Federico Cesano

Thickness of multiwalled carbon nanotubes affects their lung toxicity.

Two samples of highly pure multiwalled carbon nanotubes (MWCNTs) similar in hydrophobicity and surface reactivity were prepared with similar length, <5 μm, but markedly different diameter (9.4 vs 70 nm). The samples were compared for their cytotoxic activity, uptake, and ability to induce oxidative stress (ROS production and intracellular GSH depletion) in vitro in murine alveolar macrophages (MH-S). The in vivo toxicity was evaluated by measuring biochemical (LDH activity and total proteins) and cellular responses in bronchoalveolar lavage (BAL) after intratracheal instillation in rats. Both samples were internalized in MH-S cells. However, thin MWCNTs appeared significantly more toxic than the thicker ones, both in vitro and in vivo, when compared on a mass-dose basis. The data reported herein suggest that the nanotube diameter is an important parameter to be considered in the toxicological assessment of CNTs.

Furfuryl alcohol polymerization in H-Y confined spaces: reaction mechanism and structure of carbocationic intermediates.

The acid-catalyzed polymerization and resinification, in the 300-673 K interval, of furfuryl alcohol adsorbed in the framework of a protonic Y zeolite is studied by means of FTIR, Raman, and UV-vis spectroscopies. The idea is that restricted spaces can impose a constraint to the growth of the oligomeric chains, therefore moderating the formation of conjugated sequences responsible for the color of the products and allowing their observation by means of spectroscopic techniques. The detailed study of the evolution of UV-vis, FTIR, and Raman spectra upon dosed amount, contact time, and temperature has allowed the spectroscopic features of some of the single species, either neutral and positively charged (carbocationic intermediates), to be singled out and assigned to understand the mechanism of initiation. The vibrational assignments have been confirmed by computer simulations on model compounds and compared with the results of the mechanistic description of the reaction mechanism made in the past (Choura, et al. Macromolecules 1996, 29, 3839-3850). The spectroscopic methods have been applied in a large temperature range in order to follow also the formation of more complex products into the pores, associated with longer conjugated sequences, gradually filling the open spaces of the zeolite. For samples contacted with furfuryl alcohol at 673 K, this methodology gives information also on the incipient carbonization process, leading to the formation of a carbonaceous replica phase inside the internal porosity of the zeolite.

Model oxide supported MoS2 HDS catalysts: structure and surface properties

Supported hydrodesulfidation (HDS) MoS2/SiO2, MoS2/γ-Al2O3 and MoS2/MgO catalysts having a model character have been synthesized by using CS2 as the sulfiding agent and deeply investigated by means of several techniques. XRPD, HRTEM, Raman and UV-Vis methods have been applied to obtain information on the morphology and the structure of the catalysts as well as on the vibrational and spectroscopic properties. It is shown that, when compared with HRTEM results, XRPD, Raman and UV-Vis data give realistic information on the stacking degree, on the particle size distribution and on the heterogeneity of supported MoS2 particles on the various supports. (S K-, Mo L3- and K- edges) EXAFS and XANES spectroscopies have been also used to set up the best sulfidation procedure. UV-vis analysis under controlled atmosphere has been performed to understand the presence of sulfur vacancies and the valence state of Mo ions associated with them. To explore the structure of coordinatively unsaturated Mo sites after reducing or sulfiding treatments (with CS2 or, occasionally, with H2S), in situFTIR of adsorbed CO has been performed. It is demonstrated that CO is a sensitive probe for coordinatively unsaturated sites and that the formation of sulfur vacancies on the MoS2 surface upon reduction in pure H2 at 673 K is accompanied by an increase of the coordinative unsaturation and a decrease of the valence state of a fraction of surface Mo cations, mainly located on corner and edge sites. Furthermore, it is demonstrated that this process can be reversed upon interaction with the sulfiding agent and that this reversible behavior is really mimicking some of the elementary acts occurring in the HDS process. The complexity of the IR results suggests that the adopted reduction procedure in pure H2 at 673 K induces the formation of several types of sulfur vacancies, presumably located in different crystallographic positions. It is also concluded that the sulfiding steps are strongly involving the surface of the support and that reductive treatments at high T in H2 are causing sulfur depletion not only from supported MoS2 particles, but also from the supporting phase. The involvement of the support is particularly relevant for Al2O3 and MgO.

MoS2 Nanoparticles Decorating Titanate-Nanotube Surfaces: Combined Microscopy, Spectroscopy, and Catalytic Studies

MoS2/TNTs composites have been obtained by impregnation of titanate nanotubes (TNTs) with a centrifuged solution of nanosized MoS2 particles in isopropyl alcohol (IPA). The characterization has been performed by combining UV-vis-NIR, Raman, AFM, and HRTEM analyses, before and after impregnation. HRTEM images show that the contact between single-layer MoS2 nanoparticles and the support is efficient, so justifying the decoration concept. The volatility of IPA solvent allows the preparation of composites at low temperature and free of carbonaceous impurities. MoS2 nanoparticles have strong excitonic transitions, which are only slightly shifted with respect to the bulk because of quantum size effects. Concentrations of MoS2, less than 0.1 wt %, are enough to induce strong absorption in the visible. Photodegradation of methylene blue (MB) has been performed on TNTs and MoS2/TNTs to verify the effect of the presence of MoS2. The first layer of adsorbed MB is consumed first, followed by clustered MB in the second and more external layers. The presence of low concentrated MoS2 nanoparticles does not substantially alter the photocatalytic properties of TNTs. This result is due to poor overlapping between the high frequency of MoS2 C, D excitonic transitions and the TNTs band gap transition.

The role of iron impurities in the toxic effects exerted by short multiwalled carbon nanotubes (MWCNT) in murine alveolar macrophages.

Lung toxicity mediated by multiwalled carbon nanotubes (MWCNT) has been widely demonstrated and recently associated with induction of carcinogenic asbestos-like effects, but the chemical features that drive this toxic effect have still not been well elucidated. The presence of metals as trace contaminants during MWCNT preparation, in particular iron (Fe) impurities, plays an important role in determining a different cellular response to MWCNT. Our goal was to clarify the mechanisms underlying MWCNT-induced toxicity with correlation to the presence of Fe impurities by exposing murine alveolar macrophages to two different MWCNT samples, which differed only in the presence or absence of Fe. Data showed that only Fe-rich MWCNT were significantly cytotoxic and genotoxic and induced a potent cellular oxidative stress, while Fe-free MWCNT did not exert any of these adverse effects. These results confirm that Fe content represents an important key constituent in promoting MWCNT-induced toxicity, and this needs to be taken into consideration when planning new, safer preparation routes.

Micro-FTIR and Micro-Raman Studies of a Carbon Film Prepared from Furfuryl Alcohol Polymerization

The synthesis of a carbon film by the acid-catalyzed polymerization and resinification of furfuryl alcohol with a diluted solution of HCl is studied by combining micro-FTIR and micro-Raman spectroscopies. The detailed study of the evolution of spectra as a function of dosage of furfuryl alcohol and temperature shows that neutral and protonated species are formed at 80 degrees C, while upon gradually increasing the temperature up to 600 degrees C, the viscous polyfurfuryl alcohol resin is transformed into a carbon phase, containing a heterogeneous distribution of pores, with a size in the 100-2000 nm range, as shown by SEM and AFM analyses.

Rapid purification/oxidation of multi-walled carbon nanotubes under 300 kHz-ultrasound and microwave irradiation

The use of ultrasound (US) and microwaves (MW) in the oxidation and purification of multi-walled carbon nanotubes (MWCNTs) was investigated. These techniques, in particular US at a frequency of 300 kHz, strongly accelerate the process and avoid the heavy structural damage, observed at the 20–35 kHz classic range, even at low power. Due to the residual metal catalyst on the head of MWCNTs, MW heating is strongly absorbed, causing the rupture of the tip and the loss of the metal. All our chemico-physical treatment types were performed by suspending the CNTs in a 3 ∶ 1 H2SO4/HNO3 mixture. The resulting samples were investigated by TEM microscopy, TGA analyses and Raman spectroscopy, while the degree of oxidation was estimated by colourimetric analyses.

Association of polyalanine and polyglutamine coiled coils mediates expansion disease-related protein aggregation and dysfunction

The expansion of homopolymeric glutamine (polyQ) or alanine (polyA) repeats in certain proteins owing to genetic mutations induces protein aggregation and toxicity, causing at least 18 human diseases. PolyQ and polyA repeats can also associate in the same proteins, but the general extent of their association in proteomes is unknown. Furthermore, the structural mechanisms by which their expansion causes disease are not well understood, and these repeats are generally thought to misfold upon expansion into aggregation-prone β-sheet structures like amyloids. However, recent evidence indicates a critical role for coiled-coil (CC) structures in triggering aggregation and toxicity of polyQ-expanded proteins, raising the possibility that polyA repeats may as well form these structures, by themselves or in association with polyQ. We found through bioinformatics screenings that polyA, polyQ and polyQA repeats have a phylogenetically graded association in human and non-human proteomes and associate/overlap with CC domains. Circular dichroism and cross-linking experiments revealed that polyA repeats can form—alone or with polyQ and polyQA—CC structures that increase in stability with polyA length, forming higher-order multimers and polymers in vitro. Using structure-guided mutagenesis, we studied the relevance of polyA CCs to the in vivo aggregation and toxicity of RUNX2—a polyQ/polyA protein associated with cleidocranial dysplasia upon polyA expansion—and found that the stability of its polyQ/polyA CC controls its aggregation, localization and toxicity. These findings indicate that, like polyQ, polyA repeats form CC structures that can trigger protein aggregation and toxicity upon expansion in human genetic diseases.

Altered excitability of cultured chromaffin cells following exposure to multi-walled carbon nanotubes

Abstract We studied the effects of multi-walled carbon nanotubes (MWCNTs) on the electrophysiological properties of cultured mouse chromaffin cells, a model of spontaneously firing cells. The exposure of chromaffin cells to MWCNTs at increasing concentrations (30–263 μg/ml) for 24 h reduced, in a dose-dependent way, both the cell membrane input resistance and the number of spontaneously active cells (from 80–52%). Active cells that survived from the toxic effects of MWCNTs exhibited more positive resting potentials, higher firing frequencies and unaltered voltage-gated Ca2+, Na+ and K+ current amplitudes. MWCNTs slowed down the inactivation kinetics of Ca2+-dependent BK channels. These electrophysiological effects were accompanied by MWCNTs internalization, as confirmed by transmission electron microscopy, indicating that most of the toxic effects derive from a dose-dependent MWCNTs-cell interaction that damages the spontaneous cell activity.

Designing rGO/MoS2 hybrid nanostructures for photocatalytic applications

Graphene and its derivatives exhibit large surface area, being ideal templates to facilitate the nucleation, growth or interaction of a huge variety of structures. Among them, molybdenum disulphide, with its structural and morphological compatibility with graphene, can be a candidate for achieving an excellent integration, to make new hybrid nanocomposites with outstanding characteristics. Among the synthesis methods of graphene/MoS2 composites, the solution-phase exfoliation of a MoS2/graphite mixture, by means of ultrasounds, shows significant advantages in terms of large amount production without altering the main properties of 2D nanomaterials. Moreover MoS2, having a strong absorption in the visible, has been exploited as a novel visible light-sensitive semiconductor photocatalyst. But, due to the quick recombination of photo-generated charge carriers, the photocatalytic efficiency of MoS2 has to be further improved. Graphene and graphene related materials, as excellent electron-acceptor/transport materials, have been applied to photocatalysis, because they are able to decrease the photo-generated electron–hole recombination, thus improving the light absorption. Therefore, MoS2 and graphite oxide (GO) have been simultaneously sonicated in an ethanol/water mixture and characterized from the structure, morphology and electronic properties point of view. The composite was thermally treated in such a way to reduce GO and the photocatalytic activity of the reduced GO/MoS2 has been investigated by means of UV-vis spectroscopy, following the degradation of methylene-blue (MB) under solar-like irradiation.