| Literature DB >> 30345587 |
Maozhu Tang1, Rong Zhang1, Shiqi Li1, Jian Zeng1, Mingchao Luo1, Yun-Xiang Xu1, Guangsu Huang1.
Abstract
Natural rubber is one of most famous self-reinforced rubbers thanks to the phenomenon of strain-induced crystallization. It is usually used in a vulcanized form to enhance the mechanical strength but this results in recycling issues. Herein a thermoplastic analogue of vulcanized natural rubber is obtained as a structural mimic. Terminally functionalized polyisoprene rubber B-4A-PIP was prepared by using tetra-analine as physical crosslinking units. The strong binding of tetra-analine groups gave B-4A-PIP a high tensile strength (15 MPa) and breaking strain of 890 %, which is much higher than those of undecorated copolymer B-OH-PIP. B-4A-PIP has a similar onset strain of crystallization and crystallization index to vulcanized natural rubber. Randomly functionalized polyisoprene R-4A-PIP showed a much lower mechanical strength and SIC properties although R-4A-PIP and B-4A-PIP possessed similar molecular weights and amounts of tetra-analine groups.Entities:
Keywords: polar monomers; polyisoprene; strain-induced crystallization; terminal functionalization; toughness
Year: 2018 PMID: 30345587 DOI: 10.1002/anie.201809339
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336