Sulfur

Sulfur,  16S

Spectral lines of sulfur
General properties
Pronunciation /ˈsʌlfər/
SUL-fər
Alternative name sulphur (British spelling)
Appearance lemon yellow sintered microcrystals
Sulfur in the periodic table
O
↑
S
↓
Se
phosphorus ← sulfur → chlorine ‍
Atomic number (Z) 16
Group, period group 16 (chalcogens), period 3
Block p-block
Element category   polyatomic nonmetal
Standard atomic weight (Ar)
  • [32.059, 32.076][1]
  • conventional: 32.06
Electron configuration [Ne] 3s2 3p4
Electrons per shell
 2, 8, 6
Physical properties
Phase (at STP) solid
Melting point 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: 2.07 g/cm3
beta: 1.96 g/cm3
gamma: 1.92 g/cm3
when liquid, at m.p. 1.819 g/cm3
Critical point 1314 K, 20.7 MPa
Heat of fusion mono: 1.727 kJ/mol
Heat of vaporization mono: 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 6, 5, 4, 3, 2, 1, −1, −2 ​(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
Miscellanea
Crystal structure

​orthorhombic

Orthorhombic crystal structure for sulfur
Thermal conductivity 0.205 W/(m·K) (amorphous)
Electrical resistivity 2×1015  Ω·m (at 20 °C) (amorphous)
Magnetic ordering diamagnetic[2]
Magnetic susceptibility (χmol) (α) −15.5·10−6 cm3/mol (298 K)[3]
Bulk modulus 7.7 GPa
Mohs hardness 2.0
CAS Number 7704-34-9
History
Discovery Chinese[4] (before 2000 BCE)
Recognized as an element by Antoine Lavoisier (1777)
Main isotopes of sulfur
Iso­tope Abun­dance Half-life (t1/2) Decay mode Pro­duct
32S 94.99% stable
33S 0.75% stable
34S 4.25% stable
35S trace 87.32 d β− 35Cl
36S 0.01% stable

Sulfur or sulphur (see spelling and etymology) is a chemical element with symbol S and atomic number 16. It is abundant, multivalent, and nonmetallic. Under normal conditions, sulfur atoms form cyclic octatomic molecules with a chemical formula S8. Elemental sulfur is a bright yellow crystalline solid at room temperature. Chemically, sulfur reacts with all elements except for gold, platinum, iridium, tellurium, and the noble gases.

Though sometimes found in pure, native form, sulfur usually occurs as sulfide and sulfate minerals. Being abundant in native form, sulfur was known in ancient times, being mentioned for its uses in ancient India, ancient Greece, China, and Egypt. In the Bible, sulfur is called brimstone.[5] Today, almost all elemental sulfur is produced as a byproduct of removing sulfur-containing contaminants from natural gas and petroleum. The greatest commercial use of the element is the production of sulfuric acid for sulfate and phosphate fertilizers, and other chemical processes. The element sulfur is used in matches, insecticides, and fungicides. Many sulfur compounds are odoriferous, and the smells of odorized natural gas, skunk scent, grapefruit, and garlic are due to organosulfur compounds. Hydrogen sulfide gives the characteristic odor to rotting eggs and other biological processes.

Sulfur is an essential element for all life, but almost always in the form of organosulfur compounds or metal sulfides. Three amino acids (cysteine, cystine, and methionine) and two vitamins (biotin and thiamine) are organosulfur compounds. Many cofactors also contain sulfur including glutathione and thioredoxin and iron–sulfur proteins. Disulfides, S–S bonds, confer mechanical strength and insolubility of the protein keratin, found in outer skin, hair, and feathers. Sulfur is one of the core chemical elements needed for biochemical functioning and is an elemental macronutrient for all organisms.

Characteristics

When burned, sulfur melts to a blood-red liquid and emits a blue flame that is best observed in the dark.

Physical properties

Sulfur forms polyatomic molecules with different chemical formulas, the best-known allotrope being octasulfur, cyclo-S8. The point group of cyclo-S8 is D4d and its dipole moment is 0 D.[6] Octasulfur is a soft, bright-yellow solid that is odorless, but impure samples have an odor similar to that of matches.[7] It melts at 115.21 °C (239.38 °F), boils at 444.6 °C (832.3 °F) and sublimes easily.[5] At 95.2 °C (203.4 °F), below its melting temperature, cyclo-octasulfur changes from α-octasulfur to the β-polymorph.[8] The structure of the S8 ring is virtually unchanged by this phase change, which affects the intermolecular interactions. Between its melting and boiling temperatures, octasulfur changes its allotrope again, turning from β-octasulfur to γ-sulfur, again accompanied by a lower density but increased viscosity due to the formation of polymers.[8] At higher temperatures, the viscosity decreases as depolymerization occurs. Molten sulfur assumes a dark red color above 200 °C (392 °F). The density of sulfur is about 2 g·cm−3, depending on the allotrope; all of the stable allotropes are excellent electrical insulators.

Chemical properties

Sulfur burns with a blue flame with formation of sulfur dioxide, which has a suffocating and irritating odor. Sulfur is insoluble in water but soluble in carbon disulfide and, to a lesser extent, in other nonpolar organic solvents, such as benzene and toluene. The first and second ionization energies of sulfur are 999.6 and 2252 kJ·mol−1, respectively. Despite such figures, the +2 oxidation state is rare, with +4 and +6 being more common. The fourth and sixth ionization energies are 4556 and 8495.8 kJ·mol−1, the magnitude of the figures caused by electron transfer between orbitals; these states are only stable with strong oxidants such as fluorine, oxygen, and chlorine. Sulfur reacts with nearly all other elements with the exception of gold, platinum, iridium, nitrogen, tellurium, iodine and the noble gases. Some of those reactions need elevated temperatures.[9]

Allotropes

The structure of the cyclooctasulfur molecule, S8

Sulfur forms over 30 solid allotropes, more than any other element.[10] Besides S8, several other rings are known.[11] 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 with S7 and small amounts of S6.[12] Larger rings have been prepared, including S12 and S18.[13][14]

Amorphous or "plastic" sulfur is produced by rapid cooling of molten sulfur—for example, by pouring it into cold water. X-ray crystallography studies show that the amorphous form may have a helical structure with eight atoms per turn. The long coiled polymeric molecules make the brownish substance elastic, and in bulk this form has the feel of crude rubber. This form is metastable at room temperature and gradually reverts to crystalline molecular allotrope, which is no longer elastic. This process happens within a matter of hours to days, but can be rapidly catalyzed.

Isotopes

Sulfur has 25 known isotopes, four of which are stable: 32S (94.99 ± 0.26%), 33S (0.75 ± 0.02%), 34S (4.25 ± 0.24%), and 36S (0.01 ± 0.01%).[15][16] Other than 35S, with a half-life of 87 days and formed in cosmic ray spallation of 40Ar, the radioactive isotopes of sulfur have half-lives less than 3 hours.

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 carbonate minerals 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 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 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 δ34S values from lakes believed to be dominated by watershed sources of sulfate.

Natural occurrence

Sulfur vat from which railroad cars are loaded, Freeport Sulphur Co., Hoskins Mound, Texas (1943)
Most of the yellow and orange hues of Io are due to elemental sulfur and sulfur compounds deposited by active volcanoes.
A man carrying sulfur blocks from Kawah Ijen, a volcano in East Java, Indonesia, 2009

32S is created inside massive stars, at a depth where the temperature exceeds 2.5×109 K, by the fusion of one nucleus of silicon plus one nucleus of helium.[17] As this is part of the alpha process that produces elements in abundance, sulfur is the 10th most common element in the universe.

Sulfur, usually as sulfide, 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%. It is normally present as troilite (FeS), but there are exceptions, with carbonaceous chondrites containing free sulfur, sulfates and other sulfur compounds.[18] The distinctive colors of Jupiter's volcanic moon Io are attributed to various forms of molten, solid and gaseous sulfur.[19]

Sulfur occurs in fumaroles such as this one in Vulcano, Italy

On Earth, 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. Such deposits are polycrystalline, with the largest documented single crystal measuring 22×16×11 cm.[20] Historically, Sicily was a major source of sulfur in the Industrial Revolution.[21]

Native sulfur is synthesised by anaerobic bacteria acting on sulfate minerals such as gypsum in salt domes.[22][23] Significant deposits in salt domes occur along the coast of the Gulf of Mexico, and in evaporites in eastern Europe and western Asia. Native sulfur may be produced by geological processes alone. Fossil-based sulfur deposits from salt domes were until recently the basis for commercial production in the United States, Russia, Turkmenistan, and Ukraine.[24] Currently, commercial production is still carried out in the Osiek mine in Poland. Such sources are now of secondary commercial importance, and most are no longer worked.

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). On Earth, just as upon Jupiter's moon Io, elemental sulfur occurs naturally in volcanic emissions, including emissions from hydrothermal vents.

Compounds

Common oxidation states of sulfur range from −2 to +6. Sulfur forms stable compounds with all elements except the noble gases.

Sulfur polycations

Sulfur polycations, S82+, S42+ and S162+ are produced when sulfur is reacted with mild oxidising agents in a strongly acidic solution.[25] The colored solutions produced by dissolving sulfur in oleum were first reported as early as 1804 by C.F. Bucholz, but the cause of the color and the structure of the polycations involved was only determined in the late 1960s. S82+ is deep blue, S42+ is yellow and S162+ is red.[8]

Sulfides

Treatment of sulfur with hydrogen gives hydrogen sulfide. When dissolved in water, hydrogen sulfide is mildly acidic:[5]

H2S ⇌ HS− + H+

Hydrogen sulfide gas and the hydrosulfide anion are extremely toxic to mammals, due to their inhibition of the oxygen-carrying capacity of hemoglobin and certain cytochromes in a manner analogous to cyanide and azide (see below, under precautions).

Reduction of elemental sulfur gives polysulfides, which consist of chains of sulfur atoms terminated with S− centers:

2 Na + S8 → Na2S8

This reaction highlights a distinctive property of sulfur: its ability to catenate (bind to itself by formation of chains). Protonation of these polysulfide anions produces the polysulfanes, H2Sx where x = 2, 3, and 4.[26] Ultimately, reduction of sulfur produces sulfide salts:

16 Na + S8 → 8 Na2S

The interconversion of these species is exploited in the sodium-sulfur battery.

The radical anion S3− gives the blue color of the mineral lapis lazuli.

Lapis lazuli owes its blue color to a trisulfur radical anion (S−
3)
Two parallel sulfur chains grown inside a single-wall carbon nanotube (CNT, a). Zig-zag (b) and straight (c) S chains inside double-wall CNTs[27]

Oxides, oxoacids and oxoanions

The principal sulfur oxides are obtained by burning sulfur:

S + O2 → SO2
2 SO2 + O2 → 2 SO3

Multiple sulfur oxides are known; the sulfur-rich oxides include sulfur monoxide, disulfur monoxide, disulfur dioxides, and higher oxides containing peroxo groups.

Sulfur forms sulfur oxoacids, some of which cannot be isolated and are only known through the salts. Sulfur dioxide and sulfites (SO2−
3) are related to the unstable sulfurous acid (H2SO3). Sulfur trioxide and sulfates (SO2−
4) are related to sulfuric acid. Sulfuric acid and SO3 combine to give oleum, a solution of pyrosulfuric acid (H2S2O7) in sulfuric acid.

Thiosulfate salts (S
2O2−
3), sometimes referred as "hyposulfites", used in photographic fixing (hypo) and as reducing agents, feature sulfur in two oxidation states. Sodium dithionite (Na
2S
2O
4), contains the more highly reducing dithionite anion (S
2O2−
4).

Halides and oxyhalides

Several sulfur halides are important to modern industry. Sulfur hexafluoride is a dense gas used as an insulator gas in high voltage transformers; it is also a nonreactive and nontoxic propellant for pressurized containers. Sulfur tetrafluoride is a rarely used organic reagent that is highly toxic.[28] Sulfur dichloride and disulfur dichloride are important industrial chemicals. Sulfuryl chloride and chlorosulfuric acid are derivatives of sulfuric acid; thionyl chloride (SOCl2) is a common reagent in organic synthesis.[29]

Pnictides

An important S–N compound is the cage tetrasulfur tetranitride (S4N4). Heating this compound gives polymeric sulfur nitride ((SN)x), which has metallic properties even though it does not contain any metal atoms. Thiocyanates contain the SCN− group. Oxidation of thiocyanate gives thiocyanogen, (SCN)2 with the connectivity NCS-SCN. Phosphorus sulfides are numerous, the most important commercially being the cages P4S10 and P4S3.[30][31]

Metal sulfides

The principal ores of copper, zinc, nickel, cobalt, molybdenum, and other metals are sulfides. These materials tend to be dark-colored semiconductors that are not readily attacked by water or even many acids. They are formed, both geochemically and in the laboratory, by the reaction of hydrogen sulfide with metal salts. The mineral galena (PbS) was the first demonstrated semiconductor and was used as a signal rectifier in the cat's whiskers of early crystal radios. The iron sulfide called pyrite, the so-called "fool's gold", has the formula FeS2.[32] Processing these ores, usually by roasting, is costly and environmentally hazardous. Sulfur corrodes many metals through tarnishing.

Organic compounds

Some of the main classes of sulfur-containing organic compounds include the following:[33]

Compounds with carbon-sulfur multiple bonds are uncommon, an exception being carbon disulfide, a volatile colorless liquid that is structurally similar to carbon dioxide. It is used as a reagent to make the polymer rayon and many organosulfur compounds. Unlike carbon monoxide, carbon monosulfide is stable only as an extremely dilute gas, found between solar systems.[34]

Organosulfur compounds are responsible for some of the unpleasant odors of decaying organic matter. They are widely known as the odorant in domestic natural gas, garlic odor, and skunk spray. Not all organic sulfur compounds smell unpleasant at all concentrations: the sulfur-containing monoterpenoid (grapefruit mercaptan) in small concentrations is the characteristic scent of grapefruit, but has a generic thiol odor at larger concentrations. Sulfur mustard, a potent vesicant, was used in World War I as a disabling agent.[35]

Sulfur-sulfur bonds are a structural component used to stiffen rubber, similar to the disulfide bridges that rigidify proteins (see biological below). In the most common type of industrial "curing" or hardening and strengthening of natural rubber, elemental sulfur is heated with the rubber to the point that chemical reactions form disulfide bridges between isoprene units of the polymer. This process, patented in 1843, made rubber a major industrial product, especially in automobile tires. Because of the heat and sulfur, the process was named vulcanization, after the Roman god of the forge and volcanism.

History

Antiquity

Pharmaceutical container for sulfur from the first half of the 20th century. From the Museo del Objeto del Objeto collection

Being abundantly available in native form, sulfur was known in ancient times and is referred to in the Torah (Genesis). English translations of the Bible commonly referred to burning sulfur as "brimstone", giving rise to the term "fire-and-brimstone" sermons, in which listeners are reminded of the fate of eternal damnation that await the unbelieving and unrepentant. It is from this part of the Bible that Hell is implied to "smell of sulfur" (likely due to its association with volcanic activity). According to the Ebers Papyrus, a sulfur ointment was used in ancient Egypt to treat granular eyelids. Sulfur was used for fumigation in preclassical Greece;[36] this is mentioned in the Odyssey.[37] Pliny the Elder discusses sulfur in book 35 of his Natural History, saying that its best-known source is the island of Melos. He mentions its use for fumigation, medicine, and bleaching cloth.[38]

A natural form of sulfur known as shiliuhuang (石硫黄) was known in China since the 6th century BC and found in Hanzhong.[39] By the 3rd century, the Chinese discovered that sulfur could be extracted from pyrite.[39] Chinese Daoists were interested in sulfur's flammability and its reactivity with certain metals, yet its earliest practical uses were found in traditional Chinese medicine.[39] A Song dynasty military treatise of 1044 AD described different formulas for Chinese black powder, which is a mixture of potassium nitrate (KNO
3), charcoal, and sulfur. It remains an ingredient of black gunpowder.

Indian alchemists, practitioners of "the science of mercury" (sanskrit rasaśāstra, रसशास्त्र), wrote extensively about the use of sulfur in alchemical operations with mercury, from the eighth century AD onwards.[40] In the rasaśāstra tradition, sulfur is called "the smelly" (sanskrit gandhaka, गन्धक).

Various alchemical symbols for sulfur

Early European alchemists gave sulfur a unique alchemical symbol, a triangle at the top of a cross. In traditional skin treatment, elemental sulfur was used (mainly in creams) to alleviate such conditions as scabies, ringworm, psoriasis, eczema, and acne. The mechanism of action is unknown—though elemental sulfur does oxidize slowly to sulfurous acid, which is (through the action of sulfite) a mild reducing and antibacterial agent.[41][42][43]

Modern times

Sicilian kiln used to obtain sulfur from volcanic rock

In 1777, Antoine Lavoisier helped convince the scientific community that sulfur was an element, not a compound.

Sulfur deposits in Sicily were the dominant source for more than a century. By the late 18th century, about 2,000 tonnes per year of sulfur were imported into Marseilles, France, for the production of sulfuric acid for use in the Leblanc process. In industrializing Britain, with the repeal of tariffs on salt in 1824, demand for sulfur from Sicily surged upward. The increasing British control and exploitation of the mining, refining, and transportation of the sulfur, coupled with the failure of this lucrative export to transform Sicily's backward and impoverished economy, led to the 'Sulfur Crisis' of 1840, when King Ferdinand II gave a monopoly of the sulfur industry to a French firm, violating an earlier 1816 trade agreement with Britain. A peaceful solution was eventually negotiated by France.[44][45]

In 1867, elemental sulfur was discovered in underground deposits in Louisiana and Texas. The highly successful Frasch process was developed to extract this resource.[46]

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 used as a medicinal tonic and laxative.[24] With the advent of the contact process, the majority of sulfur today is used to make sulfuric acid for a wide range of uses, particularly fertilizer.[47]

Spelling and etymology

Sulfur is derived from the Latin word sulpur, which was Hellenized to sulphur. The spelling sulfur appears toward the end of the Classical period. (The true Greek word for sulfur, θεῖον, is the source of the international chemical prefix thio-.) In 12th-century Anglo-French, it was sulfre; in the 14th century the Latin -ph- was restored, for sulphre; and by the 15th century the full Latin spelling was restored, for sulfur, sulphur. The parallel f~ph spellings continued in Britain until the 19th century, when the word was standardized as sulphur.[48] Sulfur was the form chosen in the United States, whereas Canada uses both. The IUPAC adopted the spelling sulfur in 1990, as did the Nomenclature Committee of the Royal Society of Chemistry in 1992, restoring the spelling sulfur to Britain.[49] Oxford Dictionaries note that "in chemistry and other technical uses ... the -f- spelling is now the standard form for this and related words in British as well as US contexts, and is increasingly used in general contexts as well."[50]

Production

Sulfur mining at Ijen, Indonesia

Sulfur may be found by itself and historically was usually obtained in this form; pyrite has also been a source of sulfur.[51] In volcanic regions in Sicily, in ancient times, it was found on the surface of the Earth, and the "Sicilian process" was used: sulfur deposits were piled and stacked in brick kilns built on sloping hillsides, with airspaces between them. Then, some sulfur was pulverized, spread over the stacked ore and ignited, causing the free sulfur to melt down the hills. Eventually the surface-borne deposits played out, and miners excavated veins that ultimately dotted the Sicilian landscape with labyrinthine mines. Mining was unmechanized and labor-intensive, with pickmen freeing the ore from the rock, and mine-boys or carusi carrying baskets of ore to the surface, often through a mile or more of tunnels. Once the ore was at the surface, it was reduced and extracted in smelting ovens. The conditions in Sicilian sulfur mines were horrific, prompting Booker T. Washington to write "I am not prepared just now to say to what extent I believe in a physical hell in the next world, but a sulphur mine in Sicily is about the nearest thing to hell that I expect to see in this life."[52]

Elemental sulfur was once extracted from salt domes where it sometimes occurs in nearly pure form, but this method has been obsolete since the late 20th century. Today's sulfur production is as a side product of other industrial processes such as oil refining; in these processes, sulfur often occurs as undesired or detrimental compounds that are extracted and converted to elemental sulfur. As a mineral, native sulfur under salt domes is thought to be a fossil mineral resource, produced by the action of ancient bacteria on sulfate deposits. It was removed from such salt-dome mines mainly by the Frasch process.[24] In this method, superheated water was pumped into a native sulfur deposit to melt the sulfur, and then compressed air returned the 99.5% pure melted product to the surface. Throughout the 20th century this procedure produced elemental sulfur that required no further purification. Due to a limited number of such sulfur deposits and the high cost of working them, this process for mining sulfur has not been employed in a major way anywhere in the world since 2002.[53][54]

Sulfur recovered from hydrocarbons in Alberta, stockpiled for shipment in North Vancouver, British Columbia

Today, sulfur is produced from petroleum, natural gas, and related fossil resources, from which it is obtained mainly as hydrogen sulfide. Organosulfur compounds, undesirable impurities in petroleum, may be upgraded by subjecting them to hydrodesulfurization, which cleaves the C–S bonds:[53][54]

R-S-R + 2 H2 → 2 RH + H2S

The resulting hydrogen sulfide from this process, and also as it occurs in natural gas, is converted into elemental sulfur by the Claus process. This process entails oxidation of some hydrogen sulfide to sulfur dioxide and then the comproportionation of the two:[53][54]

3 O2 + 2 H2S → 2 SO2 + 2 H2O
SO2 + 2 H2S → 3 S + 2 H2O
Production and price (US market) of elemental sulfur

Owing to the high sulfur content of the Athabasca Oil Sands, stockpiles of elemental sulfur from this process now exist throughout Alberta, Canada.[55] Another way of storing sulfur is as a binder for concrete, the resulting product having many desirable properties (see sulfur concrete).[56] Sulfur is still mined from surface deposits in poorer nations with volcanoes, such as Indonesia, and worker conditions have not improved much since Booker T. Washington's days.[57]

The world production of sulfur in 2011 amounted to 69 million tonnes (Mt), with more than 15 countries contributing more than 1 Mt each. Countries producing more than 5 Mt are China (9.6), US (8.8), Canada (7.1) and Russia (7.1).[58] Production has been slowly increasing from 1900 to 2010; the price was unstable in the 1980s and around 2010.[59]

Applications

Sulfuric acid

Elemental sulfur is used mainly as a precursor to other chemicals. Approximately 85% (1989) is converted to sulfuric acid (H2SO4):

2 S + 3 O2 + 2 H2O → 2 H2SO4
Sulfuric acid production in 2000

In 2010, the United States produced more sulfuric acid than any other inorganic industrial chemical.[59] 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.[24]

Other important sulfur chemistry

Sulfur reacts directly with methane to give carbon disulfide, used to manufacture cellophane and rayon.[24] One of the direct uses of sulfur is in vulcanization of rubber, where polysulfide chains crosslink organic polymers. Large quantities of sulfites are used to bleach paper and to preserve dried fruit. Many surfactants and detergents (e.g. sodium lauryl sulfate) are sulfate derivatives. Calcium sulfate, gypsum, (CaSO4·2H2O) is mined on the scale of 100 million tonnes each year for use in Portland cement and fertilizers.

When silver-based photography was widespread, sodium and ammonium thiosulfate were widely used as "fixing agents." Sulfur is a component of gunpowder ("black powder").

Fertilizer

Sulfur is increasingly used as a component of fertilizers. The most important form of sulfur for fertilizer is the mineral calcium sulfate. Elemental sulfur is hydrophobic (not soluble in water) and cannot be used directly by plants. Over time, soil bacteria can convert it to soluble derivatives, which can then be used by plants. Sulfur improves the efficiency of other essential plant nutrients, particularly nitrogen and phosphorus.[60] Biologically produced sulfur particles are naturally hydrophilic due to a biopolymer coating and are easier to disperse over the land in a spray of diluted slurry, resulting in a faster update.

The botanical requirement for sulfur equals or exceeds the requirement for phosphorus. It is an essential nutrient for plant growth, root nodule formation of legumes, and immunity and defense systems. Sulfur deficiency has become widespread in many countries in Europe.[61][62][63] Because atmospheric inputs of sulfur continue to decrease, the deficit in the sulfur input/output is likely to increase unless sulfur fertilizers are used.

Fine chemicals

A molecular model of the pesticide malathion

Organosulfur compounds are used in pharmaceuticals, dyestuffs, and agrochemicals. Many drugs contain sulfur, early examples being antibacterial sulfonamides, known as sulfa drugs. Sulfur is a part of many bacterial defense molecules. Most β-lactam antibiotics, including the penicillins, cephalosporins and monolactams contain sulfur.[33]

Magnesium sulfate, known as Epsom salts when in hydrated crystal form, can be used as a laxative, a bath additive, an exfoliant, magnesium supplement for plants, or (when in dehydrated form) as a desiccant.

Fungicide and pesticide

Sulfur candle originally sold for home fumigation

Elemental 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 also be used 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 miscible.[64][65] It has similar applications and is used as a fungicide against mildew and other mold-related problems with plants and soil.

Elemental sulfur powder is used as an "organic" (i.e. "green") insecticide (actually an acaricide) against ticks and mites. A common method of application is dusting the clothing or limbs with sulfur powder.

A diluted solution of lime sulfur (made by combining calcium hydroxide with elemental sulfur in water) is used as a dip for pets to destroy ringworm (fungus), mange, and other dermatoses and parasites.

Sulfur candles of almost pure sulfur were burned to fumigate structures and wine barrels, but are now considered too toxic for residences.

Bactericide in winemaking and food preservation

Small amounts of sulfur dioxide gas addition (or equivalent potassium metabisulfite addition) to fermented wine to produce traces of sulfurous acid (produced when SO2 reacts with water) and its sulfite salts in the mixture, has been called "the most powerful tool in winemaking."[66] After the yeast-fermentation stage in winemaking, sulfites absorb oxygen and inhibit aerobic bacterial growth that otherwise would turn ethanol into acetic acid, souring the wine. Without this preservative step, indefinite refrigeration of the product before consumption is usually required. Similar methods go back into antiquity but modern historical mentions of the practice go to the fifteenth century. The practice is used by large industrial wine producers and small organic wine producers alike.

Sulfur dioxide and various sulfites have been used for their antioxidant antibacterial preservative properties in many other parts of the food industry. The practice has declined since reports of an allergy-like reaction of some persons to sulfites in foods.

Pharmaceuticals

Octasulfur
Clinical data
AHFS/Drugs.com Multum Consumer Information
Routes of
administration		 Topical, rarely oral
ATC code
Legal status
Legal status
Identifiers
CAS Number
PubChem CID
ChemSpider
ChEBI
ECHA InfoCard 100.028.839
Chemical and physical data
Formula S8
Molar mass 256.52 g/mol
3D model (JSmol)

Sulfur (specifically octasulfur, S8) is used in pharmaceutical skin preparations for the treatment of acne and other conditions. It acts as a keratolytic agent and also kills bacteria, fungi, scabies mites and other parasites.[67] Precipitated sulfur and colloidal sulfur are used, in form of lotions, creams, powders, soaps, and bath additives, for the treatment of acne vulgaris, acne rosacea, and seborrhoeic dermatitis.[68]

Common adverse effects include irritation of the skin at the application site, such as dryness, stinging, itching and peeling.[69]

Mechanism of action

Sulfur is converted to hydrogen sulfide (H2S) through reduction, partly by bacteria. H2S kills bacteria (possibly including Propionibacterium acnes which plays a role in acne,[70]) fungi, and parasites such as scabies mites.[67]

Furniture

Sulfur can be used to create decorative inlays in wooden furniture. After a design has been cut into the wood, molten sulfur is poured in and then scraped away so it is flush. Sulfur inlays were particularly popular in the late 18th and early 19th centuries, notably amongst Pennsylvania German cabinetmakers. The practice soon died out, as less toxic and flammable substances were substituted. However, some modern craftsmen have occasionally revived the technique in the creation of replica pieces.[71][72]

Biological role

Protein and organic cofactors

Sulfur is an essential component of all living cells. It is the seventh or eighth most abundant element in the human body by weight, about equal in abundance to potassium, and slightly greater than sodium and chlorine. A 70 kg (150 lb) human body contains about 140 grams of sulfur.

In plants and animals, the amino acids cysteine and methionine contain most of the sulfur, and the element is present in all polypeptides, proteins, and enzymes that contain these amino acids. In humans, methionine is an essential amino acid that must be ingested. However, save for the vitamins biotin and thiamine, cysteine and all sulfur-containing compounds in the human body can be synthesized from methionine. The enzyme sulfite oxidase is needed for the metabolism of methionine and cysteine in humans and animals.

Disulfide bonds (S-S bonds) between cysteine residues in peptide chains are very important in protein assembly and structure. These covalent bonds between peptide chains confer extra toughness and rigidity.[73] For example, the high strength of feathers and hair is due in part to the high content of S-S bonds with cysteine and sulfur. Eggs are high in sulfur to nourish feather formation in chicks, and the characteristic odor of rotting eggs is due to hydrogen sulfide. The high disulfide bond content of hair and feathers contributes to their indigestibility and to their characteristic disagreeable odor when burned.

Homocysteine and taurine are other sulfur-containing acids that are similar in structure, but not coded by DNA, and are not part of the primary structure of proteins. 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.[73] Two of the 13 classical vitamins, biotin and thiamine, contain sulfur, with the latter being named for its sulfur content.

In intracellular chemistry, sulfur operates as a carrier of reducing hydrogen and its electrons for cellular repair of oxidation. Reduced glutathione, a sulfur-containing tripeptide, is a reducing agent through its sulfhydryl (-SH) moiety derived from cysteine. The thioredoxins, a class of small proteins essential to all known life, use neighboring pairs of reduced cysteines to work as general protein reducing agents, with similar effect.

Methanogenesis, the route to most of the world's methane, is a multistep biochemical transformation of carbon dioxide. This conversion requires several organosulfur cofactors. These include coenzyme M, CH3SCH2CH2SO3−, the immediate precursor to methane.[74]

Metalloproteins and inorganic cofactors

Inorganic sulfur forms a part of iron–sulfur clusters as well as many copper, nickel, and iron proteins. Most pervasive are the ferrodoxins, which serve as electron shuttles in cells. In bacteria, the important nitrogenase enzymes contains an Fe–Mo–S cluster and is a catalyst that performs the important function of nitrogen fixation, converting atmospheric nitrogen to ammonia that can be used by microorganisms and plants to make proteins, DNA, RNA, alkaloids, and the other organic nitrogen compounds necessary for life.[75]

Sulfur metabolism and the sulfur cycle

The sulfur cycle was the first of the biogeochemical cycles to be discovered. In the 1880s, while studying Beggiatoa (a bacterium living in a sulfur rich environment), Sergei Winogradsky found that it oxidized hydrogen sulfide (H2S) as an energy source, forming intracellular sulfur droplets. Winogradsky referred to this form of metabolism as inorgoxidation (oxidation of inorganic compounds). He continued to study it together with Selman Waksman until the 1950s.

Sulfur oxidizers can use as energy sources reduced sulfur compounds, including hydrogen sulfide, elemental sulfur, sulfite, thiosulfate, and various polythionates (e.g., tetrathionate).[76] They depend on enzymes such as sulfur oxygenase and sulfite oxidase to oxidize sulfur to sulfate. Some lithotrophs can even use the energy contained in sulfur compounds to produce sugars, a process known as chemosynthesis. Some bacteria and archaea use hydrogen sulfide in place of water as the electron donor in chemosynthesis, a process similar to photosynthesis that produces sugars and utilizes oxygen as the electron acceptor. The photosynthetic green sulfur bacteria and purple sulfur bacteria and some lithotrophs use elemental oxygen to carry out such oxidization of hydrogen sulfide to produce elemental sulfur (S0), oxidation state = 0. Primitive bacteria that live around deep ocean volcanic vents oxidize hydrogen sulfide in this way with oxygen; the giant tube worm is an example of a large organism that uses hydrogen sulfide (via bacteria) as food to be oxidized.

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

Sulfur is absorbed by plants roots from soil as sulfate and transported as a phosphate ester. Sulfate is reduced to sulfide via sulfite before it is incorporated into cysteine and other organosulfur compounds.[77]

SO42− → SO32− → H2S → cysteine → methionine

Precautions

NFPA 704
fire diamond
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g., diesel fuel Health code 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g., sodium chloride Reactivity code 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g., calcium Special hazards (white): no codeNFPA 704 four-colored diamond
2
0
1
Fire diamond hazard sign for elemental sulfur[78]
Effect of acid rain on a forest, Jizera Mountains, Czech Republic

Elemental sulfur is non-toxic, as are most of the soluble sulfate salts, such as Epsom salts. Soluble sulfate salts are poorly absorbed and laxative. When injected parenterally, they are freely filtered by the kidneys and eliminated with very little toxicity in multi-gram amounts.

When sulfur burns in air, it produces sulfur dioxide. In water, this gas produces sulfurous acid and sulfites; sulfites are antioxidants that inhibit growth of aerobic bacteria and a useful food additive in small amounts. At high concentrations these acids harm the lungs, eyes or other tissues. In organisms without lungs such as insects or plants, sulfite in high concentration prevents respiration.

Sulfur trioxide (made by catalysis from sulfur dioxide) and sulfuric acid are similarly highly acidic and corrosive in the presence of water. Sulfuric acid is a strong dehydrating agent that can strip available water molecules and water components from sugar and organic tissue.[79]

The burning of coal and/or petroleum by industry and power plants generates sulfur dioxide (SO2) that reacts with atmospheric water and oxygen to produce sulfuric acid (H2SO4) and sulfurous acid (H2SO3). These acids are components of acid rain, lowering 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 that fuel producers extract sulfur from fossil fuels to prevent acid rain formation. This extracted and refined sulfur represents a large portion of sulfur production. In coal-fired power plants, flue gases are sometimes purified. More modern power plants that use synthesis gas extract the sulfur before they burn the gas.

Hydrogen sulfide is as toxic as hydrogen cyanide, and kills by the same mechanism (inhibition of the respiratory enzyme cytochrome oxidase),[80] though hydrogen sulfide is less likely to cause surprise poisonings from small inhaled amounts because of its disagreeable odor. Hydrogen sulfide quickly deadens the sense of smell and a victim may breathe increasing quantities without noticing the increase until severe symptoms cause death. Dissolved sulfide and hydrosulfide salts are toxic by the same mechanism.

See also

References

  1. ↑ Meija, J.; et al. (2016). "Atomic weights of the elements 2013 (IUPAC Technical Report)". Pure Appl. Chem. 88 (3): 265–91. doi:10.1515/pac-2015-0305.
  2. ↑ Lide, D. R., ed. (2005). "Magnetic susceptibility of the elements and inorganic compounds". CRC Handbook of Chemistry and Physics (PDF) (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  3. ↑ Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN 0-8493-0464-4.
  4. ↑ "Sulfur History". Georgiagulfsulfur.com. Retrieved 2008-09-12.
  5. 1 2 3 Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd ed.), Oxford:Butterworth-Heinemann. ISBN 0-7506-3365-4.
  6. ↑ Rettig, S. J.; Trotter, J. (15 December 1987). "Refinement of the structure of orthorhombic sulfur, α-S8". Acta Crystallographica Section C. 43 (12): 2260–2262. doi:10.1107/S0108270187088152.
  7. ↑ A strong odor called "smell of sulfur" actually is given off by several sulfur compounds, such as hydrogen sulfide and organosulfur compounds.
  8. 1 2 3 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 645–665. ISBN 0-08-037941-9.
  9. ↑ Egon Wiberg; Nils Wiberg (2001). Inorganic Chemistry. Academic Press. pp. 513–. ISBN 978-0-12-352651-9.
  10. ↑ Steudel, Ralf; Eckert, Bodo (2003). "Solid Sulfur Allotropes Sulfur Allotropes". Topics in Current Chemistry. Topics in Current Chemistry. 230: 1–80. ISBN 978-3-540-40191-9. doi:10.1007/b12110.
  11. ↑ Steudel, R. (1982). "Homocyclic Sulfur Molecules". Topics in Current Chemistry. Topics in Current Chemistry. 102: 149–176. ISBN 978-3-540-11345-4. doi:10.1007/3-540-11345-2_10.
  12. ↑ Tebbe, Fred N.; Wasserman, E.; Peet, William G.; Vatvars, Arturs; Hayman, Alan C. (1982). "Composition of Elemental Sulfur in Solution: Equilibrium of S
    6    , S7, and S8 at Ambient Temperatures". Journal of the American Chemical Society. 104 (18): 4971–4972. doi:10.1021/ja00382a050.
  13. ↑ Meyer, Beat (1964). "Solid Allotropes of Sulfur". Chemical Reviews. 64 (4): 429–451. doi:10.1021/cr60230a004.
  14. ↑ Meyer, Beat (1976). "Elemental sulfur". Chemical Reviews. 76 (3): 367–388. doi:10.1021/cr60301a003.
  15. ↑ Sulfur. Commission on Isotopic Abundances and Atomic Weights
  16. ↑ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 1.14. ISBN 1439855110.
  17. ↑ Cameron, A. G. W. (1957). "Stellar Evolution, Nuclear Astrophysics, and Nucleogenesis" (PDF). CRL-41.
  18. ↑ Mason, B. (1962). Meteorites. New York: John Wiley & Sons. p. 160. ISBN 0-908678-84-3.
  19. ↑ Lopes, Rosaly M. C.; Williams, David A. (2005). "Io after Galileo". Reports on Progress in Physics. 68 (2): 303–340. Bibcode:2005RPPh...68..303L. doi:10.1088/0034-4885/68/2/R02.
  20. ↑ Rickwood, P. C. (1981). "The largest crystals" (PDF). American Mineralogist. 66: 885–907.
  21. ↑ Kutney, Gerald (2007). Sulfur: history, technology, applications & industry. Toronto: ChemTec Publications. p. 43. ISBN 978-1-895198-37-9. OCLC 79256100.
  22. ↑ Klein, Cornelis and Cornelius S. Hurlbut, Jr., Manual of Mineralogy, Wiley, 1985, 20th ed., p. 265-6 ISBN 0-471-80580-7
  23. ↑ Sulphur on Mindat.org
  24. 1 2 3 4 5 Nehb, Wolfgang; Vydra, Karel (2006). "Sulfur". Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH Verlag. ISBN 3-527-30673-0. doi:10.1002/14356007.a25_507.pub2.
  25. ↑ Shriver, Atkins. Inorganic Chemistry, Fifth Edition. W. H. Freeman and Company, New York, 2010; pp 416
  26. ↑ Handbook of Preparative Inorganic Chemistry, 2nd ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 421.
  27. ↑ Fujimori, Toshihiko; Morelos-Gómez, Aarón; Zhu, Zhen; Muramatsu, Hiroyuki; Futamura, Ryusuke; Urita, Koki; Terrones, Mauricio; Hayashi, Takuya; Endo, Morinobu; Young Hong, Sang; Chul Choi, Young; Tománek, David; Kaneko, Katsumi (2013). "Conducting linear chains of sulphur inside carbon nanotubes". Nature Communications. 4: 2162. Bibcode:2013NatCo...4E2162F. PMC 3717502 Freely accessible. PMID 23851903. doi:10.1038/ncomms3162.
  28. ↑ Hasek, W. R. (1961). "1,1,1-Trifluoroheptane". Org. Synth. 41: 104. doi:10.1002/0471264180.os041.28.
  29. ↑ Rutenberg, M. W.; Horning, E. C. (1950). "1-Methyl-3-ethyloxindole". Org. Synth. 30: 62. doi:10.15227/orgsyn.030.0062.
  30. ↑ Heal, H. G. (1980). The Inorganic Heterocyclic Chemistry of Sulfur, Nitrogen, and Phosphorus. London: Academic Press. ISBN 0-12-335680-6.
  31. ↑ Chivers, T. (2004). A Guide To Chalcogen-Nitrogen Chemistry. Singapore: World Scientific. ISBN 981-256-095-5.
  32. ↑ Vaughan, D. J.; Craig, J. R. "Mineral Chemistry of Metal Sulfides" Cambridge University Press, Cambridge (1978) ISBN 0-521-21489-0
  33. 1 2 Cremlyn R. J.; "An Introduction to Organosulfur Chemistry" John Wiley and Sons: Chichester (1996). ISBN 0-471-95512-4.
  34. ↑ Wilson, R. W.; Penzias, A. A.; Wannier, P. G.; Linke, R. A. (15 March 1976). "Isotopic abundances in interstellar carbon monosulfide". Astrophysical Journal. 204: L135–L137. Bibcode:1976ApJ...204L.135W. doi:10.1086/182072.
  35. ↑ Banoub, Joseph (2011). Detection of Biological Agents for the Prevention of Bioterrorism. Dordrecht: Springer. p. 183. ISBN 978-90-481-9815-3. OCLC 697506461.
  36. ↑ Rapp, George Robert (4 February 2009). Archaeomineralogy. p. 242. ISBN 978-3-540-78593-4.
  37. ↑ Odyssey, book 22, lines 480–495. www.perseus.tufts.edu. Retrieved on 16 August 2012.
  38. ↑ Pliny the Elder on science and technology, John F. Healy, Oxford University Press, 1999, ISBN 0-19-814687-6, pp. 247–249.
  39. 1 2 3 Zhang, Yunming (1986). "The History of Science Society: Ancient Chinese Sulfur Manufacturing Processes". Isis. 77 (3): 487. doi:10.1086/354207.
  40. ↑ White, David Gordon (1996). The Alchemical Body — Siddha Traditions in Medieval India. Chicago: University of Chicago Press. pp. passim. ISBN 978-0-226-89499-7.
  41. ↑ Lin, A. N.; Reimer, R. J.; Carter, D. M. (1988). "Sulfur revisited". Journal of the American Academy of Dermatology. 18 (3): 553–558. PMID 2450900. doi:10.1016/S0190-9622(88)70079-1.
  42. ↑ Maibach, H. I.; Surber, C.; Orkin, M. (1990). "Sulfur revisited". Journal of the American Academy of Dermatology. 23 (1): 154–156. PMID 2365870. doi:10.1016/S0190-9622(08)81225-X.
  43. ↑ Gupta, A. K.; Nicol, K. (2004). "The use of sulfur in dermatology". Journal of drugs in dermatology : JDD. 3 (4): 427–31. PMID 15303787.
  44. ↑ Riall, Lucy (1998). Sicily and the Unification of Italy: Liberal Policy and Local Power, 1859–1866. Oxford University Press. ISBN 9780191542619. Retrieved 7 February 2013.
  45. ↑ Thomson, D. W. (April 1995). "Prelude to the Sulphur War of 1840: The Neapolitan Perspective". European History Quarterly. 25 (2): 163–180. doi:10.1177/026569149502500201.
  46. ↑ Botsch, Walter (2001). "Chemiker, Techniker, Unternehmer: Zum 150. Geburtstag von Hermann Frasch". Chemie in unserer Zeit (in German). 35 (5): 324–331. doi:10.1002/1521-3781(200110)35:5<324::AID-CIUZ324>3.0.CO;2-9.
  47. ↑ Kogel, Jessica (2006). Industrial minerals & rocks: commodities, markets, and uses (7th ed.). Colorado: Littleton. p. 935. ISBN 978-0-87335-233-8. OCLC 62805047.
  48. ↑ "sulphur". Oxford English Dictionary (3rd ed.). Oxford University Press. September 2005. (Subscription or UK public library membership required.)
  49. ↑ McNaught, Alan (1991). "Journal style update". The Analyst. 116 (11): 1094. Bibcode:1991Ana...116.1094M. doi:10.1039/AN9911601094.
  50. ↑ "sulphur – definition of sulphur in English". Oxford Dictionaries. Retrieved 2016-11-19.
  51. ↑ Riegel, Emil; Kent, James (2007). Kent and Riegel's handbook of industrial chemistry and biotechnology. 1. New York: Springer. p. 1171. ISBN 978-0-387-27842-1. OCLC 74650396.
  52. ↑ Washington, Booker T. (1912). The Man Farthest Down: A Record of Observation and Study in Europe. Doubleday, Page. p. 214.
  53. 1 2 3 Eow, John S. (2002). "Recovery of sulfur from sour acid gas: A review of the technology". Environmental Progress. 21 (3): 143–162. doi:10.1002/ep.670210312.
  54. 1 2 3 Schreiner, Bernhard (2008). "Der Claus-Prozess. Reich an Jahren und bedeutender denn je". Chemie in unserer Zeit. 42 (6): 378–392. doi:10.1002/ciuz.200800461.
  55. ↑ Hyndman, A. W.; Liu, J. K.; Denney, D. W. (1982). "Sulfur Recovery from Oil Sands". Sulfur: New Sources and Uses. ACS Symposium Series. 183. pp. 69–82. ISBN 0-8412-0713-5. doi:10.1021/bk-1982-0183.ch005.
  56. ↑ Mohamed, Abdel-Mohsen; El-Gamal, Maisa (2010). Sulfur concrete for the construction industry: a sustainable development approach. Fort Lauderdale: J. Ross Publishing. p. 109. ISBN 978-1-60427-005-1. OCLC 531718953.
  57. ↑ McElvaney, Kevin. "The Men Who Mine Volcanos". theatlantic.com. The Atlantic. Retrieved 26 February 2015.
  58. ↑ Apodaca, Lori E. (2012) Sulfur. Mineral Commodity Summaries. USGS
  59. 1 2 Apodaca, Lori E. "Mineral Yearbook 2010: Sulfur" (PDF). United States Geological Survey.
  60. ↑ Sulfur as a fertilizer. Sulphurinstitute.org. Retrieved on 16 August 2012.
  61. ↑ Zhao, F.; Hawkesford, M. J.; McGrath, S. P. (1999). "Sulphur Assimilation and Effects on Yield and Quality of Wheat". Journal of Cereal Science. 30 (1): 1–17. doi:10.1006/jcrs.1998.0241.
  62. ↑ Blake-Kalff, M. M. A. (2000). "Diagnosing sulfur deficiency in field-grown oilseed rape (Brassica napus L.) and wheat ( Triticum aestivum L.)". Plant and Soil. 225 (1/2): 95–107. doi:10.1023/A:1026503812267.
  63. ↑ Ceccotti, S. P. (1996). "Plant nutrient sulphur-a review of nutrient balance, environmental impact and fertilizers". Fertilizer Research. 43 (1–3): 117–125. doi:10.1007/BF00747690.
  64. ↑ Mohamed, Abdel-Mohsen Onsy; El Gamal, M. M (13 July 2010). Sulfur Concrete for the Construction Industry: A Sustainable Development Approach. pp. 104–105. ISBN 978-1-60427-005-1.
  65. ↑ Every, Richard L.; et al. (20 August 1968). "Method for Preparation of Wettable Sulfur" (PDF). Retrieved 20 May 2010.
  66. ↑ Spencer, Benjamin Sulfur in wine demystified. intowine.com. Retrieved 26 October 2011.
  67. 1 2 Hagers Handbuch der Pharmazeutischen Praxis (in German). 6B (4th ed.). Berlin–Heidelberg–New York: Springer. 1978. pp. 672–9. ISBN 3-540-07738-3.
  68. ↑ Arzneibuch-Kommentar. Wissenschaftliche Erläuterungen zum Europäischen Arzneibuch und zum Deutschen Arzneibuch [Pharmacopoeia Commentary. Scientific annotations to the European Pharmacopoeia and the German Pharmacopoeia] (in German) (23rd ed.). Stuttgart: Wissenschaftliche Verlagsgesellschaft. 2004. Monographie Schwefel zum äußerlichen Gebrauch [Monograph Sulfur for external use]. ISBN 978-3-8047-2575-1.
  69. ↑ Multum Consumer Information: Sulfur topical.
  70. ↑ FDA Professional Drug Information: Perrigo Sodium Sulfacetamide and Sulfur.
  71. ↑ The Worst Way To Inlay, Popular Science, January 1, 2005.
  72. ↑ Mass, Jennifer L; Anderson, Mark J (2003). "Pennsylvania German sulfur-inlaid furniture: characterization, reproduction, and ageing phenomena of the inlays". Measurement Science and Technology. 14 (9): 1598. doi:10.1088/0957-0233/14/9/311.
  73. 1 2 Nelson, D. L.; Cox, M. M. (2000). Lehninger, Principles of Biochemistry (3rd ed.). New York: Worth Publishing. ISBN 1-57259-153-6.
  74. ↑ Thauer, R. K. (1998). "Biochemistry of methanogenesis: a tribute to Marjory Stephenson:1998 Marjory Stephenson Prize Lecture". Microbiology. 144 (9): 2377–2406. PMID 9782487. doi:10.1099/00221287-144-9-2377.
  75. ↑ Lippard, S. J.; Berg, J. M. (1994). Principles of Bioinorganic Chemistry. University Science Books. ISBN 0-935702-73-3.
  76. ↑ Pronk JT; Meulenberg R; Hazeu W; Bos P; Kuenen JG (1990). "Oxidation of reduced inorganic sulphur compounds by acidophilic thiobacilli" (PDF). FEMS Microbiology Letters. 75 (2–3): 293–306. doi:10.1111/j.1574-6968.1990.tb04103.x.
  77. ↑ Heldt, Hans-Walter (1996). Pflanzenbiochemie. Heidelberg: Spektrum Akademischer Verlag. pp. 321–333. ISBN 3-8274-0103-8.
  78. ↑ Technical data for Sulfur. periodictable.com
  79. ↑ "EiC March 2007 – Feature – Exhibition chemistry: the dehydration of source". www.rsc.org. Retrieved 2016-04-30.
  80. ↑ Gresham et al, Medscape: Hydrogen sulfide toxicity

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.