This thesis provides a study of different aspects of the mechanical and vibrational properties of disordered and amorphous solids. Resorting to the theoretical framework of non-affine lattice dynamics the attention is focused on the analysis of disordered networks and lattices which serve as tractable model systems for real materials. Firstly, we discuss the static elastic response and the vibrational spectra of defective fcc crystals. The connection to different types of microstructural disorder in the form of bond-depletion and vacancies is described within the context of the inversion symmetry breaking of the local particle configurations. We identify the fluctuations of the local inversion symmetry breaking, which is directly linked to the non-affinity of the disordered solid, as the source of different scalings behaviours of the position of the boson peak. Furthermore, we describe the elastic heterogeneities occurring in a bond-depleted two- dimensional lattice with long-range interactions. The dependence of the concomitant correlations of the local elastic moduli are studied in detail in terms of the interaction range and the degree of disorder. An analytical scaling relation is derived for the radial part of the elastic correlations in the affine limit. Subsequently, we provide an argument for the change of the angular symmetry of the elastic correlation function which was observed in simulations and experiments on glasses and colloids, respectively. Moving to the dynamical behaviour of disordered solids, a framework is developed based on the kernel polynomial method for the approximate computation of the non- affine correlator of displacement fields which is the key requirement to describe the linear viscoelastic response of the system within the quasi-static non-affine formalism. This approach is then extended to the case of multicomponent polymer melts and validated against molecular dynamics simulations at low non-zero temperatures. We also consider the dynamical behaviour of metallic glasses in terms of its shear elasticity and viscosity. A theoretical scheme is suggested which links the repulsive strength of the interatomic potential to the viscoelasticity and fragility in metallic glasses in the quasi-affine limit.

L'objectif de cette thèse est l'étude des conséquences de la thermo-oxydation sur la structure chimique et le comportement mécanique d'un Ethylène Propylène Diène Monomère (EPDM). Afin de déterminer les modifications à différentes échelles structurales, quatre formulations modèles sont étudiées : la gomme pure, les matrices vulcanisées stabilisée et non stabilisée et l'élastomère industriel. L'ensemble des échantillons est vieilli entre 70 et 170°C dans l'air ou sous vide puis caractérisé par divers outils analytiques. La thermogravimétrie donne accès aux variations de masse résultant de l'incorporation d'oxygène et l'émission de composés volatils. L'analyse infrarouge permet de suivre les évolutions des espèces chimiques. Les essais de gonflement, de chromatographie et de spectrométrie mécanique permettent de calculer les nombres de coupures de chaînes et d'actes de réticulation à chaque instant. Sur la base de ces résultats, un modèle cinétique général de thermo-oxydation de la matrice EPDM est proposé et en partie validé. Les conséquences du vieillissement thermique sur le comportement mécanique de l'élastomère industriel sont mises en évidence par des essais de traction uniaxiale et de multi-relaxation à température ambiante et vitesse de déformation initiale de 10-3 s-1. L'impact du vieillissement thermique sur les propriétés ultimes et les réponses à l'équilibre et hors équilibre est examiné. Un critère prédictif de rupture basé sur la mécanique de la rupture est proposé. Enfin, le couplage vieillissement thermique - contrainte mécanique est étudié par des essais relaxation de contraintes continues entre 130 et 170°C dans l'air. Les modifications de la microstructure pendant le vieillissement thermique sont intégrées dans les équations constitutives du modèle mécanique macroscopique afin de proposer un outil de prédiction du comportement à long terme de l'élastomère industriel. La simulation numérique montre une bonne adéquation avec les résultats expérimentaux. / The aim of this work is to study the consequences of the thermal oxidation on the chemical structure and mechanical behavior of an Ethylene-Propylene-Diene Monomer (EPDM). In order to determine the structural changes at different scales, four model formulations have been considered: free additive gum, stabilized and unstabilized vulcanized matrix and industrial rubber. All samples were aged between 70 and 170°C in air or vacuum and characterized by several analytical tools. Thermogravimetry gives access to weight variations due to oxygen grafting and volatile compounds release. Infrared analysis is used to follow chemical species evolutions. Swelling tests, chromatographic and mechanical spectrometry tests allow calculating the number of chain scission and cross-linking events at any time. Based on these results, a general kinetic model is proposed and partially validated for EPDM matrix thermal oxidation. The consequences of thermal ageing on the mechanical behavior of the industrial rubber are pointed out by monotonic tensile and stress relaxation tests at room temperature and a 10-3 s-1- initial strain rate. The impact of thermal ageing on ultimate properties and equilibrium and non-equilibrium response are examined. Finally, the coupling between thermal ageing and mechanical stress is studied by continuous stress relaxation tests between 130 et 170°C in air. The microstructural modifications during thermal ageing are introduced into the constitutive equations of the macroscopic mechanical model in order to propose a predictif tool of the long time behavior of the industrial rubber. The numerical simulation is in good agreement with experimental results.

<p>The present dissertation focuses on two themes: (i) elastic instability of flow and (ii) elastic instability of microscopic filaments.</p> <p><br></p> <p>(i) The presence of macromolecules often leads to the viscoelastic nature of industrial and biological fluids. The flow of viscoelastic fluids in porous media is important in many industrial, geophysical, and biological applications such as enhanced oil recovery, groundwater remediation, biofilm formation, and drug delivery. The stretching of polymeric chains as the viscoelastic fluid passes through the microstructure of the porous media induces large elastic stresses, which leads to viscoelastic instability at the Weissenberg number greater than a critical value, where the Weissenberg number quantifies the ratio of elastic to viscous forces. Viscoelastic instability can lead to a time-dependent chaotic flow even at negligible inertia, which is sometimes also known as elastic turbulence due to its analogous features to traditional inertial turbulence. In the present thesis, we investigate the pore-scale viscoelastic instabilities and the flow states induced by the instabilities in symmetric and asymmetric geometries. We found that the topology of the polymeric stress field regulates the formation of different flow states during viscoelastic instabilities. Viscoelastic instability-induced flow states exhibit hysteresis due to the requirement of a finite time for the transformation of polymeric stress topology. Further, we study viscoelastic flows through ordered and disordered porous geometries and explore the effect of viscoelastic instability on sample-scale transport properties. Viscoelastic instability enhances transverse transport in ordered porous media and longitudinal transport in disordered porous media. We also derive a relationship between the polymeric stress field and the Lagrangian stretching field. The Lagrangian stretching field helps to predict the feature of flow states and transport in complex flows. The experimental measurement of the polymeric stress field is extremely challenging. The framework established here can be used to obtain the topology of the polymeric stress field directly from the easily measured velocity field.  </p> <p><br></p> <p><br></p> <p>(ii) The interaction between flow and elastic filaments plays an important role in sperm and bacterial motility and cell division. The sperm cells of many organisms use long elastic flagellum to propel themselves and also face complex flows and boundaries during their search for egg cells. Strong flows have the potential to mechanically inhibit flagellar motility through elastohydrodynamic interactions. We explore the effects of an extensional flow on the buckling dynamics of sperm flagella through detailed numerical simulations and microfluidic experiments. Compressional fluid forces lead to rich buckling dynamics of the sperm flagellum beyond a critical dimensionless sperm number, which represents the ratio of viscous force to elastic force. Shear flows navigate the sperm cells in complex geometries and flows. We have also studied the effect of flow strength and flagellar elastic deformation on the sperm trajectory in simple shear and Poiseuille flows.</p>