Peruvian salt mines, seaside rust, HPLC precipitates and electrospray ionization – gas-phase ionic solids: is it all the same?
>> December 2, 2009



During a trip to Peru I visited a salt mine (not really a mine), where Peruvians directed a stream of salted water that came from a mountain to “pools” where it was dry out and the salt recovered.
The region was dry, few rainy days per year. But all place was covered with salt, I exclude the possibility of spills during rain for the reason I just described. The only possibility I see is salt carried by micro droplets during evaporation. You can see a photo at left.

Last month after my vacations I came back to work and saw some crystals growing from connection on HPLC (left), outside and inside the oven. No one had a previously leaking, the crystals came from the thin film of mobile phase from connections. Time was passing and during drying out the solvent carried the salt buffers over the metal. This explains how the salt covered the metal surface without a visible leaking but don’t explain how the mobile-phase evaporated so much without we see any leaking. By the way, we have leaking detector on ovens, and they work.
Anyone out there already did a 30% NaOH solution out a hood? Did you smell anything? Well, it seems that ionic solids are not so not-volatile as they taught to us…I think it follow that universal answer on chromatography: It depends of…
Last photo: Agilent Technologies.
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