by
Victor » Tue May 16, 2006 8:59 pm
I agree with mjf's reasoning on this one, and with Peter Apps.
The problem with using wool ( are you using ordinary glass wool?) is that the increased surface area this provides may cause reversible or irreversible adsorption of strongly polar solutes. Presumably, you are not using samples with such "active" consituents, otherwise you might have encountered these problems already. It is possible that such problems might be limited somewhat if you used quartz wool, but I wouldn't bet on it. For such samples I might be inclined to start with an empty liner or even an empty liner one where the sample has to perform contortions (their are many designs available from companies like Restek) to encourage the volatilization of less volatile solutes-if that is what you are talking about by saying "less volatile material".