Sulfur

This article is about the chemical element. For other uses, see Sulfur (disambiguation).

Sulfur, ₁₆S

Sulfur
Alternative name	Sulphur (British spelling)
Allotropes	see Allotropes of sulfur
Appearance	Lemon yellow sintered microcrystals
Standard atomic weight Ar°(S)
	[32.059, 32.076] 32.06±0.02 (abridged)
Sulfur in the periodic table
Hydrogen Helium Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson O ↑ S ↓ Se phosphorus ← sulfur → chlorine
Atomic number (Z)	16
Group	group 16 (chalcogens)
Period	period 3
Block	p-block
Electron configuration	[Ne] 3s2 3p4
Electrons per shell	2, 8, 6
Physical properties
Phase at STP	solid
Melting point	alpha (α-S8): 388.36 K ​(115.21 °C, ​239.38 °F)
Boiling point	717.8 K ​(444.6 °C, ​832.3 °F)
Density (near r.t.)	alpha (α-S8): 2.07 g/cm3 beta (β-S8): 1.96 g/cm3 gamma (γ-S8): 1.92 g/cm3
when liquid (at m.p.)	1.819 g/cm3
Critical point	1314 K, 20.7 MPa
Heat of fusion	beta (β-S8): 1.727 kJ/mol
Heat of vaporization	beta (β-S8): 45 kJ/mol
Molar heat capacity	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
Oxidation states	−2, −1, 0, +1, +2, +3, +4, +5, +6 (a strongly acidic oxide)
Electronegativity	Pauling scale: 2.58
Ionization energies	1st: 999.6 kJ/mol 2nd: 2252 kJ/mol 3rd: 3357 kJ/mol (more)
Covalent radius	105±3 pm
Van der Waals radius	180 pm
Spectral lines of sulfur
Other properties
Natural occurrence	primordial
Crystal structure	alpha (α-S8): ​orthorhombic (oF128)
Lattice constants	a = 1.0460 nm b = 1.2861 nm c = 2.4481 nm (at 20 °C)
Crystal structure	beta (β-S8): ​monoclinic (mP48)
Lattice constants	a = 1.0923 nm b = 1.0851 nm c = 1.0787 nm β = 95.905° (at 20 °C)
Thermal conductivity	0.205 W/(m⋅K) (amorphous)
Electrical resistivity	2×1015  Ω⋅m (at 20 °C) (amorphous)
Magnetic ordering	diamagnetic
Molar magnetic susceptibility	alpha (α-S8): −15.5×10−6 cm3/mol (298 K)
Bulk modulus	7.7 GPa
Mohs hardness	2.0
CAS Number	7704-34-9
History
Discovery	before 2000 BCE
Recognized as an element by	Antoine Lavoisier (1777)
Isotopes of sulfur
Main isotopes Decay abun­dance half-life (t1/2) mode pro­duct 32S 94.8% stable 33S 0.760% stable 34S 4.37% stable 35S trace 87.37 d β− 35Cl 36S 0.02% stable 34S abundances vary greatly (between 3.96 and 4.77 percent) in natural samples.

Sulfur or sulphur (Template:Pron-en SUL-fər, see spelling below) is the chemical element that has the atomic number 16. It is denoted with the symbol S. It is an abundant, multivalent non-metal. Sulfur, in its native form, is a yellow crystalline solid. In nature, it can be found as the pure element and as sulfide and sulfate minerals. It is an essential element for life and is found in two amino acids, cysteine and methionine. Its commercial uses are primarily in fertilizers, but it is also widely used in black gunpowder, matches, insecticides and fungicides. Elemental sulfur crystals are commonly sought after by mineral collectors for their brightly colored polyhedron shapes. In nonscientific contexts, it can also be referred to as brimstone.

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Characteristics

Sulfur melts to a blood-red liquid. When burned, it emits a blue flame.

At room temperature, sulfur is a soft, bright-yellow solid. Elemental sulfur has only a faint odor, similar to that of matches. The odor associated with rotten eggs is due to hydrogen sulfide (H
₂S) and organic sulfur compounds rather than elemental sulfur. Sulfur burns with a blue flame that emits sulfur dioxide, notable for its peculiar suffocating odor due to dissolving in the mucosa to form dilute sulfurous acid. Sulfur itself is insoluble in water, but soluble in carbon disulfide — and to a lesser extent in other non-polar organic solvents such as benzene and toluene. Common oxidation states of sulfur include −2, +2, +4 and +6. Sulfur forms stable compounds with all elements except the noble gases. Sulfur in the solid state ordinarily exists as cyclic crown-shaped S₈ molecules.

The crystallography of sulfur is complex. Depending on the specific conditions, the sulfur allotropes form several distinct crystal structures, with rhombic and monoclinic S₈ best known.

A noteworthy property of sulfur is that the viscosity in its molten state, unlike most other liquids, increases above temperatures of 200 °C due to the formation of polymers. The molten sulfur assumes a dark red color above this temperature. At higher temperatures, however, the viscosity is decreased as depolymerization occurs.

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 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.

Allotropes

The structure of the cyclooctasulfur molecule, S₈.

Main article: Allotropes of sulfur

Sulfur forms more than 30 solid allotropes, more than any other element. Besides S₈, several other rings are known. Removing one atom from the crown gives S₇, which is more deeply yellow than S₈. HPLC analysis of "elemental sulfur" reveals an equilibrium mixture of mainly S₈, but also S₇ and small amounts of S₆. Larger rings have been prepared, including S₁₂ and S₁₈. By contrast, sulfur's lighter neighbor oxygen only exists in two states of allotropic significance: O₂ and O₃. Selenium, the heavier analogue of sulfur, can form rings but is more often found as a polymer chain.

Isotopes

Main article: Isotopes of sulfur

Sulfur has 25 known isotopes, four of which are stable: ³²S (95.02%), ³³S (0.75%), ³⁴S (4.21%), and ³⁶S (0.02%). Other than ³⁵S, the radioactive isotopes of sulfur are all short lived. ³⁵S is formed from cosmic ray spallation of ⁴⁰argon in the atmosphere. It has a half-life of 87 days.

When sulfide minerals 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 δC-13 and δS-34 of coexisting carbonates and sulfides can be used to determine the pH and oxygen fugacity of the ore-bearing fluid during ore formation.

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 hydrologic studies. Differences in the natural abundances can also be used in systems where there is sufficient variation in the ³⁴S 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.

Occurrence

Sulfur crystallites 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. Such volcanic deposits are currently mined in Indonesia, Chile, and Japan. Sicily is also famous for its sulfur mines. Sulfur deposits are polycrystalline, and the largest documented single crystal measured 22x16x11 cm³.

Significant deposits 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. The sulfur in these deposits is believed to come from the action of anaerobic bacteria on sulfate minerals, especially gypsum, although apparently native sulfur may be produced by geological processes alone, without the aid of living organisms (see below). However, fossil-based sulfur deposits from salt domes are the basis for commercial production in the United States, Poland, Russia, Turkmenistan, and Ukraine.

Sulfur recovered from hydrocarbons in Alberta, stockpiled for shipment in North Vancouver, B.C.

Sulfur production through hydrodesulfurization of oil, gas, and the Athabasca Oil Sands has produced a surplus — huge stockpiles of sulfur now exist throughout Alberta, Canada.

Common naturally occurring sulfur compounds include the sulfide minerals, such as pyrite (iron sulfide), cinnabar (mercury sulfide), galena (lead sulfide), sphalerite (zinc sulfide) and stibnite (antimony sulfide); and the sulfates, such as gypsum (calcium sulfate), alunite (potassium aluminium sulfate), and barite (barium sulfate). It occurs naturally in volcanic emissions, such as from hydrothermal vents, and from bacterial action on decaying sulfur-containing organic matter.

The distinctive colors of Jupiter's volcanic moon, Io, are from various forms of molten, solid and gaseous sulfur. There is also a dark area near the Lunar crater Aristarchus that may be a sulfur deposit.

Sulfur is present in many types of meteorites. Ordinary chondrites contain on average 2.1% sulfur, and carbonaceous chondrites may contain as much as 6.6%. Sulfur in meteorites is normally present as troilite (FeS), but other sulfides are found in some meteorites, and carbonaceous chondrites contain free sulfur, sulfates, and possibly other sulfur compounds.

Extraction and production

Extraction from natural resources

Sulfur is extracted by mainly two processes: the Sicilian process and the Frasch process. The Sicilian process, which was first used in Sicily, was used in ancient times to get sulfur from rocks present in volcanic regions. In this process, the sulfur deposits are piled and stacked in brick kilns built on sloping hillsides, and with airspaces between them. Then powdered sulfur is put on top of the sulfur deposit and ignited. As the sulfur burns, the heat melts the sulfur deposits, causing the molten sulfur to flow down the sloping hillside. The molten sulfur can then be collected in wooden buckets.

The second process used to obtain sulfur is the Frasch process. In this method, three concentric pipes are used: the outermost pipe contains superheated water, which melts the sulfur, and the innermost pipe is filled with hot compressed air, which serves to create foam and pressure. The resulting sulfur foam is then expelled through the middle pipe.

The Frasch process produces sulfur with a 99.5% purity content, and which needs no further purification. The sulfur produced by the Sicilian process must be purified by distillation.

Production from hydrogen sulfide

Chemically

The Claus process is used to extract elemental sulfur from hydrogen sulfide produced in hydrodesulfurization of petroleum or from natural gas.

Biologically

In the biological route, hydrogen sulfide (H₂S) from natural gas or refinery gas is absorbed with a slight alkaline solution in a wet scrubber, or the sulfide is produced by biological sulfate reduction. In the subsequent process step, the dissolved sulfide is biologically converted to elemental sulfur. This solid sulfur is removed from the reactor. This process has been built on commercial scale. The main advantages of this process are:

1. no use of expensive chemicals,
2. the process is safe as the H₂S is directly absorbed in an alkaline solution,
3. no production of a polluted waste stream,
4. re-usable sulfur is produced, and
5. the process occurs under ambient conditions.

The biosulfur product is different from other processes in which sulfur is produced because the sulfur is hydrophilic. Next to straightforward reuses as source for sulfuric acid production, it can also be applied as sulfur fertilizer.

Chemistry

Inorganic compounds

Sulfur powder.

When 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. Pyrite can show semiconductor properties. 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.

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 useful 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.

The sulfate anion, SO₄²⁻

• 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 (S₂O₃²⁻). Sometimes referred as thiosulfites or "hyposulfites", Thiosulfates are used in photographic fixing (HYPO) as reducing agents. Ammonium thiosulfate is being investigated as a cyanide replacement in leaching gold.[1]
• Sodium dithionite, Na
  ₂S
  ₂O
  ₄, is the highly reducing dianion derived from hyposulfurous/dithionous acid.

Peroxydisulfuric acid.

(Na₂S₂O₆).

• Polythionic acids (H₂S_nO₆), 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 (Na₂S_x)
• 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 compounds

An organic sulfur compound, dithiane.

Many of the unpleasant odors of organic matter are based on sulfur-containing compounds such as methyl mercaptan and dimethyl sulfide. Thiols and sulfides are used in the odoration of natural gas, notably, 2-methyl-2-propanethiol (t-butyl mercaptan). The odor of garlic and "skunk stink" are also caused by sulfur-containing organic compounds. Not all organic sulfur compounds smell unpleasant; for example, grapefruit mercaptan, a sulfur-containing monoterpenoid is responsible for the characteristic scent of grapefruit. It should be noted that this thiol is present in very low concentrations. In larger concentrations, the odor of this compound is that typical of all thiols, unpleasant.

Sulfur-containing organic compounds include the following (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 have the form R-S^-. Such anions arise upon treatment of thiols with base.
• Sulfoxides have the form R-S(=O)-R′. The simplest sulfoxide, DMSO, is a common solvent.
• Sulfones have the form R-S(=O)₂-R′. A common sulfone is sulfolane C₄H₈SO₂.

See also Category: sulfur compounds and organosulfur chemistry

Applications

One of the direct uses of sulfur is in vulcanization of rubber, where polysulfides crosslink organic polymers. Sulfur is a component of gunpowder. It reacts directly with methane to give carbon disulfide, which is used to manufacture cellophane and rayon.

Elemental sulfur is mainly used as a precursor to other chemicals. Approximately 85% (1989) is converted to sulfuric acid (H₂SO₄), which is of such prime importance to the world's economies that the production and consumption of sulfuric acid is an indicator of a nation's industrial development. For example, more sulfuric acid is produced in the United States every year than any other industrial chemical. The principal use for the acid is the extraction of phosphate ores for the production of fertilizer manufacturing. Other applications of sulfuric acid include oil refining, wastewater processing, and mineral extraction.

Sulfur compounds are also used in detergents, fungicides, dyestuffs, and agrichemicals. In silver-based photography sodium and ammonium thiosulfate are used as "fixing agents."

Sulfur is an ingredient in some acne treatments.[2]

An increasing application is as fertilizer. Standard sulfur is hydrophobic and therefore has to be covered with a surfactant by bacteria in the ground before it can be oxidized to sulfate. This makes it a slow release fertilizer, which cannot be taken up by the plants instantly, but has to be oxidized to sulfate over the growth season. Sulfur also improves the use efficiency of other essential plant nutrients, particularly nitrogen and phosphorus. Biologically produced sulfur particles are naturally hydrophilic due to a biopolymer coating. This sulfur is therefore easier to disperse over the land (via spraying as a diluted slurry), and results in a faster release.

Sulfites, derived from burning sulfur, are heavily used to bleach paper. They are also used as preservatives in dried fruit.

Magnesium sulfate, better known as Epsom salts, can be used as a laxative, a bath additive, an exfoliant, a magnesium supplement for plants, or a desiccant.

Specialized applications

Sulfur is used as a light-generating medium in the rare lighting fixtures known as sulfur lamps.

Historical applications

In the late 18th century, furniture makers used molten sulfur to produce decorative inlays in their craft. Because of the sulfur dioxide produced during the process of melting sulfur, the craft of sulfur inlays was soon abandoned. Molten sulfur is sometimes still used for setting steel bolts into drilled concrete holes where high shock resistance is desired for floor-mounted equipment attachment points. Pure powdered sulfur was also used as a medicinal tonic and laxative. Sulfur was also used in baths for people who had seizures.

Fungicide and pesticide

Sulfur is one of the oldest fungicides and pesticides. Dusting sulfur, elemental sulfur in powdered form, is a common fungicide for grapes, strawberry, many vegetables and several other crops. It has a good efficacy against a wide range of powdery mildew diseases as well as black spot. In organic production, sulfur is the most important fungicide. It is the only fungicide used in organically farmed apple production against the main disease apple scab under colder conditions. Biosulfur (biologically produced elemental sulfur with hydrophilic characteristics) can be used well for these applications.

Standard-formulation dusting sulfur is applied to crops with a sulfur duster or from a dusting plane. Wettable sulfur is the commercial name for dusting sulfur formulated with additional ingredients to make it water soluble. It has similar applications, and is used as a fungicide against mildew and other mold-related problems with plants and soil.

Sulfur is also used as an "organic" (i.e. "green") insecticide (actually an acaricide) against ticks and mites. A common method of use is to dust clothing or limbs with sulfur powder. Some livestock owners set out a sulfur salt block as a salt lick.

Biological role

Main article: Sulfur assimilation

See sulfur cycle for more on the inorganic and organic natural transformations of sulfur.

Sulfur is an essential component of all living cells.

Inorganic sulfur forms a part of iron-sulfur clusters, and sulfur is the bridging ligand in the Cu_A site of cytochrome c oxidase, a basic substance involved in utilization of oxygen by all aerobic life.

Sulfur may also serve as chemical food source for some primitive organisms: some forms of bacteria use hydrogen sulfide (H₂S) in the place of water as the electron donor in a primitive photosynthesis-like process in which oxygen is the electron receptor. The photosynthetic green and purple sulfur bacteria and some chemolithotrophs use elemental oxygen to carry out such oxidization of hydrogen sulfide to produce elemental sulfur (S^o), oxidation state = 0. Primitive bacteria which live around deep ocean volcanic vents oxidize hydrogen sulfide in this way with oxygen: see giant tube worm for an example of large organisms (via bacteria) making metabolic use of hydrogen sulfide as food to be oxidized.

The so-called sulfur bacteria, by contrast, "breathe sulfate" instead of oxygen. They use sulfur as the electron acceptor, and reduce various oxidized sulfur compounds back into sulfide, often into hydrogen sulfide. They also can grow on a number of other partially oxidized sulfur compounds (e. g. thiosulfates, thionates, polysulfides, sulfites). The hydrogen sulfide produced by these bacteria is responsible for the smell of some intestinal gases and decomposition products.

Sulfur is a part of many bacterial defense molecules. For example, though sulfur is not a part of the lactam ring, it is a part of most beta lactam antibiotics, including the penicillins, cephalosporins, and monobactams.

Sulfur is absorbed by plants via the roots from soil as the sulfate ion and reduced to sulfide before it is incorporated into cysteine and other organic sulfur compounds (see sulfur assimilation for details of this process).

Sulfur is regarded as secondary nutrient although plant requirements for sulfur are equal to and sometimes exceed those for phosphorus. However sulfur is recognized as one of the major nutrients essential for plant growth, root nodule formation of legumes and plants protection mechanisms. Sulfur deficiency has become widespread in many countries in Europe. Because atmospheric inputs of sulfur will continue to decrease, the deficit in the sulfur input/output is likely to increase, unless sulfur fertilizers are used.

In plants and animals the amino acids cysteine and methionine contain sulfur, as do all polypeptides, proteins, and enzymes which contain these amino acids. Homocysteine and taurine are other sulfur-containing acids which are similar in structure, but which are not coded for by DNA, and are not part of the primary structure of proteins. Glutathione is an important sulfur-containing tripeptide which plays a role in cells as a source of chemical reduction potential in the cell, through its sulfhydryl (-SH) moiety. Many important cellular enzymes use prosthetic groups ending with -SH moieties to handle reactions involving acyl-containing biochemicals: two common examples from basic metabolism are coenzyme A and alpha-lipoic acid.

Disulfide bonds (S-S bonds) formed between cysteine residues in peptide chains are very important in protein assembly and structure. These strong covalent bonds between peptide chains give proteins a great deal of extra toughness and resiliency. For example, the high strength of feathers and hair is in part due to their high content of S-S bonds and their high content of cysteine and sulfur (eggs are high in sulfur because large amounts of the element are necessary for feather formation). The high disulfide content of hair and feathers contributes to their indigestibility, and also their odor when burned.

Traditional medical role for elemental sulfur

In traditional medical skin treatment which predates modern era of scientific medicine, elemental sulfur has been used mainly as part of creams to alleviate various conditions such as psoriasis, eczema and acne. The mechanism of action is not known, although elemental sulfur does oxidize slowly to sulfurous acid, which in turn (through the action of sulfite) acts as a mild reducing and antibacterial agent.

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 organisms without lungs such as insects or plants, it otherwise prevents respiration.

Hydrogen sulfide is toxic. Although very pungent at first, it quickly deadens the sense of smell, so potential victims may be unaware of its presence until death or other symptoms occur.

Environmental impact

The burning of coal and/or petroleum by industry and power plants generates sulfur dioxide (SO₂), which reacts with atmospheric water and oxygen to produce sulfuric acid (H₂SO₄). This sulfuric acid is a component of acid rain, which lowers the pH of soil and freshwater bodies, sometimes resulting in substantial damage to the environment and chemical weathering of statues and structures. 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. In coal fired power plants, the flue gases are sometimes purified. In more modern power plants that use syngas the sulfur is extracted before the gas is burned.

See also

• Sulfur cycle
• Stratospheric sulfur aerosols
• Disulfide bond
• Sulfonium S⁺, S⁺R₃
• Ultra-low sulfur diesel
• Claus process
• Shell-Paques sulfide removal/sulfur recovery process

External links

• Sulfur phase diagram
• WebElements.com – Sulfur
• chemicalelements.com/sulfur
• Crystalline, liquid and polymerization of sulphur on Vulcano Island, Italy
• Sulfur and its use as a pesticide
• The Sulphur Institute