Re: Any Rule of Thumb for Peak Fronting
Posted: Fri Aug 24, 2012 12:48 pm
If the local pH is changed the eluant species in competition with the analyte could change. In the case of a carbonate buffer, if the analyte zone causes a decrease in pH this will increase the bicarbonate ion concentration which is a weaker displacing ion (also lower ionic strength).I fully agree with Carl, as my experience goes right in this direction: low ionic strenght in buffers in IEC causes "strange" peak behavior.
I agree with both of you that low ionic strength can alter pH "local" pH if we have mass overload, but recall that if we are dealing with an strong anion exchanger, it's behaviour should be independent of pH. So still the fundamental reason of low ionic strength eluent showing strange peak shape stands unclear.