Chemistry:Carbon tetrafluoride

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Carbon tetrafluoride
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Carbon-tetrafluoride-3D-balls-B.png
Carbon Tetrafluoride.png
Names
IUPAC names
Tetrafluoromethane
Carbon tetrafluoride
Other names
Carbon tetrafluoride, Perfluoromethane, Tetrafluorocarbon, Freon 14, Halon 14, Arcton 0, CFC 14, PFC 14, R 14, UN 1982
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
EC Number
  • 200-896-5
RTECS number
  • FG4920000
UNII
Properties
CF4
Molar mass 88.0043 g/mol
Appearance Colorless gas
Odor odorless
Density 3.72 g/L, gas (15 °C)
Melting point −183.6 °C (−298.5 °F; 89.5 K)
Boiling point −127.8 °C (−198.0 °F; 145.3 K)
0.005%V at 20 °C
0.0038%V at 25 °C
Solubility soluble in benzene, chloroform
Vapor pressure 3.65 MPa at 15 °C
106.5 kPa at −127 °C
5.15 atm-cu m/mole
1.0004823[1]
Viscosity 17.32 μPa·s[2]
Structure
Tetragonal
Tetrahedral
0 D
Hazards
Safety data sheet ICSC 0575
NFPA 704 (fire diamond)
Flash point Non-flammable
Related compounds
Other anions
 Tetrachloromethane
Tetrabromomethane
Tetraiodomethane
Other cations
 Silicon tetrafluoride
Germanium tetrafluoride
Tin tetrafluoride
Lead tetrafluoride
Related fluoromethanes
 Fluoromethane
Difluoromethane
Fluoroform
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Tetrafluoromethane, also known as carbon tetrafluoride or R-14, is the simplest perfluorocarbon (CF4). As its IUPAC name indicates, tetrafluoromethane is the perfluorinated counterpart to the hydrocarbon methane. It can also be classified as a haloalkane or halomethane. Tetrafluoromethane is a useful refrigerant but also a potent greenhouse gas.[3] It has a very high bond strength due to the nature of the carbon–fluorine bond.

Bonding

Because of the multiple carbon–fluorine bonds, and the high electronegativity of fluorine, the carbon in tetrafluoromethane has a significant positive partial charge which strengthens and shortens the four carbon–fluorine bonds by providing additional ionic character. Carbon–fluorine bonds are the strongest single bonds in organic chemistry.[4] Additionally, they strengthen as more carbon–fluorine bonds are added to the same carbon. In the one carbon organofluorine compounds represented by molecules of fluoromethane, difluoromethane, trifluoromethane, and tetrafluoromethane, the carbon–fluorine bonds are strongest in tetrafluoromethane.[5] This effect is due to the increased coulombic attractions between the fluorine atoms and the carbon because the carbon has a positive partial charge of 0.76.[5]

Preparation

Tetrafluoromethane is the product when any carbon compound, including carbon itself, is burned in an atmosphere of fluorine. With hydrocarbons, hydrogen fluoride is a coproduct. It was first reported in 1926.[6] It can also be prepared by the fluorination of carbon dioxide, carbon monoxide or phosgene with sulfur tetrafluoride. Commercially it is manufactured by the reaction of hydrogen fluoride with dichlorodifluoromethane or chlorotrifluoromethane; it is also produced during the electrolysis of metal fluorides MF, MF2 using a carbon electrode.

Although it can be made from a myriad of precursors and fluorine, elemental fluorine is expensive and difficult to handle. Consequently, CF4 is prepared on an industrial scale using hydrogen fluoride:[3]

CCl2F2 + 2 HF → CF4 + 2 HCl

Laboratory synthesis

Tetrafluoromethane and silicon tetrafluoride can be prepared in the laboratory by the reaction of silicon carbide with fluorine.

SiC + 4 F2 → CF4 + SiF4

Reactions

Tetrafluoromethane, like other fluorocarbons, is very stable due to the strength of its carbon–fluorine bonds. The bonds in tetrafluoromethane have a bonding energy of 515 kJ⋅mol−1. As a result, it is inert to acids and hydroxides. However, it reacts explosively with alkali metals. Thermal decomposition or combustion of CF4 produces toxic gases (carbonyl fluoride and carbon monoxide) and in the presence of water will also yield hydrogen fluoride.

It is very slightly soluble in water (about 20 mg⋅L−1), but miscible with organic solvents.

Uses

Tetrafluoromethane is sometimes used as a low temperature refrigerant (R-14). It is used in electronics microfabrication alone or in combination with oxygen as a plasma etchant for silicon, silicon dioxide, and silicon nitride.[7] It also has uses in neutron detectors.[8]

Environmental effects

Mauna Loa tetrafluoromethane (CF4) timeseries.
PFC-14 measured by the Advanced Global Atmospheric Gases Experiment (AGAGE) in the lower atmosphere (troposphere) at stations around the world. Abundances are given as pollution free monthly mean mole fractions in parts-per-trillion.
Atmospheric concentration of CF4 (PFC-14) vs. similar man-made gases (right graph). Note the log scale.

Tetrafluoromethane is a potent greenhouse gas that contributes to the greenhouse effect. It is very stable, has an atmospheric lifetime of 50,000 years, and a high greenhouse warming potential 6,500 times that of CO2.[9]

Tetrafluoromethane is the most abundant perfluorocarbon in the atmosphere, where it is designated as PFC-14. Its atmospheric concentration is growing.[10] As of 2019, the man-made gases CFC-11 and CFC-12 continue to contribute a stronger radiative forcing than PFC-14.[11]

Although structurally similar to chlorofluorocarbons (CFCs), tetrafluoromethane does not deplete the ozone layer[12] because the carbon–fluorine bond is much stronger than that between carbon and chlorine.[13]

Main industrial emissions of tetrafluoromethane besides hexafluoroethane are produced during production of aluminium using Hall-Héroult process. CF4 also is produced as product of the breakdown of more complex compounds such as halocarbons.[14]

Health risks

Due to its density, tetrafluoromethane can displace air, creating an asphyxiation hazard in inadequately ventilated areas. Otherwise, it is normally harmless due to its stability.

See also

References

  1. ↑ Abjean, R.; A. Bideau-Mehu; Y. Guern (15 July 1990). "Refractive index of carbon tetrafluoride (CF4) in the 300-140 nm wavelength range". Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 292 (3): 593–594. doi:10.1016/0168-9002(90)90178-9. Bibcode: 1990NIMPA.292..593A. 
  2. ↑ Kestin, J.; Ro, S.T.; Wakeham, W.A. (1971). "Reference values of the viscosity of twelve gases at 25°C". Transactions of the Faraday Society 67: 2308–2313. doi:10.1039/TF9716702308. 
  3. ↑ 3.0 3.1 Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2002). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a11_349. 
  4. ↑ O'Hagan D (February 2008). "Understanding organofluorine chemistry and in cations. An introduction to the C–F bond". Chemical Society Reviews 37 (2): 308–19. doi:10.1039/b711844a. PMID 18197347. 
  5. ↑ 5.0 5.1 Lemal, D.M. (2004). "Perspective on Fluorocarbon Chemistry". J. Org. Chem. 69 (1): 1–11. doi:10.1021/jo0302556. PMID 14703372. 
  6. ↑ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8. 
  7. ↑ K. Williams, K. Gupta, M. Wasilik. Etch Rates for Micromachining Processing – Part II J. Microelectromech. Syst., vol. 12, pp. 761–777, December 2003.
  8. ↑ Moon, Myung-Kook; Nam, Uk-Won; Lee, Chang-Hee; Em, V.T.; Choi, Young-Hyun; Cheon, Jong-Kyu; Kong, Kyung-Nam (2005). "Low efficiency 2-dimensional position-sensitive neutron detector for beam profile measurement". Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 538 (1–3): 592–596. doi:10.1016/j.nima.2004.09.020. Bibcode: 2005NIMPA.538..592M. 
  9. ↑ Artaxo, Paulo; Berntsen, Terje; Betts, Richard; Fahey, David W.; Haywood, James; Lean, Judith; Lowe, David C.; Myhre, Gunnar et al. (February 2018). "Changes in Atmospheric Constituents and in Radiative Forcing". International Panel on Climate Change. p. 212. https://www.ipcc.ch/site/assets/uploads/2018/02/ar4-wg1-chapter2-1.pdf. 
  10. ↑ "Climate change indicators - Atmospheric concentration of greenhouse gases - Figure 4". United States Environmental Protection Agency. 27 June 2016. https://www.epa.gov/climate-indicators/climate-change-indicators-atmospheric-concentrations-greenhouse-gases. 
  11. ↑ Butler J. and Montzka S. (2020). "The NOAA Annual Greenhouse Gas Index (AGGI)". NOAA Global Monitoring Laboratory/Earth System Research Laboratories. https://www.esrl.noaa.gov/gmd/aggi/aggi.html. 
  12. ↑ Cicerone, Ralph J. (1979-10-05). "Atmospheric Carbon Tetrafluoride: A Nearly Inert Gas" (in en). Science 206 (4414): 59–61. doi:10.1126/science.206.4414.59. ISSN 0036-8075. PMID 17812452. Bibcode: 1979Sci...206...59C. https://escholarship.org/content/qt5n81h9fs/qt5n81h9fs.pdf?t=obqs5d. 
  13. ↑ "Bond Energies". https://www2.chemistry.msu.edu/faculty/reusch/OrgPage/bndenrgy.htm. 
  14. ↑ Jubb, Aaron M.; McGillen, Max R.; Portmann, Robert W.; Daniel, John S.; Burkholder, James B. (2015). "An atmospheric photochemical source of the persistent greenhouse gas CF4". Geophysical Research Letters 42 (21): 9505–9511. doi:10.1002/2015GL066193. ISSN 0094-8276. Bibcode: 2015GeoRL..42.9505J. https://zenodo.org/record/1229070. 

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