yulinios:
One thing to clarify here. The analyzer indicates +/- 1,200 mg/Nm3. This is at standard conditions and the temperature and pressure conditions cited are merely the characterization of the environment the analyzer is sampling. I believe this is part of what 25362 means by his last statement, but I thought it could bear repeating and a little clarification. The theoretical equation is
(mg/m3)*(1/(1000*MW))*(0.0224m3/mol)= m3 of gas A/m3 of gas mixture
Where mg/m3 is the measured concentration from the analyzer, MW is the molecular weight of the chemical in question in grams/mol and 0.0224 is the volume of a single mole of an ideal gas at standard conditions (i.e., 0C and 1 atm.). The result of this calculation is cubic meters of the particular chemical species of interest per cubic meter of mixed gas. To convert to ppm, multiply the result by 10^6. Thus the final equation is:
(mg/m3)*(22.4/MW)= PPM or 1,200*(22.4/64.06) = 420 ppm
It appears the difference here between my result and 25362's is that I calculate a pure vapor phase density of 2.860 mg/ml, not the quantity used by 25362. I would expect this is a tabulated value based on laboratory results and is representative of the error introduced by the ideal gas assumption.