wg48temp9
National Hazard
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What is the difference between flash chromatography and dry chromatography?
I have looked up what the difference between dry vacuum chromatography and flash chromatography is. Apparently the only significant difference in the
apparatus is the column in dry chromatography is packed dry with some compression. Do I have that correct ?
So given the same amount (mass) and type of the stationary phase with identical column diameters and solvent, the separation with both will be very
similar. Is that correct?
I am wg48 but not on my usual pc hence the temp handle.
Thank goodness for Fleming and the fungi.
Old codger' lives matters, wear a mask and help save them.
Be aware of demagoguery, keep your frontal lobes fully engaged.
I don't know who invented mRNA vaccines but they should get a fancy medal and I hope they made a shed load of money from it.
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S.C. Wack
bibliomaster
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How to pack probably depends a lot on the silica gel available and the difficulty of separation. The original lit. speaks of this "cheaper" TLC-mesh
gel. Maybe it was all fines from making larger sizes then. Probably became more expensive and hard to find quick. Especially without additives. Maybe
if you own a ball mill...
There's many ways to do column chromatography. The only difference is the column is run dry, since pressure was never a requirement for other forms.
https://www.erowid.org/archive/rhodium/chemistry/index.html
the chromatography section
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Texium
Administrator
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The way that I typically set up a column is I first add the amount of silica gel that I want to use. Then I add enough solvent to the column to make a
slurry of the silica, and shake it until it has all become a nice slurry. Then I let it rest for a few minutes to equilibrate and let the solvent soak
into the silica gel (this is important because otherwise you’ll get a lot of air bubbles). Finally I apply compressed air to finish compacting the
column and push out any excess solvent until the top of the silica is exposed but not dry. Then I add my sample as a solution in as low of a polarity
of solvent as it is readily soluble in, and gently apply compressed air until it is loaded onto the column (once again, the top of the silica should
be exposed but still moist). Then I add a little sand and carefully pour in the first round of eluent, and it’s ready to run.
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