Posted by : kaushik zala Saturday, March 5, 2011


Symptoms of Column Fouling
Since many HPLC methods are run isocratically, it is not unusual to have situations where mobile phase strengths are adequate for eluting compounds of interest but are not strong enough to elute strongly retained compounds. In these cases, chromatographic performance will deteriorate as more and more non-eluting compounds build up on the column stationary phase.
Some of the symptoms of column fouling are
             increases in back pressure
 changes in retention times
 peak broadening or tailing and
 loss of resolution
Column Regeneration
The performance of a fouled, reversed-phase column can often be restored by purging the column with a strong eluting solvent such as 100% acetonitrile. If this does not restore column performance follow the column regeneration procedure described on the next page before opening or discarding the column. A procedure to regenerate normal phase columns is also included.

Regeneration Procedure for
Reversed-Phase Columns


  1. Disconnect the column and reconnect it to the chromatograph with the flow through the column in the reversed direction.
  2. Flush out any salts/buffers with HPLC grade water. Pump 25 mL of water through the column at 1 mL/min.
  3. Flush column with 25 mL of isopropanol.
  4. Flush column with 25 mL of methylene chloride.
  5. Flush column with 25 mL of hexane.
  6. Flush column again with 25 mL of methylene chloride.
  7. Flush column again with 25 mL of isopropanol.
  8. Reconnect the column to the chromatograph with the now in the proper direction. Flush the column with the mobile phase without the buffer, then re-introduce the buffer.
  9. Equilibrate the column with 25 to 50 mL of mobile phase.
  10. Inject a standard or a sample to see if performance is restored.
Note:
For some retained compounds that have fouled the column, dimethyl-formamide may be a better "cleaning" solvent than methylene chloride and hexane.

Regeneration Procedure for
Normal-Phase Columns


  1. Connect the column to the chromatograph with the flow in the reversed direction.
  2. Flush column with 50 mL of 50:50 methanol:chloroform.
  3. Flush column with 50 mL of ethyl acecate.
  4. Reconnect the column in the proper flow direction.
  5. Equilibrate the column with 50 mL of mobile phase.
  6. Inject a standard or a sample and evaluate performance.

Caution
In general, it is worth trying to clean and back flush an HPLC column with appropriate solvents before trying to replace the frit. There is always a danger that small amounts of packing material may be lost when a frit is replaced and column efficiency will decrease. In addition, the use of an 0.5 µm in-line filter to capture particulate material and routine column washes with an appropriate strong solvent are highly recommended.



1 comments

  1. માહિતી ખરેખર કામ ની છે.
    બાય ધી વે, માની લે કે એ રીતે કોલમ ને રી-જનરેટ ના કરીએ તો નવી કોલમ લેવાનો ખર્ચો કેટલો આવે?

    ReplyDelete

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