Alkylbenzene sulfonate

Class of chemical compounds

The general structure of Sodium dodecylbenzenesulfonates, prominent examples of alkylbenzene sulphonates

Alkylbenzene sulfonates are a class of anionic surfactants, consisting of a hydrophilic sulfonate head-group and a hydrophobic alkylbenzene tail-group. Along with sodium laureth sulfate, they are one of the oldest and most widely used synthetic detergents and may be found in numerous personal-care products (soaps, shampoos, toothpaste etc.) and household-care products (laundry detergent, dishwashing liquid, spray cleaner etc.).[1] They were introduced in the 1930s in the form of branched alkylbenzene sulfonates (BAS). However following environmental concerns these were replaced with linear alkylbenzene sulfonates (LAS) during the 1960s.[2] Since then production has increased significantly from about one million tons in 1980, to around 3.5 million tons in 2016, making them most produced anionic surfactant after soaps.[citation needed]

## Branched alkylbenzene sulfonates

[edit]

An example of a branched alkylbenzene sulfonate (BAS)

Extensive foaming Fremont, California \- 1972

Branched alkylbenzene sulfonates (BAS) were introduced in the early 1930s and saw significant growth from the late 1940s onwards,[3] in early literature these synthetic detergents are often abbreviated as syndets. They were prepared by the Friedel–Crafts alkylation of benzene with 'propylene tetramer' (also called tetrapropylene) followed by sulfonation. Propylene tetramer being a broad term for a mixture of compounds formed by the oligomerization of propene, its use gave a mixture of highly branched structures.[4]

Compared to traditional soaps, BAS offered superior tolerance to hard water and better foaming.[5] However, the highly branched tail made it difficult to biodegrade.[6] BAS was widely blamed for the formation of large expanses of stable foam in areas of wastewater discharge such as lakes, rivers and coastal areas (sea foams), as well as foaming problems encountered in sewage treatment[7] and contamination of drinking water.[8] As such, BAS was phased out of most detergent products during the 1960s, being replaced with linear alkylbenzene sulfonates (LAS), which biodegrade much more rapidly. BAS is still important in certain agrochemical and industrial applications, where rapid biodegradability is of reduced importance. For instance, inhibiting asphaltene deposition from crude oil.

## Linear alkylbenzene sulfonates

[edit]

An example of a linear alkylbenzene sulfonate (LAS)

Linear alkylbenzene sulfonates (LAS) are prepared industrially by the sulfonation of linear alkylbenzenes (LABs), which can themselves be prepared in several ways.[2] In the most common route benzene is alkylated by long chain monoalkenes (e.g. dodecene) using hydrogen fluoride as a catalyst.[9] The purified dodecylbenzenes (and related derivatives) are then sulfonated with sulfur trioxide to give the sulfonic acid.[10] The sulfonic acid is subsequently neutralized with sodium hydroxide.[1] The term "linear" refers to the starting alkenes rather than the final product, perfectly linear addition products are not seen, in-line with Markovnikov's rule. Thus, the alkylation of linear alkenes, even 1-alkenes such as 1-dodecene, gives several isomers of phenyldodecane.[11]

## Structure property relationships

[edit]

Under ideal conditions the cleaning power of BAS and LAS is very similar, however LAS performs slightly better in normal use conditions, due to it being less affected by hard water.[12] Within LAS itself the detergency of the various isomers are fairly similar,[13][14] however their physical properties (Krafft point, foaming etc.) are noticeably different.[15][16] In particular the Krafft point of the high 2-phenyl product (i.e. the least branched isomer) remains below 0 °C up to 25% LAS whereas the low 2-phenyl cloud point is ~15 °C.[17] This behavior is often exploited by producers to create either clear or cloudy products.

## Environmental fate

[edit]

The biodegradability of alkylbenzene sulfonates has been well studied,[6][18][19] and is affected by isomerization, in this case, branching. The salt of the linear material has an LD50 of 2.3 mg/liter for fish, about four times more toxic than the branched compound; however the linear compound biodegrades far more quickly, making it the safer choice over time. It is biodegraded rapidly under aerobic conditions with a half-life of approximately 1–3 weeks;[18] oxidative degradation initiates at the alkyl chain.[1] Under anaerobic conditions it degrades very slowly or not at all, causing it to exist in high concentrations in sewage sludge, but this is not thought to be a cause for concern as it will rapidly degrade once returned to an oxygenated environment.

## References

[edit]

1. ^ a b c Kurt Kosswig,"Surfactants" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2005, Weinheim. doi:10.1002/14356007.a25_747
2. ^ a b Kocal, Joseph A; Vora, Bipin V; Imai, Tamotsu (November 2001). "Production of linear alkylbenzenes". Applied Catalysis A: General. 221 (1–2): 295–301. doi:10.1016/S0926-860X(01)00808-0.
3. ^ Dee, Foster; Snell, Cornelia T. (August 1958). "50th ANNIVERSARY FEATURE—Fifty Years of Detergent Progress". Industrial & Engineering Chemistry. 50 (8): 48A–51A. doi:10.1021/ie50584a005.
4. ^ Scheibel, Jeffrey J. (17 December 2015). "The evolution of anionic surfactant technology to meet the requirements of the laundry detergent industry". Journal of Surfactants and Detergents. 7 (4): 319–328. doi:10.1007/s11743-004-0317-7. S2CID 93889318.
5. ^ Hill, J. A. (22 October 2008). "The Chemistry and Application of Detergents". Journal of the Society of Dyers and Colourists. 63 (10): 319–322. doi:10.1111/j.1478-4408.1947.tb02430.x.
6. ^ a b Hashim, M. A.; Kulandai, J.; Hassan, R. S. (24 April 2007). "Biodegradability of branched alkylbenzene sulphonates". Journal of Chemical Technology & Biotechnology. 54 (3): 207–214. doi:10.1002/jctb.280540302.
7. ^ McKinney, Ross E. (1957). "Syndets and Waste Disposal". Sewage and Industrial Wastes. 29 (6): 654–666. JSTOR 25033358.
8. ^ Sawyer, Clair N.; Ryckman, Devere W. (1957). "Anionic Synthetic Detergents and Water Supply Problems". American Water Works Association. 49 (4): 480–490. Bibcode:1957JAWWA..49d.480S. doi:10.1002/j.1551-8833.1957.tb16814.x. JSTOR 41254845.
9. ^ Cahn, AOCS]. Ed.: Arno (2003). 5th World Conference on Detergents: Reinventing the industry - opportunities and challenges ([Elektronische Ressource] ed.). Champaign, Ill.: AOCS Press. ISBN 1-893997-40-5.
10. ^ Roberts, David W. (May 1998). "Sulfonation Technology for Anionic Surfactant Manufacture". Organic Process Research & Development. 2 (3): 194–202. doi:10.1021/op9700439.
11. ^ Bipin V. Vora; Joseph A. Kocal; Paul T. Barger; Robert J. Schmidt; James A. Johnson (2003). "Alkylation". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.0112112508011313.a01.pub2. ISBN 0471238961.
12. ^ Matheson, K. Lee (August 1985). "Detergency performance comparison between LAS and ABS using calcium sulfonate precipitation boundary diagrams". Journal of the American Oil Chemists' Society. 62 (8): 1269–1274. doi:10.1007/BF02541841. S2CID 98677989.
13. ^ Matheson, K. Lee; Matsoim, Ted P. (September 1983). "Effect of carbon chain and phenyl isomer distribution on use properties of linear alkylbenzene sulfonate: A comparison of 'high' and 'low' 2-phenyl LAS homologs". Journal of the American Oil Chemists' Society. 60 (9): 1693–1698. doi:10.1007/BF02662436. S2CID 97659271.
14. ^ Baumgartner, F. N. (June 1954). "Relation of Molecular Structure to Detergency of Some Alkylbenzene Sulfonates". Industrial & Engineering Chemistry. 46 (6): 1349–1352. doi:10.1021/ie50534a061.
15. ^ Drozd, Joseph C.; Gorman, Wilma (March 1988). "Formulating characteristics of high and low 2-phenyl linear alkylbenzene sulfonates in liquid detergents". Journal of the American Oil Chemists' Society. 65 (3): 398–404. doi:10.1007/BF02663085. S2CID 93127857.
16. ^ Sweeney, W. A.; Olson, A. C. (December 1964). "Performance of straight-chain alkylbenzene sulfonates (LAS) in heavy-duty detergents". Journal of the American Oil Chemists' Society. 41 (12): 815–822. doi:10.1007/BF02663964. S2CID 98586085.
17. ^ Farn, Richard J. (2006). Chemistry and technology of surfactants. Oxford: Blackwell Pub. p. 96. ISBN 978-14051-2696-0.
18. ^ a b Jensen, John (February 1999). "Fate and effects of linear alkylbenzene sulphonates (LAS) in the terrestrial environment". Science of the Total Environment. 226 (2–3): 93–111. Bibcode:1999ScTEn.226...93J. doi:10.1016/S0048-9697(98)00395-7. PMID 10085562.
19. ^ Mackay, Donald; Di Guardo, Antonio; Paterson, Sally; Kicsi, Gabriel; Cowan, Christina E.; Kane, David M. (September 1996). "Assessment of chemical fate in the environment using evaluative, regional and local-scale models: Illustrative application to chlorobenzene and linear alkylbenzene sulfonates". Environmental Toxicology and Chemistry. 15 (9): 1638–1648. doi:10.1002/etc.5620150930.

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See also
Receptor/signaling modulators
GABA receptor modulators
GABAA receptor positive modulators
Ionotropic glutamate receptor modulators

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Xenobiotic-sensing receptor modulators

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* Antagonists: Ketoconazole
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See also
Receptor/signaling modulators
*[v]: View this template
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*[GlyR]: Glycine receptor
*[NMDAR]: N-Methyl-D-aspartate receptor
*[GlyT1]: Glycine transporter 1
*[GlyT2]: Glycine transporter 2
*[CAR]: Constitutive androstane receptor
*[PXR]: Pregnane X receptor