Lead

This article is about the metal. For other uses, see Lead (disambiguation).

Lead, ₈₂Pb

Lead
Pronunciation	/ˈlɛd/ ​(led)
Appearance	metallic gray
Standard atomic weight Ar°(Pb)
	[206.14, 207.94] 207.2±1.1 (abridged)
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 thallium ← lead → bismuth
Atomic number (Z)	82
Group	group 14 (carbon group)
Period	period 6
Block	p-block
Electron configuration	[Xe] 4f14 5d10 6s2 6p2
Electrons per shell	2, 8, 18, 32, 18, 4
Physical properties
Phase at STP	solid
Melting point	600.61 K ​(327.46 °C, ​621.43 °F)
Boiling point	2022 K ​(1749 °C, ​3180 °F)
Density (at 20 °C)	11.348 g/cm3
when liquid (at m.p.)	10.66 g/cm3
Heat of fusion	4.77 kJ/mol
Heat of vaporization	179.5 kJ/mol
Molar heat capacity	26.650 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 states	common: +2, +4 −4, −2,? −1,? 0, +1,? +3?
Electronegativity	Pauling 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 radius	empirical: 175 pm
Covalent radius	146±5 pm
Van der Waals radius	202 pm
Spectral lines of lead
Other properties
Natural occurrence	primordial
Crystal structure	​face-centered cubic (fcc) (cF4)
Lattice constant	a = 494.99 pm (at 20 °C)
Thermal expansion	28.73×10−6/K (at 20 °C)
Thermal conductivity	35.3 W/(m⋅K)
Electrical resistivity	208 nΩ⋅m (at 20 °C)
Magnetic ordering	diamagnetic
Molar magnetic susceptibility	−23.0×10−6 cm3/mol (at 298 K)
Young's modulus	16 GPa
Shear modulus	5.6 GPa
Bulk modulus	46 GPa
Speed of sound thin rod	1190 m/s (at r.t.) (annealed)
Poisson ratio	0.44
Mohs hardness	1.5
Brinell hardness	38–50 MPa
CAS Number	7439-92-1
History
Discovery	Middle East (7000 BCE)
Symbol	"Pb": from Latin plumbum
Isotopes of lead
Main isotopes 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

Lead (/lɛd/) is a chemical element with atomic number 82 and symbol Pb (from Template:Lang-la). It is a soft, malleable, and heavy metal. Freshly cut solid lead has a bluish-white color that soon tarnishes to a dull grayish color when exposed to air; the liquid metal has shiny chrome-silver luster. Lead's density of 11.34 g/cm³ exceeds that of most common materials. Lead has the second highest atomic number of all practically stable elements. As such, lead is located at the end of some decay chains of heavier elements, which in part accounts for the relative abundance of lead: it exceeds those of other similarly-numbered elements.

Lead is a post-transition metal, and is relatively inert unless powdered. Its weakened metallic character is illustrated by its general amphoteric nature: it and its oxides react with both acids and bases. It also displays a marked tendency toward covalent bonding. Its compounds are most commonly found in the +2 oxidation state, rather than +4, unlike the lighter group 14 elements. Exceptions are mostly limited to organolead compounds, where the positive charge on lead is dispersed and stabilized. Like the lighter group 14 elements, lead shows a tendency to bond to itself, forming complicated chain, ring, or polyhedral structures.

Lead is relatively easy to extract, and the metal was known to prehistoric people in Western Asia. While its softness and dullness prevented it from high demand, galena—a principle ore of lead—often bore silver in it, which helped initiate production of lead. Lead production peaked in ancient Rome, and lead became easily available to common people. After the fall of Rome, levels of lead production fell, and those of Rome were not surpassed anywhere until as late as the Industrial Revolution. The metal was established as poisonous as late as in the late nineteenth century, which led to its eventual displacement from many uses, and it has been or is being phased out from those which include immediate contact to people.

Lead has several properties that make it advantageous to use, alongside its commonness: high density, low melting point, ductility, and relative inertness against oxygen attack. Lead minerals are easier to mine and lead is easier to extract from its ores than many other metals, which makes the resulting metal relatively inexpensive. For example, lead is used in building construction, lead–acid batteries, bullets and shot, weights, as part of solders, pewters, fusible alloys, and as a radiation shield. Currently, lead is produced in quantities of around ten thousand tonnes annually; secondary production from recycling is gaining ground, accounting for around half of that figure. Lead's toxicity has been a reason why lead was or is being phased out for some uses. If ingested or inhaled, lead and its compounds are poisonous to animals and humans. Lead is a neurotoxin which accumulates in soft tissues and bones, damaging the nervous system and causing brain disorders. Excessive lead also causes blood disorders in mammals.

Etymology

The modern English word "lead" is of Germanic origin; it comes from the Middle English leed and Old English lēad (with the macron above the "e" signifying that the vowel sound of that letter is long). The Old English word is derived from the hypothetical Proto-Germanic *lauda- ("lead"). According to the linguistic hypothesis, this word bore descendants in most Germanic languages (with a major exception being German) of exactly the same meaning.

The origin of the Proto-Germanic *lauda- is not agreed on in the linguistic community. One hypothesis suggests it is derived from Proto-Indo-European *lAudh- ("lead"; capitalization of the vowel is equivalent to the macron). Another hypothesis suggests it is borrowed from Proto-Celtic *ɸloud-io- ("lead"). This word is related to the Latin plumbum, which gave the element its chemical symbol Pb. The origin of *ɸloud-io- presumably pre-dates the Proto-Indo-European language; while it is yet unknown, it is suggested it is also the origin of Proto-Germanic *bliwa- (which also means "lead"), from which stemmed the German Blei ("lead").

The name of the chemical element is not related to the verb of the same spelling, which is instead derived from (eventually) Proto-Germanic *laidijan- ("to lead").

Properties

Atomic

A lead atom has 82 electrons, arranged in an electronic configuration of [Xe]4f¹⁴5d¹⁰6s²6p². The combined first and second ionization energy of lead—the total energy required to remove the two 6p electrons from a neutral lead atom—is close to that of tin, its upper neighbor in group 14. This is unusual since ionization energies generally fall going down a group as an element's electrons become more distant from its nucleus. The similarity is attributable to the lanthanide contraction. This describes the greater-than-expected decrease in the radii of elements in the lanthanide series from atomic number 57, lanthanum, to 71, lutetium, and causes smaller than otherwise expected ionic radii for the subsequent elements starting with 72, hafnium. It results from poor shielding of the nucleus by the lanthanide 4f electrons; the outer electrons are drawn towards the nucleus, thus resulting in a smaller atomic radius. The combined first four ionization energies of lead exceed those of tin contrary to what the periodic trends would predict. For this reason lead, unlike tin, rarely has a +4 oxidation state in inorganic compounds. Such behavior is attributable to relativistic effects, which become particularly prominent at the bottom of the periodic table; the result is that the 6s electrons of lead become reluctant to participate in bonding, a phenomenon referred to as the inert pair effect.

All the lighter elements in group 14 have a stable or metastable allotrope in which they crystallize in the diamond cubic structure, involving covalent bonds. In this structure, each atom is tetrahedrally coordinated, indicating that all four bonds are equivalent, having each attained the lowest possible energy. To explain this, in spite of the fact that two of the electrons are in s-orbitals and the other two in higher-energy p-orbitals, orbital hybridization is invoked, in which one of the electrons is "promoted" from an s-orbital to a p-orbital, and then all form four intermediate hybrid orbitals in a process called sp³ hybridization. The inert pair effect affects the crystal structure of lead, because the promotion energy of a 6s-electron becomes larger than the amount of energy that would be released from the additional bonds formed. Thus, rather than having the diamond-cubic covalent structure, lead forms metallic bonds, in which only the p-electrons are delocalized and shared between the Pb²⁺ ions, resulting in a face-centered cubic structure like those of the similarly-sized divalent calcium and strontium.

Physical

A sample of lead freshly solidified from molten state

Lead is a bright silvery metal with a very slight shade of blue in a dry atmosphere. It tarnishes on contact with moist air, forming a complex surface mixture of compounds whose color and composition will vary depending on the prevailing conditions. Lead's characteristic properties include high density, softness, malleability, ductility, poor electrical conductivity compared to other metals, high resistance to corrosion (conferred by its surface patina), and a propensity to react with organic reagents.

Lead's face-centered cubic structure and high atomic weight give it a characteristically high density of 11.34 g/cm³, hence the idiom go down like a lead balloon. Its density exceeds that of common metals such as iron (7.87 g/cm³), copper (8.93 g/cm³), zinc (7.14 g/cm³). Some rarer metals are denser: tungsten and gold are both 19.3 g/cm³, while the densest metal known—osmium—has a density of 22.59 g/cm³, almost twice that of lead.

Lead is a very soft material with a Mohs hardness of 1.5; it can be scratched with a fingernail. It is malleable and ductile metal, with its malleability exceeding its ductility. Lead easily changes its shape, compared to most metals. Its compressive strength is high and it can therefore be rolled into extremely thin sheets. The bulk modulus—a measure of the ease of compressibility of a material—of lead is 45.8 GPa. (For comparison, that of aluminium is 75.2 GPa; copper 137.8 GPa; and mild steel 160–169 GPa.) Lead has to be treated carefully when being elongated into wire as its tensile strength is comparatively low: 12–17 MPa (that of aluminium is 6 times higher; copper 10 times higher; mild steel 15 times higher); this value is easily improved by adding small concentrations of other metals (such as antimony or copper).

The melting point of lead is 327.5 °C (621.5 °F), which is considered low from an industrial perspective. Its boiling point is 1749 °C (3180 °F). The electrical resistivity of lead at 20 °C is 208 nano-ohm-meters; this almost an order of magnitude higher than those of industrially applied metals (that of copper is 17.12 nΩ·m; gold 22.55 nΩ·m; aluminium 27.09 nΩ·m).

Chemical

Flame test: lead colors flame pale blue

As with many metals, finely divided powdered lead exhibits pyrophoricity. It burns with a bluish-white flame.

Bulk lead exposed to moist air forms a protective layer of varying composition. A common reaction is the formation of the oxide which in turn reacts with carbon dioxide to give lead carbonate. Other insoluble compounds, such the sulfate or chloride, may form the protective layer if lead is exposed to a different chemical environment.

Fluorine reacts with lead at room temperature, forming lead(II) fluoride. The reaction with chlorine is similar, but requires heating: the chloride layer diminishes the reactivity of the elements. Molten lead reacts with the chalcogens to give lead(II) chalcogenides.

The presence of carbonates or sulfates results in the formation of insoluble lead salts, which protect the metal from corrosion. So does carbon dioxide, as the insoluble lead carbonate is formed; however an excess of this gas will result in the formation of the soluble bicarbonate, which makes the use of lead pipes dangerous. Water in the presence of oxygen attacks lead to start an accelerating reaction. Lead also dissolves in concentrated alkalis (≥10%) because of the amphoteric character and solubility of plumbites.

The metal is not attacked by dilute sulfuric acid; the concentrated acid dissolves lead thanks to complexation. Lead reacts slowly with hydrochloric acid; nitric acid reacts vigorously to form nitrogen oxides and lead(II) nitrate. Organic acids, such as acetic acid, also dissolve lead, but this reaction requires oxygen as well.

Isotopes

Main article: Isotopes of lead

Lead has four stable isotopes, lead-204, lead-206, lead-207, and lead-208. The high number of stable isotopes relies on the fact that lead's atomic number of 82 is even, and is a magic number. With its high atomic number, lead is the second-heaviest element that occurs naturally in the form of isotopes regarded as stable: bismuth has a higher atomic number of 83, but its only primordial isotope was found in 2003 to be very slightly radioactive. The four stable isotopes of lead could theoretically undergo alpha decay to isotopes of mercury with a release of energy, but this has not been observed for any of them: accordingly, their predicted half-lives are extremely long, ranging up to over 10¹⁰⁰ years. As such, lead is often quoted as the heaviest stable element.

Holsinger meteorite, the largest piece of the Canyon Diablo meteorite. Uranium–lead dating and lead–lead dating on this meteorite allowed refinement of the age of the Earth to 4.55 billion ± 70 million years.

Three of these isotopes are also found in three of the four major decay chains: lead-206, lead-207, and lead-208, are the final decay products of uranium-238, uranium-235, and thorium-232, respectively; the decay chains are called the uranium series, actinium series, and thorium series. Since the amounts of them in nature depend on the presence of other elements, the isotopic composition of natural lead varies between samples: in particular, the relative amount of lead-206 may vary between 20.84% and 27.78%, and the abundance of lead-208 may vary between 52.4% in normal samples to 90% in thorium ores. (For this reason, the atomic weight of lead is given to only one decimal place.) As time passes, the ratio of lead-206 and lead-207 to lead-204 increase, since the former two are supplemented by radioactive decay of heavier elements and the latter is not; this allows for lead–lead dating. Analogously, as uranium decays (eventually) into lead, their relative amounts change; this allows for uranium–lead dating.

Apart from the stable isotopes, which make up almost all lead that exists naturally, there are trace quantities of a few radioactive isotopes. One of them is lead-210; although it has a half-life of 22.3 years, a period too short to allow any primordial lead-210 to exist, some small non-primordial quantities of it occur in nature, because lead-210 is found in the uranium series: thus, even though it constantly decays away, it is constantly regenerated by decay of its parent, polonium-214, which, while also constantly decaying, is also supplied by decay of its parent, and so on, all the way up to original uranium-238, which has been present for billions of years on Earth. Lead-210 is particularly useful for helping to identify ages of samples containing it, which is performed by measuring lead-210 to lead-206 ratios (both isotopes are present in a single decay chain). Lead-214 is also present in the decay chain of natural uranium-238, lead-212 is present in that of natural thorium-232, and lead-211 is present in that of natural uranium-235; therefore, traces of all three of these isotopes exist naturally as well. Lastly, very minute traces of lead-209 are also present from the cluster decay of radium-223, one of the daughter products of natural uranium-235. Hence, natural lead consists of not only the four stable isotopes, but also minute traces of another five short-lived radioisotopes.

In total, thirty-eight isotopes of lead have been synthesized, with mass numbers of 178–215. Lead-205 is the most stable radioisotope of lead, with a half-life of around 1.5×10⁷ years. The second-most stable radioisotope is the synthetic lead-202, which has a half-life of about 53,000 years, longer than any of the natural trace radioisotopes. Additionally, 47 nuclear isomers (long-lived excited nuclear states), of 24 lead isotopes, have been characterized. The longest-lived isomer is lead-204m2 with a half-life of about 1.1 hours).

Chemistry

See also: Compounds of lead

Lead shows two main oxidation states: +4 and +2. The tetravalent state is common for group 14. Tne divalent state is rare for carbon and silicon, minor for germanium, important (but not prevailing) for tin, and is the more important for lead: even the strongest oxidizing agents, oxygen and fluorine, initially oxidize lead only to lead(II). This is caused by relativistic effects, specifically the inert pair effect, which manifests itself when there is a large difference in electronegativity between lead and, for example, oxide, halide, or nitride anions, leading to a significant partial positive charge on lead. The result is a stronger contraction of the lead 6s orbital than is the case for the 6p orbital, making it rather inert in ionic compounds. This is not quite as applicable to compounds in which lead forms covalent bonds to elements of similar electronegativity such as carbon in organolead compounds. Here the 6s and 6p orbitals remain similarly sized and sp³ hybridization in compounds is still energetically favorable; as such, lead, like carbon, is predominantly tetravalent in organolead compounds. The 5s electron pair tends to be stereochemically active in tin(II) compounds, but is much less so in lead(II) compounds. Consequently, there are often structural similarities between lead(II) compounds and analogous compounds of the divalent cations of calcium, strontium, barium, europium, and ytterbium.

The electrode potential of lead shows that it is only slightly easier to oxidize than hydrogen. Lead can therefore dissolve in acids, but this is often impossible due to factors such as the formation of insoluble salts. Electronegativity, although often thought to be constant for each element, is a variable property; lead shows a high electronegativity difference between values for lead(II) and lead(IV) of —1.87 and 2.33, respectively. This difference marks a reversal in the trend of increasing stability of the +4 oxidation state down group 14; tin, by comparison, has electronegativities of 1.80 and 1.96 in the +2 and +4 oxidation states.

Inorganic compounds

Lead(II)

Crystalline form of lead sulfate

Lead (II) compounds are characteristic of the inorganic chemistry of lead. Even strong oxidizing agents like fluorine and chlorine react with lead at room temperature to give only PbF₂ and PbCl₂. Lead forms binary compounds with many nonmetals, but not all of them; for example there is no known lead carbide.

Most lead(II) compounds are ionic, but they are not as ionic as those of many other metals. In particular, many lead(II) compounds are water-insoluble. In solution, lead(II) ions are colorless, but under specific conditions, lead is capable of changing its color. Unlike tin(II) ions, these do not react as reducing agents in solution. Lead(II) ions partially hydrolyze in aqueous solution to form Pb(OH)⁺ and finally Pb₄(OH)₄ (in which the hydroxyls ions act as bridging ligands).

Lead monoxide exists in two allotropes, red α-PbO and yellow β-PbO, the latter being stable only above around 488 °C. It is the most commonly applicable compound of lead. Its hydroxide counterpart, lead(II) hydroxide, is not capable of existence outside of solution; in solution, it is known to form plumbite anions. Lead commonly reacts with the heavier chalcogens. Lead sulfide can only be dissolved in strong acids. It is a semiconductor, a photoconductor, and an extremely sensitive infrared radiation detector. A mixture of the monoxide and the monosulfide, when heated, forms the metal. The other two chalcogenides are likewise photo-conducting. They are quite unusual in that their color becomes lighter down the group.

  Lead and   oxygen in a tetragonal unit cell of lead(II,IV) oxide

Lead dihalides are well-characterized; this includes the diastatide, and mixed examples, such as PbFCl. The relative insolubility of the latter forms a useful basis for the gravimetric determination of fluorine. The difluoride was the first ionically conducting compound to be discovered (in 1838, by Michael Faraday). The other dihalides decompose on exposure to ultraviolet or visible light, especially the diiodide. Many pseudohalides are also known. Lead(II) forms a tremendous variety of coordination complexes, such as [PbCl₄]²⁻, [PbCl₆]⁴⁻, and the chain anion [Pb₂Cl₉]_n⁵ⁿ⁻, although most of them are not yet adequately characterized structurally.

Lead(II) sulfate is well known for its insolubility in water, like the sulfates of the other heavy divalent cations; lead(II) nitrate and lead(II) acetate, in contrast, are very soluble, and this facility is exploited in the synthesis of other lead compounds.

Lead(IV)

Few inorganic lead(IV) compounds are known, and they are typically strong oxidants or exist only in highly acidic solutions. Lead(II) oxide gives a mixed oxide on further oxidation, Pb
₃O
₄. It is described as lead(II,IV) oxide, or structurally 2PbO•PbO
₂, and is the best-known mixed valence lead compound. Lead dioxide is a strong oxidizing agent, capable of oxidizing hydrochloric acid to chlorine gas. This is because the expected PbCl₄ that would be produced is unstable and spontaneously decomposes to PbCl₂ and Cl₂. Analogously to lead monoxide, lead dioxide is capable of forming plumbate anions. Lead tetrafluoride, a yellow crystalline powder, is stable, but less stable than the difluoride. Lead tetrachloride (a yellow oil) decomposes at room temperature, lead tetrabromide is less stable still and the existence of lead tetraiodide is questionable. Lead disulfide, like the monosulfide, is a semiconductor. Lead(IV) selenide is also known.

Other oxidation states

See also: Plumbide

The capped square antiprismatic anion [Pb₉]⁴⁻ from [K(18-crown-6)]₂K₂Pb₉·(en)_1.5. This is not a simple Zintl compound, but rather contains the organic molecules 18-crown-6 and ethylenediamine (en) in order to stabilize the crystal structure.

Some lead compounds exist in formal oxidation states other than +4 or +2. Lead(III) may be obtained as an intermediate between lead(II) and lead(IV), in larger organolead complexes (rather than on its own). This oxidation state is not specifically stable, as the lead(III) ion (and, consequently, the larger complexes containing it) is a radical; the same applies for lead(I), which can also be found in such species.

Negative oxidation states can occur as Zintl phases, as either free lead anions, for example, in Ba
₂Pb, with lead formally being lead(−IV), or in oxygen-sensitive cluster ions, for example, in a trigonal bipyramidal Pb⁵⁻
₂ ion, where two lead atoms are lead(−I) and three are lead(0): this illustrates lead's proclivity towards catenation (the ability to form chains of atoms of the same element), an ability shared with all the lighter members of group 14 and more generally with most of the heavy p-block elements. In such anions, each atom is at a polyhedral vertex and contributes two electrons to each covalent bond along an edge from their sp³ hybrid orbitals, the other two being an external lone pair. The shapes of such anions may be determined by Wade's rules. They may be made by reduction of lead by sodium in liquid ammonia.

Many mixed lead(II,IV) oxides are known. When PbO₂ is heated in air, it becomes Pb₁₂O₁₉ at 293 °C, Pb₁₂O₁₇ at 351 °C, Pb₃O₄ at 374 °C, and finally PbO at 605 °C. A further sesquioxide Pb₂O₃ can be obtained at high pressure, along with several non-stoichiometric phrases. Many of them show defect fluorite structures in which some oxygen atoms are replaced by vacancies: for instance, PbO can be considered as such a structure with every alternate layer of oxygen atoms absent.

Organolead

Main article: Organolead compound

Structure of a tetraethyllead molecule:
  Carbon
  Hydrogen
  Lead

Lead can form long singly- or multiply-bonded chains—catenas—and so shares some covalent chemistry with its lighter homolog carbon. This tendency is much lower for lead because the Pb–Pb bond energy (98 kJ/mol) is much lower than for the C–C bond (356 kJ/mol). Lead atoms can build metal–metal bonds of an order up to three. Lead also forms covalent bonds with carbon to produce organolead compounds similar to but generally less stable than typical organic compounds, as the Pb–C bond is rather weak. Nevertheless, the organometallic chemistry of lead is far less wide-ranging than that of tin. Almost all are organolead(IV) compounds. Very few organolead(II) compounds are known: even starting with inorganic lead(II) reactants always results in organolead(IV) products. The most well-characterized exceptions are the purple Pb[CH(SiMe)₃)₂]₂ and lead cyclopentadienide, Pb(η⁵-C₅H₅)₂.

The simplest lead analog of an organic compound is plumbane, the lead analog of methane. It is unstable against heat, decaying in heated tubes, and thermodynamically; little is known about the chemistry of plumbane, due to its instability. A lead analog of the next alkane, ethane, is not known. Two simple plumbane derivatives, tetramethyllead and tetraethyllead, are the best-known organolead compounds. They may be made by the addition (hydroplumbation) of trimethyllead or triethyllead to alkenes or alkynes; these precursors may themselves be made from the corresponding lead halides and lithium aluminium hydride at −78 °C. These compounds are relatively stable against heating—tetraethyllead only starts to decompose at 100 °C (210 °F)—as well as sunlight or ultraviolet light. (Tetraphenyllead is even more thermally stable, decomposing only at 270 °C.) The general oxidizing nature of organolead compounds find use in chemistry: tetraethyllead is produced in larger quantities than any other organometallic compound; lead tetraacetate is an important laboratory reagent for oxidation in organic chemistry. Other organolead compounds, including homologs of the said compounds, are still less chemically stable. Polyplumbanes are not well-characterized and are generally highly thermally unstable and reactive.

Lead readily forms an equimolar alloy with sodium metal that reacts with alkyl halides to form organometallic compounds of lead such as tetraethyllead. Plumbane may be obtained in a reaction between metallic lead and atomic (not molecular) hydrogen. Atoms of chlorine or bromine displace alkyl groups in tetramethyllead and tetraethyllead; hydrogen chloride, a by-product of the previous reaction, further reacts with the halogenated molecules to complete mineralization—a chemical reaction or a series of reactions transforming an organic compound into an inorganic one—of the original compounds, yielding lead dichloride.

Origin and occurrence

In space

Chart representing the final part of the s-process from mercury to polonium. Red horizontal lines with a circle in their right ends represent neutron captures; right-upward blue arrows represent beta decays; left-downward green arrows represent alpha decays; right-downward cyan arrows represent electron captures.

Primordial lead—which comprises the isotopes lead-204, lead-206, lead-207, and lead-208—was largely created as a result of repetitive neutron capture processes occurring in stars. The two main modes of capture are the s-process and the r-process.

In the s-process (s is for "slow"), captures are separated by years or decades, allowing less stable nuclei to beta decay. For example, a stable thallium-203 nucleus captures a neutron and becomes thallium-204, which is unstable. The thallium-204 nucleus undergoes beta decay to give stable lead-204; on capturing another neutron, it becomes lead-205, which, while unstable, is stable enough to generally last longer than a capture takes (its half-life is around 15 million years). Further captures result in lead-206, lead-207, and lead-208. On capturing another neutron, lead-208 becomes lead-209, which quickly decays into bismuth-209, which on capturing another neutron becomes bismuth-210, which either undergoes an alpha decay to result in thallium-206, which would beta decay into lead-206, or a beta decay to yield polonium-210, which would inevitably alpha decay into lead-206 as well, and the cycle ends at lead-206, lead-207, lead-208, and bismuth-209.

In the r-process (r is for "rapid"), captures happen faster than nuclei can decay. This occurs in environments with a high neutron density, possibly in a supernova or during the merger of two neutron stars. The neutron flux involved may be on the order of 10²² neutrons/cm²/second. The r-process does not form as much lead as the s-process. This is because the r-process tends to subside once very neutron-rich nuclei reach 126 neutrons. At this point the neutrons are arranged in complete shells within the atomic nucleus and it becomes harder to accommodate more of them. When the neutron flux subsides, the nuclei beta decay into stable isotopes of osmium, iridium and platinum. This effect is nevertheless masked, because the lead isotopes involved are located at the end of three major decay chains (see above), and are supplemented by the decay of the fewer heavier elements created by the r-process.

Most synthesized nuclides with mass numbers just above those of stable lead and bismuth, quickly undergo alpha and beta decay to stable lead and bismuth isotopes. Nuclides with mass numbers 232, 235, and 238 and above soon decay to the extremely long-lived isotopes of thorium and uranium, which decay very slowly to lead. These decay away quite slowly and, in some quantities, still exist to this day; therefore, the amount of lead in the universe is still increasing, although noticeably only from the perspective of millions of years.

Solar System abundances

Atomic number	Element	Relative amount
42	Molybdenum	1.0
46	Palladium	0.3
50	Tin	0.9
52	Tellurium	1.6
56	Barium	1.2
80	Mercury	0.1
82	Lead	1
92	Uranium	0.0052

The isotopes at the end of the chains make up around 98.02% lead in the universe, with non-radiogenic lead-204 making up slightly less than two percent. Lead is not an abundant element in general—its per-particle abundance in the Universe is 0.06 ppb (parts per billion)—still, it is an order of magnitude more abundant than mercury, and further exceeds those of most other elements of similar atomic numbers. After element 40 (zirconium), no element is at least twofold as abundant as lead, and there is no element as abundant as lead starting after element 56 (barium). Lead is three times as abundant as platinum, ten times as mercury, and twenty times as gold. Per mass, lead's abundance is 10 ppb—the difference between the per-mass and per-particle abundances is justified by mass difference between lead isotopes and the most common elements: the most common nuclide in the Universe, hydrogen-1, has a mass of approximately one atomic mass unit, while those of lead isotopes have masses of over 200 atomic mass units.

On Earth

Lead is a quite common element in the Earth's crust for its high atomic number.

Since lead commonly reacts with sulfur (see above), it is classified as a chalcophile using the Goldschmidt classification. Lead is likely to form minerals that do not sink into the core but that stay above on Earth in its crust. Lead's abundance in the Earth's crust is 16 ppm. This results in a great availability of lead minerals and easy extraction of the metal; for this reason, the mineral form of its sulfide, galena, has been known for millennia, as was the metal itself (see below). Lead's pronounced chalcophilic character is close to those of zinc and copper; as such, it is usually found in ore and extracted together with these metals. Metallic lead does occur in nature, but it is rare. As a result of lead's chemistry, it occurs in primary minerals exclusively as lead(II), unlike tin, which always occurs as tin(IV). Lead deposits can be hydrothermal vein, impregnation, and replacement deposits; volcanogenic sedimentary deposits; and hydrothermal or marine sedimentary deposits. World resources of lead exceed 2 billion tons. Massive resources are located in Australia, China, Ireland, Mexico, Peru, Portugal, Russia, and the United States. World reserves—resources ready to be mined for which that would be economically feasible—totaled 89 million tons in 2015, of which Australia had 35 million, China had 15.8 million, and Russia had 9.2 million.

The main lead mineral is galena (PbS). Galena is mostly found with other minerals, mostly zinc ores. Most other lead minerals are normally related to galena in some way; for example, boulangerite, Pb
₅Sb
₄S
₁₁, is a mixed sulfide derived from galena; anglesite, PbSO
₄, is a product of galena oxidation; cerussite or white lead ore, PbCO
₃, is a decomposition product of galena. Zinc, copper, arsenic, tin, anitmony, silver, gold, and bismuth are common impurities in lead minerals.

History

World lead production peaking in the Roman period and the rising Industrial Revolution
(present on the picture = 1980)

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 easily smeltable. Metallic lead beads dating back to 7000–6500 BCE, if not before that, have been found in Asia Minor; this indicates lead was the first metal ever to be smelted. At that point, lead had little, if any at all, applications, as it is soft and dull. The major reason for the spread of lead production, rather than its usefulness, was its association with silver, which may be obtained by burning galena, a widespread lead mineral, even though a few minor uses for lead appeared over time: The Ancient Egyptians are thought to have used lead for sinkers in fishing nets, in glazes, glasses and enamels, and for ornaments; they also were the first to use lead for cosmetics, a use that would continue through millennia to Ancient Greece and far beyond. Various civilizations of the Fertile Crescent used lead as a writing material, as currency, and for construction. The Ancient Chinese used lead as a stimulant in the royal court, a currency, and a contraceptive; lead also had a few uses, such as making amulets, for the Indus Valley civilization and the Mesoamericans. Peoples of eastern and southern Africa are known to exercise wire drawing.

Lead Roman pipes inscribed IMP.VESP.VIIII.T.IMP.VII.COS.CN.­IULIO.AGRICOLA.LEG.AUG.PR.PR.

As silver was extensively used as a decoration material and a means for exchange, lead deposits were first worked in Asia Minor in 3000 BCE. Lead deposits were worked in 2000 BCE in the Iberian peninsula by the Phoenicians; and also in Athens, Carthage, and Sicily. With the development of mining and its territorial expansion in Europe and across the Mediterranean, Rome became the greatest producer of lead during the classical era, with an estimated annual output equaling 80,000 tonnes at its peak. The Romans obtained lead mostly as a by-product of extensive silver smelting. Lead mining occurred in Central Europe, Britain, the Balkans, Greece, Anatolia, and Hispania, which alone accounted for 40% of world production. Lead was used for making water pipes in the Roman Empire, as lead was formable and resistant to corrosion, and, consequently, the Latin word for the metal, plumbum, was the origin of the periodic table symbol Pb and the English word "plumbing" and its derivatives—even though some Romans, such as Vitruvius, were able to recognize its danger for health. Some researchers suggest lead poisoning was one of the reasons behind the fall of Rome. Lead poisoning—a condition in which one becomes dark and cynical—was called "saturnine", after the ghoulish god of Saturn; the metal was also considered the father of all metals. It was easily available in the Roman society, and as such, its social status was low.

During the ancient and classical eras, (and even far beyond them, until the 17th century), tin was often not distinguished from lead or seen as a different kind of the metal that lead is: Romans called lead plumbum nigrum (literally, "black lead"), while tin was called plumbum candidum (literally, "bright lead"). Their association through history can also be seen in other languages: the word olovo in Czech translates to "lead", but in Russian the cognate олово (olovo) means "tin". In addition to that, lead also bore a close relation to antimony: Both elements commonly occur as sulfides (galena and stibnite), often together. Pliny declared stibnite would give lead on heating, whereas the mineral on heating actually produces antimony. The originally South Asian surma—"galena" in English—spread across Asia with that meaning, and also gave its name to antimony in a number of Central Asian languages, as well as Russian.

Elizabeth I of England was one European monarch commonly depicted with a whitened face. Lead in face whiteners is thought to be one reason behind her death.

Lead plumbing in Western Europe may have been continued beyond the fall of the Western Roman Empire into the medieval era, but lead mining in Europe in general fell into decline, with the only region with noticeable production being the Arabian Iberia, and the largest lead production was conducted in South and East Asia, especially China and India, where lead output underwent a strong growth. In Europe, lead production only began to revive in the 11th and 12th centuries, and lead was again used for roofing and piping; from the 13th century, it was used to create stained glass. During the period, lead was used increasingly for wine adulteration. This practice was declared forbidden in 1498 by a papal bull, but it continued long past the date, being a reason of various mass poisonings up to late 18th century. In the wake of the Renaissance, the printing press was invented, and lead served as a key material for its parts, starting with the Johannes Gutenberg's press; lead dust was commonly inhaled by operators, causing lead poisoning. Additionally, firearms were invented approximately at the same time, and lead, despite its expense over iron, became a chief material for making bullets, because it made less damage to iron gun barrels, had a higher density (which allowed for better retention of velocity and energy), and its lower melting point made production much easier: bullets could be made on wooden fire. Lead was extensively used in cosmetics at the time in Western Europe by the aristocracy, as whitened faces were seen as a sign of modesty. The practice eventually expanded to white wigs and eyeliners, and it only faded out with the French Revolution in the late 18th century; one effect of such prolonged contacts with lead was teeth rotting and teeth replacements often were also made of lead (which temporarily gave sweet breath), inducing further damage to the organism. (A similar fashion appeared in Japan in the 18th century with the emergence of the geishas, with the practice continuing long into the 20th century and the white face becoming a "symbol of a Japanese woman"; lead was commonly used as a face whitener.)

In the New World, lead was first produced soon after the European settlers had arrived; the earliest recorded lead production dates to 1621, in the Colony of Virginia that had been founded fourteen years earlier. In Australia, mining was introduced by the colonists as well, and they opened the first mine on the continent—a lead mine—in 1841. Centuries before the Europeans were able to start the colonization of Africa in the late 19th century, lead mining was known in the Benue Trough and the lower Congo basin, where lead was used for trade with the Europeans and as a currency.

Lead mining in the upper Mississippi River region in the United States in 1865

In the second half of the 18th century, Britain and later continental Europe and then the United States entered the Industrial Revolution. During the period, lead mining proved important; the Industrial Revolution was the first time to have greater lead production rates than those of Rome. Britain was the leading producer during the period, losing the status of the greatest producer by the mid-19th century with depletion of its mines and development of lead mining in Germany, Spain, and the United States. Lead production in the United States dominated by 1900; other non-European nations—in particular, Canada, Mexico, and Australia—started their massive lead production, and by 1900, Europe's output of lead fell below that elsewhere. A great share of demand of lead came from plumbing and painting—lead paints had been invented and regularly used; with invention of gasoline in the late 19th century, lead was extensively used as an additive. At this time, more people—the working class—contacted the metal, and this led to the increase of the numbers of those poisoned by lead. This also led to research of effects of lead intake: lead was proven to be more dangerous in its fume form than as a solid metal; lead poisoning and gout were linked (Alfred Baring Garrod noted a third of his gout patients was plumbers and painters); effects of chronic ingestion of lead, including mental disorders, were all studied in the 19th century. The first political acts to decrease the degree of lead poisoning in factories followed in the 1870s and 1880s in the United Kingdom.

Promotional poster for Dutch Boy lead paint, United States, 1912

Further evidence of the threat lead posed to human organisms were revealed in the late 19th and early 20th centuries—mechanisms of the harm were better realized, and lead blindness was documented—and countries in Europe and the United States started efforts to reduce the amount of lead a regular person contacts with. The last major innovation to impose contact with lead on humans was adding tetraethyllead to gasoline, invented in the United States in 1921; it was phased out in the U.S. and the European Union by 2000. Most European countries banned usage of lead paint for interiors by 1930. The result of many regulations and bans put on lead products was significant: in the last quarter of the 20th century, percentage of people with excessive lead blood levels dropped from over three quarters of the population to slightly over two percent in the U.S. By the end of the 20th century, the main good made of lead was the lead–acid battery, which possesses no direct threat to humans. This allowed for a consistent lead production in the industrialized countries. From 1960 to 1990, lead output in the Western Bloc grew by 31%. The share of the world's lead production of the Eastern Bloc increased from 10% and 30% from 1950 to 1990, with the Soviet Union being world's largest producer during the mid- and late 1970s and the 1980s, and China started a massive lead production in the late 20th century. Unlike the European communist countries, China was largely unindustrialized by mid-20th century; in 2004, China surpassed Australia as the largest producer of lead. Similarly to European industrialization, lead has a negative effect on health in the country.

Production

Historical evolution of the production of lead, as extracted in different countries

Production and consumption of lead is increasing worldwide. Lead production generally is divided into two major categories, primary and secondary: the primary production is the production from concentrate from the previously mined ores, and the secondary production is the production from scrap. In 2013, 4.74 million metric tons came from the primary production, and 5.74 million tons came from secondary production. The top mining countries for lead in 2013 were China, Australia, Russia, India, Bolivia, Sweden, North Korea, South Africa, Poland, and Ireland. The top lead producing countries were China, United States, India, South Korea, Germany, Mexico, United Kingdom, Canada, Japan, and Australia. According to the International Resource Panel's Metal Stocks in Society report of 2010, the global per capita stock of lead in use in society is 8 kg. Much of this is in more developed countries (20–150 kg per capita) rather than less developed countries (1–4 kg per capita).

Processes of production of primary and secondary lead are similar, despite using different sources of lead—ores and scrap—and some primary production plants now also use scrap, and this trend is likely increase in the future. Given adequate techniques, secondary lead is indistinguishable from primary lead. Scrap lead from the building trade is usually fairly clean and is re-melted without the need for smelting, though some refining operations may be necessary; as such, secondary lead is also cheaper to produce than primary in terms of energy spent on production, often twice or more so.

Primary production

Most lead ores contain only a very low percentage of lead, which must be concentrated during processing. During initial ore processing, ores typically undergo crushing, dense-medium separation, grinding, froth flotation, and drying of the resulting concentrate. The resulting concentrate is the initial quantitative metric of mined lead. Sulfide concentrate is more common for subsequent lead production than oxide concentrate; it commonly has a lead content fraction of 50%–60%, occasionally varying to up to 30% or 80%.

World's largest mining countries of lead, 2015

Country	Output (thousand tons)
China	2,300
Australia	633
United States	385
Peru	300
Mexico	240
India	130
Russia	90
Bolivia	82
Sweden	76
Turkey	54
North Korea	45
Poland	40
South Africa	40
Kazakhstan	38
Ireland	33
Other countries	226

The resulting concentrate is then turned into (impure) lead metal. The main route for doing so is the two-stage process: The sulfide concentrate is roasted in the air, the main reaction occurring is oxidation of lead sulfide with oxygen:

2PbS + 3O₂ → 2PbO + 2SO₂↑

This reaction releases heat once it started. As the original concentrate was not pure lead sulfide, roasting does not yield pure oxide, producing primarily lead oxide and a mixture of sulfates and silicates of lead and other metals contained in the ore. This impure lead oxide reduced in a coke-fired blast furnace to the (again, impure) metal by a reaction with that very coke:

2PbO + C → Pb + CO₂↑

Research on a process cheaper in terms of energy spent and pollution introduced into the environment than the described one continues, with some success; a major drawback is that the alternative results in either an exceedingly high sulfur content of the resulting lead metal or too much lead lost as waste. An alternative gaining ground involves direct smelting without an intermediate compound involved; another promising alternative involves hydrometallurgical means (it is based on anodes of impure lead and cathodes of pure lead dissolved in an electrolyte).

Impurities in the resulting metal are still significant; these are mostly 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. Since lead ores contain significant concentrations of silver, the smelted metal also is commonly contaminated with silver. Metallic silver as well as gold is removed and recovered economically by means of the Parkes process, in which zinc is added to lead and adsorbs silver, which dissolves in zinc many times more actively than in lead. 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. Very pure lead can be obtained by processing smelted lead electrolytically by means of the Betts process. The process uses anodes of impure lead and cathodes of pure lead in an electrolyte of silica fluoride. Once electrical potential is applied, impure lead at the anode dissolves and then plates out in the cathode, while the impurities remain in the solution.

Secondary production

Smelting, an essential part of the primary production, is often skipped in the secondary production. The reason for that is that scrap lead itself is commonly reproduced to its metallic form. As such, smelting is only performed when metallic lead had undergone significant chemical transformation, such as oxidation/rusting. When smelting is performed, it is performed in a fashion similar to that of the primary production in either a blast furnace or a rotary furnace (though both, with the essential difference being the greater variability of what could be extracted as the final product after the latter). The Isasmemt process is a more recent method that possesses a possibility of extension to the primary production; the essence of this process is that the input battery paste is deprived of its sulfur content (by, for example, treating it with alkalies) and then treated in a coal-fueled furnace in presence of oxygen, which eventually yields impure lead with antimony being the most common impurity.

Refining of secondary lead is similar to that of primary lead; some refining processes may be skipped depending on the material recycled and its potential contamination, with bismuth and silver being skipped especially often of all major impurities.

Of the sources of lead for recycling, lead–acid batteries is the most important one; lead pipe, sheet, and cable sheathing are also significant sources.

Applications

Contrary to popular belief, pencil leads in wooden pencils have never been made from lead. The term comes from the Roman stylus, called the penicillus, a small brush used for painting. When the pencil originated as a wrapped graphite writing tool, the particular type of graphite being used was named plumbago (lit. act for lead, or lead mockup).

Elemental form

Lead bricks are commonly used as radiation shielding.

Lead metal has a number of mechanical properties that make using it advantageous in comparison with many alternatives: high density, low melting point, ductility, and relative inertness against oxygen attacks. While many metals are superior to lead in some of these aspects, lead is also more common than most of these metals; moreover, lead minerals are easier to mine and then lead is easier to extract from its ores than many other metals, which makes the resulting metal relatively inexpensive. One disadvantage of using lead is its chemical toxicity, and it has been a reason why lead was or is being phased out for some uses.

Lead has been used for bullets since their invention (see above); with the development of firearms, round bullets became pointed and later, lead was jacketed with, for example, copper. The low melting point makes casting of lead easy, and therefore small arms ammunition and shotgun pellets can be cast with minimal technical equipment. It is also inexpensive and denser than other common metals. Lead is sometimes alloyed with tin or antimony: this increases the cost and time of making the bullet, but increasing the hardness of the bullet, this makes the bullet more effective against hard targets, eases the tension on the gun barrel and does not contaminate it with lead, as simple lead bullets do. Concerns have been raised over whether lead bullets used for hunting can damage the environment.

Because of its high density and resistance to corrosion, lead is used for the ballast keel of sailboats. Its high density 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. For the same reason, it is used in scuba diving weight belts to counteract the diver's natural buoyancy and that of his equipment.

Lead crystal beads

Lead is alloyed with copper and its alloys (namely, brass and bronze) to increase their machinability and to reduce machine tool wear. Lead does not form a solid solution with copper and is found as granules within copper. It acts as a lubricant in copper; in low concentrations, it also acts as a chip breaker.

It is also 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, or sheet-lead, is used as a sound deadening layer in some areas in wall, floor and ceiling design in sound studios where levels of airborne and mechanically produced sound are targeted for reduction or virtual elimination. It is the traditional base metal of organ pipes, mixed with varying amounts of tin to control the tone of the pipe.

Lead has many uses in the construction industry (e.g., lead sheets are used as architectural metals in roofing material, cladding, flashing, gutters and gutter joints, and on roof parapets). Detailed lead moldings are used as decorative motifs used to fix lead sheet. Lead is still widely used in statues and sculptures. 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.

Apart from its mechanical properties, lead is also useful in batteries, namely lead–acid batteries. The reactions in the battery between lead, lead dioxide, and sulfuric acid provides a reliable source of voltage. This, since lead in batteries undergoes no direct contact with humans (and thus no toxicity), is a use not threatened by toxicity concerns, and has been the largest use of lead in early 21st century.

Multicolor lead-glazing in a Tang dynasty Chinese sancai ceramic cup dating from the 8th century CE

Lead is also used as electrodes in the process of electrolysis. It is used in solder for electronics, although this usage is being phased out by some countries to reduce the amount of environmentally hazardous waste, and in high voltage power cables as sheathing material to prevent water diffusion into insulation. Lead is one of three metals used in the Oddy test for museum materials, helping detect organic acids, aldehydes, and acidic gases. It is also used as shielding from radiation (e.g., in X-ray rooms). Molten lead is used as a coolant (e.g., for lead cooled fast reactors).

Compounds

Lead compounds are used as a coloring element in ceramic glazes, notably for the colors red and yellow.

Lead tetraacetate (LTA) and lead dioxide have been used as oxidizing agents in organic chemistry. Geminal diols are cleaved to a pair of carbonyl compounds by stoichiometric LTA. LTA also is a selective oxidant of 5-methyl groups in 5-methylpyrrole-2-carboxylic esters, leading to 5-acetoxymethyl groups or 5-formyl groups with one or two equivalents of oxidant, respectively, to provide important intermediates for porphyrin synthesis.

Lead is frequently used in polyvinyl chloride (PVC) plastic, which coats electrical cords.

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 alternatives such as zinc. Lead glass is composed of 12–28% lead oxide. It changes the optical characteristics of the glass and reduces the transmission of ionizing radiation.

Lead-based semiconductors, such as lead telluride, lead selenide and lead antimonide are finding applications in photovoltaic (solar energy) cells and infrared detectors.

Biological and environmental effects

Main article: Lead poisoning

Biological

Symptoms of lead poisoning

Lead is a highly poisonous metal (whether inhaled or swallowed), affecting almost every organ and system in the body. The component limit of lead (1.0 μg/g) is a test benchmark for pharmaceuticals, representing the maximum daily intake an individual should have. Even at this level, a prolonged intake can be hazardous to human beings. Exposure to lead and lead chemicals occurs primarily through ingestion, to a lesser extent through inhalation and occasionally by direct contact.

The main target for lead toxicity is the nervous system, both in adults and children, in which it crosses the blood-brain barrier by mimicking calcium. Lead causes loss of neurons' myelin sheaths, reduces numbers of neurons, interferes with neurotransmission, and decreases neuronal growth. In a child's developing brain, lead interferes with synapse formation in the cerebral cortex, neurochemical development (including that of neurotransmitters), and organization of ion channels. The primary cause of lead's toxicity is its interference with a variety of enzymes because it binds to sulfhydryl groups found on many enzymes. Part of lead's toxicity results from its ability to mimic other metals that take part in biological processes, which act as cofactors in many enzymatic reactions, displacing them at the enzymes on which they act. Lead salts are thus very quickly and efficiently absorbed by the body, accumulating in it and leading to both chronic and acute poisoning. Lead is able to bind to and interact with many of the same enzymes as these metals but, due to its differing chemistry, does not properly function as a cofactor, thus interfering with the enzyme's ability to catalyze its normal reaction or reactions. Among the essential metals with which lead interacts are calcium, iron, and zinc. Thus high levels of calcium and iron tend to protect one somewhat from lead poisoning, while low levels of these metals render one more susceptible. According to the United States Agency for Toxic Substance and Disease Registry, a small amount of ingested lead (1%) will be stored in bones, and the rest will be excreted by an adult through urine and feces within a few weeks of exposure. Only about a third of lead will be excreted by a child.

Long-term exposure of adults can result in decreased performance in some tests that measure functions of the nervous system. Long-term exposure to lead or its salts (especially soluble salts or the strong oxidant PbO₂) can cause nephropathy, and colic-like abdominal pains. It may also cause weakness in fingers, wrists, or ankles. Lead exposure also causes small increases in blood pressure, particularly in middle-aged and older people and can cause anemia. Exposure to high lead levels can cause severe damage to the brain and kidneys in adults or children and ultimately cause death. In pregnant women, high levels of exposure to lead may cause miscarriage. Chronic, high-level exposure has been shown to reduce fertility in males. Lead also damages nervous connections (especially in young children) and causes blood and brain disorders. Lead poisoning typically results from ingestion of food or water contaminated with lead, but may also occur after accidental ingestion of contaminated soil, dust, or lead-based paint. 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.

NFPA 704 safety square
3 1 0 Fire diamond for lead granules

The treatment for lead poisoning consists of dimercaprol and succimer. Acute lead poisoning is treated using disodium calcium edetate: the calcium chelate of the disodium salt of ethylenediaminetetraacetic acid (EDTA). This chelating agent has a greater affinity for lead than for calcium and so the lead chelate is formed by exchange. This is then excreted in the urine leaving behind harmless calcium.

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 learning disabilities). Most cases of adult elevated blood lead levels are workplace-related. High blood levels are associated with delayed puberty in girls. Lead has been shown many times to permanently reduce the cognitive capacity of children at extremely low levels of exposure.

Despite the toxicity of lead in significant amounts, there is some evidence that trace amounts of lead are beneficial in pigs and rats, and that its absence causes deficiency signs including depressed growth, anemia, and disturbed iron metabolism. If true in humans as well, this would make lead an essential element; nevertheless, these findings are still uncertain, and even if lead does turn out to be beneficial in small quantities, the threshold of toxicity is so low that lead toxicity would remain a much higher priority to address than lead deficiency.

Sources of exposure

Battery collection site in Dakar, Senegal, where at least 18 children died of lead poisoning in 2008

Ingestion of lead-based paint is the major source of lead exposure for children. As lead paint deteriorates, it peels, is pulverized into dust and then enters the body through hand-to-mouth contact or through contaminated food, water, or alcohol. Ingesting certain home remedy medicines may also expose people to lead or lead compounds. Lead can be ingested through fruits and vegetables contaminated by high levels of lead in the soils they were grown in. Soil is contaminated through particulate accumulation from lead in pipes, lead paint and residual emissions from leaded gasoline that was used before the Environment Protection Agency issued the regulation in 1980. The use of lead for water pipes is problematic in areas with soft or (and) acidic water. Hard water forms insoluble layers in the pipes while soft and acidic water dissolves the lead pipes.

Inhalation is the second major pathway of exposure, especially for workers in lead-related occupations. Almost all inhaled lead is absorbed into the body, the rate is 20–70% for ingested lead; children absorb more than adults.

Dermal exposure may be significant for a narrow category of people working with organic lead compounds, but is of little concern for general population, as most countries stopped using leaded gasoline by 2007. The rate of skin absorption is also low for inorganic lead.

Environmental

The extraction, production, use, and disposal of lead and its products have caused significant contamination of the Earth's soils and waters, posing a hazard to living organisms because of its toxicity. Atmospheric emissions of lead were at their peak during the Industrial Revolution and the period of leaded petrol in the second half of the twentieth century; although these periods are over, elevated concentrations of lead persist in soils and sediments in post-industrial and urban areas. Meanwhile, industrial emissions continue in many parts of the world.

Radiography of a swan found dead in Condé-sur-l'Escaut (northern France), highlighting lead shot. The amount of lead is exceptionally high (some hundreds pellets; a dozen is enough to kill an adult swan within a few days). The body will be a new source of environmental contamination of toxic lead.

Lead accumulates in soil, especially in soil with high organic contents, where it remains for a long time, hundreds and thousand of years. According to the U.S. Environmental Protection Agency, lead from soils may take places of other metals within organic matter, particularly plants. In plants, lead accumulates on the surface, thus covering the plant from the incoming carbon dioxide, reducing the rate of photosynthesis, which trump the growth of the plant or kills it. Contamination of soils and plants, in turn, affects microorganisms and animals. Affected animals have reduced ability to synthesize red blood cells. Sources of contamination of the environment with lead are thus being limited.

Research has been conducted on how to remove lead from biosystems by the means of biological organisms: Fish bones are being researched for their ability to bioremediate lead in contaminated soil. The fungus Aspergillus versicolor is known as both greatly effective and fast at removing lead ions. Several bacteria have been researched for their ability to reduce lead; including the sulfate reducing bacteria Desulfovibrio and Desulfotomaculum, which are highly effective in aqueous solutions.

Restriction of lead usage

During the 20th century, the use of lead in paint pigments was sharply reduced because of the danger of lead poisoning, especially to children. 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 Chinese brass. Old 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. Old paint should not be stripped by sanding, as this produces inhalable dust.

People can be exposed to lead in the workplace by breathing it in, swallowing it, skin contact, and eye contact. In the United States, the Occupational Safety and Health Administration has set the permissible exposure limit for lead exposure in the workplace as 0.05 mg/m³ over an 8-hour workday, which applies to metallic lead, inorganic lead compounds, and lead soaps. The National Institute for Occupational Safety and Health has set a recommended exposure limit of 0.05 mg/m³ over an 8-hour workday, and recommends that workers' blood concentrations of lead stay below 0.06 mg per 100 g blood. At levels of 100 mg/m³, lead is immediately dangerous to life and health.

See also

• 2009 Chinese lead poisoning scandal
• Adult Blood Lead Epidemiology and Surveillance
• Alquifou
• Consumer Product Safety Improvement Act
• Devon colic
• Flint water crisis
• Medical geology
• Plumbosolvency
• Restriction of Hazardous Substances Directive
• Roman lead pipe inscription

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• Kroonen, Guus (2013). Etymological Dictionary of Proto-Germanic. Leiden Indo-European Etymological Dictionary Series. Leiden, Boston: Brill.
• Rich, Vincent (1994). The International Lead Trade. Woodhead Publishing. ISBN 9781855731035.{{cite book}}: CS1 maint: ref duplicates default (link)
• Polyanskiy, N. G. (1986). Fillipova, N. A (ed.). Аналитическая химия элементов: Свинец (in Russian). Nauka. {{cite book}}: Invalid |ref=harv (help); Unknown parameter |trans_title= ignored (|trans-title= suggested) (help)
• Thornton, Iain; Rautiu, Radu; Brush, Susan (2001). Lead: the facts. Hersham, Surrey: Ian Allan Printing. ISBN 0-9542496-0-7.

Further reading

• Keisch, B.; Feller, R. L.; Levine, A. S.; Edwards, R. R. (1967). "Dating and Authenticating Works of Art by Measurement of Natural Alpha Emitters". Science. 155 (3767): 1238–1242. Bibcode:1967Sci...155.1238K. doi:10.1126/science.155.3767.1238. PMID 17847535.
• Keisch, B (1968). "Dating Works of Art Through their Natural Radioactivity: Improvements and Applications". Science. 160 (3826): 413–415. Bibcode:1968Sci...160..413K. doi:10.1126/science.160.3826.413. PMID 17740234.
• Keisch, B (1968). "Discriminating Radioactivity Measurements of Lead: New Tool for Authentication". Curator. 11 (1): 41–52. doi:10.1111/j.2151-6952.1968.tb00884.x.
• Casas, Jose S.; Sordo, Jose, eds. (2006). Lead Chemistry, Analytical Aspects. Environmental Impacts and Health Effects. Elsevier. ISBN 0-444-52945-4.

External links

• National Lead Free Wheel Weight Initiative| Waste Minimization|Wastes|US EPA
• CDC – NIOSH Pocket Guide to Chemical Hazards – Lead