Praseodymium(III) sulfate
Praseodymium sulfate octahydrate | |
Names | |
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Other names
Praseodymium sulphate, dipraseodymium trisulphate, praseodymium(III) sulfate | |
Identifiers | |
13510-41-3 10277-44-8 (octahydrate) | |
ChemSpider | 145346 |
EC number | 233-622-8 |
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Jmol-3D images | Image |
PubChem | 165851 25022097 (octahydrate) |
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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) | |
Hazards | |
Main hazards | Xi |
EU Index | 233-622-8 |
R-phrases | 36/37/38 |
S-phrases | 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 noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
Infobox references | |
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]
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
- ↑ 1.0 1.1 1.2 1.3 National Research Council (U.S.) (1919). Bulletin of the National Research Council. National Academies. pp. 3–. NAP:12020. Retrieved 14 November 2011.
- ↑ 2.0 2.1 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
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Salts and the ester of the Sulfate ion | |||||||||||||||||||
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H2SO4 | He | ||||||||||||||||||
Li2SO4 | BeSO4 | B | (RO)2SO3 | (NH4)2SO4 N2H6SO4 (NH3OH)2SO4 |
O | F | Ne | ||||||||||||
Na2SO4 NaHSO4 |
MgSO4 | Al2(SO4)3 | Si | P | SO42− | Cl | Ar | ||||||||||||
K2SO4 KHSO4 |
CaSO4 | Sc2(SO4)3 | Ti(SO4)2 | V2(SO4)3 VOSO4 |
CrSO4 Cr2(SO4)3 |
MnSO4 | FeSO4 Fe2(SO4)3 |
CoSO4, Co2(SO4)3 |
NiSO4 | CuSO4 | ZnSO4 | Ga2(SO4)3 | Ge | As | Se | Br | Kr | ||
Rb2SO4 | SrSO4 | Y | Zr(SO4)2 | Nb | Mo | Tc | Ru | Rh | PdSO4 | Ag2SO4 | CdSO4 | In2(SO4)3 | SnSO4 | Sb2(SO4)3 | Te | I | Xe | ||
Cs2SO4 | BaSO4 | Hf | Ta | W | Re | Os | Ir | Pt | Au | Hg2SO4, HgSO4 |
Tl2SO4 | PbSO4 | Bi2(SO4)3 | Po | At | Rn | |||
Fr | Ra | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Uut | Fl | Uup | Lv | Uus | Uuo | |||
↓ | |||||||||||||||||||
La | Ce2(SO4)3 Ce(SO4)2 |
Pr2(SO4)3 | Nd | Pm | Sm | Eu | Gd | Tb | Dy | Ho | Er | Tm | Yb2(SO4)3 | Lu | |||||
Ac | Th | Pa | U(SO4)2 UO2SO4 |
Np | Pu | Am | Cm | Bk | Cf | Es | Fm | Md | No | Lr |