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Lead, 82Pb
A small gray metal cube surrounded by three gray metal nuggets in front of a light gray background
Lead
Pronunciation/ˈlɛd/ (led)
Appearancemetallic gray
Standard atomic weight Ar°(Pb)
Lead in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
Sn

Pb

Fl
thalliumleadbismuth
Atomic number (Z)82
Groupgroup 14 (carbon group)
Periodperiod 6
Block  p-block
Electron configuration[Xe] 4f14 5d10 6s2 6p2
Electrons per shell2, 8, 18, 32, 18, 4
Physical properties
Phase at STPsolid
Melting point600.61 K ​(327.46 °C, ​621.43 °F)
Boiling point2022 K ​(1749 °C, ​3180 °F)
Density (at 20 °C)11.348 g/cm3[3]
when liquid (at m.p.)10.66 g/cm3
Heat of fusion4.77 kJ/mol
Heat of vaporization179.5 kJ/mol
Molar heat capacity26.650 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 978 1088 1229 1412 1660 2027
Atomic properties
Oxidation statescommon: +2, +4
−4,[4] −2,? −1,? 0,[5] +1,? +3?
ElectronegativityPauling scale: 2.33 (in +4), 1.87 (in +2)
Ionization energies
  • 1st: 715.6 kJ/mol
  • 2nd: 1450.5 kJ/mol
  • 3rd: 3081.5 kJ/mol
Atomic radiusempirical: 175 pm
Covalent radius146±5 pm
Van der Waals radius202 pm
Color lines in a spectral range
Spectral lines of lead
Other properties
Natural occurrenceprimordial
Crystal structureface-centered cubic (fcc) (cF4)
Lattice constant
Face-centered cubic crystal structure for lead
a = 494.99 pm (at 20 °C)[3]
Thermal expansion28.73×10−6/K (at 20 °C)[3]
Thermal conductivity35.3 W/(m⋅K)
Electrical resistivity208 nΩ⋅m (at 20 °C)
Magnetic orderingdiamagnetic
Molar magnetic susceptibility−23.0×10−6 cm3/mol (at 298 K)[6]
Young's modulus16 GPa
Shear modulus5.6 GPa
Bulk modulus46 GPa
Speed of sound thin rod1190 m/s (at r.t.) (annealed)
Poisson ratio0.44
Mohs hardness1.5
Brinell hardness38–50 MPa
CAS Number7439-92-1
History
DiscoveryMiddle East (7000 BCE)
Symbol"Pb": from Latin plumbum
Isotopes of lead
Main isotopes[7] Decay
abun­dance half-life (t1/2) mode pro­duct
202Pb synth 5.25×104 y ε 202Tl
204Pb 1.40% stable
205Pb trace 1.73×107 y ε 205Tl
206Pb 24.1% stable
207Pb 22.1% stable
208Pb 52.4% stable
209Pb trace 3.253 h β 209Bi
210Pb trace 22.20 y β 210Bi
211Pb trace 36.1 min β 211Bi
212Pb trace 10.64 h β 212Bi
214Pb trace 26.8 min β 214Bi
Isotopic abundances vary greatly by sample[8]
 Category: Lead
| references
Lead pipe in Roman baths

Lead (Template:PronEng) is a main group element with a symbol Pb (Template:Lang-la). 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 it is exposed to air and is a shiny chrome silver when melted into a liquid. Lead is used in building construction, lead-acid batteries, bullets and shot, weights, and is part of solder, pewter, and fusible alloys. 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.

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

A stylistic variation of the Alchemical symbol for lead, used since ancient times also for the planet Saturn.

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.[9] 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.[10][11][12] 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.

Lead mining in Wales

Lead mining dates back to at least Roman times and continued until well into the 20th century. Galena is found commonly in northeast Wales. The Northeast Wales Orefield was by far the most important source of lead and zinc in Wales and second in national importance only to the North Pennine Orefield. Galena is present in steeply dipping fissure veins and in pipes and is in Mississippi Valley-type lead-zinc-fluorite and copper-dolomite associations. The mineralisation occurs in the upper parts of the Loggerheads and Cefn Mawr Formations of the Carboniferous Limestone.[13]

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.[14]

Lead oxide from the roasting process is reduced in a coke-fired blast furnace.[15] 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.[14]

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.[14][16]

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.[17][14][16]

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.[14][16]

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.[14][16]

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.[16] Australia, China and the United States account for more than half of primary production.[18]

  • 2007 mine production: 3,595,000 tonnes
  • 2007 metal production: 8,127,000 tonnes[19]

At current use rates, the supply of lead is estimated to run out in 42 years.[20] Environmental analyst, Lester Brown, however, has suggested lead could run out within 18 years based on an extrapolation of 2% growth per year.[21] This may need to be reviewed to take account of renewed interest in recycling, and rapid progress in fuel cell technology.

Isotopes

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

Health effects

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[citation needed]). Most cases of adult elevated blood lead levels are workplace-related.[22] High blood levels are associated with delayed puberty in girls.[23]

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.[24] 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.[citation needed] 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.[25]

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.

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.[citation needed]

Leaching of lead from metal surfaces

The Pourbaix diagram for lead in a non-complexing aqueous medium (eg perchloric acid / sodium hydroxide)[26]
The Pourbaix diagram for lead in citric acid/citrate[26]

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 however they are not reliable.

Descriptive chemistry

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.[17]

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 (Pb
3
(OH)
2
(CO
3
)
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.[27]

The II oxide is also soluble in alkali hydroxide solutions to form the corresponding plumbite salt.[17]

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.[27] Lead dioxide dissolves in alkali hydroxide solutions to form the corresponding plumbates.[17]

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.[28]

Chloride complexes

Diagram showing the forms of lead in chloride media[26]

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[29]
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−[26]
Diagram for lead in sulfate media[26]

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.[26]
Pourbaix diagram for lead in chloride (0.1 M) media[26]

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

  • Lead is a major constituent of the lead-acid battery used extensively as a car battery.
  • Lead is used as a coloring element in ceramic glazes, notably in the colors red and yellow.
  • Lead is used to form glazing bars for stained glass or other multi-lit windows. The practice has become less common, not for danger but for stylistic reasons.
  • Lead is used as projectiles for firearms and fishing sinkers because of its density, low cost compared to alternative products and ease of use due to relatively low melting point.[30]
  • Lead or "sheet-lead" is used as a sound deadening layer in such areas as wall, floor and ceiling design in sound studios where levels of airborne and mechanically produced sound are targeted for reduction or virtual elimination.
  • Lead is used in some candles to treat the wick to ensure a longer, more even burn. Because of the dangers, European and North American manufacturers use more expensive alternatives such as zinc.[31]
  • Lead is used as shielding from radiation, e.g. in x-ray rooms.
  • Molten lead is used as a coolant, eg. for lead cooled fast reactors.
  • Lead glass is composed of 12-28% lead oxide. It changes the optical characteristics of the glass and reduces the transmission of radiation.
  • Lead is the traditional base metal of organ pipes, mixed with varying amounts of tin to control the tone of the pipe.
  • Lead is used as electrodes in the process of electrolysis.
  • Lead is used in solder for electronics, although this usage is being phased out by some countries to reduce the amount of environmentally unfriendly waste.
  • Lead is used in high voltage power cables as sheathing material to prevent water diffusion into insulation.
  • Lead is used for the ballast keel of sailboats. Its high weight-to-volume ratio allows it to counterbalance the heeling effect of wind on the sails while at the same time occupying a small volume and thus offering the least underwater resistance. It does not have the weight-to-volume ratio of many heavy metals, but its low cost increases its use in these and other applications.
  • Lead is added to brass to reduce machine tool wear.
  • Some artists using oil-based paints continue to use lead carbonate white, citing its properties in comparison with the alternatives.
  • Lead, in the form of strips or "tape" is used for the customization of tennis racquets. Tennis racquets of the past sometimes had lead added to them by the manufacturer to increase weight.
  • Lead has many uses in the construction industry, e.g. lead sheets are used as architectural metals in roofing material, cladding, flashings, gutters and gutter joints, and on roof parapets. Detailed lead mouldings are used as decorative motifs used to fix lead sheet.
  • Lead is frequently used in scuba diving weight belts to counteract the diver's natural buoyancy and that of his equipment.
  • Lead is often used to balance the wheels of a car; this use is being phased out in favor of other materials for environmental reasons.
  • Lead is still widely used in statues and sculptures.
  • Tetra-ethyl lead is used as an anti-knock additive for aviation fuel in piston driven aircraft.
  • Lead-based semiconductors, such as lead telluride, lead selenide and lead antimonide are finding applications in photovoltaic (solar energy) cells and infrared detectors.[32]

Former applications

  • Lead pigments were used in lead paint for white as well as yellow, orange, and red. Most have been discontinued due of the dangers of lead poisoning. However, lead chromate is still in industrial use. Lead carbonate (white) is the traditional pigment for the priming medium for oil painting, but it has been largely displaced by the zinc and titanium oxide pigments. It was also quickly replaced in water-based painting mediums.
  • Lead carbonate white was used by the Japanese geisha and in the West for face-whitening make-up, which caused ill-health in the wearer.
  • Lead was the hot metal used in hot metal typesetting.
  • Lead was used for plumbing in Ancient Rome.
  • Lead was used as a preservative for food and drink in Ancient Rome.
  • Lead was used for joining cast iron water pipes and used as a material for small diameter water pipes until the early 1970s.
  • Tetraethyl lead was used in leaded fuels to reduce engine knocking; however, this is no longer common practice in the Western world due to its incompatibility with catalytic converters.
  • The EPA banned the use of lead gasoline for highway transportation, beginning January 1st, 1996.[33]
  • Lead has been used to make "clubs" or bats more lethal by melting it into a hole drilled into the top
  • Lead was used to make bullets for slings.
  • Lead was used as a component of toys. Due to toy safety regulations, this use has been stopped in the United States.
  • Lead was used in car body filler, which was used in many custom cars in the 1940s–60s. Hence the term Leadsled.
  • Lead is a superconductor at 7.2 K and IBM tried to make a Josephson effect computer out of lead-alloy.[34]
  • Lead was also used in pesticides before the 1950s, when fruit orchards were treated (ATSDR).

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.[35] 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

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  2. ^ Prohaska, Thomas; Irrgeher, Johanna; Benefield, Jacqueline; Böhlke, John K.; Chesson, Lesley A.; Coplen, Tyler B.; Ding, Tiping; Dunn, Philip J. H.; Gröning, Manfred; Holden, Norman E.; Meijer, Harro A. J. (2022-05-04). "Standard atomic weights of the elements 2021 (IUPAC Technical Report)". Pure and Applied Chemistry. doi:10.1515/pac-2019-0603. ISSN 1365-3075.
  3. ^ a b c Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
  4. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 28. ISBN 978-0-08-037941-8.
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  6. ^ Weast, Astle & Beyer 1983, p. E110.
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  8. ^ Meija et al. 2016.
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  11. ^ "Download: Lead paint: Cautionary note". Queensland Government. {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)
  12. ^ "Lead Paint Information". Master Painters, Australia. {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)
  13. ^ Davies, J.R., Wilson, D. & Williamson, I.T. (2004). The geology of the country around Flint. Memoir of the British Geological Survey, Sheet 108. (England and Wales). British Geological Survey, Keyworth.
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  16. ^ a b c d e "Primary Lead Refining Technical Notes". LDA International. {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help) Cite error: The named reference "leadorg" was defined multiple times with different content (see the help page).
  17. ^ a b c d Pauling, Linus General Chemistry, W.H. Freeman 1947 ed.
  18. ^ "Lead Information". LDA International. Retrieved 2007-09-05.
  19. ^ "Lead and Zinc Statistics". International Lead and Zinc Study Group. {{cite web}}: |access-date= requires |url= (help); Missing or empty |url= (help); Unknown parameter |http://www.ilzsg.org/static/statistics.aspx?from= ignored (help)
  20. ^ "How Long Will it Last?". New Scientist. 194 (2605): 38–39. May 26, 2007. ISSN 0262-4079. {{cite journal}}: Check date values in: |date= (help)
  21. ^ 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.
  22. ^ "NIOSH ABLES". United States National Institute for Occupational Safety and Health. Retrieved 2007-10-04.
  23. ^ Endocrine Disruptors and Abnormalities of Pubertal Development, Schoeters G, et al. Basic & Clinical Pharmacology & Toxicology, 102, 168–175, 2008
  24. ^ Government report on lead poisoning from ceramic glazes "Government report on lead poisoning from ceramic glazes". Retrieved 2008-04-24. {{cite web}}: Check |url= value (help); Cite has empty unknown parameter: |1= (help)
  25. ^ "The Pernicious Allure of Lead". New York Times.
  26. ^ a b c d e f g Ignasi Puigdomenech, Hydra/Medusa Chemical Equilibrium Database and Plotting Software (2004) KTH Royal Institute of Technology, freely downloadable software at [1]
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  28. ^ Merck Index of Chemicals and Drugs, 9th ed., monograph 8393
  29. ^ Ward, C.H.; Hlousek, Douglas A.; Phillips, Thomas A.; Lowe, Donald F. (2000). Remediation of Firing Range Impact Berms. CRC Press. ISBN 1566704626.{{cite book}}: CS1 maint: multiple names: authors list (link)
  30. ^ Dr. Rooney, Corinne. "Contamination at Shooting Ranges" (PDF). The Lead Group, incorporated. {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)
  31. ^ Randerson, James (2002). "Candle pollution". NewScientist.com (2348). Retrieved 2007-04-07. {{cite journal}}: Unknown parameter |month= ignored (help)
  32. ^ "Applications for Lead". {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)
  33. ^ "Banning of Leaded Gasoline for Highway Use". {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)
  34. ^ Henkels, W. H.; Geppert, L. M.; Kadlec, J.; Epperlein, P. W.; Beha, H. (1985). "Josephson 4 K-bit cache memory design for a prototype signal processor". Harvard University. {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help); Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  35. ^ "A history of pencils". www.pencils.com. {{cite web}}: Unknown parameter |accessdaymonth= ignored (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)

Further reading

  • Keisch, B., Feller, R. L., Levine, A. S., and Edwards, R. R.: "Dating and Authenticating Works of Art by Measurement of Natural Alpha Emitters". In: Science, 155, No. 3767, p. 1238–1242, 1967.
  • Keisch, B: "Dating Works of Art Through their Natural Radioactivity: Improvements and Applications". In: Science, 160, p. 413–415, 1968.
  • Keisch, B: "Discriminating Radioactivity Measurements of Lead: New Tool for Authentication". In: Curator, 11, No. 1., p. 41–52, 1968.

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