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1.
    
The heterogeneous oxidation of n-decane initiated by azo-bis(isobutyronitrile) on quartz surface has been investigated in the temperature range of 80–100°C. At 100°C after the complete consumption of the initiator the oxidation proceeds at a measurable rate. Though heterogeneous oxidation is in many aspects similar to liquid phase oxidation, differences can be observed due to the specific role of the surface.
80–100°C - , - (). 100°C . , , , .
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2.
The use of hydrogen-oxygen titration method to characterize platinum-nickel supported catalysts has shown that the number of oxidized or reduced nickel layers is dependent on the atomic composition. This phenome non involves dynamic changes of the surface probably by a spillover mechanism. A surface reaction scheme based on a previous work is proposed to explain the experimental results.
- - , . , , . , .
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3.
In aqueous solution, PM12–nVnO40 –(3+n) (M=Mo,W) hetero-polyanions provide a much faster oxidation of NO than mononuclear VO 2 + ions, yielding HNO2, NO 3 and reduced HPA.
, PM12–nVnO40 –(3+n) (M=Mo,W) , VO 2 + , NO HNO2 NO 3 .
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4.
Self-oscillation found experimentally in the cool-flame combustion of a model n-heptane-i-octane mixture has been studied in dependence on the composition of the reaction mixture. Calculations based on the CSTR model are in qualitative agreement with experimental data.
--. . .
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5.
    
It has been found that there is a strong dependence of the rate of benzil hydrogenation on the structure and basicity of maines. This observation is interpreted in terms of heterolytic activation of hydrogen by cobaloxime.
. .
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6.
Catalysts with nonuniform distribution of the catalytically active component (Pt) over their porous support (Al2O3) have been studied. A nonuniform activity distribution changes not only the reaction rate but also the kinetics can be different on these catalysts.
(Pt) (Al2O3). , , .
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7.
Benzyl chloride transformation has been studied over Rh/TiO2 under SMSI state to give evidence for the transfer of electrons from support to metal.
Rh/TiO2, . .
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8.
In an attempt to explain how the calibration factor of a heat flux DSC cell depends both on the standard utilized and on the experimental variables, a study has been undertaken of the entire DSC trace.This report deals with the second half of the peak and shows that, other experimental conditons being fixed, the peak area increases with increasing heating rate.This accounts for the observed decrease in the calibration factors with increasing heating rate.
Zusammenfassung Die gesamte DSC-Kurve wurde untersucht, um zu klären, wie der Eichfaktor einer Wärmefluss-DSC vom verwendeten Eichstandard und von den Versuchsbedingungen abhängt. Der vorliegende Teil behandelt den zweiten Abschnitt eines DSC-peaks (vom Maximum an). Es wird gezeigt, dass bei Konstanthalten aller anderen Versuchsbedingungen die peak-Flächen mit steigender Aufheizgeschwindigkeit zunehmen. Das wird als Ursache für die beobachtete Verringerung des Eichfaktors mit steigender Aufheizgeschwindigkeit angesehen.

, . . , - , . .
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9.
The oxidation of ethanol on CuO, CuO/Al2O3 and Pt/Al2O3 catalysts has been studied at various concentrations of alcohol, oxygen and water vapor in the reaction mixture. The reaction order and activation energies have been determined for both complete and partial oxidation processes. A consecutive oxidation scheme is suggested.
CuO, CuO/Al2O3 Pt/Al2O3 , . . .
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10.
    
-complexes of Pd(II) and Pd(I) with benzene in sulfuric acid have been detected via NMR and electronic spectra. Their stability constants and chemical shifts have been determined and compared with the Ag(I) benzene complex.
— - PdII- PdI- . AgI-.
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