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Article

Crystalline Syndiotactic Polystyrene as Reinforcing Agent of cis-1,4-Polybutadiene Rubber

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Antonio Buonerba†‡, Cinzia Cuomo†‡, Vito Speranza§ and Alfonso Grassi*†‡
† Dipartimento di Chimica, Università di Salerno, via Ponte don Melillo, 84084 Fisciano (SA), Italy
‡ NANOMATES, Research Centre for NANOMAterials and nanoTEchnology at Salerno University, 84084 Fisciano (SA), Italy
§ Dipartimento di Ingegneria Chimica, Università di Salerno, via Ponte don Melillo, 84084 Fisciano (SA), Italy
Macromolecules, 2010, 43 (1), pp 367–374
DOI: 10.1021/ma901859e
Publication Date (Web): November 13, 2009
Copyright © 2009 American Chemical Society
*To whom correspondence should be addressed. E-mail: agrassi@unisa.it. Fax: +39089969824.
CASSection:
Synthetic Elastomers and Natural Rubber

Abstract

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Syndiotactic polystyrene (sPS), a thermoplastic polymer characterized by high crystallinity, good chemical resistance and high modulus, has been successfully tested as a reinforcing agent for cis-1,4-polybutadiene (PB) rubber. Blends of sPS and PB have been in situ synthesized using a multistep polymerization process catalyzed by monocyclopentadienyl titanium compounds activated with MAO. This procedure assures an intimate mixing of the components and homogeneous dispersion of the sPS particles having dimension from few hundreds of nanometers to micrometers. The analysis of the mechanical properties of the sPS−PB blends obtained using this process showed enhanced Young’s modulus, toughness, σbreak and ε break: these properties were found to be 1 order of magnitude higher than those of PB and comparable to those of PB charged with inorganic filler as carbon black or silica. A multiblock copolymer (sPSB) comprising segments of sPS and PB was successfully in situ synthesized with the sPS and PB homopolymers and found to be an active compatibilizer of these blends producing a novel semicrystalline phase at the interphase between the sPS particles and the PB matrix.

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History

  • Published In Issue January 12, 2010
  • Article ASAPNovember 13, 2009
  • Received: August 20, 2009
    Revised: October 28, 2009

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