Thorium(IV) nitrate explained

Thorium(IV) nitrate is a chemical compound, a salt of thorium and nitric acid with the formula Th(NO3)4. A white solid in its anhydrous form, it can form tetra- and pentahydrates. As a salt of thorium it is weakly radioactive.

Preparation

Thorium(IV) nitrate hydrate can be prepared by the reaction of thorium(IV) hydroxide and nitric acid:

Different hydrates are produced by crystallizing in different conditions. When a solution is very dilute, the nitrate is hydrolysed. Although various hydrates have been reported over the years, and some suppliers even claim to stock them, only the tetrahydrate and pentahydrate actually exist. What is called a hexahydrate, crystallized from a neutral solution, is probably a basic salt.[1]

The pentahydrate is the most common form. It is crystallized from dilute nitric acid solution.[2]

The tetrahydrate, Th(NO3)4•4H2O is formed by crystallizing from a stronger nitric acid solution. Concentrations of nitric acid from 4 to 59% result in the tetrahydrate forming.[3] The thorium atom has 12-coordination, with four bidentate nitrate groups and four water molecules attached to each thorium atom.[1]

To obtain the anhydrous thorium(IV) nitrate, thermal decomposition of Th(NO3)4·2N2O5 is required. The decomposition occurs at 150-160 °C.[4]

Properties

Anhydrous thorium nitrate is a white substance. It is covalently bound with low melting point of 55 °C.[3]

The pentahydrate Th(NO3)4•5H2O crystallizes with clear colourless crystals[5] in the orthorhombic system. The unit cell size is a=11.191 b=22.889 c=10.579 Å. Each thorium atom is connected twice to each of four bidentate nitrate groups, and to three water molecules via their oxygen atoms. In total the thorium is eleven-coordinated. There are also two other water molecules in the crystal structure. The water is hydrogen bonded to other water, or to nitrate groups.[6] The density is 2.80 g/cm3.[2] Vapour pressure of the pentahydrate at 298K is 0.7 torr, and increases to 1.2 torr at 315K, and at 341K it is up to 10.7 torr. At 298.15K the heat capacity is about 114.92 calK−1mol−1. This heat capacity shrinks greatly at cryogenic temperatures. Entropy of formation of thorium nitrate pentahydrate at 298.15K is −547.0 calK−1mol−1. The standard Gibbs energy of formation is −556.1 kcalmol−1.[7]

Thorium nitrate can dissolve in several different organic solvents[6] including alcohols, ketones, esters and ethers.[1] This can be used to separate different metals such as the lanthanides. With ammonium nitrate in the aqueous phase, thorium nitrate prefers the organic liquid, and the lanthanides stay with the water.[1]

Thorium nitrate dissolved in water lowers it freezing point. The maximum freezing point depression is −37 °C with a concentration of 2.9 mol/kg.[8]

At 25° a saturated solution of thorium nitrate contains 4.013 moles per liter. At this concentration the vapour pressure of water in the solution is 1745.2 Pascals, compared to 3167.2 Pa for pure water.[9]

Reactions

When thorium nitrate pentahydrate is heated, nitrates with less water are produced, however the compounds also lose some nitrate. At 140 °C a basic nitrate, ThO(NO3)2 is produced. When strongly heated thorium dioxide is produced.[6]

A polymeric peroxynitrate is precipitated when hydrogen peroxide combines with thorium nitrate in solution with dilute nitric acid. Its formula is Th6(OO)10(NO3)4 •10H2O.[6]

The hydrolysis of thorium nitrate solutions produces basic nitrates Th2(OH)4(NO3)4•H2O and Th2(OH)2(NO3)6•8H2O. In crystals of Th2(OH)2(NO3).6•8H2O a pair of thorium atoms are connected by two bridging oxygen atoms. Each thorium atom is surrounded by three bidentate nitrate groups and three water molecules, bringing the coordination number to 11.[6]

When oxalic acid is added to a thorium nitrate solution, insoluble thorium oxalate precipitates.[10] Other organic acids added to thorium nitrate solution produce precipitates of organic salts with citric acid; basic salts, such as tartaric acid, adipic acid, malic acid, gluconic acid, phenylacetic acid, valeric acid.[11] Other precipitates are also formed from sebacic acid and azelaic acid

Double salts

Hexanitratothorates with the generic formula M2Th(NO3)6 or MTh(NO3)6•8H2O are made by mixing other metal nitrates with thorium nitrate in dilute nitric acid solution. M can be Mg, Mn, Co, Ni, or Zn. M can be Cs, (NO)+ or (NO2)+.[6] Crystals the divalent metal thorium hexanitrate octahydrate have a monoclinic form with similar unit cell dimensions: β=97°, a=9.08 b=8.75-8 c=12.61-3.[12] Pentanitratothorates with the generic formula MTh(NO3)5•H2O are known for M being Na or K.[6]

K3Th(NO3)7 and K3H3Th(NO3)10•4H2O are also known.[1]

Complexed salts

Thorium nitrate also crystallizes with other ligands and organic solvates including ethylene glycol diethyl ether, tri(n‐butyl)phosphate, butylamine, dimethylamine, and trimethylphosphine oxide.[1]

Notes

1. Bogus hydrates include 12, 6, 5.5, 2 and 1 water molecules

Notes and References

  1. Book: Katz. Joseph j.. Seaborg. Glenn t.. The Chemistry of the Actinide and Lanthanide Elements. 2008. Springer. 978-1-4020-3598-2. 106–108. Thorium.
  2. Book: Herrmann. W. A.. Edelmann. Frank T.. Poremba. Peter. Synthetic Methods of Organometallic and Inorganic Chemistry, Volume 6, 1997: Volume 6: Lanthanides and Actinides. 1999. Georg Thieme Verlag. 9783131794611. 210. de.
  3. Book: Benz. R.. Naoumidis. A.. Brown. D.. Th Thorium: Supplement Volume C 3 Compounds with Nitrogen. Springer Science & Business Media. 9783662063309. 70–79. en. 2013-11-11.
  4. JR Ferraro, LI Katzin, G Gibson. The Reaction of Thorium Nitrate Tetrahydrate with Nitrogen Oxides. Anhydrous Thorium Nitrate. Journal of the American Chemical Society, 1955, 77(2):327-329
  5. Ueki. T.. Zalkin. A.. Templeton. D. H.. Crystal structure of thorium nitrate pentahydrate by X-ray diffraction. Acta Crystallographica. 1 November 1966. 20. 6. 836–841. 10.1107/S0365110X66001944. 96633729 . free. 1966AcCry..20..836U .
  6. Book: Brown. D.. Bailar. J.C.. Comprehensive inorganic chemistry. 1973. Pergamon Press. Oxford [u.a.]. 008017275X. 286–292. 1.. Carbonates, nitrates, sulphates, sulfites, selenates, selenites, tellurates and tellurites.
  7. Cheda. J.A.R.. Westrum. Edgar F.. Morss. Lester R.. Heat capacity of Th(NO3)4·5H2O from 5 to 350 K. The Journal of Chemical Thermodynamics. January 1976. 8. 1. 25–29. 10.1016/0021-9614(76)90146-4. 2027.42/21859. free.
  8. Apelblat. Alexander. Azoulay. David. Sahar. Ayala. Properties of aqueous thorium nitrate solutions. Part 1.—Densities, viscosities, conductivities, pH, solubility and activities at freezing point. Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases. 1973. 69. 1618. 10.1039/F19736901618.
  9. Kalinkin. A. M.. Calculation of Phase Equilibria in the Th(NO3)4-HNO3-H2O System at 25°C. Radiochemistry. 2001. 43. 6. 553–557. 10.1023/A:1014847506077. 92858856.
  10. Book: Bagnall. Kenneth W.. Th Thorium: Compounds with Carbon: Carbonates, Thiocyanates, Alkoxides, Carboxylates. Springer Science & Business Media. 9783662063156. 82. en. 2013-12-12.
  11. Book: Bagnall. Kenneth W.. Th Thorium: Compounds with Carbon: Carbonates, Thiocyanates, Alkoxides, Carboxylates. Springer Science & Business Media. 9783662063156. 66,73,74,105,107,113,122. en. 2013-12-12.
  12. Šćavničar. S.. Prodić. B.. The crystal structure of double nitrate octahydrates of thorium and bivalent metals. Acta Crystallographica. 1 April 1965. 18. 4. 698–702. 10.1107/S0365110X65001603. free. 1965AcCry..18..698S .