Perfluorooctanesulfonyl fluoride

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Perfluorooctanesulfonyl fluoride
200px
POSF molecule
Names
IUPAC name
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonyl fluoride
Identifiers
307-35-7 YesY
Abbreviations POSF, PFOSF
ChemSpider 9019 N
EC Number 206-200-6
Jmol 3D model Interactive image
PubChem 9388
  • InChI=1S/C8F18O2S/c9-1(10,3(13,14)5(17,18)7(21,22)23)2(11,12)4(15,16)6(19,20)8(24,25)29(26,27)28 N
    Key: BHFJBHMTEDLICO-UHFFFAOYSA-N N
  • InChI=1/C8F18O2S/c9-1(10,3(13,14)5(17,18)7(21,22)23)2(11,12)4(15,16)6(19,20)8(24,25)29(26,27)28
    Key: BHFJBHMTEDLICO-UHFFFAOYAY
  • C(C(C(C(C(F)(F)S(=O)(=O)F)(F)F)(F)F)(F)F)(C(C(C(F)(F)F)(F)F)(F)F)(F)F
Properties
C8F18O2S
Molar mass 502.12 g/mol
Boiling point 154 °C (309 °F; 427 K)[1]
Vapor pressure {{{value}}}
Related compounds
Related compounds
 Perfluorooctanesulfonic acid (PFOS), Perfluorooctanesulfonamide (PFOSA), Perfluorooctanoic acid (PFOA), Perfluorobutanesulfonic acid (PFBS)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Perfluorooctanesulfonyl fluoride (POSF) is a synthetic perfluorinated compound with a sulfonyl fluoride functional group. It is used to make perfluorooctanesulfonic acid (PFOS) and PFOS-based compounds. These compounds have a variety of industrial and consumer uses, but POSF-derived substances ultimately degrade to form PFOS.

Because of environmental concerns over PFOS, 3M ceased POSF use in 2002 and global production plummeted. However, Chinese production grew after 3M's phaseout. As of May 2009, POSF and PFOS are listed as persistent organic pollutants (POPs) included in Annex B of the Stockholm Convention.

Production

In 1949, 3M began producing POSF by electrochemical fluorination (ECF).[2] From 1966 to the 1990s, 3M production increased to meet demand for POSF-based compounds.[2] In 1999, 3M reported POSF was its most highly produced fluorochemical.[3] Before 2000, 3M was the largest global producer of POSF (mainly at their Decatur, AL and Antwerp facilities) and global production peaked at ~4500 tonnes per year.[2]

In 1999, the U.S. Environmental Protection Agency began investigating perfluorinated compounds after receiving data on the global distribution and toxicity of PFOS, the key ingredient in Scotchgard.[4] For these reasons, and USEPA pressure,[5] the primary American producer of PFOS, 3M, announced, in May 2000, the phaseout of the production of PFOS, PFOA, and PFOS-related products.[6] 3M stated that they would have made the same decision regardless of USEPA pressure.[7]

Immediately after the 2000–2002 3M phaseout, production plummeted, but dominant and growing production shifted to China.[8] In 2004 Chinese production of PFOS-based compounds was estimated to be <50 tonnes.[8] In 2005 global production was estimated to be between 73–162 tonnes,[9] and by 2006 Chinese production was estimated at >200 tonnes.[8] Total historical global production was estimated at ~120,000 tonnes in 2009.[2]

"[M]ost, if not all" industrially synthesized perfluorooctanesulfonyl derivatives, such as PFOS, have POSF as their precursor.[10]

Synthesis

POSF is synthesized by (ECF) of octanesulfonyl fluoride in anhydrous hydrogen fluoride by the equation:[10]

C8H17SO2F + 17 F− → C8F17SO2F + 17 H+ + 34 e−.

This reaction results in a 25% yield for POSF, less than that for shorter perfluorosulfonyl fluorides.[10] The POSF obtained is impure as it is a mixture of linear and branched isomers, with ∼70% linear.[10] POSF can also be obtained by ECF of the sulfonyl halide octanesulfonyl chloride.[10]

Reactivity

POSF and POSF-based polymers degrade to form PFOS[11] which is not known to degrade by any environmental processes.[5] POSF hydrolysis in water, however, occurs slowly.[10]

POSF reacts with bases such as potassium hydroxide to form PFOS salts:[10]

C8F17SO2F + KOH → C8F17O2SO3−K+.

Upon treatment with sulfuric acid the sulfonic acid PFOS tetrahydrate is obtained.[10]

POSF also reacts with ammonia to form perfluorooctanesulfonamide:[10]

C8F17SO2F + NH3 → C8F17O2SNH2.

Sulfonamides and sulfonamidoethanols synthesized from POSF can in turn react to form a variety of different functional groups for different applications and products.[12]

Uses

Because of multiple carbon–fluorine bonds, POSF-derivatives have chemical properties that are hydrophobic ("water-afraid"), lipophobic ("fat-afraid"), and surface tension lowering (as fluorosurfactants).[3] The main uses of chemical substances derived from POSF have been:[2]

The Stockholm Convention lists a variety of acceptable purposes and specific exemptions for POSF and PFOS (and it salts) including

  • photo-imaging;
  • photo-resist and anti-reflective coatings for semiconductors;
  • etching agent for compound semiconductors and ceramic filters;
  • aviation hydraulic fluids;
  • metal plating (hard metal plating) only in closed-loop systems;
  • certain medical devices (such as ethylene tetrafluoroethylene copolymer (ETFE) layers and radio-opaque ETFE production, in-vitro diagnostic medical devices, and CCD colour filters);
  • fire fighting foam;
  • insect baits for control of leaf-cutting ants from Atta spp. and Acromyrmex spp.;
  • photo masks in the semiconductor and liquid crystal display (LCD) industries;
  • metal plating (hard metal plating);
  • metal plating (decorative plating);
  • electric and electronic parts for some colour printers and colour copy machines;
  • insecticides for control of red imported fire ants and termites;
  • chemically driven oil production;
  • carpets;
  • leather and apparel;
  • textiles and upholstery;
  • paper and packaging;
  • coatings and coating additives; and
  • rubber and plastics.[13]

International status

At the Fourth Conference of Parties, decision SC-4/17 put POSF, along with PFOS, in the Stockholm Convention on Persistent Organic Pollutants (Annex B) in May 2009.[14][15] As such, POSF is not "banned" but has approved uses and exemptions—along with a program (SC-4/19) in Annex B that encourages reduced production.[16][17]

Environmental concern

The POSF degradation product, PFOS, is the dominant perfluorinated compound detected in biomonitoring studies,[18] where concentrations that have been detected are considered sufficient to "alter health parameters".[19][20]

See also

References

  1. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ 2.0 2.1 2.2 2.3 2.4 Lua error in package.lua at line 80: module 'strict' not found.
  3. ↑ 3.0 3.1 (1999) 3M. 1999. The science of organic fluorochemistry. 3M Company, February 5, 1999. (PDF readily accessible via a google search for the article title.)
  4. ↑ Aziz Ullah. "The Fluorochemical Dilemma: What the PFOS/PFOA fuss is all about" Cleaning & Restoration. www.ascr.org, (October, 2006). Accessed October 25, 2008.
  5. ↑ 5.0 5.1 Lua error in package.lua at line 80: module 'strict' not found.
  6. ↑ 3M: "PFOS-PFOA Information: What is 3M Doing?" Accessed October 25, 2008.
  7. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  8. ↑ 8.0 8.1 8.2 Lua error in package.lua at line 80: module 'strict' not found.
  9. ↑ (December 2006). Lua error in package.lua at line 80: module 'strict' not found.
  10. ↑ 10.0 10.1 10.2 10.3 10.4 10.5 10.6 10.7 10.8 Lua error in package.lua at line 80: module 'strict' not found.
  11. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  12. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  13. ↑ "Report of the Conference of the Parties of the Stockholm Convention on Persistent Organic Pollutants on the work of its fourth meeting" (PDF). p. 67.
  14. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  15. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  16. ↑ "Report of the Conference of the Parties of the Stockholm Convention on Persistent Organic Pollutants on the work of its fourth meeting" (PDF). pp. 67–69.
  17. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  18. ↑ Lua error in package.lua at line 80: module 'strict' not found. Supporting Information (PDF).
  19. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  20. ↑ Peden-Adams et al. (June 2008). In PFAA Days II (PDF). p. 28.

External links

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