Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Uses  





2 History  





3 Safety  





4 References  





5 See also  





6 External links  














1,1,1,2-Tetrafluoroethane: Difference between revisions






العربية
تۆرکجه
Català
Čeština
Deutsch
Español
فارسی
Français
Galego
Bahasa Indonesia
Italiano

Bahasa Melayu
Nederlands

Polski
Português
Română
Русский
Slovenščina
Српски / srpski
Srpskohrvatski / српскохрватски
Suomi
Svenska
Türkçe

 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




Print/export  







In other projects  



Wikimedia Commons
 
















Appearance
   

 





Help
 

From Wikipedia, the free encyclopedia
 


Browse history interactively
 Previous editNext edit 
Content deleted Content added
m namechange on dutch wiki
Erstats (talk | contribs)
53 edits
→‎History: Added reference.
Line 68: Line 68:

| format =

| format =

| doi =

| doi =

| accessdate =2006-01-19 }}</ref> It has insignificant ozone depletion potential ([[ozone layer]]), significant [[global warming]] potential ([[Global warming potential|GWP<sub>100</sub>]] = 1300) and negligible acidification potential ([[acid rain]]). 1,1,1,2-Tetrafluoroethane is slowly converted to [[trifluoroacetic acid]] through a [[Radical (chemistry)|radical]] [[reaction]] in the upper [[atmosphere]] and leads to a detectable amount of several ng/L in [[acid rain]].<ref>{{cite journal| author= von Sydow L, Grimvall AB, Borén HB, Laniewski K, Nielsen AT |title=Natural Background Levels of Trifluoroacetate in Rain and Snow|journal=Enviro Sci Technol |year=2000|pages=3115–3118|volume=34|doi=10.1021/es9913683}}</ref>

| accessdate =2006-01-19 }}</ref> It has insignificant ozone depletion potential ([[ozone layer]]), significant [[global warming]] potential ([[Global warming potential|GWP<sub>100</sub>]] = 1300) and negligible acidification potential ([[acid rain]]). In fact the top climate scientist at NASA, James Hansen, has advanced an alternative view of global warming wherein he argues the of 0.74±0.18°C rise in average global temperatures over the last 100 years has been driven mainly by greenhouse gases ''other'' than carbon dioxide.<ref>http://www.pnas.org/cgi/content/full/97/18/9875</ref> 1,1,1,2-Tetrafluoroethane is slowly converted to [[trifluoroacetic acid]] through a [[Radical (chemistry)|radical]] [[reaction]] in the upper [[atmosphere]] and leads to a detectable amount of several ng/L in [[acid rain]].<ref>{{cite journal| author= von Sydow L, Grimvall AB, Borén HB, Laniewski K, Nielsen AT |title=Natural Background Levels of Trifluoroacetate in Rain and Snow|journal=Enviro Sci Technol |year=2000|pages=3115–3118|volume=34|doi=10.1021/es9913683}}</ref>



==Safety==

==Safety==


Revision as of 06:48, 8 January 2009

1,1,1,2-Tetrafluoroethane, also called simply tetrafluoroethane, R-134a, Genetron 134a, Suva 134aorHFC-134a, is a haloalkane refrigerant with thermodynamic properties similar to R-12 (dichlorodifluoromethane), but without its ozone depletion potential. It has the formula CH2FCF3, and a boiling point of −26.3 °C (−15.34 °F).

Uses

1,1,1,2-Tetrafluoroethane is an inert gas used primarily as a "high-temperature" refrigerant for domestic refrigeration and automobile air conditioners. Other uses include plastic foam blowing, as a cleaning solvent and as a propellant for the delivery of pharmaceuticals (e.g. bronchodilators), gas dusters, and in air driers, for removing the moisture from compressed air. Moisture present in compressed air has a harmful effect on pneumatic systems. Tetrafluoroethane has also been used to cool computers in some overclocking attempts. It is also commonly used as a propellant for airsoft airguns.

Tetrafluoroethane, when compressed as inside gas duster cans, is a clear liquid which boils when exposed to room temperature (as seen here) and can be extracted from common canned air canisters by simply inverting them during use.

Recently, R-134a has been subject to use restrictions due to its theorized contribution to climate change. In the EU, it will be banned as from 2011 in all new cars[1]. SAE (International, an auto engineers association) has proposed HFC-134a to be best replaced by a new fluorochemical refrigerant HFO-1234yf (CF3CF=CH2) in automobile air-conditioning systems[2]. California may prohibit the sale of canned HFC-134a to individuals to avoid non-professional recharge of air conditioners. A ban has been in place in Wisconsin since Oct 1994 under ATCP 136 prohibiting sales of container sizes holding less than 15 lbs of refrigerant.[3]

History

R-134a first appeared in the early 1990s as a replacement for Dichlorodifluoromethane (R-12), which has significant ozone depleting properties.[4] R-134a has been atmospherically modeled for its impact on depleting ozone and as a contributor to global warming. Research suggests that over the past 10 years the concentration of 1,1,1,2-tetrafluoroethane has increased significantly in the Earth's atmosphere, with a recent study revealing a doubling in atmospheric concentration between 2001–2004.[5] It has insignificant ozone depletion potential (ozone layer), significant global warming potential (GWP100 = 1300) and negligible acidification potential (acid rain). In fact the top climate scientist at NASA, James Hansen, has advanced an alternative view of global warming wherein he argues the of 0.74±0.18°C rise in average global temperatures over the last 100 years has been driven mainly by greenhouse gases other than carbon dioxide.[6] 1,1,1,2-Tetrafluoroethane is slowly converted to trifluoroacetic acid through a radical reaction in the upper atmosphere and leads to a detectable amount of several ng/L in acid rain.[7]

Safety

Contact of tetrafluoroethane with flames or hot surfaces in excess of 250 °C (482 °F) may cause vapor decomposition and the emission of toxic gases including hydrogen fluoride and carbonyl halides.[8] Tetrafluoroethane itself has an LC50 (lethal concentration for 50% of subjects) in rats of 1,500 g/m³, making it relatively non-toxic. However, its gaseous form is denser than air, and will displace air in the lungs. This can result in asphyxiation if excessively inhaled.[9][10]

Aerosol cans containing tetrafluoroethane, when inverted, become effective freeze sprays. Under pressure, tetrafluoroethane is compressed into a liquid, which upon vaporization absorbs a significant amount of thermal energy. As a result, it will greatly lower the temperature of any object it contacts as it evaporates. This can result in frostbite when it contacts skin.

References

  • ^ Early Action Measure California: Use ban of canned HFC-134a
  • ^ Franklin J (1993). "The Atmospheric Degradation and Impact of 1,1,1,2-Tetrafluorethane (Hydrofluorocarbon 134a)". Chemosphere. 27: 1565–1601. doi:10.1016/0045-6535(93)90251-Y.
  • ^ "Greenhouse gas monitoring at the Zeppelin station - Annual report 2004 (TA-2110/2005)" (PDF). Norwegian Institute for Air Research. Retrieved 2006-01-19. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  • ^ http://www.pnas.org/cgi/content/full/97/18/9875
  • ^ von Sydow L, Grimvall AB, Borén HB, Laniewski K, Nielsen AT (2000). "Natural Background Levels of Trifluoroacetate in Rain and Snow". Enviro Sci Technol. 34: 3115–3118. doi:10.1021/es9913683.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ Honeywell International (2005). "MSDS # GTRN-0047 For Genetron 134aUV". {{cite journal}}: Cite journal requires |journal= (help); Unknown parameter |month= ignored (help)
  • ^ Alexander D. J, Libretto S. E. (1995). "An overview of the toxicology of HFA-134a (1,1,1,2-tetrafluoroethane)". Hum. Exp. Toxicol. 14: 715–20.
  • ^ G. E. Millward, E. Tschuikow-Roux (1972). "Kinetic analysis of the shock wave decomposition of 1,1,1,2-tetrafluoroethane". The Journal of Physical Chemistry. 76 (3): 292–298. doi:10.1021/j100647a002.
  • See also

    External links


    Retrieved from "https://en.wikipedia.org/w/index.php?title=1,1,1,2-Tetrafluoroethane&oldid=262702240"

    Categories: 
    Organofluorides
    Refrigerants
    Automotive chemicals
    Propellants
    Airsoft
    Hidden categories: 
    CS1 errors: empty unknown parameters
    CS1 maint: multiple names: authors list
    CS1 errors: unsupported parameter
    CS1 errors: missing periodical
    Commons link is locally defined
     



    This page was last edited on 8 January 2009, at 06:48 (UTC).

    This version of the page has been revised. Besides normal editing, the reason for revision may have been that this version contains factual inaccuracies, vandalism, or material not compatible with the Creative Commons Attribution-ShareAlike License.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki