by
lmh » Tue Jul 05, 2011 1:18 pm
Agreed with Peter, entirely! Gentle warming also helps the process (obviously drying solvent cools the sample; the energy for evaporation has to come from somewhere). If you can find a hot-block of some sort which fits your sample vessel(s), it will help (don't over-heat if your sample is labile).
For drying large numbers of samples of smallish volume, I once made a manifold consisting of a lunch-box attached to a nitrogen line, with loads of hypodermic needles stuck through at the correct spacing to match a dry-block heater we had in the lab. It was lethal (think compressed-air-driven explosive porcupine) but it did the job. Commercially you can get waterbaths with a nitrogen manifold fixed above them for this purpose.
When you're no longer a stressed grad student but a happy Professor, there's another bit of kit you might like to buy: it is possible to get shakers that have a hot-block that is orbitally shaken, and maintained under vacuum. The way these work is exactly the same as a rotary evaporator, but they can handle 20 samples at once.