I am using DCM ( dichloromethane) in my research, as a solvent. At the end of the day I have to separate the salute and measure it. Up until now, I have been using a constant temperature oven, set a about 65 degree Celsius (evaporation temp of DCM). The exhaust DCM is expelled into the atmosphere and the dried salute is then cooled down and measured.
I want to replace the oven with a rotary evaporator. However I have an argument with my advisor. He claims that I require two things:
- Aspirator /vacuum pump
- Draft Chamber
While I agree that a vacuum pump can be of use, I do not require my solvent to boil, therefore I do not need vacuum.
As for the draft chamber, I completely fail to see its implication. I believe that since the rotary evaporator is a completely closed system, there is no way DCM vapor could leak, rendering the draft chamber useless.