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- Posts: 106
- Joined: Tue Jun 09, 2009 9:25 pm
Ive created a calibration sequence that does a heptane blank, the 5 standards, a reagent blank, and then another heptane blank. All the chromatograms look great, sharp peaks, little noise, no peaks where there shouldn't be, theyre all increasing in the amounts they should be . And I have figured out how to integrate the peaks and clean out the noise and auto scale. But I just need help for what comes next, any tips? Any links to literature that might be helpful. I did find one agilent e seminar that was pretty helpful. Thanks!