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- Posts: 6
- Joined: Tue Jul 08, 2014 12:52 pm
I am currently trying to develop a method to separate levoglucosenone, HMF anf levoglucosan in bio-oil samples.
I am using a Zorbax SB-C18 (4.6x250mm, 5µm) column set at 40°C. I initially got the following chromatogram which shows adequate resolution of the peaks.

However, these bio-oil samples also contain a number of other sugars that co-elute with levoglucosan (I ran a lot more sugars than are included on the chromatogram). I realise that I will not get good sugar separation using a C18 column, I would just like to get the levoglucosan peak more resolved from the other sugars. I am happy for all the other sugars to elute as one peak.
By slowing down the flow rate from 1 mL/min to 0.6 mL/min I was able to move the levoglucosan peak so that it was not directly co-eluting with the other sugars but it is still not in any way resolved! It also has the detrimental effect of broadening my HMF and levoglucosenone peaks!

As you can see so far I have only run isocratic. I believe I might be able to resolve levoglucosan if I introduce a gradient at the beginning of the run, however I am not entirely sure what would work best. I was going to start very basic with something like:
0 - 85:15 H2O:MeOH
5 - 80:20
10 - 80:20
15 - 85:15
I don't know whether this would work or I'd be doing completely the wrong thing!
Any help would be greatly appreciated.
Thanks
