kappie
Chemical
- May 5, 2010
- 3
Hi,
the concept of LOC does it relate to adiabatic flame temperature?
LOC is the point in ppO2 where the gas mixture does not combust when you try to ignite it. Combustion defined as: no flames, no explosion. Slow (flame-less) oxidation is possible though below LOC.
When I have a combustible gas mixture with a vol% O2 slight above the LOC (say O2 = 12% where the LOC = 10%). When this mixture is ignited will the flames stop when the oxygen vol% has depleted to 10%? Or does the flame continue until all oxygen is depleted?
I would guess it continues because that would explain why for instance in a methane fed gas burner, the max adiabatic flame temperature is reached at stoichiometric air supply. So, apparently all methane is combusted in a burners despite the O2 falling below the LOC of methane (which is temperature dependent ofcourse) during burning.
In other words: Is the concept of LOC one-way directed?
thanks if you can shine some light here
Kappie
the concept of LOC does it relate to adiabatic flame temperature?
LOC is the point in ppO2 where the gas mixture does not combust when you try to ignite it. Combustion defined as: no flames, no explosion. Slow (flame-less) oxidation is possible though below LOC.
When I have a combustible gas mixture with a vol% O2 slight above the LOC (say O2 = 12% where the LOC = 10%). When this mixture is ignited will the flames stop when the oxygen vol% has depleted to 10%? Or does the flame continue until all oxygen is depleted?
I would guess it continues because that would explain why for instance in a methane fed gas burner, the max adiabatic flame temperature is reached at stoichiometric air supply. So, apparently all methane is combusted in a burners despite the O2 falling below the LOC of methane (which is temperature dependent ofcourse) during burning.
In other words: Is the concept of LOC one-way directed?
thanks if you can shine some light here
Kappie