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- Posts: 3
- Joined: Fri Oct 20, 2023 7:35 pm
Does anyone know a better way to clean the flow cell to get a lower LU response? Is my concern about the masking of impurity detection unfounded?
Thanks in advance,
G
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Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
Thanks for your reply. My suspicion that the flow cell was dirty was due to use of the same column on a different FLD showing a markedly different baseline starting point (around 0.3 LU).Look at the signal-to-noise ratio (average of several calculations) for one of your analytes. Compare the value you have now and the value you had a year ago. The rise of the baseline level (and noise) and the increase in the baseline slope upon gradient elution is more likeky caused by the dirty column than by the dirty FLD cell.

Indeed there is a 4uL and an 8uL flow cell. I am using the 8uL. Might be something I could look into. Thanks!Does that detector come with different flow cell options?
I'm hearing that longer cells are problem-prone... but that may just be the cells for UV/Vis.

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