Mendelevium

fermium ← mendelevium → nobelium Tm ↑ Md ↓ (Upu) 101Md Periodic table
Appearance
unknown
General properties
Name, symbol, number	mendelevium, Md, 101
Pronunciation	/ˌmɛndəˈlɛviəm/ or /ˌmɛndəˈliːviəm/
Element category	actinide
Group, period, block	n/a, 7, f
Standard atomic weight	(258)
Electron configuration	[Rn] 5f13 7s2
Electrons per shell	2, 8, 18, 32, 31, 8, 2 (Image)
Physical properties
Phase	solid
Melting point	1100 K, 827 °C, 1521 °F
Atomic properties
Oxidation states	2, 3
Electronegativity	1.3 (Pauling scale)
Ionization energies	1st: 635 kJ·mol−1
Miscellanea
Magnetic ordering	no data
CAS registry number	7440-11-1
Most stable isotopes
Main article: Isotopes of mendelevium
iso NA half-life DM DE (MeV) DP 257Md syn 5.52 h ε 0.406 257Fm α 7.558 253Es SF - - 258Md syn 51.5 d ε 1.230 258Fm 260Md syn 31.8 d SF - - α 7.000 256Es ε - 260Fm β− 1.000 260No
v · d · e · r

Mendelevium ( /ˌmɛndəˈlɛviəm/ or /ˌmɛndəˈliːviəm/) is a synthetic element with the symbol Md (formerly Mv) and the atomic number 101. A metallic radioactive transuranic element in the actinide series, mendelevium is usually synthesized by bombarding einsteinium with alpha particles. It was named after Dmitri Ivanovich Mendeleev, who created the Periodic Table. Mendeleev's periodic system is the fundamental way to classify all the chemical elements. The name "mendelevium" was accepted by the International Union of Pure and Applied Chemistry (IUPAC). On the other hand, the proposed symbol "Mv" submitted by the discoverers was not accepted, and the IUPAC selected "Md" instead.

Characteristics

Researchers have shown that mendelevium has a moderately stable dipositive (II) oxidation state in addition to the more characteristic (for actinide elements) tripositive (III) oxidation state, the latter being the more dominantly exhibited state in an aqueous solution (chromatography being the process used). Sometimes, mendelevium can even be shown to exhibit a monopositive (I) state. ²⁵⁶Md has been used to find out some of the chemical properties of this element while in an aqueous solution. There are no other known uses of mendelevium and only trace amounts of the element have ever been produced. Other isotopes of mendelevium, all radioactive, have been discovered, with ²⁵⁸Md being the most stable with a two-month half-life (about 55 days). Other isotopes range from 248 to 258 mass numbers and half-lives from a few seconds to about 51 days. The original ²⁵⁶Md had a half-life of 87 minutes.

Radioactivity

The radioactivity of the trivalent element, mendelevium, is definitely noteworthy. It was expected that the reaction would be²⁵³Es (α,n) ²⁵⁵Md, where ²⁵⁵Md was α-active with a t_½ of 5 minutes and the corresponding α-energy. No such α-activity was observed, but the 101 fraction showed spontaneous fission representing a t_½ less than 3 hours. Because spontaneous fission was also observed in the fraction containing fermium, the α-bombardment of ²⁵³Einsteinium (Es) produced ²⁵⁶Md. The latter underwent electron capture to become ²⁵⁶Fermium (Fm), which then decayed by spontaneous fission. So ²⁵⁶Fm was produced by the decays of cyclotron-synthesized mendelevium.^[1]

The metallic state

Johansson and Rosengren predicted in 1975 that Md would prefer a divalent metallic state, similar to europium (Eu) and ytterbium (Yb), rather than a trivalent one. Thermochromatographic studies conducted with trace amounts of Md concluded that Md forms a divalent metal. With the aid of empirical correlation method, a divalent metallic radius of (0.194 ± 0.010) nm has been estimated. The estimated enthalpy of sublimation is in the range of 134-142 kJ/mol.^[2]

Solution chemistry

Before the actual discovery of mendelevium, the trivalent state was the most stable one in aqueous solution. Accordingly, a similar chemical behavior to the other 3+ actinides and lanthanides was expected. The elution of Md just before Fm in the elution sequence of the trivalent actinides from the cation-exchange resin column, confirmed this prediction. Afterwards, Md in the form of insoluble hydroxides and fluorides that are quantitatively coprecipitated with trivalent lanthanides was found. The cation-exchange resin column as well as the HDEHP solvent extraction column elution date is consistent with a trivalent state for Md and an ionic radius smaller than Fm. An ionic radius of 0.0192 nm and a coordination number of 6 for Md³⁺ was predicted using empirical correlations. Using the known ionic radii for the trivalent rare earths and the linear correlation of log distribution coefficient with ionic radius, an average ionic radius of 0.089 nm was estimated for Md³⁺ and a heat of hydration of – (3654 ± 12) kJ/mol calculated using empirical models and the Born-Haber cycle. In reducing conditions, an anomalous chemical behavior of Md was found. Coprecipitation with BaSO₄ and solvent extraction chromatography experiments using HDEHP were carried out in different reducing agents. These showed that Md³⁺ could easily be reduced to a stable Md²⁺ in aqueous solution. Mendelevium can also be reduced to the monovalent state in water-ethanol solutions. The cocrystallization of Md⁺ with salts of divalent ions is due to the formation of mixed crystals. For Md⁺, an ionic radius of 0.117 nm was found. The oxidation of Md³⁺ to Md⁴⁺ was rather unsuccessful.^[1]

History

Mendelevium (for Dimitri Ivanovich Mendeleev, surname commonly transliterated into Latin script as Mendeleev, Mendeleyev, Mendeléef, or even Mendelejeff, and first name sometimes transliterated as Dmitry or Dmitriy) was first synthesized by Albert Ghiorso, Glenn T. Seaborg, Gregory R. Choppin, Bernard G. Harvey, and Stanley G. Thompson (team leader) in early 1955 at the University of California, Berkeley. The team produced ²⁵⁶Md (half-life of 87 minutes) when they bombarded an ²⁵³Es target with alpha particles (helium nuclei) in the Berkeley Radiation Laboratory's 60-inch cyclotron (²⁵⁶Md was the first isotope of any element to be synthesized one atom at a time).^[3] Element 101 was the ninth transuranic element synthesized. The first 17 atoms of this element were created and analyzed using the ion-exchange adsorption-elution method. During the process, mendelevium behaved very much like thulium, its naturally occurring homologue.

Discovery in detail

The discovery was based on a grand total of only 17 atoms. It is synthesized via the ²⁵³Es (α,n) ²⁵⁶101 reaction in the 60-Inch-Cyclotron (= 152 cm) at Berkeley (California). The target can be produced by irradiation of lighter isotopes as plutonium in the Materials Testing Reactor at the Arco Reactor Station in Idaho. Remarkable is that this target consisted of only 10⁹ atoms of highly radioactive ²⁵³Es (with a half-life of 20.5 days). By elution through a calibrated cation exchange resin column, mendelevium was separated and chemically identified.^[3]

Determining feasibility

To predict if this method would be possible, they made use of a rough calculation. The number of atoms that would be produced, would be approximately equal to the number of atoms of target material times its cross section times the ion beam intensity times the time of bombardment related to the half-life of the product when bombarding for a time of the order of its half-life). This gave 1 atom per experiment. Thus under optimum conditions, the preparation of only one atom of element 101 per experiment could be expected. This calculation demonstrated that it was feasible to go ahead with the experiment.^[3]

Recoil technique

The actual synthesis was done by a recoil technique, introduced by Albert Ghiorso. In this technique, the target element was placed on the opposite side of the target from the beam and caught the recoiling atoms on a catcher foil. This recoil target was made by an electroplating technique, developed by Alfred Chetham-Strode. This technique gave a very high yield, which is absolutely necessary when working with such a rare product as the einsteinium target material.^[3]

The recoil target consisted of 10⁻⁹ of ²⁵³Es which were deposited electrolytically on a thin gold foil (also Be, Al and Pt can be used). It was bombarded by 41 eV α-particles in the Berkeley cyclotron with a very high beam density of 6∙10¹³ particles per second over an area of 0.05 cm². The target was cooled by water or liquid helium. The use of helium, in a gaseous atmosphere, slowed down the recoil atoms. This gas could be pumped out of the reaction chamber through a small orifice to form a ‘gas-jet’. Some fraction of the nonvolatile product atoms carried along with the gas, were deposited permanently on the foil surface. The foil could be removed periodically and a new foil could be installed. The next reaction was used for the mendelevium discovery experiment:^{[3][4] 253}Es + ⁴He → ²⁵⁶Md + ¹n

Purification and isolation

The removal of the Md atoms from the collector foil was done by acid etching or total dissolution of the thin gold foil. They can be purified and isolated from other product activities by several techniques. Separation of trivalent actinides from lanthanide fission products and La carrier can be done by a cation-exchange resin column using a 90% water/10% ethanol solution saturated with HCl as eluant. To separate Md rapidly from the catcher foil, an anion-exchange chromatography using 6M HCl as eluant can be used. The gold remained on the column while the Md and other actinides passed through. A final isolation of Md³⁺ from other trivalent actinides was also required. To separate fractions containing elements 99, 100 and 101, a cation-exchange resin column (Dowex-50 exchange column) treated with ammonium salts was used. A chemical identification was made on the basis of its elution position just before Fm. In series of repetitive experiments, they made use of the eluant: α-hydroxyisobutyrate solution (α-HIB). Using the ‘gas-jet’ method, the first two steps can be eliminated. There was shown that in this method it is possible to transport and collect individual product atoms in a fraction of a second some tens of meters away from the target area. Effective transport over long distances requires the presence of large clusters (KCl aerosols) in the ‘carrier’ gas. It is used frequently in the production and isolation of transeinsteinium elements.^[1]

Another possible way to separate the 3+ actinides can be achieved by solvent extraction chromatography using bis-(2-ethylhexyl) phosphoric acid (abbreviated as HDEHP) as the stationary organic phase and HNO₃ as the mobile aqueous phase. The actinide elution sequence is reversed from that of the cation-exchange resin column. The Md separated by this method has the advantage to be free of organic complexing agent compared to the resin column. The disadvantage of this method is that Md elutes after Fm late in the sequence.^[1]

The first "Hooray!"

There was no direct detection, but by observation of spontaneous fission events arising from its electron-capture daughter ²⁵⁶Fm. These events were recorded during the night of February 19, 1955. The first one was identified with a "hooray" followed by a "double hooray" and a "triple hooray". The fourth one eventually officially proved the chemical identification of the 101st element, mendelevium. Additional analysis and further experimentation, showed the isotope to have mass 256 and to decay by electron capture with a half-life of 1.5 h.

Isotopes

Sixteen isotopes of mendelevium from mass 245 to 260 have been characterized, with the most stable being ²⁵⁸Md with a half-life of 51.5 days, ²⁶⁰Md with a half-life of 31.8 days, and ²⁵⁷Md with a half-life of 5.52 hours. All of the remaining radioactive isotopes have half-lives that are less than 97 minutes, and the majority of these have half-lives that are less than 5 minutes. This element also has 5 meta states, with the longest-lived being ^258mMd (t_½ = 58 minutes). The isotopes of mendelevium range in atomic weight from 245.091 u (²⁴⁵Md) to 262.109 u (²⁶²Md).^[5][6]

References

1. ^ ^{a b c d} Hall, Nina (2000). The new chemistry. Cambridge University Press. pp. 9–11. ISBN 0521452244. http://books.google.com/books?id=U4rnzH9QbT4C&pg=PA11. 
2. ^ Johansson, Börje; Rosengren, Anders (1975). "Generalized phase diagram for the rare-earth elements: Calculations and correlations of bulk properties". Physical Review B 11: 2836. Bibcode 1975PhRvB..11.2836J. doi:10.1103/PhysRevB.11.2836. 
3. ^ ^{a b c d e} Ghiorso, A.; Harvey, B.; Choppin, G.; Thompson, S.; Seaborg, G. (1955). "New Element Mendelevium, Atomic Number 101". Physical Review 98: 1518. Bibcode 1955PhRv...98.1518G. doi:10.1103/PhysRev.98.1518. http://books.google.com/books?id=e53sNAOXrdMC&pg=PA101. 
4. ^ Hofmann, Sigurd (2002). On beyond uranium: journey to the end of the periodic table. CRC Press&year=2002. pp. 40–42. ISBN 0415284961. http://books.google.com/books?id=4KcVj3xqsrAC&pg=PA40. 
5. ^ Audi, G (1997). "The N? evaluation of nuclear and decay properties". Nuclear Physics A 624: 1. Bibcode 1997NuPhA.624....1A. doi:10.1016/S0375-9474(97)00482-X. http://amdc.in2p3.fr/nubase/Nubase2003.pdf. 
6. ^ Lide, D. R., ed (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5. 

Further reading

• Hoffman, D.C., Ghiorso, A., Seaborg, G. T. The transuranium people: the inside story, (2000), 201-229
• Morss, L. R., Edelstein, N. M., Fuger, J., The chemistry of the actinide and transactinide element, 3, (2006), 1630–1636
• Seaborg, G. T., Les elements tranuraniens artificiels, (1967), 39-45
• Gol’danskii, V. I., Polikanov, S. M., The transuranium elements, (1973), 101-103
• Seaborg, G.T., The transcalifornium elements. Journal of Chemical Education, (1959), 36, 38-44
• Guide to the Elements - Revised Edition, Albert Stwertka, (Oxford University Press; 1998) ISBN 0-19-508083-1

External links

• Los Alamos National Laboratory - Mendelevium
• It's Elemental - Mendelevium
• WebElements.com - Mendelevium
• Environmental Chemistry- Md info