G
Ghislain David
Researcher at Centre national de la recherche scientifique
Publications - 124
Citations - 3638
Ghislain David is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Radical polymerization & Monomer. The author has an hindex of 28, co-authored 120 publications receiving 2891 citations. Previous affiliations of Ghislain David include Commissariat à l'énergie atomique et aux énergies alternatives & École Normale Supérieure.
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A simple strategy based on a highly fluorinated polymer blended with a fluorinated polymer containing phosphonic acid to improve the properties of PEMFCs
TL;DR: In this paper, a series of five blend membranes made from poly(vinylidene fluoride-co-chlorotrifluoroethylene) with a fluorinated copolymer containing phosphonic acid was synthesized.
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Determination of the cumulative degree of polymerization for the dead-end polymerization of styrene
TL;DR: In this article, a new relation correcting theoretical (DPn) with experimental values obtained in the dead-end polymerization of styrene with azocompound was explored, which fit very well in a large range of C0's, contrary to the application of the usual Mayo rule, and a discussion of validity is proposed.
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Synthesis of poly(styrene-b-dimethylsiloxane) multi-block copolymers via polyhydrosilylation reaction
TL;DR: In this paper, poly(styrene- b -siloxane) multi-block copolymers have been prepared by polyhydrosilylation reaction and the copolymer molecular weights were determined by SEC to be about 25,000g/mol.
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Use of a new crosslinking method to obtain semi-IPN membranes with phosphonic acid groups for a PEMFC application
TL;DR: In this article, the synthesis of a semi-IPN membrane was performed from a commercial fluorinated copolymer and a fluorophosphonated copolymers with pendant phosphonic acid groups.
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Advances in chitooligosaccharides chemical modifications
TL;DR: The recent developments in COS functionalization, primarily focusing on amine and hydroxyl groups and aldehyde-chain end reactions, as well as paying considerable attention to other types of modification, can be found in this paper.