Jump to content

Hafnium

Edit links
This is a good article. Click here for more information.
From Wikipedia, the free encyclopedia
(Redirected from Celtium)
For the group that caused the 2021 Microsoft Exchange Server data breach, see Hafnium (group).
Not to be confused with the compound hydrogen fluoride, formula HF.
Hafnium, 72Hf
Hafnium
Pronunciation/ˈhæfniəm/ ​(HAF-nee-əm)
Appearancesteel gray
Standard atomic weight Ar°(Hf)
Hafnium in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
Zr
↑
Hf
↓
Rf
lutetium ← hafnium → tantalum
Atomic number (Z)72
Groupgroup 4
Periodperiod 6
Block  d-block
Electron configuration[Xe] 4f14 5d2 6s2
Electrons per shell2, 8, 18, 32, 10, 2
Physical properties
Phase at STPsolid
Melting point2506 K ​(2233 °C, ​4051 °F)
Boiling point4876 K ​(4603 °C, ​8317 °F)
Density (at 20° C)13.281 g/cm3 [3]
when liquid (at m.p.)12 g/cm3
Heat of fusion27.2 kJ/mol
Heat of vaporization648 kJ/mol
Molar heat capacity25.73 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 2689 2954 3277 3679 4194 4876
Atomic properties
Oxidation statescommon: +4
−2,[4] 0,[5] +1,[6] +2,[7] +3[7]
ElectronegativityPauling scale: 1.3
Ionization energies
  • 1st: 658.5 kJ/mol
  • 2nd: 1440 kJ/mol
  • 3rd: 2250 kJ/mol
Atomic radiusempirical: 159 pm
Covalent radius175±10 pm
Color lines in a spectral range
Spectral lines of hafnium
Other properties
Natural occurrenceprimordial
Crystal structure ​hexagonal close-packed (hcp) (hP2)
Lattice constants
Hexagonal close packed crystal structure for hafnium
a = 319.42 pm
c = 505.12 pm (at 20 °C)[3]
Thermal expansion5.9 µm/(m⋅K) (at 25 °C)
Thermal conductivity23.0 W/(m⋅K)
Electrical resistivity331 nΩ⋅m (at 20 °C)
Magnetic orderingparamagnetic[8]
Molar magnetic susceptibility+75.0×10−6 cm3/mol (at 298 K)[9]
Young's modulus78 GPa
Shear modulus30 GPa
Bulk modulus110 GPa
Speed of sound thin rod3010 m/s (at 20 °C)
Poisson ratio0.37
Mohs hardness5.5
Vickers hardness1520–2060 MPa
Brinell hardness1450–2100 MPa
CAS Number7440-58-6
History
Namingafter Hafnia. Latin for: Copenhagen, where it was discovered
PredictionDmitri Mendeleev (1869)
Discovery and first isolationDirk Coster and George de Hevesy (1922)
Isotopes of hafnium
Main isotopes[10] Decay
abun­dance half-life (t1/2) mode pro­duct
172Hf synth 1.87 y ε 172Lu
174Hf 0.16% 3.8×1016 y[11] α 170Yb
176Hf 5.26% stable
177Hf 18.6% stable
178Hf 27.3% stable
178m2Hf synth 31 y IT 178Hf
179Hf 13.6% stable
180Hf 35.1% stable
182Hf synth 8.9×106 y β− 182Ta
 Category: Hafnium
| references

Hafnium is a chemical element; it has symbol Hf and atomic number 72. A lustrous, silvery gray, tetravalent transition metal, hafnium chemically resembles zirconium and is found in many zirconium minerals. Its existence was predicted by Dmitri Mendeleev in 1869, though it was not identified until 1922, by Dirk Coster and George de Hevesy. Hafnium is named after Hafnia, the Latin name for Copenhagen, where it was discovered.

Hafnium is used in filaments and electrodes. Some semiconductor fabrication processes use its oxide for integrated circuits at 45 nanometers and smaller feature lengths. Some superalloys used for special applications contain hafnium in combination with niobium, titanium, or tungsten.

Hafnium's large neutron capture cross section makes it a good material for neutron absorption in control rods in nuclear power plants, but at the same time requires that it be removed from the neutron-transparent corrosion-resistant zirconium alloys used in nuclear reactors.

Characteristics

[edit]

Physical characteristics

[edit]
Pieces of hafnium

Hafnium is a shiny, silvery, ductile metal that is corrosion-resistant and chemically similar to zirconium[12] in that they have the same number of valence electrons and are in the same group. Also, their relativistic effects are similar: The expected expansion of atomic radii from period 5 to 6 is almost exactly canceled out by the lanthanide contraction. Hafnium changes from its alpha form, a hexagonal close-packed lattice, to its beta form, a body-centered cubic lattice, at 2,388 K (2,115 °C; 3,839 °F).[13] The physical properties of hafnium metal samples are markedly affected by zirconium impurities, especially the nuclear properties, as these two elements are among the most difficult to separate because of their chemical similarity.[12]

A notable physical difference between these metals is their density, with zirconium having about one-half the density of hafnium. The most notable nuclear properties of hafnium are its high thermal neutron capture cross section and that the nuclei of several different hafnium isotopes readily absorb two or more neutrons apiece.[12] In contrast with this, zirconium is practically transparent to thermal neutrons, and it is commonly used for the metal components of nuclear reactors—especially the cladding of their nuclear fuel rods.

Chemical characteristics

[edit]
See also: Category:Hafnium compounds
Hafnium dioxide (HfO2)

Hafnium reacts in air to form a protective film that inhibits further corrosion. Despite this, the metal is attacked by hydrofluoric acid and concentrated sulfuric acid, and can be oxidized with halogens or burnt in air. Like its sister metal zirconium, finely divided hafnium can ignite spontaneously in air. The metal is resistant to concentrated alkalis.

As a consequence of lanthanide contraction, the chemistry of hafnium and zirconium is so similar that the two cannot be separated based on differing chemical reactions. The melting and boiling points of the compounds and the solubility in solvents are the major differences in the chemistry of these twin elements.[14]

Isotopes

[edit]
Main article: Isotopes of hafnium

At least 40 isotopes of hafnium have been observed, ranging in mass number from 153 to 192.[15][16][17] The five stable isotopes have mass numbers ranging from 176 to 180 inclusive. The radioactive isotopes' half-lives range from 400 ms for 153Hf[16] to 7.0×1016 years for the most stable one, the primordial 174Hf.[15][18]

The extinct radionuclide 182Hf has a half-life of 8.9±0.1 million years, and is an important tracker isotope for the formation of planetary cores.[19] The nuclear isomer 178m2Hf was at the center of a controversy for several years regarding its potential use as a weapon.

Occurrence

[edit]
Zircon crystal (2×2 cm) from Tocantins, Brazil

Hafnium is estimated to make up about between 3.0 and 4.8 ppm of the Earth's upper crust by mass.[20]: 5  [21] It does not exist as a free element on Earth, but is found combined in solid solution with zirconium in natural zirconium compounds such as zircon, ZrSiO4, which usually has about 1–4% of the Zr replaced by Hf. Rarely, the Hf/Zr ratio increases during crystallization to give the isostructural mineral hafnon (Hf,Zr)SiO4, with atomic Hf > Zr.[22] An obsolete name for a variety of zircon containing unusually high Hf content is alvite.[23]

A major source of zircon (and hence hafnium) ores is heavy mineral sands ore deposits, pegmatites, particularly in Brazil and Malawi, and carbonatite intrusions, particularly the Crown Polymetallic Deposit at Mount Weld, Western Australia. A potential source of hafnium is trachyte tuffs containing rare zircon-hafnium silicates eudialyte or armstrongite, at Dubbo in New South Wales, Australia.[24]

Production

[edit]
Melted tip of a hafnium consumable electrode used in an electron beam remelting furnace, a 1 cm cube, and an oxidized hafnium electron beam-remelted ingot (left to right)

The heavy mineral sands ore deposits of the titanium ores ilmenite and rutile yield most of the mined zirconium, and therefore also most of the hafnium.[25]

Zirconium is a good nuclear fuel-rod cladding metal, with the desirable properties of a very low neutron capture cross section and good chemical stability at high temperatures. However, because of hafnium's neutron-absorbing properties, hafnium impurities in zirconium would cause it to be far less useful for nuclear reactor applications. Thus, a nearly complete separation of zirconium and hafnium is necessary for their use in nuclear power. The production of hafnium-free zirconium is the main source of hafnium.[12]

Hafnium oxidized ingots which exhibit thin-film optical effects

The chemical properties of hafnium and zirconium are nearly identical, which makes the two difficult to separate.[26] The methods first used—fractional crystallization of ammonium fluoride salts[27] or the fractional distillation of the chloride[28]—have not proven suitable for an industrial-scale production. After zirconium was chosen as a material for nuclear reactor programs in the 1940s, a separation method had to be developed. Liquid–liquid extraction processes with a wide variety of solvents were developed and are still used for producing hafnium.[29] About half of all hafnium metal manufactured is produced as a by-product of zirconium refinement. The end product of the separation is hafnium(IV) chloride.[30] The purified hafnium(IV) chloride is converted to the metal by reduction with magnesium or sodium, as in the Kroll process.[31]

Further purification is effected by a chemical transport reaction developed by Arkel and de Boer: In a closed vessel, hafnium reacts with iodine at temperatures of 500 °C (900 °F), forming hafnium(IV) iodide; at a tungsten filament of 1,700 °C (3,100 °F) the reverse reaction happens preferentially, and the chemically bound iodine and hafnium dissociate into the native elements. The hafnium forms a solid coating at the tungsten filament, and the iodine can react with additional hafnium, resulting in a steady iodine turnover and ensuring the chemical equilibrium remains in favor of hafnium production.[14][32]

Chemical compounds

[edit]

Due to the lanthanide contraction, the ionic radius of hafnium(IV) (0.78 ångström) is almost the same as that of zirconium(IV) (0.79 angstroms).[33] Consequently, compounds of hafnium(IV) and zirconium(IV) have very similar chemical and physical properties.[33] Hafnium and zirconium tend to occur together in nature and the similarity of their ionic radii makes their chemical separation rather difficult. Hafnium tends to form inorganic compounds in the oxidation state of +4. Halogens react with it to form hafnium tetrahalides.[33] At higher temperatures, hafnium reacts with oxygen, nitrogen, carbon, boron, sulfur, and silicon.[33] Some hafnium compounds in lower oxidation states are known.[34]

Hafnium(IV) chloride and hafnium(IV) iodide have some applications in the production and purification of hafnium metal. They are volatile solids with polymeric structures.[14] These tetrachlorides are precursors to various organohafnium compounds such as hafnocene dichloride and tetrabenzylhafnium.

The white hafnium oxide (HfO2), with a melting point of 2,812 °C (3,085 K; 5,094 °F) and a boiling point of roughly 5,100 °C (5,400 K; 9,200 °F), is very similar to zirconia, but slightly more basic.[14] Hafnium carbide is the most refractory binary compound known, with a melting point over 3,890 °C (4,163 K; 7,034 °F), and hafnium nitride is the most refractory of all known metal nitrides, with a melting point of 3,310 °C (3,583 K; 5,990 °F).[33] This has led to proposals that hafnium or its carbides might be useful as construction materials that are subjected to very high temperatures. The mixed carbide tantalum hafnium carbide (Ta
4HfC
5) possesses the highest melting point of any currently known compound, 4,263 K (3,990 °C; 7,214 °F).[35] Recent supercomputer simulations suggest a hafnium alloy with a melting point of 4,400 K (4,127 °C; 7,460 °F).[36]

History

[edit]
Photographic recording of the characteristic X-ray emission lines of some elements

Hafnium's existence was predicted by Dmitri Mendeleev in 1869. In his report on The Periodic Law of the Chemical Elements, in 1869, Dmitri Mendeleev had implicitly predicted the existence of a heavier analog of titanium and zirconium. At the time of his formulation in 1871, Mendeleev believed that the elements were ordered by their atomic masses and placed lanthanum (element 57) in the spot below zirconium. The exact placement of the elements and the location of missing elements was done by determining the specific weight of the elements and comparing the chemical and physical properties.[37]

The X-ray spectroscopy done by Henry Moseley in 1914 showed a direct dependency between spectral line and effective nuclear charge. This led to the nuclear charge, or atomic number of an element, being used to ascertain its place within the periodic table. With this method, Moseley determined the number of lanthanides and showed the gaps in the atomic number sequence at numbers 43, 61, 72, and 75.[38]

The discovery of the gaps led to an extensive search for the missing elements. In 1914, several people claimed the discovery after Henry Moseley predicted the gap in the periodic table for the then-undiscovered element 72.[39] Georges Urbain asserted that he found element 72 in the rare earth elements in 1907 and published his results on celtium in 1911.[40] Neither the spectra nor the chemical behavior he claimed matched with the element found later, and therefore his claim was turned down after a long-standing controversy.[41] The controversy was partly because the chemists favored the chemical techniques which led to the discovery of celtium, while the physicists relied on the use of the new X-ray spectroscopy method that proved that the substances discovered by Urbain did not contain element 72.[41] In 1921, Charles R. Bury[42][43] suggested that element 72 should resemble zirconium and therefore was not part of the rare earth elements group. By early 1923, Niels Bohr and others agreed with Bury.[44][45] These suggestions were based on Bohr's theories of the atom which were identical to chemist Charles Bury,[42] the X-ray spectroscopy of Moseley, and the chemical arguments of Friedrich Paneth.[46][47]

Encouraged by these suggestions and by the reappearance in 1922 of Urbain's claims that element 72 was a rare earth element discovered in 1911, Dirk Coster and Georg von Hevesy were motivated to search for the new element in zirconium ores.[48] Hafnium was discovered by the two in 1923 in Copenhagen, Denmark, validating the original 1869 prediction of Mendeleev.[49][50][51] It was ultimately found in zircon in Norway through X-ray spectroscopy analysis.[52] The place where the discovery took place led to the element being named for the Latin name for "Copenhagen", Hafnia, the home town of Niels Bohr.[53][54][55] Today, the Faculty of Science of the University of Copenhagen uses in its seal a stylized image of the hafnium atom.[56]

Hafnium was separated from zirconium through repeated recrystallization of the double ammonium or potassium fluorides by Valdemar Thal Jantzen and von Hevesey.[27] Anton Eduard van Arkel and Jan Hendrik de Boer were the first to prepare metallic hafnium by passing hafnium tetraiodide vapor over a heated tungsten filament in 1924.[28][32] This process for differential purification of zirconium and hafnium is still in use today.[12]

Hafnium was one of the last two stable elements to be discovered. The element rhenium was found in 1908 by Masataka Ogawa, though its atomic number was misidentified at the time, and it was not generally recognised by the scientific community until its rediscovery by Walter Noddack, Ida Noddack, and Otto Berg in 1925. This makes it somewhat difficult to say if hafnium or rhenium was discovered last.[57]

In 1923, six predicted elements were still missing from the periodic table: 43 (technetium), 61 (promethium), 85 (astatine), and 87 (francium) are radioactive elements and are only present in trace amounts in the environment,[58] thus making elements 75 (rhenium) and 72 (hafnium) the last two unknown non-radioactive elements.

Applications

[edit]

Most of the hafnium produced is used in the manufacture of control rods for nuclear reactors.[29]

Hafnium has limited technical applications due to a few factors. First, it's very similar to zirconium, a more abundant element that can be used in most cases. Second, pure hafnium wasn't widely available until the late 1950s, when it became a byproduct of the nuclear industry's need for hafnium-free zirconium. Additionally, hafnium is rare and difficult to separate from other elements, making it expensive. After the Fukushima disaster reduced the demand for hafnium-free zirconium, the price of hafnium increased significantly from around $500–$600/kg ($227-$272/lb) in 2014 to around $1000/kg ($454/lb) in 2015.[59]

Nuclear reactors

[edit]

The nuclei of several hafnium isotopes can each absorb multiple neutrons. This makes hafnium a good material for nuclear reactors' control rods. Its neutron capture cross section (Capture Resonance Integral Io ≈ 2000 barns)[60] is about 600 times that of zirconium (other elements that are good neutron-absorbers for control rods are cadmium and boron). Excellent mechanical properties and exceptional corrosion-resistance properties allow its use in the harsh environment of pressurized water reactors.[29] The German research reactor FRM II uses hafnium as a neutron absorber.[61] It is also common in military reactors, particularly in US naval submarine reactors, to slow reactor rates that are too high.[62][63] It is seldom found in civilian reactors, the first core of the Shippingport Atomic Power Station (a conversion of a naval reactor) being a notable exception.[64]

Alloys

[edit]
Hafnium-containing rocket nozzle of the Apollo Lunar Module in the lower right corner

Hafnium is used in alloys with iron, titanium, niobium, tantalum, and other metals. An alloy used for liquid-rocket thruster nozzles, for example the main engine of the Apollo Lunar Modules, is C103 which consists of 89% niobium, 10% hafnium and 1% titanium.[65]

Small additions of hafnium increase the adherence of protective oxide scales on nickel-based alloys. It thereby improves the corrosion resistance, especially under cyclic temperature conditions that tend to break oxide scales, by inducing thermal stresses between the bulk material and the oxide layer.[66][67][68]

Microprocessors

[edit]

Hafnium-based compounds are employed in gates of transistors as insulators in the 45 nm (and below) generation of integrated circuits from Intel, IBM and others.[69][70] Hafnium oxide-based compounds are practical high-k dielectrics, allowing reduction of the gate leakage current which improves performance at such scales.[71][72][73]

Isotope geochemistry

[edit]

Isotopes of hafnium and lutetium (along with ytterbium) are also used in isotope geochemistry and geochronological applications, in lutetium-hafnium dating. It is often used as a tracer of isotopic evolution of Earth's mantle through time.[74] This is because 176Lu decays to 176Hf with a half-life of approximately 37 billion years.[75][76][77]

In most geologic materials, zircon is the dominant host of hafnium (>10,000 ppm) and is often the focus of hafnium studies in geology.[78] Hafnium is readily substituted into the zircon crystal lattice, and is therefore very resistant to hafnium mobility and contamination. Zircon also has an extremely low Lu/Hf ratio, making any correction for initial lutetium minimal. Although the Lu/Hf system can be used to calculate a "model age", i.e. the time at which it was derived from a given isotopic reservoir such as the depleted mantle, these "ages" do not carry the same geologic significance as do other geochronological techniques as the results often yield isotopic mixtures and thus provide an average age of the material from which it was derived.

Garnet is another mineral that contains appreciable amounts of hafnium to act as a geochronometer. The high and variable Lu/Hf ratios found in garnet make it useful for dating metamorphic events.[79]

Other uses

[edit]

Due to its heat resistance and its affinity to oxygen and nitrogen, hafnium is a good scavenger for oxygen and nitrogen in gas-filled and incandescent lamps. Hafnium is also used as the electrode in plasma cutting because of its ability to shed electrons into the air.[80]

The high energy content of 178m2Hf was the concern of a DARPA-funded program in the US. This program eventually concluded that using the above-mentioned 178m2Hf nuclear isomer of hafnium to construct high-yield weapons with X-ray triggering mechanisms—an application of induced gamma emission—was infeasible because of its expense. See hafnium controversy.

Hafnium metallocene compounds can be prepared from hafnium tetrachloride and various cyclopentadiene-type ligand species. Perhaps the simplest hafnium metallocene is hafnocene dichloride. Hafnium metallocenes are part of a large collection of Group 4 transition metal metallocene catalysts [81] that are used worldwide in the production of polyolefin resins like polyethylene and polypropylene.

A pyridyl-amidohafnium catalyst can be used for the controlled iso-selective polymerization of propylene which can then be combined with polyethylene to make a much tougher recycled plastic.[82]

Hafnium diselenide is studied in spintronics thanks to its charge density wave and superconductivity.[83]

Precautions

[edit]

Care needs to be taken when machining hafnium because it is pyrophoric—fine particles can spontaneously combust when exposed to air. Compounds that contain this metal are rarely encountered by most people. The pure metal is not considered toxic, but hafnium compounds should be handled as if they were toxic because the ionic forms of metals are normally at greatest risk for toxicity, and limited animal testing has been done for hafnium compounds.[84]

People can be exposed to hafnium in the workplace by breathing, swallowing, skin, and eye contact. The Occupational Safety and Health Administration (OSHA) has set the legal limit (permissible exposure limit) for exposure to hafnium and hafnium compounds in the workplace as TWA 0.5 mg/m3 over an 8-hour workday. The National Institute for Occupational Safety and Health (NIOSH) has set the same recommended exposure limit (REL). At levels of 50 mg/m3, hafnium is immediately dangerous to life and health.[85]

References

[edit]
  1. ^ "Standard Atomic Weights: Hafnium". CIAAW. 2019.
  2. ^ Prohaska, Thomas; Irrgeher, Johanna; Benefield, Jacqueline; Böhlke, John K.; Chesson, Lesley A.; Coplen, Tyler B.; Ding, Tiping; Dunn, Philip J. H.; Gröning, Manfred; Holden, Norman E.; Meijer, Harro A. J. (2022-05-04). "Standard atomic weights of the elements 2021 (IUPAC Technical Report)". Pure and Applied Chemistry. doi:10.1515/pac-2019-0603. ISSN 1365-3075.
  3. ^ a b Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
  4. ^ Hf(–2) occurs in Hf(CO)62−; see John E. Ellis (2003). "Metal Carbonyl Anions:  from [Fe(CO)4]2- to [Hf(CO)6]2- and Beyond†". Organometallics. 22 (17): 3322–3338. doi:10.1021/om030105l.
  5. ^ Hf(0) occur in (η6-(1,3,5-tBu)3C6H3)2Hf and [(η5-C5R5Hf(CO)4]−, see Chirik, P. J.; Bradley, C. A. (2007). "4.06 - Complexes of Zirconium and Hafnium in Oxidation States 0 to ii". Comprehensive Organometallic Chemistry III. From Fundamentals to Applications. Vol. 4. Elsevier Ltd. pp. 697–739. doi:10.1016/B0-08-045047-4/00062-5. ISBN 9780080450476.
  6. ^ Hf(I) has been observed in hafnium monobromide (HfBr), see Marek, G.S.; Troyanov, S.I.; Tsirel'nikov, V.I. (1979). "Кристаллическое строение и термодинамические характеристики монобромидов циркония и гафния / Crystal structure and thermodynamic characteristics of monobromides of zirconium and hafnium". Журнал неорганической химии / Russian Journal of Inorganic Chemistry (in Russian). 24 (4): 890–893.
  7. ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 28. ISBN 978-0-08-037941-8.
  8. ^ Lide, D. R., ed. (2005). "Magnetic susceptibility of the elements and inorganic compounds". CRC Handbook of Chemistry and Physics (PDF) (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  9. ^ Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN 0-8493-0464-4.
  10. ^ Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3): 030001. doi:10.1088/1674-1137/abddae.
  11. ^ Belli, P.; Bernabei, R.; Cappella, F.; Caracciolo, V.; Cerulli, R.; Incicchitti, A.; Laubenstein, M.; Leoncini, A.; Merlo, V.; Nagorny, S.S.; Nahorna, V.V.; Nisi, S.; Wang, P. (January 2025). "A new measurement of 174Hf alpha decay". Nuclear Physics A. 1053: 122976. doi:10.1016/j.nuclphysa.2024.122976. {{cite journal}}: |access-date= requires |url= (help)
  12. ^ a b c d e Schemel, J. H. (1977). ASTM Manual on Zirconium and Hafnium. Vol. STP 639. Philadelphia: ASTM. pp. 1–5. ISBN 978-0-8031-0505-8.
  13. ^ O'Hara, Andrew; Demkov, Alexander A. (2014). "Oxygen and nitrogen diffusion in α-hafnium from first principles". Applied Physics Letters. 104 (21): 211909. Bibcode:2014ApPhL.104u1909O. doi:10.1063/1.4880657.
  14. ^ a b c d Holleman, Arnold F.; Wiberg, Egon; Wiberg, Nils (1985). Lehrbuch der Anorganischen Chemie (in German) (91–100 ed.). Walter de Gruyter. pp. 1056–1057. doi:10.1515/9783110206845. ISBN 978-3-11-007511-3.
  15. ^ a b Barbalace, Kenneth L. "Periodic Table of Elements: Hf – Hafnium". environmentalchemistry.com. J.K. Barbalace Inc. Retrieved 2021-11-12.
  16. ^ a b Audi, G.; Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S. (2017). "The NUBASE2016 evaluation of nuclear properties" (PDF). Chinese Physics C. 41 (3): 030001. Bibcode:2017ChPhC..41c0001A. doi:10.1088/1674-1137/41/3/030001.
  17. ^ Haak, K.; Tarasov, O. B.; Chowdhury, P.; et al. (2023). "Production and discovery of neutron-rich isotopes by fragmentation of 198Pt". Physical Review C. 108 (34608): 034608. Bibcode:2023PhRvC.108c4608H. doi:10.1103/PhysRevC.108.034608. S2CID 261649436.
  18. ^ Caracciolo, V.; Nagorny, S.; Belli, P.; et al. (2020). "Search for α decay of naturally occurring Hf-nuclides using a Cs2HfCl6 scintillator". Nuclear Physics A. 1002 (121941): 121941. arXiv:2005.01373. Bibcode:2020NuPhA100221941C. doi:10.1016/j.nuclphysa.2020.121941. S2CID 218487451.
  19. ^ Kleine T, Walker RJ (August 2017). "Tungsten Isotopes in Planets". Annual Review of Earth and Planetary Sciences. 45 (1): 389–417. Bibcode:2017AREPS..45..389K. doi:10.1146/annurev-earth-063016-020037. PMC 6398955. PMID 30842690.
  20. ^ Haygarth, John C.; Graham, Ronald A. (2013-09-30). Mishra, Brajendra (ed.). Zirconium and Hafnium. Hoboken, NJ, USA: John Wiley & Sons, Inc. pp. 1–71. doi:10.1002/9781118788417.ch1. ISBN 978-1-118-78841-7.
  21. ^ ABUNDANCE OF ELEMENTS IN THE EARTH’S CRUST AND IN THE SEA, CRC Handbook of Chemistry and Physics, 97th edition (2016–2017), p. 14-17
  22. ^ Deer, William Alexander; Howie, Robert Andrew; Zussmann, Jack (1982). The Rock-Forming Minerals: Orthosilicates. Vol. 1A. Longman Group Limited. pp. 418–442. ISBN 978-0-582-46526-8.
  23. ^ Lee, O. Ivan (1928). "The Mineralogy of Hafnium". Chemical Reviews. 5 (1): 17–37. doi:10.1021/cr60017a002.
  24. ^ Chalmers, Ian (June 2007). "The Dubbo Zirconia Project" (PDF). Alkane Resources Limited. Archived from the original (PDF) on 2008-02-28. Retrieved 2008-09-10.
  25. ^ Gambogi, Joseph (2010). "2008 Minerals Yearbook: Zirconium and Hafnium". United States Geological Survey. Retrieved 2021-11-11.
  26. ^ Larsen, Edwin M.; Fernelius, W. Conard; Quill, Laurence (1943). "Concentration of Hafnium. Preparation of Hafnium-Free Zirconia". Ind. Eng. Chem. Anal. Ed. 15 (8): 512–515. doi:10.1021/i560120a015.
  27. ^ a b van Arkel, A. E.; de Boer, J. H. (1924). "Die Trennung von Zirkonium und Hafnium durch Kristallisation ihrer Ammoniumdoppelfluoride (The separation of zirconium and hafnium by crystallization of their double ammonium fluorides)". Zeitschrift für Anorganische und Allgemeine Chemie (in German). 141: 284–288. doi:10.1002/zaac.19241410117.
  28. ^ a b van Arkel, A. E.; de Boer, J. H. (1924-12-23). "Die Trennung des Zirkoniums von anderen Metallen, einschließlich Hafnium, durch fraktionierte Distillation" [The separation of zirconium from other metals, including hafnium, by fractional distillation]. Zeitschrift für Anorganische und Allgemeine Chemie (in German). 141 (1): 289–296. doi:10.1002/zaac.19241410118.
  29. ^ a b c Hedrick, James B. "Hafnium" (PDF). United States Geological Survey. Retrieved 2008-09-10.
  30. ^ Griffith, Robert F. (1952). "Zirconium and hafnium". Minerals yearbook metals and minerals (except fuels). The first production plants Bureau of Mines. pp. 1162–1171.
  31. ^ Gilbert, H. L.; Barr, M. M. (1955). "Preliminary Investigation of Hafnium Metal by the Kroll Process". Journal of the Electrochemical Society. 102 (5): 243. doi:10.1149/1.2430037.
  32. ^ a b van Arkel, A. E.; de Boer, J. H. (1925). "Darstellung von reinem Titanium-, Zirkonium-, Hafnium- und Thoriummetall (Production of pure titanium, zirconium, hafnium and Thorium metal)". Zeitschrift für Anorganische und Allgemeine Chemie (in German). 148: 345–350. doi:10.1002/zaac.19251480133.
  33. ^ a b c d e "Los Alamos National Laboratory – Hafnium". Retrieved 2008-09-10.
  34. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 971–975. ISBN 978-0-08-037941-8.
  35. ^ Agte, C. & Alterthum, H. (1930). "Researches on Systems with Carbides at High Melting Point and Contributions to the Problem of Carbon Fusion". Z. Tech. Phys. 11: 182–191.
  36. ^ Hong, Qi-Jun; van de Walle, Axel (2015). "Prediction of the material with highest known melting point from ab initio molecular dynamics calculations". Phys. Rev. B. 92 (2): 020104. Bibcode:2015PhRvB..92b0104H. doi:10.1103/PhysRevB.92.020104.
  37. ^ Kaji, Masanori (2002). "D. I. Mendeleev's concept of chemical elements and The Principles of Chemistry" (PDF). Bulletin for the History of Chemistry. 27: 4. Archived from the original (PDF) on 2008-12-17. Retrieved 2008-08-20.
  38. ^ Heilbron, John L. (1966). "The Work of H. G. J. Moseley". Isis. 57 (3): 336. doi:10.1086/350143. S2CID 144765815.
  39. ^ Heimann, P. M. (1967). "Moseley and celtium: The search for a missing element". Annals of Science. 23 (4): 249–260. doi:10.1080/00033796700203306.
  40. ^ Urbain, M. G. (1911). "Sur un nouvel élément qui accompagne le lutécium et le scandium dans les terres de la gadolinite: le celtium (On a new element that accompanies lutetium and scandium in gadolinite: celtium)". Comptes Rendus (in French): 141. Retrieved 2008-09-10.
  41. ^ a b Mel'nikov, V. P. (1982). "Some Details in the Prehistory of the Discovery of Element 72". Centaurus. 26 (3): 317–322. Bibcode:1982Cent...26..317M. doi:10.1111/j.1600-0498.1982.tb00667.x.
  42. ^ a b Kragh, Helge. "Niels Bohr's Second Atomic Theory." Historical Studies in the Physical Sciences, vol. 10, University of California Press, 1979, pp. 123–186, https://doi.org/10.2307/27757389.
  43. ^ Bury, Charles R. (1921). "Langmuir's Theory of the Arrangement of Electrons in Atoms and Molecules". J. Am. Chem. Soc. 43 (7): 1602–1609. Bibcode:1921JAChS..43.1602B. doi:10.1021/ja01440a023.
  44. ^ Bohr, Niels (June 2008). The Theory of Spectra and Atomic Constitution: Three Essays. Kessinger. p. 114. ISBN 978-1-4365-0368-6.
  45. ^ Niels Bohr (11 December 1922). "Nobel Lecture: The Structure of the Atom" (PDF). Retrieved 25 March 2021.
  46. ^ Paneth, F. A. (1922). "Das periodische System (The periodic system)". Ergebnisse der Exakten Naturwissenschaften 1 (in German). p. 362.
  47. ^ Fernelius, W. C. (1982). "Hafnium" (PDF). Journal of Chemical Education. 59 (3): 242. Bibcode:1982JChEd..59..242F. doi:10.1021/ed059p242. Archived from the original (PDF) on 2020-03-15. Retrieved 2009-09-03.
  48. ^ Urbain, M. G. (1922). "Sur les séries L du lutécium et de l'ytterbium et sur l'identification d'un celtium avec l'élément de nombre atomique 72" [The L series from lutetium to ytterbium and the identification of element 72 celtium]. Comptes Rendus (in French). 174: 1347. Retrieved 2008-10-30.
  49. ^ "Two Danes Discover New Element, Hafnium – Detect It by Means of Spectrum Analysis of Ore Containing Zirconium", The New York Times, January 20, 1923, p. 4
  50. ^ Coster, D.; Hevesy, G. (1923). "On the Missing Element of Atomic Number 72". Nature. 111 (2777): 79. Bibcode:1923Natur.111...79C. doi:10.1038/111079a0.
  51. ^ Hevesy, G. (1925). "The Discovery and Properties of Hafnium". Chemical Reviews. 2: 1–41. doi:10.1021/cr60005a001.
  52. ^ von Hevesy, Georg (1923). "Über die Auffindung des Hafniums und den gegenwärtigen Stand unserer Kenntnisse von diesem Element". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 56 (7): 1503–1516. doi:10.1002/cber.19230560702. S2CID 96017606.
  53. ^ Scerri, Eric R. (1994). "Prediction of the nature of hafnium from chemistry, Bohr's theory and quantum theory". Annals of Science. 51 (2): 137–150. doi:10.1080/00033799400200161.
  54. ^ Authier, André (2013). Early Days of X-ray Crystallography. Oxford: Oxford University Press. p. 153. ISBN 978-0-19-163501-4.
  55. ^ Knapp, Brian J. (2002). Francium to Polonium. Oxford: Atlantic Europe Publishing Company. p. 10. ISBN 0-7172-5677-4.
  56. ^ "University Life 2005" (pdf). University of Copenghagen. p. 43. Retrieved 2016-11-19.
  57. ^ Hisamatsu, Yoji; Egashira, Kazuhiro; Maeno, Yoshiteru (2022). "Ogawa's nipponium and its re-assignment to rhenium". Foundations of Chemistry. 24: 15–57. doi:10.1007/s10698-021-09410-x.
  58. ^ Curtis, David; Fabryka-Martin, June; Dixon, Pauland; Cramer, Jan (1999). "Nature's uncommon elements: plutonium and technetium". Geochimica et Cosmochimica Acta. 63 (2): 275–285. Bibcode:1999GeCoA..63..275C. doi:10.1016/S0016-7037(98)00282-8.
  59. ^ Albrecht, Bodo (2015-03-11). "Weak Zirconium Demand Depleting Hafnium Stock Piles". Tech Metals Insider. KITCO. Archived from the original on 2021-04-28. Retrieved 4 March 2018.
  60. ^ Noguère, G.; Courcelle, A; Palau, J.M.; Siegler, P. (2005). ""Low-neutron-energy cross sections of the hafnium isotopes"" (PDF).
  61. ^ "Forschungsreaktor München II (FRM-II): Standort und Sicherheitskonzept" (PDF). Strahlenschutzkommission. 1996-02-07. Archived from the original (PDF) on October 20, 2007. Retrieved 2008-09-22.
  62. ^ J. H. Schemel (1977). ASTM Manual on Zirconium and Hafnium. ASTM International. p. 21. ISBN 978-0-8031-0505-8.
  63. ^ World Book (2020 ed.). Chicago: Berkshire Hathaway. 2020. p. 5. ISBN 978-0-7166-0120-3.
  64. ^ C.W. Forsberg; K. Takase & N. Nakatsuka (2011). "Water Reactor". In Xing L. Yan & Ryutaro Hino (eds.). Nuclear Hydrogen Production Handbook. CRC Press. p. 192. ISBN 978-1-4398-1084-2.
  65. ^ Hebda, John (2001). "Niobium alloys and high Temperature Applications" (PDF). CBMM. Archived from the original (PDF) on 2008-12-17. Retrieved 2008-09-04.
  66. ^ Maslenkov, S. B.; Burova, N. N.; Khangulov, V. V. (1980). "Effect of hafnium on the structure and properties of nickel alloys". Metal Science and Heat Treatment. 22 (4): 283–285. Bibcode:1980MSHT...22..283M. doi:10.1007/BF00779883. S2CID 135595958.
  67. ^ Beglov, V. M.; Pisarev, B. K.; Reznikova, G. G. (1992). "Effect of boron and hafnium on the corrosion resistance of high-temperature nickel alloys". Metal Science and Heat Treatment. 34 (4): 251–254. Bibcode:1992MSHT...34..251B. doi:10.1007/BF00702544. S2CID 135844921.
  68. ^ Voitovich, R. F.; Golovko, É. I. (1975). "Oxidation of hafnium alloys with nickel". Metal Science and Heat Treatment. 17 (3): 207–209. Bibcode:1975MSHT...17..207V. doi:10.1007/BF00663680. S2CID 137073174.
  69. ^ US 6013553, Wallace, Robert M.; Stoltz, Richard A. & Wilk, Glen D., "Zirconium and/or hafnium oxynitride gate dielectric", published 2000-01-11, assigned to Texas Instruments Inc. 
  70. ^ Markoff, John (2007-01-27). "Intel Says Chips Will Run Faster, Using Less Power". New York Times. Retrieved 2008-09-10.
  71. ^ Fulton III, Scott M. (January 27, 2007). "Intel Reinvents the Transistor". BetaNews. Retrieved 2007-01-27.
  72. ^ Robertson, Jordan (January 27, 2007). "Intel, IBM reveal transistor overhaul". The Associated Press. Retrieved 2008-09-10.
  73. ^ "Atomic Layer Deposition (ALD)". Semiconductor Engineering. Retrieved 2023-04-30.
  74. ^ Patchett, P. Jonathan (January 1983). "Importance of the Lu-Hf isotopic system in studies of planetary chronology and chemical evolution". Geochimica et Cosmochimica Acta. 47 (1): 81–91. Bibcode:1983GeCoA..47...81P. doi:10.1016/0016-7037(83)90092-3.
  75. ^ Söderlund, Ulf; Patchett, P. Jonathan; Vervoort, Jeffrey D.; Isachsen, Clark E. (March 2004). "The 176Lu decay constant determined by Lu–Hf and U–Pb isotope systematics of Precambrian mafic intrusions". Earth and Planetary Science Letters. 219 (3–4): 311–324. Bibcode:2004E&PSL.219..311S. doi:10.1016/S0012-821X(04)00012-3.
  76. ^ Blichert-Toft, Janne; Albarède, Francis (April 1997). "The Lu-Hf isotope geochemistry of chondrites and the evolution of the mantle-crust system". Earth and Planetary Science Letters. 148 (1–2): 243–258. Bibcode:1997E&PSL.148..243B. doi:10.1016/S0012-821X(97)00040-X.
  77. ^ Patchett, P. J.; Tatsumoto, M. (11 December 1980). "Lu–Hf total-rock isochron for the eucrite meteorites". Nature. 288 (5791): 571–574. Bibcode:1980Natur.288..571P. doi:10.1038/288571a0. S2CID 4284487.
  78. ^ Kinny, P. D. (1 January 2003). "Lu-Hf and Sm-Nd isotope systems in zircon". Reviews in Mineralogy and Geochemistry. 53 (1): 327–341. Bibcode:2003RvMG...53..327K. doi:10.2113/0530327.
  79. ^ Albarède, F.; Duchêne, S.; Blichert-Toft, J.; Luais, B.; Télouk, P.; Lardeaux, J.-M. (5 June 1997). "The Lu–Hf dating of garnets and the ages of the Alpine high-pressure metamorphism". Nature. 387 (6633): 586–589. Bibcode:1997Natur.387..586D. doi:10.1038/42446. S2CID 4260388.
  80. ^ Ramakrishnany, S.; Rogozinski, M. W. (1997). "Properties of electric arc plasma for metal cutting". Journal of Physics D: Applied Physics. 30 (4): 636–644. Bibcode:1997JPhD...30..636R. doi:10.1088/0022-3727/30/4/019. S2CID 250746818.
  81. ^ g. Alt, Helmut; Samuel, Edmond (1998). "Fluorenyl complexes of zirconium and hafnium as catalysts for olefin polymerization". Chem. Soc. Rev. 27 (5): 323–329. doi:10.1039/a827323z.
  82. ^ Eagan, James (24 Feb 2017). "Combining polyethylene and polypropylene: Enhanced performance with PE/iPP multiblock polymers". Science. 355 (6327): 814–816. Bibcode:2017Sci...355..814E. doi:10.1126/science.aah5744. PMID 28232574. S2CID 206652330.
  83. ^ Helmholtz Association of German Research Centres (September 7, 2022). "A new road towards spin-polarized currents". Nature Communications. 13 (1). Phys.org: 4147. doi:10.1038/s41467-022-31539-2. PMC 9288546. PMID 35842436. Archived from the original on September 9, 2022. Retrieved September 8, 2023.{{cite journal}}: CS1 maint: bot: original URL status unknown (link)
  84. ^ "Occupational Safety & Health Administration: Hafnium". U.S. Department of Labor. Archived from the original on 2008-03-13. Retrieved 2008-09-10.
  85. ^ "CDC – NIOSH Pocket Guide to Chemical Hazards – Hafnium". www.cdc.gov. Retrieved 2015-11-03.

Further reading

[edit]
[edit]
Wikimedia Commons has media related to Hafnium.
Look up hafnium in Wiktionary, the free dictionary.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Hafnium&oldid=1262378572#History"