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1.
The initial stage of the Li2SO4·H2O single crystal isothermal dehydration has been studied by means of quartz crystal microbalance. As found, weight loss in the initial process may be considered as H2O molecule diffusion from a semiinfinite medium. The numerical values of the H2O molecule diffusion in Li2SO4·H2O have been calculated from the results obtained.
. - - - -. - Li2SO4·H2O.
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2.
During hydrocarbons reactions over Pt/Al2O3 the catalyst is covered by coke. It is accepted that coke formation occurs on metal and acid sites. During normal heptane and methylcyclopentane reforming it was found that the nature and the rate of coke deposited on the catalyst surface was not same, depending on the structure of the hydrocarbon feed.
Pt/Al2O3 . , . , - .
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3.
The activity of silica-molybdenum catalyts in propylene oxidation is shown to be determined by the partially dehydrated silica-molybdenum heteropolyacid stabilized by the SiO2 surface.
, , SiO2.
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4.
The activity and selectivity of copper-iron catalysts for the synthesis of light alcohols from carbon monoxide and hydrogen were studied. The suitable ratio of copper to iron and optimal chemical composition of the catalyst were determined.
- . .
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5.
The thermal curves of diatomites (kieselguhrs) in air display different profiles, depending on the type and quantity of impurities (carbonates, clays, etc.) present. TG and DTG runs can be used for a quick diagnosis of quality, but also give a nearly quantitative picture of the silica content of these minerals.
Zusammenfassung In Abhängigkeit von Art und Menge der Verunreinigungen (Karbonate, Tonerde usw.) weisen die thermischen Kurven von Diatomiten (Kieselguhr) in Luft unterschiedlichen Verlauf auf. Einfache TG- und DTG-Untersuchungen können als Schnelldiagnose zur Bestimmung der Qualität benutzt werden und geben ausserdem noch ein nahezu quantitatives Bild über den Silikatgehalt dieser Mineralien.

( ) , (, . .). , .


The authors acknowledge the financial support of this work by the Comisión Asesora de Investigatión Cientifica y Técnica, Spain, through Project No. PR84-0151.  相似文献   

6.
Decomposition of Mn3Mo2TeO12 during oxidation of toluene to benzaldehyde was observed. Depending on the surface composition of the initial catalyst, the decomposition leads to less active but highly selective MnMoTeO6 or to MnMoO4 which is not selective in toluene oxidation.
Mn3Mo2TeO12 . , MnMoTeO6, MnMoO6.
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7.
Kinetic curves measured in the oxidation of n-butenes over a SnSb=31 mixed oxide catalyst were fitted by the kinetic model put forward in a previous paper. The goodness of fitting shows that the kinetic behavior of this complex reaction system can be described by a mechanism involving acidic and redox sites on the catalyst surface.
- SnSb=31 , . , , - .
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8.
By chemical trapping, an acyl species has been evidenced in the oxidation of alcohols to carboxylate on an alumina surface. A possible reacton scheme is discussed.
. .
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9.
In contrast with expectations based upon simple collision theory, reactions of alkyl radicals with substituted allyl radicals yield cross-combination ratios of =2. Reactions of CH 3 \ with some C5 radicals give >2, in accordance with theory.
, =2. CH3 \ C5 >2, .
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10.
    
, , , : , , -, 100%. .
The liquid phase hydrogenation of furylcyclopropane at high hydrogen pressure in the presence of ruthenium catalysts is highly selective, yielding tetrahydrofurylcyclopropane. Hydrogenation in the presence of Pd catalysts affords n-propylcyclopropane. Platinum and rhodium catalysts occupy an intermediate position.
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