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what is the cause for the diffusing peak

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

17 posts Page 2 of 2

YM,
It seems the difference is setting of PDA detector and UV. Could you pls check , if you are using any reference wevlength in your PDA?? if yes turn it off and rerun your samples. I have seen if your peak of interest fall between reference wevlength range it will not show in PDA, whereas in UV there is no such setting.

JM

JM,
Thank you for the asking and I am sorry to be late.
After I check my instrument method setup I failed to see any reference wavelength though I did see "interpolate 656nm". Is this you talking about? Or would you mind let me know how to do the check or turn on/off? Thanks again
Excel
17 posts Page 2 of 2

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