par  Dervaux, Bart;Meyer, Franck  ;Raquez, Jean-Marie;Olivier, Aurore;Du Prez, Filip;Dubois, Philippe
;Raquez, Jean-Marie;Olivier, Aurore;Du Prez, Filip;Dubois, Philippe
Référence Macromolecular chemistry and physics, 213, 12, page (1259-1265)
Publication Publié, 2012
           ;Raquez, Jean-Marie;Olivier, Aurore;Du Prez, Filip;Dubois, Philippe
;Raquez, Jean-Marie;Olivier, Aurore;Du Prez, Filip;Dubois, PhilippeRéférence Macromolecular chemistry and physics, 213, 12, page (1259-1265)
Publication Publié, 2012
                                                                                                       
			Article révisé par les pairs
                                                  
        | Résumé : | Imidazolium end-functionalized poly(butyl acrylate) and polystyrene (co)polymers (Im-PnBuA, Im-PSty, and Im-PnBuA-b-PSty are synthesized via ATRP. The controlled character of the polymerization reactions is highlighted by SEC and MALDI-TOF MS analyses. Subsequently, the polymers are tested as dispersing/compatibilizing agents for CNTs in polymer matrices. When CNTs are challenged with a mixture of Im-PnBuA and Im-PSty, the CNTs are mainly located in the PnBuA phase. In contrast, the Im-PnBuA-b-PSty block copolymer enables CNT confinement in the PSty phase. By selecting the proper ω-imidazolium polymer, it is possible to direct the CNT confinement toward a specific polymer phase within polymer mixtures. | 



