Wax Column Peak Doubling

This is more than likely inlet/sample introduction related and not the column. Column problems typically result in peak shape issues and not 20 to 36 seconds between peaks of different sizes.

How big are the peaks in Scan mode - what abundance?  What is your scan threshold?  Do you get any peaks running a blank solvent injection?

Hello, 

Thanks for your reply. Yes I agree that it would be weird for the column could cause this. Usually peaks broaden and exhibit weird shapes or split a bit. I changed column as a last resort / sanity check. Note column is wax column and it was getting older / had been through some abuse. 

This is full scan mode. Scan range 35-350amu. Scan threshold is 0 (maybe I want to increase that at some point?). Blanks are very clean (especially after doing all this maintenance and rigorously troubleshooting for potential sources of contamination). No carryover has been observed during this testing and isn't normally an issue with sample analysis. Note I am using a thermal desorption unit (TDU from Gerstel) with a cooled injection system (CIS4 from Gerstel, essentially a PTV inlet) as injection / inlet. The TDU/CIS has a lot that can go wrong compared to a normal split/splitless inlet. Thermal desorption tubes / adsorbents are also potential sources of contamination / problems. I've ruled out adsorbents and thermal desorption tubes as issue. This all started after running fatty food samples at somewhat higher then recommended temperatures likely loading contaminants onto liner / beginning of column. However, initially the problem resolved after liner change but quickly came back when I was doing more method development on the difficult sample type.  

Here is an example for 2-methylpyrazine in the same standard mix before and after column change. This is similar change I've seen when changing liner. Meaning bigger 'double' peak before changing liner (when it was obviously contaminated) versus after changing. Sometimes it goes to zero and there is no double peak at all which is how it should be and how it used to be before this problem started. 

Small 'double' peak before changing column was 3% (peak area: 642848.38) relative to main peak (peak area: 22204619.8)

Small 'double' peak after changing column is 0.5% (peak area: 94081.87) relative to main peak (peak area: 19398497.65). Ignore retention time shift this is due to different column. 

Have you resolved this problem?

Sort of. Gerstel uses what are called GraphPack-2M adapters with silver seals to connect column into their CIS inlet (PTV inlet). So I removed old adapter and installed a new one with new silver seals. I also clipped and reinstalled column. The problem went away for the most part. But it came back after a few months of use. Changed liner it went away for a while but came back. Cut column and it went away for a while but came back. Changed column and it seems to have gone away again. But I'm not totally convinced its column. It could be anything from TDU/CIS liners / adapters or column. 

If performing normal user maintenance makes the problem go away for a while, that is a good clue. When this occurs, does that little peak, or any peaks, show up if you run a method blank without the peaks of interest?   The small peak is 0.7 minutes early - 42 seconds or so. Is it from a previous run leftover or contamination in a valve or vent line or somehow getting on the column before the peak of interest - like trap breakthrough or too high a temperature or.... other Gerstel related effect?  

Thanks for reply. Blanks are clean and no evidence of carryover otherwise. It could be trap breakthrough or degradation. In most recent iteration of this problem it started when using Tenax-TA thermal desorption tubes.

It could also be 'active' sites in the inlet (opposite of deactivated). The problem is a bit mysterious in that not all compounds are effected in the same manner. For example using an alkane mix (for retention index calibration) I don't see this issue. But compounds with alcohol groups or esters and especially nitrogen rings (like pyridines or pyrazines) are more effected by the problem. 

It could also be the liners / column inlet not focusing compounds properly. I've tried different liner types glass wool versus glass beads and haven't really been able to nail down if thats issue. I generally trap at -120C using glass wool liners. 

If I dilute samples I can dilute away the double peak but its proportional when you look at a range of concentrations. So it doesn't seem like an overloading issue.