EFFECT OF UNIAXIAL DEFORMATION, ANNEALING AND CARBON NANOTUBES ON THE MORPHOLOGY AND MECHANICAL PROPERTIES OF POLY (BUTYLENE TEREPHTHALATE) AND PBT NANOCOMPOSITES

ABSTRACT The goal of this investigation is to elucidate the interrelations between the strain-induced crystallization behavior, morphology and mechanical properties of poly (butylene terephthalate) PBT and its nanocomposites with multi-walled carbon nanotubes (MWNTs). The mechanical properties of semicrystalline polymers such as PBT depend upon the processing conditions, which affect the crystallization behavior and the resulting crystal morphology developed within the processed sample. PBT is observed to undergo strain-induced crystallization during uniaxial deformation, with concomitant changes in the polymer crystal as a function of the applied strain history. In the current work polymer morphology was investigated with wide angle XRD, differential scanning calorimetry (DSC) and polarized light microscopy (PLM). DSC results indicate an increase in crystallinity due to strain-induced crystallization during uniaxial cold-stretching, which was further confirmed with XRD analysis of the samples. Analyses of the samples under polarized light pre-and post-stretching clearly show that there is a transformation of the spherulitic crystals of the pre-stretch morphology into elongated oblong crystals, as the imposed strain exceeds a critical value. Annealing of PBT was done under different conditions to probe the effects of changes in the crystallinity obtained upon thermal treatment on polymer morphology and mechanical properties. The annealed samples were found to have high crystallinity, high Young's modulus, and low yield stress values as compared to unannealed samples processed under similar conditions. To investigate the effects of nanoparticle loadings on PBT crystal morphology and mechanical properties, pure PBT was melt mixed with different concentrations of multi-walled carbon nanotubes (MWNTs). Due to the increased nucleation rate effect associated with the incorporation of MWNTs, the PBT crystallization temperature was increased and the crystal size decreased with the increasing concentration of MWNTs. Tensile tests performed on PBT and their nanocomposite samples revealed decreases in the elongation at break values. Research is ongoing to understand the relationship between the MWNT loading levels and mechanical properties along with study of orientation of MWNTs under tensile load and its effect on strain-induced crystallization

Quantitative imaging of concentrated suspensions under flow

We review recent advances in imaging the flow of concentrated suspensions, focussing on the use of confocal microscopy to obtain time-resolved information on the single-particle level in these systems. After motivating the need for quantitative (confocal) imaging in suspension rheology, we briefly describe the particles, sample environments, microscopy tools and analysis algorithms needed to perform this kind of experiments. The second part of the review focusses on microscopic aspects of the flow of concentrated model hard-sphere-like suspensions, and the relation to non-linear rheological phenomena such as yielding, shear localization, wall slip and shear-induced ordering. Both Brownian and non-Brownian systems will be described. We show how quantitative imaging can improve our understanding of the connection between microscopic dynamics and bulk flow.Comment: Review on imaging hard-sphere suspensions, incl summary of methodology. Submitted for special volume 'High Solid Dispersions' ed. M. Cloitre, Vol. xx of 'Advances and Polymer Science' (Springer, Berlin, 2009); 22 pages, 16 fig

Polymer Flow Through Porous Media: Numerical Prediction of the Contribution of Slip to the Apparent Viscosity.

The flow of polymer solutions in porous media is often described using Darcy’s law with an apparent viscosity capturing the observed thinning or thickening effects. While the macroscale form is well accepted, the fundamentals of the pore-scale mechanisms, their link with the apparent viscosity, and their relative influence are still a matter of debate. Besides the complex effects associated with the rheology of the bulk fluid, the flow is also deeply influenced by the mechanisms occurring close to the solid/liquid interface, where polymer molecules can arrange and interact in a complex manner. In this paper, we focus on a repulsive mechanism, where polymer molecules are pushed away from the interface, yielding a so-called depletion layer in the vicinity of the wall. This depletion layer acts as a lubricating film that may be represented by an effective slip boundary condition. Here, our goal is to provide a simple mean to evaluate the contribution of this slip effect to the apparent viscosity. To do so, we solve the pore-scale flow numerically in idealized porous media with a slip length evaluated analytically in a tube. Besides its simplicity, the advantage of our approach is also that it captures relatively well the apparent viscosity obtained from core-flood experiments, using only a limited number of inputs. Therefore, it may be useful in many applications to rapidly estimate the influence of the depletion layer effect over the macroscale flow and its relative contribution compared to other phenomena, such as non-Newtonian effects