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Skeletal structure of PFOS, an effective and bioaccumulative fluorosurfactant
Space filling model of PFOS

Fluorosurfactants, or fluorinated surfactants, are synthetic organofluorine chemical compounds that have multiple fluorine atoms. They can be polyfluorinated or fluorocarbon-based (perfluorinated).[1] As surfactants, they are more effective at lowering the surface tension of water than comparable hydrocarbon surfactants. They have a fluorinated "tail" and a hydrophilic "head." Some fluorosurfactants, such as PFOS, are detected in humans and wildlife.

Contents

Physical and chemical properties

Fluorosurfactants can lower the surface tension of water down to a value half of what is attainable by using hydrocarbon surfactants.[2] This ability is due to the lipophobic nature of fluorocarbons, as fluorosurfactants tend to concentrate at the liquid-air interface.[3] They are not as susceptible to the London dispersion force, the basis for lipophilicity, because the electronegativity of fluorine reduces the polarizability of the surfactants' fluorinated molecular surface. Therefore, the attractive interactions resulting from the "fleeting dipoles" are reduced, in comparison to hydrocarbon surfactants. Fluorosurfactants are more stable and fit for harsh conditions than hydrocarbon surfactants because of the stability of the carbon–fluorine bond. Likewise, perfluorinated surfactants persist in the environment for that reason.

Economic role

Fluorosurfactants play a key economic role for companies such as DuPont, 3M, and Gore-Tex because they are used in emulsion polymerization to produce fluoropolymers. Also, fluorosurfactants have two main markets: a $1 billion dollar annual market for inclusion into stain repellents, and a $100 million dollar annual market for inclusion into polishes, paints, and coatings.[4] However, DuPont has had legal liabilities over the fluorosurfactant C8/PFOA due to contamination of a population.

Health and environmental concerns

Some fluorosurfactants have caught the attention of regulatory agencies because of their persistence, toxicity, and widespread occurrence in the blood of general populations[5] and wildlife, such as perfluorooctanesulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorononanoic acid (PFNA). As studies give evidence that longer fluorosurfactants are more bioaccumulative and toxic, some companies are marketing shorter fluorosurfactants.[4] For example, 3M is marketing two fluorosurfactants based upon the 4 carbon perfluorobutanesulfonic acid.[4]

References

  1. ^ Lehmler, HJ (March 2005). "Synthesis of environmentally relevant fluorinated surfactants—a review". Chemosphere 58 (11): 1471–96. doi:10.1016/j.chemosphere.2004.11.078. PMID 15694468. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2587313. 
  2. ^ Salager, Jean-Louis (2002) (PDF). Surfactants-Types and Uses. FIRP Booklet # 300-A. Universidad de los Andes Laboratory of Formulation, Interfaces Rheology, and Processes. pp. 45. http://nanoparticles.org/pdf/Salager-E300A.pdf. Retrieved 7 September 2008. 
  3. ^ "Fluorosurfactant — Structure / Function". Mason Chemical Company. http://www.masonsurfactants.com/Products/Fluorosurfactant.htm. Retrieved 1 November 2008. 
  4. ^ a b c Renner R (January 2006). "The long and the short of perfluorinated replacements". Environ. Sci. Technol. 40 (1): 12–3. doi:10.1021/es062612a. PMID 16433328. http://pubs.acs.org/doi/abs/10.1021/es062612a. 
  5. ^ Calafat AM, Wong LY, Kuklenyik Z, Reidy JA, Needham LL (Nov 2007). "Polyfluoroalkyl chemicals in the U.S. population: data from the National Health and Nutrition Examination Survey (NHANES) 2003-2004 and comparisons with NHANES 1999-2000". Environ Health Perspect. 115 (11): 1596–602. doi:10.1289/ehp.10598. PMID 18007991. 
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