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1.
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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2.
From the analysis of the detailed reaction mechanism and taking into account vanadium complex formation processes, a steady state kinetic equation has been derived to describe experimental data in a wide range of reaction conditions.
, .
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3.
Ni(II), Ni(I) Ni(O) . , , , Ni(O) Ni(I) - Ni(I) Ni(II) Ni(O).
The interaction of organoaluminium compounds with phosphine complexes of Ni(II), Ni(I) and Ni(0) has been studied under the conditions of catalytic propylene dimerization. The active complexes are formed from Ni(II) compounds, the regeneration of the latter is ensured by repeated reduction, oxidation of Ni(0) to Ni(I), and by disproportionation of Ni(I) into Ni(II) and Ni(0).
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4.
The temperature of the polymerizing system was measured with a thermistor during the bulk polymerization of acrylonitrile initiated by azoisobutyronitrile. The temperature of self-heating suddenly rises at a conversion of about 2%. This jump of temperature is presumably caused by the formation of a gel structure and, consequently, the outfall of thermal convection within the system.
, -- . , - . - , .
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5.
The equilibria and thermodynamics of a number of naturally occuring isolated compounds (e.g. proteins, amino acids, carbohydrates) have recently been studied in several laboraties in different temperature ranges, and thermoanalytical methods have been used to study structural changes of biological materials, among them human tissues.In our investigations we succeeded in appling the derivatograph for the assay of glycosaminoglycans and for the characterization of the stability of crosslinked proteins in intact human and animal tissues. By means of this method age-related and pathological changes and repair reactions were studied in various connective and vascular tissues.Other temperature-dependent techniques (DSC, polarizing microscopy) were used successfully in another series of experiments. Alterations in the characteristic order-disorder transition temperatures of human serum lipoproteins could be demonstrated in pathological conditions; the altered physical structure of lipoproteins might give an additional explanation to the assumed mechanism of different metabolic disorders.
Zusammenfassung Die Gleichgewichte und die Thermodynamik einer Reihe von natürlich vorkommenden isolierten Verbindungen (z. B. Proteine, Aminosäuren, Kohlenhydrate) wurden in verschiedenen Laboratorien in verschiedenen Temperaturbereichen untersucht. Hierbei wurden thermoanalytische Methoden zum Studium der Strukturänderungen von biologischem Material, u. a. von menschlichem Gewebe, eingesetzt.In unseren Untersuchungen gelang es den Derivatographen zur Prüfung von Glycosaminoglycanen und zur Charakterisierung der Stabilität quervernetzter Proteine in intakten menschlichen und tierischen Geweben einzusetzen. Durch diese Methode wurden altersbedingte und pathologische Änderungen sowie Reaktionen zur Wiederherstellung in verschiedenen Binde und Vasculärgeweben studiert.Andere temperaturabhängige Techniken (DSC, Polarisationsmikroskopie) wurden in anderen Versuchsserien mit Erfolg eingesetzt.

, . , , , , . . , . .


Plenary lecture  相似文献   

6.
It is shown that, in contrast to classical impregnation methods, in bimetallic catalyst production the texture of the carrier is stabilized by introducing the promoting ion on the surface of Pt/Al2O3 with vapors of CrO2Cl2 or SnCl4. This is shown by a relatively slower decrease of the specific area and the volume of the pores upon calcination.
, Pt/Al2O3- CrO2Cl2 SnCl4 . .
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7.
A kinetic equation for cyclohexane dehydrogenation at PO=1.0 MPa has been obtained.
1,0 .
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8.
The possibility of describing the kinetics of thermal degradation of PVC samples under both isothermal and nonisothermal conditions with a unique model and using the same set of parameters was investigated. Analysis of the experimental data revealed good agreement at higher temperatures (above 175 °C) when the catalytic action of generated HCl and its distribution in the sample were considered. At lower reaction temperatures, further experimental conditions and/or sample characteristics must be considered, and a modification of the model is necessary.
Zusammenfassung Es wird die Möglichkeit untersucht, die Kinetik des thermischen Abbaus von PVC sowohl unter isothermen wie unter nichtisothermen Bedingungen durch ein einziges Modell und unter Verwendung des gleichen Parametersatzes zu beschreiben. Die Analyse der Messdaten zeigt gute Übereinstimmung bei hohen Temperaturen (über 175 °C), wenn die katalytische Aktivität des entwickelten HCL und seine Verteilung in der Probe berücksichtigt werden. Bei tieferen Temperaturen müssen weitere experimentelle Bedingungen und/oder Probeneigenschaften berücksichtigt werden, was eine Modifizierung des Modells erforderlich macht.

. ( 175°), . , .
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9.
A TPD technique is described in which mass spectrometic detection and normal pressure of the carrier gas are employed. Using the thermal decomposition of MgCO3 as a test reaction, it is proved that kinetic studies of each desorbed product can be realized through the whole signal-time curve in a nonrestrictive way.
MC - . MgCO3 , , - .
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10.
Kinetic equations of the isotopic exchange in a system with one elementary reaction have been derived. A principle of quasistationarity in the isotopic kinetics has been formulated.
. .
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11.
[Cu(-C2H2)2]+, [Cu(-CCH2)2]+ and [Cu(-C2H2) (-CCH2]+ complexes have been studied by the ab initio double-zeta basis set method. It has been established that all calculated compounds are stable to decomposition into two C2H2 molecules and Cu+ cation and into one C2H2 molecules and the respective monocomplex. Calculation results suggest the possibility of intramolecular acetylene-vinylidene rearrangement in the coordination sphere of Cu+.
ab initio : [Cu(-C2H2)2]+, [Cu(-CCH2)2]+, [Cu(-C2H2) (-CCH2)]+. C2H2 Cu+ C2H2 . - Cu+.
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12.
The monooxygenation of aniline by hemin, with oxygen activation by direct electron transfer from a cathode to the catalytically active center and direct participation of the reduced oxygen species in the reaction has been carried out.
.
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13.
It has been established that the liquid-phase hydrogenation of thiophene and its alkyl derivatives in the presence of metallic or sulfurized palladium catalysts provides preparative yields of tetrahydrothiophene homologs at increased pressures of hydrogen and elevated temperatures.
.
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14.
The thermal properties of polyisobutylene and isobutylene-isoprene copolymers were studied. Thermal curves were interpreted with regard to supplementary data. It was found that the degradation of both homo- and copolymers proceeds to a much higher extent in air than in argon. It follows from the results that peroxide formation plays a significant role in the degradation of this group of polymers.This finding correlates well with the influence of dicumyl peroxide and phenyl--naphthylamine on the thermal properties of the isobutylene polymers investigated in this work.
Zusammenfassung Die thermischen Eigenschaften von Polyisobutylen- und Isobutylen-Isopren-Kopolymeren wurden untersucht. Die thermischen Kurven wurden unter Berücksichtigung ergänzender Angaben gedeutet. Es wurde festgestellt, dass die Zersetzung sowohl von Homoals auch von Kopolymeren in Luft in einem viel grösseren Ausmass verläuft, als in Argon. Aus den Ergebnissen folgt, dass die Peroxidbildung bei der Zersetzung dieser Gruppe von Polymeren eine bedeutende Rolle spielt.Diese Aussage ist in guter Übereinstimmung mit dem Einfluss von Dicumylperoxid und Phenyl- naphthylamin auf die thermischen Eigenschaften der untersuchten Isobutylenpolymere.

Résumé On a étudié les propriétés thermiques des copolymères polyisobutylène et isobutylèneisoprène. On a interprété les courbes thermiques en considérant des données supplémentaires. On a établi que la dégradation tant des homoque des copolymères s'effectue d'une manière beaucoup plus importante dans l'air que dans l'argon. Nos résultats montrent que la formation du peroxyde joue un rôle important sur la dégradation de ce groupe de polymères.Cette conclusion est en bon accord avec l'influence du peroxyde de dicumyle et de la phényl-naphtylamine sur les propriétés thermiques des polymères d'isobutylène étudiés dans notre travail.

- . . , , . , . -- .
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15.
    
2--4--2 -2. , .
The kinetics of intramolecular condensation of 2-methyl-4-phenylbutanol-2 have been studied in the presence of the strongly acidic cation exchanger KU-2. The reaction is first order with respect to the catalyst. A linear relationship is found between the rate constant and the extent of modification by sodium ions of the cation exchanger.
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16.
Effect of silylation with hexamethyldisilazane on adsorption and catalytic properties of porous glass-supported platinum catalysts has been studied. Catalytic activity decreases markedly with an increase in surface coverage by trimethylsilyl groups for all the following reactions examined: hydrogenation of benzene, dehydrogenation of cyclohexane and dehydrocyclization of n-hexane.
, . , : , -.
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17.
The oxidative dehydrogenation of ethylbenzene over a charcoal catalyst has been studied by the pulse technique. The styrene yields for the oxidation of ethylbenzene by gaseous oxygen and upon the interaction of ethylbenzene with oxygen adsorbed on charcoal are shown to be the same.
. , , , .
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18.
IR and elemental analysis data indicate that the probable structure of the title compound is MoOL2ORH or MoOL2OORH which is formed directly from the radical within the coordination sphere of the catalyst (L=ligand).
- , , , MoOL2ORH MoOL2OORH. (L=).
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19.
The influence of some irregularities in polystyrene (PS) and polyvinyl chloride (PVC) chains on their thermal stability was investigated. UV irradiation caused an increase in the content of these irregularities in the polymers. It was found that the presence of carbonyl groups and crosslinking of the polymer chains hamper the thermal dehydrochlorination of PVC and the total decomposition of both polymers. On the other hand, weak peroxy linkages (which facilitate degradation processes) and conjugated double bonds decrease the temperature of total decomposition of PS and PVC blends.
Zusammenfassung Es wurde der Einfluß von Unregmlmäßigkeiten in Polystyrol (PS)- und Polyvinylchlorid (PVC)-Ketten auf deren thermische Stabilität untersucht. UV-Bestrahlung verursacht ein Ansteigen des Gehaltes an Unregelmäßigkeiten in den Polymeren. Es wurde festgestellt, daß die Gegenwart von Carbonylgruppen und Querverbindungen der Polymerketten die thermische Dehydrochlorierung von PVC und eine vollständige Zersetzung beider Polymere verhindern. Andererseits senken Peroxidverknüpfungen (die die Degradierungsvorgänge erleichtern) und konjugierte Doppelbindungen die Temperatur für eine vollständige Zersetzung von PS und PVC Gemischen.

. - . , . , , , .
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20.
Nonlinear relaxation time has been considered as a differential characteristic determined by the reciprocal value of the relative decrease in the deviation rate of the current concentration vector of intermediates from that of their steady-state concentrations. This characteristic is used for the analysis of some model reactions.
, , .
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