External electric field, hydrostatic pressure and conduction band non-parabolicity effects on the binding energy and the diamagnetic susceptibility of a hydrogenic impurity quantum dot

Electric field, hydrostatic pressure and conduction band non-parabolicity effects on the binding energies of the lower-lying states and the diamagnetic susceptibility of an on-center hydrogenic impurity confined in a typical GaAs/Al_xGa_1−xAs spherical quantum dot is theoretically investigated, by direct diagonalization of the Hamiltonian. To this end, the effect of band non-parabolicity has been performed, by means of the Luttinger-Kohn effective mass equation. Binding energies and diamagnetic susceptibility of the hydrogenic impurity are computed as a function of the dot size, external electric field strength and hydrostatic pressure, with considering the edge-band non-parabolicity. Results show that the external electric field and the hydrostatic pressure have an obvious influence on the binding energies and the diamagnetic susceptibility of the impurity.     

Study of physical chemistry on biosorption of zinc by using Chlorella pyrenoidosa

Discharge of heavy metals from metal processing industries is known to have adverse effects on the environment. Biosorption of heavy metals by metabolically inactive biomass of microbial organisms is an innovative and alternative technology for removal of these pollutants from aqueous solution. Presence of heavy metals in the aquatic system is posing serious problems. Zinc has been used in many industries and removal of Zn ions from waste water is significant. Biosorption is one of the economic methods used for removal of heavy metals. In the present study, the biomass obtained from the dried Chlorella pyrenoidosa was used for evaluating the biosorption characteristics of Zn ions in aqueous solutions. Batch adsorption experiments were performed with this material and it was found that the amount of metal ions adsorbed increased with the increase in the initial metal ion concentration. In this study effect of agitation time, initial metal ion concentration, temperature, pH and biomass dosage were studied. Maximum metal uptake (q _max) observed at pH 5 was 101.11 mg/g. The biosorption followed both Langmuir and Freundlich isotherm model. The adsorption equilibrium was reached in about 1 h. The kinetic of biosorption followed the second-border rate. The biomass could be regenerated using 0.1 M HNO₃. A positive value of ΔH° indicated the endothermic nature of the process. A negative value of the free energy (ΔG°) indicated the spontaneous nature of the adsorption process. A positive value of ΔS° showed increased randomness at solid-liquid interface during the adsorption of heavy metals, it also suggests some structural changes in the adsorbate and the adsorbent. FTIR Spectrums of Chlorella pyrenoidosa revealed the presence of hydroxyl, amino, carboxylic and carbonyl groups. The scanning electron micrograph clearly revealed the surface texture and morphology of the biosorbent.     

Selenium heterocycles XLIV. Syntheses of 8,9‐dihydro‐1,2,3‐thiadiazolo[4,5‐a]‐4,7‐dihydroxynaphthalene and 1,2,3‐selenadiazolo[4,5‐a]‐4,7‐dimethoxynaphthalene

The reaction of thionyl chloride with the semicarbazone 2 gave 4,5‐dihydro‐6,9‐dihydroxynaphtho‐[1,2‐d][1,2,3]thiadiazole ( 3 ) instead of 4,5‐dihydro‐6,9‐dimethyoxynaphtho[1,2‐d][1,2,3]thiadiazole ( 4 ). Selenium dioxide oxidation of compound 2 gave 4,5‐dihydro‐6,9‐dimethyoxynaphtho[1,2‐d][1,2,3]selenadiazole ( 5 ). Oxidation of compound 5 with 2,3‐dichloro‐5,6‐dicyano‐1,4‐benzoquinone afforded 6,9‐dimethyoxynaphtho[1,2‐d][1,2,3]selenadiazole ( 6 ).     

Optimization by Response Surface Methodology of the Adsorption of Anionic Dye on Superparamagnetic Clay/Maghemite Nanocomposite

Russian Journal of Applied Chemistry - Magnetic nanoparticles and clay minerals combine to form a class of advanced nanocomposites that would possess exceptional adsorption, magnetism, and...     

Synthesis and Simulation Study of Right Silver Bipyramids via Seed-Mediated Growth cum Selective Oxidative Etching Approach

In this study, a simple method to synthesize right silver bipyramid (AgBP) nanostructures via the seed-mediated growth cum oxidative etching approach in aqueous solution is developed. The key strategy of this method is to control the growth and etching process by careful adjustment of the reactants concentration. Ascorbic acid (AA) is used to reduce silver precursor while cetyltrimethylammonium bromide stabilizer is used to direct the preferential growth of (100) facets. The presence of Cu²⁺ and AA in the reaction mixture also enable in-situ generation of H₂O₂, leading to selective etching of (111) facets, which is crucial to the formation of anisotropic AgBPs. The structure-properties of AgBPs is systematically investigated through a series of experiments and theoretical simulations. Transmission electron microscope images and X-ray diffraction patterns of the as-synthesized AgBPs show the formation of single crystalline twined nanostructures with a relatively high yield. These results suggest the important role of the excitation of electric dipole in enhancing the electric field at the six sharp corners of AgBPs, making them especially promising for a wide range of technological applications including surface-enhanced Raman scattering with a significant enhancement factor of 1.50 × 10⁵ as demonstrated herein.     

Simultaneous spectrophotometric determination of nitrite and nitrate by flow injection analysis.

A new catalytic spectrophotometric method is reported for the simultaneous determination of nitrite and nitrate by flow injection analysis, based on the catalytic effect of nitrite on the redox reaction between pyrogallolsulfonephthalein and potassium bromate in acidic media. Nitrate can also be on-line reduced to nitrite with a modified copper-coated cadmium reduction column. The reaction was monitored spectrophotometrically by measuring the decrease in the absorbance of pyrogallolsulfonephthalein at 465 nm. Various analytical parameters such as effects of acidity, reagent concentrations, flow rates, sample sizes, lengths of the reaction coil and temperatures were studied and were optimized. Under the optimized conditions, the calibration graph was linear for 2.4 to 160 ng ml(-1) of nitrite and 4.0 to 100 ng ml(-1) of nitrate. The influences of potential interfering cations and anions for nitrite and nitrate determination were studied. The method is successfully applied for food and water samples. Up to ten samples can be analyzed per hour.     

Hydrogen evolution reaction and formic acid oxidation by decorated nanostructural Pt/Pd on a copper-filled nanoporous stainless steel

In this work, a 304 stainless steel (SS) was anodized to prepare nanoporous SS (NPSS) with an average size of about 75 nm and then filled with copper (Cu/NPSS) using pulsed electrodeposition method. Afterward, a nanostructural Pt and Pd film was deposited by galvanic replacement (GR) on the Cu/NPSS to prepare modified electrode (PtPd/Cu/NPSS) for hydrogen evolution reaction (HER) and formic acid electrooxidation (FAO). The electrocatalytic activity of the modified electrode and its structural characterization have been studied by voltammetric methods, electrochemical impedance spectroscopy (EIS), inductively coupled plasma optical emission spectrometry (ICP-OES), and field emission scanning electron microscopy (FESEM). The results show that the nanostructural Pt₁Pd₁/Cu/NPSS composition, with low Pt loading and suitable stability, has a good electrocatalytic performance toward HER (E_Onset = + 12 mV vs. NHE) and FAO (E_Onset = ?180 mV vs. NHE). For HER observed a high mass activity of noble metals (87.54 mA cm^?2μg _Pd+Pt ^?1 ) in comparison with Pt deposited Cu/NPSS (41.5 mA cm^?2 μg _Pt ^?1 ) at the same applied potential of ? 0.25 V versus NHE. Also, the fabricated electrocatalysts with more electrochemically active surface area in comparison with Pd/Cu/NPSS and Pt/Cu/NPSS revealed more resisting to the poisoning components and good stability for FAO.     

Effect of solidification temperature of lead alloy grids on the electrochemical behavior of lead-acid battery

One of the main electrochemical characteristics of a lead-acid battery is amount of water consumption. The effect of solidification temperature on electrochemical behavior (mainly hydrogen overvoltage) of Pb–Ca–Sn–Al (0.09%, Ca; 0.9%, Sn; 0.02%, Al) and Pb–Sb–Sn (1.7%, Sb; 0.24%, Sn) alloys, which are used in making the grid of lead-acid batteries, has been studied by cyclic voltammetry (CV) and linear sweep voltammety for different concentrations of sulfuric acid (ranging from 0.5 mol L^–1 to 4.0 mol L^–1). The morphology of the grid at some solidification temperatures was studied by optical microscopy. After one sweep of CV the surface of the electrode was investigated by using scanning electron microscopy.The results show that the potential of hydrogen evolution depends on the solidification temperature of the grids during production (mold temperature of grid casting). Also, at different solidification temperatures, different passivation phenomena, electrode surface constituents, and structure were observed.     

A Thermodynamic Study on the Binding of Calcium Ion with Myelin Basic Protein

The interaction of myelin basic protein (MBP) from the bovine central nervous system with divalent calcium ion was studied by isothermal titration calorimetry at 27 °C in aqueous solution. The extended solvation model was used to reproduce the enthalpies of Ca²⁺-MBP interaction over the whole range of Ca²⁺ concentrations. The solvation parameters recovered from the solvation model were attributed to the structural change of MBP due to the metal ion interaction. It was found that there is a set of two identical and non-interacting binding sites for Ca²⁺ ions. The association equilibrium constant is 0.021 μmol⋅dm⁻³. The molar enthalpy of binding is ΔH=−15.10 kJ⋅mol⁻¹.