Tin () is a
chemical element with the symbol
Sn (for ) 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, SnO
2.
This silvery, malleable poor 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% to 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
Physical properties
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. Tin melts at a low temperature of about 232 °C, which is further reduced to 117 °C for 11-nm particles.
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. 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. 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.
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.
Tin becomes a superconductor below 3.72 K. 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.
Chemical properties
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. Tin acts as a
catalyst when
oxygen is in solution and helps accelerate chemical attack.
Isotopes
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 atomic 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 .
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. 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
The English word 'tin' is
Germanic; related words are found in the other Germanic languages—
German ''zinn'',
Swedish ''tenn'', ''etc.''—but not in other branches of
Indo-European except by borrowing (''e.g.''
Irish ''tinne''). Its origin is unknown.
The Latin name ''stannum'' originally meant an alloy of silver and lead, and came to mean 'tin' in the 4th century BCE—the earlier Latin word for it was ''plumbum candidum'' 'white lead'. ''Stannum'' apparently came from an earlier ''stāgnum'' (meaning the same thing), the origin of the Romance and Celtic terms for 'tin'. The origin of ''stannum''/''stāgnum'' is unknown; it may be pre-Indo-European. 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
Antiquity
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. 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 It was soon discovered that the addition of tin or arsenic to copper increased its hardness and made casting much easier, which revolutionized metal working techniques and brought humanity from the Copper Age or Chalcolithic to the Bronze Age around 3000 BC. Early tin exploitation appears to have been centered on placer deposits of cassiterite.
The first evidence of tin use for making bronze appears in the Near East and the Balkans around 3000 BC. It is still unclear as to where the earliest tin was mined as tin deposits are very rare and evidence of early mining is scarce. Europe's earliest mining district appears to be located in Erzgebirge, on the border between Germany and Czech Republic and is dated to 2500 BC. From there tin was traded north to the Baltic Sea and south to the Mediterranean following the Amber Road trading route. Tin mining knowledge spread to other European tin mining districts from Erzgebirge and evidence of tin mining begins to appear in Brittany, Devon and Cornwall, and in the Iberian Peninsula around 2000 BC. These deposits saw greater exploitation when they fell under Roman control between the third century BC and the first century AD. Demand for tin created a large and thriving network amongst Mediterranean cultures of Classical times. By the Medieval period, Iberia's and Germany's deposits lost importance and were largely forgotten while Devon and Cornwall began dominating the European tin market.
In the Far East, the tin belt stretching from Yunnan province in China to the Malaysian Peninsula began being exploited sometime between the third and second millennium BC. The deposits in Yunnan province were not mined until around 700 BC, but by the Han Dynasty had become the main source of tin in China according to historical texts of the Han, Jin, Tang, and Song dynasties.
Other regions of the world developed tin mining industries at a much later date. In Africa, the Bantu culture extracted, smelted and exported tin between the 11th and 15th centuries AD, in the Americas tin exploitation began around 1000 AD, and in Australia it began with the arrival of Europeans in the 17th century.
Modern times
During the Middle Ages, and again in the early 19th century,
Cornwall was the major tin producer. This changed after large amounts of tin were found in the
Bolivian tin belt and the east Asian tin belt, stretching from China through
Thailand and
Laos to
Malaya and
Indonesia.
Tasmania also hosts deposits of historical importance, most notably
Mount Bischoff and
Renison Bell.
In 1931 the tin producers founded the International Tin Committee, followed in 1956 by the International Tin Council, an institution to control the tin market. After the collapse of the market in October 1985 the price for tin nearly halved.
Tin foil was once a common wrapping material for foods and drugs; replaced in the early 20th century by the use of aluminium foil, which is now commonly referred to as ''tin foil''. Hence one use of the slang term "tinnie" or "tinny" for a small pipe for use of a drug such as cannabis or for a can of beer. Today, the word "tin" is often improperly used as a generic term for any silvery metal that comes in sheets. Most everyday materials that are commonly called "tin", such as aluminium foil, beverage cans, corrugated building sheathing and tin cans, are actually made of steel or aluminium, although tin cans (tinned cans) do contain a thin coating of tin to inhibit rust. Likewise, so-called "tin toys" are usually made of steel, and may have a coating of tin to inhibit rust. The original Ford Model T was known colloquially as the "Tin Lizzy".
Compounds and Chemistry
In the great majority of its compounds, tin has the oxidation state II or IV.
Inorganic compounds
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.
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:
: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. SnO2 is amphoteric, which means that it dissolves in both acidic and basic solutions. 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).
Hydrides
Stannane (SnH
4), where tin is in the +4 oxidation state, is unstable. Organotin hydrides are however well known, e.g.
tributyltin hydride. These compound release transient tributyl tin radicals, rare examples of compounds of tin(III).
Organotin compounds
Organotin compounds, sometimes called stannanes, are
chemical compounds with tin-carbon bonds. Of the compounds of tin, the organic derivatives are the most useful commercially. Some organotin compounds are highly toxic and have been used as
biocides. The first organotin compound to be reported was diethyltin diiodide ((C
2H
5)
2SnI
2), reported by
Edward Frankland in 1849.
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:
: + 4 RMgBr → + 4 MgBrCl
The mixed halide-alkyls, which are more common and more important commercially than the tetraorgano derivatives, are prepared by redistribution reactions:
: + → 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.
Occurrence
Tin is generated via the long S-process in low-medium mass stars (0.6 -> 10 solar masses). It arises via beta decay of heavy isotopes of indium.
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.
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.
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.
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. Below are listed the nations with the largest known reserves.
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. However Lester Brown has suggested tin could run out within 20 years based on an extremely conservative extrapolation of 2% growth per year.
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.
New deposits are reported to be in southern Mongolia,
+World tin mine reserves and reserve base in tons
|
!Country |
Reserves |
| 1,700,000 |
3,500,000
|
| 1,000,000 |
1,200,000
|
| 710,000 |
1,000,000
|
| 800,000 |
900,000
|
| 540,000 |
2,500,000
|
| 450,000 |
900,000
|
| 300,000 |
350,000
|
| 170,000 |
250,000
|
| 150,000 |
300,000
|
Other
| 180,000 |
200,000
|
+Estimated economically recoverable world tin reserves
|
!Year
|
!million tons
|
1965
|
4,265
|
1970
|
3,930
|
1975
|
9,060
|
1980
|
9,100
|
1985
|
3,060
|
1990
|
7,100
|
2008
|
6,100
|
Production
Tin is produced by reducing the
ore with
carbon in a
reverberatory furnace.
Mining and smelting
In 2006, total worldwide tin mine production was 321,000 tons, and smelter production was 340,000 tons. From its production level of 186,300 tons in 1991, around where it had hovered for the previous decades, production of tin increased 89% to 351,800 tons in 2005. Most of the increase came from China and Indonesia, with the largest spike in 2004–2005, when it increased 23%. While in the 1970s Malaysia was the largest producer, with around a third of world production, it has steadily fallen, and now remains a major smelter and market center. In 2007, the
People's Republic of China was the largest producer of tin, where the tin deposits are concentrated in the southeast Yunnan tin belt, with 43% of the world's share, followed by
Indonesia, with an almost equal share, and
Peru at a distant third, reports the
USGS.
The table below shows the countries with the largest mine production and the largest smelter output.
+Mine and smelter production (tons), 2006
|
!Country |
Mine production |
Indonesia
| 117,500 |
80,933
|
China
| 114,300 |
129,400
|
Peru
| 38,470 |
40,495
|
Bolivia
| 17,669 |
13,500
|
Thailand
| 225 |
27,540
|
Malaysia
| 2,398 |
23,000
|
Belgium
| 0 |
8,000
|
Russia
| 5,000 |
5,500
|
Democratic Republic of Congo | Congo-Kinshasa ('08) |
15,000 |
0
|
After the discovery of tin in what is now Bisie, North Kivu in the Democratic Republic of Congo in 2002, illegal production has increased there to around 15,000 tons. This is largely fueling the ongoing and recent conflicts there, as well as affecting international markets.
Industry
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,
Congo-Kinshasa, 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.
+Largest tin mining companies by production in tons
|
!Company |
Polity| | 2006 |
2007 |
%Change
|
Yunnan Tin
| China
|
52,339 |
61,129 |
PT Timah
| Indonesia
|
44,689 |
58,325 |
Minsur
| Peru
|
40,977 |
35,940 |
Malay
| China
|
52,339 |
61,129 |
Malaysia Smelting Corp
| Malaysia
|
22,850 |
25,471 |
Thaisarco
| Thailand
|
27,828 |
19,826 |
Yunnan Chengfeng
| China
|
21,765 |
18,000 |
Liuzhou China Tin
| China
|
13,499 |
13,193 |
EM Vinto
| Bolivia
|
11,804 |
9,448 |
Gold Bell Group
| China
|
4,696 |
8,000 |
Prices of tin were at $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, and have been volatile because of reliance from mining in Congo-Kinshasa.
Applications
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.
Solder
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 (WEEED) 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.
Tin plating
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. 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.
Specialized alloys
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;
Babbitt metal has a high percentage of tin as well. 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 and Canadian 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.
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.
A addition of a few percent tin is commonly used in zirconium alloys for the cladding of nuclear fuel.
Illustrative niche applications
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.
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.
Float glass production
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".
Stannous fluoride in cavity prevention
Tin(II) fluoride is added to some dental care products as
stannous fluoride (SnF
2).
Tin(II) fluoride can be mixed with calcium abrasives while the more common
sodium fluoride gradually becomes biologically inactive combined with calcium compounds. It has also been shown to be more effective than
sodium fluoride in controlling
gingivitis.
Organ pipes
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. 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.
Organotin compounds
Of all the
chemical compounds of tin, the organotin compounds are most heavily used. Worldwide industrial production probably exceeds 50,000
tonnes.
PVC stabilizers
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. Typical tin compounds are carboxylic acid derivatives of dibutyltin dichloride, such as the di
laurate.
Biocides
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.
Tributyltin oxide is used as a
wood preservative.
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. The EU banned the use of organotin compounds in 2003, while concerns over the toxicity of these compounds to marine life and their effects on the reproduction and growth of some marine species, (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. Many nations now restrict the use of organotin compounds to vessels over 25 meters long.
Organic chemistry
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.
Precautions
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.
See also
Cassiterides (the mythical Tin Islands)
Stannary
Terne
Tin pest
Tin mining in Britain
Tinning
Whisker (metallurgy) (tin whiskers)
Notes
References
Bibliography
External links
WebElements.com – Tin
Theodore Gray's Wooden Periodic Table Table: Tin samples and castings
Base Metals: Tin
The history of the Count House of Ding Dong Mine, one of the oldest tin mines in Cornwall, where Richard Trevithick carried out his first experiments with high pressure steam.
Category:Chemical elements
Category:Poor metals
Category:Tin
af:Tin
am:ቆርቆሮ
ar:قصدير
an:Estanyo (elemento)
ast:Estañu
ay:Chayanta
az:Qalay
bn:টিন
zh-min-nan:Siah
be:Волава
be-x-old:Волава
bs:Kalaj
br:Staen
bg:Калай
ca:Estany (element)
cv:Тăхлан
ceb:Tansan
cs:Cín
co:Stagnu
cy:Tun
da:Tin
de:Zinn
nv:Béésh Dildǫʼí
et:Tina
el:Κασσίτερος
myv:Валдо киве
es:Estaño
eo:Stano
eu:Eztainu
fa:قلع
hif:Tin
fr:Étain
fy:Tin (elemint)
fur:Stagn
ga:Stán
gv:Stainney
gl:Estaño
hak:Siak
xal:Цанхорһлҗн
ko:주석 (원소)
hy:Անագ
hi:त्रपु
hr:Kositar
io:Stano
id:Timah
ia:Stanno
is:Tin
it:Stagno
he:בדיל
jv:Timah
kn:ತವರ
ka:კალა (ელემენტი)
kk:Қалайы
kw:Sten
sw:Stani
kv:Озысь
ht:Eten
ku:Pîl (metal)
koi:Озісь
lbe:Къалай
la:Stannum
lv:Alva
lb:Zënn
lt:Alavas
lij:Stagno (metallo)
jbo:tinci
hu:Ón
mk:Калај
ml:വെളുത്തീയം
mr:टिन
ms:Timah
mdf:Валдакиви
my:တင်း(ဓာတုဗေဒ)
nah:Amochitl
mrj:Вулны
nl:Tin (element)
ja:スズ
no:Tinn (grunnstoff)
nn:Grunnstoffet tinn
oc:Estam
uz:Qalay
pa:ਟੀਨ
pnb:ٹن
nds:Tinn
pl:Cyna
pt:Estanho
ro:Staniu
qu:Chayanta
ru:Олово
sah:Хорҕолдьун
sa:बङ्गम्
stq:Tin
sq:Kallaj
scn:Stagnu
simple:Tin
sk:Cín
sl:Kositer
sr:Калај
sh:Kalaj
fi:Tina
sv:Tenn
tl:Lata
ta:வெள்ளீயம்
te:తగరము
th:ดีบุก
tg:Қалъ
tr:Kalay
uk:Олово
ur:قلع
ug:قەلەي
vi:Thiếc
fiu-vro:Tina
zh-classical:錫
war:Lata
wuu:锡
yi:צין
yo:Tin
zh-yue:錫
zh:锡