Chemistry:Difluoromethane

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Difluoromethane
Difluoromethane-2D-skeletal
Spacefill model of difluoromethane
Names
Preferred IUPAC name
Difluoromethane[1]
Other names
Carbon fluoride hydride

Methylene difluoride
Methylene fluoride

Freon-32
Identifiers
3D model (JSmol)
Abbreviations HFC-32

R-32
FC-32

1730795
ChEBI
ChEMBL
ChemSpider
EC Number
  • 200-839-4
259463
MeSH Difluoromethane
RTECS number
  • PA8537500
UNII
UN number 3252
Properties
CH2F2
Molar mass 52.024 g·mol−1
Appearance Colorless gas
Density 1.1 g cm−3(in liquid form)
Melting point −136 °C (−213 °F; 137 K)
Boiling point −52 °C (−62 °F; 221 K)
log P -0.611
Vapor pressure 1518.92 kPa (at 21.1 °C)
Hazards
Safety data sheet MSDS at Oxford University
GHS pictograms GHS02: FlammableGHS04: Compressed Gas
GHS Signal word Danger
H220, H221, H280
P210, P377, P381, P403, P410+403
NFPA 704 (fire diamond)
Flammability code 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneHealth code 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
4
1
0
648 °C (1,198 °F; 921 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references

Difluoromethane, also called difluoromethylene, HFC-32 Methylene Fluoride or R-32, is an organic compound of the dihalogenoalkane variety. It has the formula of CH2F2. It is a colorless gas in the ambient atmosphere and is slightly soluble in the water, with a high thermal stability.[2][failed verification] Due to the low melting and boiling point, (-136.0 °C and -51.6 °C respectively) contact with this compound may result in frostbite.[2][failed verification] In the United States, the Clean Air Act Section 111 on Volatile Organic Compounds (VOC) has listed difluoromethane as an exception (since 1997) from the definition of VOC due to its low production of tropospheric ozone.[3] Difluoromethane is commonly used in endothermic processes such as refrigeration or air conditioning.

Synthesis

Difluoromethane is primarily synthesized via batch processes, by the reaction of dichloromethane and hydrogen fluoride (HF), in the liquid phase using SbCl5 as a catalyst.[4] Due to hydrogen fluoride's hazardous properties, a new synthesis was developed. The new synthesis allows for constant flow of difluoromethane production through an isolated chamber.[4]

Applications

HFC-32 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 difluoromethane at various latitudes since year 2009.

Difluoromethane is often used as a fire extinguishant due to its ability to undergo endothermic processes.[5] Atmospheric concentration of difluoromethane at various latitudes since the year 2009 are shown to the left.

Difluoromethane is a molecule used as refrigerant that has prominent heat transfer and pressure drop performance, both in condensation and vaporization.[6] It has a 100-year global warming potential (GWP) of 675 times that of carbon dioxide, and an atmospheric lifetime of nearly 5 years.[7] It is classified as A2L - slightly flammable by ASHRAE,[8] and has zero ozone depletion potential (ODP).[9] Difluoromethane is thus a relatively low-risk choice among HFC refrigerants, most of which have higher GWP and longer persistence when leaks occur.

The common refrigerant R-410A is a zeotropic, 50/50-mass-percent mixture of difluoromethane and pentafluoroethane (R-125). Pentafluoroethane is a common replacement for various chlorofluorocarbons (i.e Freon) in new refrigerant systems, especially for air-conditioning. The zeotropic mix of difluoromethane with pentafluoroethane (R-125) and tetrafluoroethane (R-134a) is known as R-407A through R-407F depending on the composition. Likewise, R-504 is the azeotropic (48.2/51.8 mass%) mixture of difluoromethane and chlorotrifluoromethane (R13). In 2011 17,949,893 metric tons of difluoromethane were emitted into the atmosphere in the United States alone.[10]

Difluoromethane is currently used by itself in residential and commercial air-conditioners in Japan, China, and India as a substitute for R-410A. In order to reduce the residual risk associated with its mild flammability, this molecule should be applied in heat transfer equipment with low refrigerant charge such as brazed plate heat exchangers (BPHE), or shell and tube heat exchangers and tube and plate heat exchangers with tube of small diameter.[11] Many applications confirmed that difluoromethane exhibits heat transfer coefficients higher than those of R-410A under the same operating conditions but also higher frictional pressure drops.[11]

Other uses of difluoromethane include its use as aerosol propellants, blowing agents, and solvents.[3]

Environmental Effects

Every year, approximately 15 kilotons of difluoromethane are produced.[3] In gas form, the compound will degrade in the atmosphere by reaction with photochemically-produced hydroxyl radicals. This process will form carbonyl difluoride. The half-life for this process is estimated to be 4 years.[3] Difluoromethane tends to enter the environment via the gas phase and accumulates there more commonly than in soils or sediments. Volatilization half-lives of this compound are about 45 minutes for rivers and 69 hours for lakes, difluoromethane does not bioaccumulate in aquatic areas well.[3]

HFC-32 released into the environment gets broken down into CF as an intermediate product. This goes on to create HF and CO2 by hydrolysis in atmospheric water.[3]

The global warming potential (GWP) of HFC-32 is estimated at 677 on a 100-year time window.[12] This is far lower than the GWP for HFC refrigerants it is replacing, but remains sufficiently high to spur continued research into using lower-GWP refrigerants.

Difluoromethane is excluded from the list of VOCs supplied in the United States Clean Air Act due to the ODP being zero. Therefore, tropospheric ozone is not likely to be produced from this molecule. Tropospheric ozone may lead to adverse health effects such as respiratory, cardiac or neurological damage.[3] Additionally, ozone can affect plant and vegetation by inducing the bronzing of leaves.[3]

Toxicity

Difluoromethane shows slight maternal and developmental toxicity at concentrations of approximately 50,000 ppm in rats, but not in rabbits. The exposure limitations set on difluoromethane for human use are 1,000 ppm, making exposure to dangerous levels unlikely.[3]

References

  1. "Difluoromethane - Compound Summary". The PubChem Project. US: National Center of Biotechnological Information. https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=6345&loc=ec_rcs. 
  2. 2.0 2.1 "Editorial Board". Journal of Fluorine Chemistry 241: 109706. January 2021. doi:10.1016/s0022-1139(20)30404-8. ISSN 0022-1139. 
  3. 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 3.8 "Stratospheric Ozone Protection: The Montreal Protocol and Title VI of the Clean Air Act Amendments of 1990". Air & Waste 43 (8): 1066–1067. August 1993. doi:10.1080/1073161x.1993.10467184. ISSN 1073-161X. 
  4. 4.0 4.1 Shen, Tao; Ge, Xin; Zhao, Hengjun; Xu, Zhixiong; Tong, Shaofeng; Zhou, Shaodong; Qian, Chao; Chen, Xinzhi (2020-07-01). "A safe and efficient process for the preparation of difluoromethane in continuous flow" (in en). Chinese Journal of Chemical Engineering 28 (7): 1860–1865. doi:10.1016/j.cjche.2020.02.024. ISSN 1004-9541. https://www.sciencedirect.com/science/article/pii/S1004954120300902. 
  5. Blowers, Paul; Hollingshead, Kyle (2009-05-21). "Estimations of Global Warming Potentials from Computational Chemistry Calculations for CH 2 F 2 and Other Fluorinated Methyl Species Verified by Comparison to Experiment" (in en). The Journal of Physical Chemistry A 113 (20): 5942–5950. doi:10.1021/jp8114918. ISSN 1089-5639. PMID 19402663. Bibcode2009JPCA..113.5942B. https://pubs.acs.org/doi/10.1021/jp8114918. 
  6. Longo, Giovanni A.; Mancin, Simone; Righetti, Giulia; Zilio, Claudio (2015). "HFC32 vaporisation inside a Brazed Plate Heat Exchanger (BPHE): Experimental measurements and IR thermography analysis". International Journal of Refrigeration 57: 77–86. doi:10.1016/j.ijrefrig.2015.04.017. 
  7. May 2010 TEAP XXI/9 Task Force Report
  8. 2009 ASHRAE Handbook
  9. "R32". http://www.linde-gas.com/en/products_and_supply/refrigerants/hfc_refrigerants/r32/index.html. 
  10. Galka, Michael D.; Lownsbury, James M.; Blowers, Paul (2012-12-04). "Greenhouse Gas Emissions for Refrigerant Choices in Room Air Conditioner Units" (in en). Environmental Science & Technology 46 (23): 12977–12985. doi:10.1021/es302338s. ISSN 0013-936X. PMID 23136858. Bibcode2012EnST...4612977G. https://pubs.acs.org/doi/10.1021/es302338s. 
  11. 11.0 11.1 Longo, Giovanni A.; Mancin, Simone; Righetti, Giulia; Zilio, Claudio (2016). "HFC32 and HFC410A flow boiling inside a 4 mm horizontal smooth tube". International Journal of Refrigeration 61: 12–22. doi:10.1016/j.ijrefrig.2015.09.002. 
  12. IPCC AR4, summarized at https://www.ghgprotocol.org/sites/default/files/ghgp/Global-Warming-Potential-Values%20%28Feb%2016%202016%29_1.pdf

External links