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Thermotoga neapolitana is a hyperthermophilic bacterium that can metabolize glucose and several organic wastes in hydrogen and lactate at a temperature of 80°C. Their high performance in producing hydrogen at so high a temperature as 80°C suggests a potential energy application of them where hydrogen is an important element of the process. In this view, experimentation of a T.neapolitana strain is carried out in double-chamber electrochemical systems. The aim is to explore the interaction of these bacteria with the anode and the cathode, stressing their capability to survive in presence of a polarized electrode which can drastically change the pH of the media. A culture enriched of 5 g/L of glucose, under CO2 pressure (80 °C) was used to fill both the anodic and cathodic compartments of the electrochemical system, applying a voltage of 1.5 V between the anode and the cathode. The test lasted ten days. Results clearly indicate that bacteria colonize both electrodes, but the glucose metabolism is completely inhibited in the anodic compartments. On the contrary, metabolism is stimulated in the cathodic compartment. Bacteria are alive on the electrodes in the pH interval of 3 - 9.

This work investigates Reduced Titanium Oxide (RTO) in comparison with Carbon Cloth (CC) and commercial Boron Doped Diamond (BDD) as anodes in hyperthermophilic bioelectrochemical systems operating at 80°C by Thermotoga neapolitana. Two samples of RTO were synthesized by plasma electrolytic oxidation (PEO) of titanium plates and subsequent electrochemical reduction. Electrochemical performance of CC, BDD, and RTO are tested by performing cyclic voltammetry in the anodic region (0-1V, 50 mV/s), in abiotic and biotic conditions. The surface of colonized materials is observed by SEM microscopy. Results show that bacteria fast settle on all tested material, significantly affecting their electrochemical conductivity. The integration of voltammetric cycles reveals that biofilm generates capacitive effects on the anodic surfaces, particularly evident in RTO, less in CC and absent in BDD. Charge densities provided by capacitive response of RTO and CC are of the order of 5.58 and 0.77 mC/cm2, respectively.

Photoelectrocatalysis (PEC) has been already proposed as a polishing treatment for wastewater treatment plants (WWTPs) effluents. In this work, the impact of polarization reversal during PEC process has been studied and evaluated on the basis of the removal of organic substance and color, biodegradability of the matrix, and inactivation of the catalyst. Effluents were sampled from a full-scale WWTP and alternatively treated by electrochemical oxidation (EC), photolysis (PL), photocatalysis (PC), photoelectrocatalysis, and photoelectrocatalysis with reverse polarization (PECr). The efficiency and the kinetics of the process, in terms of removal of organic substance and color, were not affected by reverse polarization and very similar results were obtained by PEC and PECr. The biodegradability of the effluents strongly increased both by PECr (RSBR: 0.84 ± 0.07), and by PEC and PL (0.89 ± 0.11, and 0.78 ± 0.02, respectively). In the selected polarization reversal mode (100 s at −0.1 V every 500 s at 4 V, cell voltage), a similar photocurrent loss after PEC and PECr was observed, suggesting no effect on the activity of the TiO2 mesh. This study can serve as a base for future research on polarization reversal to optimize operation parameters and exploit the procedure to preventing fouling and inactivation of the catalyst. [ABSTRACT FROM AUTHOR]

In this study, the effects of photo-electrocatalysis (PEC) were evaluated as an innovative application of conventional photocatalysis (PC) to remediate water in a recirculating system for rainbow trout (Oncorhynchus mykiss) culture, in relation to fish welfare and health, with a multidisciplinary approach. Three tanks were employed, equipped with conventional biological filters as a control system, and three tanks equipped with the PEC purification system. The concentrations of ammonia, nitrite and nitrate ions in water were monitored, and the fish's oxidative damage and stress response were evaluated in parallel. The water of the PEC-treated experimental group showed lower ammonia (TAN) and nitrite concentrations and higher nitrate concentration, possibly deriving from TAN oxidation through PEC, also leading to gaseous N2. Histological analysis did not reveal any pathological alteration in the gills and liver of both groups. The superoxide dismutase (sod1), glutathione reductase (GR), glutathione peroxidase (GPx1), and Tumor necrosis factor (TNFα) gene expressions were significantly higher in the control group than in the PEC-treated group, while the Heat shock protein 70 (Hsp70) expression did not show any difference in the two groups. These results indicate that the use of PEC filters has a positive effect on water quality, compared to the use of conventional biological filters, inducing a high level of welfare in O. mykiss. [ABSTRACT FROM AUTHOR]

Recently, among AOPs, photoelectrocatalysis (PEC) on TiO2 is gaining interest. In this study, five different real waters sampled in four different points of the integrated urban water management (IUWM) system were tested with PEC and UV alone, for comparison. This work aims to verify the effect of the PEC suggesting the optimal position in IUWM system where the PEC should be located to obtain the best performance. In groundwaters (GWs), PEC effectively removed atrazine-based compounds (> 99%), trichloroethylene, and perchloroethylene (96%), after 15 min of reaction time. However, given the low concentrations of emerging compounds, the synergistic effect of UV radiation with the catalyst and with the polarization of the mesh was not visible, with very few differences compared with the results obtained with UV alone. Pharmaceutical industrial wastewater (IWW) showed a significant increase in biodegradability after 2 h, both if subjected to PEC or UV (200%), despite the absence of COD removal. The PEC applied on IWW from a sewage sludge treatment plant allowed to effectively remove the COD (39.6%) and increase the biodegradability (300%). Good results in terms of COD removal (33.9%) and biodegradability increase (+900%) were also achieved testing PEC on wastewater treatment plant effluent. Except for GWs, PEC allowed significant EEO savings respect to UV alone (76.2–99.1%). [ABSTRACT FROM AUTHOR]

The fast, single‐step and easily scalable production by plasma electrolytic oxidation (PEO) of large area TiO2 electrodes with excellent photoactivity in water splitting under simulated solar light is systematically investigated here. In particular, the effects that the cell voltage (100–180 V) and the processing time (0.5–15 min) have on the electrode properties are studied. The PEO‐produced oxide layers are porous, the predominant crystalline structure shifting from anatase, to an anatase‐rutile mixture, and finally to rutile by rising the cell voltage. The electrodes show a double‐layered structure, with a more compact layer at the interface with the titanium substrate and a thick porous layer on the external surface. The photocurrent density versus wavelength reflects the phase composition, with a maximum incident photon‐to‐current efficiency of 90% at 320 nm. The highest H2 production rate is attained with the mixed anatase‐rutile electrode prepared by 300 s‐long PEO at 150 V. [ABSTRACT FROM AUTHOR]

Microbial fuel cells are an emerging technology for wastewater treatment, but to be commercially viable and sustainable, the electrode materials must be inexpensive, recyclable, and reliable. In this study, recyclable polymeric supports were explored for the development of anode electrodes to be applied in single-chamber microbial fuel cells operated in field under hypersaline conditions. The support was covered with a carbon nanotube (CNT) based conductive paint, and biofilms were able to colonize the electrodes. The single-chamber microbial fuel cells with Pt-free cathodes delivered a reproducible power output after 15 days of operation to achieve 12±1 mW m−2 at a current density of 69±7 mA m−2. The decrease of the performance in long-term experiments was mostly related to inorganic precipitates on the cathode electrode and did not affect the performance of the anode, as shown by experiments in which the cathode was replaced and the fuel cell performance was regenerated. The results of these studies show the feasibility of polymeric supports coated with CNT-based paint for microbial fuel cell applications. [ABSTRACT FROM AUTHOR]

Electrochemical experimental evidence of facilitated electron transfer in a sub-micrometer biosensor is presented. Layer-by-layer self-assembled deposition provides the unique advantage to specifically control the thickness of the biosensors, allowing an oxygen-insensitive device with a film thickness of 70 nanometers to be obtained. The biosensor is based on a poly(allylamine) osmium redox mediator and glucose 1-oxidase. The immobilized enzyme contributes to the signal generation through the full biosensor thickness, with no loss of 'active enzyme' in the outer layer of the biosensor through reaction with oxygen, as reported in the case of thick redox hydrogels. The application of the biosensor in complex matrices was approached with tests in wastewater. Encapsulation of the biosensor with Nafion® membrane ensured the protection of the enzyme molecules from the external environment, allowing the successful application of the sensor in a complex matrix. [ABSTRACT FROM AUTHOR]

A selective oxygen biosensor based on bilirubin oxidase (BOx) was developed. The sensor was used for determining oxygen profiles in a membraneless, single-chamber microbial fuel cell (SCMFC), fed with raw wastewater. The linear response of the sensor was optimized by a diffusion layer of silica gel. A computer-controlled stage was used to obtain accurate and precise measurements. Oxygen concentration in biofilms covering electrodes was measured, showing 3 mg L−1 of O2 in the bulk solution, decreasing to 0 mg L−1 in the cathodic biofilm. The MFC generated power in the range of 0-0.08 mW, associated to the oxygen content. [ABSTRACT FROM AUTHOR]

Manganese oxide \ carbon nanotube (CNT) thin film electrodes were fabricated by direct growth of a carbon nanotube layer on aluminum substrate (i.e. a commercially viable material for use as current collector) by chemical vapor deposition, in the presence of an electrochemically deposited thin film nickel catalyst, followed by anodic electrodeposition of MnO2. A proof of concept of this approach is demonstrated showing that the fabrication process, even in its simplest and unsophisticated implementation - notably without any deliberate effort to control the CNT growth arrangement and consequently the composite microstructure- allows the preparation of MnO2/CNT/Al prototype electrodes having almost a three-fold increase in capacitance compared to MnO2/Ni electrodes and, more significantly, comparing favorably with composite electrodes of similar design and fabrication. MnO2/CNT/Al electrodes ensured also improved cyclic stability compared to the reference case of MnO2/Ni electrodes. The proposed scheme is an effective procedure for the fabrication of thin film composite MnO2/CNT/Al electrodes, which may be amenable to significant improvements by tailoring thickness and microstructure of the CNT scaffold and manganese oxide film. Furthermore, a similar process scheme, may be proposed for the fabrication of active electrodes of different scopes with a proper choice of the substrate. [ABSTRACT FROM AUTHOR]

The aim of this work was to assess a number of coatings developed for Mg for biomedical applications. The Mg substrates were high-purity (HP) Mg and ME10, an alloy recently developed for improved extrudability. The research utilized the new fishing-line specimen configuration to allow direct comparison to our recent in vivo and in vitro measurements. The in vitro measurements were immersion tests of fishing-line specimens immersed in Nor's solution at 37 °C. Tests of substantial duration are needed because the corrosion rates of uncoated samples are low. Nor's solution is the designation given to Hank's solution through which CO2 is bubbled at a partial pressure of 0.009 atm. In this solution, pH is maintained constant by the interaction of CO2 and the bicarbonate ions in the solution. This is the same buffer as that which maintains the pH of blood. Coatings examined were: (i) an anodization using a bio-friendly alkaline electrolyte consisting of phosphate, borate, and metasilicate, (ii) octyltrimethoxysilane (OSi), (iii) 1,2-bis[triethoxysilyl]ethane (BTSE), (iv) anodization +OSi, and (v) anodization + BTSE. The performance of coated samples was comparable to or better than that of the uncoated samples, and there was a substantially better performance for the ME10 samples after anodization +OSi. Reasons for the various performances are discussed. [ABSTRACT FROM AUTHOR]

Biodegradable cardiovascular stents in magnesium (Mg) alloys constitute a promising option for a less intrusive treatment, due to their high compatibility with the body tissue and intrinsic dissolution in body fluids. The design and fabrication aspects of this medical device require an integrated approach considering different aspects such as mechanical properties, corrosion behaviour and biocompatibility. This work gathers and summarises a multidisciplinary work carried out by three different research teams for the design and fabrication of Mg stents. In particular, the paper discusses the design of the novel stent mesh, the deformability study of the Mg alloys for tubular raw material and laser microcutting for the realisation of the stent mesh. Although, the results are not fully validated as the device has not been fully tested, they show the feasibility of the used approaches, as the first prototype stents in Mg alloy were produced successfully. [ABSTRACT FROM AUTHOR]

Equal channel angular pressing (ECAP) was performed on ZK60 alloy and pure Mg in the temperature range 150-250 °C. A significant grain refinement was detected after ECAP, leading to an ultra fine grain size (UFG) and enhanced formability during extrusion process. Comparing to conventional coarse grained samples, fracture elongation of pure Mg and ZK60 alloy were significantly improved by 130% and 100%, respectively, while the tensile strength remained at high level. Extrusion was performed on ECAP processed billets to produce small tubes (with outer/inner diameter of 4/2.5 mm) as precursors for biodegradable stents. Studies on extruded tubes revealed that even after extrusion the microstructure and microhardness of the UFG ZK60 alloy were almost stable. Furthermore, pure Mg tubes showed an additional improvement in terms of grain refining and mechanical properties after extrusion. Electrochemical analyses and microstructural assessments after corrosion tests demonstrated two major influential factors in corrosion behavior of the investigated materials. The presence of Zn and Zr as alloying elements simultaneously increases the nobility by formation of a protective film and increase the local corrosion damage by amplifying the pitting development. ECAP treatment decreases the size of the second phase particles thus improving microstructure homogeneity, thereby decreasing the localized corrosion effects. [ABSTRACT FROM AUTHOR]

In the present paper, a novel method to fabricate ordered arrays of Au/NiO/Au nanowires is described, with the aim of filling the gap between the fundamental study of the electrical properties of scattered single nanowires and the engineered fabrication of nanowire arrays. This approach mainly consists of the following steps: (a) electrodeposition of Au/Ni/Au nanowires into an ordered porous anodic aluminum oxide template; (b) mechanical polishing of the sample to expose the gold tips of Au/Ni/Au nanowires to the template surface; (c) in situ annealing of the Au/Ni/Au nanowires without removing the template. The resulting structure consists in an ordered array of Au/NiO/Au nanowires slightly protruding out of a flat aluminum oxide template. Unlike current approaches, with the described method it is not necessary to remove the template in order to oxidize the middle metal, thus allowing the availability of an entire set of metal/oxide/metal nanowires ordered in a two-dimensional matrix and where single heterojunctions can be accessed individually. [ABSTRACT FROM AUTHOR]

The aim of the present work is to investigate the synthesis of Ti–Nb alloy films obtained by the physical vapor deposition (PVD) magnetron sputtering of Nb films on Ti substrates, followed by low-energy high-current electron beam (LEHCEB) alloying treatment. Ti–Nb alloys were synthetized under two different regimes, one by varying the deposited amount of Nb (from 25 to 150 nm) and treating samples with low applied voltages and a number of pulses (three pulses at either 20 or 25 kV), the second by setting the amount of Nb (100 nm) and alloying it at a higher applied voltage with a different number of pulses (from 10 to 50 at 25 and 30 kV). The synthetized Ti–Nb alloys were characterized by XRD and GDOES for phase identification and chemical composition; SEM and optical microscopy were employed for morphology evaluation; compositional investigation was done by EDS analysis and mechanical properties were evaluated by microindentation tests. LEHCEB treatment led to the formation of metastable phases (α′, α″ and β) which, together with the grain refinement effect, was responsible for improved mechanical properties. [ABSTRACT FROM AUTHOR]

Plasma Electrolytic Oxidation (PEO) was applied to extruded ZM21 Mg alloys to improve their corrosion resistance in a chloride-containing environment. PEO was carried out in DC mode and voltage control in a fluoride-free electrolyte. Potentiodynamic polarization tests in 3.5 wt.% NaCl aqueous solution and neutral salt spray (NSS) tests were carried out. Microstructural and profilometric characterization, as well as NSS tests were performed in different conditions: (i) bare ZM21, (ii) PEO-treated ZM21, (iii) powder-coated ZM21 (without PEO interlayer), and (iv) PEO-treated ZM21 with powder coating top layer (carboxyl-functionalized polyester resin). The PEO + powder coating double layer was identified as the best-performing corrosion protection. [ABSTRACT FROM AUTHOR]

Photoelectrocatalysis (PEC), photolysis (PL), and photocatalysis (PC) were applied to increase the biodegradability of wastewaters effluents sampled from a plant collecting both municipal wastewaters and aqueous waste. In PEC, the catalyst was a porous TiO2 photoanode obtained by plasma electrolytic oxidation and electrically polarized during operation. In PC a dispersion of TiO2 powders was used. The same irradiation shielding, and similar catalyst surface areas were set for PC and PEC, allowing a straightforward evaluation of the catalytic effect of the electrical polarization of TiO2 during operation. Results showed that the chemical oxygen demand (COD) and color removal rates follow the order: PEC > PL and PEC > PC. The specific biodegradability rate (SBR) increased following the same order, the PEC process allowing SBR values more than twice higher than PL and PC. The operating costs were calculated based on the electrical energy per order of COD, color, and SBR values, demonstrating that at the laboratory scale the energy demand of PEC is significantly lower than the other two tested processes. [ABSTRACT FROM AUTHOR]

In this study, we report an investigation of the photoelectrochemical activity of TiO2 films formed by DC plasma electrolytic oxidation (PEO) at a variable potential in a sulfuric acid electrolyte at 0 and 25 °C. The surface morphology was mainly determined by the oxide-forming potential. X-Ray Diffraction and Raman analyses showed that the relative amount of the anatase and rutile phases varied from 100% anatase at low potential (110–130 V) to 100% rutile at high potential (180–200 V), while mixed-phase oxide films formed at intermediate potential. Correspondingly, the band gap of the TiO2 films decreased from about 3.20 eV (pure anatase) to 2.94 eV (pure rutile) and was red-shifted about 0.1 eV by reducing the electrolyte temperature from 25 °C to 0 °C. Glow-Discharge Optical Emission Spectroscopy (GD-OES) and X-ray Photoelectron Spectroscopy (XPS) analyses evidenced S-containing species located preferentially close to the TiO2/Ti interface. The photoelectrochemical activity was assessed by measuring the incident photon-to-current efficiency (IPCE) under Ultraviolet C (UV-C) irradiation, which showed a non-gaussian normal trend as a function of the PEO cell potential, with maximum values exceeding 80%. Photoelectrocatalytic activity was assessed by decolorization of model solutions containing methylene blue. Photoanodes having higher IPCE values showed faster decolorization kinetics. [ABSTRACT FROM AUTHOR]

Carbamazepine (CBZ) is a pharmaceutical compound recalcitrant to conventional wastewater treatment plants and widely detected in wastewater bodies. In the present study, advanced oxidation processes for carbamazepine removal are investigated, with particular regard to the degradation pathways of carbamazepine by photoelectrocatalysis and conventional photocatalysis. Photoelectrocatalysis was carried out onto TiO2 meshes obtained by Plasma Electrolytic Oxidation, a well-known technique in the field of industrial surface treatments, in view of an easy scale-up of the process. By photoelectrocatalysis, 99% of carbamazepine was removed in 55 min while only 65% removal was achieved by photolysis. The investigation of the transformation products (TPs) was carried out by means of UPLC-QTOF/MS/MS. Several new TPs were identified and accordingly reaction pathways were proposed. Above 80 min the transformation products disappear, probably forming organic acids of low-molecular weight as final degradation products. The results demonstrated that photoelectrocatalysis onto TiO2 meshes obtained by plasma electrolytic oxidation is a useful alternative to common advanced oxidation processes as wastewater tertiary treatment aimed at removing compounds of emerging concern. [ABSTRACT FROM AUTHOR]