• Carlsson Chase posted an update 7 hours, 24 minutes ago

    The most investigated conducting polymer (CP) is polyaniline (PANI)), a promising polymer due to its excellent environmental stability, simplicity of synthesis, and high electrical conductivity [1], [2], [3], [4]. In corrosion protection applications, the PANI film has shown promising potential in protecting active metals such as iron by acting as physical barrier coatings, as a primer layer and as component in a multi-layer coating system [5]. The PANI has an excellent potential to replace the toxic metal, such as chromates, in corrosion protection and is considered a green anti-corrosion candidate [5], [6], [7]. The electrochemical synthesis of PANI coatings on active metals is accomplished by the dissolution of the metal at a potential lower than the monomer oxidation potential [8], [9]. Orludodstat in vivo Therefore, electrochemical synthesis of PANI coatings on active metal requires a proper choice of the electrolyte and solvent that should strongly passivate the metal without hindering the electropolymerization process [10], [11]. The data reported here are obtained while the anodic polarization of mild steel (MS) is carried out in succinic acid, sulphanilic acid, sodium orthophosphate, sodium potassium tartrate (Na-K tartrate), and benzoic acid in 31 alcohol-water (BAW) solutions [11]. However, the results of electrolytes sodium-potassium tartrate (Na-K tartrate) and benzoic acid in alcohol-water (BAW) are reported for the polymerization of aniline onto MS [11]. The SEM image of MS sample polarized in 0.3 M oxalic acid solution and 0.1 M aniline in 0.3 M oxalic acid is reported as a dataset or a supplementary material of the main manuscript ‘The Effect of Electrolytes on the Coating of Polyaniline on Mild Steel by Electrochemical Methods and Its Corrosion Behaviour [11].’These data present the 141 intracranial arterial branches’ visibilities near the 72 cerebral aneurysms in postoperative 58 patients treated with titanium or cobalt-chromium-nickel-molybdenum (CCNM) alloy clips. The visibilities were evaluated using time-of-flight magnetic resonance angiography (TOF-MRA), pointwise encoding time reduction with radial acquisition (PETRA)-MRA, which uses MRA with ultrashort echo time (UTE-MRA) and subtraction technique between saturated and non-saturated images, and three-dimensional computed tomography angiography (3DCTA). We retrospectively acquired the data from the medical records of Suwa Red Cross Hospital. Each method’s appearance was compared, and associations between visibility on PETRA-MRA, arterial diameter, clip numbers, clip shapes, clip materials, and amounts of hematoma were summarized. Our article on PETRA-MRA’s usefulness for proximal and branched arteries evaluation after cerebral aneurysm clipping [1] was based on these data. This dataset would be useful for reference value for other neurosurgeons or radiologists for further analysis on PETRA-MRA and another UTE-MRA like SILENT-MRA after cerebral aneurysm clipping.The Notch signaling pathway is an important conserved pathway for normal homeostasis during development. However, targeted deletion of Notch4 (Notch4d1 ) or Notch3 (Notch3d1 ) in mice is not lethal. In fact, both Notch4d1 and Notch3d1 mice develop normally and are fertile. Here we present RNA seq analysis of differential gene expression in the kidneys of Notch4d1 mice versus the Notch3 d1 mice, all on FVB background. Kidneys were collected from Notch4d1 and Notch3 d1 littermates at 3 months of age. RNA sequencing was carried out. The raw data were analyzed for differential gene expression using a negative binomial generalized linear model in the DeSeq2 software package. We used P-value ≤0.05 and an absolute fold change of 1.5 or greater to identify top upregulated and downregulated genes in Notch4 d1 mice compared to Notch3 d1 mice. The data provided will indentify targets of Notch3 and Notch4 signaling, specifically in kidney diseases where Notch3 or Notch4 are abberantly or redundantly expressed.The development of waste-derived functional materials for environmental and energy applications is a sustainable approach to fight global warming, and address energy and materials challenges. In this regard, many scientists are interested in the supercapacitor, adsorbent, and catalyst applications of nitrogen-doped biochars. In this article, we report the data that was collected as a part of our research on the effects of different external nitrogenous sources on the properties of biochar [1]. The data on infrared spectra of the modified samples at various temperatures is valuable to study the changes in functional groups on biochar as a function of temperature as well as nitrogen precursors. Raw data from Time-of-flight Secondary ion mass spectroscopy, surface profilometry, and scanning electron microscopy-energy dispersive X-ray spectroscopy are also provided. We expect that the data will benefit researchers around the world working in the field of nitrogen modifications of biochar.The increase of textile factories, along with the continuous development of industrialization has led to excessive discharge of high toxicity wastewater along with a diverse range of contaminants in wastewater. In this regard, to reduce their operating costs and treatment time, in this work, two synthesized nanostructures, TiO2/Na-Y zeolite and BiVO4/Na-Y zeolite was compared to remove acid orange 10 (AO10) from the aqueous solutions. The obtained optimum operating conditions including initial dye concentration, initial pH, contact time, catalyst dosage and AO10 removal efficiency were 20 mg/L, 3, 7 min, 0.2 g/100 mL, and 99.77% for TiO2/Na-Y zeolite and 20 mg/L, 3, 200 min, 0.2 g/100 mL and 46.13% for BiVO4/Na-Y zeolite composite, respectively. The structural characteristics of the synthetized materials were also determined by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and fourier-transform infrared spectroscopy (FTIR).The fatigue damage evolution depends on the local fibre volume fraction as observed in the co-submitted publication [1]. Conventionally, fibre volume fractions are determined as an averaged overall fibre volume fraction determined from small cuts of the laminate. Alternatively, automatically stitching of scanning electron microscopy (SEM) images can make high-resolution scans of large cross-section area with large contrast between the polymer and glass-fibre phase. Therefore, local distribution of the fibre volume fraction can be characterised automatically using such scan-data. The two datasets presented here cover two large Field of Views scanning electron microscopy (SEM) images. The two images is generated from between 1200 and 1800 high-resolution scan pictures which have been stitched into two high-resolution tif-files. The resolution corresponds to between 700 and 5000 pixels covering each fibre. The datasets are coming from two different non-crimp fabric glass fibre reinforced epoxy composites typically used in the wind turbine industry.