Synthesis of arsenic sorbent by the reaction of magnesium hydroxide with aqueous iron(III) chloride solution

The reaction of magnesium hydroxide with a concentrated aqueous solution of iron(III) chloride yields a mixture of magnesium–iron layered double hydroxide and iron oxide–hydroxide in the akaganeite form. The content of these phases depends on the Mg/Fe atomic ratio in the starting reactant mixture. Iron oxide–hydroxide is the major reaction product at the Mg/Fe atomic ratio in the interval 1.5–1.75, and layered magnesium–iron layered double hydroxide, at Mg/Fe = 3–4. The ability of the synthesized products to take up As(III) from aqueous solutions was studied. These sorbents allow the arsenic concentration to be decreased from 3–5 mg L^–1 to values below MPC (0.01 mg L^–1).     

Synthesis of Decaborane by the Reaction of Sodium Undecaborate with Mild Organic Oxidants

New organic oxidants (aldehydes and ketones) allowing efficient synthesis of decaborane in a high yield via intermediate alkali metal salt were found. The sodium undecaborate oxidation process was refined, and new reaction stoichiometry was suggested.     

Distribution of Zinc Oxide Nanocrystals in a Polymer Film

The structure of polymer films modified with zinc oxide nanocrystals was studied by the optical absorption and small-angle X-ray scattering methods. Small-angle X-ray scattering allows determination of the nanoparticle size distribution function, which is the decisive factor in predicting the optical properties of heterophase materials, including filled polymer films. The optical absorption spectrum of an acrylate polymer film doped with 1.6 wt % zinc oxide nanocrystals approaches the ideal absorber spectrum, which allows this material to be recommended for use as a protective color filter.     

Effect of gas environment parameters on operation efficiency of chemical absorbents of carbon dioxide

Effect of main characteristics of the gas medium on the absorbing properties of alkaline chemical absorbents is demonstrated. The following gas flow parameters were examined as variables: carbon dioxide content of the gas flow within the range 0.2–5.0 vol %, gas humidity of 25–90 rel %, and pressure in the zone of the chemisorption process in the range from 2 to 6 MPa. As objects of study served mixed chemical absorbents based on calcium, sodium, and lithium hydroxides.     

Deposition of protective-decorative coatings onto aluminum alloys

Technique for deposition of a nickel coating onto various aluminum alloys was developed. This coating can be used both independently and as a sublayer under multilayer coatings and, in particular, under those of nickel, tin–bismuth, lustrous nickel, and lustrous chromium. The technique includes anodization, chemical treatment, and electrodeposition of nickel in a special solution. The working modes of the anodization electrolyte were chosen and the necessity for a preliminary chemical treatment of the oxide film being formed was substantiated. A composition of the acid electrolyte for the subsequent nickel plating was developed with buffer and improving additives. The thus deposited electroplated nickel coatings exhibit a high adhesion to the aluminum base without additional thermal treatment. This makes it possible not only to reduce the technological time for deposition of the subsequent multilayer coatings, but also to fully automate the whole process.     

Synthesis of basic bismuth(III) oxalate by precipitation from nitrate solutions

Conditions were determined in which basic bismuth oxalate of composition BiC₂O₄(OH) can be obtained by direct precipitation upon addition of oxalic acid from nitrate solutions used in production of bismuth compounds. The composition of the compound was confirmed by X-ray phase and chemical analyses, IR and Raman spectroscopy, and thermogravimetry. Electron microscopy was used to examine the effect of the composition of the reaction medium and temperature on the morphology of the product being obtained. It was shown that β-Bi₂O₃ can be obtained in oxidative thermolysis of basic bismuth oxalate, depending on its morphology.     

Physicochemical properties and specific features of crystal formation for complex compounds based on boric acid

New procedure for synthesis of new complex compounds on the basis of boric, aminoacetic, and citric acids was developed. Specific features of the crystal formation for boron-based complex compounds were studied. The supposed application area of these compounds is associated with their biocide activity toward pathogenic microorganisms, such as Eschericia coli (intestinal bacterium), Staphylococcus aureus (aurococcus), and Candida albicans (yeast-like fungi of Candida genus).     

Regioselective synthesis of functional tellanes from tellurium tetrahalides and 1-octene

Proceeding from TeCl₄ and 1-octene a regioselective method was developed of the synthesis of trichloro(2-chlorooctyl)tellane. At adding methanol to this compound chlorine was easily replaced at room temperature by a methoxy group affording trichloro(2-methoxyoctyl)tellane. The reaction of TeBr₄ with 1-octene in methanol resulted in tribromo(2-methoxyoctyl)tellane. A reduction of trichloro- and tribromo(2-methoxyoctyl)tellanes occurs the most selectively in the system NaBH4–water–THF giving 1,2-bis(2-methoxyoctyl)ditellane. The reactions are characterized by a high selectivity and quantitative yields of the products.     

Stereoselective synthesis of tri- and tetrasubstituted tetrahydropyrans from <Emphasis Type="Italic">syn</Emphasis>- and <Emphasis Type="Italic">anti</Emphasis>-1-R-2-(4-bromophenyl)-5-methylhex-4-en-1-ols and some chemical transformations of the products

Tri- and tetrasubstituted tetrahydropyranes fused to one and two heterocycles with various functional groups (COOEt, Br, MeC=CH₂) were synthesized in stereoselective fashion by reactions of syn- and anti-1-R-2-(4-bromophenyl)-5-methylhex-4-en-1-ols (R = Bu, PhCH₂) with trifluoromethanesulfonic acid, aldehydes in the presence of boron trifluoride–diethyl ether complex (Prins reaction), and salicylaldehydes in the presence of trimethyl orthoformate and p-toluenesulfonic acid. The obtained compounds were brought into Suzuki coupling with thiofen-2-ylboronic acid, hydrolysis, and reduction of the ester group with lithium tetrahydridoaluminate. The resulting carboxylic acid was converted to carboxamide, and the alcohol was oxidized to aldehyde which was converted to oxime. The steric configuration of substituents remained unchanged in all chemical transformations.     

<Emphasis Type="Italic">peri</Emphasis>-cyclization of 11-aroylmethyl-2,3,4,5-tetrahydro[1,3]-diazepinobenzimidazoles into 2-aryl-3,4,5,6-tetrahydro-2a,6a,10b-triazabenzo[<Emphasis Type="Italic">a</Emphasis>]cyclopenta[<Emphasis Type="Italic">cd</Emphasis>]azulenium bromides

11-Aroylmethyl-2,3,4,5-tetrahydro[1,3]diazepinobenzimidazoles at heating in conc. HBr suffer a peri-cyclization with the closure of an additional imidazole ring involving the carbonyl group of ketone and the nitrogen atom of the diazepine ring affording previously unknown 2-aryl-3,4,5,6-tetrahydro-2a,6a,10btriazabenzo[a]cyclopenta[cd]azulenium bromides.