Praseodymium(III) sulfate

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Praseodymium(III) sulfate
Praseodymium sulphate octahydrate crystals.JPG
Praseodymium sulfate octahydrate
Names
IUPAC name
praseodymium(3+); trisulfate
Other names
Praseodymium sulphate, dipraseodymium trisulphate, praseodymium(III) sulfate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.553 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 233-622-8
PubChem CID
  • 165851

  • 25022097 (octahydrate)
  • InChI=1S/3H2O4S.2Pr/c3*1-5(2,3)4;;/h3*(H2,1,2,3,4);;/q;;;2*+3/p-6
    Key: HWZAHTVZMSRSJE-UHFFFAOYSA-H
  • InChI=1S/3H2O4S.8H2O.2Pr/c3*1-5(2,3)4;;;;;;;;;;/h3*(H2,1,2,3, 4);8*1H2;;/q;;;;;;;;;;;2*+3/p-6 (octahydrate)
    Key: IJXLQIGVGZNKP-UHFFFAOYSA-H (octahyrate)
  • [O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[Pr+3].[Pr+3]

  • O.O.O.O.O.O.O.O.[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-]. [Pr+3].[Pr+3] (octahyrate)
Properties
Pr2(SO4)3
Pr2(SO4)3·nH2O, n=2,5,8
Molar mass 570.0031 g/mol
714.12534 g/mol (octahydrate)
Appearancegreen 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
GHS labelling: [2]
GHS-pictogram-exclam.svg
Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
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).
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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]

Contents

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. [3]

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. [3]

Related Research Articles

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Magnesium sulfate or Magnesium sulphate is a chemical compound, a salt with the formula MgSO4, consisting of magnesium cations Mg2+ (20.19% by mass) and sulfate anions SO2−4. It is a white crystalline solid, soluble in water but not in ethanol.

<span class="mw-page-title-main">Praseodymium</span> Chemical element, symbol Pr and atomic number 59

Praseodymium is a chemical element; it has symbol Pr and the atomic number 59. It is the third member of the lanthanide series and is considered one of the rare-earth metals. It is a soft, silvery, malleable and ductile metal, valued for its magnetic, electrical, chemical, and optical properties. It is too reactive to be found in native form, and pure praseodymium metal slowly develops a green oxide coating when exposed to air.

<span class="mw-page-title-main">Copper(II) sulfate</span> Chemical compound

Copper(II) sulfate, also known as copper sulphate, is an inorganic compound with the chemical formula CuSO4. It forms hydrates CuSO4·nH2O, where n can range from 1 to 7. The pentahydrate (n = 5), a bright blue crystal, is the most commonly encountered hydrate of copper(II) sulfate. Older names for the pentahydrate include blue vitriol, bluestone, vitriol of copper, and Roman vitriol. It exothermically dissolves in water to give the aquo complex [Cu(H2O)6]2+, which has octahedral molecular geometry. The structure of the solid pentahydrate reveals a polymeric structure wherein copper is again octahedral but bound to four water ligands. The Cu(II)(H2O)4 centers are interconnected by sulfate anions to form chains. Anhydrous copper sulfate is a light grey powder.

In chemistry, water(s) of crystallization or water(s) of hydration are water molecules that are present inside crystals. Water is often incorporated in the formation of crystals from aqueous solutions. In some contexts, water of crystallization is the total mass of water in a substance at a given temperature and is mostly present in a definite (stoichiometric) ratio. Classically, "water of crystallization" refers to water that is found in the crystalline framework of a metal complex or a salt, which is not directly bonded to the metal cation.

<span class="mw-page-title-main">Vanadyl sulfate</span> Chemical compound

Vanadyl(IV) sulfate describes a collection of inorganic compounds of vanadium with the formula, VOSO4(H2O)x where 0 ≤ x ≤ 6. The pentahydrate is common. This hygroscopic blue solid is one of the most common sources of vanadium in the laboratory, reflecting its high stability. It features the vanadyl ion, VO2+, which has been called the "most stable diatomic ion".

Indium(III) sulfate (In2(SO4)3) is a sulfate salt of the metal indium. It is a sesquisulfate, meaning that the sulfate group occurs 11/2 times as much as the metal. It may be formed by the reaction of indium, its oxide, or its carbonate with sulfuric acid. An excess of strong acid is required, otherwise insoluble basic salts are formed. As a solid indium sulfate can be anhydrous, or take the form of a pentahydrate with five water molecules or a nonahydrate with nine molecules of water. Indium sulfate is used in the production of indium or indium containing substances. Indium sulfate also can be found in basic salts, acidic salts or double salts including indium alum.

<span class="mw-page-title-main">Nickel(II) sulfate</span> Chemical compound

Nickel(II) sulfate, or just nickel sulfate, usually refers to the inorganic compound with the formula NiSO4(H2O)6. This highly soluble blue green coloured salt is a common source of the Ni2+ ion for electroplating.

<span class="mw-page-title-main">Manganese(II) sulfate</span> Chemical compound

Manganese(II) sulfate usually refers to the inorganic compound with the formula MnSO4·H2O. This pale pink deliquescent solid is a commercially significant manganese(II) salt. Approximately 260,000 tonnes of manganese(II) sulfate were produced worldwide in 2005. It is the precursor to manganese metal and many other chemical compounds. Manganese-deficient soil is remediated with this salt.

<span class="mw-page-title-main">Zirconium(IV) sulfate</span> Chemical compound

Zirconium(IV) sulfate is the name for a family of inorganic salts with the formula Zr(SO4)2(H2O)n where n = 0, 4, 5, 7. These species are related by the degree of hydration. They are white or colourless solids that are soluble in water.

<span class="mw-page-title-main">Chromium(II) sulfate</span> Chemical compound

Chromium(II) sulfate refers to inorganic compounds with the chemical formula CrSO4·n H2O. Several closely related hydrated salts are known. The pentahydrate is a blue solid that dissolves readily in water. Solutions of chromium(II) are easily oxidized by air to Cr(III) species. Solutions of Cr(II) are used as specialized reducing agents of value in organic synthesis.

Copper(I) sulfate, also known as cuprous sulfate, is an inorganic compound with the chemical formula Cu2SO4. It is a white solid, in contrast to copper(II) sulfate, which is blue in hydrous form. Compared to the commonly available reagent, copper(II) sulfate, copper(I) sulfate is unstable and not readily available.

<span class="mw-page-title-main">Cerium(III) sulfate</span> Chemical compound

Cerium(III) sulfate, also called cerous sulfate, is an inorganic compound with the formula Ce2(SO4)3. It is one of the few salts whose solubility in water decreases with rising temperature.

Langbeinites are a family of crystalline substances based on the structure of langbeinite with general formula M2M'2(SO4)3, where M is a large univalent cation, and M' is a small divalent cation. The sulfate group, SO2−4, can be substituted by other tetrahedral anions with a double negative charge such as tetrafluoroberyllate, selenate, chromate, molybdate, or tungstates. Although monofluorophosphates are predicted, they have not been described. By redistributing charges other anions with the same shape such as phosphate also form langbeinite structures. In these the M' atom must have a greater charge to balance the extra three negative charges.

Yttrium(III) sulfate is an inorganic compound with the formula Y2(SO4)3. The most common form is the anhydrate and octahydrate.

A sulfite sulfate is a chemical compound that contains both sulfite and sulfate anions [SO3]2− [SO4]2−. These compounds were discovered in the 1980s as calcium and rare earth element salts. Minerals in this class were later discovered. Minerals may have sulfite as an essential component, or have it substituted for another anion as in alloriite. The related ions [O3SOSO2]2− and [(O2SO)2SO2]2− may be produced in a reaction between sulfur dioxide and sulfate and exist in the solid form as tetramethyl ammonium salts. They have a significant partial pressure of sulfur dioxide.

<span class="mw-page-title-main">Neodymium(III) sulfate</span> Chemical compound

Neodymium(III) sulfate is a salt of the rare-earth metal neodymium that has the formula Nd2(SO4)3. It forms multiple hydrates, the octa-, penta-, and the dihydrate, which the octahydrate is the most common. This compound has a retrograde solubility, unlike other compounds, its solubility decreases with increasing temperature. This compound is used in glass for extremely powerful lasers.

Praseodymium(III) carbonate is an inorganic compound, with a chemical formula of Pr2(CO3)3. The anhydrous form is olive green, and many of its hydrates such as heptahydrate and octahydrate are known. They are all insoluble in water.

<span class="mw-page-title-main">Terbium compounds</span> Chemical compounds with at least one terbium atom

Terbium compounds are compounds formed by the lanthanide metal terbium (Tb). Terbium generally exhibits the +3 oxidation state in these compounds, such as in TbCl3, Tb(NO3)3 and Tb(CH3COO)3. Compounds with terbium in the +4 oxidation state are also known, such as TbO2 and BaTbF6. Terbium can also form compounds in the 0, +1 and +2 oxidation states.

Promethium compounds are compounds containing the element promethium, which normally take the +3 oxidation state. Promethium belongs to the cerium group of lanthanides and is chemically very similar to the neighboring elements. Because of its instability, chemical studies of promethium are incomplete. Even though a few compounds have been synthesized, they are not fully studied; in general, they tend to be pink or red in color. Treatment of acidic solutions containing Pm3+ ions with ammonia results in a gelatinous light-brown sediment of hydroxide, Pm(OH)3, which is insoluble in water. When dissolved in hydrochloric acid, a water-soluble yellow salt, PmCl3, is produced; similarly, when dissolved in nitric acid, a nitrate results, Pm(NO3)3. The latter is also well-soluble; when dried, it forms pink crystals, similar to Nd(NO3)3. The electron configuration for Pm3+ is [Xe] 4f4, and the color of the ion is pink. The ground state term symbol is 5I4. The sulfate is slightly soluble, like the other cerium group sulfates. Cell parameters have been calculated for its octahydrate; they lead to conclusion that the density of Pm2(SO4)3·8 H2O is 2.86 g/cm3. The oxalate, Pm2(C2O4)3·10 H2O, has the lowest solubility of all lanthanide oxalates.

Praseodymium(III) selenate is an inorganic compound, the salt of praseodymium and selenic acid with the chemical formula Pr2(SeO4)3. It forms green crystals when hydrated.

References

  1. 1 2 3 4 National Research Council (U.S.) (1919). Bulletin of the National Research Council. National Academies. pp.  3–. NAP:12020. Retrieved 14 November 2011.
  2. "Dipraseodymium trisulphate". pubchem.ncbi.nlm.nih.gov. Retrieved 27 December 2021.
  3. 1 2 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. doi: 10.1524/ncrs.2002.217.jg.299 . S2CID   201278521. PDF copy