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Carbon black (CB) is an old-concept but versatile carbonaceous material prone to be structurally and chemically modified under quite mild wet conditions. Recently, we exploited the potentiality of CB for the production of a highly varied array of advanced materials with applications in energetics, water remediation and sensoristic. The proposed approaches are devised to meet specific needs: low production costs, scalable synthetic approaches, flexibility i.e. easy tuning of chemico-physical properties of the carbon-based advanced materials. Two main approaches have been exploited: modification of CB at the surface and highly CB de-structuration. The former approach allows obtaining highly homogenous CB-modified nanoparticles (around 160 nm) with tunable surface properties (hydrophilicity, typology of functional groups and surface charge density, pore size distribution), supports for ionic liquid (SILP) and composites (carbon-iron oxide). The latter approach exploiting a top-down demolition of CB produces a highly versatile graphene related material (GRM), made up by stacked short graphene-like layers (GL) particularly suitable for advanced composites synthesis and ultrathin carbon-based films production.

The recent development of eumelanin pigment-based blends integrating “classical” organic conducting materials is expanding the scope of eumelanin in bioelectronics. Beyond the achievement of high conductivity level, another major goal lays in the knowledge and feasible control of structure/properties relationship. We systematically investigated different hybrid materials prepared by in situ polymerization of the eumelanin precursor 5,6-dihydroxyindole (DHI) in presence of various amounts of graphene-like layers. Spectroscopic studies performed by solid state nuclear magnetic resonance (ss-NMR), x-ray photoemission, and absorption spectroscopies gave a strong indication of the direct impact that the integration of graphene-like layers into the nascent polymerized DHI-based eumelanin has on the structural organization of the pigment itself, while infrared, and photoemission spectroscopies indicated the occurrence of negligible changes as concerns the chemical units. A tighter packing of the constituent units could represent a strong factor responsible for the observed improved electrical conductivity of the hybrid materials, and could be possible exploited as a tool for electrical conductivity tuning.

Acid-base and metal ions adsorptive properties of colloidal carbon-based nanostructured materials, bearing a variable number of oxygen-containing functional groups at the surface, were investigated and modeled. Hydrophilic carbonaceous nanoparticles (HNPs) with uniform dimensions and a good grade of dispersion in water, were obtained through the oxidation of a carbon black with nitric acid, at a temperature of 100 °C, for different reaction times (2–24 h). The acid-base properties of the functional groups were evaluated in water suspension by potentiometry and infrared spectroscopy. By means of X-ray fluorescence, infrared spectroscopy and differential pulse voltammetry the interaction properties of HNPs with Cd2+, Zn2+, Pb2+ and selected Ln3+ ions have also been investigated. The experimental data, collected in the 2.0–7.0 pH range, suggest that the adsorption of metal ions on HNPs is controlled by chemical adsorption involving the strong complexation of metal ions with the carboxylic groups on the surface of HNPs. Particularly, the high complexation of Ln3+ ions opens the exploitation of HNPs in solid phase extraction for preconcentration, separation and determination of rare earth elements and actinides.

none 10 no The exploitation of nanomaterials with antimicrobial properties has attracted an ever-growing interest in the recent years. Carbon-based materials, such as graphene and graphene family materials (GFMs), have gained most of the attention for application in many biomedical fields. Here, we describe the antimicrobial activity of graphene-like (GL) layers derived from the chemical demolition of carbon black, against the planktonic growth of Staphylococcus aureus cells, primary cause of hospital and community-acquired infections, often leading to bacteremia and sepsis. The inhibitory capabilities of GL layers on the formation of S. aureus biofilm are also assessed. The antimicrobial properties seem based mainly on the interaction between GL layers and bacteria surfaces. FESEM and AFM analyses suggest that the GL layers coat the cells as soon as they get in contact with them, as also indicated by the wettability of the GLs. Olivi, M.; Alfè, M.; Gargiulo, V.; Valle, F.; Mura, F.; Di Giosia, M.; Rapino, S.; Palleschi, C.; Uccelletti, D; Fiorito, S. Olivi, M.; Alfè, M.; Gargiulo, V.; Valle, F.; Mura, F.; Di Giosia, M.; Rapino, S.; Palleschi, C.; Uccelletti, D; Fiorito, S.

The conformational features of hyaluronic acid, a key polysaccharide with important biological properties, have been determined through the combined used of nuclear magnetic resonance (NMR) spectroscopy and molecular modeling techniques. A decasaccharide fragment of sodium hyaluronate (HA) was submitted to 3.5 ns of molecular dynamics in explicit water environment form. The same decasaccharide was prepared by hyaluronidase digestion for the experimental study. The approach consisted in the measurements of NMR residual dipolar coupling (RDC) which were used to filter the molecular dynamics data by retaining those structures which were in agreement with the experimental observations. Further analysis of the new conformer ensemble (HA(RDC)) and clustering the molecules with respect to their overall length led to seven representative structures, which were described in terms of their secondary motifs, namely the best fitting helix geometry. As a result, this protocol permitted the assessment that hyaluronic acid can adopt two different arrangements, which can be described by a three- or four-folded left-handed helix, with a higher occurrence of the first one.