Praseodymium(III) sulfate
Praseodymium(III) sulfate is a praseodymium compound with formula Pr2(SO4)3. It is an odourless whitish-green crystalline compound. The anhydrous substance readily absorbs water forming pentahydrate and octahydrate.[1]
Praseodymium sulfate octahydrate | |
Names | |
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IUPAC name
praseodymium(3+); trisulfate | |
Other names
Praseodymium sulphate, dipraseodymium trisulphate, praseodymium(III) sulfate | |
Identifiers | |
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ChemSpider | |
ECHA InfoCard | 100.030.553 |
EC Number |
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PubChem CID |
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Properties | |
Pr2(SO4)3 Pr2(SO4)3·nH2O, n=2,5,8 | |
Molar mass | 570.0031 g/mol 714.12534 g/mol (octahydrate) |
Appearance | green crystalline solid |
Density | 3.72 g/cm3[1] |
Melting point | 1,010 °C (1,850 °F; 1,280 K) (decomposes)[1] |
113.0 g/l (20 °C) 108.8 g/l (25 °C) | |
+9660·10−6 cm3/mol | |
Hazards | |
Main hazards | Xi |
R-phrases (outdated) | 36/37/38 |
S-phrases (outdated) | 26–36 |
Flash point | Non-flammable |
Related compounds | |
Other anions |
Praseodymium carbonate Praseodymium chloride |
Other cations |
Neodymium sulfate |
Related compounds |
Praseodymium(III) oxide Praseodymium(III) sulfide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Properties
Praseodymium sulfate is stable under standard conditions. At elevated temperatures, it gradually loses water and becomes more whitish. Like all rare earth sulfates, its solubility decreases with temperature, a property once used to separate it from other, non-rare earth compounds.
Pentahydrate and octahydrate have monoclinic crystal structures with densities of 3.713 and 2.813 g/cm3, respectively. The octahydrate crystals are optically biaxial, with refractive index components of nα = 1.5399, nβ = 1.5494 and nγ = 1.5607.[1] They belong to the space group C12/c1 (No. 15) and have lattice constants a = 1370.0(2) pm, b = 686.1(1) pm, c = 1845.3(2) pm, β = 102.80(1)° and Z = 4.[2]
Synthesis
Crystals of octahydrate can be grown from solution obtained by dissolving wet Pr2O3 powder with sulfuric acid. This procedure can be optimised by adding a few evaporation/dissolution steps involving organic chemicals.[2]
References
- National Research Council (U.S.) (1919). Bulletin of the National Research Council. National Academies. pp. 3–. NAP:12020. Retrieved 14 November 2011.
- Y.-Q. Zheng, Y.-J. Zhu and J.-L. Lin (2002). "Redeterminaton of the crystal structure of praseodymium sulfate octahydrate, Pr2(SO4)3·8H2O". Zeitschrift für Kristallographie – New Crystal Structures. 217: 299–300. PDF copy