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- Posts: 9
- Joined: Mon Feb 26, 2007 11:58 am
http://www.sigmaaldrich.com/europe/acet ... vings.html
There is a useful calculator and a good article about switching to Methanol.
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Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
It is almost as simple as the area math discussed by several previously.Also, has anyone tried going to 3.0 mm ID columns? If so, was it very difficult?
My "modified" Agilent 1100 prep system uses either a 70 litre ( for 50mm diameter ) or 40 litre ( for up to 30mm diameter columns ) cheap plastic garage bins ( or unused lab sharps bins ) as the column heater water tank with a 1/2" pump thermocirculator providing the temperature control. It can control to 80C OK.But I'm doing preparative HPLC work right now and it is a heck lot harder to switch over to methanol as I haven't been able to find any sensible way to heat the mobile phases up to reduce backpressure at the flow rates that the separation needs to run at.
That's something that we have in mind but as you say, its not really portable or convenient in any way (ie. corrosion, changing temp will take a long time).My "modified" Agilent 1100 prep system uses either a 70 litre ( for 50mm diameter ) or 40 litre ( for up to 30mm diameter columns ) cheap plastic garage bins ( or unused lab sharps bins ) as the column heater water tank with a 1/2" pump thermocirculator providing the temperature control. It can control to 80C OK.
I'm not entirely certain, but I think as the Fused Core columns (ascent express / halo) offer higher efficiencies then switching to a shorter column should see no loss of plate count. There is another document on the Supelco website which which compares a 250mm 5um column with a 100mm Fused Core column and the N for Diaepam is roughly the same.I don't think the calculator at the site mentioned in the last post is terribly smart. When you switch from a 25 cm 3 micron column to a 15 cm 2.7 micron column, you loose nearly half your plates. This should not be the purpose of a proper scaling exercise.
I couldn't get my old boss to understand how this was possible, even though it is a "text book" case. You have my sympathies......elute between fragrance ingredient #1 and fragrance ingredient #2. ...When we removed ACN and substituted a similar percentage of methanol, API eluted AFTER fragrance ingredient #2 and before fragrance ingredient #3...
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