Pascal Viville
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Pascal Viville has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
Roberto Lazzaroni
Contribution from the Service de Chimie des Matériaux Nouveaux (SCMN), Centre de Recherche en Sciences des Matériaux Polymères, and Service des Matériaux Polymères et Composites (SMPC), Centre de Recherche en Sciences des Matériaux Polymères, Université de Mons-Hainaut, 20, Place du Parc 7000, Mons, Belgium
3 shared publicationsAlain Deffieux
Laboratoire de Chimie des Polymères Organiques, UMR ENSCPB-CNRS 5629, Universit de Bordeaux, 16 Avenue Pey Berland 33607 Pessac, France
2 shared publicationsMichel Schappacher
Laboratoire de Chimie des Polymères Organiques, UMR ENSCPB-CNRS 5629, Universit de Bordeaux, 16 Avenue Pey Berland 33607 Pessac, France
2 shared publications- Philippe Dubois
Materia Nova Research Center, UMONS Innovation Center, Avenue Nicolas Copernic 3, B-7000 Mons, Belgium
2 shared publications - Philippe Leclère
University of Mons (UMONS)/Laboratory for Physics of Nanomaterials and Energy (LPNE), Research Institute for Materials Science and Engineering, Mons, Belgium
2 shared publications - Bruno Van Mele
Vrije Universiteit Brussels
1 shared publication
Latest Publications
- 18 April 2007
- Published by Wiley in Journal of Polymer Science Part B: Polymer Physics
- Vol. 45 (11) , 1291-1302
Interfacial interaction in EVA‐carbon nanotube and EVA‐clay nanocomposites
- 18 April 2007
- Published by Wiley in Journal of Polymer Science Part B: Polymer Physics
- Vol. 45 (11) , 1291-1302
Interfacial interaction in EVA‐carbon nanotube and EVA‐clay nanocomposites
- 1 July 2004
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 126 (29) , 9007-9012
Controlled Polymer Grafting on Single Clay Nanoplatelets
We report on the controlled chemical grafting of well-defined polymer chains onto individual montmorillonite-type clay nanoplatelets and the direct visualization of the formed hybrid material at the nanoscale level. Our approach is based on the use of a surfactant mixture that contains varying proportions of hydroxyl-substituted alkylammonium and unsubstituted alkylammonium cations to exchange the initial Na+ counterions of the natural montmorillonite. This allows for the exchange of Na+ by a tunable amount of hydroxyl functions at the surface of the clays. Those functions are then derivatized into aluminum alkoxides in order to initiate the ring-opening polymerization of ε-caprolactone directly from the clay surface that was swollen in an organic solvent. Atomic force microscopy measurements on the resulting polymer-grafted nanoplatelets demonstrate the strong dependence of the coating of the individual clay particles with the composition of the surfactant mixture used for the cationic exchange. This allows for the generation of a range of morphologies varying from polymer islands distributed over the clay surface to homogeneous polymer layers thoroughly coating the platelets. Finally, the control that is achievable over the synthesis of this new family of organic−inorganic nanohybrid materials has been extended to the surface grafting of semicrystalline poly(ε-caprolactone)−poly(lactic acid) diblock copolymers with defined compositions.
- 1 July 2004
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 126 (29) , 9007-9012
Controlled Polymer Grafting on Single Clay Nanoplatelets
We report on the controlled chemical grafting of well-defined polymer chains onto individual montmorillonite-type clay nanoplatelets and the direct visualization of the formed hybrid material at the nanoscale level. Our approach is based on the use of a surfactant mixture that contains varying proportions of hydroxyl-substituted alkylammonium and unsubstituted alkylammonium cations to exchange the initial Na+ counterions of the natural montmorillonite. This allows for the exchange of Na+ by a tunable amount of hydroxyl functions at the surface of the clays. Those functions are then derivatized into aluminum alkoxides in order to initiate the ring-opening polymerization of ε-caprolactone directly from the clay surface that was swollen in an organic solvent. Atomic force microscopy measurements on the resulting polymer-grafted nanoplatelets demonstrate the strong dependence of the coating of the individual clay particles with the composition of the surfactant mixture used for the cationic exchange. This allows for the generation of a range of morphologies varying from polymer islands distributed over the clay surface to homogeneous polymer layers thoroughly coating the platelets. Finally, the control that is achievable over the synthesis of this new family of organic−inorganic nanohybrid materials has been extended to the surface grafting of semicrystalline poly(ε-caprolactone)−poly(lactic acid) diblock copolymers with defined compositions.
- 1 March 2001
- Published by Wiley in Macromolecular Symposia
- Vol. 167 (1) , 243-256
Surface organization of hyperbranched polymer molecules, as studied by atomic force microscopy
- 1 March 2001
- Published by Wiley in Macromolecular Symposia
- Vol. 167 (1) , 243-256
Surface organization of hyperbranched polymer molecules, as studied by atomic force microscopy