New LC column pressure is too high

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

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I've been using a PEEK column (C18, 150mm, ID 4.6mm) on our lab's LC, and I tried switching the old column to a new one - it was exactly the same product with the same specifications. But my backpressure suddenly shot up with the new column - with my old column, with 50ul/min of water flow, I've been maintaining ~100bar. When I switched to the new one, now it's almost at 500bar and I don't understand how just switching the column to a system that has already been working well can dramatically increase the backpressure. Can anyone give me some suggestions?
Hello, how are you, it could be several things, it has happened to me several times.
As a guide I found this page that served me, I had low pressure actually "Faulty check valve".

It served me, I recommend it! 8)

Meaby
+Problem in pump, injector, in-line filter, or tubing.
+Obstructed guard column or analytical column.

https://whatishplc.com/hplc-troubleshooting/
What is the particle size of your column , is it sub 2 micron ?
With a flow rate of 50ul/min water flow and 100 bar pressure , it seems like you are using sub 2 micron.

If you are using a high concentration buffer as mobile phase , and connected the new column directly , a buffer precipitation might occurred and a very high pressure observed.

This is because of new columns come with a high concentration of organic solvent inside.

Before connecting the new column directly to a buffered mobile phase , a water rich wash step may be necessary.
You are using a peek column? Maybe the connection is the problem. Do you use a finger tide fitting, do you have stainless steel or peek capillaries? Just cut a little bit of your capillary and connect the capillary fresh with your column. Nothing should be wrong with the column. Don't do body building when you connect a column!

Good luck and stay healthy!
Gerhard Kratz, Kratz_Gerhard@web.de
Column probably stored in ACN, are you sure the pressure difference is just not from pushing the storage ACN off the column, then it will go down to typical levels? I would flush gently with 20 to 50 column volumes and see if the pressure decreases to typical levels as a first step. Solvent fronts can create a lot of back pressure. Especially on small 2.5µ and smaller particles.
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