Difference between revisions of "Sulfur" - New World Encyclopedia

From New World Encyclopedia
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In the eighth century B.C.E., [[Homer]] mentioned "pest-averting sulfur"; and in 424 B.C.E., the tribe of [[Boeotia]]* destroyed the walls of a city by burning a mixture of coal, sulfur, and tar under them. Sometime in the twelfth century, the [[China|Chinese]] invented [[gunpowder]]*, which is a mixture of [[potassium nitrate]]* (KNO<sub>3</sub>), [[carbon]], and sulfur. Early [[alchemy|alchemists]] gave sulfur its own alchemical symbol&mdash;a triangle at the top of a cross. In the late 1770s, [[Antoine Lavoisier]] helped convince the scientific community that sulfur was an element, not a compound.
 
In the eighth century B.C.E., [[Homer]] mentioned "pest-averting sulfur"; and in 424 B.C.E., the tribe of [[Boeotia]]* destroyed the walls of a city by burning a mixture of coal, sulfur, and tar under them. Sometime in the twelfth century, the [[China|Chinese]] invented [[gunpowder]]*, which is a mixture of [[potassium nitrate]]* (KNO<sub>3</sub>), [[carbon]], and sulfur. Early [[alchemy|alchemists]] gave sulfur its own alchemical symbol&mdash;a triangle at the top of a cross. In the late 1770s, [[Antoine Lavoisier]] helped convince the scientific community that sulfur was an element, not a compound.
 +
 +
[[Furniture]] makers of the late eighteenth century used molten sulfur to produce decorative inlays in their craft. That craft, however, was soon abandoned because of the [[sulfur dioxide]]* produced during the process of melting sulfur.
  
 
In 1867, sulfur was discovered in underground deposits in [[Louisiana]]* and [[Texas]]*. The overlying layer of earth was [[quicksand]]*, prohibiting ordinary mining operations. Therefore, it was removed by the [[Frasch process]]*&mdash;the underground sulfur was melted by pumping superheated steam through pipes set in the ground, and the molten sulfur was pumped out.
 
In 1867, sulfur was discovered in underground deposits in [[Louisiana]]* and [[Texas]]*. The overlying layer of earth was [[quicksand]]*, prohibiting ordinary mining operations. Therefore, it was removed by the [[Frasch process]]*&mdash;the underground sulfur was melted by pumping superheated steam through pipes set in the ground, and the molten sulfur was pumped out.
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[[Image:Burning-sulfur.png|thumb|left|A piece of sulfur melts to a blood-red liquid. When burned, it emits a blue flame.]]
 
[[Image:Burning-sulfur.png|thumb|left|A piece of sulfur melts to a blood-red liquid. When burned, it emits a blue flame.]]
  
In the periodic table, sulfur is located in group 16 (formerly group 6A), between [[oxygen]] and [[selenium]]. It is thus a member of the oxygen family of elements, also called the ''chalcogens''. In addition, it lies between [[phosphorus]] and [[chlorine]] in period 3. It can combine with other elements in different proportions, and it is therefore described as being [[Valency (chemistry)|multivalent]].
+
In the periodic table, sulfur is located in group 16 (formerly group 6A), between [[oxygen]] and [[selenium]]. It is thus a member of the oxygen family of elements, also called the ''chalcogens''. In addition, it lies between [[phosphorus]] and [[chlorine]] in period 3.
  
Elemental sulfur has a faint odor, similiar to that of matches. The common belief that sulfur smells like rotten eggs is actually an association with the smell of [[hydrogen sulfide]]* (H<sub>2</sub>S).
+
Elemental sulfur is odorless, as noted above. The common belief that it smells like rotten eggs is actually an association with the smell of [[hydrogen sulfide]]* (H<sub>2</sub>S) gas. When it burns, sulfur produces a blue flame and emits [[sulfur dioxide]]*&mdash;a gas that is notable for its peculiar, suffocating odor, like that of burnt matches. Sulfur is insoluble in water but [[solubility|soluble]]* in [[carbon disulfide]]* and, to a lesser extent, in other organic solvents such as [[benzene]].
  
It burns with a blue flame that emits [[sulfur dioxide]], notable for its peculiar suffocating odor. Sulfur is insoluble in water but [[solubility|soluble]] in [[carbon disulfide]] and to a lesser extent in other organic solvents such as [[benzene]]. Common [[oxidation state]]s of sulfur include &minus;2, +2, +4 and +6. Sulfur forms stable compounds with all elements except the noble gases.
+
Sulfur can combine with other elements in different proportions, and it is therefore described as being [[Valency (chemistry)|multivalent]]. Common [[oxidation state]]s of sulfur include &minus;2, +2, +4 and +6.
  
Sulfur in the solid state ordinarily exists as cyclic crown-shaped S<sub>8</sub> molecules. Sulfur has many [[allotropy|allotrope]]s besides S<sub>8</sub>. Removing one atom from the crown gives S<sub>7</sub>, which is responsible for sulfur's distinctive yellow color. Many other rings have been prepared, including S<sub>12</sub> and S<sub>18</sub>. By contrast, its lighter neighbor [[oxygen]] only exists in two states of allotropic significance: O<sub>2</sub> and O<sub>3</sub>. [[Selenium]], the heavier analogue of sulfur can form rings but is more often found as a polymer chain.
+
In the solid state, sulfur ordinarily exists as cyclic, crown-shaped S<sub>8</sub> molecules. In addition, it has many [[allotropy|allotrope]]s. Removing one atom from the crown gives S<sub>7</sub>, which is responsible for sulfur's distinctive yellow color. Many other rings have been prepared, including S<sub>12</sub> and S<sub>18</sub>. By contrast, its lighter neighbor, [[oxygen]], exists in only two significant allotropic states: O<sub>2</sub> and O<sub>3</sub>. [[Selenium]], the heavier analog of sulfur, can form rings but is more often found as a polymer chain. Depending on the specific conditions, the sulfur [[allotrope]]s form several distinct [[crystal]] structures, of which [[rhombic]]* and [[monoclinic]]* S<sub>8</sub> are best known.
  
[[Image:Sulfur-8-ring-3D-vdW.png|thumb|left|The structure of the S<sub>8</sub> molecule]]
+
[[Image:Sulfur-8-ring-3D-vdW.png|thumb|left|The structure of the S<sub>8</sub> molecule. Two of the S atoms in this structure lie in the back and cannot be seen.]]
The [[crystallography]] of sulfur is complex. Depending on the specific conditions, the sulfur [[allotrope]]s form several distinct [[crystal structure]]s, with '''[[rhombic]]''' and '''[[monoclinic]]''' S<sub>8</sub> best known.
 
  
A noteworthy property is that the [[viscosity]] of molten sulfur, unlike most other liquids, increases with temperature due to the formation of [[polymer]] chains. However, after a specific temperature is reached, the viscosity is reduced because there is enough energy to break the chains.
+
The [[viscosity]]* of molten sulfur, unlike that of most other liquids, increases with temperature because of the formation of [[polymer]] chains. Once a specific temperature is reached, the viscosity starts dropping because there is enough energy to break the chains.
  
[[Amorphous]] or "plastic" sulfur can be produced through the rapid cooling of molten sulfur. [[X-ray crystallography]] studies show that the amorphous form may have a [[helix|helical]] structure with eight atoms per turn. This form is [[metastable]] at room temperature and gradually reverts back to crystalline form. This process happens within a matter of hours to days but can be rapidly catalyzed.
+
[[Amorphous]]* or "plastic" sulfur can be produced through the rapid cooling of molten sulfur. Studies using a technique known as [[X-ray crystallography]]* show that the amorphous form may have a [[helix|helical]] structure, with eight atoms per turn. At room temperature, this form is [[metastable]]* and gradually reverts back to the crystalline state. This process happens within a matter of hours to days but can be speeded up by using a [[catalyst]].
  
 
=== Isotopes ===
 
=== Isotopes ===
  
Sulfur has 18 [[isotope]]s, of which four are stable: <sup>32</sup>S (95.02%), <sup>33</sup>S (0.75%), <sup>34</sup>S (4.21%), and <sup>36</sup>S (0.02%). Other than <sup>35</sup>S, the [[radioactive isotopes]] of sulfur are all short lived. <sup>35</sup>S is formed from [[cosmic ray]] [[spallation]] of <sup>40</sup>[[argon|Ar]] in the [[Earth's atmosphere|atmosphere]]. It has a [[half-life]] of 87 days.
+
Sulfur has 18 [[isotope]]s, of which four are stable: <sup>32</sup>S (95.02%), <sup>33</sup>S (0.75%), <sup>34</sup>S (4.21%), and <sup>36</sup>S (0.02%). The radioactive isotope <sup>35</sup>S is formed from [[cosmic ray]] [[spallation]]* of <sup>40</sup>[[argon|Ar]] in the [[Earth's atmosphere|atmosphere]]. It has a [[half-life]]* of 87 days. The other radioactive isotopes of sulfur are all short lived.
  
When sulfide [[mineral]]s are precipitated, isotopic equilibration among solids and liquid may cause small differences in the δS-34 values of co-genetic minerals. The differences between minerals can be used to estimate the temperature of equilibration. The δ[[carbon|C]]-13 and δS-34 of coexisting [[carbonate]]s and sulfides can be used to determine the [[pH]] and [[oxygen]] [[fugacity]] of the ore-bearing fluid during ore formation.
+
Sulfur with a distinctive isotopic composition has been used to identify pollution sources, and enriched sulfur has been added as a tracer in [[hydrology|hydrologic]] studies. Differences in the [[natural abundance]]s can also be used in systems where there is sufficient variation in the <sup>34</sup>S of ecosystem components.
 
 
In most [[forest]] ecosystems, sulfate is derived mostly from the atmosphere; weathering of ore minerals and evaporites also contribute some sulfur. Sulfur with a distinctive isotopic composition has been used to identify pollution sources, and enriched sulfur has been added as a tracer in [[hydrology|hydrologic]] studies. Differences in the [[natural abundance]]s can also be used in systems where there is sufficient variation in the <sup>34</sup>S of ecosystem components. [[Rocky Mountain]] lakes thought to be dominated by atmospheric sources of sulfate have been found to have different δS-34 values from lakes believed to be dominated by watershed sources of sulfate.
 
  
 
== Applications ==
 
== Applications ==
[[Image:Sulfur powder.jpg|left|thumb|150px|Sulfur powder.]]
+
[[Image:Sulfur powder.jpg|right|thumb|150px|Sulfur powder.]]
  
Sulfur has many industrial uses. Through its major derivative, [[sulfuric acid]] ([[hydrogen|H]]<sub>2</sub>S[[oxygen|O]]<sub>4</sub>), sulfur ranks as one of the more important industrial raw materials. It is of prime importance to every sector of the [[world economy|world's economies]].
+
Sulfur and its compounds have many uses. Its main derivative is [[sulfuric acid]] ([[hydrogen|H]]<sub>2</sub>S[[oxygen|O]]<sub>4</sub>), through which sulfur ranks as one of the most important industrial raw materials. The consumption of sulfuric acid has been regarded as one of the best indices of a nation's industrial development. More sulfuric acid is produced in the [[United States]] every year than any other industrial chemical.
  
Sulfuric acid production is the major end use for sulfur, and consumption of sulfuric acid has been regarded as one of the best indices of a nation's industrial development. More sulfuric acid is produced in the [[United States]] every year than any other industrial chemical.
+
Sulfur is also used in [[battery (electricity)|batteries]], [[detergent]]s, the [[vulcanization]]* of rubber, [[fungicide]]s, and the manufacture of [[phosphate]]* fertilizers. [[Sulfite]]*s are used to [[Bleach (chemical)|bleach]] [[paper]] and as preservatives in [[wine]] and dried [[fruit]]. Given its flammable nature, sulfur also finds use in [[match]]es, [[gunpowder]], and [[firework]]s. Sodium and ammonium [[sodium thiosulfate|thiosulfate]]*s are used as photographic fixing agents. [[Magnesium sulfate]]*, better known as [[Epsom salts]]*, can be used as a [[laxative]], a bath additive, an [[exfoliant]]*, or a [[magnesium]] supplement for plants. Sulfur is used as the light-generating medium in the rare lighting fixtures known as [[sulfur lamp]]*s.
  
Sulfur is also used in [[battery (electricity)|batteries]], [[detergents]], the [[vulcanization]] of rubber, [[fungicide]]s, and in the manufacture of [[phosphate]] fertilizers. [[Sulfite]]s are used to [[Bleach (chemical)|bleach]] [[paper]] and as a preservative in [[wine]] and dried [[fruit]]. Because of its flammable nature, sulfur also finds use in [[match]]es, [[gunpowder]], and [[firework]]s. Sodium or ammonium [[sodium thiosulfate|thiosulfate]] is used as photographic fixing agents. [[Magnesium sulfate]], better known as [[Epsom salts]], can be used as a [[laxative]], a bath additive, an [[exfoliant]], or a [[magnesium]] supplement for plants.  Sulfur is used as the light-generating medium in the rare lighting fixtures known as [[sulfur lamp]]s.
+
== Biological role ==
  
In the late [[1700s]], [[furniture]] makers used molten sulfur to produce decorative [[inlay]]s in their craft.  Because of the [[sulfur dioxide]] produced during the process of melting sulfur, the craft of sulfur inlays was soon abandoned.
+
The [[amino acid]]s [[cysteine]]* and [[methionine]]* contain sulfur, as do all [[peptide]]*s and [[protein]]s that contain these amino acids. In protein assembly and structure, bonds between sulfur atoms&mdash;known as "disulfide bonds"&mdash;play an important role. Thus, sulfur is a necessary component of all living [[cell (biology)|cells]].
 
 
== Biological role ==
 
  
The [[amino acid]]s [[cysteine]] and [[methionine]] contain sulfur, as do all [[polypeptide]]s, [[protein]]s, and [[enzyme]]s which contain these amino acids.  This makes sulfur a necessary component of all living [[cell (biology)|cells]]. [[Disulfide bond]]s between polypeptides are very important in protein assembly and structure. [[Homocysteine]] and [[taurine]] are also sulfur containing amino acids but are not coded for by [[DNA]] nor are they part of the [[primary structure]] of proteins. Some forms of [[bacterium|bacteria]] use [[hydrogen sulfide]] (H<sub>2</sub>S) in the place of water as the [[electron]] donor in a primitive [[photosynthesis]]-like process. Sulfur is absorbed by [[plant]]s via the [[root]]s from soil as the [[sulfate]] [[ion]] and reduced to sulfide before it is incorporated into [[cysteine]] and other organic sulfur compounds ([[sulfur assimilation]]). Inorganic sulfur forms a part of [[iron-sulfur cluster]]s, and sulfur is the bridging ligand in the [[copper|Cu]]<sub>A</sub> site of [[cytochrome c oxidase]]. Sulfur is an important component of [[CoA|coenzyme A]].
+
Some forms of [[bacterium|bacteria]] use [[hydrogen sulfide]]* (H<sub>2</sub>S) in place of water as the [[electron]] donor in a primitive, [[photosynthesis]]-like process. Sulfur is absorbed by [[plant]]s via the [[root]]s from soil as the [[sulfate]]* [[Ion (physics)|ion]] and reduced to sulfide before being incorporated into cysteine and other organic sulfur compounds&mdash;a process called [[sulfur assimilation]]*. Inorganic sulfur forms a part of [[iron-sulfur cluster]]*s, and sulfur is the bridging ligand in the [[copper|Cu]]<sub>A</sub> site of the enzyme [[cytochrome c oxidase]]*. Sulfur is also an important component of [[CoA|coenzyme A]]*. The amino acids [[homocysteine]]* and [[taurine]]* also contain sulfur, but they are not part of the [[primary structure]]* of proteins.
  
 
== Environmental impact ==
 
== Environmental impact ==
  
The burning of [[coal]] and [[petroleum]] by industry and power plants liberates huge amounts of [[sulfur dioxide]] (S[[oxygen|O]]<sub>2</sub>) which reacts with atmospheric water and oxygen to produce [[sulfuric acid]]. This sulfuric acid is a component of [[acid rain]], which lowers the [[pH]] of [[soil]] and freshwater bodies, resulting in substantial damage to the [[natural environment]] and [[chemical weathering]] of statues and architecture. Fuel standards increasingly require sulfur to be extracted from [[fossil fuel]]s to prevent the formation of acid rain. This extracted sulfur is then refined and represents a large portion of sulfur production.
+
The burning of [[coal]] and [[petroleum]] by industry and power plants liberates huge amounts of [[sulfur dioxide]]* (S[[oxygen|O]]<sub>2</sub>), which reacts with atmospheric water and oxygen to produce [[sulfuric acid]]. This acid is a component of [[acid rain]], which causes [[soil]] and freshwater bodies to become acidic, thereby harming the [[natural environment]]*. It also causes substantial damage to statues and architecture. Fuel standards increasingly require sulfur to be extracted from [[fossil fuel]]*s, to prevent the formation of acid rain. This extracted sulfur is then refined and represents a large portion of sulfur production.
  
 
== Compounds ==
 
== Compounds ==

Revision as of 15:59, 28 September 2006

16 phosphorussulfurchlorine
O

S

Se
S-TableImage.png
periodic table
General
Name, Symbol, Number sulfur, S, 16
Chemical series nonmetals
Group, Period, Block 16, 3, p
Appearance lemon yellow
Sulfur.jpg
Atomic mass 32.065(5) g/mol
Electron configuration [Ne] 3s2 3p4
Electrons per shell 2, 8, 6
Physical properties
Phase solid
Density (near r.t.) (alpha) 2.07 g/cm³
Density (near r.t.) (beta) 1.96 g/cm³
Density (near r.t.) (gamma) 1.92 g/cm³
Liquid density at m.p. 1.819 g/cm³
Melting point 388.36 K
(115.21 °C, 239.38 °F)
Boiling point 717.8 K
(444.6 °C, 832.3 °F)
Critical point 1314 K, 20.7 MPa
Heat of fusion (mono) 1.727 kJ/mol
Heat of vaporization (mono) 45 kJ/mol
Heat capacity (25 °C) 22.75 J/(mol·K)
Vapor pressure
P/Pa 1 10 100 1 k 10 k 100 k
at T/K 375 408 449 508 591 717
Atomic properties
Crystal structure orthorhombic
Oxidation states −1, ±2, 4, 6
(strongly acidic oxide)
Electronegativity 2.58 (Pauling scale)
Ionization energies
(more)
1st: 999.6 kJ/mol
2nd: 2252 kJ/mol
3rd: 3357 kJ/mol
Atomic radius 100 pm
Atomic radius (calc.) 88 pm
Covalent radius 102 pm
Van der Waals radius 180 pm
Miscellaneous
Magnetic ordering no data
Electrical resistivity (20 °C) (amorphous)
2×1015 Ω·m
Thermal conductivity (300 K) (amorphous)
0.205 W/(m·K)
Bulk modulus 7.7 GPa
Mohs hardness 2.0
CAS registry number 7704-34-9
Notable isotopes
Main article: Isotopes of sulfur
iso NA half-life DM DE (MeV) DP
32S 95.02% S is stable with 16 neutrons
33S 0.75% S is stable with 17 neutrons
34S 4.21% S is stable with 18 neutrons
35S syn 87.32 d β- 0.167 35Cl
36S 0.02% S is stable with 20 neutrons

Sulfur or sulphur (see spelling below) (chemical symbol S, atomic number 16) is a yellow crystalline solid at ordinary temperatures and pressures. It is tasteless and odorless and is classified as a nonmetal. It forms stable compounds with all elements except the noble gases. Abundant in nature, it can be found as the pure element or as sulfide and sulfate minerals.

Sulfur (incorporated into certain compounds) is an essential element for living organisms. For instance, it is part of the structure of two amino acids. It is primarily used in fertilizers, but it also useful for making gunpowder, matches, insecticides, and fungicides.

Occurrence

Sulfur crystalites at Waiotapu hot springs, New Zealand.

Elemental sulfur can be found near hot springs and volcanic regions in many parts of the world, especially along the Pacific "Ring of Fire"—a zone of frequent earthquakes and volcanic eruptions encircling the Pacific Ocean. Such volcanic deposits are currently exploited in Indonesia, Chile, and Japan.

Significant desposits of elemental sulfur also exist in salt domes along the coast of the Gulf of Mexico and in evaporites in eastern Europe and western Asia. (Evaporites are mineral sediments that are left behind after evaporation of the water they were once dissolved in.) The sulfur in these deposits is believed to come from the action of anaerobic bacteria on sulfate minerals, especially gypsum. Such deposits form the basis for commercial production in the United States, Poland, Russia, Turkmenistan, and Ukraine.

Sulfur extracted from oil, gas, and the Athabasca Oil Sands has led to a glut on the market, and huge stockpiles of sulfur can be seen throughout Alberta.

Common sulfur compounds in nature include:

  • metal sulfides, such as pyrite (iron sulfide), cinnabar (mercury sulfide), galena (lead sulfide), sphalerite (zinc sulfide), and stibnite (antimony sulfide);
  • metal sulfates, such as gypsum (calcium sulfate), alunite (potassium aluminum sulfate), and barite (barium sulfate).

Sulfur is present in many types of meteorites. In addition, the distinctive colors of Jupiter's volcanic moon Io are thought to correspond to various forms of gaseous, molten, and solid sulfur. There is also a dark area near the lunar crater Aristarchus that may be a sulfur deposit.

History

Sulfur crystal

Sulfur (Sanskrit, sulvere; Latin sulpur) was known in ancient times, and is referred to in several books of the Bible, including the book of Genesis. It has been suggested that the word may have been derived from the Arabic sufra, meaning yellow, which is the color of the naturally occurring form of the element.

In the eighth century B.C.E., Homer mentioned "pest-averting sulfur"; and in 424 B.C.E., the tribe of Boeotia destroyed the walls of a city by burning a mixture of coal, sulfur, and tar under them. Sometime in the twelfth century, the Chinese invented gunpowder, which is a mixture of potassium nitrate (KNO3), carbon, and sulfur. Early alchemists gave sulfur its own alchemical symbol—a triangle at the top of a cross. In the late 1770s, Antoine Lavoisier helped convince the scientific community that sulfur was an element, not a compound.

Furniture makers of the late eighteenth century used molten sulfur to produce decorative inlays in their craft. That craft, however, was soon abandoned because of the sulfur dioxide produced during the process of melting sulfur.

In 1867, sulfur was discovered in underground deposits in Louisiana and Texas. The overlying layer of earth was quicksand, prohibiting ordinary mining operations. Therefore, it was removed by the Frasch process—the underground sulfur was melted by pumping superheated steam through pipes set in the ground, and the molten sulfur was pumped out.

Notable characteristics

A piece of sulfur melts to a blood-red liquid. When burned, it emits a blue flame.

In the periodic table, sulfur is located in group 16 (formerly group 6A), between oxygen and selenium. It is thus a member of the oxygen family of elements, also called the chalcogens. In addition, it lies between phosphorus and chlorine in period 3.

Elemental sulfur is odorless, as noted above. The common belief that it smells like rotten eggs is actually an association with the smell of hydrogen sulfide (H2S) gas. When it burns, sulfur produces a blue flame and emits sulfur dioxide—a gas that is notable for its peculiar, suffocating odor, like that of burnt matches. Sulfur is insoluble in water but soluble in carbon disulfide and, to a lesser extent, in other organic solvents such as benzene.

Sulfur can combine with other elements in different proportions, and it is therefore described as being multivalent. Common oxidation states of sulfur include −2, +2, +4 and +6.

In the solid state, sulfur ordinarily exists as cyclic, crown-shaped S8 molecules. In addition, it has many allotropes. Removing one atom from the crown gives S7, which is responsible for sulfur's distinctive yellow color. Many other rings have been prepared, including S12 and S18. By contrast, its lighter neighbor, oxygen, exists in only two significant allotropic states: O2 and O3. Selenium, the heavier analog of sulfur, can form rings but is more often found as a polymer chain. Depending on the specific conditions, the sulfur allotropes form several distinct crystal structures, of which rhombic and monoclinic S8 are best known.

The structure of the S8 molecule. Two of the S atoms in this structure lie in the back and cannot be seen.

The viscosity of molten sulfur, unlike that of most other liquids, increases with temperature because of the formation of polymer chains. Once a specific temperature is reached, the viscosity starts dropping because there is enough energy to break the chains.

Amorphous or "plastic" sulfur can be produced through the rapid cooling of molten sulfur. Studies using a technique known as X-ray crystallography show that the amorphous form may have a helical structure, with eight atoms per turn. At room temperature, this form is metastable and gradually reverts back to the crystalline state. This process happens within a matter of hours to days but can be speeded up by using a catalyst.

Isotopes

Sulfur has 18 isotopes, of which four are stable: 32S (95.02%), 33S (0.75%), 34S (4.21%), and 36S (0.02%). The radioactive isotope 35S is formed from cosmic ray spallation of 40Ar in the atmosphere. It has a half-life of 87 days. The other radioactive isotopes of sulfur are all short lived.

Sulfur with a distinctive isotopic composition has been used to identify pollution sources, and enriched sulfur has been added as a tracer in hydrologic studies. Differences in the natural abundances can also be used in systems where there is sufficient variation in the 34S of ecosystem components.

Applications

Sulfur powder.

Sulfur and its compounds have many uses. Its main derivative is sulfuric acid (H2SO4), through which sulfur ranks as one of the most important industrial raw materials. The consumption of sulfuric acid has been regarded as one of the best indices of a nation's industrial development. More sulfuric acid is produced in the United States every year than any other industrial chemical.

Sulfur is also used in batteries, detergents, the vulcanization of rubber, fungicides, and the manufacture of phosphate fertilizers. Sulfites are used to bleach paper and as preservatives in wine and dried fruit. Given its flammable nature, sulfur also finds use in matches, gunpowder, and fireworks. Sodium and ammonium thiosulfates are used as photographic fixing agents. Magnesium sulfate, better known as Epsom salts, can be used as a laxative, a bath additive, an exfoliant, or a magnesium supplement for plants. Sulfur is used as the light-generating medium in the rare lighting fixtures known as sulfur lamps.

Biological role

The amino acids cysteine and methionine contain sulfur, as do all peptides and proteins that contain these amino acids. In protein assembly and structure, bonds between sulfur atoms—known as "disulfide bonds"—play an important role. Thus, sulfur is a necessary component of all living cells.

Some forms of bacteria use hydrogen sulfide (H2S) in place of water as the electron donor in a primitive, photosynthesis-like process. Sulfur is absorbed by plants via the roots from soil as the sulfate ion and reduced to sulfide before being incorporated into cysteine and other organic sulfur compounds—a process called sulfur assimilation. Inorganic sulfur forms a part of iron-sulfur clusters, and sulfur is the bridging ligand in the CuA site of the enzyme cytochrome c oxidase. Sulfur is also an important component of coenzyme A. The amino acids homocysteine and taurine also contain sulfur, but they are not part of the primary structure of proteins.

Environmental impact

The burning of coal and petroleum by industry and power plants liberates huge amounts of sulfur dioxide (SO2), which reacts with atmospheric water and oxygen to produce sulfuric acid. This acid is a component of acid rain, which causes soil and freshwater bodies to become acidic, thereby harming the natural environment. It also causes substantial damage to statues and architecture. Fuel standards increasingly require sulfur to be extracted from fossil fuels, to prevent the formation of acid rain. This extracted sulfur is then refined and represents a large portion of sulfur production.

Compounds

Hydrogen sulfide has the characteristic smell of rotten eggs. Dissolved in water, hydrogen sulfide is acidic and will react with metals to form a series of metal sulfides. Natural metal sulfides are common, especially those of iron. Iron sulfide is called pyrite, the so called fool's gold. Interestingly, pyrite can show semiconductor properties.[1] Galena, a naturally occurring lead sulfide, was the first semiconductor discovered, and found a use as a signal rectifier in the "cat's whiskers" of early crystal radios.

Many of the unpleasant odors of organic matter are based on sulfur-containing compounds such as methyl and ethyl mercaptan used to scent natural gas so that leaks are easily detectable. The odor of garlic and "skunk stink" are also caused by sulfur-containing organic compounds. However, not all organic sulfur compounds smell unpleasant; for example, grapefruit mercaptan, a sulfur-containing monoterpenoid is responsible for the characteristic scent of grapefruit.

Polymeric sulfur nitride has metallic properties even though it does not contain any metal atoms. This compound also has unusual electrical and optical properties. This polymer can be made from tetrasulfur tetranitride S4N4.

Phosphorus sulfides are important in synthesis. For example, P4S10 and its derivatives Lawesson's reagent and naphthalen-1,8-diyl 1,3,2,4-dithiadiphosphetane 2,4-disulfide are used to replace oxygen from some organic molecules with sulfur.

Inorganic sulfur compounds:

  • Sulfides (S2−), a complex family of compounds usually derived from S2−. Cadmium sulfide (CdS) is an example.
  • Sulfites (SO32−), the salts of sulfurous acid (H2SO3) which is generated by dissolving SO2 in water. Sulfurous acid and the corresponding sulfites are fairly strong reducing agents. Other compounds derived from SO2 include the pyrosulfite or metabisulfite ion (S2O52−).
  • Sulfates (SO42−), the salts of sulfuric acid. Sulfuric acid also reacts with SO3 in equimolar ratios to form pyrosulfuric acid (H2S2O7).
  • Thiosulfates (sometimes referred to as thiosulfites or "hyposulfites") (S2O32−). Thiosulfates are used in photographic fixing (HYPO) as reducing agents. Ammonium thiosulfate is being investigated as a cyanide replacement in leaching gold.[2]
  • Sodium dithionite, Na2S2O4, is the highly reducing dianion derived from hyposulfurous/dithionous acid.
  • Sodium dithionate (Na2S2O6).
  • Polythionic acids (H2SnO6), where n can range from 3 to 80.
  • Peroxymonosulfuric acid (H2SO5) and peroxydisulfuric acids (H2S2O8), made from the action of SO3 on concentrated H2O2, and H2SO4 on concentrated H2O2 respectively.
  • Sodium polysulfides (Na2Sx)
  • Sulfur hexafluoride, SF6, a dense gas at ambient conditions, is used as nonreactive and nontoxic propellant
  • Sulfur nitrides are chain and cyclic compounds containing only S and N. Tetrasulfur tetranitride S4N4 is an example.
  • Thiocyanates contain the SCN group. Oxidation of thiocyanoate gives thiocyanogen, (SCN)2 with the connectivity NCS-SCN.

Organic sulfur compounds (where R, R', and R are organic groups such as CH3):

  • Thioethers have the form R-S-R′. These compounds are the sulfur equivalents of ethers.
  • Sulfonium ions have the formula RR'S-'R'", i.e. where three groups are attached to the cationic sulfur center. Dimethylsulfoniopropionate (DMSP; (CH3)2S+CH2CH2COO) is a sulfonium ion, which is important in the marine organic sulfur cycle.
  • Thiols (also known as mercaptans) have the form R-SH. These are the sulfur equivalents of alcohols.
  • Thiolates ions s have the form R-S-. Such anions arise upon treatment of thiols with base.
  • Sulfoxides have the form R-S(=O)-R′. A common sulfoxide is DMSO.
  • Sulfones have the form R-S(=O)2-R′. A common sulfone is sulfolane C4H8SO2.

See also Category: sulfur compounds and organosulfur chemistry

Precautions

Carbon disulfide, carbon oxysulfide, hydrogen sulfide, and sulfur dioxide should all be handled with care.

Although sulfur dioxide is sufficiently safe to be used as a food additive in small amounts, at high concentrations it reacts with moisture to form sulfurous acid which in sufficient quantities may harm the lungs, eyes or other tissues. In creatures without lungs such as insects or plants, it otherwise prevents respiration.

Hydrogen sulfide is quite toxic (more toxic than cyanide). Although very pungent at first, it quickly deadens the sense of smell, so potential victims may be unaware of its presence until it is too late.

Spelling

The element has traditionally been spelled sulphur in the United Kingdom, Ireland, Hong Kong and India, but sulfur in the United States, while both spellings are used in Australia, Canada and New Zealand. IUPAC adopted the spelling "sulfur" in 1990, as did the Royal Society of Chemistry Nomenclature Committee in 1992. This spelling has begun to replace its variant in official use, unlike aluminum, which is not commonly used outside North America, and which IUPAC rejected in 1990 in favor of aluminium.

The Latin name of the element is sulfur with an F. Since it is an original Latin name and not a Classical Greek loan, the fricative phoneme is indeed denoted with f rather than ph (which would denote the Greek letter φ). Sulfur in Greek is thios (θιοσ), which does not bear resemblance to the Latin word.

Fire and brimstone

In the Bible, sulfur is referred to as "brimstone." The book of Genesis, in particular, mentions that God punished evildoers in Sodom and Gomorrah by raining "brimstone and fire" upon them. Accordingly, a "fire and brimstone" sermon is one in which listeners are reminded of the fate of eternal damnation that awaits the unrepentant sinner. Also, hell is implied as having the smell of sulfur, although, as mentioned above, sulfur is odorless. The "smell of sulfur" usually refers to the odor of hydrogen sulfide, which is produced by rotten eggs.

See also

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