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1.
An automated system of thermal analysis is described for the study of fast exothermic reactions (intensive burning, self-inflammation, transition from the non-equilibrium state to the equilibrium state, etc.). The system includes a complex of technical means for connecting the measuring instrument with the computer (hardware), and a special mathematical supply (software).The use of this system provides data required for thermal and chemical calculations in the high-temperature range.Two examples of DTA data-processing are presented.
Zusammenfassung Ein automatisches Thermoanalyse-System zum Studium schneller exothermer Reaktionen (intensives Brennen, Selbstzündung, Übergang vom Nicht-Gleichgewichtszustand in den Gleichgewichtszustand usw.) wird beschrieben. Das System enthält eine Reihe technischer Vorrichtungen zur Verbindung des Meßgerätes mit dem Komputer und dem speziellen mathematischen Apparat.Die Anwendung dieses Systems ermöglicht die Ermittelung von Daten, welche zu thermischen und chemischen Berechnungen im Hochtemperatur-Bereich nötig sind.Zwei Beispiele der DTA-Datenverarbeitung werden gegeben.

Résumé On décrit un système automatique d'analyse thermique pour l'étude de réactions exothermiques rapides (combustion intense, autoinflammation, transition de l'état de nonéquilibre à celui d'équilibre, etc....). Le système comprend un ensemble de moyens techniques pour coupler l'instrument de mesure à l'ordinateur et à l'appareillage mathématique spécial.L'utilisation de ce système permet d'obtenir les données nécessaires aux calculs des effets thermiques et chimiques dans le domaine des températures élevées.On présente deux exemples du traitement des données de l'ATD.

( , , .). ., , . , .
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2.
A theoretical analysis of the formation of materials with metastable microstructures under non-ideal and highly non-equilibrium conditions is presented.
Zusammenfassung Es wird eine theoretische Untersuchung der Bildung von Stoffen mit metastabilen MikroStrukturen unter nichtidealen Bedingungen weitab vom Gleichgewicht dargelegt.

.
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3.
Zusammenfassung Eine Thermowaage, mit der gleichzeitig die Masse und die Temperatur in einer Probe gemessen werden können, wurde für Lehrzwecke entwickelt. Am Beispiel der Verdunstung von Aceton, der Entwässerung von Kupfersulfat-pentahydrat, der Zersetzung von Magnesiumoxalat-dihydrat und der Pyrolyse von Weichholz werden ihre TG-Kurven diskutiert.
A thermobalance for teaching purposes was constructed which is able to measure simultaneously mass and temperature in a sample. The effectiveness of the device is discussed by the TGA curves of the evaporation of acetone, the dehydration of copper sulphate pentahydrate, the decomposition of magnesium oxalate dihydrate, and the pyrolysis of wood.

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4.
In DSC studies of liquid-quenched ternary chalcogenide glasses Te80Ge20–xA x V (AV=Sb, Bi), the characteristic temperatures (glass transition and crystallization temperatures) were determined. Changes in the thermal stabilities of these glasses, depending on the element A (Sb, Bi) from group V of the periodic table and on its content in the alloy were evaluated. Moreover, the effect of changes in the glass composition on the glass formation ability expressed by the parameter Kg1 was determined.
Zusammenfassung In DSC-Untersuchungen abgeschreckter ternärer Chalkogenidgläser des Typs Te80Ge20–xA x v (Ax=Sb, Bi) wurden die charakteristischen Temperaturen (die GlasÜbergangs- und Kristallisationstemperaturen) bestimmt. Die Änderungen der Thermostabilität dieser Gläser wurden in Abhängigkeit von dem Element A (=Sb, Bi) aus der V Gruppe der Periodensystems und von seinem Gehalt in der Legierung ausgewertet. Ausserdem wurde der Einfluß der Änderungen in der Glaszusammensetzung auf die Glasbildungsfähigkeit, ausgedrückt durch den Parameter Kg1, bestimmt.

Résumé On a déterminé par analyse calorimétrique différentielle (DSC) les températures caractéristiques (températures de transition vitreuse et de cristallisation), des verres ternaires à chalcogénures formés par trempe à partir du liquide, du type Te80Ge20–xA x v (Av=Sb, Bi). On a évalué la variation de la stabilité thermique de ces verres en fonction de l'élément A (=Sb, Bi) du Vème groupe du tableau périodique et de sa teneur dans l'alliage. De plus, on a déterminé l'effet des variations de la composition du verre sur la capacité de formation du verre qui s'exprime par le paramètreK g1.

Te80Ge20–xA x v (Av=Sb, Bi), , . A(=Sb,Bi) . , K gl, .


Research supported by the U. S. National Science Foundation under Grant No. GF 421 76  相似文献   

5.
ESR and electronic spectroscopy have reveled that in low-temperature ZnO the copper ions form Cu–O–Cu type cluster structures with highly covalent bonds and strong exchange interaction between the ions. The nearer environment of the Cu2+ ions is an octahedron with distortion towards square planar coordination.
, ZnO Cu–O–Cu . Cu2+- , .
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6.
The microwave spectrum of 1,3dioxolane (C3H6O2) in the ground and first three excited states of hindered pseudorotation was studied. The transitions corresponding to the b, c, and a components of the dipole moment were identified. The spectrum was analyzed using numerical diagonalization of the effective rotational Hamiltonian for four interacting states of hindered pseudorotation. The rotational constants, centrifugal distortion constants, the constants of interaction between general rotation and hindered pseudorotation, and the distances between the quasidegenerate vibrational levels 01 = 64840.5, 12 = 122231.7 and 23 = 119732.7 MHz are determined. From the Stark effect of microwave transitions, the dipole moment components (in Debye units) in the hinderedpseudorotation states v = 0, 1, 2, and 3 are determined: 0|b|0 = 1|b|1 = 1.22, 2|b|2 = 1.20, 3|b|3 = 1.21, 0|c|1 = 0.77, 2|c3 = 0.66, and 1|a|2 = 0.19.  相似文献   

7.
The gas phase elimination of 3-bromobutyronitrile, examined in a static system and seasoned vessel, follows a first-order rate law. The reaction in the temperature range of 370.0–420.1°C and pressure range of 54–198 torr, is homogeneous and unimolecular. The temperature dependence of the rate coefficient is given by the equation: log k1 (s–1)=(13.74±0.25)–(213.7±3.2) kJ mol–1 (2.303RT)–1. The cyano substituent has been found to retard the elimination process through its electronwithdrawing resonance effect. Most of the dehydrobromination product is cis-trans-crotonitrile, while very little of allyl cyanide is obtained. This result is rationalized in terms of electronic factors.
3- , . . 370,0–420,1°C 54–198 . : log k1 (cek–1)=(13,74±0,25)–(213,7±3,2)(/)×(2,303 RT)–1. - . --, . .
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8.
The preparation of vanadium-phosphorus catalysts is described, showing the considerable influence of phosphorus on the concentration of V4+ ions. The oxidation properties were studied by chemical analysis and electron spin resonance. Moreover, ESR spectra show a strong influence of moisture on the structure of the catalysts.
- , V+4. , . , , .
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9.
The effect of cationic surfactants (cetyltrimethylammonium bromide, cetylpyridinium bromide, and tetrabutylammonium perchlorate) and a nonionic surfactant (OP-7) on the conditions of the immobilization of 4-(2-pyridylazo)resorcinol (PAR) on three types of silica gel (Silochrom S-120 (200–350 m), Silochrom S-120 (315–500 m), and Silochrom S-80 (200–350 m)) was studied. It was found that OP-7 does not affect the adsorption of surfactants. The effect of cationic surfactants increases in the order tetrabutylammonium perchlorate < cetyltrimethylammonium bromide < cetylpyridinium bromide. The adsorption activity of silica gels increases in the order Silochrom S-120 (315–500 m) < Silochrom S-80 (200–350 m) < Silochrom S-120 (200–350 m). Cetylpyridinium bromide provides full immobilization of PAR on silica gel Silochrom S-120 (200–350 m) in the pH range 2–9.  相似文献   

10.
In the presence of zeolites, dimethyl sulfide is produced either through CH3OH interaction with H2S or via CH3SH decomposition. In accordance with their activities, in both reactions, zeolites arrange in the same sequence: HZSMHNaY>NaXNaY. Realization of the reaction CH3OH+H2S is more difficult compared to methanethiol decomposition.
CH3OH H2S CH3SH. : HZSMHNaY>NaXNaY. CH3OH+H2S , .
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11.
Contact potential differences between electrodes of Pt, Au and Ta of different surface finishing were measured by the dynamic condenser method in propylene and oxygen. Propylene is irreversibly adsorbed, thus changing the work function. This renders the electrodes unsuitable as standard electrodes for work function measurements on catalysts in the atmosphere of hydrocarbons, but they may be used in adsorption studies on oxygen.
Pt, Au Ta . , , . , .
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12.
In current textbooks fugacity is introduced according to its differential or integral mathematical formulation. In this article an alternative method of explanation is offered. It is suggested that the real state of a pure gas can be described by comparing it to a hypothetical idealized state. The differences between these two states can then be expressed in terms of a function, , defined as (T,P) = real(T,P) - ideal(T,P) where real and ideal are the chemical potentials of the gas in its real and ideal states, respectively. The function is a molar excess quantity and is expressed as (T,P) = RT1n where is the fugacity coefficient. This approach introduces fugacity deductively through the function, which leads to , the fugacity coefficient. This method is also appropriate for introducing the activity of solution components and the fugacity of a real gas in gaseous mixtures.  相似文献   

13.
Zusammenfassung Es wird eine photometrische Bestimmungsmethode beschrieben für Anilin (40–720 g/ml), Monoäthylanilin (90–1650 g/ml) und Diäthylanilin (100–1600 g/ml) mit Natriumchlorit in äthanolisch-wäßrigen Lösungen, sowie für Diäthylanilin (85–1140 g/ml) und Dimethylanilin (30–330 g/ml) neben den primären und sekundären Aminen in essigsaurer Lösung mit demselben Reagens. Das Verfahren liefert gute Ergebnisse.
Summary A photometric procedure is described for the determination of aniline (40–720 g/ml), monoethylaniline (90–1650 g/ml), and diethylaniline (100–1600 g/ml) with sodium chlorite in aqueous ethanolic solutions and of diethylaniline (85–1140 g/ml) and dimethylamline (30 to 330 g/ml) in presence of the primary and secondary amines in acetic acid solution using the same reagent. Good results have been obtained,
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14.
A series of well characterized Pt–Ru bimetallic catalysts supported on graphite has been studied by means of the electroreduction of oxygen in a supporting electrolyte of 1 N H2SO4. A synergetic effect is observed when the activity per gram of catalyst is considered. However, this effect disappears when the activity values are corrected by the active surface area.
Pt–Ru, , 1N H2SO4. 1- , . , , .
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15.
The absolute concentrations of iodine, bromine and chlorine in milk, have been determined by epithermal neutron activation followed by high resolution gamma-ray spectrometry. Two kinds of milk commonly consumed in Israel have been investigated. The concentration of iodine, bromine and chlorine were found to be 0.18–0.30 g/ml, 2.02–2.85 g/ml and 0.65 mg/ml, respectively. The method is fast, selective, accurate and highly sensitive.  相似文献   

16.
During the reactions of 8 isomeric alicyclic diols on Cu/Al and Cu catalysts, epimerization of the isomers was observed. The epimerization proceeds via a hydroxy-oxo intermediate.
8 Cu/Al Cu . -.


Part XLII of the series Study of the transformations of diols and cyclic ethers.  相似文献   

17.
With the help of the transient response method and fluorescence spectroscopy, it has been revealed that the title reaction proceeds by the catalyst redox transformation Ce(III)Ce(IV) over CeO2 in great contrast to previous observations over MgO. , Ce(III)Ce(IV) CeO2 MgO.  相似文献   

18.
Through simulation of the temperature-programmed desorption, reaction and reduction in a system of parallel reactions. it is shown that the experimental conditions influence the simultaneous or consecutive occurrence of the individual reactions of the system. Adjustment of the concentration of a gaseous reaction component or optimization of the temperature program results in a shift to the desired consecutive occurrence of the reactions. Therefore, a better resolution of the individual reactions can be achieved through a judicious choice of the experimental conditions of the temperature-programmed methods.
Zusammenfassung Durch Simulierung temperaturprogrammierter Desqrption, Reaktion und Reduzierung in einem System von Parallelreaktionen konnte gezeigt werden, daß die experimentellen Bedingungen die Simultanität bzw. Konsekutivität der Einzelreaktionen des Systems beeinflussen. Durch eine Einstellung der Konzentration der gasförmigen Reaktionsprodukte oder durch Optimalisierung des Temperaturprogrammes kann eine gewünschte Folge der Einzelreaktionen erreicht werden. Somit kann durch eine geschickte Wahl der experimentellen Bedingungen bei temperaturprogrammierten Verfahren eine bessere Separierung der Einzelreaktionen erreicht werden.

- , , , . . , - .

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19.
    
A, , . -- . - - .
The molecular sieve selectivity of cationic and decationized type A zeolite, erionite and mordenite has been investigated in cracking and hydrocracking reactions. The selectivity of sodalite catalysts conforms with, whereas that of erionite catalysts is in contrast to the correspondig activity. The substrate reactivity influences the selectivity in a variety of ways.
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20.
Isotope dilution mass spectrometry using enriched isotope96Ru as a spike was applied to the determination of ruthenium as a fission product. Ruthenium in the solution was oxidized to RuO4 by Ce/IV/ and separated from coexisting metal elements by distillation. Silica-gel technique was employed to enhance ion current of ruthenium in the mass spectrometric measurement. The lower detection limit was 0.005 g ml–1 and the relative standard deviations /n=3/ for 1.2 and 0.05 g ml–1 of ruthenium were 0.2 and 0.5%, respectively.  相似文献   

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