Overview The membrane pump that attaches to the Vapur interface used with DART should be optimized upon installation of a new unit. This document may also be referenced by a user looking to re-optimize their membrane pump. To optimize the pump we will be running the same standard while adjust the suction and then base the optimum setting off of the best signal response. Each pump setting should be run in doublet. Spot the 1-D Transmission or QuickStrip module with 3 ul of the Quinine Standard provided in your DART kit and allow samples to dry. Start with the needle valve one full turn out from all the way closed, as shown below.
Note: the valve has the 0 value facing up and is still in the red indicator of the needle valve Start an acquisition on your mass spectrometer, then using the FreeRun page on your DART, drive the first two samples through at .5mm/s and then stop the rail in between spots 2-3
Adjust the needle valve a quarter of a turn so it looks like the image below
In the same acquisition, using the FreeRun page on your DART, drive the next two samples through at .5mm/s and then stop the rail in between spots 4-5. Adjust the needle valve a quarter of a turn so it looks like the image below
In the same acquisition, using the FreeRun page on your DART, drive the next two samples through at .5mm/s and then stop the rail in between spots 6-7. Adjust the needle valve a quarter of a turn so it looks like the image below
In the same acquisition, using the FreeRun page on your DART, drive the next two samples through at .5mm/s and then stop the rail in between spots 8-9. Adjust the needle valve a quarter of a turn so it looks like the image below.
In the same acquisition, using the FreeRun page on your DART, drive the next two samples through at .5mm/s and then stop the rail at the end of the module and end the acquisition. Adjust the needle valve a quarter of a turn so it looks like the image below.
In a separate acquisition, using the FreeRun page on your DART, drive the first two samples through at .5mm/s and then stop the rail in between spots 2-3. Adjust the needle valve a quarter of a turn so it looks like the image below.
In the same acquisition, using the FreeRun page on your DART, drive the next two samples through at .5mm/s and then stop the rail in between spots 4-5. Adjust the needle valve a quarter of a turn so it looks like the image below.
In the same acquisition, using the FreeRun page on your DART, drive the next two samples through at .5mm/s and then stop the rail in between spots 6-7. Adjust the needle valve a quarter of a turn so it looks like the image below
At this point, you can end the acquisition, as you should have already passed through the optimum setting. Open up both acquisitions and pull out an extracted ion chromatogram for the 325 m/z. Determine which of the settings gave the best signal response and reset the needle valve to that value and lock it into place using the set screw (1.5 mm allen wrench )as shown below.
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