FM radio for indoor localization with spontaneous recalibration

The position of mobile users has become highly important information in pervasive computing environments. Indoor localization systems based on Wi–Fi signal strength fingerprinting techniques are widely used in office buildings with an existing Wi–Fi infrastructure. Our previous work has proposed a solution based on exploitation of a FM signal to deal with environments not covered with Wi–Fi signal or environments with only a single Wi–Fi access point. However, a general problem of indoor wireless positioning systems pertains to signal degradation due to the environmental factors affecting signal propagation. Therefore, in order to maintain a desirable level of localization accuracy, it becomes necessary to perform periodic calibrations of the system, which is either time consuming or requires dedicated equipment and expert knowledge. In this paper, we present a comparison of FM versus Wi–Fi positioning systems and a combination of both systems, exploiting their strengths for indoors positioning. We also address the problem of recalibration by introducing a novel concept of spontaneous recalibration and demonstrate it using the FM localization system. Finally, the results related to device orientation and localization accuracy are discussed.     

The effect of selenium on antioxidant system in erythrocytes and liver of the carp (Cyprinus carpio L.)

The effect of selenium‐supplemented diet (sodium selenate and selenium yeast) on antioxidant in erthrocytes and liver of the carp (Cyprinus carpio L.) fingerlings was studied. With this goal, the activities of glutathione peroxidase (GSH‐Px), catalase (CAT), superoxide dismutase (SOD), glutathione reductase (GR) and glutathione‐S‐transferase (GST), as well as glutathione (GSH + GSSG) level, were determined. In the group supplemented with sodium selenate, no significant changes in the activity of the above enzymes were recorded in both the erythrocytes and in the liver, with the exception of GST activity that was significantly reduced in the plasma compared with the controls. Glutathione content was at the control level. In the group supplemented with selenium‐yeast, the activities of GSH‐Px, CAT, and SOD were significantly increased in erythrocytes, whereas GST activity and plasma content of GSH + GSSG were reduced compared with the controls. At the same time, the activities of hepatic SOD and GST were increased compared with the controls. These results demonstrate that organically bound selenium (selenium‐yeast) acts more efficiently on antioxidant system of the carp fingerlings than inorganic selenium salts.     

Location of deuteron sites in the proton conducting perovskite BaZr0.50In0.50O3−y

High-resolution neutron powder diffraction data have been collected on deuterated and dried samples of the perovskite BaZr_0.5In_0.5O_2.75 at 5 K and room temperature, respectively. Inspection of Fourier nuclear density maps for the deuterated phase have allowed the deuteron position to be refined on a 12h (1/2, y, 0) crystallographic site, with y = 0.217(4) yielding a chemically reasonable OD distance of 0.92(2) Å. Evidence for anisotropy of the deuteron position is also found consistent with a 24k crystallographic site (0.56, 0.21, 0) indicative of displacements of the ion towards neighbouring oxygen ions. The presence of static oxygen disorder in both the dried and deuterated samples is apparent from the structural analyses. Raman spectra confirm short range deviations from cubic symmetry for both dried and hydrated samples.     

Hydrodynamics,mass transfer,and photocatalytic phenol selective oxidation reaction kinetics in a fixed TiO2 microreactor

Photocatalytic phenol dissociation was studied in a microreactor, with a TiO₂ layer immobilized on the reactor inner walls. Experiments were conducted for various residence times, initial concentrations, pH values, and UV light irradiation intensities. The intermediates and products (catechol, hydroquinone, and resorcinol) were quantitatively investigated to determine the predominant reaction pathways for the investigated anatase catalyst. A three‐dimensional mathematical model was used to simulate the heterogeneous photocatalysis reaction conditions with Langmuir–Hinshelwood mechanism, considering the adsorption/desorption thermodynamic equilibria, and for kinetic parameter estimation via regression analysis. The effectiveness factor, Thiele modulus, and the correction function were calculated to determine the pore diffusion effects. The value of pH had the dramatic effect of lowering the reaction rate due to the competitive adsorption of hydroxide ions and protons on the catalyst surface. A phenol conversion of 79.5% was achieved at the residence time of 7.22 min, but without total mineralization. © 2014 American Institute of Chemical Engineers AIChE J, 61: 572–581, 2015     

Stability of Erythrocyte-Derived Nanovesicles Assessed by Light Scattering and Electron Microscopy

Extracellular vesicles (EVs) are gaining increasing amounts of attention due to their potential use in diagnostics and therapy, but the poor reproducibility of the studies that have been conducted on these structures hinders their breakthrough into routine practice. We believe that a better understanding of EVs stability and methods to control their integrity are the key to resolving this issue. In this work, erythrocyte EVs (hbEVs) were isolated by centrifugation from suspensions of human erythrocytes that had been aged in vitro. The isolate was characterised by scanning (SEM) and cryo-transmission electron microscopy (cryo-TEM), flow cytometry (FCM), dynamic/static light scattering (LS), protein electrophoresis, and UV-V spectrometry. The hbEVs were exposed to various conditions (pH (4–10), osmolarity (50–1000 mOsm/L), temperature (15–60 °C), and surfactant Triton X-100 (10–500 μM)). Their stability was evaluated by LS by considering the hydrodynamic radius (R_h), intensity of scattered light (I), and the shape parameter (ρ). The morphology of the hbEVs that had been stored in phosphate-buffered saline with citrate (PBS–citrate) at 4 °C remained consistent for more than 6 months. A change in the media properties (50–1000 mOsm/L, pH 4–10) had no significant effect on the R_h (=100–130 nm). At pH values below 6 and above 8, at temperatures above 45 °C, and in the presence of Triton X-100, hbEVs degradation was indicated by a decrease in I of more than 20%. Due to the simple preparation, homogeneous morphology, and stability of hbEVs under a wide range of conditions, they are considered to be a suitable option for EV reference material.     

Inkjet printing of multi-layered,via-free conductive coils for inductive sensing applications

Microsystem Technologies - A new fabrication technique based on the combined printing of Ag-nanoparticles and dielectric material was developed. The processing, composed of inkjet printing and...     

Thiol‐ene photofunctionalization of 1,4‐polymyrcene

1,4‐Polymyrcene was synthesized by anionic polymerization of β‐myrcene and was subjected to photochemical functionalization with various thiols (i.e. methyl thioglycolate, methyl 3‐mercaptopropionate, butyl 3‐mercaptopropionate, ethyl 2‐mercaptopropionate and 2‐methyl‐2‐propanethiol) using benzophenone/UV light as the radical source. The yield of thiol addition to the trisubstituted double bonds of 1,4‐polymyrcene decreased in the order 1° thiol (ca 95%) > 2° thiol (ca 80%) > 3° thiol (<5%), due to the reversibility of the thiol‐ene reaction. Remarkably, thiol addition to the side‐chain double bonds was 8 ? 10 times (1° thiol) or 24 times (2° thiol) faster than to the main‐chain double bonds, which can be explained by the different accessibility of the double bonds and steric hindrance. Despite the use of a 10‐fold excess of thiol with respect to myrcene units, the thiol‐ene addition was accompanied by chain coupling reactions, which in the extreme case of 3° thiol (or in the absence of thiol) resulted in the formation of insoluble crosslinked material. As an example, a methyl‐thioglycolate‐functionalized 1,4‐polymyrcene was saponified/crosslinked to give submicron polyelectrolyte particles in dilute alkaline solution. © 2018 Society of Chemical Industry     

Properties and applications of electrodes covered with a porous diaphragm— 1. Mass transfer investigation

The use of porous coverings on counter electrodes is proposed for controlling the mass transfer rates to the electrode and therefore the extent of possible loss reactions. An experimental study was undertaken to determine the mass transfer rates to electrodes with and without coverings of porous materials (porous PVC, porous-polyethylene, non-woven polypropylene). Additionally the effect of simultaneous gas evolution was investigated. The electrochemical method, based on the measurement of the limiting current for ferricyanide reduction, was employed for most experiments with the exception of those in which gassing at the covered electrode occurred. In the latter case the mass transfer rates were calculated from the concentration change observed during the batch electrolysis with recirculation of Ce(IV) (reduction to Ce(III)).The results have been correlated for the case of the non-woven material type E 1583 with no simultaneous gassing according to

where Sh, Sc and Re are the Sherwood and Schmidt and Reynolds numbers, respectively and l, d_p and ? are the covering thickness, pore diameter and porosity, respectively.Reductions by a factor of 100 in mass transfer rate at the mass transfer surface are easily attainable through the use of porous coverings. Interestingly, the results obtained at covered gassing electrodes, showed that the mass transfer rate decreases with increasing gassing rate. This is the inverse behaviour to that obtained at uncovered gassing electrodes.The implications on the current efficiency for operation of a differential diaphragm-less electrolysis cell in which loss reactions can occur at the counter electrode are discussed. The use of porous electrode coverings on the counter electrode in diaphragm-less cells is a technique which opens up new applications for these simpler cells.     

An imidazolium based ionic liquid electrolyte for lithium batteries

An electrolyte for lithium batteries based on the ionic liquid 3-methy-1-propylimidazolium bis(trifluoromethysulfony)imide (PMIMTFSI) complexed with lithium bis(trifluoromethysulfony)imide (LiTFSI) at a molar ratio of 1:1 has been investigated. The electrolyte shows a high ionic conductivity (∼1.2 × 10⁻³ S cm⁻¹) at room temperature. Over the whole investigated temperature range the ionic conductivity is more than one order of magnitude higher than for an analogue electrolyte based on N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl)imide (Py₁₄TFSI) complexed with LiTFSI and used here as a benchmark. Raman results indicate furthermore that the degree of lithium coordinated TFSI is slightly lower in the electrolyte based on PMIMTFSI and thus that the Li⁺ charge carriers should be higher than in electrolytes based on Py₁₄TFSI. An ionic liquid gel electrolyte membrane was obtained by soaking a fibrous fully interconnected membrane, made of electrospun P(VdF-HFP), in the electrolyte. The gel electrolyte was cycled in Li/ionic liquid polymer electrolyte/Li cells over 15 days and in Li/LiFePO₄ cells demonstrating good interfacial stability and highly stable discharge capacities with a retention of >96% after 50 cycles (∼146 mAh g⁻¹).