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Alkylbenzene sulfonate

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The general structure ofSodium dodecylbenzenesulfonates,prominent examples of alkylbenzene sulphonates

Alkylbenzene sulfonatesare a class ofanionic surfactants,consisting of ahydrophilicsulfonatehead-group and ahydrophobicalkylbenzene tail-group. Along withsodium laureth sulfate,they are one of the oldest and most widely usedsynthetic detergentsand 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 aftersoaps.[citation needed]

Branched alkylbenzene sulfonates

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An example of a branched alkylbenzene sulfonate (BAS)
Extensive foamingFremont, 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 theFriedel–Crafts alkylationofbenzenewith 'propylene tetramer' (also called tetrapropylene) followed bysulfonation.Propylene tetramer being a broad term for a mixture of compounds formed by theoligomerizationofpropene,its use gave a mixture of highly branched structures.[4]

Compared to traditional soaps, BAS offered superior tolerance tohard waterand better foaming.[5]However, the highly branched tail made it difficult tobiodegrade.[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 rapidbiodegradabilityis of reduced importance. For instance, inhibitingasphaltenedeposition fromcrude oil.

Linear alkylbenzene sulfonates

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An example of a linear alkylbenzene sulfonate (LAS)

Linear alkylbenzene sulfonates (LAS) are prepared industrially by thesulfonationoflinear alkylbenzenes(LABs), which can themselves be prepared in several ways.[2]In the most common routebenzeneis alkylated by long chain monoalkenes (e.g. dodecene) usinghydrogen fluorideas a catalyst.[9]The purifieddodecylbenzenes(and related derivatives) are thensulfonatedwithsulfur trioxideto give thesulfonic acid.[10]The sulfonic acid is subsequently neutralized withsodium hydroxide.[1] The term "linear" refers to the startingalkenesrather than the final product, perfectly linear addition products are not seen, in-line withMarkovnikov's rule.Thus, the alkylation of linear alkenes, even1-alkenessuch as1-dodecene,gives several isomers of phenyldodecane.[11]

Structure property relationships

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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 byhard 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-phenylcloud pointis ~15 °C.[17]This behavior is often exploited by producers to create either clear or cloudy products.

Environmental fate

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The biodegradability of alkylbenzene sulfonates has been well studied,[6][18][19]and is affected byisomerization,in this case, branching. The salt of the linear material has anLD50of 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 ahalf-lifeof 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 insewage sludge,but this is not thought to be a cause for concern as it will rapidly degrade once returned to an oxygenated environment.

References

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  1. ^abcKurt Kosswig, "Surfactants" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2005, Weinheim.doi:10.1002/14356007.a25_747
  2. ^abKocal, 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.S2CID93889318.
  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. ^abHashim, 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.JSTOR25033358.
  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.JSTOR41254845.
  9. ^Cahn, AOCS]. Ed.: Arno (2003).5th World Conference on Detergents: Reinventing the industry - opportunities and challenges([Elektronische Ressource] ed.). Champaign, Ill.: AOCS Press.ISBN1-893997-40-5.
  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.ISBN0471238961.
  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.S2CID98677989.
  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.S2CID97659271.
  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.S2CID93127857.
  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.S2CID98586085.
  17. ^Farn, Richard J. (2006).Chemistry and technology of surfactants.Oxford: Blackwell Pub. p.96.ISBN978-14051-2696-0.
  18. ^abJensen, 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.PMID10085562.
  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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