Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl<sub>3</sub>. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl<sub>3</sub>÷6H<sub>2</sub>O. Neodymium(III) chloride is produced from minerals monazite and bastnäsite using a complex multistage extraction process. The chloride has several important applications as an intermediate chemical for production of neodymium metal and neodymium-based lasers and optical fibers. Other applications include a catalyst in organic synthesis and in decomposition of waste water contamination, corrosion protection of aluminium and its alloys, and fluorescent labeling of organic molecules (DNA).
NdCl<sub>3</sub> is a mauve colored hygroscopic solid whose color changes to purple upon absorption of atmospheric water. The resulting hydrate, like many other neodymium salts, has the interesting property that it appears different colors under fluorescent light- In the chloride's case, light yellow (see picture).
The anhydrous NdCl<sub>3</sub> features Nd in a nine-coordinate tricapped trigonal prismatic geometry and crystallizes with the UCl<sub>3</sub> structure. This hexagonal structure is common for many halogenated lanthanides and actinides such as LaCl<sub>3</sub>, LaBr<sub>3</sub>, SmCl<sub>3</sub>, PrCl<sub>3</sub>, EuCl<sub>3</sub>, CeCl<sub>3</sub>, CeBr<sub>3</sub>, GdCl<sub>3</sub>, AmCl<sub>3</sub> and TbCl<sub>3</sub> but not for YbCl<sub>3</sub> and LuCl<sub>3</sub>.
The structure of neodymium(III) chloride in solution crucially depends on the solvent: In water, the major species are Nd(H<sub>2</sub>O)<sub>8</sub><sup>3+</sup>, and this situation is common for most rare earth chlorides and bromides. In methanol, the species are NdCl<sub>2</sub>(CH<sub>3</sub>OH)<sub>6</sub><sup>+</sup> and in hydrochloric acid NdCl(H<sub>2</sub>O)<sub>7</sub><sup>2+</sup>. The coordination of neodymium is octahedral (8-fold) in all cases, but the ligand structure is different.
NdCl<sub>3</sub> is a soft paramagnetic solid, which turns ferromagnetic at very low temperature of 0.5 K. Its electrical conductivity is about 240 S/m and heat capacity is ~100 J/(mol÷K). NdCl<sub>3</sub> is readily soluble in water and ethanol, but not in chloroform or ether. Reduction of NdCl<sub>3</sub> with Nd metal at temperatures above 650 ðC yields NdCl<sub>2</sub>:
Heating of NdCl<sub>3</sub> with water vapors or silica produces neodymium oxochloride:
Reacting NdCl<sub>3</sub> with hydrogen sulfide at about 1100 ðC produces neodymium sulfide:
Reactions with ammonia and phosphine at high temperatures yield neodymium nitride and phosphide, respectively:
Whereas the addition of hydrofluoric acid produces neodymium fluoride:
NdCl<sub>3</sub> is produced from minerals monazite and bastnäsite. The synthesis is complex because of the low abundance of neodymium in the Earth's crust (38 mg/kg) and because of difficulty of separating neodymium from other lanthanides. The process is however easier for neodymium than for other lanthanides because of its relatively high content in the mineral â up to 16% by weight, which is the third highest after cerium and lanthanum. Many synthesis varieties exist and one can be simplified as follows:
The crushed mineral is treated with hot concentrated sulfuric acid to produce water-soluble sulfates of rare earths. The acidic filtrates are partially neutralized with sodium hydroxide to pH 3âÂÂ4. Thorium precipitates out of solution as hydroxide and is removed. After that the solution is treated with ammonium oxalate to convert rare earths into their insoluble oxalates. The oxalates are converted to oxides by annealing. The oxides are dissolved in nitric acid that excludes the main components, cerium, whose oxide is insoluble in HNO<sub>3</sub>. Neodymium oxide is separated from other rare-earth oxides by ion exchange. In this process, rare-earth ions are adsorbed onto suitable resin by ion exchange with hydrogen, ammonium or cupric ions present in the resin. The rare earth ions are then selectively washed out by suitable complexing agent, such as ammonium citrate or nitrilotracetate.
This process normally yields Nd<sub>2</sub>O<sub>3</sub>; the oxide is difficult to directly convert to elemental neodymium, which is often the goal of the whole technological procedure. Therefore, the oxide is treated with hydrochloric acid and ammonium chloride to produce the less stable NdCl<sub>3</sub>:
The thus produced NdCl<sub>3</sub> quickly absorbs water and converts to NdCl<sub>3</sub>÷6H<sub>2</sub>O hydrate, which is stable for storage, and can be converted back into NdCl<sub>3</sub> when necessary. Simple rapid heating of the hydrate is not practical for that purpose because it causes hydrolysis with consequent production of Nd<sub>2</sub>O<sub>3</sub>. Therefore, anhydrous NdCl<sub>3</sub> is prepared by dehydration of the hydrate either by slowly heating to 400 ðC with 4-6 equivalents of ammonium chloride under high vacuum, or by heating with an excess of thionyl chloride for several hours. The NdCl<sub>3</sub> can alternatively be prepared by reacting neodymium metal with hydrogen chloride or chlorine, though this method is not economical due to the relatively high price of the metal and is used for research purposes only. After preparation, it is usually purified by high temperature sublimation under high vacuum.
Neodymium(III) chloride is the most common starting compound for production of neodymium metal. NdCl<sub>3</sub> is heated with ammonium chloride or ammonium fluoride and hydrofluoric acid or with alkali or alkaline earth metals in vacuum or argon atmosphere at 300âÂÂ400 ðC.
An alternative route is electrolysis of molten mixture of anhydrous NdCl<sub>3</sub> and NaCl, KCl, or LiCl at temperatures about 700 ðC. The mixture melts at those temperatures, even though they are lower than the melting points of NdCl<sub>3</sub> and KCl (~770 ðC).
Although NdCl<sub>3</sub> itself does not have strong luminescence, it serves as a source of Nd<sup>3+</sup> ions for various light emitting materials. The latter include Nd-YAG lasers and Nd-doped optical fiber amplifiers, which amplify light emitted by other lasers. The Nd-YAG laser emits infrared light at 1.064 micrometres and is the most popular solid-state laser (i.e. laser based on a solid medium). The reason for using NdCl<sub>3</sub> rather than metallic neodymium or its oxide, in fabrication of fibers is easy decomposition of NdCl<sub>3</sub> during the chemical vapor deposition; the latter process is widely used for the fiber grows.
Neodymium(III) chloride is a dopant not only of traditional silica-based optical fibers, but of plastic fibers (dopedphotolime-gelatin, polyimide, polyethylene, etc.) as well. It is also used in as an additive into infrared organic light-emitting diodes. Besides, neodymium doped organic films can not only act as LEDs, but also as color filters improving the LED emission spectrum.
Solubility of neodymium(III) chloride (and other rare-earth salts) is various solvents results in a new type of rare-earth laser, which uses not a solid but liquid as an active medium. The liquid containing Nd<sup>3+</sup> ions is prepared in the following reactions:
where Nd<sup>3+</sup> is in fact the solvated ion with several selenium oxychloride molecules coordinated in the first coordination sphere, that is [Nd(SeOCl<sub>2</sub>)<sub>m</sub>]<sup>3+</sup>. The laser liquids prepared by this technique emits at the same wavelength of 1.064 micrometres and possess properties, such as high gain and sharpness of the emission, that are more characteristic of crystalline than Nd-glass lasers. The quantum efficiency of those liquid lasers was about 0.75 relative to the traditional Nd:YAG laser.
Another important application of NdCl<sub>3</sub> is in catalysisâÂÂin combination with organic chemicals, such as triethylaluminium and 2-propanol, it accelerates polymerization of various dienes. The products include such general purpose synthetic rubbers as polybutylene, polybutadiene, and polyisoprene.
Neodymium(III) chloride is also used to modify titanium dioxide. The latter is one of the most popular inorganic photocatalyst for decomposition of phenol, various dyes and other waste water contaminants. The catalytic action of titanium oxide has to be activated by UV light, i.e. artificial illumination. However, modifying titanium oxide with neodymium(III) chloride allows catalysis under visible illumination, such as sun light. The modified catalyst is prepared by chemical coprecipitationâÂÂpeptization method by ammonium hydroxide from mixture of TiCl<sub>4</sub> and NdCl<sub>3</sub> in aqueous solution). This process is used commercially on large scale on 1000 liter reactor for using in photocatalytic self-cleaning paints.
Other applications are being developed. For example, it was reported that coating of aluminium or various aluminium alloys produces very corrosion-resistance surface, which then resisted immersion into concentrated aqueous solution of NaCl for two months without sign of pitting. The coating is produced either by immersion into aqueous solution of NdCl<sub>3</sub> for a week or by electrolytic deposition using the same solution. In comparison with traditional chromium based corrosion inhibitors, NdCl<sub>3</sub> and other rare-earth salts are environment friendly and much less toxic to humans and animals.
The protective action of NdCl<sub>3</sub> on aluminium alloys is based on formation of insoluble neodymium hydroxide. Being a chloride, NdCl<sub>3</sub> itself is a corrosive agent, which is sometimes used for corrosion testing of ceramics.
Lanthanides, including neodymium are famous for their bright luminescence and therefore are widely used as fluorescent labels. In particular, NdCl<sub>3</sub> has been incorporated into organic molecules, such as DNA, which could be then easily traced using a fluorescence microscope during various physical and chemical reactions.
Neodymium(III) chloride does not seem toxic to humans and animals (approximately similar to table salt). The LD<sub>50</sub> (dose at which there is 50% mortality) for animals is about 3.7 g per kg of body weight (mouse, oral), 0.15 g/kg (rabbit, intravenous injection). Mild irritation of skin occurs upon exposure with 500 mg during 24 hrs (Draize test on rabbits). Substances with LD<sub>50</sub> above 2 g/kg are considered non-toxic.