by
vahur » Tue Aug 13, 2013 10:37 am
Details, details, details, we need details!
Mobile phases & gradiemt?
High- or low-pressure mixing?
Detector & settings?
Do the dips always occur st the same times in the run?
My apologies, thought this could be a textbook type of problem. Mobile phase is 10 mM ammoniumformiate pH=9,5/MeOH with a 90/10 start to 15min and then up to 10/90 in 5 minutes. Column is waters Xbridge c8 (150 mm 5 um). Detector is DAD (220nm). I don´t know if its High- or low-pressure mixing (machine is Agilent 1260 infinity). The dips have occured in one run only so far so I can not say if they have the same tr every time.