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Topic: Marker for Anion-Exchange Ion Chromatography  (Read 3166 times)

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Offline harmonslide

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Marker for Anion-Exchange Ion Chromatography
« on: February 07, 2010, 02:23:11 PM »
I'm trying to find a marker (unretained analyte) for an ion chromatography analysis, with little luck. We are using a NaHCO3/Na2CO3 buffer as the eluent on an anion-exchange column (quaternary ammonium) and utilizing eluent suppression at the end to replace all the cations with hydronium.

The system uses a conductivity detector, which picks up the analytes of interest (fluoride, bromide, phosphate) nicely, but it would be helpful to have an unretained marker here to be able to calculate tm and hence retention factors, selectivity factors, etc. Cations are exchanged, anions are detected but also are retained by the column; I don't know any neutral compounds that might be useful for the conductivity detector.

Is anyone here familiar with IC methods? Is there a marker that I'm just missing here? How is the void time usually calculated if not? The only other thought I have would be finding the column's void volume and flow rate and estimating from there, but that seems more cumbersome than necessary.

Offline MOTOBALL

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Re: Marker for Anion-Exchange Ion Chromatography
« Reply #1 on: February 09, 2010, 07:10:56 PM »
Can you continuously pass a low-level solution of a salt that would give a constant signal at the conductivity detector---then inject a purely covalent compound (e.g., acetone) that is not expected to be retained (and will not precipitate the inorganic salt), and that would not have a response.  Your chromatogram would then show the compound as a negative peak on the trace.

If you try this (or any variant) please let us know if it works or not.

Motoball

Offline harmonslide

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Re: Marker for Anion-Exchange Ion Chromatography
« Reply #2 on: February 15, 2010, 04:47:58 PM »
That's a good idea --- I might try that if I have a chance. We did end up observing a negative peak for the solvent front when the sample matrix composition (it was pretty simple, just various salts in a carbonate buffer) was sufficiently different from the eluent; problem *apparently* solved!

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