Thx for reply,
Some more specification,
Solvent used in the impinger is of constant volume, and it does not evoporate considerably even after 300min.
I know the volume of gas I am passing through the impinger,
Trouble is . 1) Calibration curve is obtain from the liquid solution
2) while back calculating for concentration in ppm from the impenger , I have to take into account that this will be gas phase
So If I dont consider this change I take into account :
[ A] Response Factor (RF)= Slope from calibration curve
Analyte concentration CA [mg/L] = (RF) * GC area (from impenger solution)
[C] Correct flow SC[L/min] = Sample flow * ( BP – PW / 760) * ( 293 / (273 + t) )
BP = Pressure at time of sampling , mmHg
PW = Partial pressure of water vapor at time t , mmHg
t = Ambient temperature at time of sampling , ºC
[D] Stock concentration, ppm = (CA / MW) *(22.4 / SC * ST) * 10E6
MW = Molecular weight of MeS
ST = Sampling time
Where I am going wrong !!!!?
If you make up the solvent in the impinger to a constant volume after bubbling the gas through, then the only other parameter you need to know is the volume of gas which has passed through the impinger.
The measured concentration in ppm from the GC analysis can be used to calculate the amount of MeS collected from the gas. if you know the volume of gas which passed through the impinger you can calculate the MeS concentration in the gas.
If you add a fixed volume of solvent to the impinger, you may get evaporative loss during the bubbling process which will affect your result. I've found it's always better to make up the impinger contents to a fixed volume after the fact.