Photooxidation of ABS of long-wavelengths

The evolution of the photochemical degradation of ABS has been studied in conditions of long wavelength irradiation (λ's> 300 nm). The main photoproducts involved in the oxidative evolution have been identified by using FTIR spectroscopy and chemical titrations. A particular attention has been devoted to α–β unsaturated ketones that appear as secondary photoproducts. Those ketones present a low photochemical stability when exposed in the range 300–400 nm. Conditions for their formation have been experimentally studied. Formation of oxidation photoproducts has been also studied at the macroscopic level and it has been shown that their repartition in the polymer is heterogeneous. The origins of the heterogenities have been studied.     

The reactivity of furan compounds in vapor-phase catalytic oxidation

The reactivity of furan compounds in vapor-phase oxidation with air over a vanadium-molybdenum-phosphorus catalyst on low-porosity corondum has been studied under nongradient conditions. It has been established that the rate of the over-all conversion of the furan compounds studied and the rate of accumulation of maleic anhydride in the cycle decreases in the sequence: furan > furfural > tetrahydrofuran > furfuryl alcohol > 2-methylfuran > 5-methylfurfural, and the selectivity relative to the formation of maleic anhydride decreases in the following sequence: furan > tetrahydrofuran > furfural > furfuryl alcohol > 2-methylfuran > 5-methylfurfural. Some considerations relating to the mechanism of the reaction studied has been put forward.     

Extraction of uranium(VI) and thorium(IV) from nitric acid solution by N-alkylcaprolactam

Extraction of uranium(VI), thorium(IV) from nitric acid has been studied with N-octylcaprolactam and N-(2-ethyl)hexylcaprolactam. Distribution coefficients of U(VI), Th(IV) and HNO₃ as a function of aqueous NHO₃ concentration, extractant concentration and temperature have been studied. The compositions of extracted species, thermodynamic parameters of extraction have been evaluated. Third phase formation in extraction of U(VI) has been studied. Back extraction behavior of U(VI) and Th(IV) from the organic phase has also been tested. The results obtained are compared with those obtained by using TBP under the same experimental conditions.     

Effect of Surface Treatment of Titanium Dioxide Nanoparticles on Non-Isothermal Crystallization Behavior,Viscoelastic Transitions and Cold Crystallization of Poly(Ethylene Terephthalate) Nanocomposites

The effect of untreated and tri-n-octylphosphine oxide (TOPO) surface-treated TiO₂ nanoparticles when included as filler in poly(ethylene terephthalate) on its compatibility, non-isothermal crystallization behavior, viscoelastic transitions and cold crystallization has been studied. The effectiveness of the surface treatment has been studied using infrared spectrophotometry (FTIR) and thermogravimetric analysis (TGA). The effect of the untreated and surface-treated nanofiller content in the polymer, added by an extrusion process, on the non-isothermal crystallization has been studied by differential scanning calorimetry (DSC). The influence on the viscoelastic transitions and cold crystallization of PET nanocomposites has been studied through thermomechanical analysis (TMA). The surface treatment and the concentration of nanofiller influence the non-isothermal crystallization behavior, the viscoelastic transitions and the cold crystallization of the PET nanocomposites, enables us to evaluate the compatibility and the level of dispersion/aggregation of the nanofiller in the poly(ethylene terephthalate).     

Separation of copper and bichromate ions by complex methods

Separation of Cu²⁺ and Cr₂O₇ ^2– has been studied by electrodialysis combined with preliminary adsorption on bentonite. The influence of concentration, pH, and electric current on the degree of desalination has been studied. The optimum conditions for almost complete separation of the ions studied have been found. Real galvanic sewage has been examined by this method.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1191–1193, July, 1994.     

Synergism in the extraction of scandium

Synergism in the extraction of scandium by a mixture of di-2-ethylhexyl phosphoric acid and a β-diketone has been studied. The nature of the extracted species has been investigated. The effect of temperature on extraction has been studied and synergism has been explained on the basis of thermodynamic parameters of the extraction process.     

Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens

In order to estimate the potential of steroid estrogens modification, three D-homoanalogs of estrogens have been prepared; their structures and biological properties have been studied. The expansion of D-ring in such compounds has lead to strong decrease if the uterotropic action, however, the unfavorable hypertriglyceridemic effect has been retained. The latter has been eliminated by combined action of the studied steroids and ursolic acid; therewith the hypocholesterolemic activity has been retained.     

Chemical transformations of TiAl and Ti3Al intermetallides in amonium medium

Hydrogenation, hydronitriding, disproportionation, and dispersing in the TiAl-NH₃ and Ti₃Al-NH₃ systems in the temperature range 100–500°C under a pressure of 1.5 MPa in the presence of an NH4Cl activator have been studied. Phase transitions have been studied and conditions for formation of fine intermetallide powders with a medium particle size of 0.15–0.30 μm have been determined.     

Spectral-luminescent and solvatochromic properties of 2-(3-coumarinyl)-5-(2′-(R-amino)-phenyl)-1,3,4-oxadiazoles

Spectral-luminescent properties of the newly synthesized 2-(3^′-coumarinyl)-5-(2′-(R-amino)-phenyl)-1,3,4-oxadiazoles has been investigated in solvents of various polarity and hydrogen-bonding ability. It has been found that for all the studied compounds no excited state intramolecular proton transfer occurs despite the presence of coumarinyl fragment - electron acceptor effect of the coumarinyl fragment is not sufficient to increase the excited state acidity of the amino group. It has been found that the absorption spectra of the studied compounds shift to higher energy with increase in solvent polarity, whereas corresponding fluorescence spectra shift to lower energy with solvent polarity increase. It has been suggested that long-wavelength shifts of the fluorescence spectra of the studied compounds with increase in solvent polarity is caused by the solvent relaxation. The observed solvent relaxation effect allow us to propose some of the studied compounds as potential probes to monitor changes in solvent relaxation in low-polar media and as potential probes for rigidochromic effect.     

The Effect of Substituent Groups on the Migration of Metal Ions in Thin Layer Chromatography

Abstract

A reverse phase thin layer partition chramotography has been performed on metal ions using silica gel G as an adsorbent. The effect of chlorosubstituent groups on the migration of cations has been studied. The use of aqueous solutions of acetic acid, monochloro, dichloro and trichloro acetic acid in the solvent system revealed profound effect of substituent groups on the R_f values of metal ions. The effect of concentration and pH of the mobile phases have been studied. Many qualitative ternary separations have been sucessfully achieved.     

ELECTRON SPIN RESONANCE OF TRIPLET STATES AND FREE RADICALS APPEARING IN PORPHYRINS, AROMATIC AMINO-ACIDS AND PROTEINS UNDER THE EFFECT OF LIGHT

Abstract— The electron paramagnetic resonance (EPR) of the triplet excited state of solutions of a series of porphyrins and aromatic amino-acids has been studied at 77°K. It has been shown that for some of the compounds it is possible to observe EPR for transitions with δ M =±1, ±2.
It has been shown that photoreactions in solid solutions of porphyrins and aromatic amino-acids proceed through the triplet excited state.
Reactions of photosensitized deamination of aliphatic amino-acids in solid aqueous solutions at 77°K by aromatic compounds have been studied.     

Chain scission of butyl rubber by nitrogen dioxide in absence and presence of air

The chain scission reaction suffered by butyl rubber due to NO₂ (0.01-1 mm Hg) has been studied in the presence and absence of air. It has also been studied as a function of temperature (25–65°C) at constant NO₂ pressure, again in absence and presence of 1 atm of air. Reaction mechanisms which are in good agreement with the experimental results have been formulated. The synergistic action of O₂ and NO₂ has been pointed out.     

Elucidation of the Structure of Products of Triphenylphosphine Electrooxidation in the Presence of Camphene

The structure of the products of anodic oxidation of triphenylphosphine in the presence of camphene carried out in acetonitrile with sodium perchlorate as supporting electrolyte has been studied. The major product, triphenylphosphine oxide, has been isolated from the solution in the form of cocrystals of free triphenylphosphine oxide and its complex with sodium perchlorate. The molecular structure of the cocrystals has been studied by X-ray diffraction analysis. Triphenylcamphenylphosphonium perchlorate, bornylacetamide, and a terpene compound with triphenylphosphonium and acetamide substituents in the cycle have been detected by NMR ¹³C as the electrolysis side products.

     

Radiation-initiated telomerization of tetrafluoroethylene in 1,2-dibromotetrafluoroethane

The kinetics of the radiation telomerization of tetrafluoroethylene in 1,2-dibromotetrafluoroethane has been studied. It has been shown that the process occurs very efficiently in the perfluorinated solvent; small doses of γ-radiation (~2 kGy) are required for the complete conversion of the monomer. Telomers with a chain length of 120–360 tetrafluoroethylene units and high thermal stability are formed in the reaction. The structure and properties of the telomers have been studied by IR spectroscopy, thermogravimetry, and elemental analysis.     

Polymeric Nitrofuran Derivatives. I. Radical-Initiated Homo- and Copolymerization of 5-Nitrofurfuryl Methacrylate

The radical homopolymerization of 5-nitrofurfuryl methacrylate (NFMA) and the copolymerization of NFMA with methyl methacrylate and various vinyl monomers, respectively, have been studied in dimethylformamide at 65°C. NFMA and poly(NFMA) have been characterized by ¹H-NMR, IR, and UV spectroscopy. The influence of polymerization conditions on monomer conversion and on the molecular weight of the polymers obtained has been investigated. The thermal behavior of the polymers obtained has been studied by TGA and DSC analysis.     

Quantum-Chemical Study of the Oxidative Ability of Nitro Compounds Using Decomposition of Some Simple Amines in the Presence of Triplet Nitromethane as an Example

The photooxidation of amines with triplet nitromethane has been studied using the uB3LYP/6-311g* method. The activation energies for hydrogen atom abstraction from ammonia and the amino group of methylamine or aniline have been found to be 14.1, 4.9, and 6.3 kJ mol^?1, respectively. Details of the hydrogen atom transfer mechanism have been studied, the structures of transition complexes have been revealed, and noncovalent interaction energies have been evaluated in terms of the theory of atoms in molecules.     

Experimental results relating to the metabolism of the cardiac glycosides

Summary 1. The metabolism of nine cardenolides — convallatoxin, convallatoxol, erychroside, erychrosol, securiside, securisidol, gofruside, frugoside, and erysimin — has been studied at the stage of passage through the liver and in the pathways of excretion by the kidneys.2. It has been found that the aldehyde at the C₁₉ group of the cardiac glycosides studied is reduced to an alcohol group.3. Erysimin differs in its metabolism from the other glycosides studied by the fact that in addition to the production of a form reduced at C₁₉ it undergoes hydrolytic cleavage with the production of the genin. A third metabolite has not been identified and has provisionally been called metabolite M.Khar'kov Scientific-Research Institute of Pharmaceutical Chemistry. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 658–662, September–October, 1973.     

Oxygen chemisorption by an anthracite from peñarroya (Spain). A comparative study using dynamic and isothermal gravimetric methods

The chemisorption of oxygen (P = 1 atm, flow rate, 200 ml min^?1) by an anthracite from Peñarroya and on other adsorbents prepared from the starting sample has been studied in isothermal and dynamic conditions using gravimetric methods.Hypotheses to justify the thermograms have been established and comparative information on the energetic aspects determining both gasification stages has been obtained.Some kinetic and thermodynamic aspects are studied from oxygen chemisorption isotherms.     

A Spectrophotometric Study of Fe(III) Chelates of Some Hydroxy Coumarin Derivatives

Chelates formation of Fe(III) with 7–hydroxy–4–methyl coumarin–6–carboxylic acid (HMCCH)₂ and 8–amino–7–hydroxy–4–methyl coumarin (AHMCH) have been studied. It has been observed that Fe(III) forms 1:2 (metal:ligand) chelates with HMCCH₂ and AHMCH. The stability constants of these chelates at different ionic strengths and the effect of temperature on the stability constants of these chelates have been studied. The thermodynamic parameters such as entropy change (ΔS), free energy of formation (ΔG) and enthalpy change (ΔH) have also been calculated. The effect of dielectric constant oh the stability constants of these chelates have been studied. Estimation of nanogram quantities of Fe(III) with these ligands and the effect of diverse ions have also been studied and the results have been compared with other methods used for estimation of Fe(III).     

Kinetics and mechanism of oxidation of sugars by quinquevalent vanadium in binary mixture solvents of DMSO–water and acetic acid–water in H2SO4 medium

The kinetics of oxidation of aldosugars and ketosugar by quinquevalent vanadium in binary mixtures of DMSO–water and acetic acid–water in sulfuric acid medium have been studied. The reaction is first order in both oxidant and substrate. The effect of acidity on the reaction kinetics has been determined. The effect of acidity shows a clear difference. The ketose has a unit dependence, whereas aldoses have a 0.5 dependence in H₀. The role of solvent in these reactions has also been studied, and the effect of temperature on these reactions has been determined. A suitable mechanism has been postulated taking all the observed facts into consideration.