Misplaced Pages

Bromotrifluoromethane

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from Halon gas) Organic halide used for fire suppression
Bromotrifluoromethane
Names
Preferred IUPAC name Bromotri(fluoro)methane
Other names
  • Bromotrifluoromethane
  • Trifluorobromomethane
  • Monobromotrifluoromethane
  • Trifluoromethyl bromide
  • Bromofluoroform
  • Carbon monobromide trifluoride
  • Halon 1301
  • BTM
  • Freon 13BI
  • Freon FE 1301
  • R 13B1
  • Halon 1301 BTM
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.000.807 Edit this at Wikidata
EC Number
  • 200-887-6
PubChem CID
RTECS number
  • PA5425000
UNII
UN number 1009
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CBrF3/c2-1(3,4)5Key: RJCQBQGAPKAMLL-UHFFFAOYSA-N
  • InChI=1/CBrF3/c2-1(3,4)5Key: RJCQBQGAPKAMLL-UHFFFAOYAV
SMILES
  • BrC(F)(F)F
Properties
Chemical formula CBrF3
Molar mass 148.910 g·mol
Appearance Colorless gas
Odor Odorless
Density 1.538 g/cm (at −58 °C (−72 °F))
Melting point −167.78 °C (−270.00 °F; 105.37 K)
Boiling point −57.75 °C (−71.95 °F; 215.40 K)
Solubility in water 0.03 g/L (20 °C (68 °F))
log P 1.86
Vapor pressure 1434 kPa (20 °C (68 °F))
Hazards
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
LCLo (lowest published) 834,000 ppm (rat, 15 min)
NIOSH (US health exposure limits):
PEL (Permissible) TWA 1000 ppm (6100 mg/m)
REL (Recommended) TWA 1000 ppm (6100 mg/m)
IDLH (Immediate danger) 40,000 ppm
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Bromotrifluoromethane, commonly referred to by the code numbers Halon 1301, R13B1, Halon 13B1 or BTM, is an organic halide with the chemical formula CBrF3. It is used for gaseous fire suppression as a far less toxic alternative to bromochloromethane.

Table of physical properties

Property Value
Critical temperature (Tc) 66.9 °C (340.08 K)
Critical pressure (pc) 3.956 MPa (39.56 bar)
Critical density (ρc) 5.13 mol.l
Ozone depletion potential (ODP) 10 (CCl3F = 1)
Global warming potential (GWP) 6900 (CO2 = 1)

Synthesis

Bromotrifluoromethane is commercially synthesized in a two-step process from chloroform. Chloroform is fluorinated with hydrogen fluoride.

CHCl3 + 3 HF → CHF3 + 3 HCl

The resulting Fluoroform is then reacted with elemental bromine.

CHF3 + Br2 → CF3Br + HBr

Uses

Warning sign for fire suppression system
Civilian Halon 1301 fire extinguisher, USA, 1980s

Halon 1301 was developed in a joint venture between the U.S. Army and Purdue University in the late 1940's, and became a DuPont product in 1954. It was introduced as an effective gaseous fire suppression fixed systems agent in the 1960s, and was used around valuable materials, such as aircraft, mainframe computers, and telecommunication switching centers, usually in total flooding systems. It was also widely used in the maritime industry to add a third level of protection should the main and emergency fire pumps become inoperable or ineffective. Halon 1301 was never widely used in portables outside marine, military and spacecraft applications, due to its limited range, and invisible discharge. It does not produce the characteristic white cloud like CO2 and is difficult to direct when fighting large fires. Halon 1301 is ideal for armored vehicles and spacecraft, because it produces fewer toxic by-products than does Halon 1211, which is critical for combat or space conditions where a compartment may not be able to be ventilated immediately. Halon 1301 is widely used by the U.S. Military and NASA in a 2-3/4 lb portable extinguisher with a sealed, disposable cylinder for quick recharging. Other agents such as CO2 and FE-36 (HFC-236fa) wet chemical are largely replacing halon 1301 for environmental concerns. Civilian models in 2-3/4, 3, and 4 lb sizes were also made.

It is considered good practice to avoid all unnecessary exposure to Halon 1301, and to limit exposures to concentrations of 7% and below to 15 minutes. Exposure to Halon 1301 in the 5% to 7% range produces little, if any, noticeable effect. At levels between 7% and 10%, mild central nervous system effects such as dizziness and tingling in the extremities have been reported. In practice, the operators of many Halon 1301 total flooding systems evacuate the space on impending agent discharge.

Halon systems are among the most effective and commonly used fire protection systems used on commercial aircraft. Halon 1301 is the primary agent used in commercial aviation engine, cargo compartments, and auxiliary power unit fire zones. Efforts to find a suitable replacement for Halon 1301 have not produced a widely accepted replacement.

Bromotrifluoromethane was also used as a filling of the bubble chamber in the neutrino detector Gargamelle.

Before the dangers of Halon 1301 as an ozone depleter were known, many industrial chillers used it as an efficient refrigerant gas.

H-1301 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.

Chemical reagent

It is a precursor to trifluoromethyltrimethylsilane, a popular trifluoromethylating reagent in organic synthesis.

Alternatives

Halon 1301 hazard sign, with instructions upon gas discharge.

Alternatives for normally occupied areas include (PFC-410 or CEA-410), C3F8 (PFC-218 or CEA-308), HCFC Blend A (NAF S-III), HFC-23 (FE 13), HFC-227ea (FM 200), IG-01 (argon), IG-55 (argonite), HFC-125, or HFC-134a. For normally unoccupied areas, the alternatives include carbon dioxide, powdered Aerosol C, CF3I, HCFC-22, HCFC-124, HFC-125, HFC-134a, gelled halocarbon/dry chemical suspension (PGA), blend of inert gas, high expansion foam systems and powdered aerosol (FS 0140), and IG-541 (Inergen). Perfluorocarbons, i.e., PFCs such as C3F8, have very long atmospheric lifetimes and very high global warming potentials. Hydrochlorofluorocarbons, i.e., HCFCs including HCFC containing NAF S-III, contain chlorine and are stratospheric ozone layer depleters, although less so than Halon 1301. Their selection for usage as Halon replacements should consider those factors, and is restricted in some countries.

See also

References

  1. ^ NIOSH Pocket Guide to Chemical Hazards. "#0634". National Institute for Occupational Safety and Health (NIOSH).
  2. "Trifluorobromomethane". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  3. Dagani, M. J.; Barda, H. J.; Benya, T. J.; Sanders, D. C. "Bromine Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_405. ISBN 978-3527306732.
  4. Brice, T. J.; Pearlson, W. H.; Simons, J. H. (June 1946). "Fluorocarbon Bromides". Journal of the American Chemical Society. 68 (6): 968–969. doi:10.1021/ja01210a017. ISSN 0002-7863.
  5. "Final Report on Fire Extinguishing Agents for the Period September 1, 1947, to June 30, 1950", Contract No. W44-099eng-507, Purdue Research Foundation, Lafayette, Indiana, July 1950.
  6. NFPA 12A Standard on Halon 1301 Fire Extinguishing Systems https://www.nfpa.org/codes-and-standards/1/2/a/12a?l=125
  7. Hodges and McCormick, "Fire Extinguishing Agents for Protection of Occupied Spaces in Military Ground Vehicles," 2010, DTIC ADA517470 https://apps.dtic.mil/sti/citations/ADA517470
  8. NFPA 12A Standard on Halon 1301 Fire Extinguishing Systems, 2004 Edition / Annex D, Hazards to Personnel, section D.2.2
  9. United States Environmental Protection Agency | Guidance for the EPA Halon(R) Emission Reduction Rule | Federal Aviation Administration
  10. Boeing Commercial Aeromagazine | Quarter 04, 2011 | Replacing Halon in Fire Protection Systems: a Progress report
  11. Aerospace Manufacturing and Design | Halon Alternatives for Aircraft Propulsion Systems consortium formed | January 27, 2015
  12. FAA | Task Group on Halon Options
  13. "National Refrigerants MSDS" (PDF). Archived from the original (PDF) on 2011-02-08. Retrieved 2009-07-17.
  14. Ramaiah, Pichika; Krishnamurti, Ramesh; Prakash, G. K. Surya (1995). "1-Trifluoromethyl-1-cyclhexanol". Org. Synth. 72: 232. doi:10.15227/orgsyn.072.0232.
  15. Halon 1301 Replacements Archived 2008-04-19 at the Wayback Machine

External links

Halomethanes
Unsubstituted
Monosubstituted
Disubstituted
Trisubstituted
Tetrasubstituted
* Chiral compound.
Fluorine compounds
Salts and covalent derivatives of the fluoride ion
HF ?HeF2
LiF BeF2 BF
BF3
B2F4
+BO3
CF4
CxFy
+CO3
NF3
FN3
N2F2
NF
N2F4
NF2
?NF5
OF2
O2F2
OF
O3F2
O4F2
?OF4
F2 Ne
NaF MgF2 AlF
AlF3
SiF4 P2F4
PF3
PF5
S2F2
SF2
S2F4
SF3
SF4
S2F10
SF6
+SO4
ClF
ClF3
ClF5
?ArF2
?ArF4
KF CaF
CaF2
ScF3 TiF2
TiF3
TiF4
VF2
VF3
VF4
VF5
CrF2
CrF3
CrF4
CrF5
?CrF6
MnF2
MnF3
MnF4
?MnF5
FeF2
FeF3
FeF4
CoF2
CoF3
CoF4
NiF2
NiF3
NiF4
CuF
CuF2
?CuF3
ZnF2 GaF2
GaF3
GeF2
GeF4
AsF3
AsF5
Se2F2
SeF4
SeF6
+SeO3
BrF
BrF3
BrF5
KrF2
?KrF4
?KrF6
RbF SrF
SrF2
YF3 ZrF2
ZrF3
ZrF4
NbF4
NbF5
MoF4
MoF5
MoF6
TcF4
TcF
5

TcF6
RuF3
RuF
4

RuF5
RuF6
RhF3
RhF4
RhF5
RhF6
PdF2
Pd
PdF4
?PdF6
Ag2F
AgF
AgF2
AgF3
CdF2 InF
InF3
SnF2
SnF4
SbF3
SbF5
TeF4
?Te2F10
TeF6
+TeO3
IF
IF3
IF5
IF7
+IO3
XeF2
XeF4
XeF6
?XeF8
CsF BaF2   LuF3 HfF4 TaF5 WF4
WF5
WF6
ReF4
ReF5
ReF6
ReF7
OsF4
OsF5
OsF6
?OsF
7

?OsF
8
IrF2
IrF3
IrF4
IrF5
IrF6
PtF2
Pt
PtF4
PtF5
PtF6
AuF
AuF3
Au2F10
?AuF6
AuF5•F2
Hg2F2
HgF2
?HgF4
TlF
TlF3
PbF2
PbF4
BiF3
BiF5
?PoF2
PoF4
PoF6
AtF
?AtF3
?AtF5
RnF2
?RnF
4

?RnF
6
FrF RaF2   LrF3 Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
LaF3 CeF3
CeF4
PrF3
PrF4
NdF2
NdF3
NdF4
PmF3 SmF2
SmF3
EuF2
EuF3
GdF3 TbF3
TbF4
DyF2
DyF3
DyF4
HoF3 ErF3 TmF2
TmF3
YbF2
YbF3
AcF3 ThF3
ThF4
PaF4
PaF5
UF3
UF4
UF5
UF6
NpF3
NpF4
NpF5
NpF6
PuF3
PuF4
PuF5
PuF6
AmF2
AmF3
AmF4
?AmF6
CmF3
CmF4
 ?CmF6
BkF3
BkF
4
CfF3
CfF4
EsF3
EsF4
?EsF6
Fm Md No
PF−6, AsF−6, SbF−6 compounds
AlF−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6, GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl
Chemical formulas
Categories: