期刊论文详细信息
Macromol
Aspects of the Synthesis of Poly(styrene-block-isobutylene-block-styrene) by TiCl4-Co-initiated Cationic Polymerization in Open Conditions
Dmitry G. Yakhvarov1  Giyjaz E. Bekmukhamedov1  Evgeny A. Ovcharenko2  Maria A. Rezvova2  Tatiana V. Glushkova2  Ivan A. Berezianko3  Pavel A. Nikishau3  Miraslau I. Makarevich3  Sergei V. Kostjuk3 
[1] Alexander Butlerov Institute of Chemistry, Kazan Federal University, 420008 Kazan, Russia;Research Institute for Complex Issues of Cardiovascular Diseases, 650002 Kemerovo, Russia;Research Institute for Physical Chemical Problems of the Belarusian State University, 220006 Minsk, Belarus;
关键词: cationic polymerization;    living polymerization;    isobutylene;    styrene;    polyisobutylene;    poly(styrene-block-isobutylene-block-styrene);   
DOI  :  10.3390/macromol1040017
来源: DOAJ
【 摘 要 】

The cationic polymerization of isobutylene and its block copolymerization with styrene using DiCumCl/TiCl4/2,6-lutidine initiating system has been studied in open conditions. It was shown that a higher concentration of proton trap is required in open conditions as compared to the glove box technique in order to have good control over molecular weight and polydispersity. Polyisobutylenes with Mn ≤ 50,000 g mol−1 and low polydispersity (Đ ≤ 1.2) were prepared at [Lu] = 12 mM. The synthesis of poly(styrene-block-isobutylene-block-styrene) triblock copolymer (SIBS) in open conditions required the addition of proton trap into two steps, half at the beginning of the reaction and the second half together with styrene. Following this protocol, a series of triblock copolymers with different length of central polyisobutylene block (from Mn = 20,000 g mol−1 to 50,000 g mol−1) and side polystyrene blocks (Mn = 4000 g mol−1–9000 g mol−1) with low polydispersity (Đ ≤ 1.25) were synthesized. High molecular SIBS (Mn > 50,000 g mol−1) with low polydispersity (Đ < 1.3) containing longer polystyrene blocks (Mn > 6000 g mol−1) demonstrated higher tensile strength (~13.5 MPa).

【 授权许可】

Unknown   

  文献评价指标  
  下载次数:0次 浏览次数:0次