp. 240–242. ISBN 978-0-19-850341-5.
  35. Hudson Institute of Mineralogy (1993–2018). "Mindat.org". www.mindat.org. Retrieved 14 January 2018.
  36. Hedrick, James B. "Rare-Earth Metals" (PDF). USGS. Retrieved 2009-06-06.
  37. Castor, Stephen B.; Hedrick, James B. (2006). "Rare Earth Elements" (PDF). In Jessica Elzea Kogel, Nikhil C. Trivedi and James M. Barker (ed.). Industrial Minerals and Rocks. Society for Mining, Metallurgy and Exploration. pp. 769–792. Archived from the original on 2009-10-07.{{cite book}}: CS1 maint: bot: original URL status unknown (link)
  38. Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  39. Chang, Kenneth (2023-03-08). "New Room-Temperature Superconductor Offers Tantalizing Possibilities". The New York Times. ISSN 0362-4331. Retrieved 2023-03-08.
  40. Dasenbrock-Gammon, N.; Snider, E.; McBride, R. (2023). "Evidence of near-ambient superconductivity in a N-doped lutetium hydride". Nature. 615 (7951): 244–250. Bibcode:2023Natur.615..244D. doi:10.1038/s41586-023-05742-0. PMID 36890373. S2CID 257407449.
  41. Wei, Yayi; Brainard, Robert L. (2009). Advanced Processes for 193-NM Immersion Lithography. SPIE Press. p. 12. ISBN 978-0-8194-7557-2.
  42. Nielsen, J. W.; Blank, S. L.; Smith, D. H.; Vella-Coleiro, G. P.; Hagedorn, F. B.; Barns, R. L.; Biolsi, W. A. (1974). "Three garnet compositions for bubble domain memories". Journal of Electronic Materials. 3 (3): 693–707. Bibcode:1974JEMat...3..693N. doi:10.1007/BF02655293. S2CID 98828884.
  43. Wahl, R. L. (2002). "Instrumentation". Principles and Practice of Positron Emission Tomography. Philadelphia: Lippincott: Williams and Wilkins. p. 51.
  44. Daghighian, F.; Shenderov, P.; Pentlow, K. S.; Graham, M. C.; Eshaghian, B.; Melcher, C. L.; Schweitzer, J. S. (1993). "Evaluation of cerium doped lutetium oxyorthosilicate (LSO) scintillation crystals for PET". IEEE Transactions on Nuclear Science. 40 (4): 1045–1047. Bibcode:1993ITNS...40.1045D. doi:10.1109/23.256710. S2CID 28011497.
  45. Bush, Steve (14 March 2014). "Discussing LED lighting phosphors". Electronic Weekly. Retrieved 26 January 2017.
  46. Simard-Normandin, Martine (2011). "A19 LED bulbs: What's under the frosting?". EE Times (July 18): 44–45. ISSN 0192-1541.
  47. Muriel Gargaud; Hervé Martin; Philippe Claeys (2007). Lectures in Astrobiology. Springer. p. 51. ISBN 978-3-540-33692-1.
  48. Sigel, Helmut (2004). Metal complexes in tumor diagnosis and as anticancer agents. CRC Press. p. 98. ISBN 978-0-8247-5494-5.
  49. Balter, H.; Trindade, V.; Terán, M.; Gaudiano, J.; Ferrando, R.; Paolino, A.; Rodriguez, G.; Hermida, J.; De Marco, E.; Oliver, P. (2015). "177Lu-Labeled Agents for Neuroendocrine Tumor Therapy and Bone Pain Palliation in Uruguay". Current Radiopharmaceuticals. 9 (1): 85–93. doi:10.2174/1874471008666150313112620. PMID 25771367.
  50. Carollo, A.; Papi, S.; Chinol, M. (2015). "Lutetium-177 Labeled Peptides: The European Institute of Oncology Experience". Current Radiopharmaceuticals. 9 (1): 19–32. doi:10.2174/1874471008666150313111633. PMID 25771368.
  51. Arnold, K.J.; Kaewuam, R.; Roy, A.; Tan, T.R.; Barrett, M.D. (2018). "Blackbody radiation shift assessment for a lutetium ion clock". Nature Communications. 9 (1): 1650. arXiv:1712.00240. Bibcode:2018NatCo...9.1650A. doi:10.1038/s41467-018-04079-x. PMC 5917023. PMID 29695720.
  52. Blasse, G.; Dirksen, G.; Brixner, L.; Crawford, M. (1994). "Luminescence of materials based on LuTaO4". Journal of Alloys and Compounds. 209 (1–2): 1–2. doi:10.1016/0925-8388(94)91069-3.
  53. Shionoya, Shigeo (1998). Phosphor handbook. CRC Press. p. 846. ISBN 978-0-8493-7560-6.
  54. Gupta, C. K.; Krishnamurthy, Nagaiyar (2004). Extractive metallurgy of rare earths. CRC Press. p. 32. ISBN 978-0-415-33340-5.

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