Carbon oxidation reactions could misguide the evaluation of carbon black-based oxygen-evolution electrocatalysts

2017 ◽  
Vol 53 (84) ◽  
pp. 11556-11559 ◽  
Author(s):  
Wang Wang ◽  
Jin Luo ◽  
Shengli Chen

Carbon may suffer severe oxidation during OER, leading to overestimation of the activity of carbon-black based electrocatalysts towards OER.

2021 ◽  
Vol 316 ◽  
pp. 105-109
Author(s):  
Evgeny A. Kirichenko ◽  
Pavel G. Chigrin ◽  
Anton A. Gnidenko

YFeO3-δ (δ = 0.26) and LaFeO3-δ (δ = 0.5) perovskites with a high specific surface and oxygen non-stoichiometry was firstly synthesized by pyrolysis of polymer-salt compositions. It was shown that the catalytic oxidation of carbon in the presence of these complex oxide systems proceeds in the range of 400 - 700 °С, with a maximum temperature at 556 °С for YFeO3-δ; and 380 - 620 °С ,with a maximum temperature at 501 °С for LaFeO3-δ, in one-stage mode for both. By means of thermal analysis and diffractometry, it was shown that there is no contribution to the soot oxidation mechanism by cyclic perovskite surface transformations, due to the reduction of metal oxides by the soot and their subsequent reoxidation. It has been established that the basis of the catalytic reaction mechanism for both perovskites is the presence of oxygen vacancies on the surface of complex oxides.


2021 ◽  
Author(s):  
Hua Zhou ◽  
Zhenhua Li ◽  
Lina Ma ◽  
Haohong Duan

Oxidation reactions provide a wide range of important chemicals in industry; however, most of them are produced from fossil feedstocks. As a candidate of oxygen evolution reaction (OER), the electrooxidation...


2018 ◽  
Vol 2 (9) ◽  
pp. 1905-1927 ◽  
Author(s):  
Lacey M. Reid ◽  
Tengfei Li ◽  
Yang Cao ◽  
Curtis P. Berlinguette

Organic oxidation reactions can replace the anodic oxygen evolution of water splitting for clean hydrogen generation paired with high-value product.


2020 ◽  
Vol 159 ◽  
pp. 112203 ◽  
Author(s):  
Raouia Attaallah ◽  
Amina Antonacci ◽  
Vincenzo Mazzaracchio ◽  
Danila Moscone ◽  
Giuseppe Palleschi ◽  
...  

1954 ◽  
Vol 27 (3) ◽  
pp. 695-704
Author(s):  
F. Lyon ◽  
K. A. Burgess ◽  
C. W. Sweitzer

Abstract The effect of carbon black on the autocatalytic stage of oxidation of unvulcanized rubber is shown to be specific for the type of carbon, the reaction conditions, and the polymer. Carbon black is an effective antioxidant for cold rubber when the rubber is heated in air or oxygen. The effectiveness of carbon in inhibiting oxidation increases as the volatile content of the carbon increases. The special case of low loadings of highly oxidized carbons, which completely repress gelation during Banbury mixing, is of particular interest. The opposite behavior of carbon black during rubber gelation is observed when benzoyl peroxide is used as catalyst. With cold rubber, carbon black promotes gelation, while with natural rubber increased scission results. Alteration of any one of these variables produces profound changes in the course and extent of the oxidation reactions.


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