-
- Posts: 8
- Joined: Mon Dec 10, 2007 8:56 am
The following conditions were used for the analysis: flowrate 0.7 mL/min; eluent 0.005 M HClO4 aqueous solution/CH3CN = 50/50; oven temperature 40oC; UV/vis detector 220 nm.
However, i find that the RsPak De-413L is not able to separate these compounds (phenol, and guaiacol) and when analyzed in HPLC, it will come out together as 1 peak.
I notice when i analyzed the standard phenol and guaiacol only by its own it eluate at 10.3 and 10.4 minutes. But when it is analyzed together it will come out as 1 peak at 10.44 minute. Is there any advice on how i can separate out these 2 compounds. I have tried to change the wavelength from 220 to 280 and still no effect.