Low-Temperature Plasma-Chemical Deposition of Nanocomposite Antifriction Molybdenum Disulfide (Filler)–Silicon Oxide (Matrix) Coatings

It was demonstrated experimentally that the spatial separation of two processes of chemical vapor deposition, one of which provides synthesis of filler (MoS₂) nanoparticles and the other yields the matrix (SiO₂) of the nanocomposite coating, performed ina common reactor, enables an independent control over two process rates and makes it possible to widely vary the composition of the films deposited in this way. The deposition was performed in a double-zone vertical tubular quartz reactor. Molybdenum disulfide particles were produced by pyrolysis of aerosols of ammonium thiomolybdate solutions in dimethylformamide in the upper zone of the reactor, and the plasma-chemical deposition of a nanocomposite coating occurred in the lower zone into which MoS₂ nanoparticles were transported by the gas flow and tetraethoxysilane was delivered. It was shown that the nanocomposite coatings composed of molybdenum disulfide (filler) and silicon oxide (matrix) possess improve the antifriction properties as compared with the matrix (SiO₂ layers), these properties being determined by the relative amounts of MoS₂ nanoparticles in the layer and by their average size.     

Degradation of physicomechanical properties of epoxy nanocomposites with carbon nanotubes upon heat and humidity aging

The dependence of the physicomechanical properties of epoxy nanocomposites subjected to heat and humidity aging on the type of covalently functionalized carbon nanotubes and on the uniformity of their distribution in the epoxy matrix was studied. Two types of carbon nanotubes were used: those modified with carboxy and amide groups. The elastic modulus, bending deflection, and ultimate bending strength for the initial epoxy nanocomposites with carbon nanotubes and for those subjected to heat and humidity aging were determined. The epoxy binders modified with carboxylated carbon nanotubes are more resistant to the action of aging factors. The presence of aggregates of carboxylated carbon nanotubes in the epoxy matrix positively influences the preservation of physicomechanical properties of the composite subjected to heat and humidity aging. Microscopic examination revealed structural features of the epoxy nanocomposite and their effect on the resistance of the composite to the heat and humidity aging.     

Aggregatively stable suspensions of micrometer powders of doped barium cerate for electrophoretic deposition of thin-film coatings of solid-oxide fuel cells

Potentialities of the method of electrophoretic deposition of thin-film coatings based on micrometer powders of multidoped barium cerate BaCe_0.8Sm_0.19Cu_0.01O_3–δ (BCSCuO) and BaCe_0.89Gd_0.1Cu_0.01O_3–δ (BCGCuO) were considered. Micrometer powders of BCSCuO and BCGCuO were produced by the methods of solid-phase and citrate-nitrate syntheses, respectively. The dispersity, fraction composition, and electrokinetic potential of nonaqueous suspensions of these powders and the electrokinetic parameters of the electrophoretic deposition process were examined. An ultrasonic treatment and ultracentrifugation produced aggregatively stable suspensions of BCGCuO and BCSCuO micrometer particles in a mixed (70/30 vol %) isopropanol–acetyl acetone medium. These suspensions are characterized by high positive values of the zeta potential (+24 and +28 mV, respectively). Thin film coatings of the electrolyte materials BCSCuO and BCGCuO, which are of interest for the technology of medium-temperature solid-oxide fuel cells, were produced by the electrophoretic deposition onto a dense model cathode.     

Synthesis of fused derivatives of 1,8-naphthyridine

Reactions of aromatic aldehyde, 2-aminoprop-1-ene-1,1,3-tricarbonitrile and cyclic enhydrazinoketones led to the formation of N-substituted 5-aryl-2,4-diamino-6-oxo-5,6,7,8,9,10-hexahydrobenzo[b][1,8]- naphthyridine-3-carbonitriles     

New functionalized amino derivatives of 2-hydroxyphenyl-1,3,5-triazines

4-(2-Hydroxyphenyl)-1,3,5-triazin-2-ylcyanamides reacted with sodium azide to give N-(tetrazol-5-yl)-1,3,5-triazin-2-amines, and their reaction with allyl bromide afforded allyl(1,3,5-triazin-2-yl)cyanamides. Acetylation of 4-(2-hydroxyphenyl)-1,3,5-triazin-2-amines involved only the amino group with formation of diacetylamino derivatives, whereas the phenolic hydroxy group remained intact. The reaction of triazinamines with 2,5-dimethoxytetrahydrofuran in the presence of P₂O₅ gave pyrrolyl-substituted triazines.     

Cyclopropanation and epoxidation of 2-ylidene derivatives of lupane series

Russian Journal of Organic Chemistry - Crotone condensation of allobetulone with fluorine-containing benzaldehydes afforded new α,β-unsaturated ketones of lupane series. Their...     

New chalcones containing carbazole and 3,4-ethylenedioxythiophene fragments

Russian Journal of Organic Chemistry - Acylation of 9-(2-ethylhexyl)carbazole with acetyl bromide in the presence of tin(IV) chloride gave 3-acetyl- and 3,6-diacetyl-9-(2-ethylhexyl)carbazoles...     

Halocyclization of 2-allyl(propargyl)sulfanyl-6-aminopyrimidin-4(3H)-ones

Russian Journal of Organic Chemistry - The alkylation of 6-amino-2-thiouracil with allyl, methallyl, and propargyl halides in the presence of bases gave 2-[allyl(methallyl,...     

Dynamic structure of organic compounds in solution according to NMR data and quantum chemical calculations: II. Styrene

The dynamic structure of styrene has been studied with the goal of obtaining detailed information on the internal rotation parameters. A potential energy surface has been constructed for the rotation of the vinyl group about the single bond in terms of the second-order Møller–Plesset perturbation theory with aug-cc-pvtz basis functions, and conformational dependences of ⁿ J _HH have been calculated at the FPT DFT (B3LYP) level of theory with basis functions of the same type. The vibration-averaged coupling constants have been compared with the experimental values reliably determined in this work. A high efficiency of the proposed dynamic model for structural studies of organic molecules with ultrafast internal rotation dynamics has been demonstrated.     

New eco-friendly low-cost binders for Li-ion anodes

In the production of commercial Li-ion batteries, the active materials slurries are generally prepared using polyvinylidene fluoride (PVdF) as binder because of its good adhesion properties and electrochemical stability. Unfortunately, there are some disadvantages related to the use of PVdF: the most important is the use of toxic and environmentally unfriendly solvents, such as N-methyl-pyrrolidone (NMP), and the second is the high costs. In the light of these considerations, it seemed straightforward to investigate the suitability of some water-soluble, inexpensive, and eco-friendly materials to test as alternative binders (sodium alginate, chitosan tragacanth gum, gelatin). The rheological properties of these materials have been investigated in addition to the electrochemical characterization. Furthermore, graphite electrodes with PVdF, carboxymethyl cellulose (CMC), and styrene-butadiene rubber (SBR) binders have been considered for sake of comparison. We found that some of these water-soluble binders, besides good electrochemical performances, showed a high adhesion to the current collector and a good electrochemical stability under the experimental conditions employed, which makes them interesting for the next generation of Li-ion batteries.