59
Pr
Praseodymium
Atomic Mass 140.90766
Electron Configuration [Xe]6s24f3
Oxidation States +3
Year Discovered 1885

Identifiers

Element Name Praseodymium
Element Symbol Pr
InChI InChI=1S/Pr
InChIKey PUDIUYLPXJFUGB-UHFFFAOYSA-N

Properties

Atomic Weight

140.907 66(1)

140.90766

140.9

140.90766(2)

Electron Configuration

[Xe]6s24f3

Atomic Radius

Van der Waals Atomic Radius : 239 pm (Van der Waals)

Empirical Atomic Radius : 185pm (Empirical)

Covalent Atomic Radius : 203(7) pm (Covalent)

Oxidation States

+3

5, 4, 3, 2 ​(a mildly basic oxide)

Ground Level

49/2

Ionization Energy

5.464 eV

5.4702 ± 0.0004 eV (The level was determined by interpolation or extrapolation of known experimental values or by semiempirical calculation; its absolutre accuracy is reflected in the number of significant figures assigned to it.)

Electronegativity

Pauling Scale Electronegativity : 1.13(Pauling Scale)

Atomic Spectra

Lines Holdings

Levels Holdings

Physical Description

Solid

Element Classification

Metal

Element Period Number

6

Element Group Number

- Lanthanide

Density

6.77 grams per cubic centimeter

Melting Point

1204 K (931°C or 1708°F)

935°C

Boiling Point

3793 K (3520°C or 6368°F)

3130°C

Estimated Crustal Abundance

9.2 milligrams per kilogram

Estimated Oceanic Abundance

6.4×10-7 milligrams per liter

History

The name derives from the Greek prasios for "green" and didymos for "twin" because of the pale green salts it forms. Praseodymium was discovered by the Austrian chemist Carl Auer (Baron von Welsbach) in 1885, who separated it and the element neodymium from a didymium sample (didymium had previously been thought to be a separate element).

Praseodymium was discovered by Carl F. Auer von Welsbach, an Austrian chemist, in 1885. He separated praseodymium, as well as the element neodymium, from a material known as didymium. Today, praseodymium 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 prasios, green, and didymos, twin. In 1841 Mosander extracted the rare earth didymia from lanthana; in 1879, Lecoq de Boisbaudran isolated a new earth, samaria, from didymia obtained from the mineral samarskite. Six years later, in 1885, von Welsbach separated didymia into two others, praseodymia and neodymia, which gave salts of different colors. As with other rare earths, compounds of these elements in solution have distinctive sharp spectral absorption bands or lines, some of which are only a few Angstroms wide.

Historical Atomic Weights

Year Atomic Weight (uncertainty) [u] Reference
2017 140.907 66(1) https://doi.org/10.1515/pac-2019-0603
2013 140.907 66(2) https://doi.org/10.1515/pac-2015-0305
1995 140.907 65(2) https://doi.org/10.1351/pac199668122339
1985 140.907 65(3) https://doi.org/10.1351/pac198658121677
1969 140.9077(1) https://doi.org/10.1351/pac197021010091
1961 140.907 https://doi.org/10.1021/ja00881a001
1925 140.92 https://doi.org/10.1039/CT9252700913
1916 140.9 https://doi.org/10.1021/ja02176a001
1902 140.6 https://doi.org/10.1007/BF01370337

Historical Isotopic Abundances

Year Isotope Abundance (uncertainty) Reference
1975, 141Pr, 1, doi:10.1351/pac197647010075

Description

Praseodymium is soft, silvery, malleable, and ductile. It is somewhat more resistant to corrosion in air than europium, lanthanum, cerium, or neodymium, but it does develop a green oxide coating that falls off when exposed to air. As with other rare-earth metals, it should be kept under a light mineral oil or sealed in plastic.

Users

Praseodymium's primary use is as an alloying agent with magnesium to create high-strength metals that are used in aircraft engines. Praseodymium also makes up about 5% of Misch metal, a material that is used to make flints for lighters. Praseodymium forms the core of carbon arc lights which are used in the motion picture industry for studio lighting and projector lights. Praseodymium is added to fiber optic cables as a doping agent where it is used as a signal amplifier. Praseodymium salts are used to give glasses and enamels a yellow color. Praseodymium is also a component of didymium glass, which is used to make certain types of welder's and glass blower's goggles.

Misch metal, used in making cigarette lighters, contains about 5% praseodymium metal. The rare-earth oxides, including Pr2O3 are among the most refractory substances known. Along with other rare earths, it is widely used as a core material for carbon arcs used by the motion picture industry for studio lighting and projection. Salts of praseodymium are used to color glasses and enamels; when mixed with certain other materials, praseodymium produces an intense and unusually clean yellow color in glass. Didymium glass, of which praseodymium is a component, is a colorant for welders goggles.

Sources

The element occurs along with other rare-earth elements in a variety of minerals. Monazite and bastnasite are the two principal commercial sources of the rare-earth metals. It was prepared in relatively pure form in 1931.

Compounds

See more information at the Praseodymium compound page.

Element Forms

CID Name Formula SMILES Molecular Weight
23942 praseodymium Pr [Pr] 140.90766
185491 praseodymium(3+) Pr+3 [Pr+3] 140.90766
105157 praseodymium-144 Pr [144Pr] 143.91331
167024 praseodymium-142 Pr [142Pr] 141.91005
161103 praseodymium-143 Pr [143Pr] 142.91082
167417 praseodymium-145 Pr [145Pr] 144.91452
167418 praseodymium-147 Pr [147Pr] 146.9190
177608 praseodymium-138 Pr [138Pr] 137.9108
176416 praseodymium-136 Pr [136Pr] 135.9127
177568 praseodymium-137 Pr [137Pr] 136.91068
181086 praseodymium-139 Pr [139Pr] 138.90893
10197771 praseodymium-149 Pr [149Pr] 148.9237
139035505 praseodymium-141 Pr [141Pr] 140.90766

Isotopes

Stable Isotope Count 1

Isotopes in Medicine

Because of its relatively short half-life (19.12 h) and decay primarily by beta decay (96.3 percent beta decay and 3.7 percent alpha decay), 142Pr has been proposed for two main innovative applications in medicine, namely in microsphere brachytherapy and in eye plaque brachytherapy [425]. 142Pr is advantageous because penetration of the beta fraction of the radiation is limited to a few millimeters in tissue, therefore limiting the dose of radiation to the treated site. 142Pr may be produced either by fast neutron activation or thermal neutron activation of stable 141Pr.

Research in metal-bearing radiopharmaceuticals is being conducted to determine the most efficient way to produce and process radioactive metals for in vivo tracing. This research has led to the development of a potential radionuclide generator that administers radioactive metal complexes to be observed during positron emission tomography (PET) imaging. A n(140Nd)/n(140Pr) amount-ratio radionuclide generator has been designed to administer 140Pr complexes, such as 140Pr-DTPA, to be used as a tracer during a PET scan [426]. The half-life of 140Pr is 3.4 min. The n(140Nd)/n(140Pr) ratio radionuclide generators can also be used for administering 140Pr-phosphonate complexes to identify the development of skeletal metastases. Once the skeletal metastases are found, 153Sm-EDTMP can be administered as a radiotherapeutic agent to treat bone cancer (Fig. IUPAC.59.1) [426]. The half-life of 153Sm is 1.9 days.

Fig. IUPAC.59.1: Glass microcapillary for use in brachytherapy investigations [425], composed of a mixture of silica, aluminium, oxygen, and praseodymium-141 and praseodymium-142. The glass was irradiated in a nuclear reactor to produce radioactive ¹⁴²Pr from stable ¹⁴¹Pr. Image kindly provided by Dr. Clara Ferreira (University of Oklahoma, Oklahoma City, Oklahoma, USA).

[425] M. C. Ferreira. Dosimetric Study of Beta-Minus Emitter Praseodymium-142: Applications in Microsphere Brachytherapy for Hepatocellular Carcinoma and Brachytherapy for Ocular Squamous Cell Carcinoma, East Carolina University Greenville, North Carolina, USA (2013).
[426] K. P. Zhernosekov. Radiochemical Aspects of Production and Processing of Radiometals for Preparation of Metalloradiopharmaceuticals, Johannes Gutenberg-Universität Mainz: Department of Chemistry, Pharmacy and Earth Sciences (2017), Feb. 27; https://publications.ub.uni-mainz.de/theses/volltexte/2006/1043/pdf/1043.pdf.

Isotope Mass and Abundance

Isotope Atomic Mass (uncertainty) [u] Abundance (uncertainty)
141Pr 140.907 66(1) 1
Isotope Atomic Mass (uncertainty) [u] Abundance (uncertainty)
141Pr 140.9076576(23) 1

Atomic Mass, Half Life, and Decay

Nuclide Atomic Mass and Uncertainty [u] Half Life and Uncertainty Discovery Year Decay Modes, Intensities and Uncertainties [%]
121Pr 120.955393 ± 0.000537 [Estimated] 12 ms ± 5 2005 p≈100%
122Pr 121.951927 ± 0.000537 [Estimated] 500 ms [Estimated] β+ ?; β+p ?
123Pr 122.946076 ± 0.000429 [Estimated] 800 ms [Estimated] β+ ?; β+p ?
124Pr 123.942940 ± 0.00043 [Estimated] 1.2 s ± 0.2 1986 β+=100%; β+p=?
125Pr 124.937659 ± 0.000322 [Estimated] 3.3 s ± 0.7 2002 β+=100%; β+p ?
126Pr 125.935240 ± 0.00021 [Estimated] 3.12 s ± 0.18 1983 β+=100%; β+p=?
127Pr 126.930710 ± 0.00021 [Estimated] 4.2 s ± 0.3 1995 β+=100%
127Prm 126.930710 ± 0.00021 [Estimated] 2 us [Estimated] 1998 IT ?
128Pr 127.928791000 ± 0.000032 2.85 s ± 0.09 1985 β+=100%; β+p=?
129Pr 128.925095000 ± 0.000032 30 s ± 4 1977 β+=100%
129Prm 128.925095000 ± 0.000032 26 us ± 11# [Estimated] 1997 IT=100%
130Pr 129.923590000 ± 0.000069 40.0 s ± 0.4 1977 β+=100%
130Prm 129.923590000 ± 0.000069 10 s [Estimated] 1988 β+ ?
131Pr 130.920234960 ± 0.000050451 1.50 m ± 0.03 1977 β+=100%
131Prm 130.920234960 ± 0.000050451 5.73 s ± 0.20 1996 IT=96.4±1.2%; β+=3.6±1.2%
132Pr 131.919240000 ± 0.000031 1.49 m ± 0.11 1974 β+=100%
132Prm 131.919240000 ± 0.000031 1 s [Estimated] 1990 β+ ?; IT ?
132Prn 131.919240000 ± 0.000031 2.46 us ± 0.04 2012 IT=100%
132Prp 131.919240000 ± 0.000031 486 ns ± 70 2012 IT=100%
133Pr 132.916330558 ± 0.000013416 6.5 m ± 0.3 1970 β+=100%
133Prm 132.916330558 ± 0.000013416 1.1 s ± 0.2 1995 IT=100%
134Pr 133.915696729 ± 0.00002181 17 m ± 2 1967 β+=100%
134Prm 133.915696729 ± 0.00002181 ~11 m 1973 β+=100%
135Pr 134.913111772 ± 0.000012686 24 m ± 1 1954 β+=100%
135Prm 134.913111772 ± 0.000012686 105 us ± 10 1973 IT=100%
136Pr 135.912677470 ± 0.000012296 13.1 m ± 0.1 1968 β+=100%
137Pr 136.910679183 ± 0.000008733 1.28 h ± 0.03 1958 β+=100%
137Prm 136.910679183 ± 0.000008733 2.66 us ± 0.07 1987 IT=100%
138Pr 137.910757495 ± 0.000010748 1.45 m ± 0.05 1951 β+=100%
138Prm 137.910757495 ± 0.000010748 2.12 h ± 0.04 1958 β+=100%
139Pr 138.908932700 ± 0.000003917 4.41 h ± 0.04 1951 β+=100%
140Pr 139.909085600 ± 0.000006593 3.39 m ± 0.01 1938 β+=100%; e+=48.7±2.2%; ε=51.3±2.2%
140Prm 139.909085600 ± 0.000006593 350 ns ± 20 1964 IT=100%
140Prn 139.909085600 ± 0.000006593 3.05 us ± 0.20 1964 IT=100%
141Pr 140.907659604 ± 0.000001607 Stable 1924 IS=100%
142Pr 141.910051640 ± 0.000001607 19.12 h ± 0.04 1935 β-≈100%; ε=0.0164±0.8%
142Prm 141.910051640 ± 0.000001607 14.6 m ± 0.5 1967 IT=100%
143Pr 142.910822624 ± 0.000001949 13.57 d ± 0.02 1948 β-=100%
144Pr 143.913310682 ± 0.000002907 17.28 m ± 0.05 1951 β-=100%
144Prm 143.913310682 ± 0.000002907 7.2 m ± 0.3 1970 IT≈100%; β-≈0.07%
145Pr 144.914517987 ± 0.000007674 5.984 h ± 0.010 1954 β-=100%
146Pr 145.917687630 ± 0.000036882 24.09 m ± 0.10 1953 β-=100%
147Pr 146.919007438 ± 0.00001702 13.39 m ± 0.04 1964 β-=100%
148Pr 147.922129992 ± 0.000016147 2.29 m ± 0.02 1964 β-=100%
148Prm 147.922129992 ± 0.000016147 2.01 m ± 0.07 1964 β-=64±1%; IT=36±1%
149Pr 148.923736100 ± 0.0000106 2.26 m ± 0.07 1964 β-=100%
150Pr 149.926676391 ± 0.000009677 6.19 s ± 0.16 1970 β-=100%
151Pr 150.928309066 ± 0.000012506 18.90 s ± 0.07 1990 β-=100%
151Prm 150.928309066 ± 0.000012506 50 us ± 8 2006 IT=100%
152Pr 151.931552900 ± 0.0000199 3.57 s ± 0.11 1983 β-=100%
152Prm 151.931552900 ± 0.0000199 4.16 us ± 0.10 1990 IT=100%
153Pr 152.933903511 ± 0.000012755 4.28 s ± 0.11 1987 β-=100%; β-n ?
154Pr 153.937885165 ± 0.00010736 2.30 s ± 0.09 1988 β-=100%; β-n ?
155Pr 154.940509193 ± 0.000018462 1.47 s ± 0.3 1992 β-=100%; β-n ?
156Pr 155.944766900 ± 0.0000011 444 ms ± 6 1992 β-=100%; β-n ?
157Pr 156.948003100 ± 0.0000034 307 ms ± 21 2017 β-=100%; β-n ?
158Pr 157.952603 ± 0.000322 [Estimated] 181 ms ± 14 2016 β-=100%; β-n ?
159Pr 158.956232 ± 0.000429 [Estimated] 134 ms ± 43 2017 β-=100%; β-n ?
160Pr 159.961138 ± 0.000429 [Estimated] 170 ms ± 140 2017 β-=100%; β-n ?
161Pr 160.965121 ± 0.000537 [Estimated] 90 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
    Praseodymium

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