Effect of hydrothermal treatment on catalytic properties of superhigh-silica zeolites

The effect of hydrothermal treatment of decationized superhigh-silica zeolite on the mechanism of n-hexane conversion has been studied. It has been established that thermosteam modification sharply decreases the cracking activity and increases the selectivity to aromatization reactions. Zeolite acidity markedly decreases, but its crystal structure does not become amorphous.

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Catalytic properties of initial and thermosteamed faujasites in n-hexane aromatization

Regularities in n-hexane conversion on decationized Y zeolites under cracking and aromatization conditions have been studied. Possible formation of lower olefins and benzenes in parallel reactions following different mechanisms at low conversion degrees is suggested. The effect of thermosteam treatment on the activity and selectivity of Y zeolites in n-hexane conversion has been examined.

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Catalytic and acidic properties of different metal-zeolite catalysts

Catalytic and acidic properties of bifunctional catalysts containing faujasite, superhigh-silica zeolite and mordenite have been studied in isomerization of C₈-alkylaromatic hydrocarbons.

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Specific features of solketal synthesis on KU-2-8 cation-exchange resin

Technological specific features of the solketal synthesis on a KU-2-8 cation-exchange resin were improved. Data are presented on the mutual solubility of the components in the glycerol–acetone–water and glycerol–acetone–water–ethanol systems. It is shown that use of ethanol for homogenization of the starting reagents is more than twice more efficient than performing the process with delivery of an emulsion of the reagents or reaching a full solubility of glycerol in acetone due to the 20-fold excess of the latter at 35°C. It is shown that the delivery of a glycerol emulsion in acetone to an immobile bed of a heterogeneous catalyst working in the falling-film mode leads to flooding of the reactor at spraying densities exceeding 0.15 m³ m^–2 h^–1.     

Effect of sodium chloride on the solubility and hydrolysis of epichlorohydrin in water

The mutual solubility of the components in the epichlorhydrin–water–sodium chloride system was studied in the temperature range of 20–90 °С. It was found that epichlorohydrin is salted out as the concentration of NaCl increases. The Sechenov coefficient was determined to be equal to 0.29. It was found that epichlorohydrin reacts with an aqueous solution of sodium chloride to form glycerol dichlorohydrins. Alkali formed during this reaction catalyzes the hydrolysis of epichlorohydrin to glycerol monochlorohydrin, acts as a reagent in the glycidol formation and accelerates its subsequent conversion to glycerol.     

Formation of superacid centers in the structure of zeolite ZSM-5

The structural changes and acid characteristics of the zeolite ZSM-5 modified with titanium and sulfur were studied. The modifier components were chemically bonded to the zeolite structure. The acid characteristics of zeolite changed and superacid centers appeared. A physicochemical study showed that treatment of zeolite with titanium tetrachloride and sulfuryl chloride did not change its structure and molecular-sieve properties.     

Physicochemical and catalytic characteristics of La-H-ZSM-5 zeolite in converting dimethyl ether to the mixtures of gasoline hydrocarbons: Effect of ion exchange conditions

The effect of the manner and conditions of introducing lanthanum cations into NH₄-ZSM-5 zeolite on the properties of catalysts for the conversion of dimethyl ether into the mixtures of gasoline hydrocarbons is studied. The physicochemical properties of synthesized catalysts are studied by means of temperature-programmed ammonia desorption, the adsorption of benzene, atomic absorption spectroscopy, differential scanning calorimetry, and thermogravimetry. It is shown that the degree to which lanthanum cations are replaced by ammonium cations both depends on the conditions of ion exchange in the zeolite and affects its acidity spectrum and the selectivity of the formation of paraffin hydrocarbons with isostructure. It is concluded that an increase in the amount of introduced lanthanum leads to an increase in the content of iso-paraffins from 69 to 76 wt % and a decrease in the content of aromatic hydrocarbons from 10.5 to 5.5 wt % and that of durene from 1.5 to 0.2 wt % in the products.     

Completel-groupoids and their prime spectra

We argue for the validity of the infinite ∩-distributivity law in a lattice of radical elements of an arbitrary complete l-groupoid, in particular, in the lattice of radical ideals of an arbitrary ring. The notion of a prime spectrumSpec (L) is defined, and we point out a specific place that topological spaces of typeSpec (L) hold among all T_o-spaces. Supported by the AMS grant. Translated fromAlgebra i logika, Vol. 36, No. 3, pp. 341–355, May–June, 1997.     

Conversion of Dimethyl Ether to a Mixture of Liquid Hydrocarbons with Increased Triptane Content

The influence of the structural type and of the textural and acid properties of the zeolite on the catalyst selectivity in synthesis of a mixture of liquid hydrocarbons with increased content of isoalkanes from dimethyl ether was examined. The synthesis of liquid hydrocarbons enriched in triptane in the course of gasoline production from CO and H₂ via dimethyl ether in the presence of La-H-Y zeolite was performed for the first time. Excess hydrogen in the system and relatively short contact time of the catalyst with the feed favor an increase in the triptane yield. Additional modification with palladium leads to optimization of the acid properties of the La-H-Y zeolite and, as a consequence, to an increase in the triptane content of the gasoline from 2.0 to 9.4 wt %.

     

Searching for Neutrino and Ultra-High-Energy Gamma-Ray Counterparts of the GCN Alerts

Physics of Atomic Nuclei - The Baksan Neutrino Observatory setups are currently performing search for neutrino and ultra-high-energy gamma-ray counterparts of the events on the Gamma-ray...