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- Posts: 12
- Joined: Wed Feb 12, 2014 1:32 pm
A few months ago I started observing my internal standard reducing in intensity over the first 16-24 samples by around 90 %, then after perhaps 50 + samples the signal would start to come back. (retention times remain very steady)
After a weekend of being left in standby the signal comes back to full strength and takes about 25 samples before the sensitivity starts to drop with a rate of decline is lower than if the MS gets used on consecutive days.
I’ve cleaned the source and ion tunnel numerous times (Sonicated in 50 % MeOH 20 min, followed by 100 % MeOH for 20, dried under N2) I’m careful with what I inject ensuring the divert valve only switches from waste when the analytes elute. I’ve been running the same types of sample for a long while now without seeing any change in sensitivity (apart from the usual cone contamination over time) and have not otherwise seen a gradual decline of sensitivity over a longer period.
I have a daily standard consisting of 4 compounds of varying polarity/lipophilicity (caffeine, Nalidixic acid, Glafenine, Fenofibrate) and find the same issue when running these so it’s not down to a specific compound or property.
Whilst the water is refreshed fairly often the organic phase comes from a 2.5 L bottle of MeCN which has been there for quite a while. The air inlet is filtered so there shouldn’t be anything contaminating the solvent but is there anything that could have been absorbed from the air that would cause this?? Clutching at straws I know but I’m not sure where else to look.
I’ve run a Gas collision cleanliness test with reserpine monitoring at 609.8>195.5, 1000>195.5 and 2000>195.5 with 20+ direct injections and found absolutely no cross talk between channels.
If there is contamination on the MS 1 quad (looking very likely) can this charge gradually then dissipate that charge whilst still remaining adherent? Do lipids behave like this?
Any insight or opinions would be gratefully received!
Thank you
Marcus
