Flammability limit


Mixtures of dispersed combustible materials and oxygen in the air will burn only if the fuel concentration lies within well-defined lower and upper bounds determined experimentally, referred to as flammability limits or explosive limits. Combustion can range in violence from deflagration through detonation.
Limits vary with temperature and pressure, but are normally expressed in terms of volume percentage at 25 °C and atmospheric pressure. These limits are relevant both to producing and optimising explosion or combustion, as in an engine, or to preventing it, as in uncontrolled explosions of build-ups of combustible gas or dust. Attaining the best combustible or explosive mixture of a fuel and air is important in internal combustion engines such as gasoline or diesel engines.
The standard reference work is still that elaborated by Michael George Zabetakis, a fire safety engineering specialist, using an apparatus developed by the United States Bureau of Mines.

Violence of combustion

Combustion can vary in degree of violence. A deflagration is a propagation of a combustion zone at a velocity less than the speed of sound in the unreacted medium. A detonation is a propagation of a combustion zone at a velocity greater than the speed of sound in the unreacted medium. An explosion is the bursting or rupture of an enclosure or container due to the development of internal pressure from a deflagration or detonation as defined in NFPA 69.

Limits

Lower flammability limit

Lower flammability limit : The lowest concentration of a gas or a vapor in air capable of producing a flash of fire in the presence of an ignition source. The term is considered by many safety professionals to be the same as the lower explosive level. At a concentration in air lower than the LFL, gas mixtures are "too lean" to burn.
Methane gas has an LFL of 5.0%. If the atmosphere has less than 5.0% methane, an explosion cannot occur even if a source of ignition is present. From the health and safety perspective, the LEL concentration is considered to be Immediately Dangerous to Life or Health, where a more stringent exposure limit does not exist for the flammable gas.
Percentage reading on combustible air monitors should not be confused with the LFL concentrations. Explosimeters designed and calibrated to a specific gas may show the relative concentration of the atmosphere to the LFL—the LFL being 100%. A 5% displayed LFL reading for methane, for example, would be equivalent to 5% multiplied by 5%, or approximately 0.25% methane by volume at 20 degrees C. Control of the explosion hazard is usually achieved by sufficient natural or mechanical ventilation, to limit the concentration of flammable gases or vapors to a maximum level of 25% of their lower explosive or flammable limit.

Upper flammability limit

Upper flammability limit : Highest concentration of a gas or a vapor in air capable of producing a flash of fire in the presence of an ignition source. Concentrations higher than UFL or UEL are "too rich" to burn. Operating above the UFL is usually avoided for safety because air leaking in can bring the mixture into combustibility range.

Influence of temperature, pressure and composition

Flammability limits of mixtures of several combustible gases can be calculated using Le Chatelier's mixing rule for combustible volume fractions :
and similar for UFL.
Temperature, pressure, and the concentration of the oxidizer also influences flammability limits. Higher temperature or pressure, as well as higher concentration of the oxidizer, results in lower LFL and higher UFL, hence the gas mixture will be easier to explode. The effect of pressure is very small at pressures below 10 millibar and difficult to predict, since it has only been studied in internal combustion engines with a turbocharger.
Usually atmospheric air supplies the oxygen for combustion, and limits assume the normal concentration of oxygen in air. Oxygen-enriched atmospheres enhance combustion, lowering the LFL and increasing the UFL, and vice versa; an atmosphere devoid of an oxidizer is neither flammable nor explosive for any fuel concentration. Significantly increasing the fraction of inert gases in an air mixture, at the expense of oxygen, increases the LFL and decreases the UFL.

Controlling explosive atmospheres

Gas and vapor

Controlling gas and vapor concentrations outside the flammable limits is a major consideration in occupational safety and health. Methods used to control the concentration of a potentially explosive gas or vapor include use of sweep gas, an unreactive gas such as nitrogen or argon to dilute the explosive gas before coming in contact with air. Use of scrubbers or adsorption resins to remove explosive gases before release are also common. Gases can also be maintained safely at concentrations above the UEL, although a breach in the storage container can lead to explosive conditions or intense fires.

Dusts

Dusts also have upper and lower explosion limits, though the upper limits are hard to measure and of little practical importance. Lower flammability limits for many organic materials are in the range of 10-50 g/m³, which is much higher than the limits set for health reasons, as is the case for the LEL of many gases and vapours. Dust clouds of this concentration are hard to see through for more than a short distance, and normally only exist inside process equipment.
Flammability limits also depend on the particle size of the dust involved, and are not intrinsic properties of the material. In addition, a concentration above the LEL can be created suddenly from settled dust accumulations, so management by routine monitoring, as is done with gases and vapours, is of no value. The preferred method of managing combustible dust is by preventing accumulations of settled dust through process enclosure, ventilation, and surface cleaning. However, lower flammability limits may be relevant to plant design.

Volatile liquids

Situations caused by evaporation of flammable liquids into the air-filled void volume of a container may be limited by flexible container volume or by using an immiscible fluid to fill the void volume. Hydraulic tankers use displacement of water when filling a tank with petroleum.

Examples

The flammable/explosive limits of some gases and vapors are given below. Concentrations are given in percent by volume of air.
SubstanceLFL/LEL in %
by volume of air		UFL/UEL in %
by volume of air		NFPA ClassFlash pointMinimum ignition energy in mJ
expressed at percent by volume in air
Autoignition
temperature
Acetaldehyde4.057.0IA−39 °C0.37175 °C
Acetic acid 419.9II39 °C to 43 °C463 °C
Acetic anhydrideII54 °C-
Acetone2.6–312.8–13IB−17 °C1.15 @ 4.5%465 °C, 485 °C
AcetonitrileIB2 °C524 °C
Acetyl chloride7.319IB5 °C390 °C
Acetylene2.5100IAFlammable gas0.017 @ 8.5% 305 °C
Acrolein2.831IB−26 °C0.13-
Acrylonitrile3.017.0IB0 °C0.16 @ 9.0%-
Allyl chloride2.911.1IB−32 °C0.77-
Ammonia1528IIIB11 °C680651 °C
Arsine4.5–5.178IAFlammable gas-
Benzene1.27.8IB−11 °C0.2 @ 4.7%560 °C
1,3-Butadiene2.012IA−85 °C0.13 @ 5.2%-
Butane, n-butane1.68.4IA−60 °C0.25 @ 4.7%420–500 °C
n-Butyl acetate, butyl acetate1–1.78–15IB24 °C370 °C
2-Butanol1.79.829 °C405 °C
Isobutanol1.710.922–27 °C415 °C
n-Butanol1.411.2IC35 °C340 °C
n-Butyl chloride, 1-chlorobutane1.810.1IB−6 °C1.24-
n-Butyl mercaptan1.410.2IB2 °C225 °C
Butyl methyl ketone, 2-hexanone18IC25 °C423 °C
Butylene, 1-butylene, 1-butene1.989.65IA−80 °C
Carbon disulfide1.050.0IB−30 °C0.009 @ 7.8%90 °C
Carbon monoxide1275IA−191 °C Flammable gas609 °C
Chlorine monoxideIAFlammable gas-
1-Chloro-1,1-difluoroethane6.217.9IA−65 °C Flammable gas-
Cyanogen6.0–6.632–42.6IAFlammable gas-
Cyclobutane1.811.1IA−63.9 °C426.7 °C
Cyclohexane1.37.8–8IB−18 °C to -20 °C0.22 @ 3.8%245 °C
Cyclohexanol19IIIA68 °C300 °C
Cyclohexanone1–1.19–9.4II43.9–44 °C420 °C
CyclopentadieneIB0 °C0.67640 °C
Cyclopentane1.5–29.4IB−37 to −38.9 °C0.54361 °C
Cyclopropane2.410.4IA−94.4 °C0.17 @ 6.3%498 °C
Decane0.85.4II46.1 °C210 °C
Diborane0.888IA−90 °C Flammable gas38 °C
o-Dichlorobenzene, 1,2-dichlorobenzene29IIIA65 °C648 °C
1,1-Dichloroethane611IB14 °C-
1,2-Dichloroethane616IB13 °C413 °C
1,1-Dichloroethene6.515.5IA−10 °C Flammable gas-
Dichlorofluoromethane54.7Non flammable, -36.1 °C552 °C
Dichloromethane, methylene chloride1666Non flammable-
Dichlorosilane4–4.796IA−28 °C0.015-
Diesel fuel0.67.5IIIA>62 °C 210 °C
Diethanolamine213IB169 °C-
Diethylamine1.810.1IB−23 to −26 °C312 °C
Diethyl disulfide1.2II38.9 °C-
Diethyl ether1.9–236–48IA−45 °C0.19 @ 5.1%160–170 °C
Diethyl sulfideIB−10 °C-
1,1-Difluoroethane3.718IA−81.1 °C-
1,1-Difluoroethylene5.521.3−126.1 °C-
Diisobutyl ketone1649 °C-
Diisopropyl ether121IB−28 °C-
Dimethylamine2.814.4IAFlammable gas-
1,1-DimethylhydrazineIB-
Dimethyl sulfideIA−49 °C-
Dimethyl sulfoxide2.6–342IIIB88–95 °C215 °C
1,4-Dioxane222IB12 °C-
Epichlorohydrin42131 °C-
Ethane312–12.4IAFlammable gas -135 °C515 °C
Ethanol, ethyl alcohol3–3.319IB12.8 °C 365 °C
2-Ethoxyethanol31843 °C-
2-Ethoxyethyl acetate2856 °C-
Ethyl acetate212IA−4 °C460 °C
Ethylamine3.514IA−17 °C-
Ethylbenzene1.07.115–20 °C-
Ethylene2.736IA0.07490 °C
Ethylene glycol322111 °C-
Ethylene oxide3100IA−20 °C-
Ethyl chloride3.815.4IA−50 °C-
Ethyl mercaptanIA-
Fuel oil No.10.75-
Furan214IA−36 °C-
Gasoline 1.47.6IB< −40 °C 246–280 °C
Glycerol319199 °C-
Heptane, n-heptane1.056.7−4 °C0.24 @ 3.4%204–215 °C
Hexane, n-hexane1.17.5−22 °C0.24 @ 3.8%225 °C, 233 °C
Hydrogen4/18.375/59IAFlammable gas0.016 @ 28% 500–571 °C
Hydrogen sulfide4.346IAFlammable gas0.068-
Isobutane1.89.6IAFlammable gas462 °C
Isobutyl alcohol21128 °C-
Isophorone1484 °C-
Isopropyl alcohol, isopropanol212IB12 °C398–399 °C; 425 °C
Isopropyl chlorideIA-
Kerosene Jet A-10.6–0.74.9–5II>38 °C as jet fuel210 °C
Lithium hydrideIA-
2-MercaptoethanolIIIA-
Methane 5.0 / 4.4 14.3 / 17 IAFlammable gas0.21 @ 8.5%580 °C
Methyl acetate316−10 °C-
Methyl alcohol, methanol6–6.736IB11 °C385 °C; 455 °C
MethylamineIA8 °C-
Methyl chloride10.717.4IA−46 °C-
Methyl etherIA−41 °C-
Methyl ethyl etherIA-
Methyl ethyl ketone1.810IB−6 °C505–515 °C
Methyl formateIA-
Methyl mercaptan3.921.8IA−53 °C
Mineral spirits0.76.538–43 °C258 °C
Morpholine1.810.8IC31–37.7 °C310 °C
Naphthalene0.95.9IIIA79–87 °C540 °C
Neohexane1.197.58−29 °C425 °C
Nickel tetracarbonyl2344 °C60 °C
Nitrobenzene29IIIA88 °C-
Nitromethane7.322.235 °C379 °C
Octane1713 °C-
iso-Octane0.795.94-
Pentane1.57.8IA−40 to −49 °Cas 2-Pentane 0.18 @ 4.4%260 °C
n-Pentane1.47.8IA0.28 @ 3.3%
iso-Pentane1.329.16IA420 °C
PhosphineIA-
Propane2.19.5–10.1IAFlammable gas0.25 @ 5.2% 480 °C
Propyl acetate2813 °C-
Propylene2.011.1IA−108 °C0.28458 °C
Propylene oxide2.936IA-
Pyridine21220 °C-
Silane1.598IA<21 °C
Styrene1.16.1IB31–32.2 °C490 °C
TetrafluoroethyleneIA-
Tetrahydrofuran212IB−14 °C321 °C
Toluene1.2–1.276.75–7.1IB4.4 °C0.24 @ 4.1%480 °C; 535 °C
Triethylborane−20 °C−20 °C
TrimethylamineIAFlammable gas-
TrinitrobenzeneIA-
Turpentine0.8IC35 °C-
Vegetable oilIIIB327 °C -
Vinyl acetate2.613.4−8 °C-
Vinyl chloride3.633-
Xylenes0.9–1.06.7–7.0IC27–32 °C0.2-
m-Xylene1.17IC25 °C525 °C
o-XyleneIC17 °C-
p-Xylene1.06.0IC27.2 °C530 °C