Flow synthesis of medium molecular weight polyisobutylene coinitiated by AlCl3. (July 2016)

• Record Type: Journal Article
• Authors: Zhu, Shan; Lu, Yangcheng; Wang, Kai; Luo, Guangsheng
• Is Part Of: European polymer journal. Volume 80(2016:Jul.)
• Page Start: 219
• Page End: 226
• Publication Date: 2016-07
• Subjects: Cationic polymerization -- Isobutylene -- Medium molecular weight -- Flow synthesis; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; Polymerization; Polymers; Periodicals; Electronic journals; 547.705
• DOI: 10.1016/j.eurpolymj.2016.01.034
• Languages: English
• ISSNs: 0014-3057

Abstract

Graphical abstract: Highlights: Study flow polymerization of isobutylene coinitiated by neat AlCl3 in hexane–CH2 Cl2 . Obtain 20–100 kDa polyisobutylenes at temperatures from −30 °C to −10 °C. Decrease reaction time for quantitative conversion to 6 s. Propose chain transfer dominated polymerization mechanism. Recognize effects of diluent on active species transformation. Abstract: In this work, we established a microflow reaction system, and systematically investigates the flow synthesis of medium molecular weight polyisobutylene (MPIB, 10, 000–100, 000 g mol −1 ) coinitiated by neat AlCl3 in the mixture of hexane and CH2 Cl2 . It includes (1) revealing the effects of mixing conditions and the evolution of polymer products, (2) proposing chain transfer dominated polymerization mechanism with considerations on the possibilities or rates of various chain reactions, (3) exploring the effects of diluent from the viewpoint of active species transformation to guide for the selection of diluent, (4) evaluating the effects of temperature to find a window capable of producing MPIBs with adjustable molecular weight, and (5) testing the polymerization process in high monomer concentration to enhance the productivity. Exploiting the perfect performances of a microflow system in mixing and residence time control, the adjustable molecular weight in the range from 20, 000 to 100, 000 g mol −1 was afforded at relative high temperatures (−30 °C to −10 °C). The reaction time for quantitative conversion could be decreased to 6 s. It potentially leads to a breakthrough for high efficiency MPIBs production.