Suchergebnisse

In accordance with the Concept of state family policy in the Russian Federation for the period up to 2025, the development of the system of state support for families with children is one of the main tasks of the state family policy. Despite the fact that in the years 2000-2013. there was a significant reduction of poverty, the poverty rate among families with children continues to be quite high: in 2014, 18.5% against 11% among the general population. In this regard, particularly relevant is the assessment of the impact of implemented measures of social support for families with children on their well-being. The object of study in this paper is the social support of families with children in Russia (on the example of the pilot regions - the Altai Territory and Samara Region). Spend analysis of the legislation governing the provision of social support to families with children of measures, quantitative survey of families with children and interviews with the staff of the bodies and institutions of social protection.

We present here a novel method for formation of laterally-oriented monolayers of plasmonic silver nanoplates and their electrostatic ensembles with semiconductor quantum dots. Monolayers were electrostatically deposited on the surface of thin polymeric film containing different amount of tertiary amino groups. This method allows simultaneously investigate optical properties and morphology of silver nanoplates using transmittance electron microscopy. The optical density of films and surface concentration of silver nanoplates is proportional to the percentage of tertiary amino groups in the polymeric film. A surface ligand exchange was used for functionalization of the surface of silver nanoplates toward formation of electrostatic ensembles with colloidal quantum dots. We observed a straight correlation between the red shift of surface plasmon resonances in silver nanoplates and alkyl chain length of ligand molecules.

Method of reactive polyisobutylene modification by various alkoxybenzenes (anisole and 4-phenoxybutanol) was proposed to form functionalized polyisobutylenes. Polymerization of D,L-lactide was explored on the 4-phenoxybutanol/1,5,7-triazabicyclo[4.4.0]dec-5-ene system. It led to determination of optimal conditions for gaining of poly(isobutylene-b-D,L-lactide). Such copolymers (Mn = 14 300 g/mol and Mn = 36 600 g/mol, Mw /  Mn ≤ 2.5) which were obtained by the polymerization of D,L-lactide on polyisobutylene macroinitiator shows microphase ordering. Formation of the block copolymers is confirmed by 1Н NMR spectroscopy, gel permeation chromatography, and scanning electron microscopy.

The crystalline complexes CuL2X2 and CuL4X2 , where X = Cl or X = Br were synthesized by the interaction of copper(II) chloride or bromide with 1-tert-butyl-1,2,4-triazole (L) in water or organic solvents. The structure of metal complexes have been studied by elemental analysis, X-ray analysis and IR-spectroscopy in the medium (4000 –500 cm –1 ) and long-wavelength (400–50 cm –1 ) regions. Quantum chemical calculations of the vibrational spectra of the CuL2Cl2 and CuL4Cl2 complexes have been carried out to perform the assignment of the signals in the IR-spectra. It is shown that the polymer structure of CuL2X2 complexes is formed due to bridging of one of their halide ions. In the CuL4X2 complexes, the halide ions and 1-tert-butyl-1,2,4-triazole form an island type structure. In all metal complexes 1-tert-butyl-1,2,4-triazole is coordinated by N(4) atom of heterocycle.

It has been shown that the WP04 functional in combination with moderate basic sets 6-31G(d) and SDD allows to calculate characteristics of 1H NMR-spectrum of metal complexes with ligands based on tetrazole derivatives with high accuracy, which can be used to assign signals in the NMR-spectra. The process of hydrolysis of the isomeric platinum(II) chloride complexes with (2-isopropyltetrazol-5-yl)acetic acid has been investigated using the methods of quantum chemistry and NMR-spectroscopy. An explanation of the changes of signals in the 1H NMR-spectra of the considered complexes during their hydrolysis is given.

Based on the literature data on the solubility of pymetrozine in water and organic solvents, as well as experimental data on the extraction of pymetrozine from water, soil and plant matrices, the optimal conditions for the extraction of pymetrozine from water; soil; cucumber; rape seeds, oil and green pods were selected. The conditions for cleaning extracts were selected as well. At the first stage, acetonitrile, a mixture of dichloromethane – isopropanol, or a mixture of dichloromethane – methanol in the presence or absence of inorganic salts were used for extraction of the pesticide. Pymetrozine was found to be a highly hydrophilic substance. For the purification of extracts of pymetrozine from plant matrices the extraction systems hexane – 0.02 mol/L aqueous solution of orthophosphoric acid, hexane or chloroform – aqueous solutions of ammonium sulfate were successfully used. The samples, obtained after this treatment, were pure enough to determine the residual amounts of pymetrozine in them at the maximum residue level (MRL), determined in Russia and the countries of the European Union, or lower using widespread liquid chromatography with diode-array (ultraviolet) detection.

The object of the work is to develop optimal composition of a gel with wound­healing ability based on Ag(I) complex with 2­(4,6­di­tert­butyl­2,3­dihydroxyphenylsulphanyl)acetic acid to produce a novel effective remedy. It was found that propylene glycol (PG) favours the formation of more fine suspension of Ag(I) complex, and introduction of polyvinylpyrrolidone (PVP) hinders aggregation of the particles of the complex, thus providing optimal dispersity of the gel suspension. The gels based on methyl cellulose (MC) are characterized by an acceptable degree of release of Ag(I) complex. It is the gels containing PG and PVP that are characterized by the most complete release of the active substance, which is in agreement with the data on the optimal dispersity. It was found that PG and PVP being introduced into the gel composition increase the osmotic activity of the gel considerably. The optimal composition of the ointment base was determined, %: MC – 3.5; PVP – 5.0; 0.1 mol/L citric acid solution – 5.0; PG – 20.0; water for injections – up to 100.0. The gel obtained was shown to surpass «Dermazin» cream and «Levomecol» ointment in wound­healing ability, while the content of the active substance was significantly lower (0.5 %), and to promote wounds to be cleansed of microorganisms fast and completely too. No accumulation of silver in the liver was found when the gel was used medicinally.

The nickel – phosphorus – copper functional coating was deposited on aluminum alloys substrate by chemical deposition method from malonate­glycinate nickel plating solution. The chemical and phase coatings composition was studied by X­ray fluorescence and X­ray phase analyze. Thermally stimulated phase transitions in deposited Ni – P – Cu coating were detected by differential scanning calorimetry method. The annealing at 250 and 400 °С was shown to lead to the changes in coating structure involving the transition from amorphous to amorphous­crystalline at 250 °С and to crystalline at 400 °С with Ni and Ni3P1 –  δ phases forming. Changes in the structure of Ni–P coating results in the increase of microhardness by 1.6–1.7 times and wear resistance by 3– 4 times. Annealing at 400 °С led to decreasing of corrosion stability of the coatings in 3.5 % sodium chloride solution. The optimum physical, mechanical and protective properties has the attained in the case of Ni – P – Cu coating annealed at 250 °C.

Stable ethylene glycol (EG) and propylene glycol (PG) electrolytes containing СuCl2 · 2H2O, SnCl4 · 5H2O and Trilon B have been developed, which provide electrodeposition of Cu – Sn alloy with tin content varying from 34 to 52 at. % in case of EG and from 51 to 91 at. % in case of PG electrolytes. It is found that the coatings contain phases of Cu6Sn5 и Cu10Sn3 intermetallic compounds, and metallic tin is also present in case of its highest content in the alloy. It is revealed that tin content can be simply varied by the change of current density or concentrations of tin and copper compounds in glycols. The effect of electrolyte composition, deposition conditions, a nature of a substrate on the coatings deposition rate (in the limits of 0.9‒2.9 μm ∙ h‒1), total metal current efficiency (from 40 to 95 %), the ratio of metals in the alloy (from 34 to 91 at. %), its phase composition and microstructure is determined. The conditions for the deposition of Cu – Sn alloy close to the eutectic composition have been found.

The optimal conditions for the electrochemical synthesis in the sulfate electrolyte of low-melting Sn–Ag alloy coatings used in the assembly of electronic equipment containing 7.1–8.3 at. % of silver and with total current yield of metals equal to 88.8–87.0 % are determined. It is established that electrochemical reduction of Sn(II) and Ag(I) on the surface of the alloy is accompanied by the process of contact displacement of Ag(I) with tin included into the coating. The process of contact displacement is intensified with the electrolyte temperature growth and leads to the increase in silver content in the alloy, to the appearance of dendrites on the surface of the coating due to its passivation.

The effect of aluminum coagulants composition and pH regulator dosing method on colloidal characteristics of aluminum hydroxide dispersions (diameter, particle size distribution, density and sedimentation rate of aggregates) was investigated by using of laser diffraction method. Highly basic polyaluminum chloride «Brilliant-50» was established to form aggregates of larger size and lower density than aluminum sulfate. Size and density of the aluminum sulfate aggregates were found to be a function of the pH dosing method (multi- or single-stage dosing). This effect became more evident when powdered coagulant was used as compared to its solution. According to computational study results hydration of aluminum polynuclear hydroxocomplexes increased with their molecular mass increasing, and consequently density of coagulation aggregates formed by them was suggested to decrease.

The possibility of  Na2EDTA applying as a reducing and stabilizing reagent in aqueous medium to obtain gold hydrosols from hydrogen tetrachloroaurate was studied. It was found that, depending on the pH of the reaction medium, both nanosized precipitates (~60 nm) and gold hydrosols, consisting of spherical nanoparticles of uniform size (12–15 nm), can be obtained. Stable gold sols are formed at pH ≥ 10.5. Sol formation process rate depends on the temperature and concentration of  Na2EDTA and increases with their increase. An electrochemical study of processes of  HAuCl4 reduction and Na2EDTA oxidation showed that the possibility of gold hydrosols formation in an alkaline medium is due to the kinetic inhibition of the reduction process of gold hydroxo complexes formed during this process.

Thermal treatment of ferrite magnetic nanoparticles in NaCl matrix gives an opportunity to increase their specific magnetization with preservation of nanoscale size. Composite materials based on mixed ferrites Co0.65Zn0.35Fe2O4 and Mg 0.5Zn0.5Fe2O4 were synthesized by spray-drying of aqueous suspensions in presence of NaCl and annealed at 300 –900 °C. The microstructure and phase composition of nanoparticles before and after annealing were studied by scanning and transmission electron microscopy (SEM and TEM), X-ray diffraction analysis and IR spectroscopy. The magnetic properties of nanoparticles were estimated using a ponderomotive method of measuring the specific magneti zation at room temperature in a magnetic field with an induction of 0.86 T. The increase of the annealing temperature up to 900 °C was established to lead to the increase in the specific magnetization of ferrites – from 32.79 to 91.3 emu/g (Co0.65Zn0.35Fe2O4) and from 2.76 to 22.31 emu/g (Mg 0.5 Zn 0.5Fe2O4) due to recrystallization processes and increase of crystallinity degree of the ferrites. Due to the NaCl insulating layer, the particle size increases just slightly (from ~ 10 nm before annealing to ~ 60 nm after annealing at 900 °C). This method is effective for substantial increase in specific magnetization of ferrite nanoparticles with preservation of their nanoscale size.

А new way of the free radical ROS- and HOCl-induced destruction of serine, threonine, and their peptide derivatives due to the nitrogen-centered radicals formation and their subsequent decomposition with the side chain elimination has been established. It has been shown that substances with reducing properties are inhibitors of this process, while oxygen does not affect the probability of its occurrence. The data obtained are relevant for the development of novel approaches to the search for effective free radical processes regulators.