Abstract
Evaporation paths were calculated for aqueous solutions of polyethylene oxide (PEO) and polypropylene oxide (PPO) from the phase diagram. With the exception of solutions with a predominant fraction of one of the polymers the evaporation gave rise to phase separation for intermediate water contents. With similar restrictions for the fractions of the polymers the separated phase contained greater amounts of water and of PPO. In the two-phase region two consolute points were found, one at lower water content and greater PPO content; the other one with the opposite extremes. The difference in the composition of these two points was significantly greater for the polymers, approximately 0.4, than for the water content, less than 0.1. As a consequence there was a transfer of each polymer and of water between the phases during the evaporation. The evaporation of water took place preferentially from the phase with less water and more PEO, and in addition water as well as polymers was transferred from this phase to the one with less water and greater amount of PPO. The versatility of the phase diagram approach was demonstrated by displaying the variation in phase ratios and phase compositions as function of water weight fraction, water weight, and weight of the water evaporated. Another example of the same feature was a simple equation to obtain the amount of water to be added to a mutual solution of the two polymers in order to obtain the two phases in equal amounts.
The authors express their sincere gratitude to professors Malmsten and Linse, who not only provided the original values of the phase diagrams, but also for their encouragement and valuable comments. Besides, this work was supported by the National Nature Science Foundation of China (No. 20633010 and 20773106).
Notes
Part of the special issue, Surface and Colloid Chemistry Without Borders: An International Festschrift for Professor Per Stenius on the Occasion of His 70th Birthday.