Zirconium

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Zirconium, 40Zr
Zirconium
Pronunciation/zɜːrˈkniəm/ (zur-KOH-nee-əm)
Appearancesilvery white
Standard atomic weight Ar°(Zr)
Zirconium 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
Ti

Zr

Hf
yttriumzirconiumniobium
Atomic number (Z)40
Groupgroup 4
Periodperiod 5
Block  d-block
Electron configuration[Kr] 4d2 5s2
Electrons per shell2, 8, 18, 10, 2
Physical properties
Phase at STPsolid
Melting point2125 K ​(1852 °C, ​3365 °F)
Boiling point4650 K ​(4377 °C, ​7911 °F)
Density (at 20° C)6.505 g/cm3[3]
when liquid (at m.p.)5.8 g/cm3
Heat of fusion14 kJ/mol
Heat of vaporization591 kJ/mol
Molar heat capacity25.36 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 2639 2891 3197 3575 4053 4678
Atomic properties
Oxidation states−2, 0, +1,[4][citation needed] +2, +3, +4 (an amphoteric oxide)
ElectronegativityPauling scale: 1.33
Ionization energies
  • 1st: 640.1 kJ/mol
  • 2nd: 1270 kJ/mol
  • 3rd: 2218 kJ/mol
Atomic radiusempirical: 160 pm
Covalent radius175±7 pm
Color lines in a spectral range
Spectral lines of zirconium
Other properties
Natural occurrenceprimordial
Crystal structurehexagonal close-packed (hcp) (hP2)
Lattice constants
Hexagonal close-packed crystal structure for zirconium
a = 323.22 pm
c = 514.79 pm (at 20 °C)[3]
Thermal expansion5.69×10−6/K (at 20 °C)[3][a]
Thermal conductivity22.6 W/(m⋅K)
Electrical resistivity421 nΩ⋅m (at 20 °C)
Magnetic orderingparamagnetic[5]
Young's modulus88 GPa
Shear modulus33 GPa
Bulk modulus91.1 GPa
Speed of sound thin rod3800 m/s (at 20 °C)
Poisson ratio0.34
Mohs hardness5.0
Vickers hardness820–1800 MPa
Brinell hardness638–1880 MPa
CAS Number7440-67-7
History
Namingafter zircon, zargun زرگون meaning "gold-colored".
DiscoveryMartin Heinrich Klaproth (1789)
First isolationJöns Jakob Berzelius (1824)
Isotopes of zirconium
Main isotopes[6] Decay
abun­dance half-life (t1/2) mode pro­duct
88Zr synth 83.4 d ε 88Y
γ
89Zr synth 78.4 h ε 89Y
β+ 89Y
γ
90Zr 51.5% stable
91Zr 11.2% stable
92Zr 17.1% stable
93Zr trace 1.53×106 y β 93Nb
94Zr 17.4% stable
96Zr 2.80% 2.0×1019 y[7] ββ 96Mo
 Category: Zirconium
| references

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Zirconium rod

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Zirconium (Template:PronEng, /ˌzɝˈkoʊniəm/) is a chemical element with the symbol Zr and atomic number 40. It is a lustrous, gray-white, strong transition metal that resembles titanium. Zirconium is used as an alloying agent due to its high resistance to corrosion. It is never found as a native metal, but is instead obtained mainly from the mineral zircon, which can be purified by chlorine. Zirconium was first isolated in an impure form in 1824 by Jöns Jakob Berzelius.

Zirconium has no known biological role. Zirconium forms both inorganic and organic compounds, such as zirconium dioxide and zirconocene dibromide, respectively. There are five naturally-occurring isotopes, three of which are stable. Short-term exposure to zirconium powder causes minor irritation, and inhalation of zirconium compounds can cause skin and lung granulomas.

Characteristics

Zirconium is a lustrous, grayish-white, soft, ductile, and malleable metal which is solid at room temperature, though it becomes hard and brittle at lower purities.[8][9] In powder form, zirconium is highly flammable, but the solid form is far less prone to igniting.[10] Zirconium is highly resistant to corrosion by alkalis, acids, salt water, and other agents.[11] However, it will dissolve in hydrochloric and sulfuric acid, especially when fluorine is present.[12] Alloys with zinc become magnetic below 35 K.[10]

The melting point of zirconium is at 1855°C, and the boiling point is at 4409°C.[10] Zirconium has an electronegativity of 1.33 on the Pauling scale. Of the elements within d-block, Zirconium has the fourth lowest electronegativity after yttrium, lutetium, and hafnium.[13]

Applications

Because of zirconium's excellent resistance to corrosion, it is often used as an alloying agent in materials that are exposed to corrosive agents, such as surgical appliances, explosive primers, vacuum tube getters and filaments. Zirconium dioxide (ZrO2) is used in laboratory crucibles, metallurgical furnaces, and as a refractory material.[10] Zircon (ZrSiO4) is cut into gemstones for use in jewelry. Zirconium carbonate (3ZrO2·CO2·H2O) was used in lotions to treat poison ivy, but this was discontinued as it caused bad skin reactions in some cases.[8] 90% of all zirconium produced is used in nuclear reactors because of its low neutron-capture cross-section and resistance to corrosion.[10][9] Zirconium alloys are used in space vehicle parts for their resistance to heat, an important quality given the extreme heat associated with atmospheric reentry.[14] Zirconium is also a component in some abrasives, such as grinding wheels and sandpaper.[15] Zirconium is used in weapons such as the BLU-97/B Combined Effects Bomb for incendiary effect. Zirconium in the oxidized form is also used in dentistry for crowning of the teeth because of its biocompatibility, strength and appearance.

Refining

Upon being collected from coastal waters, the solid mineral zircon is purified by spiral concentrators to remove excess sand and gravel and by magnetic separators to remove ilmenite and rutile. The byproducts can then be dumped back into the water safely, as they are all natural components of beach sand. The refined zircon is then purified into pure zirconium by chlorine or other agents, then sintered until sufficiently ductile for metalworking.[9] Zirconium and hafnium are both contained in zircon and they are quite difficult to separate due to their similar chemical properties.[14]

History

The zirconium-containing mineral zircon, or its variations (jargoon, hyacinth, jacinth, ligure), were mentioned in biblical writings.[10][14] The mineral was not known to contain a new element until 1789,[15] when Klaproth analyzed a jargoon from the island of Ceylon in the Indian Ocean. He named the new element Zirkonerde (zirconia).[11][10] Humphry Davy attempted to isolate this new element in 1808 through electrolysis, but failed.[8] Zirconium (from Syriac zargono,[16] Arabic zarkûn from Persian zargûn زرگون meaning "gold like")[14] was first isolated in an impure form in 1824 by Berzelius by heating a mixture of potassium and potassium-zirconium fluoride in a small decomposition process conducted in an iron tube.[11][10]

The crystal bar process (or Iodide process), discovered by Anton Eduard van Arkel and Jan Hendrik de Boer in 1925, was the first industrial process for the commercial production of pure metallic zirconium. The process involved thermally decomposing zirconium tetraiodide. It was superseded in 1945 by the much cheaper Kroll process developed by William Justin Kroll, in which zirconium tetrachloride is broken down by magnesium.[9][17]

Occurrence

Geological

Zirconium output in 2005
World production trend of zirconium mineral concentrates

Zirconium has a concentration of about 130 mg/kg within the earth's crust and about .026 μg/L in sea water,[18] though it is never found in nature as a native metal. The principal commercial source of zirconium is the zirconium silicate mineral, zircon (ZrSiO4),[8] which is found primarily in Australia, Brazil, India, Russia, South Africa, and the United States, as well as in smaller deposits around the world.[9] 80% of zircon mining occurs in Australia and South Africa.[8] Zircon resources exceed 60 million metric tons worldwide[19] and annual worldwide zirconium production is approximately 900,000 metric tons.[18]

Zircon is a by-product of the mining and processing of the titanium minerals ilmenite and rutile, as well as tin mining.[20] From 2003 to 2007, zircon prices have steadily increased from $360 to $840 per metric ton.[19] Zirconium also occurs in more than 140 other recognized mineral species including baddeleyite and kosnarite.[21] This metal is commercially produced mostly by the reduction of the zirconium(IV) chloride with magnesium metal in the Kroll process.[10] Commercial-quality zirconium for most uses still has a content of 1% to 3% hafnium.[8]

This element is relatively-abundant in S-type stars, and it has been detected in the sun and in meteorites. Lunar rock samples brought back from several Apollo program missions to the moon have a quite high zirconium oxide content relative to terrestrial rocks.[11]

See also zirconium minerals.

Biological

Zirconium has no known biological role, though zirconium salts are of low toxicity. The human body contains, on average, only 1 milligram of zirconium, and daily intake is approximately 50 μg per day. Zirconium content in human blood is as low as 10 parts per billion. Aquatic plants readily take up soluble zirconium, but it is rare in land plants. 70% of plants have no zirconium content at all, and those that do have as little as 5 parts per billion.[8]

Compounds

As a transition metal, zirconium forms various inorganic compounds, such as zirconium dioxide (ZrO2). This compound, also referred to as zirconia, has exceptional fracture toughness and chemical resistance, especially in its cubic form.[22] These properties make zirconia useful as a thermal barrier coating,[23] though it is also a common diamond substitute.[22] Zirconium tungstate is an unusual substance in that it shrinks in all directions when heated, whereas other elements expand when heated.[10] ZrZn2 is one of only two substances to exhibit superconductivity and ferromagnetism simultaneously, with the other being UGe2.[24] Other inorganic zirconium compounds include zirconium(II) hydride, zirconium nitride, and zirconium tetrachloride (ZrCl4), which is used in the Friedel-Crafts reaction.[25]

Organozirconium chemistry is the study of compounds containing a carbon-zirconium bond. These organozirconium compounds are often employed as polymerization catalysts. The first such compound was zirconocene dibromide, prepared in 1952 by John M. Birmingham at Harvard University.[26] Schwartz's reagent, prepared in 1970 by P. C. Wailes and H. Weigold,[27] is a metallocene used in organic synthesis for transformations of alkenes and alkynes.[28]

Isotopes

Naturally-occurring zirconium is composed of five isotopes. 90Zr, 91Zr, and 92Zr are stable. 94Zr has a half-life of 1.10×1017 years. 96Zr has half-life of 2.4×1019 years, making it the longest-lived radioisotope of zirconium. Of these natural isotopes, 90Zr is the most common, making up 51.45% of all zirconium. 96Zr is the least common, comprising only 2.80% of zirconium.[29]

28 artificial isotopes of zirconium have been synthesized, ranging in atomic mass from 78 to 110. 93Zr is the longest-lived artificial isotope, with a half-life of 1.53×106 years. 110Zr, the heaviest isotope of zirconium, is also the shortest-lived, with an estimated half-life of only 30 milliseconds. Radioactive isotopes at or above mass number 93 decay by β, whereas those at or below 89 decay by β+. The only exception is 88Zr, which decays by ε.[29]

Zirconium also has six metastable isomers, 83mZr, 85mZr, 89mZr, 90m1Zr, 90m2Zr, and 91mZr. Of these, 90m2Zr has the shortest halflife at 131 nanoseconds. 89mZr is the longest lived with a half-life of 4.161 minutes.[29]

Toxicity

Ingestion or inhalation of 93Zr, a radioactive isotope, causes a slight increase in the likelihood of developing cancer.[18] Short-term exposure to zirconium powder can cause irritation, but only contact with the eyes requires medical attention.[30] Inhalation of zirconium compounds can cause skin and lung granulomas. Zirconium aerosols can cause pulmonary granulomas. Persistent exposure to zirconium tetrachloride resulted in increased mortality in rats and guinea pigs and a decrease of blood hemoglobin and red blood cells in dogs. OSHA recommends a 5 mg/m3 time weighted average limit and a 10 mg/m3 short-term exposure limit.[31]

See also

Notes

  1. ^ "Standard Atomic Weights: Zirconium". CIAAW. 1983.
  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 c d Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
  4. ^ "Zirconium: zirconium(I) fluoride compound data". OpenMOPAC.net. Retrieved 2007-12-10.
  5. ^ 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.
  6. ^ 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.
  7. ^ Pritychenko, Boris; Tretyak, V. "Adopted Double Beta Decay Data". National Nuclear Data Center. Retrieved 2008-02-11.
  8. ^ a b c d e f g Emsley, John (2001). Nature's Building Blocks. Oxford: Oxford University Press. pp. 506–510. ISBN 0-19-850341-5.
  9. ^ a b c d e "Zirconium". How Products Are Made. Advameg Inc. 2007. Retrieved 2008-03-26.
  10. ^ a b c d e f g h i j Lide, David R., ed. (2007–2008), "Zirconium", CRC Handbook of Chemistry and Physics, vol. 4, New York: CRC Press, p. 42, 978-0-8493-0488-0
  11. ^ a b c d "Zirconium". Los Alamos Chemistry Division. 2003-12-15. Retrieved 2008-02-12.
  12. ^ Considine, Glenn D., ed. (2005), "Zirconium", Van Nostrand's Encyclopedia of Chemistry, New York: Wylie-Interscience, pp. 1778–1779, ISBN 0-471-61525-0
  13. ^ Winter, Mark (2007). "Electronegativity (Pauling)". University of Sheffield. Retrieved 2008-03-05.
  14. ^ a b c d Stwertka, Albert (1996). A Guide to the Elements. Oxford University Press. pp. 117–119. ISBN 0-19-508083-1.
  15. ^ a b Krebs, Robert E. (1998). The History and Use of our Earth's Chemical Elements. Westport, Connecticut: Greenwood Press. pp. 98–100. ISBN 0-313-30123-9.
  16. ^ Pearse, Roger (2002-09-16). "Syriac Literature". Retrieved 2008-02-11.
  17. ^ Hedrick, James B. (1998), "Zirconium", Metal Prices in the United States through 1998 (PDF), US Geological Survey, pp. 175–178, retrieved 2008-02-26
  18. ^ a b c Peterson, John; MacDonell, Margaret (2007), "Zirconium", Radiological and Chemical Fact Sheets to Support Health Risk Analyses for Contaminated Areas (PDF), Argonne National Laboratory, pp. 64–65, retrieved 2008-02-26
  19. ^ a b "Zirconium and Hafnium" (PDF). Mineral Commodity Summaries. US Geological Survey: 192–193. 2008. Retrieved 2008-02-24. {{cite journal}}: Unknown parameter |month= ignored (help)
  20. ^ Callaghan, R. (2008-02-21). "Zirconium and Hafnium Statistics and Information". US Geological Survey. Retrieved 2008-02-24.
  21. ^ Ralph, Jolyon (2008). "Minerals that include Zr". Mindat.org. Retrieved 2008-02-23. {{cite web}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  22. ^ a b "Zirconia". AZoM.com. 2008. Retrieved 2008-03-17.
  23. ^ Gauthier, V.; Dettenwanger, F.; Schütze, M. (2002-04-10). "Oxidation behavior of γ-TiAl coated with zirconia thermal barriers". Intermetallics. 10 (7). Frankfurt, Germany: Karl Winnacker Institut der Dechema: 667–674. doi:10.1016/S0966-9795(02)00036-5.
  24. ^ Day, Charles (2001). "Second Material Found that Superconducts in a Ferromagnetic State". Physics Today. 54 (9). American Institute of Physics: 16. doi:10.1063/1.1420499. ISSN 0031-9228. {{cite journal}}: Unknown parameter |month= ignored (help)
  25. ^ Bora U. (2003). "Zirconium Tetrachloride". Synlett: 1073–1074. doi:10.1055/s-2003-39323.
  26. ^ Rouhi, A. Maureen (2004-04-19). "Organozirconium Chemistry Arrives". Science & Technology. 82 (16). Chemical & Engineering News: 36–39. ISSN 0009-2347. Retrieved 2008-03-17.
  27. ^ P. C. Wailes and H. Weigold (1970). "Hydrido complexes of zirconium I. Preparation". Journal of Organometallic Chemistry. 24: 405–411. doi:10.1016/S0022-328X(00)80281-8.
  28. ^ D. W. Hart and J. Schwartz (1974). "Hydrozirconation. Organic Synthesis via Organozirconium Intermediates. Synthesis and Rearrangement of Alkylzirconium(IV) Complexes and Their Reaction with Electrophiles". J. Am. Chem. Soc. 96 (26): 8115–8116. doi:10.1021/ja00833a048.
  29. ^ a b c Audi, G (2003). "Nubase2003 Evaluation of Nuclear and Decay Properties". Nuclear Physics A. 729. Atomic Mass Data Center: 3–128. doi:10.1016/j.nuclphysa.2003.11.001.
  30. ^ "Zirconium", International Chemical Safety Cards, International Labour Organization, October 2004, retrieved 2008-03-30
  31. ^ "Zirconium Compounds". National Institute for Occupational Health and Safety. 2007-12-17. Retrieved 2008-02-17.

External links

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