A distorted peak or a sudden pressure spike can ruin a whole sequence of injections. The good news is that most HPLC column problems follow predictable patterns, and you can usually fix them in minutes once you know where to look. This guide covers the three most common issues: peak tailing, peak splitting and high backpressure, with practical causes and solutions.
Many problems blamed on the column actually come from the system. Start with these questions:
If a new column behaves normally, the old one is the culprit. If not, look at the injector, tubing, fittings, and mobile phase.
| Symptom | Most likely cause | First thing to check |
|---|---|---|
| Peak tailing | Silanol interaction, overload, dead volume | Mobile phase pH, injection amount, fittings |
| Peak splitting | Strong sample solvent, blocked frit, column void | Sample diluent, guard column |
| High backpressure | Blocked frit, buffer precipitation | Pressure with column removed |
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