hollerg
Chemical
- Mar 22, 1999
- 97
I need to control degradation when I renovate an existing evaporator to run at a lower pressure, but at a higher level of moisture removal from an organic acid. The equipment has an external exchanger, with a 100 to one circulation to product discharge rate and a 50 to one inventory to product discharge rate. Temperature rise is only a few degrees each pass. Back-pressure suppresses boiling in the tubes to prevent salts from fouling the surface.
For degradation that doubles for every 10 C rise in T, is there a relationship to apportion the relative contribution of the damage the heat exchanger surface temperature causes and the degradation in the bulk @ the flash temperature?
Your suggestions on how to deal with the heat exchanger contribution in the recycle loop, would help a great deal
I hope to perform preliminary engineering of surface area, heat transfer enhancement or volume reduction while waiting on the kinetics to be measured.
Thanks for suggestions.
Gary
For degradation that doubles for every 10 C rise in T, is there a relationship to apportion the relative contribution of the damage the heat exchanger surface temperature causes and the degradation in the bulk @ the flash temperature?
Your suggestions on how to deal with the heat exchanger contribution in the recycle loop, would help a great deal
I hope to perform preliminary engineering of surface area, heat transfer enhancement or volume reduction while waiting on the kinetics to be measured.
Thanks for suggestions.
Gary