Names | |
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IUPAC name
Silver(I) sulfate | |
Other names
Disilver sulfate Argentous sulfate | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.030.581 |
EC Number |
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PubChem CID |
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UNII | |
UN number | 3077 |
CompTox Dashboard (EPA) |
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Properties | |
Ag2SO4 | |
Molar mass | 311.79 g·mol−1 |
Appearance | Colorless solid |
Odor | Odorless |
Density | 5.45 g/cm3 (25 °C) 4.84 g/cm3 (660 °C)[1] |
Melting point | 652.2–660 °C (1,206.0–1,220.0 °F; 925.4–933.1 K)[1][2] |
Boiling point | 1,085 °C (1,985 °F; 1,358 K)[3][2] decomposition |
0.57 g/100 mL (0 °C) 0.69 g/100 mL (10 °C) 0.83 g/100 mL (25 °C) 0.96 g/100 mL (40 °C) 1.33 g/100 mL (100 °C)[4] | |
Solubility product (Ksp) |
1.2·10−5[1] |
Solubility | Dissolves in aq. acids, alcohols, acetone, ether, acetates, amides[4] Insoluble in ethanol[3] |
Solubility in sulfuric acid | 8.4498 g/L (0.1 molH2SO4/LH2O)[4] 25.44 g/100 g (13 °C) 31.56 g/100 g (24.5 °C) 127.01 g/100 g (96 °C)[3] |
Solubility in ethanol | 7.109 g/L (0.5 nEtOH/H2O)[4] |
Solubility in acetic acid | 7.857 g/L (0.5 nAcOH/H2O)[4] |
−9.29·10−5 cm3/mol[1] | |
Refractive index (nD) |
nα = 1.756 nβ = 1.775 nγ = 1.782[5] |
Structure | |
Orthorhombic, oF56[5] | |
Fddd, No. 70[5] | |
2/m 2/m 2/m[5] | |
α = 90°, β = 90°, γ = 90° | |
Thermochemistry | |
Heat capacity (C) |
131.4 J/mol·K[1] |
Std molar entropy (S⦵298) |
200.4 J/mol·K [1] |
Std enthalpy of formation (ΔfH⦵298) |
−715.9 kJ/mol[1] |
Gibbs free energy (ΔfG⦵) |
−618.4 kJ/mol [1] |
Hazards | |
GHS labelling: | |
[6] | |
Danger | |
H318, H410[6] | |
P273, P280, P305+P351+P338, P501[6] | |
NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Silver sulfate is the inorganic compound with the formula Ag2SO4. It is a white solid with low solubility in water.
Preparation and structure
Silver sulfate precipitates as a solid when an aqueous solution of silver nitrate is treated with sulfuric acid:
- 2 AgNO3 + H2SO4 → Ag2SO4 + 2 HNO3
It is purified by recrystallization from concentrated sulfuric acid, a step that expels traces of nitrate.[7] Silver sulfate and anhydrous sodium sulfate adopt the same structure.[8]
Silver(II) sulfate
The synthesis of silver(II) sulfate (AgSO4) with a divalent silver ion instead of a monovalent silver ion was first reported in 2010[9] by adding sulfuric acid to silver(II) fluoride (HF escapes). It is a black solid that decomposes exothermically at 120 °C with evolution of oxygen and the formation of the pyrosulfate.
AgF2 + H2SO4 → AgSO4 + 2 HF
4 AgSO4 → 2 Ag2S2O7 + O2
References
- 1 2 3 4 5 6 7 8 Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0.
- 1 2 3 "MSDS of Silver sulfate". Fisher Scientific, Inc. Retrieved 2014-07-19.
- 1 2 3 Anatolievich, Kiper Ruslan. "silver sulfate". Retrieved 2014-07-19.
- 1 2 3 4 5 Seidell, Atherton; Linke, William F. (1919). Solubilities of Inorganic and Organic Compounds (2nd ed.). New York: D. Van Nostrand Company. pp. 622–623.
- 1 2 3 4 5 Morris, Marlene C.; McMurdie, Howard F.; Evans, Eloise H.; Paretzkin, Boris; Groot, Johan H. de; Hubbard, Camden R.; Carmel, Simon J. (June 1976). "13". Standard X-ray Diffraction Powder Patterns. Vol. 25. Washington: Institute for Materials Research National Bureau of Standards.
- 1 2 3 Sigma-Aldrich Co., Silver sulfate. Retrieved on 2014-07-19.
- ↑ O. Glemser; R. Sauer (1963). "Silver Sulfate". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 2pages=1042. NY, NY: Academic Press.
- ↑ Zachariasen, W. H. (1932). "Note on the Crystal Structure of Silver Sulphate, Ag2SO4". Zeitschrift für Kristallographie - Crystalline Materials. 82 (1–6): 161–162. doi:10.1524/zkri.1932.82.1.161. S2CID 101362527.
- ↑ Malinowski, P.; Derzsi, M.; Mazej, Z.; Jagličić, Z.; Gaweł, B.; Lasocha, W.; Grochala, W. (2010). "Ag(II)SO(4): A Genuine Sulfate of Divalent Silver with Anomalously Strong One-Dimensional Antiferromagnetic Interactions". Angewandte Chemie International Edition in English. 49 (9): 1683–1686. doi:10.1002/anie.200906863. PMID 20084660.