Content-Transfer-Encoding: |
8bit |
Sender: |
|
Subject: |
|
From: |
|
Date: |
Fri, 28 Apr 2006 11:53:46 -0500 |
Content-Type: |
text/plain; charset="US-ASCII" |
MIME-Version: |
1.0 |
Reply-To: |
|
Parts/Attachments: |
|
|
Sue,
I can't think of anything offhand given this level of information other than
data analysis. It is possible for the chromatography to be "pretty good" but
the integration parameters for the early compounds may not be usable for the
later compounds, and this effect will be on the level of per mil in my
experience. As long as it is consistent between samples and standards there
is no analytical problem per se, but to track the effect in more detail you
will have to manually integrate the isotope peaks.
John
-----Original Message-----
From: Stable Isotope Geochemistry [mailto:[log in to unmask]] On Behalf
Of Susan Ziegler
Sent: Friday, April 28, 2006 11:29 AM
To: [log in to unmask]
Subject: [ISOGEOCHEM] GC-C-IRMS issues
Hello All:
I am seeking any possible hints to solve a problem that has developed
in our GC-IRMS system.
At the moment the suite of standards we run for d13C of FAMEs in
order to check for consistency no longer exhibits a constant
correction factor across all the compounds in each standard
chromatogram which range from 14:0 through 23:0 in size. In fact we
are seeing greater depletion in 13C for the longer (or later RT)
FAMEs by as much as a few per mil relative to the first compounds
(14:0). I have been trying to isolate the variables and this is what
I've found so far:
1. Flow is constant throughout the entire GC run (2 mL/min).
2. CO2 injected throughout the run remains constant in it isotopic
composition so does not exhibit the depletion see in compounds that
must be combusted.
3. I figured it must be the combustion column so it has been replaced
and we are again seeing the same problem.
4. Peak shape looks pretty good with widths remaining within 15-20s
and fairly sharp ratio traces. The ratio traces do become a little
broader with the last few more deplete compounds but not particularly
worse than runs where we've gotten good consistent values.
We are using an Agilent (HP) 6890 GC with a split/splitless injector
in splitless mode. I have changed the septa (done frequently
anyway), liner, and the gold seal and washer. The GC column is very
new but also has been cut (`0.5m) to see if reactive sites may have
been a problem. We are using the metal Valco cross piece and have
been now for years without a problem, could this have developed
active sites that may yield such symptoms?
Thanks for any information anyone might have regarding this
problem...I've been at this for some time now and am in danger of
pulling out all my hair!
Best regards,
Sue
|
|
|