Marino Lavorgna

Enhancing electrical conductivity of rubber composites by constructing interconnected network of self-assembled graphene with latex mixing

Vulcanized graphene/natural rubber composites with a conductive segregated network exhibiting good electrical conductivity, water vapor permeability and high mechanical strength are prepared by self-assembly in latex and static hot pressing. The composite exhibits a percolation threshold of ∼0.62 vol% and a conductivity of 0.03 S m−1 at a content of 1.78 vol%, which is ∼5 orders of magnitude higher than that of the composites made by conventional methods at the same loading fraction.

Sodium montmorillonite silylation: Unexpected effect of the aminosilane chain length

In this work, the silylation of sodium montmorillonite (Na-MMT) was performed in glycerol using 3-aminopropyltriethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane and 3-[2-(2-aminoethylamino)ethylamino]-propyl-trimethoxysilane. The effects on the d-spacing of sodium montmorillonite (Na-MMT) upon reaction with three aminosilanes of different chain length were studied in details by combining experimental and computational techniques. Infrared spectroscopy was used to monitor the grafting process, while the degree of grafting was calculated using thermogravimetric analysis. X-ray diffraction experiments were carried out to evaluate the shift of the (0 0 1) basal spacing. It was found that the degree of silylation of Na-MMT increases with increasing the length of the aminosilane organic moieties, the overall aminosilane concentration, and temperature. The same beneficial effects were observed on the silicate d-spacing, as its value increases with increasing silane concentration and reaction temperature. Remarkably, however, increasing the length of the organic chains in the silane modifiers resulted in decreasing values of the Na-MMT interlayer distance. A rationale for this behavior is proposed on the basis of atomistic molecular dynamics simulation evidences.

Active systems based on silver-montmorillonite nanoparticles embedded into bio-based polymer matrices for packaging applications.

Silver-montmorillonite (Ag-MMT) antimicrobial nanoparticles were obtained by allowing silver ions from nitrate solutions to replace the Na(+) of natural montmorillonite and to be reduced by thermal treatment. The Ag-MMT nanoparticles were embedded in agar, zein, and poly(ε-caprolactone) polymer matrices. These nanocomposites were tested in vitro with a three-strain cocktail of Pseudomonas spp. to assess antimicrobial effectiveness. The results indicate that Ag-MMT nanoparticles embedded into agar may have antimicrobial activity against selected spoilage microorganisms. No antimicrobial effects were recorded with active zein and poly(ε-caprolactone). The water content of the polymeric matrix was the key parameter associated with antimicrobial effectiveness of this active system intended for food packaging applications.

Tailoring Assembly of Reduced Graphene Oxide Nanosheets to Control Gas Barrier Properties of Natural Rubber Nanocomposites

Self-assembling of reduced graphene oxide platelets, as a tailored interconnected network within a natural rubber matrix, is proposed as a mean for obtaining nanocomposites with improved gas barrier, as compared to neat natural rubber. Interestingly, this nanocomposite structure results to be much more effective than homogeneous dispersion of graphene platelike particles, even at low graphene loadings. Such behavior is interpreted on the grounds of a theoretical model describing permeability of heterogeneous systems specifically accounting for self-segregated graphene morphology.

MMT-supported Ag nanoparticles for chitosan nanocomposites: Structural properties and antibacterial activity

Multifunctional bionanocomposites have been prepared by loading chitosan matrix with silver-montmorillonite antimicrobial nanoparticles obtained by replacing Na(+) ions of natural montmorillonite with silver ions. This filler has been chosen for its twofold advantage to serve as silver supporting material and to confer new and better performance to the obtained material. It has been proved that the achievement of the intercalation of chitosan into the silicate galleries of montomorillonite as well as the interaction between chitosan and Ag ions and silver particles lead to an enhancement of the thermal stability, to an improvement of mechanical strengths and to a reduction of the liquid water uptake of the obtained bionanocomposites. Results also show that silver ions are released in a steady and prolonged manner providing, after 24 h, a significant reduction in the microbial growth of Pseudomonas spp.

Treatment and recycling of asbestos-cement containing waste

The remediation of industrial buildings covered with asbestos-cement roofs is one of the most important issues in asbestos risk management. The relevant Italian Directives call for the above waste to be treated prior to disposal on landfill. Processes able to eliminate the hazard of these wastes are very attractive because the treated products can be recycled as mineral components in building materials. In this work, asbestos-cement waste is milled by means of a high energy ring mill for up to 4h. The very fine powders obtained at all milling times are characterized to check the mineralogical and morphological transformation of the asbestos phases. Specifically, after 120 min of milling, the disappearance of the chrysotile OH stretching modes at 3690 cm(-1), of the main crystalline chrysotile peaks and of the fibrous phase are detected by means of infrared spectroscopy and X-ray diffraction and scanning electron microscopy analyses, respectively. The hydraulic behavior of the milled powders in presence of lime is also tested at different times. The results of thermal analyses show that the endothermic effects associated to the neo-formed binding phases significantly increase with curing time. Furthermore, the technological efficacy of the recycling process is evaluated by preparing and testing hydraulic lime and milled powder-based mortars. The complete test set gives good results in terms of the hydration kinetics and mechanical properties of the building materials studied. In fact, values of reacted lime around 40% and values of compressive strength in the range of 2.17 and 2.29 MPa, are measured.

Tuning the insulator to conductor transition in a multiwalled carbon nanotubes/epoxy composite at substatistical percolation threshold

A fine tuning of the electrical conductivity from insulator to conductor behavior has been obtained for a multiwalled carbon nanotubes epoxy composite at a fixed substatistical percolation threshold content by varying the organization of the nanotubes network. A multiscale characterization has been carried out by transmission optical microscopy technique and small angle x-ray analysis that revealed a two level structure characterized by different topological arrangements for the micron sized clusters and nanosized isolated bundles, respectively. A picture of the multidimensional organization of the nanotubes network has been proposed to account for the observed transition modulation.

Combining gravimetric and vibrational spectroscopy measurements to quantify first- and second-shell hydration layers in polyimides with different molecular architectures.

In-situ Fourier transform infrared (FTIR) measurements have been carried out at different relative pressures of water vapor to study the H(2)O diffusion in three polyimides differing in their molecular structure and fluorine substitution. Spectral data have been analyzed by difference spectroscopy, least-squares curve fitting, and two-dimensional (2D) correlation spectroscopy, which provided molecular level information on the diffusion mechanism. In particular, two distinct water species were identified corresponding, respectively, to the first and second-shell hydration layers. The spectroscopic analysis demonstrated that the relative population of these species is a function of the total water content in the system. A method has been devised to quantify the water concentration in the two hydration layers, based on a combination of spectroscopic and gravimetric data. The results have been compared with those from an earlier spectroscopic approach reported in the literature and based on the analysis of the carbonyl region.

Gas-Barrier Hybrid Coatings by the Assembly of Novel Poly(vinyl alcohol) and Reduced Graphene Oxide Layers through Cross-Linking with Zirconium Adducts.

Gas-barrier materials obtained by coating poly(ethylene terephthalate) (PET) substrates have already been studied in the recent literature. However, because of the benefits of using cheaper, biodegradable, and nonpolar polymers, multilayered hybrid coatings consisting of alternate layers of reduced graphene oxide (rGO) nanosheets and a novel high amorphous vinyl alcohol (HAVOH) with zirconium (Zr) adducts as binders were successfully fabricated through a layer-by-layer (LbL) assembly approach. Atomic force microscopy analysis showed that rGO nanoplatelets were uniformly dispersed over the HAVOH polymer substrate. Scanning and transmission electron microscopies revealed that multilayer (HAVOH/Zr/rGO)n hybrid coatings exhibited a brick-wall structure with HAVOH and rGO as buildings blocks. It has been shown that 40 layers of HAVOH/Zr/rGO ultrathin films deposited on PET substrates lead to a decrease of 1 order of magnitude of oxygen permeability with respect to the pristine PET substrate. This is attributed to the effect of zirconium polymeric adducts, which enhance the assembling efficiency of rGO and compact the layers, as confirmed by NMR characterization, resulting in a significant increment of the oxygen-transport pathways. Because of their high barrier properties and high flexibility, these films are promising candidates in a variety of applications such as packaging, selective gas films, and protection of flexible electronics.

Synergistic effect of vegetable protein and silicon addition on geopolymeric foams properties

Organic–inorganic hybrid foams based on an alkali alumino-silicate matrix were prepared using different foaming methods. Firstly, silico-aluminate inorganic matrix, activated through a sodium silicate solution, was prepared at room temperature. The obtained viscous paste was expanded by means of silicon metal redox reaction in alkaline media in combination with protein-assisted foaming. The foamed systems were hardened at defined temperature and time and then characterized by FTIR, scanning electron microscopy, and compression tests. The high temperature behavior and specific surface area were also evaluated. The experimental findings highlighted that the combination of silicon metal and vegetable protein allowed tailoring hybrid foams with enhanced properties: good yield strength and thermal resistance typical of geopolymeric foam with a ductile behavior (toughness) and low density typical of organic foams.