Lead(II) sulfide: Difference between revisions
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{{Redirect|PbS|other uses|PBS (disambiguation)}} |
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| verifiedrevid = 447377289 |
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| ImageFile1 = Galena-unit-cell-3D-ionic.png |
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| verifiedrevid = 450727917 |
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| ImageSize1 = 200 |
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| ImageFile1 = Galena-unit-cell-3D-ionic.png |
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| ImageFile2 = Sulfid olovnatý.PNG |
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| ImageFile2 = Sulfid olovnatý.PNG |
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| ImageSize2 = 244 |
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| ImageSize2 = 244 |
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| ImageName = Lead(II) sulfide |
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| ImageName = Lead(II) sulfide |
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| IUPACName = |
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| IUPACName = |
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| OtherNames = Plumbous sulfide<br />[[Galena]] |
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| OtherNames = Plumbous sulfide<br />[[Galena]], Sulphuret of lead |
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| Section1 = {{Chembox Identifiers |
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| Section1 = {{Chembox Identifiers |
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| CASNo = 1314-87-0 |
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| Abbreviations = |
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| CASNo_Ref = {{cascite}} |
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| CASNo = 1314-87-0 |
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| CASNo_Comment = |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNoOther = |
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| PubChem = 14819 |
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| ChemSpiderID = 14135 |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID_Comment = |
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| EC_number = 215-246-6 |
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| RTECS = OG4550000 |
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| UNNumber = 3077 |
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| UNII = 2425D15SYM |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| DrugBank = |
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| KEGG = |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| MeSHName = |
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| ChEBI = |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEMBL = |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| SMILES = [Pb]=S |
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| InChI = |
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| StdInChI = 1S/Pb.S |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChIKey = XCAUINMIESBTBL-UHFFFAOYSA-N |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| Beilstein = |
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| Gmelin = |
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| 3DMet = |
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| Section2 = {{Chembox Properties |
| Section2 = {{Chembox Properties |
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| Formula = PbS |
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| MolarMass = 239.30{{nbsp}}g/mol |
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| Appearance = Black |
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| Density = 7.60 g/cm<sup>3</sup><ref>{{cite book | last =Patnaik | first =Pradyot | year = 2003 | title =Handbook of Inorganic Chemical Compounds | publisher = McGraw-Hill | page = | isbn =0070494398 | url= http://books.google.com/?id=Xqj-TTzkvTEC&pg=PA119 | accessdate = 2009-06-06}}</ref> |
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| Density = 7.60{{nbsp}}g/cm<sup>3</sup><ref name=crc>Haynes, p. 4.69</ref> |
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| Solubility = 2.6{{e|-11}} kg/kg (calculated, at pH=7)<ref>{{cite book|author=W. Linke|title=Solubilities. Inorganic and Metal-Organic Compounds|volume=2|page=1318|publisher= American Chemical Society|location= Washington, D.C.|year= 1965}}</ref> 8.6{{e|-7}}</sup> kg/kg<ref>{{cite book|url=http://books.google.com/?id=cl1Kry_k6ZUC&pg=PA206|title= Handbook of Chemical Risk Assessment|author=Ronald Eisler|publisher=CRC Press|year= 2000|isbn=1566705061}}</ref> |
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| Solubility = 2.6{{e|-11}}{{nbsp}}kg/kg (calculated, at pH=7)<ref>{{cite book|author=Linke, W. |title=Solubilities. Inorganic and Metal-Organic Compounds|volume=2|page=1318|publisher= American Chemical Society|location= Washington, D.C.|year= 1965}}</ref> 8.6{{e|-7}} kg/kg<ref>{{cite book|url=https://books.google.com/books?id=cl1Kry_k6ZUC&pg=PA206|title= Handbook of Chemical Risk Assessment|author=Ronald Eisler|publisher=CRC Press|year= 2000|isbn=978-1-56670-506-6}}</ref> |
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| SolubilityProduct = 9.04{{e|-29}} |
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| SolubilityProduct = |
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| MeltingPtC = 1118 |
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| MeltingPtC = 1113<ref name=crc/> |
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| BoilingPtC = 1281 |
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| MeltingPt_ref = |
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| BoilingPtC = 1281 |
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| RefractIndex = 3.91<ref>Haynes, p. 4.135</ref> |
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| MagSus = −83.6·10<sup>−6</sup>{{nbsp}}cm<sup>3</sup>/mol<ref>Haynes, p. 4.128</ref> |
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| Section3 = {{Chembox Structure |
| Section3 = {{Chembox Structure |
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| CrystalStruct = [[Halite]] (cubic), [[Pearson symbol|cF8]] |
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| SpaceGroup = Fm{{overline|3}}m, No. 225 |
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| Coordination = Octahedral (Pb<sup>2+</sup>)<br />Octahedral (S<sup>2−</sup>) |
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| LattConst_a = 5.936{{nbsp}}Å |
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| UnitCellFormulas = 4 |
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|Structure_ref= <ref>Haynes, p. 4.141</ref> |
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|Dipole = 3.59 D<ref>Haynes, p. 9.63</ref> |
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| Section4 = {{Chembox Thermochemistry |
| Section4 = {{Chembox Thermochemistry |
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|Thermochemistry_ref= <ref>Haynes, p. 5.25</ref> |
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| DeltaHf = –1.00{{e|2}} kJ/mol |
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| DeltaHf = −100.4{{nbsp}}kJ/mol |
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| DeltaGf = −98.7{{nbsp}}kJ/mol |
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| HeatCapacity = 46.02 J/degree mol |
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| Entropy = 91.2{{nbsp}}J/mol |
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| HeatCapacity = 49.5{{nbsp}}J/mol⋅K |
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}} |
}} |
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| Section7 = {{Chembox Hazards |
| Section7 = {{Chembox Hazards |
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| ExternalSDS = [http://msds.chem.ox.ac.uk/LE/lead_sulfide.html External MSDS] |
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| GHSPictograms = {{GHS07}}{{GHS08}}{{GHS09}} |
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| EUIndex = 082-001-00-6 |
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| GHSSignalWord = Danger |
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| EUClass = Repr. Cat. 1/3<br />Harmful ('''Xn''')<br />Dangerous for the environment ('''N''') |
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| HPhrases = {{H-phrases|302|332|360|373|410}} |
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| RPhrases = {{R61}}, {{R20/22}}, {{R33}}, {{R62}}, {{R50/53}} |
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| PPhrases = {{P-phrases|201|202|260|261|264|270|271|273|281|301+312|304+312|304+340|308+313|312|314|330|391|405|501}} |
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| SPhrases = {{S53}}, {{S45}}, {{S60}}, {{S61}} |
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| NFPA-H = 2 |
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| NFPA-F = 0 |
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| NFPA-R = 0 |
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| NFPA-S = |
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| FlashPt = Non-flammable |
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}} |
}} |
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| Section8 = {{Chembox Related |
| Section8 = {{Chembox Related |
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| OtherAnions = [[Lead(II) oxide]]<br />[[Lead selenide]]<br />[[Lead telluride]] |
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| OtherCations = [[Carbon monosulfide]]<br />[[Silicon monosulfide]]<br />[[Germanium(II) sulfide]]<br />[[Tin(II) sulfide]] |
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| OtherCompounds = [[Thallium sulfide]]<br />[[Lead(IV) sulfide]]<br />[[Bismuth sulfide]] |
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'''Lead(II) sulfide''' (also spelled [[Sulfur#Spelling| |
'''Lead(II) sulfide''' (also spelled ''[[Sulfur#Spelling and etymology|sulphide]]'') is an [[inorganic compound]] with the [[chemical formula|formula]] [[Lead|Pb]][[Sulfide|S]]. [[Galena]] is the principal ore and the most important compound of [[lead]]. It is a semiconducting material with niche uses. |
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==Formation, basic properties, related materials== |
==Formation, basic properties, related materials== |
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Addition of hydrogen sulfide or sulfide salts to a solution |
Addition of [[hydrogen sulfide]] or sulfide salts to a solution containing a lead salt, such as PbCl<sub>2</sub>, gives a black precipitate of lead sulfide. |
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:Pb<sup>2+</sup> + H<sub>2</sub>S |
: Pb<sup>2+</sup> + H<sub>2</sub>S → PbS↓ + 2 H<sup>+</sup> |
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The equilibrium constant for this reaction is 3{{e|6}} M.<ref>{{RubberBible86th}} |
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</ref> |
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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." |
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This reaction is used in [[qualitative inorganic analysis]]. The presence of hydrogen sulfide or sulfide ions may be tested using "lead acetate paper." |
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Like the related materials [[lead selenide|PbSe]] and [[lead telluride|PbTe]], PbS is a [[semiconductor]].<ref>{{cite book|author=Vaughan, D. J.; Craig, J. R. |title=Mineral Chemistry of Metal Sulfides|publisher= Cambridge University Press|location= Cambridge|year= 1978|isbn=0521214890}};</ref> In fact, lead sulfide was one of the earliest materials to be used as a semiconductor.<ref>C.Michael Hogan. 2011. [http://www.eoearth.org/article/Sulfur?topic=49557 ''Sulfur''. Encyclopedia of Earth, eds. A.Jorgensen and C.J.Cleveland, National Council for Science and the environment, Washington DC]</ref> Lead sulfide crystallizes in the [[sodium chloride]] motif, unlike many other [[List of semiconductor materials#Group IV-VI|IV-VI semiconductor]]s. |
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Like the related materials [[lead selenide|PbSe]] and [[lead telluride|PbTe]], PbS is a [[semiconductor]].<ref>{{cite book|author1=Vaughan, D. J. |author2=Craig, J. R. |title=Mineral Chemistry of Metal Sulfides|publisher= Cambridge University Press|location= Cambridge|year= 1978|isbn=978-0-521-21489-6}};</ref> In fact, lead sulfide was one of the earliest materials to be used as a semiconductor.<ref>Hogan, C. Michael (2011). [http://www.eoearth.org/article/Sulfur?topic=49557 "Sulfur"]. in ''Encyclopedia of Earth'', eds. A. Jorgensen and C.J. Cleveland, National Council for Science and the environment, Washington DC. {{webarchive|url=https://web.archive.org/web/20121028080550/http://www.eoearth.org/article/Sulfur?topic=49557 |date=2012-10-28 }}</ref> Lead sulfide crystallizes in the [[sodium chloride]] motif, unlike many other [[List of semiconductor materials#Group IV-VI|IV-VI semiconductor]]s. |
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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:<ref>{{cite book|author1=Sutherland, Charles A. |author2=Milner, Edward F. |author3=Kerby, Robert C. |author4=Teindl, Herbert |author5=Melin, Albert |author6=Bolt, Hermann M. |chapter=Lead|title= Ullmann's Encyclopedia of Industrial Chemistry|year= 2005 |publisher=Wiley-VCH|location= Weinheim|doi=10.1002/14356007.a15_193.pub2|isbn=978-3527306732 }}</ref> |
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: 2 PbS + 3 O<sub>2</sub> → 2 [[Lead(II) oxide|PbO]] + 2 SO<sub>2</sub> |
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: PbO + C → Pb + CO |
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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:<ref>{{cite book|author=Charles A. Sutherland, Edward F. Milner, Robert C. Kerby, Herbert Teindl, Albert Melin, Hermann M. Bolt |title=Lead. in Ullmann's Encyclopedia of Industrial Chemistry|year= 2005 |publisher=Wiley-VCH|location= Weinheim|doi=10.1002/14356007.a15_193.pub2}}</ref> |
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:2 PbS + 3 O<sub>2</sub> → 2 PbO + 2 SO<sub>2</sub> |
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:PbO + C → Pb + CO |
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The [[sulfur dioxide]] is converted to [[sulfuric acid]]. |
The [[sulfur dioxide]] is converted to [[sulfuric acid]]. |
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=== Nanoparticles === |
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Lead sulfide-containing [[nanoparticle]] and [[quantum dot]]s have been well studied.<ref>{{Cite journal|title = The Quantum Mechanics of Larger Semiconductor Clusters ("Quantum Dots")|journal = Annual Review of Physical Chemistry|date = 1990-01-01|pages = 477–496|volume = 41|issue = 1|doi = 10.1146/annurev.pc.41.100190.002401|first3 = L. E.|last3 = Brus|bibcode = 1990ARPC...41..477B}}</ref> Traditionally, such materials are produced by combining lead salts with a variety of sulfide sources.<ref>{{Cite journal|title = Coated semiconductor nanoparticles; the cadmium sulfide/lead sulfide system's synthesis and properties|journal = The Journal of Physical Chemistry|date = 2002-05-01|pages = 895–901|volume = 97|issue = 4|doi = 10.1021/j100106a015|language = EN|first1 = H. S.|last1 = Zhou|first2 = I.|last2 = Honma|first3 = H.|last3 = Komiyama|first4 = Joseph W.|last4 = Haus}}</ref><ref>{{Cite journal|title = A novel and simple one-step solid-state reaction for the synthesis of PbS nanoparticles in the presence of a suitable surfactant|journal = Materials Research Bulletin|date = 2001-09-15|pages = 1977–1984|volume = 36|issue = 11|doi = 10.1016/S0025-5408(01)00678-X|first1 = Wenzhong|last1 = Wang|first2 = Yingkai|last2 = Liu|first3 = Yongjie|last3 = Zhan|first4 = Changlin|last4 = Zheng|first5 = Guanghou|last5 = Wang}}</ref> In 2009, PbS nanoparticles have been examined for use in solar cells.<ref>{{Cite journal|title = PbS and CdS Quantum Dot-Sensitized Solid-State Solar Cells: "Old Concepts, New Results"|journal = Advanced Functional Materials|date = 2009-09-09|issn = 1616-3028|pages = 2735–2742|volume = 19|issue = 17|doi = 10.1002/adfm.200900081|language = en|first1 = HyoJoong|last1 = Lee|first2 = Henry C.|last2 = Leventis|first3 = Soo-Jin|last3 = Moon|first4 = Peter|last4 = Chen|first5 = Seigo|last5 = Ito|first6 = Saif A.|last6 = Haque|first7 = Tomas|last7 = Torres|first8 = Frank|last8 = Nüesch|first9 = Thomas|last9 = Geiger| s2cid=98631978 |doi-access = free}}</ref> |
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==Applications== |
==Applications== |
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[[File:CatWhisker.jpg|thumb|left|Galena-based [[cat's-whisker detector]] used in the early 1900s]] |
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PbS was once used as a black pigment, but current applications exploit its semiconductor properties, which have long been recognized.<ref>{{cite journal|doi=10.1088/0370-1301/64/7/110|title=Lead Sulphide – An Intrinsic Semiconductor|year=1951|author=Putley, E H|journal=Proceedings of the Physical Society Section B|volume=64|pages=616|last2=Arthur|first2=J B}}</ref> PbS is one of the oldest and most common detection element materials in various [[infrared detector]]s. 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. |
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[[File:German WWII PbS IR detector.jpg|thumb|left|World War II German PbS infrared detector]] |
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=== Photodetector === |
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A PbS element can be used to measure radiation in either of two ways: by measuring the tiny [[electrical current|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. |
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{{See also|Photoconductivity}} |
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PbS was one of the first materials used for electrical diodes that could detect electromagnetic radiation, including [[infrared light]].<ref>{{cite journal |doi=10.1088/0370-1301/64/7/110 |title=Lead Sulphide – An Intrinsic Semiconductor |year=1951 |author=Putley, E H |journal=Proceedings of the Physical Society | series = Series B | volume=64 |issue=7 |pages=616–618 |last2=Arthur |first2=J B|author-link=E. H. Putley }}</ref> As an infrared sensor, PbS directly detects light, 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 [[wavelength]]s between approximately 1 and 2.5 [[micrometre|μm]]. This range corresponds to the shorter wavelengths in the infra-red portion of the [[electromagnetic spectrum|spectrum]], the so-called short-wavelength infrared (SWIR). Only very hot objects emit radiation in these wavelengths. |
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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 [[HgCdTe|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). |
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At [[room temperature]], PbS is sensitive to radiation at [[wavelength]]s between approximately 1 and 2.5 [[micrometre|μm]]. This range corresponds to the shorter wavelengths in the infra-red portion of the [[electromagnetic spectrum|spectrum]], the so-called short-wavelength infrared (SWIR). Only very hot objects emit radiation in these wavelengths. |
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==Planetary science== |
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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 [[HgCdTe|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). |
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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 "[[Venus snow|snow]]s" 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]].<ref>{{cite news|url=http://news-info.wustl.edu/news/page/normal/633.html|access-date=2009-07-07|title='Heavy metal' snow on Venus is lead sulfide|publisher=[[Washington University in St. Louis]]|archive-date=2008-04-15|archive-url=https://web.archive.org/web/20080415000214/http://news-info.wustl.edu/news/page/normal/633.html|url-status=live}}</ref> |
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==Astronomy== |
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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 "[[Venus snow|snow]]s" 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]].<ref>{{cite news|url=http://news-info.wustl.edu/news/page/normal/633.html|accessdate=2009-07-07|title='Heavy metal' snow on Venus is lead sulfide|publisher= Washington University in St. Louis}}</ref> |
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==Safety== |
==Safety== |
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Lead(II) sulfide is |
Lead(II) sulfide is so insoluble that it is almost nontoxic, but pyrolysis of the material, as in smelting, gives dangerous toxic fumes of lead and oxides of sulfur.<ref>{{Cite web |url=http://www.espimetals.com/msds%27s/leadsulfide.pdf |title=Lead sulfide MSDS |access-date=2009-11-20 |archive-url=https://web.archive.org/web/20061111080525/http://www.espimetals.com/msds's/leadsulfide.pdf |archive-date=2006-11-11 |url-status=dead }}</ref> 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.<ref>{{cite journal |url=https://jpet.aspetjournals.org/content/34/1/85|title=Studies on the Toxicity of Various Lead Compounds Given Intravenously |author1=Bischoff, Fritz |author2=Maxwell, L. C. |author3=Evens, Richard D. |author4=Nuzum, Franklin R. |journal=Journal of Pharmacology and Experimental Therapeutics |year=1928 |volume=34 |issue=1 |pages=85–109 }}</ref> A large safety risk occurs in the synthesis of PbS using lead carboxylates, as they are particularly soluble and can cause [[Lead poisoning|negative physiological conditions.]] |
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==References== |
==References== |
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{{reflist|30em}} |
{{reflist|30em}} |
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==Cited sources== |
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*{{cite book |ref=Haynes| editor= Haynes, William M. | date = 2016| title = [[CRC Handbook of Chemistry and Physics]] | edition = 97th | publisher = [[CRC Press]] | isbn = 9781498754293}} |
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==External links== |
==External links== |
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{{Commons |
{{Commons category|Lead(II) sulfide}} |
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* [ |
* [https://www.atsdr.cdc.gov/csem/csem.html Case Studies in Environmental Medicine (CSEM): Lead Toxicity] |
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* [ |
* [https://www.atsdr.cdc.gov/toxfaqs/tfacts13.pdf ToxFAQs: Lead] |
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* [http://www.npi.gov.au/database/substance-info/profiles/50.html National Pollutant Inventory – Lead and Lead Compounds Fact Sheet] |
* [https://web.archive.org/web/20080111154608/http://www.npi.gov.au/database/substance-info/profiles/50.html National Pollutant Inventory – Lead and Lead Compounds Fact Sheet] |
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{{Lead compounds}} |
{{Lead compounds}} |
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{{Sulfides}} |
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{{DEFAULTSORT:Lead(Ii) Sulfide}} |
{{DEFAULTSORT:Lead(Ii) Sulfide}} |
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[[Category:Lead compounds]] |
[[Category:Lead(II) compounds]] |
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[[Category: |
[[Category:Monosulfides]] |
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[[Category: |
[[Category:IV-VI semiconductors]] |
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[[Category:Infrared sensor materials]] |
[[Category:Infrared sensor materials]] |
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[[Category:Rock salt crystal structure]] |
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[[cs:Sulfid olovnatý]] |
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[[de:Blei(II)-sulfid]] |
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[[fr:Sulfure de plomb(II)]] |
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[[it:Solfuro di piombo]] |
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[[pl:Siarczek ołowiu(II)]] |
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[[pt:Sulfeto de chumbo (II)]] |
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[[ru:Сульфид свинца(II)]] |
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[[fi:Lyijysulfidi]] |