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- Posts: 7
- Joined: Wed Apr 01, 2015 6:25 pm
I have some experience in chromatography but I am an absolute beginner concerning classic detectors like the FID. (I did a lot of stable isotope work using IRMS in the last years). Now I am in the position to re-establish a lab to measure CH4 in lowest amounts (4 mL of air STP, lowest concentrations: 350 ppb CH4).
What I found in that lab is a bottle with N2/O2 = 60/40. From my manual I expect AIR = N2/O2 = 80/20.
Furthermore I reconstructed that my forerunners (not available) used an old Varian GC (approx. late 1980s) with the following flow rates for the FID:
H2 = 30 mL/min
60/40 N2/O2 = 330 mL/min
N2 = 20 mL/min
Carrier = He = 5-10 mL/min
I assume N2 was used as make up gas.
Can anyone explain, why someone would use N2/O2 = 60/40?
Could it be that this increases sensitivity for lowest amounts of CH4?
Could it fade out a disturbing species (like CO)?
Could it be that N2 was not used as make up but to dilute the 60/40 mix?
Any hints are welcome. My only knowledge on this is from textbooks and the manual (saying: air, no specs on N2/O2 ratio). Please forgive if essential info is missing here, please tell me what I forgot.
My new GC will be a: Agilent 7890B equipped with a FID for capillary columns only.
Thanks!
Michael
