indium ← tin → antimony Ge ↑ Sn ↓ Pb 50Sn Periodic table
Appearance
silvery (left, beta) or gray (right, alpha)
General properties
Name, symbol, number	tin, Sn, 50
Pronunciation	/ˈtɪn/
Element category	post-transition metal
Group, period, block	14, 5, p
Standard atomic weight	118.710
Electron configuration	[Kr] 4d10 5s2 5p2
Electrons per shell	2, 8, 18, 18, 4 (Image)
Physical properties
Phase	solid
Density (near r.t.)	(white) 7.365 g·cm−3
Density (near r.t.)	(gray) 5.769 g·cm−3
Liquid density at m.p.	6.99 g·cm−3
Melting point	505.08 K, 231.93 °C, 449.47 °F
Boiling point	2875 K, 2602 °C, 4716 °F
Heat of fusion	(white) 7.03 kJ·mol−1
Heat of vaporization	(white) 296.1 kJ·mol−1
Molar heat capacity	(white) 27.112 J·mol−1·K−1
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k at T (K) 1497 1657 1855 2107 2438 2893
Atomic properties
Oxidation states	4, 2, -4 (amphoteric oxide)
Electronegativity	1.96 (Pauling scale)
Ionization energies	1st: 708.6 kJ·mol−1
	2nd: 1411.8 kJ·mol−1
	3rd: 2943.0 kJ·mol−1
Atomic radius	140 pm
Covalent radius	139±4 pm
Van der Waals radius	217 pm
Miscellanea
Crystal structure note	Tetragonal (white), diamond cubic (gray)
Magnetic ordering	(gray) diamagnetic[1], (white) paramagnetic
Electrical resistivity	(0 °C) 115 nΩ·m
Thermal conductivity	66.8 W·m−1·K−1
Thermal expansion	(25 °C) 22.0 µm·m−1·K−1
Young's modulus	50 GPa
Shear modulus	18 GPa
Bulk modulus	58 GPa
Poisson ratio	0.36
Mohs hardness	1.5
Brinell hardness	~350 MPa
CAS registry number	7440-31-5
Most stable isotopes
Main article: Isotopes of tin
iso NA half-life DM DE (MeV) DP 112Sn 0.97% 112Sn is stable with 62 neutrons 114Sn 0.66% 114Sn is stable with 64 neutrons 115Sn 0.34% 115Sn is stable with 65 neutrons 116Sn 14.54% 116Sn is stable with 66 neutrons 117Sn 7.68% 117Sn is stable with 67 neutrons 118Sn 24.22% 118Sn is stable with 68 neutrons 119Sn 8.59% 119Sn is stable with 69 neutrons 120Sn 32.58% 120Sn is stable with 70 neutrons 122Sn 4.63% 122Sn is stable with 72 neutrons 124Sn 5.79% 124Sn is stable with 74 neutrons 126Sn trace 2.3×105 y β− 0.380 126Sb
v t e · r

Tin ( /ˈtɪn/ TIN) is a chemical element with the symbol Sn (for Latin: stannum) and atomic number 50. It is a main group metal in group 14 of the periodic table. Tin shows chemical similarity to both neighboring group 14 elements, germanium and lead and has two possible oxidation states, +2 and the slightly more stable +4. Tin is the 49th most abundant element and has, with 10 stable isotopes, the largest number of stable isotopes in the periodic table. Tin is obtained chiefly from the mineral cassiterite, where it occurs as tin dioxide, SnO₂.

This silvery, malleable post-transition metal is not easily oxidized in air and is used to coat other metals to prevent corrosion. The first alloy, used in large scale since 3000 BC, was bronze, an alloy of tin and copper. After 600 BC pure metallic tin was produced. Pewter, which is an alloy of 85–90% tin with the remainder commonly consisting of copper, antimony and lead, was used for flatware from the Bronze Age until the 20th century. In modern times tin is used in many alloys, most notably tin/lead soft solders, typically containing 60% or more of tin. Another large application for tin is corrosion-resistant tin plating of steel. Because of its low toxicity, tin-plated metal is also used for food packaging, giving the name to tin cans, which are made mostly of steel.

Characteristics[link]

Physical properties[link]

Droplet of molten tin

Tin is a malleable, ductile and highly crystalline silvery-white metal. When a bar of tin is bent, a crackling sound known as the tin cry can be heard due to the twinning of the crystals.^[2] Tin melts at a low temperature of about 232 °C, which is further reduced to 177.3 °C for 11-nm particles.^[3]

β-tin (the metallic form, or white tin), which is stable at and above room temperature, is malleable. In contrast, α-tin (nonmetallic form, or gray tin), which is stable below 13.2 °C, is brittle. α-tin has a diamond cubic crystal structure, similar to diamond, silicon or germanium. α-tin has no metallic properties at all because its atoms form a covalent structure where electrons cannot move freely. It is a dull-gray powdery material with no common uses, other than a few specialized semiconductor applications.^[2] These two allotropes, α-tin and β-tin, are more commonly known as gray tin and white tin, respectively. Two more allotropes, γ and σ, exist at temperatures above 161 °C and pressures above several GPa.^[4] Although the α-β transformation temperature is nominally 13.2 °C, impurities (e.g. Al, Zn, etc.) lower the transition temperature well below 0 °C, and upon addition of Sb or Bi the transformation may not occur at all, increasing the durability of the tin.^[5][6]

Commercial grades of tin (99.8%) resist transformation because of the inhibiting effect of the small amounts of bismuth, antimony, lead and silver present as impurities. Alloying elements such as copper, antimony, bismuth, cadmium and silver increase its hardness. Tin tends rather easily to form hard, brittle intermetallic phases, which are often undesirable. It does not form wide solid solution ranges in other metals in general, and there are few elements that have appreciable solid solubility in tin. Simple eutectic systems, however, occur with bismuth, gallium, lead, thallium and zinc.^[5]

Tin becomes a superconductor below 3.72 K.^[7] In fact, tin was one of the first superconductors to be studied; the Meissner effect, one of the characteristic features of superconductors, was first discovered in superconducting tin crystals.^[8]

Chemical properties[link]

Tin resists corrosion from water but can be attacked by acids and alkalis. Tin can be highly polished and is used as a protective coat for other metals.^[2] In this case the formation of a protective oxide layer is used to prevent further oxidation. This oxide layer forms on pewter and other tin alloys.^[9] Tin acts as a catalyst when oxygen is in solution and helps accelerate chemical attack.^[2]

Isotopes[link]

Tin is the element with the greatest number of stable isotopes, ten; these include all those with atomic masses between 112 and 124, with the exception of 113, 121 and 123. Of these, the most abundant ones are ¹²⁰Sn (at almost a third of all tin), ¹¹⁸Sn, and ¹¹⁶Sn, while the least abundant one is ¹¹⁵Sn. The isotopes possessing even mass numbers have no nuclear spin while the odd ones have a spin of +1/2. Tin, with its three common isotopes ¹¹⁵Sn, ¹¹⁷Sn and ¹¹⁹Sn, is among the easiest elements to detect and analyze by NMR spectroscopy, and its chemical shifts are referenced against SnMe₄.^{[note 1][10]}

This large number of stable isotopes is thought to be a direct result of tin possessing an atomic number of 50, which is a "magic number" in nuclear physics. There are 28 additional unstable isotopes that are known, encompassing all the remaining ones with atomic masses between 99 and 137. Aside from ¹²⁶Sn, which has a half-life of 230,000 years, all the radioactive isotopes have a half-life of less than a year. The radioactive ¹⁰⁰Sn is one of the few nuclides possessing a "doubly magic" nucleus and was discovered relatively recently, in 1994.^[11] Another 30 metastable isomers have been characterized for isotopes between 111 and 131, the most stable of which being ^121mSn, with a half-life of 43.9 years.

Etymology[link]

The English word 'tin' is Germanic; related words are found in the other Germanic languages—German zinn, Swedish tenn, Dutch tin, etc.—but not in other branches of Indo-European except by borrowing (e.g. Irish tinne). Its origin is unknown.^[12]

The Latin name stannum originally meant an alloy of silver and lead, and came to mean 'tin' in the 4th century BCE^[13]—the earlier Latin word for it was plumbum candidum 'white lead'. Stannum apparently came from an earlier stāgnum (meaning the same thing),^[12] the origin of the Romance and Celtic terms for 'tin'.^[12][14] The origin of stannum/stāgnum is unknown; it may be pre-Indo-European.^[15] The Meyers Konversationslexikon speculates on the contrary that stannum is derived from Cornish stean, and is proof that Cornwall in the first centuries AD was the main source of tin.

History[link]

Ceremonial giant bronze dirk of the Plougrescant-Ommerschans type, Plougrescant, France, 1500–1300 BC.

Tin extraction and use can be dated to the beginnings of the Bronze Age around 3000 BC, when it was observed that copper objects formed of polymetallic ores with different metal contents had different physical properties.^[16] The earliest bronze objects had tin or arsenic content of less than 2% and are therefore believed to be the result of unintentional alloying due to trace metal content in the copper ore.^[17] The addition of a second metal to copper increases its hardness, lowers the melting temperature, and improves the casting process by producing a more fluid melt that cools to a denser, less spongy metal.^[17] This was an important innovation that allowed for the much more complex shapes cast in closed moulds of the Bronze Age. Arsenical bronze objects appear first in the Near East where arsenic is commonly found in association with copper ore, but the health risks were quickly realized and the quest for sources of the much less hazardous tin ores began early in the Bronze Age.^[18] This created the demand for rare tin metal and formed a trade network that linked the distant sources of tin to the markets of Bronze Age cultures.^{[citation needed]}

Cassiterite (SnO₂), the tin oxide form of tin, was most likely the original source of tin in ancient times. Other forms of tin ores are less abundant sulfides such as stannite that require a more involved smelting process. Cassiterite often accumulates in alluvial channels as placer deposits due to the fact that it is harder, heavier, and more chemically resistant than the granite in which it typically forms.^[19] These deposits can be easily seen in river banks as cassiterite is usually black, purple or otherwise dark in colour, a feature exploited by early Bronze Age prospectors. It is likely that the earliest deposits were alluvial in nature, and perhaps exploited by the same methods used for panning gold in placer deposits.^{[citation needed]}

Compounds and chemistry[link]

In the great majority of its compounds, tin has the oxidation state II or IV.

Inorganic compounds[link]

Halide compounds are known for both oxidation states. For Sn(IV), all four halides are well known: SnF₄, SnCl₄, SnBr₄, and SnI₄. The three heavier members are volatile molecular compounds, whereas the tetrafluoride is polymeric. All four halides are known for Sn(II) also: SnF₂, SnCl₂, SnBr₂, and SnI₂. All are polymeric solids. Of these eight compounds, only the iodides are coloured.^[20]

Tin(II) chloride (also known as stannous chloride) is the most important tin halide in a commercial sense. Illustrating the routes to such compounds, chlorine reacts with tin metal to give SnCl₄ whereas the reaction of hydrochloric acid and tin gives SnCl₂ and hydrogen gas. Alternatively SnCl₄ and Sn combine to stannous chloride via a process called comproportionation:^[21]

SnCl₄ + Sn → 2 SnCl₂

Tin can form many oxides, sulfides, and other chalcogenide derivatives. The dioxide SnO₂ (cassiterite) forms when tin is heated in the presence of air.^[20] SnO₂ is amphoteric, which means that it dissolves in both acidic and basic solutions.^[22] There are also stannates with the structure [Sn(OH)₆]²⁻, like K₂[Sn(OH)₆], although the free stannic acid H₂[Sn(OH)₆] is unknown. The sulfides of tin exist in both the +2 and +4 oxidation states: tin(II) sulfide and tin(IV) sulfide (mosaic gold).

Ball-and-stick models of the structure of solid stannous chloride (SnCl₂).^[23]

Hydrides[link]

Stannane (SnH₄), where tin is in the +4 oxidation state, is unstable. Organotin hydrides are however well known, e.g. tributyltin hydride (Sn(C₄H₉)₃H).^[2] These compound release transient tributyl tin radicals, rare examples of compounds of tin(III).^[24]

Organotin compounds[link]

Organotin compounds, sometimes called stannanes, are chemical compounds with tin-carbon bonds.^[25] Of the compounds of tin, the organic derivatives are the most useful commercially.^[26] Some organotin compounds are highly toxic and have been used as biocides. The first organotin compound to be reported was diethyltin diiodide ((C₂H₅)₂SnI₂), reported by Edward Frankland in 1849.^[27]

Most organotin compounds are colorless liquids or solids that are stable to air and water. They adopt tetrahedral geometry. Tetraalkyl- and tetraaryltin compounds can be prepared using Grignard reagents:^[26]

SnCl₄ + 4 RMgBr → R₄Sn + 4 MgBrCl

The mixed halide-alkyls, which are more common and more important commercially than the tetraorgano derivatives, are prepared by redistribution reactions:

SnCl₄ + R₄Sn → 2 SnCl₂R₂

Divalent organotin compounds are uncommon, although more common than related divalent organogermanium and organosilicon compounds. The greater stabilization enjoyed by Sn(II) is attributed to the "inert pair effect". Organotin(II) compounds include both stannylenes (formula: R₂Sn, as seen for singlet carbenes) and distannylenes (R₄Sn₂), which are roughly equivalent to alkenes. Both classes exhibit unusual reactions.^[28]

Occurrence[link]

Sample of cassiterite, the main ore of tin.

Granular pieces of cassiterite, which are collected by placer mining

Tin is generated via the long S-process in low-medium mass stars (with masses of 0.6 to 10 times that of Sun). It arises via beta decay of heavy isotopes of indium.^[29]

Tin is the 49th most abundant element in the Earth's crust, representing 2 ppm compared with 75 ppm for zinc, 50 ppm for copper, and 14 ppm for lead.^[30]

Tin does not occur as the native element but must be extracted from various ores. Cassiterite (SnO₂) is the only commercially important source of tin, although small quantities of tin are recovered from complex sulfides such as stannite, cylindrite, franckeite, canfieldite, and teallite. Minerals with tin are almost always associated with granite rock, usually at a level of 1% tin oxide content.^[31]

Because of the higher specific gravity of tin dioxide, about 80% of mined tin is from secondary deposits found downstream from the primary lodes. Tin is often recovered from granules washed downstream in the past and deposited in valleys or under sea. The most economical ways of mining tin are through dredging, hydraulic methods or open cast mining. Most of the world's tin is produced from placer deposits, which may contain as little as 0.015% tin.^[32]

It was estimated in January 2008 that there were 6.1 million tons of economically recoverable primary reserves, from a known base reserve of 11 million tons.^[33] Below are listed the nations with the largest known reserves.

World tin mine reserves and reserve base in tons^[33]

Country	Reserves	Reserve base
China	1,700,000	3,500,000
Malaysia	1,000,000	1,200,000
Peru	710,000	1,000,000
Indonesia	800,000	900,000
Brazil	540,000	2,500,000
Bolivia	450,000	900,000
Russia	300,000	350,000
Thailand	170,000	250,000
Australia	150,000	300,000
Other	180,000	200,000
Total	6,000,000	11,100,000

Estimates of tin production have historically varied with the dynamics of economic feasibility and the development of mining technologies, but it is estimated that, at current consumption rates and technologies, the Earth will run out of tin that can be mined in 40 years.^[34] However Lester Brown has suggested tin could run out within 20 years based on an extremely conservative extrapolation of 2% growth per year.^[35]

Secondary, or scrap, tin is also an important source of the metal. The recovery of tin through secondary production, or recycling of scrap tin, is increasing rapidly. Whereas the United States has neither mined since 1993 nor smelted tin since 1989, it was the largest secondary producer, recycling nearly 14,000 tons in 2006.^[33]

New deposits are reported to be in southern Mongolia,^[37] and in 2009, new deposits of tin were discovered in Colombia, South America, by the Seminole Group Colombia CI, SAS.^[38][39]

Production[link]

This section requires expansion.

Tin is produced by carbothermic reduction of the oxide ore with carbon or coke. Both reverberatory furnace and electric furnace can be used.^[40][41][42]

Mining and smelting[link]

Industry[link]

The ten largest companies produced most of world's tin in 2007. It is not clear which of these companies include tin smelted from the mine at Bisie, Democratic Republic of the Congo, which is controlled by a renegade militia and produces 15,000 tons. Most of the world's tin is traded on the London Metal Exchange (LME), from 8 countries, under 17 brands.^[43]

Prices of tin were at US$11,900 per ton as of Nov 24, 2008. Prices reached an all-time high of nearly $25,000 per ton in May 2008, largely because of the effect of the decrease of tin production from Indonesia.

Exchanges[link]

• London Metal Exchange (LME), contract market
• Kuala Lumpur Tin Market (KLTM), contract market
• Indonesia Tin Exchange (INATIN), the solely physical market for tin will formally launchs at January 12, 2012^[45] (postponed to February 1, 2012 due to 10 days holiday of Chinese Lunar New year)

Applications[link]

In 2006, about half of tin produced was used in solder. The rest was divided between tin plating, tin chemicals, brass and bronze, and niche uses.^[46]

Solder[link]

A coil of lead-free solder wire

Tin has long been used as a solder in the form of an alloy with lead, tin accounting for 5 to 70% w/w. Tin forms a eutectic mixture with lead containing 63% tin and 37% lead. Such solders are primarily used for solders for joining pipes or electric circuits. Since the European Union Waste Electrical and Electronic Equipment Directive (WEEE Directive) and Restriction of Hazardous Substances Directive (RoHS) came into effect on 1 July 2006, the use of lead in such alloys has decreased. Replacing lead has many problems, including a higher melting point, and the formation of tin whiskers causing electrical problems. Replacement alloys are rapidly being found, however.^[47]

Tin plating[link]

Tin bonds readily to iron and is used for coating lead or zinc and steel to prevent corrosion. Tin-plated steel containers are widely used for food preservation, and this forms a large part of the market for metallic tin. A tinplate canister for preserving food was first manufactured in London in 1812.^[48] Speakers of British English call them "tins", while speakers of American English call them "cans" or "tin cans". One thus-derived use of the slang term "tinnie" or "tinny" means "can of beer". The tin whistle is so called because it was first mass-produced in tin-plated steel.^[49][50]

Specialized alloys[link]

Pewter plate

Tin in combination with other elements forms a wide variety of useful alloys. Tin is most commonly alloyed with copper. Pewter is 85–99% tin;^[51] Babbitt metal has a high percentage of tin as well.^[52][53] Bronze is mostly copper (12% tin), while addition of phosphorus gives phosphor bronze. Bell metal is also a copper-tin alloy, containing 22% tin. Tin has also sometimes been used in coinage; for example, it once formed a single figure percentage of the American^[54] and Canadian^[55] pennies. Because copper is often the major metal in such coins, and zinc is sometimes present as well, these could technically be called bronze and/or brass alloys.

Tin plated metal from can

The niobium-tin compound Nb₃Sn is commercially used as wires for superconducting magnets, due to the material's high critical temperature (18 K) and critical magnetic field (25 T). A superconducting magnet weighing only a couple of kilograms is capable of producing magnetic fields comparable to a conventional electromagnet weighing tons.^[56]

A addition of a few percent tin is commonly used in zirconium alloys for the cladding of nuclear fuel.^[57]

Most metal pipes in a pipe organ are made of varying amounts of a tin/lead alloy, with 50%/50% being the most common. The amount of tin in the pipe defines the pipe's tone, since tin is the most tonally resonant of all metals^{[dubious – discuss]}. When a tin/lead alloy cools, the lead cools slightly faster and produces a mottled or spotted effect. This metal alloy is referred to as spotted metal. Major advantages of using tin for pipes include its appearance, its workability, and resistance to corrosion.^[58][59]

Other applications[link]

A 21st century reproduction barn lantern made of punched tin.

Punched tin, also called pierced tin, is an artisan technique originating in central Europe for creating housewares that are both functional and decorative. Decorative piercing designs exist in a wide variety, based on geography or the artisan's personal creations. Punched tin lanterns are the most common application of this artisan technique. The light of a candle shining through the pierced design creates a decorative light pattern in the room where it sits. Punched tin lanterns and other punched tin articles were created in the New World from the earliest European settlement. A well-known example is the Revere type lantern, named after Paul Revere.^[60]

Before the modern era, in some areas of the Alps, a goat or sheep's horn would be sharpened and a tin panel would be punched out using the alphabet and numbers from one to nine. This learning tool was known appropriately as "the horn". Modern reproductions are decorated with such motifs as hearts and tulips.

In America, pie safes and food safes came into use in the days before refrigeration. These were wooden cupboards of various styles and sizes - either floor standing or hanging cupboards meant to discourage vermin and insects and to keep dust from perishable foodstuffs. These cabinets had tinplate inserts in the doors and sometimes in the sides, punched out by the homeowner, cabinetmaker or a tinsmith in varying designs to allow for air circulation. Modern reproductions of these articles remain popular in North America.^[61]

Window glass is most often made by floating molten glass on top of molten tin (creating float glass) in order to produce a flat surface. This is called the "Pilkington process".^[62]

Tin is also used as a negative electrode in advanced Li-ion batteries. Its application is somewhat limited by the fact, that some tin surfaces catalyze decomposition of carbonate-based electrolytes used in Li-ion batteries.^[63]

Tin(II) fluoride is added to some dental care products^[64][65] as stannous fluoride (SnF₂). Tin(II) fluoride can be mixed with calcium abrasives while the more common sodium fluoride gradually becomes biologically inactive combined with calcium compounds.^[66] It has also been shown to be more effective than sodium fluoride in controlling gingivitis.^[67]

Organotin compounds[link]

Of all the chemical compounds of tin, the organotin compounds are most heavily used. Worldwide industrial production probably exceeds 50,000 tonnes.^[68]

PVC stabilizers[link]

The major commercial application of organotin compounds is in the stabilization of PVC plastics. In the absence of such stabilizers, PVC would otherwise rapidly degrade under heat, light, and atmospheric oxygen, to give discolored, brittle products. Tin scavenges labile chloride ions (Cl^-), which would otherwise initiate loss of HCl from the plastic material.^[69] Typical tin compounds are carboxylic acid derivatives of dibutyltin dichloride, such as the dilaurate.^[70]

Biocides[link]

Organotin compounds can have a relatively high toxicity, which is both advantageous and problematic. They have been used for their biocidal effects in/as fungicides, pesticides, algaecides, wood preservatives, and antifouling agents.^[69] Tributyltin oxide is used as a wood preservative.^[71] Tributyltin was used as additive for ship paint to prevent growth of marine organisms on ships, with use declining after organotin compounds were recognized as persistent organic pollutants with an extremely high toxicity for some marine organisms, for example the dog whelk.^[72] The EU banned the use of organotin compounds in 2003,^[73] while concerns over the toxicity of these compounds to marine life and their effects on the reproduction and growth of some marine species,^[69] (some reports describe biological effects to marine life at a concentration of 1 nanogram per liter) have led to a worldwide ban by the International Maritime Organization.^[74] Many nations now restrict the use of organotin compounds to vessels over 25 meters long.^[69]

Organic chemistry[link]

Some tin reagents are useful in organic chemistry. In the largest application, stannous chloride is a common reducing agent for the conversion of nitro and oxime groups to amines. The Stille reaction couples organotin compounds with organic halides or pseudohalides.^[75]

Precautions[link]

This section requires expansion.

Cases of poisoning from tin metal, its oxides, and its salts are "almost unknown". On the other hand, certain organotin compounds are almost as toxic as cyanide.^[26]

See also[link]

Books View or order collections of articles	Tin Period 5 elements Carbon group Chemical elements (sorted alphabetically) Chemical elements (sorted by number)
Portals Access related topics	Chemistry portal
Find out more on Wikipedia's Sister projects	Images and media from Commons Definitions from Wiktionary

Notes[link]

1. ^ Only H, F, P, Tl and Xe have a higher receptivity for NMR analysis for samples containing isotopes at their natural abundance.

References[link]

Bibliography[link]

• CRC contributors (2006). David R. Lide (editor). ed. Handbook of Chemistry and Physics (87th ed.). Boca Raton, Florida: CRC Press, Taylor & Francis Group. ISBN 0-8493-0487-3. 
• Emsley, John (2001). "Tin". Nature's Building Blocks: An A-Z Guide to the Elements. Oxford, England, UK: Oxford University Press. pp. 445–450. ISBN 0-19-850340-7. http://books.google.com/?id=j-Xu07p3cKwC&printsec=frontcover. 
• Stwertka, Albert (1998). "Tin". Guide to the Elements (Revised ed.). Oxford University Press. ISBN 0-19-508083-1. 
• Greenwood, N. N.; Earnshaw, A. (1997). Chemistry of the Elements (2nd ed.). Oxford: Butterworth-Heinemann. ISBN 0-7506-3365-4. 
• MacIntosh, Robert M. (1968). "Tin". In Clifford A. Hampel (editor). The Encyclopedia of the Chemical Elements. New York: Reinhold Book Corporation. pp. 722–732. LCCN 68-29938. 
• Heiserman, David L. (1992). "Element 50: Tin". Exploring Chemical Elements and their Compounds. New York: TAB Books. ISBN 0-8306-3018-X. 

External links[link]

• WebElements.com – Tin
• Theodore Gray's Wooden Periodic Table Table: Tin samples and castings
• Base Metals: Tin

vep:Tin

Arnold Palmer
Palmer in 1953
Personal information
Full name	Arnold Daniel Palmer
Nickname	The King
Born	(1929-09-10) September 10, 1929 (age 82) Latrobe, Pennsylvania
Height	5 ft 10 in (1.78 m)
Weight	185 lb (84 kg; 13.2 st)
Nationality	United States
Residence	Latrobe, Pennsylvania Orlando, Florida
Spouse	Winifred Walzer (m. 1954-1999) Kathleen Gawthrop (m. 2005)
Career
College	Wake Forest University
Turned professional	1954
Former tour(s)	PGA Tour Champions Tour
Professional wins	95
Number of wins by tour
PGA Tour	62 (5th all time)
European Tour	2
PGA Tour of Australasia	2
Champions Tour	10
Best results in Major Championships (Wins: 7)
Masters Tournament	Won: 1958, 1960, 1962, 1964
U.S. Open	Won: 1960
The Open Championship	Won: 1961, 1962
PGA Championship	T2: 1964, 1968, 1970
Achievements and awards
World Golf Hall of Fame	1974 (member page)
PGA Tour leading money winner	1958, 1960, 1962, 1963
PGA Player of the Year	1960, 1962
Vardon Trophy	1961, 1962, 1964, 1967
Sports Illustrated Sportsman of the Year	1960
Bob Jones Award	1971
Old Tom Morris Award	1983
PGA Tour Lifetime Achievement Award	1998
Payne Stewart Award	2000
Presidential Medal of Freedom	2004
Congressional Gold Medal	2009

Another photo of Palmer in the United States Coast Guard

Arnold Daniel Palmer (born September 10, 1929) is an American professional golfer, who is generally regarded as one of the greatest players in the history of men's professional golf. He has won numerous events on both the PGA Tour and Champions Tour, dating back to 1955. Nicknamed "The King," he is one of golf's most popular stars and its most important trailblazer, because he was the first superstar of the sport's television age, which began in the 1950s. He is part of "The Big Three" in golf, along with Jack Nicklaus and Gary Player, who are widely credited with popularizing and commercialising the sport around the world.

Palmer won the PGA Tour Lifetime Achievement Award in 1998, and in 1974 was inducted into the World Golf Hall of Fame.