Polymer Bulletin

, Volume 61, Issue 6, pp 725–736

Synthesis and aggregate formation of poly(styrenesulfonate)-b-poly(ethylene glycol)-b-poly(styrenesulfonate) triblock copolymers in aqueous solution induced by binding with aluminum ions

Authors

  • Zhiping Peng
    • Research Institute of Materials ScienceSouth China University of Technology
  • Xinxing Liu
    • Research Institute of Materials ScienceSouth China University of Technology
    • Research Institute of Materials ScienceSouth China University of Technology
Article

DOI: 10.1007/s00289-008-1004-9

Cite this article as:
Peng, Z., Liu, X. & Tong, Z. Polym. Bull. (2008) 61: 725. doi:10.1007/s00289-008-1004-9

Summary

Well-defined water-soluble poly(styrenesulfonate)-b-poly(ethylene glycol)-b- poly(styrenesulfonate) (PSS-b-PEG-b-PSS) triblock copolymers with narrow molecular weight distribution (1.29 < Mw/Mn < 1.36) were synthesized in aqueous solution at 70 oC via reversible addition-fragmentation chain transfer (RAFT) polymerization. The complex formed by the PSS-b-PEG-b-PSS triblock copolymer coordinated with aluminum ion was investigated with turbidimetry, dynamic light scattering (DSL), zeta-potential, and transmission electron microscopy (TEM). The aggregation formation was based on the neutralization of the SO3- groups in the PSS blocks with Al3+ ions. The appearance, size and stability of the PSS-b-PEG-b-PSS/Al3+ aggregates were controlled by varying the PSS block length and degree of neutralization (DN). At DN = 0.33, where the PSS-b-PEG-b-PSS copolymer was completely neutralized with Al3+, the aggregate size increased with increasing PSS block length. The transition from the shrinking coil of small size to the interchain aggregates of large size was found at DN of about 0.33.

Copyright information

© Springer-Verlag 2008