Chlorinated paraffins

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Structure of 2,3,4,5,6,8-hexachlorodecane, an example of a short-chained chlorinated paraffin (61% Cl by weight)
Structure of 2,5,6,7,8,11,15-heptachloroheptadecane, an example of a medium-chain chlorinated paraffin (52% Cl by weight)

Chlorinated paraffins (CPs) are complex mixtures of polychlorinated n-alkanes. The chlorination degree of CPs can vary between 30 and 70 wt%. CPs are subdivided according to their carbon chain length into short chain CPs (SCCPs, C10–13), medium chain CPs (MCCPs, C14–17) and long chain CPs (LCCPs, C>17). Depending on chain length and chlorine content, CPs are colorless or yellowish liquids or solids.

Production[edit]

Chlorinated paraffins are synthesized by reaction of chlorine gas with unbranched paraffin fractions (<2 % isoparaffins, <100 ppm aromatics) at a temperature of 80–100 °C.[1] The radical substitution may be promoted by UV-light.[2]

CxH(2x+2) + y Cl2 → CxH(2xy+2)Cly + y HCl

When the desired degree of chlorination is achieved, residues of hydrochloric acid and chlorine are blown off with nitrogen. Epoxidized vegetable oil, glycidyl ether or organophosphorous compounds may be added to the final product for improved stability at high temperatures.[3][4]

Commercial products have been classified as substances of unknown or variable composition. CPs are complex mixtures of chlorinated n-alkanes containing thousands of homologues and isomers[5] which are not completely separated by standard analytical methods.[6]

CP´s are produced in Europe, North Amerika, Australia, Brazil, South Afrika and Asia.[7]In China, where most of the world production capacity is located, 600.000 tons of chlorinated paraffins were produced in 2007.[8]

Industrial applications[edit]

Production of CPs for industrial use started in the 1930s.[9] Currently, over 200 CP formulations are in use for a wide range of industrial applications, such as flame retardants and plasticisers, as additives in metal working fluids, in sealants, paints, adhesives, textiles, leather fat and coatings.[10]

Safety[edit]

Short chain CPs are classified as persistent and their physical properties (octanol-water partition coefficient logKOW 4.4–8, depending on the chlorination degree) imply a high potential for bioaccumulation. Furthermore, SCCPs are classified as toxic to aquatic organisms, and carcinogenic to rats and mice. SCCPs (average chain-length of C12, chlorination degree 60 wt%) were categorised in group 2B as possibly carcinogenic to humans from the International Agency for Research on Cancer (IARC).[11] A global ban on SCCPs is being considered under the Stockholm Convention on Persistent Organic Pollutants.

References[edit]

  1. ^ Brooke 2009, pp. 4, 23.
  2. ^ Lassen 2014, p. 50.
  3. ^ Kellersohn 1998.
  4. ^ Brooke 2009, p. 5.
  5. ^ Tomy 1997, pp. 2764-2765.
  6. ^ Lassen 2014, p. 30.
  7. ^ Lassen 2014, pp. 50-51.
  8. ^ De Boer 2010, p. 8.
  9. ^ Kenne 1996.
  10. ^ De Boer 2010, p. 9.
  11. ^ IARC 1990, p. 70.

Sources[edit]

  • De Boer J., El-Sayed Ali T., Fiedler H., Legler J., Muir D. C., Nikiforov V. A., Tomy G. T., Tsunemi, K. (2010). The handbook of environmental chemistry 10: Chlorinated paraffins. Berlin: Springer-Verlag. ISBN 978-3-642-10760-3
  • Brooke, DM; Crookes, MJ; Merckel, MD (2009). Environmental risk assessment: long-chain chlorinated paraffins, Bristol, UK: Environment Agency
  • "Chlorinated paraffins" (PDF). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. 48: 55–72. 1990. ISBN 978-92-832-1248-5. PMID 2197463. 
  • Kellersohn, Thomas (1998). Chlorinated paraffins, in Ullmann’s encyclopedia of industrial chemistry, electronic release, 6th ed. Weinheim: Wiley-VCH
  • Kenne, Kerstin; Ahlborg, Ulf G (1996). Chlorinated paraffins, IPCS, Environmental Health Criteria 181; Geneva: World Health Organization. ISBN 9241571810
  • Lassen, Carsten et al. (2014). Survey of short-chain and medium-chain paraffins, Copenhagen: Danish Ministry of Environment, Environmental Protection Agency
  • Tomy, Gregg T. et al. (1997). Quantifying C10-C13 polychloroalkanes in environmental samples by high-resolution gas chromatography/electron capture negative ion high-resolution mass spectrometry, Analytical Chemistry 69, 2764-2765

Further reading[edit]

External links[edit]