The research activities of our group focus on polymer mechanical properties and interfaces and often contain both a deformation and fracture component and an interface and adhesion component. We are particularly interested in the processes where deformation of the material is in the large strain regime and in the understanding of macroscopic fracture or adhesion processes.
For all the specific topics that we have investigated, we try to establish a connection between the molecular structure or the material organization at the nano and micro level, and the macroscopic mechanical properties. Often in fracture processes, complex and inhomogeneous deformations occur before an actula macroscopic fracture takes place. The undersanding of these large deformation processes which modify the structure of the material are essential to understand the fracture process itself. In essence for deformable materials, it is not the undeformed material which fractures but it is often a highly deformed and modifed structure, which needs specific chaacterization methods.
We have developed specific techniques adapted to the investigation of the fracture of highly deformable materials, which generally use in-situ observation of deformation mechanisms and confined polymer layers. In addition of course we use standard tools of polymer science such as DSC, rheology in the linear regime, NMR and FTIR for the characterization of the chemical structure.
A second key aspect of our work is the behavior of materials at interfaces.
Because interfaces impose a boundary condition to the deforamtion, understanding
their structure and how this structure influences the boundary conditions is
essential to understand the deformation behavior. Often interfaces are also
weak mechanical points and improving, or more generally controlling the level
of adhesion at an interface, is an importat practical and scientific goal.
We present now some examples of applications where interfaces are important which will be followed by some examples of research projects.
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In coextruded polymer multilayers, several polymers are put in contact in the melt state in a specially designed die within the extruder. Once the multilayer has exited the die and cools down, it is essential for the integrity of the assembly that a good adhesion was achieved between the layers during this relatively short contact time in the melt state. In the typical food packaging application, a polar central layer acts as a barrier to oxygen and water, while the two outside layers (typically a polyolefin) impart their ductility to the assembly. Two additional tie-layers are necessary to obtain a good adhesion between the polar layer and the polyolefin. th tie-layer contains typically some modified polyolefin chains which are miscible with the polyolefin layer and can react chemically with a polar function on the center layer |
More info:Laurens, C., Ober,R., Creton, C. and Léger, L.
(2004) "Crystalline Orientation and Adhesion at polypropylene/polyamide
6 interfaces compatibilized with syndiotactic polypropylene-polyamide-6
diblock copolymers". Macromolecules, 37, 6806-6813. Laurens, C., Creton, C., Léger, L. (2004) " Adhesion
promotion mechanisms at isotactic polypropylene/polyamide 6 interfaces
: role of the copolymer architecture ", Macromolecules, 37, 6814-6822. |
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K. Landfester, R. Rothe, M. Antonietti, |
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Water-based paints are actually made from an emulsion of polymer particles with a size varying between 100 and 400 nm, stabilized by surfactants. During the drying process ,the water evaporates, the particles come in contact with each other and a good particle-particle adhesion is necessary to form a homogeneous and cohesive film. The control of the interdiffusion process of the polymers contained in the particle is essential for this good adhesion between particles and hence to obtain a paint film of good aspect and mechanical properties |
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Research Projects |
Mechanisms of adhesion of soft adhesives:In this area, we investigate the effect of systematic changes in the molecular structure or architecture of polymers typically used as pressure-sensitive-adhesives, on the micromechanisms of deformation during debonding of the adhesive layer. The main tool used in these investigations is the probe tack tester, which has been designed to test the adhesive properties of confined deformable layers in a reproducible way while observing the deformation mechanisms in real time. The rheological properties of the materials used are also of course characterized and whenever possible, tensile tests are carried out to determine the large strain deformation properties of the material.
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Mechanics of the probe tack testMechanics of the probe tack Adhesives based on acrylic statistical copolymers Adhesives based on styrene-isoprene block copolymers
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More infoShull, K.R. and Creton, C. (2004) "Deformation Behavior of Thin,
Compliant Layers Under Tensile Loading Conditions". J. Polym. Sci. Polym.
Ed. 42, 4023-4043. Lindner A, Lestriez B, Mariot S, Creton C, Maevis T, Luhmann B, Brummer R (2006) "Adhesive and rheological properties of lightly crosslinked model acrylic networks" J. Adh. 82 (3), 267-310. abstract Creton, C., A. Roos, and A. Chiche (2005) "Effect of the diblock content on the adhesive and deformation properties of PSAs based on styrenic block copolymers" in Adhesion: Current Research and Applications, W.G. Possart, Editor. Wiley-VCH: Weinheim. p. 337-364. abstract B. Lestriez, H. Lakrout, A. Chiche, A. Roos and C. Creton. "Probe tack tests as a characterization tool in pressure-sensitive-adhesives" Proceedings of the PSTC Technical Seminar TECH XXIV, Orlando, USA, 2-4 May 2001. pdf file |
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Effects of a surface modification on the failure mechanisms of soft adhesivesThe interfacial debonding of very deformable materials such as soft adhesives depends of course on the mechanical properties of the adhesive itself but depends also on the chemical composition and surface roughness of the adherent which provides a boundary condition to the deformation of the material imposed by the applied load. The surface of the adherent can be modified either chemically (by modifying the surface with functional groups or with polymers capable of entanglements with the adhesive material, or topographically through a modification of the surface roughness. In both cases the debonding mechanism will be modified and a relatively complex coupling between the deformation properties of the adhesive and the interactions at the interface will determine the observed debonding pattern. |
Effect of surface roughness on the debonding mechanisms of soft adhesives From adhesion to release with changes in rheological properties of the adhesives or in chemical composition of the surface Switchable adhesion with bicomponent polymer brushes.
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More infoH. Retsos, A. Kiriy, V. Senkovskyy, M. Stamm, M. M. Feldstein and
C. Creton (2006) "Controlling tack with Bicomponent Polymer Brushes",
Adv. Mat. 18 (19), 2624-2628. Josse, G., Sergot, P., Dorget, M. and Creton, C. (2004).
"Measuring interfacial adhesion between a soft viscoelastic layer and
a rigid surface using a probe method." Journal of Adhesion, 80
(1-2), 87-118. Chiche, A., P.Pareige and C. Creton (2000) "Role of surface roughess
in controlling the adhesion of a soft adhesive on a hard surface" Comptes
Rendus de L'Académie des Sciences, Série IV, 1: 1197-1204. C. Creton, G. Josse, A. Chiche. "Mécanismes d 'adhésion et contrôle de l 'adhérence pour les matériaux très déformables" Proceedings of the 9èmes journées de la formulation, Lyon, France, 9-10 december 2002.pdf file |
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Fracture of interfaces between polymer melts When two very entangled high molecular weight polymer melts are put in contact, polymer chains interdiffuse and entanglements are formed across the interface increasing its mechanical strength. The conditions of this reinforcement depend on the nature of the polymers, on their molecular weight and on their degree of miscibility. In order to test reproducibly this mechanical strength of the interface a specific test of fluid fracture was developed. This test confines the two fluid layers between two parallel rigid plates and fractures then the interface by applying a tensile stress. The confinement is essential to avoid excessive deformation unrelated to the interfacial strength. |
Study of the Adhesion between polymer melts
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More infoR. Schach, Y. Tran, A. Menelle, C. Creton "Adhesion at Interfaces Between Immiscible Polymer Melts" World Polymer Congress, 41' International Symposium on Macromolecules, Rio de Janeiro, Brazil, 16-21th july 2006 pdf file R. Schach and C. Creton "Adhesion between Polymeric Fluids using a Probe Method" Proceedings of the 229th ACS National Meeting, San Diego, USA, 13-17 March 2005. pdf file R.Schach, C.Creton "Polymer-polymer adhesion of uncrosslinked
elastomers at short contact times" |
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Mechanical properties of hydrogels When a water-soluble polymer is chemically crosslinked, it forms a network which swells but no longer dissolves in water. This water-swollen crosslinked polymer is then called a hydrogel. Although the equilibrium swelling properties and the elastic properties of hydrogels have been well studied, their large-strain and fracture properties remain poorly understood. More specifically, while most hydrogels are rather weak solids, certain types of hydrogels can be quite strong, due to their specific network architecture. The reasons of this exceptional toughness are poorly understood |
Synthesis and rheological properties of hydrogels containing grafted hydrophobic groups.
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More infoG. Miquelard-Garnier, C. Creton, D. Hourdet "Synthesis and rheological behaviour of new hydrophobically modified hydrogels" World Polymer Congress, 41' International Symposium on Macromolecules, Rio de Janeiro, Brazil, 16-21th july 2006 pdf file |
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