Lead

82 thalliumleadbismuth
Sn

Pb

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Pb-TableImage.png
Periodic Table - Extended Periodic Table
General
Name, Symbol, Number lead, Pb, 82
Element category Post-transition metals
Group, Period, Block 14, 6, p
Appearance bluish gray
Lead brick.jpg
Standard atomic weight 207.2(1)  g·mol−1
Electron configuration [Xe] 4f14 5d10 6s² 6p²
Electrons per shell 2, 8, 18, 32, 18, 4
Physical properties
Phase solid
Density (near r.t.) 11.34  g·cm−3
Liquid density at m.p. 10.66  g·cm−3
Melting point 600.61 K
(327.46 °C, 621.43 °F)
Boiling point 2022 K
(1749 °C, 3180 °F)
Heat of fusion 4.77  kJ·mol−1
Heat of vaporization 179.5  kJ·mol−1
Specific heat capacity (25 °C) 26.650  J·mol−1·K−1
Vapor pressure
P(Pa) 1 10 100 1 k 10 k 100 k
at T(K) 978 1088 1229 1412 1660 2027
Atomic properties
Crystal structure cubic face centered
Oxidation states 4, 2
(Amphoteric oxide)
Electronegativity 2.33 (Pauling scale)
Ionization energies
(more)
1st:  715.6  kJ·mol−1
2nd:  1450.5  kJ·mol−1
3rd:  3081.5  kJ·mol−1
Atomic radius 180  pm
Atomic radius (calc.) 154  pm
Covalent radius 147  pm
Van der Waals radius 202 pm
Miscellaneous
Magnetic ordering diamagnetic
Electrical resistivity (20 °C) 208 n Ω·m
Thermal conductivity (300 K) 35.3  W·m−1·K−1
Thermal expansion (25 °C) 28.9  µm·m−1·K−1
Speed of sound (thin rod) (r.t.) (annealed)
1190  m·s−1
Young's modulus 16  GPa
Shear modulus 5.6  GPa
Bulk modulus 46  GPa
Poisson ratio 0.44
Mohs hardness 1.5
Brinell hardness 38.3  MPa
CAS registry number 7439-92-1
Most-stable isotopes
Main article: Isotopes of lead
iso NA half-life DM DE (MeV) DP
204Pb 1.4% >1.4×1017 y Alpha 2.186 200Hg
205Pb syn 1.53×107 y Epsilon 0.051 205Tl
206Pb 24.1% 206Pb is stable with 124 neutrons
207Pb 22.1% 207Pb is stable with 125 neutrons
208Pb 52.4% 208Pb is stable with 126 neutrons
210Pb trace 22.3 y Alpha 3.792 206Hg
Beta 0.064 210Bi
References
Lead pipe in Roman baths

Lead (pronounced /ˈlɛd/) is a main group element with a symbol Pb (Latin: plumbum). Lead has the atomic number 82. Lead is a soft, malleable poor metal, also considered to be one of the heavy metals. Lead has a bluish-white color when freshly cut, but tarnishes to a dull grayish color when exposed to air. It has a shiny chrome-silver luster when melted into a liquid.

Lead is used in building construction, lead-acid batteries, bullets and shot, weights, and is part of solder, pewter, fusible alloys and radiation shields. Lead has the highest atomic number of all stable elements, although the next element, bismuth, has a half-life so long (longer than the estimated age of the universe) it can be considered stable. Like mercury, another heavy metal, lead is a potent neurotoxin that accumulates in soft tissues and bone over time.

Contents

Characteristics

Lead has a dull luster and is a dense, ductile, very soft, highly malleable, bluish-white metal that has poor electrical conductivity. This true metal is highly resistant to corrosion, and because of this property, it is used to contain corrosive liquids (e.g., sulfuric acid). Because lead is very malleable and resistant to corrosion it is extensively used in building construction, e.g., external coverings of roofing joints. Lead can be toughened by adding a small amount of antimony or other metals to it. It is a common misconception that lead has a zero Thomson effect. All lead, except 204Pb, is the end product of a complex radioactive decay (see isotopes of lead below). Lead is also poisonous.

History

Roman lead water pipes with taps

Lead has been commonly used for thousands of years because it is widespread, easy to extract and easy to work with. It is highly malleable and ductile as well as easy to smelt. Metallic lead beads have been found in Çatalhöyük dating back to 6400 B.C.[1] In the early Bronze Age, lead was used with antimony and arsenic. Lead is mentioned in the Book of Exodus (15:10).

In alchemy, lead was thought to be the oldest metal and was associated with the planet Saturn. Lead pipes that bear the insignia of Roman emperors are still in service and many Roman "pigs" (ingots) of lead figure in Derbyshire lead mining history and in the history of the industry in other English centres. The Romans also used lead in molten form to secure iron pins that held together large limestone blocks in certain monumental buildings. Lead's symbol Pb is an abbreviation of its Latin name plumbum for soft metals; originally it was plumbum nigrum (literally, "black plumbum"), where plumbum candidum (literally, "bright plumbum") was tin. The English words "plumbing" and "plumb-bob" also derive from this Latin root.

Lead also refers collectively to the organic and inorganic compounds of lead, which are toxic. Lead poisoning was documented in ancient Rome, Greece, and China. In the 20th century, the use of lead in paint pigments was sharply reduced because of the danger of lead poisoning, especially to children.[2][3][4] By the mid-1980s, a significant shift in lead end-use patterns had taken place. Much of this shift was a result of the U.S. lead consumers' compliance with environmental regulations that significantly reduced or eliminated the use of lead in non-battery products, including gasoline, paints, solders, and water systems. Lead use is being further curtailed by the European Union's RoHS directive. Lead may still be found in harmful quantities in stoneware, vinyl (such as that used for tubing and the insulation of electrical cords), and brass manufactured in China. Between 2006 and 2007 many children's toys made in China were recalled, primarily due to lead in paint used to color the product.

Occurrence

Metallic lead does occur in nature, but it is rare. Lead is usually found in ore with zinc, silver and (most abundantly) copper, and is extracted together with these metals. The main lead mineral is galena (PbS), which contains 86.6% lead. Other common varieties are cerussite (PbCO3) and anglesite (PbSO4).

Processing ore

Lead ore

Most ores contain less than 10% lead, and ores containing as little as 3% lead can be economically exploited. Ores are crushed and concentrated by froth flotation typically to 70% or more. Sulfide ores are roasted, producing primarily lead oxide and a mixture of sulfates and silicates of lead and other metals contained in the ore.[5]

Lead oxide from the roasting process is reduced in a coke-fired blast furnace.[6] This converts most of the lead to its metallic form. Three additional layers separate in the process and float to the top of the metallic lead. These are slag (silicates containing 1.5% lead), matte (sulfides containing 15% lead), and speiss (arsenides of iron and copper). These wastes contain concentrations of copper, zinc, cadmium, and bismuth that can be recovered economically, as can their content of unreduced lead.[5]

Metallic lead that results from the roasting and blast furnace processes still contains significant contaminants of arsenic, antimony, bismuth, zinc, copper, silver, and gold. The melt is treated in a reverberatory furnace with air, steam, and sulfur, which oxidizes the contaminants except silver, gold, and bismuth. The oxidized contaminants are removed by drossing, where they float to the top and are skimmed off.[5][7]

Most lead ores contain significant concentrations of silver, resulting in the smelted metal also containing silver as a contaminant. Metallic silver as well as gold is removed and recovered economically by means of the Parkes process.[8][5][7]

Desilvered lead is freed of bismuth according to the Betterton-Kroll process by treating it with metallic calcium and magnesium, which forms a bismuth dross that can be skimmed off.[5][7]

Very pure lead can be obtained by processing smelted lead electolytically by means of the Betts process. The process uses anodes of impure lead and cathodes of pure lead in an electrolyte of silica fluoride.[5][7]

Production and recycling

Worldwide production and consumption of lead is increasing. Total annual production is about 8 million tonnes; about half is produced from recycled scrap. Top lead producing countries, as of 2008, are Australia, China, USA, Peru, Canada, Mexico, Sweden, Morocco, South Africa and North Korea.[7] Australia, China and the United States account for more than half of primary production.[9]

At current use rates, the supply of lead is estimated to run out in 42 years.[11] Environmental analyst, Lester Brown, however, has suggested lead could run out within 18 years based on an extrapolation of 2% growth per year.[12] This may need to be reviewed to take account of renewed interest in recycling, and rapid progress in fuel cell technology.

Isotopes

Main article: Isotopes of lead

Lead has seven isotopes in total (3 stable, 3 unstable, 1 radiogenic). The 3 stable isotopes are 206Pb, 207Pb and 208Pb. The 3 unstable isotopes are 204Pb, 205Pb and 210Pb. The one common radiogenic isotope, 202Pb, has a half-life of approximately 53,000 years.

Health effects

Main article: Lead poisoning

Lead is a poisonous metal that can damage nervous connections (especially in young children) and cause blood and brain disorders. Because of its low reactivity and solubility, lead poisoning usually only occurs in cases when the lead is dispersed, like when sanding lead based paint, or long term exposure in the case of pewter tableware. Long term exposure to lead or its salts (especially soluble salts or the strong oxidant PbO2) can cause nephropathy, and colic-like abdominal pains. The concern about lead's role in cognitive deficits in children has brought about widespread reduction in its use (lead exposure has been linked to schizophrenia). Most cases of adult elevated blood lead levels are workplace-related.[13] High blood levels are associated with delayed puberty in girls.[14]

Older houses may still contain substantial amounts of lead paint. White lead paint has been withdrawn from sale in industrialized countries, but the yellow lead chromate is still in use; for example, Holland Colours Holcolan Yellow. Old paint should not be stripped by sanding, as this produces inhalable dust.

Lead salts used in pottery glazes have on occasion caused poisoning, when acid drinks, such as fruit juices, have leached lead ions out of the glaze.[15] It has been suggested that what was known as "Devon colic" arose from the use of lead-lined presses to extract apple juice in the manufacture of cider. Lead is considered to be particularly harmful for women's ability to reproduce. For that reason, many universities do not hand out lead-containing samples to women for instructional laboratory analyses. Lead(II) acetate (also known as sugar of lead) was used by the Roman Empire as a sweetener for wine, and some consider this to be the cause of the dementia that affected many of the Roman Emperors.[16]

Lead as a soil contaminant is a widespread issue, since lead is present in natural deposits and may also enter soil through (leaded) gasoline leaks from underground storage tanks or through a wastestream of lead paint or lead grindings from certain industrial operations.

Lead can also be found listed as a criteria pollutant in the United States Clean Air Act section 108. Lead that is emitted into the atmosphere can be inhaled, or it can be ingested after it settles out of the air. It is rapidly absorbed into the bloodstream and is believed to have adverse effects on the central nervous system, the cardiovascular system, kidneys, and the immune system.[17]

Biochemistry of lead poisoning

In the human body, lead inhibits porphobilinogen synthase and ferrochelatase, preventing both porphobilinogen formation and the incorporation of iron into protoporphyrin IX, the final step in heme synthesis. This causes ineffective heme synthesis and subsequent microcytic anemia.

Leaching of lead from metal surfaces

The Pourbaix diagram for lead in a non-complexing aqueous medium (eg perchloric acid / sodium hydroxide)[18]
The Pourbaix diagram for lead in citric acid/citrate[18]

It is clear from the Pourbaix diagram below that lead is more likely to corrode in a citrate medium than it is in a non-complexing medium. The central part of the diagram shows that lead metal is more easy to oxidise in the citrate medium than it is in normal water.

In a Pourbaix diagram, the acidity is plotted on the x axis using the pH scale, while how oxidising/reducing nature of the system is plotted on the y axis in terms of volts relative to the standard hydrogen electrode. The diagram shows the form of the element which is most chemically stable at each point, it only comments on thermodynamics and it says nothing about the rate of change (kinetics).

Occupational Exposure

It is widely used in the production of batteries, metal products (solder and pipes), ammunition and devices to shield X-rays leading to its exposure to the people working in these industries. Use of lead in gasoline, paints and ceramic products, caulking, and pipe solder has been dramatically reduced in recent years because of health concerns. Ingestion of contaminated food and drinking water is the most common source of lead exposure in human. Exposure can also occur via inadvertent ingestion of contaminated soil/dust or lead-based paint.

Testing of Lead

Water contamination can be tested with commercially available kits. Analysis of lead in whole blood is the most common and accurate method of assessing lead exposure in human. Erythrocyte protoporphyrin (EP) tests can also be used to measure lead exposure, but are not as sensitive at low blood lead levels (<20 μg/dL). Lead in blood reflects recent exposure. Bone lead measurements are an indicator of cumulative exposure. While measurements of urinary lead levels and hair have been used to assess lead exposure, they are not reliable.

Descriptive chemistry

See also: Category:Lead compounds

Various oxidized forms of lead are easily reduced to the metal. An example is heating PbO with mild organic reducing agents such as glucose. A mixture of the oxide and the sulfide heated together without any reducing agent will also form the metal.[8]

2PbO + PbS   →   3 Pb + SO2

Metallic lead is attacked only superficially by air, forming a thin layer of oxide that protects it from further oxidation. The metal is not attacked by sulfuric or hydrochloric acids. It does, however, dissolve in nitric acid with the evolution of nitric oxide gas to form dissolved Pb(NO3)2.

3 Pb + 8 H+ + 8 NO3   →   3 Pb2+ + 6 NO3 + 2 NO + 4H2O

When heated with nitrates of alkali metals, metallic lead oxidizes to form PbO (also known as litharge), leaving the corresponding alkali nitrite. PbO is representative of lead's II oxidation state. It is soluble in nitric and acetic acids, from which solutions it is possible to precipitate halide, sulfate, chromate, carbonate (PbCO3), and basic carbonate (Pb3(OH)2(CO3)2) salts of lead. The sulfide can also be precipitated from acetate solutions. These salts are all poorly soluble in water. Among the halides, the iodide is less soluble than the bromide, which, in turn, is less soluble than the chloride.[19]

The II oxide is also soluble in alkali hydroxide solutions to form the corresponding plumbite salt.[8]

PbO + 2OH + H2O   →   Pb(OH)42–

Chlorination of plumbite solutions causes the formation of lead's IV oxidation state.

Pb(OH)42– + Cl2   →   PbO2 + 2 Cl + 2 H2O

Lead dioxide is representative of the IV state, and is a powerful oxidizing agent. The chloride of this oxidation state is formed only with difficulty and decomposes readily into the II chloride and chlorine gas. The bromide and iodide of IV lead are not known to exist.[19] Lead dioxide dissolves in alkali hydroxide solutions to form the corresponding plumbates.[8]

PbO2 + 2 OH + 2 H2O   →   Pb(OH)62–

Lead also has an oxide that is a hybrid between the II and IV oxidation states. Red lead (also called minium) is Pb3O4.

Lead readily forms an equimolar alloy with sodium metal that reacts with alkyl halides to form organometallic compounds of lead such as tetraethyl lead.[20]

Chloride complexes

Diagram showing the forms of lead in chloride media[18]

Lead(II) forms a series of complexes with chloride, the formation of which alters the corrosion chemistry of the lead. This will tend to limit the solubility of lead in saline media.

Equilibrium constants for aqueous lead chloride complexes at 25 °C[21]
Pb2+ + Cl → PbCl+      K1 = 12.59
PbCl+ + Cl → PbCl20 K2 = 14.45
PbCl20 + Cl → PbCl3 K3 = 3.98 ×10−1
PbCl3 + Cl → PbCl42− K4 = 8.92 × 10−2


Phase diagrams of solubilities

Plot showing aqueous concentration of dissolved Pb2+ as a function of SO42−[18]
Diagram for lead in sulfate media[18]
See also: Phase diagram

Lead(II) sulfate is poorly soluble, as can be seen in the following diagram showing addition of SO42− to a solution containing 0.1M of Pb2+. The pH of the solution is 4.5, as above that, Pb2+ concentration can never reach 0.1M due to the formation of Pb(OH)2. Observe that Pb2+ solubility drops 10,000 fold as SO42− reaches 0.1M

Diagram showing the solubility of lead in chloride media. The lead concentrations are plotted as a function of the total chloride present.[18]
Pourbaix diagram for lead in chloride (0.1 M) media[18]

Here it can be seen that the addition of chloride can lower the solubility of lead, however in chloride rich media (such as aqua regia) the lead can become soluble again as anionic chlorocomplexes.

The Pourbaix diagram on the right is for a moderate concentration (0.1 M) of chloride.

Applications

Former applications

Contrary to popular belief, pencil "leads" have never been made from lead. The term comes from the Roman stylus, called the penicillus, which was made of lead.[27] When the pencil originated as a wrapped graphite writing tool, the particular type of graphite being used was named plumbago (lit. "act for lead"; "lead mockup").

See also

References

  1. Dennis L. Heskel (1983). "A Model for the Adoption of Metallurgy in the Ancient Middle East". Current Anthropology 24 (3): 362–366. doi:10.1086/203007. http://www.jstor.org/stable/2742674. 
  2. "NSW Multicultural Health Communication Service". NSW Health. Retrieved on 7 April 2007.
  3. "Download: Lead paint: Cautionary note". Queensland Government. Retrieved on 7 April 2007.
  4. "Lead Paint Information". Master Painters, Australia. Retrieved on 7 April 2007.
  5. 5.0 5.1 5.2 5.3 5.4 5.5 Samans, Carl H. Engineering Metals and their Alloys MacMillan 1949
  6. "Primary Extraction of Lead Technical Notes". LDA International. Retrieved on 7 April 2007.
  7. 7.0 7.1 7.2 7.3 7.4 "Primary Lead Refining Technical Notes". LDA International. Retrieved on 7 April 2007.
  8. 8.0 8.1 8.2 8.3 Pauling, Linus General Chemistry, W.H. Freeman 1947 ed.
  9. "Lead Information". LDA International. Retrieved on 2007-09-05.
  10. "Lead and Zinc Statistics". International Lead and Zinc Study Group. Retrieved on 2008-07-06.
  11. "How Long Will it Last?". New Scientist 194 (2605): 38–39. May 26, 2007. ISSN 0262-4079. 
  12. Brown, Lester (2006). Plan B 2.0: Rescuing a Planet Under Stress and a Civilization in Trouble. New York: W.W. Norton. p. 109. ISBN 0393328317. 
  13. "NIOSH ABLES". United States National Institute for Occupational Safety and Health. Retrieved on 2007-10-04.
  14. Endocrine Disruptors and Abnormalities of Pubertal Development, Schoeters G, et al. Basic & Clinical Pharmacology & Toxicology, 102, 168–175, 2008
  15. "Government report on lead poisoning from ceramic glazes Government report on lead poisoning from ceramic glazes". Retrieved on 2008-04-24.
  16. "The Pernicious Allure of Lead". New York Times.
  17. http://www3.interscience.wiley.com.offcampus.lib.washington.edu/cgi-bin/fulltext/121393911/PDFSTART
  18. 18.0 18.1 18.2 18.3 18.4 18.5 18.6 Ignasi Puigdomenech, Hydra/Medusa Chemical Equilibrium Database and Plotting Software (2004) KTH Royal Institute of Technology, freely downloadable software at [1]
  19. 19.0 19.1 Brady, James E. and Holum, John R. Descriptive Chemistry of the Elements John Wiley and Sons
  20. Merck Index of Chemicals and Drugs, 9th ed., monograph 8393
  21. Ward, C.H.; Hlousek, Douglas A.; Phillips, Thomas A.; Lowe, Donald F. (2000). Remediation of Firing Range Impact Berms. CRC Press. ISBN 1566704626. 
  22. Dr. Rooney, Corinne. "Contamination at Shooting Ranges" (PDF). The Lead Group, incorporated. Retrieved on 7 April 2007.
  23. Randerson, James (June 2002). "Candle pollution". NewScientist.com (2348). http://www.newscientist.com/article/mg17423481.900-candle-pollution.html. Retrieved on 2007-04-07. 
  24. "Applications for Lead". Retrieved on 7 April 2007.
  25. "Banning of Leaded Gasoline for Highway Use". Retrieved on 23 September 2008.
  26. Henkels, W. H.; Geppert, L. M.; Kadlec, J.; Epperlein, P. W.; Beha, H. (September 1985). "Josephson 4 K-bit cache memory design for a prototype signal processor.". Harvard University. Retrieved on 7 April 2007.
  27. "A history of pencils". www.pencils.com. Retrieved on 7 April 2007.

Further reading

External links