peak fronting
Grant </p>
Answers
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Dear Harringg,
It is most likely a bad fitting at the column inlet or outlet. Fitting become worn or are not seated properly. Please see the attached power point titled "split peaks" it contains experts from several sources. It shows several examples of poor chromatography resulting from poor fittings or other issues. I hope that you find it useful.
Patty
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Thanks for the information. I'll pass it along to the UPLC operator, and reply back. From what I've observed here in the lab, all mobile phase, s/w solvents, sample diluent, injection volume, etc... is correct. The only thing left would be either a fitting or a bad column. Putting the "old" column on the peak spliting/fronting went away. Maybe the new column isn't seating properly.
Thanks.
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