The frit assembly in a Cogent HPLC Column is a possible cause of blockage and resulting high pressures and other possible issues. For non UHPLC, the frit pore size is a distribution of sizes with an average of only 2um wide and therefore can be easily blocked by small un-dissolved sample. matrix or other particulate matter that was not filtered out during sample prep. The frits used in HPLC columns are actually compressed powders and therefore the consistency of pore size does vary a bit, with higher flow rates they become more susceptible to blockage.

Blockage is more likely at the inlet frit:. Frits can be removed and replaced but it is not recommended that you replace the frits as it is easy to disrupt the packing bed when the frit cap is off. Therefore, the best way to repair a blocked frit in your lab is to try to dislodge or dissolve the particle on the frit using solvents that the particle might be soluble in.

Place the column in a reverse direction on your HPLC system from what you were using it when it got blocked. Without creating any pressure shock, slowly and gently run 100% HPLC grade water through the column starting a 0ml/minute and holding the flow rate at 0.5ml/minute for 3.0 or 4.6mm ID columns. Hold at this flow rate for about 2-3 hours then reduce the flow rate gently back to 0ml/min. Using 100% Acetonitrile as the flow solvent, repeat the above. If this does not work, we have found the 50% Methanol: 50% Water also works for many biological samples as the flow solvent.

For 2.1mm ID columns, follow the same procedure but ramp the flow rate from 0ml/min to 0.05ml/minute.