Cerium(IV) sulfate
Names | |
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Other names
Ceric sulfate | |
Identifiers | |
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3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.033.648 |
PubChem CID |
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UNII | |
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Properties | |
Ce(SO4)2 | |
Molar mass | 332.24 g/mol (anhydrous) 404.304 (tetrahydrate) |
Appearance | Yellow solid (anhydrous) yellow-orange crystals (tetrahydrate) |
Density | 3.91 g/cm3 (tetrahydrate) |
Melting point | 350 °C (662 °F; 623 K) (decomposes) |
Boiling point | NA |
Soluble in small amounts, hydrolyzes in large amounts of water 21.4 g/100 mL (0 °C) 9.84 g/100 mL (20 °C) 3.87 g/100 mL (60 °C)[1] | |
Solubility | soluble in dilute sulfuric acid |
+37.0·10−6 cm3/mol | |
Structure | |
orthorhombic | |
Hazards | |
Main hazards | Oxidizer |
Safety data sheet | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Cerium(IV) sulfate, also called ceric sulfate, is an inorganic compound. It exists as the anhydrous salt Ce(SO4)2 as well as a few hydrated forms: Ce(SO4)2(H2O)x, with x equal to 4, 8, or 12. These salts are yellow to yellow/orange solids that are moderately soluble in water and dilute acids. Its neutral solutions slowly decompose, depositing the light yellow oxide CeO2. Solutions of ceric sulfate have a strong yellow color. The tetrahydrate loses water when heated to 180-200 °C.
Uses
The ceric ion is a strong oxidizer, especially under acidic conditions. If ceric sulfate is added to dilute hydrochloric acid, then elemental chlorine is formed, albeit slowly. With stronger reducing agents it reacts much faster. For example, with sulfite in acidic environments it reacts quickly and completely.
When ceric compounds are reduced, so-called cerous compounds are formed. The reaction taking place is:
- Ce4+ + e− → Ce3+
The cerous ion is colorless.
Ceric sulfate is used in analytical chemistry for redox titration, often together with a redox indicator.
A related compound is ceric ammonium sulfate.[2]
The solubility of Ce(IV) in methanesulfonic acid is approximately 10 times the value obtainable in acidic sulphate solutions.[3]
References
- ↑ Lide, David R., ed. (2006). CRC Handbook of Chemistry and Physics (87th ed.). Boca Raton, FL: CRC Press. ISBN 0-8493-0487-3.
- ↑ Mariappan Periasamy, Ukkiramapandian Radhakrishnan "Cerium(IV) Ammonium Sulfate" Encyclopedia of Reagents for Organic Synthesis, 2001, John Wiley & Sons. doi:10.1002/047084289X.rc040
- ↑ Kreh, Robert P. (1989). "Mediated electrochemical synthesis of aromatic aldehydes, ketones, and quinones using ceric methanesulfonate". The Journal of Organic Chemistry. 54 (7): 1526–1531. doi:10.1021/jo00268a010.
Salts and esters of the sulfate ion | |||||||||||||||||||
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H2SO4 | He | ||||||||||||||||||
Li2SO4 | BeSO4 | B | esters ROSO3− (RO)2SO2 |
(NH4)2SO4 N2H6SO4 (NH3OH)2SO4 |
O | F | Ne | ||||||||||||
Na2SO4 NaHSO4 |
MgSO4 | Al2(SO4)3 Al2SO4(OAc)4 |
Si | P | SO42− | Cl | Ar | ||||||||||||
K2SO4 KHSO4 |
CaSO4 | Sc2(SO4)3 | Ti(SO4)2 TiOSO4 |
VSO4 V2(SO4)3 VOSO4 |
CrSO4 Cr2(SO4)3 |
MnSO4 Mn2(SO4)3 |
FeSO4 Fe2(SO4)3 |
CoSO4 Co2(SO4)3 |
NiSO4 | CuSO4 Cu2SO4 |
ZnSO4 | Ga2(SO4)3 | Ge | As | Se | Br | Kr | ||
RbHSO4 Rb2SO4 |
SrSO4 | Y2(SO4)3 | 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 Tl2(SO4)3 |
PbSO4 | Bi2(SO4)3 | Po | At | Rn | |||
Fr | Ra | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Nh | Fl | Mc | Lv | Ts | Og | |||
↓ | |||||||||||||||||||
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 |