THE 2-MINUTE RULE FOR HPLC COLUMN SELECTION

The 2-Minute Rule for hplc column selection

The 2-Minute Rule for hplc column selection

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Having said that, failing to find out what clogged a column can don't just end in complications but in addition inconsistencies and inaccuracy down the road for a whole lab.

Distorted or doublet peak styles: Analyze your peaks. Doublet peaks final result from the blockage with the frit of a column, resulting in aspects of a homogenous sample to maneuver in the column at various instances.

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A related procedure is much more compact and less complicated to manage. During this webinar, we give an overview on tips on how to configure the Resolute® BioSC.

Method enhancement and production can have to deal with many different resins starting from small to huge particles, from slender to extensive distribution of particle size and from comfortable to rigid, maybe even brittle particles.

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Improved strain about several injections: This happens when sample components bit by bit accumulate in the frit or beginning in the column. Preserve a logbook of pressures prior to and immediately after operates that can help recognize these troubles.

Researchers and analysts will have to carefully pick more info the suitable column sort and situations for his or her distinct analytical demands to achieve precise and trusted final results.

Improved throughput from enhanced yields and quicker run occasions, benefitting from higher capability and ready-to-use formats

For those who detect issues with any of the above, here then it’s time to wash your HPLC column. Acquire the subsequent ways to restore the column to its former glory: Identify the events primary as much as the trouble. Did a fresh form of sample get injected? Was the strategy transformed to research a sample?

Initial, wash the column with different solvents in a lower stream level. Even so, In case your column is so clogged that it may possibly’t movement in any respect, flip the column and operate it in the alternative way.

Molecular size and condition: Bigger or irregularly shaped molecules need a wider pore size inside the stationary section.

When the column is flipped and reinstalled on 1 close, you'll be able to begin jogging your program with cleansing solution, that may be found in our guide during the website link down below.

In this kind of chromatography, retention is based on the attraction amongst solute ions and billed internet sites certain to the stationary phase.

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