A Coupled FEM-BEM Approach for the Solution of the Free-Boundary Axi-Symmetric Plasma Equilibrium Problem

In this paper we present a coupled Finite Element Method – Boundary Element Method (FEM-BEM) approach for the solution of the free-boundary axi-symmetric plasma equilibrium problem. The proposed method, obtained from an improvement of the Hagenow-Lackner coupling method, allows to efficiently model the equilibrium problem in unbounded domains by discretizing only the plasma region; the external conductors can be modelled either as 2D or 3D models, according to the problem of interest. The paper explores different iterative methods for the solution of the nonlinear Grad-Shafranov equation, such as Picard, Newton-Raphson and Newton-Krylov, in order to provide a robust and reliable tool, able to handle large-scale problems (e.g. high resolution equilibria). This method has been implemented in the FRIDA code (FRee-boundary Integro-Differential Axisimmetric – https://github. om/matteobonotto/ FRIDA), together with a suitable Adaptive Integration Technique (AIT) for the computation of the source term. FRIDA has been successfully tested and validated against experimental data from RFX-mod device, and numerical equilibria of an ITER-like device.     

Adsorptive removal of lead from aqueous solutions by amine–functionalized magMCM-41 as a low–cost nanocomposite prepared from rice husk: Modeling and optimization by response surface methodology

Amorphous silica that was extracted from rice husk was used to synthesize the magMCM-41 mesoporous silica. This was then functionalized by the APTMS group in order to produce NH₂-magMCM-41 as a novel and low–cost adsorbent. The XRD, VSM, N₂ adsorption–desorption, FT–IR, TGA, SEM and TEM analyses were utilized to characterize the produced materials. In order to optimize the adsorption of the Pb(II) ions, the RSM (response surface methodology) was applied by using the synthesized adsorbent in aqueous solutions. A rotatable CCD (central composite design) was adopted to carry out the experiments and RSM was used to analyze them. Three independent factors namely, initial solution pH (3–7), adsorbent dosage (0.1–2 g L^?1), and initial Pb(II) concentration (15–150 mg L^?1) were used to investigate the removal procedure. According to the obtained results, the initial solution pH of 5.22, adsorbent dosage of 0.1 g L^?1, and initial Pb(II) concentration of 150 mg L^?1 were considered as the optimum conditions with 64.32% removal of Pb(II) and an adsorption capacity of 540.64 mg g^?1. The maximum removal efficiency of Pb(II) ions was found to be 96.76%. The Sips isotherm model represents a better correlation with equilibrium data. It was reported by the kinetic study that data taken from the experiments fitted better to the pseudo–second–order model compared to the pseudo–first–order and intraparticle diffusion models. Finally, according to the thermodynamic study, the removal process strongly depends on temperature, which indicates an exothermic behavior and spontaneous nature of the adsorption.     

A novel fMRI paradigm to dissociate the behavioral and neural components of mixed‐strategy decision making from non‐strategic decisions in humans

During competitive interactions, such as predator–prey or team sports, the outcome of one's actions is dependent on both their own choices and those of their opponents. Success in these rivalries requires that individuals choose dynamically and unpredictably, often adopting a mixed strategy. Understanding the neural basis of strategic decision making is complicated by the fact that it recruits various cognitive processes that are often shared with non‐strategic forms of decision making, such as value estimation, working memory, response inhibition, response selection, and reward processes. Although researchers have explored neural activity within key brain regions during mixed‐strategy games, how brain activity differs in the context of strategic interactions versus non‐strategic choices is not well understood. We developed a novel behavioral paradigm to dissociate choice behavior during mixed‐strategy interactions from non‐strategic choices, and we used task‐based functional magnetic resonance imaging (fMRI) to contrast brain activation. In a block design, participants competed in the classic mixed‐strategy game, “matching pennies,” against a dynamic computer opponent designed to exploit predictability in players’ response patterns. Results were contrasted with a non‐strategic task that had comparable sensory input, motor output, and reward rate; thus, differences in behavior and brain activation reflect strategic processes. The mixed‐strategy game was associated with activation of a distributed cortico‐striatal network compared to the non‐strategic task. We propose that choosing in mixed‐strategy contexts requires additional cognitive demands present to a lesser degree during the control task, illustrating the strength of this design in probing function of cognitive systems beyond core sensory, motor, and reward processes.     

Conversion of a renewable bio-resource to a functional composite material: Product design,comprehensive characterization and adsorption of 2,4-D herbicide

Based on the opinion of “utilizing waste resources to treat waste”, a sustainable resource waste was transformed into a useful and functional material by a comprehensive experimental setup. A high surface area lentil processing waste-based activated carbon was synthesized by microwave-assisted K₂CO₃ chemical activation and then successfully converted into a ferrospinel composite. The ferrospinel composite was characterized with BET, FTIR, XRD, XPS, FE-SEM, EDX mapping, Raman and VSM techniques and the detailed characterization analysis confirmed the successful formation of the ferrospinel composite. It was also applied as an effective adsorbent material in the treatment of 2,4-dichlorphenoxyacetic acid herbicide bearing wastewater. The pseudo-second order model better defined the kinetic pathway of the adsorption while the isothermal data indicated the best suitability to Langmuir model. The maximum adsorption capacity of the ferrospinel composite towards 2,4-dichlorophenoxyacetic acid was 400 mg/g at 45 °C. Thermodynamic studies showed the favorability and spontaneity of the adsorption process.     

A 2,5-Dihydroxybenzoic Acid–Gelatin Conjugate: The Synthesis,Antiviral Activity and Mechanism of Antiviral Action Against Two Alphaherpesviruses

Various natural and synthetic polyanionic polymers with different chemical structures are known to exhibit potent antiviral activity in vitro toward a variety of enveloped viruses and may be considered as promising therapeutic agents. A water-soluble conjugate of 2,5-dihydroxybezoic acid (2,5-DHBA) with gelatin was synthesized by laccase-catalyzed oxidation of 2,5-DHBA in the presence of gelatin, and its antiviral activity against pseudorabies virus (PRV) and bovine herpesvirus type 1 (BoHV-1), two members of the Alphaherpesvirinae subfamily, was studied. The conjugate produced no direct cytotoxic effect on cells, and did not inhibit cell growth at concentrations up to 1000 µg/mL. It exhibited potent antiviral activity against PRV (IC₅₀, 1.5–15 µg/mL for different virus strains) and BoHV-1 (IC₅₀, 0.5–0.7 µg/mL). When present during virus adsorption, the conjugate strongly inhibited the attachment of PRV and BoHV-1 to cells. The 2,5-DHBA–gelatin conjugate had no direct virucidal effect on the viruses and did not influence their penetration into cells, cell-to-cell spread, production of infectious virus particles in cells, and expression of PRV glycoproteins E and B. The results indicated that the 2,5-DHBA–gelatin conjugate strongly inhibits the adsorption of alphaherpesviruses to cells and can be a promising synthetic polymer for the development of antiviral formulations against alphaherpesvirus infections.     

Kinetic and mechanistic study of methanol oxidation on a Pt(100) surface in alkaline media1

A comparative study of methanol oxidation on a Pt(100) surface was carried out in bicarbonate, carbonate and different pH values of sodium hydroxide solutions. It was shown that Pt(100) adsorbs OH and `poisoning species'. The surface activity was directly correlated to the OH<sub>ad</sub> species coverage. The `poisoning species', produced in methanol oxidation, participate in the reaction at higher potentials, but block the surface partially at lower potentials. A dual path reaction mechanism, common to all the alkaline solutions used, was proposed based on the assumptions that HCO is a reactive intermediate and that a formate is a reaction product in the main path, while CO₂ is a product of `poisoning species' oxidation in a parallel reaction path.     

Film-forming properties and viscosities of saliva substitutes and human whole saliva

Hypo-salivation, related to medical remedies, is an increasing clinical problem. Studies report a weak correlation between subjective mouth dryness and objective sialometry. This indicates that both quantity and quality of saliva are important for the surface-associated functions of saliva, such as lubrication and hydration, to be expressed. Film-forming properties and viscosities of three saliva substitutes were compared to human saliva. Adsorption to surfaces was measured by ellipsometry, infrared spectroscopy and drop-volume technique. Viscosity measurements were carried out using an oscillating rheometer. Saliva, with the lowest viscosity value and the highest protein content, presented superior film retention on both hydrophilic and hydrophobic surfaces. The carboxymethylcellulose-based MAS 84 showed intermediate values of viscosity, poorest ability to reduce surface tension, and negligible film-forming capacity. The porcine mucin-based Saliva Orthana showed about twice the viscosity of saliva and film-forming capability on preferably hydrophobic substrates. Salinum, a linseed extract, possessed the highest viscosity value and an initial surface tension close to that of saliva. The film retention on hydrophilic surfaces was not as effective as for saliva. The results indicate that the film-forming capacity of saliva substitutes is a property also to be considered in the exploration of clinically effective artificial salivas.     

Vibrational study of adsorbed phosphate ions on rhodium single crystal electrodes

The adsorption of H₂PO₄^? ions was studied on low Miller index rhodium single crystal electrodes by in situ FTIR spectroscopy. It is found that for Rh(1 0 0) and Rh(1 1 0), H₂PO₄^? ions are the major species at low potentials, but at higher potentials, some of the H₂PO₄^? ions undergo a potential induced deprotonation and probably there is a mixture of H₂PO₄^? and HPO₄^2? ions. On Rh(1 1 1) the deprotonation starts at very low potentials and at higher potentials the H₂PO₄^? is fully converted to HPO₄^2?. The behavior of the band center and of the band intensity with the applied potential was also analyzed. It is found that the adsorption increases from 0.08 V vs. a Pd–H₂ electrode up to 0.5 V and then it decreases when the OH starts to be adsorbed.     

Adsorption from black tea and red wine onto in vitro salivary pellicles studied by ellipsometry

The adsorption of black tea and red wine components onto a pellicle-like protein layer formed in vitro by adsorption from whole unstimulated saliva on hydroxyapatite discs were studied by in situ ellipsometry. It was found that components from black tea readily adsorbed to the pellicle. Subsequent exposure to saliva led to further adsorption of salivary components to give an overall increase in the amounts adsorbed. The amounts adsorbed increased still further following a third tea and saliva exposure. Components of red wine gave significantly greater amounts of adsorption to the pellicle than black tea. The adsorption of components of black tea gave a concomitant increase in colour or stain as measured by a reflectance chromameter. In all cases, the black tea- and red wine-modified pellicles were not eluted by either phosphate buffer or sodium dodecyl sulphate (SDS) rinses. Thus, black tea and red wine components have been shown to have a profound effect on in vitro pellicle maturation, causing thickened layers of stained material to build up, which are not readily removed.     

Adsorption of organic compounds and hydrophilicity of bismuth,cadmium and antimony electrodes

The adsorption behavior of various organic compounds at bismuth, antimony, cadmium, mercury and other “mercury-like” metals has been discussed. The systematic trends of the influence of the chemical nature of electrode metal and adsorbate to the molecular interaction parameter, a; limiting Gibbs adsorption, Γ_{A, max}; and Gibbs energy of adsorption, ΔG_A⁰, have been analyzed. The ingredients of the total Gibbs energy of organic compounds adsorption have been found. A new more general method for obtaining the metal-water; interaction Gibbs energy has been worked out and used. It was found that the dependence of Gibbs energy of metal-water interaction on the chemical nature of metal and aliphatic organic compound studied is weak. Only in the case of chemically very different metals, for example for Sb and Zn, the difference of Gibbs energy of metal-water interaction values is somewhat higher than the exactness of the determination of the experimental values of Gibbs energy of organic compound adsorption.