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Neodymium(III) chloride

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Neodymium(III) chloride
Names
Other names Neodymium trichloride
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.016 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/3ClH.Nd/h3*1H;/q;;;+3/p-3Key: ATINCSYRHURBSP-UHFFFAOYSA-K
  • InChI=1/3ClH.Nd/h3*1H;/q;;;+3/p-3Key: ATINCSYRHURBSP-DFZHHIFOAM
SMILES
  • Cl(Cl)Cl
Properties
Chemical formula NdCl3,
NdCl3·6H2O (hydrate)
Molar mass 250.598 g/mol
Appearance Mauve-colored powder
hygroscopic
Density 4.13 g/cm (2.3 for hydrate)
Melting point 759 °C (1,398 °F; 1,032 K)
Boiling point 1,600 °C (2,910 °F; 1,870 K)
Solubility in water 1 kg/L at 25 °C
Solubility in ethanol 0.445 kg/L
Structure
Crystal structure hexagonal (UCl3 type), hP8
Space group P63/m, No. 176
Lattice constant a = 0.73988 nm, c = 0.42423 nm
Formula units (Z) 2
Coordination geometry Tricapped trigonal prismatic
(nine-coordinate)
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H315, H319, H335
Precautionary statements P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2 0 0
Safety data sheet (SDS) External SDS
Related compounds
Other anions Neodymium(III) bromide
Neodymium(III) oxide
Other cations LaCl3, SmCl3, PrCl3, EuCl3, CeCl3, GdCl3, TbCl3, Promethium(III) chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl3. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl3·6H2O. 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).

Appearance

NdCl3 under sunlight (top) and fluorescent light (bottom)

NdCl3 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).

Structure

Solid

The anhydrous NdCl3 features Nd in a nine-coordinate tricapped trigonal prismatic geometry and crystallizes with the UCl3 structure. This hexagonal structure is common for many halogenated lanthanides and actinides such as LaCl3, LaBr3, SmCl3, PrCl3, EuCl3, CeCl3, CeBr3, GdCl3, AmCl3 and TbCl3 but not for YbCl3 and LuCl3.

Solution

The structure of neodymium(III) chloride in solution crucially depends on the solvent: In water, the major species are Nd(H2O)8, and this situation is common for most rare earth chlorides and bromides. In methanol, the species are NdCl2(CH3OH)6 and in hydrochloric acid NdCl(H2O)7. The coordination of neodymium is octahedral (8-fold) in all cases, but the ligand structure is different.

Properties

NdCl3 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). NdCl3 is readily soluble in water and ethanol, but not in chloroform or ether. Reduction of NdCl3 with Nd metal at temperatures above 650 °C yields NdCl2:

2 NdCl3 + Nd → 3 NdCl2

Heating of NdCl3 with water vapors or silica produces neodymium oxochloride:

NdCl3 + H2O → NdOCl + 2 HCl
2 NdCl3 + SiO2 → 2 NdOCl + SiCl4

Reacting NdCl3 with hydrogen sulfide at about 1100 °C produces neodymium sulfide:

2 NdCl3 + 3 H2S → 2 Nd2S3 + 6 HCl

Reactions with ammonia and phosphine at high temperatures yield neodymium nitride and phosphide, respectively:

NdCl3 + NH3 → NdN + 3 HCl
NdCl3 + PH3 → NdP + 3 HCl

Whereas the addition of hydrofluoric acid produces neodymium fluoride:

NdCl3 + 3 HF → NdF3 + 3 HCl

Preparation

Monazite

NdCl3 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 – 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 3–4. 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 HNO3. 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 Nd2O3; 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 NdCl3:

Nd2O3 + 6 NH4Cl → 2 NdCl3 + 3 H2O + 6 NH3

The thus produced NdCl3 quickly absorbs water and converts to NdCl3·6H2O hydrate, which is stable for storage, and can be converted back into NdCl3 when necessary. Simple rapid heating of the hydrate is not practical for that purpose because it causes hydrolysis with consequent production of Nd2O3. Therefore, anhydrous NdCl3 is prepared by dehydration of the hydrate either by slowly heating to 400 °C with 4-6 equivalents of ammonium chloride under high vacuum, or by heating with an excess of thionyl chloride for several hours. The NdCl3 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.

Applications

Production of neodymium metal

Nd:YAG laser with lid open showing frequency doubled 532 nm green light

Neodymium(III) chloride is the most common starting compound for production of neodymium metal. NdCl3 is heated with ammonium chloride or ammonium fluoride and hydrofluoric acid or with alkali or alkaline earth metals in vacuum or argon atmosphere at 300–400 °C.

2 NdCl3 + 3 Ca → 2 Nd + 3 CaCl2

An alternative route is electrolysis of molten mixture of anhydrous NdCl3 and NaCl, KCl, or LiCl at temperatures about 700 °C. The mixture melts at those temperatures, even though they are lower than the melting points of NdCl3 and KCl (~770 °C).

Lasers and fiber amplifiers

Although NdCl3 itself does not have strong luminescence, it serves as a source of Nd 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 NdCl3 rather than metallic neodymium or its oxide, in fabrication of fibers is easy decomposition of NdCl3 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 ions is prepared in the following reactions:

SnCl4 + 2 SeOCl2 → SnCl6 + 2 SeOCl
SbCl5 + SeOCl2 → SbCl6 + SeOCl
3 SeOCl + NdCl3 → Nd(solv) + 3 SeOCl2,

where Nd is in fact the solvated ion with several selenium oxychloride molecules coordinated in the first coordination sphere, that is . 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.

Catalysis

Another important application of NdCl3 is in catalysis—in 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 coprecipitation–peptization method by ammonium hydroxide from mixture of TiCl4 and NdCl3 in aqueous solution). This process is used commercially on large scale on 1000 liter reactor for using in photocatalytic self-cleaning paints.

Corrosion protection

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 NdCl3 for a week or by electrolytic deposition using the same solution. In comparison with traditional chromium based corrosion inhibitors, NdCl3 and other rare-earth salts are environment friendly and much less toxic to humans and animals.

The protective action of NdCl3 on aluminium alloys is based on formation of insoluble neodymium hydroxide. Being a chloride, NdCl3 itself is a corrosive agent, which is sometimes used for corrosion testing of ceramics.

Labeling of organic molecules

Lanthanides, including neodymium are famous for their bright luminescence and therefore are widely used as fluorescent labels. In particular, NdCl3 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.

Health issues

Neodymium(III) chloride does not seem toxic to humans and animals (approximately similar to table salt). The LD50 (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 LD50 above 2 g/kg are considered non-toxic.

See also

References

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Neodymium compounds
Nd(II)
Nd(III)
Nd(IV)
Salts and covalent derivatives of the chloride ion
HCl He
LiCl BeCl2 B4Cl4
B12Cl12
BCl3
B2Cl4
+BO3
C2Cl2
C2Cl4
C2Cl6
CCl4
+C
+CO3
NCl3
ClN3
+N
+NO3
ClxOy
Cl2O
Cl2O2
ClO
ClO2
Cl2O4
Cl2O6
Cl2O7
ClO4
+O
ClF
ClF3
ClF5
Ne
NaCl MgCl2 AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2 Ar
KCl CaCl
CaCl2
ScCl3 TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2 CuCl
CuCl2
ZnCl2 GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrCl Kr
RbCl SrCl2 YCl3 ZrCl2
ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3 PdCl2 AgCl CdCl2 InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsCl BaCl2 * LuCl3 HfCl4 TaCl3
TaCl4
TaCl5
WCl2
WCl3
WCl4
WCl5
WCl6
ReCl3
ReCl4
ReCl5
ReCl6
OsCl2
OsCl3
OsCl4
OsCl5
IrCl2
IrCl3
IrCl4
PtCl2
PtCl4
AuCl
(Au)2
AuCl3
Hg2Cl2
HgCl2
TlCl
TlCl3
PbCl2
PbCl4
BiCl3 PoCl2
PoCl4
AtCl Rn
FrCl RaCl2 ** LrCl3 RfCl4 DbCl5 SgO2Cl2 BhO3Cl Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* LaCl3 CeCl3 PrCl3 NdCl2
NdCl3
PmCl3 SmCl2
SmCl3
EuCl2
EuCl3
GdCl3 TbCl3 DyCl2
DyCl3
HoCl3 ErCl3 TmCl2
TmCl3
YbCl2
YbCl3
** AcCl3 ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3 PuCl3 AmCl2
AmCl3
CmCl3 BkCl3 CfCl3
CfCl2
EsCl2
EsCl3
FmCl2 MdCl2 NoCl2
Lanthanide salts of halides
La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
+4 CeF4 PrF4 NdF4 TbF4 DyF4
+3 LaF3
LaCl3
LaBr3
LaI3
CeF3
CeCl3
CeBr3
CeI3
PrF3
PrCl3
PrBr3
PrI3
NdF3
NdCl3
NdBr3
NdI3
PmF3
PmCl3
PmBr3
PmI3
SmF3
SmCl3
SmBr3
SmI3
EuF3
EuCl3
EuBr3
EuI3
GdF3
GdCl3
GdBr3
GdI3
TbF3
TbCl3
TbBr3
TbI3
DyF3
DyCl3
DyBr3
DyI3
HoF3
HoCl3
HoBr3
HoI3
ErF3
ErCl3
ErBr3
ErI3
TmF3
TmCl3
TmBr3
TmI3
YbF3
YbCl3
YbBr3
YbI3
LuF3
LuCl3
LuBr3
LuI3
+2 LaI2 CeI2 PrI2 NdF2
NdCl2
NdBr2
NdI2
SmF2
SmCl2
SmBr2
SmI2
EuF2
EuCl2
EuBr2
EuI2
GdI2 DyF2
DyCl2
DyBr2
DyI2
TmF2
TmCl2
TmBr2
TmI2
YbF2
YbCl2
YbBr2
YbI2
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