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Styrene Moiety-Carrying Diorganozinc Compound Preparation for Polystyrene-Poly(ethylene- co-1-hexene)-Polystyrene Triblock Copolymer Production
  • Lee, Jong Chul ;
  • Park, Kyung Lee ;
  • Bae, Sung Moon ;
  • Lee, Hyun Ju ;
  • Baek, Jun Won ;
  • Lee, Junseong ;
  • Sa, Seokpil ;
  • Shin, Eun Ji ;
  • Lee, Ki Soo ;
  • Lee, Bun Yeoul
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Publication Year
2020-09-08
Publisher
American Chemical Society
Citation
Macromolecules, Vol.53, pp.7274-7284
Mesh Keyword
Chain transfer polymerizationCommercial gradeCrystalline solidsLarge scale preparationMarket expansionsPoly(ethylene-co-1-butene)Styrene polymerizationToughening agents
All Science Classification Codes (ASJC)
Organic ChemistryPolymers and PlasticsInorganic ChemistryMaterials Chemistry
Abstract
Polystyrene (PS)-block-poly(ethylene-co-1-butene)-block-PS (SEBS), produced by PS-block-polybutadiene-block-PS hydrogenation, is a high-performance thermoplastic elastomer. Hydrogenation is costly and tedious, making SEBS market expansion difficult. Thus, we envisioned a new one-pot SEBS-like triblock copolymer synthetic scheme to grow PO chains from styrene moiety-carrying diorganozinc compounds by coordinative chain transfer polymerization (CCTP), followed by anionic styrene polymerization using a specially designed initiator, allowing PS chain growth from not only the styrene moieties but also the Zn-C sites. Large-scale preparation of highly pure styrene moiety-carrying diorganozinc compounds was one of the main challenges we faced, but we overcame it by synthesizing (CH2═CHC6H4CH2CH2CH2)2Zn (4), a stable and crystalline solid that worked well as a CCTP agent. This enabled the preparation of PS-block-poly(ethylene-co-1-hexene)-block-PS (SEHS), which exhibited a stress-strain curve similar to that of the commercial-grade SEBS. The SEHS dispersed better in a polypropylene (PP) matrix, allowing it to act as a better toughening agent for PP blending than the commercial-grade SEBS. Moreover, SEHS was less viscous, exhibiting better workability.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/31527
DOI
https://doi.org/10.1021/acs.macromol.0c01253
Fulltext

Type
Article
Funding
This work was supported by the Commercialization Promotion Agency for R&D Outcomes (COMPA) funded by the Ministry of Science and ICT (MSIT) and by the Korea CCS R&D Center (KCRC) grant (Grant No. 2012-0008935).
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Department of Applied Chemistry & Biological Engineering
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