Electrocatalytic selective oxidation of ethylene glycol: a concise review of catalyst development and reaction mechanism with comparison to thermocatalytic oxidation process

Author(s):  
Ji Qi ◽  
Ziying An ◽  
Chuang Li ◽  
Xiao Chen ◽  
Wenzhen Li ◽  
...  
2018 ◽  
Vol 346 ◽  
pp. 238-248 ◽  
Author(s):  
Lijuan Shen ◽  
Xiaohai Zheng ◽  
Ganchang Lei ◽  
Xiang Li ◽  
Yanning Cao ◽  
...  

1990 ◽  
Vol 6 (4) ◽  
pp. 399-407 ◽  
Author(s):  
Graham J. Hutchings ◽  
Michael S. Scurrell ◽  
Jeremy R. Woodhouse

2020 ◽  
Vol 44 (4) ◽  
pp. 1632-1639 ◽  
Author(s):  
Qi Zhao ◽  
Bing Liu ◽  
Yuebing Xu ◽  
Feng Jiang ◽  
Xiaohao Liu

Five-coordinated Rh leads to the over-oxidation of CH4, while four-coordinated Rh stabilizes CH3 and facilitates methanol formation via the CH3OOH intermediate.


1997 ◽  
Vol 153 (1-2) ◽  
pp. 217-231 ◽  
Author(s):  
U. Rodemerck ◽  
B. Kubias ◽  
H.-W. Zanthoff ◽  
G.-U. Wolf ◽  
M. Baerns

1993 ◽  
Vol 58 (3) ◽  
pp. 538-546 ◽  
Author(s):  
Refat M. Hassan ◽  
Sahr A. El-Gaiar ◽  
Abd El-Hady M. El-Summan

The kinetics of permanganate oxidation of selenium dioxide in perchloric acid solutions at a constant ionic strength of 2.0 mol dm-3 has been investigated spectrophotometrically. A first-order reaction in [MnO4-] and fractional order with respect to selenium(IV) were observed. The reaction rate was found to be pH-independent at lower acid concentrations ([H+] < 0.5 mol dm-3) and was acid-catalyzed beyond this range. Addition of Mn2+ and F- ions leads to the prediction that MnO4- is the sole reactive species in the oxidation process. A tentative reaction mechanism consistent with the reaction kinetics has been proposed.


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