Thiophene conversion in the BIMF process

Catalytic conversion of an oil distillate with the added extra amounts of thiophene over a zeolite catalyst was studied. The rate of the catalyst deactivation was found to increase with the increase in the thiophene concentration in the feed. A possible pathway of the thiophene conversion is discussed.     

Effect of the homogeneity of the column set on the performance of a simulated moving bed unit. I. Theory

Although it is impossible to manufacture identical columns for use in a simulated moving bed (SMB) process, theoretical studies assume that all the columns in an SMB unit have identical characteristics. In practice, calculations in modeling and optimization studies are made with the average values of each column parameter set. In this report, the effects on SMB process performance caused by column-to-column fluctuations of the parameters are discussed. As a first step, we show how the differences in porosity of the columns may be taken into account with a revised set of separation conditions. Reductions in the purity of the extract and the raffinate streams are quantitatively related to the column-to-column fluctuations of the retention times of the two components arising from these porosity differences. For the sake of simplicity, the discussion first addresses the case of a four-column SMB operating under linear conditions. Then, the scope is extended to the cases of SMB units incorporating several columns in each section and to SMB units operating under nonlinear conditions.     

Spectral and electrochemical study of coordination molecules Cu4OX6L4: 3-Methylpyridine and 4-Methylpyridine Cu4OBrnCl(6−n)L4 complexes

The tetranuclear Cu₄OBr_nCl_(6-n)L₄ complexes, where L = 3-methylpyridine (3-Mepy), 4-methylpyridine (4-Mepy) and n=0–6 with trigonal bipyramidal coordination of copper(II) were prepared and their infrared and electronic absorption spectra as well as cyclic voltammograms in nitromethane solutions were measured. The polyhedra in Cu₄OBr_nCl_(6−n) (3-Mepy)₄ molecules are less distorted comparing with those of 4-Mepy analogues as indicated by infrared Cu₄O absorptions, far infrared Cu—Br, Cu—Cl, and Cu—N absorptions, d—d bands in electronic spectra and potentials, measured by cyclic voltammetry. The 3-Mepy complexes exhibit strong single infrared Cu₄O absorptions, while for related 4-Mepy complexes doubly split Cu₄O bands were observed. Two strongly overlapped d—d bands in electronic absorption spectra of the 3-and 4-Mepy complexes in nitromethane were resolved by Gaussian fitting. The 4-Mepy ligand produces slightly stronger ligand field than its 3-Mepy analogue. The maxima of high-energy d—d bands are in a linear correlation with the number of bromide ligands. The correlations for corresponding low-energy bands are considerably deviated from linearity. The halfwave potentials of the complexes in nitromethane correlate with both the number of bromides and the data of electronic absorption spectra suggesting that the reducing electron at the electrode process enters the half-filled d _{z 2} orbital of the copper(II) atom. The origin of a difference between the 3-and 4-Mepy complexes in their spectral and electrochemical properties is also discussed.     

Transuranic elements alpha-particle energy analysis using nuclear track in solids methodology

This paper presents a method for the energy analysis of alpha-particles emitted by transuranic elements via a novel technique using Nuclear Tracks. The method is based on the relationship between the energy deposited in the detection material and the diameter of the track, that is formed by chemical etching. The method involves CR-39 polycarbonate as the detector material, one-step chemical etching after irradiation, and a digital image analysis system for automatic reading of the track diameters. The experimental study included alpha-particles in the energy range 5.1 MeV to 5.8 MeV emitted by²³⁹Pu,²⁴¹Am and²⁴⁴Cm. The quantitative results provide a clear signature to identify each one of the emitters based on a characteristic track diameter.     

Atomic force microscopy and solid state photolyses: phase rebuilding

Atomic force microscopy (AFM) was used for the study of the mechanism of phase rebuilding in photodimerizations in crystals and of photoreactions on polymer surfaces. The AFM features that are found upon photochemical reactions in the surface regions indicate far-reaching (up to 100 nm) molecular transport which are well directed in space and depend on the crystal face. Thus, not only proximity considerations (topochemistry) but more importantly phase-rebuilding mechanisms are crucial for solid state photoreactivity and this depends on the bulk crystal structure. 2-benzylidenecyclopentanone (d=4.123 Å) and trans-stilbene (d=5.720 Å) are not reactive, because no phase-rebuilding mechanism is available, while anthracene (d=6.038 Å) does form a photodimer. The phase-rebuilding mechanisms on two natural faces of antharacene are analysed and interpreted on the molecular level. The formation of three different photoproducts from 2,5-dibenzylidenecyclopentanone shows two different phase-rebulding mechanisms on the morphologically dominant face and there are extraordinarily wide molecular rotations of the highly skewed (46°, 131°) reactants in the crystal. Photolyses of polymeric foils of styrene-isopropyl-acrylate copolymer and polystyrene give rise to very nanostructures in the surface region that can be imaged by AFM.     

Fluorine absorption spectra and some fluorides in condensed state

The absorption spectra of liquid F₂, NF₃, N₂F₄, CF₄, BF₃, NF₃, SF₆ have been obtained at diminished temperatures in the near ultra-violet region of the spectrum. It is shown that the absorption spectrum does not differ from the spectra in the gaseous phase, therefore the elementary absorption act is characterized by the cross section of photon absorption by an individual molecule. The absorption cross sections of the above mentioned molecules are represented in the liquid phase, which do not differ strongly from absorption cross sections of these molecules in the gaseous phase. The dependence of the absorption cross sections of liquid fluorine on its concentrations in solutions with N₂, Ar, NF₃, O₂ at - 196°C has been studied. The cross sections of photon absorption by the fluoride molecule in different liquid media with small fluorine concentrations have been obtained.     

Influence of wilt infection on the gossypol pigments of seeds and roots of a cotton plant of the variety Tashkent-1

A study has been made of the gossypol pigments of the seeds and roots of a cotton plant of the variety Tashkent-1 infected with wilt in comparison with a healthy plant. The amount of gossypol in the infected plant was lower than in the healthy plant. In the diseased plant, gossypurpurin was concentrated in the roots, and in the healthy plant it was concentrated in the seeds. Gossypol possessing optical activity was detected in the seeds and roots of both the healthy and the diseased plants.Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 63–66, January–February, 1989.     

Reaction of 2-substituted 4,4-dimethyl-5-methylene-1,3-dioxolanes with dichlorocarbene and certain transformations of adducts obtained

A series of derivatives of 4,4-dimethyl-5-methylene-1,3-dioxolane has been synthesized, and their reaction with dichlorocarbene, obtained under interphase catalysis conditions, has been studied. The adducts obtained undergo thermal isomerization into dichloroethylidene derivatives.     

Reactions of heterocyclic cations with nitrogen-containing nucleophiles. 10. Synthesis of 3,5,7-triaryl-1,2-oxazepinium perchlorates by the reaction of 2,4,6-triarylpyrylium salts with nitrones and substituted hydroxylamines

2-Substituted 3,5,7-triaryl-1,2-oxazepinium perchlorates were obtained by the reaction of 2,4,6-triarylpyrylium salts in dimethylformamide with nitrones and N-arylhydroxylamines. The products are the first representatives of seven-membered cations with eight electrons.See [1] for Communication 9.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 457–460, April, 1982.     

Autocatalytic condensation of 1,2-orthoesters of sugars with 2,3-dihydroxy-1,4-naphthoquinone (isonaphthazarin)

The autocatalytic glycosylation of isonaphthazarine and its derivatives with 1,2-orthoesters of D-glucose and maltose in chlorobenzene has been studied. It has been established that the ratio of mono- and bisglycoside forms depends on the acidity of the glycosylated hydroxy group and its steric accessibility. Free monoglycosides of 2,3-dihydroxy-1,4-naphthoquinone have been synthesized by deacetylation with sodium methoxide in methanol.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, USSR Academy of Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 477–482, July–August, 1989.