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Nobelium

Nobelium,  102No
General properties
Name, symbol nobelium, No
Pronunciation or
or
Nobelium in the periodic table
Yb

No

(Upq)
mendeleviumnobeliumlawrencium
Atomic number 102
Standard atomic weight [259]
Element category actinide
Group, block group n/a, f-block
Period period 7
Electron configuration [Rn] 5f14 7s2
per shell 2, 8, 18, 32, 32, 8, 2
Physical properties
Phase solid (predicted)[1]
Melting point 1100 K ​(827 °C, ​1521 °F) (predicted)[1]
Atomic properties
Oxidation states 2, 3
Electronegativity Pauling scale: 1.3 (predicted)[2]
Ionization energies 1st: 641.6 kJ·mol−1
2nd: 1254.3 kJ·mol−1
3rd: 2605.1 kJ·mol−1
Miscellanea
CAS number 10028-14-5
History
Naming after Alfred Nobel
Discovery Joint Institute for Nuclear Research (1966)
Most stable isotopes
iso NA half-life DM DE (MeV) DP
253No syn 1.62 min 80% α 8.14, 8.06, 8.04, 8.01 249Fm
20% β+ 253Md
254No syn 51 s 90% α 250Fm
10% β+ 254Md
255No syn 3.1 min 61% α 8.12, 8.08, 7.93 251Fm
39% β+ 2.012 255Md
257No syn 25 s 99% α 8.32, 8.22 253Fm
1% β+ 257Md
259No syn 58 min 75% α 7.69, 7.61, 7.53.... 255Fm
25% ε 259Md
10% SF

Nobelium is a synthetic chemical element with symbol No and atomic number 102. It is named in honor of Alfred Nobel, the inventor of dynamite and benefactor of science. A radioactive metal, it is the tenth transuranic element and is the penultimate member of the actinide series. Like all elements with atomic number over 100, nobelium can only be produced in particle accelerators by bombarding lighter elements with charged particles. A total of twelve nobelium isotopes are known to exist; the most stable is 259No with a half-life of 58 minutes, but the shorter-lived 255No (half-life 3.1 minutes) is most commonly used in chemistry because it can be produced on a larger scale.

Chemistry experiments have confirmed that nobelium behaves as a heavier homolog to ytterbium in the periodic table. The chemical properties of nobelium are not completely known: they are mostly only known in aqueous solution. Before nobelium's discovery, it was predicted that it would show a stable +2 oxidation state as well as the +3 state characteristic of the other actinides: these predictions were later confirmed, as the +2 state is much more stable than the +3 state in aqueous solution and it is difficult to keep nobelium in the +3 state.

In the 1950s and 1960s, many claims of the discovery of nobelium were made from laboratories in Sweden, the Soviet Union, and the United States. Although the Swedish scientists soon retracted their claims, the priority of the discovery and therefore the naming of the element was disputed between Soviet and American scientists, and it was not until 1997 that International Union of Pure and Applied Chemistry (IUPAC) established nobelium as the official name for the element and credited the Soviet team with the discovery.

Contents

  • Discovery 1
  • Characteristics 2
    • Physical 2.1
    • Chemical 2.2
    • Atomic 2.3
    • Isotopes 2.4
  • Preparation and purification 3
  • References 4
  • Bibliography 5
  • External links 6

Discovery

The element was named after Alfred Nobel.

The discovery of element 102 was a complicated process and was claimed by groups from Sweden, the United States, and the former Soviet Union. The first complete and incontrovertible report of its detection only came in 1966 from the Joint Institute of Nuclear Research at Dubna (then in the Soviet Union).[3]

The first announcement of the discovery of element 102 was announced by physicists at the Nobel Institute in Sweden in 1957. The team reported that they had bombarded a curium target with carbon-13 ions for twenty-five hours in half-hour intervals. Between bombardments, ion-exchange chemistry was performed on the target. Twelve out of the fifty bombardments contained samples emitting (8.5 ± 0.1) MeV alpha particles, which were in drops which eluted earlier than fermium (atomic number Z = 100) and californium (Z = 98). The half-life reported was 10 minutes and was assigned to either 251102 or 253102, although the possibility that the alpha particles observed were from a presumably short-lived mendelevium (Z = 101) isotope created from the electron capture of element 102 was not excluded.[3] The team proposed the name nobelium (No) for the new element,[4][5] which was immediately approved by IUPAC,[6] a decision which the Dubna group later characterized in 1968 as being hasty.[7] The following year, scientists at the Lawrence Berkeley National Laboratory repeated the experiment but were unable to find any 8.5 MeV events which were not background effects.[3]

In 1959, the Swedish team attempted to explain the Berkeley team's inability to detect element 102 in 1958, maintaining that they did discover it. However, later work has shown that no nobelium isotope lighter than 259No (no heavier isotopes could have been produced in the Swedish experiments) with a half-life over 3 minutes exist, and that the Swedish team's results are most likely from thorium-225, which has a half-life of 8 minutes and quickly undergoes triple alpha decay to polonium-213, which has a decay energy of 8.53612 MeV. This hypothesis is lent weight by the fact that thorium-225 can easily be produced in the reaction used and would not be separated out by the chemical methods used. Later work on nobelium also showed that the divalent state is more stable than the trivalent one and hence that the samples emitting the alpha particles could not have contained nobelium, as the divalent nobelium would not have eluted with the other trivalent actinides.[3] Thus, the Swedish team later retracted their claim and associated the activity to background effects.[6]

The Berkeley team, consisting of John R. Walton and Torbjørn Sikkeland, then claimed the synthesis of element 102 in 1958. The team used the new heavy-ion linear accelerator (HILAC) to bombard a curium target (95% 244Cm and 5% 246Cm) with 13C and 12C ions. They were unable to confirm the 8.5 MeV activity claimed by the Swedes but were instead able to detect decays from fermium-250, supposedly the daughter of 254102 (produced from the curium-246), which had an apparent half-life of ~3 s. Later 1963 Dubna work confirmed that 254102 could be produced in this reaction, but that its half-life was actually 50 ± 10 s. In 1967, the Berkeley team attempted to defend their work, stating that the isotope found was indeed 250Fm but the isotope that the half-life measurements actually related to was californium-244, granddaughter of 252102, produced from the more abundant curium-244. Energy differences were then attributed to "resolution and drift problems", although these had not been previously reported and should also have influenced other results. 1977 experiments showed that 252102 indeed had a 2.3-second half-life. However, 1973 work also showed that the 250Fm recoil could have also easily been produced from the isomeric transition of 250mFm (half-life 1.8 s) which could also have been formed in the reaction at the energy used.[3] Given this, it is probable that no nobelium was actually produced in this experiment.[3]

In 1959 the team continued their studies and claimed that they were able to produce an isotope that decayed predominantly by emission of an 8.3 MeV alpha particle, with a half-life of 3 s with an associated 30% spontaneous fission branch. The activity was initially assigned to 254No but later changed to 252No. However, they also noted that it was not certain that nobelium had been produced due to difficult conditions.[3] The Berkeley team decided to adopt the proposed name of the Swedish team, "nobelium", for the element.[6]

244
96
Cm
+ 12
6
C
256
102
No
*
252
102
No
+ 4 1
0
n

Meanwhile in Dubna, experiments were carried out in 1958 and 1960 aiming to synthesize element 102 as well. The first 1958 experiment bombarded plutonium-239 and -241 with oxygen-16 ions. Some alpha decays with energies just over 8.5 MeV were observed, and they were assigned to 251,252,253102, although the team wrote that formation of isotopes from lead or bismuth impurities (which would not produce nobelium) could not be ruled out. While later 1958 experiments noted that new isotopes could be produced from mercury, thallium, lead, or bismuth impurities, the scientists still stood by their conclusion that element 102 could be produced from this reaction, mentioning a half-life of under 30 seconds and a decay energy of (8.8 ± 0.5) MeV. Later 1960 experiments proved that these were background effects. 1967 experiments also lowered the decay energy to (8.6 ± 0.4) MeV, but both values are too high to possibly match those of 253No or 254No.[3] The Dubna team later stated in 1970 and again in 1987 that these results were not conclusive.[3]

In 1961, Berkeley scientists claimed the discovery of element 103 in the reaction of californium with boron and carbon ions. They claimed the production of the isotope 257103, and also claimed to have synthesized an alpha decaying isotope of element 102 that had a half-life of 15 s and alpha decay energy 8.2 MeV. They assigned this to 255102 without giving a reason for the assignment. The values do not agree with those now known for 255No, although they do agree with those now known for 257No, and while this isotope probably played a part in this experiment its discovery was inconclusive.[3]

Work on element 102 also continued in Dubna, and in 1964, experiments were carried out there to detect alpha-decay daughters of element 102 isotopes by synthesizing element 102 from the reaction of a uranium-238 target with neon ions. The products were carried along a silver catcher foil and purified chemically, and the isotopes 250Fm and 252Fm were detected. The yield of 252Fm was interpreted as evidence that its parent 256102 was also synthesized: as it was noted that 252Fm could also be produced directly in this reaction by the simultaneous emission of an alpha particle with the excess neutrons, steps were taken to ensure that 252Fm could not go directly to the catcher foil. The half-life detected for 256102 was 8 s, which is much higher than the more modern 1967 value of (3.2 ± 0.2) s.[3] Further experiments were conducted in 1966 for 254102, using the reactions 243Am(15N,4n)254102 and 238U(22Ne,6n)254102, finding a half-life of (50 ± 10) s: at that time the discrepancy between this value and the earlier Berkeley value was not understood, although later work proved that the formation of the isomer 250mFm was less likely in the Dubna experiments than at the Berkeley ones. In hindsight, the Dubna results on 254102 were probably correct and can be now considered a conclusive detection of element 102.[3] One more very convincing experiment from Dubna came in 1966, again using the same two reactions, which concluded that 254102 indeed had a half-life much longer than the 3 seconds claimed by Berkeley.[3] Later work in 1967 at Berkeley and 1971 at the Oak Ridge National Laboratory fully confirmed the discovery of element 102 and clarified earlier observations.[6] In December 1966, the Berkeley group repeated the Dubna experiments and fully confirmed them, and used this data to finally assign correctly the isotopes they had previously synthesized but could not yet identify at the time, and thus claimed to have discovered nobelium in 1958 to 1961.[6]

238
92
U
+ 22
10
Ne
260
102
No
*
254
102
No
+ 6 1
0
n

In 1969, the Dubna team carried out chemical experiments on element 102 and concluded that it behaved as the heavier homologue of ytterbium. The Russian scientists proposed the name joliotium (Jo) for the new element, creating an element naming controversy that would not be resolved for several decades, which each group using its own proposed names.[6]

In 1992, the IUPAC-IUPAP Transfermium Working Group (TWG) reassessed the claims of discovery and concluded that only the Dubna work from 1966 correctly detected and assigned decays to nuclei with atomic number 102 at the time. The Dubna team are therefore officially recognised as the discoverers of nobelium although it is possible that it was detected at Berkeley in 1959.[3] This decision was criticized by Berkeley the following year, calling the reopening of the cases of elements 101 to 103 a "futile waste of time", while Dubna agreed with the IUPAC's decision.[7]

In 1994, as part of an attempted resolution to the element naming controversy, the IUPAC ratified names for elements 101–109. For element 102, it ratified the name nobelium (No) on the basis that it had become entrenched in the literature over the course of 30 years and that Flerov Laboratory of Nuclear Reactions.[9] This proposal was also not accepted, and in 1997 the name "nobelium" was restored.[8] Today, the name "flerovium", with the same symbol, now refers to element 114.[10]

Characteristics

Physical

Energy required to promote an f electron to the d subshell for the f-block lanthanides and actinides. Above around 210 kJ/mol, this energy is too high to be provided for by the greater crystal energy of the trivalent state and thus einsteinium, fermium, mendelevium form divalent metals like the lanthanides europium and ytterbium. Nobelium is also expected to form a divalent metal, but this has not yet been confirmed.[11]

In the periodic table, nobelium is located to the right of the actinide mendelevium, to the left of the actinide lawrencium, and below the lanthanide ytterbium. Nobelium metal has not yet been prepared in bulk quantities, and bulk preparation is currently impossible.[12] Nevertheless, a number of predictions and some preliminary experimental results have been done regarding its properties.[12]

The lanthanides and actinides, in the metallic state, can exist as either divalent (such as europium and ytterbium) or trivalent (most other lanthanides) metals. The former have fnd1s2 configurations, whereas the latter have fn+1s2 configurations. In 1975, Johansson and Rosengren examined the measured and predicted values for the cohesive energies (enthalpies of crystallization) of the metallic lanthanides and actinides, both as divalent and trivalent metals.[13][14] The conclusion was that the increased binding energy of the [Rn]5f136d17s2 configuration over the [Rn]5f147s2 configuration for nobelium was not enough to compensate for the energy needed to promote one 5f electron to 6d, as is true also for the very late actinides: thus einsteinium, fermium, mendelevium, and nobelium were expected to be divalent metals, although for nobelium this prediction has not yet been confirmed.[13] The increasing predominance of the divalent state well before the actinide series concludes is attributed to the relativistic stabilization of the 5f electrons, which increases with increasing atomic number: an effect of this is that nobelium is predominantly divalent instead of trivalent, unlike all the other lanthanides and actinides.[15] In 1986, nobelium metal was estimated to have an enthalpy of sublimation between 126 kJ·mol−1, a value close to the values for einsteinium, fermium, and mendelevium and supporting the theory that nobelium would form a divalent metal.[12] Divalent nobelium metal should have a metallic radius of around 197 pm.[12] Nobelium's melting point has been predicted to be 827 °C, the same value as that estimated for the neighboring element mendelevium.[16]

Chemical

The chemistry of nobelium is incompletely characterized and is known only in aqueous solution, in which it can take on the +3 or +2

  • Chart of Nuclides. nndc.bnl.gov
  • Los Alamos National Laboratory – Nobelium
  • Nobelium at The Periodic Table of Videos (University of Nottingham)

External links

  • Silva, Robert J. (2011). "Chapter 13. Fermium, Mendelevium, Nobelium, and Lawrencium". In Morss, Lester R.; Edelstein, Norman M. and Fuger, Jean. The Chemistry of the Actinide and Transactinide Elements. Netherlands: Springer.  

Bibliography

  1. ^ a b Lide, D. R., ed. (2003). CRC Handbook of Chemistry and Physics (84th ed.). Boca Raton (FL): CRC Press.  
  2. ^ J.A. Dean, ed. (1999). Lange's Handbook of Chemistry (15 ed.). McGraw-Hill. Section 4; Table 4.5, Electronegativities of the Elements. 
  3. ^ a b c d e f g h i j k l m n Barber, R. C.; Greenwood, N.N.; Hrynkiewicz, A.Z.; Jeannin, Y.P.; Lefort, M.; Sakai, M.; Ulehla, I.; Wapstra, A.P.; Wilkinson, D.H. (1993). "Discovery of the transfermium elements. Part II: Introduction to discovery profiles. Part III: Discovery profiles of the transfermium elements". Pure and Applied Chemistry 65 (8): 1757.   (Note: for Part I see Pure Appl. Chem., Vol. 63, No. 6, pp. 879–886, 1991)
  4. ^ a b Silva, pp. 1636–7
  5. ^ Fields, P. R.; Friedman, A. M.; Milsted, J.; Atterling, H.; Forsling, W.; Holm, L. W.; Åström, B. (1 September 1957). "Production of the New Element 102". Phys. Rev. 107 (5): 1460.  
  6. ^ a b c d e f John Emsley (2011). Nature's Building Blocks: An A-Z Guide to the Elements. Oxford University Press. pp. 368–9.  
  7. ^ a b Ghiorso, A.; Seaborg, G.T.; Organessian, Yu. Ts.; Zvara, I.; Armbruster, P.; Hessberger, F.P.; Hofmann, S.; Leino, M.; Munzenberg, G.; Reisdorf, W.; Schmidt, K.-H. (1993). "Responses on 'Discovery of the transfermium elements' by Lawrence Berkeley Laboratory, California; Joint Institute for Nuclear Research, Dubna; and Gesellschaft fur Schwerionenforschung, Darmstadt followed by reply to responses by the Transfermium Working Group". Pure and Applied Chemistry 65 (8): 1815–1824.  
  8. ^ a b "Names and symbols of transfermium elements". Pure & Applied Chemistry 69 (12): 2471–2473. 1997.  
  9. ^ Hoffmann, Darleane C.; Lee, Diana M.; Pershina, Valeria (2006). "Transactinides and the future elements". In Morss, L. R.; Edelstein, N. M.; Fuger, J. The Chemistry of the Actinide and Transactinide Elements (3rd ed.).  
  10. ^ "Element 114 is Named Flerovium and Element 116 is Named Livermorium" (Press release).  
  11. ^ Haire, Richard G. (2006). "Einsteinium". In Morss, Lester R.; Edelstein, Norman M.; Fuger, Jean. The Chemistry of the Actinide and Transactinide Elements 3 (3rd ed.). Dordrecht, the Netherlands: Springer. pp. 1577–1620.  
  12. ^ a b c d e f Silva, pp. 1639
  13. ^ a b Silva, pp. 1626–8
  14. ^ Johansson, Börje; Rosengren, Anders (1975). "Generalized phase diagram for the rare-earth elements: Calculations and correlations of bulk properties". Physical Review B 11 (8): 2836.  
  15. ^ Hulet, E. K. (1980). "Chapter 12. Chemistry of the Heaviest Actinides: Fermium, Mendelevium, Nobelium, and Lawrencium". In Edelstein, Norman M. Lanthanide and Actinide Chemistry and Spectroscopy.  
  16. ^ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). CRC Press. pp. 4.121–4.123.  
  17. ^ a b c d e f g h i j k l Silva, pp. 1639–41
  18. ^ Martin, W. C.; Hagan, Lucy; Reader, Joseph; Sugar, Jack (1974). "Ground Levels and Ionization Potentials for Lanthanide and Actinide Atoms and Ions". J. Phys. Chem. Ref. Data 3 (3): 771–9. Retrieved 2013-10-19. 
  19. ^ David R. Lide (ed), CRC Handbook of Chemistry and Physics, 84th Edition. CRC Press. Boca Raton, Florida, 2003; Section 10, Atomic, Molecular, and Optical Physics; Ionization Potentials of Atoms and Atomic Ions
  20. ^ a b c d e f g h Silva, pp. 1637–8
  21. ^ a b c d e f g http://www.nucleonica.net/unc.aspx
  22. ^ a b c d e f g Audi, G.; Bersillon, O.; Blachot, J.; Wapstra, A. H. (2003), evaluation of nuclear and decay properties"UBASE"The N, Nucl. Phys. A 729: 3–128,  
  23. ^ Kratz, J. V. (5 September 2011). "The Impact of Superheavy Elements on the Chemical and Physical Sciences". 4th International Conference on the Chemistry and Physics of the Transactinide Elements. Retrieved 27 August 2013. 
  24. ^ Nurmia, Matti (2003). "Nobelium". Chemical and Engineering News 81 (36). 
  25. ^ a b c d Silva, pp. 1638–9

References

Once the nobelium-255 is produced, it can be separated out in a similar way as used to purify the neighboring actinide mendelevium. The recoil hydrochloric acid as mobile aqueous phase, or using 3 M hydrochloric acid as an eluant from cation-exchange resin columns), nobelium will pass through the column and elute while the other trivalent actinides remain on the column.[25] However, if a direct "catcher" gold foil is used, the process is complicated by the need to separate out the gold using anion-exchange chromatography before isolating the nobelium by elution from chromatographic extraction columns using HDEHP.[25]

The isotopes of nobelium are mostly produced by bombarding actinide targets (uranium, plutonium, curium, californium, or einsteinium), with the exception of nobelium-262, which is produced as the daughter of lawrencium-262.[20] The most commonly used isotope, 255No, can be produced from bombarding curium-248 or californium-249 with carbon-12: the latter method is more common. Irradiating a 350 μg cm−2 target of californium-249 with three trillion (3 × 1012) 73 MeV carbon-12 ions per second for ten minutes can produce around 1200 nobelium-255 atoms.[20]

Preparation and purification

The half-lives of nobelium isotopes increase smoothly from 250No to 253No. However, a dip appears at 254No, and beyond this the half-lives of even-even nobelium isotopes drop sharply as spontaneous fission becomes the dominant decay mode. For example, the half-life of 256No is almost three seconds, but that of 258No is only 1.2 milliseconds.[20][21][22] This shows that at nobelium, the mutual repulsion of protons poses a limit to the island of relative stability of long-lived nuclei in the actinide series.[24] The even-odd nobelium isotopes mostly continue to have longer half-lives as their mass numbers increase, with a dip in the trend at 257No.[20][21][22]

Twelve isotopes of nobelium are known, with mass numbers 250–260 and 262; all are radioactive.[20] Additionally, nuclear isomers are known for mass numbers 251, 253, and 254.[21][22] Of these, the longest-lived isotope is 259No with a half-life of 58 minutes, and the longest-lived isomer is 251mNo with a half-life of 1.7 seconds.[21][22] However, the still undiscovered isotope 261No is predicted to have a still longer half-life of 170 min.[21][22] Additionally, the shorter-lived 255No (half-life 3.1 minutes) is more often used in chemical experimentation because it can be produced in larger quantities from irradiation of californium-249 with carbon-12 ions.[20] After 259No and 255No, the next most stable nobelium isotopes are 253No (half-life 1.62 minutes), 254No (51 seconds), 257No (25 seconds), 256No (2.91 seconds), and 252No (2.57 seconds).[20][21][22] All of the remaining nobelium isotopes have half-lives that are less than a second, and the shortest-lived known nobelium isotope (250No) has a half-life of only 0.25 milliseconds.[20][21][22] The isotope 254No is especially interesting theoretically as it is in the middle of a series of prolate nuclei from 231Pa to 279Rg, and the formation of its nuclear isomers (of which two are known) is controlled by proton orbitals such as 2f5/2 which come just above the spherical proton shell.[23]

Isotopes

A nobelium atom has 102 electrons, of which three can act as valence electrons. They are expected to be arranged in the configuration [Rn]5f147s2 (ground state term symbol 1S0), although experimental verification of this electron configuration had not yet been made as of 2006.[12] In forming compounds, all the three valence electrons may be lost, leaving behind a [Rn]5f13 core: this conforms to the trend set by the other actinides with their [Rn] 5fn electron configurations in the tripositive state. Nevertheless, it is more likely that only two valence electrons may be lost, leaving behind a stable [Rn]5f14 core with a filled 5f14 shell. The first ionization potential of mendelevium was measured to be at most (6.65 ± 0.07) eV in 1974, based on the assumption that the 7s electrons would ionize before the 5f ones;[18] this value has since not yet been refined further due to nobelium's scarcity and high radioactivity.[19] The ionic radius of hexacoordinate and octacoordinate No3+ had been preliminarily estimated in 1978 to be around 90 and 102 pm respectively;[17] the ionic radius of No2+ has been experimentally found to be 100 pm to two significant figures.[12] The enthalpy of hydration of No2+ has been calculated as 1486 kJ·mol−1.[17]

Atomic

The standard reduction potential of the E°(No3+→No2+) couple was estimated in 1967 to be between +1.4 and +1.5 V.[17] The positive value shows that No2+ is more stable than No3+ and that No3+ is a good oxidizing agent. While the quoted values for the E°(No2+→No0) and E°(No3+→No0) vary among sources, the accepted standard estimates are −2.61 and −1.26 V.[17] It has been predicted that the value for the E°(No4+→No3+) couple would be +6.5 V.[17] The Gibbs energies of formation for No3+ and No2+ are estimated to be −342 and −480 kJ·mol−1, respectively.[17]

Nobelium's complexing ability with chloride ions is most similar to that of barium, which complexes rather weakly.[17] Its complexing ability with citrate, oxalate, and acetate in an aqueous solution of 0.5 M ammonium nitrate is between that of calcium and strontium, although it is somewhat closer to that of strontium.[17]

In 1967, experiments were conducted to compare nobelium's chemical behavior to that of terbium, californium, and fermium. All four elements were reacted with chlorine and the resulting chlorides were deposited along a tube, along which they were carried by a gas. It was found that the nobelium chloride produced was strongly adsorbed on solid surfaces, proving that it was not very volatile, like the chlorides of the other three investigated elements. However, both NoCl2 and NoCl3 were expected to exhibit nonvolatile behavior and hence this experiment was inconclusive as to what the preferred oxidation state of nobelium was.[17] Determination of nobelium's favoring of the +2 state had to wait until the next year, when cation-exchange chromatography and coprecipitation experiments were carried out on around fifty thousand 255No atoms, finding that it behaved differently from the other actinides and more like the divalent alkaline earth metals. This proved that in aqueous solution, nobelium is most stable in the divalent state when strong oxidizers are absent.[17] Later experimentation in 1974 showed that nobelium eluted with the alkaline earth metals, between Ca2+ and Sr2+.[17]

[17]

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