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This study presents the proof-of-concept of the “Oil-Spill Snorkel”: a novel bioelectrochemical approach to stimulate the oxidative biodegradation of petroleum hydrocarbons in sediments. The “Oil-Spill Snorkel” consists of a single conductive material (the snorkel) positioned suitably to create an electrochemical connection between the anoxic zone (the contaminated sediment) and the oxic zone (the overlying O2-containing water). The segment of the electrode buried within the sediment plays a role of anode, accepting electrons deriving from the oxidation of contaminants. Electrons flow through the snorkel up to the part exposed to the aerobic environment (the cathode), where they reduce oxygen to form water. Here we report the results of lab-scale microcosms setup with marine sediments and spiked with crude oil. Microcosms containing one or three graphite snorkels and controls (snorkel-free and autoclaved) were monitored for over 400 days. Collectively, the results of this study confirmed that the snorkels accelerate oxidative reactions taking place within the sediment, as documented by a significant 1.7-fold increase (p = 0.023, two-tailed t-test) in the cumulative oxygen uptake and 1.4-fold increase (p = 0.040) in the cumulative CO2 evolution in the microcosms containing three snorkels compared to snorkel-free controls. Accordingly, the initial rate of total petroleum hydrocarbons (TPH) degradation was also substantially enhanced. Indeed, while after 200 days of incubation a negligible degradation of TPH was noticed in snorkel-free controls, a significant reduction of 12 ± 1% (p = 0.004) and 21 ± 1% (p = 0.001) was observed in microcosms containing one and three snorkels, respectively. Although, the “Oil-Spill Snorkel” potentially represents a groundbreaking alternative to more expensive remediation options, further research efforts are needed to clarify factors and conditions affecting the snorkel-driven biodegradation processes and to identify suitable configurations for field applications.

Growth by chemical vapor deposition (CVD) leads to multilayer WS2 of very high quality, based on high-resolution angle-resolved photoemission spectroscopy. The experimental valence band electronic structure is considered to be in good agreement with that obtained from density functional theory calculations. We find the spin-orbit splitting at the K-point to be 420 ± 20 meV with a hole effective mass of −0.35 ± 0.02 me for the upper spin-orbit component (the branch closer to the Fermi level) and −0.43 ± 0.07 me for the lower spin-orbit component. As predicted by theory, a thickness-dependent increase of bandwidth is observed at the top of the valence band, in the region of the Brillouin zone center. The top of the valence band of the CVD-prepared films exhibits a substantial binding energy, consistent with n-type behavior, and in agreement with transistor characteristics acquired using devices incorporating the same WS2 material

The development of novel materials for energy harvesting applications or strain sensing has generated great interest towards zinc oxide (ZnO) nanostructures, and in particular towards the synthesis of ZnO nanowires or nanorods with well controlled morphology and properties. The high-yield mass production of such nanostructures by catalyst-free methods is a crucial aspect to enable a cost-effective large-scale development of new ZnO-based piezoelectric devices and materials. In the present work, we propose a method for the mass-production of high-purity ZnO-nanorods with a uniform size distribution, based on the combination of thermal decomposition of zinc acetate dihydrate and probe sonication in acetone. The quality of the produced ZnO nanorods is assessed through multi-technique characterization using field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and photo-luminescence spectroscopy (PL). The adopted synthesis method is simple, cost effective and feasible for large-scale production. Various process parameters such as precursor amount and growth time have been found to play an important role in controlling the formation of the as grown nanostructures with high uniformity in size and morphology. Size distribution curves were employed to depict the effect of various process parameters for tailoring the morphology, homogeneity and aspect ratio of the nanorods. Our results reveal that the high crystallographic quality of ZnO nanorods grown by a long-time thermal decomposition method is not affected by probe sonication, which is proposed as a post-synthesis step necessary to produce ZnO nanorod powder with a uniform distribution of diameters and lengths

AISI 316L steel, subjected to a low temperature carburizing treatment (kolstering), has been examined by Mechanical Spectroscopy (MS) and nanoindentation to determine the Youngs modulus of the surface hardened layer (S phase). MS results showed that the average value of elastic modulus of S phase is 202 GPa, a little higher than that of the untreated material.Nanoindentation tests, carried out with loads of 5, 15 and 30 mN, evidence a modulus profile vs depth: E is ~ 400 GPa at a distance from the surface of ~ 110 nm, then decreases to reach the value of the steel substrate (190 GPa) at 33 μm.These results, together with X-ray Photoelectron Spectroscopy (XPS) and Auger Electron Spectroscopy (AES) measurements of carbon concentration profile, can be explained by considering the presence of a very thin surface layer, different from S phase and consisting of a mixed structure of Diamond-like carbon (DLC) and tetrahedral carbon (taC).Furthermore, the same experiments have been carried out also after heat treatments at 450 °C to correlate the modulus change to the decomposition of the metastable S phase leading to the formation of (Cr,Mo)C and Cr23C6 carbides in a Cr-depleted austenitic matrix.

Zinc oxide nanorods (ZnO-NRs) with high density and chemical purity were grown onto unsupported graphene nanoplatelets (GNPs) in aqueous suspensions, using two different growth approaches namely: a hydrothermal method and ultrasonic probe sonication. The size and density of the ZnO-nanorods grown onto graphene nanoplatelets were controlled through seed layer deposition and through the proper setting of the process parameters, in particular through the control of the fluidodynamics of the colloidal suspension during the growth. The highest growth density of the ZnO nanorods having a diameter of ∼45 nm was obtained onto GNPs seeded by the probe sonication method and through the hydrothermal method in dynamic conditions. XRD and XPS investigations confirmed that all produced ZnO-GNP composites are characterized by high crystallinity and purity, although solution dynamics affected their UV luminescence. The proposed approaches enable the controlled high-density growth of crystalline ZnO-NRs onto GNPs in an aqueous suspension, at a low cost, and are suitable for large scale production

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