Hydrophobic effect for anionic dye - cationic surfactant interaction in aqueous and mixed solvent

Abstract

The interaction between anionic dyes [Reactive Orange 122 (R.O 122), Reactive Blue 19 (R.B 19), Reactive Violet 5 (R.V 5) and Acid Green 20 (A.G 20)] with cationic surfactant cetyltrimethylammoniun bromide (CTAB) has been investigated by spectrophotometry and conductance technique. The used dyes are characterized by tautomeric behavior which affects the mechanism of the interaction. Various parameters such as dye structure, surfactant composition, solvent composition, temperature and pH of the medium were studied. The spectral data were applied for calculating the binding constant between dye and surfactant (K_b), fraction of micellization (?_mic), and standard free energy change of binding (ΔG°_b) in 0,10,20 and 30 v/v % acetonitile (AN). Conductance technique was constructed to estimate the ion pairing constant (K_a) at different temperatures and v/v % AN. Thermodynamic parameters (ΔG°, ΔH° and ΔS°) for ion pair formation were evaluated. The role of hydrophobic and electrostatic effect on dye-surfactant interaction was discussed.     

The Determination of Trace Elements by Flame Atomic Absorption Spectrometry: Effect of the Composition of Standard Solution Matrices

Abstract

The effect of using solution matrices in calibration standards different from those employed for the extraction steps in the determination of Cd, Cr, Cu, Ni and Zn were tested. Cu and Zn are little affected by matrix effects but, if the extractant is ammonium acetate, the use of other matrices may result in too high Cd, Cr and Ni values.     

Effects of laser irradiation on optical properties of a-Se100−x Te x thin films

The effect of laser irradiation on the optical properties of thermally evaporated Se_100?x Te _x (x=8, 12, 16) chalcogenide thin films has been studied. The result shows that the irradiation causes a shift in the optical gap. The results have been analyzed on the basis of laser irradiation-induced defects in the film. The width of the tail of localized state in the band gap has been evaluated using the Urbach edge method. As the irradiation time increases, the values of the optical energy gap for all compositions decrease, while tail energy width increases. It is also observed that the optical energy gap decreases with increasing Te content in the alloy. These changes are a consequence of an increment in disorder produced by laser irradiation in the amorphous structure of thin film.     

Size-dependent ignition temperature of metallic compounds fabricated by self-propagating high-temperature synthesis

Considering the diffusion reaction at solid interfaces, the ignition temperature of compounds fabricated by self-propagating high-temperature synthesis (SHS) is modelled with the help of size-dependent activation energy. As reactant size decreases, ignition temperature also decreases. This is because of increased contact areas between the reactants and the lowered diffusion barrier, both of which must be calculated specifically for reactants in nanoscale. The model predictions and experimental results are consistent for some metallic compounds.     

An unusual substitution reaction of an aromatic sulfonic group based on 3-carbonyl-4-phenolsulfonic acid

An unusual substitution reaction of an aromatic sulfonic group based on 3-carbonyl-4-phenolsulfonic acid was discovered in a diazo-coupling process.The reaction occurred under mild reaction conditions (pH 8.0-9.0.0-5 C,solvent:water) within a short reaction time(1h).A plausible substitution reaction mechanism by phenol-ketone resonance was proposed.     

Slater Sum in Cylindrically Symmetric Inhomogeneous Electron Liquids: Towards A Differential Equation for the Stark Effect in Hydrogen Atom

Abstract

Attention is focussed here on a variety of cylindrically symmetric inhomogeneous electron liquids. These include separable potentials in which a general variation along the (z) axis of cylindrical symmetry is combined with isotropic harmonic confinement in the (x, y) plane. in this case, an explicit differential equation is derived for the Slater sum along the z axis by projecting out of the (off-diagonal) canonical density matrix the states with zero angular momentum about the axis of symmetry. Some attention is then given to the calculation of the Slater sum for a hydrogen-like atom in a uniform electric field of arbitrary strength. the model of a separable potential with harmonic confinement, though no longer exact, is shown to lead directly to a (now approximate) equation for the Slater sum along the z axis for the Stark effect in hydrogen. Finally some further progress is shown to be possible in the extreme high field limit.     

One-step synthesis ofα,β-unsaturated arylsulfones by a novel multicomponent reaction of aromatic aldehydes,chloroacetonitrile, benzenesulfinic acid sodium salt

A new and green method for the synthesis of α,β-unsaturated arylsulfones had been achieved through the condensation of aromatic aldehydes,chloroacetonitrile,benzenesulfinic acid sodium salt in the presence of l-butyl-3-methyl imidazolium hydroxide([bmim]OH) in EtOH under reflux.The ionic liquid was recovered and recycled for subsequent reactions.The advantages of this protocol were non-toxic,easy work-up and good yields.     

Effect of solvent on the construction of Co(II) coordination polymers containing a semi-rigid bis(benzimidazole) derivative: syntheses,structures, and properties

Two Co(II) coordination polymers, [CoL(npa)]·2H₂O (1) and [CoL(Hnpa)₂] (2) (L = 1,4-bis(5,6-dimethylbenzimidazole-1-yl)benzene, H₂npa = 5-nitroisophthalic acid), have been synthesized in different solvent systems and characterized by Infrared (IR) spectroscopy, elemental analysis, and powder and single crystal X-ray diffraction. Compound 1 was synthesized under solvothermal conditions with DMF as solvent and had a pair of L ligands adopting a μ₂-bridging mode and connecting two Co²⁺ cations to generate a 26-membered Co₂L₂ loop. The npa^2? link adjacent Co₂L₂ loops via a bis(monodentate) bridging mode to create a 1-D channel-like chain structure. Compound 2 was obtained under hydrothermal conditions, and the carboxylate of the monodeprotonated Hnpa^? adopt a μ₁-η^0?:?η¹ coordination to connect adjacent Co²⁺ cations into a 2-D polymeric layer. The μ₂-bridging L ligands connect adjacent 2-D [Co(Hnpa)]_n polymeric layers into a 3-D NaCl-like framework. The Co²⁺ cations and the L ligands in compounds 1 and 2 exhibit different coordination geometries and conformations. Effects of solvents on the construction of Co(II) coordination polymers were investigated. In addition, the electrochemical behavior of carbon paste electrodes containing 1 and 2 and the thermal stabilities of 1 and 2 were investigated.