66
Dy
Dysprosium
Atomic Mass 162.500
Electron Configuration [Xe]6s24f10
Oxidation States +3
Year Discovered 1886

Identifiers

Element Name Dysprosium
Element Symbol Dy
InChI InChI=1S/Dy
InChIKey KBQHZAAAGSGFKK-UHFFFAOYSA-N

Properties

Atomic Weight

162.500(1)

162.500

162.5

162.500(1)

Electron Configuration

[Xe]6s24f10

Atomic Radius

Van der Waals Atomic Radius : 229 pm (Van der Waals)

Empirical Atomic Radius : 175pm (Empirical)

Covalent Atomic Radius : 192(7) pm (Covalent)

Oxidation States

+3

3, 2, 1 ​(a basic oxide)

Ground Level

5I8

Ionization Energy

5.939 eV

5.939061 ± 0.000006 eV

Electronegativity

Pauling Scale Electronegativity : 1.22(Pauling Scale)

Atomic Spectra

Lines Holdings

Levels Holdings

Physical Description

Solid

Element Classification

Metal

Element Period Number

6

Element Group Number

- Lanthanide

Density

8.55 grams per cubic centimeter

Melting Point

1685 K (1412°C or 2574°F)

1407°C

Boiling Point

2840 K (2567°C or 4653°F)

2562°C

Estimated Crustal Abundance

5.2 milligrams per kilogram

Estimated Oceanic Abundance

9.1×10-7 milligrams per liter

History

The name derives from the Greek dysprositos for "hard to get at", owing to the difficulty in separating this rare earth element from a holmium mineral in which it was found. It was discovered by the Swiss chemist Marc Delafontaine in the mineral samarskite in 1878 and called philippia. Philippia was subsequently thought to be a mixture of terbium and yttrium. It was later rediscovered in a holmium sample by the French chemist Paul-Emile Lecoq de Boisbaudran in 1886, who was then credited with the discovery. Dysprosium was first isolated by the French chemist Georges Urbain in 1906.

Dysprosium was discovered by Paul-Émile Lecoq de Boisbaudran, a French chemist, in 1886 as an impurity in erbia, the oxide of erbium. The metal was isolated by Georges Urbain, another French chemist, in 1906. Pure samples of dysprosium were first produced in the 1950s. Today, dysprosium is primarily obtained through an ion exchange process from monazite sand ((Ce, La, Th, Nd, Y)PO4), a material rich in rare earth elements.

From the Greek word dysprositos, meaning hard to get at. Dysprosium was discovered in 1886 by Lecoq de Boisbaudran, but not isolated. Neither the oxide nor the metal was available in relatively pure form until 1950, when the development of ion-exchange separation and metallographic reduction techniques were created by Spedding and associates. Dysprosium occurs along with other so-called rare-earth or lanthanide elements in a variety of minerals such as xenotime, fergusonite, gadolinite, euxenite, polycrase, and blomstrandine. The most important sources, however, are from monaziate and bastnasite. Dysprosium can be prepared by reduction of the trifluoride with calcium.

Historical Atomic Weights

Year Atomic Weight (uncertainty) [u] Reference
2001 162.500(1) https://doi.org/10.1351/pac200375081107
1969 162.50(3) https://doi.org/10.1351/pac197021010091
1961 162.50 https://doi.org/10.1021/ja00881a001
1955 162.51 https://doi.org/10.1021/ja01595a001
1931 162.46 https://doi.org/10.1039/JR9310001617
1925 162.52 https://doi.org/10.1039/CT9252700913
1908 162.5 https://doi.org/10.1021/ja01943a001

Historical Isotopic Abundances

Year Isotope Abundance (uncertainty) Reference
2001 156Dy 0.000 56(3) https://doi.org/10.1063/1.1836764
2001 158Dy 0.000 95(3) https://doi.org/10.1063/1.1836764
2001 160Dy 0.023 29(18) https://doi.org/10.1063/1.1836764
2001 161Dy 0.188 89(42) https://doi.org/10.1063/1.1836764
2001 162Dy 0.254 75(36) https://doi.org/10.1063/1.1836764
2001 163Dy 0.248 96(42) https://doi.org/10.1063/1.1836764
2001 164Dy 0.282 60(54) https://doi.org/10.1063/1.1836764
1997 156Dy 0.0006(1) https://doi.org/10.1351/pac199870010217
1997 158Dy 0.0010(1) https://doi.org/10.1351/pac199870010217
1997 160Dy 0.0234(8) https://doi.org/10.1351/pac199870010217
1997 161Dy 0.1891(24) https://doi.org/10.1351/pac199870010217
1997 162Dy 0.2551(26) https://doi.org/10.1351/pac199870010217
1997 163Dy 0.2490(16) https://doi.org/10.1351/pac199870010217
1997 164Dy 0.2818(37) https://doi.org/10.1351/pac199870010217
1989 156Dy 0.0006(1) https://doi.org/10.1351/pac199163070991
1989 158Dy 0.0010(1) https://doi.org/10.1351/pac199163070991
1989 160Dy 0.0234(6) https://doi.org/10.1351/pac199163070991
1989 161Dy 0.189(2) https://doi.org/10.1351/pac199163070991
1989 162Dy 0.255(2) https://doi.org/10.1351/pac199163070991
1989 163Dy 0.249(2) https://doi.org/10.1351/pac199163070991
1989 164Dy 0.282(2) https://doi.org/10.1351/pac199163070991
1979 156Dy 0.0006(1) https://doi.org/10.1351/pac198052102349
1979 158Dy 0.0010(1) https://doi.org/10.1351/pac198052102349
1979 160Dy 0.0234(4) https://doi.org/10.1351/pac198052102349
1979 161Dy 0.190(2) https://doi.org/10.1351/pac198052102349
1979 162Dy 0.255(4) https://doi.org/10.1351/pac198052102349
1979 163Dy 0.249(4) https://doi.org/10.1351/pac198052102349
1979 164Dy 0.281(4) https://doi.org/10.1351/pac198052102349
1975 156Dy 0.0006 https://doi.org/10.1351/pac197647010075
1975 158Dy 0.001 https://doi.org/10.1351/pac197647010075
1975 160Dy 0.0234 https://doi.org/10.1351/pac197647010075
1975 161Dy 0.189 https://doi.org/10.1351/pac197647010075
1975 162Dy 0.255 https://doi.org/10.1351/pac197647010075
1975 163Dy 0.249 https://doi.org/10.1351/pac197647010075
1975 164Dy 0.282 https://doi.org/10.1351/pac197647010075

Description

The element has a metallic, bright silver luster. It is relatively stable in air at room temperature, and is readily attacked and dissolved by dilute and concentrated mineral acids, to evolve hydrogen. The metal is soft enough to be cut with a knife and can be machined without sparking if overheating is avoided. Small amounts of impurities can greatly affect its physical properties.

Users

There are no commercial applications for dysprosium. Since it easily absorbs neutrons and has a high melting point, dysprosium might be alloyed with steel for use in nuclear reactors. When combined with vanadium and other rare earth elements, dysprosium is used as a laser material.

Dysprosium oxide (Dy2O3), also known as dysprosia, is combined with nickel and added to a special cement used to cool nuclear reactor rods. Other dysprosium compounds include: dysprosium fluoride (DyF3), dysprosium iodide (DyI3) and dysprosium sulfate (Dy2(SO4)3).

While we have not found many applications for dysprosium, its thermal neutron absorption cross-section and high melting point suggest metallurgical uses in nuclear control applications and for alloying with special stainless steels. A dysprosium oxide-nickel cement has found use in cooling nuclear reactor rods. This cement absorbs neutrons readily without swelling or contracting under prolonged neutron bombardment. In combination with vanadium and other rare earths, dysprosium has been used in making laser materials. Dysprosium-cadmium chalcogenides, as sources of infrared radiation, have been used for studying chemical reactions.

Compounds

See more information at the Dysprosium compound page.

Element Forms

CID Name Formula SMILES Molecular Weight
23912 dysprosium Dy [Dy] 162.500
166954 dysprosium-165 Dy [165Dy] 164.931709
167438 dysprosium-166 Dy [166Dy] 165.932813
178181 dysprosium-159 Dy [159Dy] 158.92575
6442238 dysprosium-157 Dy [157Dy] 156.92547
44152848 dysprosium-161 Dy [161Dy] 160.926939
177532 dysprosium-155 Dy [155Dy] 154.9258
177489 dysprosium-162 Dy [162Dy] 161.926805
185492 dysprosium(3+) Dy+3 [Dy+3] 162.500
10125089 dysprosium-164 Dy [164Dy] 163.929181
10419363 dysprosium-152 Dy [152Dy] 151.92473
11389607 dysprosium-167 Dy [167Dy] 166.93568
131708390 dysprosium-156 Dy [156Dy] 155.92428
131708391 dysprosium-158 Dy [158Dy] 157.92441
131708392 dysprosium-160 Dy [160Dy] 159.925204
131708393 dysprosium-163 Dy [163Dy] 162.928737

Isotopes

Stable Isotope Count 7

Isotopes in Industry

The isotopes of dysprosium are highly magnetic and have been the subject of physics research involving interactions of isotopes and the structure of lattice supersolids (spatially ordered material with superfluid properties, i.e. zero viscosity). The Magneto-Optical Trapping (MOT) chamber is used for slowing atoms (isotopes) to study the physics of neutral atoms by using a laser light to cool atoms (“Doppler cooling”) and magnetic quadrupole fields to slow and “trap” the neutral atoms (Fig. IUPAC.66.1) [462], [463].

164Dy has a large neutron absorption cross section, so dysprosium is used for control rods [464]. 161Dy has been a key isotope for studying the Mössbauer Effect, which is the resonance and absorption of gamma ray emissions on nearby atoms in a solid state [465].

Fig. IUPAC.66.1: Magneto-Optical Trapping (MOT) of isotopes of dysprosium. (Used with permission from: Prof. Benjamin Lev, Stanford University) [466].

[462] S. H. Youn, M. Lu, U. Ray, B. L. Lev. Am. Phys. Soc. Phys. Rev. A.82, 043425 (2010). https://doi.org/10.1103/PhysRevA.82.043425.
[463] C. M. Elliott. First Dysprosium MOT, Physics Illinois-University of Illinois at Urbana-Champaign (2017), Feb. 28; http://engineering.illinois.edu/news/article/2009-07-31-first-dysprosium-mot.
[464] V. E. Ceron, J. G. Hirsch. Phys. Lett. B471, 1 (1999).
[465] R. L. Cohen. Phys. Rev.137, 1809 (1965).
[466] B. Lev. Research-Announcing the World’s First Dysprosium MOT (Magneto-Optical Trap)! Stanford University (2017), Feb. 28; http://levlab.stanford.edu/news-events/worlds-first-dy-mot.

Isotopes in Medicine

165Dy (with a half-life of 140 min) is commonly used in arthritis therapy (radiosynovectomy). Rheumatic inflammation of the membranes of joints is often treated by the injection of 165Dy-ferric oxide directly into the joint space of the knee. Leakage from the joint has been shown to be minimal [467].

[467] C. B. Sledge, J. D. Zuckerman, M. R. Zalutsky, R. W. Atcher, S. Shortkroff, D. R. Lionberger, H. A. Rose, B. J. Hurson, P. A. Lankenner, R. J. Anderson, W. A. Bloomer. Arthritis Rheum.29, 153 (1986).

Isotopes Used as a Source of Radioactive Isotope(s)

164Dy is used to produce 166Dy (with a half-life of 3.4 days) via double neutron capture [468], [469], [470]. 166Dy, which decays to 166Ho, is used in cancer and arthritis therapy [468], [471].

[468] D. Ma, A. R. Ketring, G. J. Ehrhardt, W. Jia. J. Radioanal. Nucl. Chem.206, 119 (1996).
[469] S. Mirzadeh, R. E. Schenter, A. P. Callahan, F. F. Knapp. Production Capabilities in U.S. Nuclear Reactors for Medical Radioisotopes, Tm-12010, Oak Ridge National Laboratory Oak Ridge, Tenn (1992).
[470] S. Lahiri, K. J. Volkers, B. Wierczinski. Appl. Radiat. Isot.61, 1157 (2004).
[471] G. Ferro-Flores, O. Hernandez-Oviedo, C. Arteaga de Murphy, J. I. Tendilla, F. Monroy-Guzman, M. Pedraza-Lopez, K. Aldama-Alvarado. Appl. Radiat. Isot.61, 1227 (2004).

Isotope Mass and Abundance

Isotope Atomic Mass (uncertainty) [u] Abundance (uncertainty)
156Dy 155.924 284(8) 0.000 56(3) 0.00056(3)
158Dy 157.924 41(2) 0.000 95(3) 0.00095(3)
160Dy 159.925 203(5) 0.023 29(18) 0.02329(18)
161Dy 160.926 939(5) 0.188 89(42) 0.18889(42)
162Dy 161.926 804(5) 0.254 75(36) 0.25475(36)
163Dy 162.928 737(5) 0.248 96(42) 0.24896(42)
164Dy 163.929 181(5) 0.282 60(54) 0.28260(54)

Atomic Mass, Half Life, and Decay

Nuclide Atomic Mass and Uncertainty [u] Half Life and Uncertainty Discovery Year Decay Modes, Intensities and Uncertainties [%]
138Dy 137.962500 ± 0.00054 [Estimated] 200 ms [Estimated] β+ ?; β+p ?
139Dy 138.959527 ± 0.000537 [Estimated] 600 ms ± 200 1999 β+=100%; β+p≈11%
140Dy 139.954020 ± 0.00043 [Estimated] 700 ms [Estimated] 2002 β+ ?; β+p ?
140Dym 139.954020 ± 0.00043 [Estimated] 7.0 us ± 0.5 2002 IT=100%
141Dy 140.951280 ± 0.00032 [Estimated] 900 ms ± 140 1984 β+=100%; β+p=?
142Dy 141.946194 ± 0.000782 [Estimated] 2.3 s ± 0.3 1986 β+=100%; e+=90±0.4%; ε=10±0.4%; β+p=0.06±0.3%
143Dy 142.943994332 ± 0.000014 5.6 s ± 1.0 1983 β+=100%; β+p=?
143Dym 142.943994332 ± 0.000014 3.0 s ± 0.3 2003 β+=100%; β+p=?
143Dyn 142.943994332 ± 0.000014 1.2 us ± 0.3 2005 IT=100%
144Dy 143.939269512 ± 0.0000077 9.1 s ± 0.4 1986 β+=100%; β+p=?
145Dy 144.937473992 ± 0.000007 9.5 s ± 1.0 1982 β+=100%; β+p=?
145Dym 144.937473992 ± 0.000007 14.1 s ± 0.7 1982 β+=100%; β+p≈50%
146Dy 145.932844526 ± 0.000007187 33.2 s ± 0.7 1981 β+=100%
146Dym 145.932844526 ± 0.000007187 150 ms ± 20 1982 IT=100%
147Dy 146.931082712 ± 0.0000095 67 s ± 7 1975 β+=100%; β+p≈0.05%
147Dym 146.931082712 ± 0.0000095 55.2 s ± 0.5 1976 β+=68.9±2.3%; IT=31.1±2.3%
147Dyn 146.931082712 ± 0.0000095 400 ns ± 10 1985 IT=100%
148Dy 147.927149944 ± 0.000009365 3.3 m ± 0.2 1974 β+=100%
148Dym 147.927149944 ± 0.000009365 471 ns ± 20 1978 IT=100%
149Dy 148.927327516 ± 0.000009858 4.20 m ± 0.14 1958 β+=100%
149Dym 148.927327516 ± 0.000009858 490 ms ± 15 1976 IT=99.3±0.3%; β+=0.7±0.3%
150Dy 149.925593068 ± 0.000004636 7.17 m ± 0.05 1959 β+=66.4±1.8%; α=33.6±1.8%
151Dy 150.926191279 ± 0.000003486 17.9 m ± 0.3 1959 β+=94.4±0.6%; α=5.6±0.4%
152Dy 151.924725274 ± 0.00000493 2.38 h ± 0.02 1958 ε=99.900±0.7%; α=0.100±0.7%
153Dy 152.925771729 ± 0.000004295 6.4 h ± 0.1 1958 β+=99.9906±1.4%; α=0.0094±1.4%
154Dy 153.924428920 ± 0.000007977 3.0 My ± 1.5 1961 α=100%; 2β+ ?
155Dy 154.925758049 ± 0.000010354 9.9 h ± 0.2 1958 β+=100%
155Dym 154.925758049 ± 0.000010354 6 us ± 1 1970 IT=100%
156Dy 155.924283593 ± 0.00000106 Stable >1Ey 1948 IS=0.056±0.3%; α ?; 2β+ ?
157Dy 156.925469555 ± 0.000005532 8.14 h ± 0.04 1953 β+=100%
157Dym 156.925469555 ± 0.000005532 1.3 us ± 0.2 1974 IT=100%
157Dyn 156.925469555 ± 0.000005532 21.6 ms ± 1.6 1970 IT=100%
158Dy 157.924414817 ± 0.000002509 Stable 1938 IS=0.095±0.3%; α ?; 2β+ ?
159Dy 158.925745938 ± 0.000001544 144.4 d ± 0.2 1951 ε=100%
159Dym 158.925745938 ± 0.000001544 122 us ± 3 1965 IT=100%
160Dy 159.925203578 ± 0.000000751 Stable 1938 IS=2.329±1.8%
161Dy 160.926939425 ± 0.000000748 Stable 1934 IS=18.889±4.2%
161Dym 160.926939425 ± 0.000000748 760 ns ± 170 2012 IT=100%
162Dy 161.926804507 ± 0.000000746 Stable 1934 IS=25.475±3.6%
162Dym 161.926804507 ± 0.000000746 8.3 us ± 0.3 2011 IT=100%
163Dy 162.928737221 ± 0.000000744 Stable 1934 IS=24.896±4.2%
164Dy 163.929180819 ± 0.000000746 Stable 1934 IS=28.260±5.4%
165Dy 164.931709402 ± 0.000000748 2.332 h ± 0.004 1935 β-=100%
165Dym 164.931709402 ± 0.000000748 1.257 m ± 0.006 1963 IT=97.76±1.1%; β-=2.24±1.1%
166Dy 165.932812810 ± 0.000000862 81.6 h ± 0.1 1949 β-=100%
167Dy 166.935682415 ± 0.0000043 6.20 m ± 0.08 1960 β-=100%
168Dy 167.937134977 ± 0.000150303 8.7 m ± 0.3 1982 β-=100%
168Dym 167.937134977 ± 0.000150303 0.57 us ± 0.7 2019 IT=100%
169Dy 168.940315231 ± 0.000322781 39 s ± 8 1990 β-=100%
169Dym 168.940315231 ± 0.000322781 1.26 us ± 0.17 2019 IT=100%
170Dy 169.942340 ± 0.000215 [Estimated] 54.9 s ± 8.0 2010 β-=100%
170Dym 169.942340 ± 0.000215 [Estimated] 0.99 us ± 0.04 2016 IT=100%
171Dy 170.946312 ± 0.000215 [Estimated] 4.07 s ± 0.40 2012 β-=100%
172Dy 171.948728 ± 0.000322 [Estimated] 3.4 s ± 0.2 2012 β-=100%
172Dym 171.948728 ± 0.000322 [Estimated] 710 ms ± 50 2016 β-=19±0.3%; IT=81±0.3%
173Dy 172.953043 ± 0.000429 [Estimated] 1.43 s ± 0.20 2012 β-=100%; β-n ?
174Dy 173.955845 ± 0.000537 [Estimated] 1 s >300ns [Estimated] 2012 β- ?; β-n ?
175Dy 174.960569 ± 0.000537 [Estimated] 390 ms >550ns [Estimated] 2018 β- ?; β-n ?
176Dy 175.963918 ± 0.000537 [Estimated] 440 ms >550ns [Estimated] 2018 β- ?; β-n ?

Information Sources

  1. 1.  PubChem
  2. 2.  Atomic Mass Data Center (AMDC), International Atomic Energy Agency (IAEA)
  3. 3.  IUPAC Commission on Isotopic Abundances and Atomic Weights (CIAAW)
  4. 4.  Jefferson Lab, U.S. Department of Energy
    LICENSE
    Please see citation and linking information https https://www.jlab.org/privacy-and-security-notice
  5. 5.  Los Alamos National Laboratory, U.S. Department of Energy
  6. 6.  NIST Physical Measurement Laboratory
  7. 7.  IUPAC Periodic Table of the Elements and Isotopes (IPTEI)
    LICENSE
    Copyright (c) 2020 International Union of Pure and Applied Chemistry. The International Union of Pure and Applied Chemistry (IUPAC) contribution within Pubchem is provided under a CC-BY-NC-ND 4.0 license, unless otherwise stated.
    https://creativecommons.org/licenses/by-nc-nd/4.0/
  8. 8.  PubChem Elements
    Dysprosium

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