Uranium tetrachloride

Uranium tetrachloride

Names
IUPAC name Uranium(IV) chloride
Other names Tetrachlorouranium Uranium tetrachloride Uranous chloride
Identifiers
CAS Number	10026-10-5 Y
3D model (JSmol)	Interactive image
ChemSpider	19969614 Y
ECHA InfoCard	100.030.040
EC Number	233-057-7
PubChem CID	66210
UNII	8E7IB152RL Y
CompTox Dashboard (EPA)	DTXSID1064906
InChI InChI=1S/4ClH.2U/h4*1H;;/q;;;;2*+2/p-4 Y Key: AYQSGSWJZFIBLR-UHFFFAOYSA-J Y InChI=1/4ClH.2U/h4*1H;;/q;;;;2*+2/p-4 Key: AYQSGSWJZFIBLR-XBHQNQODAS
SMILES [U+4].[Cl-].[Cl-].[Cl-].[Cl-]
Properties
Chemical formula	UCl4
Molar mass	379.84 g/mol
Appearance	olive green solid
Density	4.87 g/cm3
Melting point	590 °C (1,094 °F; 863 K)
Boiling point	791 °C (1,456 °F; 1,064 K)
Solubility in water	Hydrolysis
Solubility	Soluble in hydrochloric acid
Structure
Crystal structure	Octahedral
Related compounds
Related compounds	uranium trichloride, uranium pentachloride, uranium hexachloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Uranium tetrachloride is an inorganic compound, a salt of uranium and chlorine, with the formula UCl₄. It is a hygroscopic olive-green solid. It was used in the electromagnetic isotope separation (EMIS) process of uranium enrichment. It is one of the main starting materials for organouranium chemistry.

Synthesis and structure

Uranium tetrachloride is synthesised generally by the reaction of uranium trioxide (UO₃) and hexachloropropene. Solvent UCl₄ adducts can be formed by a simpler reaction of UI₄ with hydrogen chloride in organic solvents.

Uranium tetrachloride also forms the nonahydrate, which can be produced by evaporating a mildly acidic solution of UCl₄.^[1]

According to X-ray crystallography the uranium centers are eight-coordinate, being surrounded by eight chlorine atoms, four at 264 pm and the other four at 287pm.^[2]

Chemical properties

Dissolution in protic solvents is more complicated. When UCl₄ is added to water the uranium aqua ion is formed.

UCl₄ + xH₂O → [U(H₂O)_x]⁴⁺ + 4Cl⁻

The aqua ion [U(H₂O)_x]⁴⁺, (x is 8 or 9^[3]) is strongly hydrolyzed.

[U(H₂O)_x]⁴⁺ ⇌ [U(H₂O)_x−1(OH)]³⁺ + H⁺

The pK_a for this reaction is ca. 1.6,^[4] so hydrolysis is absent only in solutions of acid strength 1 mol dm⁻³ or stronger (pH < 0). Further hydrolysis occurs at pH > 3. Weak chloro complexes of the aqua ion may be formed. Published estimates of the log K value for the formation of [UCl]³⁺(aq) vary from −0.5 to +3 because of difficulty in dealing with simultaneous hydrolysis.^[4]

With alcohols, partial solvolysis may occur.

UCl₄ + xROH ⇌ UCl_4−x(OR)_x + xHCl

Uranium tetrachloride dissolves in non-protic solvents such as tetrahydrofuran, acetonitrile, dimethyl formamide etc. that can act as Lewis bases. Solvates of formula UCl₄L_x are formed which may be isolated. The solvent must be completely free of dissolved water, or hydrolysis will occur, with the solvent, S, picking up the released proton.

UCl₄ + H₂O + S ⇌ UCl₃(OH) + SH⁺ +Cl⁻

The solvent molecules may be replaced by other ligand in a reaction such as

UCl₄ + 2Cl⁻ → [UCl₆]²⁻.

The solvent is not shown, just as when complexes of other metal ions are formed in aqueous solution.

Solutions of UCl₄ are susceptible to oxidation by air, resulting in the production of complexes of the uranyl ion.

Applications

Uranium tetrachloride is produced commercially by the reaction of carbon tetrachloride with pure uranium dioxide UO₂ at 370 °C. It has been used as feed in the electromagnetic isotope separation (EMIS) process of uranium enrichment. Beginning in 1944, the Oak Ridge Y-12 Plant converted UO₃ to UCl₄ feed for the Ernest O. Lawrence's Alpha Calutrons. Its major benefit being the uranium tetrachloride used in the calutrons is not as corrosive as the uranium hexafluoride used in most other enrichment technologies This process was abandoned in the 1950s. In the 1980s, however, Iraq unexpectedly revived this option as part of its nuclear weapons program. In the enrichment process, uranium tetrachloride is ionized into a uranium plasma.

The uranium ions are then accelerated and passed through a strong magnetic field. After traveling along half of a circle, the beam is split into a region nearer the outside wall, which is depleted, and a region nearer the inside wall, which is enriched in ²³⁵U. The large amounts of energy required in maintaining the strong magnetic fields as well as the low recovery rates of the uranium feed material and slower more inconvenient facility operation make this an unlikely choice for large scale enrichment plants.

Work is being done in the use of molten uranium chloride–alkali chloride mixtures as reactor fuels in molten salt reactors. Uranium tetrachloride melts dissolved in a lithium chloride–potassium chloride eutectic have also been explored as a means to recover actinides from irradiated nuclear fuels through pyrochemical nuclear reprocessing.^[5]

Safety

Like all water soluble uranium salts, uranium tetrachloride is nephrotoxic (poisonous to the kidney) and can cause severe renal damage and acute renal failure if ingested.

References