|Jmol-3D images||Image 1|
|Molar mass||239.30 g/mol|
|Melting point||1,118 °C; 2,044 °F; 1,391 K|
|Boiling point||1,281 °C; 2,338 °F; 1,554 K|
|Solubility in water||2.6×10−11 kg/kg (calculated, at pH=7) 8.6×10−7 kg/kg|
|Solubility product, Ksp||9.04×10−29|
|Refractive index (nD)||3.91|
|Crystal structure||Halite (cubic), cF8|
|Space group||Fm3m, No. 225|
|Lattice constant||a = 5.936 Angstroms |
heat capacity C
|46.02 J/degree mol|
|Std enthalpy of
|EU classification||Repr. Cat. 1/3
Dangerous for the environment (N)
|R-phrases||R61, R20/22, R33, R62, R50/53|
|S-phrases||S53, S45, S60, S61|
|Other anions||Lead(II) oxide
|Other cations||Carbon monosulfide
|Related compounds||Thallium sulfide
| (what is: / ?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Lead(II) sulfide (also spelled sulphide) is an inorganic compound with the formula PbS. It finds limited use in electronic devices. PbS, also known as galena, is the principal ore, and most important compound of lead.
Addition of hydrogen sulfide or sulfide salts to a solution of lead ions gives a poorly soluble black product consisting of PbS:
- Pb2+ + H2S → PbS + 2 H+
The equilibrium constant for this reaction is 3×106 M. This reaction, which entails a dramatic color change from colourless or white to black, was once used in qualitative inorganic analysis. The presence of hydrogen sulfide or sulfide ions is still routinely tested using "lead acetate paper."
Like the related materials PbSe and PbTe, PbS is a semiconductor. In fact, lead sulfide was one of the earliest materials to be used as a semiconductor. Lead sulfide crystallizes in the sodium chloride motif, unlike many other IV-VI semiconductors.
Since PbS is the main ore of lead, much effort has focused on its conversion. A major process involves smelting of PbS followed by reduction of the resulting oxide. Idealized equations for these two steps are:
- 2 PbS + 3 O2 → 2 PbO + 2 SO2
- PbO + C → Pb + CO
PbS was once used as a black pigment, but current applications exploit its semiconductor properties, which have long been recognized. PbS is one of the oldest and most common detection element materials in various infrared detectors. As an infrared detector, PbS functions as a photon detector, responding directly to the photons of radiation, as opposed to thermal detectors, which respond to a change in detector element temperature caused by the radiation.
A PbS element can be used to measure radiation in either of two ways: by measuring the tiny photocurrent the photons cause when they hit the PbS material, or by measuring the change in the material's electrical resistance that the photons cause. Measuring the resistance change is the more commonly used method.
At room temperature, PbS is sensitive to radiation at wavelengths between approximately 1 and 2.5 μm. This range corresponds to the shorter wavelengths in the infra-red portion of the spectrum, the so-called short-wavelength infrared (SWIR). Only very hot objects emit radiation in these wavelengths.
Cooling the PbS elements, for example using liquid nitrogen or a Peltier element system, shifts its sensitivity range to between approximately 2 and 4 μm. Objects that emit radiation in these wavelengths still have to be quite hot—several hundred degrees Celsius—but not as hot as those detectable by uncooled sensors. Other compounds used for this purpose include indium antimonide (InSb) and mercury-cadmium telluride (HgCdTe), which have somewhat better properties for detecting the longer IR wavelengths. The high dielectric constant of PbS leads to relatively slow detectors (compared to silicon, germanium, InSb, or HgCdTe).
Elevations above 2.6 km (1.63 mi) on the planet Venus are coated with a shiny substance. Though the composition of this coat is not entirely certain, one theory is that Venus "snows" crystallized lead sulfide much as Earth snows frozen water. If this is the case, it would be the first time the substance was identified on a foreign planet. Other less likely candidates for Venus' "snow" are bismuth sulfide and tellurium.
Lead(II) sulfide is toxic if the lead and sulfur are heated to decomposition and toxic compounds of lead and sulfur oxides are produced (such as in a fire). Lead sulfide is insoluble and a stable compound in the pH of blood and so is probably one of the less toxic forms of lead.
- Patnaik, Pradyot (2003). Handbook of Inorganic Chemical Compounds. McGraw-Hill. ISBN 0-07-049439-8. Retrieved 2009-06-06.
- W. Linke (1965). Solubilities. Inorganic and Metal-Organic Compounds 2. Washington, D.C.: American Chemical Society. p. 1318.
- Ronald Eisler (2000). Handbook of Chemical Risk Assessment. CRC Press. ISBN 1-56670-506-1.
- Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
- Vaughan, D. J.; Craig, J. R. (1978). Mineral Chemistry of Metal Sulfides. Cambridge: Cambridge University Press. ISBN 0-521-21489-0.;
- C.Michael Hogan. 2011. Sulfur. Encyclopedia of Earth, eds. A.Jorgensen and C.J.Cleveland, National Council for Science and the environment, Washington DC
- Charles A. Sutherland, Edward F. Milner, Robert C. Kerby, Herbert Teindl, Albert Melin, Hermann M. Bolt (2005). Lead. in Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_193.pub2.
- Putley, E H; Arthur, J B (1951). "Lead Sulphide – An Intrinsic Semiconductor". Proceedings of the Physical Society. Series B 64: 616. doi:10.1088/0370-1301/64/7/110.
- "'Heavy metal' snow on Venus is lead sulfide". Washington University in St. Louis. Retrieved 2009-07-07.
- Lead sulfide MSDS
- Fritz Bischoff, L. C. Maxwell, Richard D. Evens and Franklin R. Nuzum (1928). "Studies on the Toxicity of Various Lead Compounds Given Intravenously". Journal of Pharmacology and Experimental Therapeutics 34 (1): 85–109.
|Wikimedia Commons has media related to Lead(II) sulfide.|
- Case Studies in Environmental Medicine (CSEM): Lead Toxicity
- ToxFAQs: Lead
- National Pollutant Inventory – Lead and Lead Compounds Fact Sheet