shifting retention time of acetone

Discussions about gel permeation chromatography / gel filtration chromatography / size exclusion chromatography

3 posts Page 1 of 1
Hi, I am currently on a method development of GFC and I am very new on this technique. I use polystyrene sulfonate as standards and acetone as a maker of the exclusion volume of the column. However, the retention time of acetone seems different under different mobile phase. At a flow rate of 1ml/min, the retention time of acetone is 12.5 min in 100% water, 11.9min in 75% 10mM/20mM phosphate buffer + 25%ACN, 11.5min in 65%10mM/20mM phosphate buffer + 35%ACN, 13.8min in 80% (50mM phosphate buffer + 0.1M NaCl) + 20% MeOH. This is confusing me since there should be no secondary interactions between acetone and the column matrix, theoretically, the retention time should be the same, unless there are some fundamental that I missed since I never use SEC before.

Every time before changing the buffer, I flushed the column thoroughly with water and 30%ACN, it shouldn't be the retention problem (the retention times are very reproducible under each mobile phase). I also noticed that even the calibration curve made with polystyrene sulfonate are not linear at the low Mw, the slope became less steep, which also confuse me.

I wonder if acetone is a good marker for the exclusion volume, and how can I determine the exclusion volume at its optimal condition (all the secondary interactions are suppressed to the minimum)? More importantly, can anyone tell me why the calibration curve became less steep at the lower Mw?

Many thanks in advance!
This is something that is indeed fundamental to liquid chromatography. The packing support material will swell and change shape depending on what it is soaked in (the mobile phase). Those changes affect the available internal and external surface area inside the column (the packed TUBE or Cylinder). This is why changes in column void volume can be measured and why we both estimate AND measure it using the specific method conditions that we plan on using. So column void volume (and exclusion times in your case) will be constant for the same mobile phase.
PS: I should have also mentioned that to get a quick check of where the the theoretical exclusion volume (time) is for your method, watch for the injector's pressure pulse (blip) on the baseline. This hardware artifact is a reliable indicator of where the void volume is and is not subject to absorption effects.
3 posts Page 1 of 1

Who is online

In total there is 1 user online :: 0 registered, 0 hidden and 1 guest (based on users active over the past 5 minutes)
Most users ever online was 599 on Tue Sep 18, 2018 9:27 am

Users browsing this forum: No registered users and 1 guest

Latest Blog Posts from Separation Science

Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.

Subscribe to our eNewsletter with daily, weekly or monthly updates: Food, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.

Liquid Chromatography

Gas Chromatography

Mass Spectrometry