Phosgene is anorganic chemical compound with theformulaCOCl2. It is a toxic, colorless gas; in low concentrations, its musty odor resembles that of freshly cut hay or grass.[7] It can be thought of chemically as the doubleacyl chloride analog ofcarbonic acid, or structurally asformaldehyde with the hydrogen atoms replaced by chlorine atoms. In 2013, about 75–80 % of global phosgene was consumed forisocyanates, 18% forpolycarbonates and about 5% for otherfine chemicals.[8]
Phosgene is extremely poisonous and was used as achemical weapon duringWorld War I, where it wasresponsible for 85,000 deaths. It is a highly potent pulmonary irritant and quickly filled enemy trenches due to it being a heavy gas.
Phosgene is a planar molecule as predicted byVSEPR theory. The C=O distance is 1.18 Å, the C−Cl distance is 1.74 Å and the Cl−C−Cl angle is 111.8°.[10] Phosgene is acarbon oxohalide and it can be considered one of the simplest acyl chlorides, being formally derived fromcarbonic acid.
This reaction is exothermic and is typically performed between 50 and 150 °C. Above 200 °C, phosgene reverts to carbon monoxide and chlorine,Keq(300 K) = 0.05. World production of this compound was estimated to be 2.74 million tonnes in 1989.[9]
Phosgene is fairly simple to produce, but is listed as aSchedule 3 substance under theChemical Weapons Convention. As such, it is usually considered too dangerous to transport inbulk quantities. Instead, phosgene is usually produced and consumed within the same plant, as part of an "on demand" process. This involves maintaining equivalent rates of production and consumption, which keeps the amount of phosgene in the system at any one time fairly low, reducing the risks in the event of an accident. Some batch production does still take place, but efforts are made to reduce the amount of phosgene stored.[11]
Simpleorganochlorides slowly convert into phosgene when exposed toultraviolet (UV) irradiation in the presence ofoxygen.[12] Before the discovery of theozone hole in the late 1970s large quantities of organochlorides were routinely used by industry, which inevitably led to them entering the atmosphere. In the 1970-80s phosgene levels in thetroposphere were around 20-30pptv (peak 60 pptv).[12] These levels had not decreased significantly nearly 30 years later,[13] despite organochloride production becoming restricted under theMontreal Protocol.
Phosgene in the troposphere can last up to about 70 days and is removed primarily by hydrolysis with ambient humidity or cloudwater.[14] Less than 1% makes it to thestratosphere, where it is expected to have a lifetime of several years, since this layer is much drier and phosgene decomposes slowly through UVphotolysis. It plays a minor part inozone depletion.
Carbon tetrachloride (CCl4) can turn into phosgene when exposed to heat in air. This was a problem as carbon tetrachloride is an effective fire suppressant and was formerly in widespread use infire extinguishers.[15] There are reports of fatalities caused by its use to fight fires inconfined spaces.[16] Carbon tetrachloride's generation of phosgene and its own toxicity mean it is no longer used for this purpose.[15]
Phosgene was synthesized by theCornish chemistJohn Davy (1790–1868) in 1812 by exposing a mixture of carbon monoxide and chlorine tosunlight. He named it "phosgene" fromGreekφῶς (phos, light) andγεννάω (gennaō, to give birth) in reference of the use of light to promote the reaction.[18] It gradually became important in the chemical industry as the 19th century progressed, particularly in dye manufacturing.
The reaction of an organic substrate with phosgene is calledphosgenation.[9] Phosgenation ofdiols give carbonates (R =H,alkyl,aryl), which can be either linear or cyclic:
n HO−CR2−X−CR2−OH +n COCl2 → [−O−CR2−X−CR2−O−C(=O)−]n + 2n HCl
An example is the reaction of phosgene withbisphenol A to formpolycarbonates.[9] Phosgenation of diamines gives di-isocyanates, liketoluene diisocyanate (TDI),methylene diphenyl diisocyanate (MDI),hexamethylene diisocyanate (HDI), andisophorone diisocyanate (IPDI). In these conversions, phosgene is used in excess to increase yield and minimize side reactions. The phosgene excess is separated during the work-up of resulting end products and recycled into the process, with any remaining phosgene decomposed in water usingactivated carbon as the catalyst. Diisocyanates are precursors topolyurethanes. More than 90% of the phosgene is used in these processes, with the biggest production units located in the United States (Texas and Louisiana), Germany, Shanghai, Japan, and South Korea. The most important producers areDow Chemical,Covestro, andBASF. Phosgene is also used to produce monoisocyanates, used as pesticide precursors (e.g.methyl isocyanate (MIC).
Aside from the widely used reactions described above, phosgene is also used to produceacyl chlorides fromcarboxylic acids:
R−C(=O)−OH + COCl2 → R−C(=O)−Cl + HCl + CO2
For this application,thionyl chloride is commonly used instead of phosgene.
The synthesis ofisocyanates from amines illustrates theelectrophilic character of this reagent and its use in introducing the equivalentsynthon "CO2+":[19]
R−NH2 + COCl2 → R−N=C=O + 2 HCl, where R =alkyl,aryl
Such reactions are conducted on laboratory scale in the presence of a base such aspyridine that neutralizes thehydrogen chloride side-product.
In these syntheses, phosgene is used in excess to prevent formation of the correspondingcarbonate ester.
Withamino acids, phosgene (or its trimer) reacts to giveamino acid N-carboxyanhydrides. More generally, phosgene acts to link two nucleophiles by a carbonyl group. For this purpose, alternatives to phosgene such ascarbonyldiimidazole (CDI) are safer, albeit expensive.[20] CDI itself is prepared by reacting phosgene withimidazole.
Phosgene is stored inmetal cylinders. In the US, the cylinder valve outlet is a tapered thread known as "CGA 160" that is used only for phosgene.
In the research laboratory, due to safety concerns phosgene nowadays finds limited use inorganic synthesis. A variety of substitutes have been developed, notably trichloromethyl chloroformate ("diphosgene"), a liquid at room temperature, and bis(trichloromethyl) carbonate ("triphosgene"), a crystalline substance.[21]
It is listed onSchedule 3 of theChemical Weapons Convention: All production sites manufacturing more than 30 tonnes per year must be declared to theOPCW.[22] Although less toxic than many otherchemical weapons such assarin, phosgene is still regarded as a viablechemical warfare agent because of its simpler manufacturing requirements when compared to that of more technically advanced chemical weapons such astabun, a first-generationnerve agent.[23]
Phosgene was first deployed as a chemical weapon by the French in 1915 in World War I.[24] It was also used in a mixture with an equal volume of chlorine, with the chlorine helping to spread the denser phosgene.[25][26] Phosgene was more potent than chlorine, though some symptoms took 24 hours or more to manifest.
Following the extensive use of phosgene duringWorld War I, it was stockpiled by various countries.[27][28][29]
Phosgene is an insidious poison as the odor may not be noticed and symptoms may be slow to appear.[31]
At low concentrations, phosgene may have a pleasant odor of freshly mown hay or green corn,[32] but has also been described as sweet, like rotten banana peels. Theodor detection threshold for phosgene is 0.4 ppm, four times thethreshold limit value (time weighted average). Its hightoxicity arises from the action of the phosgene on the−OH,−NH2 and−SH groups of theproteins in pulmonaryalveoli (the site of gas exchange), respectively forming ester, amide and thioester functional groups in accord with the reactions discussed above. This results in disruption of theblood–air barrier, eventually causingpulmonary edema. The extent of damage in the alveoli does not primarily depend on phosgene concentration in the inhaled air, with the dose (amount of inhaled phosgene) being the critical factor.[33] Dose can be approximately calculated as "concentration" × "duration of exposure".[33][34] Therefore, persons in workplaces where there exists risk of accidental phosgene release usually wear indicator badges close to the nose and mouth.[35] Such badges indicate the approximate inhaled dose, which allows for immediate treatment if the monitored dose rises above safe limits.[35]
In case of low or moderate quantities of inhaled phosgene, the exposed person is to be monitored and subjected to precautionary therapy, then released after several hours. For higher doses of inhaled phosgene (above 150 ppm × min) apulmonary edema often develops which can be detected byX-ray imaging and regressiveblood oxygen concentration. Inhalation of such high doses can eventually result in fatality within hours up to 2–3 days of the exposure.
The risk connected to a phosgene inhalation is based not so much on its toxicity (which is much lower in comparison to modern chemical weapons likesarin ortabun) but rather on its typical effects: the affected person may not develop any symptoms for hours until an edema appears, at which point it could be too late for medical treatment to assist.[36] Nearly all fatalities as a result of accidental releases from the industrial handling of phosgene occurred in this fashion. On the other hand, pulmonary edemas treated in a timely manner usually heal in the mid- and longterm, without major consequences once some days or weeks after exposure have passed.[37][38] Nonetheless, the detrimental health effects on pulmonary function from untreated, chronic low-level exposure to phosgene should not be ignored; although not exposed to concentrations high enough to immediately cause an edema, many synthetic chemists (e.g.Leonidas Zervas) working with the compound were reported to experience chronic respiratory health issues and eventual respiratory failure from continuous low-level exposure.
If accidental release of phosgene occurs in an industrial or laboratory setting, it can be mitigated withammonia gas; in the case of liquid spills (e.g. of diphosgene or phosgene solutions) an absorbent and sodium carbonate can be applied.[39]
The first major phosgene-related incident happened in May 1928 when eleven tons of phosgene escaped from a war surplus store in centralHamburg.[40] Three hundred people were poisoned, of whom ten died.[40]
In the second half of 20th century several fatal incidents implicating phosgene occurred in Europe, Asia and the US. Most of them have been investigated by authorities and the outcome made accessible to the public. For example, phosgene was initiallyblamed for theBhopal disaster, but investigations provedmethyl isocyanate to be responsible for the numerous poisonings and fatalities.
Recent major incidents happened in January 2010 and May 2016. An accidental release of phosgene gas at aDuPont facility inWest Virginia killed one employee in 2010.[41] TheUS Chemical Safety Board released a video detailing the accident.[42] Six years later, a phosgene leak occurred in aBASF plant inSouth Korea, where a contractor inhaled a lethal dose of phosgene.[43]
^"PHOSGENE (cylinder)".Inchem (Chemical Safety Information from Intergovernmental Organizations). International Programme on Chemical Safety and the European Commission.
^Falcke, Heino; Holbrook, Simon; Clenahan, Iain; López Carretero, Alfredo; Sanalan, Teoman; Brinkmann, Thomas; Roth, Joze; Zerger, Benoit; Roudier, Serge, eds. (2017).Best Available Techniques (BAT) reference document for the production of large volume organic chemicals. Luxembourg: EU Publications Office. p. 443.ISBN978-92-79-76589-6.
^Nakata, M.; Kohata, K.; Fukuyama, T.; Kuchitsu, K. (1980). "Molecular Structure of Phosgene as Studied by Gas Electron Diffraction and Microwave Spectroscopy. Therz Structure and Isotope Effect".Journal of Molecular Spectroscopy.83:105–117.doi:10.1016/0022-2852(80)90314-8.
^Gowland, Richard (1996). "Applying inherently safer concepts to a phosgene plant acquisition".Process Safety Progress.15 (1):52–57.doi:10.1002/prs.680150113.S2CID110707551.
^Kindler, T.P.; Chameides, W.L.; Wine, P.H.; Cunnold, D.M.; Alyea, F.N.; Franklin, J.A. (20 January 1995). "The fate of atmospheric phosgene and the stratospheric chlorine loadings of its parent compounds: CCl 4, C 2 Cl 4, C 2 HCl 3, CH 3 CCl 3, and CHCl 3".Journal of Geophysical Research: Atmospheres.100 (D1):1235–1251.Bibcode:1995JGR...100.1235K.doi:10.1029/94JD02518.
^abBurke, Robert (2007-11-06).Fire Protection: Systems and Response. CRC Press. p. 209.ISBN978-0-203-48499-9.
^Pohl, Lance R.; Bhooshan, B.; Whittaker, Noel F.; Krishna, Gopal (December 1977). "Phosgene: A metabolite of chloroform".Biochemical and Biophysical Research Communications.79 (3):684–691.doi:10.1016/0006-291X(77)91166-4.PMID597296.
^John Davy (1812)."On a gaseous compound of carbonic oxide and chlorine".Philosophical Transactions of the Royal Society of London.102:144–151.doi:10.1098/rstl.1812.0008.JSTOR107310. Phosgene was named on p. 151: " ... it will be necessary to designate it by some simple name. I venture to propose that of phosgene, or phosgene gas; fromφως, light,γινομαι, to produce, which signifies formed by light; ... "
^abWerner F. Diller, Early Diagnosis of Phosgene Overexposure.Toxicology and Industrial Health, Vol.1, Nr.2, April 1985, p. 73 -80
^W. F. Diller, R. Zante : Zentralbl. Arbeitsmed. Arbeitsschutz Prophyl. Ergon. 32, (1982) 60 -368
^abW. F.Diller, E.Drope, E. Reichold:Ber. Int. Kolloq. Verhütung von Arbeitsunfällen und Berufskrankheiten Chem. Ind.6 th (1979) Chem. Abstr. 92 (1980) 168366x
^W. F. Diller:Radiologische Untersuchungen zur verbesserten Frühdiagnose von industriellen Inhalationsvergiftungen mit verzögertem Wirkungseintritt, Verlag für Medizin Dr. E. Fischer, Heidelberg. Zentralbatt für Arbeitsmedizin, Arbeitsschutz und Ergonomie, Nr. 3, Mai 2013, p. 160 - 163
^W.F. Diller, F. Schnellbächer, F. Wüstefeld : Zentralbl. Arbeitsmed. Arbeitsschutz Prophyl. 29 (1979) p.5-16
^Results From the US Industry-Wide Phosgene Surveillance "The Diller Registry" : Journal of Occ. and Env. Med., March 2011-Vol.53-iss. 3 p.239- 244
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