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Problem with separation of ketone and its diketone impurity
Posted: Tue Aug 28, 2007 11:28 am
by martas
I have problem with separation of ketone of saturated cyclic hydrogencarbon and its diketone impurity.
Does anybody have some idea how to perform GC analysis? Is derivatisation possible?
I use Ultra-II column, 50 m length.
Thank you for your comments,
Martas
Posted: Thu Aug 30, 2007 10:13 pm
by HbJ
Please tell us (the forum) your temperature program, the other dimensions of the column (internal diameter, film thickness), your injection parameters (injector temperature, split), type and pressure of carrier gas and if you can resolve the two peaks at all.
Generally speaking an OV-7 (20% phenyl/80%methylsilicone) might do the job as that phase allowed me to separate a quite similar analyte quite well.
Re: Problem with separation of ketone and its diketone
Posted: Fri Aug 31, 2007 5:23 am
by martas
Chromatographic conditions in detail:
Column: HP Ultra–2, 50 m x 0,32 mm, film 0,52 um
Carrier gas: helium, 1,2 ml/min
Injection volume: 1 µl
Temperature programme: 150 °C - 2 min, gradient 15 °C/min to 250 °C, 20 min
Injector temperature: 220 °C
Detector temperature: 280 °C
Splitter: 30 : 1
M.
Posted: Sun Sep 02, 2007 1:32 am
by HbJ
Why are you using such a steep gradient (15°/min!) with a column of 50m?
And what are the boiling points of your analytes? (hint: exploit the differences!)
What solvent do you use? (or do you inject the undiluted sample?)
But anyway you might try the following method:
150°C/5 min => 5°C/min => 250°C/20 min.
Then check if the peaks resolve and please tell us if you resolve your peaks now.
Posted: Fri Sep 07, 2007 11:37 pm
by HbJ
What's the current state of affairs?