A Smart Multisensor System for the Ash Fall-Out Monitoring

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Composite nafion-catio3-δ membranes as electrolyte component for pem fuel cells

Manufacturing new electrolytes with high ionic conductivity has been a crucial challenge in the development and large-scale distribution of fuel cell devices. In this work, we present two Nafion composite membranes containing a non-stoichiometric calcium titanate perovskite (CaTiO3−δ ) as a filler. These membranes are proposed as a proton exchange electrolyte for Polymer Electrolyte Membrane (PEM) fuel cell devices. More precisely, two different perovskite concentrations of 5 wt% and 10 wt%, with respect to Nafion, are considered. The structural, morphological, and chemical properties of the composite membranes are studied, revealing an inhomogeneous distribution of the filler within the polymer matrix. Direct methanol fuel cell (DMFC) tests, at 110◦ C and 2 M methanol concentration, were also performed. It was observed that the membrane containing 5 wt% of the additive allows the highest cell performance in comparison to the other samples, with a maximum power density of about 70 mW cm−2 at 200 mA cm−2 . Consequently, the ability of the perovskite structure to support proton carriers is here confirmed, suggesting an interesting strategy to obtain successful materials for electrochemical devices

Pt–Fe cathode catalysts to improve the oxygen reduction reaction and methanol tolerance in direct methanol fuel cells

High surface area carbon-supported Pt and bimetallic Pt–Fe catalysts are investigated for the oxygen electro-reduction reaction (ORR) in low-temperature direct methanol fuel cells (60 °C). The electrocatalysts are prepared using a combination of colloidal and incipient wetness methods allowing the synthesis of carbon-supported bimetallic nanoparticles with a particle size of about 2–3 nm. These materials are studied in terms of structure, morphology and composition using X-ray diffraction, X-ray fluorescence and transmission electron microscopy techniques. The electrocatalytic behaviour of these catalysts for ORR is investigated by employing the rotating disc technique. An enhancement of the ORR is observed with the bimetallic Pt–Fe catalyst in the oxygen-saturated electrolyte solution, with and without methanol.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

A High-Resolution Fully Inkjet Printed Resonant Mass Sensor

The rapid prototyping of low-cost sensors is assuming strategic importance in several application fields. In this paper, a fully inkjet printed mass sensor is proposed. The device consists of a poly-ethylene terephthalate (PET) cantilever beam, which is driven to its resonant mode by an electromagnetic actuation mechanism, implemented through the interaction between a current impulse flowing through a planar coil (inkjet printed on the PET beam), and a permanent magnet, facing the actuation coil. Target masses are positioned close to the beam end. The sensing methodology, based on the relationship between the beam first natural frequency and the target mass, is implemented through a strain gauge (inkjet printed across the fixed end of the cantilever). The resonant operating mode of the sensor confers intrinsic robustness against instabilities of the strain sensor structure (e.g., the residual stress of the cantilever beam), the target mass material and the magnet–coil distance. The latter indeed changes as a function of the target mass values. The friction-less actuation mode is another shortcoming of the sensor, as well as the low-cost feature arising from the adopted technology. As far as we know, the solution proposed is the first example of a low-cost fully printed mass sensor. The operating range of the device is 0–0.36 g while its resolution is in the order of 1.0 mg, thus addressing crucial application fields. A Q factor around 35 has been estimated, which confirms the suitable performances of the sensor in term of selectivity and resolution

A comparison of linear and non-linear strategies for energy harvesting from mechanical vibrations

Energy Harvesting strategies coupled with the improvement of electronics and the progressive reduction of power requirements have been widely recognized as fundamental to enable self-powered (or autonomous) devices. Among all the potential energy sources, kinetic energy stemming from mechanical vibrations has been particularly extensively investigated for EH purposes due to its characteristics of heterogeneity and ubiquity. To exploit such energy sources, a suitable coupling mechanism to convert vibrations into electric charge is required; it must take into account the wide frequency bandwidth of mechanical vibrations as encountered in everyday scenarios. This review offers an overview of linear vs. non-linear strategies for EH, with a specific focus on different approaches to implement efficient coupling mechanisms; the performances of the specific solutions covered in this work are discussed

Dry Hydrogen Production in a Tandem Critical Raw Material-Free Water Photoelectrolysis Cell Using a Hydrophobic Gas-Diffusion Backing Layer

A photoelectrochemical tandem cell (PEC) based on a cathodic hydrophobic gas-diffusion backing layer was developed to produce dry hydrogen from solar driven water splitting. The cell consisted of low cost and non-critical raw materials (CRMs). A relatively high-energy gap (2.1 eV) hematite-based photoanode and a low energy gap (1.2 eV) cupric oxide photocathode were deposited on a fluorine-doped tin oxide glass (FTO) and a hydrophobic carbonaceous substrate, respectively. The cell was illuminated from the anode. The electrolyte separator consisted of a transparent hydrophilic anionic solid polymer membrane allowing higher wavelengths not absorbed by the photoanode to be transmitted to the photocathode. To enhance the oxygen evolution rate, a NiFeOX surface promoter was deposited on the anodic semiconductor surface. To investigate the role of the cathodic backing layer, waterproofing and electrical conductivity properties were studied. Two different porous carbonaceous gas diffusion layers were tested (Spectracarb® and Sigracet®). These were also subjected to additional hydrophobisation procedures. The Sigracet 35BC® showed appropriate ex-situ properties for various wettability grades and it was selected as a cathodic substrate for the PEC. The enthalpic and throughput efficiency characteristics were determined, and the results compared to a conventional FTO glass-based cathode substrate. A throughput efficiency of 2% was achieved for the cell based on the hydrophobic backing layer, under a voltage bias of about 0.6 V, compared to 1% for the conventional cell. For the best configuration, an endurance test was carried out under operative conditions. The cells were electrochemically characterised by linear polarisation tests and impedance spectroscopy measurements. X-Ray Diffraction (XRD) patterns and Scanning Electron Microscopy (SEM) micrographs were analysed to assess the structure and morphology of the investigated materials.Authors gratefully acknowledge funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 760930 (FotoH2 project)

Optimizing the synthesis of carbon nanofiber based electrocatalysts for fuel cells

7 páginas, 2 tablas, 7 figuras.This work deals with an optimization of the platinum dispersion on low surface area carbon nanofibers (CNFs) by using different synthesis procedures and its electrocatalytic activity towards oxygen reduction. The selected CNFs were characterized by a BET surface area of ca. 100 m2 g-1 and were in-house synthesized by the decomposition of CH4 at 700ºC. Pt nanoparticles were deposited by using four different synthesis routes. A metal concentration of 20 wt% was confirmed by EDX and TGA. Two classical impregnation routes were employed, one using NaBH4 as reducing agent at 15ºC and the second one using formic acid at 80ºC. Two alternative processes consisted in a microemulsion procedure followed by reduction with NaBH4 and a colloidal route by using the sulphite complex method followed by reduction with hydrogen. The main differences regarded the platinum crystal size varying from 2.5 nm for the colloidal route to 8.1 nm for the impregnation route (formic acid). The classical impregnation procedures did not result appropriate to obtain a small particle size in the presence of this support, whereas microemulsion and colloidal methods fit the requirements for the cathodic oxygen reduction reaction in polymer electrolyte fuel cells, despite the low surface area of CNFs. The catalysts were subjected to an accelerated degradation test by continuous potential cycling. Although the initial activity was the highest for the microemulsion based catalyst, after the accelerated degradation test the colloidal based catalyst experienced a relatively lower loss of performance.The authors wish to thank FEDER and the Spanish MEC for financial support to project CTQ2011-28913-C02-01. The authors also acknowledge the support of bilateral CNR (Italy) -CSIC (Spain) joint agreement 2011-2012 (project Baglio/Lazaro 2010IT0026).Peer reviewe

Enhanced Photoelectrochemical Water Splitting at Hematite Photoanodes by Effect of a NiFe-Oxide co-Catalyst

Tandem photoelectrochemical cells (PECs), made up of a solid electrolyte membrane between two low-cost photoelectrodes, were investigated to produce “green” hydrogen by exploiting renewable solar energy. The assembly of the PEC consisted of an anionic solid polymer electrolyte membrane (gas separator) clamped between an n-type Fe2O3 photoanode and a p-type CuO photocathode. The semiconductors were deposited on fluorine-doped tin oxide (FTO) transparent substrates and the cell was investigated with the hematite surface directly exposed to a solar simulator. Ionomer dispersions obtained from the dissolution of commercial polymers in the appropriate solvents were employed as an ionic interface with the photoelectrodes. Thus, the overall photoelectrochemical water splitting occurred in two membrane-separated compartments, i.e., the oxygen evolution reaction (OER) at the anode and the hydrogen evolution reaction (HER) at the cathode. A cost-effective NiFeOx co-catalyst was deposited on the hematite photoanode surface and investigated as a surface catalytic enhancer in order to improve the OER kinetics, this reaction being the rate-determining step of the entire process. The co-catalyst was compared with other well-known OER electrocatalysts such as La0.6Sr0.4Fe0.8CoO3 (LSFCO) perovskite and IrRuOx. The Ni-Fe oxide was the most promising co-catalyst for the oxygen evolution in the anionic environment in terms of an enhanced PEC photocurrent and efficiency. The materials were physico-chemically characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM).Authors gratefully acknowledge funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 760930 (FotoH2 project)

Blocking Tumor-Educated MSC Paracrine Activity Halts Osteosarcoma Progression

Purpose: Human osteosarcoma is a genetically heterogeneous bone malignancy with poor prognosis despite the employment of aggressive chemotherapy regimens. Because druggable driver mutations have not been established, dissecting the interactions between osteosarcoma cells and supporting stroma may provide insights into novel therapeutic targets.Experimental Design: By using a bioluminescent orthotopic xenograft mouse model of osteosarcoma, we evaluated the effect of tumor extracellular vesicle (EV)-educated mesenchymal stem cells (TEMSC) on osteosarcoma progression. Characterization and functional studies were designed to assess the mechanisms underlying MSC education. Independent series of tissue specimens were analyzed to corroborate the preclinical findings, and the composition of patient serum EVs was analyzed after isolation with size-exclusion chromatography.Results: We show that EVs secreted by highly malignant osteosarcoma cells selectively incorporate a membrane-associated form of TGF\u3b2, which induces proinflammatory IL6 production by MSCs. TEMSCs promote tumor growth, accompanied with intratumor STAT3 activation and lung metastasis formation, which was not observed with control MSCs. Importantly, intravenous administration of the anti-IL6 receptor antibody tocilizumab abrogated the tumor-promoting effects of TEMSCs. RNA-seq analysis of human osteosarcoma tissues revealed a distinct TGF\u3b2-induced prometastatic gene signature. Tissue microarray immunostaining indicated active STAT3 signaling in human osteosarcoma, consistent with the observations in TEMSC-treated mice. Finally, we isolated pure populations of EVs from serum and demonstrated that circulating levels of EV-associated TGF\u3b2 are increased in osteosarcoma patients.Conclusions: Collectively, our findings suggest that TEMSCs promote osteosarcoma progression and provide the basis for testing IL6- and TGF\u3b2-blocking agents as new therapeutic options for osteosarcoma patients. Clin Cancer Res; 23(14); 3721-33. \ua92017 AACR