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- Posts: 1
- Joined: Sat Nov 12, 2011 9:28 pm
The molecules of interest range from monosaccharides to about 600 daltons.
We are using an affinity ligand to achieve a fairly high purity in a single run but would like to cycle though successive runs as fast we can without excessive zone broadening during elution.
I looked up the Van Deemter wiki page and found the relationship: linear flow rate (u) = (B/C)^0.5 where B is the diffusion coefficient, which I believe I can estimate and C is the resistance to mass transfer coefficent, which I don't know how to come up with. In fact I am not sure this is really the equation to use.
If anyone has some thoughts/suggestions to share on a theoretical approach to the problem of establishing a practical "speed limit" I would be very grateful.