Catalytic properties of nickel oxide and its solid solutions in magnesium oxide in hydrogen oxidation

1980 ◽  
Vol 15 (1) ◽  
pp. 73-78 ◽  
Author(s):  
O. I. Goncharova ◽  
T. M. Yurieva
1966 ◽  
Vol 5 (2) ◽  
pp. 271-278 ◽  
Author(s):  
A CIMINO ◽  
R BOSCO ◽  
V INDOVINA ◽  
M SCHIAVELLO

1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka

The catalytic properties of two-component catalyst nickel oxide-cadmium oxide with the proportions of the components covering the whole composition region 0-100% were examined by studying the decomposition of hydrogen peroxide in aqueous solution on it. In the range 0-25 mol.% CdO, cadmium oxide is found to affect infavourably the ability of nickel oxide to chemisorb oxygen. The amount of the chemisorbed oxygen increases several times on gamma irradiation of the samples. The effect of cadmium oxide on the catalytic activity of the system shows up in fresh samples only indirectly via the changed amount of the oxygen chemisorbed. In older samples the initial catalytic activity of the system is changed, which can be explained based on the concept of bivalent catalytic centres in terms of the co-action of the catalytic centres of the two oxides, which are in equilibrium. The irradiation of the system under study speeds up the processes leading to the establishing of this equilibrium which is thermally very stable, and results in a substantial increase of the catalytic activity of the samples investigated.


1984 ◽  
Vol 49 (1) ◽  
pp. 14-24 ◽  
Author(s):  
Viliam Múčka

Some physical and catalytic properties of cerium dioxide-nickel oxide two-component catalysts have been studied over the entire composition region, employing the decomposition of hydrogen peroxide in aqueous solution as a model catalytic process. The two oxides have been found to affect each other, particularly for NiO contents of 9.1 and 96.7 mol%; the mutual influencing, the nature of which in the conditions applied remains unaffected by heat treatment of the sample or by its exposition to ionizing radiation, is manifested by the nonmonotonic dependences of the oxidation power and of the specific activity of the catalysts on their composition. This can be interpreted in terms of the concept of bivalent catalytic centres, assuming that for nickel oxide the centres consist of Ni2+-Ni3+ ion pairs, for cerium dioxide they consist of Ce3+-Ce4+ ion pairs, and that in the region of the mutual influencing , Ni2+-Ce4+ ion pairs play a major role. Within the scope of this concept, the increase in the oxidation power of all the catalysts in question and a simultaneously decrease in the specific activity of the pure nickeloxide exposed to ionizing radiation can be explained in terms of the ionization effect.


2011 ◽  
Vol 130 (1-2) ◽  
pp. 387-391 ◽  
Author(s):  
Gaoqing Yuan ◽  
Junhua Zheng ◽  
Chang Lin ◽  
Xiaoying Chang ◽  
Huanfeng Jiang

Author(s):  
Jin-Tao Ren ◽  
Zhong-Yong Yuan

In situ-formed nickel/nickel oxide heterostructures coupled with N-doped graphitic carbon significantly promote the hydrogen oxidation and oxygen reduction reactions in alkaline water.


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