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- Posts: 25
- Joined: Fri Jul 25, 2008 1:42 pm
At this point the best peak shape and best separation has been an isothermal method.
Initial temp: 240C
Final Hold: 30 min
While the separtaion has vastly improved over the first few methods I was working with there is still quite a bit of coelution around where I expect to see the C16-C18 peaks.
Would it be easier to derivitize, dry and then return my sample to solution or have others obtained resonable results from underivitized fatty acids on PEG columns?
Another method that has provided resonable separation, less co-elution, but awful peak shape is:
Initial Temp: 120C
Initial hold: 2min
Ramp: 15deg/min
Final Temp: 240C
Final hold: 30min
All of my samples have used either DMF or Methylene chloride as a solvent. MCl seems to provided slightly clearer results on the carbowax column. Usually our derivitizing agent has been 1% TMCS. Much of this analysis was previously (and currently) done with derivitized samples on a restek Rtx-50 column.
