Colloidal synthesis and characterization of tetrapod-shaped magnetic nanocrystals

Tetrapod-shaped maghemite nanocrystals are synthesized by manipulating the decomposition of iron pentacarbonyl in a ternary surfactant mixture under mild thermal conditions. Adjustment of the reaction parameters allows for the systematic tuning of both the width and the length of the tetrapod arms, which grow preferentially along the 111 easy axis direction. Such degree of control leads to modulation of the magnetic behavior of the nanocrystals, which evolves systematically as their surface magnetization phase and shape anisotropy are progressively increased.     

Osteoblast Dysfunction in Non-Hereditary Sclerosing Bone Diseases

A review of the available literature was performed in order to summarize the existing evidence between osteoblast dysfunction and clinical features in non-hereditary sclerosing bone diseases. It has been known that proliferation and migration of osteoblasts are concerted by soluble factors such as fibroblast growth factor (FGF), platelet-derived growth factor (PDGF), transforming growth factor (TGF), bone morphogenetic protein (BMP) but also by signal transduction cascades such as Wnt signaling pathway. Protein kinases play also a leading role in triggering the activation of osteoblasts in this group of diseases. Post-zygotic changes in mitogen-activated protein kinase (MAPK) have been shown to be associated with sporadic cases of Melorheostosis. Serum levels of FGF and PDGF have been shown to be increased in myelofibrosis, although studies focusing on Sphingosine-1-phosphate receptor was shown to be strongly expressed in Paget disease of the bone, which may partially explain the osteoblastic hyperactivity during this condition. Pathophysiological mechanisms of osteoblasts in osteoblastic metastases have been studied much more thoroughly than in rare sclerosing syndromes: striking cellular mechanisms such as osteomimicry or complex intercellular signaling alterations have been described. Further research is needed to describe pathological mechanisms by which rare sclerosing non hereditary diseases lead to osteoblast dysfunction.     

Development of new catalysts for N2O-decomposition from adipic acid plant

Direct decomposition of N₂O was investigated using simulated and real industrial gas stream coming from an adipic acid plant. Two different kinds of catalysts were studied: (i) LaB_1−xB′_xO₃ and CaB_1−xCu_xO₃ (B = Mn, Fe and B′ = Cu, Ni) perovskites (PVKs) and (ii) supported PVKs (10 or 20 wt.%) on γ-Al₂O₃ and CeO₂–ZrO₂. The structural modifications induced by the composition of PVK samples affect the catalytic performances: mixed oxide formation in CaMn_0.7Cu_0.3O₃ samples allows to reach the highest values of N₂O conversion while the effect of PVK phases is more controversial. The importance of copper on catalytic activities is confirmed by the investigation on CaMn_1−xCu_xO₃ samples. The best results were obtained with a CaMn_0.6Cu_0.4O₃ catalyst calcined at 700 °C for 5 h, in which the presence of copper maximises the Ca₃CuMnO₆ phase formation. The increase in Cu-content produces a large segregation of CuO despite PVK formation. The best catalyst was tested using industrial gas stream, showing good stability also in the presence of H₂O and O₂ (8% v/v ) after 1400 h on-stream. To increase surface area, Cu-containing PVKs were deposed on γ-Al₂O₃ and CeO₂–ZrO₂, and this latter has been recognised as the best support. Indeed, the activity of the PVKs supported on ceria–zirconia is comparable to and even better than that of the bulk catalysts. A possible explanation regards the support contribution in terms of activity and/or promotion of O₂ mobility which enhances the overall activity of the catalyst.     

Traffic emission scenarios in Lombardy region in 1998-2015

This study assesses and discusses the current and future contribution of road traffic to primary PM10 and PM10 main precursors (i.e. NO(x), SO(2), NH(3), VOC) in the Lombardy region (Italy). It defines a coherent and updated set of input parameters (emission factors, mileage and fleet composition) for traffic emission estimation between 1998 and 2015. 1998-2004 emissions are assessed basing on historical data, while 2005-2015 rely on different hypothesis about mobility development and vehicular turnover rate. The work shows that road traffic emissions of PM10 and PM10 precursors are expected to decrease in the period 2005-2015, with a reduction greater than 70% in scenarios with a fast vehicle turnover and a decrease in fuel usage. Increase in fuel consumption could substantially lower the emission reduction expected, off-setting a substantial part of the new technology benefits. The introduction of DPF (diesel particulate filter) vehicles will determine a reduction of PM10 exhaust, however this could potentially be stalled by the increase in diesel usage in the vehicle fleet and an increase in mileage driven, as the latter causes a rise in the contribution of PM10 from abrasion. Concerning the total atmospheric emissions in Lombardy, SO(2) (-6%) and NH(3) (<-2%) emission will remain constant, while PM10, VOC and NO(x) emission will decrease, respectively by 2-30%, 6-15% and 2-32% in the period 2001-2015.     

Decolourisation and detoxification of textile effluents by fungal biosorption

Textile effluents, in addition to high COD, display several problems mainly due to toxicity and recalcitrance of dyestuffs. Innovative technologies effective in removing dyes from large volumes of effluents at low cost and in a timely fashion are needed. Fungi are among the most promising organisms for dye biosorption. In this study dye decolourisation, COD and toxicity decrease of three wastewater models after the treatment with inactivated biomasses of three Mucorales fungi cultured on two different media were evaluated. Fungal biomasses displayed good sorption capabilities giving rise to decolourisation percentages up to 94% and decrease in COD up to 58%. The Lemna minor toxicity test showed a significant reduction of toxicity after biosorption treatments, indicating that decolourisation corresponds to an actual detoxification of the treated wastewaters.     

Role of many body shake-up in core-valence-valence electron emission from single wall carbon nanotubes

Auger core-valence-valence transitions from single wall Carbon nanotubes are studied using a tight-binding calculational scheme with nearest neighbor overlap, hopping interactions, and a double-zeta basis set. The resulting Hamiltonian approximates the unperturbed pi and sigma bands of the nanomaterials coupled with the free electron states outside the solid and the core-hole. As a first step, the Fermi's golden rule is applied to determine the so called one-electron spectrum of emitted electrons from different tubes, in which either the neutralizing or the ejected electrons, in the initial state, lie within nearest neighboring atomic sites to the core-hole. Many-body corrections are effectively modeled using a broadening function, which accounts for dynamic screening effects involving the initial and final states. Particular attention is paid to the asymmetric component of the broadening function, responsible for the shake-up of pi electrons. Finally, the Cini-Sawatzky distortion function is used to describe the final state effect of the hole-hole interaction. A quantitative estimation of the interplay of shake-up processes is proposed by adjusting the asymmetric parameters of the broadening function to reproduce measurements of Auger electrons ejected from bundles of single wall Carbon nanotubes.     

Single‐ and Double‐Sided Chemical Functionalization of Bilayer Graphene

An experimental study on the interaction between the top and bottom layer of a chemically functionalized graphene bilayer by mild oxygen plasma is reported. Structural, chemical, and electrical properties are monitored using Raman spectroscopy, transport measurements, conductive atomic force microscopy and X‐ray photoelectron spectroscopy. Single‐ and double‐sided chemical functionalization are found to give very different results: single‐sided modified bilayers show relatively high mobility (200–600 cm² V^?1 s^?1 at room temperature) and a stable structure with a limited amount of defects, even after long plasma treatment (>60 s). This is attributed to preferential modification and limited coverage of the top layer during plasma exposure, while the bottom layer remains almost unperturbed. This could eventually lead to decoupling between top and bottom layers. Double‐sided chemical functionalization leads to a structure containing a high concentration of defects, very similar to graphene oxide. This opens the possibility to use plasma treatment not only for etching and patterning of graphene, but also to make heterostructures (through single‐sided modification of bilayers) for sensors and transistors and new graphene‐derivatives materials (through double‐sided modification).     

Ag/ZnO nanomaterials as high performance sensors for flammable and toxic gases

Ag/ZnO nanocomposites supported on polycrystalline Al2O3 were synthesized by an unprecedented approach combining plasma enhanced chemical vapor deposition (PE-CVD) of ZnO matrices and the subsequent deposition of Ag nanoparticles (NPs) by radio frequency (RF) sputtering. The system structure, composition and morphology were investigated by glancing incidence x-ray diffraction (GIXRD), secondary ion mass spectrometry (SIMS), field emission scanning electron microscopy (FE-SEM) and energy dispersive x-ray spectroscopy (EDXS). A tailored dispersion and distribution of silver particles could be obtained under mild conditions by the sole variation of the sputtering time. Gas sensing properties toward flammable and toxic gases, both reducing (CH3CH2OH, CH3COCH3) and oxidizing (O3), were investigated in the temperature range 100-400?°C. Beside the high sensitivity, the developed sensors exhibited a response proportional to Ag content, thanks to catalytic and electronic effects promoted by silver NPs. In addition, discrimination between oxidizing and reducing analytes was enabled by a suitable choice of the adopted working temperature.     

Gas sensing properties of columnar CeO2 nanostructures prepared by chemical vapor deposition

Columnar CeO2 nanostructures are grown on alumina substrates by a template- and catalyst-free Chemical Vapor Deposition (CVD) approach and subsequently tested as resistive gas sensors of CH3COCH3, H2, NO2. The sensor response is stable and reproducible throughout the whole working temperature range (200-500 degrees C) and directly dependent on the analyte gas and the adopted operating conditions. The higher sensitivity with respect to that displayed by continuous CeO2 thin films demonstrates the potential of fabricating nanostructured sensing devices characterized by improved functional performances.