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Why SEC column go

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

5 posts Page 1 of 1
Hi

Why do SEC column go “badâ€

The silica SEC columns come with a surface modification which may react. Of course the silica itself can react and thus change. Then accumulation of "dirt" can cause surface changes or plugging. I don´t see so much diffrence to columns used for adsorption chromatography.

I'm sure part of the reason lifetime may vary depends on what the actual packing material is made of. Silica packing may fail for different reasons compared to cross-linked styrene-divinyl benzene packing. I've been using a cross-linked polymer column for SEC analysis for about 3 years now, and its still kicking.

The swelling and shrinking of the cross-linked polymer packing in various solvents over time may possibly cause unwanted flow channels within the packing material. Thats my opinion, though I may be wrong.

If you use the SEC column for the seperation of biological sample, you would find the column would quite fast get dirty . :cry:
Hi,

A few years ago I was using an inline carbon analyzer as one of my detectors for SEC. At first I tried to use a Waters SEC column but it was apparently bleeding carbon steadily, and creating a high and unstable baseline in the carbon detector. However, I switched to a Tosoh Biosciences TSK column and it has undetectable bleed. Some columns are more stable than others.....

Dave
5 posts Page 1 of 1

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