Third International Conference on Polymer Behavior: “Multiphysics Approaches for the Behavior of Polymers and Polymer-Based Nanomaterials” (original) (raw)
Related papers
Parameters governing strain induced crystallization in filled natural rubber
Polymer, 2007
A series of in situ synchrotron X-ray diffraction experiments are performed during the stretching of weakly and highly vulcanized carbon black (CB), silica and grafted silica filled natural rubber sample (NR). Conversely to literature, Mullins effect observed after one stretching cycle modifies the strain induced crystallization (SIC) behaviour of the sample. The onset of crystallization is ruled by the strain amplification induced by the filler presence. Moreover, fillers (CB and silica) behave as additional crosslinks into NR network, through fillererubber interactions that either accelerate or slow down the crystallization rate depending on NR matrix chemical crosslink density. This is consistent with the assumption that effective network density, which is due to chemical crosslinks, entanglements, and fillererubber interactions, controls the crystallization rate.
Intrinsic Deformation Behavior of Semicrystalline Polymers
Macromolecules, 2004
The influence of crystallinity and lamellar thickness on the intrinsic deformation behavior of a number of semicrystalline polymers is studied: a poly(ethylene terephthalate) and two different molecular weight grades of polyethylene and polypropylene. The crystallinity and lamellar thickness are altered by varying the rate of crystallization from the melt and by cold crystallization (annealing) at elevated temperatures above T g but below the melting point. Crystallinity and lamellar thickness are determined by wide-angle X-ray diffraction and small-angle X-ray scattering measurements. Uniaxial compression tests are performed to obtain the large strain intrinsic deformation behavior, e.g., yield stress, strain softening, and strain hardening modulus. The yield stress is found to be proportional to lamellar thickness, whereas the strain hardening modulus is shown not to depend on crystallinity or lamellar thickness. Over the strain range experimentally covered, the strain hardening modulus appears to be well described by a simple neo-Hookean relation and appears to be related to the chain entanglement density. An affirmation for this relation arises from the observation that slowly melt crystallized samples exhibit a lower strain hardening, resulting from a lower chain entanglement density, which is expected to be caused by reeling in of the molecular chains in such a slow crystallization process. The similarity in the results observed on all polymers tested supports the conclusion that the crystalline phase does not contribute to strain hardening, which is primary controlled by the chain entanglement density.
A study of strain-induced crystallization of polymers
The response of polymers depends on their morphology. One of the challenges in modeling from a continuum perspective is how to incorporate the microstructural features into the homogenized continuum model. Here, we use a recent framework that associates dierent natural states and material symmetries with distinct microstructures of the body (Rajagopal, K.. We study the problem of strain-induced crystallization of polymeric materials, in particular, we study the problem of uniaxial stretching of polymeric materials and the subsequent crystallization and the predictions of the theory are compared with experimental results.
Strain-induced crystallization of natural rubber with high strain rates
Journal of Polymer Science Part B: Polymer Physics, 2012
Strain-induced crystallization (SIC) of natural rubber (NR) samples with different strain rates at a fixed strain was investigated by synchrotron radiation X-ray diffraction measurements, which provided the evolution trends of crystal sizes and crystallinity during the SIC process. It was found that the Avrami index was about 1 during the crystallization of NR after the cessation of stretch, which demonstrated that sporadic nucleation occurred during SIC process. The increase of the crystallinity was attributed to the increase of the number of new crystallites rather than the growth of the crystal size. An unexpected relationship between the final crystallinity and the strain rates was observed. The increase of physical crosslink points originated from either entanglement or crystallite was considered as the reason that leads to the nonmonotonic variation of the final crystallinity with strain rates. V
Dominating factor of strain-induced crystallization in natural rubber
Polymer, 2015
The contribution of entropy change due to stretching of polymer chains in promoting crystal nucleation is theoretically derived for strain-induced crystallization of natural rubber. The results of theoretical calculation are compared with experimental results obtained by fast time-resolved wide-angle X-ray diffraction. Usual values of surface free energies corresponding to chain-folded nuclei lead to theoretical results far from experimental measurements. Because the discrepancy comes from the large activation energy of nucleation even after the stretching of polymer chains, additional contribution of reduced surface free energies due to the formation of bundle-like nuclei was taken into account. This treatment allows to faithfully reproduce experimental results and then to conclude that nuclei formed in natural rubber during stretching are of bundle-like type. Moreover, it reveals that surface energies have a greater effect on the decrease of critical free energy than the change in entropy due to deformation.
Journal of The Mechanics and Physics of Solids, 2022
HAL is a multidisciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers. L'archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d'enseignement et de recherche français ou étrangers, des laboratoires publics ou privés. Distributed under a Creative Commons Attribution-NonCommercial| 4.0 International License