Firefighting foam

Firefighting foam is a foam used for fire suppression. Its role is to cool the fire and to coat the fuel, preventing its contact with oxygen, resulting in suppression of the combustion. Fire-fighting foam was invented by the Russian engineer and chemist Aleksandr Loran in 1902.[1]

Firefighters sprayed foam on structures in the Mammoth Hot Springs complex on 10 September 1988 during the Yellowstone Fires.

The surfactants used must produce foam in concentration of less than 1%. Other components of fire-retardant foams are organic solvents (e.g., trimethyl-trimethylene glycol and hexylene glycol), foam stabilizers (e.g., lauryl alcohol), and corrosion inhibitors.

Overview
  • Low-expansion foams such as AFFF, have an expansion rate less than 20 times are low-viscosity, mobile, and can quickly cover large areas.
  • Medium-expansion foams have an expansion ratio of 20–100.
  • High-expansion foams have an expansion ratio over 200–1000 and are suitable for enclosed spaces such as hangars, where quick filling is needed.
  • Alcohol-resistant foams contain a polymer that forms a protective layer between the burning surface and the foam, preventing foam breakdown by alcohols in the burning fuel. Alcohol-resistant foams are used in fighting fires of fuels containing oxygenates, e.g. MTBE, or fires of liquids based on or containing polar solvents.

Class A foams
A fire truck demonstrating Class A foam in a CAFS system

Class A foams were developed in mid-1980s for fighting wildfires. Class A foams lower the surface tension of the water, which assists in the wetting and saturation of Class A fuels with water. This aids fire suppression and can prevent reignition.[2] Favorable experiences led to its acceptance for fighting other types of class A fires, including structure fires.[3]

Class B foams

Class B foams are designed for class B fires—flammable liquids. The use of class A foam on a class B fire may yield unexpected results, as class A foams are not designed to contain the explosive vapors produced by flammable liquids. Class B foams have two major subtypes.

Synthetic foams

Synthetic foams are based on synthetic surfactants. They provide better flow and spreading over the surface of hydrocarbon-based liquids, for faster knockdown of flames. They have limited post-fire security and are toxic groundwater contaminants.

Protein foams

Protein foams contain natural proteins as the foaming agents. Unlike synthetic foams, protein foams are bio-degradable. They flow and spread slower, but provide a foam blanket that is more heat-resistant and more durable.

Protein foams include regular protein foam (P), fluoroprotein foam (FP), film-forming fluoroprotein (FFFP),[4] alcohol-resistant fluoroprotein foam (AR-FP), and alcohol-resistant film-forming fluoroprotein (AR-FFFP).

Applications

Every type of foam has its application. High-expansion foams are used when an enclosed space, such as a basement or hangar, must be quickly filled. Low-expansion foams are used on burning spills. AFFF is best for spills of jet fuels, FFFP is better for cases where the burning fuel can form deeper pools, and AR-AFFF is suitable for burning alcohols. The most flexibility is achieved by AR-AFFF or AR-FFFP. AR-AFFF must be used in areas where gasolines are blended with oxygenates, since the alcohols prevent the formation of the film between the FFFP foam and the gasoline, breaking down the foam, rendering the FFFP foam virtually useless.

History of fire-fighting foams

Water has long been a universal agent for suppressing fires, but is not best in all cases. For example, water is typically ineffective on oil fires, and can be dangerous. Fire-fighting foams were a development for extinguishing oil fires.

In 1902, a method of extinguishing flammable liquid fires by blanketing them with foam was introduced by Russian engineer and chemist Aleksandr Loran. Loran was a teacher in a school in Baku, the center of the Russian oil industry at that time. Impressed by large, difficult-to-extinguish oil fires that he had seen there, Loran tried to find a liquid substance that could deal effectively with them. He invented fire-fighting foam, which was successfully tested in experiments in 1902 and 1903.[1] In 1904 Loran patented his invention, and developed the first foam extinguisher the same year.[5]

The original foam was a mixture of two powders and water produced in a foam generator. It was called chemical foam because of the chemical action to create it. In general, the powders used were sodium bicarbonate and aluminium sulfate, with small amounts of saponin or liquorice added to stabilise the bubbles. Hand-held foam extinguishers used the same two chemicals in solution. To actuate the extinguisher, a seal was broken and the unit inverted, allowing the liquids to mix and react. Chemical foam is a stable solution of small bubbles containing carbon dioxide with lower density than oil or water, and exhibits persistence for covering flat surfaces. Because it is lighter than the burning liquid, it flows freely over the liquid surface and extinguishes the fire by a smothering (removal/prevention of oxygen) action. Chemical foam is considered obsolete today because of the many containers of powder required, even for small fires.

In the 1940s, Percy Lavon Julian developed an improved type of foam called Aerofoam. Using mechanical action, a liquid protein-based concentrate, made from soy protein, was mixed with water in either a proportioner or an aerating nozzle to form air bubbles with the free-flowing action. Its expansion ratio and ease of handling made it popular. Protein foam is easily contaminated by some flammable liquids, so care should be used so that the foam is applied only above the burning liquid. Protein foam has slow knockdown characteristics, but it is economical for post-fire security.

In the early 1950s, high-expansion foam was conceived by Herbert Eisner in England at the Safety in Mines Research Establishment (now the Health & Safety Laboratory) to fight coal mine fires. Will B. Jamison, a Pennsylvania Mining Engineer, read about the proposed foam in 1952, requested more information about the idea. He proceeded to work with the US Bureau of Mines on the idea, testing 400 formulas until a suitable compound was found. In 1964, Walter Kidde & Company (now Kidde) bought the patents for high expansion foam.[6]

In the 1960s, National Foam, Inc. developed fluoroprotein foam. Its active agent is a fluorinated surfactant that provides an oil-rejecting property to prevent contamination. In general, it is better than protein foam because its longer blanket life provides better safety when entry is required for rescue. Fluoroprotein foam has fast knockdown characteristics and it can also be used together with dry chemicals that destroy protein foam.

In the mid-1960s, the US Navy developed aqueous film-forming foam (AFFF). This synthetic foam has a low viscosity and spreads rapidly across the surface of most hydrocarbon fuels. A water film forms beneath the foam, which cools the liquid fuel, stopping the formation of flammable vapors. This provides dramatic fire knockdown, an important factor in crash rescue fire fighting.

In the early 1970s, National Foam, Inc. invented Alcohol-Resistant AFFF technology. AR-AFFF is a synthetic foam developed for both hydrocarbon and polar-solvent materials. Polar solvents are combustible liquids that destroy conventional fire-fighting foam. These solvents extract the water contained in the foam, breaking down the foam blanket. Hence, these fuels require an alcohol- or polar-solvent-resistant foam. Alcohol-resistant foam must be bounced off of a surface and allowed to flow down and over the liquid to form its membrane, compared to standard AFFF that can be sprayed directly onto the fire.

In 1993, Pyrocool Technologies Inc. acquired the patent rights to a wetting agent with superior cooling properties that is effective on Class A, Class B, Class D as well as pressurized and 3-dimensional fires involving both hydro carbon based fuels and polar solvents such as alcohol and ethanol. The wetting agent is marketed under the name of Pyrocool. Pyrocool Technologies Inc. was awarded the 1998 Presidential Green Chemistry Award by the USEPA. Carol Browner, the USEPA Administrator in 1998, described Pyrocool as the “Technology for the Third Millennium: The Development and Commercial Introduction of an Environmentally Responsible Fire Extinguishment and Cooling Agent”. Pyrocool lost their UL classification after Hurricane Katrina when it was discovered the original formula was no longer being used when going to a different blending company. Novacool UEF (Universal Extinguishing Foam) is the only firefighting foam on the market using the original formula invented and developed by Paul Berger of Baums Caustorine. Berger was awarded the 1998 Presidential Green Chemistry Award for his formulation.

In 2010, Orchidee International of France developed the first FFHPF, the highest performing fluorine-free foam. The foam has achieved a 97% degradability rating and is currently marketed by Orchidee International under the brand name "BluFoam". The foam is used at 3% both on hydrocarbon and polar solvent fires.

Environmental and health concerns

Studies have shown that PFOS is a persistent, bioaccumulative, and toxic pollutant.[7][8][9] It was added to Annex B of the Stockholm Convention on Persistent Organic Pollutants in May 2009.[10] Regulations in the United States, Canada, European Union, Australia, and Japan have banned the new production of PFOS-based products, including fire fighting foams.[11] 3M phased out production of PFOS in 2002 due to toxicity concerns.[12]

One study, published in 2015, found that firefighters were more likely to have fluorinated surfactants in their blood stream.[13] In 2016, the United States Air Force paid $4.3 million for a water treatment system for residents downstream of Peterson Air Force Base in Colorado.[14][15]

In the United States, discharges of AFFF by vessels to surface waters are regulated by the U.S. Environmental Protection Agency (EPA) and Department of Defense, pursuant to the Clean Water Act.[16][17]

In Australia, in 2015 a public safety announcement was issued by the New South Wales Environment Protection Authority following a water source contamination near RAAF Base Williamtown. Surface water, ground water and fish were reported to contain chemicals from firefighting foams that had been released by the local Royal Australia Air Force base prior to training protocol changes in 2008.[18] The residents of the area were advised to not consume any bore water, in addition to eggs and seafood from fauna exposed to the contaminated water.[19] The discovery led to the banning of all forms of fishing in the waters of Fullerton Cove until the beginning of October 2016.[20][21]

As of 2017 the Department of Defence is dealing with two class action suits brought by those affected by contamination at Williamtown and at Army Aviation Centre Oakey.[22][23] Along with many airports and fire services, the Department of Defence is investigating possible contamination at 18 military sites across Australia.[24] At Williamtown, it is also conducting studies on the uptake and residual contamination in plants, chickens and eggs.[25]

In December 2017, New Zealand's Minister for the Environment announced that higher than acceptable levels of PFOS and PFOA were found in groundwater at two Royal New Zealand Air Force bases, thought to be from historic use of firefighting foam containing the substances.[26] Residents residing near the airbases were told to drink bottled water until more extensive testing could be carried out.[27]

In 2020, state government agencies in the US are planning to dispose of firefighting foam, either by incineration or landfilling. Nearly 1 million US gal (3,800 kl) of foam will be disposed by the states. The potential health risks of incinerating AFFF are still being investigated by EPA and state agencies.[28]

gollark: That is a YouTube video.
gollark: * superior
gollark: Bow to my superiot TeX.
gollark: =tex \sum_{n=0}^{\infty}\frac{1}{n}
gollark: No ohio.

See also

References
  1. Loran and the fire extinguisher Archived 27 July 2011 at the Wayback Machine at p-lab.org (in Russian)
  2. Phos Chek WD881 Brochure (PDF), Phos-Chek, archived from the original (PDF) on 5 January 2009, retrieved 5 December 2008
  3. "Class A Foam: Q & A". Archived from the original on 29 September 2005.
  4. Clause 1 BS 5306-6.1
  5. The history of fire extinguisher (in Russian)
  6. Kearney, Paul (February 1966). "Shut the Windows!". Popular Mechanics. Vol. 125 no. 2. Hearst Magazines. pp. 136–139, 210–212. ISSN 0032-4558.
  7. OECD (2002). "Hazard Assessment of Perfluorooctane Sulfonate (PFOS) and its salts". ENV/JM/RD(2002)17/FINAL (page 5).
  8. "How safe is firefighting foam?". FireRescue1. Retrieved 14 February 2017.
  9. "'Dark Waters' movie poses risk for 3M, analyst says". AFFF contamination on ArmyBases. Retrieved 20 November 2019.
  10. Governments unite to step-up reduction on global DDT reliance and add nine new chemicals under international treaty. Geneva: Stockholm Convention Secretariat. 8 May 2008.
  11. "Fact Sheet on AFFF Fire Fighting Agents" (PDF). Arlington, VA: Fire Fighting Foam Coalition. 2017.
  12. Pelley, Janet. "Novel Fluorinated Surfactants Discovered In Firefighters' Blood – Chemical & Engineering News". Retrieved 19 November 2016.
  13. Rotander, Anna; Kärrman, Anna; Toms, Leisa-Maree L.; Kay, Margaret; Mueller, Jochen F.; Gómez Ramos, María José (2015). "Novel Fluorinated Surfactants Tentatively Identified in Firefighters Using Liquid Chromatography Quadrupole Time-of-Flight Tandem Mass Spectrometry and a Case-Control Approach". Environmental Science & Technology. 49 (4): 2434–2442. Bibcode:2015EnST...49.2434R. doi:10.1021/es503653n. ISSN 0013-936X.
  14. Finley, Bruce (10 May 2017). "Elevated cancer rates found south of Colorado Springs where water supplies contain toxic chemicals". Denver Post.
  15. "Tainted Water Near Colorado Bases Hints at Wider Safety Concerns". The New York Times. 26 July 2016. Retrieved 19 November 2016.
  16. U.S. Environmental Protection Agency (EPA), Washington, D.C. (12 April 2013). "Final National Pollutant Discharge Elimination System (NPDES) General Permit for Discharges Incidental to the Normal Operation of a Vessel." Federal Register. 78 FR 21938.
  17. DOD and EPA (11 January 2017). "Uniform National Discharge Standards for Vessels of the Armed Forces-Phase II Batch One." Federal Register, 82 FR 3173.
  18. "Department of Defence and NSW Government investigating chemicals around Williamtown RAAF Base". Media and information. Sydney: New South Wales Environment Protection Authority. 3 September 2015. Archived from the original on 12 September 2015.
  19. "Expert Panel recommends oyster ban end, further fish testing". Chief Scientist and Engineer. Sydney: New South Wales Government. 2 October 2015.
  20. Chris Ray (25 March 2016). "What's happening to the water in Williamtown?". The Sydney Morning Herald. Fairfax Media. Retrieved 15 August 2017.
  21. Tonkin, Emma; Cook, Carly (27 September 2016). "Fishing ban put in place due to contamination set to be lifted north of Newcastle". ABC News. Retrieved 25 October 2017.
  22. Daniel Burdon (21 April 2017). "Federal government considering phasing out toxic fire-fighting foam chemicals". The Canberra Times. Fairfax Media. Retrieved 15 August 2017.
  23. Gregory, Katherine (12 May 2017). "Williamtown residents angry over revelations Defence delayed information on contamination". ABC News (Australia). Retrieved 17 August 2017.
  24. "PFAS Investigation & Management Program". Department of Defence. Retrieved 16 August 2017.
  25. "PFAS Uptake Studies in Plants, Chicken & Eggs". Department of Defence. Retrieved 16 August 2017.
  26. "Agencies investigating potential water contamination". Radio New Zealand News. 7 December 2017. Retrieved 8 December 2017.
  27. "Defence force knew of possible contamination for months". Radio New Zealand News. 8 December 2017. Retrieved 8 December 2017.
  28. Carignan, Sylvia; Clukey, Keshia (2020-07-16). "States Must Throw Out Almost 1 Million Gallons of PFAS Foam". Environment & Energy Report. Bloomberg Law.

Further reading
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.