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- Posts: 37
- Joined: Thu Jul 19, 2012 6:21 pm
So: Dean's switch or just put two columns in and run low flow on the column not in use?
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Discussions about GC-MS, LC-MS, LC-FTIR, and other "coupled" analytical techniques.
I think we used a 0.1mm ID transfer line to be the restrictor in the setup I mentioned above. Forgot to mention that. It works similar to the old "no-vent" adapters but you can use a longer piece of transfer line for more restriction if needed.The problem with trying to set a low flow on a column going to an MS is that the minimum pressure drop is 1 bar because the end of the column is in a vacuum. If you want to have two columns connected all the time you will need a restrictor through the transfer line, with the columns T-eed onto that.
Peter
The Quickswap is an insert that screws onto the end of the transferline and is fed helium from an auxilary EPC at psi. There is a capillary that goes through the transferline that is 100um that provides flow resistance. So at 4psi and 280 deg C and 17cm 100um diameter there is ~ 1.3 ml/min going into the mass spec so you set your column flow less than that or when doing pulses you increase the aux epc pressure as well then set it back down after the pulse.Hi MSChemist - what is the agilent quickswap? I am running into problems with 2 capillary columns (one for purge and trap) and the other for SPME/headspace going to one mass spec and huge air leaks. They also have a OPD hooked up so multiple connections and am looking for a better way of doing it to limit my leak issues.
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