BHT peak in every injection

We have an Agilent 7890B GC coupled with a 5977E MSD. When we first buy the instrument, in every injection we were having a huge BHT peak covering all of the chromatogram. The support engineers tried almost every thing and at last changed the inlet. After 5 years of use we started the same problem. This time BHT is not covering the chromatogram, it is only a peak. When method parametres changed, the peak shape and retention time changes. Therefore I thought it was not comming from the Helium. Multiple injections of the same solution (even blank hexane) have BHT peaks, in the same RT but with different altitues. Sometimes it is a peak, sometimes a planar height but RT is always the same. When I checked the same solution with another equipment, no BHT.

I changed septa, liners and injectors millions of times.I changed washer and gold ring multiple times. I put a oxygen/water trap between the instrument and the helium tube. I dismantled the split/splitless inlet and clean every part of it with isopopyl alcohol and other solvents. I washed and cleaned the split vent valve tubing. But BHT is always there. Changing peak shapes and heights, but in the same RT (if method, flow, temp cahnges RT changes).

Because of BHT splitless injection and low concentration analysis is totaly imposible. In split injection, we have the BHT.

I gently want to ask you if anyone experienced the same problem.

We analyse essential oils diluted in hexane in split mode and sythetic markers in splitless mode. No BHT ever entered our lab.

Thanks in advance

Parents
  • Are you sure it's BHT?  Would you please share a spectrum of the peak?   I wonder if it is 207 amu...column background/column bleed....

    One way to see if a peak is coming from before the injection port.

    1. Edit your normal run method parameters to make two new ones. Make one with the initial oven time only 0.0 minutes and one with the initial oven time 10.0 minutes.
    2. Bake the system at the final oven temperature for a while…like an hour.
    3. Manually run the method with a 0.0 minute initial oven time.
    4. Manually run the method with the 10.0 minute initial oven time.
    5. Compare the contaminant peak areas.
    6. If the 10.0 minute hold peak area is larger, there is the possibility that the peak is being cold-trapped on the head of the column during the 10 minute time. If the peak areas are about the same, there’s a higher chance that the stuff is in the column.
Reply
  • Are you sure it's BHT?  Would you please share a spectrum of the peak?   I wonder if it is 207 amu...column background/column bleed....

    One way to see if a peak is coming from before the injection port.

    1. Edit your normal run method parameters to make two new ones. Make one with the initial oven time only 0.0 minutes and one with the initial oven time 10.0 minutes.
    2. Bake the system at the final oven temperature for a while…like an hour.
    3. Manually run the method with a 0.0 minute initial oven time.
    4. Manually run the method with the 10.0 minute initial oven time.
    5. Compare the contaminant peak areas.
    6. If the 10.0 minute hold peak area is larger, there is the possibility that the peak is being cold-trapped on the head of the column during the 10 minute time. If the peak areas are about the same, there’s a higher chance that the stuff is in the column.
Children
No Data
Was this helpful?