Chlorotrifluoromethane

Chlorotrifluoromethane
Names
Preferred IUPAC name
Chloro(trifluoro)methane
Other names
Chlorotrifluoromethane
Monochlorotrifluoromethane
Trifluorochloromethane
Trifluoromethyl chloride
Trifluoromonochlorocarbon
Arcton 3
Freon 13
Genetron 13
R-13
CFC 13
UN 1022
Identifiers
CAS Number
  • 75-72-9 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 6152 checkY
ECHA InfoCard 100.000.814 Edit this at Wikidata
EC Number
  • 200-894-4
PubChem CID
  • 6392
RTECS number
  • PA6410000
UNII
  • 7C6U91JNED ☒N
CompTox Dashboard (EPA)
  • DTXSID4052500 Edit this at Wikidata
InChI
  • InChI=1S/CClF3/c2-1(3,4)5 checkY
    Key: AFYPFACVUDMOHA-UHFFFAOYSA-N checkY
  • InChI=1/CClF3/c2-1(3,4)5
    Key: AFYPFACVUDMOHA-UHFFFAOYAV
  • ClC(F)(F)F
Properties
Chemical formula
CClF3
Molar mass 104.46 g/mol
Appearance Colorless gas with sweet odor
Density 1.526 g/cm3
Melting point −181 °C (−293.8 °F; 92.1 K)
Boiling point −81.5 °C (−114.7 °F; 191.7 K)
Solubility in water
0.009% at 25 °C (77 °F)
Vapor pressure 3.263 MPa at 21 °C (70 °F)
Thermal conductivity 0.01217 W m−1 K−1 (300 K)[1]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Ozone depletor and asphyxiant
Flash point Non-flammable
Safety data sheet (SDS) ICSC 0420
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references
Chemical compound

Chlorotrifluoromethane, R-13, CFC-13, or Freon 13, is a non-flammable, non-corrosive, nontoxic chlorofluorocarbon (CFC) and also a mixed halomethane. It is a man-made substance used primarily as a refrigerant. When released into the environment, CFC-13 has a high ozone depletion potential, and long atmospheric lifetime.[2] Only a few other greenhouse gases surpass CFC-13 in global warming potential (GWP).[3]: 2  The IPCC AR5 reported that CFC-13's atmospheric lifetime was 640 years.[4]

Production

CFC-13—like all chlorofluorocarbon compounds—contains atoms of carbon (C), chlorine (Cl), and fluorine (F).[5][6]

It can be prepared by reacting carbon tetrachloride with hydrogen fluoride in the presence of a catalytic amount of antimony pentachloride:

CCl4 + 3HF → CClF3 + 3HCl

This reaction can also produce trichlorofluoromethane (CCl3F), dichlorodifluoromethane (CCl2F2) and tetrafluoromethane (CF4).[7]

Montreal Protocol

Following the unanimous ratification of the 1987 Montreal Protocol—in response to concerns about the role of concentrations of chlorofluorocarbons (CFCs) in ozone layer-depletion in the stratosphere—a process was put into place to gradually phase out and replace CFC-13 and all the other CFCs.[8] Research in the 1980s said that these man-made CFC compound compounds had opened a hole in ozone layer in the upper atmosphere or stratosphere that protects life on earth from UV radiation.[5]

CFC-13's ozone depletion potential (ODP) is high— 1[9] (CCl3F = 1)—it is categorized as a Class I in the IPCC's list of ozone-depleting substances.[9] CFC-13's radiative efficiency is high which results in a high global warming potential (GWPs) of 13 900 GWP-100 yr that is "surpassed by very few other greenhouse gases."[3] It is categorized as a Class I in the list of ozone-depleting Substances.[9]: 2 

Increase in atmospheric abundance of CFC-13 in 2010s

Starting in the 2010s, despite a global ban on the production of CFCs, five of these ozone-damaging emissions were on the rise.[5]

The atmospheric abundance of CFC-13 rose from 3.0 parts per trillion (ppt) in year 2010 to 3.3 ppt in year 2020 based on analysis of air samples gathered from sites around the world.[10] Contrary to the Montreal Protocol, the atmospheric emissions of CFC-13 and four other chlorofluorocarbons (CFCs), increased between 2010 and 2020.[11]

As of 2023, the drivers behind the increase in CFC-13 and CFC-112a emissions were not certain.[11]

Physical properties

The IPCC AR5 reported that CFC-13's Atmospheric lifetime was 640 years.[12]

Property Value
Density (ρ) at -127.8 °C (liquid) 1.603 g⋅cm−3
Density (ρ) at boiling point (gas) 6.94 kg⋅m−3
Density (ρ) at 15 °C (gas) 4.41 g⋅cm−3
Triple point temperature (Tt)
Critical temperature (Tc) 28.8 °C (302 K)
Critical pressure (pc) 3.86 MPa (38.6 bar)
Critical density (ρc) 5.5 mol⋅L−1
Latent heat of vaporization at boiling point 149.85 kJ⋅kg−1
Specific heat capacity at constant pressure (Cp) at -34.4 °C 0.06 kJ⋅mol−1⋅K−1
Specific heat capacity at constant volume (CV) at -34.4 °C 0.051 kJ⋅mol−1⋅K−1
Heat capacity ratio (к) at -34.4 °C 1.168016
Compressibility Factor (Z) at 15 °C 0.9896
Acentric factor (ω) 0.17166
Viscosity (η) at 0 °C (gas) 13.3 mPa⋅s (0.0133 cP)
Viscosity (η) at 25 °C (gas) 14.1 mPa⋅s (0.01440 cP)
Ozone depletion potential (ODP) 1[9](CCl3F = 1)
Global warming potential (GWP) 14,000[4] (CO2 = 1)
Atmospheric lifetime 640 years[4]

See also

References

  1. ^ Touloukian, Y.S., Liley, P.E., and Saxena, S.C. Thermophysical properties of matter - the TPRC data series. Volume 3. Thermal conductivity - nonmetallic liquids and gases. Data book. 1970.
  2. ^ Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2002). "Fluorine Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a11_349. ISBN 978-3527306732.
  3. ^ a b Vollmer, Martin; Young, Dickon; Trudinger, Cathy; Mühle, Jens; Henne, Stephan; Rigby, Matt; Park, Sunyoung; Li, Shihong; Guillevic, Myriam; Mitrevski, Blagoj; Harth, Christina; Miller, Benjamin; Reimann, Stefan; Yao, Bo; Steele, L.; Wyss, Simon; Lunder, Chris; Arduini, Jgor; McCulloch, Archie; Simmonds, Peter (October 10, 2017). "Atmospheric histories and emissions of chlorofluorocarbons CFC-13 (CClF3), CFC-114 (C2Cl2F4), and CFC-115 (C2ClF5)". Atmospheric Chemistry and Physics Discussions. 2017 (39). doi:10.5194/acp-2017-935. hdl:1721.1/116270.
  4. ^ a b c "Chapter 8". AR5 Climate Change 2013: The Physical Science Basis. p. 731.
  5. ^ a b c Ashworth, James (April 3, 2023). "Mystery emissions of ozone-damaging gases are fuelling climate change". Natural History Museum. Retrieved April 3, 2023.
  6. ^ Elkins, James.W. (2013). "Halocarbons and other Atmospheric Trace Species". NOAA Global Monitoring Laboratory (Press release). Retrieved April 3, 2023 – via US Department of Commerce and NOAA.
  7. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 304. ISBN 978-0-08-037941-8.
  8. ^ Allen, Kate (April 3, 2023). "Remember ozone-destroying CFCs? They're on the rise again. And the source is a mystery". The Star. Retrieved April 3, 2023.
  9. ^ a b c d "Class I Ozone-depleting Substances". Science - Ozone Layer Protection. US EPA. 2007. Archived from the original on 2010-12-10. Retrieved 2010-12-16.
  10. ^ "AGAGE Data and Figures". Massachusetts Institute of Technology. Retrieved 2021-02-11.
  11. ^ a b Western, Luke M.; Vollmer, Martin K.; Krummel, Paul B.; Adcock, Karina E.; Fraser, Paul J.; Harth, Christina M.; Langenfelds, Ray L.; Montzka, Stephen A.; Mühle, Jens; O’Doherty, Simon; Oram, David E.; Reimann, Stefan; Rigby, Matt; Vimont, Isaac; Weiss, Ray F.; Young, Dickon; Laube, Johannes C. (April 3, 2023). "Global increase of ozone-depleting chlorofluorocarbons from 2010 to 2020". Nature Geoscience. 16 (4): 309–313. Bibcode:2023NatGe..16..309W. doi:10.1038/s41561-023-01147-w. hdl:1983/9e103fef-e61c-49c7-a1a3-902540ec1d7c. ISSN 1752-0908. S2CID 257941769. Retrieved April 3, 2023.
  12. ^ Forster, Piers; Ramaswamy, Venkatachalam; Artaxo, Paulo; Berntsen, Terje; Betts, Richard; Fahey, David W; Haywood, James; Lean, Judith; Lowe, David C; Raga, Graciela; Schulz, Michael; Dorland, Robert Van; Bodeker, G; Etheridge, D; Foukal, P; Fraser, P; Geller, M; Joos, F; Keeling, C D; Keeling, R; Kinne, S; Lassey, K; Oram, D; O’Shaughnessy, K; Ramankutty, N; Reid, G; Rind, D; Rosenlof, K; Sausen, R; Schwarzkopf, D; Solanki, S K; Stenchikov, G; Stuber, N; Takemura, T; Textor, C; Wang, R; Weiss, R; Whorf, T; Nakajima, Teruyuki; Ramanathan, Veerabhadran; Ramaswamy, V; Artaxo, P; Berntsen, T; Betts, R; Fahey, D W; Haywood, J; Lean, J; Lowe, D C; Myhre, G; Nganga, J; Prinn, R; Raga, G; Schulz, M; Dorland, R Van. "Changes in Atmospheric Constituents and in Radiative Forcing". International Panel of Climate Change (IPCC). AR4 Climate Change 2007: The Physical Science Basis.

External links

  • MSDS at mathesontrigas.com
  • International Chemical Safety Card 0420
  • Entry at Air Liquide gas encyclopaedia Archived 2011-07-07 at the Wayback Machine
  • The crystal structure of chlorotrifluoromethane, CF3Cl; neutron powder diffraction and constrained refinement[permanent dead link]
  • Termochemical data table
  • v
  • t
  • e
Unsubstituted
  • CH4
Monosubstituted
  • CH3F
  • CH3Cl
  • CH3Br
  • CH3I
  • CH3At
Disubstituted
  • CH2F2
  • CH2ClF
  • CH2BrF
  • CH2FI
  • CH2Cl2
  • CH2BrCl
  • CH2ClI
  • CH2Br2
  • CH2BrI
  • CH2I2
Trisubstituted
  • CHF3
  • CHClF2
  • CHBrF2
  • CHF2I
  • CHCl2F
  • C*HBrClF
  • C*HClFI
  • CHBr2F
  • C*HBrFI
  • CHFI2
  • CHCl3
  • CHBrCl2
  • CHCl2I
  • CHBr2Cl
  • C*HBrClI
  • CHClI2
  • CHBr3
  • CHBr2I
  • CHBrI2
  • CHI3
Tetrasubstituted
  • CF4
  • CClF3
  • CBrF3
  • CF3I
  • CCl2F2
  • CBrClF2
  • CClF2I
  • CBr2F2
  • CBrF2I
  • CF2I2
  • CCl3F
  • CBrCl2F
  • CCl2FI
  • CBr2ClF
  • C*BrClFI
  • CClFI2
  • CBr3F
  • CBr2FI
  • CBrFI2
  • CFI3
  • CCl4
  • CBrCl3
  • CCl3I
  • CBr2Cl2
  • CBrCl2I
  • CCl2I2
  • CBr3Cl
  • CBr2ClI
  • CBrClI2
  • CClI3
  • CBr4
  • CBr3I
  • CBr2I2
  • CBrI3
  • CI4
* Chiral compound.
  • v
  • t
  • e
HF He
LiF BeF2 BF
BF3
B2F4
CF4
CxFy
NF3
N2F4
OF
OF2
O2F2
O2F
F Ne
NaF MgF2 AlF
AlF3
SiF4 P2F4
PF3
PF5
S2F2
SF2
S2F4
SF4
S2F10
SF6
ClF
ClF3
ClF5
HArF
ArF2
KF CaF2 ScF3 TiF3
TiF4
VF2
VF3
VF4
VF5
CrF2
CrF3
CrF4
CrF5
CrF6
MnF2
MnF3
MnF4
FeF2
FeF3
CoF2
CoF3
NiF2
NiF3
CuF
CuF2
ZnF2 GaF3 GeF4 AsF3
AsF5
SeF4
SeF6
BrF
BrF3
BrF5
KrF2
KrF4
KrF6
RbF SrF2 YF3 ZrF4 NbF4
NbF5
MoF4
MoF5
MoF6
TcF6 RuF3
RuF4
RuF5
RuF6
RhF3
RhF5
RhF6
PdF2
Pd[PdF6]
PdF4
PdF6
AgF
AgF2
AgF3
Ag2F
CdF2 InF3 SnF2
SnF4
SbF3
SbF5
TeF4
TeF6
IF
IF3
IF5
IF7
XeF2
XeF4
XeF6
XeF8
CsF BaF2 * LuF3 HfF4 TaF5 WF4
WF6
ReF6
ReF7
OsF4
OsF5
OsF6
OsF
7

OsF8
IrF3
IrF5
IrF6
PtF2
Pt[PtF6]
PtF4
PtF5
PtF6
AuF
AuF3
Au2F10
AuF5·F2
HgF2
Hg2F2
HgF4
TlF
TlF3
PbF2
PbF4
BiF3
BiF5
PoF4
PoF6
At RnF2
RnF6
Fr RaF2 ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
* LaF3 CeF3
CeF4
PrF3
PrF4
NdF3 PmF3 SmF2
SmF3
EuF2
EuF3
GdF3 TbF3
TbF4
DyF3 HoF3 ErF3 TmF2
TmF3
YbF2
YbF3
** AcF3 ThF4 PaF4
PaF5
UF3
UF4
UF5
UF6
NpF3
NpF4
NpF5
NpF6
PuF3
PuF4
PuF5
PuF6
AmF3
AmF4
AmF6
CmF3 Bk Cf Es Fm Md No
PF6, AsF6, SbF6 compounds
  • AgPF6
  • KAsF6
  • LiAsF6
  • NaAsF6
  • HPF6
  • HSbF6
  • NH4PF6
  • KPF6
  • KSbF6
  • LiPF6
  • NaPF6
  • NaSbF6
  • TlPF6
AlF6 compounds
  • Cs2AlF5
  • K3AlF6
  • Na3AlF6
chlorides, bromides, iodides
and pseudohalogenides
SiF62-, GeF62- compounds
  • BaSiF6
  • BaGeF6
  • (NH4)2SiF6
  • Na2[SiF6]
  • K2[SiF6]
Oxyfluorides
  • BrOF3
  • BrO2F
  • BrO3F
  • LaOF
  • ThOF2
  • VOF
    3
  • TcO
    3
    F
  • WOF
    4
  • YOF
  • ClOF3
  • ClO2F3
Organofluorides
  • CBrF3
  • CBr2F2
  • CBr3F
  • CClF3
  • CCl2F2
  • CCl3F
  • CF2O
  • CF3I
  • CHF3
  • CH2F2
  • CH3F
  • C2Cl3F3
  • C2H3F
  • C6H5F
  • C7H5F3
  • C15F33N
  • C3H5F
  • C6H11F
with transition metal,
lanthanide, actinide, ammonium
  • VOF3
  • CrOF4
  • CrF2O2
  • NH4F
  • (NH4)2ZrF6
  • CsXeF7
  • Li2TiF6
  • Li2ZrF6
  • K2TiF6
  • Rb2TiF6
  • Na2TiF6
  • Na2ZrF6
  • K2NbF7
  • K2TaF7
  • K2ZrF6
  • UO2F2
nitric acids
bifluorides
  • KHF2
  • NaHF2
  • NH4HF2
thionyl, phosphoryl,
and iodosyl
  • F2OS
  • F3OP
  • PSF3
  • IOF3
  • IO3F
  • IOF5
  • IO2F
  • IO2F3
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