Novel type of oscillatory chemical reactions

Chemical oscillations occur during the uncatalyzed oxidation of a number of phenol and aniline derivatives by acidic bromate.

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Structure of vanadium phosphate anion in solutions from17O,51V and31P NMR data

¹⁷O,⁵¹V and³¹P NMR studies indicate that the anion structure of sodium vanadophosphate in an aqueous solution is close to that in crystals of the (CN₃H₆)₈HPV₁₄O₄₂ 7H₂O salt.

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¹⁷O,⁵¹V,³¹P , (CN₃H₆)₈HPV₁₄O₄₂ 7H₂O.

     

Reaction of triphenyl phosphite ozonide with thioacetals

Kinetic regularities in the reaction of triphenyl phosphite ozonide with several thioacetals in CH₂Cl₂ solution at –15°C have been studied. The consumption rate of ozonides is described by the kinetic equation W=k₀[(C₆H₅O)₃P·O₃]+k₁[(C₆H₅O)₃P·O₃][R₁R₂C(SR₃)₂] Rate constants k₀ and k₁ for the thioacetals: (CH₃H₇S)₂CH₂, (C₆H₅S)₂CH₂, (C₆H₅CH₂S)₂CH, (n=C₁₂H₂₅–S)₂CH₂, (C₃H₇S)₂C(H)CH₃, (C₃H₇S)₂C(H)C₆H₅, (C₃H₇S)₂C(CH₃)C₆H₅ and (C₃H₇S)₂C(H)C₁₀H₉, increases with increasing the electron-donating power of subtituents R_i.

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CH₂Cl₂ –15°C. : W=k₀[(C₆H₅O)₃P·O₃]+k₁[(C₆H₅O)₃P·O₃][R₁R₂C(SR₃)₂] k₀ k₁ (C₃H₇S)₂CH₂, (C₆H₅S)₂CH₂, (C₆H₅CH₂S)₂CH₂, (n-C₁₂H₂₅S)₂CH₂, (C₃H₇S)₂C(H)CH₃, (C₃H₇S)₂C(H)C₆H₅, (C₃H₇S)₂C(CH₃)C₆H₅, (C₃H₇S)₂C(H)C₁₀H₉. .

     

The thermal decomposition of phosphorus iodides

The thermal decomposition of crystalline PI₃ and P₂I₄ in nitrogen and oxygen is reported. The oxidation of PI₃ leads mainly to the formation of phosphorus pentoxide and iodine together with P_xI polymeric species as a minor product. The decomposition of the polymeric species P₃I₂O₆ in oxygen and nitrogen follows a two-stage route which precludes its involvement in the oxidation of P₂I₄.

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Zusammenfassung Es wurde die thermische Zersetzung von kristallinem PI₃ und P₂I₄ in Stickstoff und Sauerstoff untersucht. Die Oxydation von PI₃ führt zur Bildung von Phosphorpentoxyd und Jod mit wenig Polymeren der Zusammensetzung P_xI. Die Zersetzung der Polymeren P₃I₂O₄ in Sauerstoff und Stickstoff erfolgt in zwei Stufen, die eine Beteiligung in der Oxydation von P₂I₄ ausschließen.

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Résumé On décrit la décomposition thermique, dans l'azote et dans l'oxygène, de PI₃ et de P₂I₂ cristallins. L'oxydation de PI₃ conduit principalement à la formation d'iode et de pentoxyde de phosphore, avec de petites quantités de P_xI de type polymère. La décomposition de l'espèce polymère P₃I₂O₆, dans l'oxygène et dans l'azote, s'effectue suivant un processus en deux étapes excluant sa participation à l'oxydation de P₂I₄.

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I₃ P₂I₄ . I₃, , , — — _xI . ₃I₂₆ , ₂I₄.

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The author is indebted to Mrs. I. M. Walker for practical assistance with the thermoanalysis studies.     

Reduction of alkenes by hydrogen transfer over a Pd/sepiolite catalyst. Compensation effect

This paper shows the occurrence of a linear relationship between the activation energy (E_A) and the logarithm of the pre-exponential factor (ln A) in the Arrhenius equation, and between the enthalpy increment (H) and the entropy increment (S) in the Eyring equation for the reduction of olefinic double bonds by hydrogen transfer over a Pd/sepiolite catalyst. Such a relationship is known as the compensation effect or isokinetic relationship.

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Pd/ (E_a) (ln A) (H) (S) . .

     

Effect of TiO2 crystal modification on catalytic properties of cobalt-titanium dioxide catalysts for Fischer-Tropsch synthesis

CO hydrogenation on cobalt-rutile and cobalt-anatase catalysts with various amounts of cobalt at 480–570 K has been studied. C₁–C₁₅ hydrocarbons are formed on cobalt-rutile catalysts at 478–523 K. During the initial period of catalyst operation a counterclockwise hysteresis is observed. Cobalt-anatase catalysts remain inactive up to 670 K.

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CO - - - 480–570 . - 478–523 C₁–C₁₅. . - 670 .

     

Hydrogenation of CO2 on carbon-supported nickel and cobalt

The hydrogenation of CO₂ has been studied at atmospheric pressure on Co/C and Ni/C catalysts and the results are compared with those obtained on unsupported Co and Ni. Specific activites in the form of turnover frequencies for CO₂ hydrogenation decrease with increasing metal dispersity. Carbon supported Co and Ni present a smaller selectivity for methane than bulk metals. Higher specific activities and smaller activation energies are obtained on Co catalysts, compared with those determined for Ni catalysts.

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CO₂ Co/ Ni/ Co Ni . CO₂ . Co Ni , . .

     

Alcohol formation from synthesis gas: A thermodynamic study

A thermodynamic study is presented for the simultaneous synthesis of C₁–C₄ alcohols from synthesis gas. The equilibrium composition was calculated for the gaseous mixture containing Co, H₂, CH₃OH, C₂H₅OH, C₃H₇OH, n-C₄H₉OH and H₂O. Operating industrial conditions were specifically considered.

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C₁–C₄ -. , CO, H₂, CH₃OH, C₂H₅OH, C₃H₇OH, -C₄H₉OH H₂O. .

     

Adsorption of nitrous oxide on metallic copper catalysts

With the help of UPS spectroscopy, it has been shown that N₂O decomposes into N₂ and surface Cu₂O over copper catalysts in the temperature range –150, –100°C. The surface oxide oxygen dissolved into the bulk above 100°C to some extent.

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, N₂O –150° –100°C, N₂ Cu₂O. 100°C.

     

m-Xylene conversion over dealuminated Y zeolites studied by the pulse method

m-Xylene conversion was studied over dealuminated Y type zeolites in hydrogen forms, SiO₂ to Al₂O₃ ratios were varied from 4.86 to 12.95.

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- . SiO₂/Al₂O₃ 4,86 12,95.

     

A thermoanalytical study on some compounds of Zr(IV) with azopyrazolonic derivatives

Thermoanalytical data on six reagents and on their compounds with Zr(IV) are reported. Except for H acid, all reagents were azopyrazolonic derivatives obtained by synthesis. The purpose of this study was to obtain data on the thermal stabilities of the reagents and their zirconium compounds, and to establish the reagent: zirconium: water combination ratio.

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Zusammenfassung Thermoanalytische Daten von 6 Reagenzien und deren Verbindungen mit Zr(IV) werden mitgeteilt. Außer H-Säure waren alle Reagenzien durch Synthese erhaltene Azopyrazolon-Derivate. Zweck der Untersuchung war, Daten über die thermische Stabilität dieser Reagenzien und ihrer Zirkonverbindungen zu erhalten und das Verhältnis Reagens: Zirkon: Wasser festzustellen.

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. , , - . , : : .

     

Basic condensation of triphenylsilane. II. Kinetics in anhydrous isopropanol and influence of silanol

Condensation of triphenylsilane with isopropanol in presence of isopropoxide has been studied in anhydrous medium and the activation parameters have been measured. Dehydration of the medium has been obtained by means of a pre-reaction of triphenylsilane with the residual water in the solvent. In this medium the reaction is extremely slow, moreover, it is inhibited by silanol whose effect would lower the actual catalyst concentration.

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. . , .

     

Effect of quantization of molecular rotations on the rate of capture in the ion-linear dipole system

The version of transition state theory that accounts for quantization of the rotational energy of a dipole gives ion-dipole capture rate constants in good agreement with the statistical adiabatic channel model and, in the region , gives results more accurate than those obtained by numerical trajectory calculations.

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, , - . , .

     

A differential scanning calorimetric study of some phenol derivatives

Differential scanning calorimetry has been applied to derive the fusion enthalpies and entropies of series of mono and dimethylphenols, mono and dichlorophenols, and mono and dinitrophenols.

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Zusammenfassung DSC wurde verwendet zur Ermittlung der Schmelzenthalpie und Entropie der Reihen von Mono- und Dimethylphenolen, Mono- und Dichlorphenolen, Mono- und Dinitrophenolen.

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- , - , - .

     

Evaluation of triplet repulsion energies

The equation is suggested for predicting triplet repulsion energies. X=R–R^o, while R^o and¹V^o are the equilibrium bond length and the spectroscopic dissociation energy, respectively. Parameters and may be estimated from known bond properties.

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( X=R–R^o, a R^{o 1}V^o , . , .

     

Einige Anwendungen der thermometrischen Methode zur Analyse und Charakterisierung von feindispersen Kieselsäuren und Silikaten

Zusammenfassung Unter Anwendung der thermochemische Methode werden die Bestimmungen von SiO₂, Al₂O₃, Na₂O, SO₃ und Feuchte in feindispersen Kieselsäuren und Silikaten beschrieben. Besonders eingegangen wird auf die aufeinanderfolgende Bestimmung von SiO₂ und Al₂O₃ sowie der hierbei beobachteten Vorteile und Störungen. Über die Möglichkeit der Verwendung der kinetisch-katalytischen Analyse mit thermometrischer Indikation zur Bestimmung von Cu und Mn werden Ausführungen gemacht. Der zweite Teil des Vortrages befaßt sich mit der Benetzungs- und Immersionswärme von feindispersen Kieselsäuren und Angaben zur Bestimmung dieser auch unter betriebsanalytischen Bedingungen. Für verschiedene Kieselsäuretypen werden unterschiedliche Benetzungswärmen gefunden. Auf die Notwendigkeit der Weiterführung solcher Messungen wird verwiesen.

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The authors describe the determination of the SiO₂, Al₂O₃, Na₂O, SO₃ and moisture contents of finely dispersed silicic acids and silicates by means of thermochemical methods. Special interest is paid to the determination of SiO₂ and Al₂O₃ as well as to the advantages of the method and to disturbing factors. The possibility of using kinetic-catalytic analysis with thermometric end-point detection for Cu and Mn determination is discussed. In the second part of the paper the authors deal with the heat of wetting and heat of immersion of finely dispersed silicic acid, and give data for their determination under circumstances of industrial analysis too. Differences in the heats of wetting were found for the different types of silicic acid. These studies require further measurements to be made.

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, , , . , . . . . .

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Überarbeitete Fassung einer Vorlesung zum 3. Seminar über thermometrische Analyse, Marienbad, CSSR, 1983.     

Kinetic analysis of thermogravimetric data. XXVI

Ten metal and ammonium salts of the acid H₂[ReCl₆] were obtained by double decomposition reactions, and their pyrolyses in air atmosphere were studied by means of DSC measurements. The kinetic parameters of these reactions were derived and are discussed.

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Zusammenfassung 10 Metall- und Ammoniumsalze der Säure H₂[ReCl₆] wurden durch Doppelzersetzungsreaktionen erhalten. Die Pyrolyse dieser Salze in Luft wurde mittels DSC untersucht. Die kinetischen Parameter dieser Reaktionen wurden ermittelt und diskutiert.

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H₂[ReCl₆]. . .

     

A novel method for the preparation of extensively dealuminated faujasites

Open structure faujasites may be dealuminated with retention of crystallinity using phosgene (or similar reactants) provided the sample has been made ultrastable in a previous procedure.

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( ) . .

     

An Inorganic-Organic Hybrid Supramolecular Hydrogen-Bonding and π-π Stacking Network Containing Ge4S4− 10 Cluster: Synthesis and Characterization of (H2bipy)2Ge4S10⋅(bipy)⋅7H2O (bipy=4,4′-bipy)

The reactions of TMA₄Ge₄S₁₀ (TMA=tetramethylammonium), Cu(NO₃)₂3H₂Oand 4,4-bipy under hydrothermal environment result in the formation of (H₂bipy)₂Ge₄S₁₀(bipy)7H₂O (1), which has been structurally characterized by single crystal X-ray analysis. The 3-D structure of 1 can be viewed as an inorganic-organic hybrid supramolecular hydrogen-bonding (hydrogen bonds: O–HO, N–HN, C–HO, N–HO, and O–HS) and - stacking network containing Ge₄S^4– ₁₀ clusters and novel [H₂bipybipyH₂bipy] trimers.