Lead(II) oxide
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| Names | |
|---|---|
| IUPAC name
Lead(II) oxide | |
| Other names | |
| Identifiers | |
1317-36-8  | |
| PubChem | 14827 |
| RTECS number | OG1750000 |
| UN number | 3288 |
| Properties | |
| PbO | |
| Molar mass | 223.20 g/mol |
| Appearance | red or yellow powder |
| Density | 9.53 g/cm3 |
| Melting point | 888 °C (1,630 °F; 1,161 K) |
| Boiling point | 1,477 °C (2,691 °F; 1,750 K) |
| 0.017 g/L[1] | |
| Solubility | insoluble in dilute alkalis, alcohol soluble in concentrated alkalis soluble in HCl, ammonium chloride |
| Structure | |
| tetragonal, tP4 | |
| P4/nmm, No. 129 | |
| Hazards | |
| Safety data sheet | ICSC 0288 |
| EU classification (DSD) |
Repr. Cat. 1/3 Harmful (Xn) Dangerous for the environment (N) |
| R-phrases | R61, R20/22, R33, R62, R50/53 |
| S-phrases | S53, S45, S60, S61 |
| NFPA 704 | |
| Flash point | Non-flammable |
| Lethal dose or concentration (LD, LC): | |
| LDLo (Lowest published) |
1400 mg/kg (dog, oral)[2] |
| Related compounds | |
| Other anions |
Lead sulfide Lead selenide Lead telluride |
| Other cations |
Carbon monoxide Silicon monoxide Tin(II) oxide |
| Lead(II,II,IV) oxide Lead dioxide | |
| Related compounds |
Thallium(III) oxide Bismuth(III) oxide |
| 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 | |
Lead(II) oxide, also called lead monoxide, is the inorganic compound with the molecular formula PbO. PbO occurs in two polymorphs, one litharge having a tetragonal crystal structure and the other massicot having an orthorhombic crystal structure. Modern applications for PbO are mostly in lead-based industrial glass and industrial ceramics, including computer components.
Preparation
PbO may be prepared by heating lead metal in air at approx. 600 °C. At this temperature it is also the end product of oxidation of other lead oxides in air:[3]
- PbO2 –(293 °C)→ Pb12O19 –(351 °C)→ Pb12O17 –(375 °C)→ Pb3O4 –(605 °C)→ PbO
Thermal decomposition of lead(II) nitrate or lead carbonate also results in the PbO formation:
- 2 Pb(NO3)2 → 2 PbO + 4 NO2 + O2
- PbCO3 → PbO + CO2
PbO is produced on a large scale as an intermediate product in refining raw lead ores into metallic lead. The usual lead ore is galena (lead(II) sulfide). At high temperature (1000 °C) the sulfide is converted to the oxide:[4]
- 2 PbS + 3 O2 → 2PbO + 2SO2
Metallic lead is obtained by reducing the PbO with carbon monoxide at around 1200 °C:.[5]
- PbO + CO → Pb + CO2
Structure
As determined by X-ray crystallography, both polymorphs, tetragonal and orthorhombic feature a pyramidal four-coordinate Pb center. In the tetragonal form the four Pb-O bonds have the same length, but in the orthorhombic two are shorter and two longer. The pyramidal nature indicates the presence of a stereo-chemically active lone pair of electrons.[6] When PbO occurs in tetragonal lattice structure it is called litharge; and when the PbO has orthorhombic lattice structure it is called massicot. The PbO can be changed from massicot to litharge or vice versa by controlled heating and cooling.[7] The tetragonal form is usually red or orange color, while the orthorhombic is usually yellow or orange, but the color is not a very reliable indicator of the structure.[8] The tetragonal and orthorhombic forms of PbO occur naturally as rare minerals.
Reactions
The red and yellow forms of this material are related by a small change in enthalpy: PbO(red) → PbO(yellow) ΔH = 1.6 kJ/mol
PbO is amphoteric, which means that it reacts with both acids and with bases. With acids, it forms salts of Pb2+ via the intermediacy of oxo clusters such as [Pb6O(OH)6]4+. With strong base, PbO dissolves to form plumbite(II) salts:[9] PbO + H2O + OH− → [Pb(OH)3]−
Applications
The kind of lead in lead glass is normally PbO, and PbO is used extensively in making glass. Depending on the glass, the benefit of using PbO in glass can be one or more of (1) increasing the refractive index of the glass, (2) decreasing the viscosity of the glass, (3) increasing the electrical resistivity of the glass, and (4) increasing the ability of the glass to absorb X-rays. Adding PbO to industrial ceramics (as well as glass) makes the materials more magnetically and electrically inert (raises the Curie temperature) and is often used for this purpose.[10] Historically PbO was also used extensively in ceramic glazes for household ceramics, and it is still used, but not extensively any more. Other less dominating applications include the vulcanization of rubber and the production of certain pigments and paints.[11] PbO is used in cathode ray tube glass to block X-ray emission, but mainly in the neck and funnel because it can cause discoloration when used in the faceplate. Strontium oxide is preferred for the faceplate.
The consumption of lead, and hence the processing of PbO, correlates with the number of automobiles because it remains the key component of automotive lead-acid batteries.[12]
Niche or declining uses
A mixture of PbO with glycerine sets to a hard, waterproof cement that has been used to join the flat glass sides and bottoms of aquariums, and was also once used to seal glass panels in window frames. It is a component of lead paints.
In powdered tetragonal litharge form, it can be mixed with linseed oil and then boiled to create a weather-resistant sizing used in gilding. The litharge would give the sizing a dark red color that made the gold leaf appear warm and lustrous, while the linseed oil would impart adhesion and a flat durable binding surface.
PbO is used in certain condensation reactions in organic synthesis.[13]
Health issues
Lead oxide may be fatal if swallowed or inhaled. It causes irritation to skin, eyes, and respiratory tract. It affects gum tissue, central nervous system, kidneys, blood, and reproductive system. It can bioaccumulate in plants and in mammals.[14]
References
- ↑ Blei(II)-oxid. Merck
- ↑ "Lead compounds (as Pb)". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
- ↑ N.N. Greenwood, A. Earnshaw, "Chemistry of Elements", 2nd edition, Butterworth-Heinemann, 1997.
- ↑ Abdel-Rehim, A. M. (2006), "Thermal and XRD analysis of Egyptian galena", Journal of Thermal Analysis and Calorimetry 86 (2): 393–401
- ↑ Lead Processing @ Universalium.academic.ru. Alt address: Lead processing @ Enwiki.net.
- ↑ Wells, A. F. (1984), Structural Inorganic Chemistry (5th ed.), Oxford: Clarendon Press, ISBN 0-19-855370-6
- ↑ A simple example is given in A Text Book of Inorganic Chemistry, by Anil Kumar De, year 2007, page 383. A more complex example is in The Chemistry of Metal Alkoxides, published by Kluwer Academic Publishers, year 2002, section 9.4 on lead alkoxides, page 115.
- ↑ Lead manufacturing in Britain, by David John Rowe, year 1983, page 16.
- ↑ Holleman, A. F.; Wiberg, E. (2001), Inorganic Chemistry, San Diego: Academic Press, ISBN 0-12-352651-5
- ↑ Chapter 9, "Lead Compounds", in the book Ceramic and Glass Materials: Structure, Properties and Processing, published by Springer, year 2008.
- ↑ Dodd S. Carr "Lead Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinhiem. doi:10.1002/14356007.a15_249
- ↑ Charles A. Sutherland, Edward F. Milner, Robert C. Kerby, Herbert Teindl, Albert Melin, Hermann M. Bolt "Lead" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a15_193.pub2
- ↑ Corson, B. B. (1936). "1,4-Diphenylbutadiene". Org. Synth. 16: 28.; Coll. Vol. 2, p. 229
- ↑ "Lead (II) oxide". International Occupational Safety and Health Information Centre. Retrieved 2009-06-06.
External links
- Case Studies in Environmental Medicine - Lead Toxicity
- ToxFAQs: Lead
- National Pollutant Inventory - Lead and Lead Compounds Fact Sheet
- Webelements PbO
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