Effects of pairwise, donor–acceptor functional groups on polymer solubility, solution viscosity and mist control

• Published in: Polymer (Guilford) 2009-12, Vol.50 (26), p.6323-6330
• Main Authors: David, R.L. Ameri, Wei, Ming-Hsin, Kornfield, Julia A.
• Format: Article
• Language: English
• Subjects: Applied sciences; Donor–acceptor interactions; Exact sciences and technology; Extensional rheology; Mist control; Organic polymers; Physicochemistry of polymers; Properties and characterization; Solution and gel properties
• ISSN: 0032-3861; 1873-2291
• DOI: 10.1016/j.polymer.2009.10.032

Homologous series of functionalized polymers were used to compare the solution properties of donor–acceptor (DA) interpolymer mixtures with those of self-associating and non-associating polymer analogues. Polymer analogous synthesis was used to produce a series of polymers from a specific, anionically-polymerized prepolymer (1250 kg/mol polybutadiene), using thiol-ene coupling to incorporate systematically-varied contents of side groups: either tertiary amines (as proton acceptors) or carboxylic acids (both as proton donors in donor–acceptor mixtures, or as self-associating moieties in single-polymer solutions). Comparison with controls reveals that, relative to the effects of self-associations, DA interpolymer interactions more strongly affect solution properties such as phase behavior, interpolymer aggregation, shear viscosity, and elastic response in extensional flow. Specifically, DA associations lead to (i) greater reductions in polymer solubility in hydrocarbon solvents, (ii) interpolymer aggregation into larger clusters, and (iii) greater shear viscosity in solution. Nevertheless, DA associations reduced solution elasticity and mist suppression—a highly unanticipated result in light of the prior literature. [Display omitted]