I'm currently designing a continuous distillation column for the recovery of solvent from a mixture of acrylic acid and other components.
It will be operatuing under vacuum (13 kPa) with a feed vapour fraction of about 80%.
Based on this I decided a packed distillation column would be suited for this type of separation.
I'v gone through the procedures for calculating the column dimensions (Packed Colum Design, Cheresources / Coulson & Richardson volume 6) but I'm getting crazy dimensions. I'v come out with a column diameter of 58 meters and a height of 12.5.
I'v attached a diagram of this column and a snapshot of my spreadsheet, perhaps someone will spot what the problem is and lead me in the right direction.


Note: Area = mass vapour flow in rectifying section / V*w
I can't find anything wrong with my calculations so I'm guessing it's to do with my high flowrates?
This is my feed to the column

Regards
Greg
Edited by -G-, 03 March 2011 - 03:32 PM.