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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?
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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
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
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