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- Posts: 25
- Joined: Tue Jul 03, 2012 2:33 pm
Any ideas? My analytes are in the mass range of 140-200 D, which is what I've set the MS to scan for.
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Discussions about GC-MS, LC-MS, LC-FTIR, and other "coupled" analytical techniques.
I'm not sure if that was the problem, but one thing I did that really improved the signal was used 0.1% acetic acid for my ACN/H20 reverse phase LC-MS. Adding the acid really improved the signal.I assume your negative peaks are in the total ion chromatogram? What this usually means is that you have a background ion (it might be something like a phthalate from the solvent, background ions are almost impossible to exclude completely), and the ionisation of the background ion is inhibited by an analyte that is eluting. This means the signal goes down rather than up. It can happen even when the analyte doesn't itself make a signal at all.
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