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- Posts: 4
- Joined: Wed Sep 14, 2016 9:36 am
This is my first post to this forum so please excuse me if miss someting.
We are setting up a GC system to check residual solvent, however we are having some headaches.
We have made a standard solution consisting of 0,1% ethanol and 0,01% acetonitrile. Analysing this solution with our system, we are finding that the peaks from ethanol are behaving much more erratic than acetonitrile. In Our last run we had six samples, yielding a 16% RSD for ethanol and 7% for acetonitrile. This is a very typical result. We have recently had service on the system, and both injector and FID has been replaced. Switching to a new column had no effect. What are we missing. Why are ethanol giving so poor precision of the peak-area of ethanol?
The system is GC-FID
1:3 split
140 oC injector, 250 oC detektor.
program;
5 min @ 50 oC
10 degrees/min to 130 oC
2,7 ml/min helium flow
Head Space PAL system
10 ml head Space vial
4950 µl water 50 µl sample
45 min @ 80 oC incubation
90 oC Needle temp
1 ml injection volume
Syring flushed With helium between injections
