Preparation of ultrahigh molecular weight polyacrylonitrile and its terpolymers

• Published in: Journal of applied polymer science 1995-12, Vol.58 (11), p.2067-2075
• Main Authors: Zhang, C., Gilbert, R. D., Fornes, R. E.
• Format: Article
• Language: English
• Subjects: Applied sciences; Exact sciences and technology; Organic polymers; Physicochemistry of polymers; Polymerization; Preparation, kinetics, thermodynamics, mechanism and catalysts
• ISSN: 0021-8995; 1097-4628
• DOI: 10.1002/app.1995.070581119

The synthesis of high molecular weight (in excess of 106 million Daltons) poly(acrylonitrile) and poly(acrylonitrile‐co‐methylacrylate‐co‐itaconic acid) is described. An inverse emulsion polymerization formulation with AIBN as the initiator was used. However, polymer precipitation occurred early in the polymerization. In each case, the molecular weight distribution was surprisingly narrow (M̄w/M̄n ∼ 1.5). Conversion vs. time plots with monomers containing the inhibitor had the “S” shape typical of emulsion polymerizations. The terpolymer composition and molecular weight were quite uniform throughout the polymerization. With inhibitor‐free monomers, the initial molecular weights were very high (∼ 3 × 106 Daltons), but gelation occurred at ca. 50% conversion. There was an inverse relationship between the monomer inhibitor content and the polymer molecular weight. It is suggested that the growing polymer radicals are occluded in the precipitated polymer particles and are terminated by inhibitor diffusing into the particles, accounting for the narrow molecular weight distribution. © 1995 John Wiley & Sons, Inc.