1,1,1,2-TETRAFLUOROETHANE

1,1,1,2-Tetrafluoroethane
Structure
3-D structure
General
Systematic name 1,1,1,2-tetrafluoroethane
Other names Genetron 134a
HFC-134a
R-134a
Freon 134a
Molecular formula C2H2F4
SMILES FC(F)(F)C(F)
Molar mass 102.03 g/mol
Appearance Colorless gas.
CAS number
Properties
Density and phase 0.00425 g/cm³, gas.
Solubility in water Insoluble.
Melting point -103.3°C (169.85 K)
Boiling point -26.08°C (247.07 K)
Structure
Molecular shape Planar.
Dipole moment ? D
Hazards
MSDS External MSDS
Main hazards Asphyxiant.
NFPA 704
Flash point Non-flammable.
R/S statement R: ?
S: , , , .
RTECS number KI8842500
Supplementary data page
Structure and
properties
''n'', εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Related compounds
Other anions ?
Other cations ?
Related refrigerants Difluoromethane
Pentafluoroethane
Related compounds 1,1,2,2,2-pentafluoroethane
2-Chloro-
1,1,1,2-tetrafluoroethane

1,1,1-Trichloroethane
Except where noted otherwise, data are given for
materials in their standard state (at 25°C, 100 kPa)

'1,1,1,2-Tetrafluoroethane', also called simply 'tetrafluoroethane', 'R-134a', 'Genetron 134a', Freon 134a or 'HFC-134a', is a haloalkane refrigerant without an ozone depletion potential and thermodynamic properties similar to R-12 (dichlorodifluoromethane). It has the formula CH2FCF3, and a boiling point of −26.6 °C (−15.9 °F).

Contents
Uses
History
Safety
References
External links

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, that is, 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 power source for airsoft airguns.
Tetrafluoroethane is a clear liquid which boils at 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], and California may prohibit the sale of canned HFC-134a to individuals to avoid non-professional recharge of the air conditioner. [2]

History


R-134a first appeared in the early 1990s as a replacement for Dichlorodifluoromethane (R-12), which has significant ozone depleting properties. [3] 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 atmosphere, with a recent study revealing a doubling in atmospheric concentration between 2001-2004.[4] It has insignificant ozone depletion potential (ozone layer), significant global warming potential (GWP100 = 1300) and negligible acidification potential (acid rain). 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. [5]

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.[6] 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.[7][8]
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 contacting skin.

References


1. European Directive 2006/40/EC relating to emissions from air-conditioning systems in motor vehicles
2. Early Action Measure California: Use ban of canned HFC-134a
3. The Atmospheric Degradation and Impact of 1,1,1,2-Tetrafluorethane (Hydrofluorocarbon 134a), Franklin J, , , Chemosphere, 1993
4. Greenhouse gas monitoring at the Zeppelin station - Annual report 2004 (TA-2110/2005)
5. Natural Background Levels of Trifluoroacetate in Rain and Snow, von Sydow L, Grimvall AB, Borén HB, Laniewski K, Nielsen AT, , , Enviro Sci Technol, 2000
6. MSDS # GTRN-0047 For Genetron® 134aUV, Honeywell International, , , ,
7. An overview of the toxicology of HFA-134a (1,1,1,2-tetrafluoroethane), Alexander D. J, Libretto S. E., , , Hum. Exp. Toxicol., 1995
8. Kinetic analysis of the shock wave decomposition of 1,1,1,2-tetrafluoroethane, G. E. Millward, E. Tschuikow-Roux, , , , 1972

External links





Honeywell Refrigerant Data and MSDSs

MSDS at Oxford University

Concise International Chemical Assessment Document 11 at inchem.org

Quick Change R-134A MSDS

Pressure temperature calculator

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