Synergistic icephobic behaviour of swollen nitrile butadiene rubber graphene and/or carbon nanotube composites

Spontaneous change of adhesion of solidifying liquid on surfaces is of significant importance in materials technology where it finds applications such as anti-icing components operating in extreme environments like those of seals. In this work, nitrile butadiene rubber (NBR) composites reinforced with graphene, carbon nanotubes, and a mix of them after immersion in several fluids, experienced both a swelling and a reduction of the cross-link density that reduces ice adhesion, being this effect more evident for graphene containing samples. These results have been rationalized via a first principles atomistic modellization of interfaces formed by ice water of increasing thickness and graphene and scaling laws from fracture mechanics, revealing a clear synergy between swelling and nanocarbon phase in the icephobic nature of the composite, dictated by a competition between elastic modulus and adsorption energy. These findings could find an upscale in component validation readily applied to different areas where de-icing demands handling of large amount of environmental harmful agents.GG wants to thank CINECA [grant number HP10CN7DI0] and acknowledge PRACE for awarding us access to resource Marconi based in Italy at CINECA [Grant number Pra14_3664]. G.G. is similarly grateful to CARIT [grant number FCARITR17FR]” for supporting this research. MALM thanks the support from the MINECO [grant number MAT2016- 81138-R]. NMP is supported by the European Commission under the Graphene Flagship Core2 [WP14 “Composites” grant number 785219] and FET Proactive “Neurofibres” [grant number 732344]. NMP is supported by theItalian Ministry of Education, University and Research (MIUR) under the “Departments of Excellence” grant L.232/2016. LV is supported by the European Commission under the Graphene Flagship Core2 [WP14 “Composites” grant number 785219]. LV and GG rea supported by the Italian Ministry of Education, University and Research (MIUR) under the “Departments of Excellence” grant L.232/2016Peer Reviewe

Structure and properties of polylactide/natural rubber blends

International audiencePolylactide, PLA, is a biodegradable thermoplastic polyester derived from biomass that has restricted packaging applications due to its high brittleness and poor crystallisation behaviour. Here, new formulations based on natural rubber-PLA blends have been developed. The processing windows, temperature, time, and rotor rate, and the rubber content have been optimised in order to obtain a blend with useful properties. The rubber phase was uniformly dispersed in the continuous PLA matrix with a droplet size range from 1.1 to 2.0 mu m. The ductility of PLA has been significantly improved by blending with natural rubber, NR. The elongation at break improved from 5% for neat PLA to 200% by adding 10 wt% NR. In addition, the incorporation of NR not only increased the crystallisation rate but also enhanced the crystallisation ability of PLA. These materials are, therefore, very promising for industrial applications

Comparing the effect of carbon-based nanofillers on the physical properties of flexible polyurethane foams

Flexible polyurethane foams filled with a fixed amount of carbon-based nanofillers, in particular multiwall nanotubes and graphenes, have been studied to clarify the influence of the morphology and functional groups on the physical properties of these polymeric foams. The effect of the carbon nanoparticles on the microphase separation has been analyzed by FT-IR spectroscopy revealing a decrease in the degree of phase separation of the segments. Variations of the glass transition temperature and an improved thermal stability were observed due to the presence of the nanoparticles. The EMI shielding effectiveness of flexible PU foams has also been enhanced, in particular for FGS nanocomposite foams

Physicochemical properties of organoclay filled polylactic acid/natural rubber blend bionanocomposites

International audienceA novel toughened polylactic acid (PLA) bionanocomposite with tuneable properties was successfully prepared by melt mixing PEA with natural rubber and several montmorillonites (MMTs). The organoclays were preferentially located at the interface acting as compatibilisers between both polymer phases. This location resulted in a marked improvement of the physical and mechanical properties of the system. Moreover, these properties can be controlled as a function of the nanofiller nature and the mixing procedure used

Cationic photocured epoxy nanocomposites filled with different carbon fillers

In this work, the effect of several carbon fillers, exfoliated graphite (EG), functionalized graphene sheets (FGS), multi-walled carbon nanotubes (MWCNTs), and oxidized multi-walled carbon nanotubes (f-MWCNTs), were compared on the curing process and physical properties of a cationically photocurable epoxy resin. The extent of the photopolymerization was monitored by Real-Time FTIR spectroscopy. It was found that all the nanofillers delayed the curing reaction probably due to a shielding effect as well as to an increase of the resin viscosity. All the systems showed an electrical percolation threshold, but with MWCNTs was attained at a lower concentration (< 0.1 wt.%). In addition, FGS showed the best response in terms of the dynamic mechanical and microindentation performances. An increase of more than 20 C in the glass transition temperature was observed with the addition of 1 wt.% of FG