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552.3 inlet degradation of analytes

Discussions about GC and other "gas phase" separation techniques.

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has anyone run into analyte degradation in the inlet of your GC? Had the method optimized for a quick runtime, but there were a few caveats and the SOP was getting a little difficult so i went back to the method suggested oven program and gained MCAA and lost DCAA... Any ideas?
This happens many times. With pesticides, carbamates, flame retardants..

If decomposition happens in teh LINER you need to eliminate Glass wool (take a double gooseneck or a cyclosplitter), Use LOWER injection port temperatures (using splitless injection you can us eMUCH lower temperatures as you inject during long time), or use PTV or even better: cold -on-column.

If decomposition happens in the column:(you can see by peak-shape): Make sure we minimize elution temperatures by:
Using Highest flow rate , Flow programming, columns with THIN films, SHORT length and preferrable H2 as carrier gas.
For instance for the BFR's we developed a special "fast" columns based on EPA1614.

rgsd
jaap de zeeuw, Restek corporation
2 posts Page 1 of 1

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