Translator for HPLC HINTS and TIPS for Chromatographers

Showing posts with label Buffer. Show all posts
Showing posts with label Buffer. Show all posts

Saturday, October 31, 2020

Capillary Electrophoresis (CE) Troubleshooting Tips:

What follows is a short list of problems, "observations" followed by a list of areas that should be investigated, as appropriate in parenthesis (), to troubleshoot common problems seen when using the analytical technique of capillary electrophoresis, CE, CZE.

 Observation (Investigate for cause):

            Excessive Baseline Drifting up or down

·         Temperature is not stable (stabilize room and/or capillary temperature).

·         Fouling of capillary (replace or clean and wash capillary with fresh, filtered solution).

·         Current levels unstable (loose connections, partial obstruction in capillary or running out of buffer solutions).

·         Capillary may have poorly cut ends resulting in poor connections or flow (replace capillary).

Excessive Signal Noise

·         Detector has air in flow cell (purge capillary and wash flow path).

·         Current level may be too high (reduce current).

·         Detection parameters, wavelength and bandwidth, may be inappropriate for buffer solution (select appropriate detection settings which are appropriate for the buffer used and selective for the analyte).

Loss of Signal

·         Voltage/Current has turned off (turn ON or investigate if system is in “alarm” state due to an error).

·         Detector parameters not selected.

·         Capillary has not been fully equilibrated (equilibrate capillary and auto-zero the scale).

·         Baseline offset may be off-scale (after equilibration, adjust scale or auto-zero).

·         Detector lamp(s) off, not ignited or due for replacement (verify lamp operation).

Signal Peak Shape Issues

·         Truncated, clipped or ‘square’ peaks (sample overload, reduce concentration 10x, shorten load time and re-evaluate).

·         Tailing peaks often result from very high current or when the concentration of buffer is too high (lower the current and/or reduce the buffer concentration, then re-evaluate).

·         Sampling rate may be too low (measure the peak width in units of time (i.e. seconds), then configure the detector to insure that the sampling rate allows for at least 20 points to be collected per average peak width (30 points is a better target # to use).

·         No peaks observed (Many possible causes, including: Partially or fully obstructed capillary, broken capillary, out of buffer, no injection, detector settings inappropriate for analysis, current too low, pressure too low. Look for a small peak from the injection along the start of the baseline to confirm that an analysis was started, then troubleshoot the method and settings).

            General Stability and Noise Issues 

·   When the CE system has not been used in a few days, salts from the buffer solution(s) may deposit on and clog the capillary line, flow cell and/or sensors. To avoid these problems, be sure to thoroughly clean, flush and wash down the flow path before use. Take the time to prepare fresh filtered solutions (each day) and allow time for the system to equilibrate. Taking these basic steps will avoid many hours/days of frustration.

Saturday, December 26, 2015

Common pKa Values for ACIDS & BASES used in HPLC and LC/MS Method Development





pKa (25°C)                              ACID
0.3                                           Trifluoroacetic acid
2.15                                          Phosphoric acid (pK#1)
3.13                                          Citric acid (pK#1)
3.75                                          Formic acid
4.76                                          Acetic acid
4.76                                          Citric acid (pK#2)
4.86                                          Propionic acid
6.35                                          Carbonic acid (pK#1)
6.40                                          Citric acid (pK#3)
7.20                                          Phosphoric acid (pK#2)
8.06                                          Tris
9.23                                          Boric acid
9.25                                          Ammonia
9.78                                          Glycine (pK#2)
10.33                                        Carbonic acid (pK#2)
10.72                                        Triethylamine
11.27                                        Pyrrolidine
12.33                                        Phosphoric acid (pK#3)



Notes: (1) This is a general list of commonly used acids & bases for chromatography applications and not meant to be a comprehensive list of all values. (2) TFA is an overused and very strong acid for many chromatography applications. It also has strong ion pairing properties and can result in high UV noise, vacuum degasser and/or MS contamination. If you must use it, try and use the lowest concentration which results in the desired pH. Example: 0.1 % TFA ~ pH 2.0, 0.02% TFA ~ pH 2.7. (3) Formic acid is a popular alternative to TFA for many applications, esp LC/MS. (4) Not all acids/bases provide "buffering" on their own.

Reference: CRC Handbook of Chemistry & Physics.

Saturday, May 30, 2015

HPLC Peak Tailing - Some of the Most Common Reasons For it



Three easy ways to minimize chromatography peak tailing:

(1) Tailing often results from using “Type – A” HPLC silica. Type-A silica often contains more acidic silanol groups and metal impurities than Type-B. To improve peak shape, use modern “Type – B” silicas which are of higher overall purity, have less metal contamination and feature minimal silanol ionization under higher pH conditions.



(2) Minimize ionic interactions and utilize a buffer or ion pairing agent (e.g. TFA 0.02%) in your mobile phase. Select a buffer that is at least 2.0 pH units away from your sample's pKa and use the smallest concentration or amount that gets the job done. For LC/MS or MS/MS applications, remember to only use volatile buffers and avoid the use of ion pairing agents unless absolutely necessary (and if used, use at the lowest possible concentration to avoid source contamination).



(3) Always use a freshly washed and equilibrated column. Is the column fouled or the inlet frit dirty? If the head of the column is fouled from sample overloading or from a failure to wash off strongly retained compounds from many runs (much more common problem), then your peak shape and reproducibility will suffer. Incorporate a washing step in between your analysis methods which utilizes a solvent which is stronger (in concentration) than your mobile phase to wash off any strongly retained material after each run. For example, if you normally end a method with an 80% concentration of ACN, utilize a separate wash method which has 95% ACN in it. Allow enough wash time for this work.

Saturday, June 14, 2014

Popular LC/MS and HPLC Volatile Mobile Phase Modifiers

For applications which utilize an Evaporative Light Scattering Detector (E.L.S.D.), Charged Aerosol Detector (CAD) and/or Mass Spectrometer Detector with Electrospray Ionization source (e.g. LC/MS, MSD or LC/MS/MS), a fully volatile buffering system is usually required. Many of the common HPLC buffers such as sodium or potassium phosphate are not compatible.Use the smallest amount of buffer which provides buffering under the analysis conditions (e.g. 10mM). *Select a buffering agent (or modifier) which are within 2 pH units (+/- 1) of the sample's pKa and 2 pH units away from any acid's pKa. 

  • For LC/MS applications: Positive ion mode favors acidic mobile phases and Negative ion mode favors basic mobile phases. However, feel free to experiment using both ionization modes and don't forget about using adducts (e.g. ammonium and sodium) with all types of samples to improve signal response. *Maintain these buffers at or below 10 mM. Adjust the pH of the mobile phase to be 1 to 2 units away from your sample's pKa.

Table 1:  Popular examples of useful volatile mobile phase buffers, modifiers and/or additives.

BUFFERING/MODIFIER AGENT                                   USEFUL pH RANGE
  • Ammonium formate                                 2.8 - 4.8; 8.2. - 10.2
  • Formic Acid                                            3.3 - 4.3
  • Pyridine/Formic Acid                               3.3. 4.3, 4.8 - 5.8
  • Trimethylamine/Formic Acid                     3.3 - 4.3, 9.3 - 10.3
  • Ammonium Acetate                                  3.8 - 5.8; 8.2 - 10.2
  • Acetic Acid                                              4.3 - 5.3
  • Trimethylamine/Acetic Acid                      4.3 -5.3, 9.3 - 10.3
  • Ammonia/Formic Acid                              3.3 - 4.3, 8.8 - 9.8
  • Ammonia/Acetic Acid                               4.3 - 5.3, 8.8 - 9.8
  • Ammonium Bicarbonate                           5.9 - 6.9,  8.8 - 9.8
  • Ammonium Carbonate                              5.9 - 6.9, 8.8 - 9.8  
  • Carbonic Acid                                            6 - 8 (pKa 6.37/pKb 7.63)
  • 1-Methylpiperidene                                   10.0 - 12.0  

  • Trifluoroacetic Acid (TFA)                        pKa = 0.3 (WARNING when used with MS
                                                                                     systems!).  See notes #2 and #4 below.           
*Notes: (1) Formic acid (3.75) is slightly stronger and more volatile than Acetic acid (4.75). Formic acid is often available in higher purity grades and absorbs less in the UV region making it a better choice for most chromatography applications. It works well in positive mode LC/MS analysis, esp at 0.1%. (2) Trifluoroacetic acid (TFA, pKa = 0.3) is very strong and volatile, but we do not recommend its use in LC/MS applications as it can increase the background signal levels (esp. in Negative Mode) LC/MS (m/z 113), be very hard to remove from the source and result in long term instrument contamination. Difluoroacetic acid (DFA) and ammonium formate are other alternatives as they offer good ion pairing capacity with less ion suppression problems. (3) Triethylamine (TEA, pKa 11) is volatile, strong and very stable, but causes similar contamination problems resulting in high background signals when used in Positive Mode LC/MS (m/z 102). (4) Many ion-pairing reagents suppress ionization, bind to the plastics and metals used and contaminate the flow path. If you must use them, please do so using the lowest possible concentrations levels and thoroughly decontaminate the entire flow path of the system after use (or dedicate the MS system to use with them only). Minimize further contamination by labeling and using a dedicated column for the application (Do not use that same column exposed to ion pairing compounds for any other methods or applications). (5) Acids and bases alone provide little "buffering" so should be used with a secondary buffering species to resist change in pH.