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bismuth

 
Dictionary: bis·muth   (bĭz'məth) pronunciation
 
n. (Symbol Bi)

A white, crystalline, brittle, highly diamagnetic metallic element used in alloys to form sharp castings for objects sensitive to high temperatures and in various low-melting alloys for fire-safety devices. Atomic number 83; atomic weight 208.98; melting point 271.3°C; boiling point 1,560°C; specific gravity 9.747; valence 3, 5.

[Obsolete German Bismuth.]

bismuthal bis'muth·al adj.
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The metallic element, Bi, of atomic number 83 and atomic weight 208.980 belonging in the periodic table to group 15. Bismuth is the most metallic element in this group in both physical and chemical properties. The only stable isotope is that of mass 209. It is estimated that the Earth's crust contains about 0.00002% bismuth. It occurs in nature as the free metal and in ores. The principal ore deposits are in South America. However, the primary source of bismuth in the United States is as a by-product in refining of copper and lead ores. See also Periodic table.

Physical and mechanical properties of bismuth

Property

Value

Temperature

Melting point, °C

271.4

Boiling point, °C

1559

Heat of fusion, kcal/mole

2.60

Heat of vaporization, kcal/mole

36.2

Vapor pressure, mm Hg

1

 917°C

10

1067°C

100

1257°C

Density, g/cm3

9.80

  20° (solid)

10.03

 300° (liquid)

9.91

 400° (liquid)

9.66

 600° (liquid)

Mean specific heat, cal/g

0.0294

   0–270°C

0.0373

300–1000°C

Coefficient of linear expansion

13.45 × 10−6/°C

Thermal conductivity, cal/(s)(cm2)(°C)

0.018

 100° (solid)

0.041

 300° (liquid)

0.037

 400° (liquid)

Electrical resistivity, μohm-cm

106.5

   0° (solid)

160.2

 100° (solid)

267.0

 269° (solid)

128.9

 300° (liquid)

134.2

 400° (liquid)

145.3

 600° (liquid)

Surface tension, dynes/cm

376

 300°C

370

 400°C

363

 500°C

Viscosity, centipoise

1.662

 300°C

1.280

 450°C

0.996

 600°C

Magnetic susceptibility, cgs units

−1.35 × 10−6

Crystallography

Rhombohedral, a0 = 0.47457 nm

Thermal-neutron absorption cross section, barns

0.032 ± 0.003

Modulus of elasticity, lb/cm2

4.6 × 106

Shear modulus, lb/cm2

1.8 × 106

Poisson's ratio

0.33

Hardness, Brinell

4–8

The main use of bismuth is in the manufacture of low-melting alloys which are used in fusible elements in automatic sprinklers, special solders, safety plugs in compressed gas cylinders, and automatic shutoffs for gas and electric water-heating systems. Some bismuth alloys, which expand on freezing, are used in castings and in type metal. Another important use of bismuth is in the manufacture of pharmaceutical compounds.

Bismuth is a gray-white, lustrous, hard, brittle, coarsely crystalline metal. It is one of the few metals which expand on solidification. The thermal conductivity of bismuth is lower than that of any metal, with the exception of mercury. The table cites the chief physical and mechanical properties of bismuth. Bismuth is inert in dry air at room temperature, although it oxidizes slightly in moist air. It rapidly forms an oxide film at temperatures above its melting point, and it burns at red heat, forming the yellow oxide, Bi2O3. The metal combines directly with halogens and with sulfur, selenium, and tellurium; however, it does not combine directly with nitrogen or phosphorus. Bismuth is not attacked at ordinary temperatures by air-free water, but it is slowly oxidized at red heat by water vapor.

Almost all compounds of bismuth contain trivalent bismuth. However, bismuth can occasionally be pentavalent or monovalent. Sodium bismuthate and bismuth pentafluoride are perhaps the most important compounds of Bi(V). The former is a powerful oxidizing agent, and the latter a useful fluorinating agent for organic compounds.


 
Dental Dictionary: bismuth
Top
(biz′məth)
n

A reddish, crystalline, trivalent metallic element that in combination with other elements forms salts that are used in the production of many pharmaceutical compounds.

 

Semimetallic to metallic chemical element, chemical symbol Bi, atomic number 83. Hard, brittle, and lustrous, it has a distinctive gray-white colour with a reddish tinge. It is often found free in nature and also occurs in compounds and in mixed ores. Bismuth alloys are used (because of their low melting points) in making metal castings, special solders, automatic sprinkler heads, fuses, and many fire-detection devices. Bismuth phosphomolybdate is a catalyst in the production of acrylonitrile, an important raw material for fibres and plastics. Salts of bismuth are used in making soothing agents for digestive disorders (especially bismuth subsalicylate), in treating skin infections and injuries, and in lipstick, nail polish, and eye shadow, to which they impart a pearlescent quality.

For more information on bismuth, visit Britannica.com.

 
bismuth (bĭz'məth) [Ger. Weisse Masse=white mass], metallic chemical element; symbol Bi; at. no. 83; at. wt. 208.9804; m.p. 271.3°C; b.p. about 1,560°C; sp. gr. 9.75 at 20°C; valence +3 or +5. Bismuth is a silver-white, reddish-tinged, brittle metallic element with a rhombohedral crystalline structure. It exhibits more metallic properties than the other members of Group 15 of the periodic table. It occurs free in nature to a small extent. Bismuth does not tarnish in air, but when heated it burns to form yellow fumes of the trioxide. It reacts with the halogens and with sulfur and is dissolved in nitric acid and hot sulfuric acid. Its soluble compounds are poisonous, but some of its insoluble compounds are used in medicine to treat certain gastric disorders and skin injuries. Bismuth is the poorest heat conductor of all the metals except mercury; it is the most diamagnetic of all metals. The major ores of bismuth, bismuthinite (the sulfide), also called bismuth glance, and bismite (the oxide), are found extensively in South America but are rare in the United States, where bismuth is obtained as a byproduct of lead and copper refining. Bismuth expands upon solidification; this unusual property makes it useful in type-metal alloys and for castings. The most important use of bismuth is in the manufacture of low-melting alloys, such as Wood's metal, used in electrical fuses and in automatic fire alarm and sprinkler systems. Bismuth was recognized as a metal by early observers, including Georg Agricola, in the 16th cent., but was believed to be a kind of lead or tin until Claud J. Geoffroy established it as a separate element in 1753.


 

A chemical element, atomic number 83, atomic weight 208.980, symbol Bi. Several insoluble salts, including the subcarbonate and subnitrate, have been used in the management of inflammatory diseases of the stomach and intestines. Toxic doses cause kidney damage.

  • b. glycollylarsanilate — see glycobiarsol.
  • b. subgallate — used topically in wound powders and in the treatment of metritis.
  • b. subsalicylate, b. salicylate — an insoluble salt, used orally in the treatment of diarrhea and as an antacid. There is liberation of salicylic acid which acts against prostaglandin synthetase.
 
Wikipedia: Bismuth
Top
83 leadbismuthpolonium
Sb

Bi

Uup
Bismuth in the periodic table of the elements
General
Name, symbol, number bismuth, Bi, 83
Element category poor metals
Group, period, block 156, p
Appearance lustrous silver
Standard atomic weight 208.98040(1)g·mol−1
Electron configuration [Xe] 4f14 5d10 6s2 6p3
Electrons per shell 2, 8, 18, 32, 18, 5 (Image)
Physical properties
Phase solid
Density (near r.t.) 9.78 g·cm−3
Liquid density at m.p. 10.05 g·cm−3
Melting point 544.7 K
(271.5 °C, 520.7 °F)
Boiling point 1837 K
(1564 °C, 2847 °F)
Heat of fusion 11.30 kJ·mol−1
Heat of vaporization 151 kJ·mol−1
Specific heat capacity (25 °C) 25.52 J·mol−1·K−1
Vapor pressure
P/Pa 1 10 100 1 k 10 k 100 k
at T/K 941 1041 1165 1325 1538 1835
Atomic properties
Crystal structure rhombohedral
Oxidation states 3, 5
(mildly acidic oxide)
Electronegativity 2.02 (Pauling scale)
Ionization energies
(more)
1st: 703 kJ·mol−1
2nd: 1610 kJ·mol−1
3rd: 2466 kJ·mol−1
Atomic radius 160 pm
Atomic radius (calc.) 143 pm
Covalent radius 146 pm
Miscellaneous
Magnetic ordering diamagnetic
Electrical resistivity (20 °C) 1.29x10^-6Ω·m
Thermal conductivity (300 K) 7.97 W·m−1·K−1
Thermal expansion (25 °C) 13.4 µm·m−1·K−1
Speed of sound (thin rod) (20 °C) 1790 m/s
Young's modulus 32 GPa
Shear modulus 12 GPa
Bulk modulus 31 GPa
Poisson ratio 0.33
Mohs hardness 2.25
Brinell hardness 94.2 MPa
CAS registry number 7440-69-9
Most stable isotopes
Main article: Isotopes of bismuth
iso NA half-life DM DE (MeV) DP
207Bi syn 31.55 y ε, β+ 2.399 207Pb
208Bi syn 368,000 y ε, β+ 2.880 208Pb
209Bi 100% (19 ± 2) ×1018y α   205Tl
210mBi syn 3.04 ×106y IT 0.271 210Bi
References

Bismuth (pronounced /ˈbɪzməθ/) is a chemical element that has the symbol Bi and atomic number 83. This trivalent poor metal chemically resembles arsenic and antimony. Bismuth is heavy and brittle; it has a silvery white color with a pink tinge due to the surface oxide. Bismuth is the most naturally diamagnetic of all metals, and only mercury has a lower thermal conductivity. It is generally considered to be the last naturally occurring stable, non-radioactive element on the periodic table, although it is actually slightly radioactive, with an extremely long half-life.

Bismuth compounds are used in cosmetics, medicines, and in medical procedures. As the toxicity of lead has become more apparent in recent years, alloy uses for bismuth metal as a replacement for lead have become an increasing part of bismuth's commercial importance.

Contents

Characteristics

Bismuth crystal with an iridescent oxide surface

Bismuth is a brittle metal with a white, silver-pink hue, often occurring in its native form with an iridescent oxide tarnish showing many refractive colors from yellow to blue. When combusted with oxygen, bismuth burns with a blue flame and its oxide forms yellow fumes.[1] Its toxicity is much lower than that of its neighbors in the periodic table such as lead, tin, tellurium, antimony, and polonium.

Although ununpentium is theoretically more diamagnetic, no other metal is verified to be more naturally diamagnetic than bismuth.[1] (Superdiamagnetism is a different physical phenomenon.) Of any metal, it has the second lowest thermal conductivity (after mercury) and the highest Hall coefficient. It has a high electrical resistance.[1] When deposited in sufficiently thin layers on a substrate, bismuth is a semiconductor, rather than a poor metal.[2]

Elemental bismuth is one of very few substances of which the liquid phase is denser than its solid phase (water being the best-known example). Bismuth expands 3.32% on solidification; therefore, it was long an important component of low-melting typesetting alloys, which needed to expand to fill printing molds.[1]

Bismuth crystals

Though virtually unseen in nature, high-purity bismuth can form distinctive hopper crystals. These colorful laboratory creations are typically sold to collectors. Bismuth is relatively nontoxic and has a low melting point just above 271 °C, so crystals may be grown using a household stove, although the resulting crystals will tend to be lower quality than lab-grown crystals.[citation needed]

Isotopes

While bismuth was traditionally regarded as the element with the heaviest stable isotope, bismuth-209, it had long been suspected to be unstable on theoretical grounds. This was finally demonstrated in 2003 when researchers at the Institut d'Astrophysique Spatiale in Orsay, France, measured the alpha emission half-life of 209Bi to be 1.9 x 1019 years,[3] over a billion times longer than the current estimated age of the universe. Owing to its extraordinarily long half-life, for nearly all applications bismuth can be treated as if it is stable and non-radioactive. The radioactivity is of academic interest, however, because bismuth is one of few elements whose radioactivity was suspected, and indeed theoretically predicted, before being detected in the laboratory.

History

Bismuth (New Latin bisemutum from German Wismuth, perhaps from weiße Masse, "white mass") was confused in early times with tin and lead because of its resemblance to those elements. Bismuth has been known since ancient times, and so no one person is credited with its discovery. Agricola, in De Natura Fossilium states that bismuth is a distinct metal in a family of metals including tin and lead in 1546 based on observation of the metals and their physical properties.[4] Claude François Geoffroy demonstrated in 1753 that this metal is distinct from lead and tin.[1]

"Artificial bismuth" was commonly used in place of the actual metal. It was made by hammering tin into thin plates, and cementing them by a mixture of white tartar, saltpeter, and arsenic, stratified in a crucible over an open fire.[citation needed]

Bismuth was also known to the Incas and used (along with the usual copper and tin) in a special bronze alloy for knives.[5]

Occurrence and production

New York prices[6]
Time Price (USD/lb.)
Dec 2000 $3.85-$4.15
Nov 2002 $2.70-$3.10
Dec 2003 $2.60-$2.90
Jun 2004 $3.65-$4.00
Sep 2005 $4.20-$4.60
Sep 2006 $4.50-$4.75
Nov 2006 $6.00-$6.50
Dec 2006 $7.30-$7.80
Mar 2007 $9.25-$9.75
Apr 2007 $10.50-$11.00
Jun 2007 $18.00-$19.00
Nov 2007 $13.50-$15.00
Bismuth output in 2005
Bismite mineral

In the Earth's crust, bismuth is about twice as abundant as gold. It is not usually economical to mine it as a primary product. Rather, it is usually produced as a byproduct of the processing of other metal ores, especially lead, tungsten (China), tin, copper, and also silver (indirectly) or other metallic elements.

The most important ores of bismuth are bismuthinite and bismite.[1] In 2005, China was the top producer of bismuth with at least 40% of the world share followed by Mexico and Peru, reports the British Geological Survey. Native bismuth is known from Australia, Bolivia, and China.

According to the USGS, world 2006 bismuth mine production was 5,700 tonnes, of which China produced 3,000 tonnes, Mexico 1,180 tonnes, Peru 950 tonnes, and the balance Canada, Kazakhstan and other nations. World 2006 bismuth refinery production was 12,000 tonnes, of which China produced 8,500 tonnes, Mexico 1,180 tonnes, Belgium 800 tonnes, Peru 600 tonnes, Japan 510 tonnes, and the balance Canada and other nations.[7]

The difference between world bismuth mine production and refinery production reflects bismuth's status as a byproduct metal. Bismuth travels in crude lead bullion (which can contain up to 10% bismuth) through several stages of refining, until it is removed by the Kroll-Betterton process or the Betts process. The Kroll-Betterton process uses a pyrometallurgical separation from molten lead of calcium-magnesium-bismuth drosses containing associated metals (silver, gold, zinc, some lead, copper, tellurium, and arsenic), which are removed by various fluxes and treatments to give high-purity bismuth metal (over 99% Bi). The Betts process takes cast anodes of lead bullion and electrolyzes them in a lead fluosilicate-hydrofluosilicic acid electrolyte to yield a pure lead cathode and an anode slime containing bismuth. Bismuth will behave similarly with another of its major metals, copper. Thus world bismuth production from refineries is a more complete and reliable statistic.

According to the Bismuth Advocate News[6], the price for bismuth metal from year-end 2000 to September 2005 was stuck in a range from $2.60 to $4.15 per lb., but after this period the price started rising rapidly as global bismuth demand as a lead replacement and other uses grew rapidly. New mines in Canada and Vietnam may relieve the shortages, but prices are likely to remain above their previous level for the foreseeable future. The Customer-Input price for bismuth is more oriented to the ultimate consumer; it started January 2008 at US$39.40 per kilogram ($17.90 per pound) in January 2008 and reached US$35.55 per kg (US$16.15 per lb.) in September 2008. [8]

Recycling

While bismuth is most available today as a byproduct, its sustainability is more dependent on recycling. Bismuth is mostly a byproduct of lead smelting, along with silver, zinc, antimony, and other metals, and also of tungsten production, along with molybdenum and tin, and also of copper and tin production. Recycling bismuth is difficult in many of its end uses, primarily because of scattering. Probably the easiest to recycle would be bismuth-containing fusible alloys in the form of larger objects, then larger soldered objects. Half of the world solder consumption is in electronics (i.e., circuit boards).[9] As the soldered objects get smaller or contain little solder or little bismuth, the recovery gets progressively more difficult and less economic, although solder with a sizable silver content will be more worth recovering. Next in recycling feasibility would be sizeable catalysts with a fair bismuth content, perhaps as bismuth phosphomolybdate, and then bismuth used in galvanizing and as a free-machining metallurgical additive. Finally, the bismuth in the uses where it gets scattered the most, in stomach medicines (bismuth subsalicylate), paints (bismuth vanadate) on a dry surface, pearlescent cosmetics (bismuth oxychloride), and bismuth-containing bullets. The bismuth is so scattered in these uses as to be unrecoverable with present technology. Bismuth can also be available sustainably from greater efficiency of use or substitution, most likely stimulated by a rising price. For the stomach medicine, another active ingredient could be substituted for some or all of the bismuth compound[citation needed]. It would be more difficult to find an alternative to bismuth oxychloride in cosmetics to give the pearlescent effect. However, there are many alloying formulas for solders and therefore many alternatives.

The most important sustainability fact about bismuth is its byproduct status, which can either improve sustainability (i.e., Vanadium or Manganese nodules)or, for bismuth from lead ore, constrain it; bismuth is constrained. The extent that the constraint on bismuth can be ameliorated or not is going to be tested by the future of the lead storage battery, since 90% of the world market for lead is in storage batteries for gasoline or diesel-powered motor vehicles. A huge worldwide research and development effort is underway to develop and manufacture advanced (non-lead) batteries or electrical storage devices. In December 2008, it was announced that a consortium of 14 U.S. firms were seeking $1 billion in Federal aid to build a battery manufacturing plant to make Li-on batteries for electric automobiles. The plant would build the basic cell and the individual consortium firm would finish its batteries by adding their own electronics, changing the voltage, chemistry, and other parameters as required. Similar batteries are already being manufactured in several countries in the Far East, and four dozen advanced battery plants are under construction in China.[citation needed] These batteries certainly foreshadow such batteries for gasoline-powered motor vehicles. When the Li-on battery or other electrical storage devices replace the lead storage battery, the bismuth recovered from lead ore is going to drop along with the production of lead ore and bismuth is going to become more dependent on recycling.

The life-cycle assessment of bismuth will focus on solders, one of the major uses of bismuth, and the one with the most complete information. The average primary energy use for solders is around 200 MJ per kg, with the high-bismuth solder (58% Bi) only 20% of that value, and three low-bismuth solders (2% to 5% Bi) running very close to the average. The global warming potential averaged 10 to 14 kg carbon dioxide, with the high-bismuth solder about two-thirds of that and the low-bismuth solders about average. The acidification potential for the solders is around 0.9 to 1.1 kg sulfur dioxide equivalent, with the high-bismuth solder and one low-bismuth solder only one-tenth of the average and the other low-bismuth solders about average. [10] There is very little life-cycle information on other bismuth alloys or compounds.

Chemistry

Bismuth forms trivalent and pentavalent compounds. The trivalent compounds are more common. Many of its chemical properties are similar to other elements in its group; namely, arsenic and antimony.

Bismuth is stable to both dry and moist air at ordinary temperatures. At elevated temperatures, the vapours of the metal combine rapidly with oxygen, forming the yellow trioxide, Bi2O3.[11] On reaction with base, this oxide forms two series of oxyanions: BiO2, which is polymeric and forms linear chains, and BiO3−3. The anion in Li3BiO3 is actually a cubic octameric anion, Bi8O24−24, whereas the anion in Na3BiO3 is tetrameric.[12]

Bismuth sulfide, Bi2S3, occurs naturally in bismuth ores.[13] It is also produced by the combination of molten bismuth and sulfur.[11]

Unlike earlier members of group 15 elements such as nitrogen, phosphorus, and arsenic, and similar to the previous group 15 element antimony, bismuth does not form a stable hydride analogous to ammonia and phosphine. Bismuth hydride, bismuthine (BiH3), is an endothermic compound that spontaneously decomposes at room temperature. It is stable only below −60°C.[12]

The halides of bismuth in low oxidation states have been shown to have unusual structures. What was originally thought to be bismuth(I) chloride, BiCl, turns out to be a complex compound consisting of Bi5+9 cations and BiCl2−5 and Bi2Cl2−8 anions.[12][14] The Bi5+9 cation is also found in Bi10HfCl18, prepared by reducing a mixture of hafnium(IV) chloride and bismuth chloride with elemental bismuth. Other polyatomic bismuth cations are also known, such as Bi2+8, found in Bi8(AlCl4)2.[14] Bismuth also forms a low-valence bromide with the same structure as "BiCl". There is a true monoiodide, BiI, which contains chains of Bi4I4 units. BiI decomposes upon heating to the triiodide, BiI3, and elemental bismuth. A monobromide of the same structure also exists.[12]

In oxidation state +3, bismuth forms trihalides with all of the halogens: BiF3, BiCl3, BiBr3, and BiI3. All of these, except BiF3, are hydrolysed by water to form the bismuthyl cation, BiO+, a commonly encountered bismuth oxycation.[12] Bismuth(III) chloride reacts with hydrogen chloride in ether solution to produce the acid HBiCl4.[15]

Bismuth dissolves in nitric acid to form bismuth(III) nitrate, Bi(NO3)3. In the presence of excess water or the addition of a base, the Bi3+ ion reacts with the water to form BiO+, which precipitates as (BiO)NO3.[16]

The oxidation state +5 is less frequently encountered. One such compound is the pentafluoride, BiF5, a powerful oxidising agent capable of oxidising xenon tetrafluoride:[15]

BiF5 + XeF4 → XeF+3BiF6

The dark red bismuth(V) oxide, Bi2O5, is unstable, liberating O2 gas upon heating.[17]

In aqueous solution, the Bi3+ ion exists in various states of hydration, depending on the pH:

pH range Species
<3 Bi(H2O)3+6
0-4 Bi(H2O)5OH2+
1-5 Bi(H2O)4(OH)2+
5-14 Bi(H2O)3(OH)3
>11 Bi(H2O)2(OH)4

These mononuclear species are in equillibrium. Polynuclear species also exist, the most important of which is BiO+, which exists in hexameric form as the octahedral complex [Bi6O4(OH)4]6+ (or 6 [BiO+]·2 H2O).[18]

Applications

Bismuth oxychloride is sometimes used in cosmetics. Bismuth subnitrate and bismuth subcarbonate are used in medicine.[1] Bismuth subsalicylate (the active ingredient in Pepto-Bismol and (modern) Kaopectate) is used as an antidiarrheal and to treat some other gastro-intestinal diseases (oligodynamic effect). Also, the product Bibrocathol is an organic molecule containing Bismuth and is used to treat eye infections. Bismuth subgallate (the active ingredient in Devrom) is used as an internal deodorant to treat malodor from flatulence (or gas) and faeces.

Some other current uses:

  • New research by physicists has found a potential role of bismuth as an ingredient in electronic circuits and in manufacturing next-generation solar cells which would have a greater efficiency. Bismuth allows for the creation of new diodes that can reverse their direction of current flow.[1] Ordinary semiconductor diodes are fixed in their direction.
  • Many bismuth alloys have low melting points and are widely used for fire detection and suppression system safety devices.[1]
  • Bismuth is used as an alloying agent in production of malleable irons.[1]
  • It is also used a thermocouple material.[1]
  • A carrier for U-235 or U-233 fuel in nuclear reactors.[1]
  • Bismuth has also been used in solders. The fact that bismuth and many of its alloys expand slightly when they solidify make them ideal for this purpose.
  • Bismuth subnitrate is a component of glazes that produces an iridescent luster finish.
  • Bismuth telluride is an excellent thermoelectric material; it is widely used.
  • A replacement propellant for xenon in Hall effect thrusters
  • In 1997 an antibody conjugate with Bi-213, which has a 45 minute half-life, and decays with the emission of an alpha-particle, was used to treat patients with leukemia.
  • In 2001, Professor Barry Allen and Dr. Graeme Melville at St. George Hospital in Sydney successfully produced Bi-213 in linac experiments which involved bombarding radium with bremsstrahlung photons. This cancer research team used Bi-213 in its Targeted Alpha Therapy (TAT) program.
  • The delta form of bismuth oxide when it exists at room temperature is a solid electrolyte for oxygen. This form normally only exists above and breaks down below a high temperature threshold, but can be electrodeposited well below this temperature in a highly alkaline solution.

In the early 1990s, research began to evaluate bismuth as a nontoxic replacement for lead in various applications:

  • As noted above, bismuth has been used in solders; its low toxicity will be especially important for solders to be used in food processing equipment and copper water pipes.
  • A pigment in artists' oil and acrylic paint (Bismuth Vanadate)
  • Ingredient in free-machining brasses for plumbing applications
  • Ingredient in free-machining steels for precision machining properties
  • A catalyst for making acrylic fibers[1]
  • In low-melting alloys used in fire detection and extinguishing systems
  • Ingredient in lubricating greases
  • Dense material for fishing sinkers
  • In crackling microstars (dragon's eggs) in pyrotechnics, as the oxide, subcarbonate, or subnitrate
  • Replacement for lead in shot and bullets. The UK, U.S., and many other countries now prohibit the use of lead shot for the hunting of wetland birds, as many birds are prone to lead poisoning due to mistaken ingestion of lead (instead of small stones and grit) to aid digestion. Bismuth-tin alloy shot is one alternative that provides similar ballistic performance to lead. (Another less expensive but also more poorly performing alternative is "steel" shot, which is actually soft iron.)
  • Bismuth core bullets are also starting to appear for use in indoor shooting ranges, where fine particles of lead from bullets impacting the backstop can be a chronic toxic inhalant problem. Owing to bismuth's crystalline nature, the bismuth bullets shatter into a non-toxic powder on impact, making recovery and recycling easy.[citation needed] The lack of malleability does, however, make bismuth unsuitable for use in expanding hunting bullets.
  • Fabrique Nationale de Herstal uses bismuth in the projectiles for its FN 303 less-lethal riot gun.

According to the USGS, U.S. bismuth consumption in 2006 totaled 2,050 tonnes, of which chemicals (including pharmaceuticals, pigments, and cosmetics) were 510 tonnes, bismuth alloys 591 tonnes, metallurgical additives 923 tonnes, and the balance other uses.

Precautions

Bismuth is not known to be toxic, compared to its periodic table neighbours (lead, antimony, and polonium), although some compounds (including bismuth chloride due to its corrosive acidity) are toxic and should be handled with care. As with lead, overexposure to bismuth can result in the formation of a black deposit on the gingiva, known as a bismuth line[19].

Fine bismuth powder can be pyrophoric.[20]

See also

References

  1. ^ a b c d e f g h i j k l C. R. Hammond. The Elements, in Handbook of Chemistry and Physics 81th edition. CRC press. ISBN 0849304857. 
  2. ^ C. A. Hoffman, J. R. Meyer, and F. J. Bartoli, A. Di Venere, X. J. Yi, C. L. Hou, H. C. Wang, J. B. Ketterson, and G. K. Wong (1993). "Semimetal-to-semiconductor transition in bismuth thin films". Phys. Rev. B 48: 11431. doi:10.1103/PhysRevB.48.11431. 
  3. ^ Marcillac, Pierre de; Noël Coron, Gérard Dambier, Jacques Leblanc, and Jean-Pierre Moalic (April 2003). "Experimental detection of α-particles from the radioactive decay of natural bismuth". Nature 422: 876–878. doi:10.1038/nature01541. PMID 12712201. 
  4. ^ Agricola, Georgious (1546 (oring.); 1955(trans)). De Natura Fossilium. New York: Mineralogical Society of America. pp. 178. 
  5. ^ "Bismuth Bronze from Machu Picchu, Peru". http://adsabs.harvard.edu/abs/1984Sci...223..585G. 
  6. ^ a b "Bismuth Advocate News - Price and Long-Term Outlook Issue No. 29 November – December 2007". http://www.basicsmines.com/bismuth/index.html. Retrieved on 8 August 2008. 
  7. ^ Carlin, Jr., James F.. "Commodity Report 2006: Bismuth" (PDF). United States Geological Survey. http://minerals.usgs.gov/minerals/pubs/commodity/bismuth/myb1-2006-bismu.pdf. Retrieved on 2009-02-08. 
  8. ^ "CUSTOMER INPUT PRICES". http://customer-inputprices.blogspot.com. Retrieved on 2009-02-08. 
  9. ^ Taylor, Harold A.. Bismuth. Financial Times Executive Commodity Reports. p. 17. ISBN 1 84083 326 2. 
  10. ^ "IKP, Department of Life-Cycle Engineering". http://leadfree.ipc.org/files/RoHS_15.pdf. Retrieved on 2009-05-05. 
  11. ^ a b Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0070494398
  12. ^ a b c d e S. M. Godfrey; C. A. McAuliffe; A. G. Mackie; R. G. Pritchard (1998). Nicholas C. Norman. ed. Chemistry of arsenic, antimony, and bismuth. Springer. pp. 67-84. ISBN 075140389X. 
  13. ^ Ira Remsen (1886). An Introduction to the Study of Chemistry. Henry Holt and Company. p. 363. 
  14. ^ a b R. J. Gillespie; J. Passmore (1975). H. J. Emeléus, A. G. Sharp. ed. Advances in Inorganic Chemistry and Radiochemistry. Academic Press. pp. 77-78. ISBN 0120236176. 
  15. ^ a b Hitomi Suzuki; Yoshihiro Matano (2001). Organobismuth chemistry. Elsevier. p. 8. ISBN 0444205284. 
  16. ^ Charles Adolphe Wurtz; William Houston Greene; H. F. Keller (1880). William Houston Greene. ed. Elements of modern chemistry (6th ed.). J.B. Lippincott. p. 351. 
  17. ^ Thomas Scott; Mary Eagleson (1994). Concise encyclopedia chemistry. Walter de Gruyter. p. 136. ISBN 3110114518. 
  18. ^ Arnold F. Holleman; Egon Wiberg (2001). Nils Wiberg. ed. Inorganic chemistry. Academic Press. p. 771. ISBN 0123526515. 
  19. ^ "bismuth line". Farlex, Inc.. http://medical-dictionary.thefreedictionary.com/bismuth+line. Retrieved on 8 February 2008. 
  20. ^ Patnaik, Patnaik (2002). Handbook of Inorganic Chemical Compounds. McGraw-Hill Professional. ISBN 0070494398. 

External links


 
Translations: Bismuth
Top

Dansk (Danish)
n. - vismut

Nederlands (Dutch)
bismut

Français (French)
n. - bismuth

Deutsch (German)
n. - (chem.) Wismut

Ελληνική (Greek)
n. - βισμούθιο

Italiano (Italian)
bismuto

Português (Portuguese)
n. - bismuto (m) (Quím.)

Русский (Russian)
висмут

Español (Spanish)
n. - bismuto

Svenska (Swedish)
n. - vismut

中文(简体)(Chinese (Simplified))

中文(繁體)(Chinese (Traditional))
n. - 鉍

한국어 (Korean)
n. - 창연(금속원소)

日本語 (Japanese)
n. - ビスマス

العربيه (Arabic)
‏(الاسم) معدن البزموت‏

עברית (Hebrew)
n. - ‮ביסמות (מתכת)‬


 
 

 

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