Trifluoroiodomethane
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Names | |||
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Preferred IUPAC name
Trifluoro(iodo)methane | |||
Other names
Trifluoroiodomethane
Iodotrifluoromethane Monoiodotrifluoromethane Trifluoromethyl iodide Perfluoromethyl iodide Freon 13T1 | |||
Identifiers | |||
3D model (JSmol)
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ChemSpider | |||
ECHA InfoCard | 100.017.286 | ||
EC Number |
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PubChem CID
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RTECS number |
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
Chemical formula
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CF3I | ||
Molar mass | 195.91 g/mol | ||
Appearance | Colorless odorless gas | ||
Density | 2.5485 g/cm3 at -78.5 °C 2.3608 g/cm3 at -32.5 °C | ||
Melting point | −110 °C (−166 °F; 163 K) | ||
Boiling point | −22.5 °C (−8.5 °F; 250.7 K) | ||
Slightly | |||
Vapor pressure | 541 kPa | ||
Hazards | |||
Safety data sheet | See: data page | ||
GHS labelling: | |||
Signal word
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Warning | ||
H341 | |||
P201, P202, P281, P308+P313, P405, P501 | |||
Supplementary data page | |||
Structure and
properties |
Refractive index (n), Dielectric constant (εr), etc. | ||
Thermodynamic
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Phase behaviour solid–liquid–gas | ||
Spectral data
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UV, IR, NMR, MS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
what is ?) | (|||
Infobox references | |||
Trifluoroiodomethane, also referred to as trifluoromethyl iodide is a halomethane with the formula CF3I. It is an experimental alternative to Halon 1301 (CBrF3) in unoccupied areas.[1] It would be used as a gaseous fire suppression flooding agent for in-flight aircraft and electronic equipment fires.
Chemistry[]
It is used in the rhodium-catalyzed α-trifluoromethylation of α,β-unsaturated ketones.[2]
It can be used as a new generation fire extinguishing agent to replace Halon in fire protection systems.[3] The mechanism of extinguishing fires for CF3I is active and primarily based on interruption of the chain reaction in the combustion area of the flame by so-called "negative" catalytic action.[4] It is also used as an eco-friendly insulation gas to replace SF6 in electrical power industry.[5]
In the presence of sunlight or at temperatures above 100 °C it can react with water, forming hazardous by-products such as hydrogen fluoride (HF), hydrogen iodide (HI) and carbonyl fluoride (COF2).
Environmental effects[]
Trifluoroiodomethane contains carbon, fluorine, and iodine atoms. Although iodine is several hundred times more efficient at destroying stratospheric ozone than chlorine, experiments have shown that because the weak C-I bond breaks easily under the influence of water (owing to the electron-attracting fluorine atoms), trifluoroiodomethane has an ozone depleting potential less than one-thousandth that of Halon 1301 (0.008-0.01). Its atmospheric lifetime, at less than 1 month, is less than 1 percent that of Halon 1301, and less even than hydrogen chloride formed from volcanoes.
There is, however, still the problem of the C-F bonds absorbing in the atmospheric window.[6] However, the IPCC has calculated the 100-year global warming potential of trifluoroiodomethane to be 0.4 (i.e., 40% of that of CO2).[7]
Further reading[]
- Iodotrifluoromethane: Toxicity Review (2004)
- Solomon S, Burkholder J.B, Ravishankara A.R & Garcia R.R (1994) Ozone depletion and global warming potentials of CF3I. Journal of Geophysical Research: Atmospheres, 99(D10), 20929-20935.
References[]
- Duan Y. Y.; Shi L.; Sun L. Q.; Zhu M. S.; Han L. Z. (March 2000). "Thermodynamic Properties of Trifluoroiodomethane (CF3I)". International Journal of Thermophysics. 21 (2): 393–404(12). doi:10.1023/A:1006683529436. S2CID 118125837. (dead link 1 April 2019)
- Duan Y. Y.; Shi L.; Zhu M. S.; Han L. Z. (January 1999). "Surface tension of trifluoroiodomethane (CF3I)". Fluid Phase Equilibria. 154 (1): 71–77(7). doi:10.1016/S0378-3812(98)00439-7.
- Duan Y. Y.; Shi L.; Sun L. Q.; Zhu M. S.; Han L. Z. (1997). "Thermal Conductivity of Gaseous Trifluoroiodomethane (CF3I)". J. Chem. Eng. Data. 42 (5): 890–893 (4). doi:10.1021/je9700378. Retrieved 2007-06-02.
- Duan Y. Y.; Shi L.; Zhu M. S.; Han L. Z. (1999). "Critical Parameters and Saturated Density of Trifluoroiodomethane (CF3I)". J. Chem. Eng. Data. 44 (3): 501–504. doi:10.1021/je980251b. Retrieved 2007-06-02.
- Chamber Studies of Photolysis and Hydroxyl Radical Reactions of Trifluoroiodomethane
- ^ Vitali, Juan. "Halon Substitute Protects Aircrews and the Ozone Layer". www.afrlhorizons.com. Archived from the original on 11 July 2007. Retrieved 2017-09-06.
- ^ "Trifluoroiodomethane 171441". Sigma-Aldrich. Retrieved 2017-09-06.
- ^ "Fire extinguishing agents trifluoroiodomethane/CF3I". beijingyuji. Retrieved 2018-09-20.
- ^ "CFI rim seal fire protection for floating roof tanks" (PDF). 2018-09-20.
- ^ "Investigation of the Performance of CF3I Gas as a Possible Substitute for SF6". researchgate.net. Retrieved 2018-09-20.
- ^ Shimanouchi, T. (1972). "Methane, trifluoroiodo-". webbook.nist.gov. 6 (3): 993–1102. Retrieved 2017-09-06.
- ^ Ramfjord, Birgit (2012-03-05). "Listing of GWP Values as per Report IPCC WG1 AR4" (PDF). Swedish Defence Materiel Administration. Archived from the original (PDF) on 13 March 2016. Retrieved 7 September 2017.
External links[]
- Halomethanes
- Fire suppression agents
- Trifluoromethyl compounds
- Organoiodides