iPhoneOgraphy – 26 Jun 2016 (Day 178/366)
The first fire extinguisher of which there is any record was patented in England in 1723 by Ambrose Godfrey, a celebrated chemist at that time. It consisted of a cask of fire-extinguishing liquid containing a pewter chamber of gunpowder. This was connected with a system of fuses which were ignited, exploding the gunpowder and scattering the solution. This device was probably used to a limited extent, as Bradley’s Weekly Messenger for November 7, 1729, refers to its efficiency in stopping a fire in London.
The modern fire extinguisher was invented by British Captain George William Manby in 1818; it consisted of a copper vessel of 3 gallons (13.6 liters) of pearl ash (potassium carbonate) solution contained within compressed air.
The soda-acid extinguisher was first patented in 1866 by Francois Carlier of France, which mixed a solution of water and sodium bicarbonate with tartaric acid, producing the propellant CO2 gas. A soda-acid extinguisher was patented in the U.S. in 1881 by Almon M. Granger. His extinguisher used the reaction between sodium bicarbonate solution and sulfuric acid to expel pressurized water onto a fire. A vial of concentrated sulfuric acid was suspended in the cylinder. Depending on the type of extinguisher, the vial of acid could be broken in one of two ways. One used a plunger to break the acid vial, while the second released a lead stopple that held the vial closed. Once the acid was mixed with the bicarbonate solution, carbon dioxide gas was expelled and thereby pressurized the water. The pressurized water was forced from the canister through a nozzle or short length of hose.
The cartridge-operated extinguisher was invented by Read & Campbell of England in 1881, which used water or water-based solutions. They later invented a carbon tetra chlorine model called the “Petrolex” which was marketed toward automotive use.
The chemical foam extinguisher was invented in 1904 by Aleksandr Loran in Russia, based on his previous invention of fire fighting foam. Loran first used it to extinguish a pan of burning naphtha. It worked and looked similar to the soda-acid type, but the inner parts were slightly different. The main tank contained a solution of sodium bicarbonate in water, whilst the inner container (somewhat larger than the equivalent in a soda-acid unit) contained a solution of aluminium sulphate. When the solutions were mixed, usually by inverting the unit, the two liquids reacted to create a frothy foam, and carbon dioxide gas. The gas expelled the foam in the form of a jet. Although liquorice-root extracts and similar compounds were used as additives (stabilizing the foam by reinforcing the bubble-walls), there was no “foam compound” in these units. The foam was a combination of the products of the chemical reactions: sodium and aluminium salt-gels inflated by the carbon dioxide. Because of this, the foam was discharged directly from the unit, with no need for an aspirating branchpipe (as in newer foam-compound types).
In 1910, The Purene Manufacturing Company of Delaware filed a patent for using carbon tetra chloride (CTC, or CCI4) to extinguish fires. The liquid vaporized and extinguished the flames by inhibiting the chemical chain reaction of the combustion process (it was an early 20th-century presupposition that the fire suppression ability of carbon tetrachloride relied on oxygen removal). In 1911, they patented a small, portable extinguisher that used the chemical. This consisted of a brass or chrome container with an integrated handpump, which was used to expel a jet of liquid towards the fire. It was usually of 1 imperial quart (1.1 l) or 1 imperial pint (0.57 l) capacity but was also available in up to 2 imperial gallons (9.1 l) size. As the container was unpressurized, it could be refilled after use through a filling plug with a fresh supply of CTC.
Another type of carbon tetrachloride extinguisher was the fire grenade. This consisted of a glass sphere filled with CTC, that was intended to be hurled at the base of a fire (early ones used salt-water, but CTC was more effective). Carbon tetrachloride was suitable for liquid and electrical fires and the extinguishers were fitted to motor vehicles. Carbon tetrachloride extinguishers were withdrawn in the 1950s because of the chemical’s toxicity – exposure to high concentrations damages the nervous system and internal organs. Additionally, when used on a fire, the heat can convert CTC to phosgene gas, formerly used as a chemical weapon.
In the 1940s, Germany invented the liquid chlorobromomethane (CBM) for use in aircraft. It was more effective and slightly less toxic than carbon tetrachloride and was used until 1969. Methyl bromide was discovered as an extinguishing agent in the 1920s and was used extensively in Europe. It is a low-pressure gas that works by inhibiting the chain reaction of the fire and is the most toxic of the vaporizing liquids, used until the 1960s. The vapor and combustion by-products of all vaporizing liquids were highly toxic, and could cause death in confined spaces.
The carbon dioxide (CO2) extinguisher was invented (at least in the US) by the Walter Kidde Company in 1924 in response to Bell Telephone’s request for an electrically non-conductive chemical for extinguishing the previously difficult-to-extinguish fires in telephone switchboards. It consisted of a tall metal cylinder containing 7.5 pounds (3.4 kg) of CO2 with a wheel valve and a woven brass, cotton covered hose, with a composite funnel-like horn as a nozzle. CO2 is still popular today as it is an ozone-friendly clean agent and is used heavily in film and television production to extinguish burning stuntmen. Carbon dioxide extinguishes fire mainly by displacing oxygen. It was once thought that it worked by cooling, although this effect on most fires is negligible. This characteristic is well known and has led to the widespread misuse of carbon dioxide extinguishers to rapidly cool beverages, especially beer.
In 1928, DuGas (later bought by ANSUL) came out with a cartridge-operated dry chemical extinguisher, which used sodium bicarbonate specially treated with chemicals to render it free-flowing and moisture-resistant. It consisted of a copper cylinder with an internal CO2 cartridge. The operator turned a wheel valve on top to puncture the cartridge and squeezed a lever on the valve at the end of the hose to discharge the chemical. This was the first agent available for large-scale three-dimensional liquid and pressurized gas fires, and was but remained largely a specialty type until the 1950s, when small dry chemical units were marketed for home use. ABC dry chemical came over from Europe in the 1950s, with Super-K being invented in the early 60s and Purple-K being developed by the US Navy in the late 1960s.
In the 1970s, Halon 1211 came over to the United States from Europe, where it had been used since the late 40s or early 50s. Halon 1301 had been developed by DuPont and the US Army in 1954. Both 1211 and 1301 work by inhibiting the chain reaction of the fire, and in the case of Halon 1211, cooling class A fuels as well. Halon is still in use today, but is falling out of favor for many uses due to its environmental impact. Europe, and Australia have severely restricted its use, since the Montreal Protocol of 1987. Less severe restrictions have been implemented in the United States, the Middle East, and Asia.