Use of nickel (as natural meteoric nickel–iron alloy) has been traced as far back as 3500BCE. Nickel was first isolated and classified as an element in 1751 by Axel Fredrik Cronstedt, who initially mistook the ore for a coppermineral, in the cobalt mines of Los, Hälsingland, Sweden. The element's name comes from a mischievous sprite of German miner mythology, Nickel (similar to Old Nick). Nickel minerals can be green, like copper ores, and were known as kupfernickel – Nickel's copper – because they produced no copper.
Nickel is one of four elements (the others are iron, cobalt, and gadolinium)[12] that are ferromagnetic at about room temperature. Alnico permanent magnets based partly on nickel are of intermediate strength between iron-based permanent magnets and rare-earth magnets. The metal is used chiefly in alloys and corrosion-resistant plating.
About 68% of world production is used in stainless steel. A further 10% is used for nickel-based and copper-based alloys, 9% for plating, 7% for alloy steels, 3% in foundries, and 4% in other applications such as in rechargeable batteries,[13] including those in electric vehicles (EVs).[14] Nickel is widely used in coins, though nickel-plated objects sometimes provoke nickel allergy. As a compound, nickel has a number of niche chemical manufacturing uses, such as a catalyst for hydrogenation, cathodes for rechargeable batteries, pigments and metal surface treatments.[15] Nickel is an essential nutrient for some microorganisms and plants that have enzymes with nickel as an active site.[16]
Nickel is a silvery-white metal with a slight golden tinge that takes a high polish. It is one of only four elements that are ferromagnetic at or near room temperature; the others are iron, cobalt and gadolinium. Its Curie temperature is 355°C (671°F), meaning that bulk nickel is non-magnetic above this temperature.[18][12] The unit cell of nickel is a face-centered cube; it has lattice parameter of 0.352nm, giving an atomic radius of 0.124nm. This crystal structure is stable to pressures of at least 70GPa. Nickel is hard, malleable and ductile, and has a relatively high electrical and thermal conductivity for transition metals.[19] The high compressive strength of 34 GPa, predicted for ideal crystals, is never obtained in the real bulk material due to formation and movement of dislocations. However, it has been reached in Ni nanoparticles.[20]
Electron configuration dispute
Nickel has two atomic electron configurations, [Ar] 3d8 4s2 and [Ar] 3d9 4s1, which are very close in energy; [Ar] denotes the complete argon core structure. There is some disagreement on which configuration has the lower energy.[21] Chemistry textbooks quote nickel's electron configuration as [Ar] 4s2 3d8,[22] also written [Ar] 3d8 4s2.[23] This configuration agrees with the Madelung energy ordering rule, which predicts that 4s is filled before 3d. It is supported by the experimental fact that the lowest energy state of the nickel atom is a 3d8 4s2 energy level, specifically the 3d8(3F) 4s23F, J=4 level.[24][25]
However, each of these two configurations splits into several energy levels due to fine structure,[24][25] and the two sets of energy levels overlap. The average energy of states with [Ar] 3d9 4s1 is actually lower than the average energy of states with [Ar] 3d8 4s2. Therefore, the research literature on atomic calculations quotes the ground state configuration as [Ar] 3d9 4s1.[21]
The isotopes of nickel range in atomic weight from 48u (48 Ni) to 82u (82 Ni).[7]
Natural nickel is composed of five stable isotopes, 58 Ni, 60 Ni, 61 Ni, 62 Ni and 64 Ni, of which 58 Ni is the most abundant (68.077% natural abundance).[7]
Nickel-62 has the highest binding energy per nucleon of any nuclide: 8.7946MeV/nucleon.[26][27] Its binding energy is greater than both 56 Fe and 58 Fe, more abundant nuclides often incorrectly cited as having the highest binding energy.[28] Though this would seem to predict nickel as the most abundant heavy element in the universe, the high rate of photodisintegration of nickel in stellar interiors causes iron to be by far the most abundant.[28]
Nickel-60 is the daughter product of the extinct radionuclide60 Fe (half-life 2.6million years). Due to the long half-life of 60 Fe, its persistence in materials in the Solar System may generate observable variations in the isotopic composition of 60 Ni. Therefore, the abundance of 60 Ni in extraterrestrial material may give insight into the origin of the Solar System and its early history.[29]
At least 26 nickel radioisotopes have been characterized; the most stable are 59 Ni with half-life 76,000 years, 63 Ni (100 years), and 56 Ni (6 days). All other radioisotopes have half-lives less than 60 hours and most these have half-lives less than 30 seconds. This element also has one meta state.[7]
Radioactive nickel-56 is produced by the silicon burning process and later set free in large amounts in type Iasupernovae. The shape of the light curve of these supernovae at intermediate to late-times corresponds to the decay via electron capture of 56 Ni to cobalt-56 and ultimately to iron-56.[30] Nickel-59 is a long-lived cosmogenicradionuclide; half-life 76,000 years. 59 Ni has found many applications in isotope geology. 59 Ni has been used to date the terrestrial age of meteorites and to determine abundances of extraterrestrial dust in ice and sediment. Nickel-78, with a half-life of 110 milliseconds, is believed an important isotope in supernova nucleosynthesis of elements heavier than iron.[31]48Ni, discovered in 1999, is the most proton-rich heavy element isotope known. With 28 protons and 20 neutrons, 48Ni is "doubly magic", as is 78Ni with 28 protons and 50 neutrons. Both are therefore unusually stable for nuclei with so large a proton–neutron imbalance.[7][32]
Nickel-63 is a contaminant found in the support structure of nuclear reactors. It is produced through neutron capture by nickel-62. Small amounts have also been found near nuclear weapon test sites in the South Pacific.[33]
Widmanstätten pattern showing the two forms of nickel–iron, kamacite and taenite, in an octahedrite meteorite
Nickel ores are classified as oxides or sulfides. Oxides include laterite, where the principal mineral mixtures are nickeliferous limonite, (Fe,Ni)O(OH), and garnierite (a mixture of various hydrous nickel and nickel-rich silicates).[34] Nickel sulfides commonly exist as solid solutions with iron in minerals such as pentlandite and pyrrhotite with the formula Fe9-xNixS8 and Fe7-xNixS6, respectively. Other common Ni-containing minerals are millerite and the arsenideniccolite.[35][36]
Identified land-based resources throughout the world averaging 1% nickel or greater comprise at least 130million tons of nickel (about the double of known reserves). About 60% is in laterites and 40% in sulfide deposits.[37]
On geophysical evidence, most of the nickel on Earth is believed to be in Earth's outer and inner cores. Kamacite and taenite are naturally occurring alloys of iron and nickel. For kamacite, the alloy is usually in the proportion of 90:10 to 95:5, though impurities (such as cobalt or carbon) may be present. Taenite is 20% to 65% nickel. Kamacite and taenite are also found in nickel iron meteorites.[38]
Nickel is commonly found in iron meteorites as the alloys kamacite and taenite. Nickel in meteorites was first detected in 1799 by Joseph-Louis Proust, a French chemist who then worked in Spain. Proust analyzed samples of the meteorite from Campo del Cielo (Argentina), which had been obtained in 1783 by Miguel Rubín de Celis, discovering the presence in them of nickel (about 10%) along with iron.[39]
The most common oxidation state of nickel is +2, but compounds of Ni0, Ni+, and Ni3+ are well known, and the exotic oxidation states Ni2− and Ni− have been characterized.[40]
Nickel(0)
Tetracarbonyl nickel
Nickel tetracarbonyl(Ni(CO)4), discovered by Ludwig Mond,[41] is a volatile, highly toxic liquid at room temperature. On heating, the complex decomposes back to nickel and carbon monoxide:
Nickel(I) complexes are uncommon, but one example is the tetrahedral complex NiBr(PPh3)3. Many nickel(I) complexes have Ni–Ni bonding, such as the dark red diamagneticK4[Ni2(CN)6] prepared by reduction of K2[Ni2(CN)6] with sodium amalgam. This compound is oxidized in water, liberating H2.[42]
It is thought that the nickel(I) oxidation state is important to nickel-containing enzymes, such as [NiFe]-hydrogenase, which catalyzes the reversible reduction of protons to H2.[43]
Nickel(II)
Color of various Ni(II) complexes in aqueous solution. From left to right, [Ni(NH3)6], [Ni(NH2CH2CH2NH2)], [NiCl4], [Ni(H2O)6]Crystals of hydratednickel(II) sulfate
Nickel(II) forms compounds with all common anions, including sulfide, sulfate, carbonate, hydroxide, carboxylates, and halides. Nickel(II) sulfate is produced in large amounts by dissolving nickel metal or oxides in sulfuric acid, forming both a hexa- and heptahydrate[44] useful for electroplating nickel. Common salts of nickel, such as chloride, nitrate, and sulfate, dissolve in water to give green solutions of the metal aquo complex[Ni(H2O)6]2+.[45]
The four halides form nickel compounds, which are solids with molecules with octahedral Ni centres. Nickel(II) chloride is most common, and its behavior is illustrative of the other halides. Nickel(II) chloride is made by dissolving nickel or its oxide in hydrochloric acid. It is usually found as the green hexahydrate, whose formula is usually written NiCl2·6H2O. When dissolved in water, this salt forms the metal aquo complex[Ni(H2O)6]2+. Dehydration of NiCl2·6H2O gives yellow anhydrous NiCl2.[46]
Some tetracoordinate nickel(II) complexes, e.g. bis(triphenylphosphine)nickel chloride, exist both in tetrahedral and square planar geometries. The tetrahedral complexes are paramagnetic; the square planar complexes are diamagnetic. In having properties of magnetic equilibrium and formation of octahedral complexes, they contrast with the divalent complexes of the heavier group 10 metals, palladium(II) and platinum(II), which form only square-planar geometry.[40]
Nickelocene has an electron count of 20. Many chemical reactions of nickelocene tend to yield 18-electron products.[47]
Nickel(III) and (IV)
Nickel(III) antimonide
Many Ni(III) compounds are known. Ni(III) forms simple salts with fluoride[48] or oxide ions. Ni(III) can be stabilized by σ-donor ligands such as thiols and organophosphines.[42]
Ni(IV) remains a rare oxidation state and very few compounds are known. Ni(IV) occurs in the mixed oxide BaNiO3.[50][51][52][53]
History
Unintentional use of nickel can be traced back as far as 3500BCE. Bronzes from what is now Syria have been found to contain as much as 2% nickel.[54] Some ancient Chinese manuscripts suggest that "white copper" (cupronickel, known as baitong) was used there in 1700–1400BCE. This Paktong white copper was exported to Britain as early as the 17th century, but the nickel content of this alloy was not discovered until 1822.[55] Coins of nickel-copper alloy were minted by Bactrian kings Agathocles, Euthydemus II, and Pantaleon in the 2nd century BCE, possibly out of the Chinese cupronickel.[56]
Nickeline/niccolite
In medieval Germany, a metallic yellow mineral was found in the Ore Mountains that resembled copper ore. But when miners were unable to get any copper from it, they blamed a mischievous sprite of German mythology, Nickel (similar to Old Nick), for besetting the copper. They called this ore Kupfernickel from German Kupfer 'copper'.[57][58][59][60] This ore is now known as the mineral nickeline (formerly niccolite[61]), a nickel arsenide. In 1751, Baron Axel Fredrik Cronstedt tried to extract copper from kupfernickel at a cobalt mine in the village of Los, Sweden, and instead produced a white metal that he named nickel after the spirit that had given its name to the mineral.[62] In modern German, Kupfernickel or Kupfer-Nickel designates the alloy cupronickel.[19]
Originally, the only source for nickel was the rare Kupfernickel. Beginning in 1824, nickel was obtained as a byproduct of cobalt blue production. The first large-scale smelting of nickel began in Norway in 1848 from nickel-rich pyrrhotite. The introduction of nickel in steel production in 1889 increased the demand for nickel; the nickel deposits of New Caledonia, discovered in 1865, provided most of the world's supply between 1875 and 1915. The discovery of the large deposits in the Sudbury Basin in Canada in 1883, in Norilsk-Talnakh in Russia in 1920, and in the Merensky Reef in South Africa in 1924 made large-scale nickel production possible.[55]
Aside from the aforementioned Bactrian coins, nickel was not a component of coins until the mid-19th century.[63]
Canada
99.9% nickel five-cent coins were struck in Canada (the world's largest nickel producer at the time) during non-war years from 1922 to 1981; the metal content made these coins magnetic.[64] During the war years 1942–1945, most or all nickel was removed from Canadian and US coins to save it for making armor.[58] Canada used 99.9% nickel from 1968 in its higher-value coins until 2000.[65]
Switzerland
Coins of nearly pure nickel were first used in 1881 in Switzerland.[66]
United Kingdom
Birmingham forged nickel coins in c.1833 for trading in Malaysia.[67]
In the United States, the term "nickel" or "nick" originally applied to the copper-nickel Flying Eagle cent, which replaced copper with 12% nickel 1857–58, then the Indian Head cent of the same alloy from 1859 to 1864. Still later, in 1865, the term designated the three-cent nickel, with nickel increased to 25%. In 1866, the five-cent shield nickel (25% nickel, 75% copper) appropriated the designation, which has been used ever since for the subsequent 5-cent pieces. This alloy proportion is not ferromagnetic.
The US nickel coin contains 0.04 ounces (1.1g) of nickel, which at the April 2007 price was worth 6.5 cents, along with 3.75grams of copper worth about 3 cents, with a total metal value of more than 9 cents. Since the face value of a nickel is 5 cents, this made it an attractive target for melting by people wanting to sell the metals at a profit. The United States Mint, anticipating this practice, implemented new interim rules on December 14, 2006, subject to public comment for 30 days, which criminalized the melting and export of cents and nickels.[68] Violators can be punished with a fine of up to $10,000 and/or a maximum of five years in prison.[69] As of September 19, 2013, the melt value of a US nickel (copper and nickel included) is $0.045 (90% of the face value).[70]
Current use
In the 21st century, the high price of nickel has led to some replacement of the metal in coins around the world. Coins still made with nickel alloys include one- and two-euro coins, 5¢, 10¢, 25¢, 50¢, and $1 U.S. coins,[71] and 20p, 50p, £1, and £2 UK coins. From 2012 on the nickel-alloy used for 5p and 10p UK coins was replaced with nickel-plated steel. This ignited a public controversy regarding the problems of people with nickel allergy.[66]
World production
Time trend of nickel productionNickel ores grade evolution in some leading nickel producing countries or regions
An estimated 3.6million tonnes (t) of nickel per year are mined worldwide; Indonesia (1,800,000t), the Philippines (400,000t), Russia (200,000t), New Caledonia (France) (230,000t), Canada (180,000t) and Australia (160,000t) are the largest producers as of 2023.[73] The largest nickel deposits in non-Russian Europe are in Finland and Greece. Identified land-based sources averaging at least 1% nickel contain at least 130million tonnes of nickel. About 60% is in laterites and 40% is in sulfide deposits. Also, extensive nickel sources are found in the depths of the Pacific Ocean, especially in an area called the Clarion Clipperton Zone in the form of polymetallic nodules peppering the seafloor at 3.5–6km below sea level.[74][75] These nodules are composed of numerous rare-earth metals and are estimated to be 1.7% nickel.[76] With advances in science and engineering, regulation is currently being set in place by the International Seabed Authority to ensure that these nodules are collected in an environmentally conscientious manner while adhering to the United NationsSustainable Development Goals.[77]
The one place in the United States where nickel has been profitably mined is Riddle, Oregon, with several square miles of nickel-bearing garnierite surface deposits. The mine closed in 1987.[78][79] The Eagle mine project is a new nickel mine in Michigan's Upper Peninsula. Construction was completed in 2013, and operations began in the third quarter of 2014.[80] In the first full year of operation, the Eagle Mine produced 18,000 t.[80]
Production
Evolution of the annual nickel extraction, according to ores
Nickel is obtained through extractive metallurgy: it is extracted from ore by conventional roasting and reduction processes that yield metal of greater than 75% purity. In many stainless steel applications, 75% pure nickel can be used without further purification, depending on impurities.[44]
Traditionally, most sulfide ores are processed using pyrometallurgical techniques to produce a matte for further refining. Hydrometallurgical techniques are also used. Most sulfide deposits have traditionally been processed by concentration through a froth flotation process followed by pyrometallurgical extraction. The nickel matte is further processed with the Sherritt-Gordon process. First, copper is removed by adding hydrogen sulfide, leaving a concentrate of cobalt and nickel. Then, solvent extraction is used to separate the cobalt and nickel, with the final nickel content greater than 86%.[81]
A second common refining process is leaching the metal matte into a nickel salt solution, followed by electrowinning the nickel from solution by plating it onto a cathode as electrolytic nickel.[82]
Mond process
Highly purified nickel spheres made by the Mond process
The purest metal is obtained from nickel oxide by the Mond process, which gives a purity of over 99.99%. The process was patented by Ludwig Mond and has been in industrial use since before the beginning of the 20th century.[83] In this process, nickel is treated with carbon monoxide in the presence of a sulfur catalyst at around 40–80°C to form nickel carbonyl. In a similar reaction with iron, iron pentacarbonyl can form, though this reaction is slow. If necessary, the nickel may be separated by distillation. Dicobalt octacarbonyl is also formed in nickel distillation as a by-product, but it decomposes to tetracobalt dodecacarbonyl at the reaction temperature to give a non-volatile solid.[11]
Nickel is obtained from nickel carbonyl by one of two processes. It may be passed through a large chamber at high temperatures in which tens of thousands of nickel spheres (pellets) are constantly stirred. The carbonyl decomposes and deposits pure nickel onto the spheres. In the alternate process, nickel carbonyl is decomposed in a smaller chamber at 230°C to create a fine nickel powder. The byproduct carbon monoxide is recirculated and reused. The highly pure nickel product is known as "carbonyl nickel".[84]
Market value
The market price of nickel surged throughout 2006 and the early months of 2007; as of April5,2007[update], the metal was trading at US$52,300/tonne or $1.47/oz.[85] The price later fell dramatically; as of September 2017[update], the metal was trading at $11,000/tonne, or $0.31/oz.[86] During the 2022 Russian invasion of Ukraine, worries about sanctions on Russian nickel exports triggered a short squeeze, causing the price of nickel to quadruple in just two days, reaching US$100,000 per tonne.[87][88] The London Metal Exchange cancelled contracts worth $3.9billion and suspended nickel trading for over a week.[89] Analyst Andy Home argued that such price shocks are exacerbated by the purity requirements imposed by metal markets: only Grade I (99.8% pure) metal can be used as a commodity on the exchanges, but most of the world's supply is either in ferro-nickel alloys or lower-grade purities.[90]
Applications
Nickel foam (top) and its internal structure (bottom)
Global use of nickel is currently 68% in stainless steel, 10% in nonferrous alloys, 9% electroplating, 7% alloy steel, 3% foundries, and 4% other (including batteries).[13]
Nickel is used in many recognizable industrial and consumer products, including stainless steel, alnico magnets, coinage, rechargeable batteries (e.g. nickel–iron), electric guitar strings, microphone capsules, plating on plumbing fixtures,[91] and special alloys such as permalloy, elinvar, and invar. It is used for plating and as a green tint in glass. Nickel is preeminently an alloy metal, and its chief use is in nickel steels and nickel cast irons, in which it typically increases the tensile strength, toughness, and elastic limit. It is widely used in many other alloys, including nickel brasses and bronzes and alloys with copper, chromium, aluminium, lead, cobalt, silver, and gold (Inconel, Incoloy, Monel, Nimonic).[82]
Nickel is traditionally used for Kris production in Southeastern Asia.
Because nickel is resistant to corrosion, it was occasionally used as a substitute for decorative silver. Nickel was also occasionally used in some countries after 1859 as a cheap coinage metal (see above), but in the later years of the 20th century, it was replaced by cheaper stainless steel (i.e., iron) alloys, except in the United States and Canada.[63]
Nickel is an excellent alloying agent for certain precious metals and is used in the fire assay as a collector of platinum group elements (PGE). As such, nickel can fully collect all six PGEs from ores, and can partially collect gold. High-throughput nickel mines may also do PGE recovery (mainly platinum and palladium); examples are Norilsk, Russia and the Sudbury Basin, Canada.[92]
Nickel and its alloys are often used as catalysts for hydrogenation reactions. Raney nickel, a finely divided nickel-aluminium alloy, is one common form, though related catalysts are also used, including Raney-type catalysts.[95]
Nickel is naturally magnetostrictive: in the presence of a magnetic field, the material undergoes a small change in length.[96][97] The magnetostriction of nickel is on the order of 50ppm and is negative, indicating that it contracts.[98]
Nickel is used as a binder in the cemented tungsten carbide or hardmetal industry and used in proportions of 6% to 12% by weight. Nickel makes the tungsten carbide magnetic and adds corrosion-resistance to the cemented parts, though the hardness is less than those with cobalt binder.[99]
Around 27% of all nickel production is used for engineering, 10% for building and construction, 14% for tubular products, 20% for metal goods, 14% for transport, 11% for electronic goods, and 5% for other uses.[13]
Raney nickel is widely used for hydrogenation of unsaturated oils to make margarine, and substandard margarine and leftover oil may contain nickel as a contaminant. Forte et al. found that type 2 diabetic patients have 0.89ng/mL of Ni in the blood relative to 0.77ng/mL in control subjects.[103]
It was not recognized until the 1970s, but nickel is known to play an important role in the biology of some plants, bacteria, archaea, and fungi.[104][105][106] Nickel enzymes such as urease are considered virulence factors in some organisms.[107][108] Urease catalyzes hydrolysis of urea to form ammonia and carbamate.[105][104]NiFe hydrogenases can catalyze oxidation of H2 to form protons and electrons; and also the reverse reaction, the reduction of protons to form hydrogen gas.[105][104] A nickel-tetrapyrrole coenzyme, cofactor F430, is present in methyl coenzyme M reductase, which can catalyze the formation of methane, or the reverse reaction, in methanogenicarchaea (in +1 oxidation state).[109] One of the carbon monoxide dehydrogenase enzymes consists of an Fe-Ni-S cluster.[110] Other nickel-bearing enzymes include a rare bacterial class of superoxide dismutase[111] and glyoxalase I enzymes in bacteria and several eukaryotic trypanosomal parasites[112] (in other organisms, including yeast and mammals, this enzyme contains divalent Zn2+).[113][114][115][116][117]
Dietary nickel may affect human health through infections by nickel-dependent bacteria, but nickel may also be an essential nutrient for bacteria living in the large intestine, in effect functioning as a prebiotic.[118] The US Institute of Medicine has not confirmed that nickel is an essential nutrient for humans, so neither a Recommended Dietary Allowance (RDA) nor an Adequate Intake have been established. The tolerable upper intake level of dietary nickel is 1mg/day as soluble nickel salts. Estimated dietary intake is 70 to 100μg/day; less than 10% is absorbed. What is absorbed is excreted in urine.[119] Relatively large amounts of nickel – comparable to the estimated average ingestion above – leach into food cooked in stainless steel. For example, the amount of nickel leached after 10 cooking cycles into one serving of tomato sauce averages 88μg.[120][121]
The major source of nickel exposure is oral consumption, as nickel is essential to plants.[124] Typical background concentrations of nickel do not exceed 20ng/m3 in air, 100mg/kg in soil, 10mg/kg in vegetation, 10μg/L in freshwater and 1μg/L in seawater.[125] Environmental concentrations may be increased by human pollution. For example, nickel-plated faucets may contaminate water and soil; mining and smelting may dump nickel into wastewater; nickel–steel alloy cookware and nickel-pigmented dishes may release nickel into food. Air may be polluted by nickel ore refining and fossil fuel combustion. Humans may absorb nickel directly from tobacco smoke and skin contact with jewelry, shampoos, detergents, and coins. A less common form of chronic exposure is through hemodialysis as traces of nickel ions may be absorbed into the plasma from the chelating action of albumin.[citation needed]
The average daily exposure is not a threat to human health. Most nickel absorbed by humans is removed by the kidneys and passed out of the body through urine or is eliminated through the gastrointestinal tract without being absorbed. Nickel is not a cumulative poison, but larger doses or chronic inhalation exposure may be toxic, even carcinogenic, and constitute an occupational hazard.[126]
Nickel compounds are classified as human carcinogens[127][128][129][130] based on increased respiratory cancer risks observed in epidemiological studies of sulfidic ore refinery workers.[131] This is supported by the positive results of the NTP bioassays with Ni sub-sulfide and Ni oxide in rats and mice.[132][133] The human and animal data consistently indicate a lack of carcinogenicity via the oral route of exposure and limit the carcinogenicity of nickel compounds to respiratory tumours after inhalation.[134][135] Nickel metal is classified as a suspect carcinogen;[127][128][129] there is consistency between the absence of increased respiratory cancer risks in workers predominantly exposed to metallic nickel[131] and the lack of respiratory tumours in a rat lifetime inhalation carcinogenicity study with nickel metal powder.[136] In the rodent inhalation studies with various nickel compounds and nickel metal, increased lung inflammations with and without bronchial lymph node hyperplasia or fibrosis were observed.[130][132][136][137] In rat studies, oral ingestion of water-soluble nickel salts can trigger perinatal mortality in pregnant animals.[138] Whether these effects are relevant to humans is unclear as epidemiological studies of highly exposed female workers have not shown adverse developmental toxicity effects.[139]
Sensitized persons may show a skin contact allergy to nickel known as a contact dermatitis. Highly sensitized persons may also react to foods with high nickel content.[143] Patients with pompholyx may also be sensitive to nickel. Nickel is the top confirmed contact allergen worldwide, partly due to its use in jewelry for pierced ears.[144] Nickel allergies affecting pierced ears are often marked by itchy, red skin. Many earrings are now made without nickel or with low-release nickel[145] to address this problem. The amount allowed in products that contact human skin is now regulated by the European Union. In 2002, researchers found that the nickel released by 1 and 2 euro coins, far exceeded those standards. This is believed to be due to a galvanic reaction.[146] Nickel was voted Allergen of the Year in 2008 by the American Contact Dermatitis Society.[147] In August 2015, the American Academy of Dermatology adopted a position statement on the safety of nickel: "Estimates suggest that contact dermatitis, which includes nickel sensitization, accounts for approximately $1.918billion and affects nearly 72.29million people."[143]
Reports show that both the nickel-induced activation of hypoxia-inducible factor (HIF-1) and the up-regulation of hypoxia-inducible genes are caused by depletion of intracellular ascorbate. The addition of ascorbate to the culture medium increased the intracellular ascorbate level and reversed both the metal-induced stabilization of HIF-1- and HIF-1α-dependent gene expression.[148][149]
Nickel in popular culture
In the second Oz book, The Marvelous Land of Oz (by L. Frank Baum, published by Reilly & Britton, 1904), the Tin Woodman states that he has had his tin body nickel-plated. He is thereafter very careful not to allow his nickel plating to get scratched, nicked, or marred.[150]
Related Research Articles
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Platinum is a chemical element; it has symbol Pt and atomic number 78. It is a dense, malleable, ductile, highly unreactive, precious, silverish-white transition metal. Its name originates from Spanish platina, a diminutive of plata "little silver".
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Smelting is a process of applying heat and a chemical reducing agent to an ore to extract a desired base metal product. It is a form of extractive metallurgy that is used to obtain many metals such as iron, copper, silver, tin, lead and zinc. Smelting uses heat and a chemical reducing agent to decompose the ore, driving off other elements as gases or slag and leaving the metal behind. The reducing agent is commonly a fossil-fuel source of carbon, such as carbon monoxide from incomplete combustion of coke—or, in earlier times, of charcoal. The oxygen in the ore binds to carbon at high temperatures, as the chemical potential energy of the bonds in carbon dioxide is lower than that of the bonds in the ore.
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Zinc is a chemical element with the symbol Zn and atomic number 30. It is a slightly brittle metal at room temperature and has a shiny-greyish appearance when oxidation is removed. It is the first element in group 12 (IIB) of the periodic table. In some respects, zinc is chemically similar to magnesium: both elements exhibit only one normal oxidation state (+2), and the Zn2+ and Mg2+ ions are of similar size. Zinc is the 24th most abundant element in Earth's crust and has five stable isotopes. The most common zinc ore is sphalerite (zinc blende), a zinc sulfide mineral. The largest workable lodes are in Australia, Asia, and the United States. Zinc is refined by froth flotation of the ore, roasting, and final extraction using electricity (electrowinning).
Copper is a chemical element; it has symbol Cu and atomic number 29. It is a soft, malleable, and ductile metal with very high thermal and electrical conductivity. A freshly exposed surface of pure copper has a pinkish-orange color. Copper is used as a conductor of heat and electricity, as a building material, and as a constituent of various metal alloys, such as sterling silver used in jewelry, cupronickel used to make marine hardware and coins, and constantan used in strain gauges and thermocouples for temperature measurement.
Nickel carbonyl (IUPAC name: tetracarbonylnickel) is a nickel(0) organometallic compound with the formula Ni(CO)4. This colorless liquid is the principal carbonyl of nickel. It is an intermediate in the Mond process for producing very high-purity nickel and a reagent in organometallic chemistry, although the Mond Process has fallen out of common usage due to the health hazards in working with the compound. Nickel carbonyl is one of the most dangerous substances yet encountered in nickel chemistry due to its very high toxicity, compounded with high volatility and rapid skin absorption.
The platinum-group metals (PGMs), also known as the platinoids, platinides, platidises, platinum group, platinum metals, platinum family or platinum-group elements (PGEs), are six noble, precious metallic elements clustered together in the periodic table. These elements are all transition metals in the d-block.
Group 10, numbered by current IUPAC style, is the group of chemical elements in the periodic table that consists of nickel (Ni), palladium (Pd), platinum (Pt), and darmstadtium (Ds). All are d-block transition metals. All known isotopes of darmstadtium are radioactive with short half-lives, and are not known to occur in nature; only minute quantities have been synthesized in laboratories.
Nickeline or niccolite is the mineral form of nickel arsenide. The naturally-occurring mineral contains roughly 43.9% nickel and 56.1% arsenic by mass, but composition of the mineral may vary slightly.
Nickel(II) chloride (or just nickel chloride) is the chemical compound NiCl2. The anhydrous salt is yellow, but the more familiar hydrate NiCl2·6H2O is green. Nickel(II) chloride, in various forms, is the most important source of nickel for chemical synthesis. The nickel chlorides are deliquescent, absorbing moisture from the air to form a solution. Nickel salts have been shown to be carcinogenic to the lungs and nasal passages in cases of long-term inhalation exposure.
Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands. Metal carbonyls are useful in organic synthesis and as catalysts or catalyst precursors in homogeneous catalysis, such as hydroformylation and Reppe chemistry. In the Mond process, nickel tetracarbonyl is used to produce pure nickel. In organometallic chemistry, metal carbonyls serve as precursors for the preparation of other organometallic complexes.
The Mond process, sometimes known as the carbonyl process, is a technique created by Ludwig Mond in 1890, to extract and purify nickel. The process was used commercially before the end of the 19th century, and particularly by the International Nickel Company in the Sudbury Basin. This process converts nickel oxides into nickel metal with very high purity being attainable in just a single step.
Nickel(II) oxide is the chemical compound with the formula NiO. It is the principal oxide of nickel. It is classified as a basic metal oxide. Several million kilograms are produced annually of varying quality, mainly as an intermediate in the production of nickel alloys. The mineralogical form of NiO, bunsenite, is very rare. Other nickel(III) oxides have been claimed, for example: Ni 2O 3 and NiO 2, but remain unproven.
A native metal is any metal that is found pure in its metallic form in nature. Metals that can be found as native deposits singly or in alloys include antimony, arsenic, bismuth, cadmium, chromium, cobalt, indium, iron, manganese, molybdenum, nickel, niobium, rhenium, tantalum, tellurium, tin, titanium, tungsten, vanadium, and zinc, as well as the gold group and the platinum group. Among the alloys found in native state have been brass, bronze, pewter, German silver, osmiridium, electrum, white gold, silver-mercury amalgam, and gold-mercury amalgam.
Cobalt is a chemical element; it has symbol Co and atomic number 27. As with nickel, cobalt is found in the Earth's crust only in a chemically combined form, save for small deposits found in alloys of natural meteoric iron. The free element, produced by reductive smelting, is a hard, lustrous, somewhat brittle, gray metal.
Cobalt extraction refers to the techniques used to extract cobalt from its ores and other compound ores. Several methods exist for the separation of cobalt from copper and nickel. They depend on the concentration of cobalt and the exact composition of the ore used.
Nickel compounds are chemical compounds containing the element nickel which is a member of the group 10 of the periodic table. Most compounds in the group have an oxidation state of +2. Nickel is classified as a transition metal with nickel(II) having much chemical behaviour in common with iron(II) and cobalt(II). Many salts of nickel(II) are isomorphous with salts of magnesium due to the ionic radii of the cations being almost the same. Nickel forms many coordination complexes. Nickel tetracarbonyl was the first pure metal carbonyl produced, and is unusual in its volatility. Metalloproteins containing nickel are found in biological systems.
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1 2 Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on Classification, Labelling and Packaging of Substances and Mixtures, Amending and Repealing Directives 67/548/EEC and 1999/45/EC and amending Regulation (EC) No 1907/2006 [OJ L 353, 31.12.2008, p. 1]. Annex VIArchived March 14, 2019, at the Wayback Machine . Accessed July 13, 2017.
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![Structure of
[Ni2(CN)6] ion Structure of hexacyanodinickelate(I) ion.png](http://upload.wikimedia.org/wikipedia/commons/thumb/b/b5/Structure_of_hexacyanodinickelate%28I%29_ion.png/220px-Structure_of_hexacyanodinickelate%28I%29_ion.png)
![Color of various Ni(II) complexes in aqueous solution. From left to right,
[Ni(NH3)6],
[Ni(NH2CH2CH2NH2)],
[NiCl4],
[Ni(H2O)6] Color of various Ni(II) complexes in aqueous solution.jpg](http://upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Color_of_various_Ni%28II%29_complexes_in_aqueous_solution.jpg/450px-Color_of_various_Ni%28II%29_complexes_in_aqueous_solution.jpg)
