Neodymium
Neodymium | ||||||||||||||||||||||||||||||||||||||||||||||
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Pronunciation | /ˌniːoʊˈdɪmiəm/ | |||||||||||||||||||||||||||||||||||||||||||||
Appearance | silvery white | |||||||||||||||||||||||||||||||||||||||||||||
Standard atomic weight Ar°(Nd) | ||||||||||||||||||||||||||||||||||||||||||||||
Neodymium in the periodic table | ||||||||||||||||||||||||||||||||||||||||||||||
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kJ/mol | ||||||||||||||||||||||||||||||||||||||||||||||
Heat of vaporization | 289 kJ/mol | |||||||||||||||||||||||||||||||||||||||||||||
Molar heat capacity | 27.45 J/(mol·K) | |||||||||||||||||||||||||||||||||||||||||||||
Vapor pressure
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Atomic properties | ||||||||||||||||||||||||||||||||||||||||||||||
Discovery | Carl Gustaf Mosander (1841) | |||||||||||||||||||||||||||||||||||||||||||||
First isolation | Carl Auer von Welsbach (1885) | |||||||||||||||||||||||||||||||||||||||||||||
Named by | Carl Auer von Welsbach (1885) | |||||||||||||||||||||||||||||||||||||||||||||
Isotopes of neodymium | ||||||||||||||||||||||||||||||||||||||||||||||
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Neodymium is a
Neodymium compounds were first commercially used as glass dyes in 1927 and remain a popular additive. The color of neodymium compounds comes from the Nd3+ ion and is often a reddish-purple. This color changes with the type of lighting because of the interaction of the sharp light absorption bands of neodymium with ambient light enriched with the sharp visible emission bands of mercury, trivalent europium or terbium. Glasses that have been doped with neodymium are used in lasers that emit infrared with wavelengths between 1047 and 1062 nanometers. These lasers have been used in extremely high-power applications, such as in inertial confinement fusion. Neodymium is also used with various other substrate crystals, such as yttrium aluminium garnet in the Nd:YAG laser.
Neodymium
Physical properties
Metallic neodymium has a bright, silvery metallic luster.
Electron configuration
Neodymium is the fourth member of the lanthanide series. In the periodic table, it appears between the lanthanides praseodymium to its left and the radioactive element promethium to its right, and above the actinide uranium. Its 60 electrons are arranged in the configuration [Xe]4f46s2, of which the six 4f and 6s electrons are valence. Like most other metals in the lanthanide series, neodymium usually only uses three electrons as valence electrons, as afterwards the remaining 4f electrons are strongly bound: this is because the 4f orbitals penetrate the most through the inert xenon core of electrons to the nucleus, followed by 5d and 6s, and this increases with higher ionic charge. Neodymium can still lose a fourth electron because it comes early in the lanthanides, where the nuclear charge is still low enough and the 4f subshell energy high enough to allow the removal of further valence electrons.[19]
Chemical properties
Neodymium has a melting point of 1,024 °C (1,875 °F) and a boiling point of 3,074 °C (5,565 °F). Like other lanthanides, it usually has the oxidation state +3, but can also form in the +2 and +4 oxidation states, and even, in very rare conditions, +0.[4] Neodymium metal quickly oxidizes at ambient conditions,[13] forming an oxide layer like iron rust that can spall off and expose the metal to further oxidation; a centimeter-sized sample of neodymium corrodes completely in about a year. Nd3+ is generally soluble in water. Like its neighbor praseodymium, it readily burns at about 150 °C to form neodymium(III) oxide; the oxide then peels off, exposing the bulk metal to the further oxidation:[13]
- 4Nd + 3O2 → 2Nd2O3
Neodymium is an electropositive element, and it reacts slowly with cold water, or quickly with hot water, to form neodymium(III) hydroxide:[20]
- 2Nd (s) + 6H2O (l) → 2Nd(OH)3 (aq) + 3H2 (g)
Neodymium metal reacts vigorously with all the stable halogens:[20]
- 2Nd (s) + 3F2 (g) → 2NdF3 (s) [a violet substance]
- 2Nd (s) + 3Cl2 (g) → 2NdCl3 (s) [a mauve substance]
- 2Nd (s) + 3Br2 (g) → 2NdBr3 (s) [a violet substance]
- 2Nd (s) + 3I2 (g) → 2NdI3 (s) [a green substance]
Neodymium dissolves readily in dilute sulfuric acid to form solutions that contain the lilac Nd(III) ion. These exist as a [Nd(OH2)9]3+ complexes:[21]
- 2Nd (s) + 3H2SO4 (aq) → 2Nd3+ (aq) + 3SO2−4 (aq) + 3H2 (g)
Compounds
Some of the most important neodymium compounds include:
- halides:
- oxides: Nd2O3
- hydroxide: Nd(OH)3
- carbonate: Nd2(CO3)3
- sulfate: Nd2(SO4)3
- acetate: Nd(CH3COO)3
- neodymium magnets (Nd2Fe14B)
Some neodymium compounds vary in color under different types of lighting.[22]
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Neodymium compounds in fluorescent tube light—from left to right, the sulfate, nitrate, and chloride
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Neodymium compounds in compact fluorescent lamp light
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Neodymium compounds in normal daylight
Organoneodymium compounds
Organoneodymium compounds are compounds that have a neodymium–carbon bond. These compounds are similar to
Isotopes
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talk |
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Naturally occurring neodymium (60Nd) is composed of five stable
Neodymium also has 13 known
Neodymium isotopes are used in various scientific applications. 142Nd has been used for the production of short-lived Tm and Yb isotopes. 146Nd has been suggested for the production of 147Pm, which is a source of radioactive power. Several neodymium isotopes have been used for the production of other promethium isotopes. The decay from 147Sm (t1/2 = 1.06×1011 y) to the stable 143Nd allows for samarium–neodymium dating.[27] 150Nd has also been used to study double beta decay.[28]
History
In 1751, the Swedish mineralogist
Double nitrate crystallization was the means of commercial neodymium purification until the 1950s. Lindsay Chemical Division was the first to commercialize large-scale ion-exchange purification of neodymium. Starting in the 1950s, high purity (>99%) neodymium was primarily obtained through an ion exchange process from monazite, a mineral rich in rare-earth elements.[13] The metal is obtained through electrolysis of its halide salts. Currently, most neodymium is extracted from bastnäsite and purified by solvent extraction. Ion-exchange purification is used for the highest purities (typically >99.99%). Since then, the glass technology has improved due to the improved purity of commercially available neodymium oxide and the advancement of glass technology in general. Early methods of separating the lanthanides depended on fractional crystallization, which did not allow for the isolation of high-purity neodymium until the aforementioned ion exchange methods were developed after World War II.[40]
Occurrence and production
Occurrence
Neodymium is rarely found in nature as a free element, instead occurring as ores, such as monazite and bastnäsite (these are mineral group names rather than single mineral names) that contain small amounts of all rare-earth metals. In these minerals neodymium is rarely dominant; some exceptions include monazite-(Nd) and kozoite-(Nd).[41] The main mining areas are in China, United States, Brazil, India, Sri Lanka, and Australia.
The Nd3+ ion is similar in size to the early lanthanides of the cerium group (those from lanthanum up to samarium and europium) that immediately follow in the periodic table, and hence it tends to occur along with them in phosphate, silicate and carbonate minerals, such as monazite (MIIIPO4) and bastnäsite (MIIICO3F), where M refers to all the rare-earth metals except scandium and the radioactive promethium (mostly Ce, La, and Y, with somewhat less Pr and Nd).[42] Bastnäsite is usually lacking in thorium and the heavy lanthanides, and the purification of the light lanthanides from it is less involved. The ore, after being crushed and ground, is first treated with hot concentrated sulfuric acid, evolving carbon dioxide, hydrogen fluoride, and silicon tetrafluoride. The product is then dried and leached with water, leaving the early lanthanide ions, including lanthanum, in solution.[42]
Atomic number |
Element | Relative amount |
---|---|---|
42 | Molybdenum | 2.771 |
47 | Silver | 0.590 |
50 | Tin | 4.699 |
58 | Cerium | 1.205 |
59 | Praseodymium | 0.205 |
60 | Neodymium | 1 |
74 | Tungsten | 0.054 |
90 | Thorium | 0.054 |
92 | Uranium | 0.022 |
In space
Neodymium's per-particle abundance in the
In the Earth's crust
Neodymium is classified as a lithophile under the Goldschmidt classification, meaning that it is generally found combined with oxygen. Although it belongs to the rare-earth metals, neodymium is not rare at all. Its abundance in the Earth's crust is about 41 mg/kg.[44] It is similar in abundance to lanthanum.
Production
The world's production of neodymium was about 7,000 tons in 2004.
Neodymium is typically 10–18% of the rare-earth content of commercial deposits of the light rare-earth-element minerals bastnäsite and monazite.[13] With neodymium compounds being the most strongly colored for the trivalent lanthanides, it can occasionally dominate the coloration of rare-earth minerals when competing chromophores are absent. It usually gives a pink coloration. Outstanding examples of this include monazite crystals from the tin deposits in Llallagua, Bolivia; ancylite from Mont Saint-Hilaire, Quebec, Canada; or lanthanite from Lower Saucon Township, Pennsylvania. As with neodymium glasses, such minerals change their colors under the differing lighting conditions. The absorption bands of neodymium interact with the visible emission spectrum of mercury vapor, with the unfiltered shortwave UV light causing neodymium-containing minerals to reflect a distinctive green color. This can be observed with monazite-containing sands or bastnäsite-containing ore.[49]
The demand for mineral resources, such as
Applications
Magnets
Neodymium magnets appear in products such as
Glass
Neodymium glass (Nd:glass) is produced by the inclusion of neodymium oxide (Nd2O3) in the glass melt. In daylight or incandescent light neodymium glass appears lavender, but it appears pale blue under fluorescent lighting. Neodymium may be used to color glass in shades ranging from pure violet through wine-red and warm gray.[55]
The first commercial use of purified neodymium was in glass coloration, starting with experiments by Leo Moser in November 1927. The resulting "Alexandrite" glass remains a signature color of the Moser glassworks to this day. Neodymium glass was widely emulated in the early 1930s by American glasshouses, most notably Heisey, Fostoria ("wisteria"), Cambridge ("heatherbloom"), and Steuben ("wisteria"), and elsewhere (e.g. Lalique, in France, or Murano). Tiffin's "twilight" remained in production from about 1950 to 1980.[56] Current sources include glassmakers in the Czech Republic, the United States, and China.[57]
The sharp absorption bands of neodymium cause the glass color to change under different lighting conditions, being reddish-purple under
Light transmitted through neodymium glasses shows unusually sharp absorption bands; the glass is used in astronomical work to produce sharp bands by which spectral lines may be calibrated.[13] Another application is the creation of selective astronomical filters to reduce the effect of light pollution from sodium and fluorescent lighting while passing other colours, especially dark red hydrogen-alpha emission from nebulae.[59] Neodymium is also used to remove the green color caused by iron contaminants from glass.[60]
Neodymium is a component of "didymium" (referring to mixture of salts of neodymium and praseodymium) used for coloring glass to make welder's and glass-blower's goggles; the sharp absorption bands obliterate the strong sodium emission at 589 nm. The similar absorption of the yellow mercury emission line at 578 nm is the principal cause of the blue color observed for neodymium glass under traditional white-fluorescent lighting. Neodymium and didymium glass are used in color-enhancing filters in indoor photography, particularly in filtering out the yellow hues from incandescent lighting. Similarly, neodymium glass is becoming widely used more directly in incandescent light bulbs. These lamps contain neodymium in the glass to filter out yellow light, resulting in a whiter light which is more like sunlight.[61] During World War I, didymium mirrors were reportedly used to transmit Morse code across battlefields.[62] Similar to its use in glasses, neodymium salts are used as a colorant for enamels.[13]
Lasers
Certain transparent materials with a small concentration of neodymium ions can be used in lasers as
Trivalent neodymium ion Nd3+ was the first lanthanide from rare-earth elements used for the generation of laser radiation. The Nd:CaWO4 laser was developed in 1961.[65] Historically, it was the third laser which was put into operation (the first was ruby, the second the U3+:CaF laser). Over the years the neodymium laser became one of the most used lasers for application purposes. The success of the Nd3+ ion lies in the structure of its energy levels and in the spectroscopic properties suitable for the generation of laser radiation. In 1964 Geusic et al.[66] demonstrated the operation of neodymium ion in YAG matrix Y3Al5O12. It is a four-level laser with lower threshold and with excellent mechanical and temperature properties. For optical pumping of this material it is possible to use non-coherent flashlamp radiation or a coherent diode beam.[67]
The current laser at the UK
Neodymium glass
Other
Other applications of neodymium include:
- Neodymium has an unusually large cryocoolers.[70]
- Neodymium acetate can be used as a standard contrasting agent in electron microscopy (a substitute for the radioactive and toxic uranyl acetate).[71]
- Probably because of similarities to Ca2+, Nd3+ has been reported[72] to promote plant growth. Rare-earth element compounds are frequently used in China as fertilizer.[73]
- Samarium–neodymium dating is useful for determining the age relationships of rocks[74] and meteorites.[75]
- Neodymium isotopes recorded in marine sediments are used to reconstruct changes in past ocean circulation.[76][77]
Biological role and precautions
Hazards | |
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GHS labelling: | |
Warning | |
H315, H319, H335 | |
P261, P305+P351+P338[78] | |
NFPA 704 (fire diamond) |
The early lanthanides, including neodymium, as well as lanthanum, cerium and praseodymium, have been found to be essential to some
Neodymium metal dust is combustible and therefore an explosion hazard. Neodymium compounds, as with all rare-earth metals, are of low to moderate toxicity; however, its toxicity has not been thoroughly investigated. Ingested neodymium salts are regarded as more toxic if they are soluble than if they are insoluble.[82] Neodymium dust and salts are very irritating to the eyes and mucous membranes, and moderately irritating to skin. Breathing the dust can cause lung embolisms, and accumulated exposure damages the liver. Neodymium also acts as an anticoagulant, especially when given intravenously.[38]
Neodymium magnets have been tested for medical uses such as magnetic braces and bone repair, but biocompatibility issues have prevented widespread applications.[83] Commercially available magnets made from neodymium are exceptionally strong and can attract each other from large distances. If not handled carefully, they come together very quickly and forcefully, causing injuries. There is at least one documented case of a person losing a fingertip when two magnets he was using snapped together from 50 cm away.[84]
Another risk of these powerful magnets is that if more than one magnet is ingested, they can pinch soft tissues in the
See also
- Neodymium compounds
- Category:Neodymium compounds
- Lanthanides
- Period 6 elements
- Rare earth metals
Notes
- ^ The thermal expansion is anisotropic: the parameters (at 20 °C) for each crystal axis are αa = 4.8×10−6/K, αc = 10.5×10−6/K, and αaverage = αV/3 = 6.7×10−6/K.[3]
- ^ Abundances in the source are listed relative to silicon rather than in per-particle notation. The sum of all elements per 106 parts of silicon is 2.6682×1010 parts; lead comprises 3.258 parts.
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External links
- WebElements.com—Neodymium
- It's Elemental—The element Neodymium
- Neodymium at The Periodic Table of Videos(University of Nottingham)
- EnvironmentalChemistry.com – Neodymium
- Pictures and more details about Neodymium metal