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Thanks.
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Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
You are correct. An ordinary instrument can halve the plate count e.g. an ordinary HPLC gave 6000 and an optimized system gave 14,000 plates for a 100x2.1 mm i.d (home packed column). Still the reduced plate height is not near the perfect one (~ 2). The instrument is in a perfect condition for minimum extra-column effects (< 5% contribution to peak variance).Farooq, are you evaluating the 2.1-mm i.d. columns on an HPLC system that's been set up for 4.6-mm i.d. columns? If so, then peaks from the 2.1-mm i.d. column will exhibit severe fronting, due to diffusion into the excessive extracolumn volume. The column itself may be fine. The solution is to increase the flow rate - thereby reducing the time available for diffusion - or to use shorter connections with narrower i.d.'s. Also, use a detector cell with a volume of 1-2 µl instead of the more usual 8-9 µl.
Thanks. I noticed that there is another school of thought which just thinks the opposite. They use ultrahigh pressures to pack microbore and capillary columns (e.g. 25,000 psi to 60,000 psi). With normal packing pressures it seems that the wall area is too tightly packed and the central core is loose in narrow i.d. columns. This gives rise to severe tails since the wall is so close to the injected band in a narrow column.Gerhard is correct.
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