Le réseau
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L'organisation
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La structure de veille et de réflexion prospective
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Actualités
Prix de thèse GFP/SFIP 2026
Deux prix étudiants, un même dossier de candidature.
Le GFP (Groupe Français des Polymères) et la SFIP (Société Française des Ingénieurs des Plastiques) proposent un dossier de candidature identique pour les deux prix destinés à récompenser les travaux de recherche d’un étudiant ayant soutenu une thèse dans le domaine des polymères entre le 31 juillet 2025 et le 31 juillet 2026. lire plus…
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Pour cela, nous vous invitons à prendre quelques minutes pour remplir un court questionnaire consacré au site internet du GFP. Vos réponses nous aideront à identifier les points forts du site, les améliorations possibles et les contenus ou fonctionnalités à développer en priorité.
Accéder au questionnaire :
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Merci par avance pour votre participation. Vos retours sont précieux pour faire évoluer le site et mieux répondre aux besoins de la communauté du GFP.
Élastomères conducteurs supramoléculaires autoréparables à base de réseaux interpénétrés pour la peau électronique
Paru le 19 juin 2026, ce travail mené par l’Institut Parisien de Chimie Moléculaire (IPCM, CNRS/Sorbonne Université) introduit une nouvelle classe de polymères conducteurs combinant souplesse mécanique extrême et propriétés d’autoréparation autonomie à température ambiante. Les auteurs ont synthétisé un réseau interpénétré de polymères (IPN) associant une matrice polyuréthane hautement élastique, fonctionnalisée par des liaisons hydrogène dynamiques réversibles, et des micro-domaines percolants d’un polymère conjugué dopé. L’analyse rhéologique montre une récupération de 98 % des propriétés de conduction électrique et de résistance mécanique après rupture en moins de 10 minutes, sans apport d’énergie externe. L’application cible les dispositifs biomédicaux portables et les capteurs de déformation (strain-sensors) pour la robotique souple.
Dépolymérisation photo-induite contrôlée de polycarbonates biosourcés par organocatalyse sélective
Dans une étude publiée le 16 juin 2026 par une équipe du Laboratoire de Chimie des Polymères Organiques (LCPO, Bordeaux), les chercheurs ont mis au point une stratégie de recyclage chimique par dépolymérisation amorcée sous lumière visible d’un polycarbonate issu du dioxyde de carbone et d’époxydes biosourcés. Le procédé repose sur l’utilisation d’une plateforme d’organocatalyseurs (bases organiques non métalliques) hautement sélectifs qui activent spécifiquement les liaisons carbonate intrachaînes sans dégrader les fonctions périphériques. À température ambiante et après seulement quelques heures d’exposition, le taux de conversion en monomères cycliques de départ dépasse 94 %, avec une pureté optique préservée. Ce signal illustre l’excellence de la recherche française dans la conception de boucles de circularité fermées « polymère-à-monomère » à faible empreinte énergétique.
Une approche d’enchevêtrement réversible ouvre la voie à des polymères thermodurcissables hautement recyclables
Des chercheurs du Beckman Institute ont publié le 17 juin 2026 une stratégie de rupture pour le cycle de vie des plastiques thermodurcissables, essentiels dans l’aéronautique et l’électronique mais historiquement infusibles. Au lieu de s’appuyer sur une densité de réticulation covalente permanente, le procédé exploite le concept macro-moléculaire d’enchevêtrement physique de très longues chaînes polymères (analogues à des réseaux de câbles interférents partagés) combiné à un nombre restreint et contrôlé de liaisons réversibles. Cette architecture permet de maintenir d’excellentes propriétés thermomécaniques en usage, tout en offrant la possibilité de découpler chimiquement les points de jonction pour libérer les chaînes en vue d’un recyclage par fusion. La portée industrielle est majeure : elle jette les bases d’une refonte complète de la formulation des résines structurales en conciliant résistance mécanique ultime et circularité matière.
Amorçage direct de polymérisations radicalaires contrôlées (photo-ATRP) à partir de fonctions amines primaires
Dans une publication du 20 juin 2026 au Journal of the American Chemical Society, des chimistes ont démontré la possibilité d’amorcer une polymérisation radicalaire par transfert d’atomes photocontrôlée (photo-ATRP) directement depuis le carbone alpha d’amines primaires courantes, s’affranchissant ainsi des amorceurs halogénés classiques. En convertissant in situ l’amine en sels de Katritzky pour former des complexes donneur-accepteur d’électrons (EDA), l’activation sous lumière visible génère un radical alkyle propre à initier la croissance. Les polymères ainsi synthétisés affichent des indices de polymolécularité très étroits et une fidélité d’extrémité de chaîne supérieure à 99 %. Cette percée simplifie considérablement la synthèse d’architectures polymères avancées, telles que les greffages de surfaces denses ou les conjugués polymères-protéines, à partir de substrats fonctionnels bruts.
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Adhérez au GFP
Devenez un membre et découvrez les avantages d’un abonnement GFP.
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Sections locales GFP
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Les partenaires
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cnrs
http://www.ispa.asso.fr
lrccp
http://www.ispa.asso.fr
LPMC
http://www.ispa.asso.fr
ICS
https://www-ics.u-strasbg.fr/
Waters_logo_stacked_K_web-NEW
http://www.waters.com
arkema
http://www.coatex.com
hutchinson
http://www.hutchinson.com/fr
Logo-ChemSuD
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logo-ispa_coul_fond-fonce
http://www.ispa.asso.fr
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