Gabriel Gedler

Multifunctional nanocomposite foams based on polypropylene with carbon nanofillers

This work considers the preparation and characterization of polypropylene foams with variable concentrations of graphene and carbon nanofibres, focussing on the influence of the foaming process and the nanofillers on the microstructural and dynamic-mechanical-thermal properties of the foams. Great differences were found in terms of foam morphology depending on the type of foaming process, with foams prepared by physical foaming showing a vertically deformed cell structure, while chemical foams presented an isotropic-like cellular structure. The addition of graphene resulted in foams with higher cell densities and more uniform cellular structures when compared to the ones with nanofibres. Direct result of the combination of their particular cellular structure and higher expansion, polypropylene foams obtained by physical foaming presented a higher orientation of the α-monoclinic polypropylene crystal perpendicular to the foam’s surface and higher exfoliation of the nanofillers, resulting in foams with improved mechanical properties. All these considerations are of extreme importance, as some of the most promising applications of these polymer foams require a good electromagnetic interference shielding efficiency, which greatly depends on the developed foam morphology.

Novel polycarbonate-graphene nanocomposite foams prepared by CO2 dissolution

Polycarbonate foams reinforced with 0,5 wt% of graphene were obtained by firstly melt-mixing the polycarbonate and graphene in an internal mixer, compression-moulding the melt-compounded grinded material and lastly dissolving CO2 inside a high pressure vessel. The CO2 desorption behaviour in the unfilled polycarbonate and nanocomposite was studied in terms of the CO2 saturation concentration and desorption diffusion coefficient, with the graphene-filled nanocomposite displaying a higher CO2 loss rate when compared to the neat polycarbonate. The cellular structure of the foams was found to be highly dependent on the saturation/foaming temperature, with smaller cell sizes being obtained with decreasing the temperature. Another parameter that had an important influence was the residual pressure, with higher residual pressure values resulting in foams with more uniform and regular cells.

Enhanced electrical conductivity in graphene-filled polycarbonate nanocomposites by microcellular foaming with sc-CO2

Abstract Electrically conductive polycarbonate (PC) foams containing a low concentration of graphene nanoplatelets (0.5 wt.%) were produced with variable range of expansion ratio by applying a high-pressure batch foaming process using sc-CO2. The structure of the foams was assessed by means of SEM, AFM and WAXS, and the electrical conductivity was measured in the foam growing direction. Results showed that electrical conductivity of PC composite foams remarkably increased when compared to that of non-foamed PC composite, with both the electrical conductivity and the main cell size of the foams being directly affected by the resultant expansion ratio of the foam. This interesting result could be explained by the development of an interconnected graphene nanoparticle network composed by increasingly well-dispersed and reoriented graphene nanoplatelets, which was developed into the solid fraction of the foam upon foaming by sudden depressurising of the plasticised CO2-saturated PC preform. Some evidences of morphological changes in the graphene nanoplatelets after foaming were obtained by analysing variations in graphene’s (0 0 2) diffraction plane, whose intensity decreased with foaming. A reduction of the average number of layers in the graphene nanoplatelets was also measured, both evidences indicating that improved dispersion of graphene nanoparticles existed in the PC composite foams. As a result, foams with a proper combination of low density and enhanced electrical conductivity could be produced, enabling them to be used in applications such as electromagnetic interference shielding.

Diffusion of CO2 in Polymer Nanocomposites Containing Different Types of Carbon Nanoparticles for Solid-State Microcellular Foaming Applications

This work considers the study of the diffusion of carbon dioxide in polypropylene and amorphous polymers containing carbon nanoparticles, particularly carbon nanofibres and graphene, as well as nanoclays, to be used in microcellular foaming. The diffusion of CO2 out and into the nanocomposites was studied during high pressure CO2 dissolution, as the amount of CO2 dissolved into the nanocomposite and CO2 desorption rate are crucial in order to have a proper control of foaming. Comparatively, platelet-like nanoparticles slowed down the desorption of CO2 out of the nanocomposites by means of a physical barrier effect, enabling a higher concentration of CO2 to remain in the polymer and be used in foaming. As a consequence of the higher amount of CO2 retained in the polymer and the cell nucleation effect promoted by the nanoparticles, polymer nanocomposite foams presented finer microcellular structures, in the case of PMMA even sub-microcellular, and higher specific moduli and electrical conductivities when compared to their pure counterparts.