Wikipedia

Zirconium

(Redirected from Zircronium)
Not to be confused with zircon, zirconia, or cubic zirconia.

Zirconium is a chemical element; it has symbol Zr and atomic number 40. First identified in 1789, isolated in impure form in 1824, and manufactured at scale by 1925, pure zirconium is a lustrous transition metal with a greyish-white color that closely resembles hafnium and, to a lesser extent, titanium. It is solid at room temperature, ductile, malleable and corrosion-resistant. The name zirconium is derived from the name of the mineral zircon, the most important source of zirconium. The word is related to Persian zargun (zircon; zar-gun, "gold-like" or "as gold").[11] Besides zircon, zirconium occurs in over 140 other minerals, including baddeleyite and eudialyte; most zirconium is produced as a byproduct of minerals mined for titanium and tin.

Zirconium, 40Zr
Zirconium
Pronunciation/zɜːrˈkoʊniəm/ ​(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
yttrium ← zirconium → niobium
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 statescommon: +4
−2,[4] 0,[5] +1,[6] +2,[7][8] +3[6]
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 structure ​hexagonal 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[9]
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[10] 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% 2.34×1019 y β−β− 96Mo
 Category: Zirconium
| references

Zirconium forms a variety of inorganic compounds, such as zirconium dioxide, and organometallic compounds, such as zirconocene dichloride. Five isotopes occur naturally, four of which are stable. The metal and its alloys are mainly used as a refractory and opacifier; zirconium alloys are used to clad nuclear fuel rods due to their low neutron absorption and strong resistance to corrosion, and in space vehicles and turbine blades where high heat resistance is necessary. Zirconium also finds uses in flashbulbs, biomedical applications such as dental implants and prosthetics, deodorant, and water purification systems.

Zirconium compounds have no known biological role, though the element is widely distributed in nature and appears in small quantities in biological systems without adverse effects. There is no indication of zirconium as a carcinogen. The main hazards posed by zirconium are flammability in powder form and irritation of the eyes.

Characteristics

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Zirconium is a lustrous, greyish-white, soft, ductile, malleable metal that is solid at room temperature, though it is hard and brittle at lesser purities.[12] In powder form, zirconium is highly flammable, but the solid form is much less prone to ignition. Zirconium is highly resistant to corrosion by alkalis, acids, salt water and other agents.[13] However, it will dissolve in hydrochloric and sulfuric acid, especially when fluorine is present.[14] Alloys with zinc are magnetic at less than 35 K.[13]

The melting point of zirconium is 1855 °C (3371 °F), and the boiling point is 4409 °C (7968 °F).[13] Zirconium has an electronegativity of 1.33 on the Pauling scale. Of the elements within the d-block with known electronegativities, zirconium has the fourth lowest electronegativity after hafnium, yttrium, and lutetium.[15]

At room temperature zirconium exhibits a hexagonally close-packed crystal structure, α-Zr, which changes to β-Zr, a body-centered cubic crystal structure, at 863 °C. Zirconium exists in the β-phase until the melting point.[16]

Isotopes

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Main article: Isotopes of zirconium

Naturally occurring zirconium is composed of five isotopes. 90Zr, 91Zr, 92Zr and 94Zr are stable, although 94Zr is predicted to undergo double beta decay (not observed experimentally) with a half-life of more than 1.10×1017 years. 96Zr has a half-life of 2.34×1019 years, and is 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.[10]

Thirty-three artificial isotopes of zirconium have been synthesized, ranging in atomic mass from 77 to 114.[10][17] 93Zr is the longest-lived artificial isotope, with a half-life of 1.61×106 years. Radioactive isotopes at or above mass number 93 decay by electron emission, whereas those at or below 89 decay by positron emission. The only exception is 88Zr, which decays by electron capture.[10]

Thirteen isotopes of zirconium also exist as metastable isomers: 83m1Zr, 83m2Zr, 85mZr, 87mZr, 88mZr, 89mZr, 90m1Zr, 90m2Zr, 91mZr, 97mZr, 98mZr, 99mZr, and 108mZr. Of these, 97mZr has the shortest half-life at 104.8 nanoseconds. 89mZr is the longest lived with a half-life of 4.161 minutes.[10]

Occurrence

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See also: Category:Zirconium minerals
 
World production trend of zirconium mineral concentrates

Zirconium has a concentration of about 130 mg/kg within the Earth's crust and about 0.026 μg/L in sea water. It is the 18th most abundant element in the crust.[18] It is not found in nature as a native metal, reflecting its intrinsic instability with respect to water. The principal commercial source of zirconium is zircon (ZrSiO4), a silicate mineral,[12] which is found primarily in Australia, Brazil, India, Russia, South Africa and the United States, as well as in smaller deposits around the world.[19] As of 2013, two-thirds of zircon mining occurs in Australia and South Africa.[20] Zircon resources exceed 60 million tonnes worldwide[21] and annual worldwide zirconium production is approximately 900,000 tonnes.[18] Zirconium also occurs in more than 140 other minerals, including the commercially useful ores baddeleyite and eudialyte.[22]

Zirconium is relatively abundant in S-type stars, and has been detected in the sun and in meteorites. Lunar rock samples brought back from several Apollo missions to the moon have a high zirconium oxide content relative to terrestrial rocks.[23]

EPR spectroscopy has been used in investigations of the unusual 3+ valence state of zirconium. The EPR spectrum of Zr3+, which has been initially observed as a parasitic signal in Fe‐doped single crystals of ScPO4, was definitively identified by preparing single crystals of ScPO4 doped with isotopically enriched (94.6%)91Zr. Single crystals of LuPO4 and YPO4 doped with both naturally abundant and isotopically enriched Zr have also been grown and investigated.[24]

Production

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Occurrence

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Zirconium output in 2005

Zirconium is a by-product formed after mining and processing of the titanium minerals ilmenite and rutile, as well as tin mining.[25] From 2003 to 2007, while prices for the mineral zircon steadily increased from $360 to $840 per tonne, the price for unwrought zirconium metal decreased from $39,900 to $22,700 per ton. Zirconium metal is much more expensive than zircon because the reduction processes are costly.[21]

Collected from coastal waters, zircon-bearing sand is purified by spiral concentrators to separate lighter materials, which are then returned to the water because they are natural components of beach sand. Using magnetic separation, the titanium ores ilmenite and rutile are removed.[26]

Most zircon is used directly in commercial applications, but a small percentage is converted to the metal. Most Zr metal is produced by the reduction of the zirconium(IV) chloride with magnesium metal in the Kroll process.[13] The resulting metal is sintered until sufficiently ductile for metalworking.[19]

Separation of zirconium and hafnium

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Commercial zirconium metal typically contains 1–3% of hafnium,[27] which is usually not problematic because the chemical properties of hafnium and zirconium are very similar. Their neutron-absorbing properties differ strongly, however, necessitating the separation of hafnium from zirconium for nuclear reactors.[28] Several separation schemes are in use.[27] The liquid-liquid extraction of the thiocyanate-oxide derivatives exploits the fact that the hafnium derivative is slightly more soluble in methyl isobutyl ketone than in water. This method accounts for roughly two-thirds of pure zirconium production,[29] though other methods are being researched;[30] for instance, in India, a TBP-nitrate solvent extraction process is used for the separation of zirconium from other metals.[31] Zr and Hf can also be separated by fractional crystallization of potassium hexafluorozirconate (K2ZrF6), which is less soluble in water than the analogous hafnium derivative. Fractional distillation of the tetrachlorides, also called extractive distillation, is also used.[30][32]

Vacuum arc melting, combined with the use of hot extruding techniques and supercooled copper hearths, is capable of producing zirconium that has been purified of oxygen, nitrogen, and carbon.[33]

Hafnium must be removed from zirconium for nuclear applications because hafnium has a neutron absorption cross-section 600 times greater than zirconium.[34] The separated hafnium can be used for reactor control rods.[35]

Compounds

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See also the categories Zirconium compounds and Zirconium minerals

Like other transition metals, zirconium forms a wide range of inorganic compounds and coordination complexes.[36] In general, these compounds are colourless diamagnetic solids wherein zirconium has the oxidation state +4. Some organometallic compounds are considered to have Zr(II) oxidation state.[7] Non-equilibrium oxidation states between 0 and 4 have been detected during zirconium oxidation.[8]

Oxides, nitrides, and carbides

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"ZrO" redirects here. For other uses, see ZRO.

The most common oxide is zirconium dioxide, ZrO2, also known as zirconia. This clear to white-coloured solid has exceptional fracture toughness (for a ceramic) and chemical resistance, especially in its cubic form.[37] These properties make zirconia useful as a thermal barrier coating,[38] although it is also a common diamond substitute.[37] Zirconium monoxide, ZrO, is also known and S-type stars are recognised by detection of its emission lines.[39]

Zirconium tungstate has the unusual property of shrinking in all dimensions when heated, whereas most other substances expand when heated.[13] Zirconyl chloride is one of the few water-soluble zirconium complexes, with the formula [Zr4(OH)12(H2O)16]Cl8.[36]

Zirconium carbide and zirconium nitride are refractory solids. Both are highly corrosion-resistant and find uses in high-temperature resistant coatings and cutting tools.[40] Zirconium hydride phases are known to form when zirconium alloys are exposed to large quantities of hydrogen over time; due to the brittleness of zirconium hydrides relative to zirconium alloys, the mitigation of zirconium hydride formation was highly studied during the development of the first commercial nuclear reactors, in which zirconium carbide was a frequently used material.[41]

Lead zirconate titanate (PZT) is the most commonly used piezoelectric material, being used as transducers and actuators in medical and microelectromechanical systems applications.[42]

Halides and pseudohalides

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All four common halides are known, ZrF4, ZrCl4, ZrBr4, and ZrI4. All have polymeric structures and are far less volatile than the corresponding titanium tetrahalides; they find applications in the formation of organic complexes such as zirconocene dichloride.[43] All tend to hydrolyse to give the so-called oxyhalides and dioxides.[27]

Fusion of the tetrahalides with additional metal gives lower zirconium halides (e.g. ZrCl3). These adopt a layered structure, conducting within the layers but not perpendicular thereto.[44]

The corresponding tetraalkoxides are also known. Unlike the halides, the alkoxides dissolve in nonpolar solvents. Dihydrogen hexafluorozirconate is used in the metal finishing industry as an etching agent to promote paint adhesion.[45]

Organic derivatives

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Main article: Organozirconium chemistry
 
Zirconocene dichloride, a representative organozirconium compound

Organozirconium chemistry is key to Ziegler–Natta catalysts, used to produce polypropylene. This application exploits the ability of zirconium to reversibly form bonds to carbon. Zirconocene dibromide ((C5H5)2ZrBr2), reported in 1952 by Birmingham and Wilkinson, was the first organozirconium compound.[46] Schwartz's reagent, prepared in 1970 by P. C. Wailes and H. Weigold,[47] is a metallocene used in organic synthesis for transformations of alkenes and alkynes.[48]

Many complexes of Zr(II) are derivatives of zirconocene,[43] one example being (C5Me5)2Zr(CO)2.

History

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The zirconium-containing mineral zircon and related minerals (jargoon, jacinth, or hyacinth, ligure) were mentioned in biblical writings.[13][28] The mineral was not known to contain a new element until 1789,[49] when Klaproth analyzed a jargoon from the island of Ceylon (now Sri Lanka). He named the new element Zirkonerde (zirconia),[13] related to the Persian zargun (zircon; zar-gun, "gold-like" or "as gold").[11] Humphry Davy attempted to isolate this new element in 1808 through electrolysis, but failed.[12] Zirconium metal was first obtained in an impure form in 1824 by Berzelius by heating a mixture of potassium and potassium zirconium fluoride in an iron tube.[13]

The crystal bar process (also known as the 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 metallic zirconium. It involves the formation and subsequent thermal decomposition of zirconium tetraiodide (ZrI4), and was superseded in 1945 by the much cheaper Kroll process developed by William Justin Kroll, in which zirconium tetrachloride (ZrCl4) is reduced by magnesium:[19][50]

 

Applications

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Approximately 900,000 tonnes of zirconium ores were mined in 1995, mostly as zircon.[27]

Most zircon is used directly in high-temperature applications. Because it is refractory, hard, and resistant to chemical attack, zircon finds many applications. Its main use is as an opacifier, conferring a white, opaque appearance to ceramic materials. Because of its chemical resistance, zircon is also used in aggressive environments, such as moulds for molten metals.[27]

Zirconium dioxide (ZrO2) is used in laboratory crucibles, in metallurgical furnaces, and as a refractory material[13] Because it is mechanically strong and flexible, it can be sintered into ceramic knives and other blades.[51] Zircon (ZrSiO4) and cubic zirconia (ZrO2) are cut into gemstones for use in jewelry. Zirconium dioxide is a component in some abrasives, such as grinding wheels and sandpaper.[49] Zircon is also used in dating of rocks from about the time of the Earth's formation through the measurement of its inherent radioisotopes, most often uranium and lead.[52]

Further information: Zirconium alloys

A small fraction of the zircon is converted to the metal, which finds various niche applications. Because of zirconium's excellent resistance to corrosion, it is often used as an alloying agent in materials that are exposed to aggressive environments, such as surgical appliances, light filaments, and watch cases. The high reactivity of zirconium with oxygen at high temperatures is exploited in some specialised applications such as explosive primers and as getters in vacuum tubes.[53] Zirconium powder is used as a degassing agent in electron tubes, while zirconium wire and sheets are utilized for grid and anode supports.[54][55] Burning zirconium was used as a light source in some photographic flashbulbs. Zirconium powder with a mesh size from 10 to 80 is occasionally used in pyrotechnic compositions to generate sparks. The high reactivity of zirconium leads to bright white sparks.[56]

Nuclear applications

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Cladding for nuclear reactor fuels consumes about 1% of the zirconium supply,[27] mainly in the form of zircaloys. The desired properties of these alloys are a low neutron-capture cross-section and resistance to corrosion under normal service conditions.[19][13] Efficient methods for removing the hafnium impurities were developed to serve this purpose.[28]

One disadvantage of zirconium alloys is the reactivity with water, producing hydrogen, leading to degradation of the fuel rod cladding:[57]

 

Hydrolysis is very slow below 100 °C, but rapid at temperature above 900 °C. Most metals undergo similar reactions. The redox reaction is relevant to the instability of fuel assemblies at high temperatures.[58] This reaction occurred in the reactors 1, 2 and 3 of the Fukushima I Nuclear Power Plant (Japan) after the reactor cooling was interrupted by the earthquake and tsunami disaster of March 11, 2011, leading to the Fukushima I nuclear accidents. After venting the hydrogen in the maintenance hall of those three reactors, the mixture of hydrogen with atmospheric oxygen exploded, severely damaging the installations and at least one of the containment buildings.[59]

Zirconium is a constituent of uranium zirconium hydrides, nuclear fuels used in research reactors.[60]

Space and aeronautic industries

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Materials fabricated from zirconium metal and ZrO2 are used in space vehicles where resistance to heat is needed.[28]

High temperature parts such as combustors, blades, and vanes in jet engines and stationary gas turbines are increasingly being protected by thin ceramic layers and/or paintable coatings, usually composed of a mixture of zirconia and yttria.[61]

Zirconium is also used as a material of first choice for hydrogen peroxide (H2O2) tanks, propellant lines, valves, and thrusters, in propulsion space systems such as these equipping the Sierra Space's Dream Chaser spaceplane[62] where the thrust is provided by the combustion of kerosene and hydrogen peroxide, a powerful, but unstable, oxidizer. The reason is that zirconium has an excellent corrosion resistance to H2O2 and, above all, do not catalyse its spontaneous self-decomposition as the ions of many transition metals do.[62][63]

Medical uses

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Zirconium-bearing compounds are used in many biomedical applications, including dental implants and crowns, knee and hip replacements, middle-ear ossicular chain reconstruction, and other restorative and prosthetic devices.[64]

Zirconium binds urea, a property that has been utilized extensively to the benefit of patients with chronic kidney disease.[64] For example, zirconium is a primary component of the sorbent column dependent dialysate regeneration and recirculation system known as the REDY system, which was first introduced in 1973. More than 2,000,000 dialysis treatments have been performed using the sorbent column in the REDY system.[65] Although the REDY system was superseded in the 1990s by less expensive alternatives, new sorbent-based dialysis systems are being evaluated and approved by the U.S. Food and Drug Administration (FDA). Renal Solutions developed the DIALISORB technology, a portable, low water dialysis system. Also, developmental versions of a Wearable Artificial Kidney have incorporated sorbent-based technologies.[66]

Sodium zirconium cyclosilicate is used by mouth in the treatment of hyperkalemia. It is a selective sorbent designed to trap potassium ions in preference to other ions throughout the gastrointestinal tract.[67]

Mixtures of monomeric and polymeric Zr4+ and Al3+ complexes with hydroxide, chloride and glycine, called aluminium zirconium glycine salts, are used in a preparation as an antiperspirant in many deodorant products. It has been used since the early 1960s, as it was determined more efficacious as an antiperspirant than contemporary active ingredients such as aluminium chlorohydrate.[68]

Defunct applications

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Zirconium carbonate (3ZrO2·CO2·H2O) was used in lotions to treat poison ivy but was discontinued because it occasionally caused skin reactions.[12]

Safety

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Zirconium
Hazards
NFPA 704 (fire diamond)
 Health 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
1
0

Although zirconium has no known biological role, the human body contains, on average, 250 milligrams of zirconium, and daily intake is approximately 4.15 milligrams (3.5 milligrams from food and 0.65 milligrams from water), depending on dietary habits.[69] Zirconium is widely distributed in nature and is found in all biological systems, for example: 2.86 μg/g in whole wheat, 3.09 μg/g in brown rice, 0.55 μg/g in spinach, 1.23 μg/g in eggs, and 0.86 μg/g in ground beef.[69] Further, zirconium is commonly used in commercial products (e.g. deodorant sticks, aerosol antiperspirants) and also in water purification (e.g. control of phosphorus pollution, bacteria- and pyrogen-contaminated water).[64]

Short-term exposure to zirconium powder can cause irritation, but only contact with the eyes requires medical attention.[70] Persistent exposure to zirconium tetrachloride results in increased mortality in rats and guinea pigs and a decrease of blood hemoglobin and red blood cells in dogs. However, in a study of 20 rats given a standard diet containing ~4% zirconium oxide, there were no adverse effects on growth rate, blood and urine parameters, or mortality.[71] The U.S. Occupational Safety and Health Administration (OSHA) legal limit (permissible exposure limit) for zirconium exposure is 5 mg/m3 over an 8-hour workday. The National Institute for Occupational Safety and Health (NIOSH) recommended exposure limit (REL) is 5 mg/m3 over an 8-hour workday and a short term limit of 10 mg/m3. At levels of 25 mg/m3, zirconium is immediately dangerous to life and health.[72] However, zirconium is not considered an industrial health hazard.[64] Furthermore, reports of zirconium-related adverse reactions are rare and, in general, rigorous cause-and-effect relationships have not been established.[64] No evidence has been validated that zirconium is carcinogenic[73] or genotoxic.[74]

Among the numerous radioactive isotopes of zirconium, 93Zr is among the most common. It is released as a product of nuclear fission of 235U and 239Pu, mainly in nuclear power plants and during nuclear weapons tests in the 1950s and 1960s. It has a very long half-life (1.53 million years), its decay emits only low energy radiations, and it is not considered particularly hazardous.[75]

See also

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Notes

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  1. ^ The thermal expansion of a zirconium crystal is anisotropic: the parameters (at 20 °C) for each crystal axis are αa = 4.91×10−6/K, αc = 7.26×10−6/K, and αaverage = αV/3 = 5.69×10−6/K.[3]

References

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  5. ^ Zr(0) occur in (η6-(1,3,5-tBu)3C6H3)2Zr and [(η5-C5R5Zr(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.
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  15. ^ Winter, Mark (2007). "Electronegativity (Pauling)". University of Sheffield. Retrieved 2024-07-27.
  16. ^ Schnell I & Albers RC (January 2006). "Zirconium under pressure: phase transitions and thermodynamics". Journal of Physics: Condensed Matter. 18 (5): 16. Bibcode:2006JPCM...18.1483S. doi:10.1088/0953-8984/18/5/001. S2CID 56557217.
  17. ^ Sumikama, T.; et al. (2021). "Observation of new neutron-rich isotopes in the vicinity of Zr110". Physical Review C. 103 (1): 014614. Bibcode:2021PhRvC.103a4614S. doi:10.1103/PhysRevC.103.014614. hdl:10261/260248. S2CID 234019083.
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