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Ternary ABC block copolymers based on one glassy and two crystallizable blocks: polystyrene‐ block ‐polyethylene‐ block ‐poly(ε‐caprolactone)
Author(s) -
Balsamo Vittoria,
Müller A. J.,
von Gyldenfeldt Friederike,
Stadler Reimund
Publication year - 1998
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/(sici)1521-3935(19980601)199:6<1063::aid-macp1063>3.0.co;2-v
Subject(s) - polybutadiene , copolymer , polymer chemistry , materials science , polystyrene , crystallinity , caprolactone , differential scanning calorimetry , crystallization , polyethylene , polymer , miscibility , gel permeation chromatography , chemical engineering , composite material , physics , thermodynamics , engineering
The hydrogenation of polystyrene‐ block ‐polybutadiene‐ block ‐poly(ε‐caprolactone) SBC triblock copolymers was performed in the presence of the Wilkinson catalyst RhCl(P(C 6 H 5 ) 3 ) 3 . Reaction conditions (hydrogen pressure, temperature and reaction time) were varied to ensure quantitative hydrogenation without detectable side reactions. Gel permeation chromatography showed no broadening of the molecular weight distribution during hydrogenation. The efficiency of the catalyst is markedly influenced by the molecular weight of the copolymer. Due to the presence of the polyethylene (PE) block, the resulting polymers exhibit a reduced solubility in comparison to the starting materials. Using differential scanning calorimetry (DSC), preliminary results about the crystallization and melting behavior of the PE‐block were obtained. In the triblock copolymers, the PE‐block showed a marked depression of the melting point and crystallinity when compared to pure hydrogenated polybutadiene of equivalent molecular weight and microstructure or to a comparable PE‐block within a polyethylene‐ block ‐poly(ε‐caprolactone) diblock copolymer. A fractionated crystallization process of the PCL‐block was observed when the PCL component in the hydrogenated triblock copolymers was present as a minor phase.