Kinetics Solvent Effect and Mechanism of Hydrolysis of Ethyl Caprylate Ester in Aqueous Organic Solvent Media

The specific rate constant of ethyl caprylate in alkali catalised hydrolysis in water-acetone mixture covering range of 30 to 70% (v/v) of acetone has been determined at temperature 20 to 400c. The rate of reaction decreases with increase in percentage of Acetone from 30 to 70% (v/v). The observed Activation energy decreases progressively with increase in acetone content of the medium. The effect of molar concentration of water and Dielectric constant on the reaction kinetic has also been studied. The thermodynamic parameters (DG*, DH* and DS*) has been determined which showed strong dependency on solvent composition.

Cationic all-halogen bonding rotaxanes for halide anion recognition

A family of cationic halogen bonding [2]rotaxanes have been synthesised via an active-metal template synthetic strategy. 1H NMR spectroscopic anion titration investigations reveal these interlocked host systems recognize halides selectively over oxoanions in aqueous–organic solvent media. Furthermore, systematically modulating the rigidity and size of the rotaxanes’ anion binding cavities via metal complexation, as well as by varying the number of halogen bond-donor groups in the axle component, was found to dramatically influence halide anion selectivity.

Substrate Selection and Management Strategies for Aqueous EPD

Classical EPD has typically been conducted in organic solvent media. Many suitable solvents are volatile and highly flammable and this limits the industrial application of the technique on the basis of safety alone. Aqueous EPD may be seen as a safer method, but issues relating to electrolysis and surface energy phenomena become prominent and can create interferences and variability unless the substrate type and its preparation are compatible with the aqueous EPD chemistry and its deposition method. As EPD layers become thinner, factors such as substrate surface structure and wettability become more critical. Industrial processes utilising some principles of EPD for applying paint from water-based preparations are well established in the metal finishing sector. Consequently there is a significant body of practical experience available from this sector that can be of use in translating classical EPD from a solvent to an aqueous technique while avoiding interferences inherent in the use of water as the deposition medium. In this paper, substrate selection is discussed in relation to the electrolyte content of the system where phenomena such as dissolution and micro-arcing can occur. The initial wetting of the substrate must be considered prior to applying voltage. Surface preparation techniques and the methods of introducing the substrate into the EPD dispersion all can have an impact on the final result. Note: This paper is based on the authors’ personal and practical experience of industrial electrophoretic painting over more than 40 years. Only metal substrates are discussed because these have been almost exclusive in this sector during that time. Non-metal substrates such as conductive plastics, graphite and carbon fibre have also been coated with electrophoretic paints but this is not yet at any significant scale and so no general principles have been established

Acoustical Behaviour of Sodium Nitroprusside in Aquo-Organic Solvent Media at 308.15 K

Density and ultrasonic velocity have been measured for sodium nitroprusside in aqueous solutions of CH3OH, ethylene glycol, DMSO, and n-propanol solvents at 308.15 K. A quantitative relationship has been established among the acoustical properties like ultrasonic velocity (U), adiabatic compressibility (β), intermolecular free length (Lf), acoustic impedance (Z), apparent molar compressibility (Kϕ), apparent molar volume (Vϕ), limiting apparent molar compressibility (Kϕ0) limiting apparent molar volume (Vϕ0), and their constants (SK,Sv). From the obtained values, molecular interaction study has been made successfully in the light of these acoustical properties through hydrogen bonding in solute and solvent mixture.