卷 89, 编号 3 (2016)

Activated alumina desiccants modified with NaOH and KOH were synthesized from the product of a centrifugal thermal activation of gibbsite, with the subsequent hydration in an acid or alkaline medium, and their properties were studied. It was shown that the modification makes it possible to raise the dynamic capacity of desiccants produced from pseudoboehmite by up to a factor of 2 via formation of new super-strong basic centers the concentration of which grows with increasing content of an alkaline oxide. A correlation was found between the total concentration of basic centers on the surface of the desiccants and their dynamic capacity in drying of both dry and humid air. Use of the modified desiccants with high static and dynamic capacity will make it possible to improve the drying efficiency.

Sorption properties of micrometer calcium peroxide particles produced by the chemical reaction between calcium hydroxide and hydrogen peroxide were studied. The dependences of the sorption properties of CaO₂ particles on temperature and acidity of the medium were used to find the optimal values of these parameters at which the sorption of metals is at the maximum. It was shown that CaO₂ particles are nearly as good in sorption properties with hematite and goethite nanoparticles and possess antifungal properties exceeding the corresponding characteristics of sulfur and silver nanoparticles. The simplicity of the method used to obtain the product containing 73% CaO₂, low expenditure due to the application of large-tonnage starting reagents, and its good sorption and antimicrobial properties make it possible to recommend this compound for purification of wastewater, natural water basins, and soil to remove heavy metal ions, with the simultaneous detoxication of these objects.

Problems of human and environmental protection from discharges formed in out-of-balance ores dumped from nonferrous metallurgy were considered. To the most hazardous dumps belong those of metacolloid ores, discharges from which are contaminated with copper, zinc, iron, and also indium and cadmium. It was found that the most effective way to preclude the contamination is by using heap leaching of contaminant metals from ores in the chemical reclamation of the dumps. Mathematical dependences of the leaching rate of easily soluble compounds of metals (copper, zinc, indium, and cadmium) from metacolloid ores on the main technological factors of the process: sulfuric acid concentration, ore spraying density, and oxidation interval between sprayings were determined, the optimal process modes were found, and the cost-efficient production of metals in reclamation of dumps of this kind to a state in which they hardly contaminate the environment was calculated.

Morphology and structure of activated carbons produced from a wide variety of carbon-containing vegetable and mineral raw materials were studied and their physicochemical characteristics were determined. The sorption of gold from industrial solutions with various pH values with activated carbons based on birch wood, coconut shells, and even shungite was examined. Results obtained in desorption of gold from activated carbons with a NaOH solution are presented.

Method for synthesis of calcium aluminate and sorbents based on this compound was developed on its basis of the sol-gel technology. The method makes it possible to obtain the target product with specific surface areas in the range from 7 to 120 m² g^–1. The compounds obtained were characterized by scanning electron microscopy, X-ray phase analysis, and X-ray fluorescence microanalysis. It was found that the main phase of the sorbents is rhombohedral calcium monoaluminate CaAl₂O₄. The method of Hammett indicator adsorption was used to determine the content of active centers on the surface of the sorbents and the distribution of these centers over ionization constants. It was shown that the surface characteristics of the sorbents depend on their synthesis method. The retention parameters, polarities, and thermodynamic characteristics were determined for organic compounds of various classes. The possibility of using calcium aluminate modified with sodium chloride for gas-chromatographic separation of aliphatic and aromatic hydrocarbons and carbonyl compounds was demonstrated.

The results of optimization of the process parameters for preparing high-performance heterogeneous catalysts for bisphenol synthesis show that the performance of the solid acid catalyst is determined by its exchange capacity, acidity, pore structure, and specific surface area. Optimum process parameters for preparing highly active solid acid catalysts were revealed.

The effect of Amberlyst 15Dry™ cation-exchange resin on the reaction of peracetic acid formation from acetic acid and hydrogen peroxide in aqueous solution was studied. The pathways of available oxygen consumption were determined. The noncatalytic synthesis is accompanied by spontaneous decomposition of the peracid formed, which sharply decelerates on introducing Amberlyst 15Dry catalyst into the reaction mixture. Comparison of the kinetic relationships of the processes occurring in batch and flow-through reactors shows that in the latter case the process is characterized by diffusion hindrance. A kinetic model of the process with the parameters ensuring adequate mathematical description of the data obtained was suggested.

The structure and barrier properties of layers formed on the interface of steel with aniline–orthanilic acid copolymers of different compositions were determined. The structure of the protective system ensuring the best anticorrosion properties was found.

A procedure was suggested for preparing nanoparticles consisting of magnetite and poly(o-phenylenediamine) by combining the hydrolysis of a mixture of iron(II) and (III) sulfates with oxidative polymerization of o-phenylenediamine. These nanoparticles efficiently bind phenylalanine, thyrosine, tryptophan, and doxorubicin in aqueous solution.

A two-step procedure for utilization of cellulose nitrate waste accumulated at industrial enterprises of the Russian Federation was suggested and experimentally checked. The procedure involves hydrolysis of cellulose nitrate in alkaline medium and incineration of hydrolysis products. The best reagents for complete hydrolysis of cellulose nitrate are aqueous solutions of sodium hydroxide and sodium carbonate. As demonstrated by thermal analysis and thermodynamic calculations, incineration of cellulose nitrate base hydrolysis products can be performed without using hydrocarbon fuel.

Crystalline phases of polyacrylamide titanium tungstophosphate composite material has been synthesized via sol–gel method. The properties of its were determined using different technique. The ion-exchange capacities of the hybrid material for Cs⁺, Co²⁺ and Eu³⁺ ions it was found that 6.22, 2.76 and 1.38 mequiv. g^–1 respectively. The material was found that highly selective for Eu³⁺ and the selectivity sequence for sorption of Cs⁺, Co²⁺ and Eu³⁺ ions on polyacrylamide titanium tungstophosphate was found that; Eu³⁺ > Cs⁺ > Co²⁺. Thermodynamic parameters have been calculated for the studied ions showing that the overall adsorption process is spontaneous and endothermic. The experimental isotherm data were analyzed using the Langmuir and Freundlich models.

The inhibition ability of N,N′-bis(2,4-dihydroxyacetophenone)-1,3-propandiimine (DHAPP) as a schiff base against the corrosion of API-5L-X65 in 1 M HCl solution was evaluated by polarization, electrochemical impedance spectroscopy, and scanning electron microscopy. Polarization studies indicated that DHAPP retards both the cathodic and anodic reactions through chemical adsorption and blocking the active corrosion sites. The adsorption of this compound obeyed the Langmuir adsorption isotherm. The inhibition efficiency increased with inhibitor concentration and decreased with increasing temperature. EIS data analysed to equivalent circuit model showed that as the inhibitor concentration increased the charge transfer resistance of steel increased whilst double layer capacitance decreased. Kinetic and thermodynamic parameters such as activation energy, enthalpy, entropy, and Gibbs free energy of activation and adsorption were calculated. Gibbs free energy indicated that adsorption occurred through physical and spontaneous process. Scanning electron microscopy was used to study the steel surface with and without inhibitor.

N-pyridinium salt derivatives (1–5) were prepared and investigated as corrosion inhibitors for mild steel in 1 M H₂SO₄ solution at 30°C for 24 h. The corrosion inhibiting action was studied using weight loss measurements. The results demonstrated that the corrosion rate decreases, inhibition efficiencies increase, and surface coverage degree increases with increasing inhibitor concentration. Inhibition efficiencies for prepared N-pyridinium salt derivatives have highest inhibiting efficiency for even low concentration. The values of ΔG_ads^° showed physisorption effect for all prepared compounds. Molecular modeling systems were achieved for suggested inhibitors 1–5. Theoretical calculations could be used as a useful tool to obtain information for explaining the mechanism and nature of interaction between the metal surface and the organic molecule as a corrosion inhibitor.