Sulfolane

Sulfolane
	; Carbon, C Hydrogen, H Oxygen, O Sulfur, S
Names
	Preferred IUPAC name 1λ6-Thiolane-1,1-dione
	Other names Sulfolane; Tetrahydrothiophene 1,1-dioxide; Tetramethylene sulfone;
Identifiers
CAS Number	126-33-0 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:74794 ;
ChEMBL	ChEMBL3186899;
ChemSpider	29080 ;
ECHA InfoCard	100.004.349
EC Number	204-783-1;
PubChem CID	31347;
RTECS number	XN0700000;
UNII	Y5L06AH4G5 ;
UN number	3334
CompTox Dashboard (EPA)	DTXSID3027037 ;
	InChI InChI=1S/C4H8O2S/c5-7(6)3-1-2-4-7/h1-4H2 Key: HXJUTPCZVOIRIF-UHFFFAOYSA-N ; InChI=1/C4H8O2S/c5-7(6)3-1-2-4-7/h1-4H2 Key: HXJUTPCZVOIRIF-UHFFFAOYAA;
	SMILES C1CCS(=O)(=O)C1;
Properties
Chemical formula	(CH2)4SO2
Molar mass	120.17 g·mol−1
Appearance	Colorless liquid
Density	1.261 g/cm3, liquid
Melting point	27.5 °C (81.5 °F; 300.6 K)
Boiling point	285 °C (545 °F; 558 K)
Solubility in water	miscible
Viscosity	0.01007 Pa·s at 25 °C
Structure
Dipole moment	4.35 D
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302
Precautionary statements	P264, P270, P301+P312, P330, P501
NFPA 704 (fire diamond)	2 1 0
Flash point	165 °C (329 °F; 438 K)
Autoignition; temperature	528 °C (982 °F; 801 K)
Related compounds
Related compounds	Methylsulfonylmethane; Tetrahydrothiophene; Sulfolene;
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Sulfolane (also tetramethylene sulfone, systematic name: 1λ⁶-thiolane-1,1-dione) is an organosulfur compound, formally a cyclic sulfone, with the formula (C H₂)₄S O₂. It is a colorless liquid commonly used in the chemical industry as a solvent for extractive distillation and chemical reactions. Sulfolane was originally developed by the Shell Oil Company in the 1960s as a solvent to purify butadiene.^[1]^[2] Sulfolane is a polar aprotic solvent, and it is miscible with water.

Properties

Sulfolane is classified as a sulfone, a group of organosulfur compounds containing a sulfonyl functional group. The sulfone group is a sulfur atom doubly bonded to two oxygen atoms and singly bonded to two carbon centers. The sulfur-oxygen double bond is polar, conferring good solubility in water, while the four carbon ring provides non-polar stability. These properties allow it to be miscible in both water and hydrocarbons, resulting in its widespread use as a solvent for purifying hydrocarbon mixtures.

Synthesis

The original method developed by the Shell Oil Company was to first allow butadiene to react with sulfur dioxide via a cheletropic reaction to give sulfolene. This was then hydrogenated using Raney nickel as a catalyst to give sulfolane.^[3]^[4]

Shortly thereafter, it was discovered that both the product yield and the lifetime of the catalyst could be improved by adding hydrogen peroxide and then neutralizing to a pH of roughly 5-8 before hydrogenation. Developments have continued over the years, including in the catalysts used. Recently, it was found that Ni-B/MgO showed superior catalytic activity to that of Raney nickel and other common catalysts that have been used in the hydrogenation of sulfolene.

Other syntheses have also been developed, such as oxidizing tetrahydrothiophene with hydrogen peroxide. This reaction produces tetramethylene sulfoxide, which can then be further oxidized. Because the first oxidation occurs at low temperature and the second at higher temperature, the reaction can be controlled at each stage. This gives greater freedom for the manipulation of the reaction, which can potentially lead to higher yields and purity.

Uses

Sulfolane is widely used as an industrial solvent, especially in the extraction of aromatic hydrocarbons from hydrocarbon mixtures and to purify natural gas.^[3] The first large scale commercial use of sulfolane, the sulfinol process, was first implemented by Shell Oil Company in March 1964 at the Person gas plant near Karnes City, Texas. The sulfinol process purifies natural gas by removing H₂S, CO₂, COS and mercaptans from natural gas with a mixture of alkanolamine and sulfolane.

Shortly after the sulfinol process was implemented, sulfolane was found to be highly effective in separating high purity aromatic compounds from hydrocarbon mixtures using liquid-liquid extraction. This process is widely used in refineries and the petrochemical industry. Because sulfolane is one of the most efficient industrial solvents for purifying aromatics, the process operates at a relatively low solvent-to-feed ratio, making sulfolane relatively cost effective compared to similar-purpose solvents. In addition, it is selective in a range that complements distillation; where sulfolane cannot separate two compounds, distillation easily can and vice versa, keeping sulfolane units useful for a wide range of compounds with minimal additional cost.

Whereas sulfolane is highly stable and can therefore be reused many times, it does eventually degrade into acidic byproducts. A number of measures have been developed to remove these byproducts, allowing the sulfolane to be reused and increase the lifetime of a given supply. Some methods that have been developed to regenerate spent sulfolane include vacuum and steam distillation, back extraction, adsorption, and anion-cation exchange resin columns.

Sulfolane is also added to hydrofluoric acid as a vapor suppressant,^[5] commonly for use in a refinery's alkylation unit. This "modified" hydrofluoric acid is less prone to vaporization if released in its liquid form.

As a pollutant

Groundwater in parts of the city of North Pole, Alaska, has been contaminated with sulfolane due to pollution from a now-closed petroleum refinery.^[6] Due to this contamination, affected residents have been supplied with alternative potable water sources.^[6] Animal studies on the toxicity of sulfolane are ongoing, funded through the US federal government's National Toxicology Program.^[7] No long-term in vivio animal studies have been done, which prevents any firm conclusion as to whether sulfolane is a carcinogen, although in vitro studies have failed to demonstrate any cancerous changes in bacterial or animal cells. In animal studies, high doses of sulfolane have induced negative impacts on the central nervous system, including hyperactivity, convulsions and hypothermia; the impacts of lower doses, especially over the long-term, are still being studied.^[8]

References

^ Young, Eldred E. (Shell International Research) BE Patent 616856, 1962
^ Goodenbour, John W.; Carlson, George J. (Shell International Research) BE Patent 611850, 1962
^ ^a ^b Hillis O. Folkins, "Benzene" in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a03_475
^ Earl Clark, Kirk-Othmer Encyclopedia of Chemical Technology, "Sulfolane and Sulfones", John Wiley & Sons, NY, 1997
^ "Sulfolane Fact Sheet" (PDF). Chevron Phillips Chemical Company.
^ ^a ^b "Human Health and Toxicology - Sulfolane and PFAS". dec.alaska.gov. Retrieved 2020-10-23.
^ "Sulfolane". National Toxicology Program: U.S. Department of Health and Human Services. Retrieved 2020-10-23.
^ "Sulfolane: Research Efforts by the National Toxicology Program" (PDF). Alaska Department of Environmental Conservation. November 2019. Retrieved 2020-10-23.

Ge, Shaohui; Wu, Zhijie; Zhang, Minghui; Li, Wei; Tao, Keyi.Industrial & Engineering Chemistry Research,200645(7), 2229-2234,
Sharipov, A. Kh.Russian Journal of Applied Chemistry2003,76(1), 108-113.
Dunn, C. L.; Freitas, E. R.; Hill, E. S.; Sheeler, J. E. R., Jr. Proc., Ann. Conv. Nat. Gas Processors Assoc. Am.,Tech. Papers1965,44 55-8
Broughton, Donald B.; Asselin, George F. UOP Process Div., Universal Oil Prod. Co., Des Plaines, IL, USA. World Petrol. Congr., Proc., 7th1968, Meeting Date 1967,4 65-73. Publisher: Elsevier Publ. Co. Ltd., Barking, Engl
Lal, Raj Kumar Jagadamba; Bhat, Sodankoor Garadi Thirumaleshwara. (Indian Petrochemicals Corp. Ltd., India). Eur. Pat. Appl. 1989-308019 (1991)
Van der Wiel, A.Nature1960,187 142-3.
Block, E.Reactions of Organosulfur Compounds; Academic: New York, 1978
Belen'kii, L.I.Chemistry of Organosulfur Compounds; Horwood: New York, 1990

External links

[1] Young, Eldred E. (Shell International Research) BE Patent 616856, 1962

[2] Goodenbour, John W.; Carlson, George J. (Shell International Research) BE Patent 611850, 1962

[Ullmann-3] Hillis O. Folkins, "Benzene" in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a03_475

[4] Earl Clark, Kirk-Othmer Encyclopedia of Chemical Technology, "Sulfolane and Sulfones", John Wiley & Sons, NY, 1997

[5] "Sulfolane Fact Sheet" (PDF). Chevron Phillips Chemical Company.

[:0-6] "Human Health and Toxicology - Sulfolane and PFAS". dec.alaska.gov. Retrieved 2020-10-23.

[7] "Sulfolane". National Toxicology Program: U.S. Department of Health and Human Services. Retrieved 2020-10-23.

[8] "Sulfolane: Research Efforts by the National Toxicology Program" (PDF). Alaska Department of Environmental Conservation. November 2019. Retrieved 2020-10-23.

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