Experimental clues of soft glassy rheology in strained filled elastomers

International audienceTensile stress-relaxation measurements have been performed on a series of cross-linked filled elastomers. The fillers are chosen in order to investigate the effect of the filler-filler and the filler-matrix interactions on the time dependence of the tensile relaxation modulus E(t) after UP and DOWN jumps. For the carbon black filled sample (strong filler-elastomer interaction) E(t) decreases as log(t) when the strain epsilon is strictly larger than 0.2 and reached by UP jumps. For the silica filled samples in the same conditions, and for all samples after a DOWN jump including epsilon = 0.2, the experimental data can be fitted with a power law equation characterized by the exponent m. Thus, in all cases, |dE(t)⁄dt| scales as t^(-α) with α=m+1. Pertinence of the Soft Glassy Rheology (SGR) model for interpreting the present results is examined. It is shown that α could be equivalent to the effective noise temperature x and related to the polymer chain mobility

X-ray Near Field Speckle: Implementation and Critical Analysis

We have implemented the newly-introduced, coherence-based technique of x-ray near-field speckle (XNFS) at 8-ID-I at the Advanced Photon Source. In the near field regime of high-brilliance synchrotron x-rays scattered from a sample of interest, it turns out, that, when the scattered radiation and the main beam both impinge upon an x-ray area detector, the measured intensity shows low-contrast speckles, resulting from interference between the incident and scattered beams. We built a micrometer-resolution XNFS detector with a high numerical aperture microscope objective and demonstrate its capability for studying static structures and dynamics at longer length scales than traditional far field x-ray scattering techniques. Specifically, we characterized the structure and dynamics of dilute silica and polystyrene colloidal samples. Our study reveals certain limitations of the XNFS technique, which we discuss.Comment: 53 pages, 16 figure

Tuning the Mechanical Properties in Model Nanocomposites: Influence of the Polymer-Filler Interfacial Interactions

This paper presents a study of the polymer-filler interfacial effects on filler dispersion and mechanical reinforcement in Polystyrene (PS) / silica nanocomposites by direct comparison of two model systems: un-grafted and PS-grafted silica dispersed in PS matrix. The structure of nanoparticles has been investigated by combining Small Angle Neutron Scattering (SANS) measurements and Transmission Electronic Microscopic (TEM) images. The mechanical properties were studied over a wide range of deformation by plate/plate rheology and uni-axial stretching. At low silica volume fraction, the particles arrange, for both systems, in small finite size non-connected aggregates and the materials exhibit a solid-like behavior independent of the local polymer/fillers interactions suggesting that reinforcement is dominated by additional long range effects. At high silica volume fraction, a continuous connected network is created leading to a fast increase of reinforcement whose amplitude is then directly dependent on the strength of the local particle/particle interactions and lower with grafting likely due to deformation of grafted polymer.Comment: Journal Polymer Science (2011

Nearly Space-Filling Fractal Networks of Carbon Nanopores

URL:http://link.aps.org/doi/10.1103/PhysRevLett.88.115502 DOI:10.1103/PhysRevLett.88.115502Small-angle x-ray scattering, nitrogen adsorption, and scanning tunneling microscopy show that a series of activated carbons host an extended fractal network of channels with dimension Dp = 2.8-3.0 (pore fractal), channel width 15-20Å (lower end of scaling), network diameter 3000-3400Å (upper end of scaling), and porosity of 0.3-0.6. We interpret the network as a stack of quasiplanar invasion percolation clusters, formed by oxidative removal of walls between closed voids of diameter of ∼10Å and held in registry by fibrils of the biological precursor, and point out unique applications.This work was supported by the Petroleum Research Fund, Grant No. 30602-AC9,5 (P. P.); the Department of Energy, Contracts No. W-7405-ENG-36 (P. P.) and No. DE-AC04-00A185000 (T. P. R.); and the Ceramic and Non-Metallic Materials Program at AFOSR (W. P. H.)

Production of activated carbons from waste tyres for low temperature NOx control

Waste tyres were pyrolysed in a bench scale reactor and the product chars were chemically activated with alkali chemical agents, KOH, K2CO3, NaOH and Na2CO3 to produce waste tyre derived activated carbons. The activated carbon products were then examined in terms of their ability to adsorb NOx (NO) at low temperature (25°C) from a simulated industrial process flue gas. This study investigates the influence of surface area and porosity of the carbons produced with the different alkali chemical activating agents on NO capture from the simulated flue gas. The influence of varying the chemical activation conditions on the porous texture and corresponding NO removal from the flue gas was studied. The activated carbon sorbents were characterized in relation to BET surface area, micropore and mesopore volumes and chemical composition. The highest NO removal efficiency for the waste tyre derived activated carbons was ∼75% which was obtained with the adsorbent treated with KOH which correlated with both the highest BET surface area and largest micropore volume. In contrast, the waste tyre derived activated carbons prepared using K2CO3, NaOH and Na2CO3 alkali activating agents appeared to have little influence on NO removal from the flue gases. The results suggest problematic waste tyres, have the potential to be converted to activated carbons with NOx removal efficiency comparable with conventionally produced carbons