The Effect of Additionally Introduced Impurities of Fe and Pb Ions on Silver Azide Decomposition

2017 ◽  
Vol 736 ◽  
pp. 101-104
Author(s):  
A.P. Rodzevich ◽  
L.V. Kuzmina ◽  
E.G. Gazenauer ◽  
V.I. Krasheninin ◽  
D.Yu. Sozinov ◽  
...  

The experiments have emphasized that additionally introduced impurities of Fe and Pb ions are relevant to the initiation of slow and explosive decomposition of silver azide crystals by the external electric field and UV irradiation. External gas release was used for research purpose. Test-sensitivity is 10−12 mole. Time-to-explosion was measured by a stop watch. It’s been found out that the reaction of slow decomposition in silver azide under the action of electric field turns into explosion faster in samples with the additionally introduced impurities. The samples with additionally introduced Fe are the most explosive ones (time-to-explosion 3 minutes). The authors have assumed that external influence can generate non-equilibrium charge carriers (holes), which become localized on cationic vacancies and support formation of reactive sites. As soon as cut off concentration of these sites is reached, the solid-phase chain reaction turns into explosion. The growing concentration of impurity influences on the number of reactive sites, making their concentration critical. In view of the results obtained in experiments a procedure for monitoring the decomposition of crystals is suggested, which necessitates additional introduction of Fe and Pb ions.

Author(s):  
Xiaogang Liu ◽  
Wenjie Chen ◽  
Wei Wang ◽  
Zhengbo Jiao

The local polarization electric field resulting from protonation and Fe-doping in g-C3N4 can be formed, thus highly facilitating the separation and transport of charge carriers and boosting the photocatalytic activity.


2019 ◽  
Vol 6 (2) ◽  
pp. 111-114
Author(s):  
R. Kornev ◽  
P. Sennikov ◽  
V. Nazarov ◽  
A. Kut'in ◽  
A. Plekhovich

A contracted RF (40.68 MHz) arc discharge of atmospheric pressure, stabilized between two rod electrodes, was used to obtain trichlorosilane by the reaction of hydrogen reduction of silicon tetrachloride (SiCl<sub>4</sub>). In model mixtures of macro-composition in the ratio H<sub>2</sub>/SiCl<sub>4</sub>/CCl<sub>4</sub>=10/1/1, it was shown that C and SiC are the main solid-phase product which are deposited on the surface of electrodes in the form of dendrides. The temperature of the ends of the electrodes determined using emission thermometry is 1600 K. The thermodynamic analysis of H<sub>2</sub>+SiCl<sub>4</sub>+CCl<sub>4</sub> system confirms that the formation of C and SiC occurs in the temperature range of 1600 K. The deposition of solid-phase products occurs on the electrodes in the zone of high electric field strength.


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