Lead(II) fluoride is the inorganic compound with the formula PbF2. It is a white solid. The compound is polymorphic, at ambient temperatures it exists in orthorhombic (PbCl2 type) form, while at high temperatures it is cubic (Fluorite type).[2]
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Other names
Lead difluoride
plumbous fluoride | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.029.089 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
PbF2 | |
Molar mass | 245.20 g/mol |
Appearance | white powder |
Odor | odorless |
Density | 8.445 g/cm3 (orthorhombic) 7.750 g/cm3 (cubic) |
Melting point | 824 °C (1,515 °F; 1,097 K) |
Boiling point | 1,293 °C (2,359 °F; 1,566 K) |
0.057 g/100 mL (0 °C) 0.0671 g/100 mL (20 °C)[1] | |
Solubility product (Ksp)
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2.05 x 10−8 (20 °C) |
Solubility | soluble in nitric acid and hydrochloric acid; insoluble in acetone and ammonia |
−-58.1·10−6 cm3/mol | |
Structure | |
Fluorite (cubic), cF12 | |
Fm3m, No. 225 | |
Hazards | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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3031 mg/kg (oral, rat) |
Related compounds | |
Other anions
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Lead(II) chloride Lead(II) bromide Lead(II) iodide |
Other cations
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Difluorocarbene Difluorosilylene Difluorogermylene Stannous fluoride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Preparation
editLead(II) fluoride can be prepared by treating lead(II) hydroxide or lead(II) carbonate with hydrofluoric acid:[3]
- Pb(OH)2 + 2 HF → PbF2 + 2 H2O
Alternatively, it is precipitated by adding hydrofluoric acid to a lead(II) salt solution, or by adding a fluoride salt to a lead salt, such as potassium fluoride to a lead(II) nitrate solution,[4]
- 2 KF + Pb(NO3)2 → PbF2 + 2 KNO3
or sodium fluoride to a lead(II) acetate solution.
- 2 NaF + Pb(CH3COO)2 → PbF2 + 2 NaCH3COO
It appears as the very rare mineral fluorocronite.[5][6]
Uses
editLead(II) fluoride is used in low melting glasses, in glass coatings to reflect infrared rays, in phosphors for television-tube screens, and as a catalyst for the manufacture of picoline.[3] The Muon g−2 experiment uses PbF
2 scintillators in conjunction with silicon photomultipliers.[7]
It also serves as a oxygen scavenger in high-temperature fluorine chemistry, as plumbous oxide is relatively volatile.[8]
References
edit- ^ NIST-data review 1980
- ^ Haines, J.; Léger, J. M.; Schulte, O. (1998-04-01). "High-pressure isosymmetric phase transition in orthorhombic lead fluoride". Physical Review B. 57 (13). American Physical Society (APS): 7551–7555. Bibcode:1998PhRvB..57.7551H. doi:10.1103/physrevb.57.7551. ISSN 0163-1829.
- ^ a b Carr, Dodd S. "Lead Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_249. ISBN 978-3527306732.
- ^ Arnold Hollemann, Egon Wiberg, 101st ed., de Gruyter 1995 Berlin; ISBN 3-11-012641-9
- ^ "Fluorocronite".
- ^ "List of Minerals". 21 March 2011.
- ^ Grange, J.; et al. (Muon g−2 Collaboration) (Jan 27, 2015). Muon (g−2) Technical Design Report. Fermi National Accelerator Laboratory (Report). arXiv:1501.06858. Bibcode:2015arXiv150106858G. FERMILAB-FN-0992-E. Via inSPIRE
- ^ Beeks, Kjeld; Sikorsky, Tomas; Rosecker, Veronika; Pressler, Martin; Schaden, Fabian; Werban, David; Hosseini, Niyusha; Rudischer, Lukas; Schneider, Felix; Berwian, Patrick; Friedrich, Jochen; Hainz, Dieter; Welch, Jan; Sterba, Johannes H.; Kazakov, Georgy; Schumm, Thorsten (2023). "Growth and characterization of thorium‑doped calcium fluoride single crystals" (PDF). Scientific Reports. 13 (1): 3897–. Bibcode:2023NatSR..13.3897B. doi:10.1038/s41598-023-31045-5. PMC 9995343. PMID 36890210.