Article
Licensed
Unlicensed Requires Authentication

Devolatilization with Chemical Reaction in Polymer Solutions

  • , and
Published/Copyright: May 28, 2013
Become an author with De Gruyter Brill

Abstract

It has been observed previously [1] that under the specific conditions prevailing in a reflux flask reactor, the overall rate of the transesterification reaction between an ethylene and vinyl acetate copolymer and 3-phenyl 1-propanol can be enhanced appreciably by the introduction of boiling inert hydrocarbon solvents. In the present study, the same reaction carried out under a controlled removal of vapors in a simulator emulating a non-intermeshing counter-rotating devolatilization twin screw extruder, a significant acceleration of the reaction rate has also been observed. In agreement with the previous work [1], the intrinsic reaction mechanism and the chemical equilibrium do not appear to be affected by boiling of the inert hydrocarbon solvents, nor does the additional mechanical agitation due to the rapid bubble growth contribute to the increase of the overall reaction rate. Theoretical analysis of the results confirms that the acceleration of the reaction rate originates from the localized mass transfer effect connected to the presence of the bubble vapor-liquid interface films induced by devolatilization.


* Mail address: Prof. J. Th. Lindt, Department of Materials Science and Engineering, University of Pittsburgh, 848 Benedum Hall, Pittsburgh, PA 15261, U.S.A.

Received: 1993-12-1
Accepted: 1995-11-3
Published Online: 2013-05-28
Published in Print: 1996-09-01

© 1996, Carl Hanser Verlag, Munich

Downloaded on 5.4.2026 from https://www.degruyterbrill.com/document/doi/10.3139/217.960228/html
Scroll to top button