I was initially hired to GCMS and HPLC for my position. We’ve received an HPIC Integrion later on which I’ve been so happy to work on to learn a new instrument. Unfortunately, things get busy on the GCMS/HPLC side and we don’t use HPIC for a lot of projects. I feel like HPIC has fallen on the back burner as a result of the demands of my job. No one touches the instrument when I’m away either, which I later learned was a big no-no for HPIC. Lately, I’ve found carryover/contamination in some of my runs and I haven’t been able to figure out why. Part of the reason is the nature of my work and I think the stress/overwhelm from my job is also clouding my judgement. I’ve been able to figure out the following with what I know but I cannot come to a conclusion yet:
- The peak shows up in almost every run, even after equilibriating the system for more than an hour.
- I do see carryover of other analytes in my runs, but they are so small, the results are practically zero. And they don’t show up as frequently as sodium. The sodium is the only thing that remains consistently present.
- We hand wash a lot of glassware. I suspect the contamination is from the injection side or sample prep. Sometimes, we use salt for certain extractions
for GC
- and I do think
that people leave salt on the bench at times
- . It’s hard to say if we rinse the glassware efficiently enough because everyone washes and rinses differently. I even prerinse my glassware
with 18 M Ohm water too
. I also tried to fill deionized water in a glass bottle that’s
for single use purposes and
I
- still see the peak in my runs.
I know sample storage isn’t always recommended in glass… but we don’t have much else at the moment.
4. My method is calibrated to Push Full at the moment. I have considered doing Push Partial but I haven’t had the time to look into it.
5. We used to run an end method with high eluent concentration and still saw the sodium peak when starting a new sequence.