by
JA » Mon Sep 01, 2008 8:45 pm
Chandrasekhar,
Perhaps you can clarify on what you have observed experimentally? I agree with CPGuy that what you have asked is rather ambiguous but I will take a shot at a few possibilities. Further info on these can be found by using the search utility on this forum;
- strong solvent effect (mismatch with mobile phase)
- analyte lability (reaction)
- analyte/impurity solubility (ppt after injection)
Depending on the specific shape of your distorted peaks and anything you have seen to improve the situation, e.g. use of alternative diluent, injection volume or sample concentration, people might be able to better answer your question.