Search

Your search keyword '"Saint-Loup, René"' showing total 37 results
Start Over Author "Saint-Loup, René"
37 results on '"Saint-Loup, René"'

6. Résine biosourcée pour une composition cosmétique et son procédé de fabrication

Author

Poupon, Andy, Laubé, Florian, Saint-Loup, René, Nouguerede, Olivier, Roussel, Joël, Rataj, Véronique, Zinck, Philippe, Université de Lille, CNRS, Centrale Lille, ENSCL, Univ. Artois, Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS], Roquette Frères, Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis
Abstract

La présente invention concerne une résine polyester biosourcée comprenant un mélange de diols et de polyacides, son procédé de préparation ainsi qu’une composition filmogène et un vernis à ongles comprenant ladite résine. La résine polyester peut notamment être utile en tant que liant dans un vernis à ongles.

Published
2021

11. Solvant biosourcé non-toxique pour la réalisation de revêtements polyuréthanes

Author

Jacquel, Nicolas, Saint-Loup, René, Pascault, Jean-Pierre, Blache, Héloïse, Rousseau, Alain, Méchin, Françoise, Fleury, Etienne, Méchin, Françoise, Roquette Frères, Ingénierie des Matériaux Polymères (IMP), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), and Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.POLY] Chemical Sciences/Polymers, [CHIM.POLY]Chemical Sciences/Polymers, [SPI.MAT] Engineering Sciences [physics]/Materials, humanities, [SPI.MAT]Engineering Sciences [physics]/Materials
Abstract

The present invention relates to a crosslinkable polyurethane coating composition that comprises a polyol moiety, a polyisocyanate moiety, isosorbide, and a solvent comprising dimethyl isosorbide, as well as to a method for producing a polyurethane coating from said composition on a substrate, and the coating obtained in this manner. The invention also relates to the use of dimethyl isosorbide as a compatibilizer for a mixture comprising isosorbide and an aliphatic polyisocyanate.

Published
2019

12. New Cure – Study of the carbamate-aldehyde reaction : toward new thermosetting resins

Author

Gérard, David, Méchin, Françoise, Saint-Loup, René, Pascault, Jean-Pierre, Fleury, Etienne, Méchin, Françoise, Ingénierie des Matériaux Polymères (IMP), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Roquette Frères

Subjects
[CHIM.MATE] Chemical Sciences/Material chemistry, [CHIM.MATE]Chemical Sciences/Material chemistry, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

14. Caractérisations structurale et thermomécanique de dérivés d'amidon

Author

David, Adélina, Meimoun, Julie, Wiatz, Vincent, Saint-Loup, René, Parcq, Julien, Descamps, Nicolas, Favrelle, Audrey, Bonnet, Fanny, Delaunay, Thierry, Stoclet, Grégory, Lourdin, Denis, Zinck, Philippe, GAUCHER, Valérie, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Unité Matériaux et Transformations - UMR 8207 (UMET), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Supérieure de Chimie de Lille (ENSCL)-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Unité de Catalyse et de Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Ecole Centrale de Lille-Ecole Nationale Supérieure de Chimie de Lille (ENSCL)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université de Lille-Ecole Nationale Supérieure de Chimie de Lille (ENSCL)-Institut National de la Recherche Agronomique (INRA), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, and Institut de Chimie du CNRS (INC)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Lille-Ecole Nationale Supérieure de Chimie de Lille (ENSCL)

Subjects
[CHIM.POLY]Chemical Sciences/Polymers, [SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering, [CHIM.MATE]Chemical Sciences/Material chemistry, ComputingMilieux_MISCELLANEOUS, [SPI.MAT]Engineering Sciences [physics]/Materials
Abstract

National audience

Published
2018

15. Synthesis and Characterization of New Thermosetting Polyurethanes coatings obtained from Biobased Dihydroxytelechelic Oligocarbonates

Author

Ben Chrait, Imen, Saint-Loup, René, Woisel, Patrice, Zinck, Philippe, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Unité Matériaux et Transformations - UMR 8207 (UMET), Institut de Chimie du CNRS (INC)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Lille-Ecole Nationale Supérieure de Chimie de Lille (ENSCL), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), and Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Supérieure de Chimie de Lille (ENSCL)-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2018

16. Modification of starch by graft copolymerization

Author

Meimoun, Julie, Wiatz, Vincent, Saint-Loup, René, Parcq, Julien, Favrelle, Audrey, Bonnet, Fanny, Zinck, Philippe, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Institut Français des Matériaux Agro-Sourcés (IFMAS), Division recherche, Roquette Frères, Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, ENSCL, CNRS, INRA, Centrale Lille, Univ. Artois, Université de Lille, Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS], Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181, and Unité de Catalyse et de Chimie du Solide (UCCS) - UMR 8181

Subjects
[CHIM.POLY]Chemical Sciences/Polymers, ring-opening polymerization, food and beverages, grafted starch, coupling agents, radical polymerization
Abstract

International audience; Research toward bio-based and biodegradable polymers has received a lot of attention these last years, due to environmental concerns and the need to replace fossil resources. Starch is in this frame an interesting starting material due to its abundance and low cost. Native starch displays however, poor mechanical properties and is highly hydrophilic. New starch-based thermoplastic materials can be prepared to overcome these drawbacks by chemical modification, and notably graft copolymerization. A large range of polymers can be grafted on starch by ring-opening and radical polymerizations of various monomers in order to modulate the properties of the final product. Polymers can also be directly grafted onto starch using coupling strategies. This review presents the state of the art in the field.

Published
2018

19. Isosorbide as a chain extender for thermoplastic polyurethanes

Author

Blache, Héloïse, Méchin, Françoise, Alain, Rousseau, Fleury, Etienne, Pascault, Jean-Pierre, Saint-Loup, René, Jacquel, Nicolas, Ingénierie des Matériaux Polymères (IMP), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon, Roquette Frères, Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Université Claude Bernard Lyon 1 (UCBL), and Méchin, Françoise

Subjects
[CHIM.MATE] Chemical Sciences/Material chemistry, [CHIM.MATE]Chemical Sciences/Material chemistry, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2017

20. La chimie en Région Hauts-de-France : Chimie de la biomasse

Author

Kovensky, José, Lebeuf, Raphael, Len, Christophe, Monflier, Eric, Nardello-Rataj, Véronique, Ontiveros Ontiveros, Jesus, Paul, Sébastien, Saint-Loup, René, Sauthier, Mathieu, Suisse, Isabelle, Visseaux, Marc, Wadouachi, Anne, Woisel, Patrice, Zinck, Philippe, Beaulieu, Remi, Bonnet, Fanny, Delaunay, Thierry, Dumeignil, Franck, Epoune Lingome, Cédric, Favrelle, Audrey, Gauvin, Régis, Hapiot, Frédéric, Jacquel, Nicolas, Laboratoire de Glycochimie, des Antimicrobiens et des Agro-ressources - UMR CNRS 7378 (LG2A ), Université de Picardie Jules Verne (UPJV)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Université de Technologie de Compiègne (UTC), UCCS Équipe Catalyse Supramoléculaire, Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Roquette Frères, Unité Matériaux et Transformations - UMR 8207 (UMET), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Supérieure de Chimie de Lille (ENSCL)-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS), Semences Innovation Protection Recherche et Environnement, Chimie Organique et Bioorganique : Réactivité et Analyse (COBRA), Institut de Chimie Organique Fine (IRCOF), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Université de Rouen Normandie (UNIROUEN), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Université Le Havre Normandie (ULH), Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Caen Normandie (UNICAEN), Normandie Université (NU)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), and Normandie Université (NU)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM]Chemical Sciences
Abstract

International audience

Published
2017

25. Structure-Properties Relationship of In Situ Synthesized Poly(Butylene Succinate)/Silica Nanocomposites: Application in Extrusion Blowing of Films

Author

Jacquel, Nicolas, Saint-Loup, René, Pascault, Jean-Pierre, Rousseau, Alain, Fenouillot, Françoise, Ingénierie des Matériaux Polymères (IMP), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet [Saint-Étienne] (UJM)-Centre National de la Recherche Scientifique (CNRS), Division recherche, Roquette Frères, Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Claude Bernard Lyon 1 (UCBL), and Université de Lyon

Subjects
[CHIM.POLY]Chemical Sciences/Polymers, film blowing, silica, nanocomposites, poly(butylene succinate), [CHIM.MATE]Chemical Sciences/Material chemistry
Abstract

International audience; The melt synthesis of poly(butylene succinate)/silica (PBS/SiO2) nanocomposites is investigated via an in situ approach. The use of two types of nanosilica, fumed (or pyrogenic) silica and colloidal silica, is described. In all cases, the addition of silica favors an increase of the melt viscosity during the polycondensation step. This behavior is attributed to both polymer-silica interactions and PBS chain coupling via possible reaction with silica silanols. Biodegradable film is a promising application for PBS. In this context, it is proved that silica greatly facilitates PBS processing by extrusion blowing (a longitudinal draw ratio of 16 is attained). Moreover, tensile tests performed on films demonstrate significant reinforcement of the material with the addition of the nanofiller. The dispersion of the particles into the polymer matrix is assessed by transmission electron microscopy and further characterized by image analysis. It appears that pyrogenic and colloidal silica particles are regularly dispersed in the polymer matrix and that this dispersion is stable upon film blowing.

Published
2014

26. Efficiency of Organometal- and Metal Oxide- based Catalysts during the Synthesis of Poly(butylene succinate): a Biodegradable Potentially Fully Bio-based Polyester

Author

Alain, Rousseau, Jacquel, Nicolas, Freyermouth, Floriane, Fenouillot, Françoise, Pascault, Jean-Pierre, Fuertes, Patrick, Saint-Loup, René, Ingénierie des Matériaux Polymères (IMP), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon, Division recherche, Roquette Frères, and Doucet, Florian

Subjects
[CHIM.POLY] Chemical Sciences/Polymers, [CHIM.MATE] Chemical Sciences/Material chemistry, [CHIM.POLY]Chemical Sciences/Polymers, [CHIM.MATE]Chemical Sciences/Material chemistry, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2012

27. Efficiency Increase of Poly(ethylene terephthalate-co-isosorbide terephthalate) Synthesis using Bimetallic Catalytic Systems

Author

Bersot, Jean-Christophe, Jacquel, Nicolas, Saint-Loup, René, Fuertes, Patrick, Rousseau, Alain, Pascault, Jean-Pierre, Spitz, Roger, Fenouillot, Françoise, Monteil, Vincent, Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Macromoléculaires (IMP-LMM), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet [Saint-Étienne] (UJM)-Centre National de la Recherche Scientifique (CNRS), Institut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier (ICGM ICMMM), Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie, Catalyse, Polymères et Procédés, R 5265 (C2P2), Centre National de la Recherche Scientifique (CNRS)-École supérieure de Chimie Physique Electronique de Lyon (CPE)-Université Claude Bernard Lyon 1 (UCBL), and Université de Lyon-Université de Lyon-Institut de Chimie du CNRS (INC)

Subjects
[CHIM.POLY]Chemical Sciences/Polymers, isosorbide, bimetallic catalysts, [CHIM.MATE]Chemical Sciences/Material chemistry, polyesters, polycondensation, transesterification
Abstract

International audience; New catalytic systems are developed to increase the transesterification efficiency during the synthesis of poly(ethylene terephthalate-co-isosorbide terephthalate) with the aim of compensating for the lack of reactivity of the isosorbide and to reduce the coloration of the polymer. The combination of antimony oxide with a second metal (lithium-, magnesium-, or aluminium-based compounds) is investigated, leading to the discovery of innovative antimony-based bimetallic catalytic systems that exhibit a higher polymerization efficiency, even at high isosorbide contents (20%) and, in some cases, lower coloration.

Published
2011

35. Synthesis of Poly[(ethylene terephthalate)-co-(ɛ-caprolactone)]‐Poly(propylene oxide) Block Copolyester by Direct Polyesterification of Reactive Oligomers

Author

Saint-Loup, René and Robin, Jean-Jacques

Abstract

Summary: The objective of this study was to synthesize thermoplastic elastomers by the direct copolyesterification of reactive oligomers of poly[(ethylene terephthalate)-co-(ɛ-caprolactone)] (PET) and poly(propylene oxide) (PPO). The synthesis of hard segment oligomers was achieved in two steps. The first step consisted of the glycolysis of PET leading to α,ω‐hydroxyl functionalized oligomers. The second step corresponded to the ring opening polymerization of ɛ‐caprolactone onto the hydroxyl end groups of the PET oligomers. Commercially available hydroxytelechelic poly(propylene oxide) was modified to obtain carboxytelechelic poly(propylene oxide). The chemical structure of the product was investigated by 1H NMR and size exclusion chromatography (SEC). Multiblock poly(ester‐ether) was then synthesized by polyesterification of hydroxytelechelic poly[(ethylene terephthalate)‐co‐(ɛ‐caprolactone)] with carboxytelechelic poly(propylene oxide) oligomers, using different catalysts and reaction conditions. The best stoichiometric ratio for the reaction was determined in order to obtain the highest possible $\overline M _{\rm n}$. The chemical structure of the synthesized poly(ester‐ether) was investigated by size exclusion chromatography and 1H NMR. The thermal and thermomechanical behavior of the synthesized poly(ester‐ether) was investigated by differential scanning calorimetry and dynamic mechanical analysis, which showed that the poly(ester‐ether) behaved as a thermoplastic elastomer. This product could also be an interesting way for chemical recycling of PET waste.Synthesis of multiblock co-poly(ester-ether).

Published
2005
Full Text
View/download PDF

36. Synthesis of Poly(ethylene terephthalate)-<TOGGLE>block</TOGGLE>-Poly(tetramethylene oxide) Copolymer by Direct Polyesterification of Reactive Oligomers

Author

Saint-Loup, René, Robin, Jean-Jacques, and Boutevin, Bernard

Abstract

The object of this study was the synthesis of thermoplastic elastomer compounds by direct copolyesterification of reactive oligomers of poly(ethylene terephthalate) (PET) and of poly(tetramethylene oxide) (PTMO). PET was glycolysed to synthesise hydroxytelechelic oligomers of PET. Commercially available hydroxytelechelic PTMO was modified to synthesise carboxytelechelic oligomers. The chemical structures of these oligomers were investigated by 1H NMR and size exclusion chromatography. Multiblock poly(ester-ether) was then obtained by polyesterification of the hydroxytelechelic and carboxytelechelic oligomers, using different catalysts and different reaction conditions. The best stoichiometric ratio was determined to lead to the highest Mn. The chemical structure of the synthesised poly(ester-ether) was investigated by size exclusion chromatography and 1H NMR. The thermal and thermomechanical behaviour of the synthesised poly(ester-ether) was investigated by differential scanning calorimetry and by dynamic mechanical analysis, and showed a thermoplastic elastomer behaviour. This product could also be an interesting way of chemically recycling PET waste. Polyesterification of hydroxytelechelic PET with carboxytelechelic PTMO.

Published
2003
Full Text
View/download PDF

37. Synthesis of hydroxytelechelic ɛ-caprolactone/poly(ethylene terephthalate) co-oligomers, 1

Author

Saint-Loup, René, Robin, Jean-Jacques, Boutevin, Bernard, Argalon, Morgane, and Michel, Alain

Abstract

In the presence of ethylene glycol, poly(ethylene terephthalate) (PET) undergoes chain scissions with the formation of α,ω-hydroxyl oligomers, through classical transesterification by alcoholysis. ɛ-Caprolactone was subsequently added on the hydroxyl end groups of PET oligomers by ring-opening polymerization at different molar ratios of ɛ-caprolactone to PET oligomers. The chemical structure of the products was investigated by size exclusion chromatography, 1H NMR spectroscopy, and differential scanning calorimetry. A large majority of these products are soluble in common organic solvents. The thermal and 1H NMR analyses reveal that the transesterification between base units of PET oligomers and ɛ-caprolactone during the synthesis is always present whatever the reaction conditions. This phenomenon leads to copolymers having thermal properties different from those of PET. However, some co-oligomers present the interest of keeping properties close to those of PET. The main purpose of this study was the synthesis of PET co-oligomers that are soluble in some organic solvents that would make their use easier, and so that they can be used further as hard segment precursers for polycondensation reactions. Ring-opening polymerization of ɛ-caprolactone onto hydroxytelechelic oligomers of PET.

Published
2002
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results