The Imaginary Point Spectrum and Hypercyclicity

Let A be a generator of a C₀-semigroup T(·) on a separable Banach space. Under suitable conditions on the imaginary point spectrum of A, we show that T(·) is hypercyclic.     

Effect of Microalgae Polysaccharides on Biochemical and Metabolomics Pathways Related to Plant Defense in Solanum lycopersicum

Applied Biochemistry and Biotechnology - Microalgae are photosynthetic microorganisms that produce several bioactive molecules that have received considerable attention in scientific and industrial...     

Simulation and Experimental Study for Degradation of Organic Dyes Using Dual pin‐to‐plate Corona Discharge Plasma reactors for Industrial Wastewater Treatment

This work researches the possibility of increasing the dye removal efficiency from wastewater using nonthermal plasma. A study for the optimal air gap distance between dual pin and surface of Acid Blue 25 dye solution and thickness of ground plate is carried out using 3D‐EM simulator to find maximum electric field intensity at the tip of both pins. The consequences display that the best gap for corona discharge is approximately 5 mm using 15 kV source. In addition, the optimum plate thickness is 0.1 mm. These distance and thickness were mentioned are constant during the study of other factors. Dual pin‐to‐plate high‐voltage corona discharge plasma system is presented to investigation experimentally the gap distance, thickness of ground plate, initial dye concentration, pH solution and conductivity on the amount of Acid Blue 25 dye color removal efficiency from wastewater. There is a large consensus among the simulation and experimental work in the air gap and thickness of ground plate. Where the decolorization for air gap 5 mm is 95.74 at time 35 min compared with 91% and 17% for 1 mm and 20 mm gap distance respectively. Also, the discharge energy at each air gap are calculated. Measurement results for the impact of thickness of an Aluminum ground plate on color removal competence showed color removal efficiencies of 86.3%, 90.78% and 98.06%, after treatment time 15 min for thicknesses of 2, 0.5 and 0.1 mm respectively. The decolorization behavior utilizing dual pin‐to‐plate corona discharge plasma system display 82% pigment evacuation proficiency inside 11min. The complete decolorization was accomplished within 28min for distinctive examined introductory color focuses 5 ppm up to 100 ppm. Likewise, the impacts of conductivity by utilizing diverse salts as AlCl3, CaCl2, KCl and NaCl and with distinctive focuses have been explored. The rising of the solution conductivity leads to the reduction of decolorization efficiency. The decolorization efficiency and discharge energy are calculated at different concentration molarity for AlCl3, CaCl2, KCl and NaCl. It was observed that the presence of salts at the same concentration level substantially decreased the rate and the extent of decolorization. The results indicate that the optimum pH for the decolorization of Acid Blue 25 dye is in the range between 3 and 6. Furthermore the conductivity and discharge energy were measurement at each value of pH. Energy yield for decolorization and Electrical Energy per Order (EE/O) under different initial pH value were calculated. A kinetic model is used to define the performance of corona discharge system under different value of pH. The model of pseudo ‐zero, pseudo‐first order, and pseudo‐second order reactions kinetic are utilized to investigate the decolorization of Acid Blue 25 dye. The rate of degradation of Acid Blue 25 dye follows the pseudo‐first order kinetics in the dye concentration. Energy consumption requirements for decolorization was considered. The outcomes will be useful for designing the plasma treatment systems suitable for industrial wastewaters. (© 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Disordering in Pyridine at High Pressures

JETP Letters - Pyridine has recently attracted significant attention because of its polymorphism and capability to form polymerized hydrocarbons at high pressures that have great technological...     

Monte Carlo study of the spin-1 Blume–Capel Ising film

Using Monte Carlo simulations with the Metropolis algorithm, we have studied the influence of crystal-field interaction on the critical behavior of magnetic spin-1 Ising film on a cubic lattice structure. The phase diagrams in the (_kBTc/J,R=_Js/J)$(k_{\mathrm{B}}{T}_{\mathrm{c}}/J,R=J_{\mathrm{s}}/J)$ plane are obtained for different values of the crystal-field interaction. We found that the special point _Rsp(_Rc)$R_{\mathrm{sp}}(R_{\mathrm{c}})$, at which the critical temperature is independent of the film thickness N, is independent of the crystal-field interaction and that the system may exhibit a tricritical behavior.     

Structural and magnetic characterisation of the perovskite oxides La0.7Ca0.3−x Na x MnO3

X-ray powder diffraction (XRD) and magnetic measurements were performed in order to investigate the effect of Na⁺ ion substitution for Ca²⁺ ions on the crystallographic structure, the character of magnetic ordering, and the effect of transition temperature in La_0.7Ca_0.3−x Na _x MnO₃ manganites series (0 ⩽ × ⩽ 0.2). All samples crystallise in an orthorhombic structure with the Pnma space group. We have found a strong dependence of structural and magnetic properties on the cation-size disorder parameter σ ². The temperature dependence of magnetization of all samples obeys the Bloch T ^3/2 law. The values of the spin wave constant at low temperature B increase with the increase of x and the Curie temperature decreases. It is concluded that the substitution of Ca by Na⁺ ions causes a decrease in total exchange integral Aof the samples.      

Spectrofluorometric Determination of Methocarbamol in Pharmaceutical Preparations and Human Plasma

A simple, sensitive and rapid spectrofluorometric method for determination of methocarbamol in pharmaceutical formulations and spiked human plasma has been developed. The proposed method is based on the measurement of the native fluorescence of methocarbamol in methanol at 313 nm after excitation at 277 nm. The relative fluorescence intensity-concentration plot was rectilinear over the range of 0.05–2.0 μg/mL, with good correlation (r = 0.9999), limit of detection of 0.007 μg/ mL and a lower limit of quantification of 0.022 μg/ mL. The described method was successfully applied for the determination of methocarbamol in its tablets without interference from co-formulated drugs, such as aspirin, diclofenac, paracetamol and ibuprofen, The results obtained were in good agreement with those obtained using the official method (USP 30).The high sensitivity of the method allowed the determination of the studied drug in spiked human plasma with average percentage recovery of 99.42 ± 3.84.     

H2O + Fe(NO3)3 + Ni(NO3)2 ternary system isotherms at 0 °C and 30 °C

H₂O + Ni(NO₃)₂ binary system were investigated in the temperature range from −25 °C to 55 °C. The solid-liquid equilibria of the ternary system H₂O + Fe(NO₃)₃ + Ni(NO₃)₂ were studied using a synthetic method based on conductivity measurements. Tow isotherms were established at 0 °C and 30 °C, and the appearing stable solid phases are iron nitrate nonahydrate (Fe(NO₃)₃·9H₂O), iron nitrate hexahydrate (Fe(NO₃)₃·6H₂O), nickel nitrate hexahydrate (Ni(NO₃)₂·6H₂O) and nickel nitrate tetrahydrate (Ni(NO₃)₂·4H₂O).     

Development and validation of a sensitive UHPLC‐MS/MS method for the simultaneous analysis of tramadol,dextromethorphan chlorpheniramine and their major metabolites in human plasma in forensic context: application to pharmacokinetics

The prerequisites for forensic confirmatory analysis by LC/MS/MS with respect to European Union guidelines are chromatographic separation, a minimum number of two MS/MS transitions to obtain the required identification points and predefined thresholds for the variability of the relative intensities of the MS/MS transitions (MRM transitions) in samples and reference standards. In the present study, a fast, sensitive and robust method to quantify tramadol, chlorpheniramine, dextromethorphan and their major metabolites, O‐desmethyltramadol, dsmethyl‐chlorpheniramine and dextrophan, respectively, in human plasma using ibuprofen as internal standard (IS) is described. The analytes and the IS were extracted from plasma by a liquid–liquid extraction method using ethyl acetate–diethyl‐ether (1:1). Extracted samples were analyzed by ultra‐high‐performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry (UHPLC‐ESI‐MS/MS). Chromatographic separation was performed by pumping the mobile phase containing acetonitrile, water and formic acid (89.2:11.7:0.1) for 2.0 min at a flow rate of 0.25 μL/min into a Hypersil‐Gold C₁₈ column, 20 × 2.0 mm (1.9 µm) from Thermoscientific, New York, USA. The calibration curve was linear for the six analytes. The intraday precision (RSD) and accuracy (RE) of the method were 3–9.8 and ?1.7–4.5%, respectively. The analytical procedure herein described was used to assess the pharmacokinetics of the analytes in 24 healthy volunteers after a single oral dose containing 50 mg of tramadol hydrochloride, 3 mg chlorpheniramine maleate and 15 mg of dextromethorphan hydrobromide. Copyright © 2014 John Wiley & Sons, Ltd.