Einsteinium
not relevantEinsteinium has no water story: made in milligram amounts for research, it has no measurable occurrence in water, no guideline and no treatment role.
1 · Identity
- Symbol, number
- Es, 99
- Oxidation states in water
- +3 (book entry); never measured in natural water
- Note
- Identity from the book entry; nothing measured in water.
Sources
Identity
- Name and symbol
- Einsteinium, Es
- Atomic number
- 99 protons
- Position
- no group (f-block) · period 7 · f-block · actinide
- CAS number
- 7429-92-7
Atomic structure
- Atomic mass
- 252 u
- Electron configuration
- 1s² 2s² 2p⁶ 3s² 3p⁶ 4s² 3d¹⁰ 4p⁶ 5s² 4d¹⁰ 5p⁶ 6s² 4f¹⁴ 5d¹⁰ 6p⁶ 7s² 5f¹¹
[Rn] 7s²⁵f¹¹ - Electrons per shell
- 2, 8, 18, 32, 29, 8, 2
- Valence electrons
- 13 ns, (n-1)d and (n-2)f
| nuclide | half-life | decay |
|---|---|---|
| 252Es | 471.7 d | α=78±0.2%; ε=22±0.2% |
| 254Es | 275.7 d | α≈100%; ε ?; β-=1.74e-4±0.8%; SF<3e-6% |
| 255Es | 39.8 d | β-=92.0±0.4%; α=8.0±0.4%; SF=0.0041±0.2% |
| 253Es | 20.47 d | α=100%; SF=8.7e-6±0.3% |
Physical properties
- State at room temperature
- Solid
- Melting point
- 1,133 K (859.85 °C)
- Boiling point
- 996 K (722.85 °C)
- Density
- not in sources
- Appearance
- silvery; glows blue in the dark
- Thermal conductivity
- not in sources
- Electrical resistivity
- not in sources
- Electrical conductivity
- not in sources
- Crystal structure
- face-centered cubic
- Molar heat capacity
- not in sources
Chemical properties
- Oxidation states
- +3
- Electronegativity
- 1.3 (Pauling Scale)
- Ionisation energy
- 6.42 eV
1st 619 kJ/mol - Electron affinity
- not in sources
- Atomic radius
- van der Waals 245 pm
- Ionic radius
- Es³⁺ 84 pm
- Reactivity
- A soft, silvery, rather reactive late actinide and the heaviest element studied in bulk: +3 dominates in solids and in solution (pale pink), and it is the first actinide in which a +2 state is firmly established, made by reducing Es(III) with samarium(II) chloride.
- with water
- The sources do not describe the metal with water; Es3+ is the stable aqueous ion and the trihalides react with water vapor to oxyhalides such as EsOCl.
- with oxygen, air
- The sources do not describe the metal with oxygen; the oxide Es2O3 was obtained by burning the nitrate and exists in cubic, monoclinic and hexagonal forms that interconvert under self-irradiation.
- with acids
- Tracer studies show trivalent actinide behavior in acid solution, giving the pale pink Es3+ ion whose luminescence has been observed in hydrochloric acid.
- with halogens
- No reaction of the metal with the halogens is reported; the trihalides EsF3, EsCl3, EsBr3 and EsI3 are made from the oxide or from solution, and hydrogen reduces them to the dihalides: .
- Typical compounds
- Es₂O₃ einsteinium(III) oxide colorless cubic crystals, from burning the nitrate
- EsF₃ einsteinium(III) fluoride precipitated from Es(III) chloride solution with fluoride
- EsCl₃ einsteinium(III) chloride orange, from the oxide in dry hydrogen chloride
- EsCl₂ einsteinium(II) chloride divalent, from hydrogen reduction of the trichloride
Occurrence, production and use
- Crustal abundance
- Not Applicable
- Oceanic abundance
- Not Applicable
- Occurrence and sources
- synthetic only milligram quantities from neutron bombardment of plutonium in a reactor
- Extraction, production
- not in sources
- Uses
Since only small amounts of einsteinium have ever been produced, it currently has no uses outside of basic scientific research.
- Safety, toxicity
- not in sources
Discovery and name
- Discovered by
- Lawrence Berkeley National Laboratory
- Discovered
- 1952
- First isolated
- not in sources
- Named by
- not in sources
- Origin of the name
- after Albert Einstein
Einsteinium does not occur naturally in the Earth’s crust. It was first identified in December 1952 by American scientists from the Argonne National Laboratory near Chicago, Illinois, the Los Alamos National Laboratory in Los Alamos, New Mexico, and The University of California Laboratory in Berkeley, California in the debris of thermonuclear weapons. The element was named for Albert Einstein (Fig. IUPAC.99.1). 253Es was the first isotope identified; it has a half-life of 20.47 days. The isotope with the longest half-life is 252Es, with a half-life of 472 days [630], [631].
There are no uses for isotopes of einsteinium outside of basic scientific research for the production of higher transuranic elements and studies of actinide science. Due to the radiation and heat given off by einsteinium isotopes, it is difficult to use them in experiments and studies [631].
Tracer studies using 253Es show that einsteinium has chemical properties typical of a heavy trivalent, actinide element. Oxidation states of II and III for einsteinium have been reported and oxidation state IV has been postulated from vapor transport studies but not established unequivocally. Einsteinium is the first divalent metal in the actinide series (two bonding electrons rather than three). The self-irradiation properties of einsteinium make it extremely difficult, for example, to obtain x-ray crystallographic data. The intense gamma and x-rays from einsteinium decay to daughter products over-exposes the x-ray film/detector. This intense self-irradiation can be exploited however to study accelerated aging and radiation damage studies, and for targeted radiation medical treatments. An example of einsteinium chemical studies is the chemical consequences of radioactive decay. With the relatively short half-life of Es-253 (20.47 days) one can study the in-growth of daughter Bk-249 (half-life 330 days) and grand-daughter Cf-249 (half-life 351 years). Evidence suggests that divalent Es might decay into a divalent Bk daughter and subsequently into as of yet unknown divalent Cf. There are no commercial uses for einsteinium however it is the heaviest element for which bulk studies can be performed that allows for fundamental studies of the role of 5-f electrons in actinide systematics.
Further reading:
Richard G. Haire (2006) Chapter 12, The Chemistry of the Actinide and Transactinide Elements, Third Edition, L. R. Morss, J. Fuger, and N. M. Edelstein, Eds, Springer Publishers.
This element reviewed and Updated by Dr. David Hobart, 2011
Conventions
Valence electrons are counted by the usual convention: the outer shell for s- and p-block elements, ns and (n-1)d for the d-block, ns, (n-1)d and (n-2)f for the f-block. Lanthanides and actinides are placed in the f-block with no group number. Electrical conductivity is the reciprocal of the printed resistivity. Ionic radii are Shannon effective radii, six-coordinate unless noted. Where a field reads “not in sources” the value was not found; it is a gap, not a zero. Regulatory limits are the published values and change often, so check the standard in force at your site and the numbers written into your own permit before you design to them.
Data
Element records, isotopes, radii and the descriptive text come from PubChem (NCBI), the Los Alamos National Laboratory periodic table, IUPAC CIAAW and the IAEA Atomic Mass Data Center. Appearance, thermal conductivity, electrical resistivity, crystal structure, discovery and the origin of each name come from Wikipedia and Periodic-Table-JSON, used under CC BY-SA 4.0. Hazard classifications come from the ECHA C&L inventory via PubChem. Ionic radii follow R. D. Shannon (1976). The water chapters cite their own sources at the foot of each entry, and are written to the level of Snoeyink and Jenkins, Stumm and Morgan, MWH's Water Treatment and Metcalf and Eddy.