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Purpose The study aimed to identify the environmental hotspots of lab-scale preparation of high purity porous Al2O3 pellets with suitable feature to work properly as metal layer-based deposition substrates for hydrogen separation membranes. The work intention was providing hints that may help the designing of upscaled systems, fundamental for the development of a possible future industrial production of hydrogen separation metal layer-based membranes technology. Methods The goal of this study was achieved assessing and analyzing environmental impacts of Al2O3 pellet production at lab scale. Primary data were collected in Padua laboratories of National Research Council of Italy. Secondary data were retrieved from Ecoinvent 3.7 database. Life cycle assessment (LCA) was performed using Environmental Footprint 3.0 method employing SimaPro 9.3 as software. Moreover, the CML LCIA method v. 4.7 was used to verify the robustness analysis of characterized results. Results Life cycle impact assessment highlighted as the main driver of environmental impacts was mainly associated to the pellet consolidation process and their morphological characterization stage. In particular, the impact of the first energy consuming process resulted strictly related to the peculiar energy mix used (linked to the laboratory geographical location). Conversely, morphological characterization stage was found to affect mainly the mineral resource depletion category due to the Au coating used for performing scanning electron microscope (SEM) analyses. Conclusions The study identified the environmental hotspots related to lab-scale preparation of porous alumina pellets as substrate for hydrogen separation metal layer-based membranes. The optimization strategies evaluated in this work were addressed to improve the environmental profile of experimental activities considering several scenarios, in view of a possible industrial scale-up.

Ultrafast high-temperature sintering (UHS) is a recently proposed technique able to synthesize and sinter dense materials within seconds. Although UHS has already proved its effectivity with a large set of materials, spanning from refractory ceramics to complex metal alloys, any application to thermoelectric materials is today still lacking. Mg2Si is a well-established thermoelectric material. It is based on wide available non-critical raw materials, it is non-toxic, lightweight and it expresses its best thermoelectric performances in the intermediate temperature range (up to about 600 °C). Mg2Si is typically produced with powder processing by Spark Plasma Sintering (SPS), partially limiting its widespread diffusion also due to the costly production technique. Here we present a simple route to sinter Mg2Si pressed powders by UHS. The process allowed to obtain dense samples (with relative densities >95%) with 20 s heating up to about 1080 °C followed by a rapid free cooling, a total thermal history below 1 min, and with energy demand at the Wh scale. The high process rate proved its efficacy in preventing grain growth and in avoiding any significant Mg evaporation. A full thermoelectric functional characterization is presented for Mg2Si and Bi-doped Mg2Si, together with a comparison with SPS-produced properties.

Phase change material emulsions (PCMEs) were largely investigated as potential working fluids for various applications as in HVAC systems, solar thermal storage, and heat transfer. They basically contain water and phase change materials, possess much larger energy storage capacity than currently used chilled water based systems and exploit higher thermal conductivity than bulk PCM reservoirs. Main barriers to their application are the difficulty in maintaining emulsion stability and the undercooling effect. In this work, a new solvent-assisted route was developed to produce nano-emulsions of commercial paraffin waxes in water. Concentrations from 2 to 10 wt% were obtained starting from two commercial paraffin waxes, with nominal melting temperatures around 55 °C and 70 °C. The droplet dimensions were verified and resulted below 100 nm for lower concentrations and around 180–220 nm for 10 wt%. The stability of emulsions was verified by long-term tests. An undercooling effect was verified and strongly reduced by testing some nucleating agents (a paraffin melting at 70 °C in the paraffin melting at 55 °C or a carbon nanostructure, single wall carbon nanohorns). The heat of melting was lower than expected, probably due to PCM molecules on the surface of the nanoparticles anchored to the surfactant. However, calculating the thermal capacity of PCMEs with respect to pure water, a gain up to 40% for operating temperatures close to PCM melting temperature was estimated. Optical properties of single wall carbon nanohorns/paraffin composites were also measured.

In the present work, surface engineering of Ti6Al4V, produced via selective laser melting parts, was carried out with the aim of investigating how surface features of substrate may improve the coupling with AlTiN coatings deposited by physical vapor deposition reactive high-power impulse magnetron sputtering. In particular, the work highlighted how vacuum thermal treatments at 800 °C induced peculiar mesoscale morphology and surface chemical modifications of the Ti6Al4V, which contributed to improve the adhesion of the deposited AlTiN thin films. Chemical composition, crystallographic structure, and surface properties of both substrates and coatings were analyzed by field emission scanning electron microscopy (equipped with energy dispersive spectroscopy), atomic force microscopy, x-ray photoelectron spectroscopy, x-ray diffraction, nanoindentation, and scratch test measurements.

This work analyzes the dynamic viscosity, surface tension and wetting behavior of phase change material nano–emulsions (PCMEs) formulated at dispersed phase concentrations of 2, 4 and 10 wt.%. Paraffin–in–water samples were produced using a solvent–assisted route, starting from RT21HC technical grade paraffin with a nominal melting point at ~293–294 K. In order to evaluate the possible effect of paraffinic nucleating agents on those three properties, a nano–emulsion with 3.6% of RT21HC and 0.4% of RT55 (a paraffin wax with melting temperature at ~328 K) was also investigated. Dynamic viscosity strongly rose with increasing dispersed phase concentration, showing a maximum increase of 151% for the sample containing 10 wt.% of paraffin at 278 K. For that same nano–emulsion, a melting temperature of ~292.4 K and a recrystallization temperature of ~283.7 K (which agree with previous calorimetric results of that emulsion) were determined from rheological temperature sweeps. Nano–emulsions exhibited surface tensions considerably lower than those of water. Nevertheless, at some concentrations and temperatures, PCME values are slightly higher than surface tensions obtained for the corresponding water+SDS mixtures used to produce the nano–emulsions. This may be attributed to the fact that a portion of the surfactant is taking part of the interface between dispersed and continuous phase. Finally, although RT21HC–emulsions exhibited contact angles considerably inferior than those of distilled water, PCME sessile droplets did not rapidly spread as it happened for water+SDS with similar surfactant contents or for bulk–RT21HC.

Nowadays, the use of lasers has become commonplace in everyday life, and laser protection has become an important field of scientific investigation, as well as a security issue. In this context, optical limiters are receiving increasing attention. This work focuses on the identification of the significant parameters affecting optical limiting properties of aqueous suspensions of pristine single-wall carbon nanohorns. The study is carried out on the spectral range, spanning from ultraviolet to near-infrared (355, 532 and 1064 nm). Optical nonlinear properties are systematically investigated as a function of nanohorn morphology, concentration, dimensions of aggregates, sample preparation procedure, nanostructure oxidation and the presence and concentration of surfactants to identify the role of each parameter in the nonlinear optical behavior of colloids. The size and morphology of individual nanoparticles were identified to primarily determine optical limiting. A cluster size effect was also demonstrated, showing more effective optical limiting in larger aggregates. Most importantly, we describe an original approach to identify the dominant nonlinear mechanism. This method requires simple transmittance measurements and a fitting procedure. In our suspensions, nonlinearity was identified to be of electronic origin at a 532 nm wavelength, while at 355 nm, it was found in the generation of bubbles.

Oxidized carbon nanohorn water based nanofluids are attracting more and more attention for solar harvesting applications because of their peculiar features: stable suspension without any surfactant, higher solar absorbance values as compared to the base fluid, etc. However, these nanofluids are still matter of research because not all their properties have been comprehensively studied yet. This paper is focused on the wettability properties of the carbon nanohorn water based nanofluids on different metal surfaces. The static contact angle was measured for ten nanofluids with concentrations ranging from 0.002%wt to 0.1% wt, five of those used non-oxidized carbon nanohorns while the other five used oxidized carbon nanohorns. Moreover, this work investigates a novel use of the oxidized carbon nanohorn nanofluids to deposit an ultra-thin layer via pool boiling. The realized coating was proved to be stable and found to slightly affect the wettability of the nanofluids. Finally, the solar reflectance of the coated aluminum sample was measured and found to be from 2 to 10 times lower as compared to a reference aluminum surface.

Nanolubricants, thanks to their ability to reduce friction and wear, are increasingly studied in the transport and automotive sectors. These systems are generally produced with a two-step procedure by dispersing nanoparticles into base oils. Very recently, one-step methods have received increasing attention for the production of highly stable nanosuspensions at lower cost. Degradation-decomposition of the base oil can however occur during the synthesis affecting the final performances. In this work, copper-based nanolubricants were produced using a new procedure that preserves the base oil from the degradation induced by the synthesis and allows producing highly stable nanolubricant. The produced fluid showed a monodisperse distribution of nanometric particles and a good stability up to at least 60 days from its production. The as-produced nanolubricants showed notable performance reducing the friction coefficient even up to 32.7% for Cu concentration of 0.01 vol% at 80°C.

In this work, powders of Single Wall Carbon Nanohorns (SWCNHs), a typical hydrophobic material, were oxidized with concentrated HNO3 with the aim of surface carboxylation and consequent improved hydrophilicity and dispersibility in polar solvents. Dynamic Light Scattering and zeta-potential measurements demonstrated that very stable colloidal suspensions of SWCNH in water were obtained in total absence of stabilizers. By properly optimizing the reaction parameters, the suspensions achieved stability even higher than colloids with similar composition but prepared with the use of surfactants. Surface damage and oxidation degree of SWCNHs were evaluated by SEM microscopy, Thermogravimetric Analysis, Residual Gas Analysis, XPS and UV-visible spectroscopy.

Lithium wall conditioning has improved the performance of many magnetic fusion devices. Li conditioning in the RFX-mod device was performed by: (1) a single Li pellet injector and (2) a multi-Li pellet injector during He plasma discharges; (3) a Li evaporator after He glow discharge cleaning and He plasma discharge exposure. This report compares the spatial and depth distributions of Li deposited on polycrystalline graphite witness samples at different locations in RFX-mod and the elemental and chemical compositions of the resulting surfaces. The sample surfaces were analyzed ex situ using secondary ion mass spectrometry (SIMS) and high-resolution X-ray photoelectron spectroscopy (HR-XPS). The results showed that Li pellet injection provided a relatively uniform toroidal coverage while Li evaporation produced highly localized Li deposition. A Li 1s HR-XPS peak at 56.5 eV binding energy (BE) characteristic of lithium-intercalated graphite was only observed with the sample exposed to Li evaporation. All of the samples exhibited a HR-XPS C 1s peak at 285.1–285.2 eV BE that is largely attributed to hydrogenated graphite. This finding suggests that hydrogenation of fresh graphite occurs during He plasma discharge exposures. Our results have implications for density control and the selection of Li conditioning techniques in magnetic fusion devices.

Goethite (α-FeOOH) nanorods have been synthesized using two different methods, by aging at different temperatures of ferrihydrite suspensions obtained through co-precipitation, or by fast conversion of ferrihydrite through ultrasonic irradiation. The synthesis method and parameters influenced the size and shape of nanoparticles. Stable colloidal suspensions of nanorods have been prepared by purification of the precipitates and subsequent dispersion in deionised water by sonication. The synthesized nanopowders have been characterized by Powder X-ray Diffraction and Scanning Electron Microscopy and the colloidal suspensions by Dynamic Light Scattering and ζ-potential measurements. The magnetic field at nuclei level has been investigated by Mossbauer spectroscopy. Moreover, since a colloidal suspension of goethite is a mineral liquid crystal and due to its peculiar magnetic properties, polarized radiation transmittance of colloids in the UV-vis-NIR range has been determined under different magnetic field directions and intensities. It has been found that the transmittance in the NIR range can be tuned by changing magnetic field direction and strength.

International audience; Droplet volume and temperature affect contact angle significantly. Phase change heat transfer processes of nanofluids – suspensions containing nanometre-sized particles – can only be modelled properly by understanding these effects. The approach proposed here considers the limiting contact angle of a droplet asymptotically approaching zero-volume as a thermophysical property to characterise nanofluids positioned on a certain substrate under a certain atmosphere.Graphene oxide, alumina, and gold nanoparticles are suspended in deionised water. Within the framework of a round robin test carried out by nine independent European institutes the contact angle of these suspensions on a stainless steel solid substrate is measured with high accuracy. No dependence of nanofluids contact angle of sessile droplets on the measurement device is found. However, the measurements reveal clear differences of the contact angle of nanofluids compared to the pure base fluid.Physically founded correlations of the contact angle in dependency of droplet temperature and volume are obtained from the data. Extrapolating these functions to zero droplet volume delivers the searched limiting contact angle depending only on the temperature. It is for the first time, that this specific parameter, is understood as a characteristic material property of nanofluid droplets placed on a certain substrate under a certain atmosphere. Together with the surface tension it provides the foundation of proper modelling phase change heat transfer processes of nanofluids.

Ceria was deposited onto boron doped polycrystalline diamond (BDD) cathodes, through electrochemically induced precipitation from nitrate-based solutions. The deposits were characterized using SEM-EDS, HRTEM, XRD and XPS. The morphology, thickness and composition of ceria films, which besides CeO2 contained Ce(OH)(3) when prepared at very negative potential, were controlled by tuning the deposition parameters. Thin Ce(OH)(3)-free ceria films allowed CO2 electrochemical reduction at overpotentials below 50 mV, yielding formic acid with faradaic yield higher than 40% and stable performance for many hours. Ceria seemed to act as a co-catalyst that activated CO2 for reduction at the H-terminated BDD surface, because comparable results were not obtained with ceria-coated glassy carbon electrodes.

Membranes based on zeolites have been extensively studied and used to purify/separate H2 or CO2 or other gases, depending on their composition. The deposition of zeolite films onto porous, chemically and thermally stable, substrates can increase their stability, but the production process may require lengthy two-step procedures. In this work, a single-step method was developed for the production of homogeneous hydroxy-sodalite (HS) zeolite films, without seeding and by direct deposition during hydrothermal treatment on cheap and porous alumina substrates. Alumina substrates have been developed with fine porosity (> 35% porosity, 500-600 nm of mean pore diameter), with low resistance to gas flow but reduced surface porosity to favour the deposition of dense films. The single-step growth of HS films with a thickness ranging from a few to 28 ?m on alumina was successfully achieved. These membranes have been tested in hydrogen, methane, carbon dioxide and nitrogen, and good results in terms of hydrogen permeance and separation performance were achieved for 10-12-?m-thick HS films on alumina.

The goal of the study was to identify the environmental hotspots of an experimental research work at lab scale consisting in the physical vapor deposition magnetron sputtering of aluminum titanium nitride based thin coatings onto commercial laminated steel. The findings can provide useful insights for supporting the design of future experimental research campaigns, or instrumentation set-ups, with lower environmental impacts. Results highlighted that the main driver of impacts in the analyzed laboratory activities was the electricity used for instruments operations, in particular for the vacuum keeping. Thus, several optimization strategies were evaluated to reduce the overall electricity consumption, and to improve the environmental profile of experimental activities.

Enhancing the tribological performance of lubricants with nanoparticle additives is a recent challenge. The purpose of this study was to investigate the potential advantage of nanolubricants, a new class of advanced lubricants integrating nano-sized materials, to reduce friction and wear processes, in view of applications in compressors for refrigeration. An investigation of tribological and thermal properties of nanolubricants for vane-on-roller systems was carried out through ball-on-disk wear tests and thermal diffusivity photo-acoustic measurements from room temperature to 70 °C. Nanofluids containing different concentrations of graphene based nanostructures in oil were tested. Poly-alkylene glycol was selected as the oil, being a lubricant suitable for compressors operating with CO2 refrigerants. The suspensions resulted stable with time. The dispersed nanostructures played an important role in protecting surfaces against wear phenomena and in improving the friction properties and load carrying capability of raw oil. A maximum decrease of 18% for friction coefficient and over 70% for worn volume were estimated in boundary lubrication conditions, the most severe for tribological couplings. Finally, durability experiments and Stribeck tests confirmed the benefits produced by nano-additives in different lubrication regimes. Thermal investigation proved also the advantage of using nanolubricants in heat exchange properties in laminar flow conditions, e.g. during compressor power-up phases.

Galvanic displacement reactions between sacrificial oxide layers and metal cations, leading to the formation of secondary oxide layers, have been studied with the aim of collecting new experimental evidence on their mechanism. The study has been carried out by combining electrochemical methods, SEM-EDS and XPS depth profiling. Both porous and compact PbO2 layers have been used as sacrificial oxides and reacted, in different experiments, with: (i) a single low-valent cation, (ii) two cations in sequential exchange reactions or (iii) two cations simultaneously. The experimental results converged to show (i) a lack of correlation between the reaction driving force and the secondary oxide growth rate, (ii) the incorporation of cations from solution at the secondary oxide/electrolyte interface, (iii) the transport of Pb species through the growing secondary oxide layer and (iv) a major effect of mass transport on the growth rate.

The electrochemiluminescence (ECL) performances were comparatively investigated at flat and nanoporous gold (NPG) electrodes of different thicknesses (120 and 200 nm) and roughness factors (fr). The phenomena were studied using either tripropylamine (TPrA) or peroxydisulfate (S2O82−) as sacrificial coreactant and Ruthenium (II)-tris(2,2′-bipyridine) as emitting species. The experiments performed using TPrA showed, at first glance, a linear dependence of the ECL emission with respect to the effective surface area of the NPG electrodes. However, ECL signals were not stable in the measuring conditions, presumably due to amine absorption on the metal surface, leading to electrode corrosion and modification of the surface morphology. The experiments made using peroxydisulfate as coreactant provided conversely a stable ECL response, about proportional to the effective electrode surface area, in the considered range of thicknesses.

The study of electric breakdown in magnetic nanofluid is one of the basic characterizations from the dielectric point of view. In this article we put effort to study dielectric breakdown strength of the transformer oil doped with goethite rod-shape nanoparticles. We use oscilloscope technique to catch the breakdown value for DC and AC applied potential, respectively. The investigated sample was exposed to both, DC and AC electric potential. We point out that for DC dielectric strength there is a positive influence of goethite nanorods on dielectric strength till electrode gap doesn't exceed critical value. Otherwise, for AC electric potential there was practically no effect on dielectric strength of the investigated nanofluid. In the result and discussion we present more complex description of the measured data. We also provide information about preparation processes of the fluid and detailed description of the measurement setup.

The development of hydrogen purification membranes that meet market demands such as high purity, dynamic hydrogen production even at small scale, and reduced costs is still an open question. With this view, the present study aims at developing, for the first time, a method based on high power impulse magnetron sputtering for the deposition of Pd77Ag23 (wt%) films onto porous alumina substrates to achieve composite membranes with high hydrogen permeability and stability. This technique allows the deposition of films also on complex geometries and can be easily scaled up, thus making this technology a potential candidate for preparing high performing membranes. Membranes made by stable and porous alumina supports and metallic, dense and crystalline Pd77Ag23 layers, from 3.5 μm to 17 μm thick, have been prepared and tested. The membranes showed good hydrogen permeability values, showing flux values up to a maximum of 0.62 molH2 m−2 s−1 at 450 °C and ΔP of 300 kPa. The resistance to hydrogen embrittlement and the chemical inertness to syngas were also demonstrated.

Thanks to their high hydrogen permeability, vanadium based alloys can be a valuable and sustainable alternative to palladium alloys, commonly employed in commercial membranes for hydrogen purification/separation. In this work, the unprecedented deposition of micrometric vanadium-based multilayers and their investigation as hydrogen selective membranes have been reported. In particular, this work describes the use of High Power Impulse Magnetron Sputtering, a technique easily scalable also for complex geometries, for the deposition of dense and crystalline Pd/V93Pd7/Pd multilayers with total thickness

This work is devoted to the study of composite system of liquid crystal 4-(trans-4-n-hexylcyclohexyl)-isothiocyanato-benzene (6CHBT) doped with lath-like goethite magnetic nanoparticles with the concentration of 0.01 vol%. The structural transitions in ferronematic samples were observed by dielectric measurements in a capacitor made of ITO-coated glass electrodes as well as by polarizing optical microscopy. Due to the presence of magnetic particles a decrease of the magnetic Freedericksz transition was observed. The response of ferronematics to very low magnetic fields is also presented which opens the door towards application possibilities such as low magnetic fields sensors.

The addition of nanoparticles in lubricating oils recently demonstrated to reduce the coefficient of friction and to increase the load-carrying capability of lubricant in coupled surfaces. In this work, different kinds of nanoparticles were tested as additives to engine oil to improve lubrication: copper and titanium oxide nanoparticles and single walled carbon nanohorns (SWCNHs). Two nanoparticle sizes were also tested in case of copper. The tribological properties of these nanofluids were evaluated by Stribeck tests, in order to compare the effect of nanoparticles on friction coefficient and electric contact resistance in different lubrication regimes. Stribeck curves showed that the coefficient of friction was reduced, compared to raw oil, by the action of Cu nanoparticles having 130 nm diameter, leading to a mean decrease of about 17%, and by SWCNHs, with a mean decrease of about 12%. Conversely, no significant changes were detected in presence of Cu nanoparticles having 50 nm diameter or of TiO2. The suspension viscosity and stability were also tested. Wear tests were also carried out, showing a reduction of wear rate up to nearly 50% for Cu nanoparticles (150 nm diameter) and around 30% for SWCNHs. The measurements showed that nanoparticles having size comparable to the mean roughness of coupled surfaces significantly improved the tribological properties of bare oil. An explanation of nanoparticle action is proposed.

BaCe0.65Zr0.2Y0.15O3-δ (BCZY) have been recently proposed for IT-SOFCs due to its high proton conductivity. On the other hand considerable efforts are directed towards the development of metal-supported cells. The combination of the potential advantages offered by either proton conductors based cells and metal supported configuration has never been explored. In this work the technological issues to produce proton conducting BCZY-Ni anodes stainless steel-supported were carefully investigated. A tailored porous metal support was produced by tape casting. Afterwards the anode was deposited by screen printing and the resulting bilayer sintered in reducing atmosphere. Each step of the production process was thoroughly investigated. A cations interdiffusion between the metallic support and the anodic layer was observed in all range of temperatures considered. The influence of a CeO2 barrier layer and anode thickness on the cations diffusion and a successful production of planar crack-free anode was deeply analyzed.

An experimental investigation on the use of nanofluids as working fluids and direct absorbers in a full-scale concentrating collector is presented. The nanofluid consists of a suspension of single wall carbon nanohorns in distilled water with a concentration of 0.02 g L−1. The thermo-physical properties are the same as those of the base fluid, but the presence of carbon nanoparticles greatly enhances the optical characteristics. A direct absorption receiver has been designed and set up to investigate the capability of the nanofluid to absorb the concentrated sunlight. The receiver exhibits a flat geometry and has been designed for installation on an asymmetric parabolic trough, where the concentrated solar flux locally reaches 100 kW m−2 under clear-sky conditions. Results show that the application of a carbon nanohorn-based nanofluid in a concentrating collector displays an efficiency comparable to that obtained with a surface receiver tested in the same system. However, such performance is not maintained for a long time because of lack of stability of the absorbing fluid.

Pt-based structured catalysts for the low-temperature combustion of methanol have been prepared by electrochemical methods, using Fe-Cr-Al alloy (Fecralloy) foam supports. Among the strategies investi- gated, pulsed electrodeposition of Pt nanoparticles from an H2PtCl6 solution, followed by cathodic elec- trodeposition of CeO2 thin films from a nitrate bath was the most successful. Pt loading and surface area were measured by ICP-MS and cyclic voltammetry, respectively. Although the presence of a CeO2 film decreased the Pt surface area accessible to electrolyte it enhanced the performance of the catalysts towards methanol combustion, without affecting the activation energy of the process, due to the forma- tion of additional active sites along the interface of CeO2-coated Pt nanoparticles

This research aims at studying the stability and thermophysical properties of nanofluids designed as dispersions of sulfonic acid-functionalized graphene nanoplatelets in an (ethylene glycol + water) mixture at (10:90)% mass ratio. Nanofluid preparation conditions were defined through a stability analysis based on zeta potential and dynamic light scattering (DLS) measurements. Thermal conductivity, dynamic viscosity, and density were experimentally measured in the temperature range from 283.15 to 343.15 K and nanoparticle mass concentrations of up to 0.50% by using a transient plate source, a rotational rheometer, and a vibrating-tube technique, respectively. Thermal conductivity enhancements reach up to 5% without a clear effect of temperature while rheological tests evidence a Newtonian behavior of the studied nanofluids. Different equations such as the Nan, Vogel-Fulcher-Tamman (VFT), or Maron-Pierce (MP) models were utilized to describe the temperature or nanoparticle concentration dependences of thermal conductivity and viscosity. Finally, different figures of merit based on the experimental values of thermophysical properties were also used to compare the heat transfer capability and pumping power between nanofluids and base fluid. Ministerio de Economía y Competitividad | Ref. ENE2014-55489-C2-2-R

The work illustrates the preparation of stable suspensions of single-walled carbon nano-horns (SWCNHs) in engine oil and shows their tribological behavior at different temperatures. The suspension stability was verified by dynamic light scattering, and the viscosity of suspensions was measured. Stribeck test was used to evaluate the tribological performances of nano-lubricants in the 25-80 °C temperature range. The coefficient of friction was reduced with the addition of SWCNHs at all temperatures and concentrations. In particular, at T = 25 °C, the coefficient friction was reduced up to about 12 % in boundary regime even with a very low SWCNH concentration (0.01 vol%). Wear tests were carried out to verify results obtained from Stribeck characterization. A decrease in mean wear rate was observed at each temperature, between 25 and 30 %. In particular, at 25 °C, a decrease of about 30 % in wear rate was estimated. Friction coefficient decrease was also observed during all wear tests, probably due to the ball-bearing effect played by SWCNHs spherical aggregates. Therefore, SWCNHs revealed the potential to be promising candidates as additives, to develop a new class of lubricants that are suitable and effective in different operating environments. © 2014 Springer Science+Business Media New York.

The dependence of polarized optical properties of colloidal suspensions of goethite (α-FeOOH) nanorods in water and PAO base fluids under the action of an applied magnetic field are investigated in the ultraviolet, visible and near infrared from 300 to 1500 nm wavelength. We found that the transmittance in the NIR range can be tuned by changing magnetic field direction and strength. Moreover, we found that the magnetic field dependence of optical properties is strongly connected to the base fluid where magnetic nanoparticles are suspended. The obtained results show that the optical properties of goethite-based suspensions are very sensitive to even weak external magnetic fields, with promising perspectives for sensing applications.

In this study, new phase change material nanoemulsions (PCMEs) were designed and characterized as possible storage and heat transfer media for low-temperature thermal uses. Water- and (ethylene glycol + water)-based emulsions with fine droplets of n-heptadecane and RT21HC commercial paraffin were produced by a solvent-assisted emulsification method. No phase separation or significant growth in PCM drops were observed for the prepared emulsions through storage, after freeze–thaw cycles and under mechanical shear. Phase change transitions were characterized and a significant sub-cooling was observed, with solidification temperatures up to 13 K below the melting point. One pure alkane and two commercial paraffin waxes with higher melting points were considered as nucleating agents to reduce sub-cooling effect. Although the emulsions exhibited diminutions in thermal conductivity up to 9% with respect to the carrier fluids used as base fluid, enhancements in energy storage capacity (considering an operational temperature interval equal to the sub-cooling) reached 26% in the case of RT21HC nanoemulsion based on the (ethylene glycol + water) mixture that contained 10% in mass of paraffin. In addition, the thermal reliability of the nanoemulsions was verified analyzing the changes in latent heat after storage and throughout 1000 thermal cycles.

Cu nanoparticles (NPs) are widely studied to understand how they work in lubricant oils to improve its tribological properties. This paper describes the synthesis and characterization of Cu NPs of different size (φ = 60 and 130 nm) carried out in EG and the dispersion procedure used to prepare nanolubricants containing different amounts of NPs (0.005 vol% -0.01 vol% -0.02 vol%). The base oil was a commercially available lubricant oil for internal combustion engines. In order to study the influence of different parameters such as particles size and concentration on tribological properties of nanolubricants, the Stribeck curves were recorded at 25°C in the three lubrication regions (elasto-hydrodynamic, mixed lubrication, and boundary lubrication) and the results discussed. It was found that Cu NPs with a 130-nm mean diameter were more effective in reducing the coefficient of friction in all the lubrication regimes with respect to smaller ones.

This paper describes the cathodic electrodeposition of nickel hydroxides from NiCl2 at constant potentials. In a single-compartment electrochemical cell, the procedure yields black films that have the appearance of glassy carbon. XPS analyses reveal that the films consist of a mixture of Ni(OH)2 and NiOOH in a proportion that depends on the deposition potential; furthermore, SIMS analyses indicate that the coatings are richer in NiOOH in the inner regions towards the support. The electrochemical behavior has been compared with data obtained on electrodes based on pure Ni(OH)2 prepared by cathodic electrodeposition from Ni(NO3)2, following literature procedures. This comparison confirms the composite nature of black nickel hydroxide (BN) coatings, adding that Ni(OH)2 and NiOOH are present in nearly equal amounts. The electrocatalytic activity of BN electrodes was tested in the oxidation of methanol in alkaline solutions. Experimental results are consistent with a mechanism previously proposed in literature for the oxidation of organic compounds on nickel electrodes. Comparison with electrodes based on pure Ni(OH)2 shows that, in the low potentials region, the presence of a high amount of NiOOH causes a decrease of activity, while an opposite effect is observed when the potential is increased. The black nickel electrodes show a remarkable stability in repeated cycles of oxidation of methanol and O2 evolution; under similar conditions, conventional Ni(OH)2 films show an appreciable decrease in thickness, as evidenced by the decrease of peak charge in cyclic voltammetry experiments.

The higher manganese silicides (HMS), represented by MnSix (x = 1.71 to 1.75), are promising p-type leg candidates for thermoelectric energy harvesting systems in the middle-high temperature range. They are very attractive as they could replace lead-based compounds due to their nontoxicity, low-cost starting materials, and high thermal and chemical stability. Dense pellets were obtained through direct reaction between Mn and Si powders during the spark plasma sintering process. The tetragonal HMS and cubic MnSi phase amounts and the functional properties of the material such as the Seebeck coefficient and electrical and thermal conductivity were evaluated as a function of the SPS processing conditions. The morphology, composition, and crystal structure of the samples were characterized by scanning electron microscopy, energy-dispersive x-ray spectroscopy, and x-ray diffraction analyses, respectively. Differential scanning calorimetry and thermogravimetric analysis were performed to evaluate the thermal stability of the final sintered material. A ZT value of 0.34 was obtained at 600°C for the sample sintered at 900°C and 90 MPa with 5 min holding time.

Magnesium silicide (Mg2Si)-based alloys are promising candidates for thermoelectric (TE) energy conversion for the middle to high range of temperature. These materials are very attractive for TE research because of the abundance of their constituent elements in the Earth’s crust. Mg2Si could replace lead-based TE materials, due to its low cost, nontoxicity, and low density. In this work, the role of aluminum doping (Mg2Si:Al = 1:x for x = 0.005, 0.01, 0.02, and 0.04 molar ratio) in dense Mg2Si materials was investigated. The synthesis process was performed by planetary milling under inert atmosphere starting from commercial Mg2Si pieces and Al powder. After ball milling, the samples were sintered by means of spark plasma sintering to density >95%. The morphology, composition, and crystal structure of the samples were characterized by field-emission scanning electron microscopy, energy-dispersive spectroscopy, and x-ray diffraction analyses. Moreover, Seebeck coefficient analyses, as well as electrical and thermal conductivity measurements were performed for all samples up to 600°C. The resultant estimated ZT values are comparable to those reported in the literature for these materials. In particular, the maximum ZT achieved was 0.50 for the x = 0.01 Al-doped sample at 600°C.

A high temperature test rig to simultaneously measure electrical conductivity and thermopower is described. The apparatus allows to perform measurements in controlled atmosphere or vacuum to protect oxygen sensitive materials. A spring load mounting placed in a cold zone permits to reduce the thermal contact resistance between the sample and two metallic blocks (the hot side and the heat sink) even at high temperature. The hot side metal block is periodically heated to obtain the thermopower from the slope of the ?V vs ?T line. Conductivity is measured before each thermopower measurement by a linear four-wire method. The automatic data acquisition and analysis is controlled by a LabView-based interface. Two interchangeable setups are possible. The first one uses silver blocks and K-type thermocouples and is suitable for temperatures from 300 to about 1100 K. The second one uses W blocks and S-type thermocouples to allow higher temperatures measurements since all the hot zone parts are made of Al2O3, Pt or W. The device was tested using PdAg alloy and Ni rods and, for the low temperatures range, the NIST Standard Reference Material 3451 (bismuth telluride), strictly confirming the reference data.

International audience; New 3D electrodes are prepared and tested in reductive herbicide dechlorination as the first step of an environmental remediation process. Commercial nickel foams are modified through the spontaneous deposition of silver nanoparticles. Some of the solutions of Ag+ ions employed in the galvanic displacement reactions contain complexing agents, such as thiosulfate or thiocyanate, and a capping agent, polyvinylpyrrolidone (PVP), which influences the morphology and growth kinetics of the silver deposits. Modified foams are used as cathodes for the reductive dechlorination of Alachlor(TM), a common chloroacetanilide herbicide, in a series of tests that confirm the catalytic activity of silver. Electrodes prepared in a thiosulfate solution containing PVP allow extensive reduction of Alachlor(TM) to give deschloroalachlor as the only dechlorinated product.

Magnesium silicide (Mg2Si) is a promising candidate for thermoelectric energy conversion due to its low toxicity, the abundance of its raw constituents and its low density, allowing manufacturing of light, sustainable and relatively cheap devices. Mg2Si needs to be doped in order to increase its efficiency, making this material competitive among materials operating in the intermediate temperature range. In this work, a synthesis procedure based on melting of the raw elements in easily available and cheap Al2O3 crucibles was developed to obtain polycrystalline Sb doped Mg2Si materials in a wide range of compositions. Powders from the crushed lumps were consolidated via spark plasma sintering and then thermally annealed to obtain dense pellets of Sb:Mg2Si with Sb = 0.0, 0.1, 0.3, 0.5, 0.7, 1.0 and 1.5 at%. The effects of Sb doping and of the synthesis and sintering technique on composition, morphology and stability of n-type Mg2Si are discussed. Transport properties (Seebeck coefficient, electrical and thermal conductivity, charge carrier density) were evaluated in order to elucidate the composition–property relationship within this material system and find the optimal doping amount to optimize its thermoelectric properties.

Modified Reversed-Field eXperiment is an experiment of magnetic confinement of thermonuclear plasma in the Reversed-Field Pinch configuration. The toroidal device is designed to operate with hydrogen plasmas, and the most internal wall is entirely covered with polycrystalline graphite tiles. The disadvantage of graphite walls is the progressive hydrogen accumulation in graphite during operation. To overcome this problem, some graphite conditioning procedures are necessary (e.g. boronization, lithization and glow discharge). The critical role of graphite walls on plasma control suggested the use of secondary ion mass spectrometry (SIMS) technique for the evaluation of conditioning procedures efficacy. SIMS analyses of graphite samples after their exposure to plasmas or wall conditioning treatments are presented in this work. The SIMS technique resulted fundamental on the investigation of the boron distribution in the graphite tiles, and sample comparisons indicated the need for glow discharge cleaning system upgrading to improve the conditioning process and boronization uniformity. Copyright © 2012 John Wiley & Sons, Ltd.

A method for large-scale production of Single Wall Carbon Nanohorns (SWCNH) in a prototype reactor was tested with optimal thermodynamic conditions that favour high quality material formation at rates of about 100 g/h. The first productions demonstrated the excellent capability and flexibility of the approach. The plant typology that can be easily scaled up to tens the present scale, making possible to propose materials based on SWCNHs for real uses such as in hydrogen storage. In this framework, pristine and oxidized materials were characterized and tested.

In the RFX-mod Reversed Field Pinch experiment the wall is entirely covered by graphite tiles. The disadvantage of a graphite wall is that, except after wall conditioning procedures, such as boronization, lithization or glow discharge cleaning, the graphite becomes saturated with trapped Hydrogen, causing that during the discharge the particle recycling factor is approximately one and plasma density is entirely sustained by particle fluxes coming from the wall. In the paper the results of the analyses of graphite samples after their exposure to plasmas or wall conditioning treatments are presented. The topics addressed are: the deposition of Boron during different boronization treatments; the erosion and re-deposition of the Boron layer by Hydrogen plasmas; some remarks about the presence of Lithium in the wall since the beginning of lithization treatments.

In this work, BaCe0.65Zr0.20Y0.15O3−δ powders with a perovskite-type structure were successfully synthesized by a microwave-assisted sol–gel Pechini method (SGP). By comparison, powders having the same nominal stoichiometry were also prepared without the microwave assistance. For the syntheses, nitrates were used as metal precursors, and ethylenediaminetetraacetic acid and ethylene glycol were used as complexing and polymerizing agents, respectively. An extensive structural and morphological investigation by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM) has been performed. Moreover, in order to check the phase transitions, simultaneous thermogravimetric and differential thermal analyses were (TG-DTA) performed on gels. With respect to the conventional Pechini method, the microwave-assisted process guaranteed a faster, energy-saving procedure for obtaining single-phase nanopowders of high purity. Moreover, a significant increase in pellet densities was achieved owing to a higher grain coalescence.

The La0.75Sr0.25Cr0.5Mn0.5O3-δ (LSCM) catalyst and the novel Ru/La0.75Sr0.25Cr0.5Mn0.5O3-δ composite were investigated as alternative anodes for the direct utilization of propane in anode-supported solid oxide fuel cells. In particular, their synthesis and performance in direct propane reforming were studied. The LSCM powders were prepared by a sol–gel method based on a modified Pechini procedure. Single-phase LSCM perovskite powders were obtained. SEM micrographs of the LSCM powders revealed particles in the 200–300 nm range with a homogeneous grain distribution. The deposition of 5 wt.% metallic ruthenium nanoparticles on the LSCM perovskite powders was carried out by a microwave-assisted procedure. TEM investigations of Ru/LSCM composites showed a homogeneous distribution of metallic ruthenium nanoparticles with a mean grain size of around 2–3 nm. The catalytic activity of these potential anode materials was investigated for the following propane reforming processes: steam reforming (SR), autothermal reforming (ATR) and partial oxidation (POX) at 600, 700 and 800 °C. Very high propane conversion rates were observed under POX and ATR conditions at 700 and 800 °C for both the LSCM and Ru/LSCM compounds (> 92 at 700 °C and > 98% at 800 °C), whereas in the steam reforming environment, a satisfactory conversion was achieved only at 800 °C. The ruthenium presence was found to strongly improve the selectivity for H2 and syngas production for all of the experiments performed, reaching an approximately 90% syngas yield. Finally, good chemical stability after the catalytic tests was demonstrated for the LSCM and Ru/LSCM anode materials.