Ring opening polymerization of ε-caprolactone ...
Type de document :
Article dans une revue scientifique
DOI :
URL permanente :
Titre :
Ring opening polymerization of ε-caprolactone in the presence of wet β-cyclodextrin: effect of the operative pressure and of water molecules in the β-cyclodextrin cavity
Auteur(s) :
Galia, Alessandro [Auteur]
Scialdone, Onofrio [Auteur]
Spanò, Tiziana [Auteur]
Valenti, Maria Grazia [Auteur]
Grignard, Bruno [Auteur]
Lecomte, Philippe [Auteur]
Monflier, Eric [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Tilloy, Sebastien [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Rousseau, Cyril [Auteur]
Scialdone, Onofrio [Auteur]
Spanò, Tiziana [Auteur]
Valenti, Maria Grazia [Auteur]
Grignard, Bruno [Auteur]
Lecomte, Philippe [Auteur]
Monflier, Eric [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Tilloy, Sebastien [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Rousseau, Cyril [Auteur]
Titre de la revue :
RSC Adv.
Numéro :
6
Pagination :
90290-90299
Date de publication :
2016-09-12
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
The ring opening polymerization (ROP) of ε-caprolactone (CL) in the presence of β-cyclodextrin (β-CD) was performed in batch reactors both at room pressure and with the reaction system pressurized with CO2, N2 or Ar. ...
Lire la suite >The ring opening polymerization (ROP) of ε-caprolactone (CL) in the presence of β-cyclodextrin (β-CD) was performed in batch reactors both at room pressure and with the reaction system pressurized with CO2, N2 or Ar. Significant enhancements of the polymerization rate was observed when the ROP was carried out with wet β-CD under pressure. For example, after 24 hours at 120 °C with a β-CD/CL molar ratio of about 1/100, the monomer conversion increased from 4 to 98–99% when the pressure was changed from 0.1 to 12.5–13.0 MPa independent of the nature of the compressing gas. MALDI-TOF analyses indicated that a major fraction of polymer chains obtained in pressurized systems was initiated by water molecules. The collected results suggest that at 12–13 MPa wet β-CD can catalyse both the ring opening of ε-caprolactone and the polymerization of the obtained linear species and that high energy water molecules located inside the cavity of the cyclic oligosaccharide must play a role in initiating the polymerization. The trend of number average molecular weight and the results of MALDI-TOF analyses obtained in polymerizations performed for long reaction times and in a hydrolysis test of commercial poly(ε-caprolactone) indicate that wet β-CD can work as an artificial lipase enzyme under the adopted conditions.Lire moins >
Lire la suite >The ring opening polymerization (ROP) of ε-caprolactone (CL) in the presence of β-cyclodextrin (β-CD) was performed in batch reactors both at room pressure and with the reaction system pressurized with CO2, N2 or Ar. Significant enhancements of the polymerization rate was observed when the ROP was carried out with wet β-CD under pressure. For example, after 24 hours at 120 °C with a β-CD/CL molar ratio of about 1/100, the monomer conversion increased from 4 to 98–99% when the pressure was changed from 0.1 to 12.5–13.0 MPa independent of the nature of the compressing gas. MALDI-TOF analyses indicated that a major fraction of polymer chains obtained in pressurized systems was initiated by water molecules. The collected results suggest that at 12–13 MPa wet β-CD can catalyse both the ring opening of ε-caprolactone and the polymerization of the obtained linear species and that high energy water molecules located inside the cavity of the cyclic oligosaccharide must play a role in initiating the polymerization. The trend of number average molecular weight and the results of MALDI-TOF analyses obtained in polymerizations performed for long reaction times and in a hydrolysis test of commercial poly(ε-caprolactone) indicate that wet β-CD can work as an artificial lipase enzyme under the adopted conditions.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
ENSCL
CNRS
Centrale Lille
Univ. Artois
Université de Lille
CNRS
Centrale Lille
Univ. Artois
Université de Lille
Collections :
Équipe(s) de recherche :
Catalyse et chimie supramoléculaire (CASU)
Date de dépôt :
2019-09-25T14:05:02Z